Post-Intensive Care Syndrome A41.8 F06.3 F32.9 F06.7 G62.8 G72.8
Conditions
Interventions
Group 1: Patient:inside after intensive medical treatment
Sponsors
Charité - Universitätsmedizin Berlin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age = 18 years Intensive care treatment > 72h
Exclusion criteria
Exclusion criteria: non
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the diagnosis of PICS by at least one abnormality in one of the domains | — |
Secondary
| Measure | Time frame |
|---|---|
| - Subdomains of the PICS or number of PICS domains affected. - Physical function (including Barthel index, timed Up-and-Go, Short Physical Performance Battery Test (SPPB), hand strength, bioimpedance analysis). - Quality of life (e.g. European Quality of Life 5 Dimensions 5 Level (EQ5D-5L)) - Cognitive function (e.g. MiniCog, animal naming test, Trail Making Test A+B) - Disability (WHO Disability Assessment Schedule 2.0 (WHODAS 2.0)) - Mental health (Patient Health Questionnaire-4 (PHQ-4) and Patient Health Questionnaire-8 (PHQ-8) Generalized Anxiety Disorder Scale-7 (GAD-7), Impact of Event Scale - Revised (IES-R)) - Swallowing disorders - Health care needs (duration of ventilation, intensive care and hospital stay, rehabilitation duration, nursing care needs, medication needs) - Nutritional status (including MNA short/long, NRS 2002, MUST, SGA, PG-SGA, weight change, abdominal circumference, skin thickness) - If other tests are added to survey for PICS, they will also be included - Exploratory evaluation of routine clinical data will be performed | — |
Countries
Germany
Contacts
Public ContactClaudia Spies
Klinik für Anästhesiologie und Intensivmedizin CCM/CVK
Outcome results
None listed