The influence of cardiopulmonary bypass on pediatric pharmacokinetics

被引:3
|
作者
van Saet, Annewil [1 ,3 ]
Tibboel, Dick [2 ]
机构
[1] Erasmus MC, Dept Anesthesiol, Rotterdam, Netherlands
[2] Erasmus MC, Dept Intens Care & Pediat Surg, Rotterdam, Netherlands
[3] Erasmus MC, Dept Anesthesiol, Dr Molewaterplein 40,Room Na1717, NL-3015 GD Rotterdam, Netherlands
关键词
Cardiopulmonary bypass; congenital heart disease; pediatric; pharmacokinetics; Population pharmacokinetic modeling; OPEN-HEART-SURGERY; POPULATION PHARMACOKINETICS; CARDIAC-SURGERY; PLASMA-CONCENTRATIONS; TRANEXAMIC ACID; DRUG DISPOSITION; PROTEIN-BINDING; SEQUESTRATION; CHILDREN; PROPOFOL;
D O I
10.1080/17425255.2023.2227556
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IntroductionEvery year thousands of children undergo surgery for congenital heart disease. Cardiac surgery requires the use of cardiopulmonary bypass, which can have unexpected consequences for pharmacokinetic parameters.Areas coveredWe describe the pathophysiological properties of cardiopulmonary bypass that may influence pharmacokinetic parameters, with a focus on literature published in the last 10 years. We performed a PubMed database search with the keywords 'Cardiopulmonary bypass' AND 'Pediatric' AND 'Pharmacokinetics'. We searched related articles on PubMed and checked the references of articles for relevant studies.Expert opinionInterest in the influence of cardiopulmonary bypass on pharmacokinetics has increased over the last 10 years, especially due to the use of population pharmacokinetic modeling. Unfortunately, study design usually limits the amount of information that can be obtained with sufficient power and the best way to model cardiopulmonary bypass is yet unknown. More information is needed on the pathophysiology of pediatric heart disease and cardiopulmonary bypass. Once adequately validated, PK models should be integrated in the patient electronic database integrating covariates and biomarkers influencing PK, making it possible to predict real-time drug concentrations and guide further clinical management for the individual patient at the bedside.
引用
收藏
页码:333 / 344
页数:12
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