Fluticasone propionate powder: Oral corticosteroid-sparing effect and improved lung function and quality of life in patients with severe chronic asthma

被引:62
作者
Nelson, HS
Busse, WW
deBoisblanc, BP
Berger, WE
Noonan, MJ
Webb, DR
Wolford, JP
Mahajan, PS
Hamedani, AG
Shah, T
Harding, SM
机构
[1] Natl Jewish Med & Res Ctr, Denver, CO 80206 USA
[2] Univ Wisconsin, Ctr Clin Canc, Madison, WI USA
[3] Louisiana State Univ, Med Ctr, New Orleans, LA USA
[4] So Calif Res Ctr, Mission Viejo, CA USA
[5] Allergy Associates PC, Portland, OR USA
[6] Allergy & Asthma Associates, Kirkland, WA USA
[7] Glaxo Wellcome Inc, Res Triangle Pk, NC 27709 USA
关键词
asthma; Diskus; fluticasone propionate; oral corticosteroid-sparing;
D O I
10.1016/S0091-6749(99)70501-4
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Many patients with severe asthma are dependent on oral corticosteroids for maintenance control of their disease. Treatments that allow patients to be weaned off oral corticosteroids may help to minimize the risk of side effects associated with their chronic use. Objective: This study evaluated whether inhaled fluticasone propionate powder could maintain pulmonary function while reducing the dose of oral prednisone in patients with chronic, severe asthma. Methods: Oral prednisone-dependent (5 to 40 mg/day) adolescents and adults with asthma (n = 111; mean FEV1 = 61% of predicted value) were randomized to placebo or twice daily fluticasone propionate 500 or 1000 mu g administered by means of a multidose powder inhaler for 16 weeks in a double-blind, parallel-group study, Patients underwent controlled prednisone reduction on the basis of predetermined asthma stability criteria. Results: Oral prednisone was eliminated by 75% and 89% of patients in the twice daily 500 and 1000 mu g fluticasone propionate groups, respectively, versus 9% of the placebo group (P < .001). FEV1, morning and evening peak expiratory flow, asthma symptoms, albuterol use, and nighttime awakenings improved with fluticasone propionate treatment, achieving statistical significance (P less than or equal to .009) primarily in the 1000 mu g twice daily group. Hypothalamic-pituitary-adrenal axis suppression observed at baseline improved when patients were weaned off oral prednisone to fluticasone propionate. Adverse events ascribed to drug treatment were primarily topical effects of inhaled corticosteroids or those associated with prednisone withdrawal. Patient quality of life assessed by means of the Asthma Quality of Life Questionnaire was clinically and significantly improved after fluticasone propionate treatment (P less than or equal to .003). Conclusion: Fluticasone propionate powder (500 or 1000 mu g twice daily) effectively improved lung function, adrenal function, and asthma-specific quality of life in patients with severe chronic asthma previously treated with oral prednisone while allowing most patients to be weaned off oral corticosteroid therapy.
引用
收藏
页码:267 / 275
页数:9
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