Kales A, Bixler E O, Vela-Bueno A, Soldatos C R, Niklaus D E, Manfredi R L
Clin Pharmacol Ther. 1986 Oct;40(4):378-86. doi: 10.1038/clpt.1986.194.
Two benzodiazepine hypnotics, triazolam, 0.25 mg, with a short elimination t1/2, and quazepam, 15 mg, with a long t1/2, were evaluated in 22-night sleep laboratory studies. Quazepam improved sleep significantly during both short- and intermediate-term use. Daytime sleepiness, which decreased with continued use, was the side effect most often associated with quazepam dosing. In contrast, triazolam dosing did not significantly improve any of the major sleep efficiency parameters, and there was a rapid development of tolerance for the drug's slight initial effectiveness. In addition, there were a number of behavioral side effects including amnesia, confusion, and disinhibition. Withdrawal of triazolam was associated with sleep and mood disturbances (rebound insomnia and rebound anxiety), whereas quazepam exerted carryover effectiveness. Thus the data in this study show that the 0.25 mg dose of triazolam, which is being prescribed increasingly, has a profile of side effects that is similar to that of the 0.5 mg dose.
在一项为期22晚的睡眠实验室研究中,对两种苯二氮䓬类催眠药进行了评估,一种是消除半衰期短的三唑仑(0.25毫克),另一种是半衰期长的夸西泮(15毫克)。夸西泮在短期和中期使用期间均能显著改善睡眠。白天嗜睡是与夸西泮给药最常相关的副作用,随着持续使用会有所减轻。相比之下,三唑仑给药并未显著改善任何主要的睡眠效率参数,而且对该药轻微的初始疗效很快就产生了耐受性。此外,还出现了一些行为副作用,包括失忆、意识模糊和去抑制。停用三唑仑会出现睡眠和情绪障碍(反弹性失眠和反弹性焦虑),而夸西泮则具有持续疗效。因此,本研究中的数据表明,越来越常被处方的0.25毫克剂量三唑仑的副作用情况与0.5毫克剂量相似。