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Use of livers with microvesicular fat safely expands the donor pool

T M Fishbein1, M I Fiel, S Emre

  • 1Division of Abdominal Organ Transplantation, The Mount Sinai Medical Center, New York, New York 10029, USA.

Transplantation
|July 27, 1997
PubMed
Abstract

Insights

Transplanting livers with moderate to severe microvesicular steatosis is safe and effective. Fatty liver grafts, identified by frozen-section biopsy, show good patient and graft survival rates post-transplant.

Area of Science:

  • Hepatology
  • Transplantation immunology
  • Surgical pathology

Background:

  • The safety of using donor livers with moderate to severe microvesicular steatosis for transplantation remains largely unknown.
  • Fatty liver allografts are frequently discarded, potentially limiting organ availability.
  • Frozen-section biopsy is a novel method to differentiate microvesicular from macrovesicular steatosis.

Purpose of the Study:

  • To evaluate the safety and efficacy of transplanting donor livers with moderate to severe microvesicular steatosis.
  • To assess early graft function, patient survival, and graft survival in this cohort.
  • To determine the reliability of frozen-section biopsy in evaluating steatosis and its reversibility.

Main Methods:

  • A retrospective review of 426 liver transplants, identifying 40 cases with ≥30% microvesicular steatosis.
  • Analysis of early graft function, patient/graft survival, and donor risk factors.
  • Comparison with non-fatty allografts and assessment of frozen-section biopsy reliability and steatosis persistence via follow-up biopsies.

Main Results:

  • Primary nonfunction occurred in 5% and poor early graft function in 10% of cases.
  • One-year patient and graft survival rates were 80% and 72.5%, respectively.
  • Donor obesity and traumatic death were common risk factors; frozen-section biopsy was reliable, and microsteatosis resolved in most grafts within 1 year.

Conclusions:

  • Donor livers with moderate to severe microvesicular steatosis can be safely transplanted.
  • Despite initial poor graft function, outcomes are not compromised.
  • Microsteatosis is often linked to donor risk factors and is typically reversible post-transplant.

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