Pinot Juliette, Rigal Laurent, Granger Bernard, Sidorkiewicz Stéphanie, Jaury Philippe
Département de Médecine Générale, Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Département de Médecine Générale, Université Paris Sud, Paris Saclay, Faculté de Médecine, Paris, France.
Front Psychiatry. 2018 Oct 8;9:486. doi: 10.3389/fpsyt.2018.00486. eCollection 2018.
More information is needed about the efficacy and safety of long-term baclofen in the treatment of alcohol use disorders. The objective of this study was to assess the effect of treatment with tailored-dose baclofen on alcohol consumption in patients with alcohol use disorders followed for 3 years after first initiating baclofen treatment. This retrospective descriptive cohort included outpatients followed in a French general practice clinic for 3 years and treated with tailored-dose baclofen to reduce or eliminate alcohol consumption. At 3 years, treatment was considered successful if alcohol consumption was at or below levels defined as low-risk by the WHO (≤ 40 g/d in men and ≤ 20 g/d in women). The study population included 144 patients (88 men and 56 women). The participants' mean age was 46 ± 11 years and mean daily alcohol intake before treatment was 167 ± 77 grams. At the end of the study, treatment was successful for 91 (63.2%) patients. Participants' mean dose of baclofen at the end of study period was 100 ± 101 mg/d. We identified 75 (52.1%) patients for whom treatment was successful at each annual follow-up appointment: at 1, 2, and 3 years. The mean maximum dose of baclofen over follow-up of the 144 patients was 211 ± 99 mg/d (dose range: 40 mg/d to 520 mg/d). In this study, tailored-dose baclofen appears to be an effective treatment in patients with alcohol use disorders, with sustainable effect over time (3 years). There are many adverse effects but they are consistent with those already described in the literature.
关于长期使用巴氯芬治疗酒精使用障碍的疗效和安全性,还需要更多信息。本研究的目的是评估首次开始使用巴氯芬治疗后,对酒精使用障碍患者进行为期3年的量身定制剂量巴氯芬治疗对酒精摄入量的影响。这项回顾性描述性队列研究纳入了在法国一家普通诊所接受为期3年随访并接受量身定制剂量巴氯芬治疗以减少或消除酒精摄入的门诊患者。3年后,如果酒精摄入量达到或低于世界卫生组织定义的低风险水平(男性≤40克/天,女性≤20克/天),则认为治疗成功。研究人群包括144名患者(88名男性和56名女性)。参与者的平均年龄为46±11岁,治疗前平均每日酒精摄入量为167±77克。研究结束时,91名(63.2%)患者治疗成功。研究期结束时,参与者的巴氯芬平均剂量为100±101毫克/天。我们确定了75名(52.1%)患者在每次年度随访预约(第1、2和3年)时治疗成功。144名患者随访期间巴氯芬的平均最大剂量为211±99毫克/天(剂量范围:40毫克/天至520毫克/天)。在本研究中,量身定制剂量的巴氯芬似乎是治疗酒精使用障碍患者的一种有效疗法,且随着时间推移(3年)效果可持续。有许多不良反应,但与文献中已描述的一致。