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Clinical Investigations: ASTHMA |

Zafirlukast Treatment for Acute Asthma*: Evaluation in a Randomized, Double-Blind, Multicenter Trial

Robert A. Silverman, MD; Richard M. Nowak, MD; Phillip E. Korenblat, MD; Emil Skobeloff, MD; Yusong Chen, PhD; Catherine M. Bonuccelli, MD; Christopher J. Miller, MStat; Steven G. Simonson, MD, FCCP
Author and Funding Information

*From the Long Island Jewish Medical Center (Dr. Silverman), New Hyde Park, NY; the Henry Ford Health System (Dr. Nowak), Detroit, MI; Barnes-Jewish Hospital (Dr. Korenblat), St. Louis, MO; Crozer-Chester Medical Center (Dr. Skobeloff), Upland, PA; and AstraZeneca Pharmaceuticals LP (Drs. Chen, Bonuccelli, and Simonson, and Mr. Miller), Wilmington, DE.

Correspondence to: Robert A. Silverman, MD, Long Island Jewish Medical Center, 270–05 76th Ave, New Hyde Park, NY 11042; e-mail: aresilv@aol.com



Chest. 2004;126(5):1480-1489. doi:10.1378/chest.126.5.1480
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Context: Acute asthma causes nearly 2 million hospital emergency department (ED) visits in the United States annually, and hospitalization after an ED visit and relapse after ED discharge are common.

Objective: To evaluate the adding of therapy with zafirlukast to standardized care for patients with acute asthma in the ED and a 28-day follow-up period.

Design and patients: A total of 641 patients presenting to the ED with acute asthma were randomized to receive either single-dose zafirlukast, 160 mg (Z160) [162 patients], zafirlukast, 20 mg (Z20) [158 patients]), or placebo (321 patients) as adjunct treatment to standard care in this double-blind, multicenter trial. Assessments, including spirometry and symptom scores, were obtained before each albuterol treatment and at 4 h. Patients who were discharged from the ED after 4 h continued outpatient therapy over a 28-day period and received either Z20 bid (276 patients) or placebo (270 patients) in addition to prednisone, albuterol, and their previous asthma medications. FEV1 was measured at clinic visits on days 10 and 28. Patients recorded outpatient clinical data twice daily on a home diary card.

Main outcome measures: the effect of zafirlukast on relapse after ED discharge. Other assessments were the rate of extended care (ie, ED stay for > 4 h or hospitalization), FEV1, and symptoms.

Results: At the end of the outpatient period, 65 of 276 patients (23.6%) treated with zafirlukast and 78 of 270 patients (28.9%) treated with placebo relapsed (p = 0.047; absolute reduction, 5.3%; relative reduction, 18.3%). At the end of the ED period, 16 of 162 patients (9.9%) treated with Z160, 26 of 158 patients (16.5%) treated with Z20, and 48 of 321 patients (15.0%) treated with placebo required extended care (p = 0.052; absolute reduction with Z160 compared to placebo, 5.1%; relative reduction, 34%). These findings were supported by a significant improvement in FEV1 and dyspnea in the ED with the use of Z160 therapy, and by greater improvement in FEV1 and symptoms during the outpatient period for patients treated with Z20.

Conclusions: When added to standardized care, therapy with Z20 bid reduced the risk of relapse compared with placebo over a 28-day treatment period. One dose of Z160 in the ED also reduced the rate of extended care.

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