Multicenter, randomized open label clinical trial to evaluate IEM and HS as concomitant therapy for respiratory tract infection in patients under artificial ventilation in the ICU. Lung infection is a serious complication that may occur during hospital stay and may need artificial respiration or even develop during artificial ventilation for other causes. Current specific treatment consists of intravenous antibiotics. The current study evaluated whether aspiration and drainage of infected sputum helps curing this severe complication and whether nebulized HS has additional benefits, like loosening of secretions, eradicating bacteria or reducing inflammation.
Open label, randomized, multicenter (7 ICUs at 7 hospitals in Spain). The study has 2 main arms, pneumonia and tracheobronchitis. If the diagnosis is pneumonia, subjects will be randomization to one of 3 study groups: 1. IV Antibiotic therapy 2. IV Antibiotic therapy + mechanical insufflation-Exsugglation (MI-E) 3. IV Antibiotic therapy + MI-E + nebulized hypertonic saline-hyaluronic acid (HS) If the diagnosis is tracheobronchitis,subjects will be randomization to one of 3 study groups: 1. No specific therapy (recommendation of the Infectious Diseases Society of America) 2. IV Antibiotic therapy (common practice to prevent progressión to pneumona and shorten duration of intubation) 3. MI-E + HS Safety will be compared by number of adverse events, severe adverse events and mortality between study groups in each main arm. Efficacy will be compared by duration of respiratory support and number of cases with worsening organ dysfunction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Combined use of mechanical insufflation-exsufflation with nebulized hypertonic saline in intubated patients with nosocomial respiratory tract infection
systemic antibiotic therapy and catheter suctioning of secretions as recommended by guidelines
Commercially available combination of 7% hypertonic saline with 0.1% hyaluronic acid given as nebulization during the MI-E session
Hospital Vall d´Hebrón.
Barcelona, Barcelona, Spain
Hospital Nuestra Señora de la Candelaria.
Santa Cruz de Tenerife, Las Palmas, Spain
Hospital Clinico San Carlos
Madrid, Madrid, Spain
Hospital Clínico San Carlos
Madrid, Madrid, Spain
Hospital de la Princesa
Madrid, Madrid, Spain
Hospital Doce de Octubre
Madrid, Madrid, Spain
Hospital Álvaro Cunqueiro.
Vigo, Pontevedra, Spain
Virgen de la Salud
Toledo, Toledo, Spain
Median SOFA score increase >2 points on day 4
Increase in organ dysfunction score from baseline to day 4 after randomization.
Time frame: inclusion to day 4 after randomization
Median respiratory support-free days increase at day 28
28 minus duration in days on high-flow nasal cannula + invasive ventilation.
Time frame: Inclusion to day 28 after randomization
Percentage of subjects surviving/dying day 28
crude mortality on day 28 after randomization
Time frame: Inclusion to day 28 after randomization
Subjects with bacterial eradication in respiratory samples at day 4 after randomization
Negative tests for causal microorganism in day 4 samples
Time frame: Day 3 to 5 after randomization
Subjects with bacterial eradication in respiratory samples at end of systemic antibiotic therapy
Negative culture and molecular test for causative bacteria in samples at end of therapy
Time frame: 7 and 14 days after randomization
Median Length of ICU stay
Duration of ICU stay from admission to discharge or death
Time frame: ICU admission to discharge or death in days
Median antibiotic-free days at 28 days
28 minus days without systemic antibiotic therapy
Time frame: from study inclusion to day 28
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