Cargando…
Time from symptoms to definitive diagnosis of idiopathic pulmonary arterial hypertension: The delay study
Survival rates for patients with idiopathic pulmonary arterial hypertension (IPAH) have improved with the introduction of PAH-specific therapies. However, the time between patient-reported onset of symptoms and a definitive diagnosis of IPAH is consistently delayed. We conducted a retrospective, mul...
Autores principales: | Strange, Geoff, Gabbay, Eli, Kermeen, Fiona, Williams, Trevor, Carrington, Melinda, Stewart, Simon, Keogh, Anne |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641745/ https://www.ncbi.nlm.nih.gov/pubmed/23662179 http://dx.doi.org/10.4103/2045-8932.109919 |
Ejemplares similares
-
Hemodynamics in pulmonary arterial hypertension (PAH): do they explain long-term clinical outcomes with PAH-specific therapy?
por: Steele, Peter, et al.
Publicado: (2010) -
Integrated care and optimal management of pulmonary arterial hypertension
por: Strange, Geoff, et al.
Publicado: (2009) -
Pulmonary hypertension: prevalence and mortality in the Armadale echocardiography cohort
por: Strange, Geoff, et al.
Publicado: (2012) -
Exercise Intolerance in Pulmonary Arterial Hypertension
por: Fowler, Robin M., et al.
Publicado: (2012) -
Review of bosentan in the management of pulmonary arterial hypertension
por: Gabbay, Eli, et al.
Publicado: (2007)