Nuijten Mascha, Blanken Peter, van den Brink Wim, Hendriks Vincent
Parnassia Addiction Research Centre (PARC, Brijder Addiction Treatment), PO Box 53002, 2505 AA The Hague, The Netherlands.
Parnassia Addiction Research Centre (PARC, Brijder Addiction Treatment), PO Box 53002, 2505 AA The Hague, The Netherlands.
Drug Alcohol Depend. 2014 May 1;138:177-84. doi: 10.1016/j.drugalcdep.2014.02.024. Epub 2014 Feb 26.
Crack-cocaine dependence is a complex disorder with limited treatment options. Topiramate is one of the promising medications with reported reductions in cocaine use and craving in former studies. The present study evaluated the acceptance and effectiveness of topiramate as an add-on to cognitive behavioral therapy (CBT) in crack-cocaine dependent patients.
Seventy-four crack-cocaine dependent outpatients participated in an open-label, randomized feasibility trial. They were randomized to receive either 12-week CBT plus topiramate (200mg/day) or 12-week CBT only. The primary outcome measure was treatment retention. Secondary outcomes included medication adherence, safety, cocaine and other substance use, health, social functioning, and patient satisfaction.
Adherence to topiramate treatment was low. In the intent-to-treat analyses, topiramate neither improved treatment retention nor reduced cocaine and other substance use. Post hoc, exploratory analyses suggested a moderation effect of comorbid opioid dependence, with a significant effect of topiramate on cocaine use reduction only in crack-cocaine dependent patients with comorbid opioid dependence.
Topiramate was safe and well-tolerated in this sample of crack-cocaine dependent patients, but efficacy was not supported probably due to low acceptance of the treatment. Given the equivocal results of previous studies and the negative findings in our study, the potential of topiramate in the treatment of cocaine dependence seems limited.
可卡因成瘾是一种复杂的疾病,治疗选择有限。托吡酯是一种有前景的药物,在先前的研究中报告其可减少可卡因使用和渴望。本研究评估了托吡酯作为认知行为疗法(CBT)辅助治疗对可卡因成瘾患者的接受度和有效性。
74名可卡因成瘾门诊患者参与了一项开放标签的随机可行性试验。他们被随机分为接受12周CBT加托吡酯(200mg/天)或仅接受12周CBT。主要结局指标是治疗保留率。次要结局包括药物依从性、安全性、可卡因及其他物质使用、健康状况、社会功能和患者满意度。
托吡酯治疗的依从性较低。在意向性分析中,托吡酯既未改善治疗保留率,也未减少可卡因及其他物质的使用。事后探索性分析表明,共病阿片类药物依赖有调节作用,仅在合并阿片类药物依赖的可卡因成瘾患者中,托吡酯对减少可卡因使用有显著效果。
在该可卡因成瘾患者样本中,托吡酯安全且耐受性良好,但可能由于治疗接受度低而未显示出疗效。鉴于先前研究结果不明确以及本研究的阴性结果,托吡酯在治疗可卡因成瘾方面的潜力似乎有限。