Lahtinen Pasi, Kokki Hannu, Hynynen Markku
Department of Anesthesiology and Intensive Care, University of Kuopio, Kuopio, Finland.
J Cardiothorac Vasc Anesth. 2008 Apr;22(2):225-9. doi: 10.1053/j.jvca.2007.07.004. Epub 2007 Oct 29.
Remifentanil is being used increasingly during fast-track cardiac surgery. Postoperative hyperalgesia and opioid tolerance have been reported in volunteer studies and in patients after major abdominal surgery with remifentanil infusion. In the present study, the authors evaluated whether high-dose remifentanil infusion induces opioid tolerance in 90 patients undergoing coronary artery bypass surgery with sternotomy.
Prospective, randomized, and double-blind study.
Single-institution, tertiary level, university hospital.
Ninety patients undergoing coronary artery bypass surgery.
Patients were randomized to receive a 3-hour infusion of remifentanil (0.3 microg/kg/min, n = 45) or placebo (n = 45) intraoperatively as adjunct to a standardized sufentanil/propofol-based general anesthesia.
Opioid consumption, pain, and sedation scores, as well as adverse events and patients' satisfaction with pain therapy, were recorded for 48 postoperative hours. There were no differences in postoperative opioid consumption between the groups (median oxycodone consumption in the remifentanil group, 98 mg [range, 29-166] and in the placebo group, 99 mg [42-219]). Pain scores were comparable at rest, but during a deep breath pain scores were lower in the remifentanil group (p = 0.020). Sedation scores, satisfaction with analgesia, and adverse events were similar between the 2 groups. The most common adverse event was nausea, with a 33% incidence in the placebo and 40% incidence in the remifentanil group.
Three-hour remifentanil infusion did not increase postoperative pain or opioid consumption in cardiac surgery patients. The present results suggest that high-dose remifentanil does not elicit opioid tolerance when given during cardiac surgery.
瑞芬太尼在快通道心脏手术中的应用日益广泛。在志愿者研究以及接受瑞芬太尼输注的腹部大手术患者中,均有术后痛觉过敏和阿片类药物耐受的报道。在本研究中,作者评估了高剂量瑞芬太尼输注是否会在90例行胸骨切开冠状动脉搭桥手术的患者中诱导阿片类药物耐受。
前瞻性、随机、双盲研究。
单机构、三级大学医院。
90例行冠状动脉搭桥手术的患者。
患者被随机分为两组,术中作为基于舒芬太尼/丙泊酚的标准化全身麻醉的辅助用药,一组接受3小时的瑞芬太尼输注(0.3微克/千克/分钟,n = 45),另一组接受安慰剂输注(n = 45)。
记录术后48小时的阿片类药物消耗量、疼痛和镇静评分,以及不良事件和患者对疼痛治疗的满意度。两组术后阿片类药物消耗量无差异(瑞芬太尼组羟考酮消耗量中位数为98毫克[范围29 - 166],安慰剂组为99毫克[42 - 219])。静息时疼痛评分相当,但深呼吸时瑞芬太尼组疼痛评分较低(p = 0.020)。两组的镇静评分、镇痛满意度和不良事件相似。最常见的不良事件是恶心,安慰剂组发生率为33%,瑞芬太尼组为40%。
3小时的瑞芬太尼输注并未增加心脏手术患者的术后疼痛或阿片类药物消耗量。目前的结果表明,在心脏手术期间给予高剂量瑞芬太尼不会引发阿片类药物耐受。