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Buprenorphine maintenance versus placebo or methadone maintenance for opioid dependence

丁丙诺啡 美沙酮 医学 安慰剂 美沙酮维持 科克伦图书馆 随机对照试验 置信区间 类阿片 相对风险 荟萃分析 阿片剂替代治疗 麻醉 内科学 替代医学 受体 病理
作者
Richard P. Mattick,Courtney Breen,Jo Kimber,Marina Davoli
出处
期刊:The Cochrane library [Elsevier]
卷期号:2014 (2) 被引量:1459
标识
DOI:10.1002/14651858.cd002207.pub4
摘要

Background Buprenorphine maintenance treatment has been evaluated in randomised controlled trials against placebo medication, and separately as an alternative to methadone for management of opioid dependence. Objectives To evaluate buprenorphine maintenance compared to placebo and to methadone maintenance in the management of opioid dependence, including its ability to retain people in treatment, suppress illicit drug use, reduce criminal activity, and mortality. Search methods We searched the following databases to January 2013: Cochrane Drugs and Alcohol Review Group Specialised Register, Cochrane Central Register of Controlled Trials, MEDLINE, EMBASE, Current Contents, PsycLIT, CORK, Alcohol and Drug Council of Australia, Australian Drug Foundation, Centre for Education and Information on Drugs and Alcohol, Library of Congress, reference lists of identified studies and reviews. We sought published/unpublished randomised controlled trials (RCTs) from authors. Selection criteria Randomised controlled trials of buprenorphine maintenance treatment versus placebo or methadone in management of opioid‐dependent persons. Data collection and analysis We used Cochrane Collaboration methodology. Main results We include 31 trials (5430 participants), the quality of evidence varied from high to moderate quality. There is high quality of evidence that buprenorphine was superior to placebo medication in retention of participants in treatment at all doses examined. Specifically, buprenorphine retained participants better than placebo: at low doses (2 ‐ 6 mg), 5 studies, 1131 participants, risk ratio (RR) 1.50; 95% confidence interval (CI) 1.19 to 1.88; at medium doses (7 ‐ 15 mg), 4 studies, 887 participants, RR 1.74; 95% CI 1.06 to 2.87; and at high doses (≥ 16 mg), 5 studies, 1001 participants, RR 1.82; 95% CI 1.15 to 2.90. However, there is moderate quality of evidence that only high‐dose buprenorphine (≥ 16 mg) was more effective than placebo in suppressing illicit opioid use measured by urinanalysis in the trials, 3 studies, 729 participants, standardised mean difference (SMD) ‐1.17; 95% CI ‐1.85 to ‐0.49, Notably, low‐dose, (2 studies, 487 participants, SMD 0.10; 95% CI ‐0.80 to 1.01), and medium‐dose, (2 studies, 463 participants, SMD ‐0.08; 95% CI ‐0.78 to 0.62) buprenorphine did not suppress illicit opioid use measured by urinanalysis better than placebo. There is high quality of evidence that buprenorphine in flexible doses adjusted to participant need,was less effective than methadone in retaining participants, 5 studies, 788 participants, RR 0.83; 95% CI 0.72 to 0.95. For those retained in treatment, no difference was observed in suppression of opioid use as measured by urinalysis, 8 studies, 1027 participants, SMD ‐0.11; 95% CI ‐0.23 to 0.02 or self report, 4 studies, 501 participants, SMD ‐0.11; 95% CI ‐0.28 to 0.07, with moderate quality of evidence. Consistent with the results in the flexible‐dose studies, in low fixed‐dose studies, methadone (≤ 40 mg) was more likely to retain participants than low‐dose buprenorphine (2 ‐ 6 mg), (3 studies, 253 participants, RR 0.67; 95% CI: 0.52 to 0.87). However, we found contrary results at medium dose and high dose: there was no difference between medium‐dose buprenorphine (7 ‐ 15 mg) and medium‐dose methadone (40 ‐ 85 mg) in retention, (7 studies, 780 participants, RR 0.87; 95% CI 0.69 to 1.10) or in suppression of illicit opioid use as measured by urines, (4 studies, 476 participants, SMD 0.25; 95% CI ‐0.08 to 0.58) or self report of illicit opioid use, (2 studies, 174 participants, SMD ‐0.82; 95% CI ‐1.83 to 0.19). Similarly, there was no difference between high‐dose buprenorphine (≥ 16 mg) and high‐dose methadone (≥ 85 mg) in retention (RR 0.79; 95% CI 0.20 to 3.16) or suppression of self‐reported heroin use (SMD ‐0.73; 95% CI ‐1.08 to ‐0.37) (1 study, 134 participants). Few studies reported adverse events ; two studies compared adverse events statistically, finding no difference between methadone and buprenorphine, except for a single result indicating more sedation among those using methadone. Authors' conclusions Buprenorphine is an effective medication in the maintenance treatment of heroin dependence, retaining people in treatment at any dose above 2 mg, and suppressing illicit opioid use (at doses 16 mg or greater) based on placebo‐controlled trials. However, compared to methadone, buprenorphine retains fewer people when doses are flexibly delivered and at low fixed doses. If fixed medium or high doses are used, buprenorphine and methadone appear no different in effectiveness (retention in treatment and suppression of illicit opioid use); however, fixed doses are rarely used in clinical practice so the flexible dose results are more relevant to patient care. Methadone is superior to buprenorphine in retaining people in treatment, and methadone equally suppresses illicit opioid use.
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