ARDS, Multi-organ Failure
Conditions
Keywords
Acute respiratory distress syndrome (ARDS), Extracorporeal membrane oxygenation (ECMO), biomarker
Brief summary
The goal of this project is to find a marker expression that the investigators can use to trace symptom progression and develop a more efficient therapy to enhance ARDS patient survival rate and better post-ICU life quality.
Detailed description
The investigators will first identify acute respiratory distress syndrome (ARDS) patients receiving ECMO support in ICU at National Taiwan University Hospital, and then collect blood, urine and bronchioalveolar lavage fluid (BALF) samples at different time points: before setting up ECMO, 2, 6, 12, 24, 72 hours,5 and 14 days after ECMO installment, time to wean ECMO and the day removing ECMO and leaving ICU. From the samples, the free radicals, cytokines (IL-1, IL-6, IL-8, IL-18,tumor necrosis factor-α, transforming growth factor-β), and inflammasome- related markers, immune cell responses and other biochemical markers would be measured. The novel biomarkers to predict the outcome of the patient will be identified.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
1. \>18 years old 2. ARDS, needing ECMO support
Exclusion criteria
1. pre-existing sepsis 2. pre-existing chronic renal failure (dialysis dependent), liver failure other diseases precluding chance of survival.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mortality or multi-organ failure | 7 days | Patients who survived for more than 7 days after ECMO treatment were defined as survival, and non-survival patients were defined as expired or multiple organ failure incompatible with life within 7 days after ECMO installation. |
Countries
Taiwan