高压布比卡因用于成年患者的脊髓麻醉:0.5%等压布比卡因在80mg/Ml和40mg/Ml葡萄糖溶液中的比较

Nehme Pw, Maalouli Jm, Merheb Mt, Gharios Em
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引用次数: 0

摘要

背景:布比卡因的Baricity是影响局部麻醉剂分布特征和阻断剂传播的最重要因素之一。布比卡因通过添加葡萄糖而具有高压作用。不同程度的高胆血症在脊髓麻醉阻滞方面的效果仍有待评估。方法:在一项双盲、随机、平行组的前瞻性研究中,将100名接受下腹、髋关节和下肢手术的患者随机分为两组。第一组接受0.5%的等压布比卡因和80mg/ml的葡萄糖,而第二组接受0.5%等压布哌卡因和40mg/ml的葡萄糖。坐位于L3-4和L4-L5间隙中线位置鞘内注射。测量的感觉阻滞和运动阻滞是开始和持续时间。感觉阻滞的持续时间是指从最高阻滞时间回归到S2皮肤组的时间。结果:两组感觉阻滞的成功率、范围和持续时间相似。两组中感觉阻滞的最高中位数水平为T3(T2-T7)(中位数(第10/90个百分位数))。达到T10的时间在各组之间没有差异。功率分析表明,两组共需要100名成年人,才能有90%的机会在0.05的显著性水平上检测到组间10%的成功差异。分类数据采用卡方检验。对于连续数据,使用Mann-Whitney检验。结果以中位数(10-90个百分位数)、病例数(%)表示,显著性设定为P<0.05。结论:80mg/ml葡萄糖溶液中的布比卡因与40mg/ml葡萄糖溶液相比,可提供持续时间更短、低血压更少的可靠脊麻。考虑到在日间病例环境中进行了更多的手术,罗哌卡因的恢复情况可能令人感兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyperbaric Bupivacaine for Spinal Anaesthesia in Adults Patients: Comparison of Isobaric Bupivacaine 0.5% in 80mg/Ml and 40 Mg/Ml Glucose Solutions
Background: The Baricity of bupivacaine is one of the most important factors to influence the characteristics of distribution of the local anaesthetic and spread of the blockade. Bupivacaine is rendered hyperbaric by adding glucose. The effect of differing degrees of hyperbaricity remains to be evaluated in term of spinal anesthesia blockade. Methods: Hundred patients who underwent lower abdominal, hips, and lower extremity surgeries were randomized into two groups in a double-blind, randomised, parallel group, prospective study. Group I received 0.5% isobaric bupivacaine with 80 mg/ml of glucose, while Group II received 0.5% isobaric bupivacaine with 40 mg/ml of glucose. Injection was made intrathecally in midline position at L3-4 and L4-L5 interspace in sitting position. The measured sensory blockade and motor blockade are the onset and duration. Duration of sensory block was the time measured from the time of the highest block for the regression to the S2 dermatome. Results: Success rate, spread and duration of sensory block were similar in both groups. The highest median level of sensory block was T3 (T2-T7) (median (10th/90th percentiles)) in both groups. Time to reach T10 did not differ between the groups. Power analysis suggested that a total number of 100 adults were required in both groups for a 90% chance at the 0.05 level of significance of detecting a10% difference in success between groups. Categorical data were tested using the chi square test. For continuous data the Mann–Whitney test was used. Results are presented as median (10–90th percentiles), number (%) of cases, the significance was set as P<0.05. Conclusion: These results demonstrate that bupivacaine in 80mg/ml glucose provides reliable spinal anaesthesia of shorter duration and with less hypotension than bupivacaine in 40 mg/ml glucose. The recovery profile for ropivacaine may be of interest given that more surgery is being performed in the day-case setting.
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