Acute Respiratory Distress Syndrome, Acute Respiratory Failure
Conditions
Brief summary
This is an observational study to evaluate the clinical impact of respiratory virus in the patients with acute respiratory failure
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Male or female aged ≥ 19 years * Written informed consent by the patient or legally authorized representative * Critical illness consistent with acute respiratory failure, to be enrolled within 24 hours of presentation
Exclusion criteria
* No informed consent * A patient who is judged to be unable to make a voluntary decision by understanding information about this research due to cognitive vulnerability
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of respiratory viral infections | within 24 hours after intensive care unit (ICU) admission | Rate of respiratory viral infections in patients with acute respiratory failure |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| ICU mortality rate | Through study completion, an average of 1 year | Association between respiratory viral infections and death in ICU and risk factors of death in patients with ARF |
| Hospital mortality rate | Through study completion, an average of 1 year | Association between respiratory viral infections and death in hospital and risk factors of death in patients with ARF |
Countries
South Korea