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DOI 10.1093/infdis/jiae374

Медицинская библиотека · The Journal of infectious diseases · 2025

A Prospective Evaluation of the Diagnostic Accuracy of the Point-of-Care VISITECT CD4 Advanced Disease Test in 7 Countries.

Gils Tinne, Hella Jerry, Jacobs Bart K M, Sossen Bianca, Mukoka Madalo, Muyoyeta Monde, Nakabugo Elizabeth, Van Nguyen Hung, Ubolyam Sasiwimol, Macé Aurélien, Vermeulen Marcia, Nyangu Sarah, Sanjase Nsala, Sasamalo Mohamed, Dinh Huong Thi, Ngo The Anh, Manosuthi Weerawat, Jirajariyavej Supunnee, Denkinger Claudia M, Nguyen Nhung Viet, Avihingsanon Anchalee, Nakiyingi Lydia, Székely Rita, Kerkhoff Andrew D, MacPherson Peter, Meintjes Graeme, Reither Klaus, Ruhwald Morten

СтатьяМногоцентровое исследованиеОценочное исследованиеПеревод в очереди

Аннотация

BACKGROUND

CD4 measurement is pivotal in the management of advanced human immunodeficiency virus (HIV) disease. VISITECT CD4 Advanced Disease (VISITECT; AccuBio, Ltd) is an instrument-free, point-of-care, semiquantitative test allowing visual identification of CD4 ≤ 200 cells/µL or >200 cells/ µL from finger-prick or venous blood.

METHODS

As part of a diagnostic accuracy study of FUJIFILM SILVAMP TB LAM, people with HIV ≥18 years old were prospectively recruited in 7 countries from outpatient departments if a tuberculosis symptom was present, and from inpatient departments. Participants provided venous blood for CD4 measurement using flow cytometry (reference standard) and finger-prick blood for VISITECT (index text), performed at point-of-care. Sensitivity, specificity, and positive and negative predictive values of VISITECT to determine CD4 ≤ 200 cells/ µL were evaluated.

RESULTS

Among 1604 participants, the median flow cytometry CD4 was 367 cells/µL (interquartile range, 128-626 cells/µL) and 521 (32.5%) had CD4 ≤ 200 cells/µL. VISITECT sensitivity was 92.7% (483/521; 95% confidence interval [CI], 90.1%-94.7%) and specificity was 61.4% (665/1083; 95% CI, 58.4%-64.3%). For participants with CD4 0-100, 101-200, 201-300, 301-500, and >500 cells/µL, VISITECT misclassified 4.5% (95% CI, 2.5%-7.2%), 12.5 (95% CI, 8.0%-18.2%), 74.1% (95% CI, 67.0%-80.5%), 48.0% (95% CI, 42.5%-53.6%), and 22.6% (95% CI, 19.3%-26.3%), respectively.

CONCLUSIONS

VISITECT's sensitivity, but not specificity, met the World Health Organization's minimal sensitivity and specificity threshold of 80% for point-of-care CD4 tests. VISITECT's quality needs to be assessed and its accuracy optimized. VISITECT's utility as CD4 triage test should be investigated. Clinical Trials Registration. NCT04089423.

Для цитирования: Gils Tinne, Hella Jerry, Jacobs Bart K M, Sossen Bianca, Mukoka Madalo, Muyoyeta Monde, Nakabugo Elizabeth, Van Nguyen Hung, Ubolyam Sasiwimol, Macé Aurélien, Vermeulen Marcia, Nyangu Sarah, Sanjase Nsala, Sasamalo Mohamed, Dinh Huong Thi, Ngo The Anh, Manosuthi Weerawat, Jirajariyavej Supunnee, Denkinger Claudia M, Nguyen Nhung Viet, Avihingsanon Anchalee, Nakiyingi Lydia, Székely Rita, Kerkhoff Andrew D, MacPherson Peter, Meintjes Graeme, Reither Klaus, Ruhwald Morten. A Prospective Evaluation of the Diagnostic Accuracy of the Point-of-Care VISITECT CD4 Advanced Disease Test in 7 Countries.. The Journal of infectious diseases. 2025. DOI: 10.1093/infdis/jiae374.

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