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右美托咪定减少双频谱指数引导闭环麻醉期间丙泊酚和瑞芬太尼的需求:一项双盲、安慰剂对照试验。

Dexmedetomidine reduces propofol and remifentanil requirements during bispectral index-guided closed-loop anesthesia: a double-blind, placebo-controlled trial.

机构信息

From the *Department of Anesthesiology, Hôpital Foch, Suresnes, France; †UVSQ-UFR des Sciences de la Santé Simone Veil, Montigny-le-Bretonneux, France; ‡Outcomes Research Consortium, Cleveland, Ohio; §Department of Anesthesiology and Intensive Care, Hôpital Tenon, Paris, France; ‖Pharmacy, Hôpital Foch, Suresnes, France; ¶Department of Anesthesiology, Leeds General Infirmary, Leeds, United Kingdom; #UPMC, Paris, France; and **Department of Outcomes Research, Cleveland Clinic, Cleveland, Ohio.

出版信息

Anesth Analg. 2014 May;118(5):946-55. doi: 10.1213/ANE.0000000000000185.

Abstract

BACKGROUND

The α2-adrenergic agonist dexmedetomidine is a sedative and can be used as an adjunct to anesthetics. Our primary goal was thus to determine the extent to which dexmedetomidine reduces the requirement for propofol and remifentanil.

METHODS

This double-blinded, randomized study (NCT00921284) used an automated dual closed-loop administration to maintain the Bispectral Index between 40 and 60. Sixty-6 ASA physical status I and II patients were given either dexmedetomidine (1 μg/kg over 10 minutes followed by a continuous infusion of 0.5 μg/kg/h throughout surgery) or comparable volumes of saline as a placebo. Propofol and remifentanil requirements were compared using nonparametric tests and expressed as medians (interquartile ranges).

RESULTS

Twenty-eight patients in each group completed the study. Patients given dexmedetomidine required less propofol (1.0 [0.7-1.3] vs 1.3 [1.0-1.7] mg/kg, P = 0.002) and remifentanil (1.2 [1.0-1.4] vs 1.6 [1.1-2.8] μg/kg, P = 0.02) for anesthetic induction. The propofol dosage required for anesthetic maintenance was 29% (with a 95% confidence interval, 18-40) lower in patients given dexmedetomidine (2.2 [1.5-3.0] vs 3.1 [2.4-4.5] mg/kg/h, P = 0.005), whereas the remifentanil dosage was not significantly different (0.16 [0.09-0.17] vs 0.14 [0.13-0.21] μg/kg/h with P = 0.3). The incidence of adverse events, including hemodynamic instability and delayed recovery, was comparable with and without dexmedetomidine. The first postoperative request for morphine analgesia was delayed in patients given dexmedetomidine (median fourth hour vs first hour, P = 0.008).

CONCLUSIONS

Dexmedetomidine administration significantly reduced the requirement for both propofol and remifentanil during anesthetic induction and reduced propofol use during maintenance of anesthesia. Dexmedetomidine also delayed postoperative analgesic use. Dexmedetomidine is a useful adjuvant that reduces anesthetic requirement and provides postoperative analgesia.

摘要

背景

α2-肾上腺素能激动剂右美托咪定是一种镇静剂,可用作麻醉的辅助剂。我们的主要目标是确定右美托咪定减少丙泊酚和瑞芬太尼需求的程度。

方法

这是一项双盲、随机研究(NCT00921284),使用自动双闭环给药来维持脑电双频指数在 40 到 60 之间。66 名 ASA 身体状况 I 和 II 级的患者接受右美托咪定(1μg/kg 静脉输注 10 分钟,然后以 0.5μg/kg/h 的速度持续输注直至手术结束)或安慰剂(等容量生理盐水)。使用非参数检验比较丙泊酚和瑞芬太尼的需求,并以中位数(四分位距)表示。

结果

每组 28 名患者完成了研究。给予右美托咪定的患者需要更少的丙泊酚(1.0[0.7-1.3]mg/kg 与 1.3[1.0-1.7]mg/kg,P=0.002)和瑞芬太尼(1.2[1.0-1.4]μg/kg 与 1.6[1.1-2.8]μg/kg,P=0.02)用于麻醉诱导。给予右美托咪定的患者维持麻醉所需的丙泊酚剂量降低了 29%(95%置信区间,18-40)(2.2[1.5-3.0]mg/kg/h 与 3.1[2.4-4.5]mg/kg/h,P=0.005),而瑞芬太尼剂量没有显著差异(0.16[0.09-0.17]μg/kg/h 与 0.14[0.13-0.21]μg/kg/h,P=0.3)。有和没有右美托咪定的不良事件发生率,包括血流动力学不稳定和恢复延迟,相当。给予右美托咪定的患者术后第一次吗啡镇痛要求的时间延迟(中位数第四小时与第一小时,P=0.008)。

结论

右美托咪定给药可显著减少麻醉诱导期间丙泊酚和瑞芬太尼的需求,并减少麻醉维持期间丙泊酚的使用。右美托咪定还延迟了术后镇痛的使用。右美托咪定是一种有用的辅助剂,可减少麻醉需求并提供术后镇痛。

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