Evidence map›Paper›PMID 35771878›Full record

ArticlePloS one2022

HIV viral load assays when used with whole blood perform well as a diagnostic assay for infants.

Charles Kiyaga, Youyi Fong, Christopher Okiira, Grace Esther Kushemererwa, Ismail Kayongo, Iga Tadeo, Christine Namulindwa, Victor Bigira, Isaac Ssewanyana, Trevor Peter and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

13 authors at 3 institutions in 2 countries.

Charles KiyagaCentral Public Health Laboratory, Kampala, Uganda.
Youyi FongFred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
Christopher OkiiraUganda National Health Laboratory Services, Kampala, Uganda.
Grace Esther KushemererwaCentral Public Health Laboratory, Kampala, Uganda.
Ismail KayongoCentral Public Health Laboratory, Kampala, Uganda.
Iga TadeoCentral Public Health Laboratory, Kampala, Uganda.
Christine NamulindwaCentral Public Health Laboratory, Kampala, Uganda.
Victor BigiraUganda National Health Laboratory Services, Kampala, Uganda.
Isaac SsewanyanaCentral Public Health Laboratory, Kampala, Uganda.
Trevor PeterClinton Health Access Initiative, Boston, MA, United States of America.
Meg DohertyWorld Health Organization, Geneva, Switzerland.
Jilian A SacksClinton Health Access Initiative, Boston, MA, United States of America.
Lara VojnovWorld Health Organization, Geneva, Switzerland.ORCID 0000-0003-0488-1012
Clinton Health Access Initiative · USWorld Health Organization · CHFred Hutch Cancer Center · US

Funding

World Health Organization 001
6 · The paper itself

Abstract

objectiveOver the past several years, only approximately 50% of HIV-exposed infants received an early infant diagnosis test within the first two months of life. While high attrition and mortality account for some of the shortcomings in identifying HIV-infected infants early and putting them on life-saving treatment, fragmented and challenging laboratory systems are an added barrier. We sought to determine the accuracy of using HIV viral load assays for infant diagnosis of HIV.

methodsWe enrolled 866 Ugandan infants between March-April 2018 for this study after initial laboratory diagnosis. The median age was seven months, while 33% of infants were less than three months of age. Study testing was done using either the Roche or Abbott molecular technologies at the Central Public Health Laboratory. Dried blood spot samples were prepared according to manufacturer-recommended protocols for both the qualitative and quantitative assays. Viral load test samples for the Roche assay were processed using two different buffers: phosphate-buffered saline (PBS: free virus elution viral load protocol [FVE]) and Sample Pre-Extraction Reagent (SPEX: qualitative buffer). Dried blood spot samples were processed for both assays on the Abbott using the manufacturer's standard infant diagnosis protocol. All infants received a qualitative test for clinical management and additional paired quantitative tests.

results858 infants were included in the analysis, of which 50% were female. Over 75% of mothers received antiretroviral therapy, while approximately 65% of infants received infant prophylaxis. The Roche SPEX and Abbott technologies had high sensitivity (>95%) and specificity (>98%). The Roche FVE had lower sensitivity (85%) and viral load values.

conclusionsTo simplify and streamline laboratory practices, HIV viral load may be used to diagnose HIV infection in infants, particularly using the Roche SPEX and Abbott technologies.

Indexed as

HIV-1HIV InfectionsFemaleHIV TestingHumansInfantMaleRNA, ViralSensitivity and SpecificityViral LoadRNA, Viral

Identifiers

PMID35771878
PMCPMC9246233
OpenAlexW4283728121

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.