Rosenkranz, S. (2014). Cor pulmonale and pulmonary hypertension. Update after the world conference in Nice. Herz, 39 (1). S. 58 - 66. MUNICH: URBAN & VOGEL. ISSN 1615-6692

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Abstract

Pulmonary hypertension (PH) is a common phenomenon which may occur as a consequence of various diseases (e.g. heart failure, chronic lung diseases and pulmonary embolism), as a distinct disease of the small pulmonary arterioles or a combination of both. Independent from the origin, PH has an important impact on patient symptoms and prognosis. Establishment of an exact diagnosis and classification as well as an understanding of the hemodynamic interrelationships provide the basis for often challenging treatment decisions. Recently, the fifth World Symposium on PH took place in Nice, France, where important standards and definitions were specified. The most relevant results including the rating of novel treatment options are summarized in this article.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Rosenkranz, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-446233
DOI: 10.1007/s00059-014-4058-5
Journal or Publication Title: Herz
Volume: 39
Number: 1
Page Range: S. 58 - 66
Date: 2014
Publisher: URBAN & VOGEL
Place of Publication: MUNICH
ISSN: 1615-6692
Language: German
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
PRESERVED EJECTION FRACTION; ARTERIAL-HYPERTENSION; HEART-FAILURE; PHOSPHODIESTERASE-5 INHIBITION; TREATMENT ALGORITHM; IMATINIB MESYLATE; RIOCIGUAT; MACITENTAN; PRESSURE; SURVIVALMultiple languages
Cardiac & Cardiovascular SystemsMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/44623

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