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Plasmapheresis in primary dysfunction of hepatic transplants
1Department of Medicine, Mount Sinai Medical Center, New York 10029-6574, USA.
Journal of Clinical Apheresis
|January 1, 1996
Summary
Plasmapheresis did not significantly improve liver graft survival in primary graft dysfunction. However, it reduced elevated cytokines and showed a trend toward improved survival in patients with renal failure.
Area of Science:
- Hepatology
- Transplantation immunology
- Critical care medicine
Background:
- Primary graft dysfunction affects ~5% of liver transplants, often necessitating retransplantation.
- Elevated cytokines (interleukin-6, tumor necrosis factor) are linked to hepatic graft dysfunction.
- Plasmapheresis has historical benefit in fulminant hepatic failure, suggesting potential in graft dysfunction.
Purpose of the Study:
- To evaluate plasmapheresis effectiveness in primary liver graft dysfunction.
- To compare clinical outcomes, patient, and graft survival with historical controls.
Main Methods:
- 18 liver transplant patients with primary graft dysfunction received four daily plasma exchange procedures.
- Outcomes were compared to a historical control group.
Main Results:
- No significant difference in graft survival at 10 days or patient survival at 100 days between groups.
- Plasmapheresis group showed higher dialysis incidence, indicating more severe dysfunction.
- Significant reduction in tumor necrosis factor (66.0%) and interleukin-6 (55.2%) after one procedure.
Conclusions:
- Plasmapheresis did not significantly improve graft survival in primary graft dysfunction.
- A non-significant trend towards increased patient survival was observed in severe cases with renal failure.
- Documented reduction of elevated cytokines (TNF and IL-6) suggests a potential role in managing specific aspects of graft dysfunction.