Hartofilakidis George, Yiannakopoulos Christos K, Babis George C
Department of Orthopaedics, University of Athens Medical School, Byzantiou 2, Athens, Nea Smyrni, 17121, Greece.
Clin Orthop Relat Res. 2008 Apr;466(4):820-4. doi: 10.1007/s11999-008-0131-9. Epub 2008 Feb 21.
Three different types of congenital hip disease in adults have been distinguished based upon the position of the femoral head relative to the acetabulum and the underlying pathoanatomy of the joint: (1) dysplasia; (2) low dislocation; and (3) high dislocation. To facilitate classification of borderline or ambiguous cases, we studied the morphologic variations of low and high dislocation as observed on the radiographs of 101 hips with low and 74 hips with high dislocation. In low dislocation, 54 hips (53.5%) had extended coverage of the true acetabulum (Type B1) and 47 hips (46.5%) had limited coverage (Type B2). Among the cases with high dislocation, a false acetabulum with an adjacent femoral head occurred in 46 hips (62.2%) (Type C1), and the femoral head was floating within the gluteal muscles in 28 hips (37.8%) (Type C2). The kappa value for interobserver agreement between two raters who made radiographic measurements was 0.963, and for intraobserver agreement between the two evaluations of the same observer it was 0.946 and 0.971, respectively. The two types of low and high dislocation were associated with high intra- and interobserver agreement. Whether these distinctions have clinical utility requires further validation.
Level III, diagnostic study. See the Guidelines for Authors for a complete description of levels of evidence.
根据股骨头相对于髋臼的位置以及关节潜在的病理解剖结构,区分出了三种不同类型的成人先天性髋关节疾病:(1)发育不良;(2)低位脱位;(3)高位脱位。为便于对临界或不明确的病例进行分类,我们研究了101例低位脱位髋关节和74例高位脱位髋关节的X线片上观察到的低位和高位脱位的形态学变异。在低位脱位中,54例髋关节(53.5%)真髋臼覆盖范围扩大(B1型),47例髋关节(46.5%)覆盖范围有限(B2型)。在高位脱位病例中,46例髋关节(62.2%)出现假髋臼并伴有相邻股骨头(C1型),28例髋关节(37.8%)股骨头漂浮于臀肌内(C2型)。进行X线测量的两名评估者之间的观察者间一致性kappa值为0.963,同一观察者的两次评估之间的观察者内一致性kappa值分别为0.946和0.971。低位和高位脱位的两种类型在观察者内和观察者间具有高度一致性。这些区分是否具有临床实用性需要进一步验证。
III级,诊断性研究。有关证据水平的完整描述,请参阅作者指南。