sedativum op IC na cardiochirurgische ingreep eris geen sprake van een te bestuderen aandoening
Conditions
Interventions
During study A, 21 ICU patients will be sedated using a target controlled
infusion of propofol at one of 3 fixed target propofol concentrations in
addition to a target controlled infusion of S(+) ke
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Scheduled for ventilation and sedation at the ICU post cardiac surgery. Aged 18-80 years. Being able to give written informed consent.
Exclusion criteria
Exclusion criteria: Unable to give written informed consent. Increased intracranial pressure Poor ventricular function Epilepsy Psychosis Glaucoma History of cerebrovascular incident 35).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| • Ramsay score • BIS score • Cardiac Output (Vigileo) • Cardiac Index (Vigileo) • RRsys • RRdias • MAP • CVP • HR • SVV • SVR • Saturation | — |
Secondary
| Measure | Time frame |
|---|---|
| Concentration of propofol and ketamine from the several blood draws. | — |
Countries
Netherlands
Outcome results
None listed