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The goal of this observational prospective cohort study is to explore the clinical characteristics, treatment strategies, and outcomes of adult patients with acute respiratory distress syndrome (ARDS) admitted to the medical intensive care unit of Asan Medical Center. The main questions it aims to answer are:
Participants will:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Acute respiratory distress syndrome (ARDS) |
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| Measure | Description | Time Frame |
|---|---|---|
| Ventilator-free days within 28 days | Number of days alive and free from invasive mechanical ventilation during the first 28 days after enrollment. Patients who die within 28 days will be assigned zero ventilator-free days. | From enrollment to Day 28 |
| Measure | Description | Time Frame |
|---|---|---|
| 28-day mortality | All-cause mortality within 28 days after enrollment. | From enrollment to Day 28 |
| 90-day mortality | All-cause mortality within 90 days after enrollment. |
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Inclusion Criteria:
Exclusion Criteria:
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This study will enroll participants from among patients with acute respiratory failure who are admitted to the medical intensive care unit of Asan Medical Center in Seoul, Korea.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Director, Medical Intensive Care Unit, Asan Medical Center | Contact | 82-2-3010-3130 | ggaamang24@amc.seoul.kr | |
| Su Yeon Lee, MD, PhD | Contact | 82-2-3010-6809 | lsy5013@amc.seoul.kr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Asan Medical Center | Seoul | 05505 | South Korea |
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| ID | Term |
|---|---|
| D012128 | Respiratory Distress Syndrome |
| ID | Term |
|---|---|
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D012120 | Respiration Disorders |
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| From enrollment to Day 90 |
| ICU mortality | Death occurring during the index ICU stay. | From enrollment until ICU discharge, up to 90 days |
| Hospital mortality | Death occurring during the index hospital admission. | From enrollment until hospital discharge, up to 90 days |
| Duration of invasive mechanical ventilation | Total number of days patients require invasive mechanical ventilation. | From enrollment to Day 90 |
| ICU length of stay | Total number of days spent in the ICU. | From enrollment until ICU discharge, up to 90 days |
| Hospital length of stay | Total number of days spent in the hospital. | From enrollment until hospital discharge, up to 90 days |
| Ventilator-associated pneumonia (VAP) | Incidence of VAP diagnosed according to standard clinical criteria during the index ICU stay. | From enrollment until ICU discharge, up to 90 days |
| Central line-associated bloodstream infection (CLABSI) | Incidence of CLABSI diagnosed according to CDC/NHSN criteria during the index ICU stay. | From enrollment until ICU discharge, up to 90 days |
| Barotrauma | Incidence of pneumothorax, pneumomediastinum, or subcutaneous emphysema documented by imaging or clinical assessment during the index ICU stay. | From enrollment until ICU discharge, up to 90 days |
| Quality of life at hospital discharge | Health-related quality of life assessed using the 5-level European Quality of Life 5 Dimensions version (EQ-5D-5L) questionnaire at the time of hospital discharge for survivors. Scores range from -0.066 to 1.0 (based on Korean Time Trade-Off value set), with higher scores indicating better health status. | From enrollment until hospital discharge, up to 90 days |
| Disposition at hospital discharge | Patient's destination at hospital discharge (e.g., home, rehabilitation, long-term care facility, or death). | From enrollment until hospital discharge, up to 90 days |