Retrospective Review of Outcomes of Total Hip Arthroplasty in Developmental Dysplasia of the Hip in Adults

被引:0
作者
Chaudhry, Faran [1 ,2 ,3 ]
Bridger, Adam [1 ,2 ]
Daud, Anser [2 ,3 ]
Greenberg, Arieh [2 ,3 ]
Safir, Oleg A. [2 ,3 ]
Gross, Allan E. [2 ,3 ]
Kuzyk, Paul R. [2 ,3 ]
机构
[1] Univ Toronto, Temerty Fac Med, Toronto, ON, Canada
[2] Mt Sinai Hosp, Dept Orthopaed Surg, Toronto, ON, Canada
[3] Univ Toronto, Dept Surg, Div Orthopaed Surg, Toronto, ON, Canada
关键词
total hip arthroplasty; developmental dysplasia of the hip; Hartofilakidis classification; survivorship; adult; LEG LENGTH INEQUALITY; OSTEOARTHRITIS; ETIOLOGY; DISEASE; RISK;
D O I
10.1016/j.arth.2025.03.070
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Developmental dysplasia of the hip (DDH) is a major cause of hip arthritis in young adults. Total hip arthroplasty (THA) is an effective treatment for DDH, but few studies have examined mid-(5 to 10 years) to long-term (> 10 years) outcomes. This study reports the long-term survivorship, clinical, and radiographic outcomes of THA in DDH patients. Methods: A total of 255 patients were included from our retrospective review of THAs from January 2004 to January 2022. Among these cases, 214 (83.9%) were women; the mean age at the time of surgery was 46 years (range, 18 to 87), and the mean follow-up was 8.3 (range, 0.05 to 21.1) years. Kaplan-Meier survivorship analysis was conducted with failure defined as revision surgery for any reason. Results: Kaplan-Meier survivorship for patients who underwent THA to treat DDH due to all-cause failure was 93.4% (95% confidence interval (CI): 90.3 to 96.5) at 5 years, 92.5% (95% CI: 89.0 to 95.6) at 10 years, and 90.9% (95% CI: 86.2 to 94.0) at 15 years. The overall rate of revision of the index surgery was 18 of 255 (7.1%). These complications included pain (seven), dislocation (four), aseptic loosening of the cup (three), periprosthetic fracture (two), complete foot drop (one), and infection (one). Kaplan-Meier all-cause survivorship for Hartofilakidis A, B, and C was also conducted and showed no significant differences. The mean femoral offset improved from a preoperative value of 12.2 cm (SD 1.4) to a postoperative value of 11.7 cm (SD 1.1) (P < 0.001). The rate of femoral nerve palsy was 0.78%. Conclusions: Our study suggests THA for DDH is a viable treatment, providing excellent mid-term to long-term survivorship, clinical, and radiographic outcomes with a low complication rate. Future research should evaluate patient-reported outcomes and long-term follow-up in larger cohorts. (c) 2025 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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收藏
页码:S236 / S242
页数:7
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