Evidence map›Paper›PMID 26161864›Full record

ArticlePloS one2015

Accounting for False Positive HIV Tests: Is Visceral Leishmaniasis Responsible?

Leslie Shanks, Koert Ritmeijer, Erwan Piriou, M Ruby Siddiqui, Jarmila Kliescikova, Neil Pearce, Cono Ariti, Libsework Muluneh, Johnson Masiga, Almaz Abebe

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  6. The evaluation of low cut-off index values of ElecsysJournal of clinical laboratory analysis · 2020
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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

10 authors at 5 institutions in 3 countries.

Leslie ShanksMédecins Sans Frontières, Amsterdam, The Netherlands.
Koert RitmeijerMédecins Sans Frontières, Amsterdam, The Netherlands.
Erwan PiriouMédecins Sans Frontières, Amsterdam, The Netherlands.
M Ruby SiddiquiMédecins Sans Frontières, London, United Kingdom.
Jarmila KliescikovaMédecins Sans Frontières, Amsterdam, The Netherlands.
Neil PearceLondon School of Hygiene and Tropical Medicine, London, United Kingdom.
Cono AritiLondon School of Hygiene and Tropical Medicine, London, United Kingdom.
Libsework MulunehEthiopian Health and Nutrition Research Institute, Addis Ababa, Ethiopia.
Johnson MasigaMédecins Sans Frontières, Amsterdam, The Netherlands.
Almaz AbebeEthiopian Health and Nutrition Research Institute, Addis Ababa, Ethiopia.
Médecins Sans Frontières · NLEthiopian Public Health Institute · ETLondon School of Hygiene & Tropical Medicine · GBMédecins Sans Frontières‎ · GBUniversity of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCo-infection with HIV and visceral leishmaniasis is an important consideration in treatment of either disease in endemic areas. Diagnosis of HIV in resource-limited settings relies on rapid diagnostic tests used together in an algorithm. A limitation of the HIV diagnostic algorithm is that it is vulnerable to falsely positive reactions due to cross reactivity. It has been postulated that visceral leishmaniasis (VL) infection can increase this risk of false positive HIV results. This cross sectional study compared the risk of false positive HIV results in VL patients with non-VL individuals. METHODOLOGY/PRINCIPAL

findingsParticipants were recruited from 2 sites in Ethiopia. The Ethiopian algorithm of a tiebreaker using 3 rapid diagnostic tests (RDTs) was used to test for HIV. The gold standard test was the Western Blot, with indeterminate results resolved by PCR testing. Every RDT screen positive individual was included for testing with the gold standard along with 10% of all negatives. The final analysis included 89 VL and 405 non-VL patients. HIV prevalence was found to be 12.8% (47/ 367) in the VL group compared to 7.9% (200/2526) in the non-VL group. The RDT algorithm in the VL group yielded 47 positives, 4 false positives, and 38 negatives. The same algorithm for those without VL had 200 positives, 14 false positives, and 191 negatives. Specificity and positive predictive value for the group with VL was less than the non-VL group; however, the difference was not found to be significant (p = 0.52 and p = 0.76, respectively).

conclusionThe test algorithm yielded a high number of HIV false positive results. However, we were unable to demonstrate a significant difference between groups with and without VL disease. This suggests that the presence of endemic visceral leishmaniasis alone cannot account for the high number of false positive HIV results in our study.

Indexed as

AdolescentAdultAgedChildDemographyFalse Positive ReactionsFemaleHIV InfectionsHumansLeishmaniasis, VisceralMaleMiddle AgedSensitivity and SpecificityYoung Adult

Identifiers

PMID26161864
PMCPMC4498794
OpenAlexW2122594136

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.