Idiopathic pulmonary arterial hypertension and co-existing lung disease: is this a new phenotype?
idiopathic pulmonary arterial hypertension (IPAH)
lung disease
survival
treatment response
Journal
Pulmonary circulation
ISSN: 2045-8932
Titre abrégé: Pulm Circ
Pays: United States
ID NLM: 101557243
Informations de publication
Date de publication:
Historique:
received:
30
10
2019
accepted:
23
02
2020
entrez:
15
4
2020
pubmed:
15
4
2020
medline:
15
4
2020
Statut:
epublish
Résumé
Patients classified as idiopathic pulmonary arterial hypertension (defined as Group 1 on European Respiratory Society (ERS)/European Cardiac Society (ESC) criteria) may have evidence of minor co-existing lung disease on thoracic computed tomography. We hypothesised that these idiopathic pulmonary arterial hypertension patients (
Identifiants
pubmed: 32284847
doi: 10.1177/2045894020914851
pii: 10.1177_2045894020914851
pmc: PMC7132795
doi:
Types de publication
Journal Article
Langues
eng
Pagination
2045894020914851Informations de copyright
© The Author(s) 2020.
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