The objective of this study is to determine the incidence of delirium in adults patients who are admitted at the critical care unit of a Dutch University Hospital. The primary aim is to determine the incidence of delirium and to determine risk factors for this group of patients to develop a prediction model. A secondary aim is to find differences between delirious patients and non-delirious patients on different aspects of diagnostics, treatment and care, outcome, length of stay, and inflammation. According to Dutch law, the need to obtain informed consent was waived by the Committee on Research Involving Human Subjects (CMO) of Nijmegen for this observational study (2007/283).
Study Type
OBSERVATIONAL
Enrollment
700
Radboud University Nijmegen Medical Centre, Critical Care
Nijmegen, Gelderland, Netherlands
delirium
Time frame: during admission at the critical care
markers of inflammation
Time frame: within 24 hours of delirium diagnosis
biomarkers
Time frame: within 24 hours of delirium diagnosis
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