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Impact of increasing CD4 count threshold eligibility for antiretroviral therapy initiation on advanced HIV disease and tuberculosis prevalence and incidence in South Africa

An interrupted time series analysis

Bibliographic Data

ID21879198
AuthorsKwabena Asare (0000-0002-5074-2315, Centre for the AIDS Programme of Research in South Africa), Lara Lewis (0000-0001-5373-2086, Centre for the AIDS Programme of Research in South Africa), Johan van der Molen (0000-0002-6233-479X, Centre for the AIDS Programme of Research in South Africa), Yukteshwar Sookrajh (0000-0001-9029-5153, eThekwini Municipality), Thokozani Khubone (0000-0002-2488-6454, eThekwini Municipality), Thulani Ngwenya (Addington Hospital), Ntokozo Siyabonga Mkhize (Addington Hospital), Richard Lessells (0000-0003-0926-710X, Centre for the AIDS Programme of Research in South Africa), Kogieleum Naidoo (0000-0002-8874-6661, Centre for the AIDS Programme of Research in South Africa), Phelelani Sosibo (eThekwini Municipality), Christian Bottomley (0000-0002-5241-8412, London School of Hygiene & Tropical Medicine), Nigel Garrett (0000-0002-4530-234X, Centre for the AIDS Programme of Research in South Africa), Jienchi Dorward (0000-0001-6072-1430, Centre for the AIDS Programme of Research in South Africa)
Year2025
Volume10
Issue4
Pagese016631
Publication date2025-04-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueBMJ Global Health (JOURNAL)
Journal identifiersISSN: 2059-7908 • E-ISSN: 2059-7908
PublisherBMJ (PUBLISHER • GB)
DOI10.1136/bmjgh-2024-016631
PMID40204463
OpenAlexW4409287634
LanguageEN
Citations received2
References cited36

INTRODUCTION: We investigated the impact of increasing CD4 count eligibility for antiretroviral therapy (ART) initiation on advanced HIV disease (AHD) and tuberculosis (TB) prevalence and incidence among people living with HIV (PLHIV) in South Africa. METHODS: We conducted an interrupted time series analysis with de-identified data of PLHIV aged ≥15 years initiating ART between April 2012 and February 2020 at 65 primary healthcare clinics in KwaZulu-Natal, South Africa. Outcomes included monthly proportions of new ART initiators presenting with AHD (CD4 count <200 cells/μL) and TB disease. We created a cohort of monthly ART initiators without TB and evaluated the cumulative incidence of TB within 12 months follow-up. We used segmented binomial regression models to estimate relative risks (RR) of outcomes, allowing for a step and slope change after expanding the ART initiation CD4 count eligibility from <350 to <500 cells/μL in January 2015 and following Universal Test and Treat (UTT) implementation in September 2016. RESULTS: Among 209 984 participants, median age was 32 (range: 26-38), and 141 499 (67.4%) were female. After January 2015, the risk of AHD at initiation decreased in step by 25.0% (RR=0.750, 95% CI 0.688 to 0.812) and further reduced by 26.9% following UTT implementation (RR=0.731, 95% CI 0.681 to 0.781). The risk of TB at initiation also decreased in step by 27.6% after January 2015 (RR=0.724, 95% CI 0.651 to 0.797) and further decreased by 17.4% after UTT implementation (RR=0.826, 95% CI 0.711 to 0.941) but remained stable among initiators with AHD. Among the incidence cohort, we saw a step decrease in the risk of new TB by 31.4% (RR=0.686, 95% CI 0.465 to 0.907) following UTT implementation. Among the incidence cohort with AHD, there was weak evidence of a step decrease in the risk of new TB (RR=0.755, 95% CI 0.489 to 1.021), but the slope decreased by 9.7% per month (RR=0.903, 95% CI 0.872 to 0.934) following UTT implementation. CONCLUSIONS: Our data support the added benefit of decreased TB co-burden with expanded ART access. Early diagnosis and immediate linkage to care should be prioritised among PLHIV

Antiretroviral therapy · Cohort · Cohort study · Confidence interval · Cumulative incidence · Interrupted time series · Psychological intervention · Relative risk · Tuberculosis · Viral load · Demography · HIV/AIDS drug development and treatment · HIV/AIDS Research and Interventions · Medicine · Tuberculosis Research and Epidemiology · Immunology · Internal Medicine · Pediatrics

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Unique citing works2
Citations per year2
Citation span2026 - 2026 (1)
Citation velocitycurrent
Highly citedNo
Citation typesNeutral: 2
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