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Perioperative intravenous lidocaine infusion for postoperative pain control: a meta-analysis of randomized controlled trials.

机译:围手术期静脉利多卡因输注以控制术后疼痛:一项随机对照试验的荟萃分析。

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INTRODUCTION: Various strategies have been proposed for postoperative pain control. Among those, intravenous lidocaine infusion (IVLI) has gained in interest. However, its clinical benefit remains unclear. This systematic review is an evaluation of the analgesic efficacy and safety of IVLI during general anesthesia. METHODS: A systematic search was performed using MEDLINE, EMBASE, Cochrane, and SCOPUS databases, likewise, grey literature. The review included all randomized controlled trials that used a placebo or any comparator and evaluated IVLI during general anesthesia for any type of surgery. Primary outcomes were pain control and opioid requirement. Secondary outcomes were mortality, length of stay, ileus recovery time, nausea/vomiting, and adverse events. Random effects models were used and heterogeneity was assessed using the I2 index. RESULTS: From 5,472 citations retrieved, 29 studies involving a total of 1,754 patients met eligibility. At six hours postoperatively, intravenous lidocaine infusion reduced pain at rest (weighted mean difference [WMD]-8.70, 95% confidence intervals [CI] -16.19 to -1.21), during cough (WMD -11.19, 95% CI -17.73 to -4.65), and during movement (WMD -9.56, 95% CI -17.31 to-1.80). Intravenous lidocaine infusion also reduced opioid requirement (morphine) (WMD -8.44 mg, 95% CI -11.32 to -5.56), time to first flatus (WMD -7.62 hr, 95% CI-10.78 to -4.45), time to first feces (WMD -10.71 hr, 95% CI -16.14 to -5.28), nausea/vomiting (risk ratios = 0.71, 95% CI 0.57-0.90), and hospital length of stay (WMD -0.17 days, 95% CI -0.41 to 0.07). Abdominal surgery was strongly associated with benefit. For the 12 studies that systematically screened adverse events, the incidence of cardiac and neurologic adverse events was comparable. Eight studies observed toxic plasma levels. DISCUSSION: Perioperative IVLI reduced postoperative pain and opioid requirement, as well as ileus recovery time, hospital length of stay, and nausea/vomiting. Intravenous lidocaine infusion was effective mainly in abdominal surgery populations. Considering that toxic levels were detected and that adverse events were not systematically screened for in most studies, dose and safety of IVLI should be established before recommending its use.
机译:引言:已经提出了多种用于术后疼痛控制的策略。其中,利多卡因静脉输注(IVLI)引起了人们的兴趣。但是,其临床益处尚不清楚。该系统评价是对全身麻醉期间IVLI的镇痛效果和安全性的评估。方法:使用MEDLINE,EMBASE,Cochrane和SCOPUS数据库以及灰色文献进行系统的搜索。该评价包括所有使用安慰剂或任何比较剂并在全身麻醉期间对任何类型的手术进行IVLI评估的随机对照试验。主要结果是控制疼痛和阿片类药物需求。次要结果是死亡率,住院时间,肠梗阻恢复时间,恶心/呕吐和不良事件。使用随机效应模型,并使用I2指数评估异质性。结果:从检索到的5472篇文献中,有29项研究(总计1754例患者)符合资格。术后六小时,静脉注射利多卡因可减轻咳嗽时的静息疼痛(加权平均差异[WMD] -8.70,95%置信区间[CI] -16.19至-1.21),WMD -11.19,95%CI -17.73至- 4.65)和运动期间(WMD -9.56,95%CI -17.31 to-1.80)。静脉注射利多卡因还减少了阿片类药物的需求量(吗啡)(WMD -8.44 mg,95%CI -11.32至-5.56),首次肠胃胀气的时间(WMD -7.62 hr,95%CI-10.78至-4.45),首次粪便的时间(WMD -10.71小时,95%CI -16.14至-5.28),恶心/呕吐(风险比= 0.71,95%CI 0.57-0.90),以及住院时间(WMD -0.17天,95%CI -0.41至0.07)。腹部手术与获益密切相关。对于系统筛选不良事件的12项研究,心脏和神经系统不良事件的发生率具有可比性。八项研究观察到有毒血浆水平。讨论:围手术期IVLI减少了术后疼痛和阿片类药物需求,以及肠梗阻恢复时间,住院时间和恶心/呕吐。静脉注射利多卡因主要在腹部手术人群中有效。考虑到在大多数研究中都检测到了毒性水平并且没有系统筛查不良事件,因此在建议使用IVLI之前应确定其剂量和安全性。

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