A5007897287- Congenital Heart Disease Studies
- Cardiac Arrhythmias and Treatments
- Cardiovascular Issues in Pregnancy
- Cardiac Structural Anomalies and Repair
- Coronary Artery Anomalies
- Vascular anomalies and interventions
- Cardiovascular Function and Risk Factors
- Cardiovascular Conditions and Treatments
- Prenatal Screening and Diagnostics
- COVID-19 Impact on Reproduction
- Cerebrovascular and Carotid Artery Diseases
- Cardiac pacing and defibrillation studies
- Mechanical Circulatory Support Devices
- Cardiomyopathy and Myosin Studies
- Renal and Vascular Pathologies
- Cardiac Imaging and Diagnostics
- Acute Ischemic Stroke Management
- Congenital heart defects research
- Tracheal and airway disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Congenital Anomalies and Fetal Surgery
- Liver Disease and Transplantation
- Parvovirus B19 Infection Studies
- Dysphagia Assessment and Management
- Tuberous Sclerosis Complex Research
Northwestern University
2018-2025
Lurie Children's Hospital
2017-2025
University of North Carolina at Chapel Hill
2024
University of Florida
2021-2023
Florida College
2023
United States Food and Drug Administration
2022
Box (United States)
2021
Alberta Health Services
2020
Royal Brompton Hospital
2018
Lucile Packard Children's Hospital
2017
Although most congenital heart defects (CHDs) are asymptomatic at birth, certain CHD lesions significant risk of severe hemodynamic instability and death if emergent cardiac interventions not performed in a timely fashion. Therefore, accurate identification at-risk fetuses appropriate delivery resource planning according to the degree anticipated is crucial. Fetal echocardiography has increased prenatal detection recent years due advancements ultrasound techniques improved obstetrical...
Intraatrial Mustard baffle repair of dextro-transposition the great arteries (d-TGA) is vulnerable to complications, typically obstruction and leaks. Because patients often require pacemakers or intracardiac electrophysiology studies (EPS)/ablation for arrhythmias, narrowed obstructed baffles restrict cardiac access hindering procedures. Current guidelines recommend clinical as well comprehensive transthoracic echocardiographic/Doppler (TTE) identify problems. This study reviews...
Hyperuricemia is associated with development of gout, hypertension, and renal disease. The impact allopurinol, a urate-lowering therapy, on function unclear, especially in patients chronic kidney disease who are at higher risk hypersensitivity reaction.The aim this study was to determine the effect allopurinol hyperuricemic male veterans.This retrospective cohort using pharmacy, medical, laboratory records veterans enrolled Veterans Administration New York Harbor Healthcare System, Brooklyn...
Background Fetal diagnosis of congenitally corrected transposition the great arteries (ccTGA) has been increasingly reported; however, predictors clinical outcomes remain underexplored. We undertook a multicenter, retrospective study to investigate natural history, associated anomalies, and fetal ccTGA. Methods Results Fetuses with ccTGA diagnosed from January 2004 July 2020 within 20 North American programs were included. severe ventricular hypoplasia thought definitively preclude...
Turner syndrome (TS) is associated with abnormalities across several organ systems, including the visual system. There a relative paucity of literature describing ophthalmic manifestations TS. We sought to investigate eye in our cross-sectional population pediatric TS patients.All patients managed by program tertiary children's hospital were identified. Patients documentation at least one exam included for analysis. Chart review was retrospectively performed identify all documented ocular as...
Congenital complete heart block (CCHB) is associated with high intrauterine and post-natal mortality. Prenatal detection management, as well appropriate delivery planning, may improve the outcomes in CCHB. We describe a rare case of CCHB that initially presented fetal ascites high-grade second-degree noted on echocardiography. The mother was to be positive for anti-SSA antibodies, treatment maternal steroids started an effort reverse cardiac conduction abnormality. However, rhythm progressed...
<title>Abstract</title> Staged palliation of single ventricle congenital heart disease culminating in complete cavo-pulmonary anastomosis (“Fontan”) is life preserving but associated with long term morbidity frequently including Fontan-associated liver (FALD). Markers early FALD are lacking. We sought to measure hepatic venous oxygen saturation (ShVO2) obtained during surveillance cardiac catheterization Fontan patients, as a potential marker FALD. patients ShVO2 measurements between 2018...
Background: Patients born with single ventricle anatomy palliated the Fontan procedure are at risk of lymphatic complications (LC), including plastic bronchitis, protein losing enteropathy, ascites, and hypoalbuminemia. The mechanism LC, associated factors, impact on outcomes not well understood. Aim: We aimed to describe prevalence Fontan-related expand their association previously reported explore mortality transplantation. Methods: performed a single-center, retrospective, cross-sectional...
Background: Fetal cardiomyopathy (FCM) affects 8 per 100,000 live births, often with unknown etiology. Progress in fetal cardiac screening, genetic testing and management may have impacted historically poor outcomes. Aims: We sought to investigate associations clinical outcomes of FCM the current era. Methods: This was a retrospective Heart Society Research Collaborative cohort study cases diagnosed from January 2017-December 2021 39 centers. Cases myocardial disease attributable maternal...