Mechanical failure of 113 uncemented modular revision femoral components

Author:

Krueger D. R.1,Guenther K-P.2,Deml M. C.3,Perka C.1

Affiliation:

1. Center for Musculoskeletal Surgery (CMSC), Charité – Universitätsmedizin Berlin, Berlin, Germany.

2. Center for Orthopaedic and Trauma Surgery, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

3. Department of Orthopaedic and Trauma Surgery, University of Bern, Inselspital, Bern, Switzerland.

Abstract

Aims We evaluated a large database with mechanical failure of a single uncemented modular femoral component, used in revision hip arthroplasty, as the end point and compared them to a control group treated with the same implant. Patient- and implant-specific risk factors for implant failure were analyzed. Methods All cases of a fractured uncemented modular revision femoral component from one manufacturer until April 2017 were identified and the total number of implants sold until April 2017 was used to calculate the fracture rate. The manufacturer provided data on patient demographics, time to failure, and implant details for all notified fractured devices. Patient- and implant-specific risk factors were evaluated using a logistic regression model with multiple imputations and compared to data from a previously published reference group, where no fractures had been observed. The results of a retrieval analysis of the fractured implants, performed by the manufacturer, were available for evaluation. Results There were 113 recorded cases with fracture at the modular junction, resulting in a calculated fracture rate of 0.30% (113/37,600). The fracture rate of the implant without signs of improper use was 0.11% (41/37,600). In 79% (89/113) of cases with a failed implant, either a lateralized (high offset) neck segment, an extralong head, or the combination of both were used. Logistic regression analysis revealed male sex, high body mass index (BMI), straight component design, and small neck segments were significant risk factors for failure. Investigation of the implants (76/113) showed at least one sign of improper use in 72 cases. Conclusion Implant failure at the modular junction is associated with patient- and implant-specific risk factors as well as technical errors during implantation. Whenever possible, the use of short and lateralized neck segments should be avoided with this revision system. Implantation instructions and contraindications need to be adhered to and respected. Cite this article: Bone Joint J 2020;102-B(5):573–579.

Publisher

British Editorial Society of Bone & Joint Surgery

Subject

Orthopedics and Sports Medicine,Surgery

Reference54 articles.

1. Revisionsendoprothetik der Hüfte

2. Grimberg A, Jansson V, Liebs T, et al. German Arthroplasty Registry EPRD. Annual Report 2017. Berlin 2018. https://www.eprd.de/fileadmin/user_upload/Dateien/Publikationen/Berichte/EPRD-Jahresbericht_2017_Einzelseiten_Online-Version.pdf (date last accessed 27 February 2020).

3. IQTIG.[Annual report 2017. Hip arthroplasty. Quality indicators]. Institute for quality assurance and transparency in healthcare. 2018. https://iqtig.org/downloads/berichte/2018/IQTIG_Qualitaetsreport-2019_2019-09-25.pdf (date last accessed 27 February 2020).

4. Current Epidemiology of Revision Total Hip Arthroplasty in the United States: National Inpatient Sample 2009 to 2013

5. Future Young Patient Demand for Primary and Revision Joint Replacement: National Projections from 2010 to 2030

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