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比较丁丙诺啡和美沙酮在减少甲基苯丙胺渴求方面的效果:一项随机临床试验。

Comparing the effect of buprenorphine and methadone in the reduction of methamphetamine craving: a randomized clinical trial.

作者信息

Ahmadi Jamshid, Razeghian Jahromi Leila

机构信息

Substance Abuse Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Trials. 2017 Jun 6;18(1):259. doi: 10.1186/s13063-017-2007-3.

DOI:10.1186/s13063-017-2007-3
PMID:28587620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5461765/
Abstract

BACKGROUND

We sought to test the effectiveness of methadone and buprenorphine in the treatment of methamphetamine withdrawal craving over a 17-day treatment period.

METHODS

Patients were randomized into one of two groups. The study sample comprised 40 male subjects dependent on methamphetamine who met criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, for methamphetamine dependence and withdrawal and were seeking treatment. Furthermore, they should have a history of daily methamphetamine use for at least 6 months and should have discontinued their use just before starting the protocol. Patients received 40 mg of methadone or 8 mg of buprenorphine per day and were treated in an inpatient psychiatric hospital. We used methamphetamine craving score, negative urine drug screening test (thin-layer chromatography) during the study, and retention in treatment.

RESULTS

All 40 patients completed the study. Both drugs were effective in decreasing methamphetamine craving during methamphetamine withdrawal. Reduction of craving in the buprenorphine group was significantly more than in the methadone group (P < 0.05).

CONCLUSIONS

The results favor the efficacy and safety of buprenorphine as a short-term treatment for methamphetamine withdrawal craving. We should mention that it is to be expected that craving declines over time without any medication. Therefore, the conclusion may not be that methadone and buprenorphine both reduce the craving. Because buprenorphine is superior to methadone, only buprenorphine surely reduces craving.

TRIAL REGISTRATION

Iranian Registry of Clinical Trials identifier: IRCT2015112125160N1 . Registered on 4 June 2016.

摘要

背景

我们试图测试美沙酮和丁丙诺啡在17天治疗期内治疗甲基苯丙胺戒断渴求的有效性。

方法

患者被随机分为两组。研究样本包括40名依赖甲基苯丙胺的男性受试者,他们符合《精神障碍诊断与统计手册》第五版中甲基苯丙胺依赖和戒断的标准且正在寻求治疗。此外,他们应有至少6个月的每日甲基苯丙胺使用史,且应在开始方案前刚停用甲基苯丙胺。患者每天接受40毫克美沙酮或8毫克丁丙诺啡治疗,并在一家住院精神病医院接受治疗。我们使用甲基苯丙胺渴求评分、研究期间的阴性尿液药物筛查试验(薄层色谱法)以及治疗保留率。

结果

所有40名患者均完成了研究。两种药物在减少甲基苯丙胺戒断期间的渴求方面均有效。丁丙诺啡组的渴求减少显著多于美沙酮组(P < 0.05)。

结论

结果支持丁丙诺啡作为甲基苯丙胺戒断渴求短期治疗的有效性和安全性。我们应提及,预计即使不使用任何药物,渴求也会随时间下降。因此,结论可能并非美沙酮和丁丙诺啡都能减少渴求。因为丁丙诺啡优于美沙酮,只有丁丙诺啡肯定能减少渴求。

试验注册

伊朗临床试验注册中心标识符:IRCT2015112125160N1。于2016年6月4日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/fe9ae9eb3420/13063_2017_2007_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/6a018734886f/13063_2017_2007_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/956a19e276ca/13063_2017_2007_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/fe9ae9eb3420/13063_2017_2007_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/6a018734886f/13063_2017_2007_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/956a19e276ca/13063_2017_2007_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dec/5461765/fe9ae9eb3420/13063_2017_2007_Fig3_HTML.jpg

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