RECRUITINGOBSERVATIONAL
LUNG INFECTION in ICU (LUNG-I3)
LUNG INFECTION in ICU
About This Trial
objective of LUNG-I3 study is to assess the quantitative and functional differences in cells between blood and bronchoalveolar lavage (BAL) fluid after an infection, with a special focus on alveolar macrophages and neutrophils
Who May Be Eligible (Plain English)
Who May Qualify:
All the following criteria
- Age 18 years or greater
- Severe ICU patients hospitalized for one of the above diseases:
- Septic shock (requirement of vasopressor to maintain a mean arterial pressure of 65 mm Hg or greater and serum lactate level greater than 2 mmol/L (\>18 mg/dL) in the absence of hypovolemia) caused either by pneumonia (n=20) or another source n=20)
- Severe trauma (level I and II), Injury Severity Score ≥ 25 OR
- Burn with TBSA over 20%
- NAD \> 0.1 µg/kg/min
- At least 2 SOFA criteria ≥ 2 points
Who Should NOT Join This Trial:
- Aspiration pneumonia
- Unable to obtain a valid and written consent from a patient or their legally authorized representative in accordance with the local regulatory instances (this includes in FR: Person not affiliated to a health insurance scheme, or not a beneficiary of such a scheme. Persons who are the subject of a legal protection order. Person with restricted freedom following a legal or administrative decision and a person admitted without their consent pursuant to Articles L.3212-1 and 3213-1, which are not included in Article L.1121-8 of the French Public Health Code.)
- COPD
- Smoke inhalation in burn patients
- Participation in an intervention study
- Pregnant or breastfeeding women
- Immunocompromised patients, defined as
- patients with solid tumors with chemotherapy in the last 3 months or a progressive metastatic disease
- hematologic malignancies
- solid organ transplantation
- HIV infection with or without AIDS
- treatment with corticosteroids (\> 3 months at any dosage or ≥ 1 mg/kg prednisone equivalent per day for \> 7 day)
- treatment with other immunosuppressive drugs.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
All the following criteria
* Age 18 years or greater
* Severe ICU patients hospitalized for one of the above diseases:
* Septic shock (requirement of vasopressor to maintain a mean arterial pressure of 65 mm Hg or greater and serum lactate level greater than 2 mmol/L (\>18 mg/dL) in the absence of hypovolemia) caused either by pneumonia (n=20) or another source n=20)
* Severe trauma (level I and II), Injury Severity Score ≥ 25 OR
* Burn with TBSA over 20%
* NAD \> 0.1 µg/kg/min
* At least 2 SOFA criteria ≥ 2 points
Exclusion Criteria:
* Aspiration pneumonia
* Unable to obtain a valid and written consent from a patient or their legally authorized representative in accordance with the local regulatory instances (this includes in FR: Person not affiliated to a health insurance scheme, or not a beneficiary of such a scheme. Persons who are the subject of a legal protection order. Person with restricted freedom following a legal or administrative decision and a person admitted without their consent pursuant to Articles L.3212-1 and 3213-1, which are not included in Article L.1121-8 of the French Public Health Code.)
* COPD
* Smoke inhalation in burn patients
* Participation in an intervention study
* Pregnant or breastfeeding women
* Immunocompromised patients, defined as
* patients with solid tumors with chemotherapy in the last 3 months or a progressive metastatic disease
* hematologic malignancies
* solid organ transplantation
* HIV infection with or without AIDS
* treatment with corticosteroids (\> 3 months at any dosage or ≥ 1 mg/kg prednisone equivalent per day for \> 7 day)
* treatment with other immunosuppressive drugs.
Locations (1)
Hopital Edouard Herriot
Lyon, France