Health Outcomes Research in Medicine
Volume 1, Issue 2 , Pages e93-e102, December 2010

Incidence of Exacerbations and Hospitalizations Is Reduced and Time to Exacerbations Is Prolonged with Mometasone Furoate Dry Powder Inhaler Versus Beclomethasone Dipropionate Hydrofluoroalkane Aerosol in Patients with Mild Asthma

  • Prakash Navaratnam, RPh, MPH, PhD

      Affiliations

    • Eympres Research, LLC, Hilliard, Ohio
    • Corresponding Author InformationCorresponding Author: Prakash Navaratnam, RPh, MPH, PhD, Eympres Research, LLC, 4660 Stonehill St., Hilliard, OH 43026.
  • ,
  • Eduardo Urdaneta, MD

      Affiliations

    • Schering-Plough Corporation, Kenilworth, New Jersey
  • ,
  • John McLaughlin, MSPH

      Affiliations

    • Informagenics, LLC, Worthington, Ohio
  • ,
  • Howard S. Friedman, PhD, MMS

      Affiliations

    • Analytic Solutions, LLC, New York, New York

published online 01 September 2010.

Abstract 

Objective

To compare the incidence and time to onset of exacerbations among mild asthmatic non-controller-naive patients who began treatment with mometasone furoate via a dry powder inhaler (MF-DPI) or a beclomethasone dipropionate-hydrofluoroalkane (BDP-HFA) aerosol inhaler.

Study Design

An administrative claims database was retrospectively examined from January 1, 2005 through June 30, 2008. Patients with mild asthma aged 12-65 years who were US residents and enrolled in their health plan for ≥1 year before and after the index date for MF-DPI or BDP-HFA treatment initiation were included (n=1273 matched patients per cohort). Primary evaluations included the incidence of and time to any asthma exacerbations and several asthma exacerbation subtypes. Multivariate generalized linear regression modeling analyses were used to compare the postindex incidence of exacerbations between cohorts. Cox regression analyses were conducted to control for the impact of input variables and evaluate the time to exacerbations.

Results

Significantly fewer MF-DPI patients experienced an exacerbation compared with BDP-HFA patients (9.7% vs 11.5%, respectively; P=.0002). At all time points examined, fewer MF-DPI patients compared with BDP-HFA patients experienced any exacerbation or an exacerbation requiring inpatient hospitalization. The difference between cohorts in the incidence of inpatient exacerbations increased over time. MF-DPI patients experienced prolonged time to any asthma exacerbation (hazard ratio=0.77; P=.0414) or exacerbations requiring inpatient hospitalization (hazard ratio=0.51; P=.0191) compared with BDP-HFA patients.

Conclusion

These analyses suggest that patients (previously receiving asthma-related therapy) with mild asthma receiving MF-DPI are at lower risk for asthma exacerbations compared with those receiving BDP-HFA.

Keywords: Adherence, Asthma-related therapy, Inhaled corticosteroids

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 This work was supported by Merck & Co., Kenilworth, New Jersey.

 Prakash Navaratnam is a paid consultant for Merck & Co.; Eduardo Urdaneta was an employee of Merck & Co. (then Schering-Plough Corporation) when this study was conducted; John McLaughlin is a paid consultant for Merck & Co and is employed as a research scientist at Informagenics, LLC; Howard S. Friedman is the owner of Analytic Consulting, LLC, which performs consulting work in the pharmaceutical industry, including Merck & Co.

PII: S1877-1319(10)00011-X

doi:10.1016/j.ehrm.2010.08.001

Health Outcomes Research in Medicine
Volume 1, Issue 2 , Pages e93-e102, December 2010