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利用密歇根关节置换登记协作质量倡议(MARCQI)的数据对全髋关节置换植入物进行早期基准测试。

Early Benchmarking Total Hip Arthroplasty Implants Using Data from the Michigan Arthroplasty Registry Collaborative Quality Initiative (MARCQI).

作者信息

Chubb Heather A, Cornish Eric R, Hallstrom Brian R, Hughes Richard E

机构信息

Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.

Department of Orthopedic Surgery, MidMichigan Health, Alpena, MI, USA.

出版信息

Orthop Res Rev. 2021 Nov 24;13:215-228. doi: 10.2147/ORR.S325042. eCollection 2021.

Abstract

BACKGROUND

Benchmarking arthroplasty implant revision risk is an informative way to address implant performance. National benchmarking efforts exist in the United Kingdom, Netherlands, and Australia. Recently, the International Prosthesis Benchmarking Working Group, including representatives from industry, academia, and national registries, produced a guideline describing arthroplasty benchmarking methodology. The proposal was applied to data from the Michigan Arthroplasty Registry Collaborative Quality Initiative (MARCQI) to assess its feasibility for benchmarking implants in the United States.

METHODS

Primary elective total hip arthroplasty procedures performed for osteoarthritis between 2/15/2012 and 12/31/2018 and their associated revisions were identified in the MARCQI registry. The guidelines recommend that all prostheses combinations receive an early benchmark if they have at least 250 procedures at risk and the revision rate does not exceed the pre-determined standard of 2% at 2 years and 3% at 5 years.

RESULTS

A total of 72,949 primary cases met the inclusion criteria. Of these, 1369 had revisions. Twenty-nine and six stem/cup combinations satisfied the minimum case requirement at 2 and 5 years, respectively. Three implant combinations would not receive a benchmark at 2 years: Secur-Fit/Trident, Anthology/Reflection 3, Taperloc 133/G7.

CONCLUSION

The guideline can be implemented in the United States by a regional registry. Moreover, not all hip implants currently in use would receive an early benchmark. This raises concern as these implant combinations represent a significant number of cases in Michigan, some with increasing utilization.

摘要

背景

对关节置换植入物翻修风险进行基准评估是评估植入物性能的一种有效方式。英国、荷兰和澳大利亚都有全国性的基准评估工作。最近,由行业、学术界和国家登记处代表组成的国际假体基准评估工作组制定了一项指南,描述关节置换基准评估方法。该提议被应用于密歇根关节置换登记协作质量倡议(MARCQI)的数据,以评估其在美国对植入物进行基准评估的可行性。

方法

在MARCQI登记处确定了2012年2月15日至2018年12月31日期间因骨关节炎进行的初次择期全髋关节置换手术及其相关翻修手术。该指南建议,如果所有假体组合至少有250例有风险的手术,且翻修率在2年时不超过预先确定的2%的标准,在5年时不超过3%的标准,则应进行早期基准评估。

结果

共有72949例初次病例符合纳入标准。其中,1369例进行了翻修。分别有29种和6种柄/髋臼杯组合在2年和5年时满足最低病例要求。三种植入物组合在2年时不会获得基准评估:Secur-Fit/Trident、Anthology/Reflection 3、Taperloc 133/G7。

结论

该指南可由地区登记处在美国实施。此外,并非所有目前使用的髋关节植入物都会获得早期基准评估。这引发了担忧,因为这些植入物组合在密歇根州代表了大量病例,其中一些病例的使用量在增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98d2/8627892/57024d20e635/ORR-13-215-g0001.jpg

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