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Population Pharmacokinetics of Caffeine in Neonates with Congenital Heart Disease and Associations with Acute Kidney Injury.

Elizabeth J ThompsonKanecia O ZimmermanDaniel GonzalezHenry P FooteSangah ParkKevin D HillJillian H HurstChi D HornikReid C ChamberlainRasheed A GbadegesinChristoph P Hornik
Published in: Journal of clinical pharmacology (2023)
Cardiac surgery-associated acute kidney injury (CS-AKI) occurs in ∼65% of neonates undergoing cardiac surgery on cardiopulmonary bypass and contributes to morbidity and mortality. Caffeine may reduce CS-AKI by counteracting adenosine receptor upregulation after bypass, but pharmacokinetics (PK) in this population are unknown. The goal of our analysis is to address knowledge gaps in age-, disease-, and bypass-related effects on caffeine disposition and explore preliminary associations between caffeine exposure and CS-AKI using population PK (PopPK) modelling techniques and an opportunistic, electronic health record-integrated trial design. We prospectively enrolled neonates receiving pre-operative caffeine per standard of care and collected PK samples. We retrospectively identified neonates without caffeine exposure undergoing surgery on bypass as a control cohort. We followed FDA guidance for PopPK model development using NONMEM. Effects of clinical covariates on PK parameters were evaluated. We simulated peri-operative exposures and used multivariable logistic regression to evaluate the association between caffeine exposure and CS-AKI. Twenty-seven neonates were included in model development. A 1-compartment model with bypass time as a covariate on clearance and volume of distribution best fit the data. Twenty-three neonates with caffeine exposure and 109 controls were included in the exposure-response analysis. Over half of neonates developed CS-AKI. On multivariable analysis, there were no significant differences between CS-AKI based on caffeine exposure. Neonates with single ventricle heart disease without CS-AKI had consistently higher simulated caffeine exposures. Our results highlight areas for further study to better understand disease- and bypass-specific effects on drug disposition and identify populations where caffeine may be beneficial. This article is protected by copyright. All rights reserved.
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