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Published on: November 8, 2015
Once daily calcineurin inhibitor monotherapy in pediatric liver transplantation
U D Ekong1, H Bhagat1, E M Alonso1
1Siragusa Transplant Center, Children's Memorial Hospital, Northwestern University Feinberg School of Medicine, Chicago, IL.
Insights
Pediatric liver transplant patients on reduced-dose, once-daily calcineurin inhibitor (CNI) monotherapy showed successful outcomes. A longer interval post-transplant improved the success rate of this safe therapeutic strategy.
Area of Science:
- Pediatric Transplant Medicine
- Immunosuppression Therapy
- Hepatology
Background:
- Calcineurin inhibitors (CNIs) are crucial for preventing organ rejection post-transplant.
- Optimizing CNI dosing is essential to balance efficacy and minimize toxicity in pediatric liver recipients.
Purpose of the Study:
- To evaluate the safety and efficacy of reduced-dose, once-daily CNI monotherapy in pediatric liver transplant recipients.
- To identify factors influencing the success of CNI dose reduction and simplified dosing regimens.
Main Methods:
- Retrospective analysis of 147 pediatric liver transplant recipients (2001-2008).
- Fifty-six patients meeting specific criteria transitioned to once-daily CNI at half their previous dose.
- Success defined as normal liver enzymes at 1 year post-dose change with sustained normal levels.
Main Results:
- Fifty out of 56 patients (89%) successfully achieved the reduced-dose, once-daily CNI regimen.
- Graft loss did not occur in any patients undergoing this therapy.
- Successful dose change was associated with a significantly longer interval from initial liver transplantation (p < 0.05).
Conclusions:
- Reduced-dose, once-daily CNI monotherapy is a safe and effective strategy for carefully selected pediatric liver transplant recipients.
- A longer post-transplant period is a key factor predicting successful CNI dose reduction and simplified immunosuppression.
Abstract:
This report describes a group of pediatric liver transplant recipients who have undergone once daily calcineurin inhibitor (CNI) monotherapy at Children's Memorial Hospital, Chicago, between January 1, 2001 and November 30, 2008. We defined success as normal liver enzymes at 1 year after dose change, with normal enzymes throughout all follow-up. Patients who did not meet the set criteria or had lost an organ to chronic rejection were not considered for this therapeutic strategy. There were 147 patients in our organ transplant tracking record (OTTR) who were > or = 5 years post liver transplant. Of these, 56 underwent reduced dose, once daily CNI monotherapy. Patients who met the set criteria were placed on once daily calcineurin inhibitor at half their previous dose. Fifty patients successfully achieved this dose change, while six patients failed at a mean of 3.7 +/- 3.2 months following the dosing change. The mean interval from transplant was significantly longer in those patients who were successful compared to those who failed dose change (p < 0.05). Importantly, there have been no graft losses. Reduced dose, once daily CNI monotherapy is safe in carefully selected recipients, with a longer interval post liver transplantation increasing the likelihood of success.
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