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首页> 外文期刊>Acta orthopaedica. >Implant survival after primary total hip arthroplasty due to childhood hip disorders Results from the Danish Hip Arthroplasty Registry
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Implant survival after primary total hip arthroplasty due to childhood hip disorders Results from the Danish Hip Arthroplasty Registry

机译:儿童髋关节疾患导致的原发性全髋关节置换术后的植入物存活丹麦髋关节置换注册处的结果

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Background Childhood hip disorders including acetabular dysplasia, congenital hip dislocation, epiphysiolysis, and morbus Calvé-Legg-Perthes are well-established risk factors for the development of early osteoarthritis of the hip. These patients have an increased risk of undergoing a total hip arthroplasty (THA) operation early in their life. However, there are very few data on implant survival in such patients. Methods We used data from the Danish Hip Arthroplasty Registry to identify patients who had been treated with a primary THA in Denmark between 1995 and 2005. Implant survival during early and late postoperative follow-up (6 months, respectively) was assessed for patients treated with a primary THA due to childhood hip disorders, and compared with implant survival for THA patients with primary osteoarthritis. Results 56,087 THA procedures included 53,694 (96%) hips with primary osteoarthritis, 890 (1.6%) with acetabular dysplasia, 565 (1.0%) with congenital hip dislocation, 267 (0.5%) with epiphysiolysis, and 404 (0.7%) hips with morbus Calvé-Legg-Perthes Patients with acetabular dysplasia had an increased risk of revision during the 0–6-month postoperative period compared to patients with primary osteoarthritis (adjusted relative risk (RR)=1.9 (95% CI: 1.2–3.1)). These revisions were mainly performed due to dislocation of the THA, providing an adjusted RR of revision due to dislocation of 2.8 (95% CI: 1.6–4.9) compared to patients operated due to primary osteoarthritis. We found no statistically significant differences in risk of revision for the other childhood hip disorder groups during the early postoperative phase. In addition, we found no substantial differences in revision risk during later follow-up (0.5–12 years) for any of the childhood hip disorders compared to patients with primary osteoarthritis. Interpretation We found an encouraging rate of long-term implant survival for patients with childhood hip disorders. The major concern is the increased risk of revision because of dislocation in the first 6 postoperative months for patients with acetabular dysplasia. However, the advent of alternative bearings and the use of large-diameter femoral heads may improve the outcome after primary THA in these patients.
机译:背景技术儿童髋关节疾病包括髋臼发育异常,先天性髋关节脱位,骨physi松解和morbusCalvé-Legg-Perthes是早发性髋关节炎的公认危险因素。这些患者在生命早期经历全髋关节置换术(THA)的风险增加。但是,关于这类患者植入物存活的数据很少。方法我们使用丹麦髋关节置换术注册中心的数据来确定1995年至2005年间在丹麦接受原发性THA治疗的患者。对术后早期和晚期随访(分别为6个月)的植入物存活率进行了评估。因儿童髋关节疾病而导致的原发性THA,并与原发性骨关节炎的THA患者的植入物生存率进行了比较。结果56,087例THA手术包括53,694例(96%)的髋关节原发性骨关节炎,890例(1.6%)的髋臼发育不良,565例(​​1.0%)的先天性髋关节脱位,267例(0.5%)的表皮软化和404例(0.7%)的髋关节与原发性骨关节炎患者相比,髋臼发育不良的morbusCalvé-Legg-Perthes患者在术后0-6个月内翻修的风险增加(调整后的相对风险(RR)= 1.9(95%CI:1.2-3.1)) 。这些修订主要是由于THA脱位而进行的,与因原发性骨关节炎手术的患者相比,由于脱位2.8(95%CI:1.6–4.9)而提供了调整后的修订版RR。我们发现,在术后早期,其他儿童髋关节疾病组的翻修风险没有统计学上的显着差异。此外,与原发性骨关节炎患者相比,对于任何儿童髋关节疾病,在后续随访(0.5至12岁)中,翻修风险均无显着差异。解释我们发现儿童髋关节疾病患者的长期植入物存活率令人鼓舞。主要问题是髋臼发育不良患者术后前6个月因脱位而翻修的风险增加。但是,在这些患者中,初次THA后替代轴承的使用和大直径股骨头的使用可能会改善预后。

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