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骨骼发育异常患者下肢全关节置换术的疗效:一项系统评价。

Outcomes of Lower Extremity Total Joint Arthroplasty in Patients With Skeletal Dysplasia: A Systematic Review.

作者信息

Guirguis Paul, Fowler Lucas, Ricciardi Benjamin F

机构信息

Department of Orthopaedic Surgery, Center for Musculoskeletal Research, University of Rochester School of Medicine, Rochester, NY.

出版信息

Arthroplast Today. 2024 Aug 9;29:101405. doi: 10.1016/j.artd.2024.101405. eCollection 2024 Oct.

Abstract

BACKGROUND

Patients with genetic skeletal dysplasias often require lower extremity total joint arthroplasty (TJA) due to early joint degeneration; however, little data exists regarding the outcomes of TJA in this population. Our purpose was to review the literature to determine the complication rates, revision rates, implant survivorship, and patient-reported outcomes of total knee arthroplasty and total hip arthroplasty (THA) in those with genetic skeletal dysplasias.

METHODS

A systematic literature review of online databases (PubMed and Google Scholar) was conducted. Studies that reported the outcomes of THA or total knee arthroplasty in patients with genetically confirmed skeletal dysplasias were included. Case reports and studies that defined dysplasia based on height alone were excluded. Fourteen studies met the criteria for data extraction and analysis.

RESULTS

Our review yielded a sample of 596 skeletal dysplasia patients with a median follow-up of 6.01 years (1.7-15.9). Mean age was 54.04 years, and mean body mass index was 29.1 kg/m. Cementless fixation was utilized in 65.7% of THAs, while all knees were cemented. Hip implant survivorship was 79% at 10 years and 56% at 20 years. Knee implant survivorship was 92% at 10 years and 46% at 20 years. Hip and knee revisions were 15.3% and 13.5%, respectively. The most common indication was aseptic loosening and polyethylene wear. Patient-reported outcomes improved across all domains.

CONCLUSIONS

The literature regarding lower extremity TJA in those with genetic skeletal dysplasias demonstrates appropriate 10-year implant survivorship and improvement in patient-reported outcomes across all survey domains.

摘要

背景

由于早期关节退变,遗传性骨骼发育不良患者常需进行下肢全关节置换术(TJA);然而,关于该人群TJA结局的数据很少。我们的目的是回顾文献,以确定遗传性骨骼发育不良患者全膝关节置换术和全髋关节置换术(THA)的并发症发生率、翻修率、植入物生存率以及患者报告的结局。

方法

对在线数据库(PubMed和谷歌学术)进行系统的文献综述。纳入报告经基因确诊的骨骼发育不良患者THA或全膝关节置换术结局的研究。排除仅根据身高定义发育不良的病例报告和研究。14项研究符合数据提取和分析标准。

结果

我们的综述纳入了596例骨骼发育不良患者,中位随访时间为6.01年(1.7 - 15.9年)。平均年龄为54.04岁,平均体重指数为29.1kg/m²。65.7%的THA采用非骨水泥固定,而所有膝关节置换均采用骨水泥固定。髋关节植入物10年生存率为79%,20年生存率为56%。膝关节植入物10年生存率为92%,20年生存率为46%。髋关节和膝关节翻修率分别为15.3%和13.5%。最常见的原因是无菌性松动和聚乙烯磨损。患者报告的所有领域结局均有所改善。

结论

关于遗传性骨骼发育不良患者下肢TJA的文献表明,植入物10年生存率合适,患者报告的所有调查领域结局均有所改善。

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