Midfoot Arthrodesis after Failed Lisfranc Open Reduction and Internal Fixation.

IF 1.6 3区 医学 Q3 ORTHOPEDICS
Megan L Campbell, Oliver C Sroka, Tyler Thorne, Anne Hakim, Matthew J Siebert, Justin M Haller, Lucas S Marchand
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引用次数: 0

Abstract

Objectives: To determine the incidence and risk factors for secondary arthrodesis (SA) and compare patients who underwent primary arthrodesis (PA) versus SA following ORIF for Lisfranc injuries.

Methods: Design : Retrospective cohort.

Setting: Single tertiary level 1 trauma center.

Patient selection criteria: Adult patients treated surgically for Lisfranc injuries AO/OTA 85.1A-C +/- 85.2.A-C, 85.3A-C; 87.1.1A-C-87.5.1A-C; 89B) between 2003-2023 were included.

Outcome measures and comparisons: Patients who underwent index PA were compared to those who underwent index ORIF and subsequent SA. A composite primary outcome was used for comparison which included the development of adjacent midfoot arthrosis, midfoot collapse, or mal/nonunion rated satisfactory, suboptimal, poor, or severe; secondary outcomes were PROMIS measures of physical function (PF) and pain interference (PI). Descriptive and comparative statistics, multivariable analysis, and logistic regression were utilized to compare groups.

Results: Of 489 Lisfranc injuries (482 patients), index treatment for 98 (20%) was PA. Average age was 37.7y (SD 15.6); mean follow up was 2.3y (SD 8.8). Fifty six percent of patients were men. There were thirty-four SAs (8.7% of index ORIF group). Patients who underwent SA were more likely to develop a poor (21.9% vs. 6.5% p=0.021) or severe outcome (12.5% vs. 1.1%, p=0.015) compared to those who underwent PA (OR 5.1, CI 1.4-18.5; OR 12.7, CI 1.1-12.8). Patients requiring SA also had significantly higher PI and significantly lower PF at final follow-up (p=0.018, p<0.001). Divergent injuries had higher odds of needing a SA compared to homolateral injuries (OR 6.9, p=0.006), as did index treatment with a tightrope (OR 4.6, p=0.003).

Conclusions: Nine percent of patients underwent SA after index ORIF of their Lisfranc injury, and outcomes fared substantially worse than those treated with PA. This emphasizes the importance of identifying risk factors for patients that may fail ORIF. Further work is needed to clearly delineate which patients may best be served with PA.

Level of evidence: Level 3.

Lisfranc切开复位和内固定失败后的中足关节融合术。
目的:确定继发性关节融合术(SA)的发生率和危险因素,并比较Lisfranc损伤ORIF后接受原发性关节融合术(PA)和SA的患者。方法:设计:回顾性队列。地点:单一三级创伤中心。患者选择标准:手术治疗Lisfranc损伤的成人患者AO/OTA 85.1A-C +/- 85.2。得了,得了85.3;87.1.1A-C-87.5.1A-C;(89B) 2003-2023年期间。结果测量和比较:将接受指数PA的患者与接受指数ORIF和随后的SA的患者进行比较。采用复合主要结局进行比较,包括相邻足中部关节的发展、足中部塌陷或畸形/不愈合分为满意、次优、差或严重;次要结果是PROMIS测量的身体功能(PF)和疼痛干扰(PI)。采用描述性和比较统计、多变量分析和逻辑回归进行组间比较。结果:489例Lisfranc损伤(482例)中,98例(20%)采用PA治疗。平均年龄37.7岁(SD 15.6);平均随访时间为2.3y (SD 8.8)。56%的患者是男性。SAs 34例(占指数ORIF组的8.7%)。与接受PA的患者相比,接受SA的患者更有可能发生不良(21.9%对6.5% p=0.021)或严重的结果(12.5%对1.1%,p=0.015) (or 5.1, CI 1.4-18.5;或12.7,ci 1.1-12.8)。在最终随访时,需要SA的患者PI也显著升高,PF显著降低(p=0.018, p)。结论:9%的患者在Lisfranc损伤指数ORIF后接受SA治疗,其结果明显差于接受PA治疗的患者。这强调了识别可能导致ORIF失败的风险因素的重要性。需要进一步的工作来明确哪些患者最好接受PA治疗。证据等级:三级。
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来源期刊
Journal of Orthopaedic Trauma
Journal of Orthopaedic Trauma 医学-运动科学
CiteScore
3.90
自引率
8.70%
发文量
396
审稿时长
3-8 weeks
期刊介绍: Journal of Orthopaedic Trauma is devoted exclusively to the diagnosis and management of hard and soft tissue trauma, including injuries to bone, muscle, ligament, and tendons, as well as spinal cord injuries. Under the guidance of a distinguished international board of editors, the journal provides the most current information on diagnostic techniques, new and improved surgical instruments and procedures, surgical implants and prosthetic devices, bioplastics and biometals; and physical therapy and rehabilitation.
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