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dc.contributor.author
Hita, Alejandro
dc.contributor.author
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
dc.rights.uri
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
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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
dc.description.fil
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
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