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拇外翻手术后持续性伤口浸润。

Continuous Wound Infiltration After Hallux Valgus Surgery.

机构信息

1 Department of Orthopedic Surgery, Medical University of Innsbruck, Innsbruck, Austria.

2 Department of Anesthesiology and Critical Care, Medical University of Innsbruck, Innsbruck, Austria.

出版信息

Foot Ankle Int. 2018 Feb;39(2):180-188. doi: 10.1177/1071100717736292. Epub 2017 Oct 27.

Abstract

BACKGROUND

Hallux valgus surgery is associated with significant early postoperative pain. The aim of this study was to investigate the use of continuous wound infiltration (CWI) with ropivacaine for pain management after hallux valgus surgery.

METHODS

In this prospective, randomized, double-blind, and placebo-controlled single-center trial, 50 patients undergoing distal metatarsal osteotomy for idiopathic hallux valgus were allocated to CWI with ropivacaine 2 mg/mL at a rate of 2 mL/h or placebo for 24 hours postoperatively. Average and peak pain levels on the verbal numeric rating scale (NRS; 1-10) during the first 48 hours after surgery were recorded as primary outcome parameters. Secondary outcome parameters included consumption of narcotics, clinical outcome, incidence of postoperative complications, and patient satisfaction.

RESULTS

No significant difference in mean ( P = .596) and peak ( P = .353) postoperative pain level was found for CWI with either ropivacaine (mean NRS 1.9 ± 0.8; peak NRS 3.5 ± 2.0) or placebo (mean NRS 2.0 ± 0.7; peak NRS 3.9 ± 1.7) during the early postoperative course. Furthermore, no significant difference between both groups was detected regarding narcotic consumption ( P = .354) and all other secondary outcome parameters. Two severe complications (local dysesthesia with CWI, catheter accidentally fixed by a suture) and 5 catheter dislocations were observed.

CONCLUSION

CWI with ropivacaine 2 mg/mL at a rate of 2 mL/h for 24 hours after hallux valgus surgery did not reduce postoperative pain level in an inpatient setting.

LEVEL OF EVIDENCE

Level I, prospective randomized trial.

摘要

背景

拇外翻手术后会出现明显的早期术后疼痛。本研究旨在探讨罗哌卡因持续切口浸润(CWI)在拇外翻手术后疼痛管理中的应用。

方法

在这项前瞻性、随机、双盲、安慰剂对照的单中心试验中,50 例行远端跖骨切开术治疗特发性拇外翻的患者被分配到术后 24 小时内以 2 mL/h 的速度接受 2 mg/mL 罗哌卡因的 CWI 或安慰剂。记录术后前 48 小时内数字评分量表(NRS;1-10)的平均和峰值疼痛水平作为主要结局参数。次要结局参数包括阿片类药物的消耗、临床结果、术后并发症的发生率和患者满意度。

结果

在 CWI 罗哌卡因组(平均 NRS 1.9 ± 0.8;峰值 NRS 3.5 ± 2.0)和安慰剂组(平均 NRS 2.0 ± 0.7;峰值 NRS 3.9 ± 1.7)中,术后早期的平均(P =.596)和峰值(P =.353)疼痛水平没有显著差异。此外,两组之间在阿片类药物消耗(P =.354)和所有其他次要结局参数方面也没有显著差异。观察到 2 例严重并发症(CWI 局部感觉异常,导管意外被缝线固定)和 5 例导管脱位。

结论

在住院环境下,拇外翻手术后以 2 mL/h 的速度持续输注 2 mg/mL 罗哌卡因 24 小时并不能降低术后疼痛水平。

证据等级

I 级,前瞻性随机试验。

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