Bronchopulmonary Dysplasia Clinical Trial
Official title:
Randomized Clinical Trial: Use of Azithromycin to Prevent Lung Damage in Preterm Newborns Under Mechanical Ventilation
The introduction of invasive mechanical ventilation in the treatment of preterm infants works
as an adjuvant in the treatment of acute respiratory failure, which has resulted in
significantly significant survival rates. In recent years there has been an increase in the
number of evidence that mechanical factors can cause lung injury through inflammatory cells
and soluble mediators.
The alveolar and airway epithelium is an important source of cytokine release. Cytokines are
very low molecular weight proteins or glycoproteins with hormone-like actions. They
contribute to the pathogenesis of various diseases through the ability to induce other
inflammatory mediators Mechanical ventilation strategies can increase pulmonary and systemic
cytokines and lead to dysfunction of multiple organs and systems.
Azithromycin has a potent anti-inflammatory and immunomodulatory effect It suppresses the
production of proinflammatory cytokines (IL-6, IL-1, and TNF-α), has effective antimicrobial
properties against Ureaplasma and, best of all, few side effects The hypothesis of this study
is that azithromycin would reduce pulmonary inflammation induced by mechanical ventilation in
premature infants, conferring a protective character.Randomized clinical trial: use of
azithromycin in preventing pulmonary damage newborn preterm undergoing mechanical ventilation
The nature of lung injury induced by mechanical ventilation is clearly established, including
the release of immunoinflammatory mediators. However, safe drug therapy that decreases its
severity is not available. Azithromycin is a macrolide antibiotic with potent
anti-inflammatory effects, but has been poorly studied in preterm infants except for very few
studies in extreme preterms for the prevention of bronchopulmonary dysplasia.
The aim of this study was to evaluate the effect of azithromycin on the prevention of
cytokine-mediated MV-induced injury in cytokine plasma levels (IL-1β, IL-2, IL-6, IL-8, IL-10
and TNF- α) in preterm newborns, submitted to mechanical ventilation in the first 72 hours of
life.
It is a double-blind placebo controlled clinical trial. When the use of azithromycin was
considered, after signing the informed consent, a randomization was performed by the
intravenous mixtures center of Hospital de clinicas de porto alegre where a group of newborns
will receive azithromycin EV at the dose of 10mg / kg / day and another group will receive
placebo (SF 0.9%) in the same volume, a blood aliquot of 300μL will be collected in all ETDA
for cytokine analysis and PCR for Ureaplasma. After 5 days of starting azithromycin or
placebo, a new sample will be collected for cytokines along with blood collection from the
patient's routine. There will be no blood collection exclusively for the study.
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