Journal Home
Search for

Volume 104, Issue 6, Pages 780-787 (June 2010)


View previous. 3 of 24 View next.

Controller medications and their effects on asthma exacerbations temporally associated with upper respiratory infections

Charlene M. Prazmaa, Kenneth M. Krala, Nadeem Gulb, Steve W. Yanceya, David A. StempelaCorresponding Author Informationemail address

Received 19 November 2009; accepted 8 February 2010. published online 08 March 2010.

Summary 

Background

Exacerbations are a major risk and a cause of asthma morbidity and healthcare utilization. Viral-induced upper respiratory tract infections are the most frequent trigger of asthma-related exacerbations. Studies have traditionally assessed exacerbations without documentation regarding exacerbation etiology. Therefore, it remains unknown whether asthma medications can alter exacerbation susceptibility based on a specific etiology.

Objective

To examine whether treatment with inhaled corticosteroids plus long-acting beta2-agonists reduced the number of exacerbations associated with upper respiratory tract infections versus inhaled corticosteroids alone.

Methods

Two large datasets comparing treatment with fluticasone propionate and fluticasone propionate plus salmeterol were analyzed, including the number of clinically reported upper respiratory tract infections, asthma-related exacerbations, and the presence of an exacerbation and concurrent report of an upper respiratory tract infection.

Results

Both treatment groups had similar incidences of upper respiratory tract infections. Of those reporting an upper respiratory tract infection, statistically significantly fewer reported an asthma-related exacerbation comparing fluticasone propionate plus salmeterol with fluticasone propionate (p=0.0057).

Discussion

This retrospective analysis suggests that therapy with fluticasone propionate plus salmeterol provides protection against asthma exacerbations temporally associated with upper respiratory tract infections. This retrospective analysis supports the hypothesis that specific therapeutic approaches to mitigate virus-associated exacerbations may benefit asthma care. Well-controlled prospective studies are warranted.

a Respiratory Medical Development Center, GlaxoSmithKline, Research Triangle Park, Five Moore Drive, NC 27709, USA

b GlaxoSmithKline, Stockley Park, London, UK

Corresponding Author InformationCorresponding author. Tel.: +1 919 483 5325; fax: +1 919 483 4300.

 This study was funded by GlaxoSmithKline.

PII: S0954-6111(10)00058-2

doi:10.1016/j.rmed.2010.02.007


View previous. 3 of 24 View next.