HIV-infected prisoners fare poorly after release. Though rarely available,
opioid agonist
therapy (OAT) may be one way to improve HIV and
substance abuse treatment outcomes after release. Of the 69 HIV-infected prisoners enrolled in a randomized controlled trial of directly administered antiretroviral
therapy, 48 (70%) met DSM-IV criteria for
opioid dependence. Of these, 30 (62.5%) selected OAT, either as
methadone (N = 7, 14.5%) or
buprenorphine/naloxone (BPN/NLX; N = 23, 48.0%). Twelve-week HIV and
substance abuse treatment outcomes are reported as a sub-study for those selecting BPN/NLX. Retention was high: 21 (91%) completed BPN/NLX induction and 17 (74%) remained on BPN/NLX after 12 weeks. Compared with baseline, the proportion with a non-detectable viral load (61% vs 63% log(10) copies/mL) and mean CD4 count (367 vs 344 cells/mL) was unchanged at 12 weeks.
Opiate-negative urine testing remained 83% for the 21 who completed induction. Using means from 10-point Likert scales,
opioid craving was reduced from 6.0 to 1.8 within 3 days of BPN/NLX induction and satisfaction remained high at 9.5 throughout the 12 weeks. Adverse events were few and mild. BPN/NLX
therapy was acceptable, safe and effective for both HIV and
opioid treatment outcomes among released HIV-infected prisoners. Future randomized controlled trials are needed to affirm its benefit in this highly vulnerable population.