J80.0
Conditions
Interventions
Group 1: In sedated patients with ARDS, sedation depth and regional oxygen saturation are measured during the sedation period using non-invasive monitoring techniques (adhesive electrodes applied to t
Sponsors
Universitätsmedizin GöttingenKlinik für Anästhesiologie
Eligibility
Sex/Gender
All
Age
18 Years to 91 Years
Inclusion criteria
Inclusion criteria: Patient of Ward 0119 (w / m / d) Age> 18 years <91 years Diagnosis of an ARDS Existence of valid information There is a valid consent
Exclusion criteria
Exclusion criteria: Rejection of participation Lack of consent Age 91 years Lack of cooperativity in JH-ACE testing (vigilance disorder, delirium, aphasia) Impossibility of JH-ACE testing due to limited knowledge of the German language
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cognitive performance at the end of the intensive care stay by means of a cognitive questionnaire (John Hopkins' Adapted Cognitive Exam) | — |
Secondary
| Measure | Time frame |
|---|---|
| Depth of sedation during the sedation phase in the intensive care unit recorded using non-invasive technology (Sedline, Masimo) Cumulative sedative dose as a summation of all sedatives during the intensive care stay taken from the digital documentation system Regional oxygen saturation during the sedation phase in the intensive care unit is measured using non-invasive technology (O3, Masimo). | — |
Countries
Germany
Contacts
Public ContactLars-Olav Harnisch
Universitätsmedizin GöttingenKlinik für Anästhesiologie
Outcome results
None listed