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首页> 外文期刊>Anesthesiology research and practice >A Comparative Study of 0.25% Levobupivacaine, 0.25% Ropivacaine, and 0.25% Bupivacaine in Paediatric Single Shot Caudal Block
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A Comparative Study of 0.25% Levobupivacaine, 0.25% Ropivacaine, and 0.25% Bupivacaine in Paediatric Single Shot Caudal Block

机译:小儿单发尾C阻滞中0.25%左旋布比卡因,0.25%罗哌卡因和0.25%布比卡因的比较研究

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Aim. There are limited data comparing levobupivacaine, ropivacaine, and bupivacaine in paediatric patients. So, this study was performed to evaluate the caudal effectiveness of all the three drugs in paediatric patients undergoing infraumbilical surgeries and associated complications with these drugs. Material and Methods. 90 patients of ASA grade I and II posted for elective infraumbilical surgeries were randomly divided into three groups of 30 each. A standardized anaesthetic protocol was used. Patients received 0.25% levobupivacaine in group 1, 0.25% ropivacaine in group 2, and 0.25% bupivacaine in group 3. The effectiveness of block was assessed using caudal effectiveness score. Postoperative pain relief was assessed with modified Hannallah pain score. Haemodynamic parameter monitoring was done. The duration of analgesia and associated complications were studied. Statistical analysis was done using the chi-square test for nonparametric data. Parametric data were analysed using ANOVA for intergroup comparison and Tukey’s HSD for intragroup comparison. Results. Demographic data were comparable. Haemodynamic parameters remained within normal range. Mean caudal effectiveness score in all the three groups was statistically insignificant (). The duration of analgesia provided by bupivacaine (145.31 ± 26.17?min) was longer than levobupivacaine (126.15 ± 15.15?min) and ropivacaine (114.68 ± 11.32?min) (). Mean postoperative pain scores were lower in group 3 as compared to group 1 and group 2. Conclusion. We conclude that levobupivacaine and ropivacaine provide similar intraoperative quality with minimal haemodynamic variability and shorter duration of postoperative analgesia without any significant complications when compared with racemic bupivacaine. This trial is registered with CTRI/2018/03/012402.
机译:目标。儿科患者比较左氧布比卡因,罗哌卡因和布比卡因的数据有限。因此,本研究旨在评估所有三种药物在接受脐带下手术及这些药物相关并发症的儿科患者的尾椎有效性。材料与方法。将90例ASAⅠ级和Ⅱ级进行选择性的脐下手术的患者随机分为三组,每组30例。使用标准化的麻醉方案。患者在第1组中接受了0.25%左旋布比卡因,在第2组中接受了0.25%的罗哌卡因,而在第3组中接受了0.25%的布比卡因。使用尾椎有效性评分评估阻滞效果。使用改良的Hannallah疼痛评分评估术后疼痛缓解。进行血液动力学参数监测。研究了镇痛的持续时间和相关并发症。使用卡方检验对非参数数据进行统计分析。参数数据的分析使用ANOVA进行组间比较,Tukey的HSD进行组内比较。结果。人口数据具有可比性。血液动力学参数保持在正常范围内。三组中的平均尾椎有效性评分在统计学上均不显着()。布比卡因提供的镇痛持续时间(145.31±26.17?min)大于左旋布比卡因(126.15±15.15?min)和罗哌卡因(114.68±11.32?min)()。与第1组和第2组相比,第3组的平均术后疼痛评分较低。我们得出的结论是,与消旋布比卡因相比,左旋布比卡因和罗哌卡因具有相似的术中质量,血流动力学变异性最小,术后镇痛时间更短,且无任何明显并发症。该试验已在CTRI / 2018/03/012402中注册。

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