Evidence map›Paper›PMID 24558359›Full record

SynthesisPloS one2014

Systematic review of the performance of HIV viral load technologies on plasma samples.

Kimberly A Sollis, Pieter W Smit, Susan Fiscus, Nathan Ford, Marco Vitoria, Shaffiq Essajee, David Barnett, Ben Cheng, Suzanne M Crowe, Thomas Denny and 5 more

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 3 pooled it
4.4field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 3 syntheses or guidelines pooled it, 58 citations in OpenAlex.

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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

15 authors at 8 institutions in 5 countries.

Kimberly A SollisDepartment of Clinical Research, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Pieter W SmitDepartment of Clinical Research, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Susan FiscusDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Nathan FordDepartment of HIV/AIDS, World Health Organization, Geneva, Switzerland.
Marco VitoriaDepartment of HIV/AIDS, World Health Organization, Geneva, Switzerland.
Shaffiq EssajeeHIV, Medicine and Science, Clinton Health Access Initiative, New York, New York, United States of America.
David BarnettDepartment of Haematology, United Kingdom National External Quality Assessment Service (UK NEQAS) for Leucocyte Immunophenotyping, Sheffield, United Kingdom.
Ben ChengDepartment of Technology and Innovation, Pangaea Global AIDS Foundation, San Fransisco, California, United States of America.
Suzanne M CroweCentre for Biomedical Research, Burnet Institute, Melbourne, Australia.
Thomas DennyDepartment of Medicine, Duke Human Vaccine Institute and Center for HIV/AIDS Vaccine Immunology, Durham, North Carolina, United States of America.
Alan LandayDepartment of Immunology- Microbiology, Rush University Medical Center, Chicago, Illinois, United States of America.
Wendy StevensDepartment of Molecular Medicine and Haematology, University of the Witwatersrand, Johannesburg, South Africa.
Vincent HabiyambereDepartment of HIV/AIDS, World Health Organization, Geneva, Switzerland.
Jos PerrinsDepartment of HIV/AIDS, World Health Organization, Geneva, Switzerland.
Rosanna W PeelingDepartment of Clinical Research, London School of Hygiene & Tropical Medicine, London, United Kingdom.
World Health Organization · CHLondon School of Hygiene & Tropical Medicine · GBBurnet Institute · AUClinton Health Access Initiative · USPangaea Global AIDS Foundation · USRush University Medical Center · USUniversity of North Carolina at Chapel Hill · USUniversity of the Witwatersrand · ZA

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
NIAID NIH HHS P30 AI050410World Health Organization 001
6 · The paper itself

Abstract

backgroundViral load (VL) monitoring is the standard of care in developing country settings for detecting HIV treatment failure. Since 2010 the World Health Organization has recommended a phase-in approach to VL monitoring in resource-limited settings. We conducted a systematic review of the accuracy and precision of HIV VL technologies for treatment monitoring. METHODS AND

findingsA search of Medline and Embase was conducted for studies evaluating the accuracy or reproducibility of commercially available HIV VL assays. 37 studies were included for review including evaluations of the Amplicor Monitor HIV-1 v1.5 (n = 25), Cobas TaqMan v2.0 (n = 11), Abbott RealTime HIV-1 (n = 23), Versant HIV-1 RNA bDNA 3.0 (n = 15), Versant HIV-1 RNA kPCR 1.0 (n = 2), ExaVir Load v3 (n = 2), and NucliSens EasyQ v2.0 (n = 1). All currently available HIV VL assays are of sufficient sensitivity to detect plasma virus levels at a lower detection limit of 1,000 copies/mL. Bias data comparing the Abbott RealTime HIV-1, TaqMan v2.0 to the Amplicor Monitor v1.5 showed a tendency of the Abbott RealTime HIV-1 to under-estimate results while the TaqMan v2.0 overestimated VL counts. Compared to the Amplicor Monitor v1.5, 2-26% and 9-70% of results from the Versant bDNA 3.0 and Abbott RealTime HIV-1 differed by greater than 0.5log10. The average intra and inter-assay variation of the Abbott RealTime HIV-1 were 2.95% (range 2.0-5.1%) and 5.44% (range 1.17-30.00%) across the range of VL counts (2log10-7log10).

conclusionsThis review found that all currently available HIV VL assays are of sufficient sensitivity to detect plasma VL of 1,000 copies/mL as a threshold to initiate investigations of treatment adherence or possible treatment failure. Sources of variability between VL assays include differences in technology platform, plasma input volume, and ability to detect HIV-1 subtypes. Monitoring of individual patients should be performed on the same technology platform to ensure appropriate interpretation of changes in VL. Prospero registration # CD42013003603.

Indexed as

Viral LoadAlgorithmsDeveloping CountriesHIV-1HIV InfectionsHIV SeropositivityHumansMolecular Diagnostic TechniquesPlasmaPolymerase Chain ReactionReagent Kits, DiagnosticReproducibility of ResultsSensitivity and SpecificitySerologic TestsWorld Health OrganizationReagent Kits, Diagnostic

Identifiers

PMID24558359
PMCPMC3928047
OpenAlexW1989372408

What OpenQuestion holds

Textmetadata
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.