Implementation of the advanced HIV disease care package with point-of-care CD4 testing during tuberculosis case finding: A mixed-methods evaluation.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 25 09 2023
accepted: 12 11 2023
medline: 22 12 2023
pubmed: 22 12 2023
entrez: 22 12 2023
Statut: epublish

Résumé

During TB-case finding, we assessed the feasibility of implementing the advanced HIV disease (AHD) care package, including VISITECT CD4 Advanced Disease (VISITECT), a semiquantitative test to identify a CD4≤200cells/μl. Adult participants with tuberculosis symptoms, recruited near-facility in Lesotho and South-Africa between 2021-2022, were offered HIV testing (capillary blood), Xpert MTB/RIF and Ultra, and MGIT culture (sputum). People living with HIV (PLHIV) were offered VISITECT (venous blood) and Alere tuberculosis-lipoarabinomannan (AlereLAM, urine) testing. AHD was defined as a CD4≤200cells/μl on VISITECT or a positive tuberculosis test. A CD4≤200cells/μl on VISITECT triggered Immy cryptococcal antigen (Immy CrAg, plasma) testing. Participants were referred with test results. To evaluate feasibility, we assessed i) acceptability and ii) intervention delivery of point-of-care diagnostics among study staff using questionnaires and group discussions, iii) process compliance, and iv) early effectiveness (12-week survival and treatment status) in PLHIV. Predictors for 12-week survival were assessed with logistic regression. Thematic content analysis and triangulation were performed. Among PLHIV (N = 676, 48.6% of 1392 participants), 7.8% were newly diagnosed, 81.8% on ART, and 10.4% knew their HIV status but were not on ART. Among 676 PLHIV, 41.7% had AHD, 29.9% a CD4≤200cells/μl and 20.6% a tuberculosis diagnosis. Among 200 PLHIV tested with Immy CrAg, 4.0% were positive. The procedures were acceptable for study staff, despite intervention delivery challenges related to supply and the long procedural duration (median: 73 minutes). At 12 weeks, among 276 PLHIV with AHD and 328 without, 3.3% and 0.9% had died, 84.8% and 92.1% were alive and 12.0% and 7.0% had an unknown status, respectively. Neither AHD nor tuberculosis status were associated with survival. Implementing AHD care package diagnostics was feasible during tuberculosis-case finding. AHD was prevalent, and not associated with survival, which is likely explained by the low specificity of VISITECT. Challenges with CD4 testing and preventive treatment uptake require addressing.

Identifiants

pubmed: 38134020
doi: 10.1371/journal.pone.0296197
pii: PONE-D-23-29770
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0296197

Informations de copyright

Copyright: © 2023 Gils et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Tinne Gils (T)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Global Health Institute, University of Antwerp, Wilrijk, Belgium.

Mashaete Kamele (M)

SolidarMed, Partnerships for Health, Butha-Buthe, Lesotho.

Thandanani Madonsela (T)

Centre for Community Based Research, Human Sciences Research Council, Pietermaritzburg, South Africa.

Shannon Bosman (S)

Centre for Community Based Research, Human Sciences Research Council, Pietermaritzburg, South Africa.

Thulani Ngubane (T)

Centre for Community Based Research, Human Sciences Research Council, Pietermaritzburg, South Africa.

Philip Joseph (P)

Centre for Community Based Research, Human Sciences Research Council, Pietermaritzburg, South Africa.

Klaus Reither (K)

Clinical Research Unit, Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
Medical Outpatient Department, University of Basel, Basel, Switzerland.

Moniek Bresser (M)

Clinical Research Unit, Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
Medical Outpatient Department, University of Basel, Basel, Switzerland.

Erika Vlieghe (E)

Global Health Institute, University of Antwerp, Wilrijk, Belgium.

Tom Decroo (T)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Irene Ayakaka (I)

SolidarMed, Partnerships for Health, Butha-Buthe, Lesotho.

Lutgarde Lynen (L)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Alastair Van Heerden (A)

Centre for Community Based Research, Human Sciences Research Council, Pietermaritzburg, South Africa.
MRC/Wits Developmental Pathways for Health Research Unit, University of the Witwatersrand, Johannesburg, South Africa.

Classifications MeSH