Ionic and Cellular Basis of Antiarrhythmic Drug Therapy and Its Proarrhythmic Risks [0.03%]
抗心律失常药的作用机制及促心律失常风险
Ibrahim Alameh,Farid Farkouh,Mohammed Kamareddine et al.
Ibrahim Alameh et al.
This review explores the ionic and cellular mechanisms that underlie antiarrhythmic drug therapy, focusing on how modulation of ionic currents influences cardiac action potentials and refractory periods. Reentrant arrhythmias, the most comm...
Complex Arrhythmias in Pediatrics and Congenital Heart Disease: Case Review [0.03%]
儿科及先天性心脏病的复杂心律失常：病例分析
Reina Bianca Tan,Maully J Shah
Reina Bianca Tan
The Growing Tie Between Congenital Heart Disease and Electrophysiology [0.03%]
先天性心脏病与电生理学之间的联系越来越紧密
Michael Lloyd,Jayanthi Koneru
Michael Lloyd
Translating Adult Electrophysiology Technology to Pediatric and Congenital Electrophysiology [0.03%]
成人电生理学技术在儿科和先天性心脏病电生理学中的应用
Edward O&#x;Leary,Natasja M S de Groot
Edward O&#x;Leary
This review intends to summarize the present landscape of translating electrophysiologic therapies designed for adults to the pediatric and congenital heart disease (CHD) populations. Unique challenges faced by pediatric and congenital elec...
Elizabeth DeWitt,Dominic Abrams
Elizabeth DeWitt
Arrhythmogenic cardiomyopathy is an inherited myocardial disorder increasingly recognized in pediatric patients. It is characterized by arrhythmias that often precede structural abnormalities and can involve the right, left, or both ventric...
M Cecilia Gonzalez Corcia,Stephanie F Chandler
M Cecilia Gonzalez Corcia
In the pediatric cardiology clinic, Brugada syndrome (BrS) most commonly presents through cascade screening following the diagnosis of a parent or sibling. However, some children may present for evaluation of syncope, or with documented atr...
Cardiac Channelopathies in the Pediatric Patient: The Ryanodine Receptor Related Inherited Cardiac Syndromes [0.03%]
儿科钙释放偶联紊乱导致的心脏离子通道病：ryanodine受体相关遗传性心脏综合征
Iqbal El Assaad,Thomas Roston,Vassilios Bezzerides
Iqbal El Assaad
The ryanodine receptor-related inherited-cardiac syndromes are a group of disorders characterized predominantly by variants associated with both gain of function and loss of function in the ryanodine receptor type 2 (RyR2) gene. The prototy...
Reina Bianca Tan,Maully J Shah
Reina Bianca Tan
Short QT Syndrome is a rare inherited arrhythmia disorder marked by accelerated repolarization and a short QT interval. It carries a high risk of atrial and ventricular arrhythmias, including sudden cardiac arrest. Genetic mutations are ide...
Christopher W Follansbee,Andrew P Landstrom,Peter F Aziz
Christopher W Follansbee
Congenital long QT syndrome is the most common inherited arrhythmia syndrome and is characterized by prolongation of the QT interval in the absence of structural heart disease or external factors. Disease will often manifest during childhoo...
Adrianna Costello,A Sami Chaouki,Jason R Imundo
Adrianna Costello
In this article, we will discuss the risk factors for postoperative arrhythmias following pediatric congenital heart disease surgeries. Factors in preventing postoperative arrhythmias as well as key tools in identifying and distinguishing b...