Clinical Research Development, Center of Valiasr Hospital, Arak University of Medical Sciences, Arak, Iran.
Students Research Committee, Arak University of Medical Sciences, Arak, Iran.
Med Gas Res. 2022 Jul-Sep;12(3):77-82. doi: 10.4103/2045-9912.330690.
This trial-based paper strives to address the comparative efficacy of some ropivacaine adjuvant options, comprising dexmedetomidine, granisetron, and nitroglycerin, on pain and hemodynamic changes in intravenous anesthesia for forearm surgeries. This double-blind, placebo-controlled study enrolled four block-randomized eligible groups with patients (overall, n=128) undergoing orthopedic forearm surgeries in the dexmedetomidine, nitroglycerin, granisetron, and placebo groups. Intra- and post-operative vital signs (mean arterial pressure/heart rate/ oxygen saturation) were monitored at baseline and captured every 10 minutes until the end of the surgery, as well as the onset of sensory and motor block and length and duration of the block and mean opioid use within 24 hours. Lastly, pain was noted after tourniquet inflation (at 15, 30, and 45 minutes every 15 minutes until the end of surgery) and after deflation (every 30 minutes to 2 hours at 30, 60, 90, and 120 minutes), as well as 6, 12, and 24 hours after the tourniquet was deflated. The dexmedetomidine-sedated subjects appeared to demonstrate quicker onset and longer length and duration of sensory and motor block, plus less pain and opioid use at all scheduled times (both P = 0.0001). Dexmedetomidine is recommended as an adjuvant to regional anesthesia (Bier's block), while being coupled with the rapid onset and prolonged length and duration of sensory and motor blocks, in addition to soothed pain and diminished opioid use within postoperative 24 hours. The study was approved by Ethics Committee of Arak University of Medical Sciences (approval No. IR.ARAKMU.REC.1398.112) on July 21, 2019, and registered at Iranian Registry of Clinical Trials (registration number IRCT20141209020258N123) on November 2, 2019.
本基于试验的论文旨在探讨一些罗哌卡因佐剂选项(包括右美托咪定、格拉司琼和硝酸甘油)在静脉麻醉下用于前臂手术中的比较疗效,包括疼痛和血液动力学变化。这项双盲、安慰剂对照研究纳入了 4 个块随机分组的患者(总体 n=128),他们接受骨科前臂手术,分别在右美托咪定、硝酸甘油、格拉司琼和安慰剂组。术中及术后生命体征(平均动脉压/心率/血氧饱和度)在基线和每隔 10 分钟监测一次,直至手术结束,以及感觉和运动阻滞的开始和长度和持续时间,以及术后 24 小时内阿片类药物的平均使用量。最后,在止血带充气后(每隔 15 分钟在 15、30 和 45 分钟记录一次,直至手术结束)和充气后(在 30、60、90 和 120 分钟时每隔 30 分钟记录一次至 2 小时)记录疼痛,以及在止血带充气后 6、12 和 24 小时记录疼痛。与其他组相比,右美托咪定镇静组的患者在所有预定时间内似乎表现出更快的感觉和运动阻滞的开始、更长的长度和持续时间,以及更少的疼痛和阿片类药物使用(均 P = 0.0001)。右美托咪定被推荐作为区域麻醉(Bier 阻滞)的佐剂,同时具有快速起效和延长感觉和运动阻滞的长度和持续时间,以及减轻术后 24 小时内的疼痛和减少阿片类药物使用的作用。该研究于 2019 年 7 月 21 日获得阿拉克医科大学伦理委员会的批准(批准号 IR.ARAKMU.REC.1398.112),并于 2019 年 11 月 2 日在伊朗临床试验注册中心(注册号 IRCT20141209020258N123)注册。