Evidence map›Paper›PMID 42615132›Full record

ArticleThe Journal of antimicrobial chemotherapy2026

Performance of plasma separation cards for HIV drug-resistance genotyping in a resource-limited setting: comparison with plasma samples.

Thang Hong Pham, Hanh Thi Hong Ngo, Tram Thi Phuong Pham, Nhung Thi Hong Le, Mai Thi Nguyen, Tuan Anh Nguyen, Huyen Thi Do, Duong Nhu Tran, Lan Trong Phan, Yoann Madec

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In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Thang Hong PhamNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.
Hanh Thi Hong NgoNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.ORCID 0000-0001-5188-4043
Tram Thi Phuong PhamNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.
Nhung Thi Hong LeNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.
Mai Thi NguyenVietnam Administration of Disease Prevention (VADP), Hanoi, Vietnam.
Tuan Anh NguyenNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.
Huyen Thi DoInstitute of Biotechnology, Vietnam Academy of Science and Technology, Hanoi, Vietnam.
Duong Nhu TranNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.
Lan Trong PhanNational Institute of Hygiene and Epidemiology (NIHE), Hanoi 100000, Vietnam.
Yoann MadecEpidemiology of Emerging Diseases, Institut Pasteur, Université de Paris, Paris F-75015, France.

Funding

RocheVingroup Innovation Foundation (VINIF) VINIF.2023.ThS.140
6 · The paper itself

Abstract

backgroundHIV drug resistance (HIVDR) threatens the effectiveness of antiretroviral therapy (ART) programmes in low- and middle-income countries. The Cobas Plasma Separation Card (PSC) is a recently developed specimen collection tool with potential to expand access to HIVDR genotyping in remote settings. This study evaluates PSC performance for HIVDR genotyping compared with plasma.

methodsPaired plasma and PSC specimens were selected from 250 people living with HIV (PLHIV) on ART ≥6 months with viral load (VL) ≥1000 copies/mL. HIVDR genotyping followed CDC Atlanta in-house protocol; resistance interpretation used the Stanford HIVdb algorithm. Paired sequences were compared for subtype, nucleotide similarity, mutation profile and drug-resistance classification.

resultsTwenty paired specimens met inclusion criteria. Amplification of the HIV-1 Pol gene succeeded in 19/20 (95%) PSC samples. Of 19 paired sequences, nucleotide similarity was 98.5% (IQR 98.0%-99.3%). Eleven plasma samples showed 37 major drug-resistance mutations (MDM); 35 (94.6%) concordant MDM were identified in PSC. Discordances in four pairs were limited to mixed versus single bases and did not alter drug-resistance classification. Only one pair showed a clinically significant discordance (K103N detected in plasma but not initially in PSC).

conclusionsPSC demonstrated good concordance with plasma for HIVDR genotyping and has potential as an alternative specimen type for clinical practice and surveillance in resource-limited settings.

Indexed as

Drug Resistance, ViralGenotyping TechniquesHIV-1HIV InfectionsPlasmaSpecimen HandlingGenotypeHumansResource-Limited SettingsViral Load

Identifiers

PMID42615132
PMCPMC13487323

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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.