Key result
Initiation of dronedarone in a kidney transplant recipient on stable sirolimus resulted in a more than 3-fold increase in sirolimus trough concentration to 38.6 ng/mL.
Why the study?
Does dronedarone interact with sirolimus to increase its trough concentration in a kidney transplant recipient?
Case Report (n=1)
Does dronedarone interact with sirolimus to increase its trough concentration in a kidney transplant recipient?
Effect estimate: >3-fold increase
Dronedarone significantly increases sirolimus trough concentrations, necessitating a 50-75% dose reduction of sirolimus if concurrent administration cannot be avoided.
Potential sirolimus-dronedarone interaction may elevate levels; leaves open need for confirmatory studies before practice change.
OBJECTIVE: To report the potential clinically significant pharmacokinetic interaction between sirolimus and dronedarone. CASE SUMMARY: A 67-year-old man status post-kidney transplant in 2004 was maintained on an immunosuppressive regimen consisting of sirolimus, mycophenolate mofetil, and prednisone. He had been maintained for more than 1 year on a stable dose of sirolimus (5 mg/day), with concentrations ranging between 5 and 13.5 ng/mL. The patient was admitted to the hospital with a complaint of bloody diarrhea; shortly after admission, he developed atrial fibrillation for which dronedarone 400 mg twice daily was initiated. Sirolimus concentrations obtained 3 days after initiation of dronedarone revealed a trough concentration that was increased by more than 3-fold (38.6 ng/mL) from his baseline trough concentration. After sirolimus was held for 6 days, the trough concentration was 7.8 ng/mL. The dosage was reduced to 1 mg/day; there was no need for further adjustment. DISCUSSION: While the potential for an interaction between sirolimus and dronedarone is listed in the package insert of dronedarone, there are no documented reports of this interaction in the peer-reviewed literature. Since sirolimus is a narrow therapeutic index medication, information about the severity and magnitude of the interaction with dronedarone may help clinicians avoid therapeutic misadventures when this combination is employed. Our case clearly demonstrates a significant pharmacokinetic interaction between sirolimus and dronedarone. The Horn Drug Interaction Probability Scale indicates that the occurrence of an interaction between sirolimus and dronedarone in our case is probable. CONCLUSIONS: Due to the potential for sirolimus toxicity and excessive immunosuppression, the concurrent use of dronedarone and sirolimus should be avoided when possible. If concurrent administration cannot be avoided, we suggest close monitoring and a 50-75% dose reduction of sirolimus prior to dronedarone initiation.
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Tichy et al. (2010) conducted a case report in Kidney transplant recipient with atrial fibrillation (n=1). Dronedarone vs. Baseline (prior to dronedarone initiation) was evaluated on Sirolimus trough concentration (>3-fold increase). Initiation of dronedarone in a kidney transplant recipient on stable sirolimus resulted in a more than 3-fold increase in sirolimus trough concentration to 38.6 ng/mL.
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