F05
Conditions
Interventions
Group 1: control group: standard of care (regular guideline-based routine care)
Group 2: structured multimodal approach to delirium prevention by a specialized team (non-pharmacological preventive mea
Sponsors
Universitätsmedizin Greifswald
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: - aged 65 yrs and over - planned elective general surgery or orthopaedic operation
Exclusion criteria
Exclusion criteria: - known neurological or psychiatric disorder - no consent given
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Delirium incidence, measured as the occurrence of post-operative delirium during the hospital stay (postoperatively tested by CAM (Confusion-Assessment-Method), clinical evaluation and chart review) | — |
Secondary
| Measure | Time frame |
|---|---|
| Prevalence of drug-related problems (drug-drug interactions, ADRs (adverse drug reactions), over/underdosing, untreated indications, drugs without indications, drug therapy in spite of contraindications), PIM (potentially inadequate medication) and delirogenic drugs | — |
Countries
Germany
Outcome results
None listed