A Randomized Double-Blind Trial Comparing the Efficacy of Dexamethasone vs. Clonidine as an Adjunct to Ropivacaine in Ultrasound Guided Continuous Interscalene Block for Arthroscopic Shoulder Surgery

Vaibhav Taneja, S. Mitra, Jasveer Singh, S. Jindal, Ravi Gupta
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Abstract

Background: Ultrasound-Guided Continuous Interscalene Block (USGCISB) decreases postoperative morbidity following arthroscopic shoulder surgery. Both dexamethasone and clonidine have been shown to prolong the duration of analgesia when added with ropivacaine in peripheral nerve blocks. However, there is no head-to-head comparison between dexamethasone and clonidine as an adjuvant using USG-CISB. Methods: In this randomized double-blinded controlled trial, 60 ASA grade 1-2 patients, 18-65 years, scheduled for arthroscopic shoulder surgery under general Anaesthesia following USG-CISB with perineural catheter using 30 ml of 0.5% ropivacaine were randomly allocated to Group 1 (adjunct dexamethasone 8 mg) or Group 2 (adjunct clonidine 150 μg). Primary outcome was duration of postoperative analgesia, as measured (in min) from the achievement of adequate sensory block till the first bolus of 0.2% ropivacaine by patient controlled regional analgesia. Secondary outcomes were measures of the pain ratings, total postoperative analgesic consumption, patient satisfaction, and adverse effects over 48h postoperatively. Results: The median duration of analgesia in Group 1 was significantly longer than Group 2 (1432 min vs. 751 min; P < 0.001). Median total postoperative analgesic consumption in Group 1 was significantly less than Group 2 (84 ml vs. 120 ml; P < 0.001). Median patient satisfaction score in Group 1 was significantly more than Group 2 (90 vs. 84; P = 0.001). Postoperative adverse effects were few and comparable. Conclusion: Compared to clonidine, dexamethasone significantly prolonged the duration of analgesia, decreased postoperative analgesic consumption, and increased patient satisfaction following USG-CISB when used as an adjunct to ropivacaine for arthroscopic shoulder surgery.
超声引导下肩关节镜手术中地塞米松与可乐定辅助罗哌卡因的随机双盲试验比较
背景:超声引导的连续斜角肌间阻滞(USGCISB)降低肩关节镜手术后的术后发病率。当周围神经阻滞中加入罗哌卡因时,地塞米松和可乐定均可延长镇痛持续时间。然而,在USG-CISB的辅助治疗中,地塞米松和可乐定没有正面比较。方法:随机双盲对照试验,60例ASA级1-2级患者,年龄18-65岁,USG-CISB术后全身麻醉行关节镜肩关节手术,经神经周导管置入0.5%罗哌卡因30 ml,随机分为1组(辅助地塞米松8 mg)和2组(辅助克拉定150 μg)。主要终点是术后镇痛的持续时间,从达到足够的感觉阻滞到通过患者控制的局部镇痛第一次注射0.2%罗哌卡因(以分钟为单位)。次要结局是测量疼痛评分、术后总止痛药用量、患者满意度和术后48小时的不良反应。结果:组1中位镇痛时间明显长于组2 (1432 min vs. 751 min;P < 0.001)。组1术后镇痛总用量中位数显著低于组2 (84 ml vs 120 ml;P < 0.001)。组1患者满意度中位数明显高于组2(90分vs. 84分;P = 0.001)。术后不良反应少且具有可比性。结论:与克拉定相比,地塞米松作为罗哌卡因关节镜肩关节手术的辅助用药,显著延长了镇痛持续时间,减少了术后镇痛消耗,提高了USG-CISB术后患者满意度。
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