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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Preoperative gabapentin for postoperative analgesia: a meta-analysis.
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Preoperative gabapentin for postoperative analgesia: a meta-analysis.

机译:术前加巴喷丁用于术后镇痛的荟萃分析。

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摘要

PURPOSE: Gabapentin's role in the treatment of chronic neuropathic pain is well known. What is less well established is its role for managing postoperative pain. In order to clarify whether gabapentin's utility in acute pain control is more than just theoretical, we conducted a meta-analysis of all randomized trials that addressed gabapentin's role in acute postoperative pain control. We specifically addressed whether gabapentin reduces pain scores, analgesia consumption, and/or analgesia-related side effects in the first 24 hr following surgery. SOURCE: We identified eight placebo-controlled, randomized controlled trials and conducted a meta-analysis using the primary outcomes of pain scores, total analgesia consumption, and side effects over a 24-hr period. PRINCIPLE FINDINGS: Patients who received gabapentin preoperatively reported significantly lower pain scores (-11.9 at rest and -11.0 with movement on a 100-point visual analogue scale) and opioid consumption (-14.7 mg of morphine in 24 hr) with no difference in the incidence of side effects. CONCLUSION: Although gabapentin given preoperatively decreases pain scores and analgesic consumption in the first 24 hr after surgery, the clinical significance of this finding has yet to be determined. This meta-analysis could not demonstrate a significant reduction in the incidence of side effects. Due to the small numbers enrolled in the studies, larger randomized control trials are warranted.
机译:目的:加巴喷丁在治疗慢性神经性疼痛中的作用是众所周知的。还不太清楚的是它在管理术后疼痛中的作用。为了阐明加巴喷丁在急性疼痛控制中的作用是否仅是理论上的,我们对所有涉及加巴喷丁在术后急性疼痛控制中作用的随机试验进行了荟萃分析。我们专门研究了加巴喷丁是否在术后24小时内降低了疼痛评分,镇痛消耗和/或与镇痛有关的副作用。资料来源:我们确定了八项安慰剂对照,随机对照试验,并使用疼痛评分,总镇痛消耗量和在24小时内的副作用的主要结局进行了荟萃分析。原则发现:术前接受加巴喷丁的患者报告的疼痛评分(静息-11.9,运动至100点视觉模拟量表时为-11.0)和阿片类药物(24小时-14.7 mg吗啡)的疼痛评分均明显降低,两者之间无差异。副作用的发生率。结论:尽管术前给予加巴喷丁可以减轻术后24小时的疼痛评分和止痛药的使用,但这一发现的临床意义尚待确定。这项荟萃分析不能证明副作用的发生率显着降低。由于研究人数少,因此需要进行较大的随机对照试验。

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