节点文献

阿坎酸治疗酒依赖的12周多中心随机双盲对照研究

A 12-week randomized,double-blind,placebo-controlled multicenter clinical trial of acamprosate for the treatment of alcohol dependence

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 孙伟许秀峰黄继忠谭庆荣邓河晃栗克清高俊钰邱宇甲李冰

【Author】 SUN Wei1,XU Xiu-Feng2,HUANG Ji-Zhong3,TAN Qing-Rong4,DENG He-Huang5, LI Ke-Qing6,GAO Jun-Yu7,QIU Yu-Jia1,LI Bing1 1Peking University Institute of Mental Health,Key Laboratory of Ministry of Health(Peking University),Beijing 100191,China 2First Affiliated Hospital of Kunming Medical University,Kunming 650032,China 3Shanghai Mental Health Center,Shanghai 200030,China 4First Affiliated Hospital of Fourth Military Medical University,Xian 710032,China 5Guangzhou Psychiatric Hospital,Guangzhou 510370,China 6The Mental Health Center of Hebei Province,Baoding 071000,Hebei Province,China 7Affiliated Hospital of Academy of Military Medical Sciences,Beijing 100071,China

【机构】 北京大学精神卫生研究所,卫生部精神卫生学重点实验室(北京大学)昆明医学院第一附属医院上海市精神卫生中心第四军医大学第一附属医院广州市精神病院河北省精神卫生中心军事医学科学院附属医院

【摘要】 目的:评价阿坎酸治疗酒依赖的疗效和安全性。方法:本研究采用随机、双盲、安慰剂对照的多中心临床试验设计。研究对象是符合美国精神障碍诊断与统计手册第4版(DSM-IV)酒依赖诊断标准的门诊或者住院患者。共入组230例,一组(n=116)用阿坎酸(体质量<60 kg,1332 mg/d;≥60kg,1998 mg/d)治疗,另一组(n=114)接受安慰剂治疗,连续治疗12周。以累计戒酒天数(CAD)与校正累积戒酒持续时间(CCAD)、每次访视的复饮率、首次复饮时间作为评价疗效的主要指标。以饮酒次数、饮酒量、可视渴求量表评分、血γ-谷氨酰转移酶水平为评价疗效的次要指标。根据生命体征、实验室及心电图检查、不良事件报告评价安全性。结果:阿坎酸组与安慰剂组在累计戒酒天数[(43.7±34.7)d vs.(38.9±35.8)d]、校正累积戒酒持续时间[(52.0±41.3)%vs.(46.3±42.6)%]、每次访视的复饮率以及首次复饮时间分布等主要疗效评价指标均无统计学差异(均P>0.05)。但在治疗12周后,阿坎酸组患者饮酒量的等级为戒除和小于5标准杯/d的比例(88.1%vs.78.7%)高于安慰剂组,可视渴求量表分[(2.6±2.3)vs.(3.3±2.9)]低于安慰剂组(均P<0.05)。阿坎酸组和安慰剂组的不良事件发生率差异无统计学意义(22.6%vs.19.3%,P>0.05)。阿坎酸组最常见的不良反应是腹泻和皮疹,与安慰剂组相比腹泻发生率(4.9%vs.3.2%)和皮疹发生率(3.9%vs.2.1%)无统计学差异(均P>0.05)。结论:阿坎酸对减少酒依赖患者饮酒量、降低渴求等方面的疗效优于安慰剂,并且安全性良好。

【Abstract】 Objective:To evaluate the efficacy and safety of acamprosate in treating patients with alcohol dependence.Methods:A randomized,double-blind,placebo-controlled multicenter clinical trial was conducted.The diagnosis of alcohol dependence was made according to the Diagnostic and Statistical Manual of Mental Disorders,Fourth Edition(DSM-IV) criteria.All 230 patients received 12 weeks treatment with either acamprosate(weight<60 kg,1332 mg/d;weight ≥ 60 kg,1998 mg/d.n=116) or placebo(n=114).The primary efficacy measures were the cumulative abstinence duration(CAD) and corrected cumulative abstinence duration(CCAD),relapse rate of every visit,time to first drink.The secondary efficacy measures were the drinking times,the number of drinks per drinking day,visual analog scale(VAS) for alcohol craving,γ-glutamyl transferase.The safety measures were the vital signs,laboratory tests,electrocardiography and adverse event report.Results:There were no significant differences of all the primary efficacy measures and adverse event report rates(22.6% vs.19.3%) between acamprosate group and placebo group.But the rate of withdraw and less than 5 standard drinks per day(88.1% vs.78.7%) was higher and the points of visual analog scale for alcohol craving [(2.6±2.3) vs.(3.3±2.9)]was lower in acamprosate group at the last visit(Ps<0.05).The most common treatment-related adverse events in acamprosate group were diarrhea and erythra.Conclusion:The results show that acamprosate appears to be more efficacious for decreasing the number of drinks per drinking day and alcohol craving than placebo.It has similar safety to placebo in treatment of alcohol dependence.

  • 【文献出处】 中国心理卫生杂志 ,Chinese Mental Health Journal , 编辑部邮箱 ,2012年12期
  • 【分类号】R749.62
  • 【被引频次】12
  • 【下载频次】150
节点文献中: 

本文链接的文献网络图示:

本文的引文网络