Treatment of full-thickness femoral cartilage lesions using condyle resurfacing prosthesis

Jens Ole Laursen1, Martin Lind2

  • 1Department of Orthopedic Surgery, County Hospital of South Jutland, Sønderborg, Denmark.

Insights

Femoral resurfacing with the HemiCAP implant improved knee function and reduced pain for cartilage lesions. However, a significant 23% reoperation rate requiring arthroplasty was observed within seven years.

Area of Science:

  • Orthopedic surgery
  • Biomaterials science
  • Regenerative medicine

Background:

  • Cartilage lesions in the knee joint can lead to pain and osteoarthritis.
  • Femoral resurfacing offers a potential treatment option for focal cartilage defects.
  • The HemiCAP implant is a device designed for femoral resurfacing.

Purpose of the Study:

  • To evaluate the outcomes of HemiCAP implant for femoral resurfacing in patients with trochleal and condylar cartilage lesions.
  • To assess subjective outcomes, pain levels, and reoperation rates following HemiCAP implantation.

Main Methods:

  • A prospective cohort study of 61 patients treated with HemiCAP implants between 2007 and 2012.
  • Patients had symptomatic ICRS grade 3-4 cartilage lesions less than 4 cm².
  • Follow-up included Knee Society scores (KSS), pain assessments, and radiographic evaluations for 2 years, with 7-year follow-up for complications.

Main Results:

  • Significant improvements in mean KSS (52 to 90) and KSS function score (45 to 92) were observed at 2-year follow-up.
  • Mean pain scores decreased from 7.1 to 1.8 at 2 years.
  • Twenty-three percent of implants were revised to arthroplasty within 7 years due to lesion progression, osteoarthritis, or pain.

Conclusions:

  • HemiCAP femoral resurfacing provides short-term improvement in subjective outcomes and pain for cartilage lesions.
  • A substantial reoperation rate (23%) requiring conversion to arthroplasty highlights limitations.
  • This treatment may serve as a temporary solution for younger patients or those not yet candidates for arthroplasty.
Abstract

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