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

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dc.date.accessioned 2024-02-29T13:04:42Z
dc.date.available 2024-02-29T13:04:42Z
dc.date.issued 2024-02-09 en
dc.identifier.issn 1932-6203 en
dc.identifier.uri http://hdl.handle.net/20.500.11910/22891
dc.description.abstract 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/ul. 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/ul on VISITECT or a positive tuberculosis test. A CD4<200cells/ul 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/ul 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. en
dc.format.medium Print en
dc.subject TUBERCULOSIS en
dc.subject HIV INFECTIONS en
dc.subject CLINICAL TESTS AND MEASUREMENTS en
dc.subject LESOTHO en
dc.subject SOUTH AFRICA en
dc.title Implementation of the advanced HIV disease care package with point-of-care CD4 testing during tuberculosis case finding: a mixed-methods evaluation en
dc.type Journal Article en
dc.description.version Y en
dc.ProjectNumber PUAXAA en
dc.Volume 18(12) en
dc.BudgetYear 2023/24 en
dc.ResearchGroup Public Health, Societies and Belonging en
dc.SourceTitle PLoS One en
dc.ArchiveNumber 9814231 en
dc.PageNumber 1-18 en
dc.outputnumber 14888 en
dc.bibliographictitle Gils , T., Kamele, M., Madonsela , T., Bosman, S., Ngubane, T., Joseph, P., Reither, K., Bresser, M., Vlieghe, E., Decroo, T., Ayakaka, I., Lynen, L. & Van Heerden, A. (2023) Implementation of the advanced HIV disease care package with point-of-care CD4 testing during tuberculosis case finding: a mixed-methods evaluation. PLoS One. 18(12):1-18. http://hdl.handle.net/20.500.11910/22891 en
dc.publicationyear 2023 en
dc.contributor.author1 Gils , T. en
dc.contributor.author2 Kamele, M. en
dc.contributor.author3 Madonsela , T. en
dc.contributor.author4 Bosman, S. en
dc.contributor.author5 Ngubane, T. en
dc.contributor.author6 Joseph, P. en
dc.contributor.author7 Reither, K. en
dc.contributor.author8 Bresser, M. en
dc.contributor.author9 Vlieghe, E. en
dc.contributor.author10 Decroo, T. en
dc.contributor.author11 Ayakaka, I. en
dc.contributor.author12 Lynen, L. en
dc.contributor.author13 Van Heerden, A. en


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