F05.8
Conditions
Interventions
Group 1: PROPDESC is a prospective observational study and therefore all included patients are observed identically according to the study protocol. There is no intervention.
The evaluation distinguis
Sponsors
Klinik für AnästhesieUniversitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
60 Years to No maximum
Inclusion criteria
Inclusion criteria: - Age over 60 years - At least 60 minutes of surgery - Signed declaration of consent of the patients
Exclusion criteria
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint is the diagnosis of postoperative delirium. This is diagnosed postoperatively by the 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. For the Intensive Care unit the Confusion Assesment Method for Intensive Care Units (CAM-ICU) and the Delirium Observation Scale (DOS) will be used. Testing takes place from the first to the fifth day after an operation respectively after cessation of sedation. | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Germany
Contacts
Public ContactJan Menzenbach
Klinik und Poliklinik für Anästhesie und operative Intensivmedizin, Universitätsklinikum Bonn
Outcome results
None listed