One-stage release by double surgical approach for neglected congenital vertical talus: results in a series of walking children in Tanzania.

I. Sanzarello, M. Nanni, F. Perna, F. Traina, C. Faldini
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引用次数: 6

Abstract

Congenital vertical talus is an uncommon rigid flatfoot deformity present at birth, producing pain and disability if untreated. This study reports results and complications in a series of walking children affected by neglected congenital vertical talus treated by one-stage release through a double surgical approach in a hospital sited in the Tanzanian rural outback. Between 2009 and 2014, nine consecutive congenital vertical talus were observed in five patients (three males and two females) aged between 2 and 4 years. In two children, the deformity was idiopathic, in two it was associated to distal arthrogryposis and in one to Larsen syndrome. The surgical procedure was performed through a posteromedial and a lateral incision and included extensive soft tissue release and reduction of talo-navicular and subtalar joint, pinned with percutaneous Kirschner wires. The talar axis-first metatarsal base angle (TAMBA) was measured preoperatively and at follow-up. Results were summarized using the Adelaar score and the PODCI (Pediatric Outcomes Data Collection Instrument) questionnaire. The mean follow-up was 2.6 years (2-4). No major intraoperative complications were observed. The TAMBA passed from 74.4º (range 68-82º) to 20.2º (range 18-24º). No talar osteonecrosis was observed. The results were excellent in three cases, good in five cases and fair in one (Adelaar score). The mean postoperative PODCI score was 48 (range 38-60). None of the patients underwent further surgery. In case of neglected congenital vertical talus and limited health resources, this surgical technique has proved to be a viable option, providing satisfactory results, with low rate of surgical and postsurgical complications.
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通过双手术入路一期解除被忽视的先天性垂直距骨:结果在坦桑尼亚的一系列步行儿童。
先天性垂直距骨是一种罕见的刚性平足畸形,在出生时就存在,如果不治疗,会产生疼痛和残疾。本研究报告了在坦桑尼亚农村内陆的一家医院,通过双手术方法一期释放治疗被忽视的先天性垂直距骨的一系列行走儿童的结果和并发症。2009 ~ 2014年,5例2 ~ 4岁患者(男3例,女2例)连续9例先天性距骨。在两名儿童中,畸形是特发性的,其中两名与远端关节挛缩有关,一名与拉森综合征有关。手术通过后内侧和外侧切口进行,包括广泛的软组织释放和距舟关节和距下关节复位,经皮克氏针固定。术前和随访时测量距骨轴-第一跖底角(TAMBA)。使用Adelaar评分和PODCI(儿科结局数据收集工具)问卷对结果进行总结。平均随访时间为2.6年(2-4年)。术中未见重大并发症。TAMBA从74.4º(68-82º)到20.2º(18-24º)。未见距骨骨坏死。结果3例为优秀,5例为良好,1例为一般(Adelaar评分)。术后平均PODCI评分为48分(范围38-60)。所有患者均未接受进一步手术。对于被忽视的先天性垂直距骨和有限的医疗资源,该手术技术已被证明是一种可行的选择,提供满意的结果,手术和术后并发症的发生率低。
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