Thrombus formation in the native aortic root in patients with hypoplastic left heart syndrome.

abstract：:The reported prenatal detection rates (PDRs) for significant congenital heart disease (sCHD) have been suboptimal, even in the current era. Changes in prenatal ultrasound policy and training may lead to improved prenatal detection of sCHD. This study analyzed the results of a policy to assess fetal cardiac outflow tra...

journal_title：Pediatric cardiology

authors： Levy DJ,Pretorius DH,Rothman A,Gonzales M,Rao C,Nunes ME,Bendelstein J,Mehalek K,Thomas A,Nehlsen C,Ehr J,Burchette RJ,Sklansky MS

更新日期：2013-03-01 00:00:00

abstract：:Cardiac surgery for congenital heart disease often necessitates a period of myocardial ischemia during cardiopulmonary bypass and cardioplegic arrest, followed by reperfusion after aortic cross-clamp removal. In experimental models, myocardial ischemia-reperfusion is associated with significant oxidative stress and ve...

journal_title：Pediatric cardiology

authors： Sznycer-Taub N,Mackie S,Peng YW,Donohue J,Yu S,Aiyagari R,Charpie J

更新日期：2016-04-01 00:00:00

abstract：:Restrictive cardiomyopathy (RCM) is characterized by irreversible diastolic dysfunction with preserved systolic function. The aim of this study was to investigate the presence of impaired ventricular contractility even in the presence of normal ejection fraction (EF) in children with RCM. Longitudinal Doppler tissue v...

journal_title：Pediatric cardiology

authors： Sasaki N,Garcia M,Lytrivi I,Ko H,Nielsen J,Parness I,Srivastava S

更新日期：2011-06-01 00:00:00

abstract：:Coronary artery anatomy represents a challenging and, often, determining predictor of outcome in an arterial switch operation (ASO). Impact of specific coronary artery variants, such as single, intramural and inverted, on time-related events following ASO, is, yet, to be determined. We sought to compare early and late...

journal_title：Pediatric cardiology

authors： Al Anani S,Fughhi I,Taqatqa A,Elzein C,Ilbawi MN,Polimenakos AC

更新日期：2017-03-01 00:00:00

abstract：:Electrocardiograms (heart rate, QRS voltage, QRS axis in the frontal plane. Q-Tc interval) echocardiograms [left ventricular fractional shortening (LVFS); preejection period (PEP); PEP/left ventricular ejection time (PEP/LVET) ratio; end-diastolic left ventricular free wall and interventricular septum thickness; prese...

journal_title：Pediatric cardiology

authors： Balducci G,Acquafredda A,Amendola F,Natuzzi M,Laforgia N,Cavallo L

更新日期：1991-01-01 00:00:00

abstract：:The data on the outcomes of children with heart disease and Down syndrome receiving extracorporeal membrane oxygenation (ECMO) for cardiac or respiratory failure are limited. This study aimed to evaluate morbidity and mortality associated with ECMO in children with Down syndrome and heart disease. Children younger tha...

journal_title：Pediatric cardiology

authors： Gupta P,Gossett JM,Rycus PT,Prodhan P

更新日期：2014-12-01 00:00:00

abstract：:Transcatheter pulmonary valve implantation in the setting of right ventricle-to-pulmonary artery conduit dysfunction is a relatively new procedure with encouraging early and midterm results. Malpositioning of the valve during implantation is a potentially serious complication. This report describes a case in which val...

journal_title：Pediatric cardiology

authors： Berman DP,Burke R,Zahn EM

更新日期：2012-06-01 00:00:00

abstract：:We report our experience with asymptomatic valvar aortic stenosis diagnosed during infancy. During the period between November 1, 1986 and October 31, 1992 a total of 13 infants were diagnosed with asymptomatic aortic stenosis, 5 of whom showed rapid progression over the first 2 years of life. Two of these asymptomati...

journal_title：Pediatric cardiology

authors： Anand R,Mehta AV

更新日期：1997-01-01 00:00:00

abstract：:Sinus node disease is a problem encountered in patients after the Mustard surgery, requiring a pacemaker implantation. The knowledge of the complexity anatomy is crucial because of the possible challenges associated with this procedure. We report a case of a 24-year-old woman presented with symptomatic bradycardia, in...

journal_title：Pediatric cardiology

authors： Cabrera-Ortega M,Díaz-Ramírez F,Benítez-Ramos DB

更新日期：2015-08-01 00:00:00

abstract：:Aortic atresia and interrupted aortic arch is a rare cardiac combination. Review of the literature revealed nine cases. We present two patients with this combination and the additional finding of quadricuspid pulmonary valves, one of which was severely stenotic. In the latter patient, an aortopulmonary window was pres...

journal_title：Pediatric cardiology

authors： Yew G,Coleman D,Calder L

更新日期：2005-07-01 00:00:00

abstract：:Common arterial trunk is relatively a straightforward diagnosis on echocardiography. We describe a neonate who was referred to our centre as a case of common arterial trunk but on evaluation was found to have pulmonary atresia with ventricular septal defect and aortopulmonary window, for which he underwent repair with...

journal_title：Pediatric cardiology

authors： Shah S,Kavya,Saraf R,Rao S

更新日期：2012-10-01 00:00:00

abstract：:Kawasaki disease (KD) is an acute febrile disease of unknown etiology that develops in children and is sometimes accompanied by myocardial dysfunction and systemic vasculitis. However, myocardial repolarization lability has not yet been fully investigated. Thus, the objective of this study was to evaluate myocardial r...

journal_title：Pediatric cardiology

authors： Kuriki M,Fujino M,Tanaka K,Horio K,Kusuki H,Hosoi M,Eryu Y,Kato T,Yamazaki T,Hata T

更新日期：2011-04-01 00:00:00

abstract：:The occurrence of familial heart disease in association with tricuspid atresia is rare. The first reported instance of tricuspid atresia and Ebstein's anomaly in siblings is presented. The presence of these two distinct pathologic variants of tricuspid valve malformations in siblings suggests that these malformations ...

journal_title：Pediatric cardiology

authors： Grant JW

更新日期：1996-09-01 00:00:00

abstract：:The neonatal Marfan syndrome is an autosomal dominantly inherited disease with an extremely poor prognosis. This report gives a clinical and echocardiographic description of an infant with a mutation in exon 29 of the fibrillin-1 gene (FBN1), a region in which this severe form of Marfan syndrome seems to cluster. The ...

journal_title：Pediatric cardiology

authors： Weidenbach M,Brenner R,Rantamäki T,Redel DA

更新日期：1999-09-01 00:00:00

abstract：OBJECTIVES:The aim of this article is to examine the frequency, timing of formation of aneurysm of the ventricular membranous septum (AVMS), and prognosis in patients with a perimembranous ventricular septal defect (VSD). PATIENTS:One hundred forty-eight patients were diagnosed with a perimembranous VSD within 90 days...

journal_title：Pediatric cardiology

authors： Miyake T,Shinohara T,Nakamura Y,Fukuda T,Tasato H,Toyohara K,Tanihira Y

更新日期：2004-07-01 00:00:00

abstract：:Magnetic resonance imaging (MRI) is a powerful tool which enables the visualization of anatomy and the assessment of many physiological aspects of organ function. MRI and magnetic resonance angiography and magnetic resonance spectroscopy will play critical roles in cardiac applications during the next millennium. Thus...

journal_title：Pediatric cardiology

authors： Mulkern RV,Chung T

更新日期：2000-01-01 00:00:00

abstract：:Enlarged bronchial arteries and/or systemic-to-pulmonary collaterals have been frequently demonstrated in association with transposition of the great arteries. They are usually clinically silent, although they might be large enough to cause accelerated pulmonary vascular obstructive disease or symptomatic cardiac volu...

journal_title：Pediatric cardiology

authors： Santoro G,Carrozza M,Russo MG,Calabrò R

更新日期：2008-07-01 00:00:00

abstract：:Noonan syndrome is an autosomal dominant disease that manifests a wide variety of clinical characteristics. The syndrome is also associated with some cardiac defects. Half of all Noonan syndrome cases are caused by mutations in the PTPN11 gene, but only limited data are available regarding aortic involvement in these ...

journal_title：Pediatric cardiology

authors： Jefferies JL,Belmont JW,Pignatelli R,Towbin JA,Craigen WJ

更新日期：2010-01-01 00:00:00

abstract：:Non-invasive evaluation of right ventricular (RV) systolic function in neonates with pulmonary hypertension (PH) with traditional metrics including RV fractional area change (FAC) and tricuspid annular systolic plane excursion (TAPSE) has improved outcomes. Apical three-chamber (3C) RV-FAC, a novel tripartite assessme...

journal_title：Pediatric cardiology

authors： Chikkabyrappa SM,Critser P,Roane J,Buddhe S,Tretter JT

更新日期：2020-08-01 00:00:00

abstract：:Dilated cardiomyopathy (DCM) is an important cause of chronic congestive cardiac failure in children. In patients with idiopathic DCM, endothelium vasomotor function is disturbed. There are many studies on the roles of nitric oxide (NO) and adrenomedullin (AM) in adult patients with DCM. However, to our knowledge, no ...

journal_title：Pediatric cardiology

authors： Kilinç M,Balat A,Cekmen M,Yürekli M,Yilmaz K,Sahinöz S

更新日期：2003-07-01 00:00:00

abstract：:Right ventricular (RV) function as assessed by deformation has been evaluated prenatally and after palliation in hypoplastic left heart syndrome (HLHS). However, limited data exist about the immediate postnatal cardiac adaptation and RV function in HLHS. We compared echocardiographic measures of cardiac performance in...

journal_title：Pediatric cardiology

authors： Altit G,Bhombal S,Chock VY,Tacy TA

更新日期：2019-01-01 00:00:00

abstract：:A case report of a neonate with cardiac tumors in association with tuberous sclerosis is presented. The rare complication of pulmonary embolism and its successful treatment by anticoagulation and thrombolytic therapy is described. The treatment of these cardiac tumors is conservative, because the tumors regress sponta...

journal_title：Pediatric cardiology

authors： Kuwabara N,Kuwahara T,Takahashi K,Goto H

更新日期：2001-07-01 00:00:00

abstract：:In 19 consecutive children with aortic valve stenosis, the left ventricle was entered retrogradely with a Gensini catheter guided by a tip-deflector guidewire which could produce any desirable degree of curvature at its tip. In all patients, the aortic valve was retrogradely traversed for measurement of the pressure g...

journal_title：Pediatric cardiology

authors： Lau KC,Leung MP,Lo RN

更新日期：1986-01-01 00:00:00

abstract：:The Norwood procedure with a modified Blalock-Taussig shunt (MBTS) is the first of the three-stage surgical palliation for infants with hypoplastic left heart syndrome. We report a patient with schistocytic hemolytic anemia that developed following a right MBTS with a Gore-Tex graft. Hemolysis associated with a MBTS h...

journal_title：Pediatric cardiology

authors： Ryerson LM,Wechsler SB,Ohye RG

更新日期：2007-05-01 00:00:00

abstract：:The etiology and pathogenesis of Kawasaki disease (KD) is largely unknown. Certain demographic factors and laboratory findings are predictive of the development of coronary artery (CA) aneurysms. The objectives of this study were to determine the epidemiology of KD patients in an urban hospital and determine risk fact...

journal_title：Pediatric cardiology

authors： Porcalla AR,Sable CA,Patel KM,Martin GR,Singh N

更新日期：2005-11-01 00:00:00

abstract：:The nuclear cross-sectional area of the muscular fibers from a series of myocardial bridges was analyzed and compared to both the adjacent and underlying myocardial fibers. The series came from 12 hearts of children, ranging in age from 24 h to 2 years, with diverse forms of congenital heart disease, which caused left...

journal_title：Pediatric cardiology

authors： Reig J,Ruiz de Miguel C,Moragas A

更新日期：1990-10-01 00:00:00

abstract：:With the advent of cardiac magnetic resonance imaging and high-resolution echocardiography, cardiac catheterization is unnecessary in clinical protocols in the "routine" single ventricle patient. Catheterization adds little to clinical care in these cases, and there are significant risks and costs associated with it. ...

journal_title：Pediatric cardiology

authors： Fogel MA

更新日期：2005-03-01 00:00:00

abstract：:Changes in ventricular geometry are often seen in patients with right ventricular hypertension secondary to pulmonary hypertension (PH). Progressive systolic bowing of the inter-ventricular septum occurs with increasing right ventricular pressure (RVp) and can be quantified with the left ventricular end-systolic eccen...

journal_title：Pediatric cardiology

authors： Averin K,Michelfelder E,Sticka J,Cash M,Hirsch R

更新日期：2016-03-01 00:00:00

abstract：:Radiation exposure from pediatric cardiac catheterization may be substantial, although published estimates vary. We sought to report patient radiation dose across a range of diagnostic and interventional cases in a modern, high-volume pediatric catheterization laboratory. We retrospectively reviewed diagnostic and int...

journal_title：Pediatric cardiology

authors： Glatz AC,Patel A,Zhu X,Dori Y,Hanna BD,Gillespie MJ,Rome JJ

更新日期：2014-06-01 00:00:00

abstract：:An aneurysm of the fossa ovalis was identified at autopsy in 17 infants. In each case the aneurysm of the fossa ovalis was considered to have resulted from excessive elevation of pressure in that atrium contralateral to the side into which the aneurysm bulged. The aneurysms were divided into two types: intrinsic (thre...

journal_title：Pediatric cardiology

authors： Topaz O,Feigl A,Edwards JE

更新日期：1985-01-01 00:00:00