Cardiac surgery for Kartagener syndrome.

abstract：:Aortic aneurysm may develop after surgery for coarctation of aorta especially patch aortoplasty. The size of patch and of adjacent native aortic wall was analyzed to determine whether aortic dilatation represents a true aneurysm. Electron beam tomography (EBT) was done on 19 patients, three months to 17.5 years after ...

journal_title：Pediatric cardiology

authors： Al-Hroob A,Husayni TS,Freter A,Chiemmongkoltip P,Ilbawi MN,Arcilla RA

更新日期：2003-01-01 00:00:00

abstract：:Use of extracorporeal membrane oxygenation (ECMO) in infants with congenital heart disease is becoming more frequent. We present the first reported use of balloon atrial septostomy during ECMO support and describe possible complications of such procedures unique to ECMO therapy. ...

journal_title：Pediatric cardiology

authors： O'Connor TA,Downing GJ,Ewing LL,Gowdamarajan R

更新日期：1993-07-01 00:00:00

abstract：:There is a higher incidence of sudden death in patients with Rett syndrome than individuals in the general population. Previous studies have implicated cardiac dysautonomia and a long QT interval as causative factors. Because carnitine plays a critical role in cellular metabolism and may have beneficial effects on car...

journal_title：Pediatric cardiology

authors： Guideri F,Acampa M,Hayek Y,Zappella M

更新日期：2005-09-01 00:00:00

abstract：:Recurrent congestive heart failure (CHF) attributable to myocarditis is a seldom-discussed entity in the scientific literature. This report describes the case of an 8-year-old girl who had three clinically identical episodes of CHF, beginning at the age of 5 years, with each episode preceded by a viral prodrome. The c...

journal_title：Pediatric cardiology

authors： Lee AF,Chiasson DA,Smythe JF,Sanatani S

更新日期：2012-01-01 00:00:00

abstract：:This study aimed to clarify the characteristics of pulmonary arterial resistance (Rp)-compliance (Cp) coupling in individuals with Down syndrome (DS), who have increased risks of pulmonary arterial hypertension (PAH). We performed cardiac catheterization before and after corrective surgery in 85 DS infants and 85 cont...

journal_title：Pediatric cardiology

authors： Iwaya Y,Muneuchi J,Inoue Y,Watanabe M,Okada S,Ochiai Y

更新日期：2019-04-01 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：: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 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：: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：: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：:Cor triatriatum sinistrum (division of the left atrium) is a recognized clinical and surgical entity. Division of the right atrium, also known as cor triatriatum dexter, is an extremely rare congenital abnormality in which persistence of the right valve of the embryonic systemic sinus venosus divides the right atrium ...

journal_title：Pediatric cardiology

authors： Choudhary D,Sivasankaran S,Venkateshwaran S,Sasidharan B

更新日期：2013-01-01 00:00:00

abstract：:Magnetocardiographic mapping was performed on a 2-year-old boy who suffered from the Wolff-Parkinson-White syndrome in association with a complex congenital heart defect. The pre-excitation site was determined noninvasively from the measured cardiac magnetic fields. The location was in the same anatomic region as foun...

journal_title：Pediatric cardiology

authors： Nenonen J,Rovamo L,Toivonen L,Ilmoniemi R,Järvinen A,Leiniö M,Montonen J,Nisula L

更新日期：1995-01-01 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：:This case discusses a Shone's variant with small left ventricle and mitral valve, bicuspid aortic valve, coarctation of the aorta, an unusual arrangement of atrial appendages, and partially anomalous pulmonary venous drainage due to a deviated atrial septum. The left atrial appendage could be directly entered from the...

journal_title：Pediatric cardiology

authors： Kurio GH,Gulati R,Bichell DP,Perry JC

更新日期：2006-09-01 00:00:00

abstract：:Myocardial contractility and relaxation are highly dependent on calcium homeostasis. Immature myocardium, as in pediatric patients, is thought to be more dependent on extracellular calcium for optimal function. For this reason, intravenous calcium chloride infusions may improve myocardial function in the pediatric pat...

journal_title：Pediatric cardiology

authors： Averin K,Villa C,Krawczeski CD,Pratt J,King E,Jefferies JL,Nelson DP,Cooper DS,Ryan TD,Sawyer J,Towbin JA,Lorts A

更新日期：2016-03-01 00:00:00

abstract：BACKGROUND:In 2017, the AHA published revised guidelines for the diagnosis of Kawasaki disease (KD). In the absence of compelling data supporting or refuting the utility of lack of tapering (LT) and perivascular brightness (PB), expert panel consensus removed LT and PB from consideration. We hypothesize that LT and PB ...

journal_title：Pediatric cardiology

authors： Rabinowitz EJ,Rubin LG,Desai K,Hayes DA,Tugertimur A,Kwon EN,Dhanantwari P,Misra N,Stoffels G,Blaufox AD,Mitchell E

更新日期：2019-01-01 00:00:00

abstract：:We sought to document morbidities and growth for patients with hypoplastic left heart syndrome (HLHS) to inform the initial surgical decision and understand healthcare needs. Data were obtained on 137 patients with HLHS, born between 1989 and 1994, who survived staged surgery ( n = 62) or transplantation ( n = 75) and...

journal_title：Pediatric cardiology

authors： Jenkins PC,Flanagan MF,Jenkins KJ,Sargent JD,Canter CE,Chinnock RE,Vincent RN,O'Connor GT

更新日期：2004-01-01 00:00:00

abstract：:Ionizing radiation exposure is a necessary risk entailed during congenital cardiac catheterizations. The congenital catheterization lab at Yale New Haven Children's Hospital employed quality improvement strategies to minimize radiation exposure in this vulnerable population. In two phases, we implemented six intervent...

journal_title：Pediatric cardiology

authors： Patel C,Grossman M,Shabanova V,Asnes J

更新日期：2019-03-01 00:00:00

abstract：:We describe a patient diagnosed with a small atrial septal defect (3-4 mm) that had grown to 24 mm in diameter over a six-year period. Timing of transcatheter intervention may be affected by growth of the atrial septal defect and this reports the first case of an atrial septal defect outgrowing the possibility of tran...

journal_title：Pediatric cardiology

authors： Tortoriello TA,McMahon C,Kovalchin JP,Bricker JT,Grifka RG

更新日期：2002-09-01 00:00:00

abstract：:Congenital heart defects (CHD) are the third leading cause of death in children <1 year of age in Mexico where there is a high prevalence of the 677C → T polymorphism of the MTHFR gene. This is important because the homozygous 677T/T MTHFR gene and deficiency of folic acid (FA) intake have been associated with CHD. Ou...

journal_title：Pediatric cardiology

authors： Balderrábano-Saucedo NA,Sánchez-Urbina R,Sierra-Ramírez JA,García-Hernández N,Sánchez-Boiso A,Klunder-Klunder M,Arenas-Aranda D,Bravo-Hernández G,Noriega-Zapata P,Vizcaíno-Alarcón A

更新日期：2013-01-01 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：: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

abstract：:In chronic aortic insufficiency (AI), left-ventricular (LV) dysfunction must be detected early to allow timely surgery. Strain and strain rate have been used for this purpose in adults, but the value of this method in pediatric AI has not been established. Forty patients with moderate to severe AI were included in thi...

journal_title：Pediatric cardiology

authors： Lowenthal A,Tacy TA,Behzadian F,Punn R

更新日期：2013-08-01 00:00:00

abstract：:M-mode and 2-dimensional (2D) echocardiographic imaging are routinely used to quantify left-ventricular (LV) size and function in pediatric patients with dilated cardiomyopathy (DCM). The reproducibility of and correlation between these techniques are unknown. This analysis sought to compare interreader, intrareader, ...

journal_title：Pediatric cardiology

authors： Lee CK,Margossian R,Sleeper LA,Canter CE,Chen S,Tani LY,Shirali G,Szwast A,Tierney ES,Campbell MJ,Golding F,Wang Y,Altmann K,Colan SD,Pediatric Heart Network Investigators.

更新日期：2014-04-01 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：:This paper reviews the initial experience of radical correction of truncus arteriosus in the Soviet Union. The anatomy, hemodynamics, diagnosis and surgical technique are described in detail. Five patients were operated on; three survived. The two deaths in this series were due to mistakes in evaluating the indication...

journal_title：Pediatric cardiology

authors： Burakovsky VI,Falkovsky GE,Ivanitsky AV

更新日期：1984-04-01 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：:Thrombocytopenia can be a real challenge during cardiac surgery in children with cyanotic congenital heart disease. This report describes a 7-year-old girl with d-transposition of the great arteries, ventricular septal defect, pulmonary hypertension, chronic thrombocytopenia, polycythemia, and chronic renal impairment...

journal_title：Pediatric cardiology

authors： Al-Biltagi M,Ismail MF,Al-Radi OO,Baho H

更新日期：2013-01-01 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：:Fetal interventions have been performed for some congenital heart diseases. However, these procedures have not gained wide acceptance due to concerns about their efficacy and safety. The aim of this study was to report on a preliminary experience with fetal cardiac interventions in Brazil. Twenty-two cardiac intervent...

journal_title：Pediatric cardiology

authors： Pedra SR,Peralta CF,Crema L,Jatene IB,da Costa RN,Pedra CA

更新日期：2014-03-01 00:00:00