Dexamethasone as an additive to bupivacaine in an ultrasound-guided adductor canal block for the management of persistent pain after arthroscopic reconstruction of the anterior cruciate ligament: a randomized, double-blind study.

IF 2.3 3区 医学 Q2 ANESTHESIOLOGY
Saeid Elsawy, Amani Abdelwahab, Yara Hamdi, Rasha Ahmed Ali Hamed
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Abstract

Background: Pain is a protective response to noxious stimuli to prevent further damage. The surgical incision results in several events that lead to pain that outlasts its benefits. Persistent postsurgical pain (PPSP) is defined as "pain that persists for three months after surgical intervention.

Objectives: To investigate the effect of dexamethasone as an adjuvant to adductor canal block on persistent postsurgical pain after ACL reconstruction.

Patients and methods: Ninety patients who underwent arthroscopic reconstruction of the anterior cruciate ligament and who completed the study were randomly allocated into two groups. Forty-five patients in each group received ultrasound-guided adductor canal block at the end of surgery. G I (Dexa group): Forty-five patients received a 20 ml mixture of 0.25% bupivacaine and 8 mg dexamethasone (2 ml). G II (control group): Patients received a 20 ml mixture of 0.25% bupivacaine and 2 ml of normal saline.

Results: No significant differences in demographic data, intraoperative hemodynamics or surgery duration were detected between the two groups. The duration of postoperative analgesia was significantly longer in the dexamethasone group (10 h ± 3 vs. 6 h ± 1) than in the control group. Additionally, 24 h postoperative consumption of meperidine was significantly lower in the dexamethasone group (65 ± 23 vs. 104 ± 27) than in the control group. Postoperative VAS scores at 6 and 12 h were also lower in the dexamethasone group than in the control group. Three-month follow-up revealed a significantly lower incidence of PPSP in the dexamethasone group (20% versus 33% in the control group). Moreover, the severity of PPSP was significantly lower in the dexamethasone group than in the control group. Additionally, Codeine consumption was significantly lower in the dexamethasone group than in the control group.

Conclusion: Perineural dexamethasone in ultrasound-guided adductor canal block reduced the severity of PPSP and opioid analgesia consumption in the first three months following arthroscopic reconstruction of the ACL.

Clinical trial registration: The study was registered on clinical trial registration (NCT04631822) in October 2020.

地塞米松加布比卡因在超声引导下内收管阻滞治疗关节镜下前交叉韧带重建后持续性疼痛:一项随机双盲研究
背景:疼痛是对有害刺激的一种保护性反应,以防止进一步的损害。手术切口会导致一些事件,这些事件导致的疼痛超过了手术的益处。持续性术后疼痛(PPSP)被定义为“手术干预后持续三个月的疼痛”。目的:探讨地塞米松辅助内收管阻滞治疗前交叉韧带重建术后持续性疼痛的效果。患者和方法:90例接受关节镜下前交叉韧带重建并完成研究的患者随机分为两组。每组45例患者术后行超声引导下内收管阻滞。G I(地塞米松组):45例患者给予0.25%布比卡因+地塞米松8mg (2ml)的混合物20ml。G组(对照组):患者给予0.25%布比卡因和生理盐水混合20 ml。结果:两组在人口学数据、术中血流动力学和手术时间方面无显著差异。地塞米松组术后镇痛时间(10 h±3比6 h±1)明显长于对照组。此外,地塞米松组术后24 h哌替啶用量(65±23比104±27)明显低于对照组。地塞米松组术后6、12 h VAS评分也低于对照组。三个月的随访显示,地塞米松组PPSP发生率显著降低(20%,对照组33%)。此外,地塞米松组PPSP的严重程度明显低于对照组。此外,地塞米松组的可待因消耗量明显低于对照组。结论:超声引导下内收管阻滞术中应用神经周围地塞米松可降低关节镜下前交叉韧带重建术后前三个月PPSP的严重程度和阿片类镇痛药物的消耗。临床试验注册:本研究已于2020年10月进行临床试验注册(NCT04631822)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Anesthesiology
BMC Anesthesiology ANESTHESIOLOGY-
CiteScore
3.50
自引率
4.50%
发文量
349
审稿时长
>12 weeks
期刊介绍: BMC Anesthesiology is an open access, peer-reviewed journal that considers articles on all aspects of anesthesiology, critical care, perioperative care and pain management, including clinical and experimental research into anesthetic mechanisms, administration and efficacy, technology and monitoring, and associated economic issues.
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