D. Morita, Department of Orthopaedic Surgery, Hamamatsu Medical Center, Hamamatsu City, Shizuoka, Japan D. Morita, T. Seki, Y. Takegami, T. Kasai, Y. Higuchi, N. Ishiguro, Department of Orthopedic Surgery, Nagoya University Graduate School of Medicine, Nagoya City, Aichi, Japan Y. Hasegawa, Department of Physical Therapy, Kansai University of Welfare Sciences, Osaka, Japan T. Amano, Department of Orthopaedic Surgery, Shizuoka Saiseikai General Hospital, Shizuoka, Japan.
Clin Orthop Relat Res. 2018 Nov;476(11):2157-2166. doi: 10.1097/CORR.0000000000000458.
Patients with comparable severities of developmental dysplasia of the hip (DDH) may variably progress to osteoarthritis (OA) over time. Although joint congruency may be associated with OA progression in patients with DDH, it has only been assessed subjectively. We assessed the gap between the rotational centers of the acetabulum and femoral head (center gap) as a possible predictive measure of OA progression in patients with DDH.
QUESTIONS/PURPOSES: In patients with bilateral DDH, we asked: (1) What is the probability of OA progression (Tönnis grade) or symptom development (pain) in the asymptomatic contralateral hip of patients with DDH undergoing unilateral joint-preserving surgery? (2) Is the center gap measurement associated with OA progression or symptom development in these hips? (3) Is the center gap measurement correlated with previous radiographic parameters?
A total of 297 patients (319 hips) underwent unilateral eccentric rotational acetabular osteotomy at our institution between July 1989 and December 1999. We performed no other joint-preserving surgery to treat patients with DDH during this timeframe. The inclusion criteria for the study were patients younger than 55 years of age, the contralateral hip classified as Tönnis Grade 0, no previous surgical interventions, and asymptomatic at the time of eccentric rotational acetabular osteotomy (155 patients, 155 hips). The exclusion criteria were a contralateral hip without dysplasia (four patients, four hips), loss to followup before 10 years (42 patients, 42 hips [27%]), or missing medical records or radiographs (21 patients, 21 hips [14%]). The remaining 88 patients (88 hips; 11 males and 77 females) with a mean age of 39 years (range, 17-53 years) and mean followup of 20 years (range, 10-27 years) were analyzed. From the institutional database, radiographic parameters including the center gap in the AP view were assessed using radiographs at the time of eccentric rotational acetabular osteotomy, and the Tönnis grade was recorded 1 year postoperatively and annually thereafter retrospectively. We defined migration of the rotational center of the femoral head based on the rotational center of the acetabulum in the horizontal plane as center gap X (mm) and in the vertical plane as center gap Y (mm) and defined the absolute value between the centers as center gap distance (mm). Using κ statistics, intra- and interobserver reliabilities were determined to be 0.896 and 0.857 for center gap X, 0.912 and 0.874 for center gap Y, and 0.912 and 0.901 for the center gap distance, respectively. When patients reported any contralateral ipsilateral hip pain during clinic visits, the hip was considered symptomatic. Kaplan-Meier survivorship analyses were performed with OA progression or symptom development in the nonoperative hip as the endpoint. Multivariate analyses were performed to assess risk factors for each outcome using the Cox proportional hazards model. Correlation analyses between the center gap and other parameters including lateral center-edge angle, femoral head extrusion index, acetabular depth-to-width index, femoral head lateralization, minimum width of the joint space, head sphericity, and joint congruency were performed using Pearson's correlation coefficient.
At 20 years postoperatively, the probability of OA progression in the nonoperative hip was 13% (95% confidence interval [CI], 7.1-22.1) and the probability of symptom development was 34% (95% CI, 24.7-46.1). The center gap X measurements in the groups with OA progression (lateral 2.0 ± 2.1 [SD] mm) or symptom development (lateral 0.9 ± 2.4 mm) took a more lateral direction than those in the group without OA progression (medial 0.4 ± 2.1 mm) or symptom development (medial 0.5 ± 2.0 mm) (OA progression, p < 0.001; symptom development, p = 0.005). The center gap Y measurements in the groups with OA progression (distal 2.7 ± 7.1 mm) or symptom development (distal 2.1 ± 6.0 mm) took a more distal direction than those in the group without OA progression (proximal 1.6 ± 6.2 mm) or symptom development (proximal 2.5 ± 6.1 mm) (OA progression, p = 0.027; symptom development, p = 0.001). Independent risk factors for OA progression were the femoral head extrusion index (hazard ratio [HR], 1.11; 95% CI, 1.01-1.22; p = 0.028) and the center gap X (HR, 1.52; 95% CI, 1.07-2.16; p = 0.019), whereas no independent risk factors for symptom development were found. The center gap in the horizontal plane had no correlations with any other radiographic parameter studied.
The center gap in the horizontal plane had a modest association with OA progression in this group of patients with DDH. Future studies are needed to determine the normal value of the center gap for patients without DDH and to assess the center gap in lateral radiographic views.
Level IV, prognostic study.
患有发育性髋关节发育不良(DDH)的患者病情严重程度相似,但随着时间的推移,他们可能会进展为骨关节炎(OA)。虽然关节一致性可能与 DDH 患者的 OA 进展有关,但仅进行了主观评估。我们评估了髋臼和股骨头旋转中心之间的间隙(中心间隙)作为 DDH 患者 OA 进展的预测指标。
问题/目的:在双侧 DDH 患者中,我们提出以下问题:(1)接受单侧关节保留手术的 DDH 患者中,无症状对侧髋关节发生 OA 进展(Tönnis 分级)或症状发展(疼痛)的概率是多少?(2)中心间隙测量与这些髋关节的 OA 进展或症状发展是否相关?(3)中心间隙测量与以前的放射学参数是否相关?
1989 年 7 月至 1999 年 12 月期间,我们机构对 297 例患者(319 髋)进行了偏心旋转髋臼截骨术。在此期间,我们没有对 DDH 患者进行任何其他关节保留手术。研究的纳入标准为年龄小于 55 岁,对侧髋关节 Tönnis 分级为 0 级,在偏心旋转髋臼截骨术前无症状(155 例患者,155 髋)。排除标准为对侧髋关节无发育不良(4 例患者,4 髋)、随访 10 年前丢失(42 例患者,42 髋[27%])或缺少病历或影像学资料(21 例患者,21 髋[14%])。其余 88 例(88 髋;11 名男性和 77 名女性)患者平均年龄为 39 岁(范围 17-53 岁),平均随访时间为 20 年(范围 10-27 年)。从机构数据库中,我们使用偏心旋转髋臼截骨术前的影像学资料评估了包括 AP 视图中心间隙在内的放射学参数,术后 1 年及此后每年根据 Tönnis 分级进行回顾性记录。我们将股骨头旋转中心的平移定义为髋臼在水平面的中心间隙 X(mm)和垂直面的中心间隙 Y(mm),并定义中心之间的绝对值为中心间隙距离(mm)。使用 κ 统计量,我们确定了中心间隙 X 的组内和组间可靠性分别为 0.896 和 0.857,中心间隙 Y 的可靠性分别为 0.912 和 0.874,中心间隙距离的可靠性分别为 0.912 和 0.901。当患者在就诊时报告任何对侧同侧髋关节疼痛时,该髋关节被认为有症状。使用 OA 进展或非手术侧髋关节症状发展作为终点,我们进行了 Kaplan-Meier 生存分析。使用 Cox 比例风险模型对每个结局的危险因素进行了多变量分析。我们使用 Pearson 相关系数分析了中心间隙与其他参数(外侧中心边缘角、股骨头外展指数、髋臼深度与宽度指数、股骨头外侧化、关节间隙最小宽度、头球形度和关节一致性)之间的相关性。
术后 20 年,非手术侧髋关节的 OA 进展概率为 13%(95%置信区间[CI],7.1-22.1),症状发展概率为 34%(95% CI,24.7-46.1)。发生 OA 进展(外侧 2.0 ± 2.1 [SD] mm)或症状发展(外侧 0.9 ± 2.4 mm)的患者的中心间隙 X 测量值比未发生 OA 进展(内侧 0.4 ± 2.1 mm)或症状发展(内侧 0.5 ± 2.0 mm)的患者更偏向外侧(OA 进展,p<0.001;症状发展,p=0.005)。发生 OA 进展(远端 2.7 ± 7.1 mm)或症状发展(远端 2.1 ± 6.0 mm)的患者的中心间隙 Y 测量值比未发生 OA 进展(近端 1.6 ± 6.2 mm)或症状发展(近端 2.5 ± 6.1 mm)的患者更偏向远端(OA 进展,p=0.027;症状发展,p=0.001)。OA 进展的独立危险因素是股骨头外展指数(HR,1.11;95% CI,1.01-1.22;p=0.028)和中心间隙 X(HR,1.52;95% CI,1.07-2.16;p=0.019),而症状发展无独立危险因素。水平方向的中心间隙与我们研究的其他任何放射学参数均无相关性。
在这组 DDH 患者中,水平方向的中心间隙与 OA 进展有一定的相关性。未来的研究需要确定无 DDH 患者的中心间隙正常值,并评估侧位放射影像学的中心间隙。
IV 级,预后研究。