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

被引:4
|
作者
Gils, Tinne [1 ,2 ]
Kamele, Mashaete [3 ]
Madonsela, Thandanani [4 ]
Bosman, Shannon [4 ]
Ngubane, Thulani [4 ]
Joseph, Philip [4 ]
Reither, Klaus [5 ,6 ]
Bresser, Moniek [5 ,6 ]
Vlieghe, Erika [2 ]
Decroo, Tom [1 ]
Ayakaka, Irene [3 ]
Lynen, Lutgarde [1 ]
Van Heerden, Alastair [4 ,7 ]
机构
[1] Inst Trop Med, Dept Clin Sci, Antwerp, Belgium
[2] Univ Antwerp, Global Hlth Inst, Antwerp, Belgium
[3] SolidarMed, Partnerships Hlth, Butha Buthe, Lesotho
[4] Human Sci Res Council, Ctr Community Based Res, Pietermaritzburg, South Africa
[5] Swiss Trop & Publ Hlth Inst, Clin Res Unit, Allschwil, Switzerland
[6] Univ Basel, Med Outpatient Dept, Basel, Switzerland
[7] Univ Witwatersrand, Wits Dev Pathways Hlth Res Unit, MRC, Johannesburg, South Africa
来源
PLOS ONE | 2023年 / 18卷 / 12期
关键词
ANTIRETROVIRAL THERAPY; INFECTION; FRAMEWORK;
D O I
10.1371/journal.pone.0296197
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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/mu l. 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/mu l on VISITECT or a positive tuberculosis test. A CD4 <= 200cells/mu l 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/mu l 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.
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页数:18
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