The improvement of pulmonary artery pressure after bosentan therapy in patients with β-thalassemia and Doppler-defined pulmonary arterial hypertension

INTRODUCTION: Pulmonary arterial hypertension (PAH) is relatively prevalent in patients with thalassemia. PAH treatment is necessary as the prevalence of Doppler-estimated PAH and the resultant mortality is high in such patients. MATERIALS AND METHODS: This study aimed at evaluating the effect of bo...

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Detalles Bibliográficos
Autores principales: Karami, Hossein, Darvishi-Khezri, Hadi, Kosaryan, Mehrnoush, Akbarzadeh, Rosetta, Dabirian, Mojdeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301293/
https://www.ncbi.nlm.nih.gov/pubmed/30588128
http://dx.doi.org/10.2147/IMCRJ.S180602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301293/
https://www.ncbi.nlm.nih.gov/pubmed/30588128
http://dx.doi.org/10.2147/IMCRJ.S180602

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