Summary: international consensus statement on nomenclature and classification of the congenital bicuspid aortic valve and its aortopathy, for clinical, surgical, interventional and research purposes
Abstract This International evidence-based nomenclature and classification consensus on the congenital bicuspid aortic valve and its aortopathy recognizes 3 types of bicuspid aortic valve: 1. Fused type, with 3 phenotypes: right-left cusp fusion, right-non cusp fusion and left-non cusp fusion; 2. 2-...
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Veröffentlicht in: | European journal of cardio-thoracic surgery 2021-09, Vol.60 (3), p.481-496 |
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creator | Michelena, Hector I Della Corte, Alessandro Evangelista, Arturo Maleszewski, Joseph J Edwards, William D Roman, Mary J Devereux, Richard B Fernández, Borja Asch, Federico M Barker, Alex J Sierra-Galan, Lilia M De Kerchove, Laurent Fernandes, Susan M Fedak, Paul W M Girdauskas, Evaldas Delgado, Victoria Abbara, Suhny Lansac, Emmanuel Prakash, Siddharth K Bissell, Malenka M Popescu, Bogdan A Hope, Michael D Sitges, Marta Thourani, Vinod H Pibarot, Phillippe Chandrasekaran, Krishnaswamy Lancellotti, Patrizio Borger, Michael A Forrest, John K Webb, John Milewicz, Dianna M Makkar, Raj Leon, Martin B Sanders, Stephen P Markl, Michael Ferrari, Victor A Roberts, William C Song, Jae-Kwan Blanke, Philipp White, Charles S Siu, Samuel Svensson, Lars G Braverman, Alan C Bavaria, Joseph Sundt, Thoralf M Khoury, Gebrine El De Paulis, Ruggero Enriquez-Sarano, Maurice Bax, Jeroen J Otto, Catherine M Schäfers, Hans-Joachim |
description | Abstract
This International evidence-based nomenclature and classification consensus on the congenital bicuspid aortic valve and its aortopathy recognizes 3 types of bicuspid aortic valve: 1. Fused type, with 3 phenotypes: right-left cusp fusion, right-non cusp fusion and left-non cusp fusion; 2. 2-sinus type with 2 phenotypes: Latero-lateral and antero-posterior; and 3. Partial-fusion or forme fruste. This consensus recognizes 3 bicuspid-aortopathy types: 1. Ascending phenotype; root phenotype; and 3. extended phenotypes. |
doi_str_mv | 10.1093/ejcts/ezab039 |
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This International evidence-based nomenclature and classification consensus on the congenital bicuspid aortic valve and its aortopathy recognizes 3 types of bicuspid aortic valve: 1. Fused type, with 3 phenotypes: right-left cusp fusion, right-non cusp fusion and left-non cusp fusion; 2. 2-sinus type with 2 phenotypes: Latero-lateral and antero-posterior; and 3. Partial-fusion or forme fruste. This consensus recognizes 3 bicuspid-aortopathy types: 1. Ascending phenotype; root phenotype; and 3. extended phenotypes.</description><identifier>ISSN: 1010-7940</identifier><identifier>EISSN: 1873-734X</identifier><identifier>DOI: 10.1093/ejcts/ezab039</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>European journal of cardio-thoracic surgery, 2021-09, Vol.60 (3), p.481-496</ispartof><rights>This article has been co-published with permission in the European Journal of Cardio-Thoracic Surgery, The Annals of Thoracic Surgery, the Journal of Thoracic and Cardiovascular Surgery, and in Radiology: Cardiothoracic Imaging. All rights reserved. © 2021 Jointly between the European Association for Cardio-Thoracic Surgery, The Society of Thoracic Surgeons, the American Association for Thoracic Surgery, and the Radiological Society of North America. The articles are identical except for minor stylistic and spelling differences in keeping with each journal’s style. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-bca1fa6679db252b534802ec33e6e6b1a20ea5ca7102b6c8ab7287219f460d403</citedby><cites>FETCH-LOGICAL-c342t-bca1fa6679db252b534802ec33e6e6b1a20ea5ca7102b6c8ab7287219f460d403</cites><orcidid>0000-0002-2341-5247</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids></links><search><creatorcontrib>Michelena, Hector I</creatorcontrib><creatorcontrib>Della Corte, Alessandro</creatorcontrib><creatorcontrib>Evangelista, Arturo</creatorcontrib><creatorcontrib>Maleszewski, Joseph J</creatorcontrib><creatorcontrib>Edwards, William D</creatorcontrib><creatorcontrib>Roman, Mary J</creatorcontrib><creatorcontrib>Devereux, Richard B</creatorcontrib><creatorcontrib>Fernández, Borja</creatorcontrib><creatorcontrib>Asch, Federico M</creatorcontrib><creatorcontrib>Barker, Alex J</creatorcontrib><creatorcontrib>Sierra-Galan, Lilia M</creatorcontrib><creatorcontrib>De Kerchove, Laurent</creatorcontrib><creatorcontrib>Fernandes, Susan M</creatorcontrib><creatorcontrib>Fedak, Paul W M</creatorcontrib><creatorcontrib>Girdauskas, Evaldas</creatorcontrib><creatorcontrib>Delgado, Victoria</creatorcontrib><creatorcontrib>Abbara, Suhny</creatorcontrib><creatorcontrib>Lansac, Emmanuel</creatorcontrib><creatorcontrib>Prakash, Siddharth K</creatorcontrib><creatorcontrib>Bissell, Malenka M</creatorcontrib><creatorcontrib>Popescu, Bogdan A</creatorcontrib><creatorcontrib>Hope, Michael D</creatorcontrib><creatorcontrib>Sitges, Marta</creatorcontrib><creatorcontrib>Thourani, Vinod H</creatorcontrib><creatorcontrib>Pibarot, Phillippe</creatorcontrib><creatorcontrib>Chandrasekaran, Krishnaswamy</creatorcontrib><creatorcontrib>Lancellotti, Patrizio</creatorcontrib><creatorcontrib>Borger, Michael A</creatorcontrib><creatorcontrib>Forrest, John K</creatorcontrib><creatorcontrib>Webb, John</creatorcontrib><creatorcontrib>Milewicz, Dianna M</creatorcontrib><creatorcontrib>Makkar, Raj</creatorcontrib><creatorcontrib>Leon, Martin B</creatorcontrib><creatorcontrib>Sanders, Stephen P</creatorcontrib><creatorcontrib>Markl, Michael</creatorcontrib><creatorcontrib>Ferrari, Victor A</creatorcontrib><creatorcontrib>Roberts, William C</creatorcontrib><creatorcontrib>Song, Jae-Kwan</creatorcontrib><creatorcontrib>Blanke, Philipp</creatorcontrib><creatorcontrib>White, Charles S</creatorcontrib><creatorcontrib>Siu, Samuel</creatorcontrib><creatorcontrib>Svensson, Lars G</creatorcontrib><creatorcontrib>Braverman, Alan C</creatorcontrib><creatorcontrib>Bavaria, Joseph</creatorcontrib><creatorcontrib>Sundt, Thoralf M</creatorcontrib><creatorcontrib>Khoury, Gebrine El</creatorcontrib><creatorcontrib>De Paulis, Ruggero</creatorcontrib><creatorcontrib>Enriquez-Sarano, Maurice</creatorcontrib><creatorcontrib>Bax, Jeroen J</creatorcontrib><creatorcontrib>Otto, Catherine M</creatorcontrib><creatorcontrib>Schäfers, Hans-Joachim</creatorcontrib><title>Summary: international consensus statement on nomenclature and classification of the congenital bicuspid aortic valve and its aortopathy, for clinical, surgical, interventional and research purposes</title><title>European journal of cardio-thoracic surgery</title><description>Abstract
This International evidence-based nomenclature and classification consensus on the congenital bicuspid aortic valve and its aortopathy recognizes 3 types of bicuspid aortic valve: 1. Fused type, with 3 phenotypes: right-left cusp fusion, right-non cusp fusion and left-non cusp fusion; 2. 2-sinus type with 2 phenotypes: Latero-lateral and antero-posterior; and 3. Partial-fusion or forme fruste. This consensus recognizes 3 bicuspid-aortopathy types: 1. 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This International evidence-based nomenclature and classification consensus on the congenital bicuspid aortic valve and its aortopathy recognizes 3 types of bicuspid aortic valve: 1. Fused type, with 3 phenotypes: right-left cusp fusion, right-non cusp fusion and left-non cusp fusion; 2. 2-sinus type with 2 phenotypes: Latero-lateral and antero-posterior; and 3. Partial-fusion or forme fruste. This consensus recognizes 3 bicuspid-aortopathy types: 1. Ascending phenotype; root phenotype; and 3. extended phenotypes.</abstract><pub>Oxford University Press</pub><doi>10.1093/ejcts/ezab039</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-2341-5247</orcidid><oa>free_for_read</oa></addata></record> |
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title | Summary: international consensus statement on nomenclature and classification of the congenital bicuspid aortic valve and its aortopathy, for clinical, surgical, interventional and research purposes |
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