Sleep and Respiratory Unit, Grenoble University Hospital, Grenoble, France.
Clin Drug Investig. 2004;24(11):625-32. doi: 10.2165/00044011-200424110-00001.
This open, non-comparative, multicentre study was designed to evaluate zolpidem consumption and evolution of its use for the treatment of insomnia on an 'as-needed' basis, under the real conditions of routine general practice.
1938 patients (aged >18 years) with insomnia (mean +/- SD duration: 3.0 +/- 15.2 months; median duration: 1 month) were enrolled. A maximum of 21 doses were prescribed for the treatment period (3 weeks maximum) and patients were instructed to take zolpidem according to their sleep disturbance ('as needed'). The main criteria were number of doses/week and consumption evolution over the treatment period. Secondary criteria included the evolution of disease severity, the evolution of parameters of sleep quality and factors predictive of the evolution of zolpidem consumption.
Consumption decreased steadily during the study, from 5.1 +/- 1.9 doses/week during week 1 to 3.7 +/- 2.5 doses/week during week 3. A prior sleep-disorder episode (p = 0.02), high initial zolpidem consumption with 6-7 doses/week (p < 0.001) or insomnia having started >3 weeks before the inclusion (p < 0.001) were predictive of stable or increased zolpidem consumption. Global clinical improvement showed moderate to very marked improvement for 90% of the patients. Other sleep-quality and clinical-improvement parameters indicated overall satisfaction. Nature, incidence and severity of safety data reported during the study were consistent with the safety experience reported to date.
During zolpidem 'as-needed' administration in general practice, patients adapted the treatment to their needs and to the evolution of their insomnia. The treatment had a good safety profile and was effective.
本开放性、非对照、多中心研究旨在评估唑吡坦在常规一般实践中的按需使用情况下的消耗情况及其治疗失眠的使用演变。
共纳入 1938 例失眠患者(年龄>18 岁;平均+/-标准差持续时间:3.0+/-15.2 个月;中位数持续时间:1 个月)。治疗期(最长 3 周)最多开具 21 剂药物,并根据患者的睡眠障碍(按需)指导患者服用唑吡坦。主要标准是每周剂量数和治疗期间的消耗演变。次要标准包括疾病严重程度的演变、睡眠质量参数的演变以及预测唑吡坦消耗演变的因素。
在研究过程中,消耗稳步下降,从第 1 周的 5.1+/-1.9 剂量/周降至第 3 周的 3.7+/-2.5 剂量/周。先前的睡眠障碍发作(p=0.02)、初始唑吡坦消耗较高(每周 6-7 剂量)(p<0.001)或失眠开始时间超过 3 周前(p<0.001)是稳定或增加唑吡坦消耗的预测因素。90%的患者总体临床改善为中度至非常显著改善。其他睡眠质量和临床改善参数表明总体满意度。研究期间报告的安全性数据的性质、发生率和严重程度与迄今为止报告的安全性经验一致。
在一般实践中唑吡坦按需给药时,患者根据自己的需求和失眠的演变调整治疗。该治疗具有良好的安全性和有效性。