Prevalence and Risk Factors for Pulmonary Arterial Hypertension in a Large Group of β-Thalassemia Patients Using Right Heart Catheterization
Author(s) -
Giorgio Derchi,
Renzo Galanello,
Patrizio Bina,
Maria Domenica Cappellini,
Antonio Piga,
Maria-Eliana Lai,
Antonella Quarta,
Gavino Casu,
Silverio Perrotta,
Valeria Maria Pinto,
Khaled M. Musallam,
Gian Luca Forni
Publication year - 2013
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.113.002124
Subject(s) - medicine , odds ratio , cardiology , pulmonary hypertension , confidence interval , thalassemia , cardiac catheterization , blood pressure , surgery
Pulmonary arterial hypertension (PAH) remains a concern in patients with β-thalassemia major (TM) and intermedia (TI); however, studies evaluating its prevalence and risk factors using systematic confirmation on right heart catheterization are lacking.
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