Evidence map›Paper›PMID 29996876›Full record

ArticleInternational journal of health geographics2018

Capturing the spatial variability of HIV epidemics in South Africa and Tanzania using routine healthcare facility data.

Diego F Cuadros, Benn Sartorius, Chris Hall, Adam Akullian, Till Bärnighausen, Frank Tanser

Abstract read
In one paragraph

Article in International journal of health geographics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. BMJ open · 2024
    Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Diego F CuadrosDepartment of Geography and Geographic Information Science, University of Cincinnati, Cincinnati, OH, 45221, USA. diego.cuadros@uc.edu.
Benn SartoriusDepartment of Public Health Medicine, School of Nursing and Public Health, University of KwaZulu-Natal, Durban, South Africa.
Chris HallGeographical Information Systems and Science Program, Kingston University, London, UK.
Adam AkullianInstitute for Disease Modeling, 3150 139th Ave SE, Bellevue, USA.
Till BärnighausenAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Frank TanserAfrica Health Research Institute, University of KwaZulu-Natal, Durban, South Africa.

Funding

Training Tanzanian Researchers for HIV/AIDS Implementation ScienceD43TW009775 · FIC · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Wafaie W Fawzi, Christopher Sudfeld · 2015 to 2026
$3.0M
New Methods for the design and evaluation of large HIV prevention interventionsR01AI112339 · NIAID · YALE UNIVERSITY · PI SPIEGELMAN, DONNA L · 2014 to 2017
$2.7M
Causal Pathways to population health impact of HIV antiretroviral treatmentR01HD084233 · NICHD · UNIVERSITY OF KWAZULU-NATAL · PI BARNIGHAUSEN, TILL, TANSER, FRANK COURTENEY · 2015 to 2021
$2.3M
Can HIV Hot-Spots be eradicated? An intervention to decrease HIV transmission to young women in rural KwaZulu-Natal South AfricaR01AI124389 · NIAID · UNIVERSITY OF KWAZULU-NATAL · PI BARNIGHAUSEN, TILL, TANSER, FRANK COURTENEY · 2016 to 2020
$2.1M
FIC NIH HHS D43 TW009775NIAID NIH HHS R01 AI112339NIAID NIH HHS R01 AI124389NICHD NIH HHS R01 HD084233NIH HHS R01-AI124389NIH HHS R01AI124389NIH HHS R01-HD084233NIH HHS R01HD084233South African Medical Research Council MRC-RFA-UFSP-01-2013/UKZN HIVEPIUK Academy of Medical Sciences Newton Advanced Fellowship NA150161Wellcome Trust
6 · The paper itself

Abstract

backgroundLarge geographical variations in the intensity of the HIV epidemic in sub-Saharan Africa call for geographically targeted resource allocation where burdens are greatest. However, data available for mapping the geographic variability of HIV prevalence and detecting HIV 'hotspots' is scarce, and population-based surveillance data are not always available. Here, we evaluated the viability of using clinic-based HIV prevalence data to measure the spatial variability of HIV in South Africa and Tanzania.

methodsPopulation-based and clinic-based HIV data from a small HIV hyper-endemic rural community in South Africa as well as for the country of Tanzania were used to map smoothed HIV prevalence using kernel interpolation techniques. Spatial variables were included in clinic-based models using co-kriging methods to assess whether cofactors improve clinic-based spatial HIV prevalence predictions. Clinic- and population-based smoothed prevalence maps were compared using partial rank correlation coefficients and residual local indicators of spatial autocorrelation.

resultsRoutinely-collected clinic-based data captured most of the geographical heterogeneity described by population-based data but failed to detect some pockets of high prevalence. Analyses indicated that clinic-based data could accurately predict the spatial location of so-called HIV 'hotspots' in > 50% of the high HIV burden areas.

conclusionClinic-based data can be used to accurately map the broad spatial structure of HIV prevalence and to identify most of the areas where the burden of the infection is concentrated (HIV 'hotspots'). Where population-based data are not available, HIV data collected from health facilities may provide a second-best option to generate valid spatial prevalence estimates for geographical targeting and resource allocation.

Indexed as

Data AnalysisEpidemicsHealth FacilitiesSpatial AnalysisHealth SurveysHIV InfectionsHumansSouth AfricaTanzaniaHealthcare facilitiesHigh resolution mapsHIV prevalenceSpatial analysisSub-Saharan Africa

Identifiers

PMID29996876
PMCPMC6042209

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.