Sirolimus and mirabegron interaction in a hematopoietic cell transplant patient

2017 ◽  
Vol 24 (8) ◽  
pp. 627-631 ◽  
Author(s):  
Jeff A Engle ◽  
Christina Fair

Purpose Hematopoietic cell transplant patients are exposed to numerous classes of medications. Transplant practitioners must vigilantly monitor for drug interactions especially involving immunosuppressants. We report a hematopoietic cell transplant patient receiving sirolimus who developed supratherapeutic serum concentrations after initiating mirabegron. Summary A 31-year-old, 98 kg female received a second umbilical cord blood transplant four years after the first transplant for relapsed acute myeloid leukemia. Mycophenolate mofetil and sirolimus were utilized for graft versus host disease prophylaxis. The patient was receiving sirolimus 2 mg daily and the serum concentration on day 26 post-transplant (day + 26) was within therapeutic range (6.7 μg/L, goal range 3–12 μg/L). Her post-transplant course was complicated by BK viruria-associated cystitis for which she was started on mirabegron. Six days after starting the new medication (day + 33), the sirolimus serum concentration increased to 19.2 μg/L. Thus mirabegron was discontinued and sirolimus was held. Sirolimus was restarted once the serum concentration was within goal and subsequently stabilized with a combination of 1 mg and 2 mg daily for a total weekly dose of 10 mg. The proposed mechanisms of interaction include: (1) sirolimus inhibition of organic anion transporting polypeptide leading to increased mirabegron in the intestinal lumen; (2) mirabegron inhibition of P-glycoprotein leading to increased absorption of sirolimus and; (3) increased sirolimus absorption leading to increased sirolimus serum concentrations. Conclusion To our knowledge, this is the first report of a potential drug interaction between sirolimus and mirabegron. Transplant specialists should be aware of this potential interaction when considering the concurrent use of these medications.

2020 ◽  
Vol 25 (5) ◽  
pp. 451-454
Author(s):  
Deni J. Trone ◽  
Elizabeth A. Hall

There are no widely accepted dose alterations for inhaled tobramycin in the setting of renal dysfunction, and serum concentrations are not typically monitored. Herein we describe a case report of a 16-year-old female with a history of 2 hematopoietic cell transplants and a kidney transplant who received inhaled tobramycin for chronic Pseudomonas aeruginosa management. The patient developed chronic kidney disease, and tobramycin concentrations were monitored. Initially she received a reduced dose of inhaled tobramycin, with repeated doses based on serum concentrations. The dose was increased, but serum concentrations obtained the following day remained higher than desired, leading to a suspicion of delayed systemic absorption. Tobramycin administration was changed from immediately prior to dialysis to the evening prior to the next day's dialysis session, and serum concentrations were consistently <1 mg/L postdialysis. In conclusion, systemic absorption of inhaled tobramycin in non–cystic fibrosis (CF) patients may differ compared to that observed in CF patients. Renal dysfunction may lead to systemic accumulation of inhaled tobramycin, and the timing of inhaled tobramycin administration with respect to dialysis has a potentially significant influence on drug clearance. Thus, monitoring may be required. Further cases are required to verify these observations.


Author(s):  
Giaimo Mariateresa ◽  
Prezioso Lucia ◽  
Cambo Benedetta ◽  
Palma Benedetta Dalla ◽  
Falcioni Federica ◽  
...  

2020 ◽  
Vol 26 (3) ◽  
pp. S354-S355
Author(s):  
Brendan L. Mangan ◽  
Dilan A. Patel ◽  
Heidi Chen ◽  
Katie S. Gatwood ◽  
Michael T. Byrne ◽  
...  

2018 ◽  
Vol 40 (6) ◽  
pp. e364-e368 ◽  
Author(s):  
Claire J. Detweiler ◽  
Sarah B. Mueller ◽  
Anthony D. Sung ◽  
Jennifer L. Saullo ◽  
Vinod K. Prasad ◽  
...  

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