Joo Hwan S, Salasidis Gary C, Kataoka Mark T, Mazer C David, Naik Viren N, Chen Robert B, Levene Richard G
Department of Anesthesia, St. Michael's Hospital, University of Toronto, Toronto, Canada.
J Cardiothorac Vasc Anesth. 2004 Jun;18(3):263-8. doi: 10.1053/j.jvca.2004.03.003.
Large bolus-dose remifentanil may be advantageous for use during induction of anesthesia because of its short duration of effect. Currently, there are little data on the use of large bolus-dose remifentanil because of reports of severe bradycardia and hypotension. The purpose of this study is to compare the hemodynamic effects of bolus remifentanil versus fentanyl with glycopyrrolate for induction of anesthesia in patients with heart disease.
A randomized, double-blinded study.
A tertiary-care academic medical center.
One hundred patients for coronary artery bypass or valvular surgery.
Subjects received either (1) remifentanil, 5 microg/kg, with glycopyrrolate, 0.2 mg, or (2) fentanyl, 20 microg/kg, with 0.2 mg of glycopyrrolate, and both groups also received midazolam, 70 microg/kg, for induction of anesthesia.
Heart rate, mean arterial pressure, systemic vascular resistance, and cardiac output were similar between the 2 groups during induction of anesthesia and tracheal intubation. The incidence of adverse events such as bradycardia (remifentanil 10%, fentanyl 10%), hypotension (remifentanil 16%, fentanyl 10%), and ischemia (remifentanil 0%, fentanyl 2%) were also similar. A greater percentage of patients in the remifentanil group lost consciousness within 1 minute of opioid administration (86% v 66%, p = 0.034).
Remifentanil with glycopyrrolate is associated with rapid and predictable clinical anesthetic effect, cardiac stability, and the ability to blunt the hemodynamic responses to tracheal intubation. Bolus remifentanil may be a feasible alternative to bolus fentanyl for induction of anesthesia in patients with heart disease because of its short duration of action and its ability to blunt the hemodynamic responses to tracheal intubation.
大剂量推注瑞芬太尼因其作用持续时间短,可能有利于麻醉诱导期使用。目前,由于有严重心动过缓和低血压的报道,关于大剂量推注瑞芬太尼使用的数据较少。本研究的目的是比较推注瑞芬太尼与芬太尼联合格隆溴铵用于心脏病患者麻醉诱导时的血流动力学效应。
一项随机双盲研究。
一家三级医疗学术中心。
100例接受冠状动脉搭桥术或瓣膜手术的患者。
受试者接受以下两种方案之一:(1)瑞芬太尼5μg/kg加格隆溴铵0.2mg,或(2)芬太尼20μg/kg加格隆溴铵0.2mg,两组均接受咪达唑仑70μg/kg用于麻醉诱导。
麻醉诱导期和气管插管期间,两组的心率、平均动脉压、全身血管阻力和心输出量相似。心动过缓(瑞芬太尼组10%,芬太尼组10%)、低血压(瑞芬太尼组16%,芬太尼组10%)和缺血(瑞芬太尼组0%,芬太尼组2%)等不良事件的发生率也相似。瑞芬太尼组中更大比例的患者在给予阿片类药物后1分钟内失去意识(86%对66%,p = 0.034)。
瑞芬太尼联合格隆溴铵具有快速且可预测的临床麻醉效果、心脏稳定性以及减轻气管插管血流动力学反应的能力。由于其作用持续时间短且能减轻气管插管的血流动力学反应,推注瑞芬太尼可能是心脏病患者麻醉诱导时推注芬太尼的一种可行替代方案。