Ropivacaine for Continuous Wound Infusion for Postoperative Pain Management: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

被引:34
作者
Raines, Shane [1 ]
Hedlund, Cecilia [2 ]
Franzon, Malin [2 ]
Lillieborg, Stefan [2 ]
Kelleher, Glen [4 ]
Ahlen, Kjell [3 ]
机构
[1] AstraZeneca R&D, Dept Biometr & Informat Sci, Wilmington, DE USA
[2] AstraZeneca R&D, Dept Biometr & Informat Sci, Sodertalje, Sweden
[3] AstraZeneca R&D, Dept Med Sci, Sodertalje, Sweden
[4] AstraZeneca, Dept Med, N Ryde, NSW, Australia
关键词
Continuous wound infusion; Postoperative analgesia; Ropivacaine; Systematic review; PROVIDES EFFECTIVE ANALGESIA; LOCAL-ANESTHETICS; DOUBLE-BLIND; EFFICACY; INSTILLATION; SURGERY; BUPIVACAINE; INFILTRATION; PLACEBO; PHARMACOKINETICS;
D O I
10.1159/000363233
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: The use of continuous wound infusion (CWI) of local anaesthetics has been suggested as a safe and effective alternative technique to epidural anaesthesia/analgesia that allows surgeons to provide postoperative pain relief while reducing opioid consumption and associated adverse events. A previous meta-analysis by Liu et al. [Am Coll Surg 2006; 203: 914-932] reported results mainly from studies of bupivacaine. Subsequently, several new randomized controlled trials (RCTs) of ropivacaine have been published. This systematic review and quantitative meta-analysis evaluates the efficacy of ropivacaine for CWI. Methods: Systematic literature searches (EMBASE, MEDLINE) were performed to retrieve studies which met the following criteria: double-blind RCT of ropivacaine versus either placebo or an active comparator; use of ropivacaine solution without added active agents, and prohibition of other routine analgesics during the study period except rescue patient-controlled analgesia. For each included study, standardized effect sizes for ropivacaine versus placebo were calculated for opioid rescue use, pain score at rest, and pain score at mobilization. Meta-analyses were conducted for each endpoint. Results: Fourteen RCTs comparing ropivacaine (n = 376) versus placebo (n = 380) were identified. Effect size estimates revealed significantly less opioid rescue use for ropivacaine patients (-1.3; 95% CI -1.5 to -1.1) and significantly less pain for ropivacaine patients both at rest (-1.1; 95% CI -1.3 to -0.9) and on mobilization (-1.5; 95% CI -1.7 to -1.3). The weighted mean reduction in opioid rescue use was 22.4 mg. Conclusion: This systematic review and meta-analysis presents substantial evidence that ropivacaine provides clinically meaningful reductions in opioid use and pain outcomes. Ropivacaine CWI is effective for postoperative pain management in a wide range of surgical procedures. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:43 / 60
页数:18
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