Cargando…
Adverse health consequences in COPD patients with rapid decline in FEV(1 )- evidence from the UPLIFT trial
BACKGROUND: The rate of decline in forced expiratory volume in 1 second (FEV(1)) is representative of the natural history of COPD. Sparse information exists regarding the associations between the magnitude of annualised loss of FEV(1 )with other endpoints. METHODS: Retrospective analysis of UPLIFT(®...
Autores principales: | Kesten, Steven, Celli, Bartolome, Decramer, Marc, Liu, Dacheng, Tashkin, Donald |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190346/ https://www.ncbi.nlm.nih.gov/pubmed/21955733 http://dx.doi.org/10.1186/1465-9921-12-129 |
Ejemplares similares
-
Risk of Nonlower Respiratory Serious Adverse Events Following COPD Exacerbations in the 4-year UPLIFT(®) Trial
por: Halpin, David M. G., et al.
Publicado: (2011) -
Acute bronchodilator responsiveness and health outcomes in COPD patients in the UPLIFT trial
por: Hanania, Nicola A, et al.
Publicado: (2011) -
Exacerbation frequency and course of COPD
por: Halpin, David MG, et al.
Publicado: (2012) -
Defining a COPD composite safety endpoint for demonstrating efficacy in clinical trials: results from the randomized, placebo-controlled UPLIFT® trial
por: Celli, Bartolomé R., et al.
Publicado: (2016) -
Tiotropium HandiHaler(®) in the treatment of COPD: A safety review
por: Kesten, Steven, et al.
Publicado: (2009)