46 The rationale for pulsed therapy was mainly driven by the concerns about the emergence of resistance with long-term continuous use of antibiotics. Pulsed therapy would allow time for the normal flora to recover and therefore potentially prevent or delay the emergence of resistant strains.33 Moxifloxacin was selected for the study

based on its potent in vitro activity against the major COPD pathogens, excellent penetration into respiratory tissues, high oral bioavailability and proven efficacy in increasing the exacerbation-free interval. 46, 55 and 88 Pulsed therapy with moxifloxacin was found to significantly reduce the risk of an exacerbation by 25% (per protocol population) in patients with moderate-to-severe COPD, while in a post-hoc analysis, this reduction was 45% in patients with purulent/mucopurulent sputum at randomisation. 46 These studies suggest that long-term antibiotic Selleckchem Regorafenib treatment in COPD patients reduces exacerbation frequency, though evidence for a reduction in inflammation is limited. Long-term antibiotic therapy appears to be well tolerated, though not all studies reported safety.81 Nevertheless, gastrointestinal events were more common in patients

receiving pulsed moxifloxacin versus placebo (4.7% vs 0.7%, respectively)46 and 12-month azithromycin treatment resulted in a higher incidence of hearing loss (25% of patients with azithromycin vs 20% of patients with placebo).45 Although long-term (daily) azithromycin treatment led to a decrease in the incidence of colonisation by respiratory pathogens, such treatment was Selleck Z-VAD-FMK also associated with an increased prevalence of macrolide-resistant bacteria colonising the airways, though there was no evidence that this colonisation increased the number of exacerbations or the incidence of pneumonia.45 No relevant resistance was reported in

the study with pulsed (with one cycle lasting for only 5 days in every 8 weeks) moxifloxacin treatment,46 Acyl CoA dehydrogenase while in others resistance development was minimal85 and 86 or not reported.81 and 82 Although the studies described above suggest that use of prophylactic oral antibiotic therapy is well tolerated, some macrolides are known to be proarrhythmic and even 5-day treatment with azithromycin has been associated with a small absolute increase in cardiovascular deaths.89 This issue, coupled with concerns of increased antibiotic resistance, indicates that such treatment should be reserved for those with severe COPD who experience frequent exacerbations requiring multiple antibiotic treatments, in spite of adequate management of their COPD with standard treatments.90 Use of inhaled antibiotics is expected to have a future role in the long-term management of patients with COPD since this route of administration has the ability to target drug delivery directly to respiratory tract.