patienten aan ECMO heart-lung machine
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
2 Years to 17 Years
Inclusion criteria
Inclusion criteria: neonates and children 0-18 year on ECMO
Exclusion criteria
Exclusion criteria: Witheld informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Karacterizing the Pharmacokinetics of different drugs (analgesia, sedatives, antibiotics, inotropic agents, PGE5 inhibitor, and diuretics) routinely used in patients undergoing ECMO. Describing the relationship between pharmacokinetics and demografical, physiological, pathophysiological factors like diagnosis, genotype, PRISM/PIM scores, liver and kidney function albumin concentrations, different ECMO modi, ECMO flow, dialysis, bloodtransfusions and ventilator settings. | — |
Secondary
| Measure | Time frame |
|---|---|
| Karacterizing the relationship between pharmacokinetics and clinical effects of the above mentioned medication. Describing the relationship between pharmacodynamics and demografical, physiological, pathophysiological factors. Formulating dosing regimes for the studied medication for patients treated with ECMO. | — |
Countries
Netherlands
Outcome results
None listed