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Cardiovascular disease is the major cause of mortality and morbidity around the world. While significant progress has been made in treating a major sub-category of cardiac disease and arrhythmias, significant unmet needs remain. Every day, thousands of patients die due to arrhythmias in the U.S. alone, and atrial fibrillation is the most common arrhythmia that affects millions of Americans at any given time. Therefore, there is an urgent public need to continue to develop new and better therapies for arrhythmias. This book reviews key research methods and protocols in cardiac electrophysiology with a focus on advantages and pitfalls. It will discuss new developments as well as traditional treatments and methods. Chapters will focus on practical implementation and collaborative cross-functional research methods. The book will contain contributions from scientists and clinicians from various academic and industrial research institutions. The inclusion of industrial experts expands the scope and potential audience of this book, and provides important perspective beyond basic science. Contributors will include researchers and clinicians from academic institutions such as the University of Minnesota, Harvard, Washington University, Case Western, Indiana University, and Manchester University. Methods and Models in Cardiac Electrophysiology will be a must-have resource for clinical academic scientists, engineers from industry (Biotech, Pharma, and Medical Device), undergraduate and graduate students, physicians, biomedical engineers, and high school and college teachers interested in studying cardiac electrophysiology and cardiac function. The book may also be of interest to students in the fields of physiology, molecular biology, cellular biology, biomedical engineering, mechanical engineering, electrical engineering, and related areas.

This reference work aims to be the primary resource in the field of heart disease in children and adult congenital heart disease. It contains nearly 100 chapters covering all aspects of heart disease in three populations: fetus with acquired and congenital heart diseases, children with acquired and congenital heart diseases, and adults with congenital heart diseases. Divided into five main sections, the book provides a comprehensive, up-to-date, and continuously revised overview of what is known in the field as well as resources for practical use such as normal values, medication information, and review of published guidelines. The first section of the book includes historical background on congenital heart disease and the evolution of medical, surgical, and catheter therapeutics. The fetal heart disease section comes next and covers cardiovascular embryogenesis, etiological mechanisms, diagnostic tools, presentation and management, cardiomyopathies, arrhythmias, perinatal management, and emergencies. The bulk of the book lies in the third section on pediatric cardiology, which examines not only basic science, assessment, and therapies but also a wide variety of specific acquired and congenital diseases such as valvular lesions, arterial diseases, cyanotic heart diseases, cardiomyopathies, cardiac tumors, and pulmonary hypertension. This is followed by the section on adult congenital heart diseases, discussing echocardiography, electrophysiology, neurodevelopment, and a variety of unique aspects of congenital heart disease in the adult years. The final section of the book focuses on pharmacology with chapters on inotropes, vasopressors, diuretics, and more. Pediatric Cardiology: Fetal and Pediatric Heart Diseases & Adult Congenital Heart Diseases is an essential reference for physicians, residents, fellows, medical students, nurse-practitioners, and allied health professionals in cardiology, pediatrics, cardiac surgery, and imaging/radiology.

The coronaries are the first branches of the ascending aorta. They arise from their respective sinuses of Valsalva, and gradually branch distally to the myocardium. Abnormalities of the coronary arteries, either congenital or acquired, can be characterized as a lack of origin, abnormal origin, anomalous course, lack of patency, abnormal connections, and/or abnormal drainage of the coronary vessels. Interruptions to or lack of flow can cause significant morbidity and mortality due to ischemia, infarction and fistulous connections, which can lead to cardiac failure, endocarditis and ischemia. Coronary artery anomalies are rare in general populations. Although they can be benign and asymptomatic, they can also be malignant due to their origin and course and can cause sudden cardiac death. As such, an understanding of how to analyze, diagnose and treat them is vital. This book presents the latest advances in congenital anomalies of coronary arteries. It offers a comprehensive overview of the field, including illustrative angiograms and diagrams that demonstrate all possible anomalies and clarify what is abnormal, and also provides practical insights to guide practitioners in their everyday practice.

This book provides a comprehensive overview of the physiology, pathophysiology, diagnosis, medical and surgical management, and future therapies for tricuspid valve disease. It is divided into two sections. The first section covers the basics of the tricuspid valve, including anatomy, epidemiology, and clinical diagnosis with individual chapters focused on hemodynamics, echocardiography, MRI, and CT assessment. The second section examines current treatments for tricuspid valve disease including both surgical and medical management. It discusses special clinical scenarios of tricuspid valve pathology such as tricuspid regurgitation in patients with ICD and pacemaker implants and the role of tricuspid valve disease in patients with heart failure and LVAD therapy. Tricuspid Valve Disease: A Comprehensive Guide to Evaluation and Management is an essential resource for general cardiologists, interventional cardiologists, cardiac surgeons, and innovators in the field of structural heart disease.