a Sleep Disorders and Research Center , Henry Ford Health System , Detroit , Michigan.
Traffic Inj Prev. 2014;15(5):439-45. doi: 10.1080/15389588.2013.830211.
The use of hypnotics is prevalent in the general population. Though these drugs have been shown to be effective, their residual effects may cause significant impairment to the user's driving ability. The objective of this meta-analysis is to determine whether there is a residual effect on driving and better evaluate the safety of hypnotics.
Randomized double-blind placebo-controlled studies were selected that employed a commonly used and valid driving measure to determine the user's driving ability the day after drug administration. The primary outcome measure for the driving task in all included studies was the Standard Deviation of Lateral Position (SDLP). Fixed effects model meta-analyses were performed.
Fourteen studies, published from 1984 to 2013 (295 subjects), were included in this meta-analysis. Overall, significant impairment was found when morning testing (i.e., 10-11 h after initiating sleep) was compared to afternoon testing (i.e., 16-17 h after initiating sleep; P = .0001). Twice the standard dose also showed significant impairment (P = .0001) relative to the standard dose. The time of the test, morning versus afternoon, also had an impact on individual drugs. Middle of the night administration (MOTN) of zolpidem and zopiclone caused significant impairment the following morning, though no such impairment was seen with zaleplon. Finally, half-life was also assessed (short: <6 h, intermediate: 6-12 h, long: >12 h) and both intermediate- and long-acting drugs caused significant impairment the morning after bedtime administration, whereas short acting hypnotics did not.
These analyses indicate that the half-life, dose of the hypnotic, as well as time between treatment and driving, as measured by SDLP, all significantly impact the ability to drive a car after taking hypnotic drugs.
催眠药在普通人群中使用较为普遍。虽然这些药物已被证明是有效的,但它们的残留作用可能会对使用者的驾驶能力造成严重损害。本荟萃分析的目的是确定催眠药是否对驾驶有残留作用,并更好地评估催眠药的安全性。
选择了随机、双盲、安慰剂对照的研究,这些研究采用了常用且有效的驾驶测量方法,以确定药物使用后第二天使用者的驾驶能力。所有纳入研究中驾驶任务的主要结局测量指标是侧向位置标准差(SDLP)。进行固定效应模型荟萃分析。
纳入了 14 项研究,这些研究发表于 1984 年至 2013 年(295 名受试者)。总体而言,与下午测试(即起始睡眠后 16-17 小时)相比,早上测试(即起始睡眠后 10-11 小时)发现明显的驾驶能力受损(P =.0001)。与标准剂量相比,两倍标准剂量也显示出明显的损伤(P =.0001)。测试时间,早上和下午,也会对个别药物产生影响。唑吡坦和佐匹克隆的午夜给药(MOTN)导致次日早上明显受损,而扎来普隆则未出现这种损伤。最后,还评估了半衰期(短:<6 h,中:6-12 h,长:>12 h),中效和长效催眠药在睡前给药后第二天早上都会导致明显的驾驶能力受损,而短效催眠药则不会。
这些分析表明,半衰期、催眠药剂量以及治疗与驾驶之间的时间(通过 SDLP 测量)都会显著影响服用催眠药后驾驶汽车的能力。