Preventing of nonunion in congenital pseudarthrosis of the tibia cases of Crawford Type I and II through the use of allograft bypass and a brace: Midterm findings
Chao Dong, Chengxiang Li, Ute Brückner, Hermann Hellmich, A. Krieg
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引用次数: 0
Abstract
Congenital pseudarthrosis of the tibia is a limb deformity, which can be distressing for the affected patients and the pediatric orthopedic surgeons involved. We hypothesized that the modified McFarland procedure would avoid fractures and even have a corrective effect on the affected tibia in congenital pseudarthrosis of the tibia patients. Toward this end, we evaluated the midterm results of treating congenital pseudarthrosis of the tibia patients of Crawford Type I and II with allograft bypass combined with long-term bracing. This study retrospectively evaluated 7 patients with congenital pseudarthrosis of the tibia who were treated with allograft bypass combined with long-term bracing between 2009 and 2018. The median follow-up was 7.0 years (range 3.8–10.0 years). The medical records and radiographs were reviewed for demographic data, clinical characteristics, outcomes, and complications. At the time of the last follow-up, all allografts revealed complete consolidation in the patients’ tibiae at both ends. All patients presented no functional restriction of the lower limbs and no amputation or non-union has occurred. Most of the obvious deformities of the tibia diaphysis or ankle joint were corrected. Two complications occurred that required successful revision surgery. In this series of seven congenital pseudarthrosis of the tibia patients, the allograft bypass technique showed satisfactory midterm results and validated our hypothesis. For congenital pseudarthrosis of the tibia patients of Crawford Type I and II, this procedure combined with long-term bracing, which involves the affected leg only, can delay or possibly prevent fractures, decrease tibial malalignment, and preserve leg length. level IV.
通过使用同种异体移植旁路和支架,防止克劳福德 I 型和 II 型先天性胫骨假关节的不愈合:中期研究结果
先天性胫骨假关节是一种肢体畸形,会给患者和小儿骨科医生带来痛苦。我们假设改良麦克法兰手术可以避免骨折,甚至对先天性胫骨假关节患者受影响的胫骨有矫正作用。为此,我们评估了对克劳福德 I 型和 II 型先天性胫骨假关节患者进行同种异体移植旁路术联合长期支具治疗的中期效果。本研究回顾性评估了2009年至2018年间接受异体移植搭桥术联合长期支具治疗的7例先天性胫骨假关节患者。中位随访时间为 7.0 年(范围为 3.8-10.0 年)。研究人员查阅了病历和X光片,以了解人口统计学数据、临床特征、疗效和并发症。在最后一次随访时,所有同种异体移植物都显示患者胫骨两端完全愈合。所有患者均未出现下肢功能受限,也未发生截肢或不愈合。大部分胫骨干骺端或踝关节的明显畸形都得到了矫正。有两例并发症需要成功进行翻修手术。在这一系列七例先天性胫骨假关节患者中,同种异体移植旁路技术显示出令人满意的中期效果,验证了我们的假设。对于克劳福德Ⅰ型和Ⅱ型先天性胫骨假关节患者,该手术结合仅涉及患腿的长期支具,可以延缓或可能预防骨折,减少胫骨错位,并保持腿的长度。