Evidence map›Paper›PMID 42902167›Full record

ArticleBMC infectious diseases2026

Evaluation of the diagnostic validity of the HIV VISITECT CD4 point-of-care rapid diagnostic test in Uganda.

Oliver Nakamaanya, Bernard Bagaya, Willy Ssengooba, Erick Thokerunga, Henry Zamarano

Abstract readEvaluation Study
In one paragraph

Article in BMC infectious diseases, 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

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Oliver NakamaanyaDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda. olivecurtis1@gmail.com.
Bernard BagayaDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda.
Willy SsengoobaDepartment of Medical Microbiology, Makerere University, Kampala, Uganda.
Erick ThokerungaInfectious Diseases Institute (IDI), Kampala, Uganda.
Henry ZamaranoUganda Protestant Medical Bureau, Kampala, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHIV remains highly prevalent in Uganda, where CD4 T-cell counts are central to identifying and managing Advanced HIV Disease (AHD). Instrument-based point-of-care (POC) CD4 platforms face cost and operational constraints in resource-limited settings. The VISITECT CD4 lateral flow immunoassay (LFA) offers a non-instrument-based alternative, but its diagnostic validity against the Pima Analyzer had not been evaluated in Uganda.

objectivesTo compare diagnostic validity of the VISITECT CD4 LFA against the Pima Analyzer at the 200 cells/µL AHD threshold and explore factors influencing performance.

methodsA comparative cross-sectional study was conducted between June and August 2023 at three Kampala health centres. Venous blood from 351 HIV-positive adults was tested simultaneously on both platforms. Sensitivity, specificity, PPV, NPV, and likelihood ratios were calculated with 95% CIs using the Pima Analyzer-a point-of-care, not gold-standard, platform-as reference; estimates reflect relative, not absolute, performance.

resultsMost participants were female (68.11%), median age 31 years; mean CD4 count was 482 cells/µL (± 283.9) and AHD prevalence 22.79%. VISITECT CD4 LFA showed sensitivity of 86.25% (95% CI: 76.73-92.93), specificity of 90.41% (95% CI: 86.26-93.64), PPV of 72.63% (95% CI: 64.57-79.44), NPV of 95.70% (95% CI: 92.78-97.48), and inter-rater agreement κ = 0.957. No assessed factor significantly modified performance.

conclusionsThe VISITECT CD4 LFA performed reliably as an AHD screening tool relative to the Pima Analyzer in resource-limited settings, particularly where instrument-based platforms are unavailable. It should complement, not replace, confirmatory testing; improvements in sensitivity and PPV remain warranted.

Indexed as

HIV InfectionsPoint-of-Care SystemsPoint-of-Care TestingAdultCD4 Lymphocyte CountCross-Sectional StudiesFemaleHumansImmunoassayMaleMiddle AgedRapid Diagnostic TestsSensitivity and SpecificityUgandaYoung AdultAdvanced HIV diseaseCD4Diagnostic accuracyHIVPIMAPoint-of-care testingUgandaVISITECT

Identifiers

PMID42902167
PMCPMC13685150

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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.