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丁丙诺啡与曲马多在阿片类(海洛因)依赖者脱毒治疗中的疗效比较。

Comparison of efficacy between buprenorphine and tramadol in the detoxification of opioid (heroin)-dependent subjects.

作者信息

Chawla Jatinder Mohan, Pal Hemraj, Lal Rakesh, Jain Raka, Schooler Nina, Balhara Yatan Pal Singh

机构信息

Department of Psychiatry, SUNY Downstate Medical Center, Brooklyn, NY, USA.

出版信息

J Opioid Manag. 2013 Jan-Feb;9(1):35-41. doi: 10.5055/jom.2013.0145.

Abstract

AIM/BACKGROUND: Tramadol is a synthetic opiate and a centrally acting weak m-opioid receptor agonist. The potential advantages of tramadol include ease of administration, low abuse potential, and being nonscheduled. This study compared tramadol and buprenorphine for controlling withdrawal symptoms in patients with opioid dependence syndrome.

METHODS

Consenting male subjects between 20 and 45 years of age who fulfilled the ICD-10-DCR criteria for opiate dependence syndrome were randomly assigned in a double-blind, double-dummy placebo-controlled trial for detoxification. Those with multiple drug dependence, abnormal cardiac, renal and hepatic functions, psychosis, or organic mental illness were excluded. Assessments included Subjective Opiate Withdrawal Scale (SOWS), Objective Opiate Withdrawal Scale (OOWS), Visual Analog Scale (VAS), and Side Effect Check List. Subjects were evaluated daily and study duration was 10 days.

RESULTS

Sixty two subjects were enrolled. The mean SOWS and OOWS and VAS were significantly lower in the buprenorphine group on second and third day of detoxification as compared to the tramadol group. Although the retention rate was higher for buprenorphine group throughout the study, when compared with tramadol the difference was not significant on any day. Three subjects in the tramadol group had seizures.

CONCLUSIONS

Tramadol was found to have limited detoxification efficacy in moderate to severe opioid withdrawal and substantial risk of seizures as compared to buprenorphine. Further studies are warranted to examine its efficacy in mild opioid withdrawal symptoms and its potential use in outpatient settings where its administration advantages may be valuable.

摘要

目的/背景:曲马多是一种合成阿片类药物,是一种中枢作用的弱μ-阿片受体激动剂。曲马多的潜在优势包括给药方便、滥用可能性低且无需处方。本研究比较了曲马多和丁丙诺啡在控制阿片类药物依赖综合征患者戒断症状方面的效果。

方法

年龄在20至45岁之间、符合国际疾病分类第10版药物依赖综合征诊断标准且同意参与研究的男性受试者,被随机分配到一项双盲、双模拟安慰剂对照的戒毒试验中。排除有多种药物依赖、心脏、肾脏和肝脏功能异常、精神病或器质性精神疾病的受试者。评估包括主观阿片类药物戒断量表(SOWS)、客观阿片类药物戒断量表(OOWS)、视觉模拟量表(VAS)和副作用检查表。每天对受试者进行评估,研究持续时间为10天。

结果

共招募了62名受试者。与曲马多组相比,丁丙诺啡组在戒毒的第二天和第三天,SOWS、OOWS和VAS的平均值显著更低。尽管在整个研究过程中丁丙诺啡组的保留率更高,但与曲马多组相比,在任何一天的差异均无统计学意义。曲马多组有3名受试者发生癫痫发作。

结论

与丁丙诺啡相比,曲马多在中度至重度阿片类药物戒断中的戒毒效果有限,且癫痫发作风险较大。有必要进一步研究其在轻度阿片类药物戒断症状中的疗效,以及在门诊环境中的潜在应用,因为其给药优势可能具有重要价值。

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