曲唑酮对睡眠的影响:系统回顾与元分析》。

IF 7.4 2区 医学 Q1 CLINICAL NEUROLOGY
CNS drugs Pub Date : 2024-10-01 Epub Date: 2024-08-09 DOI:10.1007/s40263-024-01110-2
Maria Kokkali, Elisavet Pinioti, Andreas S Lappas, Nikolaos Christodoulou, Myrto T Samara
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引用次数: 0

摘要

背景和目的:睡眠问题和失眠症很常见,治疗起来具有挑战性,并且超越了特定的诊断。虽然曲唑酮(Trazodone)是一种常用药物,但目前尚缺乏可靠的荟萃分析证据。本系统综述和荟萃分析调查了曲唑酮治疗睡眠障碍的有效性和安全性,反映了失眠诊断和治疗的最新进展:我们检索了Medline、Embase、APA PsycINFO、Cochrane对照试验中央注册中心(CENTRAL)、ClinicalTrials.gov和世界卫生组织(WHO)国际临床试验注册平台(ICTRP)截至2024年5月1日的随机对照试验(RCT),比较了曲唑酮与安慰剂,并报告了睡眠相关结果。最短药物治疗时间为 5 天。纳入的所有 RCT 均不考虑盲法(开放标签、单盲或双盲),但排除了准随机研究。科克伦随机试验偏倚风险工具对偏倚进行了评估。分析采用随机效应模型,以意向治疗(ITT)为基础。二分结果采用风险比(RR),连续结果采用加权平均差(WMD)。如果使用不同的单位或量表,则计算 Hedge's 调整 g 标准化平均差 (SMD)。亚组分析和预先计划的敏感性分析探讨了异质性,并评估了研究结果的强度和一致性:结果:共纳入 44 项 RCT,3935 名参与者。曲唑酮对主观总睡眠时间(TST)没有明显影响[WMD = 0.73 min,95% 置信区间(CI)- 24.62; 26.07,p = 0.96],但改善了睡眠质量(SQ)(SMD = - 0.58,95% CI - 0.87; - 0.28,p 结论:曲唑酮能延长患者的总睡眠时间:曲唑酮可延长总睡眠时间,但不会影响感知睡眠时间。曲唑酮可改善睡眠质量和连续性,但对睡眠潜伏期、睡眠效率和日间障碍的影响较小。曲唑酮会产生不良反应,因此有必要进行谨慎的风险效益评估。有限的数据限制了该药物的普遍性,因此需要进行更多的研究:注册:PROSPERO 注册号:CRD42022383121。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of Trazodone on Sleep: A Systematic Review and Meta-analysis.

Effects of Trazodone on Sleep: A Systematic Review and Meta-analysis.

Background and objectives: Sleep problems and insomnia are common, challenging to treat, and transcend specific diagnoses. Although trazodone is a popular choice, robust meta-analytic evidence is lacking. This systematic review and meta-analysis investigates the efficacy and safety of trazodone for sleep disturbances, reflecting recent updates in insomnia diagnosis and treatment.

Methods: We searched Medline, Embase, APA PsycINFO, the Cochrane Central Register of Controlled Trials (CENTRAL), ClinicalTrials.gov, and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) up to 1 May 2024, for Randomized Controlled Trials (RCTs) comparing trazodone with placebo and reporting sleep-related outcomes. The minimum pharmacotherapy duration was 5 days. Included were all RCTs regardless of blinding (open-label or single- or double-blind), while quasi-randomized studies were excluded. The Cochrane Risk of Bias Tool for Randomized Trials assessed bias. Analyses used a random-effects model on an intention-to-treat (ITT) basis. Risk ratio (RR) was used for dichotomous outcomes and weighted mean difference (WMD) for continuous outcomes. When different units or scales were used, Hedge's adjusted g standardized mean difference (SMD) was calculated. Subgroup and preplanned sensitivity analyses explored heterogeneity and evaluated findings' strength and consistency.

Results: In total, 44 RCTs with 3935 participants were included. Trazodone did not significantly impact subjective total sleep time (TST) [WMD = 0.73 min, 95% confidence interval (CI) - 24.62; 26.07, p = 0.96] but improved sleep quality (SQ) (SMD = - 0.58, 95% CI - 0.87; - 0.28, p < 0.01) and secondary outcomes. These included the number of nocturnal awakenings (SMD = - 0.57, 95% CI - 0.85; - 0.30], p < 0.01), nocturnal time awake after sleep onset (WMD = - 13.47 min, 95% CI - 23.09; - 3.86], p < 0.01), objective TST by polysomnography (WMD = 27.98 min, 95% CI 4.02; 51.95, p = 0.02), and sleep efficiency (WMD = 3.32, 95% CI 0.53; 1.57, p = 0.02). Tolerability issues included more dropouts owing to adverse effects (RR = 2.30, 95% CI 1.45; 3.64, p < 0.01), any sleep-related adverse effects (RR = 3.67, 95% CI 1.07; 12.47, p = 0.04), more adverse effects in general (RR = 1.18, 95% CI 1.03; 1.33, p = 0.02), and more sleep-related adverse effects (RR = 4.31, 95% CI 2.29; 8.13, p < 0.01).

Conclusion: Trazodone extends total sleep time but does not affect perceived sleep duration. It may improve sleep quality and continuity but has minor effects on sleep latency, efficiency, and daytime impairment. Trazodone is associated with adverse effects, necessitating a careful risk-benefit assessment. Limited data restrict generalizability, underscoring the need for more research.

Registration: PROSPERO registration number,CRD42022383121.

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来源期刊
CNS drugs
CNS drugs 医学-精神病学
CiteScore
12.00
自引率
3.30%
发文量
82
审稿时长
6-12 weeks
期刊介绍: CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes: - Overviews of contentious or emerging issues. - Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses. - Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. - Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry. - Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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