Birch John G, Paley Dror, Herzenberg John E, Morton Anne, Ward Shana, Riddle Russ, Specht Stacy, Cummings Don, Tulchin-Francis Kirsten
Texas Scottish Rite Hospital for Children, Dallas, Texas.
Paley Orthopedic and Spine Institute, West Palm Beach, Florida.
JB JS Open Access. 2019 Apr 5;4(2):e0053. doi: 10.2106/JBJS.OA.18.00053. eCollection 2019 Apr-Jun.
Fibular hemimelia, a congenital disorder characterized by the partial or complete absence of the fibula, tibial growth inhibition, and foot and ankle deformity and deficiency, is the most common deficiency of long bones. The purpose of the present study of children with congenital fibular hemimelia was to examine the functional and psychosocial outcomes at a minimum of 2 years after treatment either with amputation and a prosthesis or with reconstruction and lengthening.
Twenty children who were managed with primary amputation were compared with 22 children who were managed with staged limb reconstruction. The average age of the patients at the time of evaluation was 9 years (range, 5 to 15 years). Patients and parents completed psychosocial, quality-of-life, and satisfaction surveys. Patients underwent instrumented gait analysis and a timed 25 or 50-yard dash. The number and nature of surgical procedures were recorded from a retrospective chart review.
Families of children managed with amputation had lower economic and educational levels and were more ethnically diverse compared with the families of children managed with limb reconstruction. Scores on psychosocial and quality-of-life surveys were comparable with those from healthy patient populations. Parents of males treated with amputation perceived a lower school-related quality of life for their child; socioeconomic and ethnic differences between groups might account for this finding. Statistically but not clinically significant differences were measured during instrumented gait analysis at a self-selected walking speed and during a timed 25 or 50-yard dash. The majority of patients and parents reported satisfaction with the treatment method selected and would select the same treatment method again.
At this interim stage of growth, there were no significant functional or psychological differences between groups. Both groups were satisfied with the outcome in mid-childhood, irrespective of the selection of amputation or limb reconstruction.
Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.
腓骨半侧发育不全是一种先天性疾病,其特征为腓骨部分或完全缺失、胫骨生长抑制以及足踝畸形和缺损,是最常见的长骨缺损。本研究针对先天性腓骨半侧发育不全患儿的目的是,在采用截肢并安装假肢或重建与延长治疗后至少2年,检查其功能和心理社会结局。
将20例接受一期截肢治疗的患儿与22例接受分期肢体重建治疗的患儿进行比较。评估时患者的平均年龄为9岁(范围为5至15岁)。患者及其父母完成了心理社会、生活质量和满意度调查。患者接受了仪器化步态分析以及25码或50码定时短跑测试。通过回顾性病历审查记录手术程序的数量和性质。
与接受肢体重建治疗的患儿家庭相比,接受截肢治疗的患儿家庭经济和教育水平较低,种族更为多样化。心理社会和生活质量调查得分与健康患者群体相当。接受截肢治疗的男性患儿的父母认为其孩子与学校相关的生活质量较低;两组之间的社会经济和种族差异可能解释了这一发现。在仪器化步态分析中,在自选步行速度以及25码或50码定时短跑测试期间,测量到有统计学意义但无临床意义的差异。大多数患者及其父母对所选治疗方法表示满意,并会再次选择相同的治疗方法。
在这个生长中期阶段,两组之间在功能或心理方面没有显著差异。两组对童年中期的治疗结果均感到满意,无论选择截肢还是肢体重建。
治疗性III级。有关证据水平的完整描述,请参阅作者指南。