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Factors associated with antiretroviral treatment initiation amongst HIV-positive individuals linked to care within a universal test and treat programme

Early findings of the ANRS 12249 TasP trial in rural South Africa

Bibliographic Data

ID19443141
AuthorsSimon Boyer (0000-0002-7567-5200, Inserm, corresponding author), Collins Iwuji (0000-0003-2045-1717, Africa Health Research Institute), Andréa Gosset (0000-0003-0743-2458, Inserm), Camelia Protopopescu (0000-0003-0164-7917, Inserm), Nonhlanhla Okesola (Africa Health Research Institute), Mélanie Plazy (0000-0002-8971-6878, Université de Bordeaux), Bruno Spire (0000-0002-3546-8020, Inserm), Joanna Orne-Gliemann (0000-0003-0359-4089, Université de Bordeaux), Nicky Mcgrath (0000-0002-1039-0159, Africa Health Research Institute), Deenan Pillay (0000-0003-3640-2573, Faculty (United Kingdom)), François Dabis (0000-0002-1614-8857, Université de Bordeaux), Joseph Larmarange (0000-0001-7097-700X, Université Paris Cité)
Year2016
Volume28
Issuesup3
Pages39-51
Publication date2016-06-02
Open AccessYes
TypeARTICLE
VenueAIDS Care (JOURNAL)
Journal identifiersISSN: 0954-0121 • E-ISSN: 1360-0451
PublisherInforma UK Limited (PUBLISHER • GB)
DOI10.1080/09540121.2016.1164808
PMID27421051
OpenAlexW2426257378
LanguageEN
Citations received11
References cited31

Prompt uptake of antiretroviral treatment (ART) is essential to ensure the success of universal test and treat (UTT) strategies to prevent HIV transmission in high-prevalence settings. We describe ART initiation rates and associated factors within an ongoing UTT cluster-randomized trial in rural South Africa. HIV-positive individuals were offered immediate ART in the intervention arm vs. national guidelines recommended initiation (CD4≤350 cells/mm(3)) in the control arm. We used data collected up to July 2015 among the ART-eligible individuals linked to TasP clinics before January 2015. ART initiation rates at one (M1), three (M3) and six months (M6) from baseline visit were described by cluster and CD4 count strata (cells/mm(3)) and other eligibility criteria: ≤100; 100-200; 200-350; CD4>350 with WHO stage 3/4 or pregnancy; CD4>350 without WHO stage 3/4 or pregnancy. A Cox model accounting for covariate effect changes over time was used to assess factors associated with ART initiation. The 514 participants had a median [interquartile range] follow-up duration of 1.08 [0.69; 2.07] months until ART initiation or last visit. ART initiation rates at M1 varied substantially (36.9% in the group CD4>350 without WHO stage 3/4 or pregnancy, and 55.2-71.8% in the three groups with CD4≤350) but less at M6 (from 85.3% in the first group to 96.1-98.3% in the three other groups). Factors associated with lower ART initiation at M1 were a higher CD4 count and attending clinics with both high patient load and higher cluster HIV prevalence. After M1, having a regular partner was the only factor associated with higher likelihood of ART initiation. These findings suggest good ART uptake within a UTT setting, even among individuals with high CD4 count. However, inadequate staffing and healthcare professional practices could result in prioritizing ART initiation in patients with the lowest CD4 counts

Antiretroviral therapy · Family medicine · Interquartile range · Pregnancy · Viral load · Demography · HIV Research and Treatment · HIV, Drug Use, Sexual Risk · HIV/AIDS Research and Interventions · Medicine · Internal Medicine · Pediatrics

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Citations per year1.22
Citation span2017 - 2027 (11)
Highly citedNo

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