评估全膝关节置换术后的功能结果和疼痛强度变化:疼痛阻滞技术的比较分析。

IF 2 Q2 ORTHOPEDICS
Mor Kliger-Tendler, Michal Elboim-Gabyzon, Einal Bathish, Haim Shtarker
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引用次数: 0

摘要

目的:本研究旨在比较股骨神经阻滞(FNB)、关节内阻滞和对照组在全膝关节置换术(TKA)后的结果(功能、疼痛和股四头肌力量)。此外,它还试图确定术后功能能力的预测因素。方法:对54例TKA患者进行评价。术前评估包括股四头肌力量和牛津膝关节评分。术后第1天和第3/4天的评估包括计时起走(TUG)、老年人活动能力量表和5次坐立测试。同时记录疼痛程度、住院时间、手术时间、并发症和跌倒情况。结果:FNB组、关节内阻滞组和对照组在功能结局、疼痛水平或股四头肌力量方面均无显著差异,但第3/4天的TUG测试显示FNB组更有利(P < 0.01)。术前股四头肌力量是早期功能结局的重要预测指标,FNB可改善第3/4天的TUG评分。讨论:疼痛阻滞技术的选择对tka后的短期功能结果影响有限,除了在第3/4天通过TUG测试测量的早期活动能力。术前股四头肌强度显著预测初始功能表现。需要进一步的研究来加强术后疼痛管理和早期康复策略。临床试验注册号:NCT05478005。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing Functional Outcomes and Pain Intensity Variations After Total Knee Arthroplasty: A Comparative Analysis of Pain Block Techniques.

Objective: This study aimed to compare post-total knee arthroplasty (TKA) outcomes (function, pain, and quadriceps strength) between femoral nerve block (FNB), intra-articular block, and a control group. In addition, it sought to identify predictors of postoperative functional capacity.

Methods: Fifty-four TKA patients were evaluated. Preoperative assessments included quadriceps strength and the Oxford knee score. Postoperative assessments on days 1 and 3/4 included the timed up and go (TUG), Elderly Mobility Scale, and Five Times Sit-to-Stand tests. Pain levels, hospitalization duration, surgical time, complications, and falls were also recorded.

Results: No significant differences in functional outcomes, pain levels, or quadriceps strength were found between the FNB, intra-articular block, and control groups, except for the TUG test on day 3/4, which favored FNB (P < 0.01). Preoperative quadriceps strength was a valuable predictor of early functional outcomes, with FNB improving TUG scores on day 3/4.

Discussion: The choice of pain block technique had limited effect on short-term functional outcomes post-TKA, except for early mobility as measured by the TUG test on day 3/4. Preoperative quadriceps strength markedly predicted initial functional performance. Additional research is needed to enhance postoperative pain management and early rehabilitation strategies.

Clinical trial registration number: NCT05478005.

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来源期刊
CiteScore
2.60
自引率
6.70%
发文量
282
审稿时长
8 weeks
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