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.
引用
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页数:18
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