The effect of fenspiride on the number of exacerbations and the time of first exacerbation in patients with chronic bronchitis

Pirozyński, M.ł; Skucha, W.; Słomiński, M.; Chyczewska, E.; Malinowski, J.; Nowak, D.; Bartmińiski, W.; Pachocki, R.

Polski Merkuriusz Lekarski Organ Polskiego Towarzystwa Lekarskiego 19(110): 139-143

2005


ISSN/ISBN: 1426-9686
PMID: 16245418
Document Number: 594284
The aim of the work was evaluation of efficacy of fenspiride b.i.d. on the number of exacerbations and the time to the first exacerbation in patients with chronic bronchitis. Randomized, multicentre study controlled versus placebo was carried out in 12 centers in Poland. All patients, 89 females and 68 males aged between 20 and 74, were treated with fenspiride at the dose of 160 mg/day for a period of 6 months. The following symptoms were recorded every month in order to evaluate the therapeutic efficacy: sputum quality and quantity, cough intensity, dyspnea and bronchospasm. Based on these symptoms diagnosis of exacerbation was performed according to American Thoracic Society criteria. Quality and quantity of sputum and cough significantly improved in the fenspiride group (comparing to the placebo group p= 0.027 and p = 0.049 adequately for sputum and cough). A significant difference between groups was observed in the number of exacerbation episodes and their duration. In the fenspiride group there were 0.53 episodes of exacerbation compared with 1.12 episodes in the placebo group (p = 0.038). Mean duration of exacerbation was 3.3 days in the fenspiride group and 7.3 days in the placebo treated patients (p = 0.034). Time to the first exacerbation differed between groups, but this difference was not statistically significant. Number of side effects observed did not differ between groups. Fenspiride treatment was assessed as relatively effective in terms of influence on exacerbations, and well tolerated during six month therapy.

Document emailed within 1 workday
Secure & encrypted payments