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口服可乐定与口服加巴喷丁对蛛网膜下腔阻滞持续时间和术后镇痛需求的比较分析

Comparative Analysis of Oral Clonidine Versus Oral Gabapentin on Subarachnoid Block Duration and Postoperative Analgesic Needs.

作者信息

Bagle Aparna, Garud Ishan G

机构信息

Anesthesiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Dr. D.Y. Patil Vidyapeeth (Deemed to be University) Pimpri, Pune, IND.

出版信息

Cureus. 2024 Sep 6;16(9):e68834. doi: 10.7759/cureus.68834. eCollection 2024 Sep.

DOI:10.7759/cureus.68834
PMID:39376826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11456692/
Abstract

INTRODUCTION

Pain, an inherently subjective experience, plays a pivotal role in the body's defence mechanism by signalling tissue damage or potential harm. Thus, optimal postoperative pain management is a cornerstone of modern surgical practice, essential for improving recovery outcomes and overall patient well-being.

METHODS

In this study, a total of 60 patients were randomly assigned to two groups of 30 each: Group C (clonidine) and Group G (gabapentin). Group C received oral clonidine 100 mcg and Group G received oral gabapentin 600 mg one hour prior to the subarachnoid block. Duration of sensory and motor block, hemodynamic parameters, Visual Analog Scale (VAS) scores, time to rescue analgesia and any side effect of both drugs were assessed in both groups.

RESULTS

The duration of motor and sensory blockade, as well as intraoperative hemodynamics and respiratory rates, were comparable between the two groups. Group G exhibited significantly lower VAS scores from 150 minutes postoperatively up to 12 hours (p < 0.001). Additionally, Group G experienced longer duration of postoperative analgesia (16.8±3.9 hours) compared to Group C (9.27±1.7 hours). About 26.6% of the patients in Group C and 6.7% of the patients in Group G presented with postoperative nausea and vomiting (PONV).

CONCLUSION

Oral gabapentin at a dosage of 600 mg demonstrates superior efficacy as a premedication compared to oral clonidine 100 mcg for patients undergoing lower abdominal and lower limb surgeries under spinal anesthesia. Group G demonstrated extended postoperative analgesia, lower VAS scores, and a reduced incidence of PONV, indicating its superiority over clonidine as an analgesic adjunct.

摘要

引言

疼痛是一种内在的主观体验,通过发出组织损伤或潜在伤害的信号,在身体的防御机制中起着关键作用。因此,优化术后疼痛管理是现代外科实践的基石,对于改善恢复结果和患者整体健康至关重要。

方法

在本研究中,总共60例患者被随机分为两组,每组30例:C组(可乐定)和G组(加巴喷丁)。C组在蛛网膜下腔阻滞前1小时口服100微克可乐定,G组在蛛网膜下腔阻滞前1小时口服600毫克加巴喷丁。评估两组的感觉和运动阻滞持续时间、血流动力学参数、视觉模拟评分(VAS)、补救镇痛时间以及两种药物的任何副作用。

结果

两组之间的运动和感觉阻滞持续时间以及术中血流动力学和呼吸频率相当。G组术后150分钟至12小时的VAS评分显著较低(p<0.001)。此外,与C组(9.27±1.7小时)相比,G组术后镇痛持续时间更长(16.8±3.9小时)。C组约26.6%的患者和G组6.7%的患者出现术后恶心呕吐(PONV)。

结论

对于在脊髓麻醉下接受下腹部和下肢手术的患者,600毫克剂量的口服加巴喷丁作为术前用药,与100微克口服可乐定相比,显示出更好的疗效。G组术后镇痛时间延长、VAS评分较低且PONV发生率降低,表明其作为镇痛辅助药物优于可乐定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9d3/11456692/2d90a94e9e24/cureus-0016-00000068834-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9d3/11456692/2d90a94e9e24/cureus-0016-00000068834-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9d3/11456692/2d90a94e9e24/cureus-0016-00000068834-i01.jpg

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