两种不同剂量的硫酸镁作为布比卡因在脊柱麻醉下脐下(膝盖以下)骨科手术中的辅助剂

S. Chaudhary, R. Verma, S. Rana, Jai P Singh, A. Danesh
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Materials and methods This study was carried out on 90 American Society of Anesthesiology I and II patients of both sexes in the age group of 20–60 years scheduled for below knee surgeries under subarachnoid block. Group 1 (n = 30) patients received intrathecal 0.5% heavy bupivacaine (2.8 ml) +0.2 ml normal saline; group 2 (n = 30) received intrathecal 0.5% heavy bupivacaine (2.8 ml) +50 mg (0.1 ml) magnesium sulfate +0.1 ml normal saline; and group 3 (n = 30) received intrathecal 0.5% heavy bupivacaine (2.8 ml)+100 mg (0.2 ml) magnesium sulfate. The primary outcome measure was the duration of postoperative analgesia, and secondary outcomes included the number of supplemental analgesic requirements, block characteristics, and hemodynamic stability. Results The onset of sensory and motor block was delayed in the magnesium group (100 mg>50 mg). 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引用次数: 3

摘要

背景硫酸镁作为神经轴阻滞的辅助用药已得到广泛应用,其目的是改善和提高麻醉质量和麻醉时间,延缓术后疼痛的发生,从而减少术后抢救镇痛药的需求。然而,直到今天,关于硫酸镁作为蛛网膜下腔阻滞佐剂的理想剂量还没有达成共识。本研究旨在探讨鞘内添加硫酸镁(50和100 mg)是否会增强鞘内布比卡因的镇痛效果。我们假设硫酸镁作为布比卡因在蛛网膜下腔阻滞中的辅助剂的加性作用是剂量依赖性的。材料与方法本研究选取了90例年龄在20 ~ 60岁的美国麻醉学学会I、II级患者,男女均为,拟行蛛网膜下腔阻滞下膝下手术。第一组(n = 30)患者鞘内注射0.5%重布比卡因(2.8 ml) +0.2 ml生理盐水;2组(n = 30)鞘内注射0.5%重布比卡因(2.8 ml) +50 mg硫酸镁(0.1 ml) +生理盐水0.1 ml;第三组(n = 30)鞘内注射0.5%重布比卡因(2.8 ml)+硫酸镁100 mg (0.2 ml)。主要结局指标是术后镇痛持续时间,次要结局包括补充镇痛需求的次数、阻滞特征和血流动力学稳定性。结果镁组(100 mg>50 mg)感觉和运动阻滞的发生时间明显延迟。镁组患者术后镇痛时间明显延长,且呈剂量依赖性,100 mg组患者术后镇痛总需要剂量明显延迟。各组患者血流动力学稳定,无不良反应。结论与对照组和硫酸镁50 mg组相比,硫酸镁100 mg作为布比卡因蛛网膜下腔阻滞的辅助剂可延长镇痛时间,减少对抢救镇痛药物的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnesium sulfate at two different doses as an adjuvant to bupivacaine in infraumblical (below knee) orthopedic surgeries under spinal anesthesia
Background The use of magnesium sulfate as an adjuvant in neuraxial block has gained popularity, with the aim of improving and enhancing the quality and duration of anesthesia, delaying the onset of postoperative pain, and thus reducing the demand for postoperative rescue analgesics. However, until today, there has been no consensus as regards the ideal dose of magnesium sulfate as an adjuvant in the subarachnoid block. The present study was designed to examine whether the addition of intrathecal magnesium sulfate (50 and 100 mg) would enhance the analgesic efficacy of intrathecal bupivacaine. We hypothesized that the additive effect of magnesium sulfate as an adjuvant to bupivacaine in subarachnoid block is dose dependent. Materials and methods This study was carried out on 90 American Society of Anesthesiology I and II patients of both sexes in the age group of 20–60 years scheduled for below knee surgeries under subarachnoid block. Group 1 (n = 30) patients received intrathecal 0.5% heavy bupivacaine (2.8 ml) +0.2 ml normal saline; group 2 (n = 30) received intrathecal 0.5% heavy bupivacaine (2.8 ml) +50 mg (0.1 ml) magnesium sulfate +0.1 ml normal saline; and group 3 (n = 30) received intrathecal 0.5% heavy bupivacaine (2.8 ml)+100 mg (0.2 ml) magnesium sulfate. The primary outcome measure was the duration of postoperative analgesia, and secondary outcomes included the number of supplemental analgesic requirements, block characteristics, and hemodynamic stability. Results The onset of sensory and motor block was delayed in the magnesium group (100 mg>50 mg). There was a significant prolongation of postoperative analgesia in the magnesium group in a dose-dependent manner, and total dose of rescue analgesic requirement was found to be significantly delayed in the 100 mg group. Patients in all groups remained hemodynamically stable without any adverse effects. Conclusion Magnesium sulfate (100 mg) as an adjuvant to bupivacaine in subarachnoid block prolongs the duration of analgesia and decreases the demand for rescue analgesics compared with the control and the magnesium sulfate 50 mg group.
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