Macrolide antibiotics for cystic fibrosis
A number of anecdotal reports in the 1990's suggested that macrolide antibiotics, most notably azithromycin, may have the potential for improving respiratory function in young people with cystic fibrosis. Subsequent randomised controlled trials examined the impact of azithromycin on a number of clinical outcomes, primarily on forced expiratory volume in one second (FEV1). A meta-analysis of these data at several different time-points confirmed a small but significant improvement in FEV1. This analysis was published in the first Cochrane review looking at the use of macrolide antibiotics in cystic fibrosis in 2000. The authors of this review found it more challenging to obtain data and details from trials examining clarithromycin. To some degree this probably reflects the negative results o...