PRe-Operative Prediction of postoperative DElirium by appropriate SCreening
- Conditions
- F05.8Other delirium
- Registration Number
- DRKS00015715
- Lead Sponsor
- Klinik für AnästhesieUniversitätsklinikum Bonn
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 1000
Inclusion Criteria
Age over 60 years
- At least 60 minutes of surgery
- Signed declaration of consent of the patients
Exclusion Criteria
- Patients who undergo emergency surgery
- Patients with language barriers
- Any disease that, in the opinion of the investigator could compromise patient safety or compliance with the study protocol.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary endpoint is the diagnosis of postoperative delirium. <br>This is diagnosed postoperatively by the <br>Delirium Observation Scale (DOS) and the Confusion Assesment Method (CAM) as well as the Alertness, Attention, Abbreviated Mental Test (4AT) and the Attention Screening Examination (ASE-Test) on the normal ward.<br>For the Intensive Care unit the Confusion Assesment Method for Intensive Care Units (CAM-ICU) and the Delirium Observation Scale (DOS) will be used.<br> Testing takes place from the first to the fifth day after an operation respectively after cessation of sedation.
- Secondary Outcome Measures
Name Time Method Telefon-Follow-up measuring Persistent postoperative cognitive dysfunction and quality of life at 180 days after surgery using Informant Questionnaire on Cognitive Decline in the Elderly (IQ-Code) and the Euro Qol Group 5 Dimensions - 5 Level (EQ-5D-5L) Test.<br>