| Literature DB >> 30073637 |
E Jennifer Edelman1,2,3, Brent A Moore4,5, Stephen R Holt4, Nathan Hansen6,7, Tassos C Kyriakides8, Michael Virata4, Sheldon T Brown9, Amy C Justice4,5, Kendall J Bryant10, David A Fiellin4,6, Lynn E Fiellin4,6,11.
Abstract
We sought to test the efficacy of extended-release naltrexone (XR-NTX) on HIV-related and drinking outcomes. From April 2011-February 2015, we conducted a 4-site randomized double-blind placebo controlled clinical trial involving 51 HIV-positive patients with heavy drinking and < 95% antiretroviral (ART) adherence. All participants received counseling. The primary outcome was proportion with ≥ 95% ART adherence. Secondary outcomes included HIV biomarkers, VACS Index score, and past 30-day heavy drinking days. Based on receipt of ≥ 5 injections, 23 participants were retained at 24 weeks. We did not detect an effect of XR-NTX on ART adherence (p = 0.38); undetectable HIV viral load (p = 0.26); CD4 cell count (p = 0.75) or VACS Index score (p = 0.70). XR-NTX was associated with fewer heavy drinking days (p = 0.03). While XR-NTX decreases heavy drinking days, we did not detect improvements in ART adherence or HIV outcomes. Strategies to improve retention in alcohol treatment and HIV-related outcomes among heavy drinking HIV-positive patients are needed.Entities:
Keywords: Alcohol; Extended-release naltrexone; HIV; Randomized clinical trial
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Year: 2019 PMID: 30073637 PMCID: PMC6476298 DOI: 10.1007/s10461-018-2241-z
Source DB: PubMed Journal: AIDS Behav ISSN: 1090-7165