Benzodiazepine-Free Cardiac Anesthesia for Reduction of Postoperative Delirium: A Cluster Randomized Crossover Trial.

IF 14.9 1区 医学 Q1 SURGERY JAMA surgery Pub Date : 2025-01-29 DOI:10.1001/jamasurg.2024.6602
Jessica Spence,P J Devereaux,Shun-Fu Lee,Frédérick D'Aragon,Michael S Avidan,Richard P Whitlock,C David Mazer,Nicolas Rousseau-Saine,Raja Ramaswamy Rajamohan,Kane O Pryor,Rael Klein,Edmund Tan,Matthew J Cameron,Emily Di Sante,Erin DeBorba,Mary E Mustard,Etienne J Couture,Raffael Pereira Cezar Zamper,Michael W Y Law,George Djaiani,Tarit Saha,Stephen Choi,Peter Hedlin,D Ryan Pikaluk,Wing Lam,Alain Deschamps,Chinthanie F Ramasundarahettige,Jessica Vincent,William F McIntyre,Simon J W Oczkowski,Braden J Dulong,Christopher Beaver,Shelley A Kloppenburg,Andre Lamy,Eric Jacobsohn,Emilie P Belley-Côté,
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Abstract

Importance Delirium is common after cardiac surgery and associated with adverse outcomes. Intraoperative benzodiazepines may increase postoperative delirium but restricting intraoperative benzodiazepines has not yet been evaluated in a randomized trial. Objective To determine whether an institutional policy of restricted intraoperative benzodiazepine administration reduced the incidence of postoperative delirium. Design, Setting, and Participants This pragmatic, multiperiod, patient- and assessor-blinded, cluster randomized crossover trial took place at 20 North American cardiac surgical centers. All adults undergoing open cardiac surgery at participating centers during the trial period were included through a waiver of individual patient consent between November 2019 and December 2022. Intervention Institutional policies of restrictive vs liberal intraoperative benzodiazepine administration were compared. Hospitals (clusters) were randomized to cross between the restricted and liberal benzodiazepine policies 12 to 18 times over 4-week periods. Main Outcomes and Measures The primary outcome was the incidence of delirium within 72 hours of surgery as detected in routine clinical care, using either the Confusion Assessment Method-Intensive Care Unit or the Intensive Care Delirium Screening Checklist. Intraoperative awareness by patient report was assessed as an adverse event. Results During the trial, 19 768 patients (mean [SD] age, 65 [12] years; 14 528 [73.5%] male) underwent cardiac surgery, 9827 during restricted benzodiazepine periods and 9941 during liberal benzodiazepine periods. During restricted periods, clinicians adhered to assigned policy in 8928 patients (90.9%), compared to 9268 patients (93.2%) during liberal periods. Delirium occurred in 1373 patients (14.0%) during restricted periods and 1485 (14.9%) during liberal periods (adjusted odds ratio [aOR], 0.92; 95% CI, 0.84-1.01; P = .07). No patient spontaneously reported intraoperative awareness. Conclusions and Relevance In intention-to-treat analyses, restricting benzodiazepines during cardiac surgery did not reduce delirium incidence but was also not associated with an increase in the incidence of patient-reported intraoperative awareness. Given that smaller effect sizes cannot be ruled out, restriction of benzodiazepines during cardiac surgery may be considered. Research is required to determine whether restricting intraoperative benzodiazepines at the patient level can reduce the incidence of postoperative delirium. Trial Registration ClinicalTrials.gov Identifier: NCT03928236.
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无苯二氮卓类心脏麻醉减少术后谵妄:一项随机交叉试验。
心脏手术后谵妄很常见,并与不良结局相关。术中苯二氮卓类药物可能增加术后谵妄,但限制术中苯二氮卓类药物尚未在随机试验中进行评估。目的探讨术中限制苯二氮卓类药物的制度性政策是否能降低术后谵妄的发生率。设计、环境和参与者这项实用、多期、患者和评估者盲法、集群随机交叉试验在20个北美心脏外科中心进行。在2019年11月至2022年12月期间,所有在参与中心接受开放式心脏手术的成年人都通过放弃个人患者同意的方式被纳入。比较术中限制与自由给药苯二氮卓类药物的机构政策。在4周的时间内,医院(集群)随机在限制和自由苯二氮卓药物政策之间交叉12至18次。主要结局和措施主要结局是在常规临床护理中检测到的手术72小时内谵妄的发生率,使用混淆评估方法-重症监护病房或重症监护谵妄筛查清单。患者报告的术中意识被评估为不良事件。结果在试验期间,19 768例患者(平均[SD]年龄65岁;14 (528例[73.5%]男性)接受心脏手术,9827例在限制苯二氮卓类药物使用期间,9941例在自由苯二氮卓类药物使用期间。在限制期,临床医生有8928例(90.9%)患者遵守了指定的政策,而在自由期有9268例(93.2%)患者遵守了指定的政策。限制期1373例(14.0%)患者出现谵妄,自由期1485例(14.9%)患者出现谵妄(调整优势比[aOR], 0.92;95% ci, 0.84-1.01;p = .07)。无患者自发报告术中意识。在意向治疗分析中,心脏手术期间限制苯二氮卓类药物并没有降低谵妄的发生率,但也与患者报告的术中意识的发生率增加无关。鉴于不能排除较小的效应量,可以考虑在心脏手术期间限制苯二氮卓类药物的使用。术中在患者层面限制苯二氮卓类药物是否能降低术后谵妄的发生率,尚需进一步研究。临床试验注册号:NCT03928236。
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来源期刊
JAMA surgery
JAMA surgery SURGERY-
CiteScore
20.80
自引率
3.60%
发文量
400
期刊介绍: JAMA Surgery, an international peer-reviewed journal established in 1920, is the official publication of the Association of VA Surgeons, the Pacific Coast Surgical Association, and the Surgical Outcomes Club.It is a proud member of the JAMA Network, a consortium of peer-reviewed general medical and specialty publications.
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