Population pharmacokinetics of intravenous clonidine for sedation during paediatric extracorporeal membrane oxygenation and continuous venovenous hemofiltration

• Published in: British journal of clinical pharmacology Vol. 83; no. 6; pp. 1227 - 1239
• Main Authors: Kleiber, Niina, Mathôt, Ron A. A., Ahsman, Maurice J., Wildschut, Enno D., Tibboel, Dick, Wildt, Saskia N.
• Format: Journal Article
• Language: English
• Published: England John Wiley and Sons Inc 01.06.2017
• Subjects: Adolescent; Aging - metabolism; Child; Child, Preschool; clonidine; Clonidine - administration & dosage; Clonidine - pharmacokinetics; Computer Simulation; Disease Progression; dosing guideline; extracorporeal membrane oxygenation; Extracorporeal Membrane Oxygenation - methods; Female; Hemofiltration - methods; Humans; Hypnotics and Sedatives - administration & dosage; Hypnotics and Sedatives - pharmacokinetics; Infant; Infant, Newborn; Injections, Intravenous; Male; Models, Statistical; paediatric intensive care; Pharmacokinetics; Population; sedation; Sex Characteristics; α‐agonist; dosing guideline; paediatric intensive care; clonidine; pharmacokinetics; extracorporeal membrane oxygenation; α-agonist; sedation
• ISSN: 0306-5251; 1365-2125
• DOI: 10.1111/bcp.13235

Aims Clonidine is used for sedation in the paediatric intensive care unit. Extracorporeal membrane oxygenation (ECMO) provides temporary support if respiratory and cardiac function is threatened. ECMO influences the pharmacokinetics of drugs. Clonidine during paediatric ECMO cannot be effectively titrated as PK data are lacking. The aim of this study is to describe clonidine PK in a particular ECMO system and propose dosing guidelines for children on this particular ECMO circuit. Methods All children below the age of 18 years who received clonidine during ECMO were eligible. The pharmacokinetic analysis was conducted by nonlinear mixed effect modelling, which enables to establish the separate influences of determinants on drug blood level and to provide individualized dosing. Results Twenty‐two patients, median age 1 month (IQR 6.4) and weight at inclusion 4 kg (IQR 3.1) were included of whom 90% in addition to ECMO received pre‐emptive continuous venovenous hemofiltration to optimize fluid balance. The clonidine clearance rate was two‐fold that measured in patients not on ECMO. Clearance increased steeply with postnatal age: at days 6, 8 and 10, respectively 30%, 50% and 70% of the adult clearance rate was reached. The use of diuretics was associated with a lower clearance. The volume of distribution increased by 55% during ECMO support. Conclusion Our findings suggest that a higher dose of clonidine may be needed during ECMO. The PK parameters on ECMO and the dosing guidelines proposed hold the potential to improve sedation practices on ECMO but need to be repeated with different ECMO systems.