A novel flexible fixation technique for Lisfranc injuries: clinical outcomes and radiographic follow-up

Eitan M. Ingall, F. Raduan, John Y. Kwon
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Abstract

Objectives: The purpose of this investigation is to present the follow-up results and patient-reported outcome measures (PROMs) of a continuous series of surgically managed Lisfranc injuries whose constructs included a novel technique. Methods: Our billing database was retrospectively queried by Current Procedural Terminology (CPT) codes to identify all Lisfranc injuries managed operatively between 2018 and 2021. Basic demographic data were collected. Clinical notes and radiographs were reviewed. Patients were contacted prospectively to complete the Foot and Ankle Ability Measurement – Activities of Daily Living (FAAM-ADL), Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity, PROMIS Pain Interference, and PROMIS Depression surveys. Descriptive statistics were calculated. Results: Sixteen patients were included. While all patients underwent flexible fixation (FF), nine of them underwent concomitant open reduction internal fixation (ORIF) and seven, concomitant primary arthrodesis. Median radiographic and PROMs follow-up time was 7.3 months (IQR 4.4–11.6) and 25.8 (IQR 9.5–32.4), respectively. All fusion patients had evidence of joint fusion, and 8/9 of ORIF patients maintained articular congruity without evidence of arthritis at final follow-up. Median PROMs were 85 (64.75–93.5), 53.1 (49.7–57.75), 45.7 (37.7–51.3), and 46 (43.3–52.28) for the FAAM-ADL, PROMIS Pain Interference, PROMIS Pain Intensity, and PROMIS Depression scores, respectively. Conclusion: The novel FF technique proposed for residual tarsometatarsal subluxation in Lisfranc injuries appears to be safe and effective, with good PROMs at two-year follow-up and low complication rates, obviating the need for hardware removal. Level of Evidence IV; Therapeutics Studies; Cases Series.
用于治疗 Lisfranc 损伤的新型柔性固定技术:临床疗效和影像学随访
研究目的本研究的目的是介绍一系列连续手术治疗的 Lisfranc 损伤的随访结果和患者报告的结果指标(PROMs),这些损伤的构建包括一项新技术。研究方法通过当前程序术语(CPT)代码对我们的账单数据库进行回顾性查询,以确定 2018 年至 2021 年期间所有经手术治疗的 Lisfranc 损伤。收集了基本人口统计学数据。对临床笔记和X光片进行了审查。前瞻性地联系了患者,让他们完成足踝能力测量-日常生活活动(FAAM-ADL)、患者报告结果测量信息系统(PROMIS)疼痛强度、PROMIS疼痛干扰和PROMIS抑郁调查。计算了描述性统计数字。结果共纳入 16 名患者。所有患者均接受了柔性固定术(FF),其中九人同时接受了开放复位内固定术(ORIF),七人同时接受了原发性关节固定术。中位X光片和PROMs随访时间分别为7.3个月(IQR 4.4-11.6)和25.8个月(IQR 9.5-32.4)。所有融合患者都有关节融合的证据,8/9 的 ORIF 患者在最终随访时保持了关节的一致性,没有关节炎的证据。FAAM-ADL、PROMIS疼痛干扰、PROMIS疼痛强度和PROMIS抑郁评分的PROM中位数分别为85(64.75-93.5)、53.1(49.7-57.75)、45.7(37.7-51.3)和46(43.3-52.28)。结论针对 Lisfranc 损伤中的残余跖跗关节脱位提出的新型 FF 技术似乎是安全有效的,在两年的随访中具有良好的 PROMs 和较低的并发症发生率,从而避免了拆除硬件的需要。证据等级 IV;治疗研究;病例系列。
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