Department of Psychiatry, Charité Campus Mitte, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Pharmacopsychiatry. 2010 Jul;43(5):184-9. doi: 10.1055/s-0030-1249098. Epub 2010 May 25.
Anticonvulsant drugs are increasingly being used for alcohol detoxification in in- and outpatient settings. The aim of this study was to examine the efficacy, medical safety and mid-term outcome of levetiracetam, a drug with no marked liver toxicity, for outpatient alcohol detoxification.
This was an open-label observational study. After screening eligibility for outpatient alcohol detoxification, patients were seen daily for 5 days and received levetiracetam in a flexible dosage regime between 500 and 4 000 mg/d for a maximum of 7 days. Diazepam was used as a rescue medication. The severity of alcohol withdrawal was evaluated daily using the ALCOHOL WITHDRAWAL SYNDROME SCALE (AWSS). Mid-term treatment outcome was assessed at a 6-month follow-up.
A total number of 131 consecutively admitted alcohol-dependent patients received an outpatient detoxification treatment, 122 (93.1%) completed the programme successfully. The mean initial dose of levetiracetam was 1 850 mg/d. Alcohol withdrawal syndrome as indicated by the AWSS score decreased clearly over 5 days. Overall, the medication was well tolerated. There was no treatment discontinuations due to side effects of levetiracetam. No serious medical complications, especially seizures or deliria, were observed during the detoxification. At the 6-month follow-up, 57 patients (43.5%) were still abstinent. Patients with previous detoxifications had a significant higher risk for relapse (HR=1.88; p=0.016; CI 95%: 1.12-3.14) than patients without previous treatments.
The findings of this study provide some evidence that levetiracetam is an efficacious and safe treatment option for outpatient alcohol detoxification. Further randomised, controlled trials including mid- and long-term follow-ups are needed to confirm these findings.
越来越多的抗惊厥药物被用于住院和门诊环境中的酒精解毒。本研究的目的是研究无明显肝毒性的左乙拉西坦在门诊酒精解毒中的疗效、医疗安全性和中期结果。
这是一项开放标签的观察性研究。在筛选出适合门诊酒精解毒的条件后,患者每天接受治疗,连续 5 天,并根据需要在灵活的剂量范围内接受左乙拉西坦治疗,剂量为 500 至 4000mg/d,最长 7 天。安定被用作解救药物。使用酒精戒断综合征量表(AWSS)每日评估酒精戒断的严重程度。在 6 个月的随访时评估中期治疗结果。
共有 131 名连续入院的酒精依赖患者接受了门诊解毒治疗,其中 122 名(93.1%)成功完成了治疗。左乙拉西坦的初始剂量平均为 1850mg/d。AWSS 评分表明,酒精戒断综合征在 5 天内明显减轻。总体而言,该药物耐受性良好。没有因左乙拉西坦的副作用而停药的情况。在解毒过程中没有观察到严重的医疗并发症,特别是癫痫发作或谵妄。在 6 个月的随访时,57 名患者(43.5%)仍保持戒酒状态。有既往解毒治疗史的患者复发的风险显著增加(HR=1.88;p=0.016;95%CI:1.12-3.14),高于无既往治疗的患者。
本研究的结果提供了一些证据表明,左乙拉西坦是一种有效的、安全的门诊酒精解毒治疗选择。需要进一步进行随机、对照试验,包括中期和长期随访,以证实这些发现。