Transplantation Proceedings
Volume 36, Issue 6 , Pages 1747-1752, July 2004

The impact of thymoglobulin on renal function and calcineurin inhibitor initiation in recipients of orthotopic liver transplant:

A retrospective analysis of 298 consecutive patients

  • J.I. Tchervenkov

      Affiliations

    • Department of Surgery, Section of Transplantation, Royal Victoria Hospital, McGill University Health Center, Montreal
    • Corresponding Author InformationAddress reprint requests to Jean I. Tchervenkov, MD, Director of Transplantation, 687 Pine Ave. West, S 10.26, Montreal, Quebec H3A 1A1 Canada
  • ,
  • G.N. Tzimas

      Affiliations

    • Department of Surgery, Section of Transplantation, Royal Victoria Hospital, McGill University Health Center, Montreal
  • ,
  • M. Cantarovich

      Affiliations

    • Department of Medicine, Royal Victoria Hospital, McGill University Health Center, Montreal, Quebec, Canada
  • ,
  • J.S. Barkun

      Affiliations

    • Department of Surgery, Section of Transplantation, Royal Victoria Hospital, McGill University Health Center, Montreal
  • ,
  • P. Metrakos

      Affiliations

    • Department of Surgery, Section of Transplantation, Royal Victoria Hospital, McGill University Health Center, Montreal

Abstract 

Background

Renal dysfunction remains the Achilles' heel of calcineurin inhibitor (CI)use. The purpose of this study was to assess our institutional, renal-sparing strategy using thymoglobulin (TMG) in recipients of orthotopic liver transplants.

Methods

We performed a retrospective analysis of data from 298 adult recipients who were transplanted between 1991 and 2002. The patients were divided into two groups: those induced with TMG (group 1) and those that were not treated with this agent (group 2). A subgroup analysis was performed of patients with baseline serum creatinine values above 1.5 mg/dL (group 1A received TMG; group 2A did not). All patients received tacrolimus or cyclosporine (CyA) maintenance immunosuppression.

Results

Indications and demographics were similar between the two groups. Although there was no difference in patient and graft survivals, there was a statistically significant benefit in the rejection-free graft survival at 1 year for group 1 (51% vs 39%; P = .02). Furthermore, serum creatinine at 6 months was lower for group 1, despite a similar baseline creatinine. Subgroup analysis for patients with baseline abnormal serum creatinines showed that group 1A displayed an improved rejection-free graft survival at 1 month but not at 1 year.

Conclusions

Thymoglobulin induction therapy may allow a delay in the initiation of CI therapy without compromising patient and graft survival, while preventing early rejection, even among patients with baseline renal dysfunction.

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 This work was supported by the Lois and Byron Dolgin Liver Transplant Fellowship, and by the Michael Cohen Liver Transplant Fellowship, of the Royal Victoria Liver Transplant Fund.

PII: S0041-1345(04)00679-7

doi:10.1016/j.transproceed.2004.06.014

Transplantation Proceedings
Volume 36, Issue 6 , Pages 1747-1752, July 2004