Literature DB >> 12205570

Effectiveness and tolerability of high-dose salmeterol in cystic fibrosis.

Nancy L Hordvik1, Paul H Sammut, C Gerald Judy, John L Colombo.   

Abstract

The efficacy and tolerability of high-dose salmeterol (100 mcg, BID) and albuterol (2.5 mg, BID) were compared with those of albuterol (2.5 mg, BID) in outpatients with cystic fibrosis in a randomized, double-blind, double-dummy, placebo-controlled, crossover study with both short- (4 weeks of each) and long-term (24 weeks of each) treatment periods. The primary outcome measure was the difference in mean change in forced expired volume in 1 sec (FEV(1)) from baseline to the end of each treatment, and secondary measures included changes in forced vital capacity (FVC), forced expiratory flow between 25-75% of FVC (FEF(25-75)), patient-rated weekly symptom scores, number of extra (rescue) albuterol treatments, and number of antibiotic treatments. Tolerability was evaluated by changes in vital signs and adverse events.Thirty-six out of 44 patients enrolled finished the short-term treatment period, and 19 out of 23 who continued the study also finished the long-term treatment period. There was no significant difference in the mean % change in FEV(1) from baseline to completion of 4 weeks with each drug in the short-term treatment period (0.1% vs. 0.06%, albuterol vs. salmeterol; respectively). In the long-term treatment period, there was a significant decrease from baseline in FEV(1) with albuterol vs. salmeterol, as measured after both 12 and 24 weeks of each treatment (-6.2% vs. 1.8%, P = 0.013 after 12 weeks, and -6.5% vs. 1.7%, P = 0.002, after 24 weeks, respectively). In both treatment periods, salmeterol was well-tolerated. While there were more rescue treatments per patient per week with albuterol than with salmeterol treatment in both the short- and long-term periods (0.67 vs. 0.40 and 1.76 vs. 0.74, respectively), rescue treatments were needed significantly more often for only the long-term period with albuterol compared to salmeterol (P = 0.022). Also, there were more antibiotic interventions with albuterol than with salmeterol treatment in both the short- and long-term periods (25 vs. 10 and 56 vs. 42, respectively); however, antibiotics were needed significantly more often for only the short-term period (P = 0.011). In addition, there was a significantly higher symptom score with albuterol vs. salmeterol treatment during the second half of the long-term period (1.24 vs. 0.89, P = 0.001).In conclusion, long-term high-dose salmeterol was equally safe and was associated with better pulmonary function, fewer interventions, and fewer respiratory symptoms compared to standard therapy with albuterol in a population of outpatients with mild to moderate CF. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12205570     DOI: 10.1002/ppul.10162

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  4 in total

Review 1.  Asthma in cystic fibrosis.

Authors:  Ian M Balfour-Lynn
Journal:  J R Soc Med       Date:  2003       Impact factor: 5.344

2.  Salmeterol restores secretory functions in cystic fibrosis airway submucosal gland serous cells.

Authors:  Franck Delavoie; Michael Molinari; Magali Milliot; Jean-Marie Zahm; Christelle Coraux; Jean Michel; Gérard Balossier
Journal:  Am J Respir Cell Mol Biol       Date:  2008-10-17       Impact factor: 6.914

3.  Testing two different doses of tiotropium Respimat® in cystic fibrosis: phase 2 randomized trial results.

Authors:  Judy M Bradley; Paul Koker; Qiqi Deng; Petra Moroni-Zentgraf; Felix Ratjen; David E Geller; J Stuart Elborn
Journal:  PLoS One       Date:  2014-09-04       Impact factor: 3.240

4.  Pulmonary function parameters and use of bronchodilators in patients with cystic fibrosis.

Authors:  Lucia Harumi Muramatu; Roberto Stirbulov; Wilma Carvalho Neves Forte
Journal:  J Bras Pneumol       Date:  2013 Jan-Feb       Impact factor: 2.624

  4 in total

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