Evaluation of geospatial methods to generate subnational HIV prevalence estimates for local level planning

  • The Subnational Estimates Working Group of the HIV Modelling Consortium

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: There is evidence of substantial subnational variation in the HIV epidemic. However, robust spatial HIV data are often only available at high levels of geographic aggregation and not at the finer resolution needed for decision making. Therefore, spatial analysis methods that leverage available data to provide local estimates of HIV prevalence may be useful. Such methods exist but have not been formally compared when applied to HIV. Design/methods: Six candidate methods-including those used by the Joint United Nations Programme on HIV/AIDS to generate maps and a Bayesian geostatistical approach applied to other diseases-were used to generate maps and subnational estimates of HIV prevalence across three countries using cluster level data from household surveys. Two approaches were used to assess the accuracy of predictions: internal validation, whereby a proportion of input data is held back (test dataset) to challenge predictions; and comparison with location-specific data from household surveys in earlier years. Results: Each of the methods can generate usefully accurate predictions of prevalence at unsampled locations, with the magnitude of the error in predictions similar across approaches. However, the Bayesian geostatistical approach consistently gave marginally the strongest statistical performance across countries and validation procedures. Conclusions: Available methods may be able to furnish estimates of HIV prevalence at finer spatial scales than the data currently allow. The subnational variation revealed can be integrated into planning to ensure responsiveness to the spatial features of the epidemic. The Bayesian geostatistical approach is a promising strategy for integrating HIV data to generate robust local estimates.

Original languageEnglish
Pages (from-to)1467-1474
Number of pages8
JournalAIDS
Volume30
Issue number9
DOIs
StatePublished - 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.

Funding

S.J.A. received personal fees from the Bill & Melinda Gates Foundation and Anansi Health outside of the submitted work. C.B. was supported by US Agency for International Development (USAID) with support for travel from USAID and UNAIDS. D.F. reports consultant fees from Imperial College Consultants. P.W.G. is a Career Development Fellow (#K00669X) jointly funded by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement and receives support from the Bill and Melinda Gates Foundation (#OPP1068048). These grants also support S.B. T.B.H. received grants and personal fees from the Bill & Melinda Gates Foundation during the conduct of the study; grants and personal fees (prior to the conduct of the work) from World Bank; grants from UNAIDS, and The Rush Foundation; personal fees from the University of Washington, New York University, and Global Fund outside of the submitted work. J.L. is supported by IRD, and reports personal fees from UNAIDS and grants from ANRS.

ASJC Scopus Subject Areas

  • Immunology and Allergy
  • Immunology
  • Infectious Diseases

Keywords

  • Health planning/organization and administration
  • Health policy
  • HIV infections/epidemiology
  • HIV seroprevalence
  • HIV/infections prevention and control
  • Population surveillance/methods

Disciplines

  • Immunology and Infectious Disease
  • Medical Immunology
  • Infectious Disease

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