Abstract

BackgroundWe studied which factor could predict aseptic loosening in ABG I hip prosthesis with hydroxyapatite coating. Aseptic loosening and periprosthetic osteolysis are believed to be caused, at least in part, by increased polyethylene (PE) wear rate via particle disease. Based on it, increased PE wear rate should be associated with aseptic loosening regardless of the type of implant.MethodsWe analyzed data from 155 revisions of ABG I hip prostheses to examine the influence of patient, implant, surgery, and wear related factors on the rate of aseptic loosening at the site of the cup. This was calculated by stepwise logistic regression analysis. The stability of the implant and severity of bone defects were evaluated intraoperatively.ResultsWe found that men (odds ratio, OR = 5.6; p = 0.004), patients with Charnley class C (OR = 6.71; p = 0.013), those having more severe acetabular bone defects (OR = 4 for each degree of severity; p = 0.002), and longer time to revision surgery (OR = 1.51 for each additional year; p = 0.012) had a greater chance of aseptic loosening of the cup. However, aseptic loosening was not directly predicted by polyethylene wear rate in our patients.ConclusionSeverity of bone defects predicts the risk for aseptic loosening in ABG I cup. Factors potentially associated with the quality of bone bed and biomechanics of the hip might influence on the risk of aseptic loosening in this implant.

Highlights

  • We studied which factor could predict aseptic loosening in ABG I hip prosthesis with hydroxyapatite coating

  • We found a significant association between wear rate and severity of osteolysis in ABG I prosthesis, and an unacceptably high rate of aseptic loosening in ABG I cups [12,13]

  • We found that only linear polyethylene wear rate predicts the risk for complete revision (OR = 36.94 per each mm/year; 95% CI 4.69290.66; R2 = 0.252)

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Summary

Introduction

We studied which factor could predict aseptic loosening in ABG I hip prosthesis with hydroxyapatite coating. Aseptic loosening and periprosthetic osteolysis are believed to be caused, at least in part, by increased polyethylene (PE) wear rate via particle disease. Based on it, increased PE wear rate should be associated with aseptic loosening regardless of the type of implant. Aseptic loosening is the most frequent cause of total hip arthroplasty (THA) failure [1]. Both mechanical and biological mechanisms are potentially involved. Known influences on aseptic loosening include variables related to polyethylene wear rate, size of periprosthetic osteolysis, design-related variables (i.e. prosthetic material and shape, fixation surface, etc.), surgical experience and technique (quality of implant settlements), and primary diagnosis [7,8,9]. Other factors that may be important, but are not readily analyzed, include interactions between the implant and its surroundings such as composition of joint fluid, type of lubrication, individual motion/stress pattern, and genetic predisposition [10]

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