Adult Congenital Heart Disease

This book describes the most popular topics concerning adult congenital heart disease (ACHD), especially focusing on indications and re-intervention procedures for some major ACHDs.

Thanks to advances in medical and surgical therapy for congenital heart disease over the last half century, many patients who underwent surgical correction reached adulthood. However, as can be seen from the explosive increase in the number of ACHD patients, postoperative residua and sequelae have also become apparent.

The purpose of this book is to highlight complicated problems in connection with ACHD, including its present status, as well as methods for its management including medical and surgical treatment. The content primarily focuses on two areas general information for cardiologists, and information on re-intervention for interventionists and cardiac surgeons , setting it apart from the majority of books on congenital heart disease.

Written by both leading cardiac surgeons and cardiologists Includes in-depth information on sequelae following surgical procedures Provides new insights to promote comprehensive understanding of ACHD management

Autorentext
Prof. Munetaka Masuda Chief Professor, Department of Surgery, Yokohama City University

Prof. Koichiro Niwa Executive Advisor, Cardiovascular Center, St Luke's International Hospital

Inhalt

Part I: Background and Facilities.- Chapter 1: Historical perspective.- Chapter 2: Facilities for patients' care.- Part II: Medical consideration.- Chapter 3: Post-operative residua and sequelae.- Chapter 4: Heart failure.- Chapter 5: Rhythm disturbance / sudden death.- Part III: Intervention / Re-intervention considerations.- Chapter 6: Anesthesia for ACHD.- Chapter 7: Therapeutic catheter intervention (ASD, PDA, CoA, etc).- Chapter 8: Repaired tetralogy of Fallot.- Chapter 9: Post RV-PA conduit repair (PA + VSD, TGA III, etc).- Chapter 10: Repaired complete transposition of the great arteries.- Chapter 11: Corrected TGA.- Chapter 12: Post right heart bypass operation.- Chapter 13: Aortopathy including hereditary disease (Marfan syndrome, bicuspid aortic valve, etc).- Chapter 14: Ebstein anomaly.