Tuesday, 28th of January 2014 |
THE SURVIVAL BENEFITS OF ANTIRETROVIRAL THERAPY IN SOUTH AFRICA
J Infect Dis. (2014) 209 (4): 491-499. doi: 10.1093/infdis/jit584 First published online: December 3, 2013
Kenneth A. Freedberg2,3,4,5,6,7,9 and
Rochelle P. Walensky2,3,5,6,7,11
+ Author Affiliations
1Department of Emergency Medicine, San Antonio Uniformed Services Health Education Consortium, Texas
2Harvard Medical School
3Center for AIDS Research
4Department of Health Policy and Management, Harvard School of Public Health, Harvard University
5The Medical Practice Evaluation Center
6Division of Infectious Diseases
7Division of General Medicine, Massachusetts General Hospital
8Department of Biostatistics
9Department of Epidemiology, Boston University
10Department of Orthopedic Surgery
11Division of Infectious Diseases, Brigham and Womens Hospital, Boston, Massachusetts
12Yale School of Public Health, New Haven, Connecticut
13Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine
14Department of Medicine, University of Cape Town, Cape Town, South Africa
15INSERM, Centre 897
16Université Bordeaux Segalen, Bordeaux, France
17Programme PAC-CI/ANRS Research Site in Abidjan, Côte dIvoire
Correspondence: Michael D. April, MD, DPhil, MSc, Medical Practice Evaluation Center, Massachusetts General Hospital, 50 Staniford St, 9th Fl, Boston, MA 02114 (michael.d.april@post.harvard.edu).
Presented in part: 20th Conference on Retroviruses and Opportunistic Infections, Atlanta, Georgia, 3 March 2013 (poster Y-144); 66th Annual Meeting of the MGH Scientific Advisory Committee, Boston, Massachusetts 19 March 2013; 2nd Annual San Antonio Uniformed Services Health Education Consortium, San Antonio, Texas 25 April 2013.
Abstract below; full text is at http://jid.oxfordjournals.org/content/209/4/491.full
Background. We sought to quantify the survival benefits attributable to antiretroviral therapy (ART) in South Africa since 2004.
Methods. We used the Cost-Effectiveness of Preventing AIDS Complications–International model (CEPAC) to simulate 8 cohorts of human immunodeficiency virus (HIV)–infected patients initiating ART each year during 2004–2011. Model inputs included cohort-specific mean CD4+ T-cell count at ART initiation (112–178 cells/µL), 24-week ART suppressive efficacy (78%), second-line ART availability (2.4% of ART recipients), and cohort-specific 36-month retention rate (55%–71%). CEPAC simulated survival twice for each cohort, once with and once without ART. The sum of the products of per capita survival differences and the total numbers of persons initiating ART for each cohort yielded the total survival benefits.
Results. Lifetime per capita survival benefits ranged from 9.3 to 10.2 life-years across the 8 cohorts. Total estimated population lifetime survival benefit for all persons starting ART during 2004–2011 was 21.7 million life-years, of which 2.8 million life-years (12.7%) had been realized by December 2012. By 2030, benefits reached 17.9 million life-years under current policies, 21.7 million life-years with universal second-line ART, 23.3 million life-years with increased linkage to care of eligible untreated patients, and 28.0 million life-years with both linkage to care and universal second-line ART.
Conclusions. We found dramatic past and potential future survival benefits attributable to ART, justifying international support of ART rollout in South Africa.
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