Pattern of recovery for transient complete heart block after open heart surgery for congenital heart disease: duration alone predicts risk of late complete heart block.

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：:A five-day-old infant with transposition of the great arteries, ventricular septal defect, and an interrupted right aortic arch underwent successful balloon septostomy, pulmonary artery banding, and aortic arch repair. The infant also had abnormal facies with severe refractory hypocalcemia and depressed T-lymphocyte n...

journal_title：Pediatric cardiology

authors： Duncan WJ,Tyrrell MJ,Bharadwaj B,Rosenberg AM,Schroeder ML,Bingham WT

更新日期：1984-07-01 00:00:00

abstract：:Marfan syndrome (MS) is a connective tissue disease involving the cardiovascular, ocular, and the musculoskeletal systems. MS has variable phenotypic expression and is most often diagnosed in adult life. Infantile-onset MS is rare and is associated with severe cardiovascular manifestations; there is an extremely high ...

journal_title：Pediatric cardiology

authors： Strigl S,Quagebeur JM,Gersony WM

更新日期：2007-09-01 00:00:00

abstract：:In the classic scimitar syndrome, a pulmonary vein draining all or part of the right lung enters the inferior vena cava. A variant is described with the same roentgenographic appearance, but with drainage of the anomalous pulmonary vein into both the inferior vena cava and the left atrium; the atrial septum was intact...

journal_title：Pediatric cardiology

authors： Pearl W

更新日期：1987-01-01 00:00:00

abstract：:Assessment of ventricular dysfunction and asynchrony is very important in predicting the outcome for children with a single right ventricle. However, the assessment is inaccurate and subjective because of the unusual ventricular shape. This study aimed to evaluate the feasibility and clinical value of velocity vector ...

journal_title：Pediatric cardiology

authors： Wu YR,Zhang YQ,Chen LJ,Wang SS,Zhong SW,Zhang ZF

更新日期：2014-10-01 00:00:00

abstract：:Many different types of potassium channels with various functions exist in pulmonary artery smooth muscle cells, contributing to many physiological actions and pathological conditions. The deep involvement of these channels in the onset and exacerbation of pulmonary arterial hypertension (PAH) also continues to be rev...

journal_title：Pediatric cardiology

authors： Hayabuchi Y

更新日期：2017-01-01 00:00:00

abstract：:Plastic bronchitis (PB) is a poorly understood disease that can complicate any underlying pulmonary disease. However, it appears to most often occur in patients with surgically palliated congenital heart disease, particularly after the Fontan procedure. Few data exist about the prevalence and etiology of PB in this po...

journal_title：Pediatric cardiology

authors： Caruthers RL,Kempa M,Loo A,Gulbransen E,Kelly E,Erickson SR,Hirsch JC,Schumacher KR,Stringer KA

更新日期：2013-02-01 00:00:00

abstract：:This study was conducted to determine the efficacy of procainamide therapy for rapid rate control of postoperative junctional tachycardia (JT). Postoperative JT is one of the most difficult forms of tachycardia to manage. Reported success with a variety of treatments of JT in infants and children has been inconsistent...

journal_title：Pediatric cardiology

authors： Mandapati R,Byrum CJ,Kavey RE,Smith FC,Kveselis DA,Hannan WP,Brandt B 3rd,Gaum WE

更新日期：2000-03-01 00:00:00

abstract：:Sudden death accounts for up to 43% of all deaths in patients with familial dysautonomia (FD). The classic features of FD, namely, autonomic dysfunction, high blood pressure, and blood pressure labiality, are all risk factors for cardiac remodeling and hypertrophy. Myocardial remodeling and hypertrophy are independent...

journal_title：Pediatric cardiology

authors： Nussinovitch U,Katz U,Nussinovitch M,Blieden L,Nussinovitch N

更新日期：2009-11-01 00:00:00

abstract：:Internationally, there have been isolated case reports published of children presenting with dilated cardiomyopathy (DCM) in the setting of undiagnosed rickets. Although there has been an increased prevalence of rickets in the United States, there has been only one documented case of associated DCM. At our institution...

journal_title：Pediatric cardiology

authors： Brown J,Nunez S,Russell M,Spurney C

更新日期：2009-08-01 00:00:00

abstract：:Current guidelines recommend that all neonates with Down syndrome (DS) be screened for congenital heart disease (CHD) with an echocardiogram. We sought to determine the effectiveness of a more accessible and less expensive screening strategy consisting of physical examination, electrocardiogram (ECG), and chest X-ray....

journal_title：Pediatric cardiology

authors： Bogarapu S,Pinto NM,Etheridge SP,Sheng X,Liesemer KN,Young PC,Saarel EV

更新日期：2016-10-01 00:00:00

abstract：:Kawasaki disease (KD) is a self-limiting systemic vasculitis of unknown etiology. KD is often complicated by coronary artery aneurysms (CAAs), which develop in about 20-25% of untreated children and 3-5% of children treated with intravenous immunoglobulin therapy. To identify the risk loci for CAA susceptibility in pa...

journal_title：Pediatric cardiology

authors： Kwon YC,Kim JJ,Yu JJ,Yun SW,Yoon KL,Lee KY,Kil HR,Kim GB,Han MK,Song MS,Lee HD,Ha KS,Sohn S,Hong YM,Jang GY,Lee JK,Korean Kawasaki Disease Genetics Consortium.

更新日期：2019-03-01 00:00:00

abstract：:The authors present an unusual complication of the balloon atrial septostomy procedure performed in a neonate with D-transposition of the great arteries. Cardiac tamponade developed shortly after the balloon atrial septostomy procedure and the infant was found to have a tear in the superior aspect of the left atrium, ...

journal_title：Pediatric cardiology

authors： Blanchard WB,Knauf DG,Victorica BE

更新日期：1983-04-01 00:00:00

abstract：:Sleep-disordered breathing (SDB) is described in patients with acquired heart failure but its prevalence in adults with congenital heart disease is not well documented. It is likely that single-ventricle patients who have undergone Fontan palliation poorly tolerate the additional stress of SDB on their fragile cardiac...

journal_title：Pediatric cardiology

authors： Cg S,Rm J,Ad K,E Y,M K,G M,J K

更新日期：2020-10-01 00:00:00

abstract：:Right ventricular (RV) pacing can be associated with impairment of left ventricular (LV) function due to electrical dyssynchrony and myocardial remodeling (Janousek et al. in J Cardiovasc Electrophysiol 15:470-474, 2004). RV-pacing induced ventricular dysfunction is reversible by techniques such as biventricular pacin...

journal_title：Pediatric cardiology

authors： Garg S,Balaji S

更新日期：2017-08-01 00:00:00

abstract：:This study identified tracheobronchial cartilage calcification in children with congenital heart disease. Calcification of the tracheobronchial airways has been found previously in adults receiving warfarin and in children receiving warfarin after mitral valve replacement. A 9-year-old girl who had received a Fontan r...

journal_title：Pediatric cardiology

authors： Eckersley L,Stirling J,Occleshaw C,Wilson N

更新日期：2014-08-01 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

abstract：:Cardiac rhabdomyoma (CR) is the most common cardiac tumor in newborns. Approximately 75% of cases are associated with tuberous sclerosis complex. Although these tumors usually spontaneously regress after 2 years of age, they can be life-threatening when they obstruct major cardiac inflow or outflow pathways. Everolimu...

journal_title：Pediatric cardiology

authors： Chang JS,Chiou PY,Yao SH,Chou IC,Lin CY

更新日期：2017-10-01 00:00:00

abstract：:Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a heritable cardiomyopathy characterized by fibro-fatty replacement of right ventricular myocardium. Diagnostic criteria, established in 1994 and modified in 2010, are based on predominately adult manifestations of ARVC/D. The goal of this paper is ...

journal_title：Pediatric cardiology

authors： Deshpande SR,Herman HK,Quigley PC,Shinnick JK,Cundiff CA,Caltharp S,Shehata BM

更新日期：2016-04-01 00:00:00

abstract：:Severe atrioventricular valve (AVV) or semilunar valve (SLV) regurgitation in the setting of a single ventricle physiology may proceed to valve replacement if repair strategies fail. Outcome data for these children are limited. We present transplant-free survival of a case series of children with single ventricle phys...

journal_title：Pediatric cardiology

authors： Alshami N,Sarvestani AL,Thomas AS,St Louis J,Kochilas L,Raghuveer G

更新日期：2020-01-01 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：:Cardiac involvement of Duchenne and Becker muscular dystrophies (DMD/BMD) is the most common cause of fatal outcomes. It is still unclear whether some DMD/BMD gene mutations might be predictive of cardiac involvement. In this study, we provide a comprehensive overview on genotypes of cardiac disease in DMD/BMD. We sys...

journal_title：Pediatric cardiology

authors： Zhou H,Fu M,Mao B,Yuan L

更新日期：2020-10-09 00:00:00

abstract：:The clinical and pathological features of primary pulmonary artery sarcoma in two children are reported. The first patient presented with right ventricular outflow obstruction and underwent successful surgical resection of his tumor. The second patient developed cardiac arrest following a relatively short period of sy...

journal_title：Pediatric cardiology

authors： Farooki ZQ,Chang CH,Jackson WL,Clapp SK,Hakimi M,Arciniegas E,Pinsky WW

更新日期：1988-01-01 00:00:00

abstract：:The epidemiologic data for pediatric hypertrophic cardiomyopathy (HCM) needs to be periodically updated as diagnostic techniques and management strategies improve. Herein, the incidence, prevalence, and mortality rates of pediatric HCM in a population-based treatment system are described. Patients aged ≤ 17 years and ...

journal_title：Pediatric cardiology

authors： Nandi D,Hayes EA,Wang Y,Jerrell JM

更新日期：2020-10-03 00:00:00

abstract：:Eighteen of 25 survivors of aortic valvotomy in infancy were reinvestigated by cross-sectional echocardiography a mean of 7.5 (2.3-13.4) years after surgery. They had been operated at a median age of 38 (5-330) days. At the follow-up examination the gradient across the aortic valve was 41 +/- 19 (15-85) mmHg and the e...

journal_title：Pediatric cardiology

authors： Vogel M,Sebening F,Sauer U,Bühlmeyer K

更新日期：1992-01-01 00:00:00

abstract：:This report describes an unusual case with tortuosity of the great vessels in a neonate who presented at birth with cyanosis. The diagnosis was made with magnetic resonance imaging (MRI), then confirmed by genetic analysis. ...

journal_title：Pediatric cardiology

authors： Pilati M,Luciani GB,Prioli MA,Puppini G

更新日期：2009-11-01 00:00:00

abstract：:Since its first description in Japan 30 years ago, Kawasaki disease has been reported worldwide. Although an infectious etiology is suspected based on the epidemiology and clinical features, a causative agent has not been identified. The majority of the morbidity and mortality associated with this condition is attribu...

journal_title：Pediatric cardiology

authors： Laupland KB,Dele Davies H

更新日期：1999-05-01 00:00:00

abstract：:The morphology and natural history of anomalous right ventricular muscle bundles (ARVMB) have been described in a number of postnatal studies. Whether this is a congenital or acquired cardiac lesion remains obscure. A fetal echocardiogram performed in a 32-week gestation mother showed a large ventricular septal defect...

journal_title：Pediatric cardiology

authors： Leandro J,Dyck JD,Smallhorn JF

更新日期：1994-09-01 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：:Left atrial tumor, diagnosed as myxoma at first investigation, was later demonstrated to be a malignant fibrosarcoma with myxoid change. Myxoma should be diagnosed and managed carefully because of its wide range of histopathologic features. ...

journal_title：Pediatric cardiology

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

更新日期：2001-05-01 00:00:00