| Literature DB >> 34304894 |
Hector I Michelena1, Alessandro Della Corte2, Arturo Evangelista3, Joseph J Maleszewski4, William D Edwards5, Mary J Roman6, Richard B Devereux6, Borja Fernández7, Federico M Asch8, Alex J Barker9, Lilia M Sierra-Galan10, Laurent De Kerchove11, Susan M Fernandes12, 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 Chandrasekaran25, Patrizio Lancellotti26, Michael A Borger27, John K Forrest28, John Webb29, Dianna M Milewicz18, Raj Makkar28, Martin B Leon29, Stephen P Sanders30, Michael Markl31, Victor A Ferrari32, William C Roberts33, Jae-Kwan Song34, Philipp Blanke35, Charles S White36, Samuel Siu37, Lars G Svensson38, Alan C Braverman39, Joseph Bavaria40, Thoralf M Sundt41, Gebrine El Khoury11, Ruggero De Paulis42, Maurice Enriquez-Sarano25, Jeroen J Bax15, Catherine M Otto43, Hans-Joachim Schäfers44.
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.Entities:
Keywords: Aortopathy; Bicuspid aortic valve; Classification; Nomenclature
Mesh：
Year: 2021 PMID： 34304894 DOI： 10.1016/j.jtcvs.2021.05.008
Source DB: PubMed Journal: J Thorac Cardiovasc Surg ISSN： 0022-5223 Impact factor: 5.209