Bosentan for pulmonary hypertension secondary to idiopathic pulmonary fibrosis

Pulmonary hypertension is a poor prognostic factor in patients with interstitial lung disease. No established treatment exists for pulmonary hypertension secondary to interstitial pneumonia. We describe the case of an 81-year-old woman with idiopathic pulmonary fibrosis (IPF), who was admitted to ou...

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Podrobná bibliografie
Vydáno v:Respir Med Case Rep
Hlavní autoři: Onda, Naomi, Tanaka, Yosuke, Hino, Mitsunori, Gemma, Akihiko
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2014
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4356039/
https://ncbi.nlm.nih.gov/pubmed/26029570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2014.11.008
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