F05.8
Conditions
Interventions
Group 1: Pre-operative routinely available baseline parameters and two items of the MoCA (Montreal Cognitive Assessment) questionnaire will be documented. Postoperative delirium assessments will be pe
Sponsors
Universitätsklinikum Bonn Klinik für Anästhesiologie und Operative Intensivmedizin
Eligibility
Sex/Gender
All
Age
60 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. patients aged 60 years and older 2. planned elective surgery or re-surgery lasting at least 60 minutes 3. written informed consent 4. patients capable of giving consent 5. planned overnight stay in hospital after surgery
Exclusion criteria
Exclusion criteria: 1. emergency surgery 2. intracranial surgery 3. patients who are not proficient in the German language 4. concurrent participation in an interventional clinical trial on POD 5. previous participation in PROPDESC-Val 6. anticipated lack of compliance with the study protocol (which prevents adequate cognitive testing and delirium assessment and precludes contractual capacity to consent)
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints: Length of stay in hospital (LOS) and intensive care unit (ICU-LOS). In-hospital mortality | — |
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint: Validity of the PROPDESC score for preoperative assessment of risk of postoperative delirium. | — |
Countries
Germany
Contacts
Public ContactVera Guttenthaler
Universitätsklinikum Bonn Klinik für Anästhesiologie und Operative Intensivmedizin
Outcome results
None listed