Zhou Yang, Yang Tu-Bao, Wei Jie, Zeng Chao, Li Hui, Yang Tuo, Lei Guang-Hua
Department of Social Medicine, School of Public Health, Central South University, Changsha, 410008, Hunan Province, China.
Department of Orthopaedics, Xiangya Hospital, Central South University, #87 Xiangya Road, Changsha, 410008, Hunan Province, China.
Knee Surg Sports Traumatol Arthrosc. 2016 May;24(5):1651-9. doi: 10.1007/s00167-015-3656-y. Epub 2015 Jun 7.
PURPOSE: The purpose of this study was to appraise the efficacy and safety of single-dose intra-articular ropivacaine administered for pain relief after arthroscopic knee surgery. METHODS: PubMed, Embase, and Cochrane Library databases were searched in October 2014 to identify randomized controlled trials of single-dose intra-articular ropivacaine for post-operative pain relief. Post-operative pain intensity, the amount of rescue analgesia required, and side effects including local anaesthetic toxicity were assessed. The relative risk (RR), the weighted mean difference (WMD), and their corresponding 95 % confidence intervals (CIs) were calculated. RESULTS: Eight randomized controlled trials were included in the analysis. Statistically significant differences in the visual analogue scale for pain intensity value were observed during the immediate post-operative period (WMD -10.35, 95 % CI -17.12 to -3.59, p = 0.003) and the early post-operative period (WMD -11.90, 95 % CI -18.12 to -5.69, p = 0.0002), but not during the late post-operative period (WMD -2.89, 95 % CI -7.46 to 1.68, n.s.). There was no significant difference in the amount of rescue analgesia required (RR 0.76, 95 % CI 0.52-1.11, n.s.). Only two trials reported the incidence of drug-related side effects (including nausea and vomiting): the incidence in the ropivacaine groups was no higher than that in the control groups. Only one trial assessed local anaesthetic toxicity as an outcome, but it was not detected. CONCLUSIONS: Single-dose intra-articular ropivacaine administered at the end of arthroscopic knee surgery provides effective pain relief in the immediate and early post-operative periods without increasing short-term side effects.
目的:本研究旨在评估单剂量关节腔内注射罗哌卡因用于膝关节镜手术后镇痛的疗效和安全性。 方法:2014年10月检索了PubMed、Embase和Cochrane图书馆数据库,以确定单剂量关节腔内注射罗哌卡因用于术后镇痛的随机对照试验。评估术后疼痛强度、所需的补救性镇痛量以及包括局部麻醉药毒性在内的副作用。计算相对风险(RR)、加权平均差(WMD)及其相应的95%置信区间(CI)。 结果:八项随机对照试验纳入分析。术后即刻(WMD -10.35,95%CI -17.12至-3.59,p = 0.003)和术后早期(WMD -11.90,95%CI -18.12至-5.69,p = 0.0002)疼痛强度视觉模拟量表有统计学显著差异,但术后晚期无差异(WMD -2.89,95%CI -7.46至1.68,无统计学意义)。所需的补救性镇痛量无显著差异(RR 0.76,95%CI 0.52 - 1.11,无统计学意义)。仅两项试验报告了药物相关副作用(包括恶心和呕吐)的发生率:罗哌卡因组的发生率不高于对照组。仅一项试验将局部麻醉药毒性作为结果进行评估,但未检测到。 结论:膝关节镜手术结束时单剂量关节腔内注射罗哌卡因在术后即刻和早期能有效镇痛,且不增加短期副作用。
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