Deiner Stacie, Luo Xiaodong, Lin Hung-Mo, Sessler Daniel I, Saager Leif, Sieber Frederick E, Lee Hochang B, Sano Mary, Jankowski Christopher, Bergese Sergio D, Candiotti Keith, Flaherty Joseph H, Arora Harendra, Shander Aryeh, Rock Peter
Department of Anesthesiology, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, New York.
JAMA Surg. 2017 Aug 16;152(8):e171505. doi: 10.1001/jamasurg.2017.1505.
Postoperative delirium occurs in 10% to 60% of elderly patients having major surgery and is associated with longer hospital stays, increased hospital costs, and 1-year mortality. Emerging literature suggests that dexmedetomidine sedation in critical care units is associated with reduced incidence of delirium. However, intraoperative use of dexmedetomidine for prevention of delirium has not been well studied.
To evaluate whether an intraoperative infusion of dexmedetomidine reduces postoperative delirium.
DESIGN, SETTING, AND PARTICIPANTS: This study was a multicenter, double-blind, randomized, placebo-controlled trial that randomly assigned patients to dexmedetomidine or saline placebo infused during surgery and for 2 hours in the recovery room. Patients were assessed daily for postoperative delirium (primary outcome) and secondarily for postoperative cognitive decline. Participants were elderly (>68 years) patients undergoing major elective noncardiac surgery. The study dates were February 2008 to May 2014.
Dexmedetomidine infusion (0.5 µg/kg/h) during surgery and up to 2 hours in the recovery room.
The primary hypothesis tested was that intraoperative dexmedetomidine administration would reduce postoperative delirium. Secondarily, the study examined the correlation between dexmedetomidine use and postoperative cognitive change.
In total, 404 patients were randomized; 390 completed in-hospital delirium assessments (median [interquartile range] age, 74.0 [71.0-78.0] years; 51.3% [200 of 390] female). There was no difference in postoperative delirium between the dexmedetomidine and placebo groups (12.2% [23 of 189] vs 11.4% [23 of 201], P = .94). After adjustment for age and educational level, there was no difference in the postoperative cognitive performance between treatment groups at 3 months and 6 months. Adverse events were comparably distributed in the treatment groups.
Intraoperative dexmedetomidine does not prevent postoperative delirium. The reduction in delirium previously demonstrated in numerous surgical intensive care unit studies was not observed, which underscores the importance of timing when administering the drug to prevent delirium.
clinicaltrials.gov Identifier NCT00561678.
术后谵妄发生在10%至60%接受大手术的老年患者中,与住院时间延长、住院费用增加以及1年死亡率相关。新出现的文献表明,重症监护病房中使用右美托咪定镇静与谵妄发生率降低有关。然而,术中使用右美托咪定预防谵妄尚未得到充分研究。
评估术中输注右美托咪定是否能降低术后谵妄的发生率。
设计、地点和参与者:本研究是一项多中心、双盲、随机、安慰剂对照试验,将患者随机分为术中及恢复室2小时输注右美托咪定组或生理盐水安慰剂组。每天评估患者的术后谵妄(主要结局),其次评估术后认知功能下降情况。参与者为年龄大于68岁的接受重大择期非心脏手术的患者。研究时间为2008年2月至2014年5月。
术中输注右美托咪定(0.5μg/kg/h),并在恢复室持续输注2小时。
检验的主要假设是术中给予右美托咪定可降低术后谵妄的发生率。其次,该研究考察了右美托咪定的使用与术后认知变化之间的相关性。
总共404例患者被随机分组;390例完成了住院期间的谵妄评估(年龄中位数[四分位间距]为74.0[71.0 - 78.0]岁;51.3%[390例中的200例]为女性)。右美托咪定组和安慰剂组术后谵妄发生率无差异(12.2%[189例中的23例]对11.4%[201例中的23例],P = 0.94)。在对年龄和教育水平进行调整后,治疗组在3个月和6个月时的术后认知表现无差异。不良事件在治疗组中的分布相当。
术中使用右美托咪定不能预防术后谵妄。在众多外科重症监护病房研究中先前证明的谵妄发生率降低情况未被观察到,这突出了给药时间对预防谵妄的重要性。
clinicaltrials.gov标识符NCT00561678。