Addictive Behaviors Unit, Clinic Hospital, University of Barcelona, Barcelona, Spain.
Addictive Behavior Unit, Psychiatry Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Clin Drug Investig. 2018 Feb;38(2):147-155. doi: 10.1007/s40261-017-0590-4.
Alcohol dependence remains a major health problem from both a public health and clinical perspective. Harm reduction strategies have been increasingly recognized as suitable treatment goals. Nalmefene has been recently approved for this precise therapeutic indication after completion of phase III trials. However, more data from routine practice settings are needed in order to obtain evidence with high external validity. The aim of this study was to conduct a single-arm, phase IV study with alcohol-dependent outpatients starting nalmefene for the first time.
An observational, multisite, single-arm, phase IV study was conducted among adult alcohol-dependent outpatients who received nalmefene for the first time. The study consisted of four visits: baseline, 4 weeks (referred to as 1 month hereafter), 6 and 12 months. At each visit, drinking variables were obtained from the Timeline Followback regarding the previous month. Satisfaction with medication was also assessed for both patients and professionals, with the Medication Satisfaction Questionnaire. A repeated measures mixed model was performed for effectiveness analysis regarding drinking outcomes (reduction in total alcohol consumption and number of heavy drinking days). Regression analyses were performed in order to find predictors of response to nalmefene.
A total of 110 patients were included, with 88 reporting data at the 1-month visit. On average, patients took nalmefene 68% of the days. The number of heavy drinking days decreased from 13.5 to 6.8 days/month, and total alcohol consumption decreased from 169 to 79 units. For both outcomes, significant reductions at 1 month were found, with no other significant variables reaching significance. Thirty-seven patients were considered medication responders, but given the high presence of low-risk drinkers in our sample, no significant predictors could be found. Satisfaction was globally high for both professionals and patients, and overall nalmefene was well tolerated, with no serious adverse events reported.
The data provided by this phase IV study suggest nalmefene is an effective, well-tolerated treatment for alcohol dependence in real-world, clinical settings.
从公共卫生和临床角度来看,酒精依赖仍然是一个主要的健康问题。减少伤害策略已越来越被认为是合适的治疗目标。在完成 III 期试验后,纳美芬最近被批准用于这一确切的治疗适应症。然而,为了获得具有高度外部有效性的证据,还需要来自常规实践环境的更多数据。本研究的目的是对首次接受纳美芬治疗的酒精依赖门诊患者进行单臂、IV 期研究。
在首次接受纳美芬治疗的成年酒精依赖门诊患者中进行了一项观察性、多地点、单臂、IV 期研究。该研究包括四次就诊:基线、4 周(以下简称 1 个月)、6 个月和 12 个月。在每次就诊时,通过时间线回溯法获得前一个月的饮酒变量。使用药物满意度问卷评估患者和专业人员对药物的满意度。对于饮酒结局(总饮酒量和重度饮酒天数的减少),采用重复测量混合模型进行效果分析。进行回归分析以寻找对纳美芬反应的预测因子。
共纳入 110 例患者,其中 88 例在 1 个月就诊时报告数据。平均而言,患者服用纳美芬的天数为 68%。重度饮酒天数从 13.5 天/月减少到 6.8 天/月,总饮酒量从 169 单位减少到 79 单位。对于这两个结局,在 1 个月时均发现显著减少,没有其他显著变量达到显著水平。37 例患者被认为是药物反应者,但由于我们的样本中低风险饮酒者的存在率较高,因此没有发现显著的预测因子。专业人员和患者的满意度都很高,总体而言,纳美芬耐受性良好,未报告严重不良事件。
这项 IV 期研究提供的数据表明,纳美芬是一种有效的、可耐受的治疗酒精依赖的方法,适用于真实世界的临床环境。