Impact of CYP3A5 phenotype on tacrolimus time in therapeutic range and clinical outcomes in pediatric renal and heart transplant recipients
Author:
Affiliation:
1. Department of Clinical Pharmacy College of Pharmacy University of Michigan Ann Arbor Michigan USA
Funder
National Center for Advancing Translational Sciences
Publisher
Wiley
Subject
Pharmacology (medical)
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/phar.2601
Reference42 articles.
1. OPTN / SRTR 2018 Annual Data Report: Kidney
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1. Evaluating the evidence for genotype‐informed Bayesian dosing of tacrolimus in children undergoing solid organ transplantation: A systematic literature review;British Journal of Clinical Pharmacology;2024-08-15
2. Cost-effectiveness analysis of CYP3A5 genotype-guided tacrolimus dosing in solid organ transplantation using real-world data;The Pharmacogenomics Journal;2024-05-15
3. External assessment and refinement of a population pharmacokinetic model to guide tacrolimus dosing in pediatric heart transplant;Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy;2023-06-22
4. Impact of CYP3A5 genotype on de-novo LCP tacrolimus dosing and monitoring in kidney transplantation;Pharmacogenetics and Genomics;2023-02-17
5. Predictive Capacity of Population Pharmacokinetic Models for the Tacrolimus Dose Requirements of Pediatric Solid Organ Transplant Recipients;Therapeutic Drug Monitoring;2023-02
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