• Drug Alcohol Depend · Nov 2015

    Randomized Controlled Trial

    Buprenorphine dose induction in non-opioid-tolerant pre-release prisoners.

    • Frank J Vocci, Robert P Schwartz, Monique E Wilson, Michael S Gordon, Timothy W Kinlock, Terrence T Fitzgerald, Kevin E O'Grady, and Jerome H Jaffe.
    • Friends Research Institute, 1040 Park Avenue, Suite 103, Baltimore, MD 21201, USA. Electronic address: fvocci@friendsresearch.org.
    • Drug Alcohol Depend. 2015 Nov 1; 156: 133-138.

    BackgroundIn a previously reported randomized controlled trial, formerly opioid-dependent prisoners were more likely to enter community drug abuse treatment when they were inducted in prison onto buprenorphine/naloxone (hereafter called buprenorphine) than when they received counseling without buprenorphine in prison (47.5% vs. 33.7%, p=0.012) (Gordon et al., 2014). In this communication we report on the results of the induction schedule and the adverse event profile seen in pre-release prisoners inducted onto buprenorphine.MethodThis paper examines the dose induction procedure, a comparison of the proposed versus actual doses given per week, and side effects reported for 104 adult participants who were randomized to buprenorphine treatment in prison. Self-reported side effects were analyzed using generalized estimated equations to determine changes over time in side effects.ResultsStudy participants were inducted onto buprenorphine at a rate faster than the induction schedule. Of the 104 (72 males, 32 females) buprenorphine recipients, 64 (37 males, 27 females) remained on medication at release from prison. Nine participants (8.6%) discontinued buprenorphine because of unpleasant opioid side effects. There were no serious adverse events reported during the in-prison phase of the study. Constipation was the most frequent symptom reported (69 percent).ConclusionOur findings suggest that buprenorphine administered to non-opioid-tolerant adults should be started at a lower, individualized dose than customarily used for adults actively using opioids, and that non-opioid-tolerant pre-release prisoners can be successfully inducted onto therapeutic doses prior to release.Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

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