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Correction and Prevention of Deformity in Type II Tibialis Posterior Dysfunction

机译:Ⅱ型胫骨后功能障碍的畸形矫正和预防

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摘要

Cobb described a method of reconstruction in Johnson and Strom Type II tibialis posterior dysfunction (TPD) using a split tibialis anterior musculotendinous graft. We assessed patient function and satisfaction after a modified Cobb reconstruction in a group of patients with a narrow spectrum of dysfunction, examined a modification of the Johnson and Strom classification to emphasize severity of deformity, and assessed the ability of the technique to prevent subsequent fixed deformity. We prospectively followed 32 patients managed by this technique and a translational os calcis osteotomy with early flexible deformity after failed conservative treatment. There were 28 women and four men with unilateral disease. The average followup was 5.1 years. Staging was confirmed clinically and with imaging. The modified surgery involved a bone tunnel in the navicular rather than the medial cuneiform with plaster for 8 weeks followed by orthotics and physiotherapy. All of the osteotomies healed and 29 of the 32 patients could perform a single heel rise test at 12 months. The mean postoperative American Orthopaedic Foot and Ankle Society hindfoot score was 89. One patient had a superficial wound infection and one a temporary dysesthesia of the medial plantar nerve; both resolved. The observations suggest the technique is a comparable method of treating early Johnson and Strom Type II TPD.>Level of Evidence: Level IV, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.
机译:Cobb描述了一种使用拆分后的胫骨前肌腱移植物重建Johnson和Strom II型胫骨后功能障碍(TPD)的方法。我们对一组功能障碍狭窄的患者进行改良Cobb重建后评估了患者的功能和满意度,检查了Johnson和Strom分类的改进以强调畸形的严重性,并评估了该技术预防随后发生的固定畸形的能力。我们前瞻性地追踪了32例接受此技术和保守治疗失败后的早期弹性畸形的平直型输尿管结石截骨术的患者。有28名妇女和4名男子患有单方面疾病。平均随访时间为5.1年。临床和影像学证实了分期。改良后的手术需要在石膏骨沟而不是内侧楔形骨上进行8周的矫正和物理治疗。所有截骨术均已治愈,在32例患者中有29例可以在12个月进行一次脚跟抬起测试。术后美国矫形足踝学会后足平均评分为89。1例患者有浅表伤口感染,1例为a内侧神经暂时性感觉异常。都解决了。观察结果表明该技术是治疗早期Johnson和Strom II型TPD的可比方法。>证据级别: IV级,治疗研究。有关证据水平的完整说明,请参见《作者指南》。

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