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首页> 外文期刊>North American Journal of Medical Sciences >A randomized double-blind placebo-controlled study to compare preemptive analgesic efficacy of novel antiepileptic agent lamotrigine in patients undergoing major surgeries
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A randomized double-blind placebo-controlled study to compare preemptive analgesic efficacy of novel antiepileptic agent lamotrigine in patients undergoing major surgeries

机译:一项随机双盲安慰剂对照研究,比较新型抗癫痫药拉莫三嗪的先发镇痛药在接受大手术的患者中的作用

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Background: If postoperative acute pain remains unrelieved, it may result in significant morbidity and mortality. Preemptive analgesic initiated before surgery offers premature analgesia even before exposure to an initial noxious stimulus bestowing effective postoperative analgesia. In developed countries, it is regularly practiced as a part of well-defined protocol. In our country however, only a few centers practice it and that too irregularly and with undefined protocol. Few studies support preemptive analgesic efficacy of novel antiepileptic agent gabapentin. Though lamotrigine is a proven analgesic in animal models of chronic pain and clinical studies of gabapentin-resistant neuropathic pain, a literature search revealed scarce data on its preemptive analgesic efficacy. Aims: The present study is designed to study the preemptive analgesic efficacy of lamotrigine in comparison with diclofenac sodium in postoperative pain control. Materials and Methods: This randomized clinical trial included 90 patients of both sexes, between 18 years and 70 years undergoing major surgeries. Patients were randomly allocated into placebo, control, and test groups and received the respective treatment 30 min before the induction of anesthesia. Aldrete score and pain score were recorded using visual analog scale (VAS), facial rating scale (FRS), and behavioral rating scale (BRS) at awakening and at 1 h, 2 h, 4 h, 6 h, and 24 h. Postoperative rescue analgesic consumption for 24 h was recorded. Results: Significantly higher pain scores were observed in the placebo group postoperatively for 2 h on all pain scales (P P 0.05). The test group patients were more comfortable throughout the study and postoperative analgesic requirement was significantly less (P Conclusions: The study recommends the use of single oral dose lamotrigine as preemptive analgesic for effective postoperative pain control.
机译:背景:如果术后急性疼痛仍未缓解,则可能导致明显的发病率和死亡率。在手术之前开始的先发性镇痛药即使在暴露于给予有效术后镇痛作用的初始有害刺激之前,也能提供过早镇痛作用。在发达国家,通常将其作为定义明确的协议的一部分进行实践。但是,在我们国家,只有很少的中心实行这种做法,而且这种做法过于不定期,而且协议不明确。很少有研究支持新型抗癫痫药加巴喷丁的先发镇痛作用。尽管拉莫三嗪在慢性疼痛的动物模型和加巴喷丁耐药性神经性疼痛的临床研究中已被证明具有镇痛作用,但文献检索显示,关于其先发性镇痛作用的数据很少。目的:本研究旨在研究拉莫三嗪与双氯芬酸钠在术后疼痛控制中的先发性镇痛效果。材料和方法:这项随机临床试验包括90名男女患者,年龄在18岁至70岁之间,接受了大手术。将患者随机分为安慰剂组,对照组和测试组,并在麻醉诱导前30分钟接受相应的治疗。使用视觉模拟量表(VAS),面部评定量表(FRS)和行为评定量表(BRS)在清醒时以及在1 h,2 h,4 h,6 h和24 h记录Aldrete评分和疼痛评分。记录术后24小时的急救镇痛药消耗量。结果:在所有疼痛量表上,安慰剂组术后2 h的疼痛评分均显着较高(P P 0.05)。测试组患者在整个研究过程中更加舒适,术后镇痛要求明显减少(P结论:研究建议使用单剂量拉莫三嗪作为先行镇痛剂,以有效地控制术后疼痛。

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