Abstract:
:Cystic fibrosis affects 1/2500 individuals and is the most common lethal autosomal recessive disease in people of northern European descent. It is characterized by chronic infections with mucoid Pseudomonas aeruginosa and progressive deterioration of respiratory function. Much research has focused on the inflammatory component of the disease. Macrolide antibiotics are postulated to suppress inflammatory mediators and interfere with biofilm formation produced by P. aeruginosa. In vitro studies show promising results, and a limited number of human studies reported improvements in respiratory function with the drugs. Macrolide antibiotics are generally safe and well tolerated and may prove to be effective in patients with cystic fibrosis.
journal_name
Pharmacotherapyjournal_title
Pharmacotherapyauthors
Gaylor AS,Reilly JCdoi
10.1592/phco.22.3.227.33544subject
Has Abstractpub_date
2002-02-01 00:00:00pages
227-39issue
2eissn
0277-0008issn
1875-9114journal_volume
22pub_type
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