布比卡因-利多卡因与布比卡因-利多卡因加地塞米松治疗锁骨上臂丛阻滞

A. Abdelrazik, A. Ali, I. Youssef, Sohair A. Megalla
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摘要

背景:评价地塞米松辅助布比卡因-利多卡因混合治疗锁骨上臂丛阻滞是否比单独布比卡因-利多卡因混合治疗能增强阻滞,延长作用时间,改善术后镇痛。患者和方法60例患者在锁骨上臂丛阻滞下接受选择性和紧急上肢矫形手术(肩关节下),手术由神经刺激器引导。患者随机分为两组:C组(对照组,n=30)给予仅含局麻药的溶液40 ml。D组(地塞米松组,n=30)给予局麻药加地塞米松4mg溶液40 ml。主要结局是感觉和运动阻滞的发生时间,以及感觉和运动阻滞的持续时间,以分钟为单位进行评估。次要结果是使用基于视觉模拟量表的评分系统进行疼痛评估,到达首次镇痛要求的时间和总镇痛消耗。结果地塞米松组感觉阻滞时间明显长于对照组(753±68.04∶565±30.85∶733.66±69.77∶547.16±29.38);在视觉模拟量表上,两组在术后9、12、18 h比较,地塞米松组差异有统计学意义。与对照组相比,地塞米松组首次要求镇痛的时间明显更长。与对照组相比,地塞米松组的总镇痛需求也显著降低。结论4 mg地塞米松辅助局麻药可有效延长感觉和运动阻滞持续时间,延长首次镇痛请求时间,减少总镇痛消耗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bupivacaine–lidocaine versus bupivacaine–lidocaine plus dexamethasone in supraclavicular brachial plexus block
Background To evaluate whether dexamethasone as an adjuvant to bupivacaine–lidocaine mixture in supraclavicular brachial plexus block can enhance the block, prolong the duration of action, and improve postoperative analgesia than a mixture of bupivacaine–lidocaine only. Patients and methods In all, 60 patients were posted for elective and emergent upper limb orthopedic surgery (below shoulder joint), under supraclavicular brachial plexus block guided by a nerve stimulator. Patients were randomly divided into two equal groups: group C (the control group, n=30) received 40 ml solution containing local anesthetics only. Group D (the dexamethasone group, n=30) received a 40 ml solution containing local anesthetics plus 4 mg dexamethasone. Primary outcomes were onset time of sensory and motor block, and duration of sensory and motor block, which were assessed in minutes. Secondary outcomes were pain assessment using a scoring system based on the visual analog scale, time to first analgesic requirement, and total analgesic consumption. Results Duration of sensory and motor block in the dexamethasone group were significantly longer than the control group (753±68.04 vs. 565±30.85 min and 733.66±69.77 vs. 547.16±29.38 min, respectively). For visual analog scale, while comparing the two groups, the differences were significant at 9, 12, and 18 h after surgery in favor of the dexamethasone group. The time to first analgesic request was significantly longer in the dexamethasone group in comparison to the control group. The total analgesic requirement was also significantly lower in the dexamethasone group in comparison to the control group. Conclusion The use of dexamethasone at a dose of 4 mg as an adjuvant to local anesthetics provided effective prolongation in the duration of sensory and motor block, prolonged time to first analgesic request, and reduced the total analgesic consumption.
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