PRe-Operative Prediction of postoperative DElirium by appropriate SCreening” (PROPDESC) Score-VALidatio
Recruiting
- Conditions
- F05.8Other delirium
- Registration Number
- DRKS00028712
- Lead Sponsor
- niversitätsklinikum Bonn Klinik für Anästhesiologie und Operative Intensivmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 2400
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
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)
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary endpoint:<br>Validity of the PROPDESC score for preoperative assessment of risk of postoperative delirium.
- Secondary Outcome Measures
Name Time Method Secondary endpoints:<br>Length of stay in hospital (LOS) and intensive care unit (ICU-LOS).<br>In-hospital mortality