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The Right Ventricle in Adults with Tetralogy of Fallot

ISBN-13: 9788847023574 / Angielski / Twarda / 2012 / 194 str.

Massimo Chessa;Alessandro Giamberti
The Right Ventricle in Adults with Tetralogy of Fallot Massimo Chessa, Alessandro Giamberti 9788847023574 Springer Verlag - książkaWidoczna okładka, to zdjęcie poglądowe, a rzeczywista szata graficzna może różnić się od prezentowanej.

The Right Ventricle in Adults with Tetralogy of Fallot

ISBN-13: 9788847023574 / Angielski / Twarda / 2012 / 194 str.

Massimo Chessa;Alessandro Giamberti
cena 201,72 zł
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Tetralogy of Fallot is the most common form of cyanotic congenital heart disease, and one of the first to be successfully repaired by congenital heart surgeons. Although "fixed," patients born with tetralogy of Fallot cannot be considered "cured." Improving survival and quality of life for this ever-increasing adult population will continue to challenge the current and future generations of cardiologists. Adult patients with tetralogy of Fallot should be seen by a cardiologist specializing in the care of adults with congenital heart disease, to be monitored for late complications. They need to be checked regularly for any subsequent complications or disturbances of heart rhythm. This monograph is intended as both an introduction to the subject and a timely, comprehensive review, and will be welcomed by adult cardiologists, pediatric cardiologists, internists, surgeons, obstetricians, and intensivists who wish to learn about the most recent discoveries and advances concerning tetralogy of Fallot in adults. It will also be of interest to advanced undergraduates wanting to learn more about the subject.

Tetralogy of Fallot is the most common form of cyanotic congenital heart disease, and one of the first to be successfully repaired by congenital heart surgeons. Although fixed , Patients born with tetralogy of Fallot are not "cured". Improving survival and quality of life for this ever-increasing adult population will continue to challenge the current and future generations of cardiologists. §Adult patients with tetralogy of Fallot should be seen by a cardiologist specializing in the care of adults with congenital heart disease, to be monitored for late complications. They need to be checked regularly for any subsequent complications or disturbances of heart rhythm. The most common late complication is a right ventricular failure, which may require subsequent surgery.§This monograph is intended as both an introduction to the subject and a timely, comprehensive review more extensive than a review article and more up to date than a textbook.

Kategorie:
Nauka, Medycyna
Kategorie BISAC:
Medical > Kardiologia
Medical > Surgery - Cardiothoracic
Education > General
Wydawca:
Springer Verlag
Język:
Angielski
ISBN-13:
9788847023574
Rok wydania:
2012
Dostępne języki:
Angielski
Wydanie:
2012
Ilość stron:
194
Waga:
0.49 kg
Wymiary:
23.523.5 x 15.5
Oprawa:
Twarda
Wolumenów:
01

From the reviews:

"This book offers both a historical perspective and overview of recent advances in the management of tetralogy of Fallot. ... Medical students, advanced practice clinicians, physicians in training, cardiologists caring for adults with congenital heart disease are the intended audience. ... This innovative book does an excellent job of addressing the full spectrum of diagnostic and management issues in adults with tetralogy of Fallot." (Sylvia Alicia Oleck, Doody's Book Reviews, February, 2013)

Introduction.- Anatomy of Tetralogy of Fallot.- Genetics.- Stem Cells and the Right Ventricle.- Pathophysiology in Tetralogy of Fallot.- Tetralogy of Fallot: Late Outcome.- Tetralogy of Fallot: the Failing Right Ventricle.-Imaging Evaluation.- Timing for RVOT Management.- Percutaneous Pulmonary Valve.-Other Transcatheter Procedures.- Surgical Pulmonary Valve Implantation.- Other Surgical Procedures.- Late Arrhythmias: Current Approaches.- Perioperative Right Ventricular Management.         

Tetralogy of Fallot is the most common form of cyanotic congenital heart disease, and one of the first to be successfully repaired by congenital heart surgeons. Although “fixed”, patients born with tetralogy of Fallot cannot be considered “cured”. Improving survival and quality of life for this ever-increasing adult population will continue to challenge the current and future generations of cardiologists.

Adult patients with tetralogy of Fallot should be seen by a cardiologist specializing in the care of adults with congenital heart disease, to be monitored for late complications. They need to be checked regularly for any subsequent complications or disturbances of heart rhythm.

This monograph is intended as both an introduction to the subject and a timely, comprehensive review, and will be welcomed by adult cardiologists, pediatric cardiologists, internists, surgeons, obstetricians, and intensivists who wish to learn about the most recent discoveries and advances concerning tetralogy of Fallot in adults. It will also be of interest to advanced undergraduates wanting to learn more about the subject.



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