2011 - ISBTS 2011 Symposium


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Oral Communications 4: Intestinal Immunosuppression / Rejection

6.132 - Sirolimus and low dose Tacrolimus combined immunosuppression for the small bowel transplants with compromised renal function

Presenter: Myung-Duk, Lee, Seoul, Korea
Authors: Myung-Duk Lee1, Dong Goo Kim1, In Sung Moon1, Ji Il Kim2, Deuk Young Oh3, Sang Il Kim4, Shinn Young Kim2, Chong Young Choi5, Jae Myung Park5, Seung Eun Nha6, Eun Sun Chung7

132
Sirolimus and low dose Tacrolimus combined immunosuppression for the small bowel transplants with compromised renal function

Myung-Duk Lee1, Dong Goo Kim1, In Sung Moon1, Ji Il Kim2, Deuk Young Oh3, Sang Il Kim4, Shinn Young Kim2, Chong Young Choi5, Jae Myung Park5, Seung Eun Nha6, Eun Sun Chung7

1Department of Surgery, The Catholic University of Korea, Seoul, Korea; 2Department of Surgery, The Catholic University of Korea, Seoul, Korea; 3Department of Plastic Surgery, The Catholic University of Korea, Seoul, Korea; 4Department of Infectious Disease, The Catholic University of Korea, Seoul, Korea; 5Department of Gastroenterology, The Catholic University of Korea, Seoul, Korea; 6Department of Radiology, The Catholic University of Korea, Seoul, Korea; 7Department of Pathology, The Catholic University of Korea, Seoul, Korea

Background: To reverse the deteriorated renal function of the small bowel transplants (SBTx) under the Tacrolimus monotherapy, Sirolimus combined immunosuppression with lowered dose  Tacrolimus was administered.

Patients and Method: A total of 5 SBTx of this institution since 2004 were included in this study. Two were living-related donor transplants(LDTx) and 3 deceased donor transplants(DDTx). Tacrolimus was the primary immunosuppressant and the induction was Daclizumab, Basiliximab, Thymoglobulin or Alemtuzumab depending on the situation. Target serum trough level of Tacrolimus for the first 3 months of transplantation was 10 to 15 ng/dL, then 5 to 10 ng/dL. When serum BUN/Cr concentration was persistent above 30/1.8 mg/dL, Sirolimus (targeted above 10 ng/dL) was administered with lowered dose Tacrolimus (targeted 5-10 ng/dL for the first 3 months post-transplant, and then 2-5 afterwards).

Result: After acute rejection episode in Tacrolimus monotherapy of the #1 DDTx, BUN/Cr stayed above the criteria. Sirolimus was administered from the 5th month post-transplant, and BUN/Cr decreased below 20/1.2 mg/dL. In #2 DDTx, Sirolimus combination from a month post-transplant resulted in normalized BUN/Cr, but the patient died after 3 months due to unresolved septic complications. In #3 DDTx, Sirolimus combination from a month post-transplant returned renal function to normal. The #2 LDTx of a 3-year-old girl had been in good renal function for 5 years of transplantation, when segmental graft resection was performed for chronic rejection. Postoperative electrolyte imbalance and elevated BUN/Cr returned to normal after Sirolimus combination. The #1 LDTx has been in marginal chronic renal failure with proteinuria for 6 years post-transplant, when Sirolimus combination regimen was applied. Her renal function improved clearly, but could not stay alone within normal limits.

Summary: Sirolimus combination with low dose Tacrolimus was effective for the graft safety and recovery of the compromised renal function of the SBTx with Tacrolimus monotherapy.  


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