4.8 Article

Tiotropium versus Salmeterol for the Prevention of Exacerbations of COPD

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 364, Issue 12, Pages 1093-1103

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1008378

Keywords

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Funding

  1. Boehringer Ingelheim
  2. AstraZeneca
  3. Biotherapeutics
  4. GlaxoSmithKline
  5. Janssen
  6. Merck
  7. Novartis
  8. Nycomed
  9. Talecris Biotherapeutics
  10. Almirall
  11. Novartis, Mundipharma
  12. Cytos Biotechnology
  13. Pfizer
  14. Revotar Biopharmaceuticals
  15. Roche
  16. Chiesi Farmaceutici
  17. Sigma-Tau Pharmaceuticals
  18. Menarini
  19. Schering-Plough
  20. SigmaTau Pharmaceuticals
  21. Union Chimique Belge

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BACKGROUND Treatment guidelines recommend the use of inhaled long-acting bronchodilators to alleviate symptoms and reduce the risk of exacerbations in patients with moderate-tovery- severe chronic obstructive pulmonary disease (COPD) but do not specify whether a long-acting anticholinergic drug or a beta(2)-agonist is the preferred agent. We investigated whether the anticholinergic drug tiotropium is superior to the beta(2)-agonist salmeterol in preventing exacerbations of COPD. METHODS In a 1-year, randomized, double-blind, double-dummy, parallel-group trial, we compared the effect of treatment with 18 mu g of tiotropium once daily with that of 50 mu g of salmeterol twice daily on the incidence of moderate or severe exacerbations in patients with moderate-to-very-severe COPD and a history of exacerbations in the preceding year. RESULTS A total of 7376 patients were randomly assigned to and treated with tiotropium (3707 patients) or salmeterol (3669 patients). Tiotropium, as compared with salmeterol, increased the time to the first exacerbation (187 days vs. 145 days), with a 17% reduction in risk (hazard ratio, 0.83; 95% confidence interval [CI], 0.77 to 0.90; P<0.001). Tiotropium also increased the time to the first severe exacerbation (hazard ratio, 0.72; 95% CI, 0.61 to 0.85; P<0.001), reduced the annual number of moderate or severe exacerbations (0.64 vs. 0.72; rate ratio, 0.89; 95% CI, 0.83 to 0.96; P = 0.002), and reduced the annual number of severe exacerbations (0.09 vs. 0.13; rate ratio, 0.73; 95% CI, 0.66 to 0.82; P<0.001). Overall, the incidence of serious adverse events and of adverse events leading to the discontinuation of treatment was similar in the two study groups. There were 64 deaths (1.7%) in the tiotropium group and 78 (2.1%) in the salmeterol group. CONCLUSIONS These results show that, in patients with moderate-to-very-severe COPD, tiotropium is more effective than salmeterol in preventing exacerbations.

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