Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/34194
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorANDRADE, Ana Cristina
dc.contributor.authorJEROSCH-HEROLD, Michael
dc.contributor.authorWEGNER, Philip
dc.contributor.authorGABBERT, Dominik Daniel
dc.contributor.authorVOGES, Inga
dc.contributor.authorMinh Pham
dc.contributor.authorSHAH, Ravi
dc.contributor.authorHEDDERICH, Juergen
dc.contributor.authorKRAMER, Hans-Heiner
dc.contributor.authorRICKERS, Carsten
dc.date.accessioned2019-11-06T18:52:27Z-
dc.date.available2019-11-06T18:52:27Z-
dc.date.issued2019
dc.identifier.citationJOURNAL OF THE AMERICAN HEART ASSOCIATION, v.8, n.17, article ID e009618, 13p, 2019
dc.identifier.issn2047-9980
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/34194-
dc.description.abstractBackground-The aim of this study was to identify in asymptomatic patients with repaired tetralogy of Fallot the prevalence and determinants of impaired left-sided cardiac function and adverse ventricular remodeling and the relation of left ventricular (LV) dysfunction and remodeling with cardiopulmonary exercise capacity. Methods and Results-In a cross-sectional study, 103 patients with tetralogy of Fallot (median age, 16.3 years) in New York Heart Association class 1, with surgical repair at a median age of 1.1 years, and 63 age-matched controls were studied. LV, right ventricular function and geometry, LV myocardial extracellular volume (n=57), and left atrial function were quantified with cardiac magnetic resonance. Peak oxygen consumption was measured by a standardized cardiopulmonary exercise test (n=70). Patients with tetralogy of Fallot had lower LV ejection fraction (P=0.001; 49% below age-adjusted fifth percentile for controls), lower LV mass index (P=0.003), lower LV mass/volume ratio (P<0.01), and impaired left atrial function. Right ventricular mass/volume ratio was the best predictor for LV systolic dysfunction and for a lower LV mass/volume ratio. Compared with controls, LV extracellular volume was higher (P<0.001), particularly in female patients, and associated with subnormal peak oxygen consumption (P=0.037). A peak oxygen consumption below the third percentile reference level was more likely with decreasing LV ejection fraction (P=0.008), and lower LV mass index (P=0.024), but independent of right ventricular ejection fraction. Conclusions-In New York Heart Association class 1 patients with tetralogy of Fallot, frequent impaired systolic and diastolic LV function, LV adverse remodeling with LV atrophy, a decreased mass/volume ratio, and extracellular matrix expansion suggest cardiomyopathic changes. The best predictor for LV systolic dysfunction was the right ventricular mass/volume ratio. The subnormal peak oxygen consumption indicates that monitoring of LV status may be important for long-term prognosis.eng
dc.description.sponsorshipCoordination of Improvement of Higher Education Personnel of Brazil [6619-10-0]
dc.description.sponsorshipfoundation ""Kinderherzen-wollenleben e.V.""
dc.language.isoeng
dc.publisherWILEYeng
dc.relation.ispartofJournal of the American Heart Association
dc.rightsopenAccesseng
dc.subjectcardiac magnetic resonance imagingeng
dc.subjectcardiopulmonary exercise testeng
dc.subjectheart failureeng
dc.subjectleft ventricular remodelingeng
dc.subjecttetralogy of Falloteng
dc.subject.othercardiac magnetic-resonanceeng
dc.subject.otherrepaired tetralogyeng
dc.subject.otherdiastolic functioneng
dc.subject.otherpressure-overloadeng
dc.subject.otheradultseng
dc.subject.otherchildreneng
dc.subject.otherassociationeng
dc.subject.otherarrhythmiaeng
dc.subject.othermechanicseng
dc.subject.otheroutcomeseng
dc.titleDeterminants of Left Ventricular Dysfunction and Remodeling in Patients With Corrected Tetralogy of Falloteng
dc.typearticleeng
dc.rights.holderCopyright WILEYeng
dc.identifier.doi10.1161/JAHA.118.009618
dc.identifier.pmid31474177
dc.subject.wosCardiac & Cardiovascular Systemseng
dc.type.categoryoriginal articleeng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalJEROSCH-HEROLD, Michael:Brigham & Womens Hosp, Dept Radiol, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.author.externalWEGNER, Philip:Univ Hosp Schleswig Holstein, Dept Congenital Heart Dis & Pediat Cardiol, Kiel, Germany
hcfmusp.author.externalGABBERT, Dominik Daniel:Univ Hosp Schleswig Holstein, Dept Congenital Heart Dis & Pediat Cardiol, Kiel, Germany
hcfmusp.author.externalVOGES, Inga:Univ Hosp Schleswig Holstein, Dept Congenital Heart Dis & Pediat Cardiol, Kiel, Germany
hcfmusp.author.externalMinh Pham:Univ Hosp Schleswig Holstein, Dept Congenital Heart Dis & Pediat Cardiol, Kiel, Germany
hcfmusp.author.externalSHAH, Ravi:Brigham & Womens Hosp, Dept Radiol, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.author.externalHEDDERICH, Juergen:Univ Hosp Schleswig Holstein, Dept Med Informat & Stat, Kiel, Germany
hcfmusp.author.externalKRAMER, Hans-Heiner:Univ Hosp Schleswig Holstein, Dept Congenital Heart Dis & Pediat Cardiol, Kiel, Germany
hcfmusp.author.externalRICKERS, Carsten:Univ Hosp Hamburg Eppendorf, Adult Congenital Heart Dis Unit, Univ Heart Ctr, Martinistr 52, D-20246 Hamburg, Germany
hcfmusp.description.articlenumbere009618
hcfmusp.description.issue17
hcfmusp.description.volume8
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000484586800001
hcfmusp.origem.id2-s2.0-85071765549
hcfmusp.publisher.cityHOBOKENeng
hcfmusp.publisher.countryUSAeng
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dc.description.indexMEDLINEeng
hcfmusp.citation.scopus16-
hcfmusp.scopus.lastupdate2024-03-29-
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