Department of Orthopedic Surgery, Henry Ford Hospital, Detroit, MI.
J Arthroplasty. 2020 Jun;35(6S):S241-S245. doi: 10.1016/j.arth.2020.02.020. Epub 2020 Feb 14.
The purpose of this randomized controlled trial is to identify if a fascia iliaca block reduces postoperative pain and narcotic consumption and improves early functional outcomes in primary total hip arthroplasty (THA) performed through the mini-posterior approach.
Patients were recruited from September 2017 to September 2019. Eligible patients received a primary THA using a mini-posterior approach with epidural anesthesia. Postoperatively, patients were randomized to receive a fascia iliaca compartment block or a placebo block. Numeric Rating Scale pain scores, narcotic consumption, and functional outcomes were recorded at regular intervals postoperatively.
Upon study completion, 122 patients were available for final analysis. There was no difference in the average pain scores at any time interval between the placebo and block groups during the first 24 hours (P = .21-.99). There was no difference in the morphine equivalents consumed between the groups during any time interval postoperatively (P = .06-.95). Functional testing showed no difference in regards to distance walked during the first therapy session (67.1 vs 68.3 ft., P = .92) and timed-up-and-go testing (63.7 vs 66.3 seconds, P = .86). There was an increased incidence of quadriceps weakness in the block group (22% vs 0%, P = .004) requiring alterations in therapy protocols.
This randomized trial shows that a fascia iliaca compartment block does not improve functional performance and does not decrease pain levels or narcotic usage after mini-posterior THA, but does increase the risk of quadriceps weakness postoperatively. Based on these results we do not recommend routine fascia iliaca compartment blocks after THA performed with the mini-posterior approach.
本随机对照试验的目的是确定在经迷你后外侧入路行初次全髋关节置换术(THA)时,股外侧肌筋膜室阻滞是否能减轻术后疼痛、减少阿片类药物用量并改善早期功能结果。
本研究于 2017 年 9 月至 2019 年 9 月期间招募患者。纳入的患者接受经迷你后外侧入路联合硬膜外麻醉行初次 THA。术后,患者随机接受股外侧肌筋膜室阻滞或安慰剂阻滞。术后定期记录数字评分法(NRS)疼痛评分、阿片类药物用量和功能结果。
研究完成时,122 例患者可进行最终分析。在术后 24 小时内的任何时间点,安慰剂组和阻滞组的平均疼痛评分均无差异(P 值为 0.21-0.99)。两组在术后任何时间点的吗啡等效消耗量均无差异(P 值为 0.06-0.95)。功能测试显示,在首次治疗期间的行走距离(67.1 英尺对 68.3 英尺,P 值为 0.92)和起立-行走测试(63.7 秒对 66.3 秒,P 值为 0.86)方面,两组之间无差异。阻滞组的股四头肌无力发生率更高(22%对 0%,P 值为 0.004),需要改变治疗方案。
本随机试验表明,在经迷你后外侧入路行初次 THA 后,股外侧肌筋膜室阻滞不能改善功能表现,不能降低疼痛程度或阿片类药物用量,但会增加术后股四头肌无力的风险。基于这些结果,我们不建议在经迷你后外侧入路行初次 THA 后常规行股外侧肌筋膜室阻滞。