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Osteonecrosis of the hip in the sickle-cell diseases. Treatment and complications

G J Hanker1, H C Amstutz

  • 1Southern California Orthopedic and Sports Medical Group, Van Nuys 91405-3641.

Insights

Hip arthroplasty in patients with sickle cell disease and osteonecrosis yields poor outcomes. High complication rates and early failure necessitate careful consideration for these surgical procedures.

Area of Science:

  • Orthopedic Surgery
  • Hematology
  • Bone Diseases

Background:

  • Sickle cell disease (SCD) and sickle cell trait (SCT) can lead to osteonecrosis of the femoral head.
  • Surgical interventions like hip arthroplasty are sometimes considered for managing femoral head osteonecrosis in these patients.

Observation:

  • This study reviewed nine patients with SCD or SCT and femoral head osteonecrosis who underwent hip arthroplasty or other surgical procedures.
  • Follow-up averaged 6.5 years, revealing a high incidence of complications.

Findings:

  • Five of eight hip arthroplasties required revision or excision due to mechanical loosening, sepsis, or prosthetic stem fracture.
  • All patients experienced significant perioperative blood loss, prolonged hospital stays, and medical/surgical complications, irrespective of SCD/SCT severity.
  • Survivorship analysis predicted a 50% failure rate by 5.4 years postoperatively.

Implications:

  • Hip arthroplasty in patients with sickle cell disease and osteonecrosis is associated with a high failure rate and severe complications.
  • These findings suggest that current surgical approaches may not be optimal for this patient population.
  • Further research is needed to explore alternative or modified treatment strategies for femoral head osteonecrosis in sickle cell patients.

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