| Literature DB >> 34293102 |
Hector I Michelena1, Alessandro Della Corte2, Arturo Evangelista3, Joseph J Maleszewski4, William D Edwards4, Mary J Roman5, Richard B Devereux5, Borja Fernández6, Federico M Asch7, Alex J Barker8, Lilia M Sierra-Galan9, Laurent De Kerchove10, Susan M Fernandes11,12, Paul W M Fedak13, Evaldas Girdauskas14, Victoria Delgado15, Suhny Abbara16, Emmanuel Lansac17, Siddharth K Prakash18, Malenka M Bissell19, Bogdan A Popescu20, Michael D Hope21, Marta Sitges22, Vinod H Thourani23, Phillippe Pibarot24, Krishnaswamy Chandrasekaran1, Patrizio Lancellotti25,26, Michael A Borger27, John K Forrest28, John Webb29, Dianna M Milewicz18, Raj Makkar30, Martin B Leon31, Stephen P Sanders32,33, Michael Markl34, Victor A Ferrari35, William C Roberts36, Jae-Kwan Song37, Philipp Blanke38, Charles S White39, Samuel Siu40, Lars G Svensson41, Alan C Braverman42, Joseph Bavaria43, Thoralf M Sundt44, Gebrine El Khoury10, Ruggero De Paulis45, Maurice Enriquez-Sarano1, Jeroen J Bax15, Catherine M Otto46, Hans-Joachim Schäfers47.
Abstract
This International Consensus Classification and Nomenclature for the congenital bicuspid aortic valve condition recognizes 3 types of bicuspid valves: 1. The fused type (right-left cusp fusion, right-non-coronary cusp fusion and left-non-coronary cusp fusion phenotypes); 2. The 2-sinus type (latero-lateral and antero-posterior phenotypes); and 3. The partial-fusion (forme fruste) type. The presence of raphe and the symmetry of the fused type phenotypes are critical aspects to describe. The International Consensus also recognizes 3 types of bicuspid valve-associated aortopathy: 1. The ascending phenotype; 2. The root phenotype; and 3. Extended phenotypes. 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.Entities:
Keywords: Aortopathy; Bicuspid aortic valve; Classification; Nomenclature
Year: 2021 PMID: 34293102 DOI: 10.1093/ejcts/ezab038
Source DB: PubMed Journal: Eur J Cardiothorac Surg ISSN: 1010-7940 Impact factor: 4.191