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首页> 外文期刊>Bulletin of Emergency and Trauma >Comparison of Intravenous Regional Anesthesia with Single-Cuff Forearm Tourniquet and Hematoma Block and Traditional Method in Patients with Distal Radius Fractures; A Randomized Clinical Trial
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Comparison of Intravenous Regional Anesthesia with Single-Cuff Forearm Tourniquet and Hematoma Block and Traditional Method in Patients with Distal Radius Fractures; A Randomized Clinical Trial

机译:静脉区域麻醉与单袖叉脑径腹部血肿和远端半径骨折患者的传统方法的比较;随机临床试验

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Objective: To investigate the effect of intravenous regional anesthesia with single-cuff forearm tourniquet and hematoma block on intraoperative and postoperative pain intensity of patients with distal radial bone fracture. Methods: In this randomized clinical trial, a total number of 52 patients with distal radius fractures were randomly assigned to receive either a traditional Bier block with 3 mg.kg-1 lidocaine (D group) or a single-cuff forearm tourniquet intravenous regional anesthesia with 1.5 mg.kg-1 lidocaine and a hematoma block with 10 mL 0.5% bupivacaine (S group). Pain intensity score of numerical rating scale (NRS) was measured hourly for 6 hours, then every two hours till 12th hour and every 4 hours until 24th postoperative hour. Total morphine consumption in the first 24 hours after surgery, its side effects and the patients’ global satisfaction were assessed in each group. Results: Mean total morphine consumption during the first 24 hours after surgery was 11.68±7.88 mg in group D and 7.12±4.42 mg in group S (p=0.13). Pain intensity score of NRS both during recovery room and surgical ward stay was less in S group compared to D group (0.016 and 0.02, respectively). Conclusion: Intravenous regional anesthesia with single cuff forearm tourniquet and hematoma block compared to the traditional Bier block reduced intraoperative and postoperative pain intensity more effectively in patients with distal fracture of the radius bone and also reduced morphine consumption during the first 24 hours after surgery. Clinical Trial Registry: IRCT201604223213N4
机译:目的:探讨静脉内麻醉与单箍前臂止血带和血肿段对远侧径向骨折患者术中和术后疼痛强度的影响。方法:在该随机临床试验中,随机分配了52例远端半径骨折的总数,以接收3毫克kg-1利多卡因(d组)或单袖前腹部静脉内麻醉的传统bier块1.5毫克kg-1利多卡因和血肿块,10ml 0.5%bupivacaine(s组)。每小时测量数值额定量表(NRS)的疼痛强度评分6小时,然后每两周一次,每4小时一次,术后每小时每4小时。在手术后的前24小时内总体吗啡消费,其副作用和患者的全球满意度在每组中评估。结果:平均在D组后24小时内的平均吗啡消耗量为-11.68±7.88mg,群体中的7.12±4.42mg(P = 0.13)。与D组相比,恢复室内恢复室和外科病房停留期间NRS的疼痛强度得分较少(分别为0.016和0.02)。结论:静脉内麻醉与单袖前臂止血带和血肿块相比,传统的Bier块在半径骨远端骨折患者中更有效地降低了术中和术后疼痛强度,并且在手术后的前24小时内降低了吗啡消费。临床试验登记处:IRCT201604223213n4

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