Inhaled mometasone furoate reduces oral prednisone requirements while improving respiratory function and health-related duality of life in patients with severe persistent asthma

Citation
Je. Fish et al., Inhaled mometasone furoate reduces oral prednisone requirements while improving respiratory function and health-related duality of life in patients with severe persistent asthma, J ALLERG CL, 106(5), 2000, pp. 852-860
Citations number
25
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
ISSN journal
00916749 → ACNP
Volume
106
Issue
5
Year of publication
2000
Pages
852 - 860
Database
ISI
SICI code
0091-6749(200011)106:5<852:IMFROP>2.0.ZU;2-P
Abstract
Background: Inhaled corticosteroid therapy in severe persistent asthma has been shown to reduce or eliminate oral corticosteroid (OCS) use while retai ning effective asthma control. Objective: We sought to evaluate the ability of mometasone furoate (MF) del ivered by means of dry powder inhaler to reduce daily oral prednisone requi rements in OCS-dependent patients with severe persistent asthma. Methods: We performed a 12-week, double-blind, placebo-controlled trial (21 centers, 132 patients) comparing 2 doses of MF (400 and 800 mug administer ed tu ice daily) with placebo, followed by a 9-month open-label phase in wh ich 128 patients received treatment with MF. Results: At the endpoint of the double-blind trial, MF 400 and 800 mg twice daily reduced daily OCS requirements by 46.0 % and 23.9%, respectively, wh ereas placebo increased OCS requirements by 164.4% (P <.01). Oral steroids were eliminated in 40%, 37%, and 0% of patients in the MF 400 and 800 mg tw ice daily and placebo groups, respectively. Pulmonary function and quality of life significantly increased for MF-treated patients. Further reductions in OCS requirements were achieved with long-term MF treatment in the open- label phase. Conclusion: MF inhaled orally as a dry powder is an effective alternative t o systemic corticosteroids in patients with severe persistent asthma.