...
首页> 外文期刊>Thoracic cancer. >Preventive skin analgesia with lidocaine patch for management of post-thoracotomy pain: Results of a randomized, double blind, placebo controlled study
【24h】

Preventive skin analgesia with lidocaine patch for management of post-thoracotomy pain: Results of a randomized, double blind, placebo controlled study

机译:预防性皮肤镇痛与利多卡因贴片治疗后胸骨切断疼痛:随机,双盲,安慰剂对照研究的结果

获取原文

摘要

To evaluate whether pre-emptive skin analgesia using a lidocaine patch 5% would improve the effects of systemic morphine analgesia for controlling acute post-thoracotomy pain. This was a double-blind, placebo controlled, prospective study. Patients were randomly assigned to receive lidocaine 5% patch (lidocaine group) or a placebo (placebo group) three?days before thoracotomy. Postoperative analgesia was induced in all cases with intravenous morphine analgesia. The intergroup differences were assessed in order to evaluate whether the lidocaine patch 5% would have effects on pain intensity when at rest and after coughing (primary end-point) on morphine consumption, on the recovery of respiratory function, and on peripheral painful pathways measured with N2 and P2 laser-evoked potential (secondary end-points). A total of 90 patients were randomized, of whom 45 were allocated to the lidocaine group and 45 to the placebo group. Lidocaine compared with the placebo group showed a significant reduction in pain intensity both at rest (P?=?0.013) and after coughing (P?=?0.015), and in total morphine consumption (P?=?0.001); and also showed a better recovery of flow expiratory volume in one?second (P?=?0.025) and of forced vital capacity (P?=?0.037). The placebo group compared with the lidocaine group presented a reduction in amplitude of N2 (P?=?0.001) and P2 (P?=?0.03), and an increase in the latency of N2 (P?=?0.023) and P2 (P?=?0.025) laser-evoked potential. The preventive skin analgesia with lidocaine patch 5% seems to be a valid adjunct to intravenous morphine analgesia for controlling post-thoracotomy pain. However, our initial results should be corroborated/confirmed by larger studies. ? 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:为了评估使用利多卡因补丁的先发制人皮肤镇痛5%将改善全身式吗啡镇痛对控制急性后胸部疼痛的影响。这是一项双盲,安慰剂控制,前瞻性研究。患者被随机分配接受利多卡因5%蛋白(利多卡因组)或安慰剂(安慰剂组)三个?胸廓切开术前天。在所有静脉内吗啡镇痛的所有病例中诱导术后镇痛。评估杂交差异,以评估LIDOCaine贴剂5%是否会对疼痛强度产生影响,并且在咳嗽(初级终点)对吗啡消费中的咳嗽(初级终点),对呼吸功能的恢复以及测量外周疼痛途径使用N2和P2激光诱发电位(次要终点)。共有90例患者随机分配到Lidocaine组和45名患者中。利多卡因与安慰剂组相比,休息(P?= 0.013)和咳嗽后的疼痛强度显着降低(p?= 0.015),并且总体吗啡消耗(p?= 0.001);并且还显示出更好地恢复流量呼气量在一个?第二(p?= 0.025)和强制生命能力(p?= 0.037)。与利多卡因组相比,安慰剂组提出了N 2(P?= 0.001)和P2(p≤X.03)的幅度的降低,并增加了N2的潜伏量(p?= 0.023)和P2( P?=?0.025)激光诱发电位。具有利多卡因补丁的预防性皮肤镇痛5%似乎是静脉内吗啡镇痛的有效辅助,用于控制后胸胸部疼痛。但是,我们的初步结果应通过更大的研究证实/确认。 ? 2019年的作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号