Ulusaloglu Armagan Can, Asma Ali, Rogers Kenneth J, Shrader Michael Wade, Graham H Kerr, Howard Jason J
Nemours Children's Hospital, Delaware, Wilmington, DE, USA.
Department of Orthopaedic Surgery, University of Melbourne, Melbourne, VIC, Australia.
J Child Orthop. 2022 Apr;16(2):121-127. doi: 10.1177/18632521221084184. Epub 2022 Apr 30.
The aim of this article was to compare longitudinal changes in hip morphology in cerebral palsy (hypertonic) and spinal muscular atrophy (hypotonic) to examine the influence of muscle tone on development of hip displacement.
Children with spinal muscular atrophy (Types I and II) and cerebral palsy (Gross Motor Function Classification System IV and V) with hip displacement (migration percentage >30%) were included. Head shaft angle, migration percentage, and acetabular index were measured at T1 (1-2.5 years), T2 (3-5 years), and T3 (6-8 years). Analysis of variance testing and linear regression were utilized.
Sixty patients (cerebral palsy, N = 41; spinal muscular atrophy, N = 19) were included. Hip displacement occurred earlier in spinal muscular atrophy (34 months) than cerebral palsy (49 months) (p = 0.003). Head shaft angle was high and did not change between T1, T2, and T3, but significant changes in migration percentage were found (cerebral palsy: 23%, 36%, 45% (p < 0.01) and spinal muscular atrophy: 37%, 57%, 61% (p = 0.02)). Migration percentage increased by age in cerebral palsy (r = 0.41, p < 0.001), but not in spinal muscular atrophy (r = 0.18, p = 0.09). Acetabular index increased with migration percentage (cerebral palsy: r = 0.41, p < 0.001; spinal muscular atrophy: r = 0.48, p < 0.001).
Persistent lateral physeal tilt by head shaft angle was found for both spinal muscular atrophy and cerebral palsy. Abnormal physeal alignment may be causally related to weakness of the hip abductor muscles rather than spasticity or muscle imbalance, resulting in coxa valga and secondary acetabular dysplasia.
III (case-control study).
本文旨在比较脑瘫(高张力型)和脊髓性肌萎缩症(低张力型)患儿髋关节形态的纵向变化,以研究肌张力对髋关节移位发展的影响。
纳入患有脊髓性肌萎缩症(Ⅰ型和Ⅱ型)和脑瘫(粗大运动功能分级系统Ⅳ级和Ⅴ级)且存在髋关节移位(移位百分比>30%)的患儿。在T1(1 - 2.5岁)、T2(3 - 5岁)和T3(6 - 8岁)时测量头干角、移位百分比和髋臼指数。采用方差分析测试和线性回归分析。
共纳入60例患者(脑瘫41例;脊髓性肌萎缩症19例)。脊髓性肌萎缩症患者髋关节移位出现时间(34个月)早于脑瘫患者(49个月)(p = 0.003)。头干角较高,在T1、T2和T3之间无变化,但移位百分比有显著变化(脑瘫:23%、36%、45%(p < 0.01);脊髓性肌萎缩症:37%、57%、61%(p = 0.02))。脑瘫患者的移位百分比随年龄增加(r = 0.41,p < 0.001),而脊髓性肌萎缩症患者则不然(r = 0.18,p = 0.09)。髋臼指数随移位百分比增加(脑瘫:r = 0.41,p < 0.001;脊髓性肌萎缩症:r = 0.48,p < 0.001)。
脊髓性肌萎缩症和脑瘫患者均存在头干角导致的持续性外侧骨骺倾斜。异常的骨骺排列可能与髋外展肌无力有因果关系,而非痉挛或肌肉失衡,从而导致髋外翻和继发性髋臼发育不良。
Ⅲ(病例对照研究)。