M Guillot, M. Amiour, El Hachem C, S Harchaoui, Ribault, C. Paris
Abstract
Long-term low dose azithromycin treatment in cystic fibrosis patients with chronic Pseudomonas aeruginosa infection is safe and reduces the decline in lung function, the number of acute exacerbations and improves nutritional status; underlying efficacy mechanisms are multiple and synergistic.
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Long-term low dose azithromycin treatment in cystic fibrosis patients with chronic Pseudomonas aeruginosa infection is safe and reduces the decline in lung function, the number of acute exacerbations and improves nutritional status; underlying efficacy mechanisms are multiple and synergistic.
Key concepts: Cystic fibrosis, Azithromycin, Pseudomonas aeruginosa, Medicine, Lung function, Lung infection, Lung, Fibrosis