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阿片类药物成瘾的药物辅助治疗:美沙酮和丁丙诺啡。

Medication-assisted treatment for opioid addiction: methadone and buprenorphine.

作者信息

Saxon Andrew J, Hser Yih-Ing, Woody George, Ling Walter

出版信息

J Food Drug Anal. 2013 Dec;21(4):S69-S72. doi: 10.1016/j.jfda.2013.09.037.

Abstract

Among agents for treatment of opioid addiction, methadone is a full mu-opioid receptor agonist, whereas buprenorphine is a partial agonist. Both are long-acting. Buprenorphine has a superior safety profile. Methadone is formulated for oral administration and buprenorphine for sublingual administration. A subdermal buprenorphine implant with a 6-month duration of action is being considered for approval by the U.S. Food and Drug Administration. Both medications reduce mortality rates and improve other outcomes. Data from a recent randomized controlled comparison of both medications (N = 1269) show better treatment retention with methadone but reduced illicit opioid use early in treatment with buprenorphine. Human immunodeficiency virus (HIV) risk behaviors were measured using the Risk Behavior Survey at baseline, 12 weeks, and 24 weeks for study completers. In the 30 days prior to treatment entry, 14.4% of the completers randomized to treatment with buprenorphine (n = 340) and 14.1% of the completers randomized to methadone treatment (n = 391) shared needles. The percent sharing needles decreased to 2.4% for buprenorphine and 4.8 for methadone in the 30 days prior to Week 24 ( < 0.0001). In the 30 days prior to treatment entry, 6.8% of the completers randomized to buprenorphine and 8.2% of the completers randomized to methadone had multiple sexual partners, with only 5.2% and 5.1%, respectively, reporting multiple partners at Week 24 ( < 0.04).

摘要

在用于治疗阿片类药物成瘾的药物中,美沙酮是一种完全μ-阿片受体激动剂,而丁丙诺啡是一种部分激动剂。两者都是长效药物。丁丙诺啡具有更好的安全性。美沙酮为口服制剂,丁丙诺啡为舌下含服制剂。一种作用持续时间为6个月的皮下丁丙诺啡植入剂正在等待美国食品药品监督管理局的批准。两种药物都能降低死亡率并改善其他预后。最近一项对两种药物进行随机对照比较的研究(N = 1269)数据显示,美沙酮的治疗保留率更高,但在治疗早期,丁丙诺啡能减少非法阿片类药物的使用。对于完成研究的患者,在基线、12周和24周时使用风险行为调查来测量人类免疫缺陷病毒(HIV)风险行为。在进入治疗前的30天内,随机接受丁丙诺啡治疗的完成研究患者(n = 340)中有14.4%、随机接受美沙酮治疗的完成研究患者(n = 391)中有14.1%共用针头。在第24周前的30天内,丁丙诺啡组共用针头的比例降至2.4%,美沙酮组降至4.8%(P < 0.0001)。在进入治疗前的30天内,随机接受丁丙诺啡治疗的完成研究患者中有6.8%、随机接受美沙酮治疗的完成研究患者中有8.2%有多个性伴侣,在第24周时分别只有5.2%和5.1%报告有多个性伴侣(P < 0.04)。

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