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WHAT'S NEW THIS WEEKEND: CDC MALARIA POSITIONS, PREDICTORS OF CHILD SURVIVAL, SIMPLIFIED ARV DELIVERY MODELS, USE OF LAY PERSONNEL FOR ROUTINE IMMUNIZATION

Friday, 12th of August 2011 Print

 ·        

  • WHAT’S NEW THIS WEEKEND: FUTURE TRENDS IN LEPROSY, CHINA AND INDIA AS MEDICAL SUPPLIERS, REVISED RECS ON RUBELLA VACCINATION, TB VACCINE RESEARCH, POLIO OUTBREAK IN POINTE-NOIRE, CONGO
  • FUTURE TRENDS IN LEPROSY

The strategy will not immediately reduce the prevalence of G2D, but if it is applied consistently over the next 25 years, its long-term effect can be substantial.’ 

Best viewed at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127268/?tool=pubmed

Potential effect of the World Health Organization’s 2011–2015 global leprosy strategy on the prevalence of grade 2 disability: a trend analysis

 

  • CHINA AND INDIA AS MEDICAL SUPPLIERS

China and India as Suppliers of Affordable Medicines to Developing Countries

Abstract and full text .pdf are at http://papers.nber.org/papers/w17249



Tamara Hafner, David Popp

National Bureau of Economic Research Working Paper No. 17249, issued in July 2011

As countries reform their patent laws to be in compliance with the Trade Related Intellectual Property Rights Agreement, an important question is how increased patent protection will affect drug prices in low-income countries. Using pharmaceutical trade data from 1996 to 2005, we examine the role of China and India as suppliers of medicines to other middle- and low-income countries and evaluate the competitive effect of medicine imports from these countries on the price of medicines from high- income countries. We find that imports of antibiotics and unspecified medicaments from India and China significantly depress the average price of these commodities imported from high-income trading partners, suggesting that India and China are not only important sources of inexpensive medicines but also have an indirect effect by lowering prices through competition. As India is the leading supplier of medicines in Sub-Saharan Africa, this region will likely be affected most adversely.

 

  • WHO REVISED RECOMMENDATIONS ON RUBELLA VACCINATION

 ‘WHO recommends that countries take the opportunity offered by accelerated measles control and elimination activities to introduce rubella containing vaccines.’

Full text, with figures, is at http://www.who.int/wer/2011/wer8629.pdf

Since 1996, when only 83 WHO Member States used RCVs in their national immunization schedules, there has been a steady increase in the number of countries introducing vaccination against rubella, which is delivered in most countries as MMR during the second year of life. The level of introduction varies by WHO region, however: as of December 2009, a total of 130 of 193 Member States used RCVs in national immunization schedules, including 2 (4%) of 46 Member States in the African Region, 35 (100%) in Region of the Americas, 15 (71%) of 21 in the Eastern Mediterranean Region, 53 (100%) in the European Region, 4 (36%) of 11 in the South-East Asia Region, and 21 (78%) of 27 in the Western Pacific Region.51 Of the remaining 63 countries that have not yet introduced the vaccine, all are providing 2 doses of measles vaccine through a combination of routine immunization and supplementary immunization activities (SIAs) as part of accelerated efforts to reduce measles mortality or regional elimination efforts.

The Region of the Americas and the European Region have established goals to eliminate rubella by 2010 and 2015, respectively; the Western Pacific Region has established an accelerated rubella and CRS prevention goal (<1 case per 100 000 live births); the Eastern Mediterranean Region has established a goal of CRS prevention without a target date for countries that have introduced national rubella vaccination programmes; the African Region and the South-East Asia Region have not established goals for rubella control or elimination. The African and South-East Asia regions have the highest estimated number of CRS cases and are also the regions with the lowest uptake of vaccine. However, in some countries within these regions high birth rates or high rubella transmission rates, or both, will result in a lower average age of infection that will likely result in a lower incidence of CRS.10

WHO position on rubella vaccines

In light of the remaining global burden of CRS and proven efficacy and safety of RCVs, WHO recommends that countries take the opportunity offered by accelerated measles control and elimination activities to introduce RCVs. These measles vaccine delivery strategies provide an opportunity for synergy and a platform for advancing rubella and CRS elimination.

All countries that have not yet introduced rubella vaccine, and are providing 2 doses of measles vaccine using routine immunization or SIAs, or both, should consider including RCVs in their immunization programme.

There are 2 general approaches to the use of rubella vaccine. One approach focuses exclusively on reducing CRS by immunizing adolescent girls or women of childbearing age, or both, to provide individual protection.

The second approach is more comprehensive, focusing on interrupting rubella virus transmission and thereby eliminating rubella as well as CRS. To ensure the success of this approach, rubella vaccination should be integrated with measles-vaccine delivery strategies through the use of MR or MMR vaccines.

Countries planning to introduce RCVs should review the epidemiology of rubella, including the susceptibility profile of the population; assess the burden of CRS; and

establish rubella and CRS prevention as a public health priority. Cost–benefit studies are not needed in every country before rubella vaccination is implemented; results from studies in countries with similar sociodemographic circumstances can be informative. Depending on the burden of CRS and available resources, countries should define their goal and the time frame for achieving it (Table 1).

Introducing rubella vaccine into childhood immunization programmes implies a long-term commitment to achieving and maintaining sufficient immunization coverage to ensure a sustained reduction in the incidence of CRS and ultimately the elimination of rubella and CRS. Strong political commitment to the elimination of rubella and CRS, and sustainable financing for vaccination and surveillance activities, should be in place before introducing rubella vaccination into the childhood immunization programme.

For countries undertaking the strategy of CRS reduction alone, adolescent and adult females should be vaccinated through either routine services or SIAs. This option will provide direct protection to women of childbearing age; however, the impact of this strategy is limited by the coverage achieved and the age groups targeted. In the absence of a programme that vaccinates infants and young children, rubella will continue to circulate, resulting in ongoing exposure of pregnant women and the associated risk of CRS.

For countries undertaking the elimination of rubella and CRS, the preferred approach is to begin with MR vaccine or MMR vaccine in a campaign targeting a wide range of ages that is followed immediately by the introduction of MR or MMR vaccine into the routine programme. The first dose of an RCV can be delivered at 9 months or 12 months, depending on the level of measles virus transmission.23 All subsequent follow-up campaigns should use MR vaccine or MMR vaccine. In addition, countries should make efforts to reach women of childbearing age by immunizing adolescent girls or women of childbearing age, or both, either through routine services or mass campaigns.

Sustained low coverage of rubella immunization in infants and young children (for example, when rubella vaccine is used only in the private sector) can result in an increase in susceptibility among women of childbearing age that may increase the risk of CRS above levels prior to the vaccine being introduced (known as a paradoxical effect). However, if vaccination coverage is sufficiently high, rubella transmission will be markedly reduced or interrupted, thereby removing the risk of rubella exposure for pregnant women.

 

 

  • TB VACCINE RESEARCH

‘The increased research activities into tuberculosis vaccines are the result of increased public and private funding. Within the past decade, funding has at least quadrupled, reaching more than half a billion US dollars for tuberculosis research.31—33 Of this funding, roughly a fifth is devoted to vaccine research and nearly a third to basic research. This effort is highly commendable, but insufficient. Estimates suggest that about four-times this amount of financial support is needed to reach the goal of production of improved vaccines within the next decade.10, 15, 32

Best viewed at

http://www.thelancet.com/journals/laninf/article/PIIS1473-3099(11)70146-3/fulltext

Fact and fiction in tuberculosis vaccine research: 10 years later

Original Text

Dr Stefan HE Kaufmann PhD a

Summary

Tuberculosis is one of the most deadly infectious diseases. The situation is worsening because of co-infection with HIV and increased occurrence of drug resistance. Although the BCG vaccine has been in use for 90 years, protection is insufficient; new vaccine candidates are therefore needed. 12 potential vaccines have gone into clinical trials. Ten are aimed at prevention of tuberculosis and, of these, seven are subunit vaccines either as adjuvanted or viral-vectored antigens. These vaccines would be boosters of BCG-prime vaccination. Three vaccines are recombinant BCG constructs—possible replacements for BCG. Additional vaccine candidates will enter clinical trials in the near future, including postexposure vaccines for individuals with latent infection. In the long term, vaccines that prevent or eradicate infection with Mycobacterium tuberculosis would be the best possible option. Improved knowledge of immunology, molecular microbiology, cell biology, biomics, and biotechnology has paved the way towards an effective and safe vaccine against tuberculosis. The pipeline of new vaccine candidates from preclinical to clinical testing could be accelerated by development of biomarkers that can predict the clinical outcome of tuberculosis.

 

  • POLIO OUTBREAK, POINTE-NOIRE, CONGO, 2010-2011

Best viewed at http://www.cdc.gov/eid/content/17/8/110195.htm

Volume 17, Number 8–August 2011

Dispatch

Poliomyelitis Outbreak, Pointe-Noire, Republic of the Congo, September 2010–February 2011

Arnaud Le Menach, Augusto E. Llosa, Isabelle Mouniaman-Nara, Felix Kouassi, Joseph Ngala, Naomi Boxall, Klaudia Porten, and Rebecca F. Grais
Author affiliations: Health Protection Agency, London, UK (A. Le Menach, N. Boxall); European Centre for Disease Control and Prevention, Stockholm, Sweden (A. Le Menach); Epicentre, Paris, France (A.E. Llosa, K. Porten, R. F. Grais); Médecins Sans Frontières, Paris (I. Mouniaman-Nara, F. Kouassi); Médecins Sans Frontières, Brazzaville, Republic of the Congo (I. Mouniaman-Nara, F. Kouassi); and Ministry of Health, Pointe-Noire, Republic of the Congo (J. Ngala)

Suggested citation for this article

Abstract
On November 4, 2010, the Republic of the Congo declared a poliomyelitis outbreak. A cross-sectional survey in Pointe-Noire showed poor sanitary conditions and low vaccination coverage (55.5%), particularly among young adults. Supplementary vaccination should focus on older age groups in countries with evidence of immunity gaps.

On November 4, 2010, the Ministry of Health of the Republic of the Congo officially declared a poliomyelitis outbreak centered in Pointe-Noire following the laboratory identification of poliovirus type 1 in a patient with acute flaccid paralysis (AFP) (1,2). A provisional total of 554 AFP case-patients that included a high proportion (68%) of male patients was identified nationally, with paralysis onset from September 20, 2010, through February 27, 2011 (3). During this same period, 451 cases (81.4%), which included 184 deaths, were reported in Pointe-Noire. Most cases were found in the young adult population (57.4% in patients 15–24 years of age), which had a higher case-fatality ratio (CFR) of 40.8% compared with the general population of the country (3).

In most developing countries, prevention and control of poliomyelitis relies on oral polio vaccine (OPV). Routine vaccination focuses on infants <11 months of age with trivalent OPV, and supplementary immunization activities (SIAs) provide additional opportunities for vaccination for children <5 years of age (4,5). In response to the epidemic, the Ministry of Health, in collaboration with the World Health Organization, launched 4 rounds of national SIAs that used monovalent type 1 and bivalent types 1 and 3 OPV during November 12–16, 2010, December 3–7, 2010, January 11–15, 2011, and February 22–26, 2011 (3). To assess risk factors for infection and estimate vaccination coverage, Epicentre and Médecins Sans Frontières implemented a cross-sectional survey in 1 affected neighborhood of Pointe-Noire.

The Study

Figure 1

 

Figure 1. Pointe-Noire, Republic of the Congo, representing the 4 districts, Lumuba, MvouMvou, Tie-Tie, and Loandjili...

 

Figure 2

 

Figure 2. Routine vaccination coverage and acute flaccid paralysis (AFP) rate by birth cohort...

This survey was a single-community rapid assessment of epidemiologic conditions potentially contributing to the outbreak, including vaccination coverage. The survey was done in Mbota, a neighborhood composed of 4 sectors, comprising 9.5% of the city population. This neighborhood was selected from Loandjili district (Figure 1) on the basis of local expert consultation to ensure socioeconomic diversity and representativeness. To estimate vaccination coverage of 80% among children with 5% precision at a 95% confidence level, we aimed to sample at least 246 households. We assumed each household had on average 1 child <5 years of age. We also assumed 5 persons per household on average, which corresponds to ≈1,230 persons overall. Households were selected in each sector of the neighborhood. From a starting point on the border of the sector, interviews focused on every fifth household, following a predefined direction toward the center of the sector, subsequently covering the entire neighborhood. Data were collected through face-to-face interviews December 9–10, 2010, by using a structured questionnaire. The questions included household demographics, water supply, and sanitary conditions. In addition, information for each person in the household was collected about vaccination history (routine and SIAs), any previous illness, and access to health care during the past 3 months. Vaccination coverage was estimated on the basis of reported personal history or documentary evidence of vaccination: a fingernail marked with ink indicating vaccination during SIAs or a vaccination card indicating routine vaccination.

Data were eventually collected from 1,849 persons in 317 households of Mbota with all ages and both genders represented. Following the 2 first rounds of SIAs, most surveyed persons (1,812 [98%], 95% confidence interval [CI] 97.3%–98.6%) reported having been vaccinated with monovalent OPV and 1,769 (95.7%, 95% CI 94.7%–96.6%) received 2 doses in November and December 2010. Among vaccinated persons, 627 (33.9%, 95% CI 31.7%–36.1%) had fingernails marked with ink; the rest were absent during the interview or ink had already worn off. There were no significant differences in SIA vaccine coverage by gender or age. Routine vaccination coverage was estimated as 55.5% (95% CI 53.3%–57.8%) among the surveyed persons (Table 1). Among reported vaccinated persons, 21.3% (95% CI 18.8%–23.8%) showed their vaccination card, and among those, 78.7% (95% CI 73.1%–84.4%) were vaccinated >3 times. Routine vaccination coverage did not vary significantly by gender but decreased with age (p <0.0001). For persons younger than 5 years, it was 87.5% (95% CI 83.6%–91.4%) and <52% for anyone >15 years of age. In the most affected age groups, 15–19 and 20–24 years, vaccination coverage was estimated to be respectively 49.3% (95% CI 42.4%–56.1%) and 46.2% (95% CI 39.3%–53.1%) (Figure 2). By comparison, administrative vaccination coverage varied since 1986 between a reported 21% in 1997 and 112% in 2009 (Table 2).

The number of persons per bedroom, an indicator of crowding, ranged between 1 and 9, and there were >4 persons per bedroom for 12.1% (95% CI 8.4%–15.7%) of all households with no statistical differences among sectors. Tap water either from a neighbor's house (41.9%, 95% CI 35.9%–47.8%) or within the house (30.7%, 95% CI 25.2%–36.3%) was the primary potable water source recorded. Wells were also common (23.3%, 95% CI 18.3%–28.4%). When the primary source of potable water was unavailable, wells were the most frequently mentioned alternative source (37.8%, 95% CI 32.0%–43.6%). Most households reported use of a latrine shared with neighbors (57.4%, 95% CI 51.8%–63.1%) or within their house (31.4%, 95% CI 26.1%–36.7%). Few surveyed persons (16.1%, 95% CI 14.4%–17.7%) reported illness during the recall period, but if sick, 73.3% (95% CI 67.4%–79.2%) they sought health care, which suggests little underreporting of AFP cases.

Conclusions

The cross-sectional survey confirmed administrative estimates of low routine vaccination decreasing with age. Specifically, in the surveyed young adult population (15–29 years of age) it varied between a reported 46.2% and 52.6%. According to administrative data, the reported vaccination coverage varies between 41.7% and 79% in young adults between 15 and 24 years of age. Civil conflicts spanning the 1990s have potentially undermined vaccination efforts, especially affecting those currently 10–20 years of age. A further method of protection for a person is past exposure to wildtype strains. To our knowledge, no polio transmission had been reported in Pointe-Noire since the last outbreak in the city in 1969 (6). Low vaccination coverage and no previous exposure to wild virus likely led to an accumulation of susceptible persons. Once introduced, the disease spread quickly through this highly susceptible, undervaccinated, and underexposed young adult population, with disease spread facilitated by frequent flooding and poor to medium household sanitation conditions, i.e., crowding sleeping areas, shared latrines between households, and common sources for water consumption.

Poliovirus infections lead to clinical disease more frequently in older age groups, (7), which partially explains the observed shift of AFP cases toward young adult populations. Moreover, children were better protected with higher vaccination coverage. Death is more frequent when infection occurs in older age groups (8,9), which explains part of the high observed CFR. Clinical manifestations of poliovirus infections are more common in boys and men than in girls and women (10), as observed, and even though males and females share similar vaccination coverage, women in the young adult age groups may have additionally benefitted from exposure to excreted OPV while caring for the young (11).

As seen in the Republic of the Congo, or previously in Namibia (12), Cape-Verde (13), any country with no recent wild-type polio transmission and a similarly low level of vaccination coverage may face similar outbreaks characterized by a large proportion of cases in older age groups and a high CFR (14). Avoiding outbreaks will rely on ensuring vaccination of the at-risk population. Routine vaccination activities should be reinforced by SIAs punctually focusing on older age groups (especially among persons 15–35 years of age) when evidence of immunity gaps are documented by serologic surveys or low historical vaccination coverage data. Lessons from the epidemic should benefit health authorities in better prevention and response to further outbreaks on the road to eradication.

Acknowledgments

We thank the Ministry of Health for support and collaboration, the hospital directors and laboratory director in Pointe-Noire, and colleagues from World Health Organization and the Centers for Disease Control and Prevention for the harmonization of the database and stimulating technical discussions.

Dr Le Menach is an epidemiologist specialized in infectious diseases modeling, surveillance, prevention, and control. He works at London Regional Epidemiology Unit of the Health Protection Agency, as part of the European program for intervention epidemiology (EPIET).

References

  1. Grard G, Drexler JF, Lekana-Douki S, Caron M, Lukashev A, Nkoghe D, et al. Type 1 wild poliovirus and putative enterovirus 109 in an outbreak of acute flaccid paralysis in Congo, October–November 2010. Euro Surveill. 2010;15:pii:19723.
  2. Roberts L. Infectious disease. Polio outbreak breaks the rules. Science. 2010;330:1730–1. PubMed DOI
  3. Centers for Disease Control and Prevention. Poliomyelitis outbreak—Republic of the Congo, September 2010–February 2011. MMWR Morb Mortal Wkly Rep. 2011;60:312–3.
  4. Global Polio Eradication Initiative. Strategy. 2010 [cited 2010 Nov 22]. http://www.polioeradication.org/Aboutus/Strategy.aspx
  5. World Health Organization. Immunization surveillance, assessment and monitoring. 2011 [cited 2011 Jan 12]. http://www.who.int/immunization_monitoring/en/
  6. Heraut L, Rousseau E, Aubry P. Poliomyelitis epidemic at Pointe-Noire [in French]. Med Trop (Mars). 1969;29:362–4.
  7. Gawne AC, Halstead LS. Post-polio syndrome: pathophysiology and clinical management. Crit Rev Phys Rehabil Med. 1995;7:147–88.
  8. Weinstein L. Influence of age and sex on susceptibility and clinical manifestations in poliomyelitis. N Engl J Med. 1957;257:47–52. PubMed DOI
  9. Weinstein L, Shelokov A, Seltser R, Winchell GD. A comparison of the clinical features of poliomyelitis in adults and in children. N Engl J Med. 1952;246:297–302. PubMed DOI
  10. Froeschle JE, Feorino PM, Gelfand HM. A continuing surveillance of enterovirus infection in healthy children in six United States cities. II. Surveillance enterovirus isolates 1960–1963 and comparison with enterovirus isolates from cases of acute central nervous system disease. Am J Epidemiol. 1966;83:455–69.
  11. Alexander JP Jr, Gary HE Jr, Pallansch MA. Duration of poliovirus excretion and its implications for acute flaccid paralysis surveillance: a review of the literature. J Infect Dis. 1997;175(Suppl 1):S176–82. PubMed DOI
  12. Sidley P. Seven die in polio outbreak in Namibia. BMJ. 2006;332:1408. PubMed DOI
  13. Outbreak of poliomyelitis, Cape Verde. Wkly Epidemiol Rec. 2000;75:401.
  14. Nathanson N, Kew OM. From emergence to eradication: the epidemiology of poliomyelitis deconstructed. Am J Epidemiol. 2010;172:1213–29. PubMed DOI

Figures

Figure 1. Pointe-Noire, Republic of the Congo, representing the 4 districts, Lumuba, MvouMvou, Tie-Tie, and Loandjili...
Figure 2. Routine vaccination coverage and acute flaccid paralysis (AFP) rate by birth cohort...

Tables

Table 1. Persons vaccinated against poliomyelitis (routine vaccination), by age and gender, Mbota, Pointe-Noire, Republic of the Congo, December 2010
Table 2. Cumulative age-specific AFP rate and vaccination coverage from administrative data and a cross-sectional survey conducted in December 2010, by age group, Mbota, Pointe-Noire, Republic of the Congo

Suggested Citation for this Article

Le Menach A, Llosa AE, Mouniaman-Nara I, Kouassi F, Ngala J, Boxall N, et al. Poliomyelitis outbreak, Pointe-Noire, Republic of the Congo, September 2010–February 2011. Emerg Infect Dis [serial on the Internet]. 2011 Aug [date cited]. http://www.cdc.gov/EID/content/17/8/110195.htm

 

 

 


  • POTPOURRI THIS WEEK: TWO ON MALARIA IN AFRICA, ONE ON CHINA’S ONE CHILD POLICY; TWO JOBS, 1 CALL FOR FIELD EPIDEMIOLOGY PAPERS, AFRICA

‘Along with other key child survival interventions, increased ITNs/IRS coverage has significantly contributed to child mortality reduction since 2002. ITN/IRS scale-up can be more efficiently prioritized to countries where malaria is a major cause of child deaths to save greater number of lives with available resources.’

  • ·         EFFECT OF INVESTMENT IN MALARIA CONTROL ON CHILD MORTALITY IN SUB-SAHARAN AFRICA IN 2002–2008 

Full text, with figures, is at http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0021309

 

Around 8.8 million children under-five die each year, mostly due to infectious diseases, including malaria that accounts for 16% of deaths in Africa, but the impact of international financing of malaria control on under-five mortality in sub-Saharan Africa has not been examined.

We combined multiple data sources and used panel data regression analysis to study the relationship among investment, service delivery/intervention coverage, and impact on child health by observing changes in 34 sub-Saharan African countries over 2002–2008. We used Lives Saved Tool to estimate the number of lives saved from coverage increase of insecticide-treated nets (ITNs)/indoor residual spraying (IRS). As an indicator of outcome, we also used under-five mortality rate. Global Fund investments comprised more than 70% of the Official Development Assistance (ODA) for malaria control in 34 countries. Each $1 million ODA for malaria enabled distribution of 50,478 ITNs [95%CI: 37,774–63,182] in the disbursement year. 1,000 additional ITNs distributed saved 0.625 lives [95%CI: 0.369–0.881]. Cumulatively Global Fund investments that increased ITN/IRS coverage in 2002–2008 prevented an estimated 240,000 deaths. Countries with higher malaria burden received less ODA disbursement per person-at-risk compared to lower-burden countries ($3.90 vs. $7.05). Increased ITN/IRS coverage in high-burden countries led to 3,575 lives saved per 1 million children, as compared with 914 lives in lower-burden countries. Impact of ITN/IRS coverage on under-five mortality was significant among major child health interventions such as immunisation showing that 10% increase in households with ITN/IRS would reduce 1.5 [95%CI: 0.3–2.8] child deaths per 1000 live births.

Abstract

Yoko Akachi1, Rifat Atun1,2*

1 Strategy, Performance and Evaluation Cluster, The Global Fund to Fight AIDS, Tuberculosis and Malaria, Geneva, Switzerland, 2 Imperial College Business School, Imperial College, London, United Kingdom

Abstract 

Background

Around 8.8 million children under-five die each year, mostly due to infectious diseases, including malaria that accounts for 16% of deaths in Africa, but the impact of international financing of malaria control on under-five mortality in sub-Saharan Africa has not been examined.

Methods and Findings

We combined multiple data sources and used panel data regression analysis to study the relationship among investment, service delivery/intervention coverage, and impact on child health by observing changes in 34 sub-Saharan African countries over 2002–2008. We used Lives Saved Tool to estimate the number of lives saved from coverage increase of insecticide-treated nets (ITNs)/indoor residual spraying (IRS). As an indicator of outcome, we also used under-five mortality rate. Global Fund investments comprised more than 70% of the Official Development Assistance (ODA) for malaria control in 34 countries. Each $1 million ODA for malaria enabled distribution of 50,478 ITNs [95%CI: 37,774–63,182] in the disbursement year. 1,000 additional ITNs distributed saved 0.625 lives [95%CI: 0.369–0.881]. Cumulatively Global Fund investments that increased ITN/IRS coverage in 2002–2008 prevented an estimated 240,000 deaths. Countries with higher malaria burden received less ODA disbursement per person-at-risk compared to lower-burden countries ($3.90 vs. $7.05). Increased ITN/IRS coverage in high-burden countries led to 3,575 lives saved per 1 million children, as compared with 914 lives in lower-burden countries. Impact of ITN/IRS coverage on under-five mortality was significant among major child health interventions such as immunisation showing that 10% increase in households with ITN/IRS would reduce 1.5 [95%CI: 0.3–2.8] child deaths per 1000 live births.

Conclusions

Along with other key child survival interventions, increased ITNs/IRS coverage has significantly contributed to child mortality reduction since 2002. ITN/IRS scale-up can be more efficiently prioritized to countries where malaria is a major cause of child deaths to save greater number of lives with available resources.

Citation: Akachi Y, Atun R (2011) Effect of Investment in Malaria Control on Child Mortality in Sub-Saharan Africa in 2002–2008. PLoS ONE 6(6): e21309. doi:10.1371/journal.pone.0021309

Editor: Abdisalan Mohamed Noor, Kenya Medical Research Institute - Wellcome Trust Research Programme, Kenya

 

  • CURRENT DECLINE IN MALARIA IN SUB-SAHARAN AFRICA

Thursday, 28th of July 2011

  • IS THE CURRENT DECLINE IN MALARIA BURDEN IN SUB-SAHARAN AFRICA DUE TO A DECREASE IN VECTOR POPULATION?

Full text is best viewed at

http://www.malariajournal.com/content/pdf/1475-2875-10-188.pdf

Dan W Meyrowitsch , Erling M Pedersen , Michael Alifrangis , Thomas H Scheike , Mwelecele N Malecela , Stephen M Magesa , Yahya A Derua , Rwehumbiza T Rwegoshora , Edwin Michael and Paul E Simonsen

Malaria Journal 2011, 10:188doi:10.1186/1475-2875-10-188

 

Published:

13 July 2011

Abstract (provisional)

Background

In sub-Saharan Africa (SSA), malaria caused by Plasmodium falciparum has historically been a major contributor to morbidity and mortality. Recent reports indicate a pronounced decline in infection and disease rates which are commonly ascribed to large-scale bed net programmes and improved case management. However, the decline has also occurred in areas with limited or no intervention. The present study assessed temporal changes in Anopheline populations in two highly malaria-endemic communities of NE Tanzania during the period 1998-2009.

Methods

Between 1998 and 2001 (1st period) and between 2003 and 2009 (2nd period), mosquitoes were collected weekly in 50 households using CDC light traps. Data on rainfall were obtained from the nearby climate station and was used to analyze the association between monthly rainfall and malaria mosquito populations.

Results

The average number of Anopheles gambiae and Anopheles funestus per trap decreased by 76.8% and 55.3%, respectively over the 1st period, and by 99.7% and 99.8% over the 2nd period. During the last year of sampling (2009), the use of 2368 traps produced a total of only 14 Anopheline mosquitoes. With the exception of the decline in An. gambiae during the 1st period, the results did not reveal any statistical association between mean trend in monthly rainfall and declining malaria vector populations.

Conclusion

A longitudinal decline in the density of malaria mosquito vectors was seen during both study periods despite the absence of organized vector control. Part of the decline could be associated with changes in the pattern of monthly rainfall, but other factors may also contribute to the dramatic downward trend. A similar decline in malaria vector densities could contribute to the decrease in levels of malaria infection reported from many parts of SSA.

 

  • CHINA'S ONE CHILD POLICY

Saturday, 30th of July 2011

FROM  THE ECONOMIST: CHINA’S ONE CHILD POLICY

Best viewed at http://www.economist.com/node/18988926

The Economist, Jul 21st 2011 | BEIJING | from the print edition

 

CONTROVERSIAL when it began a generation ago, China’s one-child policy is stirring yet more contention. Until recently most discussion in China has been confined to academic demographers. Many of them argue that the policy did little good when it began and is increasingly damaging now that the fertility rate is below the replacement level and China’s population structure—the balance between young, middle-aged and old—is becoming so skewed.

This month the debate became political. A provincial official went public with a request to let Guangdong—China’s most populous province, with 104m people—loosen the rules. Speaking to newspapers, Zhang Feng, director of Guangdong’s Population and Family Planning Commission, said he had applied for “approval to be the leader in the country in the relaxation of the family-planning policy”.

 

China’s one-child policy is a bit of a misnomer. In most cities couples are allowed only one child, but there are exceptions. Couples in which both partners are single children may be allowed two. Some parents are allowed a second child if their first is a girl or if they suffer “hardship”, a criterion determined by local officials. Minorities (such as Tibetans or Uighurs) are permitted a second—and sometimes a third—child, whatever the sex of the first-born (see map).

For all the attention that his appeal has secured, Mr Zhang’s proposal is in fact rather modest. Under the relaxation he seeks, couples would be allowed an extra child if only one parent were a singleton, not both. In practice, this would apply to a relatively small number of people. Most young urbanites in Guangdong are likely to be singletons anyway, so the exemption would be mainly for “mixed” couples, that is those involving a marriage between a local and a migrant worker from a rural area.

Because requests to the central government are seldom aired in public, some people suspect Mr Zhang of opportunism. “He smelled the air and is making a move,” says one demographer. According to another, Mr Zhang reckons he will be seen as a hero no matter what. If his demand is accepted, he will have brought about reform; if it is rejected, at least he will have tried.

Whatever lies behind it, Mr Zhang’s demand is significant both because it is an implied public criticism of the one-child policy and because Guangdong was always likely to be in the forefront of any campaign for change. The province suffers many of the worst problems attributable to China’s population control, notably a grossly skewed gender imbalance among newborns. The combination of a strong cultural preference for boys and prenatal ultrasound imaging has led to couples identifying and aborting female fetuses so that their sole permitted child is male. This is a nationwide problem, but Guangdong has consistently had some of the worst sex ratios. Normally, 105 boys are born for every 100 girls. In 2010, Guangdong had 119 male babies for every 100 girls. Ten years earlier, the ratio was a shocking 130.

The province also has big worries about the balance between its working-age population and their dependants in the decades to come. Guangdong’s boom has sucked in huge numbers of young migrants from elsewhere (children and elderly migrants are deterred from moving by the household-registration system, or hukou). But as economic growth spreads to new areas, potential migrants may opt to stay at home, leaving Guangdong’s labour-intensive export industries vulnerable to labour shortages. This is a microcosm of China’s broader worries about ageing and the coming rise in the number of dependants for each working-age adult.

Zheng Zizhen, a demographer at the Guangdong Academy of Social Sciences (GASS), says even a modest change would help. “Every couple, in Guangdong and all over China, should be able to have two children. But before we take a second step or a third step in that direction, we need to at least take a first step like this one.”

Most demographers think the one-child policy has imposed huge costs on the country. The 2010 census showed that population growth was even slower than expected, rising just 0.57% a year over the past decade. The policy has caused conflicts with ordinary people and been a target of intense foreign criticism, worries Peng Peng of GASS (who nevertheless worries about relaxing it too fast). The costs were highlighted recently by revelations of a long-running scandal in Hunan province, where officials are accused of brutalising parents who violate the policy by confiscating “illegal” babies and putting them up for sale in the adoption market.

Few expect significant reforms soon. The family-planning bureaucracy is a vast and entrenched interest group defending the status quo at all levels of government. Senior officials fear that any change would unleash a population boom, despite predictions to the contrary by most experts. With only a year to go until China’s first leadership change in a decade, no high-level figure in the central government is likely to back significant changes now. “If the government has political reasons for not being able to change the policy, then there is nothing I can do,” says Zheng Zizhen. “I can only say that from a scientific point of view, it is clear the policy needs to change.” Guangdong thinks so, too.

·         EMERGENCY HEALTH SPECIALIST, UNICEF/SOMALIA, NAIROBI OFFICE

Saturday, 30th of July 2011

Send cover lettr and cv or P 11 to Bandjougou Magassa bmagassa@unicef.org

Emergency Health Specialist

L4 TA – 6 months

 

Under the supervision of the Chief health, the incumbent will be responsible for the overall planning and management of UNICEF’s health response to the emergency and crisis

 

Programme Coordination

  • Undertake and assist with the assessment and analysis of the emergency and crisis situation in the Somalia affecting children and women with a view to designing appropriate priorities for UNICEF health interventions.
  • Identify partners for implementation
  • Represent UNICEF in the cluster coordination meetings
  • Support the development of programmatic and reporting tools and approaches that can be mainstreamed across partner operations.
  • Ensure and enhance program quality by providing detailed technical input and innovations to service delivery and activities
  • Organize periodic meetings with all partners

Project Administration

  • Manage UNICEF’s relations with its partners, taking administrative actions such as renewing partner contracts Project Cooperation Agreements (PCA), managing program finances,
  • Oversee project supply chain in coordination with UNICEF operations staff.

Information Management, Monitoring and Evaluation

  • Work with Information Management colleague to refine key information systems and products related to the response
  • In close consultation with the M&E team, contribute to the office M&E mechanism
  • Responsible for results tracking and improvement of monitoring systems.

Advocacy and fundraising

  • Help draft donor reports and project proposals related to the response and draft donor updates
  • Contribute to drafting of press releases as deemed necessary
  • Working with the communication unit, ensure visibility of UNICEF’s action in health

Requirements

  • Advanced university degree in social sciences or public health or related field
  • A minimum of eight (8) years of progressively responsible experience in planning and implementing health programmes
  • Experience in emergencies required
  • Oral and written skills in English is required
  • Judgment, maturity, ability to work in a team, cope under stressful and difficult conditions, and political/cultural sensitivity
  • Current knowledge of development issues, policies, as well as social programming policies and procedures in international development cooperation
  • Good analytical, negotiating, communication and advocacy skills. Ability to synthesize and present complex information to external partners and media

 

·         CALL FOR PAPERS, FIELD EPIDEMIOLOGY IN AFRICA

Saturday, 30th of July 2011

Also at http://www.panafrican-med-journal.com/content/series/announcement/afenet_supplement_2011.php

 

Call for papers

PAMJ - AFENET Supplement: Field Epidemiology in Africa

The Pan African Medical Journal (PAMJ) and the African Field Epidemiology Network (AFENET) are glad to invite papers for the first sponsored supplement to be considered by PAMJ.

We welcome submissions of manuscripts for this special supplement to mark the fifth anniversary of AFENET. The anniversary will be marked during the 4th AFENET Regional Conference to be held in Dar es Salaam, Tanzania in December 2011.

The theme of this supplement is “Field Epidemiology in Africa”.

The intent of this supplement is to showcase the work of Field Epidemiology Training Programs (FETPs) in Africa and highlight AFENET’s impact during the 5 years of its existence.

Deadline for submission: August 31, 2011

The anticipated date of publication of the supplement is November 15, 2011

The Guest Editors for this supplement are:

  • · Prof. Mufuta Tshimanga, University of Zimbabwe, Harare, Zimbabwe
  • · Prof. Fred Wabwire, Makerere University, Kampala, Uganda
  • · Dr. Peter Nsubuga, CDC, Atlanta, USA
  • · Dr. Sheba N. Gitta, African Field Epidemiology Network, Kampala, Uganda

 

AFENET is a networking alliance incorporated in November 2005 with a mission to improve the health of Africans through strengthening and expanding field epidemiology and laboratory capacity. AFENET’s goal is to ensure effective prevention and control of epidemics and other priority public health problems on the continent. The networking alliance consists of 12 member Field Epidemiology and (Laboratory) Training Programs (FELTPs) spread across 19 countries in Africa.

More details about AFENET can be accessed at www.afenet.net.

Manuscript Requirements

The editors seek manuscripts from AFENET Programs, Field Epidemiology and Laboratory Training Program (FELTP) trainees, affiliated training institutions and alumni that shall advance knowledge and understanding of field epidemiology training and practice in Africa.

The manuscripts should address areas such as:

  • · Field Epidemiology and Laboratory Training Programs: Their role and impact on strengthening health systems in Africa, contexts, approaches and effects
  • · Outbreak investigations of peculiar or significant public health importance
  • · Disease surveillance
  • · Innovative laboratory techniques for example; in early diagnosis of disease outbreaks, HIV screening, etc
  • · Public health policy addressing changing trends such as non-communicable diseases
  • · HIV/AIDS, Tuberculosis and Malaria
  • · Immunization, Maternal and Child Health
  • · Non-Communicable Diseases
  • · Zoonotic and emerging/re-emerging pandemic threats such as avian influenza and ebola
  • · Neglected Tropical Diseases
  • · Diagnostics and Laboratory techniques for disease surveillance and disease prevention
  • · Health, climate and the environment
  • · Public Health Leadership

Manuscripts submitted should be of original work that has not been published or made available for consideration to any other journal.

Submissions must be in either English or French.

Articles in PAMJ are on average between 1500-5000 words.

Only manuscripts that conform to the PAMJ submission guidelines shall be considered for review. (Access PAMJ Instructions for authors page)

Manuscripts should be submitted through PAMJ Online Manuscript Submission System. As manuscript type, choose “Supplement-AFENET 2011”.

Applicants will be notified via email by the special editorial committee constituted for this supplement.

Each submission shall be assessed by the Special Editorial Committee (SEC).

The committee shall assess the following:

  • · Relevance/public health significance of the study
  • · Suitability of methods used
  • · Clarity of the results and their interpretation
  • · Overall clarity and conciseness of the manuscript
  • · Potential public health impact of the study findings and consequent recommendations

The editorial committee will determine which manuscripts shall be published in the supplement and all published papers will be subjected to external peer review. The PAMJ supplement will be available ahead of the AFENET scientific conference, in December 2011.

The manuscripts will also be printed in a special catalogue that will be made available during the AFENET conference.

Additionally, the author with the best manuscript will be given an award during the conference.

If you have any questions about this supplement, please contact:

Dr. Sheba N. Gitta at sgitta@afenet.com
Dr. Raoul Kamadjeu at editor@panafican-med-journal.com

  • M & E SPECIALIST (POLIO COMMUNICATION) SPECIALIST, UNICEF/KINSHASA (FLUENT FRENCH AND ENGLISH)

Saturday, 30th of July 2011

M&E Specialist (Polio Communication) Specialist

Duty Station: Kinshasa, DRC    Application Deadline: August 4, 2011

 

If you are a communication, social mobilization or monitoring & evaluation expert passionate about making a lasting difference for children, the world's leading children's rights organization would like to hear from you.   Help UNICEF accelerate its response to the Global Polio Eradication Initiative (GPEI) and eradicate polio.  

 

Communication plays a crucial role in polio eradication, fostering understanding of the disease and acceptance of the vaccine.  UNICEF has key communication and social mobilization responsibilities in the endemic countries and also in effectively responding to outbreaks, and we are looking for experienced communication and monitoring & evaluation professionals.

Purpose of the Position

Under the supervision of the Communication for Development Specialist (P4), responsible for the planning, development and implementation of the integrated monitoring and evaluation strategies in support of the communication for polio eradication in DRC.

 

Key Expected Results

1. Contributes towards the preparation of an integrated monitoring, evaluation and research plan for the communication for polio eradication activities.
2. Designs data collection methodologies and research related to communication for polio eradication and in support of immunization interventions: rapid surveys, CAP study, and other behavioral and social analysis.
3. Assist UNICEF and Governmental EPI programme in developing and maintaining data base of communication and social indicators of the national EPI programme.

4. Assists Government authorities to plan and organize M&E training programmes in the area of communication for polio eradication.

5. Participates in programme planning, mid-term review, annual reviews, other meetings.  Analyzes and evaluates data to ensure achievement of objectives and recommends corrective actions, when necessary. 
6. Participates in the development of the Child Survival programme workplan, ensures compliance to specific assigned objectives. 

7. Prepares the programme status reports required for management, board, donors, budget reviews, programme analysis, annual reports, etc.

 

Qualifications

Advanced university degree in Social Sciences, Demography, Development Planning, Statistics or a related technical field. A first level university degree in combination with qualifying experience may be accepted in lieu of the advanced university degree.
Five years of progressively responsible professional work experience at national and international levels in programme monitoring and evaluation. Practical experience in community-based research.
Fluency in French and English is required.

 

To Apply

Visit us at www.unicef.org/about/employ to register in our e-Recruitment system, and search using keyword “Kinshasa” for additional details/to apply before deadline.

 

In the selection of its staff, UNICEF is committed to diversity and gender equality and without distinction as to race, sex or religion, and without discrimination of persons with disabilities: Women, nationals of developing countries, and all well qualified candidates are strongly encouraged to apply.

 



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BMC Public Health has devoted an entire supplement, with 35 articles, to the Lives Saved Tool.

This tool permits the decision maker at the country level to make data driven choices for the integration of different disease prevention interventions into the country’s armamentarium.

Specialists in child and maternal mortality reduction will not be surprised by the inclusion of articles on vaccination and supplementation. What about emerging interventions against respiratory syncytial virus? Read the table of contents at http://www.biomedcentral.com/bmcpublichealth/11?issue=S3

to see how many interventions your country is currently implementing.

 

  • ASSUMPTIONS  AND METHODS IN THE LIVES SAVED TOOL

Introduction

Assumptions and methods in the Lives Saved Tool (LiST)

Monica J Fox1 , Reynaldo Martorell2 , Nynke van den Broek3 and Neff Walker1

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, 615 N Wolfe Street, Baltimore, MD 21205, USA

Hubert Department of Global Health, Rollins School of Public Health, Emory University, 1518 Clifton Road. Atlanta, Georgia 30322, USA

Maternal Newborn Health Unit, Liverpool School of Tropical Medicine, Pembroke Place Liverpool L3 5QA, UK

author email corresponding author email

from

BMC Public Health 2011, 11(Suppl 3):I1doi:10.1186/1471-2458-11-S3-I1

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/11/S3/I1

Published:

13 April 2011

© 2011 Fox et al; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

The Lives Saved Tool (LiST) is a computer-based model that estimates the impact of increasing coverage of interventions on maternal, neonatal and child mortality. The model has its origins in earlier work from the Lancet Series papers that looked at estimating the impact of increasing coverage of proven interventions on child mortality [1] and neonatal mortality [2] as well as the impact of interventions related to nutrition and nutritional status of mothers and children [3]. During the past four years, LiST has been developed into a free, publically available software tool that has been used by programs or organizations to estimate the impact of scaling up different interventions and thereby help in the health planning process. [4-6]

The development of LiST is closely linked to the work of the Child Health Epidemiology Reference Group (CHERG) of WHO and UNICEF. The CHERG provides technical inputs to the assumptions and procedures used in the model and also guides the on-going development of the model. As part of this process, this journal issue, along with a previous supplement [7], is being published to ensure that the methods and assumptions in the model are peer reviewed and made publicly available for comments, criticism and feedback.

In addition to the fact that the model now includes 75 interventions, LiST also continues to expand in terms of the scope of the program, including two major functionality additions in the current version. First, the new version of LiST estimates the impact of interventions on stillbirths. Second, the new version of LiST allows users the ability to add future interventions, thereby judging the impact of these interventions in conjunction with existing interventions. For example, one could put in a vaccine for malaria, set the efficacy of the vaccine and then estimate the impact that this vaccine would have on malaria deaths with or without the scale up of an existing malaria intervention, such as insecticide-treated nets or indoor residual spraying. More details about the Lives Saved Tool, (LiST) including documentation, training materials, and background information is available at http://www.jhsph.edu/IIP webcite.

This supplement includes 35 articles, the majority of which present reviews and meta-analyses that are used to estimate the effectiveness of interventions. In addition there are several articles that either look at the possible impact of future interventions or deal with methodological issues related to the Lives Saved Tool.

The effectiveness review articles in the supplement are organized into three broad categories. First, there are seven papers that focus on the impact of interventions on the risk of stillbirth for pregnant women, an output new to LiST. The second section has nine articles that look at the impact of interventions related to maternal, neonatal and child mortality. These articles expand the number of interventions for which effectiveness estimates are available from the previous supplement and also, in the case of rotavirus vaccine, provide an updated estimate of effectiveness based on new trial data.

The third section of the supplement contains nine reviews of nutritional interventions. Previous versions of LiST have used estimates of effectiveness drawn from the Lancet Maternal and Child Undernutrition Series [3], but the papers presented here provide new, updated reviews of the effectiveness of nutrition-related interventions.

The six papers contained in the fourth section of the issue estimate the potential impact of emerging interventions against pneumonia and meningitis utilizing a modified CHRNI methodology [8]. In the past, LiST had a large, but defined set of interventions in the model. Because the interventions discussed in this section are not proven interventions, they are not included in LiST. The most recent version of LiST, however, allows users to enter new or future interventions into the LiST model and then see what additional impact these new interventions would have in conjunction with existing interventions.

The final section of the supplement presents 4 articles that look at methodological issues related to LiST. These papers either compare LiST to other models or measured outputs or provide more detailed explanation of the underlying calculations and methods used in LiST.

The review papers in this supplement provide estimates of the effectiveness for 100 intervention-outcome combinations that were 1) interventions that are already in LiST, 2) new interventions that have been proposed for inclusion in LiST, or 3) pairings of existing interventions to new outcomes, such as stillbirth rate that were not included in earlier versions of LiST.

The quality of the data available to make these estimates varies dramatically. For 23 of the 100 intervention-outcome combinations, the data available to estimate effectiveness were rated as high using a modified GRADE approach.[9] At the other extreme, the estimates of effectiveness for 28 intervention-outcome combinations were made by using a Delphi approach [10] because there were insufficient data available from existing studies. This is in effect a method to seek consensus expert opinion. For the remaining 49 intervention-outcome combinations, the reviewers considered the estimates of effect to be based on studies with low or moderate levels of data quality.

Based on these reviews, some intervention-outcome combinations, such as those where there was a non-significant effect, will not be entered into LiST. Likewise, while Delphi analyses were run for all combinations when insufficient data were available to do a meta-analysis, many of these intervention–outcome combinations will not be included in LiST. These estimates will only be used in cases where there is overwhelming belief in the efficacy of an intervention and ethical constraints rule out studies to estimate the effects. For example, it is difficult to directly estimate the impact of caesarean-sections on cause-specific maternal and neonatal mortality or the effect of skilled birth attendance on maternal and newborn outcomes and it is unlikely that controlled trials can be designed to investigate these issues. For these situations, LiST will use the estimates of effectiveness from the Delphi processes and/or use historical data.

Similarly, in some cases such as the availability and uptake of Emergency (or Essential) Obstetric Care, the intervention consists of a ‘package’ of multiple possible separate interventions. Evaluation of the effect of such complex packages is difficult and should not be confused with the effect (or not) of the individual components of the package on the sought outcomes. Finally it must be recognized that in many studies the sought outcomes are not well defined e.g. a number of studies report on perinatal mortality (using a variety of definitions) but do not separately report on stillbirths as outcome.

Thus, the reviews presented here not only serve to improve the scope and the quality of the assumptions of the Lives Saved Tool, but they also highlight areas where further research is needed on effectiveness of interventions. Many of the interventions where insufficient data exist to estimate impact are being used in countries and/or promoted for wider use. Clearly if better health policy decisions are to be made, additional efforts to collect data on the efficacy and effectiveness of these interventions needs to be prioritized.

 

  • PREVENTIVE ZINC SUPPLEMENTATION IN DEVELOPING COUNTRIES: IMPACT ON MORTALITY AND MORBIDITY DUE TO DIARRHEA, PNEUMONIA AND MALARIA

 This article is part of the supplement: Technical inputs, enhancements and applications of the Lives Saved Tool (LiST) .

BMC Public Health 2011, 11(Suppl 3):S23doi:10.1186/1471-2458-11-S3-S23

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/11/S3/S23

Abstract

Background

Zinc deficiency is commonly prevalent in children in developing countries and plays a role in decreased immunity and increased risk of infection. Preventive zinc supplementation in healthy children can reduce mortality due to common causes like diarrhea, pneumonia and malaria. The main objective was to determine all-cause mortality and cause-specific mortality and morbidity in children under five in developing countries for preventive zinc supplementation.

Data sources/ review methods

A literature search was carried out on PubMed, the Cochrane Library and the WHO regional databases to identify RCTs on zinc supplementation for greater than 3 months in children less than 5 years of age in developing countries and its effect on mortality was analyzed.

Results

The effect of preventive zinc supplementation on mortality was given in eight trials, while cause specific mortality data was given in five of these eight trials. Zinc supplementation alone was associated with a statistically insignificant 9% (RR = 0.91; 95% CI: 0.82, 1.01) reduction in all cause mortality in the intervention group as compared to controls using a random effect model. The impact on diarrhea-specific mortality of zinc alone was a non-significant 18% reduction (RR = 0.82; 95% CI: 0.64, 1.05) and 15% for pneumonia-specific mortality (RR = 0.85; 95% CI: 0.65, 1.11). The incidence of diarrhea showed a 13% reduction with preventive zinc supplementation (RR = 0.87; 95% CI: 0.81, 0.94) and a 19% reduction in pneumonia morbidity (RR = 0.81; 95% CI: 0.73, 0.90). Keeping in mind the direction of effect of zinc supplementation in reducing diarrhea and pneumonia related morbidity and mortality; we considered all the outcomes for selection of effectiveness estimate for inclusion in the LiST model. After application of the CHERG rules with consideration to quality of evidence and rule # 6, we used the most conservative estimates as a surrogate for mortality. We, therefore, conclude that zinc supplementation in children is associated with a reduction in diarrhea mortality of 13% and pneumonia mortality of 15% for inclusion in the LiST tool. Preventive zinc supplementation had no effect on malaria specific mortality (RR = 0.90; 95% CI: 0.77, 1.06) or incidence of malaria (RR=0.92; 95 % CI 0.82-1.04)

Conclusion

Zinc supplementation results in reductions in diarrhea and pneumonia mortality.

 

 

An evaluation of emerging vaccines for childhood pneumococcal pneumonia

BMC Public Health 2011, 11(Suppl 3):S26doi:10.1186/1471-2458-11-S3-S26

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/11/S3/S26

Abstract

Background

Pneumonia is the leading cause of child mortality worldwide. Streptococcus pneumoniae (SP) or pneumococcus is estimated to cause 821,000 child deaths each year. It has over 90 serotypes, of which 7 to 13 serotypes are included in current formulations of pneumococcal conjugate vaccines that are efficacious in young children. To further reduce the burden from SP pneumonia, a vaccine is required that could protect children from a greater diversity of serotypes. Two different types of vaccines against pneumococcal pneumonia are currently at varying stages of development: a multivalent pneumococcal conjugate vaccine covering additional SP serotypes; and a conserved common pneumococcal protein antigen (PPA) vaccine offering protection for all serotypes.

Methods

We used a modified CHNRI methodology for setting priorities in health research investments. This was done in two stages. In Stage I, we systematically reviewed the literature related to emerging SP vaccines relevant to several criteria of interest: answerability; efficacy and effectiveness; cost of development, production and implementation; deliverability, affordability and sustainability; maximum potential for disease burden reduction; acceptability to the end users and health workers; and effect on equity. In Stage II, we conducted an expert opinion exercise by inviting 20 experts (leading basic scientists, international public health researchers, international policy makers and representatives of pharmaceutical companies). The policy makers and industry representatives accepted our invitation on the condition of anonymity, due to sensitive nature of their involvement in such exercises. They answered questions from CHNRI framework and their “collective optimism” towards each criterion was documented on a scale from 0 to 100%.

Results

The experts expressed very high level of optimism (over 80%) that low-cost polysaccharide conjugate SP vaccines would satisfy each of the 9 relevant CHNRI criteria. The median potential effectiveness of conjugate SP vaccines in reduction of overall childhood pneumonia mortality was predicted to be about 25% (interquartile range 20-38%, min. 15%, max 45%). For low cost, cross-protective common protein vaccines for SP the experts expressed concerns over answerability (72%) and the level of development costs (50%), while the scores for all other criteria were over 80%. The median potential effectiveness of common protein vaccines in reduction of overall childhood pneumonia mortality was predicted to be about 30% (interquartile range 26-40%, min. 20%, max 45%).

Conclusions

Improved SP vaccines are a very promising investment that could substantially contribute to reduction of child mortality world-wide.

 

  • ROTAVIRUS VACCINE AND DIARRHEA MORTALITY: QUANTIFYING REGIONAL VARIATION IN EFFECT SIZE

Christa L Fischer Walker and Robert E Black

Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205, USA

BMC Public Health 2011, 11(Suppl 3):S16

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/11/S3/S16

Abstract

Background

Diarrhea mortality remains a leading cause of child death and rotavirus vaccine an effective tool for preventing severe rotavirus diarrhea. New data suggest vaccine efficacy may vary by region.

Methods

We reviewed published vaccine efficacy trials to estimate a regional-specific effect of vaccine efficacy on severe rotavirus diarrhea and hospitalizations. We assessed the quality of evidence using a standard protocol and conducted meta-analyses where more than 1 data point was available.

Results

Rotavirus vaccine prevented severe rotavirus episodes in all regions; 81% of episodes in Latin America, 42.7% of episodes in high-mortality Asia, 50% of episodes in sub-Saharan Africa, 88% of episodes low-mortality Asia and North Africa, and 91% of episodes in developed countries. The effect sizes observed for preventing severe rotavirus diarrhea will be used in LiST as the effect size for rotavirus vaccine on rotavirus-specific diarrhea mortality.

Conclusions

Vaccine trials have not measured the effect of vaccine on diarrhea mortality. The overall quality of the evidence and consistency observed across studies suggests that estimating mortality based on a severe morbidity reduction is highly plausible.

Rotavirus vaccine and diarrhea mortality: quantifying regional variation in effect size

 

Christa L Fischer Walker and Robert E Black

Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205, USA

BMC Public Health 2011, 11(Suppl 3):S16

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/11/S3/S16

Abstract

Background

Diarrhea mortality remains a leading cause of child death and rotavirus vaccine an effective tool for preventing severe rotavirus diarrhea. New data suggest vaccine efficacy may vary by region.

Methods

We reviewed published vaccine efficacy trials to estimate a regional-specific effect of vaccine efficacy on severe rotavirus diarrhea and hospitalizations. We assessed the quality of evidence using a standard protocol and conducted meta-analyses where more than 1 data point was available.

Results

Rotavirus vaccine prevented severe rotavirus episodes in all regions; 81% of episodes in Latin America, 42.7% of episodes in high-mortality Asia, 50% of episodes in sub-Saharan Africa, 88% of episodes low-mortality Asia and North Africa, and 91% of episodes in developed countries. The effect sizes observed for preventing severe rotavirus diarrhea will be used in LiST as the effect size for rotavirus vaccine on rotavirus-specific diarrhea mortality.

Conclusions

Vaccine trials have not measured the effect of vaccine on diarrhea mortality. The overall quality of the evidence and consistency observed across studies suggests that estimating mortality based on a severe morbidity reduction is highly plausible.

 

  • AN EVALUATION OF EMERGING VACCINES FOR CHILDHOOD MENINGOCOCCAL DISEASE

BMC Public Health 2011, 11(Suppl 3):S29doi:10.1186/1471-2458-11-S3-S29

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/11/S3/S29

Abstract

Background

Meningococcal meningitis is a major cause of disease worldwide, with frequent epidemics particularly affecting an area of sub-Saharan Africa known as the “meningitis belt”. Neisseria meningitidis group A (MenA) is responsible for major epidemics in Africa. Recently W-135 has emerged as an important pathogen. Currently, the strategy for control of such outbreaks is emergency use of meningococcal (MC) polysaccharide vaccines, but these have a limited ability to induce herd immunity and elicit an adequate immune response in infant and young children. In recent times initiatives have been taken to introduce meningococcal conjugate vaccine in these African countries. Currently there are two different types of MC conjugate vaccines at late stages of development covering serogroup A and W-135: a multivalent MC conjugate vaccine against serogroup A,C,Y and W-135; and a monovalent conjugate vaccine against serogroup A. We aimed to perform a structured assessment of these emerging meningococcal vaccines as a means of reducing global meningococal disease burden among children under 5 years of age.

Methods

We used a modified CHNRI methodology for setting priorities in health research investments. This was done in two stages. In the first stage we systematically reviewed the literature related to emerging MC vaccines relevant to 12 criteria of interest. In Stage II, we conducted an expert opinion exercise by inviting 20 experts (leading basic scientists, international public health researchers, international policy makers and representatives of pharmaceutical companies). They answered questions from CHNRI framework and their “collective optimism” towards each criterion was documented on a scale from 0 to 100%.

Results

For MenA conjugate vaccine the experts showed very high level of optimism (~ 90% or more) for 7 out of the 12 criteria. The experts felt that the likelihood of efficacy on meningitis was very high (~ 90%). Deliverability, acceptability to health workers, end users and the effect on equity were all seen as highly likely (~ 90%). In terms of the maximum potential impact on meningitis disease burden, the median potential effectiveness of the vaccines in reduction of overall meningitis mortality was estimated to be 20%; (interquartile range 20-40% and min. 8%, max 50 %). For the multivalent meningococcal vaccines the experts had similar optimism for most of the 12 CHNRI criteria with slightly lower optimism in answerability and low development cost criteria. The main concern was expressed over the cost of product, its affordability and cost of implementation.

Conclusions

With increasing recognition of the burden of meningococcal meningitis, especially during epidemics in Africa, it is vitally important that strategies are taken to reduce the morbidity and mortality attributable to this disease. Improved MC vaccines are a promising investment that could substantially contribute to reduction of child meningitis mortality world-wide.

GREATEST HITS OF 2011

Dear All,

Please see below, in descending order by number of hits, the updates most often consulted by you, my readers, from January through June 2011. Thanks to IT whiz Anthony Kaguimah for assisting me in generating this list.

It is customary for me to ask you, on such occasions, which areas you would like to see better represented. May I put the question on its head and ask those of you with nutrition interests to forward items from the nutrition literature which I, in my ignorance, have overlooked.

http://www.childsurvival.net/?content=com_articles&artid=672

BTW, to find an item, type the title into the search engine at the upper right hand corner of the site.

Cheers, BD

  • TWO ON IVERMECTIN AGAINST MALARIA 

Ivermectin is best known for its use in mass drug administration against onchocerciasis (river blindness). These studies from west Africa point to an action against malaria, as well.

 

1)                 IVERMECTIN MASS DRUG ADMINISTRATION TO HUMANS DISRUPTS MALARIA PARASITE TRANSMISSION IN SENEGALESE VILLAGES

 

  1. 1.   Kevin C. Kobylinski*,
  2. 2.   Massamba Sylla*,
  3. 3.   Phillip L. Chapman,
  4. 4.   Moussa D. Sarr and
  5. 5.   Brian D. Foy*

+ Author Affiliations

  1. 1.    Arthropod-borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado; Department of Statistics, Colorado State University, Fort Collins, Colorado; Ministère de la Santé et de la Prévention Médicale, Dakar, Senegal

+ Author Notes

       Authors' addresses: Kevin C. Kobylinski, Massamba Sylla, and Brian D. Foy, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, E-mails: kobylinskikevin@yahoo.com, massamba.sylla@colostate.edu, and brian.foy@colostate.edu. Phillip L. Chapman, Department of Statistics, Fort Collins, CO, E-mail: pchapman@stat.colostate.edu. Moussa D. Sarr, Ministère de la Santé et de la Prévention Médicale, Dakar, Senegal, E-mail: mdiensarr@yahoo.fr.

  1. *Address correspondence to Kevin C. Kobylinski, Massamba Sylla, and Brian D. Foy, Department of Microbiology, Immunology and Pathology, 1692 Campus delivery, Fort Collins, CO 80523-1692. E-mails: kobylinskikevin@yahoo.com, massamba.sylla@colostate.edu, and brian.foy@colostate.edu
  2. †These authors contributed equally to this work.

Abstract.

Ivermectin mass drug administration (MDA) to humans is used to control onchocerciasis and lymphatic filariasis. Recent field studies have shown an added killing effect of ivermectin MDA against malaria vectors. We report that ivermectin MDA reduced the proportion of Plasmodium falciparum infectious Anopheles gambiae sensu stricto (s.s.) in treated villages in southeastern Senegal. Ivermectin MDA is a different delivery method and has a different mode of action from current malaria control agents. It could be a powerful and synergistic new tool to reduce malaria transmission in regions with epidemic or seasonal malaria transmission, and the prevalence and intensity of neglected tropical diseases.

Footnotes

       Financial support: This work was supported by the NIH grant R21 AI079528, Grand Challenges Explorations grant 51995 from the Bill and Melinda Gates Foundation, and CRC grant 1686174 from Colorado State University.

       Reprint requests: Brian D. Foy Department of Microbiology, Immunology and Pathology, 1692 Campus delivery, Fort Collins, CO 80523-1692, E-mail: brian.foy@colostate.edu.

       Received March 21, 2011.

       Accepted April 4, 2011.  

Abstract above; full text available to subscribers of AJTMH

 

  • MASS DRUG ADMINISTRATION OF IVERMECTIN IN SOUTH-EASTERN SENEGAL REDUCES THE SURVIVORSHIP OF WILD-CAUGHT, BLOOD FED MALARIA VECTORS

 

Best read at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3016374/?tool=pubmed

In south-eastern Senegal, malaria and onchocerciasis are co-endemic. Onchocerciasis in this region has been controlled by once or twice yearly mass drug administration (MDA) with ivermectin (IVM) for over fifteen years. Since laboratory-raised Anopheles gambiae s.s. are susceptible to ivermectin at concentrations found in human blood post-ingestion of IVM, it is plausible that a similar effect could be quantified in the field, and that IVM might have benefits as a malaria control tool.

Methods

In 2008 and 2009, wild-caught blood fed An. gambiae s.l. mosquitoes were collected from huts of three pairs of Senegalese villages before and after IVM MDAs. Mosquitoes were held in an insectary to assess their survival rate, subsequently identified to species, and their blood meals were identified. Differences in mosquito survival were statistically analysed using a Glimmix model. Lastly, changes in the daily probability of mosquito survivorship surrounding IVM MDAs were calculated, and these data were inserted into a previously developed, mosquito age-structured model of malaria transmission.

Results

Anopheles gambiae s.s. (P < 0.0001) and Anopheles arabiensis (P = 0.0191) from the treated villages had significantly reduced survival compared to those from control villages. Furthermore, An gambiae s.s. caught 1-6 days after MDA in treated villages had significantly reduced survival compared to control village collections (P = 0.0003), as well as those caught pre-MDA (P < 0.0001) and >7 days post-MDA (P < 0.0001). The daily probability of mosquito survival dropped >10% for the six days following MDA. The mosquito age-structured model of malaria transmission demonstrated that a single IVM MDA would reduce malaria transmission (Ro) below baseline for at least eleven days, and that repeated IVM MDAs would result in a sustained reduction in malaria Ro.

Conclusions

Ivermectin MDA significantly reduced the survivorship of An. gambiae s.s. for six days past the date of the MDA, which is sufficient to temporarily reduce malaria transmission. Repeated IVM MDAs could be a novel and integrative malaria control tool in areas with seasonal transmission, and which would have simultaneous impacts on neglected tropical diseases in the same villages.

  • ·         FREEDOM, INCOME EQUALITY, AND HEALTH

'The total proportion of free years from 1972-2005, the duration of current freedom level, and the Gini coefficient show independent positive associations with health indicators, which remain after the adjustment for national wealth, total government expenditure, and spending on health.'

Both political freedom and low Gini coefficients are independent predictors of improved health outcomes.
Why?

Good reading.

Bob Davis

Best read at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890539/?tool=pubmed

 

 

A PROGRAM TO DELAY CHILD MARRIAGE IN RURAL ETHIOPIA

 

Best read at http://www.guttmacher.org/pubs/journals/3500609.html 

 

Evaluation of Berhane Hewan: A Program to Delay Child Marriage in Rural Ethiopia

By Annabel S. Erulkar and Eunice Muthengi

CONTEXT: Early marriage limits girls' opportunities and compromises their health, yet in Sub-Saharan Africa many girls are married before the age of 18, and few programs have sought to increase the age at marriage on the continent.

METHODS: Berhane Hewan was a two-year pilot project conducted in 2004–2006 that aimed to reduce the prevalence of child marriage in rural Ethiopia, through a combination of group formation, support for girls to remain in school and community awareness. A quasi-experimental research design with baseline and endline surveys was used to measure changes in social and educational participation, marriage age, reproductive health knowledge and contraceptive use. Chi-square tests, proportional hazards models and logistic regressions were conducted to assess changes associated with the project.

RESULTS: The intervention was associated with considerable improvements in girls' school enrollment, age at marriage, reproductive health knowledge and contraceptive use. Particularly among girls aged 10–14, those exposed to the program were more likely than those in the control area to be in school at the endline survey (odds ratio, 3.0) and were less likely to have ever been married (0.1). However, among girls aged 15–19, those in the intervention area had an elevated likelihood of having gotten married by the endline (2.4). Sexually experienced girls exposed to the intervention had elevated odds at endline of having ever used contraceptives (2.9).

CONCLUSIONS: The success of the Berhane Hewan program, one of the first rigorously evaluated interventions to delay marriage in Sub-Saharan Africa, suggests that well-designed and effectively implemented programs can delay the earliest marriages until later adolescence.

International Perspectives on Sexual and Reproductive Health, 2009, 35(1):6–14

  • IMB REPORT

    The Independent Monitoring Board of the Global Polio Eradication Initiative, chaired by Sir Liam Donaldson, has issued the report of its most recent meeting, recently concluded in London. Full text is to appear at www.polioeradication.org. Below, I reproduce the executive summary and recommendations.

Good reading.

Bob Davis

 

EXECUTIVE SUMMARY

 

1. Our first report, in April 2011, took a broad, frank look at the task of interrupting polio transmission– its historical context, the factors critical to success, the key remaining countries. The Global Polio Eradication Initiative (GPEI) achieved a 99% reduction in polio cases worldwide between 1988 (the year of the GPEI’s founding) and 2000, but this was followed by a decade of ‘stalemate’ with no further headway being made. Evidently, eradicating the final 1% of polio is the greatest challenge yet. Nothing short of excellence will complete this task.

 

2. By our current assessment, the GPEI is not on track to interrupt polio transmission by the end of 2012 because:

 

The programme is performing poorly in controlling polio in countries with re-established transmission (DR Congo, Chad and Angola)

 

The programme is weak in anticipating and preventing outbreaks in high-risk countries

previously free of polio; 14 such countries have suffered outbreaks since the beginning of 2010

 

The polio numbers in Pakistan are going in the wrong direction: the number of cases this year has doubled compared to the same period in 2010

 

The urgency and power of the response of the programme to the situations in Chad and DR Congo has not been commensurate with the serious problems of capacity, capability and quality control on the ground in these countries

 

There are too many examples of failure to ensure consistently high quality of vaccine campaigns and surveillance in key areas

 

3. If the question is asked: “What will be done differently next month to completely transform progress against the stubborn persistence of active polio?” there is no convincing answer. More of the same will not deliver the polio eradication goal.

 

4. But polio eradication is still possible, in the near term, if there is enhanced political commitment, secure funding, strengthened technical capacity, and if the concerns below can be swiftly tackled.

 

5. This report identifies key areas of immediate risk. Listing these, we ask the GPEI to ensure that it has a clear plan to deal urgently with each.

 

6. We highlight areas of inconsistency, dysfunction and weakness in the programme, and provide recommendations to break through these.

 

7. We raise key long-term issues relating to serious resource shortfalls and the need for a clear polio endgame plan.

 

8. We update our assessment of the global milestones (see next page) and of progress in each of the seven countries with persistent transmission:

 

India has made strong progress and is on track to interrupt transmission this year.

Afghanistan is making good progress, but has not yet sufficiently overcome its access challenges.

Recent national elections set back Nigeria’s strong progress, which now needs to be resurrected.

High-level commitment is evident in Pakistan, but the country needs to get to grips with serious local level performance issues.

We welcome the additional technical support being afforded to Chad, where the situation is alarming. The surge teams of WHO and UNICEF need to become swiftly functional.

We are deeply concerned by DR Congo, where visible commitment of the President is much needed.

Angola is making good progress but needs to retain its focus on the province of Luanda.

 

9. Our view remains that stopping polio transmission needs to be treated as a global health emergency. Failure would allow this vicious disease to resurge. We will continue to provide a frank and independent assessment of the progress being made. Our next meeting will be held in London on 28-30 September 2011.

 

RECOMMENDATIONS

On the basis of our preceding analysis,

1. We recommend that the heads of the spearheading partner agencies ensure that a clear plan is in place to address each of the seven key risks that we have highlighted

 

2. We recommend the creation of twinning mechanisms, through which a country explicitly commits technical expertise and financial assistance in support of a named polio-affected country. Such arrangements should be agreed at ministerial level. The country with polio should retain primary control over what technical assistance it requests. We recommend that the GPEI seek to establish at least two such

arrangements urgently, such that the agreements and the technical assistance are in place within the next three months.

 

3. We recommend that the GPEI spearheading partners and country programmes mandate that all sections of AFP (i.e. possible polio) case investigation forms must be completed in full, notably the social data sections. Any forms in which information is missing should be returned to the individual who filed them to be completed.

 

4. We recommend that Rotary International pilots the use of a short team-based checklist by vaccination teams at the start and finish of each vaccination day. The items on the checklist should reflect the accepted best practices that are taught to teams.

The day’s work should not start or finish until the team has talked through the checklist, and committed to each of its items.

 

5. We recommend that UNICEF pilots and rapidly implements a simple tool that field staff can use in immunisation debrief sessions to identify, record, and locally disseminate effective micro-innovations.

 

We recommend that UNICEF establishes an expectation that this tool will be used after each immunisation round, and that very brief reports are compiled globally and shared rapidly.

 

6. We recommend that UNICEF creates or commissions textual and audiovisual materials (including short films) that use case studies to communicate the power of micro-innovations, and empower vaccinators and social mobilisers to be creative in tackling the challenges that they meet. These videos should be widely distributed

for viewing at vaccination team training days. The GPEI may wish to use this opportunity to communicate other key messages, such as the global view of polio eradication and the vital role of front-line workers.

 

7. We recommend that, at its next meeting, SAGE examines the potential for a combined IPV/OPV approach to be used in appropriate settings

 

8. We recommend that the spearheading partners identify leading disability advocates and explore their interest in learning more about polio eradication, with a potential view to advocating for enhanced financial and political support.

 

9. We recommend that the spearheading partners formally explore with GAVI whether a portion of its recent large funding package could be allocated to activities that further the goals of both GAVI and of the GPEI

 

10. We recommend that Pakistan, Afghanistan, DR Congo, Chad and Angola each establish a system with the same four key elements as the Abuja Commitments, to enhance and track the commitment of the key individuals at state/province and local level.

 

11. We recommend that each of the seven countries with established transmission should set out a timeline of milestones en route to interrupting transmission.

18. We recommend that the spearheading partners secure the engagement of the President of DR Congo as the leader of this country’s emergency actions to interrupt polio transmission

 

19. We recommend that DR Congo, with CDC and WHO, amend the Major Process Indicator for end-2011 that is based on vaccination, to reflect the need for good coverage across the recently affected areas

 

20. We recommend that within the next month each state of India completes its risk analysis to identify areas and populations at high risk of importation and spread of polio, setting out a clear plan to address the vulnerabilities identified

 

21. We recommend that the Indian national programme critically updates its own view of risk in light of the state analyses, to discover whether any areas need further intervention

 

22. We recommend that Nigeria works with CDC and WHO to agree and introduce an additional Major Process Indicator, based on independent monitoring data, for end-2011

 

12. We recommend that the GPEI’s endgame plan should incorporate a phase-by-phase plan to optimise the GPEI’s public health and health service delivery legacy. This should list out the benefits that are achievable and define how each can be reached, setting clear objectives, milestones and indicators. We recommend that the GPEI

identifies a named individual or group who has clear authority to lead this part of the work. This might involve recruitment. It could alternatively involve identifying existing capability elsewhere within WHO or UNICEF. Such an arrangement would allow the core current teams to concentrate on completing the eradication of polio, whilst

ensuring that the broader focus is also given the attention that it needs.

 

And from earlier in the report,

 

13. We recommend that WHO appoint, at the earliest, an epidemiologist on a long-term contract to support the Angolan national government

 

14. We recommend that the heads of WHO, CDC and UNICEF pay personal attention to ensuring that arrangements are in place to enable their agencies’ new teams in Chad to begin functioning effectively at the soonest possible time

 

15. We recommend that Chad’s emergency action plan is reviewed to (i) establish a clearer priority focus in the areas identified as being high risk, (ii) establish performance indicators that can be monitored as the technical teams increase in size

 

16. We recommend that the Chad programme incorporates collaborative working with the animal health sector in order to enhance vaccination amongst remote and difficult-to-reach populations.

 

17. We ask to receive fortnightly updates on the implementation of Chad’s emergency plan, with a particular focus on progress made in establishing a functional WHO/CDC/UNICEF team. 

 

  • GRAND ROUNDS IN CHILD SURVIVAL, NOW ON YOUTUBE

CDC's Grand Rounds in Public Health are now on Youtube.

Their program on child survival is at http://www.youtube.com/watch?v=DOdDhxD6Da4

A visit to Youtube with search item ‘child survival’ will also pick up items on the same topic from other sources. 

  • THREE DECADES OF PAHO’S EPI NEWSLETTER

For three decades, the PAHO EPI Newsletter -- first in paper form, now also on the Internet -- has kept the reading public up to date on breaking issues in immunization in the Region of the Americas.

The newsletter is not just for the Americas. Ideas which move forward globally -- smallpox eradication, polio eradication, measles eradication, and, most recently introduction of  HPV, rotavirus and pneumococcal vaccines -- often trace their roots to the Region of the Americas. To find out what's the next big thing in global immunization, one can do far worse than to read the PAHO newsletter.

Good reading, BD

Immunization Newsletter: Over 30 Years Reaching Every Corner of the Americas Launch of electronic book that compiles 2,500 articles published in the newsletter since 1979 Washington, D.C., 11 July 2011

(PAHO/WHO)–In its over 30 years of existence, the Immunization Newsletter of the Pan American Health Organization/World Health Organization (PAHO/WHO) has managed to reach thousands of health workers in the most remote locations in the Americas to share information on the vaccination programs with them. To celebrate its more than three decades, the e-book “Thirty Years of the Immunization Newsletter: History of the Expanded Program on Immunization in the Americas” was launched on 8 July. This book compiles over 2,500 articles on debates, new developments, projects, and research related to immunization. These notes, published from 1979 to the present, describe each stage of implementation of the Expanded Program on Immunization (EPI) in the Americas, a program that is considered to be one of the most successful in the world. The notes are also a testimony of the lessons learned about the subject of immunization during these years, as well as the efforts being made to introduce new vaccines in the region. “It is a witness to the milestones achieved in the history of immunization of a continent that is highly diverse, but united in a spirit of equity and solidarity, or Pan-Americanism, in order to achieve common goals in seeking to control and eliminate vaccine-preventable diseases,” stated the Director of PAHO/WHO, Dr. Mirta Roses, in the preface of this book. The Immunization Newsletter e-book describes step-by-step how the countries in the Americas have been leaders on the worldwide level in elimination or reduction of vaccine-preventable diseases. The different notes describe the advances and challenges the region faced in elimination of polio, which was achieved in 1991.They also show the efforts to combat other diseases: the last endemic case of measles was reported in 2002 and the last endemic case of rubella was reported in 2009. Although imported cases are still recorded, mass vaccination has prevented their expansion. Therefore, it is considered to be essential to maintain elimination of these diseases.

The Immunization Newsletter is prepared by the PAHO/WHO Comprehensive Family Immunization Project. It is the oldest newsletter in the world, which is published every two months in Spanish, English, and French. It has been published in French since 2003. The newsletter reaches over 7,500 people in the region and in the world free of charge. Since it began, its purpose has been to facilitate the exchange of ideas and information on the vaccination programs implemented in the region, so that more people in the health sector learn about the problems and possible solutions that have been attempted in other places. Up until the present the aim has been for the Newsletter to reach all people that are in some way associated with or work with the subject of immunization: from vaccination program managers, pediatricians, infectious disease specialists, epidemiologists, and nurses to health workers that provide vaccines in remote or isolated areas of the Americas. For a long time, the print version of the newsletter has reached the most remote zip codes in the Americas by subscription. At present, it can also be accessed electronically.

With publication of this e-book, the Immunization Newsletter relaunches its electronic and paper subscriptions for all those who are interested in knowing about the advances and challenges of vaccination in the Americas. To subscribe:

http:/new.paho.org/hq/index.php?option=com_content&task=view&id=3130&Itemid=35 04&lang=es

Links: Book Thirty Years of the Immunization Newsletter: History of the Expanded Program on Immunization in the Americas:

www.paho.org/inb Immunization Newsletter: www.paho.org/immunization/boletin (Spanish) www.paho.org/immunization/newsletter (English)

PAHO Immunization: http:/new.paho.org/hq/index.php?option=com_content&task=blogcategory&id=956&Itemid=358

The countries of the Americas are pioneers in vaccination in the world, according to the experts: http:/new.paho.org/hq/index.php?option=com_content&task=view&id=5640&Itemid=1926

Contact: Leticia Linn, PAHO/WHO Media and Communication,

Telephone: 202-974-3440; Mobile phone: 202-701-4005;

E-mail: linn@paho.org–www.paho.org 

  • ECOLOGICAL ANALYSIS OF HEALTH CARE UTILIZATION FOR CHINA'S RURAL POPULATION

‘This study highlights that richer rural households with a greater ability to pay are more able to use health services in China.’

Ecological analysis of health care utilisation for China's rural population: association with a rural county's socioeconomic characteristics

 

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/10/664

 

Kam Ling Chau

London Health Observatory, London, UK

author email corresponding author email

BMC Public Health 2010, 10:664doi:10.1186/1471-2458-10-664

Abstract

Background

The problem of accessibility and affordability of health care is reported to be a major social concern in modern China. It is pronounced in rural households which represent 60% of China's population. There are a few large scale studies which have been conducted into socioeconomic inequalities in health care utilisation for rural populations. Those studies that exist are mainly bivariate analyses. The aim of this study is to examine the relationship between socioeconomic characteristics and health service utilisation among rural counties, using aggregated data from a nationally representative dataset, within a multivariate regression analysis framework.

Methods

Secondary data analysis was conducted on China's National Health Services Survey (NHSS) 2003. Aggregated data on health care utilisation, socioeconomic position, demographic characteristics and health status were used. The samples included 67 rural counties. Multivariate linear regression analyses were performed.

Results

The results of the ecological multivariate analyses showed a positive relationship between private insurance coverage and the use of outpatient care (p-value < 0.05, standardised coefficient = 0.22). Annual income was positively correlated with annual medical expenditure (p-value < 0.01, standardised coefficient = 0.56). A rural county's area socioeconomic stratum, a composite measure frequently used in bivariate studies including the NHSS analysis report, could not explain any association with the use of health care.

Conclusions

This study highlights that richer rural households with a greater ability to pay are more able to use health services in China. The findings suggest that the scope of medical insurance might be restrictive, or the protection provided might be limited, and the health care costs might still be too high. Additional efforts are required to ensure that poorer Chinese rural households are able to utilise health care according to their needs, regardless of their income levels or private insurance coverage. This would require targeted strategies to assist low income families and a broad spectrum of interventions to address the social determinants of health.

  • ·        PAHO/WHO BLOG ON SOCIAL DETERMINANTS OF HEALTH

The blog:

http://new.paho.org/blogs/dss/          

WHO Technical Paper on the Social Determinants of Health: http://bit.ly/ruzJlM

  • SOCIAL MOBILIZATION APPROACHES TO POLIO ERADICATION IN NORTHERN INDIA

Uttar Pradesh and Bihar have seen no wild poliovirus in 2011. Would they have gotten this far without tailored approaches to social mobilization?

Those interested in the experience of northern India may also be interested in the Pakistan article 'Polio Eradication from their Perspective,' at http://www.childsurvival.net/?content=com_articles&artid=339

Outcomes of polio eradication activities in Uttar Pradesh, India: the Social Mobilization Network (SM Net) and Core Group Polio Project (CGPP)

William M Weiss1 , MH Rahman1 , Roma Solomon2 , Vibha Singh3 and Dora Ward4

Department of International Health, Johns Hopkins Bloomberg School of Public Health, 615 North Wolfe Street, Suite E8132, Baltimore, MD 21205, USA

CORE Group Polio Project - India, 45/201 Heritage City, MG Road, Gurgaon, India

CORE Group Polio Project - India, 106A/1, Gautam Nagar, New Delhi, India

CORE Group Polio Project, 151 Ellis Street, NE, Atlanta, GA 30303, USA

author email corresponding author email

BMC Infectious Diseases 2011, 11:117doi:10.1186/1471-2334-11-117

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2334/11/117

© 2011 Weiss et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

The primary strategy to interrupt transmission of wild poliovirus in India is to improve supplemental immunization activities and routine immunization coverage in priority districts with a focus on 107 high-risk blocks of western Uttar Pradesh and central Bihar. Villages or urban areas with a history of wild poliovirus transmission, or hard-to-reach or resistant populations are categorized as high-risk areas within blocks. The Social Mobilization Network (SM Net) was formed in Uttar Pradesh in 2003 to support polio eradication efforts through improved planning, implementation and monitoring of social mobilization activities in those high-risk areas. In this paper, we examine the vaccination outcomes in districts of SM Net where the CORE Group works.

Methods

We carried out a secondary data analysis of routine monitoring information collected by the SM Net and the Government of India. These data include information about vaccination outcomes in SM Net areas and non-SM Net areas within the districts where the CORE Group operates. Statistical analysis was used to compare, between SM Net and non-SM Net areas, vaccination outcomes considered sensitive to social mobilization efforts of the SM Net. We employed Generalized Estimating Equations (GEE) statistical method to account for Intra-cluster Correlation (ICC), and used 'Quasi-likelihood under the independence model criterion (QIC)' as the model selection method.

Results

Vaccination outcomes in SM Net areas were as high as or higher than in non-SM Net areas. There was considerable variation in vaccination outcomes between districts.

Conclusions

While not conclusive, the results suggest that the social mobilization efforts of the SM Net and the CORE Group are helping to increase vaccination levels in high-risk areas of Uttar Pradesh. Vaccination outcomes in CORE Group areas were equal or higher than in non-CORE, non-SM Net areas. This occurred even though SM Net areas are those with more community resistance to polio vaccination and/or are have harder-to-reach populations than non-SM Net areas. Other likely explanations for the relatively good vaccination performance in SM Net areas are not apparent.

 

  • WHERE THERE IS NO DOCTOR

Now in its eleventh printing, 'Where There is no Doctor' is a practical guide for community health workers. Originally published in paper editions in English and Spanish, it has now appeared in both electronic and paper editions in several dozen languages.

For details about paper and electronic editions, consult the Hesperian Foundation homepage at
http://www.hesperian.org/mm5/merchant.mvc?Store_Code=HB&Screen=PROD&Product_Code=B010R

Other publications from the same publisher are available at www.hesperian.org

Good reading.

 

  • ·         LAURIE GARRETT SPEAKS ON LESSONS FROM THE FLU PANDEMIC OF 1918

Another offering from www.ted.com

 

http://www.ted.com/talks/lang/eng/laurie_garrett_on_lessons_from_the_1918_flu.html

 

  • ·         TWO VIEWS ON THE ADVANCE MARKET COMMITMENT 

Query to readers: why is it that the second generation meningococcal meningitis vaccine, unique among the vaccines new to the world since 2000, is priced at <<$1? Comments welcome.

 

 One view from California:

http://www.landesbioscience.com/journals/vaccines/News-HV7-2-policy.pdf

 One view from Kenya:

 

Human Vaccines 7:3, 302-302; March 2011; © 2011 Landes Bioscience

NEWS

Human Vaccines Volume 7 Issue 3

Why the AMC Matters

Frederick Were. Email: fwere@hcc.or.ke

Donald Light’s recent piece criticizing the Pneumococcal Vaccine Advance Market Commitment (AMC) caught my attention just days before Kenya became the first developing country to benefit from the AMC. While I do not feel qualified to respond to his criticisms of the mechanism’s structure, as a pediatrician in my home country of Kenya for more than twenty years, I am qualified to say that I have witnessed far too many children lose their fight against pneumonia, the world’s leading killer of children. Furthermore, I firmly believe the AMC is going to make an enormously positive impact on families and children in my country by preventing much of this needless suffering and death.

 Nearly one in 10 children born in Kenya die before their fifth birthday,1 a statistic to which pneumonia is a significant contributor. The disease claims the lives of more than 30,0002 Kenyan children under age five per year. The burden of the pneumonia case load also places a tremendous strain on our medical system, as tens of thousands of children battling a preventable disease crowd our fragile public hospitals, often requiring choices to be made about who receives adequate care.

 Dr. Light speculates on whether this is really an important disease to address by suggesting that funds be directed to other health interventions and questions the significant body of evidence on the efficacy and effectiveness of pneumococcal conjugate vaccines.

It has been shown, however, that the primary cause of severe pneumonia in Kenya is the pneumococcus and that most of the circulating disease-causing serotypes will be prevented by the newest pneumococcal conjugate vaccines.3,4

Each year, more than 14.5 million cases of serious pneumococcal disease occur, resulting in more than half a million deaths among children under five years of age worldwide, 95 percent of which occur in the developing world.5 A Kenyan child is 160 times more likely to die of pneumococcal disease than an American child.6 This gap is evidence of the great inequality in access to preventive measures like immunization. Historically, 15 or 20 years have passed before new vaccines reached the developing world, largely because of high costs and limited vaccine supplies. Thanks to the Advance Market Commitment (AMC), Kenya introduced PCV-10, an advanced-protection pneumococcal conjugate vaccine, this February—and within months of the US adopting a similar next-generation vaccine. Kenya has thus become one of the first of many developing countries to directly benefit from the support of the AMC.

 Access to life-saving pneumococcal vaccines would have been impossible for us without this historic innovation. Tackling child mortality in my country and throughout Africa requires an approach to preventing and controlling the childhood diseases with the most significant disease burden—pneumonia and diarrhea—that encourages research and development, fosters investment and allows countries to access vaccines at affordable prices. The AMC is now doing just that.

 While the AMC may have its critics, they won’t be among the children and families benefiting from the vaccine in my country, or the 19 other countries to which GAVI has already committed AMC funds. The AMC is taking a systematic approach to disease prevention—one that holds the promise of delivering vaccines to the most needy, as well as helping to strengthen critical health infrastructure that will ultimately enable a deeper and more seamless deployment for future immunization programs to battle other deadly infectious diseases in the future.

 For families in developing countries like ours, the AMC promises to level the playing field by finally open access to the most needed vaccines, providing for the first time an early opportunity to significantly reduce suffering, disease burden and child mortality.

 

References

1. http://data.worldbank.org/indicator/SI.POV.2DAY

2. http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)60549-1/fulltext

3. O’Brien KL, et al. Lancet. 2009; 374:893-902.

4. Johnson HL, et al. PLoS Med. 2010; 7:e1000348.

5. World Health Organization. World health statistics 2006. Geneva: World Health Organization; 2006. http://www.who.int/whosis/whostat2006.pdf. Accessed

September 6, 2009.

6. O’Brien KL, et al. Lancet. 2009; 374:893-902.

 

 

WHAT’S NEW THIS WEEKEND: THREE ON EQUITY, ONE ON PERDIEMITIS

If you would like to get a bird’s eye view of equity issues from your own country, there are few better sources than the International Journal for Equity in Health, edited until recently by the late, great Professor Barbara Starfield, and accessible at http://www.equityhealthj.com/

  • GLOBAL CHALLENGES OF IMPLEMENTING HUMAN

PAPILLOMAVIRUS VACCINES

 

Full text at http://www.equityhealthj.com/content/pdf/1475-9276-10-27.pdf

 

 

Janice E Graham 1*§, Amrita Mishra*2

1 Department of Bioethics, Dalhousie University, Faculty of Medicine, 1459 Oxford

Street, Halifax, Nova Scotia, Canada B3H 4R2

Phone: (902) 494-1897, Fax: (902) 494-3865.

2 Technoscience and Regulation Research Unit, 1459 Oxford Street, Halifax, Nova

Scotia, Canada B3H 4R2, Phone: (902) 494-6733, Fax: (902) 494-3865.

 

* These authors contributed equally to this work

§Corresponding author

Email addresses:

JG: janice.graham@dal.ca

AM: amrita.mishra@dal.ca

 

Abstract

 

Human Papillomavirus vaccines are widely hailed as a sweeping pharmaceutical

innovation for the universal benefit of all women. The implementation of the

vaccines, however, is far from universal or equitable. Socio-economically

marginalized women in emerging and developing, and many advanced economies

alike, suffer a disproportionately large burden of cervical cancer. Despite the

marketing of Human Papillomavirus vaccines as the solution to cervical cancer, the

market authorization (licensing) of the vaccines has not translated into universal

equitable access. Vaccine implementation for vulnerable girls and women faces

multiple barriers that include high vaccine costs, inadequate delivery infrastructure,

and lack of community engagement to generate awareness about cervical cancer and

early screening tools. For Human Papillomavirus vaccines to work as a public health

solution, the quality-assured delivery of cheaper vaccines must be integrated with

strengthened capacity for community-based health education and screening.

 

 

  • VIEWING THE KENYAN HEALTH SYSTEM THROUGH AN EQUITY LENS

 

'The Kenyan health system is highly inequitable and policies aimed at promoting equity and addressing the needs of the poor and vulnerable have not been successful. Some progress has been made towards addressing equity challenges, but universal coverage will not be achieved unless the country adopts a systemic approach to health financing reforms.'


International Journal for Equity in Health

Viewing the Kenyan health system through an equity lens: Implications for universal coverage

Jane Chuma and Vincent Okungu

International Journal for Equity in Health 2011, 10:22 doi:10.1186/1475-9276-10-22

Full text is at http://www.equityhealthj.com/content/10/1/22/abstract

Published: 26 May 2011

Abstract (provisional)

Introduction

Equity and universal coverage currently dominate policy debates worldwide. Health financing approaches are central to universal coverage. The way funds are collected, pooled, and used to purchase or provide services should be carefully considered to ensure that population needs are addressed under a universal health system. The aim of this paper is to assess the extent to which the Kenyan health financing system meets the key requirements for universal coverage, including income and risk cross-subsidisation. Recommendations on how to address existing equity challenges and progress towards universal coverage are made.

Methods

An extensive review of published and gray literature was conducted to identify the sources of health care funds in Kenya. Documents were mainly sourced from the Ministry of Medical Services and the Ministry of Public Health. Country level documents were the main sources of data. In cases where data were not available at the country level, they were sought from the World Health Organisation website. Each financing mechanism was analysed in respect to key functions namely, revenue generation, pooling and purchasing.

Results

The Kenyan health sector relies heavily on out-of-pocket payments. Government funds are mainly allocated through historical incremental approach. The sector is largely underfunded and health care contributions are regressive (i.e. the poor contribute a larger proportion of their income to health care than the rich). Health financing in Kenya is fragmented and there is very limited risk and income cross-subsidisation. The country has made little progress towards achieving international benchmarks including the Abuja target of allocating 15% of government's budget to the health sector.

Conclusions

The Kenyan health system is highly inequitable and policies aimed at promoting equity and addressing the needs of the poor and vulnerable have not been successful. Some progress has been made towards addressing equity challenges, but universal coverage will not be achieved unless the country adopts a systemic approach to health financing reforms. Such an approach should be informed by the wider health system goals of equity and efficiency.

‘North African countries have still a long way to go to reduce social inequalities and health inequity at different levels: rural-urban, advantaged-marginalised regions and cities, between groups of different level of income and wealth.’

equityhealthj.com/article

  

 

  • SOCIAL INEQUALITIES, REGIONAL DISPARITIES AND HEALTH INEQUITY IN NORTH AFRICAN COUNTRIES. 

Abdesslam Boutayeb and Uwe Helmert

International Journal for Equity in Health 2011, 10:23 doi:10.1186/1475-9276-10-23

 

Full text is at

http://www.equityhealthj.com/content/pdf/1475-9276-10-23.pdf

 

Abstract (provisional)

Background

During the last decades, North African countries have substantially improved economic, social and health conditions of their populations in average. In all countries, human development in general and life expectancy, literacy and per capita income in particular have increased. However, improvement was not equally shared between groups of different milieu, regions or level of income. Social inequalities and health inequity have persisted or even worsened. Data are generally scarce and few studies were devoted to this topic in North Africa as a region. In this paper, we carry out a comparative study on the achievements of these countries, not only in terms of human development and its components but also in terms of inequalities reduction and health equity.

Method

This study is based on data available for comparison between North African countries. The main data sources are provided by reports released by the World Health Organization(WHO), United Nations Development Programme(UNDP), United Nations Children's Fund (UNICEF), the World Bank, surveys such as Demographic Health Surveys (DHS) and Multiple Indicator Cluster Surveys (MICS) and finally recent papers published on equity in different countries of the region.

Results and discussion

There is no doubt that education, health and human development in general have improved in North Africa during the last decades. Improvement was, however, uneven and unequally enjoyed by different socioeconomic groups. Indeed, each country included in this study shows large urban-rural disparities, discrepancies between advantaged and disadvantaged regions and cities; and unacceptable differences between rich and poor. Health inequity is particularly seen through access to health services and infant mortality.

Conclusion

During the last decades, North African decision makers have endeavoured to improve social and economic conditions of their populations. Globally, health, education and living standard in general have substantially improved in average. However, North African countries have still a long way to go to reduce social inequalities and health inequity at different levels: rural-urban, advantaged-marginalised regions and cities, between groups of different level of income and wealth. The challenge for the next decade is not only to improve economic, social and health conditions in average but also and mainly to reduce avoidable inequalities in parallel.

 

  • PERDIEMITIS

 

Per diems undermine health interventions, systems and research in Africa: burying our heads in the sand

Valéry Ridde1,2,3

Article first published online: 28 JUL 2010

Tropical Medicine & International Health

Early View (Online Version of Record published before inclusion in an issue)

Additional Information(Show All)

How to CiteAuthor InformationPublication History

How to Cite

Ridde, V. (2011), Per diems undermine health interventions, systems and research in Africa: burying our heads in the sand. Tropical Medicine & International Health, 16: no. doi: 10.1111/j.1365-3156.2010.02607.x

Author Information

1

 Research Centre of the University of Montreal Hospital Centre, Montreal, QC, Canada

2

 Department of Social and Preventive Medicine, University of Montreal, QC, Canada

3

 Institut de Recherche en Sciences de la Santé, CNRST, Burkina Faso

*Correspondence: Corresponding Author Valéry Ridde, CRCHUM, 3875 St-Urbain, 507, Montréal, QC H2W 1V1, Canada. Tel.: +1 514 890–8156; Fax: +1 514 412 7108; E-mail: valery.ridde@umontreal.ca

Acute ‘perdiemitis’ is decidedly one of the most prevalent illnesses in African public health projects. When a novice (African or Westerner) first undertakes a research project or implements a public health intervention, he will encounter the diplomatically phrased question: ‘What are the administrative modalities?’ These days, anyone attending a research results presentation workshop, a training session, or an intervention expects that the organizers will pay him a premium – a per diem – for his participation. While per diems appear to have been originally used to compensate for the loss of time and income caused by such participation, today they have become political instruments that taint research and intervention activities. If some expect that Africa will not achieve the Millennium Development Goals by 2015 (Murray et al. 2007), we believe per diems are contributing to that expected failure (without, of course, explaining it entirely), because they reduce the potential effectiveness of interventions and dilute health sector resources. While this commentary is focused on the health sector, it should be clearly noted that the issue of per diems also affects other areas such as housing construction (Bähre 2005), economic development (Phonphakdee et al. 2009) and water supply (Bradley & Karunadasa 1989). The aim of this commentary is not to throw stones at anyone in particular. Rather, it is to bring to light this phenomenon, known to all but seldom mentioned and little studied (Vian 2009), to suggest a deliberative process (Culyer & Lomas 2006) to find an equitable treatment for this long-neglected disease.

The arrival of per diems and the reasons behind them

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

References

While the history of per diems remains to be written, it appears these practices arose at the end of the 1970s with the growth of development aid. Up to then, health workers carried out their activities and were remunerated with their salaries and no other payments except for travel costs. They were often hosted in remote regions by their colleagues or by villagers, who housed and fed them. Then, the massive arrival of the development industry gave rise to new funding modalities. In these development projects, very well-paid expatriate aid workers carried out activities with their African colleagues who were much less well paid. Thus, the aid workers introduced these per diems, perhaps out of ethical concerns, but mainly motivated by a desire for effectiveness, to ensure these activities would take place. As the years went by, habits were formed, and the practice was institutionalized; even the Financial Times called it ‘the culture of the ‘per diem’’ (Jack 2009). Today, it has practically become a right, and some States (e.g. Niger, Mali, Burkina Faso) even legislate on the subject.

For example, in 2007 in Burkina Faso, five presidential decrees dealt with project functioning and the standardization of per diem rates. The hierarchy of per diems was established, with drivers receiving less than project coordinators, even though they might be assumed to have the same needs for food and lodging. However, donor agencies were not willing to ‘align’ themselves (to use the Paris Declaration terminology) with these amounts; nor were they able to agree on an alternative. In early 2010, in Mali, the United Nations agencies standardized their rates by distributing an official rate schedule for the country’s civil servants. They thereby formalized the fact, for instance, that someone attending a training session in the capital, his city of residence, must receive an amount equivalent to $10 US (5000 F CFA) for transportation costs. Article four of Decree 779 in Burkina Faso, in 2007, ratified exactly the same principles and the same amount. It thus became difficult to organize training sessions without paying the attendees, or to hold a press conference without paying the journalists.

‘The tyranny of per diem’ (Jack 2009) has made it impossible to do much of anything without these payments. The competition among projects, public servants’ low salaries in the face of an ever-growing cost of living (and for some, the desire for display) and the need to maintain one’s social status have all contributed to the generalization of this practice. Jaffré (2003), like Dujardin (2003), thus explains that in West Africa, health workers’ inadequate salaries do not allow them to undertake inter-community communication ‘upon which mutual support among families or ‘colleagues’ is based.’ Structural adjustment programs, the demands of maintaining and even reducing salary costs (Chêne 2009) and the weakening of the role of the States in Africa (Olivier de Sardan 2000) have led to a situation in which these per diems have become essential for civil servants. Per diems have progressively become supplementary sources of income (Muula & Maseko 2006; McCoy et al. 2008) that are never taxed. One study in two districts of Burkina Faso showed that health workers’ median annual income from per diems exceeded their salaries ($1900 vs. $1500 US) (Ensor et al. 2006).

Reducing the effectiveness of public health interventions

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

References

Fifteen years of observations allow me to bring to light certain abuses. Some project leaders will offer higher daily rates than a competing project to be sure they will have more public servants at their training sessions. Sometimes a workshop will be organized in a remote region because per diem rates are higher outside the capital (Vian 2009). Civil servants will sign attendance sheets in several different workshops on the same day to obtain several per diems. This has been called the ‘leapfrog’ strategy (Muula & Maseko 2006), or ‘hunting and gathering’ (Swidler & Watkins 2009). Some officials will sign for a colleague to obtain and share the income. One person with whom I discussed this practice called per diems ‘legalized corruption’. Per diems’ corruptive role was well explained in a study carried out in a neighbourhood of Cape Town in South Africa (Bähre 2005). The use of per diems could thus be seen as a form of corruption (Chêne 2009) that helps to make sense of, among other things, ‘the entire functioning (or rather, dysfunctioning) of the State’ (Blundo & Olivier de Sardan 2000).

It is also well understood that the per diem problem is not confined to Africans or Asians (Chêne 2009). Many expatriates, international experts and researchers from prosperous countries blithely take advantage as well, which partly explains the negotiated order (Strauss 1978) and the total absence of debate on per diems. This order is a construct that is social, negotiated and temporal, within a context of interactions between the societal actors that, for the time being, favours the status quo. The per diem rate for travel greatly exceeds the cost of living in the countries these workers visit, even when, for the sake of representation, they require more commodious lodging. But, as was explained to me by someone criticized by his colleagues for organizing more overseas missions than necessary and for living in precarious conditions on these missions, ‘this allows me to save some money’. These examples could be endlessly multiplied, although it is important to point out that not all actors adopt these practices. Fortunately, there are still some researchers, nurses and senior officials who do not play this game.

Contributing to healthcare systems dysfunction

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

References

Very often, these practices have dramatic impacts on the healthcare system. The players plan their actions around the primary goal of acquiring per diems, rather than of effecting changes among the publics targeted by their intervention. We are witnessing the notorious ‘workshop syndrome’ (Foster 1987), dubbed ‘trainingism’ in the 1970s (Schaffer 1974). ‘It can happen that bureaucrats will go through five identical training sessions. And after all that, they have learned nothing.’ (Hakizimana 2007). While health workers reap the benefit of per diems, the general population is not blind. People are fully aware of this way of operating, even as health policies stress the importance of their volunteering to serve on health centres’ management committees. Comparing these health workers’ salaries to the incomes of the rural population, we are justified in considering these practices unethical on the part of those who have sworn to serve the State and to respect the Hippocratic oath. Some health workers have even coined a vulgar expression for when the rate provided is too low: a ‘merdiem’ (‘crap diem’). Health workers will rarely go out to vaccinate children if they do not ‘get something in return’, such as on National Vaccination Days.

The impact of the per diem practice described in our article, as well as in other studies in Mozambique (Pfeiffer 2003), Nigeria (Smith 2003), Mali (Berche 1998) and Burkina Faso (Nguyen 2002; Ridde 2008), is deleterious to the organization of health systems in Africa. For example, Jacquemot (2007), considers that per diems are the cause of poor morale among civil servants in Ghana who do not have access to them and who, being thus disillusioned, do not take part in development processes. Yet there are very few studies on per diems, and we know little about the underground economy and the financial contribution of such practices to the healthcare system. This subject is off-limits, and researchers would rather study performance-based bonuses than raise the sensitive question of per diems. Certainly, the amount spent on per diems at the level of an entire country could be applied to improving workers’ performance. For example, in Tanzania, the budget allocated to daily allowances (per diems) for the 2008/09 fiscal year came to $390 million US (Chêne 2009).

Questions around research ethics and knowledge transfer

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

References

These per diem practices that have been around for a long time and that corrupt public health interventions are finding their way into research ethics. A woman is given ‘soap money’ as a reward for completing a questionnaire on maternal mortality. The village residents are not fools; they are perfectly aware of the salaries of the surveyors who come to question them, while they rarely see the results of the studies and their living conditions do not change. Some ethics committees in Africa now demand per diems to analyse the ethical qualities of research protocols. These days, when we organize a meeting to share the results of a study that are useful for action, which is now part of the researchers’ responsibility (Ridde 2009), we must pay per diems to decision-makers to ensure their attendance. The practice of paying per diems in research is also detrimental; it is therefore important to pay attention to their consequences to ensure our research practices are ethical (Nuffield Council on Bioethics 2005).

Finding a solution together

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

References

Obviously, there are no simple solutions to such a complex problem. Ideas for solutions can only emerge if there is a public and participative process involving all stakeholders, because even the donor agencies are not aligned on this subject, contrary to the Paris Declaration. Given the stakes, quick decisions will not work. Everyone has buried their head in the sand. Who will dare to bring this phenomenon out into the open? To find a solution for any given problem requires that it be acknowledged, first, as a public problem (Rochefort & Cobb 1994). Yet, for the time being, the question of per diems does not figure at any discussion table in the international arena of research and development projects. At some point, we will need to consider how to address this problem. Should we

• 

ask the donor agencies to convert per diem budgets to financial support for improving salaries and working conditions?

• 

legislate the rates for per diems to harmonize practices and make the system transparent?

• 

pay per diems in accordance with needs rather than administrative hierarchies?

• 

insist on more effective governance models?

• 

review the salaries of staff in High Income Countries institutions to make them more reasonable?

All of these are questions that are worth presenting dispassionately to the development community for serious consideration.

Acknowledgements

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

References

V. Ridde is a Canadian Institutes for Health Research (CIHR) New Investigator. Thanks to Emilie Robert for literature search and Donna Riley for translation and editing support.

References

Top of page

The arrival of per diems and the reasons behind them

Reducing the effectiveness of public health interventions

Contributing to healthcare systems dysfunction

Questions around research ethics and knowledge transfer

Finding a solution together

Acknowledgements

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  • PROJECTIONS OF GLOBAL HEALTH OUTCOMES FROM 2005 TO 2060 

Full text, with graphics, is at

http://www.who.int/bulletin/volumes/89/7/10-083766.pdf

Projections of global health outcomes from 2005 to 2060 using the International Futures integrated forecasting model

Barry B Hughes,a Randall Kuhn,a Cecilia M Peterson,a Dale S Rothman,a José R Solórzano,a Colin D Mathersb & Janet R Dicksona

Objective To develop an integrated health forecasting model as part of the International Futures (IFs) modelling system.

Methods

The IFs model begins with the historical relationships between economic and social development and cause-specific mortality used by the Global Burden of Disease project but builds forecasts from endogenous projections of these drivers by incorporating forward linkages from health outcomes back to inputs like population and economic growth. The hybrid IFs system adds alternative structural formulations for causes not well served by regression models and accounts for changes in proximate health risk factors. Forecasts are made to 2100 but findings are reported to 2060.

Findings

The base model projects that deaths from communicable diseases (CDs) will decline by 50%, whereas deaths from both non-communicable diseases (NCDs) and injuries will more than double. Considerable cross-national convergence in life expectancy will occur. Climate-induced fluctuations in agricultural yield will cause little excess childhood mortality from CDs, although other climate−health pathways were not explored. An optimistic scenario will produce 39 million fewer deaths in 2060 than a pessimistic one. Our forward linkage model suggests that an optimistic scenario would result in a 20% per cent increase in gross domestic product (GDP) per capita, despite one billion additional people. Southern Asia would experience the greatest relative mortality reduction and the largest resulting benefit in per capita GDP.

 

Conclusion Long-term, integrated health forecasting helps us understand the links between health and other markers of human progress and offers powerful insight into key points of leverage for future improvements.

  • ·         SCALING UP GLOBAL HEALTH INTERVENTIONS

Summary Points

The rise in international aid to fund large-scale global health programs over the last decade has catalyzed interest in improving the science of scale-up.

This Essay draws upon key themes in the emerging science of large-scale change in global health to propose a framework for explaining successful scale-up.

Success factors for scaling up were identified from interviews with implementation experts and from the published literature.

These factors include the following: choosing a simple intervention widely agreed to be valuable, strong leadership and governance, active engagement of a range of implementers and of the target community, tailoring the scale-up approach to the local situation, and incorporating research into implementation.

Best viewed at http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1001049


Scaling Up Global Health Interventions: A Proposed Framework for Success

Drawing upon interviews with experts and a review of the literature, Gavin Yamey proposes a new framework for scaling up global health interventions.

Gavin Yamey*

Evidence-to-Policy Initiative, Global Health Group, San Francisco, California, United States of America

Citation: Yamey G (2011) Scaling Up Global Health Interventions: A Proposed Framework for Success. PLoS Med 8(6): e1001049. doi:10.1371/journal.pmed.1001049

 

  • MASS DRUG TREATMENT AGAINST TRACHOMA IN TANZANIA

‘Country programs in trachoma-endemic regions must realistically expect that several years of annual mass treatment may be necessary to eliminate trachoma.’

Best viewed at http://jid.oxfordjournals.org/content/204/2/268.full?etoc

Journal of Infectious Diseases

Number of Years of Annual Mass Treatment With Azithromycin Needed to Control Trachoma in Hyper-endemic Communities in Tanzania

1. 1.   Sheila K. West1, Beatriz Munoz1, Harran Mkocha4, Charlotte A. Gaydos2 and Thomas C. Quinn2,3

+ Author Affiliations

1. 1.    1Department of Opthalmology, Dana Center for Preventive Ophthalmology

2. 2.    2International Chlamydia Laboratory, Division of Infectious Diseases, Johns Hopkins Medical Institutions, Baltimore

3. 3.    3Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland

4. 4.    4Kongwa Trachoma Project, Kongwa, Tanzania

5. Correspondence: Sheila K. West, PhD, Wilmer Rm 129, Wilmer Eye Institute, Johns Hopkins Hospital, 600 N Wolfe St, Baltimore, MD 21287 (shwest@jhmi.edu).

 

Abstract

Background. The World Health Organization recommends mass treatment as part of a trachoma control strategy. However, scant empirical data from hyperendemic communities exist on the number of rounds of treatment needed to reach a goal of <5% prevalence in children. We determined the prevalence of trachoma and infection with Chlamydia trachomatis in communities after 3–7 years of annual mass treatment in Tanzania.

Methods. Seventy-one communities with trachoma and annual azithromycin coverage data were enrolled. A cross-sectional survey of ≥100 randomly selected children aged <5 years in each community was performed. Children were examined for clinical trachoma, and swab samples were taken for determination of ocular C. trachomatis infection.

Results. After 3 years of mass treatment, the prevalence of trachoma decreased in a linear fashion with number of years of mass treatment, whereas decreased prevalences of C. trachomatis infection were related to the extent of the previous year’s azithromycin coverage. Our model suggests that, for communities with baseline trachoma prevalence of 50% and annual treatment coverage of 75%, >7 years of annual mass treatment will be needed to reach a prevalence of trachoma of <5%.

Conclusions Country programs in trachoma-endemic regions must realistically expect that several years of annual mass treatment may be necessary to eliminate trachoma.

     MIDWIFERY, MATERNAL MORTALITY REDUCTION, AND MDG 5

This UNFPA report, the result of collaborative efforts by 30 partners, shows the links between midwifery and reductions in maternal mortality.

Full text, http://www.unfpa.org/sowmy/report/home.html#

From  the Executive Summary, The State of the World’s Midwifery 2011

It is a responsibility of governments and their political leaders and an investment that is key to reducing maternal and newborn mortality and morbidity. In addition to saving lives and preventing disability, the benefits of quality midwifery services extend to all members of society in farreaching ways, including contributing to a country’s human and economic development.

There is much that needs to be done. Every year approximately 350,000 women die while pregnant or giving birth, up to 2 million newborns die within the first 24 hours of life, and there are 2.6 million stillbirths. The overwhelming majority of these deaths occur in low-income countries and most of them could have been prevented. They happen because women — usually the poor and marginalized — have no access to functioning health facilities or to qualified health professionals.

Quality midwifery services that are coordinated and integrated within communities and within

the health system ensure that a continuum of essential care can be provided throughout pregnancy, birth and beyond. Midwifery services also facilitate referrals of mothers and newborns from the home or health centre to the hospital and to the care of obstetricians, paediatricians and other specialists when required.

The State of the World’s Midwifery 2011: Delivering Health, Saving Lives, coordinated by the United Nations Population Fund (UNFPA), is the result of the collaborative efforts of 30 agencies and organizations and hundreds of individuals working at national, subnational, regional and global levels.

It responds to the ‘Global Call to Action’ issued at the Symposium on Strengthening Midwifery.  Increasing women’s access to quality midwifery services has become a focus of global efforts to realize the right of every woman to the best possible health care during pregnancy and childbirth.

The diversity of responses confirms that there are significant gaps in data and strategic intelligence. However, three key points have emerged from a synthesis of the available evidence relating to the status of the profession and the many challenges and barriers that affect the midwifery workforce, its development and its effectiveness.

There is a triple gap, consisting of competencies, coverage and access. In most countries there are not enough fully-qualified midwives and others with midwifery competencies to manage the estimated number of pregnancies, the subsequent number of births, and the 15 percent of births that generally result in obstetric complications. WHO estimates that 38 countries have severe shortages. A few countries will need more than a 10-fold increase in the number of midwives, with most needing to either double, triple or qadruple their midwifery workforce to improve quality and coverage. Second, coverage of emergency obstetric and newborn care facilities is low; and existing facilities are often insufficiently staffed and poorly equipped. This is most acute in rural and/or remote communities. Third, access issues from women’s perspectives are often not addressed.

 [complete executive summary at http://www.unfpa.org/sowmy/resources/docs/main_report/en_SOWMR_ExecSum.pdf ]

  • OF CIGARETTES, RATS AND TRANS FATS: CDC DIRECTOR THOMAS FRIEDEN ON LEADING IN PUBLIC HEALTH, WHEN SUCCESS IS WHAT YOU DON’T SEE 

 Washington Post, Posted at 12:25 PM ET, 06/21/2011

 By Tom Fox

Dr. Thomas R. Frieden became the director of the Centers for Disease Control and Prevention (CDC), and administrator of the Agency for Toxic Substances and Disease Registry in June 2009, following a seven-year stint as New York City Health Department Commissioner. He has worked on tuberculosis issues in New York and India and spent 12 years with the CDC earlier in his career.

What management lessons did you learn while serving as New York City Health Commissioner?

One was the importance of data. This is really core. We live and die in public health based on how good our data is. Take tobacco control in New York City. I was surprised to find in the epidemiologic information that tobacco was still, by far, the leading preventable cause of death. When I was approached for the job I said, "I've looked at the epidemiology and it's clear that tobacco is your number one problem and there's a way of addressing tobacco that's not being done. It will be very controversial. Are you willing to do that?" Mayor Bloomberg said, "Absolutely, yes." The first thing he did was increase the tobacco tax.

Next, I proposed we make all workplaces smoke free. Data showed that going smoke-free would save over 10,000 lives. We also showed that the level of pollution in a smoky bar was more than 50 times worse than the level of pollution in the most polluted place that people in New York City can think of: the entrance to the Holland Tunnel. It was a simple study done with a low-cost tool.

In six years, tobacco use went down by 25 percent among adults and 52 percent among kids. When the city started facing huge budget cuts, I was excoriated by the city council for spending so much money on anti-tobacco advertising when we had to reduce our staffing levels. Yet surveys allowed me to say, under oath, with complete certainty, that for every $1 million in anti-tobacco ads we spend, we save at least 1,500 lives. The data at every point in the effort was essential to define the problem, delineate the solution, determine if what we did was working and defend the program. Another example was the community health survey. We did a 10,000-respondent, random digit-dial survey in 43 neighborhoods. We learned that our educational activities about West Nile virus were completely ineffective. Instead, we just handed out mosquito repellant at senior centers. We were able to cut out an ineffective program and pay for the survey by reducing the ineffective educational efforts.

Another lesson was the importance of focus. There is a wide variety of issues in public health — communicable diseases, environmental risks, injuries, chronic diseases. You have to manage them all or they will manage you. You have to focus on where you can make a difference.

Where do you get your program ideas and how do you work to involve employees?

You build on the culture of the organization and support the front-line staff and managers so they’re free to suggest, “I think there's a better or cheaper way to do this.” We opened public health offices in the three sickest, poorest neighborhoods in New York City — Bedford-Stuyvesant, Harlem, including East Harlem and the South Bronx. We canvassed the community asking, “What's your biggest problem?” This may not be the greatest thing to talk about but, resoundingly, we got back something we never would have expected: rat control. Widespread infestations gave people a sense their community was not being attended to or valued. It's not so easy to get rid of rats. But through a multi-year effort, we found the best urban rodentologist in the world and piloted new ways to implement programs. The approach seems to be having significant success.

Great ideas are everywhere. We accomplished a lot in New York, but very little originated with us. California had gone smoke free previously. Denmark had eliminated trans fats. The menu labeling idea was around for a long time. We did a lot of innovative things, but we didn’t have to invent a new mouse trap.

How do you manage and motivate employees, and get their feedback?

I manage by walking around and interacting with staff. We’ve had great feedback resulting in better processes. Cash awards and bonuses are important. We also want to make sure that our evaluation system recognizes excellence. I highlight effective programs from around the agency, things that people may not know about that are exciting. But if managers don't address performance problems, it undermines morale throughout the federal government.

At CDC there's a real sense we're not here to worship what's known, but to question it. If someone gets up and gives a fancy talk they're really proud of, it's not rude to stand up and say, "So what? How is this going to help people?" We're here to have the maximum health impact, so that irreverence is important. We promote an atmosphere of openness and encourage people to bring up issues or problems. We have an internal blog and if people have concerns...bring 'em on, even if they’re challenging. Let's have free and open debate.

What are your top challenges?

Besides the budget, it’s that prevention is often invisible. Each year in the U.S. 40,000 people don't die because of the immunization program. Twenty million infectious disease cases don't happen. Fourteen billion dollars in medical care costs and $69 billion in societal costs are averted. Making that clear and maintaining support for programs are big challenges.

  • LAURIE GARRETT SPEAKS ON LESSONS FROM THE FLU PANDEMIC OF 1918

Another offering from www.ted.com
http://www.ted.com/talks/lang/eng/laurie_garrett_on_lessons_from_the_1918_flu.html



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ANOTHER HAT TRICK

  • THE BREAST MILK CURE 

New York Times, 22 June 2011

Also at http://www.nytimes.com/2011/06/23/opinion/23kristof.html?_r=1&hp

[This article cites the 2008 Lancet series on maternal and child nutrition, accessible at

http://www.thelancet.com/series/maternal-and-child-undernutrition

The WHO recommendations on exclusive breastfeeding for at last six months are at

http://www.who.int/topics/breastfeeding/en/ ]

Nicholas Kristof on Malnutrition, and Its Cure

What if nutritionists came up with a miracle cure for childhood malnutrition? A protein-rich substance that doesn’t require refrigeration? One that is free and is available even in remote towns like this one in Niger where babies routinely die of hunger-related causes?

Impossible, you say? Actually, this miracle cure already exists. It’s breast milk.

When we think of global poverty, we sometimes assume that the challenges are so vast that any solutions must be extraordinarily complex and expensive. Well, some are. But almost nothing would do as much to fight starvation around the world as the ultimate low-tech solution: exclusive breast-feeding for the first six months of life. That’s the strong recommendation of the World Health Organization.

The paradox is that while this seems so cheap and obvious — virtually instinctive — it’s also rare. Here in Niger, only 9 percent of babies get nothing but breast milk for the first six months of life, according to a 2007 national nutrition survey. At least that’s up from just 1 percent in 1998.

(In the United States, about 13 percent of babies are exclusively breast-fed for six months, according to the federal Centers for Disease Control and Prevention. Then again, most of the rest get formula, which is pretty safe in America.)

Next door to Niger in Burkina Faso, fewer than 7 percent of children get breast milk exclusively for six months. In Senegal it’s 14 percent; in Mauritania, 3 percent.

These are some of the countries we’re passing through on my annual win-a-trip journey, this year with a medical student from Atlanta, Saumya Dave, and a teacher from Newark, Noreen Connolly. It’s heartbreaking to see severely malnourished children and to meet mother after mother who has buried children when such a simple life-saving solution is not applied.

The biggest problem is that many mothers believe that breast milk isn’t enough, and that, on a hot day, a child needs water as well.

On a rural road near the remote town of Dogon Doutchi, in southern Niger, we ran into a family of Tuareg nomads traveling north.

“On a hot day, babies need water,” Gayshita Abdullah, the mother, told me. She said she tries to get water from a well, but if there is no well nearby she gets it from a mud puddle.

In fact, most nutritionists are adamant that babies are best off with nothing but breast milk for the first six months of life (they used to recommend four months, but now say six months). And water in poor countries is often contaminated and dangerous for a baby.

Even when the mother is herself malnourished, her body will normally provide enough milk for a baby, nutritionists say.

A 2008 report in The Lancet, the British medical journal, found that a baby that is partially breast-fed is 2.8 times as likely to die as a baby that is exclusively breast-fed for at least five months. A child that is not breast-fed at all is 14.4 times as likely to die.

Over all, The Lancet said, 1.4 million child deaths could be averted each year if babies were breast-fed properly. That’s one child dying unnecessarily every 22 seconds.

“As far as nutritional interventions that have been studied, we have crushing evidence of breast-feeding’s efficacy in reducing child mortality,” said Shawn Baker, a nutrition specialist with Helen Keller International, an aid organization that works on these issues.

“It’s the oldest nutritional intervention known to our species, and it’s available to everybody,” Baker added. “But for a development community too focused on technological fixes, it hasn’t gained the traction it should.”

The challenges with breast-feeding in poor countries are not the kinds that Western women face, and many women in the developing world continue nursing their babies for two years. The biggest problem is giving water or animal milk to babies, especially on hot days. Another is that mothers often doubt the value of colostrum, the first milk after childbirth (which is thick and yellowish and doesn’t look much like milk), and delay nursing for a day or two.

One mother near the town of Dosso, Fati Halidou, who has lost four of her seven children, told me that after childbirth, it is best to give a baby sugar water or Koranic water. This is water made by writing a verse of the Koran on a board and then washing it off; the inky water is thought to protect the child.

It’s not clear why a human instinct to nurse went awry. Does it have something to do with the sexualization of breasts? Or with infant formula manufacturers, who irresponsibly peddled their products in the past but are more restrained now? Or is it just that moms worry that their babies need water on hot days? Nobody really knows.

But what is clear is that there’s a marvelous low-tech solution to infant malnutrition all around us.

I invite you to visit my blog, On the Ground. Please also join me on Facebook, watch my YouTube videos and follow me on Twitter.

A version of this op-ed appeared in print on June 23, 2011, on page A27 of the New York edition with the headline: The Breast Milk Cure.

 


'Family planning is documented to prevent mother-child transmission of human immunodeficiency virus, contribute to birth spacing, lower infant mortality risk, and reduce the number of abortions, especially unsafe ones. It is also shown to significantly lower maternal mortality and maternal morbidity associated with unintended pregnancy.'




  • FAMILY PLANNING AND THE BURDEN OF UNINTENDED PREGNANCIES 
  1. 1.      Amy O. Tsui*,
  2. 2.      Raegan McDonald-Mosley and
  3. 3.      Anne E. Burke
  4. *Correspondence to Dr. Amy O. Tsui, Population, Family and Reproductive Health Department, Johns Hopkins Bloomberg School of Public Health, 615 North Wolfe Street, W4041, Baltimore, MD 21205 (e-mail: atsui@jhsph.edu).

Abstract and introduction below; full text is at http://epirev.oxfordjournals.org/content/32/1/152.full

Abstract

Family planning is hailed as one of the great public health achievements of the last century, and worldwide acceptance has risen to three-fifths of exposed couples. In many countries, however, uptake of modern contraception is constrained by limited access and weak service delivery, and the burden of unintended pregnancy is still large. This review focuses on family planning's efficacy in preventing unintended pregnancies and their health burden. The authors first describe an epidemiologic framework for reproductive behavior and pregnancy intendedness and use it to guide the review of 21 recent, individual-level studies of pregnancy intentions, health outcomes, and contraception. They then review population-level studies of family planning's relation to reproductive, maternal, and newborn health benefits. Family planning is documented to prevent mother-child transmission of human immunodeficiency virus, contribute to birth spacing, lower infant mortality risk, and reduce the number of abortions, especially unsafe ones. It is also shown to significantly lower maternal mortality and maternal morbidity associated with unintended pregnancy. Still, a new generation of research is needed to investigate the modest correlation between unintended pregnancy and contraceptive use rates to derive the full health benefits of a proven and cost-effective reproductive technology.

 

  • TWO COCHRANE REVIEWS ON MALARIA VECTOR CONTROL 

Below, two Cochrane reviews on malaria vector control; one recent one on IRS, one (slightly dated) one on bednets.

There is a proposed Cochrane review, still in the protocol stage, on larvivorous fish for malaria control. Do any readers know of published evaluations on this subject?

Good reading.

BD

Indoor residual spraying for preventing malaria

Pluess B, Tanser FC, Lengeler C, Sharp BL

Also at http://www2.cochrane.org/reviews/en/ab006657.html

Indoor residual spraying for preventing malaria

Spraying houses with insecticides (indoor residual spraying; IRS) to kill mosquitoes is one of the main methods that have been used to control malaria on a large scale. IRS has helped to eliminate malaria from great parts of Asia, Russia, Europe, and Latin America, and successful IRS programmes have also been run in parts of Africa.

Another successful method of mosquito control relies on the use of physical barriers such as bednets or curtains that can also be sprayed with insecticides (insecticide treated nets; ITN). This review aims to look at the health benefits of IRS and to compare this method with ITNs.

This review does not assess the potentially adverse effects of insecticides used for IRS, and it includes not only randomized controlled trials (RCTs), but also controlled before-and-after studies (CBA) and interrupted time series (ITS), as these methods were considered suitably rigorous.

Six studies were identified for inclusion (four cluster RCTs, one CBA and one ITS). Four of these studies were conducted in sub-Saharan Africa, one in India and one in Pakistan. IRS reduced malaria transmission in young children by half compared to no IRS in Tanzania (an area where people are regularly exposed to malaria), and protected all age groups in India and Pakistan (where malaria transmission is more unstable and where more than one type of malaria is found).  

When compared with ITNs, IRS appeared more protective (according to the outcome chosen) in one trial conducted in an area of stable malaria transmission, but ITN seemed to be more protective than IRS in unstable areas. Unfortunately, the level of evidence is very limited and no firm conclusions should be drawn on the basis of this review.

In conclusion, although IRS programmes have shown impressive success in malaria reduction throughout the world, there are too few well-run trials to be able to quantify the effects of IRS in areas with different malaria transmission, or to properly compare IRS and ITN.  High-quality and long-duration trials on a large scale, done in areas where there has been little or no mosquito control are still urgently required. New trials should include an IRS arm and an ITN arm, and should also assess the combined effect of ITN and IRS, a very important question in view of malaria elimination.

This is a Cochrane review abstract and plain language summary, prepared and maintained by The Cochrane Collaboration, currently published in The Cochrane Database of Systematic Reviews 2011 Issue 6, Copyright © 2011 The Cochrane Collaboration. Published by John Wiley and Sons, Ltd.. The full text of the review is available in The Cochrane Library (ISSN 1464-780X).

This record should be cited as: Pluess B, Tanser FC, Lengeler C, Sharp BL. Indoor residual spraying for preventing malaria. Cochrane Database of Systematic Reviews 2010, Issue 4. Art. No.: CD006657. DOI: 10.1002/14651858.CD006657.pub2

This version first published online: April 14. 2010
Last assessed as up-to-date: March 16. 2010

Abstract

Background

Primary malaria prevention on a large scale depends on two vector control interventions: indoor residual spraying (IRS) and insecticide-treated mosquito nets (ITNs). Historically, IRS has reduced malaria transmission in many settings in the world, but the health effects of IRS have never been properly quantified. This is important, and will help compare IRS with other vector control interventions.

Objectives

To quantify the impact of IRS alone, and to compare the relative impacts of IRS and ITNs, on key malariological parameters.

Search strategy

We searched the Cochrane Infectious Diseases Group Specialized Register (September 2009), CENTRAL (The Cochrane Library 2009, Issue 3), MEDLINE (1966 to September 2009), EMBASE (1974 to September 2009), LILACS (1982 to September 2009), mRCT (September 2009), reference lists, and conference abstracts. We also contacted researchers in the field, organizations, and manufacturers of insecticides (June 2007).

Selection criteria

Cluster randomized controlled trials (RCTs), controlled before-and-after studies (CBA) and interrupted time series (ITS) of IRS compared to no IRS or ITNs. Studies examining the impact of IRS on special groups not representative of the general population, or using insecticides and dosages not recommended by the World Health Organization (WHO) were excluded.

Data collection and analysis

Two authors independently reviewed trials for inclusion. Two authors extracted data, assessed risk of bias and analysed the data. Where possible, we adjusted confidence intervals (CIs) for clustering. Studies were grouped into those comparing IRS with no IRS, and IRS compared with ITNs, and then stratified by malaria endemicity.

Main results

IRS versus no IRS

Stable malaria (entomological inoculation rate (EIR) > 1): In one RCT in Tanzania IRS reduced re-infection with malaria parasites detected by active surveillance in children following treatment; protective efficacy (PE) 54%. In the same setting, malaria case incidence assessed by passive surveillance was marginally reduced in children aged one to five years; PE 14%, but not in children older than five years (PE -2%). In the IRS group, malaria prevalence was slightly lower but this was not significant (PE 6%), but mean haemoglobin was higher (mean difference 0.85 g/dL).

In one CBA trial in Nigeria, IRS showed protection against malaria prevalence during the wet season (PE 26%; 95% CI 20 to 32%) but not in the dry season (PE 6%; 95% CI -4 to 15%). In one ITS in Mozambique, the prevalence was reduced substantially over a period of 7 years (from 60 to 65% prevalence to 4 to 8% prevalence; the weighted PE before-after was 74% (95% CI 72 to 76%).

Unstable malaria (EIR < 1): In two RCTs, IRS reduced the incidence rate of all malaria infections;PE 31% in India, and 88% (95% CI 69 to 96%) in Pakistan. By malaria species, IRS also reduced the incidence of P. falciparum (PE 93%, 95% CI 61 to 98% in Pakistan) and P. vivax (PE 79%, 95% CI 45 to 90% in Pakistan); There were similar impacts on malaria prevalence for any infection: PE 76% in Pakistan; PE 28% in India. When looking separately by parasite species, for P. falciparum there was a PE of 92% in Pakistan and 34% in India; for P. vivax there was a PE of 68% in Pakistan and no impact demonstrated in India (PE of -2%).

IRS versus Insecticide Treated Nets (ITNs)

Stable malaria (EIR > 1): Only one RCT was done in an area of stable transmission (in Tanzania). When comparing parasitological re-infection by active surveillance after treatment in short-term cohorts, ITNs appeared better, but it was likely not to be significant as the unadjusted CIs approached 1 (risk ratio IRS:ITN = 1.22). When the incidence of malaria episodes was measured by passive case detection, no difference was found in children aged one to five years (risk ratio = 0.88, direction in favour of IRS). No difference was found for malaria prevalence or haemoglobin.

Unstable malaria (EIR < 1): Two studies; for incidence and prevalence, the malaria rates were higher in the IRS group compared to the ITN group in one study. Malaria incidence was higher in the IRS arm in India (risk ratio IRS:ITN = 1.48) and in South Africa (risk ratio 1.34 but the cluster unadjusted CIs included 1). For malaria prevalence, ITNs appeared to give better protection against any infection compared to IRS in India (risk ratio IRS:ITN = 1.70) and also for both P. falciparum (risk ratio IRS:ITN = 1.78) and P. vivax (risk ratio IRS:ITN = 1.37).

Authors' conclusions

Historical and programme documentation has clearly established the impact of IRS. However, the number of high-quality trials are too few to quantify the size of effect in different transmission settings. The evidence from randomized comparisons of IRS versus no IRS confirms that IRS reduces malaria incidence in unstable malaria settings, but randomized trial data from stable malaria settings is very limited. Some limited data suggest that ITN give better protection than IRS in unstable areas, but more trials are needed to compare the effects of ITNs with IRS, as well as to quantify their combined effects. Ideally future trials should try and evaluate the effect of IRS in areas with no previous history of malaria control activities.

 

Insecticide-treated bed nets and curtains for preventing malaria

Also at http://www2.cochrane.org/reviews/en/ab000363.html

Lengeler C

Insecticide-treated nets can reduce deaths in children by one fifth and episodes of malaria by half.

Sleeping under mosquito nets treated with insecticide aims to prevent malaria in areas where the infection is common. They are widely promoted by international agencies and governments to reduce the bad effects of malaria on health. This review showed that good quality studies of impregnated nets markedly reduce child deaths and illnesses from malaria.

This is a Cochrane review abstract and plain language summary, prepared and maintained by The Cochrane Collaboration, currently published in The Cochrane Database of Systematic Reviews 2011 Issue 6, Copyright © 2011 The Cochrane Collaboration. Published by John Wiley and Sons, Ltd.. The full text of the review is available in The Cochrane Library (ISSN 1464-780X).

This record should be cited as: Lengeler C. Insecticide-treated bed nets and curtains for preventing malaria. Cochrane Database of Systematic Reviews 2004, Issue 2. Art. No.: CD000363. DOI: 10.1002/14651858.CD000363.pub2

Editorial Group: Infectious Diseases Group

Abstract

Background

Malaria is an important cause of illness and death in many parts of the world, especially in sub-Saharan Africa. There has been a renewed emphasis on preventive measures at community and individual levels. Insecticide-treated nets (ITNs) are the most prominent malaria preventive measure for large-scale deployment in highly endemic areas.

Objectives

To assess the impact of insecticide-treated bed nets or curtains on mortality, malarial illness (life-threatening and mild), malaria parasitaemia, anaemia, and spleen rates.

Search strategy

I searched the Cochrane Infectious Diseases Group trials register (January 2003), CENTRAL (The Cochrane Library, Issue 1, 2003), MEDLINE (1966 to October 2003), EMBASE (1974 to November 2002), LILACS (1982 to January 2003), and reference lists of reviews, books, and trials. I handsearched journals, contacted researchers, funding agencies, and net and insecticide manufacturers.

Selection criteria

Individual and cluster randomized controlled trials of insecticide-treated bed nets or curtains compared to nets without insecticide or no nets. Trials including only pregnant women were excluded.

Data collection and analysis

The reviewer and two independent assessors reviewed trials for inclusion. The reviewer assessed the risk of bias in the trials, and extracted and analysed data.

Main results

Fourteen cluster randomized and eight individually randomized controlled trials met the inclusion criteria. Five trials measured child mortality: ITNs provided 17% protective efficacy (PE) compared to no nets (relative rate 0.83, 95% confidence interval (CI) 0.76 to 0.90), and 23% PE compared to untreated nets (relative rate 0.77, 95% CI 0.63 to 0.95). About 5.5 lives (95% CI 3.39 to 7.67) can be saved each year for every 1000 children protected with ITNs. In areas with stable malaria, ITNs reduced the incidence of uncomplicated malarial episodes in areas of stable malaria by 50% compared to no nets, and 39% compared to untreated nets; and in areas of unstable malaria: by 62% for compared to no nets and 43% compared to untreated nets for Plasmodium falciparum episodes, and by 52% compared to no nets and 11% compared to untreated nets for P. vivax episodes. When compared to no nets and in areas of stable malaria, ITNs also had an impact on severe malaria (45% PE, 95% CI 20 to 63), parasite prevalence (13% PE), high parasitaemia (29% PE), splenomegaly (30% PE), and their use improved the average haemoglobin level in children by 1.7% packed cell volume.

Authors' conclusions

ITNs are highly effective in reducing childhood mortality and morbidity from malaria. Widespread access to ITNs is currently being advocated by Roll Back Malaria, but universal deployment will require major financial, technical, and operational inputs.


HAT TRICK

This week, three winning entries.

First, a global online forum on integrated service delivery of immunization and family planning. As immunization levels rise, child mortality tends to decline. Then, couples are ready to practice family planning, which produces the long birth intervals associated with further gains in child survival. Note the Email address for those wishing to participate.

Second, a review of cervical cancer epidemiology and control in sub-Saharan Africa. Only Rwanda, of the 46 countries in WHO’s Africa region, is launching nationwide HPV vaccination.

Third, a second look at the Haitian cholera epidemic and how to avoid future catastrophes of the same kind.

Note as well, from last week, two communication for health vacancies in the UNICEF office, Dakar, Senegal.

Good reading.

BD

 

  • ·         EVENT ANNOUNCEMENT: GLOBAL ONLINE FORUM ON INTEGRATED SERVICE DELIVERY OF IMMUNIZATION AND FAMILY PLANNING, JULY 6-15

 Please join MCHIP and the Immunization/Family Planning Integration Working Group for a global online discussion forum highlighting new and emerging field experiences, lessons learned, and opportunities for Immunization and Family Planning Integrated Service Delivery.  The discussion will highlight opportunities for integrated programming, recent developments in Immunization/FP integration and how to make integration a win/win for both immunization and family planning outcomes.

Experts representing a variety of organizations will share field experiences and provide insights on successes and lessons learned from integrated programs within these key areas, along with potential strategies for scale-up and recommendations for future work in this area. MCHIP welcomes all interested participants to join in this rich discussion.

During the forum, you will receive one or two emails per day (during July 6-15) from the forum administrators, with all contributions screened and presented as a single, well organized digest.

If you are interested in participating, please send your Name, Title, Organization and Email address to Elizabeth Sasser at esasser@jhpiego.net .

  • ·         HPV AND CERVICAL CANCER IN SUBSAHARAN AFRICA

'ICC incidence in SSA is one of the highest in the world with an age-standardized incidence rate of 31 per 100,000 women.'

Of the 46 countries in WHO's African region, only Rwanda is introducing HPV vaccination into its national vaccination programme. One down, 45 to go.

Good reading.
Bob Davis

Best viewed at
http://onlinelibrary.wiley.com/doi/10.1111/j.1365-3156.2009.02372.x/full

Epidemiology and prevention of human papillomavirus and cervical cancer in sub-Saharan Africa: a comprehensive review

Karly S. Louie1,2,

Silvia De Sanjose2,3,

Philippe Mayaud1

Article first published online: 14 SEP 2009

Tropical Medicine & International Health

Volume 14, Issue 10, pages 1287–1302, October 2009

How to Cite

Louie, K. S., De Sanjose, S. and Mayaud, P. (2009), Epidemiology and prevention of human papillomavirus and cervical cancer in sub-Saharan Africa: a comprehensive review. Tropical Medicine & International Health, 14: 1287–1302. doi: 10.1111/j.1365-3156.2009.02372.x

Author Information

1 Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK

2 Unit of Infections and Cancer, Cancer Epidemiology Research Program, Institut Catalá d’Oncologia, Barcelona, Spain

3 CIBER en Epidemiología y Salud Pública (CIBERESP), Barcelona, Spain

*Correspondence: Corresponding Author Karly S. Louie, Department of Infectious & Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK. Tel.: 44 20 7927 2291; Fax: 44 20 7637 4314; E-mail: Karly.Louie@lshtm.ac.uk

Publication History

Issue published online: 14 SEP 2009

Article first published online: 14 SEP 2009

Objectives To identify the gaps of knowledge and highlight the challenges and opportunities for controlling cervical cancer in sub-Saharan Africa (SSA).

Methods A comprehensive review of peer-reviewed literature to summarize the epidemiological data on human papillomavirus (HPV) and invasive cervical cancer (ICC) by HIV status, to review feasible and effective cervical screening strategies, and to identify barriers in the introduction of HPV vaccination in SSA.

Results ICC incidence in SSA is one of the highest in the world with an age-standardized incidence rate of 31.0 per 100 000 women. The prevalence of HPV16/18, the two vaccine preventable-types, among women with ICC, does not appear to differ by HIV status on a small case series. However, there are limited data on the role of HIV in the natural history of HPV infection in SSA. Cervical screening coverage ranges from 2.0% to 20.2% in urban areas and 0.4% to 14.0% in rural areas. There are few large scale initiatives to introduce population-based screening using cytology, visual inspection or HPV testing. Only one vaccine safety and immunogenicity study is being conducted in Senegal and Tanzania. Few data are available on vaccine acceptability, health systems preparedness and vaccine cost-effectiveness and long-term impact.

Conclusions Additional data are needed to strengthen ICC as a public health priority to introduce, implement and sustain effective cervical cancer control in Africa.

 

  • ·         UNDERSTANDING THE HAITIAN CHOLERA EPIDEMIC

'Our epidemiologic study provides several additional arguments confirming an importation of cholera in Haiti. There was an exact correlation in time and places between the arrival of a Nepalese battalion from an area experiencing a cholera outbreak and the appearance of the first cases in Meille a few days after. The remoteness of Meille in central Haiti and the absence of report of other incomers make it unlikely that a cholera strain might have been brought there another way. DNA fingerprinting of V. cholerae isolates in Haiti (1) and genotyping (7,21) corroborate our findings because the fingerprinting and genotyping suggest an introduction from a distant source in a single event (22).'

From Emerging Infectious Diseases, www.cdc.gov/eid

EID Journal Home > Volume 17, Number 7–July 2011

Volume 17, Number 7–July 2011

Synopsis

Understanding the Cholera Epidemic, Haiti

Renaud Piarroux, Robert Barrais, Benoît Faucher, Rachel Haus, Martine Piarroux, Jean Gaudart, Roc Magloire, and Didier Raoult
Author affiliations: Université de la Méditerranée, Marseilles, France (R. Piarroux, B. Faucher, J. Gaudart, D. Raoult); Ministère de la Santé Publique et de la Population, Port-au-Prince, Haiti (R. Barrais, R. Magloire); Service de Santé des Armées, Paris, France (R. Haus); and Martine Piarroux Université de Franche-Comté, Besançon, France (M. Piarroux)

Suggested citation for this article

Abstract
After onset of a cholera epidemic in Haiti in mid-October 2010, a team of researchers from France and Haiti implemented field investigations and built a database of daily cases to facilitate identification of communes most affected. Several models were used to identify spatiotemporal clusters, assess relative risk associated with the epidemic's spread, and investigate causes of its rapid expansion in Artibonite Department. Spatiotemporal analyses highlighted 5 significant clusters (p<0.001): 1 near Mirebalais (October 16–19) next to a United Nations camp with deficient sanitation, 1 along the Artibonite River (October 20–28), and 3 caused by the centrifugal epidemic spread during November. The regression model indicated that cholera more severely affected communes in the coastal plain (risk ratio 4.91) along the Artibonite River downstream of Mirebalais (risk ratio 4.60). Our findings strongly suggest that contamination of the Artibonite and 1 of its tributaries downstream from a military camp triggered the epidemic.


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  • EVERYTHING YOU WANTED TO KNOW ABOUT MEASLES BUT WERE AFRAID TO ASK

Many thanks to the indispensable Jane Wachira, who, on the eve of her holiday, assembled 35 pages of abstracts from the forthcoming supplement to the Journal of Infectious Diseases, with abstracts on all aspects of measles epidemiology, control and eradication.

Many firmly held beliefs will not survive the appearance of this supplement. If you think that measles vaccine efficacy is 85 percent, read the piece by Uzicanin and Zimmermann. If you think that measles eradication is poor bang for the buck, read the piece by Levin and colleagues. If you think that outbreak response immunization comes too little and too late, read the piece by Cairns and colleagues. If you think that measles eradication will undermine health systems, try the piece by Griffiths and colleagues.

Subscribers to JID can access the full text of all articles at http://jid.oxfordjournals.org/content/204/suppl_1.toc

 

Good reading.

  • THE ROLE OF RESEARCH IN VIRAL DISEASE ERADICATION AND ELIMINATION PROGRAMS

Summary Points

‘Lessons from the smallpox, poliomyelitis, and measles eradication/elimination initiatives (in particular, the importance of starting laboratory, clinical, and field research early in the program and continuing research in parallel) should be incorporated into any malaria eradication initiative from the onset.

‘Vaccines are likely to be the lynchpin interventions of elimination/eradication programs, but ongoing research will be needed to improve formulations, delivery, and immunization schedules.

‘Surveillance will be critical throughout any elimination/eradication initiative, coupled with improved diagnostic methods to detect asymptomatic infections and low rates of transmission.

‘Because socio-cultural, religious, and local politics can impede eradication efforts, it is prudent to support research into improving ways to communicate effectively with local populations about the disease and the interventions to eradicate it.

‘A cross-cutting theme among the viral disease programs is that interrupting the last vestiges of transmission is particularly problematic and requires allocation of many resources including support for focused “last kilometre” research activities.’

Full text is at http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1000405

 

  • ACCELERATING MEASLES CONTROL IN INDIA: OPPORTUNITY AND OBLIGATION TO ACT NOW 

T JACOB JOHN*AND PANNA CHOUDHURY􀁧


INDIAN PEDIATRICS 939 VOLUME 46

 

*Past President, Indian Academy of Pediatrics, and Co-Chair, NTAGI, 439 Civil Supplies Godown Lane, Kamalakshipuram,

Vellore, Tamil Nadu; and 􀁧President, Indian Academy of Pediatrics (IAP), and Chairman,

IAP Committee on Immunization, DII/M 2753 Netaji Nagar, New Delhi, India. pannachoudhury@gmail.com

E D I T O R I A L

 Two major milestones in the history of measles control have recently been achieved. Since November 2002, measles is no longer endemic in the Western Hemisphere(1) and the 2005 goal set by the World Health Assembly (WHA) to halve measles deaths worldwide (compared to 1999 levels) was achieved on time(2). The main intervention that led to these achievements was the tactical scaling-up of measles vaccination.

 In May 2005, the WHA welcomed the goal of reducing measles deaths by 90% by 2010 compared to 2000 levels, as part of the Global Immunization Vision and Strategy (GIVS)(3). This global goal was endorsed unanimously by the WHA in May, 2008. This editorial explores the potential impacts of measles control strategies on child survival in India and on the global goal of reduction in measles mortality.

 

MEASLES IN INDIA

Measles continues to be an important cause of childhood morbidity and mortality in many states in India. At a workshop convened jointly by Government of India (GoI), WHO, and UNICEF on measles, in May 2007, it was estimated that between 100,000 and 160,000 children die from measles in India each year and that over 90% of deaths occur in 10 states – Uttar Pradesh (UP), Bihar, Rajasthan, Madhya. Pradesh, Jharkhand, Assam, West Bengal, Andhra Pradesh (AP), Orissa and Gujarat (preliminary results from a workshop held at National Polio Surveillance Unit, New Delhi, May 2007). A recent (2006) vaccination coverage survey in India showed overall 71% coverage for measles vaccine (given during 9 to 12 months of age) (4).

 

Accepting 85% vaccine effectiveness for vaccination at 9 months, actual protection was offered to only 60% of annual birth cohorts (71% × 85% = 60%). In other words, 40% remained susceptible to measles. Coverage of measles vaccine was less than 50% in UP, Bihar, Assam and Nagaland and between 50% and 80% in 13 other states(4). Worldwide, of the estimated 26.2 million infants who missed receiving their first dose of measles vaccine by age 12 months through routine immunization services in 2006, 10.5 million were in India (5).

 Six states (AP, Gujarat, Karnataka, Kerala, Tamil Nadu, West Bengal) conduct measles surveillance through clinical and laboratory outbreak investigations. In these states, nearly 80% cases occur in children less than 10 years old (data available at National Polio Surveillance Project [NPSP], New Delhi). Even in the states with moderate routine immunization coverage, many under-five children with measles had not been given measles vaccine (e.g. West Bengal 72%, Karnataka 38%, Gujarat 35%). According to the Registrar General and Census Commissioner of India, UP, Bihar and Assam together had 114 million children under 15 years of age, in 2006(6). More than half of them had not received measles vaccine – providing fertile ground for continued intense transmission of measles virus.

 Studies in India have shown median case-fatality ratio (CFR) of 3.8% (range: 0% to 30%) among children with measles(7). UP had recorded measles CFR of 4.1% in 1996, through routine reporting(8).  Actually the present surveillance method tends to under-report measles deaths.  Given the formidable challenges of wide interregional disparities of immunization coverage, a huge unvaccinated child population and the large disease burden, can India reduce its enormous measles morbidity and mortality?

  • ·         BILL GATES LOOKS AT THE LEGACY OF JAMES P. GRANT

 Writing in www.TheGatesNotes.com Bill Gates remembers the work of James P. Grant, executive director of UNICEF in the 1980s, in placing Universal Childhood Immunization on the world’s agenda.

For more on the work of Jim Grant, go to  http://www.unicef.org/publications/index_4402.html

 

 Jim Grant - UNICEF Visionary

Jim Grant's 'Child Survival Revolution'

Posted 02/16/2011

If ever anyone ever deserved the title “Miracle Worker” it would be Jim Grant, who as head of UNICEF for 15 years mobilized the global community to immunize millions of children. The story of Grant’s remarkable achievements is chronicled in an out-of-print book that Bill recently read.

I recently came across a book that tells the amazing story of Jim Grant, whose influence in making vaccines widely available in the developing world is credited with saving the lives of 25 million children.

Because of the work the foundation is doing on vaccine-preventable diseases, I’ve read quite a bit about the history of global immunization. But until I read Jim Grant—UNICEF Visionary (an out-of-print book available for free download), I didn’t appreciate what a remarkable visionary and results-driven leader he was. I talk more about the impact of Jim Grant’s contributions in the foundation’s annual letter.

Grant was executive director of UNICEF—the United Nations Children’s Fund—from 1980 to 1995. Prior to that time, UNICEF was already well regarded for its global work—begun in the aftermath of World War II—preventing epidemics and malnutrition among children. In 1965, for example, UNICEF was awarded the Nobel Peace Prize.

But when Grant became head of UNICEF, he saw an opportunity to address a problem that was not high on the priority list of world leaders or international development organizations. At the time, about 14 million children were dying every year of readily preventable illnesses such as measles, tetanus, whooping cough, pneumonia and diarrheal disease. Virtually all of the deaths were occurring in the developing world; Europe and North America had mostly conquered the diseases with low-cost means of prevention or cure developed in the first half of the 20th century.

Grant decided to focus UNICEF’s mission on halving child deaths in the developing world through a massive effort to introduce the same immunizations already available in developed countries, along with other highly-effective low-cost strategies, such as packets of oral rehydration salts for people suffering from diarrheal disease, educating women about the benefits of breast feeding, and monitoring the growth of children. Collectively, these efforts were known as UNICEF’s Child Survival and Development Revolution.

Although we still face many difficulties today getting vaccines to the people who need them, the challenges Grant faced were an order of magnitude greater. No organization had ever tried tackling a global health issue on such a large scale and there were many skeptics, including within UNICEF.

But as Peter Adamson, who worked closely with Grant, writes in one of the book’s chapters, “…who could not be struck by the sheer unforgiveableness of millions upon millions of children dying…when the means to prevent it were at hand.”

  • BEST PRACTICES IN MALARIA BEDNET DISTRIBUTION

Best practices for an insecticide-treated bed net distribution programme in sub-Saharan eastern Africa

When initial bednet coverage is low, can anyone defend the step by step approach to raising it? Those who reject the mass campaign approach to quick gains in coverage are on the back foot.  

‘ [Bednet] distribution should employ a catch up/keep up programme strategy. The catch-up programme rapidly scales up coverage, while the keep-up programme maintains coverage levels.’

 Malaria Journal 2011, 10:157 doi:10.1186/1475-2875-10-157

Alexis R Sexton (arsexton@gmail.com)

Article URL http://www.malariajournal.com/content/10/1/157

This peer-reviewed article was published immediately upon acceptance. It can be downloaded, printed and distributed freely for any purposes (see copyright notice below).

Malaria Journal

© 2011 Sexton ; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Best practices for an insecticide-treated bed net distribution programme in sub-Saharan

eastern Africa

Alexis R Sexton1

1Graduate School of Public Health, College of Health and Human Services, San Diego State

University, 5500 Campanile Drive, San Diego, CA 92182-4162, USA, Tel 858-603-2946

arsexton@gmail.com

Abstract

Insecticide-treated bed nets are the preeminent malaria control means; though there is no consensus as to a best practice for large-scale insecticide-treated bed net distribution. In order to determine the paramount distribution method, this review assessed literature on recent insecticide treated bed net distribution programmes throughout sub-Saharan Eastern Africa. Inclusion criteria were that the study had taken place in sub-Saharan Eastern Africa, targeted malaria prevention and control, and occurred between 1996 and 2007. Forty-two studies were identified and reviewed. The results indicate that distribution frameworks varied greatly; and consequently so did outcomes of insecticide-treated bed net use. Studies revealed consistent inequities between urban and rural populations; which were most effectively alleviated through a free insecticide treated bed net delivery and distribution framework. However, cost sharing through subsidies was shown to increase programme sustainability, which may lead to more long-term coverage.

Thus, distribution should employ a catch up/keep up programme strategy. The catch-up programme rapidly scales up coverage, while the keep-up programme maintains coverage levels.

Future directions for malaria should include progress toward distribution of long-lasting insecticide-treated nets.

  • THE POLIO ENDGAME

The view from WHO and BMGF.

Also at http://healthpolicyandreform.nejm.org/?p=14698&query=home

NEJM | June 15, 2011 | Topics: International, Public Health

Bruce Aylward, M.D., and Tadataka Yamada, M.D.

Infection with poliovirus can have devastating consequences, including paralysis and death. In 1988, a year when an estimated 350,000 or more children were paralyzed by polio, the World Health Assembly initiated a global effort to eradicate the infection once and for all. It was an audacious undertaking, given that the virus circulates largely undetected, requires laborious cell-culture techniques to confirm infection, and is tackled with vaccines that provide imperfect protection in the gut.

Cases of Poliomyelitis Caused by Wild Poliovirus Types 1 and 3, January 1–May 24, 2011.

Initially, the number of polio cases and countries with infections fell rapidly, particularly as financing and political support increased in the mid-1990s. The last case of paralytic poliomyelitis caused by the serotype 2 wild poliovirus was detected in 1999. The number of new polio cases caused by the two remaining wild serotypes had decreased by 99% between 1988 and 2005, but progress had stalled and there was a danger of failure when wild polio viruses were reintroduced into large areas of Africa and Asia. By the end of 2009, sustained investments in innovation had produced a new bivalent oral poliovirus vaccine (OPV)1 and novel tactics for reaching children who had been missed consistently by vaccination campaigns. A new independent monitoring process was established for overseeing the program and guiding course corrections. Since January 2010, new polio cases have decreased by 95% in the world’s largest remaining reservoirs of indigenous virus in northern India and northern Nigeria; the number of cases caused by serotype 3 has fallen by 92% globally; and most countries where poliovirus had been reintroduced have again become polio-free (see map and interactive map).

Declines in the intensity of poliovirus transmission in India and Nigeria are key to interrupting wild poliovirus globally, since viruses originating in these countries have been responsible for all the recent importation-associated outbreaks in previously polio-free countries. Besides India and Nigeria, indigenous polioviruses now survive only in Pakistan and one part of Afghanistan, with just eight other countries currently responding to outbreaks caused by imported viruses. However, in three of these countries — Angola, Chad, and the Democratic Republic of Congo — transmission was reestablished (i.e., at least one imported virus continued to circulate for more than 12 months). All three countries then became secondary wild-poliovirus reservoirs, with onward spread to other previously polio-free countries. The logistic challenges of reaching more than 90% of young children in mass OPV immunization campaigns in countries with reestablished transmission are similar in scale to those faced in the remaining countries with endemic disease, where conflict, insecurity, and weak public services complicate eradication operations.

Although there is still much distance to cover to eradicate the remaining wild polioviruses, recent progress has generated new confidence in the eradication effort, and talk of the polio “endgame” has intensified. However, preventing new polio outbreaks in a “post-eradication era” will require more than biocontainment measures to prevent the reintroduction of wild virus from laboratory stocks or sites where inactivated (Salk) polio vaccine (IPV) is produced. Achieving a polio-free world will eventually require stopping routine immunization with OPV and eliminating vaccine-derived polioviruses (VDPVs), particularly circulating VDPVs, which are Sabin-strain viruses that have acquired both neurovirulence and the capacity to circulate.2

Of the three risks associated with OPV, the most frequently realized one is vaccine-associated paralytic poliomyelitis (VAPP). This risk will disappear with the cessation of use of OPV. Outbreaks caused by circulating VDPVs are rarer than VAPP cases, but new diagnostic tests have confirmed their regular emergence, particularly that of serotype 2 circulating VDPVs, which were found in eight of the nine countries reporting VDPV outbreaks between 2008 and 2010. The persistence of such an outbreak for more than 4 years in Nigeria highlights the importance of reducing the risk of VDPV outbreaks when OPV use ceases and of actively managing any persisting outbreaks.

The rarest risk associated with OPV use is chronic VDPV excretion by people with severe primary B-cell immune disorders. All but one of these chronic immunodeficiency-associated VDPVs to date have occurred in industrialized countries that no longer use OPV. However, people with such infections may excrete virulent virus for years and are themselves at risk for fatal disease (see Brief Report by DeVries et al. in this issue of the Journal, pages 2316–2323). Although industrialized countries now use IPV and will therefore no longer generate new immunodeficiency-associated VDPVs, additional strategies and tools are required to mitigate the associated risk. Ongoing studies in nine low- and low-middle-income countries should help to inform more robust surveillance and, if necessary, case-management strategies for chronic immunodeficiency-associated VDPVs in such settings.

Stopping routine immunization with OPV globally after wild poliovirus is eradicated will eliminate VAPP immediately and halt the generation of new circulating and immunodeficiency-associated VDPVs. The challenge will be to synchronize global cessation of OPV immunization and then manage the transition, potentially lasting several years, to the point where residual VDPVs have been eliminated. Five years ago, the tools for executing this endgame didn’t exist. Today, 12 monovalent OPVs, at least 1 for each serotype, are licensed, and a global stockpile is being built to facilitate a rapid response to any circulating VDPVs that persist after OPV immunization ceases.

It is important to decrease the risk of emergence and transmission of circulating VDPVs in low-income countries, as well as the transmission of any wild viruses introduced through breaks in laboratory containment. Low-cost solutions have been sought to facilitate routine immunization with IPV in such settings and thereby maintain some immunity to polio through at least the first 5 to 10 years after cessation of OPV administration, when risk would probably be highest. It now appears increasingly feasible to create an IPV administration schedule that costs no more than existing OPV schedules, through some combination of reducing the number of doses, delivering one fifth the amount of antigen per dose by intradermal administration, using adjuvants, and introducing seed strains (e.g., Sabin strains) that can be produced safely by low-cost manufacturers in developing countries.3,4 To help address the problem of chronic shedding of immunodeficiency-associated VDPV and reduce the potential for emergence of resistance, there are at least two antiviral candidates in early stages of development. Given the potentially fatal outcome of chronic infection, the availability of such treatments should also facilitate screening of at-risk but asymptomatic people.

Of course, none of these tools is perfect. Using monovalent OPVs to combat residual circulating VDPVs incurs the small risk of generating a new circulating VDPV — a risk that could increase with time after OPV use ceases. Since IPV does not induce the same level of intestinal mucosal immunity as OPV, we don’t yet know how effective IPV would be in terminating transmission of a circulating VDPV in tropical settings. Even if an antiviral drug is successfully developed, viral resistance may be encountered in the treatment of chronic shedders of immunodeficiency-associated VDPVs. Further research is providing additional tools and strategies that may be necessary for managing the risks in the posteradication era. Already the availability of these new tools has allowed serious discussions to begin regarding replacing trivalent OPV with bivalent OPV in routine vaccination programs, to take advantage of the apparent eradication of wild poliovirus type 2 and eliminate the VDPV risks associated with continued routine use of live vaccines with a type 2 component.

Uncertainties about the risks associated with cessation of OPV use have contributed to arguments that continued OPV immunization might be a more prudent approach to the polio endgame. However, there is accumulating evidence that intelligent application of innovative tools and strategies has shifted the balance of risk so that sustaining routine OPV immunization after the eradication of wild-type virus would present a greater risk to society and cost much more5 than eventual cessation of OPV immunization as a critical step in eradicating all polio disease.

 

  • ADDRESSING THE VACCINE CONFIDENCE GAP

Key messages

  • Public concerns about vaccines are not merely about vaccine safety, but are also about vaccine policies and recommendations, vaccine costs, and new research findings.
  • Public decision making related to vaccine acceptance is complex and is neither driven by scientific nor economic evidence alone, but is also driven by a mix of scientific, psychological, sociocultural, and political reasons, all of which need to be better understood.
  • The internet and new forms of social media have not only allowed for rapid and ubiquitous sharing of information—and misinformation—but have also allowed new methods of self-organisation and empowerment of newly founded online communities that argue against or for vaccines.
  • Although communication of positive, evidence-based information about the safety of specific vaccines and their benefit—risk ratios to the public is crucial, communication alone will not stop public distrust and dissent against vaccines.
  • Levels of public trust in vaccines are highly variable and context specific. To sustain or restore confidence in vaccines, a thorough understanding is needed of the population's—or subpopulation's—specific vaccine concerns, historical experiences, religious or political affiliation, and socioeconomic status.
  • Core principles to be followed by all health providers, experts, health authorities, policy makers, and politicians include: engagement with and listening to stakeholders, being transparent about decision making, and being honest and open about uncertainty and risks.



Also at
http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(11)60678-8/fulltext

The Lancet, Early Online Publication, 9 June 2011

Addressing the vaccine confidence gap

Original Text

Dr Heidi J Larson PhD a , Prof Louis Z Cooper MD b, Juhani Eskola MD c, Prof Samuel L Katz MD d, Scott Ratzan MD e f

Summary

Vaccines—often lauded as one of the greatest public health interventions—are losing public confidence. Some vaccine experts have referred to this decline in confidence as a crisis. We discuss some of the characteristics of the changing global environment that are contributing to increased public questioning of vaccines, and outline some of the specific determinants of public trust. Public decision making related to vaccine acceptance is neither driven by scientific nor economic evidence alone, but is also driven by a mix of psychological, sociocultural, and political factors, all of which need to be understood and taken into account by policy and other decision makers. Public trust in vaccines is highly variable and building trust depends on understanding perceptions of vaccines and vaccine risks, historical experiences, religious or political affiliations, and socioeconomic status. Although provision of accurate, scientifically based evidence on the risk—benefit ratios of vaccines is crucial, it is not enough to redress the gap between current levels of public confidence in vaccines and levels of trust needed to ensure adequate and sustained vaccine coverage. We call for more research not just on individual determinants of public trust, but on what mix of factors are most likely to sustain public trust. The vaccine community demands rigorous evidence on vaccine efficacy and safety and technical and operational feasibility when introducing a new vaccine, but has been negligent in demanding equally rigorous research to understand the psychological, social, and political factors that affect public trust in vaccines.

This is the fifth in a Series of five papers about the new decade of vaccines

  • SYPHILIS SCREENING IN PREGNANCY: A SYSTEMATIC REVIEW AND META-ANALYSIS

‘Interventions to improve the coverage and effect of screening programmes for antenatal syphilis could reduce the syphilis-attributable incidence of stillbirth and perinatal death by 50%. The resources required to roll out antenatal screening programmes would be a worthwhile investment for reduction of adverse pregnancy outcomes and improvement of neonatal and child survival.’

Best viewed at http://www.thelancet.com/journals/laninf/article/PIIS1473-3099(11)70104-9/fulltext

The Lancet Infectious Diseases, Early Online Publication, 16 June 2011

doi:10.1016/S1473-3099(11)70104-9 Cite or Link Using DOI

Effectiveness of interventions to improve screening for syphilis in pregnancy: a systematic review and meta-analysis

Original Text

Dr Sarah Hawkes PhD a , Nashaba Matin MRCP b, Nathalie Broutet PhD c, Prof Nicola Low MD d

Summary

Background

About 2·1 million pregnant women have active syphilis every year. Without screening and treatment, 69% of these women will have an adverse outcome of pregnancy. The objectives of this study were to review the literature systematically to determine the effectiveness of screening interventions to prevent congenital syphilis and other adverse pregnancy outcomes.

Methods

We searched four electronic databases and selected studies to examine evidence for effectiveness of interventions on three outcomes: increased uptake of syphilis testing, increased treatment rates, and reduction in adverse pregnancy outcomes. We used fixed effects meta-analysis to estimate pooled relative risks if no or little evidence of heterogeneity between trials existed.

Findings

Ten studies met the inclusion criteria, including two randomised trials. Only two studies aimed to encourage women to seek care earlier in pregnancy. Nine studies included decentralisation of screening and treatment. The effects of the interventions on uptake of testing for antenatal syphilis and receiving at least one dose of penicillin were variable and could not be combined statistically. Study interventions were associated with a reduction in perinatal death (pooled risk ratio [RR] from three studies 0·46, 95% CI 0·26—0·82) and stillbirth (pooled RR from three studies 0·42, 95% CI 0·19—0·93). The incidence of congenital syphilis was reduced in all four studies that measured this outcome with heterogeneous results.

Interpretation

Interventions to improve the coverage and effect of screening programmes for antenatal syphilis could reduce the syphilis-attributable incidence of stillbirth and perinatal death by 50%. The resources required to roll out antenatal screening programmes would be a worthwhile investment for reduction of adverse pregnancy outcomes and improvement of neonatal and child survival.

 

  • DOES EXTERNAL AID LEAD TO SHIFTING OF GOVERNMENT EXPENDITURE?

'[A]id needs to be structured in a way that better aligns donors’ and recipient governments’ incentives, using innovative approaches such as performance-based aid financing. Differing donor and government priorities lead to donor funds partly replacing government resources, especially in poor countries.'


Does Funding From Donors Displace Government Spending For Health In Developing Countries? 1. Marwa Farag, 2. A.K. Nandakumar, 3. Stanley S. Wallack, 4. Gary Gaumer and 5. Dominic Hodgkin + Author Affiliations 1. Schneider Institutes for Health Policy, Heller School for Social Policy and Management, Brandeis University, in Waltham, Massachusetts 1. Marwa Farag (marwa@brandeis.edu)

Best viewed at http://content.healthaffairs.org/content/28/4/1045.long

 

Abstract The notable increases in funding from various donors for health over the past several years have made examining the effectiveness of aid all the more important. We examine the extent to which donor funding for health substitutes for—rather than complements—health financing by recipient governments. We find evidence of a strong substitution effect. The proportionate decrease in government spending associated with an increase in donor funding is largest in low-income countries. The results suggest that aid needs to be structured in a way that better aligns donors’ and recipient governments’ incentives, using innovative approaches such as performance-based aid financing. Differing donor and government priorities lead to donor funds partly replacing government resources, especially in poor countries.

'The number of women who die during pregnancy or childbirth has decreased by more than a third globally since 1990, . . . the overall downward trend is insufficient to achieve the Millennium Development Goal (MDG) of a 75% reduction in maternal mortality between 1990 and 2015.'

  • ARE WE MAKING PROGRESS IN MATERNAL MORTALITY?

Anne  Paxton, Dr.P.H., and Tessa Wardlaw, Ph.D.

N Engl J Med 2011; 364:1990-1993May 26, 2011

Best viewed, with graphics, at http://www.nejm.org/doi/full/10.1056/NEJMp1012860?query=featured_home

The number of women who die during pregnancy or childbirth has decreased by more than a third globally since 1990, according to new estimates from the United Nations1 — from nearly 550,000 deaths in that year to roughly 350,000 in 2008. Yet progress has been uneven: while some countries have seen significant improvements, others have seen marked increases in maternal mortality. Furthermore, the overall downward trend is insufficient to achieve the Millennium Development Goal (MDG) of a 75% reduction in maternal mortality between 1990 and 2015 (see table Trends in Maternal Mortality Ratios, 1990–2008.). In the United States, where women's chances of surviving pregnancy and childbirth are far greater than in other parts of the world (see map Maternal Mortality Ratios, 2008., and interactive map, available with the full text of this article at NEJM.org) — the lifetime risk of pregnancy-related death for a U.S. woman is 1 in 2100, as compared with 1 in 31 for a woman in sub-Saharan Africa — maternal mortality actually increased during this period, according to United Nations estimates. Despite spending more money on health care than any other country, the United States has higher maternal mortality than many other developed countries. How do we interpret these data and conflicting impressions of progress and decline?

. . .

Where does all this leave us? Should we celebrate the global improvements in maternal mortality or chide ourselves for not being on target to meet the MDGs for maternal health? The overall picture is one of gradual but steady reduction in maternal deaths in most areas of the world — a global public health improvement that calls for cautious optimism. The attention that has been paid to the plight of women at risk of dying during pregnancy or childbirth and increased investments in health care systems, especially in basic and comprehensive emergency obstetrical care, have paid off. The dramatic improvements in China and gains in other Asian countries, which are associated with economic improvement, decreasing fertility rates, and strengthening of health systems, contrast with sharp increases in countries experiencing the chaos and destruction of war and HIV epidemics. The overall rate of decline in global maternal mortality, 2.3%, is lower than the 5.5% MDG target but is heartening nonetheless. We believe that continued focus on national and district-level planning to make pregnancy and delivery safer and to improve treatment of obstetrical complications, with particular attention to disadvantaged women, including those with HIV, will accelerate progress over the next decade.


Seven mistakes and potential solutions in epidemiology, including a call for a World Council of Epidemiology and Causality

Raj Bhopal

The electronic version of this article is the complete one and can be found online at:

http://www.ete-online.com/content/6/1/6

 

  • DIARRHEAL DISEASE RISK IN RURAL BANGLADESH DECREASES AS TUBEWELL DENSITY INCREASES

‘Increasing the amount of drinking water available to households through increased density of tubewells contributed to lower reports of cholera and shigellosis events in rural Bangladesh.’

 Abstract below; provisional .pdf file with full text is accessible from

http://www.ij-healthgeographics.com/content/10/1/41/abstract

 Diarrheal disease risk in rural Bangladesh decreases as tubewell density increases: a zero-inflated and geographically weighted analysis

Margaret Carrel, Veronica Escamilla, Jane Messina, Sophia Giebultowicz, Jennifer Winston, Mohammad Yunus, P. KIM Streatfield and Michael Emch

International Journal of Health Geographics 2011, 10:41 doi:10.1186/1476-072X-10-41

Published: 15 June 2011

Abstract (provisional)

Background

This study investigates the impact of tubewell user density on cholera and shigellosis events in Matlab, Bangladesh between 2002 and 2004. Household-level demographic, health, and water infrastructure data were incorporated into a local geographic information systems (GIS) database. Geographically-weighted regression (GWR) models were constructed to identify spatial variation of relationships across the study area. Zero-inflated negative binomial regression models were run to simultaneously measure the likelihood of increased magnitude of disease events and the likelihood of zero cholera or shigellosis events. The aim of this study was to examine the effect of tubewell density on both the occurrence of diarrheal disease and the magnitude of diarrheal disease incidence.

Results

In Matlab, households with greater tubewell density were more likely to report zero cholera or shigellosis events. Results for both cholera and shigellosis GWR models suggest that tubewell density effects are spatially stationary and the use of non-spatial statistical methods is appropriate.

Conclusions

Increasing the amount of drinking water available to households through increased density of tubewells contributed to lower reports of cholera and shigellosis events in rural Bangladesh. Our findings demonstrate the importance of tubewell installation and access to groundwater in reducing diarrheal disease events in the developing world.

 

 

 

Author Affiliations

Public Health Sciences, Centre for Population Health Sciences, University of Edinburgh, Edinburgh, EH9 8AG, UK

 Emerging Themes in Epidemiology 2009, 6:6 doi:10.1186/1742-7622-6-6

 © 2009 Bhopal; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

  • ·         SEVEN MISTAKES THAT EPIDEMIOLOGISTS MAKE

Abstract

All sciences make mistakes, and epidemiology is no exception. I have chosen 7 illustrative mistakes and derived 7 solutions to avoid them. The mistakes (Roman numerals denoting solutions) are:

1. Failing to provide the context and definitions of study populations. (I Describe the study population in detail)

2. Insufficient attention to evaluation of error. (II Don't pretend error does not exist.)

3. Not demonstrating comparisons are like-for-like. (III Start with detailed comparisons of groups.)

4. Either overstatement or understatement of the case for causality. (IV Never say this design cannot contribute to causality or imply causality is ensured by your design.)

5. Not providing both absolute and relative summary measures. (V Give numbers, rates and comparative measures, and adjust summary measures such as odds ratios appropriately.)

6. In intervention studies not demonstrating general health benefits. (VI Ensure general benefits (mortality/morbidity) before recommending application of cause-specific findings.)

7. Failure to utilise study data to benefit populations. (VII Establish a World Council on Epidemiology to help infer causality from associations and apply the work internationally.)

Analysis of these and other common mistakes is needed to benefit from the increasing discovery of associations that will be multiplying as data mining, linkage, and large-scale scale epidemiology become commonplace.

Introduction: epidemiological mistakes and solutions

All sciences and scientists make mistakes, and epidemiology and epidemiologists (including this writer) are no exception. Epidemiological mistakes may maim and kill, and sometimes the toll can be massive. The contemporary exemplar of this is hormone replacement therapy (HRT), used by millions of women in the hope of reducing cancer and heart disease [1,2]. Fortunately, the saving of life and health benefits arising from epidemiology, despite its mistakes, seem to outweigh the harm. The lives saved from epidemiological studies of tobacco, for example, possibly outweigh all our mistakes, and the information will save even more lives as tobacco control spreads globally, particularly in Asia[3]. This judgement, however, needs and deserves quantitative evaluation.

Mistakes in epidemiology are mostly simple, but they are often challenging, though only occasionally impossible, to avoid. Every study presents a dilemma on the balance between efficiency and accuracy. More generally, we have the puzzle of why mistakes continue to occur despite much guidance. Mistakes are rarely deliberate, and usually avoidable. I have chosen seven mistakes to illustrate how epidemiology goes wrong, and seven solutions are derived (these numbers were chosen to match the title of the presentation on which this paper is based - seven sins and seven commandments of epidemiology - which chimes with our wider culture on right and wrong). My chosen seven mistakes are a sample on which I have been reflecting [4], and against which I have personally battled, but there is scope for several papers of this kind. Phillipe Grandjean's paper on the seven deadly sins of environmental epidemiology covered human frailties, [5] so this one focuses on the scientific discipline, although the two perspectives overlap. Grandjean constructed his paper around the original sins (gluttony, sloth etc.) as shown in Table 1. The seven mistakes I have chosen illustrate some of the dilemmas facing all of us, and they focus us on principles. These mistakes call for better education and training. I have chosen one or two examples for illustration.

Table 1. Common vices in environmental epidemiology

Analysis

Mistake 1: Failing to provide the context and definitions of study populations

Textbooks tell us that epidemiology is a population science, though few discuss why [6], leading me to write a full chapter on the topic in my own textbook [6,7]. Populations differ by place, their characteristics and time. The results may not generalise easily between populations, within subgroups of the same population, or within the same population at different times. This applies particularly to the burden of disease and risk factors, but also to causal understanding. Thus, understanding the kind of population studied is essential. There is nothing more elementary in epidemiology but, nonetheless, this is possibly the commonest of the seven mistakes chosen for this paper.

The solution is:

(I) State the location and timing of fieldwork and describe the study population in detail, especially age, sex, socio-economic status and ethnic composition.

Rarely, the study location might be disguised to hide the identity of study participants, especially for rare, stigmatising conditions. If so, authors should use their discretion on the level of detail and, exceptionally, even hide the location. Authors need to justify the decision and inform the reader of why they took it. Otherwise, contextual detail must be given. Timing of fieldwork is essential for examining time trends as the date of publication is a sorry substitute. It is not enough to say the study was done in the USA or even New York, except when the work was indeed national and/or city-wide, respectively. Authors should be specific about the district of the city. Without the study population's details it is not possible to draw appropriate conclusions. This is obvious in relation to applied epidemiology used for health service/public health purposes. It also applies to causal research, where understanding the biological processes, presence of co-risk factors and competing risks of disease and death are so important to generalisation. An association may vary in its strength in different populations, reflecting the presence or absence of co-factors.

Examples

When answering specific questions, it is surprising how sparse the scientific literature is, and this applies particularly in low income countries as well as in relation to minority populations within the high income countries. As shown in table 2, in recent reviews my colleagues and I have found that information on time of fieldwork was present in every North American and European cardiovascular cohort study we examined, [8] but missing in a high proportion of studies on minorities and in West Africa [9-12]. By contrast, the cardiovascular cohort studies, particularly those in Europe, were lacking in information on the ethnic composition of the samples. Absence of such basics, especially as investigators move posts and are not always easy to contact, can undermine interpretation of individual publications and weaken both traditional and systematic reviews.

Table 2. Missing fieldwork dates and absence of information on ethnicity

Mistake 2: Insufficient attention to evaluation of error

Measurement is always imperfect in the empirical sciences, and especially in humans. The most fundamental error is mismeasurement, which is ubiquitous and often unavoidable. We have motivations to ignore error. We want a rapid, inexpensive and conclusive outcome. Seeking out and rectifying errors requires scarce time and resources, and funding (for pilot studies, for example) is not easy to obtain. We want (and need) publication. While acknowledging errors and limitations is good scholarship, openness can lead to rejection of manuscripts during review, particularly if errors could, in retrospect, have been avoided. Where publication is associated with direct financial rewards and prestige, the temptation to gloss over errors is strong. The solution arising is, again, a basic one, but one that needs reinforcement, for it is widely ignored.

Solution II: Don't act as if measurement error does not exist. If possible quantify it. If not, identify that as a limitation of the work. (Remember that lack of cross-cultural validity of measures may lead to serious errors.)

Examples

Our potential actions are to ignore errors, acknowledge them but do nothing, make qualitative adjustments in the interpretation - probably through qualifying words such as 'may', 'could', etc. (this is perhaps the commonest response) - or make quantitative adjustments to summary measures. Maldonado argues that making no quantitative adjustment equates to the assumption that the study's imperfections have no important impact on study results, which is mostly untrue. He demonstrates how to quantitatively adjust relative risk using error terms [13]. Such adjustments increase the uncertainty of the summary measures (widening confidence intervals). This makes conclusions more tentative, which is good science but potentially an obstacle to publication and implementation.

The need for cross-cultural validity of self report data is self evident but often ignored [14]. It is less obvious, and more controversial, that the interpretation of physical measures such as BMI, waist, birth weight, and fetal and childhood growth may differ across different populations, particularly by ethnic group [15]. The differential performance of clinical measures, such as the electrocardiogram, is reasonably well established, but has not led to any substantial programme of research to improve matters [16]. The cross-cultural, cross-national validity of biochemical measures, for example, the biological effect of a particular level of cholesterol, and normal values of glucose during the oral glucose tolerance test, has hardly been discussed.

Implementing this solution is a major challenge. The mistake is to ignore the problem.

Mistake 3: Not demonstrating comparisons are like-for-like, and the problem of confounding

Epidemiologists are fortunate that they study humans. This privilege comes at a price: the (relatively) easy route to causal knowledge through experimentation is largely barred for ethical reasons; the scientific principle of splitting a tissue specimen or a sample of cloned/inbred animals into a control or study group, permitting rigorous like-for-like comparisons, is rarely possible.

The closest practical alternatives in human epidemiology are randomised controlled trials, but even these have error. Even if like-for-like comparison is achieved by randomisation and blinding (both are needed), many factors including the selection of populations, may preclude causal inference to the target population, i.e. external validity. Only a small fraction of epidemiological questions are answerable using trials, either for ethical or resource- and time-related reasons. If comparing like-with-like is not possible, confounding is inevitable. The epidemiological mistake, however, is neither confounding nor failing to control for it - these are not fully in our hands. The mistake is not demonstrating whether comparisons are unlikely or likely to be like-for-like. Like mistakes 1 and 2 this one is also fundamental, and the solution is clear cut.

Solution III: Prepare a detailed, prior specification of the data to be collected in order to demonstrate the similarities and differences of comparison populations. Start the analysis with such detailed comparisons.

The paradox is that the first part of this solution is nearly always applied in trials (usually table 1), where it is not essential if the randomisation has worked, but is often missed out in other study designs, where it is imperative for data interpretation. The analysis must not proceed straight to comparisons of risk factor-disease outcome relationships. The strategy of controlling confounding within the (usually) multivariable analysis is not sufficient. The reason for this is that the variables entered are not comprehensive enough and that they are imprecisely measured and categorised. While the idea of residual confounding is known it is not taken seriously enough [17]. How often do authors conclude that the confounders cannot be controlled and that they have refrained from a multivariable analysis because causal conclusions cannot be drawn? That is a rare conclusion, but it should be a common one.

Example: alcohol

Behaviours are linked to other behaviours, social circumstances, age, sex and, of course, diseases. We might therefore assume that control of confounding is nigh impossible when we are looking for associations between single behaviours and disease outcomes. Instead of that, we find ourselves in almost endless controversies over repeated studies demonstrating a variety of associations that, in the paraphrased words of the late Petr Skrabanek, can be likened to punching a pillow, whereby the dimple so formed disappears, at which point we then punch it again, and again [18]. An example is the association between alcohol and cardiovascular diseases (CVD), which has been studied intensively for decades. Thousands of papers have resulted, many of them debating the evidence, which remains controversial. The study by Naimi et al. of the potential confounding factors using the 2003 Behavioural Risk Factor Surveillance System is illustrative [19]. This large telephone survey permitted examination of moderate drinkers (men 2 drinks, and women 1 drink, per day) and non-drinkers. The study showed that 27 out of 30 CVD-associated factors were significantly more prevalent in non-drinkers. Given imprecision in measurement of confounders, and the many other potential confounders not included in a telephone survey, is it not impossible to adjust for confounders in this and similar contexts? We need to confront such harsh realities. Implementing this solution will be a major advance in interpreting associations.

Mistake 4: Either overstatement or understatement of the case for causality based on associations

Overstatement of the case for causality is perennial, much discussed but not resolved. The problem is that causal reasoning is not suitable for an algorithm based approach. Counter-factual reasoning clarifies the underpinnings of causal reasoning in epidemiology, but it is theoretical [20-23]. The closest we come to the counterfactual ideal is trials, which are often not possible for ethical, financial or time-related reasons. Whenever possible, we should test out causal hypotheses using trials, but unless we envisage an age of unethical research, based on human experimentation, we will need to improve our conceptual frameworks for causal reasoning, particularly for non-trial epidemiology [20-23]. Causal frameworks in epidemiology, often founded on those of other disciplines, [4] have served us well and deserve to be improved through research rather than being subjected to the destabilising effects of attack and counter-attack. The interpretation of associations needs to be done with great rigour. In relation to mistake 7, and in my conclusion, I recommend that we set up a World Council in Epidemiology and Causality that compiles and evaluates evidence on associations.

Recently, a new problem has emerged: the understatement of the case for causality. Typically, the authors declare that a finding is not causal because the data come from a study of population statistics, or of cross-sectional, case-control or even cohort design. This arises from the too simplistic equating of study design with causal reasoning. As soon as epidemiologists postulate an association, never mind demonstrate that one exists, they are somewhere on the pathway of causal analysis. The key question is where we are on this path, surely the toughest one in epidemiology, and not one that can be evaded. It is made even tougher when trials and observational studies contradict each other. There are many good reasons why this contradiction happens, including the problem of confounding, insufficient study size (power) to demonstrate effects, the possibility that trials have not provided the duration and amount of exposure to the factor of interest to lead to an effect, the possibility that the exposure needs to be at a critical period of life that cannot be mimicked in a trial (for example, the first year), and, of course, that trials may be done in different kinds of populations to those studied in observational studies. The problem of causality is tough and deserves 7 solutions on its own, but I have chosen one.

Solution IV: Never say that a particular study design cannot contribute to causality or imply that causality is ensured by your design, but provide a judgement based on a theoretical perspective on causality and the world's empirical and theoretical literature.

Causal understanding may hold firm on the flimsiest of evidence (or even none that we recognise as epidemiology) and be demolished when it derives from large empirical data sets with strong designs (for example, cohorts), as in the example of HRT above [1,2]. A judgement that arises from the world's empirical and theoretical literature demands a discipline to avoid selective reading and rapid production of 'knowledge'. It demands a return to a chronological and thorough review as in a PhD, at least where causality is relevant. Ideas around causation are likely to be in commentaries and reviews, reports and theses, and introductory and discussion sections of empirical writings (not in the data in the results section). Such traditional reviews are surely more suited to in-depth causal thinking, while systematic reviews are better suited to quantifying effects, which is no more than the first step in the long path to declaring an association as causal.

Examples

In 1971 Herbst et al reported that their case-control study of adenocarcinoma of the vagina in young women showed an association with maternal use of stilbestrol [24]. The case group consisted of 8 girls born in New England hospitals between 1946 - 1951 and treated between 1966 - 1969. They selected 4 controls per case. The data on oestrogens given to mothers in the relevant pregnancy were as follows:

Cases: 7/8

Controls: 0/32

P < 0.00001 (chi squared)

Herbst et al's discussion of their findings was integrated in terms of epidemiology, biology and clinical medicine. Their understated but clear-cut conclusion was that "... the results of this study suggest it is unwise to administer stilbestrol to women early in pregnancy." They did not flinch from the challenge because the case group was so small and the power of the study was low. Equally, they did not hedge their bets by saying case-control studies do not produce causal evidence. Let us contrast this with a recent case-control study.

Ismail et al studied risk factors for myocardial infarction (MI) in Pakistan in a case-control study [25]. They highlighted 8 risk factors in the abstract. Of these, six had odds ratios (ORs) = 3 and one had an OR = 0.04 (95% CI: 0.01 - 0.35). They concluded:

"...While this study does not establish a cause-effect relation ... it raises the possibility that several of the associated factors may be modifiable risk factors ...". "Based on our findings, we suggest that stringent ...". They then listed six public health actions based on their risk factors. This claim that the study design does not permit a causal interpretation, while proceeding to interpret it as causal, is not good epidemiology. This kind of contradictory reasoning is common, as shown in the abstracts of the Society for Epidemiological Research (SER) Conference 2008; examples include abstract 77 and abstract 378 [26].

Each risk factor needs to be interpreted using an appropriate causal framework, and with reference to the full scientific literature and not just the study's data. Implementing this solution will be tough, as it requires deep scholarship that transcends the disciplines that underpin causal understanding, including biology, pathology, epidemiology, statistics, social science and philosophy. Authors may be pressured by editors, referees and their own institutions into these mistakes on causality, but they remain responsible for them, so need to resist external pressures.

Mistake 5: Not providing appropriate, and appropriately adjusted, absolute and relative measures

Accurate age- and sex-specific rates underpin virtually everything we value highly in epidemiology. Other data summaries distort the basic epidemiological reality of such rates. How much time do we spend looking at age- and sex-specific rates, the building blocks of epidemiology? How much do we reflect on the distortions of other forms of data presentation? By choosing one pathway to analysis - usually relative measures such as the relative risk and the odds ratio - we close off other options. As a minimum, however, in recognition of their different messages, we should give absolute and relative measures. Relative measures are particularly prone to distortion, and some, such as the odds ratio, have an inbuilt exaggeration of the association. When we use measures such as ORs we should ensure they are adjusted to give valid relative measures [7,27].

The solution is important for epidemiology:

Solution V. Give numbers, rates and comparative measures - rates hold primacy - and adjust the summary measure if appropriate.

Examples

I have emphasised the importance of absolute measures, especially for health needs assessment, for more than 20 years [28]. The data in table 3, showing how different priorities seem when examined from an absolute compared to relative risk perspective, continue to surprise both practitioners and researchers [28-30]. The topic remains controversial, especially in the health inequalities arena [31,32].

Table 3. Deaths and SMRs* in male immigrants from the indian sub continent (aged 20 and over; total deaths = 4,352)

The odds ratio is particularly prone to giving results that are interpreted very differently (and often wrongly) from the corresponding absolute measure and even the corresponding relative measure. One of many examples that has drawn critical comment, diverting from the main message of the paper, is the work of Barnes and Bero, reporting that there was a strong association between conclusions of review articles and authors' affiliations with the tobacco industry [33]. The published odds ratio was 88.4 (95% CI: 16.4 -476.5). The actual data were that 10 of 75 (13.3%) reviews by non-tobacco-affiliated authors concluded that passive smoking was not harmful to health. By contrast 29 of 31 (96.1%) reviews by tobacco-affiliated authors reached this conclusion. The result from the odds ratio is at odds with actual data, the prevalence ratio (7.3), and the absolute risk difference (82.8%). This odds ratio was misinterpreted in the BMJ as a risk ratio.

The question of what odds ratios measure in case-control studies has been reviewed recently, with the conclusion that there is insufficient attention to this issue [34]. My work with Katherine MacGilchrist and Robin Prescott has shown that about 50% of the reports of odds ratios in four major medical journals in the year 2000 were contrary to epidemiological guidance on their presentation and/or interpretation (unpublished).

Mistake 6: Making public health recommendations from intervention studies that show specific benefits but not do not demonstrate general health benefits

We live in a specialist's world. We have cardiologists and cardiovascular epidemiologists who want to control cardiovascular disorders. But there is no point if there is no net benefit, for example, if costs and side-effects balance or even outweigh the benefits. We really need, at least from a health and health care perspective, a life expectancy and health expectancy specialism to dominate the scene. Conclusions from research on specific outcomes draw important but still-limited conclusions, and these should be tested against the goal of general benefits. Of course, specific outcomes help in the causal endeavour, where contradictory results are particularly informative, raising questions about why a particular factor increases one disease or outcome, while decreasing another. The solution here is obvious but it has wide-ranging repercussions.

Solution VI. Ensure general benefits (e.g. mortality/morbidity) exceed the general costs before recommending a public health or clinical application of a study showing a specific benefit.

Examples

The benefits and costs of HRT in relation to post-menopausal symptoms (beneficial), and cardiovascular disease and cancer (not beneficial) are well known and were discussed earlier. Vitamin A at birth reduces mortality, at least in many Asian populations. However, it does not seem to produce the same benefits in Guinea-Bissau in Africa [35-37]. Even in India and Pakistan, the benefits are contested now, and it will not be beneficial in that setting for ever [35-37]. A recent study reported that reducing glycated haemoglobin to 6% in the elderly will improve control of diabetes, much desired by diabetes specialists, but increase mortality, an unfortunate and unexpected side-effect [38,39]. By contrast, Gaede et al reported a multifactorial intervention for people with diabetes that reduced non-fatal cardiovascular disease, progression to end-stage renal failure, and all cause mortality - perhaps an exemplary set of outcomes [40].

Following this solution would require larger trials, but in return the results would be more readily applicable in population settings. Where a trial can only demonstrate cause-specific benefits, the authors need to temper their public health-related conclusions, and consider the possibility of harmful effects that negate the benefits. Further, the net benefit of an intervention will be dependent on the mix of conditions in each population. To take a simple example, if an intervention reduces CHD but increases cancer, it will probably have net benefits in populations where CHD is common and cancer rare, but probably net harm where the opposite applies. In reality, trials will often not be powered to demonstrate general health benefits (except when these are claimed for the intervention), so information on harm may need to come from alternative sources, such as health monitoring data. Public health recommendations should be tentative until such data are available.

Mistake 7: Failure by investigators and local health systems to utilise study data correctly to benefit health - a need for a higher authority providing a unified voice

Interpreting data correctly is among the highest intellectual endeavours in science, perhaps on a par with generating worthwhile hypotheses. Making health care and public health recommendations from data extends this skill. People who combine these skills are rare. The first skill needs razor sharp thinking on the scientific aspects of data, the second, similar capacity in relation to politics, policy, leadership, management and clinical care and public health. We can fail to apply data in two main ways - misapplication arising from misinterpretation, and non-application because the information has been set aside, or not brought to attention, or ignored.

There is an ethical imperative to act where it is warranted. Academic epidemiologists are, however, under pressure to research and teach, not to serve, and service-based clinicians and public health staff are under pressure to deliver services. The two worlds have been parting ways for some time [41,42]. The solution here is organisational.

Solution VII

Epidemiology needs to provide partners who apply research, including politicians, doctors, and public health specialists, with a unified voice. Is it not time for a World Council in Epidemiology and Causality that provides authoritative statements on epidemiological evidence and makes recommendation on when and how epidemiological data on associations are ready for application? I return to this question in the conclusions.

Example

The need for a unified voice is shown by 'Causality: A Frank Statement to Cigarette Smokers', the 1954 advertisement in US newspapers by 14 tobacco companies and trade associations, recently reprinted in the Lancet [43]. Among the statements about the relationship between tobacco and lung cancer were these:

"... experiments on mice have given wide publicity to a theory ...".

"... eminent doctors and research scientists have publicly questioned the claimed significance of these experiments."

"Distinguished authorities point out: That there is no agreement among the authorities regarding what the cause is "

(and 5 more points are made in a similar vein).

There will always be dissenting voices, and controversy can be exploited easily unless there is an authoritative voice that is trusted and independent. Such a voice is required to help apply important causal evidence, even when there is national hesitancy. Witness, for example, the failure to apply the knowledge that infants should be placed on their backs to sleep, to halve the risk of sudden infant death syndrome. Many European countries failed to apply this, leading to the unnecessary deaths of thousands of infants in Europe alone [44].

Conclusion

There are numerous guidelines, published over some decades, on how to undertake and publish epidemiological research [45,46], available at the EQUATOR website http://www.equator-network.org/index.aspx?o=1032; accessed 14/8/08 webcite. These enjoy interesting acronyms such as CONSORT, STROBE, PRISMA, etc. Journals provide detailed guidance to authors and referees. Books summarise these for students. So why do we not apply the guidance? I think that our human frailties, the innate limitations of our science, insufficient education and training, and pressures of time and resources combine, making it hard to avoid the kind of fundamental mistakes illustrated in this paper. If so, the lessons are that:

1. we need to pay attention to the development of ethical and rigorous epidemiologists of high integrity [5,47] with high-level conceptual, theoretical and technical skills;

2. we make the innate limitations of our discipline more explicit;

3. we reorganise our scientific endeavour to make a collective, focused and more unified approach possible.

The seventh solution asks us to create a unified voice by pooling our intellectual resources, and creating a new global authority, to which I have given a provisional title. A World Council on Epidemiology and Causality could, however, dampen innovation. Alternatively, it could hasten advances, and counter the onslaught of undigested associations that bewilder us and will be multiplying as computerised data mining, data linkage, genetic epidemiology, and grand-scale epidemiology on millions of study participants become commonplace. (The analogy here is to do for associations and causality what the Cochrane collaboration, and the UK National Institute for Clinical Excellence, is doing for effectiveness of interventions.) Epidemiologists guard their academic freedom zealously and are mistrustful, sceptical people, particularly in relation to institutions. Nonetheless, to counter criticisms about false findings [18], advance epidemiology, and properly engage the public, we need to try out such a Council, learn from the experience and find workable, collaborative, global solutions to the kinds of problems illustrated here.

Competing interests

The author declares that they have no competing interests.

Authors' contributions

The author is solely responsible for this manuscript from conceptualisation to writing.

Acknowledgements

This manuscript develops a presentation at the 18th IEA World Congress of Epidemiology, Brazil 2008: Course on Epidemiologic Research and New Directions

Session Theme: Dilemmas and conundrums from epidemiologic research: have we learned the lessons?

Paper title: Conundrums and Dilemmas in Epidemiology: 7 sins and 7 commandments

I thank my colleagues Dr Charles Agyemang (a self-acknowledged epidemiological sinner like me) for helpful advice, and Professor Aziz Sheikh for detailed critical commentary on an earlier draft. I also thank several referees for helpful criticisms.

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WHAT’S NEW IN MALE CIRCUMCISION: ITEMS FROM WWW.CHILDSURVIVAL.NET

The three published RCTs on reduction of HIV acquisition through male circumcision laid the basis for the UN recommendations in favor of medical circumcision of males. More recent research (see below) points to a protective effect against HPV as well.

Remarkably, the growth of medical circumcision in African countries continues even as San Francisco prepares to vote on a blanket ban on pediatric circumcisions, with no religious exemptions.  Who is proceeding on data based decision making: the governments of Africa, or the intactivists of California?

  • NEW ESTIMATES OF THE POPULATION IMPACT OF CIRCUMCISION INTERVENTIONS 

‘Communities, and especially women, may benefit much more from circumcision interventions than had previously been predicted, and these results provide an even greater imperative to increase scale-up of safe male circumcision services.’

Sex Transm Infect 2011;87:88-93; Volume 87, Issue 2

This article is best viewed at http://sti.bmj.com/content/87/2/88.long

Abstract

Background

Mathematical modelling has indicated that expansion of male circumcision services in high HIV prevalence settings can substantially reduce population-level HIV transmission. However, these projections need revision to incorporate new data on the effect of male circumcision on the risk of acquiring and transmitting HIV.

Methods

Recent data on the effect of male circumcision during wound healing and the risk of HIV transmission to women were synthesised based on four trials of circumcision among adults and new observational data of HIV transmission rates in stable partnerships from men circumcised at younger ages. New estimates were generated for the impact of circumcision interventions in two mathematical models, representing the HIV epidemics in Zimbabwe and Kisumu, Kenya. The models did not capture the interaction between circumcision, HIV and other sexually transmitted infections.

Results

An increase in the risk of HIV acquisition and transmission during wound healing is unlikely to have a major impact of circumcision interventions. However, it was estimated that circumcision confers a 46% reduction in the rate of male-to-female HIV transmission. If this reduction begins 2 years after the procedure, the impact of circumcision is substantially enhanced and accelerated compared with previous projections with no such effect—increasing by 40% the infections averted by the intervention overall and doubling the number of infections averted among women.

 

  • LESSONS LEARNED FROM THE FIRST YEAR OF MC IMPLEMENTATION IN NYANZA, KENYA

The authors reviewed health facilities for seven criteria for provision of male circumcision services:

  1.       Room available for surgery (e.g., minor theater)
  2.       Room available for recovery
  3.       Trained and available staff
  4.       Sterilization and infection control compliance
  5.       HIV voluntary counseling and testing (VCT) and risk-reduction counseling
  6.       STI syndromic diagnosis and treatment
  7.       Provision and promotion of male and female condoms

Countries considering the promotion of male circumcision should consider doing likewise.

Best viewed at http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0018299

  • MALE CIRCUMCISION IN EIGHT AFRICAN COUNTRIES 

EXCERPT FROM THE UN REPORT, 'AIDS AT 30: NATIONS AT THE CROSSROADS'

Medical circumcisions in eight African countries have risen to 350,000 per year from low baseline levels, according to this UN report. This, however, leaves millions of at risk males in eastern and southern Africa uncircumcised. Text below and at http://www.unaids.org/unaids_resources/aidsat30/aids-at-30.pdf page 66.

TEXT FROM UN REPORT:

'Over the past decade, a major tool for HIV prevention has emerged: voluntary medical male circumcision. To date, introduction of this breakthrough strategy has been slow, underscoring the need for urgent action to bring circumcision services to scale.

'At the time of the 2001 United Nations General Assembly Special Session, epidemiological patterns suggested that circumcised men might be less likely to become infected by HIV. However, no clinical trials had been performed that would provide definitive scientific evidence that medical circumcision of adult men reduced the odds of female-to-male sexual transmission.

'Beginning in 2005, a series of randomized controlled trials in sub-Saharan Africa found that circumcising adult men reduced their risk of infection by about 60%. These findings resulted in a major effort to introduce circumcision in settings with both high HIV prevalence and low levels of male circumcision. Male circumcision offers a partial reduction in HIV risk. Its main advantage is that, once performed, the risk reduction is life-long.

'The prevalence of circumcision varies considerably in sub-Saharan Africa. Although it is common in many areas, especially in West and Central Africa, most men are not circumcised in the Southern African countries most heavily affected by HIV. In nine countries in Southern Africa and four in Eastern Africa, less than 80% of adult men are circumcised. Outside Eastern and Southern Africa, only in the Central African Republic and Sudan are less than 80% of men circumcised.

  • LOW RISK HPV AND MALE CIRCUMCISION IN YOUNG SOUTH AFRICAN MALES

‘This study shows a reduction in LR-HPV infection among circumcised men.’

Best read at http://www.ncbi.nlm.nih.gov/pubmed/21584275

 

  • MALE CIRCUMCISION AND LOWER PREVALENCE OF HPV LESIONS IN KENYAN MEN

‘This study suggests that circumcision reduces the prevalence of HPV-associated flat lesions and may ultimately reduce male to female HPV transmission.’

Abstract below; full text, to subscribers, at http://onlinelibrary.wiley.com/doi/10.1002/ijc.26196/pdf

 International Journal of Cancer

Abstract

Human papillomavirus (HPV)-associated penile lesions in men may increase the risk of HPV transmission to their female partners. Risk factor data on HPV-associated penile lesions are needed from regions with a high burden of cervical cancer. Visual inspection of the penis was conducted using a colposcope at the 24-month visit among participants in a randomized controlled trial of male circumcision in Kenya, from May 2006 to October 2007. All photos were read independently by two observers for quality control.

Penile exfoliated cells sampled from the glans/coronal sulcus and the shaft were tested for HPV DNA using GP5+/6+ PCR and for HPV16, 18 and 31 viral loads using a real time PCR assay. Of 275 men, 151 were circumcised and 124 uncircumcised. The median age was 22 years.

Circumcised men had a lower prevalence of flat penile lesions (0.7%) versus uncircumcised (26.0%); adjusted odds ratio [OR]=0.02; 95% confidence interval [CI]: 0.003-0.1). Compared to men who were HPV-negative, men who were HPV DNA positive (OR=6.5; 95%CI: 2.4-17.5) or who had high HPV16/18/31 viral load (OR=5.2; 95%CI: 1.1-24.4) had higher odds of flat penile lesions. Among men with flat penile lesions, HPV56 (29.0%) and 16 (25.8%) were the most common types. Flat penile lesions are much more frequent in uncircumcised men, and associated with higher prevalence of HPV and higher viral loads. This study suggests that circumcision reduces the prevalence of HPV-associated flat lesions and may ultimately reduce male to female HPV transmission. © 2011 Wiley-Liss, Inc.

  • EFFECT OF CIRCUMCISION OF HIV SERONEGATIVES ON HPV TRANSMISSION TO SERONEGATIVE WOMEN IN THE UGANDA
    • ·Bottom of Form

 ‘Our findings indicate that male circumcision should now be accepted as an efficacious intervention for reducing the prevalence and incidence of HPV infections in female partners. However, protection is only partial; the promotion of safe sex practices is also important.’

 Best viewed in full at

 http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)61967-8/fulltext

 

  • CIRCUMCISION IN INDIA: TAKING THE ROAD LESS TRAVELED 

‘There is an immediate need to focus on circumcision as an important public health intervention at least coupled with the other preventive strategies like condom use, delayed sex onset, lesser number of partners, STDs management, HIV testing and counseling, and it can adequately reinforce our fight in preventing the HIV epidemic.’

Gude D. Circumcision in India: Taking the road less traveled. Indian J Public Health 54:228.

Full text: http://www.ijph.in/text.asp?2010/54/4/228/77268

 

  • RISK COMPENSATION AMONG CIRCUMCISED MEN IN KENYA

‘The results of this study illustrate that MC does not necessarily lead to risk compensation, and that there are different behavior change outcomes.’

“When I Was Circumcised I Was Taught Certain Things”: Risk Compensation and Protective Sexual Behavior among Circumcised Men in Kisumu, Kenya

Best viewed at http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0012366

 

  • ROLL-OUT OF ADULT CIRCUMCISION PRACTICES IN SOUTH AFRICA

As recently as 10 years ago, the Republic of South Africa had a president who denied the causal link between HIV and AIDS, and a health minister who promoted herbal remedies in preference to ARVs.

As Lissouba and colleagues show, things change.

Good reading.
 

A Model for the Roll-Out of Comprehensive Adult Male Circumcision Services in African Low-Income Settings of High HIV Incidence: The ANRS 12126 Bophelo Pele Project

Best viewed at http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1000309

  • RECOMMENDATIONS ON MALE CIRCUMCISION IN SOUTH AFRICA

This desk review of literature on male circumcision, also available at

http://www.malecircumcision.org/programs/documents/Review_MC_research_services_SA.pdf

comes from the first country in Africa to publish a randomized clinical trial on the impact of male circumcision on HIV acquisition in sexually active males. Given the progress of MC in neighboring countries, South Africa’s position is proof positive that ‘the first shall be last, and the last first.’

 Recommendations are at the foot of this Email.

 Country updates from other African countries are available online at

http://www.malecircumcision.org/programs/country_implementation_updates.html#progress_in_scaleup2

 

RECOMMENDATIONS

 The following recommendations from this review should be taken into consideration in

expanding, promoting and integrating MC into existing health services:

          Future expansion of circumcision services must be embedded within comprehensive HIV prevention programming, including informed consent, confidentiality, a stigma free environment, HIV counselling and testing and risk-reduction counselling.

         MC programmes should be designed to increase uptake of HCT and partner disclosure, as well as counselling to minimise MC in HIV positive men; priority should be placed on pairing MC roll-out with successful/innovative approaches such as home-based testing, integration of HCT with family planning clinics, male-oriented services).

          A plan for introduction of voluntary neonatal MC services within the provisions of the Children’s Act  of 2005 and integration of neonatal MC into existing maternal, women, neonatal and child health programmes must be drawn up.        

          MC must be delivered as part of a recommended minimum package which includes     counselling about risks and benefits of MC, counselling around risk reduction, HIV counselling and testing, couple counselling, condom promotion and provision, and STI management.

          A plan for reciprocal linking of traditional and medical MC is required. MC in traditional settings should include standards for infection control, pain management, and counselling on HIV prevention, sexual and reproductive health and rights of women and mechanisms to train traditional MC providers are urgently required. In addition, messaging around reduction of stigma and discrimination for males who opt for circumcision in clinical settings and before the age of traditional initiation is necessary.

          A forum be set up to ensure structured coordination and communication of activities and resources of donors and other stakeholders including policymakers, technical teams, private and public sector health providers.

         A culturally sensitive communications strategy for promoting acceptability and access to both adult and neonatal MMC and targeting both men and women for dissemination of consistent and correct packaging of messages around MC is critical.

         In order to address human resource challenges; service integration, task sharing, standardisation of methods and equipment, large scale training of health workers and integration of private health providers must be undertaken.

         The absence of existing mechanisms to monitor and evaluate the impact of the proposed national MC policy such as indicators for monitoring and evaluation, and quality assurance standards must be urgently addressed.

         Consideration should be given to the expansion of dedicated sexual and reproductive health services in SA, targeted at young men through schools and health facilities which could include MC as well as counselling on sexual health, substance abuse etc.

 

  • TWO ON THE RESULTS OF THE LONDON PLEDGING CONFERENCE

 

1) GAVI PRESS RELEASE FROM THE LONDON PLEDGING CONFERENCE

GAVI Alliance poised to immunise more than 250 million children in developing countries by 2015 LONDON, 13 June 2011 – Major public and private donors achieved a milestone in global health today by committing funding to immunise more than 250 million of the world’s poorest children against life-threatening diseases by 2015 and prevent more than four million premature deaths. Donors committed US$ 4.3 billion at the first pledging conference held by the GAVI Alliance. This exceeds an initial target of $3.7 billion, enabling GAVI to reach more children faster than planned and to accelerate the introduction of new vaccines. A portion of the pledges are conditional upon GAVI raising additional funds from new donors in the future. Today’s pledges bring GAVI’s total available resources for the period 2011 to 2015 to $ 7.6 billion. The increased support is timely. GAVI recently reported a record 50 countries applied for vaccine funding during the Alliance’s latest application round – nearly double the previous record in 2007. This new support will allow GAVI to fully fund approved applications. “Today is an important moment in our collective commitment to protecting children in developing countries from disease,” said President of Liberia Ellen Johnson Sirleaf. “But every 20 seconds, a child still dies of a vaccine-preventable disease. There’s more work to be done.” The meeting convened prime ministers, ministers and high-level officials from donor and developing countries, leaders of UN Agencies, CEOs from private companies and senior civil society leaders to make commitments to support GAVI’s life-saving work. The meeting was hosted by the governments of the United Kingdom and Liberia and the Bill & Melinda Gates Foundation. Governments more than doubled their previous commitments and new donors will also give for the first time, including Japan and Brazil. GAVI’s largest corporate donor, “la Caixa” Foundation, extended its financial commitment and new donors Anglo American plc and Absolute Return for Kids (ARK) made their first pledges. Developing countries committed to maintain or increase the co-financing of their vaccine programmes and leverage the partnership to immunise their children. GAVI estimates that the total level of co-financing will triple to US$ 100 million by 2015. Vaccine manufacturers announced last week they will contribute by offering lower prices on a range of life-saving vaccines supported by GAVI, including a two-thirds reduction on the rotavirus vaccine, which combats the leading cause of diarrhea deaths. Co-financing and lower prices will enhance the sustainability of immunisation programmes. “GAVI was one of the very top performers in our root-and-branch review of the agencies that deliver British aid because it demonstrates tangible results. Britain will play its full part and our support to GAVI will help vaccinate over 80 million children and save 1.4 million lives. That’s one child vaccinated every two seconds for five years,” said David Cameron, UK Prime Minister. "For the first time in history, children in developing countries will receive the same vaccines against diarrhea and pneumonia as children in rich countries,” said Bill Gates, co-chair of the Bill & Melinda Gates Foundation. “Together we must do more to ensure that all children – no matter where they live – have equal access to life-saving vaccines.” Conference participants agreed that the momentum to reach more children with vaccines must be maintained and they encouraged GAVI to expand coverage of immunisation programmes and accelerate the introduction of new vaccines. It was also recognised that vaccine manufacturers should continue to deliver and expand on their promises to reduce vaccine prices and provide greater access, while the countries themselves should continue to meet their co-financing commitments. Participants also agreed to meet in two years time to review GAVI’s progress in immunisation and resource mobilisation. “Today was a vote of confidence for GAVI. But it was also a challenge to us: to keep delivering on our mission and to do even more. Nearly two million children die from vaccine-preventable diseases every year. The day will come when malaria and other killer diseases can be beaten with a simple shot in the arm. We must prepare for that day. Working with partners, GAVI will need to continue to raise the necessary resources to tackle all vaccine-preventable diseases,” said GAVI Alliance Board Chair Dagfinn Høybråten.

2) QUERY TO READERS

The London pledging meeting saw pledges to the GAVI Alliance of $4.3 billion. If you were on the GAVI Board, how would you propose  to spend the $600 million pledged today, over and above the $3.7 billion targeted primarily for pneumococcal and rotavirus vaccines? Reply to rdavis@africamail.com

 

WHAT’S NEW ON WWW.CHILDSURVIVAL.NET: THE 30TH ANNIVERSARY OF AIDS

This month marks the thirtieth anniversary of the first detected case of AIDS. The UN has hosted a three day conference on the subject, with a report at http://www.unaids.org/unaids_resources/aidsat30/aids-at-30.pdf

  • THE 30 YEARS’ WAR AGAINST AIDS

The Economist, Monday June 6th 2011

The 30 years war: Hard pounding is gradually bringing AIDS under control

‘[T]his is the sort of area where a single scientific breakthrough might, like the invention of AIDS-suppressing drugs and the discovery that those drugs could be used to break the chain of transmission, change everything.’

This article is best viewed at http://www.economist.com/node/18772276

  • AIDS, 30 YEARS ON: A PODCAST FROM THE BBC WORLD SERVICE

Podcast,  http://www.bbc.co.uk/iplayer/console/p00gzd9c

 

  • AIDS IN RETROSPECT: A PODCAST FROM THE ECONOMIST

A summary of three decades' experience, at http://www.economist.com/blogs/multimedia/2011/06/end-aids

  • COVERAGE OF ANTIRETROVIRAL THERAPY AT THE END OF 2009 (WHO 2010 GUIDELINES, CD4<350)

Coverage of antiretroviral therapy at the end of 2009 (WHO 2010 Guidelines, CD4<350)

Burundi and Rwanda, neighboring countries at similar socio-economic levels. One is in the top quintile; the other, at the bottom.

Below, top and bottom quintiles; all quintiles and countries listed on page 45, AIDS AT 30, http://www.unaids.org/unaids_resources/aidsat30/aids-at-30.pdf

>80% COVERAGE

Botswana

Cambodia

Cuba

Guyana

Oman

Romania

Rwanda                  

 

0-20% COVERAGE

Burundi

Central African Republic

Colomiba

DRC

Djibouti

Egypt

Gambia

Iran

Kyrgyzstan

Latvia

Lebanon

Liberia

Madagascar

Maldives

Mongolia

Myanmar

Nepal

Pakistan

Republic of Moldova

Russian Federation

Sierra Leone

Somalia

Sri Lanka

Sudan

Tajikistan

Ukraine

  • ANTIRETROVIRALS PROTECT PARTNERS FROM HIV

 

A randomized clinical trial in developed and developing countries has shown dramatic declines in HIV transmission among serodiscordant heterosexual couples when ARVs are started early in HIV seropositives.

'This breakthrough is a serious game changer and will set the prevention revolution forward,' according to Michel Sidibe, head of UNAIDS.

This update should be read in tandem with two others, 'HIV prevalence in Zimbabwe,' which calls for early inception of ARV treatment, and 'Provider Initiated HIV Testing.' According to the latter article, '‘The introduction of routine PITC using lay counsellors into health-care clinics in Lusaka, Zambia, dramatically increased the uptake and acceptability of HIV testing.’

Timely and early treatment cannot begin when at risk persons remain ignorant of their serostatus. Provider initiated HIV testing may have to supplement VCT if the proportion of those getting themselves tested is to rise.

Top of Form

National Institute of Allergy and Infectious Diseases (NIAID)
http://www.niaid.nih.gov

Treating HIV-infected People with Antiretrovirals Protects Partners from Infection

Findings Result from NIH-funded International Study

Men and women infected with HIV reduced the risk of transmitting the virus to their sexual partners by taking oral antiretroviral medicines when their immune systems were relatively healthy, according to findings from a large-scale clinical study sponsored by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.

  • HIV TREATMENT AS PREVENTION

Lancet editorial:

Last week any doubts around treatment as an approach to halt the spread of the HIV epidemic were allayed. An international study showed that antiretroviral treatment can prevent the sexual transmission of HIV among heterosexual couples in whom one partner is HIV-infected and the other is not. UNAIDS described the result as a “serious game changer” for HIV prevention. The phase 3 clinical trial, HPTN 052, was done by the HIV Prevention Trials Network and funded by the US National Institutes of Health. It was due to run until 2015, but compelling interim results led the international data and safety monitoring board to recommend the results be publicly released as soon as possible. Although the results are unsurprising given the extensive ecological data supporting the prevention benefi ts of treatment, this is the first large randomised trial to provide a true impact evaluation. The study showed a 96% reduction in risk of HIV transmission—the primary outcome. The trial began in 2005 and enrolled 1763 HIV serodiscordant couples across 13 sites in nine countries in Asia, Africa, and the USA. At enrolment, the HIVpositive partner was required to have a CD4 cell count between 350 and 550 cells per μL. The median CD4 count at enrolment was 436 cells per μL. This level is higher than WHO’s recommendation to start treatment, which is at 350 cells per μL or less. This diff erence is important because the HIV-positive individuals were asymptomatic, did not require treatment, and certainly would not have been eligible for treatment, according to most national guidelines. Couples were randomised so that the HIVpositive partner received antiretrovirals immediately, or delayed treatment until their CD4 counts fell below 250 cells per μL, or had an AIDS-related event such as pneumocystis pneumonia. Throughout the study both groups received the same amount of HIV-related care and counselling. Among the 877 couples in the delayed group, 27 HIV transmissions occurred compared with one transmission in the immediate group. This diff erence was highly statistically signifi cant (p<0•0001). Furthermore, the new infections were confi rmed as being genetically linked to the HIV-positive partners, though there were a cluster of unlinked cases, raising the issue of concurrency. The study also found a statistically signifi cant reduction in extrapulmonary tuberculosis with 17 cases in the delayed group versus three cases in the immediate group. Study participants and investigators have been informed of the results and all participants off ered the appropriate care. All study participants will be followed for at least 1 more year. Clearly, treating sooner rather than later results in both a clinical benefi t for the individual and has a potentially enormous public health benefi t in slowing the spread of infection. These results are likely to provide a new level of dialogue between physician and patient. Besides emphasising the benefit of medication adherence to the patient, clinicians could stress how it has the potential to benefit others alongside other altruistic practices such as condom use. Indeed, one of the most interesting observations was that most patients adhered to treatment and 95% had viral load suppressed at all times, which is a rare outcome for an HIV clinical trial. Treatment as prevention should decrease stigma and improve uptake of testing because there is more of an incentive for people to know their status with the reassurance of knowing that if treated early they are unlikely to infect others. Many interesting research questions now lie ahead. But most urgent will be the assessment of the practical impact of these fi ndings and their public health importance in generalised epidemics. Another immediate issue will be to refl ect these fi ndings in ongoing and future prevention trials. Certainly in discordant couples it will be unethical not to offer treatment to infected people. Findings now need to be translated into policy and action. Agencies such as President’s Emergency Plan For AIDS Relief and the Global Fund to Fight AIDS, Tuberculosis and Malaria need to reassess their prevention portfolios and consider diverting funds from programmes with poor evidence (such as behavioural change communication) to treatment for prevention. There is now an ethical imperative for guidelines to be revised to start treatment much earlier than recommended. But, with 6 million people on treatment and another 9 million needing treatment, how to fund and sustain such an endeavour with functioning health systems and a suffi cient workforce will be a huge challenge. One needs to take this data yet to be peer reviewed and published with caution. But if true, these findings present an opportunity to make a big difference in the epidemic over the next few years. ■ The Lancet

Editorial www.thelancet.com Vol 377 May 21, 2011 1719
For the National Institutes of Health news release on the HPTN 052 trial see
http://www.niaid.nih.gov/news/newsreleases/2011/Pages/HPTN052.aspx

 
For more on the HPTN 052 trial see

http://www.hptn.org/web%20documents/PressReleases/HPTN052PressRelease FINAL5_12_118am.pdf

  • UNDER-FIVE MORTALITY FROM AIDS: REGIONAL TRENDS

[I]n 2009, HIV accounted for roughly 2.1% (1.2–3.0%) of under-5 deaths in low- and middle-income countries and 3.6% (2.0–5.0%) in sub-Saharan Africa. The percentage of under-5 deaths due to HIV has been falling in the last decade. . . .

‘The fall in under-5 deaths due to HIV has been driven by a combination of factors, including scale-up of prevention of mother-to-child transmission and treatment for pregnant women and children as well as a decrease in HIV prevalence among pregnant women.’

Best viewed at http://sti.bmj.com/content/86/Suppl_2/ii56.long

  • THE HISTORY OF AIDS: HEROES AND VILLAINS

The history of AIDS : Heroes and villains

The story of AIDS involves many larger-than-life characters, good and bad

The Economist, Jun 2nd 2011 | from the print edition

http://www.economist.com/node/18772268

  • THE END OF AIDS?

A video from The Economist, at http://www.economist.com/blogs/multimedia/2011/06/end-aids
with a retrospective look at 30 years of HIV/AIDS.

  • TOWARDS AN IMPROVED INVESTMENT APPROACH FOR AN EFFECTIVE RESPONSE TO HIV/AIDS

 ‘Our framework incorporates major efficiency gains through community mobilisation, synergies between programme elements, and benefits of the extension of antiretroviral therapy for prevention of HIV transmission.. . .  Implementation of the new investment framework would avert 12·2 million new HIV infections and 7·4 million deaths from AIDS between 2011 and 2020 compared with continuation of present approaches, and result in 29·4 million life-years gained. The framework is cost effective at $1060 per life-year gained, and the additional investment proposed would be largely offset from savings in treatment costs alone.’

 The Lancet, Early Online Publication, 3 June 2011

Best viewed at http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(11)60702-2/fulltext

  • HIV SURVEILLANCE, UNITED STATES – 1981—2008

'At the end of 2008, an estimated 1,178,350 persons aged ≥13 years in the United States were living with HIV infection, including 20.1% whose infections had not been diagnosed. HIV prevalence per 100,000 population was 1,819 among blacks or African Americans, 593 among Hispanics or Latinos, and 238 among whites. Nearly 50% of those living with HIV infection were men who have sex with men.’

The first medical publication on HIV was in the Morbidity and Mortality Weekly Report, 1981. This retrospective view is from the MMWR.

 Best viewed at http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6021a2.htm?s_cid=mm6021a2_w

 

WHAT’S NEW BEFORE THE LONDON DONORS’ MEETING

 

In the run-up to the GAVI sponsored pledging meeting for new and underused vaccines, which starts on 13 June, I am highlighting, from the media and from the medical literature, five items on vaccine pricing. Among vaccines currently prequalified by WHO, those most likely to impact MDG 4 and MDG 5 are pneumococcal vaccine, rotavirus vaccine, and human papillomavirus vaccine.

All articles are at www.childsurvival.net

  • TWO ON VACCINE PRICING

1)      UNICEF’s recent publication of vaccine prices paid to individual manufacturers, accessible at

http://www.unicef.org/supply/index_57476.html , is a step forward in transparency in vaccine procurement, and will assist other vaccine purchasers in doing price comparisons. Industrialized countries should bear in mind that ‘tiered pricing’ makes unit prices much lower for developing than for developed countries.

2)      FOR FIRST TIME, UNICEF REVEALS DIFFERENCES IN PRICES IT PAYS DRUG COMPANIES FOR VACCINES

By DONALD G. McNEIL Jr.

Published: New York Times, May 27, 2011

The United Nations Children’s Fund on Friday publicly listed for the first time the price it pays for vaccines.

The decision — which immediately revealed wide disparities in what vaccine makers charge — could lead to drastic cuts in prices for vaccines that save millions of children’s lives.

Unicef paid $747 million for vaccines last year, buying over two billion doses for 58 percent of the world’s children.

This Bloomberg News item on price cuts to GAVI and to 'graduating GAVI' countries. In terms of current GAVI expenditure, the cuts in the cost of pentavalent are most important. Will HPV, as well as pneumo and rotavirus vaccines, now become affordable to GAVI eligible and GAVI 'graduating' countries?

 

GlaxoSmithKline Plc (GSK) and Merck & Co. agreed to lower prices for vaccines to protect children against potentially deadly diarrhea, supporting an international effort to help least-developed nations fight diseases. The GAVI Alliance, set up by Microsoft Corp. (MSFT) founder Bill Gates to give the world’s poorest people better access to life- saving immunizations, also received commitments from India-based drugmakers Serum Institute of India Ltd. and Panacea Biotec Ltd. (PNCB) to cut the price of a key pediatric vaccine, it said today. The agreements will help the alliance prevent an extra 4 million deaths by 2015 by rolling out new vaccines to tackle the main killers of children: pneumonia and diarrhea. The Geneva- based group’s donors and partners are meeting in London next week as they seek $3.7 billion to expand immunization programs over the next five years.

 

  • GAVI REACTION TO VACCINE PRICE CUTS

GAVI welcomes lower prices for life-saving vaccines

www.gavialliance.org

Manufacturer commitments will help GAVI vaccinate millions of children in least-developed countries

Geneva, 6 June 2011 – In the lead up to its first pledging conference on June 13, the GAVI Alliance announced today it has achieved commitments from two emerging market vaccine manufacturers to lower prices for the life-saving pentavalent vaccine, which protects against five deadly diseases. Developed country manufacturers have also offered price reductions on rotavirus and human papillomavirus, or HPV, vaccines.

 

  • COST AND FINANCING ISSUES LIMIT ACCESS TO THE HPV VACCINE

‘Cervical cancer . . . is the leading cancer in women in half the countries of the world and mostly affects relatively young poor women. But the vaccine cost is too high. With the availability of cost-effective, safe vaccine, there is real hope for reducing the global burden of cervical cancer.’

  • HPV VACCINATION FOR GHANA?

 

Ghana Med J. 2010 June; 44(2): 70–75.

Copyright © Ghana Medical Association 2010

Is Routine Human Papillomavirus Vaccination an Option for Ghana?

A K Edwin


Text is at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994148/?tool=pubmed

Summary

Cervical cancer remains an important public health problem in developing countries where over 80% of the global burden occurs annually but screening has been ineffective. In a polygamous country like Ghana with a high incidence of cervical cancer but no national screening program, the Human Papilloma Virus (HPV) vaccine presents a unique opportunity to reduce the burden of HPV infection and cervical cancer in Ghanaian women. The evidence so far indicates that the vaccines are safe and efficacious. Although routine HPV vaccination of girls raises several religious, political, socioeconomic and ethical challenges, the emphasis of this paper will be on addressing the ethical challenges using the principles of autonomy, beneficence, non-maleficence and justice as a framework. Parental autonomy can be preserved with judicious exemptions for those who decline the vaccine on religious and philosophical grounds. This promotes public health without trampling parental authority. Routine HPV vaccination confers several benefits to individuals and society by preventing HPV infection. Instead of causing harm; it reduces harm by preventing the development of about 70% of cervical cancers and removing the negative physical and psychological impact of a cervical cancer diagnosis. It also has the potential to reduce the disparities in cervical cancer rates and its cost effectiveness will ensure considerable cost savings in terms of the money spent on diagnosis and treatment. Consequently, the HPV vaccine is an important public health landmark and achievement in women's health that must be heralded, especially in developing countries where the bulk of the disease and death occur.

 

  • VACCINES AGAINST CANCER: THE GAVI VIEW

While hep B vaccine is now given in almost all countries, HPV is given, to my knowledge, only in one African country.

Will the London pledging conference of 9 June find funds for HPV?

http://www.gavialliance.org/media_centre/statements/2010_02_04_uicc.php 

Increasing access to vaccines will reduce the global burden of cancer

The GAVI Alliance, the American Cancer Society, and LIVESTRONG® welcome the campaign Cancer can be prevented,  which the International Union Against Cancer (UICC) is launching on February 4, World Cancer Day. On this occasion, the UICC will also release a new report on cancer prevention with a specific focus on cancers caused by infections.

  • PROJECTIONS OF GLOBAL HEALTH OUTCOMES FROM 2005 TO 2060 USING THE INTERNATIONAL FUTURES INTEGRATED FORECASTING MODEL

‘The base model projects that deaths from communicable diseases (CDs) will decline by 50%, whereas deaths from both non-communicable diseases (NCDs) and injuries will more than double. Considerable cross-national convergence in life expectancy will occur.’

Full text is at http://www.who.int/bulletin/online_first/10-083766.pdf

  • DOES RECESSION REDUCE GLOBAL HEALTH AID? EVIDENCE FROM 15 HIGH-INCOME COUNTRIES, 1975–2007

‘Any important decrease in overall DAH following the current economic recession would have little historical precedent and claims of inevitability would be unjustifiable.’

Full text is at http://www.who.int/bulletin/volumes/89/4/10-080663/en/index.html

Objective To test the hypothesis that economic recessions lead to reduced global development assistance for health (DAH).

Methods Data obtained from the Creditor Reporting System of the Organisation for Economic Co-operation and Development (OECD) for 15 OECD countries were used to model the percentage change (relative difference) in commitments and disbursements for DAH as a function of three measures of economic recession: recessionary year (as a dummy variable with 0 for no recession and 1 for recession), percentage change in per capita gross domestic product and percentage point change in unemployment rate for recessionary cycles from 1975 through 2007. We looked for an association both during the concurrent recessionary year and one and two years later.

 Findings No statistically significant association was found in the short or long run between measures of economic recession and the amount of official DAH committed or disbursed.

 Conclusion Any important decrease in overall DAH following the current economic recession would have little historical precedent and claims of inevitability would be unjustifiable.

 

  • ·         EFFECT OF DEEP TUBE WELL USE ON CHILDHOOD DIARRHOEA IN BANGLADESH

The introduction of deep tube wells to reduce arsenic in drinking water in rural Bangladesh had the additional benefit of lowering the incidence of diarrhoea among young children.’

‘A 1°C increase in temperature at 4 months lag resulted in a 2-fold increase of cholera cases, and an increase of 200 mm of rainfall at 2 months lag resulted in a 1.6-fold increase of cholera cases.’

Abstract below; full text online to subscribers of Am J Trop Med Hyg

  • CLIMATE VARIABILITY AND THE OUTBREAKS OF CHOLERA IN ZANZIBAR, EAST AFRICA: A TIME SERIES ANALYSIS

Abstract.

Global cholera incidence is increasing, particularly in sub-Saharan Africa. We examined the impact of climate and ocean environmental variability on cholera outbreaks, and developed a forecasting model for outbreaks in Zanzibar. Routine cholera surveillance reports between 1997 and 2006 were correlated with remotely and locally sensed environmental data. A seasonal autoregressive integrated moving average (SARIMA) model determined the impact of climate and environmental variability on cholera. The SARIMA model shows temporal clustering of cholera. A 1°C increase in temperature at 4 months lag resulted in a 2-fold increase of cholera cases, and an increase of 200 mm of rainfall at 2 months lag resulted in a 1.6-fold increase of cholera cases. Temperature and rainfall interaction yielded a significantly positive association (P < 0.04) with cholera at a 1-month lag. These results may be applied to forecast cholera outbreaks, and guide public health resources in controlling cholera in Zanzibar.

 

 Full text is at http://www.who.int/bulletin/online_first/10-085530.pdf

 CIRCUMCISED HIV-INFECTED MEN AND HPV TRANSMISSION

 ‘Male circumcision is important for reduction of not only HIV infection but also HPV infection in HIV-negative men and their female partners. However, its efficacy in reducing HPV transmission seems restricted to HIV-negative men; thus, the results of increasing numbers of reports suggest the need for early circumcision to achieve maximum effectiveness in populations with a high incidence of HIV and cervical cancer. To achieve maximum reductions in HIV and HPV infections and their related diseases in women, both male circumcision and HPV vaccination of the population should be delivered before sexual debut.’

The Lancet Infectious Diseases, Early Online Publication, 12 April 2011

This comment by Guiliano and colleagues, text also at http://www.thelancet.com/journals/laninf/article/PIIS1473-3099(11)70038-X/fulltext
refers to a study by Tobian and colleagues, text and graphics available at
http://www.thelancet.com/journals/laninf/article/PIIS1473-3099(11)70038-X/fulltext

Acccess this item at http://www.childsurvival.net/?content=com_articles&artid=550

  • TWO ON VACCINE PRICING

A)      VACCINE PRICING: THE UNICEF EXPERIENCE

One has to be cautious about generalizations. The world is moving from the ‘nickel and dime’ vaccines of the 1970s, when WHO created EPI, to a new ball game, where both increased transparency and the entry of new players in the game may serve to reduce the relative rigidities which have characterized pricing of some vaccines provided through the GAVI Alliance.

One has to wonder what will happen to prices in the polio posteradication era if UNICEF procures either IPV or hexavalent vaccine (pentavalent with IPV) on a large scale. Many believe that IPV is essential to stopping circulating vaccine derived poliovirus (cVDPV).

B) http://www.nytimes.com/2011/05/28/health/28vaccine.html?emc=tnt&tntemail1=y

Access this item at http://www.childsurvival.net/?content=com_articles&artid=557

  • DECLINES IN HOUSEHOLD SMOKING AND IN OTITIS MEDIA, US

With No Tobacco Day on 31 May,  another item on tobacco and kids

 ‘This is the first study to quantify average annual decreases in paediatric encounters for OM over the past decade and a half. The observed steadily increasing trend in smoke-free households since the mid-1990s is the main explanatory factor whose influence cannot be excluded over this entire time period. The importance of smoke-free rules in homes to protect children from exposure to SHS has further significance, given the range of adverse effects that SHS exposure has on child health.’

 Article best viewed at http://tobaccocontrol.bmj.com/content/20/3/207.full

Access this item at http://www.childsurvival.net/?content=com_articles&artid=558

  • ·         TRENDS IN SELECTIVE ABORTION OF GIRLS IN INDIA

The Lancet, Early Online Publication, 24 May 2011

Trends in selective abortions of girls in India: analysis of nationally representative birth histories from 1990 to 2005 and census data from 1991 to 2011

Prof Prabhat Jha DPhil a , Maya A Kesler MSc a, Prof Rajesh Kumar MD b, Prof Faujdar Ram PhD c, Usha Ram PhD a c, Lukasz Aleksandrowicz MSc a, Diego G Bassani PhD a, Shailaja Chandra IAS d, Jayant K Banthia PhD e

This article is best viewed at http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(11)60649-1/fulltext

Summary

Background

India's 2011 census revealed a growing imbalance between the numbers of girls and boys aged 0—6 years, which we postulate is due to increased prenatal sex determination with subsequent selective abortion of female fetuses. We aimed to establish the trends in sex ratio by birth order from 1990 to 2005 with three nationally representative surveys and to quantify the totals of selective abortions of girls with census cohort data.

Methods

We assessed sex ratios by birth order in 0·25 million births in three rounds of the nationally representative National Family Health Survey covering the period from 1990 to 2005. We estimated totals of selective abortion of girls by assessing the birth cohorts of children aged 0—6 years in the 1991, 2001, and 2011 censuses. Our main statistic was the conditional sex ratio of second-order births after a firstborn girl and we used 3-year rolling weighted averages to test for trends, with differences between trends compared by linear regression.

Findings

The conditional sex ratio for second-order births when the firstborn was a girl fell from 906 per 1000 boys (99% CI 798—1013) in 1990 to 836 (733—939) in 2005; an annual decline of 0·52% (p for trend=0·002). Declines were much greater in mothers with 10 or more years of education than in mothers with no education, and in wealthier households compared with poorer households. By contrast, we did not detect any significant declines in the sex ratio for second-order births if the firstborn was a boy, or for firstborns. Between the 2001 and 2011 censuses, more than twice the number of Indian districts (local administrative areas) showed declines in the child sex ratio as districts with no change or increases. After adjusting for excess mortality rates in girls, our estimates of number of selective abortions of girls rose from 0—2·0 million in the 1980s, to 1·2—4·1 million in the 1990s, and to 3·1—6·0 million in the 2000s. Each 1% decline in child sex ratio at ages 0—6 years implied 1·2—3·6 million more selective abortions of girls. Selective abortions of girls totalled about 4·2—12·1 million from 1980—2010, with a greater rate of increase in the 1990s than in the 2000s.

Access this item at http://www.childsurvival.net/?content=com_articles&artid=548

  • ·         RAPID IMPLEMENTATION OF AN INTEGRATED LARGE-SCALE HIV COUNSELING AND TESTING, MALARIA, AND DIARRHEA PREVENTION CAMPAIGN IN RURAL KENYA

'Through integrated campaigns it is feasible efficiently to cover large proportions of eligible adults in rural underserved communities with multiple disease preventive services simultaneously achieving various national and international health development goals.'

This article is best read at http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0012435

Access this item at http://www.childsurvival.net/?content=com_articles&artid=553

Background

Integrated disease prevention in low resource settings can increase coverage, equity and efficiency in controlling high burden infectious diseases. A public-private partnership with the Ministry of Health, CDC, Vestergaard Frandsen and CHF International implemented a one-week integrated multi-disease prevention campaign.

Method

Residents of Lurambi, Western Kenya were eligible for participation. The aim was to offer services to at least 80 percent of those aged 15-49. 31 temporary sites in strategically dispersed locations offered: HIV counseling and testing, 60 male condoms, an insecticide treated bednet, a household water filter for women or an individual filter for men, and, for those testing positive, a 3 month supply of cotrimoxazole and referral for follow-up care and treatment.

Findings

Over 7 days, 47,311 people attended the campaign with a 96 percent uptake of the multi-disease preventive package. Of these, 99.7 percent were tested for HIV (87 percent in the target 15-49 age group); 80 percent had previously never tested. 4 percent of those tested were positives, 61 percent were women (5 percent of women and 3 percent of men), 6 percent had median CD4 counts of 541cell/ml (IQR; 356, 374). 386 certified counselors attended to an average 17 participants per day, consistent with recommended national figures for mass campaigns. Among women, HIV infection varied by age, and was more likely with an ended marriage (e.g. widowed vs. never married, OR 3.91; 95 percent VCI, 2.8705.34), and lack of occupation.

In men, quantitatively stronger relationships were found (e.g. widowed vs. never married, OR 7.0; 95 percent VI 3.5-13.9). always using condoms with a non-steady partners was more common among HIV infected women participants who knew their status compared to those who did not (OR 5.4, 95 percent CI, 2.3-128.).

Conclusion

Through integrated campaigns it is feasible to efficiently cover large proportions of eligible adults in rural underserved communities with multiple disease preventive services simultaneously achieving various national and international health development goals.

 

 

The way to go after 2015? Full text is  also at

http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1001031 

Summary Points

  • A coalition of civil society organizations and academics are initiating a Joint Action and Learning Initiative on National and Global Responsibilities for Health (JALI) to research key conceptual questions involving health rights and responsibilities, with the goal of securing a global health agreement and supporting civil society mobilization around the human right to health.
  • This agreement—such as a Framework Convention on Global Health—would inform post-Millennium Development Goal (MDG) global health commitments.
  • Using broad partnerships and an inclusive consultation process, JALI seeks to clarify the health services to which everyone is entitled under the right to health, the national and global responsibilities for securing this right, and global governance structures that can realize these responsibilities and close major health inequities.
  • Mutual benefits to countries in the Global South and North would come from a global health agreement that defines national and global health responsibilities.
  • JALI aims to respond to growing demands for accountability, and to create the political space that could make a global health agreement possible.

 

The Joint Action and Learning Initiative: Towards a Global Agreement on National and Global Responsibilities for Health

Lawrence Gostin and colleagues discuss their work on the Joint Action and Learning Initiative on National and Global Responsibilities for Health (JALI), which aims to secure a global health agreement (such as a Framework Convention on Global Health) that would inform post-Millennium Development Goal global health commitments.

Top of Form

Lawrence O. Gostin1*, Eric A. Friedman1, Gorik Ooms2, Thomas Gebauer3, Narendra Gupta4, Devi Sridhar5, Wang Chenguang6, John-Arne Røttingen7, David Sanders8

1 O'Neill Institute for National and Global Health Law, Georgetown University Law Center, Washington, D.C., United States of America, 2 Institute of Tropical Medicine, Antwerp, Belgium, 3 Medico International, Frankfurt, Germany, 4 Prayas, Chittorgarh, India, 5 Oxford University, Oxford, United Kingdom, 6 Tsinghua University Law School, Beijing, China, 7 Norwegian Knowledge Centre for the Health Services, Oslo, Norway and Institute of Health and Society, University of Oslo, Oslo, Norway, 8 School of Public Health, University of the Western Cape, Bellville, South Africa

Citation: Gostin LO, Friedman EA, Ooms G, Gebauer T, Gupta N, et al. (2011) The Joint Action and Learning Initiative: Towards a Global Agreement on National and Global Responsibilities for Health. PLoS Med 8(5): e1001031. doi:10.1371/journal.pmed.1001031

Published: May 10, 2011

Copyright: © 2011 Gostin et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Funding: No direct funding was received for this study.

Competing interests: Thomas Gebauer works for Medico International, a Germany-based nongovernmental organization. No other author declares a competing interest.

Abbreviations: JALI, Joint Action and Learning Initiative on National and Global Responsibilities for Health; MDG, Millennium Development Goal; NGO, nongovernmental organization; UN, United Nations; WHO, World Health Organization

* E-mail: gostin@law.georgetown.edu

Provenance: Not commissioned; externally peer reviewed.

Summary Points

  • A coalition of civil society organizations and academics are initiating a Joint Action and Learning Initiative on National and Global Responsibilities for Health (JALI) to research key conceptual questions involving health rights and responsibilities, with the goal of securing a global health agreement and supporting civil society mobilization around the human right to health.
  • This agreement—such as a Framework Convention on Global Health—would inform post-Millennium Development Goal (MDG) global health commitments.
  • Using broad partnerships and an inclusive consultation process, JALI seeks to clarify the health services to which everyone is entitled under the right to health, the national and global responsibilities for securing this right, and global governance structures that can realize these responsibilities and close major health inequities.
  • Mutual benefits to countries in the Global South and North would come from a global health agreement that defines national and global health responsibilities.
  • JALI aims to respond to growing demands for accountability, and to create the political space that could make a global health agreement possible.

Introduction Top

A decade into the 21st century, billions of people have yet to benefit from the health advances of the 20th century. Life expectancy at birth in sub-Saharan Africa is 53 years [1]—only two years higher than in the United States a century ago [2], and 27 years lower than in high-income countries today [1]. The most basic human needs continue to elude the world's poorest people. In 2010, approximately 925 million people were suffering from chronic hunger [3], 884 million people lacked access to clean water, and 2.6 billion people were without access to proper sanitation facilities [4].

Such global health disparities will likely persist until there is fair and effective global governance for health—the organization of national and global norms, institutions, and processes that collectively shape the health of the world's population. Global governance for health goes beyond the health sector. It requires remediating the currently unfair and detrimental health impacts of international regimes (e.g., trade, intellectual property, and finance), and developing stable, responsive, democratic political institutions.

A coalition of civil society and academics, with a shared vision of the “right of everyone to the enjoyment of the highest attainable standard of physical and mental health” [5] (“right to health”), is therefore launching the Joint Action and Learning Initiative on National and Global Responsibilities for Health (JALI). JALI seeks to develop a post–Millennium Development Goal (MDG) framework for global health, one rooted in the right to health and aimed at securing universal health coverage for all people. We seek to clarify the health goods and services to which all people are entitled, national and global responsibilities to secure the health of the world's population, and governance structures required to realize these responsibilities. Our goal is a global agreement, such as a Framework Convention on Global Health, which sets priorities, clarifies national and international responsibilities, ensures accountability, and develops corresponding institutions, such as a Global Health Fund [6],[7].

Partnerships with Civil Society Organizations Top

JALI will draw inspiration from, and collaborate with, civil society movements, which are central to securing and ensuring adherence to a global health agreement. Such movements have spurred momentous transformations in health. Advocates changed the world's response to AIDS from one marked by discrimination to one focused on empowering marginalized people and scaling up HIV services. The Campaign to Ban Landmines drove a process that culminated in a treaty banning this indiscriminate weapon.

Civil society campaigns for the right to health, such as those through the People's Health Movement, are already underway [8]. Nongovernmental organizations (NGOs) from the South and North launched a Declaration of Solidarity for a Unified Movement for the Right to Health [9]. JALI is developing the partnerships required to undertake an inclusive process involving research, analysis, and extensive online and regional consultations to gain insight into and build consensus around answers to four foundational questions, and to stimulate coordinated action to reduce health inequities. This bottom-up, research-focused process will develop a detailed understanding of health rights and state obligations, clear targets and benchmarks for success, and effective monitoring and accountability mechanisms. These will add precision to and enhance the effectiveness of international human rights law, which could in turn enhance civil society efforts to hold their own governments to account. By drawing on the voices of civil society and disadvantaged communities, JALI could have the legitimacy and the political support to transform global governance for health.

Four Defining Questions in Global Health Top

The four defining questions, and preliminary directions on answers, are:

1. What are the services and goods guaranteed to every person under the human right to health?

The World Health Organization (WHO) has placed universal health coverage high on the global health agenda [10], defining three dimensions of coverage: 1) the proportion of the population served; 2) the level of services; and 3) the proportion of health costs covered by prepaid pooled funds [11]. WHO has defined universal coverage “as access to key promotive, preventive, curative and rehabilitative health interventions for all at an affordable cost” [12].

The human right to health, an international treaty obligation, provides critical insight into how states should work towards universal coverage (Figure 1). Core obligations offer benchmarks to assess progress towards universal coverage, such as non-discrimination, equitable distribution of health facilities, and essential services for all, including those addressing underlying determinants of health [13].

Figure 1. Universal health coverage and the right to health.

The pooled funds represent the total amount of funding that states have available to expand universal health coverage along three dimensions: 1) who is covered, and the proportion of population covered; 2) what services are covered; and 3) the extent to which the state covers the cost of these services. Under a right to health approach, this total level of funding will be derived from the maximum of available resources that states are required to dedicate to the right to health and other rights.

doi:10.1371/journal.pmed.1001031.g001

The core principle of equality requires states to prioritize covering 100% of their populations. Although 100% coverage of all health services will not be possible immediately, full coverage of “key” health interventions should be an initial benchmark towards universal coverage. The right to health framework militates against a narrow definition of “key” services. Rather, these should encompass WHO's health system building blocks (e.g., services, workforce, information, financing, and governance); essential vaccines, medicines, and technologies; and fundamental human needs (e.g., sanitation, nutritious food, potable water, safe housing, vector abatement, tobacco control, and healthy environments).

Critically, universal coverage should be re-conceptualized to encompass fundamental human needs given their major impact on health. Within this framework, specific services would be determined nationally through participatory processes [14].

The provision of each of these core entitlements—health systems, essential vaccines and medicines, and fundamental human needs—should represent only one significant step towards achieving the highest attainable standard of health. States, even wealthy ones, will need to continue to progress towards universal coverage. The right to health requires states to spend the “maximum of…available resources” towards progressively realizing health and other socioeconomic rights [5]. Thus, under international law, states have a duty “to move as expeditiously and effectively as possible towards” fully realizing the right to health [13].

2. What responsibilities do all states have for the health of their own populations?

The right to health places the primary responsibility on governments to ensure the health needs of all their inhabitants. National responsibility includes health sector funding, addressing the socioeconomic determinants of health, and good governance.

There is no universally agreed level of health sector funding adequate to meet the population's needs. African heads of state agreed to a benchmark of at least 15% of national budgets devoted to the health sector [15], and to allocating at least 10% of their national budgets for agricultural development [16]. Additionally, 32 African countries set a target, as an aspiration, to have public sector budget allocations for sanitation and hygiene programs reach at least 0.5% of gross domestic product [17].

These benchmarks set a minimum bar for national funding responsibilities, which extend beyond the health sector. National health responsibilities should comply with well-defined, measurable international standards, balanced against the flexibility necessary to respect national priorities, health profiles, and needs.

States also have a responsibility to govern well, derived from central human rights tenets such as participatory processes, transparent and accountable government, and non-discrimination and equality. Well-designed legal rules and institutional arrangements can facilitate honest administrations, openness, and accountability, along with meaningful civil society and community participation in decision-making. The law, moreover, should guarantee equality and non-discrimination on the basis of race, sex, religion, disability, and other statuses. Measures to enhance accountability to communities in India's National Rural Health Mission [18], and Brazilian policies to reduce health disparities [19], offer instructive lessons.

3. What duties do states owe to people beyond their borders in securing the right to health?

Resource-poor states lack capacity to ensure all of their people even core health goods and services, much less a fuller realization of the right to health. Countries in a position to assist are obliged to do so under principles of international law and global social justice. The Committee on Social, Economic and Cultural Rights has declared that cooperation towards realizing the right to health is “an obligation of all States,” particularly those “in a position to assist others” [13],[20]. All countries have mutual responsibilities towards ensuring the health of the world's most disadvantaged.

Beyond development assistance, coordination and coherence is required across sectors, as global health can be improved or harmed through state and international policies and rules that govern areas such as trade, intellectual property, health worker migration, international financing, and debt relief. These responsibilities extend to the exercise of state power and influence over multilateral institutions such as the World Bank, International Monetary Fund, and World Trade Organization.

International aspects of the right to health are ill-defined. With limited exceptions, such as the commitment of wealthy countries to spend 0.7% of gross national product on official development assistance, health and development commitments are framed collectively, vaguely, or not at all. Even when countries make commitments, they often fail to follow through. For example, only one month after countries at the 2010 United Nations (UN) MDG Summit committed to provide “adequate funding” for the Global Fund to Fight AIDS, Tuberculosis and Malaria, pledges at the replenishment conference fell billions of dollars short [21],[22]. The Summit called for accelerated development assistance for health, though the rate of increase in assistance dropped during the global recession [21],[23]. Budget shortfalls in the aftermath of the financial downturn further threaten assistance levels.

4. What kind of global governance for health is needed to ensure that all states live up to their mutual responsibilities?

Translating a shared understanding of national and global responsibilities into new realities requires effective and democratic global governance for health. Notwithstanding the Paris Declaration on Aid Effectiveness, global health faces challenges of weak leadership, poor coordination, underfunded priorities, and a lack of transparency, accountability, and enforcement [24].

Innovative global governance and enhanced funding would empower WHO to exercise effective leadership in the health sector and persuasive advocacy on agriculture, finance, and trade. Moreover, state policies (e.g., agricultural subsidies, intellectual property, and foreign affairs) can powerfully affect health in resource-poor countries. States, therefore, should adopt a “health-in-all-policies” approach where all ministries address the health impacts of their policies and programs. Effective governance must include active citizen participation to ensure transparency, collaboration, and accountability while maximizing creativity and resource mobilization by states, international organizations, businesses, and civil society.

Most importantly, the global health architecture must hold stakeholders accountable, with clear standards for success, monitoring progress, and enforcement—all of which have been lacking. Lack of sufficiently precise obligations and compliance mechanisms under the right to health hinders accountability, though promising approaches exist. Human rights bodies and UN special rapporteurs are adding clarity to state responsibilities under the right to health, which is required for meaningful accountability, as are constitutional court decisions in Argentina, India, and South Africa [25],[26].

Innovations in human rights law and practice hold potential for greater accountability. Regional right-to-health special rapporteurs could be established, enabling more effective national engagement. An empowered human rights sector could learn from international regimes with more vigorous adjudication and enforcement mechanisms, such as trade. Actions to ensure that social movements and voters are well-informed about their countries' commitments could strengthen political accountability.

The Global South, where most of the world's least healthy people reside, should lead in shaping global governance for health policies, where community priorities drive global action. New governance requires the full participation of, and support for, marginalized populations.

Towards a Hopeful Future for Global Health Top

Why would states agree to greater accountability when so many countries fail to adhere to existing commitments? We do not underestimate the gravity of the challenge, yet JALI offers possibilities for success. Social mobilization could ignite new possibilities, as the AIDS movement has done, unleashing the collective power of health advocates and empowered communities.

The framework of mutual responsibilities that emerges from JALI should prove attractive to both Southern and Northern governments, creating incentives to develop a far-reaching global health agreement. Mutual responsibilities come with mutual benefits. Southern countries will benefit from increased respect for their strategies, greater and more predictable funding from more coordinated and accountable development partners, reform of policies that harm health, such as those in trade and agriculture, and most importantly, better health for their populations. Countries in the North will benefit from increased confidence that development assistance is spent effectively and the prospect of reduced financing needs over time as host countries increase their own health spending and build sustainable health systems. All will benefit from lessons on shared health challenges, from the economic and educational gains that will come with improved global health, and from increased protection for their populations from global public health threats—and from mutual goodwill derived from participating in an historic venture to make unprecedented progress towards global health equity.

This is also a moment of rare opportunity. The post-MDG global health framework is yet to be developed. Demand for accountability is growing. The right to health is increasingly motivating not only civil society, but also governments. The Pan American Health Organization passed a resolution on health and human rights [27], and the UN General Assembly explicitly recognized the right to clean water and sanitation [4]. Universal coverage, primary health care, and socioeconomic determinants are receiving renewed focus. Global health remains prominent on the international agenda, evidenced by the attention to global health and foreign policy and the upcoming UN high-level summit on non-communicable diseases.

In January 2011, WHO's Executive Board called on the Organization to assume a “more active and effective role” in “directing and coordinating” international health activities [28]. The agency initiated a reform process to strengthen its “central role in global health governance” [28],[29]. JALI supports WHO leadership, but also governance reforms extending beyond WHO, and even beyond the health sector, for a deeper understanding of the multiple forms of injustice that adversely affect health and development.

We invite readers to join JALI (http://www.section27.org.za/2010/11/23/j​ali) to develop widely shared understandings of national and global responsibilities for health to inform post-MDG commitments and create an innovative global agreement. It is time to define—and to meet—these responsibilities.

Author Contributions Top

Wrote the first draft: EAF LO. Contributed to writing the paper: LOG EAF GO TG NG DS WC J-AR DS. ICMJE criteria for authorship read and met: LOG EAF GO TG NG DS WC J-AR DS. Agree with the manuscript’s results and conclusions: LOG EAF GO TG NG DS WC J-AR DS.

References Top

  1. World Health Organization (2010) World health statistics. Geneva: Available: http://www.who.int/whosis/whostat/EN_WHS​10_Part2.pdf. Accessed 22 September 2010.
  2. Arias E (2010) United States life tables 2006. National Vital Statistics Reports 58: 1–40. Available: http://www.cdc.gov/nchs/data/nvsr/nvsr58​/nvsr58_21.pdf. Accessed 22 October 2010.
  3. Food and Agricultural Organization (2010) 925 million in chronic hunger worldwide. Rome: Available: http://www.fao.org/news/story/en/item/45​210/icode/. Accessed 10 October 2010.
  4. United Nations General Assembly (28 July 2010) The human right to water and sanitation: U.N. Doc. A/Res/64/292. New York: Available: http://www.un.org/en/ga/64/resolutions.s​html. Accessed 19 December 2010.
  5. International Covenant on Economic, Social and Cultural Rights (1976) G.A. Res. 2200A (XXI), U.N. Doc. A/6316: Available: http://www1.umn.edu/humanrts/instree/b2e​sc.htm. Accessed 15 December 2010.
  6. Gostin LO (2008) Meeting basic survival needs of the world's least healthy people: toward a Framework Convention on Global Health. Georgetown Law Journal 96: 331–392. Available: http://ssrn.com/abstract=1014082. Accessed 28 October 2010.
  7. Cometto G, Ooms G, Starrs A, Zeitz P (2008) A global fund for the health MDGs? Lancet 373: 1500–1502. Find this article online
  8. People's Health Movement (2010) PHM Right to Health and Health Care Campaign update January 2010. Available: http://www.phmovement.org/en/node/2769. Accessed 23 October 2010.
  9. Partners In Health (2009) Declaration of solidarity for a unified movement for the right to health. Available: http://act.pih.org/page/s/declaration. Accessed 23 October 2010.

10.  World Health Assembly (2010) Primary health care, including health system strengthening: WHA62.12. Geneva: Available: http://apps.who.int/gb/ebwha/pdf_files/W​HA62-REC1/WHA62_REC1-en-P2.pdf. Accessed 15 December 2010.

11.  World Health Organization (2010) World health report: health systems financing: the path to universal coverage. Geneva: Available: http://www.who.int/whr/2010/en/index.htm​l. Accessed 15 December 2010.

12.  World Health Assembly (7 April 2005) Social health insurance: sustainable health financing, universal coverage and social health insurance: report by the Secretariat: A58/20: Available: http://apps.who.int/gb/ebwha/pdf_files/W​HA58/A58_20-en.pdf. Accessed 11 February 2011.

13.  United Nations Committee on Economic, Social and Cultural Rights (2000) General comment no. 14: the right to the highest attainable standard of health, E/C.12/2000. New York: Available: http://www.unhchr.ch/tbs/doc.nsf/%28symb​ol%29/E.C.12.2000.4.En. Accessed 9 September 2010.

14.  Frenk J, Gómez-Dantés O (2009) Ideas and ideals: ethical basis for health reform in Mexico. Lancet 373: 1406–1408. Find this article online

15.  Organization of African Unity (2001) Abuja declaration on HIV/AIDS, tuberculosis and other related infectious diseases. Abuja (Nigeria): Available: http://www.un.org/ga/aids/pdf/abuja_decl​aration.pdf. Accessed 1 September 2010.

16.  African Union Assembly (2003) Maputo declaration on agriculture and food security in Africa. Maputo (Mozambique): Available: http://www.africa-union.org/Official_doc​uments/Decisions_Declarations/Assembly%2​0final/Assembly%20%20DECLARATIONS%20%20-​%20Maputo%20-%20FINAL5%2008-08-03.pdf. Accessed 1 November 2010.

17.  Second African Conference on Sanitation and Hygiene (2008) eThekwini declaration. Durban (South Africa): Available: http://www.wsp.org/wsp/sites/wsp.org/fil​es/publications/eThekwiniAfricaSan.pdf. Accessed 1 November 2010.

18.  Ministry of Health and Family Welfare, Government of India (2010) National rural health mission. New Delhi: Available: http://mohfw.nic.in/nrhm.htm. Accessed 10 October 2010.

19.  Bhutta Z, Chopra M, Axelson H, Berman P, Boerma T, et al. (2010) Countdown to 2015 decade report (2000-10): taking stock of maternal, newborn, and child survival. Lancet 375: 2032–2044. Find this article online

20.  United Nations Committee on Economic, Social and Cultural Rights (1990) General comment no. 3: the nature of States' parties obligations, E/1991/23. New York: Available: http://www1.umn.edu/humanrts/gencomm/epc​omm3.htm. Accessed 14 February 2011.

21.  United Nations General Assembly (2010) Keeping the promise: united to achieve the Millennium Development Goals: A/65/L.1. New York: Available: http://www.un.org/en/mdg/summit2010/pdf/​mdg%20outcome%20document.pdf. Accessed 5 November 2010.

22.  McNeil D (6 October 2010) Global fight against AIDS falters as pledges fail to reach goal of $13 billion. New York Times: Available: http://www.nytimes.com/2010/10/06/world/​africa/06aids.html. Accessed 5 November 2010.

23.  Institute for Health Metrics and Evaluation, University of Washington (2010) Financing global health 2010: development assistance and country spending in economic uncertainty. Seattle: Institute for Health Metrics and Evaluation, University of Washington. Available: http://www.healthmetricsandevaluation.or​g/publications/policy-report/financing-g​lobal-health-2010-development-assistance​-and-country-spending-economic-uncertain​t. Accessed 9 February 2011.

24.  Gostin LO, Mok EA (2009) Grand challenges in global health governance. Br Med Bull 90: 7–18. Available: http://bmb.oxfordjournals.org/content/90​/1/7.full.pdfhtml. Accessed 9 September 2010.

25.  Hogerzeil HV, Samson M, Casanovas, Rahmani-Ocora L (2006) Is access to essential medicines as part of the fulfilment of the right to health enforceable through the courts? Lancet 368: 305–311. Available http://www.who.int/medicines/news/Lancet​_EssMedHumanRight.pdf. Accessed 22 February 2011.

26.  Gauri V, Brinks DM, editors. (2008) Courting social justice: judicial enforcement of social and economic rights in the developing world. New York: Cambridge University Press.

27.  Pan American Health Organization (29 September 2010) Resolution CD50.R8 health and human rights. 50th Directing Council, 62nd Session. Regional Committee. Available: http://www.un.org/disabilities/documents​/paho_mh_resolution.pdf. Accessed 9 February 2011.

28.  WHO Executive Board (2011) The future of financing for WHO. WHO Executive Board, 128th Session. EB128/INF.DOC./3. Available: http://apps.who.int/gb/ebwha/pdf_files/E​B128/B128_ID3-en.pdf. Accessed 9 February 2011.

29.  Sridhar D, Gostin LO (2011) Reforming the World Health Organization. JAMA. E-pub ahead of print 29 March 2011. doi:10.1001/jama.2011.418. Find this article online

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  • MEASLES EDITION

 

I will not place on page 1 the measles updates (see next paragraph), but encourage you to click, on the red line, ‘measles edition.’  From the first page of the measles edition:

COCHRANE REVIEWS

I am placing on page 1, for your reading pleasure, each of the highly popular Cochrane reviews, none of them registering fewer than 95 visits so far this year. The review on ITN impact in pregnant women tops the league table, with 333 visits, followed by the reviews on hand washing impact and on vitamin A.

 

For those unfamiliar with the Cochrane reviews, consult http://www.cochrane.org/about-us/history/archie-cochrane

 

 

Good reading.

BD

 

AFTER 2015: POST-MDG RESPONSIBILITIES

 

The way to go after 2015? Full text is at

http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1001031

 

Summary Points

  • A coalition of civil society organizations and academics are initiating a Joint Action and Learning Initiative on National and Global Responsibilities for Health (JALI) to research key conceptual questions involving health rights and responsibilities, with the goal of securing a global health agreement and supporting civil society mobilization around the human right to health.
  • This agreement—such as a Framework Convention on Global Health—would inform post-Millennium Development Goal (MDG) global health commitments.
  • Using broad partnerships and an inclusive consultation process, JALI seeks to clarify the health services to which everyone is entitled under the right to health, the national and global responsibilities for securing this right, and global governance structures that can realize these responsibilities and close major health inequities.
  • Mutual benefits to countries in the Global South and North would come from a global health agreement that defines national and global health responsibilities.
  • JALI aims to respond to growing demands for accountability, and to create the political space that could make a global health agreement possible.

 

  • ·         GAME CHANGER IN HIV PREVENTION?

A randomized clinical trial in developed and developing countries has shown dramatic declines in HIV transmission among serodiscordant heterosexual couples when ARVs are started early in HIV seropositives.

'This breakthrough is a serious game changer and will set the prevention revolution forward,' according to Michel Sidibe, head of UNAIDS.

This update should be read in tandem with two others, 'HIV prevalence in Zimbabwe,' which calls for early inception of ARV treatment, and 'Provider Initiated HIV Testing.' According to the latter article, '‘The introduction of routine PITC using lay counsellors into health-care clinics in Lusaka, Zambia, dramatically increased the uptake and acceptability of HIV testing.’

Timely and early treatment cannot begin when at risk persons remain ignorant of their serostatus.

http://www.childsurvival.net/?content=com/articles&artid=534

  • PREVENTION PROVIDER INITIATED HIV TESTING IN ZAMBIA

‘The introduction of routine PITC using lay counsellors into health-care clinics in Lusaka, Zambia, dramatically increased the uptake and acceptability of HIV testing.’ 

Full text, with figures, is at http://www.who.int/bulletin/volumes/89/5/10-084442.pdf

 Opt-out provider-initiated HIV testing and counselling in primary care outpatient clinics in Zambia

Stephanie M Topp,a Julien M Chipukuma,a Matimba M Chiko,b Chibesa S Wamulume,b Carolyn Bolton-Moorea & Stewart E Reida

Objective To increase case-finding of infection with human immunodeficiency virus (HIV) in Zambia and their referral to HIV care and treatment by supplementing existing client-initiated voluntary counselling and testing (VCT), the dominant mode of HIV testing in the country.

Methods Lay counsellors offered provider-initiated HIV testing and counselling (PITC) to all outpatients who attended primary clinics and did not know their HIV serostatus. Data on counselling and testing were collected in registers. Outcomes of interest included HIV testing coverage, the acceptability of testing, the proportion testing HIV-positive (HIV+), the proportion enrolling in HIV care and treatment and the time between testing and enrolment.

Findings After the addition of PITC to VCT, the number tested for HIV infection in the nine clinics was twice the number undergoing VCT alone. Over 30 months, 44 420 patients were counselled under PITC and 31 197 patients, 44% of them men, accepted testing. Of those tested, 21% (6572) were HIV+; 38% of these HIV+ patients (2515) enrolled in HIV care and treatment. The median time between testing and enrolment was 6 days. The acceptability of testing rose over time.

Conclusion The introduction of routine PITC using lay counsellors into health-care clinics in Lusaka, Zambia, dramatically increased the uptake and acceptability of HIV testing. Moreover, PITC was incorporated rapidly into primary care outpatient departments. Maximizing the number of patients who proceed to HIV care and treatment remains a challenge and warrants further research.’

http://www.childsurvival.net/?content=com_articles&artid=519

  • ·         HIV PREVALENCE IN ZIMBABWE

HIV in Zimbabwe is disappearing like ‘snow in the desert’, in dramatic contrast to its neighbouring countries, mystifying epidemiologists, one of whom firmly believes the anomaly can be attributed to the country’s relatively high level of education.

. . . ‘Williams made a strong case to his colleagues in Cape Town for the introduction of ART immediately after testing positive as a powerful and long-term cost-effective prevention tool for both HIV and TB. . . .’

Full text also at http://www.samj.org.za/index.php/samj/article/viewFile/4672/3050

  • ·         GOOD GOVERNANCE AND NEW VACCINE INTRODUCTION

 I found this article the same week that I read about Merck's donation of HPV vaccine to Rwanda, the first country in central Africa to introduce HPV on a nationwide scale. Rwanda was also the first country in central Africa to introduce pneumococcal vaccine. This is a hypothesis with legs.

 ‘[G]ood country-level governance is an imperative pre-requisite for the successful early introduction of new vaccines into poor African nations.’

Abstract below; full text, with figures, is at http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0013802

  • DETERMINANTS  OF EXCLUSIVE BREAST FEEDING IN NIGERIA

‘The EBF rate in Nigeria is low and falls well short of the expected levels needed to achieve a substantial reduction in child mortality. Antenatal care was strongly associated with an increased rate of EBF.’

Best viewed at http://www.biomedcentral.com/1471-2393/11/2

Abstract Background Exclusive breast feeding (EBF) has important protective effects on the survival of infants and decreases risk for many early-life diseases. The purpose of this study was to assess the factors associated with EBF in Nigeria. Methods Data on 658 children less than 6 months of age were obtained from the Nigeria Demographic and Health Survey (NDHS) 2003.

The 2003 NDHS was a multi-stage cluster sample survey of 7864 households. EBF rates were examined against a set of individual, household and community level variables using a backward stepwise multilevel logistic regression method. Results The average EBF rate among infants younger than 6 months of age was 16.4% (95%CI: 12.6%-21.1%) but was only 7.1% in infants in their fifth month of age. After adjusting for potential confounders, multivariate analyses revealed that the odds of EBF were higher in rich (Adjusted Odds Ratios (AOR) = 1.15, CI = 0.28-6.69) and middle level (AOR = 2.45, CI = 1.06-5.68) households than poor households. Increasing infant age was associated with significantly less EBF (AOR = 0.65, 95%CI: 0.51-0.82). Mothers who had four or more antenatal visits were significantly more likely to engage in EBF (AOR = 2.70, 95%CI = 1.04-7.01). Female infants were more likely to be exclusively breastfed than male infants (AOR = 2.13, 95%CI = 1.03-4.39). Mothers who lived in the North Central geopolitical region were significantly more likely to exclusively breastfeed their babies than those mothers who lived in other geopolitical regions.

 

  • TWO ON ROAD SAFETY

1) GLOBAL PLAN FOR THE DECADE OF ACTION FOR ROAD SAFETY

In six languages, at http://www.who.int/roadsafety/decade_of_action/plan/en/index.html

Country profiles, in alphabetical order, at http://www.who.int/violence_injury_prevention/road_safety_status/country_profiles/en/index.html

2) CHILDREN'S TRAFFIC EDUCATION, BANGLADESH

These 1998 documents give an interesting idea of how to attack the problem of death and injury from road traffic accidents.


By the way, do you know the word describing a Kigali motorcyclist without a helmet? Starts with a 'j.'

Scroll down to the end for the answer.

http://www.schoolsandhealth.org/Documents/Government%20of%20Bangladesh_Children%27s%20Traffic%20Education%20in%20Bangladesh.pdf


http://www.schoolsandhealth.org/Documents/Government%20of%20Bangladesh_Development%20of%20Road%20Safety%20Education%20Materials.pdf




From the Executive Summary

Research shows that human error plays a large part in road accidents, being a contributory factor in around 95 percent of accidents. Teaching safety skills to children can provide life long benefits to society. However, to develop safe road user behavior, children need to be taught skills rather than focus simply on rules, regulations and knowledge of traffic signs. By helping to develop positive, safe attitudes years as they become teenager and the adult road users.

Developing pedestrian safety is one of the main requirements of children’s traffic education in Bangladesh, especially in young children, as this will often be their primary mode of travel. The road crossing task is complex and requires a range of fundamental skills. . . .

Although immediate improvements in road user behavior are unlikely, many attitudes are developed early in life and road safety education should be seen as a longer term investment. The children of today are the adult road users of tomorrow.


What do you call a Kigali motorcyclist without a helmet? Jailbird!

 

  • ·         AGAINST EUPHORIA

Those who believe that Africa is within shooting distance of malaria elimination may wish to reconsider their position after reading this article.

One should qualify this Ugandan article in several ways:

1)      Local insurgency in the area under consideration

2)      Hiccoughs with the GF over misappropriation of resources

3)      Autocratic gerontocracy at the national level

Unfortunately, these three factors are not peculiar to Uganda.

Good reading.

BD

Abstract from the American Journal of Tropical Medicine and Hygiene.  Full text available to subscribers

Continuing Intense Malaria Transmission in Northern Uganda

Carla Proietti, Davide D. Pettinato, Bernard N. Kanoi, Edward Ntege, Andrea Crisanti, Eleanor M. Riley, Thomas G. Egwang, Chris Drakeley*, AND Teun Bousema

Department of Immunology and Infection, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; Microtest Matrices, Imperial College London, London, United Kingdom; Med Biotech Laboratories, Kampala, Uganda; Department of Experimental Medicine and Biochemical Science, University of Perugia, Perugia, Italy

Abstract.: Recent reports of reductions in malaria transmission in several African countries have resulted in optimism that malaria can be eliminated in parts of Africa where it is currently endemic. It is not known whether these trends are global or whether they are also present in areas where political instability has hindered effective malaria control. We determined malaria parasite carriage and age-dependent antibody responses to Plasmodium falciparum antigens in cross-sectional surveys in Apac, northern Uganda that was affected by political unrest. Under-five parasite prevalence was 55.8% (115/206) by microscopy and 71.9% (41/57) by polymerase chain reaction. Plasmodium ovale alone, or as a co-infection, was detected in 8.6% (12/139) and Plasmodium malariae in 4.3% (6/139) of the infections. Age seroprevalence curves gave no indication of recent changes in malaria transmission intensity. Malaria control remains a tremendous challenge in areas that have not benefited from large-scale interventions, illustrated here by the district of Apac.

 

  • ·         PRINCIPLES OF EPIDEMIOLOGY

Epidemiology is the queen of the sciences. Here, Philip Brachman of CDC lays down the principles of epidemiology.

Best viewed at  http://www.ncbi.nlm.nih.gov/pubmed/21413284

Chapter 9

Epidemiology 

Philip S. Brachman.

General Concepts

Definitions

Epidemiology is the study of the determinants, occurrence, and distribution of health and disease in a defined population. Infection is the replication of organisms in host tissue, which may cause disease. A carrier is an individual with no overt disease who harbors infectious organisms. Dissemination is the spread of the organism in the environment.

Chain of Infection

There are three major links in disease occurrence: the etiologic agent, the method of transmission (by contact, by a common vehicle, or via air or a vector), and the host.

Epidemiologic Methods

Epidemiologic studies may be (1) descriptive, organizing data by time, place, and person; (2) analytic, incorporating a case-control or cohort study; or (3) experimental. Epidemiology utilizes an organized approach to problem solving by: (1) confirming the existence of an epidemic and verifying the diagnosis; (2) developing a case definition and collating data on cases; (3) analyzing data by time, place, and person; (4) developing a hypothesis; (5) conducting further studies if necessary; (6) developing and implementing control and prevention measures; (7) preparing and distributing a public report; and (8) evaluating control and preventive measures.

Introduction

This chapter reviews the general concepts of epidemiology, which is the study of the determinants, occurrence, distribution, and control of health and disease in a defined population. Epidemiology is a descriptive science and includes the determination of rates, that is, the quantification of disease occurrence within a specific population. The most commonly studied rate is the attack rate: the number of cases of the disease divided by the population among whom the cases have occurred. Epidemiology can accurately describe a disease and many factors concerning its occurrence before its cause is identified. For example, Snow described many aspects of the epidemiology of cholera in the late 1840s, fully 30 years before Koch described the bacillus and Semmelweis described puerperal fever in detail in 1861 and recommended appropriate control and prevention measures a number of years before the streptococcal agent was fully described. One goal of epidemiologic studies is to define the parameters of a disease, including risk factors, in order to develop the most effective measures for control. This chapter includes a discussion of the chain of infection, the three main epidemiologic methods, and how to investigate an epidemic.

 

  • MALARIA RESEARCH IN AFRICA, 1948-2007

The majority of malaria RCT conducted in Africa report on drug treatment and prevention in children; there is need for more research done in pregnant women. Sources of funding, informed consent and trial quality were often poorly reported. Overall, clearer reporting of trials is needed.

Randomized controlled trials of malaria intervention trials in Africa, 1948 to 2007: a descriptive analysis

Malaria Journal 2011, 10:61doi:10.1186/1475-2875-10-61

The electronic version of this article is the complete one and can be found online at: http://www.malariajournal.com/content/10/1/61

 

  • VACCINATION: RATTLING THE SUPPLY CHAIN

The introduction of new vaccines, combined with a push to expand immunization globally to reach every child, is straining vaccine supply chains to the limit. New thinking on the way vaccines are delivered is needed. Gary Humphreys reports. Text, with photos, best viewed at http://www.who.int/bulletin/volumes/89/5/11-030511.pdf The first decade of this century was perhaps the most productive in the history of vaccine development, seeing the release of a plethora of new life-saving vaccines for rotavirus diarrhoea, types of meningitis and pneumonia, and for human papillomavirus (HPV) infections that cause cervical cancer. “We are in a very different situation now compared to 10 years ago,” says Dr Osman Mansoor at the United Nations Children’s Fund (UNICEF) in New York. Mansoor, who is UNICEF’s senior health adviser for the Expanded Programme on Immunization and New Vaccines, notes that more vaccines are in the pipeline. In fact more than 80 vaccines are in the late stages of clinical testing, and 30 of them are designed to protect against major diseases including dengue and malaria. At the same time, the global vaccine market is booming: since 2000, global revenue from the sale of vaccines has almost tripled reaching more than US$ 17 billion by mid-2008. While most of this expansion is accounted for by sales of new and more costly vaccines in industrialized countries, more vaccines are also reaching developing countries due to the efforts of the GAVI Alliance (formerly the Global Alliance for Vaccines and Immunization), a public–private partnership established in 2000 to increase immunization in poor countries. The World Health Organization (WHO) and UNICEF estimate that just over 80% of the world’s children now have access to immunization, as measured by coverage of the third dose of DTP (diphtheria, tetanus and pertussis) vaccine, while an increasing number also have access to powerful new vaccines. “In the past, countries relied on a package of vaccines against six diseases,” says Project Optimize Coordinator Modibo Dicko, referring to WHO’s Expanded Programme on Immunization, which was launched in 1974. “Now some countries are doubling the number of vaccines they offer.” As encouraging as all this seems, the scaling up of immunization programmes and the introduction of new vaccines is putting an unprecedented strain on delivery systems that have not changed in decades.

Best read at http://www.who.int/bulletin/volumes/89/5/11-030511/en/index.html

  • ECONOMIC VALUE OF DENGUE VACCINE IN THAILAND

‘A 50% efficacious vaccine was highly cost-effective [< 1x per capita gross domestic product (GDP) ($4,289)] up to a total vaccination cost of $60 and cost-effective [< 3x per capita GDP ($12,868)] up to a total vaccination cost of $200. When the total vaccine series was $1.50, many scenarios were cost saving.’

  • From the authors’ conclusions: ‘As vaccine candidates get closer to licensure, now is the ideal time to further examine the economic value of a dengue vaccine.’

Best viewed at  http://www.ajtmh.org/cgi/content/full/84/5/764

 

  • ·         USE OF MASS MEDIA CAMPAIGNS TO CHANGE HEALTH BEHAVIOR

[M]ass media campaigns can produce positive changes or prevent negative changes in health-related behaviours across large populations.’

 Best read at http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)60809-4/fulltext

 Good reading. For those focusing on child survival, the relevant section is reproduced here.

 ‘Child survival

‘In many low-income countries, a substantial portion of premature mortality and associated morbidity occurs between birth and age 5 years. Major causes of poor child survival include inadequate treatment of dehydration resulting from diarrhoea, non-vaccination for preventable diseases, and failure to breastfeed exclusively and for sufficient time.71, 72 Each of these causes has been the target of mass media campaigns, with mixed evidence for success.

One review found four of six childhood vaccination programmes that used mass media achieved substantial improvements in vaccine use, and the effects were incremental with increasing exposure to the campaign.73, 74 One cost-effectiveness analysis in Bangladesh attributed increasing use of immunisation services to national campaign exposure.75 A later review of vaccination interventions found no additional examples of mass media campaigns alone.76 Rather, mass media was a strategy widely used in multicomponent vaccination campaigns worldwide, and substantial improvements in childhood vaccination were repeatedly recorded. As with other campaigns, effects cannot be specifically attributed to the mass media campaign component.77

  • ·         THE BROAD STREET PUMP

Wikipedia article below; also at http://en.wikipedia.org/wiki/1854_Broad_Street_cholera_outbreak

See also ‘On the Mode of Communication of Cholera,’ by John Snow, available online at http://www.deltaomega.org/snowfin.pdf

  • ·         PROVIDER INITIATED HIV TESTING, AN ALTERNATIVE TO CONVENTIONAL VCT

‘The introduction of routine PITC using lay counsellors into health-care clinics in Lusaka, Zambia, dramatically increased the uptake and acceptability of HIV testing.’ 

Full text, with figures, is at http://www.who.int/bulletin/volumes/89/5/10-084442.pdf

 Opt-out provider-initiated HIV testing and counselling in primary care outpatient clinics in Zambia

Stephanie M Topp,a Julien M Chipukuma,a Matimba M Chiko,b Chibesa S Wamulume,b Carolyn Bolton-Moorea & Stewart E Reida

Objective To increase case-finding of infection with human immunodeficiency virus (HIV) in Zambia and their referral to HIV care and treatment by supplementing existing client-initiated voluntary counselling and testing (VCT), the dominant mode of HIV testing in the country.

 Methods Lay counsellors offered provider-initiated HIV testing and counselling (PITC) to all outpatients who attended primary clinics and did not know their HIV serostatus. Data on counselling and testing were collected in registers. Outcomes of interest included HIV testing coverage, the acceptability of testing, the proportion testing HIV-positive (HIV+), the proportion enrolling in HIV care and treatment and the time between testing and enrolment.

 Findings After the addition of PITC to VCT, the number tested for HIV infection in the nine clinics was twice the number undergoing VCT alone. Over 30 months, 44 420 patients were counselled under PITC and 31 197 patients, 44% of them men, accepted testing. Of those tested, 21% (6572) were HIV+; 38% of these HIV+ patients (2515) enrolled in HIV care and treatment. The median time between testing and enrolment was 6 days. The acceptability of testing rose over time.

 Conclusion The introduction of routine PITC using lay counsellors into health-care clinics in Lusaka, Zambia, dramatically increased the uptake and acceptability of HIV testing. Moreover, PITC was incorporated rapidly into primary care outpatient departments. Maximizing the number of patients who proceed to HIV care and treatment remains a challenge and warrants further research.’

 

  • ·         SCHISTOSOMIASIS ELIMINATION

This article, originally published in 2010, continues to generate editorial correspondence. The article and letters to the editor, with authors’ reply, are best viewed online at

http://www.thelancet.com/journals/laninf/article/PIIS1473-3099(10)70099-2/fulltext

This article, which originally appeared in 2010, has generated much correspondence to the editor. Article and correspondence are best viewed at http://www.thelancet.com/journals/laninf/article/PIIS1473-3099(10)70099-2/fulltextoutline goes here

The Lancet Infectious Diseases, Volume 10, Issue 10, Pages 733 - 736, October 2010

Schistosomiasis elimination: lessons from the past guide the future

Original Text

Dr Darren J Gray PhD a b c , Prof Donald P McManus DSc c, Prof Yuesheng Li MD c d, Prof Gail M Williams PhD b, Prof Robert Bergquist MD e, Prof Allen G Ross MD a

Summary

Schistosomiasis is a major neglected tropical disease, with more than 200 million people infected and close to 800 million at risk. The disease burden is estimated to exceed 70 million disability-adjusted life-years. The anthelmintic drug praziquantel is highly effective in killing adult schistosome worms, but it is unable to kill developing schistosomes and so does not prevent reinfection. As a result, current praziquantel-based control programmes in Asia and sub-Saharan Africa are not effective or sustainable in the long term. The control of neglected tropical diseases, including schistosomiasis, is a funding priority for several donor agencies, with over US$350 million committed until 2013. Here we put forward an argument that donor funds would be more effectively spent on the development of a multi-faceted, integrated control programme, which would have a greater and longer lasting effect on disease transmission than the current chemotherapy-based programmes. The development of a transmission-blocking vaccine is also of great importance. A multi-faceted integrated control programme that incorporates a vaccine, even if only partly effective, has the potential to eliminate schistosomiasis. This integrated-approach model has the potential to improve the health of a billion of the world's poorest people and its effect cannot be underestimated.

 

  • ·         PLASMODIUM KNOWLESI MALARIA IN MALAYSIAN CHILDREN

‘P. knowlesi is the most common cause of childhood malaria in Kudat. Although infection is generally uncomplicated, anemia is common and thrombocytopenia universal. Transmission dynamics in this region require additional investigation.’

Another contribution from Emerging Infectious Diseases.

Best  read, with figures, at http://www.cdc.gov/eid/content/17/5/814.htm

  • IMPACT OF VITAMIN A SUPPLEMENTATION

As the world moves towards 2015 and MDG4, how can we increase the coverage for routine vitamin A supplementation?

Amid the positive results, the absence of impact on measles mortality is notable. This means that strict adherence to the WHO guidelines for measles treatment, with vitamin A on Days 1 and 2 of treatment, is necessary to reduce the case fatality rate from measles.

‘Pooled results for preventive vitamin A supplementation showed that it reduced all-cause mortality by 25% [RR 0.75; 95 % CI 0.64-0.88] in children 6-59 months of age. Vitamin A supplementation also reduced diarrhea specific mortality by 30% [RR 0.70; 95 % CI 0.58-0.86] in children 6-59 months. This effect has been recommended for inclusion in the Lives Saved Tool.’ 

Best viewed at
http://jid.oxfordjournals.org/content/203/4/464.full?sid=0aa3a9d2-e733-465e-a8aa-3940870d3158

  • LOW TITERS OF MEASLES ANTIBODY IN MOTHERS WHOSE INFANTS SUFFERED FROM MEASLES BEFORE ELIGIBLE AGE FOR MEASLES VACCINATION 

‘The mean measles neutralizing titer in 18 vaccinated mothers without natural boosting were significantly lower than that in 13 age-match women with the histories of clinical measles.’

Are these results unique to China? Probably not. What will happen to maternal antibody interference and to measles vaccine seroconversion among younger infant vaccinees if, in countries with declining measles incidence, there is no natural boosting?

Our floor ages for measles vaccination are largely based on studies from another era. Do they need a review, based on more recent evidence?

Full text is at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874774/?tool=pubmed

 

  • MASS CAMPAIGN BEDNET DISTRIBUTION IN MADAGASCAR

The phrase 'mass campaign' raises hackles among some advocates of integrated health services. But if you are trying rapidly to increase bednet coverage in malarious airways, is there any faster way to do so than through mass campaigns?

From the abstract: ‘Equity of campaign net ownership was evident. Post-campaign, the LLIN use target of 80% by children less than five years of age and a high level of LLIN use (69%) by pregnant women were attained. Targeted LLIN distribution further contributed to total population coverage (60%) through use of campaign nets by all age groups.’

From the text: ‘This study demonstrates the significant achievement of 80% insecticide-treated net use among children less than five years of age after an integrated campaign that distributed free LLINs to children less than five years of age in 59 districts of Madagascar. Although LLIN use by pregnant women (69%) did not achieve the 80% level, it still represents one of the highest reported use rates for this target group in sub-Saharan Africa.’

Full text, with figures, is at http://www.ajtmh.org/cgi/content/full/82/3/420

  • TWO ON RABIES

With intradermal vaccination of rabies vaccine in fractionated doses, vaccination of high risk groups (here, rag pickers in Himachal Pradesh) is becoming more affordable.

Cross posted, with thanks, from www.technet21.org

http://www.technet21.org/index.php/forum/technet21/general-discussion/1906-225-rag-pickers-given-free-antirabies-vaccination.html

 Here are weblinks to the new WHO guidelines on rabies vaccination.

http://www.technet21.org/index.php/forum/technet21/general-discussion/2613-new-guidelines-for-anti-rabies-vaccination-prophylaxis-by-who-2010.html

 

  • MORTALITY TRENDS IN A NIGERIAN TEACHING HOSPITAL OVER THREE DECADES

 

Death from infectious disease and trauma declined from 1,048 and 1,441 in the first decade (1977 – 1986) to 478 and 133 in the last decade respectively, while death from neoplasia increased from 112 in the first decade to 354 in the last decade of the study period.

 Full text is at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035961/?tool=pubmed

  • ·         CDC GRAND ROUNDS: THE OPPORTUNITY FOR AND CHALLENGES TO MALARIA ERADICATION

Note, in particular, the graphics showing changes over time in bednet utilization in countries which have measured this twice.

Can we do better than 60 percent bednet utilization rates? 

Best viewed at http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6015a3.htm?s_cid=mm6015a3_w

  • PMTCT IN KISUMU, KENYA

From the editors’ summary: 

What Do These Findings Mean?

Although these findings are limited by the single-arm design, they support the idea that giving breastfeeding women a triple-ARV regimen from late pregnancy to 6 months is a safe, feasible way to reduce MTCT in resource-limited settings. The HIV transmission rates in this study are comparable to those recorded in similar trials in other resource-limited settings and are lower than MTCT rates observed previously in Kisumu in a study in which no ARVs were used. Importantly, the KiBS mothers took most of the ARVs they were prescribed and most sped breastfeeding by 6 months as advised. 

Best viewed at http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1001015

 

 

  • DOES IMPROVING MATERNAL KNOWLEDGE OF VACCINES IMPACT INFANT IMMUNIZATION RATES?

Aatekah Owais and colleagues, writing in BMC Public Health, point to a cheap, easy way to raise completion rates. This is the second article of its kind from Pakistan; see also CSU 115/2011, ‘Redesigned vaccination cards.’ Full text of this article is available online at http://www.biomedcentral.com/content/pdf/1471-2458-11-239.pdf

 

 

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