血友病患者全髋关节置换术后假体存活情况及并发症:系统回顾。

IF 2.2 3区 医学 Q2 ORTHOPEDICS
Lei Chen, Shineng Lin, Wenlu Zhou, Yiqing Ling, Zhenyu Shi, Qinwen Ge, Wenbin Liu, Ju Li, Peijian Tong, Huihui Li, Taotao Xu
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引用次数: 0

摘要

背景:血友病关节病是血友病患者复发性关节出血引起的,通常需要全髋关节置换术(THA)来缓解疼痛和改善关节功能。然而,血友病带来的独特挑战,包括凝血功能障碍和骨骼健康受损,导致出血、感染和假体松动等并发症的风险增加。方法:系统检索截至2024年9月的PubMed、Cochrane Library、EMBASE和Web of Science数据库。研究报告了血友病患者接受人工髋关节置换术后的假体存活或并发症。方法学质量采用非随机研究方法学指数(minor)标准进行评估。结果:纳入14项回顾性队列研究,包括190例THA病例。共有190例THA病例,其中175例假体存活,无菌性松动(57%)是失败的主要原因。并发症包括出血(34.8%)、感染(19.7%)和无菌性松动(15.1%)。主要的危险因素包括骨密度降低、复发性关节炎和因凝血因子输注引起的免疫功能障碍(HIV)。术前优化凝血因子和骨质量等策略是改善预后的关键。结论:本文证实了既往研究的发现,THA是晚期血友病关节病的有效治疗方法,可显著缓解疼痛并改善功能。然而,通过正确的围手术期止血和良好的手术技术,可以降低其并发症的发生率。这种类型的手术只能在血友病治疗中心由髋关节假体植入专家团队进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prosthesis survival situation and complications following total hip arthroplasty in hemophilic patients: a systematic review.

Background: Hemophilic arthropathy, resulting from recurrent joint bleeding in patients with hemophilia, often necessitates total hip arthroplasty (THA) to alleviate pain and improve joint function. However, the unique challenges posed by hemophilia, including coagulopathy and compromised bone health, result in increased risks of complications such as bleeding, infection, and prosthesis loosening.

Methods: A systematic search of PubMed, Cochrane Library, EMBASE, and Web of Science was conducted up to September 2024. Studies reporting prosthesis survival or complications in hemophilia patients undergoing THA were included. Methodological quality was assessed using the Methodological Index for Non-Randomized Studies (MINORS) criteria.

Results: Fourteen retrospective cohort studies, encompassing 190 THA cases, were included. A total of 190 THA cases were involved, of which 175 prostheses survived, with aseptic loosening (57%) being the leading cause of failure. Complications included bleeding (34.8%), infections (19.7%), and aseptic loosening (15.1%). Key risk factors included reduced bone mineral density, recurrent hemarthrosis, and immune dysfunction (HIV) due to clotting factor infusions. Strategies such as preoperative optimization of clotting factors and bone quality were highlighted as crucial for improving outcomes.

Conclusions: This paper confirms the findings of previous studies that THA is an effective treatment for advanced-stage haemophilic arthropathy, offering significant pain relief and improved function. However, its high rate of complications has to be reduced with a correct perioperative hemostasis and a good surgical technique. This type of surgery should only be performed in centers specialized in the treatment of haemophilia by a team of surgeons expert in the implantation of hip prostheses.

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来源期刊
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders 医学-风湿病学
CiteScore
3.80
自引率
8.70%
发文量
1017
审稿时长
3-6 weeks
期刊介绍: BMC Musculoskeletal Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of musculoskeletal disorders, as well as related molecular genetics, pathophysiology, and epidemiology. The scope of the Journal covers research into rheumatic diseases where the primary focus relates specifically to a component(s) of the musculoskeletal system.
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