Abstract

BackgroundTotal hip arthroplasty is the traditional treatment for osteoarthritis in the hip joint. Hip resurfacing arthroplasty, with metal on metal bearing, is a modern concept initially developed mainly for young active people. The metal-on-metal hip arthroplasty implant, Articular Surface Replacement (ASR), was implanted in approximately 93,000 patients before it was recalled in 2010 due to a high complication rate. This study aimed to evaluate patients’ own experiences living with an implant that they knew had a high complication rate and had been recalled from the market.MethodsA total of 14 patients, still living with the implant, of a cohort of 34 patients were available for follow-up. Qualitative semi-structured interviews were conducted with 14 patients where a majority actively sought for metal-on-metal hip resurfacing arthroplasty (HRA), and subsequently underwent HRA with an ASR prosthesis between 11/21/2006 and 09/28/2009. The responses were analyzed using content analysis described by Graneheim and Lundman to compress text and identify categories and subcategories.ResultsThe results showed that most patients had already decided that they wanted a metal-on-metal HRA implant before meeting the surgeon. They expressed that the implant made it possible to live an active life. A majority did not think about the fact that they had a hip implant, because they lacked subjective pain. Most of the patients were positive about the annual exams at the hospital and wanted them to continue. None of them felt that their trust towards the healthcare system had changed after the implant recall. They expressed a belief that they would need new surgery sooner than they first thought.ConclusionsDespite all the attention when the ASR prosthesis was recalled, patients with ASR-HRA did not report themselves negatively affected by the recall in this group of patients where a majority had actively sought for an HRA procedure. The healthcare system has an obligation to continue the annual exams, even if the implant provider does not continue reimbursement.

Highlights

  • Total hip arthroplasty is the traditional treatment for osteoarthritis in the hip joint

  • The present study focuses on a recalled metal-onmetal hip arthroplasty implant, Articular Surface Replacement (ASR) by DePuy/Johnson&Johnson (Leeds, United Kingdom)

  • The implant was developed in two options, hip resurfacing arthroplasty (HRA) and total hip arthroplasty (THA)

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Summary

Introduction

Total hip arthroplasty is the traditional treatment for osteoarthritis in the hip joint. With metal on metal bearing, is a modern concept initially developed mainly for young active people. The metal-on-metal hip arthroplasty implant, Articular Surface Replacement (ASR), was implanted in approximately 93,000 patients before it was recalled in 2010 due to a high complication rate. This study aimed to evaluate patients’ own experiences living with an implant that they knew had a high complication rate and had been recalled from the market. The present study focuses on a recalled metal-onmetal hip arthroplasty implant, Articular Surface Replacement (ASR) by DePuy/Johnson&Johnson (Leeds, United Kingdom). The implant was developed in two options, hip resurfacing arthroplasty (HRA) and total hip arthroplasty (THA). From the introduction of the ASR hip system in July 2003 to its recall in August 2010, approximately 93,000 patients received this implant worldwide, including both HRA and THA [2]. Since 1996, more than 1,000,000 different metal-on-metal hip implants have been implanted worldwide [3]

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