Evidence map›Paper›PMID 25203158›Full record

ArticleAIDS (London, England)2014

Assessing and adjusting for differences between HIV prevalence estimates derived from national population-based surveys and antenatal care surveillance, with applications for Spectrum 2013.

Kimberly Marsh, Mary Mahy, Joshua A Salomon, Daniel R Hogan

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in AIDS (London, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

4 authors.

Kimberly MarshaUNAIDS, Geneva, Switzerland bDepartment of Global Health and Population, Harvard University, Boston, Massachusetts, USA cDepartment of Health Statistics and Information Systems, World Health Organization, Geneva, Switzerland.
Mary Mahy
Joshua A Salomon
Daniel R Hogan

Funding

World Health Organization 001
6 · The paper itself

Abstract

OBJECTIVE(S): To assess differences between HIV prevalence estimates derived from national population surveys and antenatal care (ANC) surveillance sites and to improve the calibration of ANC-derived estimates in Spectrum 2013 to more appropriately account for differences between these data.

designRetrospective analysis of national population survey and ANC surveillance data from 25 countries with generalized epidemics in sub-Saharan Africa and 8 countries with concentrated epidemics.

methodsAdult national population survey and ANC surveillance HIV prevalence estimates were compared for all available national population survey data points for the years 1999-2012. For sub-Saharan Africa, a mixed-effects linear regression model determined whether the relationship between national population and ANC estimates was constant across surveys. A new calibration method was developed to incorporate national population survey data directly into the likelihood for HIV prevalence in countries with generalized epidemics. Results were used to develop default rules for adjusting ANC data for countries with no national population surveys.

resultsANC surveillance data typically overestimate population prevalence, although a wide variation, particularly in rural areas, is observed across countries and survey years. The new calibration method yields similar point estimates to previous approaches, but leads to an average 44% increase in the width of 95% uncertainty intervals.

conclusionImportant biases remain in ANC surveillance data for HIV prevalence. The new approach to model-fitting in Spectrum 2013 more appropriately accounts for this bias when producing national estimates in countries with generalized epidemics. In countries with concentrated epidemics, local sex ratios should be used to calibrate ANC surveillance estimates.

Indexed as

Epidemiological MonitoringAdolescentAdultAfrica South of the SaharaFemaleHIV InfectionsHumansMaleMiddle AgedPrenatal CarePrenatal DiagnosisPrevalenceRetrospective StudiesYoung Adult

Identifiers

PMID25203158
PMCPMC4247262

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