Department of Psychiatry, Tsyr-Huey Mental Hospital, Kaohsiung Jen-Ai's Home, Kaohsiung, Taiwan; Institute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan.
Institute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan; Prospect Clinic for Otorhinolaryngology & Neurology, Kaohsiung, Taiwan; Department of Psychology, College of Medical and Health Science, Asia University, Taichung, Taiwan.
Sleep Med Rev. 2021 Jun;57:101469. doi: 10.1016/j.smrv.2021.101469. Epub 2021 Mar 11.
This network meta-analysis aimed at investigating efficacy/tolerability of pharmacologic/hormonal interventions for menopausal sleep disturbances. Major databases were searched for randomized controlled trials (RCTs) examining pharmacologic or hormonal interventions with either placebo or active controlled designs. Primary outcomes were improvements in sleep disturbance severity/tolerability (i.e., overall dropout rates), whereas secondary outcome was adverse event-related discontinuation rates. Analysis of 43 RCTs with 25 treatment arms involving 32,271 women during/after menopausal transition (age: 61.24 ± 4.23, duration: 90.83 ± 66.29 wks) showed therapeutic effect of melatonin-fluoxetine [SMD = -2.47 (95% CI:-4.19-0.74)] against sleep disturbances compared to placebo. Subgroup analysis of 15 RCTs on vasomotor symptoms demonstrated superior benefits of gabapentin [SMD = -1.04 (95% CI:-1.90-0.18)], oral combined hormone therapy [SMD = -0.62 (95% CI:-1.06-0.18)], and bazedoxifene-conjugated estrogens [SMD = -0.50 (95% CI:-0.96-0.04)] to placebo/control. Despite benefits of raloxifene-only [SMD = -1.86 (95% CI:-3.09-0.63)] and raloxifene-oral estrogen [SMD = -2.64 (95% CI:-4.64-0.63)], patient selection may be a confounder. Dropout rates were comparable between interventions and placebo/control. Eszopiclone [RR = 3.84 (95% CI: 1.14-12.87)] and oral combined hormone therapy [RR = 2.51 (95% CI: 1.04-6.07)] were associated with higher rates of adverse event-related discontinuation. The results support combined estrogen-progesterone therapy for menopausal sleep disturbances associated with vasomotor symptoms but showed no significant effects of hypnotics in this clinical setting.
这项网络荟萃分析旨在研究药物/激素干预措施治疗绝经后睡眠障碍的疗效/耐受性。主要数据库检索了随机对照试验(RCT),这些试验检查了药物或激素干预措施与安慰剂或阳性对照设计的疗效。主要结局是睡眠障碍严重程度/耐受性的改善(即总体停药率),次要结局是与不良事件相关的停药率。分析了 43 项 RCT 共 25 个治疗组,涉及 32271 名绝经后过渡(年龄:61.24±4.23 岁,持续时间:90.83±66.29 周)的女性,结果显示褪黑素-氟西汀(SMD=-2.47,95%CI:-4.19-0.74)与安慰剂相比对睡眠障碍有治疗作用。对 15 项关于血管舒缩症状的 RCT 的亚组分析表明,加巴喷丁(SMD=-1.04,95%CI:-1.90-0.18)、口服联合激素治疗(SMD=-0.62,95%CI:-1.06-0.18)和巴多昔芬结合雌激素(SMD=-0.50,95%CI:-0.96-0.04)优于安慰剂/对照。尽管雷洛昔芬(SMD=-1.86,95%CI:-3.09-0.63)和雷洛昔芬-口服雌激素(SMD=-2.64,95%CI:-4.64-0.63)仅具有获益,但患者选择可能是混杂因素。干预措施与安慰剂/对照之间的停药率相似。佐匹克隆(RR=3.84,95%CI:1.14-12.87)和口服联合激素治疗(RR=2.51,95%CI:1.04-6.07)与更高的不良事件相关停药率相关。结果支持联合雌激素-孕激素治疗与血管舒缩症状相关的绝经后睡眠障碍,但在这种临床情况下,催眠药没有显著效果。