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Journal of the American Heart Association, Ahead of Print. The increasing prevalence of atrial fibrillation (AF) in adults with congenitalheartdisease raises significant questions regarding its management. Emerging imaging modalities and ablation techniques might have a role to play.
Circulation, Ahead of Print. Over the past decade, new research has advanced scientific knowledge of neurodevelopmental trajectories, factors that increase neurodevelopmental risk, and neuroprotective strategies for individuals with congenitalheartdisease.
Circulation, Ahead of Print. With continued medical and surgical advancements, most children and adolescents with congenitalheartdisease are expected to survive to adulthood.
Journal of the American Heart Association, Ahead of Print. BackgroundFontan circulation (FC) in complex congenitalheartdisease is characterized by altered hemodynamics and associated with Fontanassociated liver disease.
Circulation, Ahead of Print. Wearable biosensors (wearables) enable continual, noninvasive physiologic and behavioral monitoring at home for those with pediatric or congenitalheartdisease. Wearables allow patients to access their personal data and monitor their health.
More than a decade of new knowledge about neurodevelopmental risk in people with congenitalheartdisease has changed the thinking about who is most at risk and the factors that impact neurological development, learning, emotions and behaviors, according to a new American Heart Association statement published in Circulation.
Cardiac device therapy is frequently required for individuals with adult congenitalheartdisease (ACHD), whether it be for bradyarrhythmia, ventricular tachyarrhythmia, or cardiac resynchronization therapy (CRT).
In fact the Circulation article cited is on Complete Transposition of the Great Vessels. All these features together in a cyanotic congenitalheartdisease is characteristic of tricuspid atresia. The sign has been described in VSD with biventricular hypertrophy in children.
Circulation, Volume 150, Issue Suppl_1 , Page A4147236-A4147236, November 12, 2024. Background/Introduction:Adults with congenitalheartdisease have higher rates of anxiety, depression, and suicide, compared to those without congenitalheartdisease.
Circulation: Cardiovascular Interventions, Ahead of Print. BACKGROUND:Current metrics used to adjust for case mix complexity in congenital cardiac catheterization are becoming outdated due to the introduction of novel procedures, innovative technologies, and expanding patient subgroups.
Journal of the American Heart Association, Ahead of Print. BackgroundThe Fontan operation is the current standard of care for singleventricle congenitalheartdisease. Almost all patients with Fontan operation develop liver fibrosis at a young age, known as Fontanassociated liver disease (FALD).
Objective To evaluate for correlation between exercise capacity as assessed by peak oxygen consumption (pVO 2 ) measurement during a cardiopulmonary exercise test (CPET) and smartwatches reporting this parameter in patients with adult congenitalheartdisease (ACHD) complex lesions.
Circulation: Cardiovascular Interventions, Ahead of Print. Background:Neonates with complex congenitalheartdisease and pulmonary overcirculation have been historically treated surgically. However, subcohorts may benefit from less invasive procedures. kilograms [IQR, 2.1–3.3])
Circulation: Genomic and Precision Medicine, Volume 16, Issue 5 , Page 415-420, October 1, 2023. BACKGROUND:Rapid genome sequencing (rGS) has been shown to improve care of critically ill infants.
Introduction:Fontan surgery performed during childhood enhances the lifespan and quality of life of patients with critical congenitalheartdisease. Post-Fontan circulation may impact function in multiple organ systems, but its long term effects on the brain microvasculature are not well characterized.
Transpulmonary exosomal miRs offer valuable insights into pulmonary circulation microenvironments. Exosomes containing microRNAs (miRs) have emerged as a novel biomarker.
Patients with pulmonary hypertension associated with a left-right shunt include a wide spectrum of pathophysiological substrates, ranging from those characterized by pulmonary over-circulation to those with advanced pulmonary vascular disease.
Circulation: Cardiovascular Interventions, Ahead of Print. Background:There are limited data about changes in cardiac function (cardiac reverse remodeling) and heart failure indices after transcatheter tricuspid valve-in-valve replacement (TT-VIVR).
Circulation, Ahead of Print. Pathogeneses include connective tissue disorders, smooth muscle contraction disorders, and congenitalheartdisease, including bicuspid aortic valve, among others. The American Heart Association has published guidelines for diagnosis and management of thoracic aortic disease.
tim.hodson Mon, 03/17/2025 - 14:56 March 17, 2025 Being born with a heart defect may be associated with an increased cancer risk for babies and their moms, according to new research published today in the American Heart Associations flagship journal Circulation. are forms of congenitalheart defects (CHD).
Circulation, Ahead of Print. Environmental toxicants and pollutants are causes of adverse health consequences, including well-established associations between environmental exposures and cardiovascular diseases.
Circulation: Cardiovascular Imaging, Ahead of Print. Disorders of the pulmonic valve (PV) receive considerably less attention than other forms of valvular heartdisease.
Circulation, Volume 150, Issue Suppl_1 , Page A4146967-A4146967, November 12, 2024. Objectives:Physically active lifestyles are important for patients with congenitalheartdisease, including Fontan.
Transcript of video: Hypoplastic Left Heart Syndrome is a very severe form of congenitalheartdisease, in which, the left ventricle, aorta and mitral and aortic valves are hypoplastic and valves may be atretic as well. This is diagrammatic representation of hypoplastic left heart syndrome.
In preparation for the ABIM Cardiovascular Disease exam, check out the BoardVitals Cardiology Board Review Question Bank and we’ll make sure you’re well versed in the following 13 areas covered on the exam: Multiple-Choice Component Arrhythmias 15% Coronary Artery Disease 23% Heart Failure and Cardiomyopathy 17% Valvular Disease 15% Pericardial (..)
Circulation: Cardiovascular Imaging, Ahead of Print. METHODS:Retrospective study of adults with congenitalheartdisease who underwent AVR at Mayo Clinic (20032023). METHODS:Retrospective study of adults with congenitalheartdisease who underwent AVR at Mayo Clinic (20032023).
Circulation, Volume 150, Issue Suppl_1 , Page A4139192-A4139192, November 12, 2024. Background:Asynchronous remote patient monitoring (RPM) is increasingly common in healthcare models for infants with congenitalheartdisease (CHD).
Circulation, Volume 150, Issue Suppl_1 , Page A4134622-A4134622, November 12, 2024. Background:Pregestational diabetes is an established risk factor for congenitalheartdisease (CHD), including heterotaxy syndrome, which results from abnormal left-right (L-R) axis.
Circulation, Volume 150, Issue Suppl_1 , Page A4146466-A4146466, November 12, 2024. Background:Without timely intervention, pressure-overloading left ventricular (poLV) remodeling may become progressive and readily degenerate into heart failure.
Circulation: Arrhythmia and Electrophysiology, Ahead of Print. BACKGROUND:A growing number of patients with tetralogy of Fallot develop left ventricular systolic dysfunction and heart failure, in addition to right ventricular dysfunction. years) with tetralogy of Fallot and CRT were enrolled.
Circulation: Cardiovascular Interventions, Ahead of Print. BACKGROUND:Maldistribution of pulmonary blood flow in patients with congenitalheartdisease impacts exertional performance and pulmonary artery growth.
Circulation, Volume 150, Issue Suppl_1 , Page A4147910-A4147910, November 12, 2024. A single study has shown this translates to humans with 22q11 and structurally normal hearts. Background:Individuals with 22q11 deletion syndrome have a mutation in the TBX1 gene which is associated with the formation of cardiac outflow tracts.
Circulation, Ahead of Print. BACKGROUND:The United Network of Organ Sharing made changes to the priority for allocation of hearts for transplantation (HT) in 2016 for pediatric patients and 2018 for adult patients.
Circulation: Genomic and Precision Medicine, Ahead of Print. BACKGROUND:Genetic disorders are prevalent in patients with congenitalheartdisease (CHD), but genetic evaluations are underutilized and nonstandardized.
Circulation, Volume 150, Issue Suppl_1 , Page A4148156-A4148156, November 12, 2024. Background:Patients with adult congenitalheartdisease (ACHD) form a unique subset of patients with complex ventricular tachycardia (VT).Objective:To These patients were younger compared to the non-ACHD subtype.(Table
Background Iron deficiency (ID) has been reported in patients with congenitalheartdisease. There is, however, a scarcity of data on its prevalence in patients with a Fontan circulation. Conclusion ID is highly prevalent among patients with a Fontan circulation. by 5-fold (p=0.035).
Circulation, Volume 150, Issue Suppl_1 , Page A4147717-A4147717, November 12, 2024. Background:SGLT2 inhibitors have demonstrated efficacy in reducing cardiovascular death and hospitalization and are recommended as first-line therapy for hear failure (HF) in adults due to acquired heartdiseases.
Circulation, Volume 150, Issue Suppl_1 , Page A4118671-A4118671, November 12, 2024. Background:Climate change is intricately linked to human health, and the cardiovascular system is particularly susceptible to suboptimal temperatures, causing premature mortality.
Circulation, Volume 150, Issue Suppl_1 , Page A4140019-A4140019, November 12, 2024. Introduction:The number of adults with congenitalheartdiseases (CHD) is rapidly increasing, who are frequently associated with cardiovascular morbidities and may result in poor outcomes.
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