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Fewer out-of-sequence vaccinations and reduction of child mortality in Northern Ghana

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“It is recommended not to give DTP with MV or DTP after MV.”

Vaccine. 2017 Apr 25;35(18):2496-2503. doi: 10.1016/j.vaccine.2017.03.004. Epub 2017 Mar 22.

Fewer out-of-sequence vaccinations and reduction of child mortality in Northern Ghana

Welaga P1, Oduro A2, Debpuur C2, Aaby P3, Ravn H4, Andersen A4, Binka F5, Hodgson A6.

Author information

1 Navrongo Health Research Centre, P.O. Box 114, Navrongo, Ghana; OPEN, Institute of Clinical Research, University of Southern Denmark, Odense, Denmark. Electronic address: pwelaga@gmail.com.

2 Navrongo Health Research Centre, P.O. Box 114, Navrongo, Ghana.

3 Bandim Health Project, Indepth Network, Apartado 861, Bissau, Guinea-Bissau.

4 Bandim Health Project, Statens Serum Institut, 2300 Copenhagen, Denmark.

5 University of Health and Allied Sciences, Ho, Ghana.

6 Research and Development Division, Ghana Health Service, Accra, Ghana.

Abstract below; full text is at http://www.sciencedirect.com/science/article/pii/S0264410X17303109

BACKGROUND:

Studies suggest that diphtheria-tetanus-pertussis (DTP) vaccine administered simultaneously with measles vaccine (MV) or DTP administered after MV are associated with higher child mortality than having MV-after-DTP3 as most recent vaccination. We tested this in Northern Ghana where the prevalence of such out-of-sequence vaccinations has declined.

METHODS:

Using annual cohort data of children aged 12-23months from 1996 to 2012 and Cox proportional hazards models, we assessed survival in relation to the most recent vaccination status within the next 12months and until five years of age. We assessed whether mortality in children aged 12-59months was higher when the most recent vaccine was non-live (DTP) rather than live (MV or OPV).

RESULTS:

Out-of-sequence vaccinations with DTP-containing vaccines and MV declined from 86% in 1989 to 24% in 1996 and 0.7% in 2012. Between 1996 and 2012, 38 070 children had their vaccinations status assessed: the adjusted hazard ratio (HR) for out-of-sequence vaccinations (DTP>=MV) compared with the recommended sequence of MV-after-DTP3 was 1.42(1.06-1.90) during the first 12months after assessment of vaccination status and 1.29(1.03-1.60) with follow-up to five years of age; the HR was 2.58(1.14-5.84) before OPV or MV campaigns and 1.37(1.02-1.85) after the campaigns.

CONCLUSION:

Out-of-sequence vaccinations with DTP and MV are associated with higher mortality than MV as most recent vaccination; the effect is unlikely to be due to confounding. Hence, the reduction in out-of-sequence vaccinations may have lowered child mortality. It is recommended not to give DTP with MV or DTP after MV.

Copyright © 2017 Elsevier Ltd. All rights reserved.