Affiliation:
1. Department of Anesthesiology and Pain Medicine Seoul National University Hospital, Seoul National University College of Medicine Seoul Korea
2. Department of Anesthesiology and Pain Medicine, Asan Medical Center Ulsan College of Medicine Seoul Korea
3. Department of Clinical Pharmacology and Therapeutics Seoul National University College of Medicine Seoul Korea
Abstract
AbstractBackgroundCardiopulmonary bypass can affect the pharmacokinetics of anesthetic agents.AimsWe aimed to evaluate the pharmacokinetics of dexmedetomidine for infants and small children undergoing cardiac surgery with cardiopulmonary bypass based on population pharmacokinetics.MethodsWe enrolled 30 pediatric cardiac surgical patients in this study. After anesthetic induction with atropine (0.02 mg/kg), thiopental sodium (5 mg/kg), and fentanyl (2–3 μg/kg), we administered 1 μg/kg of dexmedetomidine for 10 min, followed by administration of 0.5 μg/kg of dexmedetomidine per hour during surgery. At the initiation of cardiopulmonary bypass, 1 μg/kg of dexmedetomidine was infused over 5 min. Arterial blood was obtained at predefined time points. A pharmacokinetic model was developed using NONMEM. Theory‐based allometric scaling with fixed exponents was applied. Weight, age, post‐menstrual age, fat‐free mass, whether to implement cardiopulmonary bypass and temperature were explored as covariates.ResultsA total of 376 blood samples were obtained from 29 children (age: 20.3 ± 19.3 months, weight: 9.7 ± 4.1 kg). A two‐compartment mammillary model with third compartment associated cardiopulmonary bypass procedure best explained the pharmacokinetics of dexmedetomidine. The pharmacokinetic parameter estimates (95% CI) standardized to a 70‐kg person were as follows: V1 (L) = 31.6 (17.9–39.5), V2 (L) = 90.1 (44.0–330), Cl (L/min) = 1.08 (0.70–1.25), Q (L/min) = 2.0 (1.05–3.46). Volume for third compartment associated cardiopulmonary bypass procedure (L) = 39.4 (19.3–50.9). Clearance was not influenced by the presence of cardiopulmonary bypass in this model.ConclusionWhen cardiopulmonary bypass is applied, the plasma concentration of dexmedetomidine decreases due to an increase in the volume of distribution, so a loading dose is required to maintain the previous concentration.
Subject
Anesthesiology and Pain Medicine,Pediatrics, Perinatology and Child Health