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既往关节融合术后的髋关节置换术。

Hip arthroplasty after previous arthrodesis.

作者信息

Peterson Erik D, Nemanich Joseph P, Altenburg Aaron, Cabanela Miguel E

机构信息

Orthopaedic Consultants, Sioux Falls, SD, USA.

出版信息

Clin Orthop Relat Res. 2009 Nov;467(11):2880-5. doi: 10.1007/s11999-009-1027-z. Epub 2009 Aug 19.

Abstract

UNLABELLED

Total hip arthroplasty after previous arthrodesis has been associated with increased complications and decreased survivorship of the prosthesis. We evaluated pain, function, and the factors influencing survivorship of total hip arthroplasties after previous arthrodesis between 1985 and 2000 and compared these results with those obtained in prior years with the same procedure and in the same institution. We retrospectively reviewed 30 patients who had previous spontaneous or surgical arthrodesis. The minimum followup was 2 years (mean, 10.4 years; range 2-20.5 years). Seven failures were identified (23%). The overall survival free of failure was 86% at 5 years and 75% at 10 years. At last followup, 27 of the 30 patients (91%) had no or slight pain, 26 (87%) had a limp, and 18 (61%) needed a gait aid. Surgical arthrodesis, age younger than 50 years at the time of arthroplasty, and length of arthrodesis less than 30 years independently predicted failure. Conversion of arthrodesis to hip arthroplasty reliably decreases pain and improves function, but many patients will limp and require a gait aid. Our outcomes were similar to those after revision rather than after primary hip arthroplasty.

LEVEL OF EVIDENCE

Level IV, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.

摘要

未标注

既往关节融合术后行全髋关节置换术与并发症增加及假体生存率降低相关。我们评估了1985年至2000年间既往关节融合术后全髋关节置换术的疼痛、功能及影响假体生存率的因素,并将这些结果与该机构此前同期行相同手术的结果进行比较。我们回顾性分析了30例既往有自发或手术关节融合术史的患者。最小随访时间为2年(平均10.4年;范围2 - 20.5年)。确定有7例失败(23%)。5年时无失败的总体生存率为86%,10年时为75%。在末次随访时,30例患者中有27例(91%)无疼痛或仅有轻微疼痛,26例(87%)有跛行,18例(61%)需要助行器。手术关节融合术、置换术时年龄小于50岁以及关节融合时间小于30年是失败的独立预测因素。关节融合术转换为髋关节置换术确实能减轻疼痛并改善功能,但许多患者仍会跛行且需要助行器。我们的结果与翻修术后而非初次髋关节置换术后的结果相似。

证据水平

IV级,治疗性研究。有关证据水平的完整描述,请参见作者指南。

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