The Tricuspid Valve In Congenital Heart Disease

This book is devoted solely to the tricuspid valve and its role in congenital heart disease. Tricuspid valve anomalies are part of the pathological spectrum in various congenital heart diseases, including Ebstein anomaly and tricuspid valve dysplasia, with different pathophysiology and clinical implications. This book covers all relevant aspects of such anomalies, including diagnosis, therapy and follow-up. Further topics addressed include the way in which the tricuspid valve may become the “systemic” valve in some congenital diseases, with important consequences and the involvement of the tricuspid valve in the right-sided heart complications often seen in adults with congenital heart disease. All of the chapters are written by internationally recognized experts and are designed to deliver state of the art knowledge of practical value. This book will be an important addition to the library for surgeons, cardiologists and other practitioners involved in the management of patients with congenital heart disease.

Over the last 50 years, there have been remarkable developments in the diagnosis and treatment of congenital heart defects. This book addresses some of these developments, including the role of echocardiography in improving the prognosis of fetal heart defects, benefits of new echo techniques, cardiac screening of participants in sports, management of premature babies with patent ductus arteriosus, and advantages of stenting the right ventricular outflow tract. It also discusses several types of heart defects, including ventricular septal defect, atrioventricular septal defect, hypoplastic left heart syndrome, and Ebstein’s anomaly of the tricuspid valve. Finally, the book discusses the treatment of congenital aortic valve disease and issues related to managing congenital heart disease in developing countries.

From the earliest days of medicine to the present, case reports have been a critical aspect of clinical education and knowledge development. In this comprehensive volume, Dr. William C. Roberts, a renowned expert in the field, explores the rich history and ongoing importance of case reports in cardiology. Through engaging and insightful analysis, the book demonstrates how case reports have provided physicians with crucial insights into rare diseases, complex conditions, and groundbreaking treatments. Drawing on a vast range of sources, from ancient manuscripts to cutting-edge journals, it offers a unique perspective on the role of case reports in medical education and practice of congenital heart diseases and associated cardiac complications. It underscores how case reports can be used to enhance diagnostic accuracy, identify new treatment options, and promote innovation in the field. In addition, the book provides valuable insights into the process of writing and publishing case reports, including tips for young physicians looking to break into the field. The book will be an indispensable guide to the history, practice, and ongoing significance of case reports for medical students, physicians, and researchers alike. Key features: Provides a rich repository of diverse case reports in cardiology published by the editor and his colleagues over 61 years Features 52 clinical case studies related to Congenital Heart Disease useful for medical students and practicing cardiologists Valuable resource for young physicians seeking to establish a foothold in medical research and academics

Expressly created to assist with decision making for surgical treatment of congenital heart defects, this new reference covers all relevant aspects. The congenital heart defects are presented with each chapter devoted to a single malformation, with incidence, morphology, associated anomalies, pathophysiology, diagnosis (including clinical pattern, electrocardiogram, chest X-ray, echocardiogram, cardiac catheterization with angiography), indications for surgical treatment, details of surgical treatment, potential complications and literature references. Morphology, pathophysiology and surgical treatment of the defects are explained with schematic drawings, while images taken from morphologic specimens, echocardiographic and angiographic investigations as well as from intra-operative photographs illustrate better than any words the key points of the decision-making process for the surgical treatment of congenital heart defects.

In the United States, there are approximately 1 million adults with congenital heart disease, with 20,000 new patients reaching adolescence each year. With early pediatric diagnosis, improved medical, surgical and post operative care, it is now expected that 90% of patients born with congenital heart disease (CHD) will survive to adulthood. Therefore, the number of adult CHD (ACHD) patients will continue to rise. In fact, it is now estimated that for the first time in history, there are more adults living with CHD than children. The cardiologist who deals with these patients must therefore be familiar with congenital heart lesions in their uncomplicated state and know appropriate testing and follow-up methods. Also the inherent complexity of this type of cardiovascular disease really needs a comprehensive, multimedia included, practical and case base approach and assessment. The aim of this book is to provide a case base approach to adult patients with congenital heart disease including all diagnostic and treatment methods focus on physical exam, ECG, chest X-Ray, heart sounds, advanced echocardiography including of TTE & TEE, cardiac CT, CMR, catheterization, interventional procedures, surgery and also anesthesia highlights in these patients.

'Congenital Heart Disease in the Right Heart' is an exhaustive review of the malformations of the right ventricle with particular emphasis on the ability of the ventricle to support circulation and the results of right heart malformations on circulation. Edited by the world’s foremost authorities on the subject, the book benefits from an international team of contributors.