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苏沃雷生联合或不联合雷美尔酮预防谵妄的系统评价和荟萃分析。

Suvorexant with or without ramelteon to prevent delirium: a systematic review and meta-analysis.

机构信息

Department of Anaesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Psychogeriatrics. 2022 Mar;22(2):259-268. doi: 10.1111/psyg.12792. Epub 2021 Dec 8.

Abstract

Delirium is a common and serious neurobehavioral syndrome, associated with prolonged hospital stays, and increased morbidity and mortality. As it remains unclear whether suvorexant with or without ramelteon prevents delirium in elderly hospitalized patients, we conducted a systematic review and meta-analysis to evaluate, searching the PubMed, Cochrane Library, Web of Science, EMBASE, and EBSCOhost databases for all randomized controlled trials (RCTs), case-control studies, and cohort studies that investigated the effects of suvorexant with or without ramelteon on delirium in adult hospitalized patients. The primary outcome was the incidence of delirium. Two randomized controlled trials, 7 cohort studies and 2 case-control studies involving 2594 patients were included in this meta-analysis. The results showed that both suvorexant alone (odds ratio (OR) = 0.30, 95% confidence interval (CI): 0.14-0.65, P = 0.002) and suvorexant with ramelteon (OR = 0.39, 95% CI 0.23-0.65, P = 0.0003) reduced the incidence of delirium in adult hospitalized patients. Six studies involved the use of benzodiazepines; subgroup analysis performed separately in the suvorexant alone and suvorexant with ramelteon groups indicated that when benzodiazepine was administered, suvorexant with ramelteon was effective at reducing the incidence of delirium (OR = 0.53, 95% CI 0.37-0.74, P = 0.0002), but no significant difference was observed for suvorexant alone (OR = 0.40, 95% CI 0.11-1.53, P = 0.18). The current literature thus supports the effectiveness of suvorexant with or without ramelteon for delirium prevention, although suvorexant alone failed to significantly reduce the incidence of delirium when benzodiazepine was administered. The present study was limited by the significant heterogeneity among the included studies, and caution should be exercised when interpreting the results. This study was registered in the PROSPERO database (CRD4202017964).

摘要

谵妄是一种常见且严重的神经行为综合征,与住院时间延长以及发病率和死亡率增加有关。由于目前尚不清楚苏沃雷生联合或不联合雷美替胺是否可预防老年住院患者发生谵妄,我们进行了一项系统评价和荟萃分析,以评估苏沃雷生联合或不联合雷美替胺对成年住院患者谵妄的影响,检索了 PubMed、Cochrane 图书馆、Web of Science、EMBASE 和 EBSCOhost 数据库中的所有随机对照试验(RCT)、病例对照研究和队列研究。主要结局是谵妄的发生率。本荟萃分析纳入了 2 项 RCT、7 项队列研究和 2 项病例对照研究,共涉及 2594 例患者。结果显示,苏沃雷生单药治疗(比值比(OR)=0.30,95%置信区间(CI):0.14-0.65,P=0.002)和苏沃雷生联合雷美替胺治疗(OR=0.39,95%CI 0.23-0.65,P=0.0003)均可降低成年住院患者谵妄的发生率。有 6 项研究涉及苯二氮䓬类药物的使用;在苏沃雷生单药和苏沃雷生联合雷美替胺组分别进行的亚组分析表明,当使用苯二氮䓬类药物时,苏沃雷生联合雷美替胺可有效降低谵妄发生率(OR=0.53,95%CI 0.37-0.74,P=0.0002),但苏沃雷生单药治疗无显著差异(OR=0.40,95%CI 0.11-1.53,P=0.18)。目前的文献支持苏沃雷生联合或不联合雷美替胺预防谵妄的有效性,尽管苏沃雷生单药治疗在使用苯二氮䓬类药物时未能显著降低谵妄发生率。本研究受到纳入研究之间显著异质性的限制,在解释结果时应谨慎。本研究已在 PROSPERO 数据库(CRD4202017964)中注册。

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