Double right coronary artery and its clinical implications.

Abstract:

:Congenital anomalies of the coronary arteries are present in 0.2-1.4% of the general population. These anomalies represent one of the most confusing issues in the field of cardiology and challenges for interventional cardiologists and cardiac surgeons if the anomalies are unrecognised. Double right coronary artery is one of the rarest coronary arteries. Previously, the probability of developing atherosclerotic changes in patients with a double right coronary artery was considered to be equal to that in those without it. In reality, however, a high prevalence of atherosclerotic coronary artery disease was found in patients with a double right coronary artery originating from a single ostium after our comprehensive literature search through the PubMed database. Owing to the fact that double right coronary artery is both a congenital and potentially atherosclerotic coronary artery disease at diagnosis, coronary intervention or cardiac operation is more complicated than previously believed. Individuals with a double right coronary artery may be unaware of its presence until an accidental finding during coronary angiography or cardiac operation and are at risk for unsuspected complications of atherosclerotic coronary artery disease or during cardiac operation. Therefore, it is important to obtain information on the anatomic variants of this congenital coronary anomaly in patients who are undergoing either coronary intervention, aortic root operation or myocardial revascularisation. To our knowledge, this is the first comprehensive article to discuss the anomalies and their clinical implications.

journal_name

Cardiol Young

journal_title

Cardiology in the young

authors

Chien TM,Chen CW,Chen HM,Lee CS,Lin CC,Chen YF

doi

10.1017/S1047951113000176

subject

Has Abstract

pub_date

2014-02-01 00:00:00

pages

5-12

issue

1

eissn

1047-9511

issn

1467-1107

pii

S1047951113000176

journal_volume

24

pub_type

杂志文章,评审
  • Kawasaki disease with tsutsugamushi disease: two case reports.

    abstract::A number of microorganisms were hypothesised as an aetiology of the Kawasaki disease. Unfortunately, no specific agent that provides reproducible evidence has yet been reported. We report two cases of extremely rare Kawasaki disease with tsutsugamushi disease. These case reports suggest that Kawasaki disease can rarel...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120000931

    authors: Hwang HS,Kim YJ,Song MS

    更新日期:2020-06-01 00:00:00

  • Coarctation of the aorta in dizygotic twins.

    abstract::The incidence of congenital heart disease is higher in monozygotic than dizygotic twins, with a higher concordance rate. Although coarctation of the aorta has previously been reported in monozygotic twins, to the best of our knowledge it has not been described in dizygotic twins. We report here such a concurrence in d...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951100006375

    authors: Caldas M,Dhillon R

    更新日期:2000-01-01 00:00:00

  • An echocardiographic study of tetralogy of Fallot in the fetus and infant.

    abstract:OBJECTIVE:To document the echocardiographic features of tetralogy of Fallot during fetal and postnatal life. Correlation of echocardiographic findings with the requirement for early intervention prior to definitive repair. DESIGN:Retrospective observational study. SETTING:A tertiary fetal cardiology unit. PATIENTS:F...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:

    authors: Pepas LP,Savis A,Jones A,Sharland GK,Tulloh RM,Simpson JM

    更新日期:2003-06-01 00:00:00

  • Outcome for patients with isolated atrial septal defects in the oval fossa diagnosed in infancy.

    abstract:OBJECTIVE:Our aim was to investigate the change in diameter of holes within the oval fossa, and the role of aneurismal formation in reducing the size of the hole, in patients diagnosed during infancy with isolated defects in the floor of the fossa. PATIENTS:In a retrospective study, we included 100 patients diagnosed ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951107001692

    authors: Demir T,Oztunç F,Eroğlu AG,Saltik L,Ahunbay G,Kutluğ S,Güzeltaş A,Altun G

    更新日期:2008-02-01 00:00:00

  • Characteristics and outcomes of children with congenital heart disease needing diaphragm plication.

    abstract:BACKGROUND:Diaphragm dysfunction following surgery for congenital heart disease is a known complication leading to delays in recovery and increased post-operative morbidity and mortality. We aimed to determine the incidence of and risk factors associated with diaphragm plication in children undergoing cardiac surgery a...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,多中心研究

    doi:10.1017/S1047951119002671

    authors: Foster CB,Cabrera AG,Bagdure D,Blackwelder W,Moffett BS,Holloway A,Mishcherkin V,Bhutta A

    更新日期:2020-01-01 00:00:00

  • Extensive coronary and systemic arterial aneurysm development in severe refractory Kawasaki disease.

    abstract::We describe the case of an 8-week-old infant with late presentation of severe refractory atypical Kawasaki disease. In addition to developing giant coronary arterial aneurysms and coronary thrombosis, she formed extensive bilateral arterial aneurysms throughout her systemic circulation. ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116001967

    authors: Johnston N,Coleman D,McMahon CJ

    更新日期:2017-03-01 00:00:00

  • Developmental considerations with regard to so-called absence of the leaflets of the arterial valves.

    abstract:BACKGROUND:Absent arterial valve leaflets are rare anomalies. On the basis of our understanding of the normal development of the arterial valves, we draw inferences that might offer clues to their morphogenesis. METHODS:We describe the findings from four human fetal autopsies with so-called "absent" arterial valvar le...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116000524

    authors: Tretter JT,Steffensen T,Westover T,Anderson RH,Spicer DE

    更新日期:2017-03-01 00:00:00

  • Ultrasound assessment of mesenteric blood flow in neonates with hypoplastic left heart before and after hybrid palliation.

    abstract:BACKGROUND:Altered mesenteric perfusion may be a contributor to the development of necrotising enterocolitis in patients with hypoplastic left heart syndrome. The goal of this study was to document mesenteric flow patterns in patients with hypoplastic left heart syndrome pre- and post-hybrid procedure. METHODS:A prosp...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951114001607

    authors: Cozzi CT,Galantowicz M,Cheatham JP,Nicholson L,Fernandez R,Backes CH,McCaw C,Cua CL

    更新日期:2015-08-01 00:00:00

  • Levels of vasopressin in children undergoing cardiopulmonary bypass.

    abstract:OBJECTIVES:It is accepted treatment to give vasopressin to adults in postcardiotomy shock, but such use in children is controversial. Cardiopulmonary bypass is presumed to attenuate the normal endogenous vasopressin response to shock. We hypothesized that levels of vasopressin in children are altered by bypass, and tha...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951108001881

    authors: Morrison WE,Simone S,Conway D,Tumulty J,Johnson C,Cardarelli M

    更新日期:2008-04-01 00:00:00

  • Family history of associated disorders in patients with postural tachycardia syndrome.

    abstract:INTRODUCTION:Postural tachycardia syndrome is more frequently being recognised in adolescents and adults. However, its pathophysiology remains undefined. We evaluated our database for patterns in family history of clinical symptoms and associated disorders in these patients. MATERIALS AND METHODS:Patients with postura...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120000165

    authors: Boris JR,Huang J,Shuey T,Bernadzikowski T

    更新日期:2020-03-01 00:00:00

  • Atrioventricular valve repair along with Fontan completion.

    abstract::Atrioventricular valve regurgitation is widely known as a risk factor for Fontan completion in patients with univentricular physiology. To date, indications and timing for atrioventricular valve repair remain unclear and different surgical techniques have been advocated. Since 2013, 50 consecutive patients underwent e...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951114002352

    authors: Gil-Jaurena JM,González-López MT,Pérez-Caballero R,Pita A

    更新日期:2015-10-01 00:00:00

  • An evaluation of heart rate variability and its modifying factors in children with type 1 diabetes.

    abstract:OBJECTIVE:To evaluate heart rate variability by Holter monitoring in type 1 diabetic children compared with a healthy control group and determine the factors modifying heart rate variability. METHODS:This was designed as a prospective study comparing 28 patients, diagnosed with type 1 diabetes and under follow-up, wit...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951113001224

    authors: Özgür S,Ceylan Ö,Şenocak F,Örün UA,Doğan V,Yılmaz O,Keskin M,Aycan Z,Okutucu S,Karademir S

    更新日期:2014-10-01 00:00:00

  • Effects of chronic treprostinil treatment on experimental right heart hypertrophy and failure.

    abstract:BACKGROUND:Right heart function is an important predictor of morbidity and mortality in pulmonary arterial hypertension and many CHD. We investigated whether treatment with the prostacyclin analogue treprostinil could prevent pressure overload-induced right ventricular hypertrophy and failure. METHODS:Male Wistar rats...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116000160

    authors: Axelgaard S,Holmboe S,Ringgaard S,Hillgaard TK,Andersen S,Hansen MS,Andersen A,Nielsen-Kudsk JE

    更新日期:2017-01-01 00:00:00

  • Critical coarctation in an extremely low birth weight pre-term infant.

    abstract::Neonatal interventions for critical aortic coarctation may be associated with considerable morbidity and mortality if the patient is extremely premature. We report the successful treatment of critical coarctation in a 25-week, 740-gram infant using initial clipping of the duct until continued prostaglandin E1 infusion...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111000679

    authors: Bialkowski A,Baden W,Franz AR,Poets CF,Hofbeck M,Ziemer G

    更新日期:2012-02-01 00:00:00

  • Single right coronary artery with right ventricular fistula and congenital absence of left coronary artery: an extremely rare combination.

    abstract::We report an extremely rare case of a 14-month-old girl who was diagnosed with a single right coronary artery with coronary artery fistula communicating with the right ventricle and congenital absence of left coronary artery. Angiography showed a dilated and tortuous single right coronary artery draining into the righ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951119002105

    authors: Yoldaş T,Beyazal M,Örün UA

    更新日期:2019-11-01 00:00:00

  • Fetal echocardiographic features of twisted atrioventricular connections.

    abstract::We present an example of corrected transposition with twisted discordant atrioventricular connections in which both fetal and postnatal echocardiograms were obtained. We correlate the fetal echocardiograms with the postnatal echocardiograms, placing emphasis on the echocardiographic clues to the diagnosis which were p...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951100009732

    authors: Abdullah M,Yoo SJ,Hornberger L

    更新日期:2000-10-01 00:00:00

  • A premature low-birth-weight infant with congenital complete atrioventricular block and myocarditis successfully treated by staged pacemaker implantation.

    abstract::Congenital complete atrioventricular block is a known lethal condition. Although antenatal diagnosis and the technical advances of pacemaker treatment have reduced its mortality, treatment of premature babies with significant myocardial damage remains a challenge. In this paper, we report the case of a premature low-b...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116000433

    authors: Fujioka T,Nii M,Tanaka Y

    更新日期:2016-06-01 00:00:00

  • Neo-aortic valvar function after the arterial switch.

    abstract:OBJECTIVES:The purpose of our study was to assess the prevalence and progression, during childhood and adolescence, of dilation of the neo-aortic root, and neo-aortic valvar regurgitation, and to identify risk factors for such dilation and regurgitation, after the arterial switch operation. METHODS:We included all pat...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951106000953

    authors: Marino BS,Wernovsky G,McElhinney DB,Jawad A,Kreb DL,Mantel SF,van der Woerd WL,Robbers-Visser D,Novello R,Gaynor JW,Spray TL,Cohen MS

    更新日期:2006-10-01 00:00:00

  • What is the diagnostic value of the paediatric exercise tolerance test? Results from a UK centre.

    abstract::Purpose The aim of this study was to determine whether the exercise tolerance test can provide diagnostic and prognostic information regarding children and young adults and help predict outcome. METHODS:A total of 87 patients, aged 7-29 years (median 13, mean 13.4) were selected retrospectively. They underwent exerci...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951117000233

    authors: Sajnach-Menke MA,Walpole SC

    更新日期:2017-09-01 00:00:00

  • How implantable cardioverter-defibrillators work and simple programming.

    abstract::Following the sudden death of a friend in 1966, Dr Michel Mirowski began pioneering work on the first implantable cardioverter-defibrillator. By 1969 he had developed an experimental model and performed the first transvenous defibrillation. In 1970 he reported on the use of a "standby automatic defibrillator" that was...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951116002353

    authors: Bryant RM

    更新日期:2017-01-01 00:00:00

  • Radiofrequency catheter ablation of atrial tachyarrhythmias after an atrial switch operation in a patient with univentricular heart combined with transposition of the great arteries.

    abstract::A 31-year-old patient previously underwent a Mustard operation presented with palpitations. Atrial tachycardia and paroxysmal atrial fibrillation were documented on the surface electrocardiogram. Under the guidance of a three-dimensional electroanatomic mapping system, ablation of the isolated left-sided pulmonary vei...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951114001851

    authors: Ban JE,Park SW,Kim YH

    更新日期:2015-08-01 00:00:00

  • Severe tortuosity and stenosis of the systemic, pulmonary and coronary vessels in 12 patients with similar phenotypic features: a new syndrome?

    abstract::We describe what is, to the best of our knowledge, a previously unreported association in patients with similar facial features, skin and joint laxity, of lengthening and tortuosity of systemic, pulmonary and coronary vessels. We evaluated 12 patients with similar phenotypes, from eight different families. Detailed ec...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951100008854

    authors: Al Fadley F,Al Manea W,Nykanen DG,Al Fadley A,Bulbul Z,Al Halees Z

    更新日期:2000-11-01 00:00:00

  • Dilated cardiomyopathy due to premature ductus arteriosus constriction.

    abstract::Herein, we present the first case of dilated cardiomyopathy due to premature constriction of the ductus arteriosus. A fetal echocardiography showed narrowing in the ductus arteriosus, and colour Doppler flow mapping could not identify blood flow through the ductus. Neonatal echocardiography revealed a left ventricular...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951118001002

    authors: Okada S,Muneuchi J,Iwaya Y

    更新日期:2018-09-01 00:00:00

  • A new approach to hypoplastic left heart syndrome with an intact atrial septum.

    abstract::An intact atrial septum places infants with hypoplasia of the left heart into a group with an extremely high rate of mortality. We report a neonate, diagnosed antenatally, who was delivered by Caesarian section in the cardiac theatre, urgently placed onto cardiopulmonary bypass, and who then underwent an atrial septec...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951107000819

    authors: Barker C,Moscuzza F,Anderson D

    更新日期:2007-08-01 00:00:00

  • A rare association of major aorto-pulmonary collaterals with right isomerism and totally anomalous pulmonary venous drainage.

    abstract::A female neonate, born at term, presented with complex cardiac anatomy dominated by right isomerism and infra-diaphragmatic totally anomalous pulmonary venous connection. Surgical repair was performed using circulatory arrest under deep hypothermia. In the postoperative period, the patient could not be weaned off mech...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951105001836

    authors: Kumar S,Ansari J,Weerasena N

    更新日期:2005-12-01 00:00:00

  • Individual and joint effects of genetic polymorphisms in microRNA-machinery genes on congenital heart disease susceptibility.

    abstract::Single-nucleotide polymorphisms in miRNA-machinery genes may alter the biogenesis of miRNAs affecting disease susceptibility. In this case-control study, we aimed to evaluate the impact of three single-nucleotide polymorphisms (DICER rs1057035, DROSHA rs10719, and XPO5 rs11077) and their combined effect in a genetic r...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120004874

    authors: Borghini A,Vecoli C,Mercuri A,Turchi S,Andreassi MG

    更新日期:2021-01-11 00:00:00

  • Aortic rupture during stenting for recurrent aortic coarctation in an adult: live-saving, emergency, NuDEL all-in-one covered stent implantation.

    abstract::We report a case of successful, life-saving implantation of a covered Cheatham Platinum stent, an all-in-one NuDEL catheter system, in an adult with aortic rupture after bare-metal stenting for re-coarctation of the aorta. ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951117000142

    authors: Eicken A,Georgiev S,Ewert P

    更新日期:2017-08-01 00:00:00

  • Closure of a secundum atrial septal defect in two infants with chronic lung disease using the Gore HELEX Septal Occluder.

    abstract::Children with a secundum atrial septal defect are usually asymptomatic and are referred for elective closure after 3-4 years of age; however, in premature infants with chronic lung disease, bronchopulmonary dysplasia, or pulmonary hypertension, increased pulmonary blood flow secondary to a left-to-right atrial shunt, ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951114002650

    authors: Zussman ME,Freire G,Cupp SD,Stapleton GE

    更新日期:2016-01-01 00:00:00

  • Systemic hypertension in an infant with unrepaired tetralogy of Fallot: case report.

    abstract::Patients with severe right ventricular outflow tract obstruction in tetralogy of Fallot typically have right-to-left shunting, resulting in low pulmonary blood flow and cyanosis. Here we present the case of an infant with tetralogy of Fallot and severe pulmonary valve stenosis, complicated by systemic hypertension, th...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951112001837

    authors: Khoury M,Kallile M,May J,Punn R

    更新日期:2013-10-01 00:00:00

  • Factors affecting vascular access complications in children undergoing congenital cardiac catheterization.

    abstract:BACKGROUND:Complications at the vascular access sites are among the most common adverse events in congenital cardiac catheterization. The use of small-gauge catheters may reduce these events; however, other factors can contribute to the development of vascular complications. OBJECTIVES:To determine factors associated ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111000989

    authors: Roushdy AM,Abdelmonem N,El Fiky AA

    更新日期:2012-04-01 00:00:00