Effect of Pharmacotherapy on Rate of Decline of Lung Function in Chronic Obstructive Pulmonary Disease: Results from the TORCH Study
St. Elizabeth's Medical Center · GlaxoSmithKline (United Kingdom) · +9 more institutions
Abstract
In a post hoc analysis of the Toward a Revolution in COPD Health (TORCH) study, we investigated the effects of combined salmeterol 50 microg plus fluticasone propionate 500 microg, either component alone or placebo, on the rate of post-bronchodilator FEV(1) decline in patients with moderate or severe COPD.
A randomized, double-blind, placebo-controlled study was conducted from September 2000 to November 2005 in 42 countries. Of 6,112 patients from the efficacy population, 5,343 were included in this analysis. MEASUREMENTS AND MAIN RESULTS: Spirometry was measured every 24 weeks for 3 years. There were 26,539 on-treatment observations. The adjusted rate of decline in FEV(1) was 55 ml/year for placebo, 42 ml/year for salmeterol, 42 ml/year for fluticasone propionate, and 39 ml/year for salmeterol plus fluticasone propionate. Salmeterol plus fluticasone propionate reduced the rate of FEV(1) decline by 16 ml/year compared with placebo (95% confidence interval [CI], 7-25; P
Citation impact
- FWCI
- 60.65
- Percentile
- 100%
- References
- 43
Authors
10- BRBartolomé R. CelliCorresponding
St. Elizabeth's Medical Center
- NENicola E. Thomas
GlaxoSmithKline (United Kingdom), GlaxoSmithKline (Germany)
- JAJulie A. Anderson
GlaxoSmithKline (United Kingdom), GlaxoSmithKline (Germany)
- GTGary T. Ferguson
Airflow Sciences (United States)
- CJChristine Jenkins
Woolcock Institute of Medical Research
Topics & keywords
- Salmeterol
- Fluticasone propionate
- Medicine
- Placebo
- COPD
- Fluticasone
- Internal medicine
- Bronchodilator
- Good health and well-being