A prospective evaluation of the diagnostic accuracy of the point-of-care VISITECT CD4 Advanced Disease test in seven countries.

AIDS-Related Opportunistic Infections HIV sensitivity and specificity

Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
24 Jul 2024
Historique:
received: 20 03 2024
revised: 10 07 2024
accepted: 22 07 2024
medline: 24 7 2024
pubmed: 24 7 2024
entrez: 24 7 2024
Statut: aheadofprint

Résumé

CD4 measurement is pivotal in the management of advanced HIV disease. VISITECT® CD4 Advanced Disease (AccuBio Limited, Alva, UK; VISITECT) is an instrument-free, point-of-care, semi-quantitative test allowing visual identification of a CD4 ≤200 cells/µl, or >200 cells/µl from finger-prick or venous blood. As part of a diagnostic accuracy study of FUJIFILM SILVAMP TB LAM (clinicaltrials.gov: NCT04089423), people living with HIV of ≥18 years old were prospectively recruited in seven 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 a CD4 ≤200 cells/µl were evaluated. Among 1604 participants, the median flow cytometry CD4 was 367 (IQR 128-626) cells/µl and 521 (32.5%) had a CD4 ≤200 cells/µl. VISITECT sensitivity was 92.7% (483/521, 95% CI 90.1-94.7%) and specificity was 61.4% (665/1083, 95% CI 58.4-64.3%). For participants with a CD4 between 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. 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.

Sections du résumé

BACKGROUND BACKGROUND
CD4 measurement is pivotal in the management of advanced HIV disease. VISITECT® CD4 Advanced Disease (AccuBio Limited, Alva, UK; VISITECT) is an instrument-free, point-of-care, semi-quantitative test allowing visual identification of a CD4 ≤200 cells/µl, or >200 cells/µl from finger-prick or venous blood.
METHODS METHODS
As part of a diagnostic accuracy study of FUJIFILM SILVAMP TB LAM (clinicaltrials.gov: NCT04089423), people living with HIV of ≥18 years old were prospectively recruited in seven 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 a CD4 ≤200 cells/µl were evaluated.
RESULTS RESULTS
Among 1604 participants, the median flow cytometry CD4 was 367 (IQR 128-626) cells/µl and 521 (32.5%) had a CD4 ≤200 cells/µl. VISITECT sensitivity was 92.7% (483/521, 95% CI 90.1-94.7%) and specificity was 61.4% (665/1083, 95% CI 58.4-64.3%). For participants with a CD4 between 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 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.

Identifiants

pubmed: 39046150
pii: 7719076
doi: 10.1093/infdis/jiae374
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04089423']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Auteurs

Tinne Gils (T)

Department of Clinical Sciences, Institute of Tropical Medicine, Nationalestraat 155, 2000 Antwerp, Belgium.
Global Health Institute, University of Antwerp, Doornstraat 331, 2610 Wilrijk, Belgium.

Jerry Hella (J)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Bart K M Jacobs (BKM)

Department of Clinical Sciences, Institute of Tropical Medicine, Nationalestraat 155, 2000 Antwerp, Belgium.

Bianca Sossen (B)

Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.

Madalo Mukoka (M)

Public Health Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
Department of Pathology, Kamuzu University of Health Sciences, Blantyre, Malawi.

Monde Muyoyeta (M)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Elizabeth Nakabugo (E)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Hung Van Nguyen (H)

National Lung Hospital, Ha Noi, Viet Nam.

Sasiwimol Ubolyam (S)

HIV-NAT, Thai Red Cross AIDS Research Centre and Center of Excellence in Tuberculosis, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Aurélien Macé (A)

FIND, the global alliance for diagnostics, Geneva, Switzerland.

Marcia Vermeulen (M)

Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.

Sarah Nyangu (S)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Nsala Sanjase (N)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Mohamed Sasamalo (M)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Huong Thi Dinh (HT)

National Lung Hospital, Ha Noi, Viet Nam.

The Anh Ngo (TA)

Viet Tiep Hospital, Hai Phong, Viet Nam.

Weerawat Manosuthi (W)

Bamrasnaradura Infectious Diseases Institute, Nonthaburi, Thailand.

Supunnee Jirajariyavej (S)

Taksin Hospital, Bangkok, Thailand.

Claudia M Denkinger (CM)

FIND, the global alliance for diagnostics, Geneva, Switzerland.
Division of Infectious Disease and Tropical Medicine, Heidelberg University Hospital and Faculty of Medicine, Heidelberg University, Heidelberg, Germany.
German Centre for Infection Research (DZIF), Partner site Heidelberg University Hospital, Heidelberg, Germany.

Nhung Viet Nguyen (NV)

National Lung Hospital, Ha Noi, Viet Nam.

Anchalee Avihingsanon (A)

HIV-NAT, Thai Red Cross AIDS Research Centre and Center of Excellence in Tuberculosis, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Lydia Nakiyingi (L)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Rita Székely (R)

FIND, the global alliance for diagnostics, Geneva, Switzerland.

Andrew D Kerkhoff (AD)

Division of HIV, Infectious Diseases and Global Medicine, Zuckerberg San Francisco General Hospital and Trauma Center, University of California San Francisco, San Francisco, CA, United States of America.

Peter MacPherson (P)

Public Health Group, Malawi-Liverpool-Wellcome Programme, Blantyre, Malawi.
School of Health & Wellbeing, University of Glasgow, Glasgow, United Kingdom.
Clinical Research Department, London School of Hygiene & Tropical Medicine, London, United Kingdom.

Graeme Meintjes (G)

Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.

Klaus Reither (K)

Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
University of Basel, Basel, Switzerland.

Morten Ruhwald (M)

FIND, the global alliance for diagnostics, Geneva, Switzerland.

Classifications MeSH