Rozbruch S Robert, Zonshayn Samuel, Muthusamy Saravanaraja, Borst Eugene W, Fragomen Austin T, Nguyen Joseph T
Limb Lengthening and Complex Reconstruction Service, Department of Orthopaedic Surgery, Hospital for Special Surgery, Weill Cornell Medical College, Cornell University, 535 East 70th Street, New York, NY, 10021, USA,
Clin Orthop Relat Res. 2014 Dec;472(12):3842-51. doi: 10.1007/s11999-014-3526-9.
Tibial lengthening is frequently associated with gastrocsoleus contracture and some patients are treated surgically. However, the risk factors associated with gastrocsoleus contracture severe enough to warrant surgery during tibial lengthening and the consistency with which gastrocsoleus recession (GSR) results in a plantigrade foot in this setting have not been well defined.
QUESTIONS/PURPOSES: We compared patients treated with or without GSR during tibial lengthening with respect to (1) clinical risk factors triggering GSR use, (2) ROM gains and patient-reported outcomes, and (3) complications after GSR.
Between 2002 and 2011, 95 patients underwent tibial lengthenings excluding those associated with bone loss; 82 (83%) were available for a minimum followup of 1 year. According to our clinical algorithm, we performed GSR when patients had equinus contractures of greater than 10° while lengthening or greater than 0° before or after lengthening. Forty-one patients underwent GSR and 41 did not. Univariate analysis was performed to assess independent associations between surgical characteristics and likelihood of undergoing GSR. A multivariate regression model and receiver operating characteristic curves were generated to adjust for confounders and to establish risk factors and any threshold for undergoing GSR. Chart review determined ROM, patient-reported outcomes, and complications.
Amount and percentage of lengthening, age, and etiology were risk factors for GSR. Patients with lengthening of greater than 42 mm (odds ratio [OR]: 4.13; 95% CI: 1.82, 9.40; p = 0.001), lengthening of greater than 13% of lengthening (OR: 3.88; 95% CI: 1.66, 9.11; p = 0.001), and congenital etiology (OR: 1.90; 95% CI: 0.86, 4.15; p = 0.109) were more likely to undergo GSR. Adjusting for all other variables, increased amount lengthened (adjusted OR: 1.05; 95% CI: 1.02, 1.07; p < 0.001) and age (adjusted OR: 1.02; 95% CI: 0.99, 1.05; p = 0.131) were associated with undergoing GSR. Patients gained 24° of ankle dorsiflexion after GSR. Self-reported functional outcomes were similar between patients with or without GSR. Complications included stretch injury to the posterior tibial nerve leading to temporary and partial loss of plantar sensation in two patients.
Dorsiflexion was maintained and/or restored similarly among patients with or without GSR when treated under our algorithm. Functional compromise was not seen after GSR. Identification of patients at risk will help surgeons indicate patients for surgery. Acute dorsiflexion should be avoided to minimize risk of injury to the posterior tibial nerve.
Level IV, therapeutic study. See Instructions for Authors for a complete description of levels of evidence.
胫骨延长术常伴有小腿三头肌挛缩,部分患者需接受手术治疗。然而,胫骨延长过程中导致小腿三头肌挛缩严重到需要手术治疗的危险因素,以及在此情况下小腿三头肌松解术(GSR)使足部达到跖屈位的一致性,目前尚未明确。
问题/目的:我们比较了胫骨延长术期间接受或未接受GSR治疗的患者,涉及以下方面:(1)触发使用GSR的临床危险因素;(2)关节活动度增加情况及患者报告的结果;(3)GSR后的并发症。
2002年至2011年期间,95例患者接受了胫骨延长术(不包括与骨丢失相关的手术);82例(83%)患者获得了至少1年的随访。根据我们的临床方案,当患者在延长期间马蹄足挛缩大于10°,或在延长前或延长后大于0°时,我们进行GSR。41例患者接受了GSR,41例未接受。进行单因素分析以评估手术特征与接受GSR可能性之间的独立关联。生成多因素回归模型和受试者工作特征曲线,以调整混杂因素并确定接受GSR的危险因素及任何阈值。通过查阅病历确定关节活动度、患者报告的结果及并发症。
延长的量和百分比、年龄及病因是GSR的危险因素。延长超过42mm的患者(比值比[OR]:4.13;95%置信区间:1.82,9.40;p = 0.001)、延长超过延长量13%的患者(OR:3.88;95%置信区间:1.66,9.11;p = 0.001)以及先天性病因的患者(OR:1.90;95%置信区间:0.86,4.15;p = 0.109)更有可能接受GSR。在调整所有其他变量后,延长量增加(调整后OR:1.05;95%置信区间:1.02,1.07;p < 0.001)和年龄(调整后OR:1.02;95%置信区间:0.99,1.05;p = 0.131)与接受GSR相关。GSR后患者踝关节背屈增加24°。接受或未接受GSR的患者自我报告的功能结果相似。并发症包括2例患者胫后神经牵拉伤,导致足底感觉暂时部分丧失。
按照我们的方案进行治疗时,接受或未接受GSR的患者背屈维持和/或恢复情况相似。GSR后未出现功能损害。识别有风险的患者将有助于外科医生确定手术患者。应避免急性背屈,以尽量降低胫后神经损伤的风险。
IV级,治疗性研究。有关证据水平的完整描述,请参阅作者指南。