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Effect of perioperative systemic α2 agonists on postoperative morphine consumption and pain intensity: Systematic review and meta-analysis of randomized controlled trials

机译:围手术期全身性α2激动剂对术后吗啡消耗和疼痛强度的影响:随机对照试验的系统评价和荟萃分析

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Background: Systemic α2 agonists are believed to reduce pain and opioid requirements after surgery, thus decreasing the incidence of opioid-related adverse effects, including hyperalgesia. Methods: The authors searched for randomized placebo-controlled trials testing systemic α2 agonists administrated in surgical patients and reporting on postoperative cumulative opioid consumption and/or pain intensity. Meta-analyses were performed when data from 5 or more trials and/or 100 or more patients could be combined. Results: Thirty studies (1,792 patients, 933 received clonidine or dexmedetomidine) were included. There was evidence of postoperative morphine-sparing at 24 h; the weighted mean difference was-4.1 mg (95% confidence interval,-6.0 to-2.2) with clonidine and-14.5 mg (-22.1 to-6.8) with dexmedetomidine. There was also evidence of a decrease in pain intensity at 24 h; the weighted mean difference was-0.7 cm (-1.2 to-0.1) on a 10-cm visual analog scale with clonidine and-0.6 cm (-0.9 to-0.2) with dexmedetomidine. The incidence of early nausea was decreased with both (number needed to treat, approximately nine). Clonidine increased the risk of intraoperative (number needed to harm, approximately nine) and postoperative hypotension (number needed to harm, 20). Dexmedetomidine increased the risk of postoperative bradycardia (number needed to harm, three). Recovery times were not prolonged. No trial reported on chronic pain or hyperalgesia. Conclusions: Perioperative systemic α2 agonists decrease postoperative opioid consumption, pain intensity, and nausea. Recovery times are not prolonged. Common adverse effects are bradycardia and arterial hypotension. The impact of α2 agonists on chronic pain or hyperalgesia remains unclear because valid data are lacking.
机译:背景:据信全身性α2激动剂可减少术后的疼痛和阿片类药物需求,从而降低与阿片类药物相关的不良反应(包括痛觉过敏)的发生率。方法:作者搜寻了安慰剂对照试验,以测试在手术患者中使用的全身性α2激动剂,并报告术后累积的阿片类药物消耗量和/或疼痛强度。当可以合并来自5个或更多试验和/或100个或更多患者的数据时,进行荟萃分析。结果:纳入三十项研究(1,792例患者,933例接受可乐定或右美托咪定)。术后24小时有吗啡保留的证据。可乐定的加权平均差为-4.1 mg(95%置信区间,-6.0至-2.2),右美托咪定的加权平均差为-14.5 mg(-22.1至-6.8)。也有证据表明24小时疼痛强度降低。在可乐定的10厘米视觉模拟量表上,加权平均差为-0.7厘米(-1.2至-0.1),而右美托咪定的加权平均差为-0.6厘米(-0.9至-0.2)。两者均降低了早期恶心的发生率(需要治疗的数量大约为9)。可乐定增加了术中(需要伤害的数量,大约9)和术后低血压(需要伤害的数量,20)的风险。右美托咪定增加了术后心动过缓的风险(需要伤害的数字为三)。恢复时间没有延长。没有关于慢性疼痛或痛觉过敏的试验报告。结论:围手术期全身性α2激动剂可减少术后阿片类药物的消耗,疼痛强度和恶心。恢复时间不会延长。常见的不良反应是心动过缓和动脉低血压。由于缺乏有效数据,α2激动剂对慢性疼痛或痛觉过敏的影响尚不清楚。

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