Coarctation of the aorta, aortic valvar stenosis, and supravalvar aortic stenosis with left coronary artery ostial stenosis: management using a staged hybrid approach.

abstract：:For premature infants with congenital heart disease (CHD), it may be unclear when the burdens of treatment outweigh potential benefits. Parents may thus have to choose between comfort care at birth and medical stabilization until surgical repair is feasible. Better defined outcome data, including risk factors for mort...

journal_title：Pediatric cardiology

authors： Lynema S,Fifer CG,Laventhal NT

更新日期：2016-06-01 00:00:00

abstract：:The objective of this study is to identify predictors of prolonged hospital length of stay (LOS) for single ventricle patients following stage 2 palliation (S2P), excluding patients who underwent a hybrid procedure. We explore the impact of demographic features, stage 1 palliation (S1P), interstage I (IS1) management,...

journal_title：Pediatric cardiology

authors： Baker-Smith CM,Goldberg SW,Rosenthal GL

更新日期：2015-12-01 00:00:00

abstract：:DiGeorge syndrome (DGS) is commonly associated with both congenital heart disease (CHD) and immunologic abnormalities. While CHD may prompt consideration for heart transplantation (HTx), little is known about HTx management or outcomes in this group. The aim of this study was to describe the spectrum of patients with ...

journal_title：Pediatric cardiology

authors： Woolman P,Bearl DW,Soslow JH,Dodd DA,Thurm C,Hall M,Feingold B,Godown J

更新日期：2019-04-01 00:00:00

abstract：:Color-coded two-dimensional (2D) echocardiography confirmed the presence of severe congenital mitral regurgitation in an 8-month-old infant. Intraoperative inspection revealed an isolated perforation in the anterior leaflet. ...

journal_title：Pediatric cardiology

authors： Schranz D,Oelert H,Iversen S,Schuind A,Huth R,Jüngst BK,Stopfkuchen H,Erbel R

更新日期：1990-04-01 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 39-week-old phenotypically female infant was born with hypoplastic left heart syndrome and expired on the third day of life. An autopsy revealed the patient to also have male pseudohermaphroditism and uterus bicornis bicollis. The association of hypoplastic left heart syndrome and male pseudohermaphroditism has been...

journal_title：Pediatric cardiology

authors： Calaluce RD,Huang TH,Quesenberry JT,Evans ML,Luger AM,O'Connor TA

更新日期：1995-09-01 00:00:00

abstract：:The importance of myocardial bridging of a coronary artery in the setting of hypertrophic cardiomyopathy is controversial, although we have previously reported an association with myocardial ischemia and sudden death in children. We report five symptomatic children in whom symptoms or evidence of myocardial ischemia r...

journal_title：Pediatric cardiology

authors： Downar J,Williams WG,McDonald C,Wigle ED,McCrindle BW

更新日期：2004-07-01 00:00:00

abstract：:The inauguration of Sequential Segmental Analysis (SSA) a few decades ago provides basic conditions to establish a universally applicable classification system for cardiac malformations. To gain practical experience, we used this method to classify a collection of 292 congenitally malformed human hearts. Our aims were...

journal_title：Pediatric cardiology

authors： Craatz S,Künzel E,Spanel-Borowski K

更新日期：2002-09-01 00:00:00

abstract：:In case of progressive cyanosis after modified Fontan procedure, intrahepatic shunting should be considered. Ligation of the hepatic vein is safe and effective in managing this condition, and it is important to ensure that the pressure difference between superior vena cava and the portal vein system remains minimal af...

journal_title：Pediatric cardiology

authors： Hishitani T,Ogawa K,Hoshino K,Nakamura Y

更新日期：1999-11-01 00:00:00

abstract：:14-year-old white male with a past medical history of congenital bicuspid aortic valve, Streptococcus viridans endocarditis, and pulmonary valve homograft presented with culture-negative endocarditis. Molecular studies identified the causative organism as Bartonella henselae and subsequent serologic studies supported ...

journal_title：Pediatric cardiology

authors： Pitchford CW,Creech CB 2nd,Peters TR,Vnencak-Jones CL

更新日期：2006-11-01 00:00:00

abstract：:The aim of this study was to evaluate by Doppler echocardiography whether administration of transdermal nitroglycerin (NTG) to children with congestive heart failure could modify mitral flow velocity profile with redistribution of left ventricular filling to late diastole, suggesting preload reduction of the left vent...

journal_title：Pediatric cardiology

authors： Vaksmann G,Pariente-Khayat A,Godart F,Francart C,Rey E,D'Athis P,Pons G,Rey C

更新日期：2001-01-01 00:00:00

abstract：:Vasculopathy has been identified in young individuals with Turner syndrome (TS). No studies in young individuals with TS have investigated whether this vasculopathy progresses over time. The objective of this study is to describe the changes in vasculopathy over time in a cohort of young individuals with TS. Repeat ul...

journal_title：Pediatric cardiology

authors： Blunden CE,Urbina EM,Lawson SA,Gutmark-Little I,Shah AS,Khoury PR,Backeljauw PF

更新日期：2020-11-26 00:00:00

abstract：:In our institute, 1100 patients with a history of Kawasaki disease have been catheterized for selective coronary arteriography. Their age at examination ranged from four months to 13 years. Coronary artery lesions (CAL) were found in 262 patients. As far as the type of the CAL was concerned, occlusion was noted in 20 ...

journal_title：Pediatric cardiology

authors： Suzuki A,Kamiya T,Kuwahara N,Ono Y,Kohata T,Takahashi O,Kimura K,Takamiya M

更新日期：1986-01-01 00:00:00

abstract：:Congenital diverticulum of the left ventricle, a rare malformation, is usually associated with midline thoracoabdominal defect. We describe a case with congenital left ventricular diverticulum presenting as an isolated lesion. The lesion was suspected on two-dimensional echocardiography and was confirmed by cardiac ca...

journal_title：Pediatric cardiology

authors： Wu JM,Yu CY

更新日期：1996-07-01 00:00:00

abstract：:We describe the first report of an infant who was born with hypoplastic left heart syndrome and significant pulmonary stenosis. He was successfully palliated with multiple cardiac catheterization interventions while waiting for cardiac transplantation. This unusual constellation of heart defects is an entity that is r...

journal_title：Pediatric cardiology

authors： Farra H,Kort HW

更新日期：2005-09-01 00:00:00

abstract：:Increased risk of perioperative hemorrhage has been described in patients with Turner syndrome and coarctation of the aorta. We have operated on 11 patients with Turner syndrome and coarctation of the aorta, two of whom developed bleeding. One patient died. End-to-end anastomosis was performed in all patients. Histolo...

journal_title：Pediatric cardiology

authors： Brandt B 3rd,Heintz SE,Rose EF,Ehrenhaft JL,Clark EB

更新日期：1984-07-01 00:00:00

abstract：:Left ventricular hypertrophy is an adaptive mechanism in children undergoing chronic dialysis to improve contractility at rest. The aim of this study was to determine the left ventricular performance and contractility reserve by "dobutamine stress echocardiography" in children undergoing chronic dialysis. Thirty-five ...

journal_title：Pediatric cardiology

authors： Mese T,Guven B,Yilmazer MM,Serdaroglu E,Tavli V,Haydar A,Bak M

更新日期：2010-10-01 00:00:00

abstract：:A very rare combination including tetralogy of Fallot (TOF), absent pulmonary valve, and isolated left pulmonary artery is described. A 4-month-old girl presented with mild cyanosis and severe dyspnea. Echocardiography established the diagnosis of TOF and absent pulmonary valve with severe pulmonary regurgitation and ...

journal_title：Pediatric cardiology

authors： Wu L

更新日期：2008-11-01 00:00:00

abstract：:The current pulse-oximetry screening (POS) protocol for detection of critical congenital heart defects (CCHDs) is recommended only for newborns in well-infant and intermediate care nurseries, and there is no evidence-based protocol for infants discharged from the neonatal intensive care unit (NICU). The objectives of ...

journal_title：Pediatric cardiology

authors： Iyengar H,Kumar P,Kumar P

更新日期：2014-03-01 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：:This report aims to summarize and evaluate the efficacy and experience of reintervention for children with postoperative pulmonary venous restenosis. Clinical data from 61 patients with postoperative pulmonary venous restenosis who underwent reintervention at Shanghai Children's Medical Center (SCMC) from September 20...

journal_title：Pediatric cardiology

authors： Kai L,Xiaoyang Z,Jinghao Z,Zhongqun Z,Qi S,Xiaomin H,Zhiwei X,Jinfen L

更新日期：2019-06-01 00:00:00

abstract：:The observation that endocardial fibroelastosis (EFE) can result from an immune response to maternal autoantibody deposition in the fetal myocardium raises the possibility that the fetal immune system may contribute to the pathogenesis of idiopathic EFE and dilated cardiomyopathy (DCM). This study sought to characteri...

journal_title：Pediatric cardiology

authors： Fernandes NM,Taylor GP,Manlhiot C,McCrindle BW,Ho M,Miner SE,Atkinson A,Jaeggi ET,Nield LE

更新日期：2011-12-01 00:00:00

abstract：:We aimed to investigate the complications after epicardial pacemaker (PM) implantation in neonates and infants and their relationship with factors such as device size and patient size. Between May 2010 and July 2018, 55 patients under 1 year of age who underwent epicardial PM placement were retrospectively evaluated. ...

journal_title：Pediatric cardiology

authors： Ergün S,Kafalı HC,Genç SB,Yildiz O,Güneş M,Onan İS,Ergül Y,Güzeltaş A,Haydin S

更新日期：2020-04-01 00:00:00

abstract：:The outcome in a series of 23 cases of tetralogy of Fallot diagnosed prenatally was compared to published figures for this condition when (a) identified postnatally or (b) treated surgically. There was a marked difference in the survival between these groups, with the highest mortality (75%) occurring when the diagnos...

journal_title：Pediatric cardiology

authors： Allan LD,Sharland GK

更新日期：1992-01-01 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：:Modifications of the Fontan operation can afford excellent palliation for many patients with a variety of forms of single ventricle. In properly selected patients who are good candidates, early and late survival can be as high as 95-97%. However, mortality is considerably higher for patients with risk factors for poor...

journal_title：Pediatric cardiology

authors： Driscoll DJ

更新日期：2007-11-01 00:00:00

abstract：:We report our findings in the microscopic examination of the conduction system in four infants with glycogen storage disease, one of whom had adequate electrophysiologic studies. The electrophysiologic studies in the latter case showed P-A and A-H intervals at the lower limits of normal, but the H-V interval was just ...

journal_title：Pediatric cardiology

authors： Bharati S,Serratto M,DuBrow I,Paul MH,Swiryn S,Miller RA,Rosen K,Lev M

更新日期：1982-01-01 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：:A ventriculoseptal defect (VSD) usually is present in patients with a double-outlet right ventricle. This report describes a case of double-outlet right ventricle with a completely shrouded inlet VSD and no interventricular shunting. This was associated with a severely regurgitant dysplastic mitral valve. The anatomy ...

journal_title：Pediatric cardiology

authors： Singla M,Al-Radi O,Mertens L

更新日期：2013-01-01 00:00:00

abstract：:This prospective observational study conducted in a neonatal intensive care unit aimed to evaluate echocardiographic changes provoked by anemia and transfusion of packed red blood cells (pRBCs) in premature infants. In this study, 32 anemic premature infants had serial echocardiographic assessment of left ventricular ...

journal_title：Pediatric cardiology

authors： Radicioni M,Troiani S,Mezzetti D

更新日期：2012-04-01 00:00:00