» Articles » PMID: 18245142

Superiority of "triple" Therapy with Salmeterol/fluticasone Propionate and Tiotropium Bromide Versus Individual Components in Moderate to Severe COPD

Overview
Journal Thorax
Date 2008 Feb 5
PMID 18245142
Citations 55
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The combination of salmeterol and fluticasone propionate (SFC) and tiotropium bromide (TIO) are commonly used treatments in chronic obstructive pulmonary disease (COPD) but there are few data on their effectiveness when used together. We compared the effects of SFC 50/500 microg twice daily in addition to TIO 18 microg once daily with the individual treatments alone.

Methods: 41 patients with COPD participated in a randomised, double blind, double dummy, three way crossover study with 2 week washout periods between treatments. Lung function assessment included plethysmography and spirometry. The primary end point was post-dose specific airways conductance (sGaw) area under the curve (AUC(0-4 h)) on day 14.

Results: AUC(0-4 h) sGaw was significantly higher on day 14 after SFC+TIO compared with TIO (22%) or SFC alone (27%) (both p<0.001). SFC+TIO significantly improved trough forced expiratory volume in 1 s compared with TIO alone (212 ml, p<0.001) and SFC alone (110 ml, p = 0.017) on day 14. Inspiratory capacity measurements also showed significant benefits for triple therapy over individual components on day 14. Subjects receiving SFC+TIO had clinically relevant improvements in Transition Dyspnoea Index (TDI) total score of 2.2 compared with TIO alone (p<0.001) (but not SFC alone, 0.7; NS) and used significantly less rescue medication (1.0 occasion less daily than TIO (p<0.001) and 0.6 less than SFC (p = 0.01)).

Conclusion: SFC+TIO triple therapy led to greater improvements in bronchodilation compared with TIO and SFC alone. The advantages of triple therapy are observed across a range of physiologically important parameters, including airway conductance and lung volumes. Triple therapy also led to patient related benefits by improving TDI and use of rescue medication.

Citing Articles

Development of Novel Fluticasone/Salmeterol/Tiotropium-Loaded Dry Powder Inhaler and Bioequivalence Assessment to Commercial Products in Rats.

Cho H, Lee H, Hwang D Pharmaceutics. 2025; 17(1).

PMID: 39861751 PMC: 11769347. DOI: 10.3390/pharmaceutics17010103.


Outcomes Following Initiation of Triple Therapy with Fluticasone Furoate/Umeclidinium/Vilanterol versus Multiple-Inhaler Triple Therapy Among Medicare Advantage with Part D Beneficiaries and Those Commercially Enrolled for Health Care Insurance in....

Bogart M, Bengtson L, Johnson M, Bunner S, Gronroos N, DiRocco K Int J Chron Obstruct Pulmon Dis. 2024; 19:97-110.

PMID: 38226396 PMC: 10789573. DOI: 10.2147/COPD.S424497.


Investigation of the Methodology of Specific Airway Resistance Measurements in COPD.

Dean J, Singh D Int J Chron Obstruct Pulmon Dis. 2023; 18:2555-2563.

PMID: 38022825 PMC: 10655747. DOI: 10.2147/COPD.S424696.


Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution.

Braido F, Corsico A, Paleari D, Piraino A, Cavalieri L, Scichilone N Ther Adv Respir Dis. 2022; 16:17534666211066063.

PMID: 35044875 PMC: 8796083. DOI: 10.1177/17534666211066063.


Early chronic obstructive pulmonary disease: A new perspective.

Lu H, Zeng H, Chen Y Chronic Dis Transl Med. 2021; 7(2):79-87.

PMID: 34136767 PMC: 8180470. DOI: 10.1016/j.cdtm.2021.02.003.