Comparison of racemic albuterol and levalbuterol for treatment of acute asthma☆
Abstract
Objective
To determine whether levalbuterol resulted in fewer hospital admissions than racemic albuterol when used for treatment of acute asthma.
Study design
A randomized, double-blind, controlled trial was conducted in the emergency department (ED) and inpatient asthma care unit of an urban tertiary children's hospital. Children age 1 to 18 years (n
=
482) provided a total of 547 enrollments. Patients received a nebulized solution of either 2.5 mg racemic albuterol or 1.25 mg levalbuterol every 20 minutes (maximum six doses). Patients admitted to the asthma care unit were treated in a standardized fashion by using the same blinded drug assigned in the ED. Hospitalization rate was the primary outcome.
Results
Hospitalization rate was significantly lower in the levalbuterol group (36%) than in the racemic albuterol group (45 %, P
=
.02). The adjusted relative risk of admission in the racemic group compared with the levalbuterol group was 1.25 (95% confidence interval, 1.01-1.57). Hospital length of stay was not significantly shorter in the levalbuterol group (levalbuterol, 44.9 hours; racemic albuterol, 50.3 hours; P
=
.63). No significant adverse events occurred in either group.
Conclusions
Substituting levalbuterol for racemic albuterol in the ED management of acute asthma significantly reduced the number of hospitalizations.
Abbreviations: ACA, Asthma care algorithm, ACU, Asthma care unit, CI, Confidence interval, ED, Emergency department, GEE, Generalized estimating equation, LOS, Length of stay, PICU, Pediatric intensive care unit
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☆ Supported by an unrestricted research grant from Sepracor, Marlborough, Massachusetts. The study design, conduct, interpretation, and analysis of data were conducted solely by the investigators. Sepracor supplied racemic albuterol and levalbuterol. Salter (Irvine, Calif) supplied Nebutech nebulizers. Dr Carl, Dr Kercsmar, and Mr Myers have received honoraria for speaking engagements provided by Sepracor in the form of unrestricted educational grants.Portions of this work were presented at the Annual Meeting of the American Academy of Pediatrics, San Francisco, California, October 2001.
PII: S0022-3476(03)00493-1
doi:10.1067/S0022-3476(03)00493-1
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