Aortopulmonary window coexisting with tetralogy of Fallot: echocardiographic diagnosis.

abstract：:The original version of this article unfortunately contained a mistake. The presentation of Table 2 was incorrect .The corrected table is given below. ...

journal_title：Pediatric cardiology

authors： Collins JLG,Law MA,Borasino S,Erwin WC,Cleveland DC,Alten JA

更新日期：2018-03-01 00:00:00

abstract：:Magnesium sulfate was given to pediatric cardiac surgical patients during cardiopulmonary bypass period in an attempt to reduce the occurrence of postoperative junctional ectopic tachycardia (PO JET). We reviewed our data to evaluate the effect of magnesium on the occurrence of JET and assess a possible relationship b...

journal_title：Pediatric cardiology

authors： He D,Sznycer-Taub N,Cheng Y,McCarter R,Jonas RA,Hanumanthaiah S,Moak JP

更新日期：2015-08-01 00:00:00

abstract：:The HOXA1 gene plays a fundamental role in embryonic morphogenesis. Recent studies in humans and mice have indicated that HOXA1 plays a previously unrecognized role in cardiovascular system development. Congenital heart disease (CHD), particularly ventricular septal defect (VSD), might be a clinically isolated manifes...

journal_title：Pediatric cardiology

authors： Liu J,Wang B,Chen X,Li H,Wang J,Cheng L,Ma X,Gao B

更新日期：2013-02-01 00:00:00

abstract：:Unilateral absence of a pulmonary artery is a rare anomaly. Patients may present with hemoptysis, recurrent respiratory infections, pulmonary hypertension, or congestive heart failure. This report describes the case of a missing right pulmonary artery associated with anomalous left pulmonary venous connection not prev...

journal_title：Pediatric cardiology

authors： Binnetoğlu K,Ayabakan C,Sarisoy O,Tokel K

更新日期：2012-01-01 00:00:00

abstract：:Venous correction for complete transposition with intact ventricular septum remains the preferred surgical option in most centers (Mustard or Senning procedures). The long-term function of the morphologically right ventricle and tricuspid valve, which continue to sustain the systemic circulation thereafter, remains a ...

journal_title：Pediatric cardiology

authors： Smith A,Wilkinson JL,Anderson RH,Arnold R,Dickinson DF

更新日期：1986-01-01 00:00:00

abstract：:Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare condition. The majority of cases present with impaired left ventricular function. We report on a premature infant who was diagnosed at a gestational age near term with ALCAPA during routine cardiac examination. The patient showed...

journal_title：Pediatric cardiology

authors： Grosse-Wortmann L,Wenzl T,Hoevels-Guerich HH

更新日期：2006-03-01 00:00:00

abstract：:A vascular approach for balloon aortic dilatation in infants is of major concern due to the high risk of femoral artery injury. To overcome this problem, a surgical right carotid artery (RCA) approach has been advocated. No reports are available on RCA after neonatal cutdown. Since 1990, RCA cutdown has been performed...

journal_title：Pediatric cardiology

authors： Borghi A,Agnoletti G,Poggiani C

更新日期：2001-05-01 00:00:00

abstract：:When the common pulmonary vein fails to develop, the embryonic connections of the pulmonary veins to one or more of the systemic veins almost always persist. Anomalous pulmonary venous connections to the inferior vena cava (IVC) are typically characterized by hypoplasia of the involved pulmonary veins and pulmonary ar...

journal_title：Pediatric cardiology

authors： Juraszek AL,Cohn H,Van Praagh R,Van Praagh S

更新日期：2005-11-01 00:00:00

abstract：:In 810 schoolchildren (aged 5-14 years) the prevalence of a grade 1-3/6 vibratory innocent heart murmur (VIHM) is 41%. Restricted to a grade 2 or 3 VIHM, the prevalence is 14%, decreasing from 21% in the age-class 5-6 years to 8% for children 13-14 years of age. The prevalence of a grade 3 VIHM is 1%. Together with a ...

journal_title：Pediatric cardiology

authors： Van Oort A,Hopman J,De Boo T,Van Der Werf T,Rohmer J,Daniëls O

更新日期：1994-11-01 00:00:00

abstract：:Exercise testing can highlight repolarisation abnormalities in adults with coronary artery disease. Late after Kawasaki disease (KD), increased QT dispersion (QTd) has been reported on resting ECG in children, but there are no reported studies of QTd during exercise. Our objective was to determine the pattern of QTd r...

journal_title：Pediatric cardiology

authors： Gravel H,Dahdah N,Fournier A,Mathieu MÈ,Curnier D

更新日期：2012-06-01 00:00:00

abstract：:For adults with sickle cell disease (SCD), cardiac changes are well described and may account for up to one-fourth of disease-related mortality. Much less is known about heart disease in pediatric SCD patients. This retrospective study analyzed a contemporary cohort of children with SCD followed at a single tertiary c...

journal_title：Pediatric cardiology

authors： Doshi AR,Pauliks LB

更新日期：2013-04-01 00:00:00

abstract：:Acute myopericarditis is a major cause of acquired heart disease worldwide in pediatric patients. Various viruses have been reported as the etiology, of which varicella zoster virus was first reported in 1953. However, since nationwide administration of the varicella vaccine, reports of varicella-associated myopericar...

journal_title：Pediatric cardiology

authors： Kao KL,Yeh SJ,Chen CC

更新日期：2010-07-01 00:00:00

abstract：:A 16-year-old boy with anomalous origin of the left coronary artery from the pulmonary artery, Bland-White-Garland syndrome, underwent a mammary artery bypass grafting to the left coronary artery (LCA) together with closure of the stenosed origin of the left coronary artery. A residual LCA to pulmonary artery fistula ...

journal_title：Pediatric cardiology

authors： Beitzke A,Luha O,Gamillscheg A

更新日期：2000-03-01 00:00:00

abstract：:The outcome of children born with cyanotic congenital heart disease has markedly improved over the years. Follow up is recommended for most post-operated cases as complications may occur over long term. One of the complications is the development of ventricular dysfunction, often seen after a successful Fontan surgery...

journal_title：Pediatric cardiology

authors： Priyadarshini A,Saxena A,Patel C,Paul VK,Lodha R,Airan B

更新日期：2013-04-01 00:00:00

abstract：:This report describes a case involving the rare combination of persistent truncus arteriosus type A2, double aortic arch, and mitral stenosis. At the age of 26 days, the patient underwent division of the right-sided aortic arch with tracheal compression and bilateral pulmonary banding. Fontan completion was successful...

journal_title：Pediatric cardiology

authors： Imai K,Tsukuda K,Sakazaki H,Fujiwara K

更新日期：2013-01-01 00:00:00

abstract：:Patients with anomalies of the heart frequently suffer from arrhythmias that either are associated with a congenital heart defect or result from the course of the disease. For most of the bradyarrhythmias, appropriate timing of the initiation of treatment is more challenging than its eventual execution. In the case of...

journal_title：Pediatric cardiology

authors： Hebe J,Hansen P,Ouyang F,Volkmer M,Kuck KH

更新日期：2000-11-01 00:00:00

abstract：:Antenatal diagnosis of right heart enlargement has a wide spectrum of differential diagnosis from maternal, placental and fetal causes, and outcomes of all are not known. Coarctation of the aorta is in the differential diagnosis of right heart enlargement. In our study, we focused to measure multiple cardiac dimension...

journal_title：Pediatric cardiology

authors： Sivanandam S,Nyholm J,Wey A,Bass JL

更新日期：2015-10-01 00:00:00

abstract：:In this report, we describe a case of coarctation of the aorta, congenital aortic stenosis with bicuspid valve, and supravalvar aortic stenosis with left coronary artery ostial stenosis. The child underwent staged treatment using a hybrid approach employing both surgical and interventional cardiology methods. A single...

journal_title：Pediatric cardiology

authors： Goel P,Madhu Sankar N,Rajan S,Cherian KM

更新日期：2001-01-01 00:00:00

abstract：:Embryonic development is a tightly regulated process, and many families of genes functions to provide a regulatory genetic network to achieve such a program. The homeobox genes are an extensive family that encodes transcription factors with a characteristic 60-amino acid homeodomain. Mutations in these genes or in the...

journal_title：Pediatric cardiology

authors： Liu H,Espinoza-Lewis RA,Chen C,Hu X,Zhang Y,Chen Y

更新日期：2012-08-01 00:00:00

abstract：:Sudden cardiac death in young competitive athletes is tragic and usually due to unsuspected cardiovascular disease. Screening programs for athletes remain debatable, and restriction of athletes from sports can have physical, emotional, and legal ramifications. In this article, we review the epidemiology of the more co...

journal_title：Pediatric cardiology

authors： Vaseghi M,Ackerman MJ,Mandapati R

更新日期：2012-03-01 00:00:00

abstract：:Ruptured sinus Valsalva aneurysm (SVA) in a patient with tetralogy of Fallot is a very rare cardiac complication. This report describes the case of a 10-year-old Hispanic girl who presented to her cardiologist for a routine transthoracic echocardiography (TTE), which showed a ruptured sinus of Valsalva, with left-to-r...

journal_title：Pediatric cardiology

authors： Mithani AA,Polimenakos AC,Santucci BA

更新日期：2013-01-01 00:00:00

abstract：:It is unclear if neonatal tetralogy of Fallot repair offers better outcomes compared to repair later in infancy. We therefore conducted a meta-analysis comparing outcomes of neonatal and non-neonatal repair. Manuscripts were identified and reviewed for quality and bias with favorably scored manuscripts being included ...

journal_title：Pediatric cardiology

authors： Loomba RS,Buelow MW,Woods RK

更新日期：2017-06-01 00:00:00

abstract：:Dilated cardiomyopathy in children still has a poor prognosis with high rates of mortality and cardiac transplantation (resp. around 20 and 25%). Awaiting transplantation or possible recovery, these pediatric patients are mechanically supported with extracorporeal membrane oxygenation or a paracorporeal ventricular as...

journal_title：Pediatric cardiology

authors： Mets G,Panzer J,De Wolf D,Bové T

更新日期：2017-06-01 00:00:00

abstract：:Transcatheter closure of atrial septal defects (ASDs) has become a routine procedure in many countries of the world. It spares many patients cardiac surgery and has proven efficacy in long-term studies. Device improvements have resulted in a continuous reduction of complications and of residual shunt frequency. ASD cl...

journal_title：Pediatric cardiology

authors： Hein R,Bayard Y,Taaffe M,Büscheck F,Ostermayer S,Billinger K,Reschke M,Trepels T,Lissmann-Jensen H,Lang K,Römer A,Wilson N,Sievert H

更新日期：2005-05-01 00:00:00

abstract：:Crossed pulmonary arteries (CPAs) are a rare abnormality in which the ostium of the left pulmonary artery originates superior to the right pulmonary artery and to its right. Recognition of this rare pathology is important because it generally is accompanied by other congenital heart defects, extracardiac anomalies, an...

journal_title：Pediatric cardiology

authors： Babaoğlu K,Altun G,Binnetoğlu K,Dönmez M,Kayabey Ö,Anık Y

更新日期：2013-01-01 00:00:00

abstract：:Numerous RNA-binding proteins (RBPs) are expressed in the heart, and mutations in several RBPs have been implicated in cardiovascular disease through genetic associations, animal modeling, and mechanistic studies. However, the functions of many more cardiac RBPs, and their relevance to disease states, remain to be elu...

journal_title：Pediatric cardiology

authors： Akerberg AA,Burns CE,Burns CG

更新日期：2019-10-01 00:00:00

abstract：:Controversy exists as to whether a hemodynamically significant left-to-right shunt due to a patent ductus arteriosus (PDA) affects ventricular contractility. Load-dependent indices such as ejection fraction and shortening fraction have traditionally been used to assess contractility, but the relationship between the r...

journal_title：Pediatric cardiology

authors： Barlow AJ,Ward C,Webber SA,Sinclair BG,Potts JE,Sandor GG

更新日期：2004-03-01 00:00:00

abstract：:While exercise stress testing (EST) is an important tool, little is known about its use for determining ischemia in patients with hypoplastic left heart syndrome (HLHS) and Fontan palliation. We sought to determine the frequency of ST segment changes during EST in HLHS patients after Fontan and examine results of furt...

journal_title：Pediatric cardiology

authors： Kyle WB,Denfield SW,Valdes SO,Penny DJ,Bolin EH,Lopez KN

更新日期：2016-03-01 00:00:00

abstract：:A patient with pulmonary valve stenosis associated with pseudohypertrophic muscular dystrophy is reported. The anomalies were detected by two-dimensional echocardiography and elevated serum enzymes, conformed by right ventriculography and muscles biopsy. The association between these two pathologies is unknown. ...

journal_title：Pediatric cardiology

authors： Xie CH,Xia CS

更新日期：2002-03-01 00:00:00

abstract：:Novel COstatus system (Transonic Systems, Inc., NY), based on ultrasound dilution (UD), works off in situ arterial and central venous catheters in pediatric patients to measure cardiac output (CO). The purpose of the present study was to validate CO measurement by UD (COUD) with pulmonary artery (PA) thermodilution (C...

journal_title：Pediatric cardiology

authors： Darling E,Thuramalla N,Searles B

更新日期：2011-06-01 00:00:00