4.7 Article

Does Omalizumab Make a Difference to the Real-life Treatment of Asthma Exacerbations? Results From a Large Cohort of Patients With Severe Uncontrolled Asthma

Journal

CHEST
Volume 143, Issue 2, Pages 398-405

Publisher

ELSEVIER
DOI: 10.1378/chest.12-1372

Keywords

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Funding

  1. INSERM (French National Institutes of Health and Medical Research)
  2. Novartis Pharma SAS
  3. LA-SEE
  4. AstraZeneca
  5. Pfizer, Inc
  6. Takeda Pharmaceuticals International GmbH
  7. Actelion Pharmaceuticals Ltd
  8. Aerocrine
  9. Bayer AG
  10. Chiesi Farmaceutici SpA
  11. GlaxoSmithKline plc
  12. Eli Lilly and Company
  13. Merck Co, Inc
  14. Mundipharma International
  15. Stallergenes S.A.
  16. Teva Pharmaceuticals Industries, Ltd
  17. United Therapeutics Corporation
  18. Merck Sharp Dohme Corp
  19. Sanofi (formerly named Sanofi-Aventis)
  20. LA-SER

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Background: Omalizumab has been shown to decrease the risk of hospitalization or ED visits in patients with uncontrolled severe allergic asthma compared with placebo. This longitudinal study observed the conditions under which omalizumab is prescribed in real-life settings and assessed whether its use as an add-on therapy alongside standard treatments decreases the risk of severe asthmatic exacerbations. Methods: A cohort of adult patients with uncontrolled severe asthma despite optimal treatment with inhaled and oral corticosteroids and a long-acting beta(2)-agonist but no treatment with omalizumab upon entry was assembled. Risk of hospitalization or ED visits for asthma exacerbation was assessed using the Andersen-Gill extension of the Cox model for repeated events, controlling for age, sex, smoking history, BMI, gastroesophageal reflux, allergic status, allergic rhinitis, treatment, and hospitalization or ED visits for asthma in the 2 months prior to omalizumab treatment. Results: Overall, 163 physicians recruited 767 patients, of whom 374 took omalizumab at least once (mean observation period, 20.4 months). Omalizumab use was associated with an adjusted relative risk of 0.57 (95% CI, 0.43-0.78) for hospitalization or ED visits for asthma. In users of omalizumab, the adjusted relative risk of hospitalization or ED visits for asthma during omalizumab treatment vs nontreatment periods was 0.40 (95% CI, 0.28-0.58). Conclusions: Add-on omalizumab is associated with a significantly decreased risk of hospitalization or ED visits in patients with uncontrolled severe asthma in real-life practice. CHEST 2013; 143(2):398-405

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