Care of the Critically Ill Pediatric Hematopoietic Cell Transplant Patient

2021 ◽  
pp. 1207-1241
Author(s):  
Sajad Jawad Khazal ◽  
Dristhi Ragoonanan ◽  
Janet Hume ◽  
Courtney Marie Rowan ◽  
Kris Michael Mahadeo
Author(s):  
Giaimo Mariateresa ◽  
Prezioso Lucia ◽  
Cambo Benedetta ◽  
Palma Benedetta Dalla ◽  
Falcioni Federica ◽  
...  

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

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.


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