269 results match your criteria: "Children's Heart Centre[Affiliation]"

Obesity factors into hypertrophic cardiomyopathy (HCM)-related risk as a disease modifying environmental factor. Behaviours such as diet and sleep are seldom reported upon in children with HCM. It was our aim to report on these factors in this population.

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The COVID-19 pandemic had an unprecedented impact on healthcare systems and exists globally. To control pandemic progression, COVID-19 vaccines were developed and licensed for use in the adult population in early 2021 and became available in paediatric cohorts several months later. Since then, several studies have reported adverse events and severe adverse events in the adult and paediatric cohorts.

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Article Synopsis
  • Paediatric hypertrophic cardiomyopathy (HCM) is linked to a higher risk of sudden cardiac death, leading to restrictions on physical activity; this inactivity, combined with rising youth obesity, may negatively impact cardiovascular health in these patients.* -
  • The study involved 56 Canadian HCM patients aged 10-19 and evaluated their cardiovascular health using standardized questionnaires; results showed that many had poor health scores similar to those of the general Canadian youth population.* -
  • Findings indicate a significant number of HCM patients have intermediate or poor cardiovascular health, underscoring the need for targeted interventions to encourage healthier lifestyles and improve overall cardiovascular wellbeing.*
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Article Synopsis
  • Researchers studied children in Ireland admitted to pediatric ICU for COVID-19 or related conditions between January 2020 and August 2022 to understand illness severity and outcomes.
  • Out of 127 children, the majority had acute COVID-19 (68.5%) or Pediatric Inflammatory Multisystem Syndrome (30.7%), with those in the PIMS-TS group requiring more intensive cardiac support.
  • Despite the high incidence of cardiac issues during hospitalization, all patients survived and showed normal heart function upon discharge.
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Pediatric Chronic Heart Failure: Age-Specific Considerations of Medical Therapy.

Physiol Res

November 2024

Children's Heart Centre, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czech Republic.

Chronic heart failure (CHF) is a rare entity in children but carries a burden of high mortality and morbidity. Medical treatment of pediatric CHF is largely based on guidelines for the adult population. In contrast to adults, evidence for the efficacy of medications in treating CHF in children is sparse.

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Vascular Dysfunction Across the Lifespan-Why Cardiovascular Risk Reduction Is Important in Congenital Heart Disease.

Can J Cardiol

January 2025

Faculty of Medicine (Pediatrics), University of British Columbia, Vancouver, Canada; Children's Heart Centre, British Columbia Children's Hospital, Vancouver, Canada. Electronic address: https://twitter.com/KevinHarris.

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Non-invasive pressure-volume loops show high arterial elastance in children with repaired tetralogy of Fallot.

Scand Cardiovasc J

December 2024

Clinical Physiology, Department of Clinical Sciences Lund, Skåne University Hospital, Lund University, Lund, Sweden.

Article Synopsis
  • Children with repaired tetralogy of Fallot (rToF) exhibit distinct changes in left ventricular (LV) function and right ventricular (RV) size compared to healthy peers, including larger RV volumes and smaller LV volumes.
  • The study measured haemodynamic variables using non-invasive techniques, revealing higher arterial elastance and heart rates in children with rToF, suggesting a compensatory response to impaired LV filling.
  • Further research is needed to understand the implications for cardiovascular health and the potential increased risk for adverse events in these patients.
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Optimal Timing of Pulmonary Valve Replacement-The Holy Grail in Tetralogy of Fallot.

Can J Cardiol

December 2024

Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada; Children's Heart Centre, BC Children's Hospital, Vancouver, British Columbia, Canada. Electronic address:

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Implantable cardioverter defibrillators in paediatric patients: yet another example of healthcare divergence?

Europace

August 2024

Boise St. Luke's Pediatric Cardiology, Boise ID and Division of Pediatric Cardiology Department of Pediatrics, Stanford University, Stanford, CA, USA.

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Atrial septal defect closure in children at young age is beneficial for left ventricular function.

Eur Heart J Imaging Methods Pract

January 2024

Clinical Physiology, Department of Clinical Sciences, Lund, Lund University, Box 188, 221 00 Lund, Sweden.

Aims: Atrial septal defects (ASDs) lead to volume-loaded right ventricles (RVs). ASD closure does not always alleviate symptoms or improve exercise capacity, which is possibly explained by impaired left ventricular (LV) haemodynamics. This study evaluated the effect of ASD closure in children using non-invasive LV pressure-volume (PV) loops derived from cardiac magnetic resonance (CMR) imaging and brachial blood pressure, compared with controls.

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The cardiovascular risks of overweight or obesity in childhood but normal weight in adulthood.

Acta Paediatr

October 2024

School of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

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Objectives The coronavirus disease 2019 (COVID-19) pandemic has impacted public health systems and individuals' behaviour, with decreasing survival rates among out-of-hospital cardiac arrest (OHCA) patients. Bystander cardiopulmonary resuscitation (CPR) improves OHCA outcomes, which may have been affected by COVID-19. We sought to understand the impacts of COVID-19 on bystanders' willingness to administer CPR in three Canadian provinces.

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Importance: Congenital heart disease (CHD) is the most common human organ malformation, affecting approximately 1 of 125 newborns globally.

Objectives: Assessing the performance of 2 diagnostic tests using minimal amounts of dried blood spots (DBS) to identify high-risk CHD compared with controls in a Swedish cohort of neonates.

Design, Setting, And Participants: This diagnostic study took place in Sweden between 2019 and 2023 and enrolled full-term babies born between 2005 and 2023.

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Background: Hypertrophic cardiomyopathy is a burdensome condition that inflicts both physical and psychological impairment on those with the disease, negatively impacting health-related quality of life (HRQoL). Given the abundance of evidence suggesting a role of physical activity (PA) in modulating HRQoL in healthy populations of children, we sought to determine the relationship between HRQoL and PA in children diagnosed with hypertrophic cardiomyopathy.

Methods And Results: A multicenter prospective observational cohort study was conducted, with patients with hypertrophic cardiomyopathy aged 10 to 19 years being provided a wrist-worn activity tracker (Fitbit Charge HR) to wear for 14 days.

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Hydraulic force aids diastolic filling of the left ventricle (LV) by facilitating basal movement of the atrioventricular plane. The short-axis atrioventricular area difference (AVAD) determines direction and magnitude of this force. Patients with atrial septal defect (ASD) have reduced LV filling due to the left-to-right shunt across the atrial septum and thus potentially altered hydraulic force.

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A hydraulic force aids diastolic filling of the left ventricle (LV) and is proportional to the difference in short-axis area between the left ventricle and atrium; the atrioventricular area difference (AVAD). Patients with repaired Tetralogy of Fallot (rToF) and pulmonary regurgitation (PR) have reduced LV filling which could lead to a negative AVAD and a hydraulic force impeding diastolic filling. The aim was to assess AVAD and to determine whether the hydraulic force aids or impedes diastolic filling in patients with rToF and PR, compared to controls.

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Infants with concurrent severe hypertriglyceridemia and complex congenital heart disease are a rare occurrence and can have life-threatening consequences when undergoing surgical intervention. This case series outlines two instances involving infants undergoing total anomalous pulmonary venous connection repair and surgical closure of a ventricular septal defect. The study explores troubleshooting the effects of hypertriglyceridemia on perioperative outcomes.

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Article Synopsis
  • Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a serious congenital heart defect, typically existing on its own and rarely linked to other heart issues.
  • The report discusses a successful surgical repair in an infant with a rare combination of ALCAPA, a ventricular septal defect (VSD), and a double aortic arch (DAA).
  • This case is notable as it is only the second documented instance of ALCAPA occurring alongside VSD and DAA in medical literature.
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Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) may cause sudden cardiac death (SCD) despite medical therapy. Therefore, implantable cardioverter-defibrillators (ICDs) are commonly advised. However, there is limited data on the outcomes of ICD use in children.

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Background: Long-term survival after single-ventricle palliation and the effect of dominant ventricle morphology in large, unselected series of patients are scarcely reported.

Methods And Results: This nationwide cohort study included all children undergoing operation with single-ventricle palliation during their first year of life in Sweden between January 1994 and December 2019. Data were obtained from institutional records and assessment of underlying cardiac anomaly and dominant ventricular morphology was based on complete review of medical records, surgical reports, and echocardiographic examinations.

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Deep Learning-Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome.

JAMA Cardiol

April 2024

Center for Cardiovascular Innovation, Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Importance: Congenital long QT syndrome (LQTS) is associated with syncope, ventricular arrhythmias, and sudden death. Half of patients with LQTS have a normal or borderline-normal QT interval despite LQTS often being detected by QT prolongation on resting electrocardiography (ECG).

Objective: To develop a deep learning-based neural network for identification of LQTS and differentiation of genotypes (LQTS1 and LQTS2) using 12-lead ECG.

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Background: There is limited data on the organisation of paediatric echocardiography laboratories in Europe.

Methods: A structured and approved questionnaire was circulated across all 95 Association for European Paediatric and Congenital Cardiology affiliated centres. The aims were to evaluate: (1) facilities in paediatric echocardiography laboratories across Europe, (2) accredited laboratories, (3) medical/paramedical staff employed, (4) time for echocardiographic studies and reporting, and (5) training, teaching, quality improvement, and research programs.

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Article Synopsis
  • - This study explored the long-term outcomes and factors that predict mortality in children under 18 with hypertrophic cardiomyopathy (HCM) associated with various RASopathy syndromes, including Noonan syndrome and others.
  • - Researchers analyzed data from 149 patients over an average follow-up of about 16 years, finding that 15.43% of these children died, with survival rates differing significantly based on the specific RASopathy syndrome.
  • - Key predictors of mortality and sudden cardiac death included the type of RASopathy, symptoms at diagnosis, heart failure presence, and certain heart function measurements, particularly highlighting a milder HCM type within Noonan-like syndrome that still had poorer survival rates.
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Background And Objectives: Extracorporeal membrane oxygenation (ECMO) serves as cardiopulmonary therapy in critically ill patients with respiratory/heart failure and often necessitates multiple blood product transfusions. The administration of platelet transfusions during ECMO is triggered by the presence or risk of significant bleeding. Most paediatric ECMO programmes follow guidelines that recommend a platelet transfusion threshold of 80-100 × 10/L.

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