JAIDS Journal of Acquired Immune Deficiency Syndromes · 2018 · 55 citations · 33 references
MedicinePharmacologyPharmacotherapyClinical PharmacologySubstance Use DisordersSubstance Use PreventionAntiretroviral TherapyDrug Efficacy AssessmentEfficacy EvaluationPsychosocial InterventionsRelapse PreventionSubstance Abuse PreventionExtended-release NaltrexoneIncarcerated PopulationsNaltrexone TreatmentPlacebo ComparatorsPlacebo-controlled Efficacy AssessmentProgram Outcomes EvaluationSubstance Abuse TreatmentViral Disease Suppression
OBJECTIVE: To determine whether extended-release naltrexone (XR-NTX) would improve or maintain viral suppression (VS) among incarcerated individuals with HIV and alcohol use disorders (AUDs) transitioning to the community. DESIGN: A randomized, double-blind, placebo-controlled trial was conducted among incarcerated individuals with HIV and AUDs transitioning to the community from 2010 through 2016. METHODS: Eligible participants (N = 100) were randomized 2:1 to receive 6 monthly injections of XR-NTX (n = 67) or placebo (n = 33) starting at release and continued for 6 months. The primary and secondary outcomes were the proportion that maintained or improved VS at <200 and <50 copies per milliliter from baseline to 6 months, respectively, using an intention-to-treat analysis. RESULTS: Participants allocated to XR-NTX improved VS from baseline to 6 months for <200 copies per milliliter (48.0%-64.2%, P = 0.024) and for <50 copies per milliliter (31.0%-56.7%, P = 0.001), whereas the placebo group did not (<200 copies/mL: 64%-42.4%, P = 0.070; <50 copies/mL: 42.0%-30.3%, P = 0.292). XR-NTX participants were more likely to achieve VS than the placebo group at 6 months (<200 copies/mL: 64.2% vs. 42.4%; P = 0.041; <50 copies/mL: 56.7% vs. 30.3%; P = 0.015). XR-NTX independently predicted VS [<200 copies/mL: adjusted odds ratio (aOR) = 2.68, 95% confidence interval (CI) = 1.01 to 7.09, P = 0.047; <50 copies/mL: aOR = 4.54; 95% CI = 1.43 to 14.43, P = 0.009] as did receipt of ≥3 injections (<200 copies/mL: aOR = 3.26; 95% CI = 1.26 to 8.47, P = 0.010; <50 copies/mL: aOR = 6.34; 95% CI = 2.08 to 19.29, P = 0.001). Reductions in alcohol consumption (aOR = 1.43, 95% CI = 1.03 to 1.98, P = 0.033) and white race (aOR = 5.37, 95% CI = 1.08 to 27.72, P = 0.040) also predicted VS at <50 copies per milliliter. CONCLUSIONS: XR-NTX improves or maintains VS after release to the community for incarcerated people living with HIV and AUDs.
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John B. Saunders, Olaf Gjerløw Aasland, Thomas F. Babor et al. · Addiction · 1993 · 13.3K citations
Efficacy and Tolerability of Long-Acting Injectable Naltrexone for Alcohol Dependence
James C. Garbutt, Henry R. Kranzler, Stephanie S. O’Malley et al. · JAMA · 2005 · 624 citations
Melanie Thompson, Michael J. Mugavero, K. Rivet Amico et al. · Annals of Internal Medicine · 2012 · 595 citations · Full text
Public Health, Infectious Disease Control, Evidence-based Practice +15