TY - JOUR
T1 - Variability of symptoms in mild persistent asthma
T2 - Baseline data from the MIAMI study
AU - Zeiger, Robert S.
AU - Baker, James W.
AU - Kaplan, Michael S.
AU - Pearlman, David S.
AU - Schatz, Michael
AU - Bird, Steven
AU - Hustad, Carolyn
AU - Edelman, Jonathan
AU - Carl, John C.
AU - Corren, Jonathan
AU - Harden, Kathleen
AU - Mendoza, Guillermo R.
AU - Rand, Cynthía
N1 - Funding Information:
The following are members of the MIAMI Study Research Group Steering Committee: James W. Baker, MD; Steven Bird, MS; John C. Carl, MD; Jonathan Corren, MD; Jonathan Edelman, MD; Kathleen Harden, RN; Michael S. Kaplan, MD; Guillermo R. Mendoza, MD; David S. Pearlman, MD; Cynthia Rand, PhD; Michael Schatz, MD, MS; Robert Zeiger, MD, PhD. We thank Arvin Mokha, MD, for his assistance in reviewing the spirometry data. We would also like to acknowledge the Medical Program Coordinator Elizabeth Desrosiers, MS, and the writing contributions of, William Gough, PhD. Supported by a grant from Merck & Co., Inc., Whitehouse Station, New Jersey.
PY - 2004/9
Y1 - 2004/9
N2 - Objective: To describe the variability of the asthma phenotype in patients with mild persistent asthma enrolled in the Mi Asthma Montelukast versus Inhaled Corticosteroid (MIAMI) study. Methods: The variability of asthma rescue-free days, asthma symptoms, albuterol use, medical resource use, and exercise limitations among patients with documented mild persistent asthma was compared between the month before study enrollment and the last 2 weeks of the run-in period. Results: Patients eligible for randomization (n=400), aged 15-85 years, exhibited symptoms (mean±sd) 3.6±1.3 days/week, β-agonist use 3.5±1.3 days/week, and normal FEV1 (94.0±9.9% predicted) during the last 2 weeks of the run-in period. In the year before enrollment, medical intervention for asthma flares was common: 38.5% made office visits, 15.8% had oral corticosteroids, and 8.3% required emergency room or hospitalized care. In the month before enrollment, 11.8% experienced daily symptoms, and 28.3% had limitations of normal activity. Patients with daily symptoms in the month before study enrollment, compared with those having less-than-daily symptoms, experienced fewer rescue-free days (P=0.024) and had more days per week with symptoms (P=0.008) and requiring albuterol (P=0.048) during the run-in; FEV1 was similar for both groups (93.1% vs. 94.2% predicted, respectively). Conclusion: Patients with mild persistent asthma reported a substantial disease burden in the year before enrollment. The asthma burden experienced by these patients both before and during the run-in period was of sufficient severity to support the recommendation that mild persistent asthma should be managed with daily controller therapy.
AB - Objective: To describe the variability of the asthma phenotype in patients with mild persistent asthma enrolled in the Mi Asthma Montelukast versus Inhaled Corticosteroid (MIAMI) study. Methods: The variability of asthma rescue-free days, asthma symptoms, albuterol use, medical resource use, and exercise limitations among patients with documented mild persistent asthma was compared between the month before study enrollment and the last 2 weeks of the run-in period. Results: Patients eligible for randomization (n=400), aged 15-85 years, exhibited symptoms (mean±sd) 3.6±1.3 days/week, β-agonist use 3.5±1.3 days/week, and normal FEV1 (94.0±9.9% predicted) during the last 2 weeks of the run-in period. In the year before enrollment, medical intervention for asthma flares was common: 38.5% made office visits, 15.8% had oral corticosteroids, and 8.3% required emergency room or hospitalized care. In the month before enrollment, 11.8% experienced daily symptoms, and 28.3% had limitations of normal activity. Patients with daily symptoms in the month before study enrollment, compared with those having less-than-daily symptoms, experienced fewer rescue-free days (P=0.024) and had more days per week with symptoms (P=0.008) and requiring albuterol (P=0.048) during the run-in; FEV1 was similar for both groups (93.1% vs. 94.2% predicted, respectively). Conclusion: Patients with mild persistent asthma reported a substantial disease burden in the year before enrollment. The asthma burden experienced by these patients both before and during the run-in period was of sufficient severity to support the recommendation that mild persistent asthma should be managed with daily controller therapy.
KW - Airway inflammation
KW - Clinical trial
KW - Fluticasone
KW - Inhaled corticosteroids
KW - Leukotriene receptor antagonist
KW - Mild persistent asthma
KW - Montelukast
KW - Severity variability
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U2 - 10.1016/j.rmed.2004.02.016
DO - 10.1016/j.rmed.2004.02.016
M3 - Article
C2 - 15338804
AN - SCOPUS:4043079298
SN - 0954-6111
VL - 98
SP - 898
EP - 905
JO - Respiratory Medicine
JF - Respiratory Medicine
IS - 9
ER -