Physical activity and obesity in children with congenital cardiac disease.

Abstract:

BACKGROUND:Children with congenital cardiac disease experience challenges in developing healthy patterns of physical activity due to decreased exercise capacity and parental fear and confusion about what is permissible. The purpose of this study was to describe physical activity habits in children 10-14 years of age with congenital cardiac disease and the relationship of those habits to obesity as defined by body mass index. METHODS:This cross-sectional study used self-report measures and clinical data to describe the association between physical activity participation and body mass index in 10- to 14-year-old children with congenital cardiac disease. Further, physical activity levels were compared between children who were overweight or obese and those who were not. RESULTS:Children (n = 84; 51 males; 33 females) reported low rates of physical activity compared to reports on healthy children. Only 9.5% were overweight (body mass index between the 85th and 94th percentile), and alarmingly 26% were obese (body mass index at or above the 95th percentile). Physical activity and body mass index were not significantly correlated (r = -0.11, p = 0.45) and there was no significant difference in mean physical activity (t = 0.67) between children who were overweight or obese and those who were not. CONCLUSIONS:Children in this study reported low rates of physical activity and a higher obesity rate than was reported in previous studies. However, the two were not significantly correlated. Further research is indicated to determine the specific factors contributing to obesity and to test interventions to combat obesity in children with congenital cardiac disease.

journal_name

Cardiol Young

journal_title

Cardiology in the young

authors

Ray TD,Green A,Henry K

doi

10.1017/S1047951111000540

subject

Has Abstract

pub_date

2011-12-01 00:00:00

pages

603-7

issue

6

eissn

1047-9511

issn

1467-1107

pii

S1047951111000540

journal_volume

21

pub_type

杂志文章
  • How should we diagnose and differentiate hearts with double-outlet right ventricle?

    abstract::Many, if not most, of the controversies regarding the description of the congenitally malformed heart have been resolved over the turn of the 20th century. A group of lesions that remains contentious is the situation in which both arterial trunks, in their greater part, are supported by the morphologically right ventr...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951116001190

    authors: Bharucha T,Hlavacek AM,Spicer DE,Theocharis P,Anderson RH

    更新日期:2017-01-01 00:00:00

  • Current outcomes of the bi-directional cavopulmonary anastomosis in single ventricle patients: analysis of risk factors for morbidity and mortality, and suitability for Fontan completion.

    abstract:OBJECTIVES:The bi-directional cavopulmonary anastomosis forms an essential staging procedure for univentricular hearts. This review aims to identify risk factors for morbidity, mortality, and suitability for Fontan completion. METHODS:A total of 114 patients undergoing cavopulmonary anastomosis between 1992 and 2012 w...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951115000153

    authors: François K,Vandekerckhove K,De Groote K,Panzer J,De Wolf D,De Wilde H,Bové T

    更新日期:2016-02-01 00:00:00

  • Isolated retroaortic innominate vein and right aortic arch: a case report and review of literature.

    abstract::Retroaortic course of left innominate vein is a rare venous anomaly which is usually associated with CHD. Isolated retroaortic innominate vein is exceedingly rare with only a handful of reported cases. We report an otherwise healthy newborn with isolated retroaortic innominate vein and right aortic arch, a combination...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951119001380

    authors: Kohli U

    更新日期:2019-08-01 00:00:00

  • The role of the cardiologist in the evaluation of dysautonomia.

    abstract::Dysfunction of the autonomic nervous system, or dysautonomia, is an uncommon disease. Postural orthostatic tachycardia syndrome is one of the several types of dysautonomia. Postural orthostatic tachycardia syndrome, also known as chronic orthostatic intolerance, is the most common but least severe of the dysautonomic ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951110001198

    authors: Boris JR

    更新日期:2010-12-01 00:00:00

  • Transcatheter baffle leak closure via an amplatzer septal occluder in a senning-operated child.

    abstract::Senning operation is a surgical treatment for transposition of great arteries that can be complicated by post-procedural atrial or caval baffle leaks. We present a 6-year-old boy with a history of Senning repair for transposition of great arteries, who developed a pulmonary venous baffle leak. Percutaneous baffle leak...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120002255

    authors: Çetiner N,Yıldırım Baştuhan I,Çeliker A

    更新日期:2020-10-01 00:00:00

  • BNP in children with congenital cardiac disease: is there now sufficient evidence for its routine use?

    abstract::Interest in brain natriuretic peptide (BNP) and N-terminal pro-brain natriuretic peptide (NT-proBNP) in the management of children with CHD has increased. There are, however, no current guidelines for their routine use. The aim of this review article is to provide an update on the data regarding the use of BNP/NT-proB...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951114002133

    authors: Cantinotti M,Walters HL,Crocetti M,Marotta M,Murzi B,Clerico A

    更新日期:2015-03-01 00:00:00

  • Is the function of all cardiac valves after the arterial switch operation influenced by an associated ventricular septal defect?

    abstract::A ventricular septal defect in transposition of the great arteries is frequently closely related to the cardiac valves. The valvar function after arterial switch operation of patients with transposition of the great arteries and ventricular septal defect or intact ventricular septum was compared. We analysed the funct...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111000084

    authors: Gabriel J,Scheld HH,Tjan TD,Osada N,Krasemann T

    更新日期:2011-08-01 00:00:00

  • Repair of tetralogy of Fallot associated with atrioventricular septal defect.

    abstract::Tetralogy of Fallot, when associated with atrioventricular septal defect permitting shunting at ventricular level, represents a complex cyanotic congenital malformation. Experience with surgical repair is limited, and results vary considerably. Between 1984 and 1996, we repaired 14 consecutive patients with this combi...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951100004728

    authors: Tláskal T,Hucín B,Kostelka M,Chaloupecký V,Marek J,Tax P,Janouàek J,Kuèera V,Hruda J,Reich O,Skovránek J

    更新日期:1998-01-01 00:00:00

  • Management of late presentation congenital heart disease.

    abstract::In many parts of the world, mostly low- and middle-income countries, timely diagnosis and repair of congenital heart diseases (CHDs) is not feasible for a variety of reasons. In these regions, economic growth has enabled the development of cardiac units that manage patients with CHD presenting later than would be idea...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951117002591

    authors: Iyer PU,Moreno GE,Fernando Caneo L,Faiz T,Shekerdemian LS,Iyer KS

    更新日期:2017-12-01 00:00:00

  • Factors prolonging length of stay in the cardiac intensive care unit following the arterial switch operation.

    abstract::The arterial switch operation has become the preferred procedure for surgical management of transposition, defined on the basis of concordant atrioventricular and discordant ventriculo-arterial connections. We conducted a retrospective evaluation of our experience in 61 infants with this segmental combination, seen fr...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951107001746

    authors: Wheeler DS,Dent CL,Manning PB,Nelson DP

    更新日期:2008-02-01 00:00:00

  • Intraoperative rescue by placement of a stent following a surgical coronary arterial injury in a child.

    abstract::An acute injury to a coronary artery was recognized during the surgical construction of the Fontan circulation. Surgical manipulation of the site of injury was not successful in restoring normal myocardial blood flow. A stent was therefore placed intraoperatively under direct vision, with restoration of normal coronar...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951104001180

    authors: Duncan WJ,LeBlanc JG,Human DG

    更新日期:2004-02-01 00:00:00

  • Severe airway obstruction from a bronchial cast after cardiac transplantation.

    abstract::Plastic bronchitis is a rare and difficult to treat disease process in patients with congenital heart disease. Cardiac transplantation has been used increasingly to reverse this process, especially in single ventricle physiology. This case report demonstrates a foreseeable complication after cardiac transplantation in...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951113001066

    authors: Parent JJ,Darragh RK

    更新日期:2014-08-01 00:00:00

  • Asymmetrically short tendinous cords causing congenital tricuspid regurgitation: improved understanding of tricuspid valvar dysplasia in the era of color flow echocardiography.

    abstract:BACKGROUND:Tricuspid regurgitation as a manifestation of an isolated congenital anomaly of the tricuspid valve is rare. Cross-sectional and color Doppler echocardiography allow improved evaluation of tricuspid valvar function. As a result, the heterogeneous category of congenital tricuspid valvar dysplasia may be bette...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951100004972

    authors: McElhinney DB,Silverman NH,Brook MM,Hanley FL,Stanger P

    更新日期:1999-05-01 00:00:00

  • Thoracoscopic treatment of left-to-right shunt in a child with scimitar syndrome.

    abstract::Scimitar syndrome represents a rare variant of partial anomalous pulmonary venous connection with right lung hypoplasia, dextrocardia, and concomitant airway-vessel abnormalities. Surgical correction is preferred in symptomatic patients or in patients with increased left-to-right shunt. In this report, the first case ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951117001603

    authors: Dokumcu Z,Divarci E,Erdener A

    更新日期:2018-01-01 00:00:00

  • Role of toxicological determinations of amphetamines and cannabinoids in hair of adolescent patients in cardiologic diagnostic management.

    abstract:BACKGROUND:Parental suspicions that the child may possibly take narcotics may be substantiated by hair analysis, which may not only identify the narcotic abuse profile, but also define the minimum period of narcotic usage. OBJECTIVE:A toxicological hair analysis aiming at detecting the presence of amphetamines and can...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111000667

    authors: Kłys M,Szydłowski L,Rojek S

    更新日期:2012-02-01 00:00:00

  • Are children with protein-losing enteropathy after the Fontan operation at increased risk of cytomegalovirus enteropathy? A report of two cases.

    abstract:INTRODUCTION:Aetiology of protein-losing enteropathy in single-ventricle type CHD is multi-factorial. REPORT:We describe two Fontan patients with protein-losing enteropathy who presented with cytomegalovirus-associated colitis. DISCUSSION:Fontan patients display risk factors for cytomegalovirus-induced gastroenteropa...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120000049

    authors: Bauer C,Tulzer G

    更新日期:2020-03-01 00:00:00

  • Significance of red cell distribution width in the differential diagnosis between neurally mediated syncope and arrhythmic syncope in children.

    abstract:OBJECTIVES:The aim of the present study was to explore the predictive value of red cell distribution width as a means to differentiate between neurally mediated syncope and arrhythmic syncope in children. METHOD:Patients were divided into a neurally mediated syncope group (n=72) and an arrhythmic syncope group (n=21) ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116001098

    authors: Zhang Q,Li Y,Liao Y,Du J

    更新日期:2017-05-01 00:00:00

  • Time course of appearance of markers of arrhythmia in patients with tetralogy of Fallot before and after surgery.

    abstract::Sudden death and ventricular tachycardia are known to occur late after correction of tetralogy of Fallot. Abnormal dispersion of the QT interval, ventricular late potentials, and prolongation of the QRS complex, alone or in combination, are useful markers of the risk for such complications. Our present prospective stu...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951104004020

    authors: Balkhi RA,Beghetti M,Friedli B

    更新日期:2004-08-01 00:00:00

  • Comparative risk of cardiac catheterisations performed on low birth weight neonates.

    abstract::To determine whether cardiac catheterisation procedures for low birth weight neonatesr < or = 2.5 kg carries a greater risk of complications compared with neonates > 2.5 kg, we conducted a single-centre retrospective case–control study. From 01/03 to 01/09, 46 consecutive neonates < 2.5 kg at the time of cardiac cathe...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951112002247

    authors: Mobley MM,Stroup RE,Kaine SF

    更新日期:2013-10-01 00:00:00

  • Balloon angioplasty is preferred to surgery for aortic coarctation.

    abstract:OBJECTIVE:We sought to use techniques of decision analysis to compare values or preferences for balloon angioplasty versus surgery for treatment of aortic coarctation in children. BACKGROUND:Balloon angioplasty and surgery for aortic coarctation have a differing spectrum and prevalence of outcomes and complications, m...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,meta分析,评审

    doi:10.1017/S1047951107001795

    authors: Wong D,Benson LN,Van Arsdell GS,Karamlou T,McCrindle BW

    更新日期:2008-02-01 00:00:00

  • Anomalous origin of the pulmonary artery from the aorta: early diagnosis and repair leading to immediate physiological correction.

    abstract:INTRODUCTION:Anomalous origin of one pulmonary artery from the ascending aorta is a rare cardiac anomaly in which the pulmonary artery abnormally arises from the ascending aorta. Physiologically, most patients develop signs of cardiac failure due to high flow to both lungs, with systemic or supra-systemic pressures in ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951110000892

    authors: Amir G,Frenkel G,Bruckheimer E,Dagan T,Katz J,Berant M,Vidne B,Birk E

    更新日期:2010-12-01 00:00:00

  • Aortic dilatation in patients with Turner's syndrome without structural cardiac anomaly.

    abstract:INTRODUCTION:Dilatation of the ascending aorta is described in Turner's syndrome with variable prevalence (6.8-32%). Reported series typically include patients with associated cardiac anomalies. OBJECTIVE:To characterise the prevalence, age of onset, and the progress of dilatation of the ascending aorta in Turner's sy...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951115000682

    authors: Alami Laroussi N,Dahdah N,Dallaire F,Thérien J,Fournier A

    更新日期:2016-03-01 00:00:00

  • Mild or subclinical intravascular haemolysis subsequent to transcatheter occlusion of the patent arterial duct.

    abstract::One of the important complications of transcatheter occlusion of the patent duct by insertion of either the Rashkind double umbrella or coil devices is intravascular haemolysis, particularly the severe form which occurs in 0.5-0.6% of cases. The incidence of subclinical or mild intravascular haemolysis including morph...

    journal_title:Cardiology in the young

    pub_type: 临床试验,杂志文章

    doi:10.1017/s1047951100007393

    authors: Jamjureeruk V,Kirawittaya T,Ningsnondh V

    更新日期:1999-01-01 00:00:00

  • Extended survival and re-hospitalisation among paediatric patients requiring extracorporeal membrane oxygenation for primary cardiac dysfunction.

    abstract:BACKGROUND:Although survival to hospital discharge among children requiring extracorporeal membrane oxygenation support for medical and surgical cardio-circulatory failure has been reported in international registries, extended survival and re-hospitalisation rates have not been well described in the literature. MATER...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951112000777

    authors: Erwin N,Zuk J,Kaufman J,Pan Z,Carpenter E,Mitchell MB,da Cruz EM

    更新日期:2013-04-01 00:00:00

  • Stenting across head and neck vessels using covered stents for persisting aortic arch obstruction.

    abstract:OBJECTIVE:To describe endovascular stent placement using partially covered stents to preserve flow in head and neck vessels. BACKGROUND:Endovascular stent placement has become established as a first-line therapy for native coarctation of the aorta or re-coarctation in older children and adults. Increasingly covered st...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951112000236

    authors: Bentham JR,Oswal N,Yates R

    更新日期:2012-10-01 00:00:00

  • Ventricular tachycardia secondary to prolongation of the QT interval in a fetus with autoimmune mediated congenital complete heart block.

    abstract::We report a case where fetal echocardiography identified both complete heart block and ventricular tachycardia. The mother tested positive for anti-Ro antibodies. Prenatal detection of this unusual combination of arrhythmias prompted early postnatal evaluation, which revealed prolongation of the QT interval. Autoimmun...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951105000673

    authors: Duke C,Stuart G,Simpson JM

    更新日期:2005-06-01 00:00:00

  • Fever without a source in children with congenital heart disease.

    abstract::Two paediatric congenital heart disease patients presented with a brief history of low-grade fever without any focal symptoms. Their clinical features and laboratory tests were unremarkable; however, their blood cultures were positive that prompted further work-up. Infective endocarditis should be considered in any pa...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S104795112000195X

    authors: DonaireGarcia A,Burke B,Latifi SQ,Agarwal HS

    更新日期:2020-09-01 00:00:00

  • Counselling strategies for parents of infants with congenital heart disease.

    abstract::Congenital heart disease is a significant cause of morbidity and mortality in the newborn. Its diagnosis may lead to a crisis in the affected families; there are the perceived implications of having an abnormality of so vital an organ. To that may be added the assumed guilt or blame, grief and at times anger, frequent...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/s104795110000696x

    authors: Menahem S

    更新日期:1998-07-01 00:00:00

  • Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) and acute pulmonary hypertension post cardiopulmonary bypass in children with congenital cardiac diseases.

    abstract:BACKGROUND:Intra-cardiac repair of congenital cardiac diseases in children with left-right shunt is often associated with acute elevation of pulmonary artery pressure following cardiopulmonary bypass. We studied the correlation between the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and pulmona...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951110001630

    authors: Loukanov T,Hoss K,Tonchev P,Klimpel H,Arnold R,Sebening C,Karck M,Gorenflo M

    更新日期:2011-04-01 00:00:00

  • Involvement of patients and parents in research undertaken by the Australian and New Zealand Fontan Registry.

    abstract::Research that is closely connected with the population it is studying and in which the translational value to healthcare is high is a laudable goal, but it is not often achieved. The Australian and New Zealand Fontan Registry has developed a model for involving patients and parents of children with a Fontan circulatio...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951117001494

    authors: d'Udekem Y,Forsdick V,du Plessis K

    更新日期:2018-04-01 00:00:00