Late pulmonary venous obstruction after surgical repair of infradiaphragmatic total anomalous pulmonary venous return.

abstract：:We present a 2-month-old male infant with thrombosis in the superior vena cava and pericardium due to transient protein C deficiency. Protein C deficiency was related to sepsis and hepatitis-induced liver function impairment. The patient's cardiac anatomy was otherwise normal. The patient was referred to us with signs...

journal_title：Pediatric cardiology

authors： Demir T,Celkan T,Ahunbay G,Babaoglu A,Besikci R

更新日期：2006-07-01 00:00:00

abstract：:Chylous effusions frequently occur after cardiac surgery due to severe damage to the lymphatic system, thus indicating that the insertion of a chest tube may be necessary. Factor XIII (FXIII) is discussed as being essential for wound healing. The aim of this retrospective study was to evaluate whether the application ...

journal_title：Pediatric cardiology

authors： Schroth M,Meißner U,Cesnjevar R,Weyand M,Singer H,Rascher W,Klinge J

更新日期：2006-01-01 00:00:00

abstract：:Accessory atrioventricular pathways (AP) are the most common substrate for paroxysmal supraventricular tachycardia in infants and small children. Up-to-date data on AP ablation in infants and small children are limited. The aim of the present study was to gain additional insight into radiofrequency (RF) catheter ablat...

journal_title：Pediatric cardiology

authors： Backhoff D,Klehs S,Müller MJ,Schneider H,Kriebel T,Paul T,Krause U

更新日期：2016-06-01 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：:Mammalian cardiomyocytes withdraw from the cell cycle soon after birth. This process is called terminal differentiation. The c-kit, a receptor tyrosine kinase, is expressed on cardiomyocytes immediately after birth but for only a few days. In mice with genetic c-kit dysfunction, adult cardiomyocytes are phenotypically...

journal_title：Pediatric cardiology

authors： Naqvi N,Li M,Yahiro E,Graham RM,Husain A

更新日期：2009-07-01 00:00:00

abstract：:A 6-year-old girl with evidence of a parahisian accessory pathway on a baseline electrocardiogram underwent successful catheter ablation using magnetic navigation. Magnetic remote controlled ablation eliminated the parahisian pathway with the first radiofrequency application. A second anterolaterally located concealed...

journal_title：Pediatric cardiology

authors： Mantziari L,Rigby M,Till J,Ernst S

更新日期：2013-03-01 00:00:00

abstract：:Very young mammals have an impressive cardiac regeneration capacity. In contrast, cardiac regeneration is very limited in adult humans. The hearts of young children have a higher regenerative capacity compared with adults, as, for example, seen after surgical correction of an anomalous left coronary artery arising fro...

journal_title：Pediatric cardiology

authors： Rupp S,Schranz D

更新日期：2015-04-01 00:00:00

abstract：:Right ventricular (RV) remodeling in hypoplastic left heart syndrome (HLHS) begins prenatally and continues through staged palliations. However, it is unclear if the most marked observed remodeling post-Norwood is secondary to cardiopulmonary bypass (CPB) exposure or if it is an adaptation intrinsic to the systemic RV...

journal_title：Pediatric cardiology

authors： Mah K,Serrano Lomelin J,Colen T,Tham EB,Lin L,Eckersley L,Smallhorn JF,Becher H,Mertens L,Khoo NS

更新日期：2020-10-10 00:00:00

abstract：:Children and adolescents with congenital heart disease often do not have the opportunity, inclination, or education to participate in safe and effective exercise. The consequences of this behavioral pattern affect not only cardiopulmonary parameters, but also psychosocial factors, especially when lack of participation...

journal_title：Pediatric cardiology

authors： Gauthier N,Curran T,O'Neill JA,Alexander ME,Rhodes J

更新日期：2020-12-01 00:00:00

abstract：:Conotruncal heart defect is a complex form of congenital heart disease and usually has a poor prognosis. Although previous studies have identified several missense variants in GATA4 gene that may cause CTD, it remains unclear whether they are involved in CTD pathogenesis because the study population was limited. The a...

journal_title：Pediatric cardiology

authors： Liu Y,Li B,Xu Y,Sun K

更新日期：2017-03-01 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：:A 9-year-old boy whose past history was remarkable for a heart murmur was diagnosed with abdominal angina due to acute occlusion of a simple coarctation of the aorta. Using a single cross-clamp, we accomplished an end-to-end anastomosis after resection of the coarctation. Paradoxical hypertension and abdominal angina ...

journal_title：Pediatric cardiology

authors： Ingu A,Morikawa M,Fuse S,Abe T

更新日期：2003-09-01 00:00:00

abstract：:Thrombus formation in the native aortic root is a rare but potentially life-threatening complication in patients with hypoplastic left heart syndrome. The native aortic root in these patients serves as a conduit for the retrograde filling of the coronary arteries. Thrombus in this location could result in myocardial i...

journal_title：Pediatric cardiology

authors： Owens ST,Gomez-Fifer C,Ensing GJ

更新日期：2006-05-01 00:00:00

abstract：:This report describes the case of two pediatric patients who demonstrated echocardiographic evidence of pulmonary hypertension (PH) during the acute phase of Kawasaki disease. The etiology of PH development in this setting is currently unknown, but the authors hypothesize that pulmonary vasculitis may play a significa...

journal_title：Pediatric cardiology

authors： Nicholson GT,Samai C,Kanaan U

更新日期：2013-01-01 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 commonly used Darling classification for total anomalous pulmonary venous connection (TAPVC) consists of supracardiac, cardiac, infracardiac, and mixed types (Craig et al., Lab Invest 6:44-64, 1967). In supracardiac TAPVC, the common pulmonary vein drains superiorly into the left innominate vein, the superior vena...

journal_title：Pediatric cardiology

authors： Shah S,Singh M,John C,Maheshwari S

更新日期：2009-10-01 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：:Long-term neurodevelopmental sequelae are commonly detectable in children after open-heart surgery with cardiopulmonary bypass (CPB). The objective of the study was to determine the neurodevelopmental outcome in these children in relation to postoperative inflammatory reaction. This is a prospective, observational stu...

journal_title：Pediatric cardiology

authors： Gessler P,Schmitt B,Prètre R,Latal B

更新日期：2009-04-01 00:00:00

abstract：:Protein-losing enteropathy (PLE) and plastic bronchitis (PB) are major causes of long-term mortality after Fontan operation. The objective of this study was to determine early clinical risk factors before the onset of PLE and PB. In a cohort study, 106 Fontan patients between 2005 and 2013 were examined. A median of 5...

journal_title：Pediatric cardiology

authors： Unseld B,Stiller B,Borth-Bruhns T,du Bois F,Kroll J,Grohmann J,Fleck T

更新日期：2017-08-01 00:00:00

abstract：:Vitamin D has anti-inflammatory properties, and deficiency is prevalent in children. There is a paucity of data regarding vitamin D status and its correlation with low-grade inflammation and vasculature. We prospectively enrolled 25 children, 9-11 years old (13 male); 21 obese. Eight atherosclerosis-promoting risk fac...

journal_title：Pediatric cardiology

authors： Singh J,Merrill ED,Sandesara PB,Schoeneberg L,Dai H,Raghuveer G

更新日期：2015-10-01 00:00:00

abstract：:Ischemic myocardial damage was identified as a complicating feature in the clinical course of 12 newborn infants who died in congestive failure with cerebral arteriovenous malformation. Electrocardiograms of 11 patients showed signs of chamber hypertrophy and T wave and ST segment features of varying degree compatible...

journal_title：Pediatric cardiology

authors： Jedeikin R,Rowe RD,Freedom RM,Olley PM,Gillan JE

更新日期：1983-01-01 00:00:00

abstract：:In a patient with single ventricle, mitral atresia, common atrium, pulmonary stenosis, azygos continuation of the inferior vena cava and bilateral systemic artery--pulmonary artery anastomoses, the systemic veins were connected directly to the pulmonary arteries to achieve physiologic repair; the child was discharged ...

journal_title：Pediatric cardiology

authors： Waldman JD,Lamberti JJ

更新日期：1986-01-01 00:00:00

abstract：:A 6-year-old girl presented with respiratory distress. Chest radiographs exhibited calcifications in the mediastinum. Further imaging revealed extensive cardiac calcifications on computed tomography of the chest. The laboratory parameters were consistent with findings of secondary hyperparathyroidism. Detailed review ...

journal_title：Pediatric cardiology

authors： Zaidi AN,Ceneviva GD,Phipps LM,Dettorre MD,Mart CR,Thomas NJ

更新日期：2005-07-01 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：:Various echocardiographic parameters are determined in the assessment and evaluation of a patent ductus arteriosus. In isolation, many of these parameters have a low sensitivity and specificity for ductal hemodynamic significance compared with ductal size. This study aimed to correlate various echocardiographic parame...

journal_title：Pediatric cardiology

authors： Sehgal A,Menahem S

更新日期：2013-06-01 00:00:00

abstract：:We present an infant with unusual anatomy and physiology of a persistent left superior vena cava (LSVC). The adverse physiologic consequences of the LSVC were corrected with percutaneous placement of vascular plugs. ...

journal_title：Pediatric cardiology

authors： Lennox EG,Velvis H

更新日期：2010-05-01 00:00:00

abstract：:The response to warfarin is highly variable among individuals and such variability is likely to have some genetic basis. We evaluted the effect of VKORC1 polymorphisms on warfarin response among Japanese, taking advantage of its unique population structure in which CYP2C9 *2 and *3 alleles are relatively rare. Thirty-...

journal_title：Pediatric cardiology

authors： Kosaki K,Yamaghishi C,Sato R,Semejima H,Fuijita H,Tamura K,Maeyama K,Yamagishi H,Sugaya A,Dodo H,Tanigawara Y,Takahashi T

更新日期：2006-11-01 00:00:00

abstract：:The authors hypothesized that prospective, systematic Internet searches could identify occurrences of sudden cardiac death (SCD) in athletes and would be useful for establishing a system of active surveillance. Weekly advanced Google searches of the Internet were conducted for cases of SCD in young athletes during a 1...

journal_title：Pediatric cardiology

authors： Choi K,Pan YP,Pock M,Chang RK

更新日期：2013-01-01 00:00:00

abstract：:Two fetuses of approximately 11 weeks development with aplasia of the pulmonary as well as the aortic valve leaflets are reported. Both cases showed additional cardiac malformations. Case 1, with all leaflets missing, also had double-outlet right ventricle, hypoplastic left ventricle, large ventricular septal defect, ...

journal_title：Pediatric cardiology

authors： Hartwig NG,Vermeij-Keers C,De Vries HE,Gittenberger-De Groot AC

更新日期：1991-04-01 00:00:00

abstract：:Rhabdomyoma is the most common primary cardiac tumor in infants and children and is often associated with tuberous sclerosis. Surgical resection may be indicated and, if so, is usually curative. We describe a rhabdomyoma in an infant who presented with severe myocardial ischemia necessitating orthotopic heart transpla...

journal_title：Pediatric cardiology

authors： Demkow M,Sorensen K,Whitehead BF,Rees PG,Sullivan ID,Elliott MJ,de Leval MR

更新日期：1995-07-01 00:00:00