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Effects of pregabalin on postoperative pain after hysterectomy under spinal anesthesia with intrathecal morphine: a randomized controlled trial

机译:普瑞巴林对鞘内变质脊髓麻醉下子宫切除术后术后疼痛的影响:随机对照试验

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Abstract Purpose To determine if preoperative pregabalin could decrease 24-h postoperative morphine consumption after spinal anesthesia with intrathecal morphine compared with placebo. Methods A randomized, double-blind, controlled trial was performed in the tertiary care center. Patients aged between 18 and 65?years who were American Society of Anesthesiologists class I–II and scheduled for abdominal hysterectomy with or without salpingo-oophorectomy were randomly allocated to a placebo or a pregabalin group. Patients received pregabalin 150?mg or placebo 1?h prior to anesthesia. Spinal anesthesia was achieved with 0.5% hyperbaric bupivacaine with morphine 0.2?mg. Intravenous patient-controlled analgesia morphine was provided postoperatively. Postoperative morphine consumption at 6, 12, and 24?h, time to first analgesic rescue, pain scores, adverse effects, and patient satisfaction were evaluated at 24?h after the operation. Results One hundred twenty-five patients were recruited and 119 patients (placebo N ?=?58, pregabalin N ?=?61) were included in the analysis. Forty-seven (81.0%) patients in the placebo group and 53 (86.9%) patients in the pregabalin group required morphine in the first 24?h. Median [IQR] 24-h morphine consumption was 4.0 [1.8, 10.0] mg in the placebo group and 5.0 [2.0, 11.0] mg in the prebagalin group, p ?=?0.60. There were no differences in cumulative morphine consumption at 6, 12, and 24?h postoperatively. The two groups also did not differ in time to first analgesic rescue, pain scores at rest and on movement, and side effects. Conclusion A single preoperative dose of pregabalin 150?mg did not reduce 24-h postoperative morphine consumption or pain scores or prolong the time to first analgesic rescue in spinal anesthesia with intrathecal morphine.
机译:摘要目的,以确定术前普瑞巴林是否可以减少24小时术后吗啡消费,与安慰剂相比,鞘内混合物术后脊柱麻醉后。方法在三级护理中心进行随机,双盲控制试验。 18至65岁的患者是美国麻醉学家II-II类的岁月,并预定有或没有Salpingo-Oophorectomy的腹部子宫切除术,随机分配给安慰剂或普瑞巴林组。患者在麻醉之前接受普瑞巴林150?Mg或安慰剂1?H.用10.5%高压布瓦帕卡因与吗啡0.2μmg,实现脊髓麻醉。术后提供静脉内患者控制的镇痛吗啡。术后吗啡消费6,12和24?H,在操作后24μl评估第一次镇痛救援,疼痛评分,不利影响和患者的满意度。结果分析中均招募一百二十五名患者,119名患者(安慰剂N?58,Praetabalin N?=β61)。安慰剂组中的四十七(81.0%)患者,普瑞巴林组的53名(86.9%)患者在前24岁时需要吗啡。中位数[IQR] 24-H吗啡消耗量为4.0 [1.8,10.0] mg,在预备植物组中为5.0 [2.0,11.0] mg,p?= 0.60。术后6,12和24次累积吗啡消费没有差异。两组也没有及时对先镇痛救援,疼痛分数在休息和运动中的痛苦和副作用。结论单一术前剂量的PREGABALIN 150?MG没有减少24-H术后吗啡消费或疼痛评分或延长与鞘内吗啡的脊髓麻醉中首先镇痛救援的时间。

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