Clinical Impact of Main Pulmonary Artery Dilatation on Outcome in Pediatric Idiopathic and Heritable Pulmonary Arterial Hypertension
Author:
Affiliation:
1. Department of Pediatrics, Toho University Omori Medical Center
Publisher
Japanese Circulation Society
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
https://www.jstage.jst.go.jp/article/circj/82/2/82_CJ-17-0092/_pdf
Reference12 articles.
1. 2. Demerouti EA, Manginas AN, Athanassopoulos GD, Karatasakis GT. Complications leading to sudden cardiac death in pulmonary arterial hypertension. Respir Care 2013; 58: 1246–1254.
2. 3. Albadri K, Jensen JM, Christiansen EH, Mellemkjær S, Nielsen-Kudsk JE. Left main coronary artery compression in pulmonary arterial hypertension. Pulm Circ 2015; 5: 734–736.
3. 4. Tang BT, Pickard SS, Chan FP, Tsao PS, Taylor CA, Feinstein JA. Wall shear stress is decreased in the pulmonary arteries of patients with pulmonary arterial hypertension: An imagebased, computational fluid dynamics study. Pulm Circ 2012; 2: 470–476.
4. 5. Schäfer M, Ivy DD, Barker AJ, Kheyfets V, Shandas R, Abman SH, et al. Characterization of CMR-derived haemodynamic data in children with pulmonary arterial hypertension. Eur Heart J Cardiovasc Imaging 2017; 18: 424–431.
5. 6. Lupi E, Dumont C, Tejada VM, Horwitz S, Galland F. A radiologic index of pulmonary arterial hypertension. Chest 1975; 68: 28–31.
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1. Bosentan for Treatment of Pediatric Idiopathic Pulmonary Arterial Hypertension: State-of-the-Art;Frontiers in Pediatrics;2019-07-23
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