Analgesic effect of local anesthesia in total knee arthroplasty: protocol of a randomized controlled clinical trial.

IF 1.1 Q3 SURGERY
International Journal of Surgery Protocols Pub Date : 2025-08-07 eCollection Date: 2025-09-01 DOI:10.1097/SP9.0000000000000056
Weilong Diwu, Wenhao Tang, Ming Yan, Wenrui Ma, Yisheng Han, Min Yang
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引用次数: 0

Abstract

Background: Postoperative pain management remains a critical determinant of functional recovery following total knee arthroplasty (TKA). While local infiltration analgesia (LIA) is commonly employed, its clinical utility is limited by inconsistent analgesic duration (median duration of 8-12 hours), technical variability among surgeons, and systemic toxicity risks associated with high-volume injections. This phase II randomized controlled trial evaluates a dual-optimization strategy combining anatomic mapping-guided periarticular cutaneous nerve (PCN) blockade with a sustained-release triamcinolone-ropivacaine formulation to address these limitations.

Method: In this single-center, assessor-blinded, 2 × 2 factorial design, 120 adults undergoing primary unilateral TKA were randomized to four intervention arms: Group 1: Conventional iPACK (interspace between the popliteal artery and posterior knee capsule) site + novel formulation (1% ropivacaine + 40 mg triamcinolone); Group 2: PCN block site + standard formulation (1% ropivacaine + 5 mg dexamethasone); Group 3: PCN block + novel formulation; Group 4: Control (iPACK + standard formulation). Triamcinolone acetonide replaces dexamethasone in the new formulation due to its prolonged anti-inflammatory effect and demonstrated efficacy in periarticular analgesia. Primary endpoints included: resting/movement-induced pain intensity (Visual Analog Scale) at 6, 24, and 48 h postoperatively, cumulative opioid consumption (morphine milligram equivalents), functional recovery metrics (knee flexion angle, Timed Up-and-Go test). Secondary outcomes assessed safety through adverse event rates (infection, neurologic symptoms, hemodynamic instability).

Conclusions: Anatomic mapping-guided PCN blockade combined with triamcinolone-ropivacaine formulation significantly improves postoperative analgesia and functional outcomes compared to conventional LIA techniques. This dual-optimization approach may redefine periarticular infiltration standards in TKA, particularly for patients at high risk of opioid-related complications.

全膝关节置换术中局部麻醉的镇痛效果:一项随机对照临床试验方案。
背景:术后疼痛管理仍然是全膝关节置换术(TKA)后功能恢复的关键决定因素。虽然局部浸润镇痛(LIA)是常用的方法,但其临床应用受到不一致的镇痛持续时间(中位持续时间为8-12小时)、外科医生的技术差异以及与大剂量注射相关的全身毒性风险的限制。这项II期随机对照试验评估了一种双重优化策略,结合解剖定位引导的关节周围皮神经(PCN)阻断和曲安奈德-罗哌卡因缓释制剂来解决这些局限性。方法:在这个单中心、评估盲、2 × 2因子设计中,120名接受原发性单侧TKA的成年人被随机分为四个干预组:1组:传统的iPACK(腘动脉和膝关节后囊之间的间隙)部位+新配方(1%罗哌卡因+ 40 mg曲安奈德);第二组:PCN阻滞部位+标准配方(1%罗哌卡因+ 5mg地塞米松);第三组:PCN块+新配方;第4组:对照组(iPACK +标准制剂)。曲安奈德取代地塞米松在新的配方,由于其持久的抗炎作用,并证明有效的关节周围镇痛。主要终点包括:术后6、24和48小时静置/运动引起的疼痛强度(视觉模拟量表),阿片类药物的累积消耗(吗啡毫克当量),功能恢复指标(膝关节屈曲角度,计时起-走测试)。次要结局通过不良事件发生率(感染、神经系统症状、血流动力学不稳定)评估安全性。结论:与传统的LIA技术相比,解剖定位引导的PCN阻断联合曲安奈德-罗哌卡因制剂显著改善了术后镇痛和功能结果。这种双重优化方法可能重新定义TKA的关节周浸润标准,特别是对于阿片类药物相关并发症高风险的患者。
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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期刊介绍: IJS Protocols is the first peer-reviewed, international, open access journal seeking to publish research protocols across across the full breadth of the surgical field. We are aim to provide rapid submission to decision times whilst maintaining a high quality peer-review process.
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