Anomalous origin of the left coronary artery from the pulmonary artery in a premature infant with preserved left ventricular function.

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 no signs of myocardial ischemia and is doing well after corrective surgery. This is the youngest patient reported with ALCAPA and preserved myocardial function.

journal_name

Pediatr Cardiol

journal_title

Pediatric cardiology

authors

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

doi

10.1007/s00246-004-0878-z

subject

Has Abstract

pub_date

2006-03-01 00:00:00

pages

269-71

issue

2

eissn

0172-0643

issn

1432-1971

journal_volume

27

pub_type

杂志文章
  • High-dose intravenous immunoglobulin in recurrent postpericardiotomy syndrome.

    abstract::Postpericardiotomy syndrome is a frequent complication following cardiac surgery. It is characterized by fever, chest pain, pericardial friction rub or pericardial effusion, and laboratory signs of inflammation. Treatment includes the use of nonsteroidal antiinflammatory agents, corticosteroids, and pericardial draina...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-007-9025-y

    authors: Wendelin G,Fandl A,Beitzke A

    更新日期:2008-03-01 00:00:00

  • Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.

    abstract::Congenital heart defects (CHDs) are the most prevalent of all birth defects and the leading cause of death in the first year of life. The molecular causes of most CHDs remain largely unknown. The LIM homeodomain transcriptor factor ISL1 is a marker for undifferentiated cardiac progenitor cells that give rise to both t...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0578-z

    authors: Cresci M,Vecoli C,Foffa I,Pulignani S,Ait-Ali L,Andreassi MG

    更新日期:2013-04-01 00:00:00

  • Myocardial perfusion abnormalities in patients occurring more than 1 year after successful univentricular (Fontan surgery) and biventricular repair (complete repair of tetralogy of Fallot).

    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

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0531-1

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

    更新日期:2013-04-01 00:00:00

  • Unusual differential diagnosis of common arterial trunk.

    abstract::Common arterial trunk is relatively a straightforward diagnosis on echocardiography. We describe a neonate who was referred to our centre as a case of common arterial trunk but on evaluation was found to have pulmonary atresia with ventricular septal defect and aortopulmonary window, for which he underwent repair with...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0240-9

    authors: Shah S,Kavya,Saraf R,Rao S

    更新日期:2012-10-01 00:00:00

  • Large anomalous systemic arterial supply to the left lung without pulmonary sequestration: a rare cause of heart failure in a child.

    abstract::A 10-month-old boy was referred for tachypnea and heart murmur. An echocardiogram showed unexplained left heart dilation without evidence of an intracardiac shunt. A 64-slice computed tomographic contrast-enhanced angiography showed a large tortuous anomalous artery arising from the descending thoracic aorta and suppl...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-008-9287-z

    authors: Wong MN,Joshi P,Sim KH

    更新日期:2009-01-01 00:00:00

  • Restricting sports for athletes with heart disease: are we saving lives, avoiding lawsuits, or just promoting obesity and sedentary living?

    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

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-012-0170-6

    authors: Vaseghi M,Ackerman MJ,Mandapati R

    更新日期:2012-03-01 00:00:00

  • Hemodynamic assessment in patients with one-and-a-half ventricle repair revealed by four-dimensional flow magnetic resonance imaging.

    abstract::We report hemodynamic findings in two patients with pulmonary atresia and intact ventricular septum (PAIVS) after "one-and-a-half ventricle repair" and placement of a bidirectional Glenn shunt using four-dimensional (4D) flow magnetic resonance imaging. Quantification of flow and analysis of flow patterns revealed the...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0288-6

    authors: Uribe S,Bächler P,Valverde I,Crelier GR,Beerbaum P,Tejos C,Irarrazaval P

    更新日期:2013-02-01 00:00:00

  • Effects of transdermal nitroglycerin in children with congestive heart failure: a Doppler echocardiographic study.

    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

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/s002460010144

    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

  • Device closure of secundum atrial septal defects in infants weighing less than 8 kg.

    abstract::This study aimed to assess the technical aspects of atrial septal defect (ASD) closure using the Amplatzer septal occluder (ASO) and the Gore Helex septal occluder (GHSO) for infants weighing less than 8 kg and to determine the safety, effectiveness, and near-to-intermediate-term outcome of the closure. The Mid-Atlant...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00246-014-0905-7

    authors: Bishnoi RN,Everett AD,Ringel RE,Owada CY,Holzer RJ,Chisolm JL,Radtke WA,Scott Lim D,Rhodes JF Jr,Coulson JD

    更新日期:2014-10-01 00:00:00

  • Surgical repair of truncus arteriosus.

    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

    pub_type: 杂志文章

    doi:10.1007/BF02424960

    authors: Burakovsky VI,Falkovsky GE,Ivanitsky AV

    更新日期:1984-04-01 00:00:00

  • Insights into the characteristics of mammalian cardiomyocyte terminal differentiation shown through the study of mice with a dysfunctional c-kit.

    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

    pub_type: 杂志文章

    doi:10.1007/s00246-008-9366-1

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

    更新日期:2009-07-01 00:00:00

  • Rehospitalization Following Pediatric Heart Transplantation: Incidence, Indications, and Risk Factors.

    abstract::Rehospitalization following pediatric heart transplantation is common. However, existing data remain somewhat limited. Using a novel linkage between administrative and clinical databases, pediatric heart transplant (HT) recipients from 29 centers who survived to discharge were retrospectively reviewed to determine the...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-020-02326-x

    authors: Lambert AN,Weiner JG,Hall M,Thurm C,Dodd DA,Bearl DW,Soslow JH,Feingold B,Smith AH,Godown J

    更新日期:2020-03-01 00:00:00

  • Temporary atrial pacing for cardiac output after pediatric cardiac surgery.

    abstract::Pediatric cardiothoracic surgery is often associated with low cardiac output in the postoperative period. This study sought to determine whether increasing heart rate via temporary atrial pacing is beneficial in augmenting cardiac output. Patients younger than 18 years who underwent cardiothoracic surgery and had no p...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-013-0687-3

    authors: Barker GM,Affolter J,Saenz J,Cox CS,Forbess JM,Scott WA,Zeltser I

    更新日期:2013-10-01 00:00:00

  • The role of transesophageal echocardiography during surgery for patients with tetralogy of Fallot.

    abstract::Routine use of intraoperative transesophageal echocardiography (TEE) is a safe monitoring and diagnostic method during pediatric congenital cardiac surgery. However, the question of whether intraoperative TEE is accurate and cost effective for patients with tetralogy of Fallot (TOF) has not been raised. This study aim...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0423-4

    authors: Kim SJ,Park SA,Song J,Shim WS,Choi EY,Lee SY

    更新日期:2013-02-01 00:00:00

  • Elevated homocysteine and asymmetric dimethyl arginine levels in pulmonary hypertension associated with congenital heart disease.

    abstract::Pulmonary arterial hypertension (PAH) is a major cause of morbidity and mortality among patients with congenital heart disease (CHD). This study was designed to determine biomarker levels in patients with PAH associated with CHD (PAH-CHD) and CHD patients without PAH and to investigate the relationship of these potent...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0321-9

    authors: Sanli C,Oguz D,Olgunturk R,Tunaoglu FS,Kula S,Pasaoglu H,Gulbahar O,Cevik A

    更新日期:2012-12-01 00:00:00

  • Trends in Infant Mortality After TAPVR Repair over 18 Years in Texas and Impact of Hospital Surgical Volume.

    abstract::For some congenital heart lesions, higher institutional surgical volume has been associated with better survival than in lower volume centers. The relationship between institutional surgical volume and mortality in infants after total anomalous pulmonary vein return (TAPVR) repair has not been well explored. The Texas...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-019-02224-x

    authors: Lahiri S,Wang Y,Caldarone CA,Morris SA

    更新日期:2020-01-01 00:00:00

  • Closure of symptomatic ventricular septal defects: how early is too early?

    abstract::With improvements in technology and surgical technique, pediatric cardiologists are challenging surgeons to close symptomatic ventricular septal defects (VSDs) in ever smaller patients. Although delaying surgery may facilitate operative repair, early intervention decreases the period of time these patients require the...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-007-9016-z

    authors: Kogon B,Butler H,Kirshbom P,Kanter K,McConnell M

    更新日期:2008-01-01 00:00:00

  • 1173C>T polymorphism in VKORC1 modulates the required warfarin dose.

    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

    pub_type: 杂志文章

    doi:10.1007/s00246-005-1150-x

    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

  • Diagnostic Effect of the Single BP Cut-Offs for Identifying Elevated BP and Hypertension in Adolescents Aged 13-17 Years.

    abstract::In contrast to the percentile-based definitions of elevated blood pressure (BP) and hypertension for children and adolescents of all ages in the 2004 fourth report, the 2017 American Academy of Pediatrics (AAP) BP guideline recommends a change to single BP cut-offs for clinical diagnosis (120/< 80-129/< 80 mmHg for el...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-019-02058-7

    authors: Liu Q,Hou Y,Yang L,Zhao M,Li S,Xi B

    更新日期:2019-04-01 00:00:00

  • Fetal Echocardiographic Dimension Indices: Important Predictors of Postnatal Coarctation.

    abstract::The aim of the study is to identify reliable quantitative fetal echocardiographic predictors for postnatal development of coarctation (CoA). In this retrospective study, we included 65 fetuses with a prenatally suspected, isolated CoA, born 2010-2018. Dimensions of the cardiac structures, aortic, and ductal arches exp...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-020-02509-6

    authors: Fricke K,Liuba P,Weismann CG

    更新日期:2020-12-23 00:00:00

  • Height, VKORC1 1173, and CYP2C9 Genotypes Determine Warfarin Dose for Pediatric Patients with Kawasaki Disease in Southwest China.

    abstract::Long-term oral warfarin is recommended in pediatric Kawasaki disease patients with large coronary artery aneurysms; however, heterogeneity is considerable. This study aimed to determine variables affecting warfarin dosage in Kawasaki disease. The enrolled individuals (194 children) were divided into four groups: (1) C...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-018-1957-x

    authors: Yang D,Kuang H,Zhou Y,Cai C,Lu T

    更新日期:2019-01-01 00:00:00

  • Catecholaminergic Ventricular Tachycardia, Pregnancy and Teenager: Are They Compatible?

    abstract::Arrhythmias in pregnancy are becoming more common given more available and effective medical, ablation and device treatment options. Several changes associated with pregnancy, increased blood volume, cardiac output, and heart rate secondary to an increased sympathetic state, facilitate more frequent occurrences of arr...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-015-1232-3

    authors: Friday KP,Moak JP,Fries MH,Iqbal SN

    更新日期:2015-10-01 00:00:00

  • Dual-catheter balloon occlusion aortography in pulmonary atresia with ventricular septal defect and major aorto-pulmonary collaterals.

    abstract::Angiography remains the gold standard in the preoperative evaluation of complex pulmonary blood supply in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries. In neonates, balloon occlusion aortography using a Berman balloon catheter is a very effective technique. H...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-003-0634-9

    authors: Lim JS,Desai T,Stumper O

    更新日期:2004-09-01 00:00:00

  • A triple challenge: thrombocytopenia in a 7-year-old girl with unrepaired d-transposition of the great arteries, ventricular septal defect, and pulmonary hypertension.

    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

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0570-7

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

    更新日期:2013-01-01 00:00:00

  • Patent foramen ovale and left atrial appendage: new devices and methods for closure.

    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

    pub_type: 杂志文章

    doi:10.1007/s00246-005-1011-7

    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

  • Heart transplantation in an infant with rhabdomyoma.

    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

    pub_type: 杂志文章

    doi:10.1007/BF00794197

    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

  • Isolated left-sided scimitar vein connecting all left pulmonary veins to the right inferior vena cava.

    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

    pub_type: 杂志文章

    doi:10.1007/s00246-005-0920-9

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

    更新日期:2005-11-01 00:00:00

  • School-Age Developmental and Educational Outcomes Following Cardiac Procedures in the First Year of Life: A Population-Based Record Linkage Study.

    abstract::The purpose of the study was to evaluate school-age developmental and educational outcomes for children with and without a cardiac procedure in the first year of life to improve understanding of longer-term neurodevelopmental outcomes in children who have had a cardiac procedure for congenital heart disease, the most ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-018-2029-y

    authors: Lawley CM,Winlaw DS,Sholler GF,Martin A,Badawi N,Walker K,Nassar N,Lain SJ

    更新日期:2019-03-01 00:00:00

  • Cardiac regeneration in children.

    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

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-015-1120-x

    authors: Rupp S,Schranz D

    更新日期:2015-04-01 00:00:00

  • Does treatment of patent ductus arteriosus with cyclooxygenase inhibitors affect neonatal regional tissue oxygenation?

    abstract::The effect of patent ductus arteriosus (PDA) treatment with cyclooxygenase (COX) inhibitors (indomethacin [INDO] and ibuprofen [IBU]) on regional oxygenation requires further clarification. The authors hypothesized that both INDO and IBU reduce regional tissue oxygenation in preterm neonates with PDA but that the risk...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0309-5

    authors: Bhatt M,Petrova A,Mehta R

    更新日期:2012-12-01 00:00:00