Mauri M C, Gianetti S, Pugnetti L, Altamura A C
Department of Clinical Psychiatry, University of Milan, Italy.
Int J Clin Pharmacol Res. 1993;13(3):173-7.
Quazepam, a recently introduced long-half-life benzodiazepine, seems to have a more specific hypnotic activity and a physiological mechanism of action. The present study evaluated clinical efficacy and eventually rebound symptoms after the treatment with quazepam and triazolam. Sixty-five patients, affected by sleep disorders, were entered into the study. Patients were treated with a placebo for four days and, if no amelioration of insomnia was observed, they were allocated randomly to receive 15 mg of quazepam (32 patients) or 0.5 mg triazolam (33 patients) for eight weeks and finally the placebo for another week. The sleep quality, the sleep efficacy, the unwanted effects and the rebound effects had been assessed by specific evaluation scales. Both of the drugs showed a hypnogenic efficacy but patients treated with quazepam had significantly less night awakenings; at the treatment's interruption, only the patients treated with triazolam had longer awakenings and rebound symptoms. In conclusion, quazepam seems to have a good hypnotic effect without inducing rebound effects. On the contrary, triazolam turned out to be just a hypnoinducent drug with higher risks of rebound effects after withdrawal.
夸西泮是一种最近推出的长半衰期苯二氮䓬类药物,似乎具有更具特异性的催眠活性和生理作用机制。本研究评估了夸西泮和三唑仑治疗后的临床疗效以及最终的反跳症状。65名患有睡眠障碍的患者参与了该研究。患者先接受4天的安慰剂治疗,若未观察到失眠症状改善,则将他们随机分配,32名患者接受15毫克夸西泮治疗,33名患者接受0.5毫克三唑仑治疗,为期8周,最后再接受1周的安慰剂治疗。通过特定评估量表对睡眠质量、睡眠效果、不良反应和反跳效应进行了评估。两种药物均显示出催眠效果,但接受夸西泮治疗的患者夜间觉醒次数明显较少;在治疗中断时,只有接受三唑仑治疗的患者觉醒时间更长且出现了反跳症状。总之,夸西泮似乎具有良好的催眠效果且不会引起反跳效应。相反,三唑仑只是一种诱导睡眠的药物,停药后出现反跳效应的风险更高。