Results 31 to 40 of about 107,561 (313)

Severe Fontan‐Associated Liver Disease and Its Association With Mortality

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2023
Background Data are rare about the incidence of severe Fontan‐associated liver disease (FALD) and its association with mortality. We sought to: (1) estimate the probability of developing severe FALD in patients who undergo the Fontan procedure (Fontan ...
Carlos‐Eduardo Guerrero‐Chalela, Judith Therrien, Yoni Grossman, Liming Guo, Aihua Liu, Ariane Marelli   +5 more
doaj   +1 more source

Utility of deep learning networks for the generation of artificial cardiac magnetic resonance images in congenital heart disease

BMC Medical Imaging, 2020
Background Deep learning algorithms are increasingly used for automatic medical imaging analysis and cardiac chamber segmentation. Especially in congenital heart disease, obtaining a sufficient number of training images and data anonymity issues remain ...
Gerhard-Paul Diller, Julius Vahle, Robert Radke, Maria Luisa Benesch Vidal, Alicia Jeanette Fischer, Ulrike M. M. Bauer, Samir Sarikouch, Felix Berger, Philipp Beerbaum, Helmut Baumgartner, Stefan Orwat, for the German Competence Network for Congenital Heart Defects Investigators   +11 more
doaj   +1 more source

Treatment of arrhythmia disorders in the adult with congenital heart disease: A lesion-specific review

, 2022
There are now more adults living with a history of congenital heart disease than there are children. Modern electrophysiologists must familiarize themselves with the most common congenital lesions requiring electrophysiologic care as adults. Advancements
Lloyd, Michael S; Emory University Adult Congenital Heart Center, Atlanta, GA, United States, Knijnik, Leonardo; Emory University Adult Congenital Heart Center, Atlanta, GA, United States   +1 more
core   +1 more source

Thromboembolic characteristics and role of anticoagulation in long-standing Fontan circulation

International Journal of Cardiology Congenital Heart Disease, 2022
Introduction: The risk of thromboembolism increases with duration of Fontan circulation. Preventive drug strategies are still discussed controversially. We aimed to characterize clinical relevant thromboembolism in long-standing Fontan circulation and to
Mechthild Westhoff-Bleck, Carolin Klages, Carolin Zwadlo, Kristina Sonnenschein, Jan-Thorben Sieweke, Johann Bauersachs, Harald Bertram, Urte Grosser   +7 more
doaj   +1 more source

The end-of-life experience for adults with congenital heart disease: Resource utilization, functional decline, and circumstances surrounding death

International Journal of Cardiology Congenital Heart Disease, 2020
Background: Advance care planning is essential for patient-centered care at the end of life, yet little is known about the end-of-life experience for adults with congenital heart disease.
Adam J. Small, Anisha S. Fernando, Weiyi Tan, Daniel Karlin, Jamil A. Aboulhosn   +4 more
doaj   +1 more source

Infective Endocarditis in Adults With Congenital Heart Disease

JACC: Case Reports, 2023
A challenging case of infective endocarditis in a young woman with repaired tetralogy of Fallot and a diagnosis of ankylosing spondylitis is described.
Anna Selvaggia Roma, MD, Flavia Fusco, MD, Davide D’Arienzo, MD, Maria Luisa De Rimini, MD, Giancarlo Scognamiglio, MD, PhD, Berardo Sarubbi, MD, PhD   +5 more
doaj   +1 more source

Lipoprotein(a) concentrations in adult congenital heart disease patients

, 2014
Introduction. Lipoprotein(a) (Lp(a)) contributes to the formation to atherosclerosis, promotes inflammation and stimulates prothrombotic processes. Methods.
Rodríguez-González, Fayna, Martínez Quintana, Efrén   +1 more
core   +1 more source

Adult congenital heart disease and pregnancy [PDF]

BJA Education, 2018
Cardiac disease has remained the leading cause of maternal mortality since the 2000-2002 triennium. Between 2009–2014 the deaths of 189 women who died from heart disease associated with, or aggravated by, pregnancy were reported by MBRRACE-UK (Mothers and Babies: Reducing Risk through Audits and Confidential Enquiries across the UK).
L, Bishop, A, Lansbury, K, English
openaire   +2 more sources

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

Serum and 24-hour urine analysis in adult cyanotic and noncyanotic congenital heart disease patients

, 2009
Introduction. Glomerulopathy is a complication of congenital heart disease patients. The risk of developing renal impairment is particularly high in cyanotic patients. Objective. The aim of this study was to determine the prevalence of renal dysfunction
Fábregas-Brouard, Marian, Rodríguez-González, Fayna, Martínez-Quintana, Efrén, Nieto-Lago, Vicente   +3 more
core   +1 more source