Echocardiography in Pulmonary Arterial Hypertension View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-04

AUTHORS

Francesco Ferrara, Xiao Zhou, Luna Gargani, Karina Wierzbowska-Drabik, Olga Vriz, Bahaa M. Fadel, Anna Agnese Stanziola, Jaroslaw Kasprzak, Mani Vannan, Eduardo Bossone

ABSTRACT

PURPOSE OF REVIEW: Pulmonary arterial hypertension (PAH) is a devastating disease which can result in right heart (RH) failure and death. Herein, we discuss the current clinical applications of echocardiography in PAH. RECENT FINDINGS: Advanced echocardiographic techniques (strain, strain rate, 2D-speckle tracking strain, and three-dimensional echocardiography) may reveal in the near future additional important insights into RH structure and function. Although right-heart catheterization is mandatory for a definitive diagnosis, echocardiography (resting and exercise) represents a key noninvasive imaging test on the diagnostic-prognostic-therapeutic PAH algorithm. More... »

PAGES

22

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11886-019-1109-9

DOI

http://dx.doi.org/10.1007/s11886-019-1109-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1112510187

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30828743


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