F05.0
Conditions
Interventions
Group 1: Arm 1 (intervention arm): Preoperative frailty assessment, blood pressure profile, transcranial Doppler examination
Group 2: Arm 2 (control arm): Preoperative frailty assessment, blood pressu
Sponsors
Institut für Anästhesiologie, Herz- und Diabeteszentrum NRW
Eligibility
Sex/Gender
All
Age
70 Years to No maximum
Inclusion criteria
Inclusion criteria: Planned operation with use of the heart-lung machine
Exclusion criteria
Exclusion criteria: Lack of capacity to consent, refusal of the study by the patient, already proven cerebral perfusion obstacles, pre-existing delirium, unplanned operations and participation in other studies, especially drug studies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative delirium rate recorded on the 1st, 2nd and 3rd postoperative day using CAM-ICU and Delta Scan EEG | — |
Secondary
| Measure | Time frame |
|---|---|
| Stroke rate during the entire hospital stay recorded by ICD-10 coding; Length of hospitalisation measured in days until transfer to home, rehabilitation facility or death 1-year mortality rate, collected from routine data | — |
Countries
Germany
Contacts
Public ContactVera von Dossow
Institut für Anästhesiologie, Herz- und Diabateszentrum NRW
Outcome results
None listed