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Effectiveness of non-benzodiazepine hypnotics in treatment of adult insomnia: meta-analysis of data submitted to the Food and Drug Administration

机译:非苯二氮卓类催眠药治疗成人失眠的有效性:提交给食品药品监督管理局的数据的荟萃分析

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摘要

>Objectives To investigate the effectiveness of non-benzodiazepine hypnotics (Z drugs) and associated placebo responses in adults and to evaluate potential moderators of effectiveness in a dataset used to approve these drugs.>Design Systematic review and meta-analysis.>Data source US Food and Drug Administration (FDA).>Study selection Randomised double blind parallel placebo controlled trials of currently approved Z drugs (eszopiclone, zaleplon, and zolpidem).>Data extraction Change score from baseline to post-test for drug and placebo groups; drug efficacy analysed as the difference of both change scores. Weighted raw and standardised mean differences with their confidence intervals under random effects assumptions for polysomnographic and subjective sleep latency, as primary outcomes. Secondary outcomes included waking after sleep onset, number of awakenings, total sleep time, sleep efficiency, and subjective sleep quality. Weighted least square regression analysis was used to explain heterogeneity of drug effects.>Data synthesis 13 studies containing 65 separate drug-placebo comparisons by type of outcome, type of drug, and dose were included. Studies included 4378 participants from different countries and varying drug doses, lengths of treatment, and study years. Z drugs showed significant, albeit small, improvements (reductions) in our primary outcomes: polysomnographic sleep latency (weighted standardised mean difference, 95% confidence interval −0.57 to −0.16) and subjective sleep latency (−0.33, −0.62 to −0.04) compared with placebo. Analyses of weighted mean raw differences showed that Z drugs decreased polysomnographic sleep latency by 22 minutes (−33 to −11 minutes) compared with placebo. Although no significant effects were found in secondary outcomes, there were insufficient studies reporting these outcomes to allow firm conclusions. Moderator analyses indicated that sleep latency was more likely to be reduced in studies published earlier, with larger drug doses, with longer duration of treatment, with a greater proportion of younger and/or female patients, and with zolpidem.>Conclusion Compared with placebo, Z drugs produce slight improvements in subjective and polysomnographic sleep latency, especially with larger doses and regardless of type of drug. Although the drug effect and the placebo response were rather small and of questionable clinical importance, the two together produced to a reasonably large clinical response.
机译:>目标:研究非苯二氮卓类催眠药(Z药)和相关安慰剂对成人的有效性,并评估用于批准这些药物的数据集中潜在的调节剂。>设计系统评价和荟萃分析。>数据来源美国食品和药物管理局(FDA)。>研究选择当前批准的Z药物(依佐匹克隆, >数据提取:将药物和安慰剂组的评分从基线更改为测试后;将药物疗效分析为两个变化得分的差异。在以多导睡眠图和主观睡眠潜伏期为主要结果的随机效应假设下,加权原始和标准化均值差及其置信区间。次要结果包括入睡后醒来,觉醒次数,总睡眠时间,睡眠效率和主观睡眠质量。加权最小二乘回归分析用于解释药物作用的异质性。>数据合成包括13个研究,其中按结局类型,药物类型和剂量进行了65次单独的药物-安慰剂比较。研究包括来自不同国家的4378名参与者,药物剂量,治疗时间和研究年份各不相同。 Z药物在我们的主要结局中显示出显着的改善(减少),尽管有微小改善:多导睡眠图睡眠潜伏期(加权标准平均差,95%置信区间-0.57至-0.16)和主观睡眠潜伏期(-0.33,-0.62至-0.04)与安慰剂相比。加权平均原始差异分析表明,与安慰剂相比,Z药物可将多导睡眠图睡眠潜伏期缩短22分钟(-33至-11分钟)。尽管在次要结果中未发现显着影响,但尚无足够的研究报告这些结果以得出肯定的结论。主持人的分析表明,在较早发表的研究中,更大剂量的药物,更长的治疗时间,更多的年轻和/或女性患者以及唑吡坦使用唑吡坦,睡眠潜伏期更有可能减少。>结论 strong>与安慰剂相比,Z药物对主观和多导睡眠图睡眠潜伏期的影响稍有改善,尤其是大剂量使用时,无论使用哪种药物。尽管药物作用和安慰剂反应很小,并且在临床上有可疑的意义,但两者合起来产生了相当大的临床反应。

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