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Low Follow-Up Rates After a Total Hip Arthroplasty Prosthesis Recall.

Leo H Cooper1, Stephen Wahl2, Jeffrey B Stambough1

  • 1Department of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

The Journal of Arthroplasty
|December 11, 2025
PubMed
Summary
This summary is machine-generated.

Less than 60% of patients followed up after a hip implant recall, despite outreach efforts. This highlights a need for better systems to ensure patients with recalled devices receive necessary follow-up care.

Keywords:
adherencedemographicsfollow-uprecalltotal hip arthroplasty

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Area of Science:

  • Orthopedic Surgery
  • Biomaterials Science
  • Patient Safety

Background:

  • A hip arthroplasty liner recall was issued due to premature polyethylene wear, risking osteolysis and implant failure.
  • Physicians and hospitals must inform patients about recalled implants.
  • A protocol was implemented to contact patients with recalled implants for follow-up.

Purpose of the Study:

  • To evaluate the effectiveness of a patient outreach protocol following a hip arthroplasty device recall.
  • To identify risk factors associated with patient nonresponse to recall notifications.

Main Methods:

  • Retrospective cohort study involving 763 patients who received hip arthroplasty with the recalled liner.
  • Standardized letters were used to notify patients of the implant recall.
  • Demographic data were collected to analyze predictors of follow-up.

Main Results:

  • A follow-up rate of 58.8% was achieved after recall letters were sent.
  • Significant predictors of follow-up included patient proximity to the institution, the performing surgeon, and health literacy.
  • Age, sex, BMI, and race were not associated with follow-up rates.

Conclusions:

  • Despite organized outreach, less than 60% of patients followed up after the hip implant recall.
  • A significant number of patients did not attend follow-up, increasing the risk of undetected implant failure.
  • Improved patient contact systems are necessary to ensure appropriate follow-up for recalled medical devices.