Soares Bernardo, Lima Reisser Anelise Arl, Farrell Michael, Silva de Lima Mauricio
Brazilian Cochrane Centre, Universidade Federal de São Paulo, Rua Pedro de Toledo 598, São Paulo, SP, Brazil, 04039-001.
Cochrane Database Syst Rev. 2010 Feb 17(2):CD003352. doi: 10.1002/14651858.CD003352.pub2.
Cocaine dependence is a common and serious condition, which has become a substantial public health problem. There is a wide and well documented range of consequences associated to chronic use of cocaine, such as medical, psychological and social problems.. Therapeutic management of the cocaine addicts includes an initial period of abstinence from the drug. During this phase the subjects may experience, besides the intense craving for cocaine, symptoms such as depression, fatigue, irritability, anorexia, and sleep disturbances. It was demonstrated that the acute use of cocaine may enhance dopamine transmission and chronically it decreases dopamine concentrations in the brain. Pharmacological treatment that affects dopamine could theoretically reduce these symptoms and contribute to a more successful therapeutic approach.
To evaluate the efficacy and acceptability of dopamine agonists for treating cocaine dependence.
Electronic searches of Cochrane Library, EMBASE, MEDLINE, PsycLIT, Biological Abstracts and LILACS; reference searching; personal communication; conference abstracts; unpublished trials from pharmaceutical industry; book chapters on treatment of cocaine dependence, was performed for the primary version of this review in 2001. Another search of the electronic databases was done in December of 2002 for this update. The specialised register of trials of the Cochrane Group on Drugs and Alcohol was searched until February 2003.
The inclusion criteria for all randomised controlled trials were that they should focus on the use of dopamine agonists on the treatment of cocaine dependence.
The reviewers extracted the data independently and Relative Risks, weighted mean difference and number needed to treat were estimated. The reviewers assumed that people who died or dropped out had no improvement and tested the sensitivity of the final results to this assumption.
Seventeen studies were included, with 1224 participants randomised. Amantadine, bromocriptine, and pergolide were the drugs evaluated. The main outcomes evaluated were positive urine sample for cocaine metabolites, for efficacy, and retention in treatment, as an acceptability measure. There were no significant differences between interventions, and in trials where participants had primary cocaine dependence or had additional diagnosis of opioid dependence and/or were in methadone maintenance treatment.
AUTHORS' CONCLUSIONS: Current evidence does not support the clinical use of dopamine agonists in the treatment of cocaine dependence. Given the high rate of dropouts in this population, clinicians may consider adding other supportive measures aiming to keep patients in treatment.
可卡因依赖是一种常见且严重的状况,已成为一个重大的公共卫生问题。长期使用可卡因会带来广泛且有充分文献记载的一系列后果,如医学、心理和社会问题。对可卡因成瘾者的治疗管理包括药物戒断的初始阶段。在此阶段,除了对可卡因的强烈渴望外,受试者可能还会出现抑郁、疲劳、易怒、厌食和睡眠障碍等症状。已证实急性使用可卡因可增强多巴胺传递,而长期使用会降低大脑中的多巴胺浓度。从理论上讲,影响多巴胺的药物治疗可以减轻这些症状,并有助于采取更成功的治疗方法。
评估多巴胺激动剂治疗可卡因依赖的疗效和可接受性。
2001年对本综述的初版进行了检索,检索了Cochrane图书馆、EMBASE、MEDLINE、PsycLIT、生物学文摘和LILACS;参考文献检索;个人交流;会议摘要;制药行业未发表的试验;关于可卡因依赖治疗的书籍章节。2002年12月为本次更新对电子数据库进行了另一轮检索。检索了Cochrane药物与酒精研究组的专门试验注册库,直至2003年2月。
所有随机对照试验的入选标准是,试验应聚焦于多巴胺激动剂在可卡因依赖治疗中的应用。
综述作者独立提取数据,并估计相对风险、加权平均差和需治疗人数。综述作者假设死亡或退出的人没有改善,并检验了最终结果对该假设的敏感性。
纳入了17项研究,1224名参与者被随机分组。评估的药物有金刚烷胺、溴隐亭和培高利特。评估的主要结局为可卡因代谢物尿样呈阳性作为疗效指标,以及治疗保留率作为可接受性指标。各干预措施之间无显著差异,在参与者为原发性可卡因依赖或有阿片类药物依赖附加诊断和/或正在接受美沙酮维持治疗的试验中也是如此。
目前的证据不支持多巴胺激动剂用于可卡因依赖的临床治疗。鉴于该人群的高退出率,临床医生可考虑增加其他支持性措施以帮助患者坚持治疗。