
A retrospective database study comparing treatment outcomes and cost associated with choice of fixed‐dose inhaled corticosteroid/long‐acting β 2 ‐agonists for asthma maintenance treatment in Germany
Author(s) -
Aballéa S.,
Cure S.,
Vogelmeier C.,
Wirén A.
Publication year - 2008
Publication title -
international journal of clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 98
eISSN - 1742-1241
pISSN - 1368-5031
DOI - 10.1111/j.1742-1241.2008.01895.x
Subject(s) - medicine , formoterol , salmeterol , budesonide , fluticasone , asthma , budesonide/formoterol , medical prescription , corticosteroid , retrospective cohort study , propensity score matching , pediatrics , pharmacology
Summary Aims: This retrospective, observational cohort study aimed to compare treatment outcomes and healthcare costs in the year after initiation of maintenance treatment with budesonide/formoterol or salmeterol/fluticasone in a German healthcare setting. Methods: Data on German asthma patients initiating treatment with budesonide/formoterol or salmeterol/fluticasone between June 2001 and June 2005 were obtained from the IMS Disease Analyzer database. The primary outcome was the probability of treatment success, defined according to short‐acting β 2 ‐agonist prescriptions and switches or addition of controller medications, during the postindex year. A secondary definition of treatment success included hospitalisations and oral corticosteroid (OCS) prescriptions. Secondary outcomes included severe asthma exacerbations, defined as ≥1 OCS prescription, asthma‐related hospitalisation and/or referral. The effect of treatment on costs was estimated using generalised linear models, adjusting for patient and physician characteristics. Results: There were no significant differences between the budesonide/formoterol ( n = 1456) and salmeterol/fluticasone ( n = 982) groups in disease severity markers in the pre‐index year. Patients on budesonide/formoterol had a 44% greater probability of treatment success [odds ratio (OR): 1.44; p = 0.0003] according to the primary definition and a 26% greater probability (OR: 1.26; p = 0.0119) according to the secondary definition, fewer severe exacerbations (−33.4%; p = 0.0123) and fewer OCS prescriptions (−31.5%; p = 0.0082) compared with salmeterol/fluticasone, after controlling for baseline characteristics. Adjusting for covariates, budesonide/formoterol had a significant inverse relationship on asthma‐related costs compared with salmeterol/fluticasone (−13.4%; p < 0.001). Total cost (asthma‐ and non‐asthma‐related costs) was 12.6% lower for budesonide/formoterol (p < 0.0001). Conclusion: This study suggests that for patients with chronic asthma in Germany, budesonide/formoterol rather than salmeterol/fluticasone had a higher likelihood of treatment success, and that budesonide/formoterol is the less costly option. Although the cohorts appeared to be well matched at baseline, the results should be interpreted with caution given the observational nature of the study.