Renal-sparing immunosuppressive protocol using OKT3 after liver transplantation: a 19-year single-institution

Peter T W Kim1, Srinath Chinnakotla, Gary Davis

  • 1Annette C. and Harold C. Simmons Transplant Institute, Baylor University Medical Center at Dallas. Dr. Kim is now a hepatobiliary fellow in Canada.

Proceedings (Baylor University. Medical Center)
|November 3, 2011
PubMed

Insights

Muromonab-CD3 (OKT3) in liver transplant patients with acute renal failure (ARF) showed similar long-term survival for those on renal replacement therapy (RRT). This approach allowed critically ill patients to achieve comparable outcomes.

Area of Science:

  • Nephrology
  • Immunology
  • Transplantation

Background:

  • Acute renal failure (ARF) is common in liver transplant recipients.
  • Muromonab-CD3 (OKT3) is used at our institution for ARF with delayed calcineurin inhibitor initiation.
  • Outcomes of OKT3 use in liver transplant patients with ARF require evaluation.

Purpose of the Study:

  • To compare outcomes in liver transplant patients with ARF who received muromonab-CD3 (OKT3) versus those who did not.
  • To assess the impact of OKT3 on survival and renal recovery in liver transplant recipients with ARF.

Main Methods:

  • Retrospective cohort study from 1988 to 2007.
  • Included 1685 liver transplant patients with ARF (65% of total).
  • Compared 109 patients receiving OKT3 (OKT3 group) with 1416 patients on low-dose calcineurin inhibitors (control group).

Main Results:

  • The OKT3 group was more critically ill.
  • Long-term survival was similar for OKT3 and control groups on renal replacement therapy (RRT).
  • OKT3 group had higher complete renal recovery but no improved long-term survival in non-RRT patients. Increased bacterial/fungal infections observed, but no increased malignancy or hepatitis C recurrence mortality.

Conclusions:

  • Muromonab-CD3 (OKT3) use in liver transplant patients with ARF enables critically ill patients on RRT to achieve survival rates similar to controls.
  • OKT3 may offer a viable immunosuppressive strategy for select liver transplant recipients with ARF, particularly those requiring RRT.

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