Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
Conditions
Interventions
None.
Sponsors
None. Investigator initiated study.
Eligibility
Inclusion criteria
Inclusion criteria: - Intensive care admission with signs and symptoms of a viral infection - Intubated and mechanically ventilated - PCR positive for SARS-CoV-2 and/or a chest CT scan scored positive based on a CORADS-score of 4-5 by a radiologist
Exclusion criteria
Exclusion criteria: None.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical data, laboratory results, EIT measurements and vital parameters will be collected within the MaastrICCht cohort. As multiple hypotheses can be investigated within the observational cohort, no predefined primary outcome for the whole cohort will be defined. Rather, investigators have to submit a data request including a predefined analysis plan according to reporting guidelines appropriate for the type of study (i.e., STROBE for observational studies, STARD for diagnostic studies, TRIPOD for prognostic studies; see the Enhancing the QUAlity and Transparency Of health Research network at www.equator-network.org for detailed information). All external researchers submitting a data request will be required to produce a statistical analysis plan that will be reviewed by the cohort steering committee. | — |
Contacts
Public ContactBas van Bussel
Maastricht Universitair Medisch Centrum
Outcome results
None listed