膝关节损伤初次关节固定术与二次关节固定术后的功能效果和患者满意度:采用单一手术方法。

Foot & ankle international Pub Date : 2025-01-01 Epub Date: 2024-11-06 DOI:10.1177/10711007241288853
Esmee Wilhelmina Maria Engelmann, Jens Anthony Halm, Tim Schepers
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引用次数: 0

摘要

背景:在治疗急性Lisfranc损伤时,如何在初次关节固定术(PA)和开放复位内固定术(ORIF)之间做出选择仍存在争议。除初次治疗外,关节固定术还经常用于治疗慢性Lisfranc损伤,包括初次ORIF或非手术治疗失败的患者。本研究旨在比较 PA 和二次关节置换术(SA)的并发症和功能结果:方法:对 2010 年 7 月 1 日至 2020 年 7 月 1 日期间在一级创伤中心接受治疗的 Lisfranc 损伤创伤患者进行了一项回顾性队列研究。部分患者在门诊接受了评估并接受了调查。对人口统计学、损伤特征、处理、并发症和患者报告结果(美国骨科足踝协会中足评分、足部功能指数)进行了分析:37名潜在患者中有29名(78.4%;PA n = 11,SA n = 18)完成了调查,中位随访时间为7.1年(PA)至9.3年(SA)(P = .01)。大多数患者为女性(n = 18,62.1%);PA 患者的平均年龄为 57.1 岁(SD 14.2),而 SA 患者的平均年龄为 43.5 岁(SD 17.1)(P = .04)。在 PA 组中,11 位患者中的 5 位没有发生感染,100% 植体结合,植体被移除。在 SA 组中,11.1%(n = 2)的患者发生了感染,不良结合率为 11.1%,33.3%(n = 6)的患者移除了植入物,22.2% 的患者需要进行翻修手术。PA 的 AOFAS 为 "良好"(77.7,SD 17.3),SA 为 "一般"(67.1,SD 21.3,P = .19)。PA 的 FFI(26.0,SD 26.2)优于 SA(37.6,SD 30.8,P = .32),超过了最小重要临床差异:结论:虽然这项研究受到样本量的限制,但总体结果表明,与二次关节置换术相比,一次关节置换术治疗 Lisfranc 损伤患者的功能结果、疼痛和治疗满意度相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional Outcome and Patient Satisfaction After Primary vs Secondary Arthrodesis for Lisfranc Injuries: Toward a Single-Surgery Approach.

Background: The choice between primary arthrodesis (PA) and open reduction and internal fixation (ORIF) for acute Lisfranc injuries remains contentious. Apart from primary treatment, arthrodesis is often used for treating chronic Lisfranc injuries, including patients in whom initial ORIF or nonoperative treatment failed. The aim of this study was to compare PA and secondary arthrodesis (SA) in terms of complications and functional outcome.

Methods: A retrospective cohort study was conducted on trauma patients with Lisfranc injuries treated at a level 1 trauma center between July 1, 2010, and July 1, 2020. Selected patients were evaluated at the outpatient clinic and received a survey. Demographics, injury characteristics, management, complications, and patient-reported outcomes (American Orthopaedic Foot & Ankle Society midfoot score, Foot Function Index) were analyzed.

Results: Twenty-nine of 37 potential patients (78.4%; PA n = 11, SA n = 18) completed the survey with a median follow-up of 7.1 (PA) to 9.3 (SA) years (P = .01). The majority were female (n = 18, 62.1%); the mean age of PA patients was 57.1 years (SD 14.2) compared with 43.5 years (SD 17.1) in SA patients (P = .04). In the PA group, there was no infection, 100% union, and implants were removed in 5 of 11 patients. In the SA group, 11.1% (n = 2) developed infection, malunion rate was 11.1%, implants were removed in 33.3% (n = 6), and 22.2% required revision surgery. AOFAS was "good" in PA (77.7, SD 17.3) compared with rated "fair" in SA (67.1, SD 21.3, P = .19). FFI was better in PA (26.0, SD 26.2) than SA (37.6, SD 30.8, P = .32), which exceeded the minimally important clinical difference.

Conclusion: Although this study was limited by sample size, the overall results suggest equivalent functional outcome, pain and treatment satisfaction in primary arthrodesis compared with secondary arthrodesis patients for treatment of Lisfranc injury.

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