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Respiratory infections are common and sometimes very severe. An insufficient dosage of the antibiotic could lead to a treatment failure A correct plasmatic antibiotic concentration is not a guarantee of a clinical success as it could not be a reflect of pulmonary concentration. The aim of this study is to determinate the predictive factors of pulmonary penetration of antibiotics in patients with a beta lactamines failure and who undergoes a flexible bronchoscopy.
To check if pulmonary concentrations of antibiotic are enough we will measure antibiotic concentration in the broncho-alveolar lavage (BAL). This technique which is clinically relevant and reliable could determinate the pulmonary diffusion level for antibiotics by calculating the ratio between plasmatic and intra-alveolar antibiotic concentration. This ratio will be correlated with potential limitation factors of pulmonary diffusion as respiratory diseases (COPD, cystic fibrosis, fibrosis…), sepsis, hypoalbuminemia. We have chosen to study the beta lactamin antibiotics because they are the most frequently used in pneumonia. Moreover, the beta lactamins pulmonary diffusion is likely to be the lowest. Finally, for patients with a known pathogen, we will divide this pulmonary concentration with minimal inhibitory concentration (MIC). Indeed, in severe pneumonia, to be sure of bactericidal activity, a pulmonary concentration of beta lactamines should be always higher than 4 to 5 times MIC.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| measure of intra-alveolar antibiotic concentration in µg/ml | Biological | included patients will have a broncho-alveolar lavage (BAL) to measure intra-alveolar antibiotic concentration, and a blood test to measure plasmatic concentration | ||
| broncho-alveolar lavage (BAL) | Procedure | included patients will have a broncho-alveolar lavage (BAL) to measure intra-alveolar antibiotic concentration, and a blood test to measure plasmatic concentration | ||
| blood test to measure plasmatic antibiotic concentration in µg/ml | Biological | included patients will have a broncho-alveolar lavage (BAL) to measure intra-alveolar antibiotic concentration, and a blood test to measure plasmatic |
| Measure | Description | Time Frame |
|---|---|---|
| pulmonary diffusion level for beta lactamins | pulmonary diffusion level for beta lactamins is determined by ratio between bronchoalveolar concentration and plasmatic concentration of tested antibiotics | on the day of the bronco-alveolar lavage |
| Measure | Description | Time Frame |
|---|---|---|
| measure of apyrexia duration in days | measure of apyrexia duration in days | from day of inclusion to 15 days after inclusion |
| duration in days for regression of the biological inflammatory syndrome |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Claire Andrejak, Pr | CHU Amiens | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Amiens | Amiens | 80480 | France |
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duration in days for regression of the biological inflammatory syndrome (CRP concentration in mg/l divided by 2)
| from day of inclusion to 15 days after inclusion |
| measure of length of hospitalisation | measure of length of hospitalisation in days | from day of inclusion to 15 days after inclusion |
| Number of deaths at 28-day | 28-day mortality will be measured | 28 days after inclusion |
| virus presence in BAL | virus presence will be detected in bronchoalveolar lavage (BAL) | day of bronchoalveolar lavage (BAL) |
| ID | Term |
|---|---|
| D011014 | Pneumonia |
| ID | Term |
|---|---|
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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| ID | Term |
|---|---|
| D018893 | Bronchoalveolar Lavage |
| ID | Term |
|---|---|
| D007507 | Therapeutic Irrigation |
| D008919 | Investigative Techniques |
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