Long-term results of revision total hip arthroplasties using cementless stems and allografts for paprosky type IIIB and IV femoral defects short title: Revision hip arthroplasty in type IIIB and IV femoral defects.

IF 2 3区 医学 Q2 ORTHOPEDICS International Orthopaedics Pub Date : 2025-01-01 Epub Date: 2024-11-18 DOI:10.1007/s00264-024-06367-2
Young-Hoo Kim, Jang-Won Park, Young-Soo Jang, Eun-Jung Kim
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引用次数: 0

Abstract

Purpose: We determined long-term (1) clinical results of revision total hip arthroplasty (THA) in the presence of Paprosky type IIIB and IV femoral defects using validated scoring instrument; (2) osseointegration and bone remodeling; (3) the fate of cortical strut onlay allograft; (4) rates of revision and osteolysis; and (5) survivorship of the cementless stem.

Methods: We reviewed the results of 240 revision THAs in 220 patients (mean age, 59 years, range, 36-67 years) performed with an extensively porous-coated femoral stem (Solution stem; DePuy, Warsaw, Indiana) combined with a cortical strut onlay allografts for Paprosky Type IIIB and IV femoral diaphyseal bone defects from February 1994 to June 2003. Demographic data, Harris hip score, WOMAC score, UCLA activity score, and radiographic data were recorded. We determined the fate of strut cortical strut allograft and component survival rates at a mean of 26.5 years using revision and aseptic loosening as end points. Minimum follow-up was 21 years (range, 21-30 years).

Results: The clinical results improved significantly for the Harris hip score, WOMAC, and UCLA activity scores (p < 0.001). At the final follow-up, mean Harris hip, WOMAC, and UCLA activity scores were 83 ± 15 (34-100), 20 ± 15 (11-52) and 6.7 ± 1.3 (5-8) points, respectively. Of the 240 femoral stems, 218 (91%) had bone ingrowth, and 22 (9%) were unstable. Allografts were well incorporated in the host femur in all hips. The resorption of allografts was graded as mild in 192 hips (80%) and moderate in 48 hips (20%). A Kaplan-Meier survivorship analysis at a mean of 26.5 years follow-up showed that the survival rate of the femoral component was 91% (95% CI, 0.88-0.96) with re-revision for any reason as the endpoint for failure. The survival rate at a mean of 26.5 years for worst case scenario was 76% (95% CI, 0.71-0.88).

Conclusion: We found good results at a mean of 26.5 years after the revision surgery in terms of longevity and functional outcome using an extensively porous-coated stem combined with cortical strut allografts in the Paprosky Type IIIB and IV femoral diaphyseal defects. We agree that the initial quality of an uncomplicated revision of THA using supportive cortical strut allografts maintains relatively well beyond minimum 21 years of follow-up. Future studies might compare this approach with allograft-prosthesis composites, proximal femoral replacement, or modular fluted tapered stems.

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使用无骨水泥柄和同种异体材料对Paprosky IIIB型和IV型股骨缺损进行翻修全髋关节置换术的长期效果简标题:IIIB型和IV型股骨缺损的翻修髋关节置换术。
目的:我们使用有效的评分工具确定了:(1) 存在Paprosky IIIB型和IV型股骨缺损时翻修全髋关节置换术(THA)的长期临床结果;(2) 骨结合和骨重塑;(3) 皮质支柱内嵌异体移植的命运;(4) 翻修率和骨溶解率;(5) 无骨水泥柄的存活率:我们回顾了1994年2月至2003年6月期间220名患者(平均年龄59岁,年龄范围36-67岁)的240例翻修THA手术结果,这些患者均采用广泛多孔涂层股骨柄(Solution柄;DePuy,Warsaw,Indiana)结合皮质支柱衬垫同种异体移植物治疗Paprosky IIIB型和IV型股骨骺端骨缺损。我们记录了人口统计学数据、Harris髋关节评分、WOMAC评分、UCLA活动度评分和放射学数据。我们以翻修和无菌性松动为终点,确定了平均 26.5 年的支柱皮质异体移植和组件存活率。最短随访时间为 21 年(21-30 年不等):结果:Harris髋关节评分、WOMAC和UCLA活动度评分的临床结果均有明显改善(P 结论:在平均26.5年的随访中,我们发现了良好的效果:我们发现,在Paprosky IIIB型和IV型股骨骺缺损的翻修手术后平均26.5年,使用广泛多孔涂层柄结合皮质支柱异体移植物,在寿命和功能结果方面取得了良好的效果。我们一致认为,使用支持性皮质支柱同种异体移植的无并发症翻修THA的初始质量在至少21年的随访后仍能保持相对较好。未来的研究可能会将这种方法与异体移植物-假体复合材料、股骨近端置换或模块化凹槽锥形柄进行比较。
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来源期刊
International Orthopaedics
International Orthopaedics 医学-整形外科
CiteScore
5.50
自引率
7.40%
发文量
360
审稿时长
1 months
期刊介绍: International Orthopaedics, the Official Journal of the Société Internationale de Chirurgie Orthopédique et de Traumatologie (SICOT) , publishes original papers from all over the world. The articles deal with clinical orthopaedic surgery or basic research directly connected with orthopaedic surgery. International Orthopaedics will also link all the members of SICOT by means of an insert that will be concerned with SICOT matters. Finally, it is expected that news and information regarding all aspects of orthopaedic surgery, including meetings, panels, instructional courses, etc. will be brought to the attention of the readers. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted. Reports of animal experiments must state that the "Principles of laboratory animal care" (NIH publication No. 85-23, revised 1985) were followed, as well as specific national laws (e.g. the current version of the German Law on the Protection of Animals) where applicable. The editors reserve the right to reject manuscripts that do not comply with the above-mentioned requirements. The author will be held responsible for false statements or for failure to fulfil the above-mentioned requirements.
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