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Receipt of opioid agonist treatment halves the risk of HIV-1 RNA viral load rebound through improved ART adherence for HIV-infected women who use illicit drugs

•Most studies aren’t powered to examine risk factors for HIV viral rebound specifically for women.•Longitudinal analyses for a cohort of women living with HIV who use illicit drugs.•Opioid agonist treatment in the past six months halved the hazard of viral rebound.•Recent stimulant use more than dou...

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Bibliographic Details
Published in:Drug and alcohol dependence 2020-01, Vol.206, p.107670-107670, Article 107670
Main Authors: Adams, Joëlla W., Marshall, Brandon D.L., Mohd Salleh, Nur Afiqah, Barrios, Rolando, Nolan, Seonaid, Milloy, M.-J.
Format: Article
Language:English
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Summary:•Most studies aren’t powered to examine risk factors for HIV viral rebound specifically for women.•Longitudinal analyses for a cohort of women living with HIV who use illicit drugs.•Opioid agonist treatment in the past six months halved the hazard of viral rebound.•Recent stimulant use more than doubled hazard of viral rebound. Women living with HIV who use illicit drugs may be particularly vulnerable to HIV-1 RNA viral load (VL) rebound. We used longitudinal data from 2006 to 2017 to evaluate the impact of sociodemographic, behavioral, social-structural, and clinical factors on the hazard of viral rebound for women enrolled in the ACCESS study, a prospective cohort with systematic VL monitoring. Women were included if they achieved VL suppression ( 1000 copies/mL). Cox regressions using a recurrent events framework, time-varying covariates, robust standard errors, and a frailty component were used. Of the 185 women included, 62 (34%) experienced at least one viral rebound event over an 11-year period, accumulating a total of 87 viral rebound events. In adjusted analysis, stimulant use more than doubled the hazard of viral rebound (adjusted hazard ratio [AHR]: 2.35, 95% confidence interval [CI]: 1.07–5.14) while the only factor protective against viral rebound was receipt of opioid agonist treatment (OAT) in the past six months (AHR: 0.46, 95% CI: 0.26–0.81). After adjusting for ART adherence in the past six months, the effect of OAT was attenuated (AHR: 0.57, 95% CI: 0.32–1.02). Efforts to improve access to and retention within OAT programs and decrease stimulant use may improve rates of viral suppression for HIV-positive women who use illicit drugs.
ISSN:0376-8716
1879-0046
1879-0046
DOI:10.1016/j.drugalcdep.2019.107670