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dc.contributor.author
Hita, Alejandro  
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Baratta, Sergio  
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Vaccarino, Guillermo  
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Navia, José  
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Olano, Daniel  
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Telayna, Juan Manuel  
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Costantini, Ricardo  
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Chejtman, Demian  
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Matoso, Miriam  
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Gelpi, Ricardo Jorge  
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Donato, Pablo Martín  
dc.contributor.author
Morales, Maria Celina  
dc.date.available
2018-03-19T20:59:33Z  
dc.date.issued
2015-06  
dc.identifier.citation
Hita, Alejandro; Baratta, Sergio; Vaccarino, Guillermo; Navia, José; Olano, Daniel; et al.; Severe aortic stenosis with preserved ejection fraction and evidence of impairment in structure, myocardial strain and ventricular function: A new contribution to clinical decision making; Via Medica; Cardiology Journal; 22; 6; 6-2015; 613-621  
dc.identifier.issn
1897-5593  
dc.identifier.uri
http://hdl.handle.net/11336/39281  
dc.description.abstract
Background: Left ventricular ejection fraction (LVEF) is among the parameters that are usually employed to define surgical timing of severe aortic stenosis (AS). Our hypothesis states that even when their LVEF is preserved, patients with severe symptomatic AS have impaired myocardial structure and function, and such impairment is related to the deleterious progression of left ventricular hypertrophy (LVH) from the compensated to the decompensated stage, as shown by the changes in diastolic function and the increase in left ventricular end-diastolic pressure (LVEDP). Methods and Results: A total of 26 patients with severe AS and LVEF > 50% referred for aortic valve replacement underwent catheterization, echocardiography and an intraoperative biopsy. Patients with severe symptomatic AS were classified as: group 1 (G1; compensated LVH, LVEDP < 15 mm Hg without coronary artery disease [CAD], n = 7), group 2a (G2a, decompensated LVH, without CAD, n = 7), and group 2b (G2b, decompensated LVH with CAD, n = 12). Differences were seen in the following: myocyte area [μm2]: G1: 328 ± 66, G2a: 376 ± 22, G2b: 385 ± 13, p < 0.01; collagen volume [%]: G1: 4.77 ± 1.27, G2a: 8.40 ± 1.27, G2b: 11.05 ± 3.08, p < 0.01; LVEDP normalized by diastolic diameter [mm Hg/mm]: G1: 0.27 ± 0.01, G2a: 0.39 ± 0.06, G2b: 0.44 ± 0.11, p < 0.02; +dP/dtmax/LVEDP [mm Hg/s/mm Hg]: G1: 176 ± 45, G2a: 89.6 ± 20, G2b: 113.1 ± 41, p < 0.01; two-dimensional peak systolic longitudinal strain [%]: G1: –17.7 ± 4.75, G2a: –13.4 ± 3.04, G2b: –13.5 ± 3.13, p < 0.05. Conclusions: Patients with severe symptomatic AS and preserved ejection fraction who develop decompensated LVH characterized by increased LVEDP, exhibit an abnormal myocardial structure and diastolic and systolic impairment.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Via Medica  
dc.rights
info:eu-repo/semantics/openAccess  
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https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
Aortic Stenosis  
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Function  
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Hypertrophy  
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Medicina Critica y de Emergencia  
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Medicina Clínica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Severe aortic stenosis with preserved ejection fraction and evidence of impairment in structure, myocardial strain and ventricular function: A new contribution to clinical decision making  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-03-13T18:14:11Z  
dc.journal.volume
22  
dc.journal.number
6  
dc.journal.pagination
613-621  
dc.journal.pais
Polonia  
dc.description.fil
Fil: Hita, Alejandro. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
dc.description.fil
Fil: Baratta, Sergio. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Vaccarino, Guillermo. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Navia, José. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Olano, Daniel. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Telayna, Juan Manuel. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Costantini, Ricardo. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Chejtman, Demian. Universidad Austral. Facultad de Ciencias Biomédicas; Argentina  
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Fil: Matoso, Miriam. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina  
dc.description.fil
Fil: Gelpi, Ricardo Jorge. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Bioquímica y Medicina Molecular; Argentina  
dc.description.fil
Fil: Donato, Pablo Martín. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
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Fil: Morales, Maria Celina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina  
dc.journal.title
Cardiology Journal  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.5603/CJ.a2015.0034  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://journals.viamedica.pl/cardiology_journal/article/view/CJ.a2015.0034/31501