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夸西泮和氟西泮:长期使用及延长撤药期

Quazepam and flurazepam: long-term use and extended withdrawal.

作者信息

Kales A, Bixler E O, Soldatos C R, Vela-Bueno A, Jacoby J, Kales J D

出版信息

Clin Pharmacol Ther. 1982 Dec;32(6):781-8. doi: 10.1038/clpt.1982.236.

Abstract

Two investigation benzodiazepine hypnotics with long half-lifes, (30 and 15 mg quazepam and 30 mg flurazepam) were evaluated in 47-night sleep laboratory studies. The effectiveness and side effects of these benzodiazepines were assessed during short-, intermediate-, and long-term use. Subjects were also assessed for presence of rebound insomnia during the 15 days following abrupt withdrawal. Quazepam, 15 and 30 mg, and flurazepam, 30 mg, each were effective in sleep induction and maintenance after short- and intermediate-term use. Some loss of effectiveness was noted during long-term use of both doses of quazepam and, to a lesser extent, of flurazepam. Subjective reports of improvement in sleep latency and total sleep time were in general agreement with the objective data. During the 15 nights after abrupt withdrawal of these two long-half-life drugs there was no rebound insomnia, either immediate or delayed. Both drugs exerted carry-over effectiveness on the first 2 to 3 nights after withdrawal; with quazepam this effect persisted throughout the withdrawal period. Quazepam, 30 mg, induced frequent side effects related to sleepiness. Side effects noted with 30 mg flurazepam were less frequent and severe, while the side effects with 15 mg quazepam were minimal. These data suggest that the optimal dose of quazepam is 15 mg.

摘要

对两种半衰期较长的苯二氮䓬类催眠药(30毫克和15毫克夸西泮以及30毫克氟西泮)进行了47个夜晚的睡眠实验室研究评估。在短期、中期和长期使用期间评估了这些苯二氮䓬类药物的有效性和副作用。还评估了受试者在突然停药后的15天内是否存在反弹性失眠。15毫克和30毫克的夸西泮以及30毫克的氟西泮在短期和中期使用后对诱导睡眠和维持睡眠均有效。在长期使用两种剂量的夸西泮以及程度较轻的氟西泮期间,发现有效性有所下降。关于睡眠潜伏期和总睡眠时间改善的主观报告与客观数据总体一致。在突然停用这两种半衰期较长的药物后的15个夜晚,没有立即或延迟的反弹性失眠。两种药物在停药后的前2至3个夜晚都有持续效应;对于夸西泮,这种效应在整个停药期间都持续存在。30毫克的夸西泮会引发频繁的与嗜睡相关的副作用。30毫克氟西泮引起的副作用较少且较轻,而15毫克夸西泮的副作用最小。这些数据表明,夸西泮的最佳剂量是15毫克。

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