Nishino S, Mignot E
Stanford Center for Narcolepsy, Stanford University, School of Medicine, Palo Alto, California 94304, USA.
Clin Pharmacokinet. 1999 Oct;37(4):305-30. doi: 10.2165/00003088-199937040-00003.
Insomnia and excessive daytime sleepiness (EDS) are frequently observed conditions in the general public. A national survey in the USA in 1979 indicated that 35% of American adults experience insomnia in the course of a year. The prevalence of EDS varies depending on the survey (0.3 to 13.3%), but a recent study stated that 2.4% of individuals reported that they continually fell asleep at work. These problems are often long term and negatively affect the individuals' quality of life. People with these sleep problems often have difficulties maintaining high levels of productivity at work or pursuing their daily activities; individuals with insomnia lack the feeling of being rested or refreshed in the morning and EDS is unavoidable in most cases. Behavioural therapy has been shown to be effective for many people affected with insomnia and EDS. However, pharmacological treatments using hypnosedatives and central nervous system (CNS) stimulants are usually necessary, and effective, for those with more severe cases. These compounds have thus been widely prescribed in clinical practice (e.g., 2.6% of all adults surveyed used medically prescribed hypnosedatives and 4.5% used over-the-counter drugs to promote sleep). The onset and duration of action of these hypnosedatives and CNS stimulant drugs are important factors to be considered when prescribing these compounds. These factors primarily depend on physicochemical properties (lipid solubility and protein binding), as well as the pharmacokinetic profile (absorption, distribution, elimination and clearance) of the compounds. Significant differences in profile exist amongst hypnosedatives and CNS stimulants, and these differences may account for the observed variations in clinical action and adverse effects during and after treatment. In this review, we will introduce recently obtained knowledge of the pharmacokinetics of hypnosedatives and CNS stimulants and their applications for patients affected with insomnia and EDS.
失眠和日间过度嗜睡(EDS)是普通人群中常见的状况。1979年美国的一项全国性调查表明,35%的美国成年人在一年中经历过失眠。EDS的患病率因调查而异(0.3%至13.3%),但最近一项研究指出,2.4%的人报告称他们在工作时会持续入睡。这些问题往往是长期的,会对个人生活质量产生负面影响。有这些睡眠问题的人在工作中往往难以保持高生产率或进行日常活动;失眠的人早上缺乏休息好或恢复精力的感觉,而且在大多数情况下,日间过度嗜睡是不可避免的。行为疗法已被证明对许多受失眠和EDS影响的人有效。然而,对于病情较严重的患者,通常需要使用催眠镇静剂和中枢神经系统(CNS)兴奋剂进行药物治疗,且这种治疗是有效的。因此,这些药物已在临床实践中广泛使用(例如,在所有接受调查的成年人中,2.6%使用过医生开的催眠镇静剂,4.5%使用过非处方药来促进睡眠)。在开这些药物时,这些催眠镇静剂和CNS兴奋剂药物的起效时间和作用持续时间是需要考虑的重要因素。这些因素主要取决于化合物的物理化学性质(脂溶性和蛋白结合率)以及药代动力学特征(吸收、分布、消除和清除)。不同的催眠镇静剂和CNS兴奋剂在药代动力学特征上存在显著差异,这些差异可能解释了治疗期间及治疗后观察到的临床作用和不良反应的变化。在本综述中,我们将介绍最近获得的关于催眠镇静剂和CNS兴奋剂药代动力学的知识及其在受失眠和EDS影响患者中的应用。