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“Through the most current embryological and genetic research, the book attempts to define and explain the development of the conotruncal anomalies. ... for advanced practitioners, it is a current, quick reference. ... Many of the illustrations are in color to enhance the appearance and increase comprehension. Overall, this is an impressive book with advanced, detailed information on some of the most complicated and difficult cardiac anomalies currently amenable to surgical correction.” (Robert M. Arensman, Doody's Book Reviews, May, 2016)
Francois Lacour-Gayet, Pediatric Cardiac Surgery Consultant, Professor of Surgery, Imperial College, London, Royal Brompton Hospital, Department of Cardiac Surgery, London, UK
Edward L. Bove, MD, Professor of Cardiac Surgery, Chairman, Cardiac Surgery Department, University of Michigan, C.S. Mott Children’s Hospital, Department of Cardiac Surgery, Ann Arbor, Michigan, USA
Viktor Hraška, MD, PhD, Asklepios Clinic Sankt Agustin, German Pediatric Heart Center, Sankt Augustin, Germany
Victor O. Morell, MD, Eugene S. Wiener Professor and Chair, Pediatric Cardiothoracic Surgery, Vice Chair & Director of Cardiovascular Services, Dept. Cardiothoracic Surgery, University of Pittsburgh Medical School, Department of Cardiothoracic Surgery, Pittsburgh, Pennsylvania, USA
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Book Description Condition: New. Seller Inventory # 39553406
Book Description Buch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This book addresses the most technically demanding but life-changing techniques in the treatment of conotruncal heart defects, as many repairs are performed on small infants. Each chapter reviews surgical anatomy (the anatomical classification that the surgeon is using), preoperative evaluation (the surgeon's check list before doing the surgery), and surgical techniques (clear drawings and videos, minimal text). It is an essential reference book for newly qualified surgeons when performing these complex cases. Conotruncal heart defects (CTHDs) are a group of complex congenital anomalies of the cardiovascular system that are a major cause of symptomatic cardiac disease at birth. They may account for up to 30% of all congenital cardiac anomalies. In many instances, patients with CTHD are symptomatic in the first days or weeks of life, with severe cyanosis or heart failure, requiring surgery in the neonatal period or in infancy. Most CHTD are today diagnosed in utero by fetal ultrasound. CHTDs are usually defined as malformations of the cardiac outflow tracts and presumably result in disturbance in the development of the cono-truncal apparatus of the embryonic heart, as well as of the primitive aortic arches. CTHDs include the following: truncus arteriosus, tetralogy of Fallot, double outlet right (or left) ventricle, transposition of the arteries, corrected transposition of the great arteries, interrupted aortic arch. The outcomes of CHTD surgery has considerably improved in the past 20 years, with quite fascinating innovations. 627 pp. Englisch. Seller Inventory # 9783319230566
Book Description Buch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book addresses the most technically demanding but life-changing techniques in the treatment of conotruncal heart defects, as many repairs are performed on small infants. Each chapter reviews surgical anatomy (the anatomical classification that the surgeon is using), preoperative evaluation (the surgeon's check list before doing the surgery), and surgical techniques (clear drawings and videos, minimal text). It is an essential reference book for newly qualified surgeons when performing these complex cases. Conotruncal heart defects (CTHDs) are a group of complex congenital anomalies of the cardiovascular system that are a major cause of symptomatic cardiac disease at birth. They may account for up to 30% of all congenital cardiac anomalies. In many instances, patients with CTHD are symptomatic in the first days or weeks of life, with severe cyanosis or heart failure, requiring surgery in the neonatal period or in infancy. Most CHTD are today diagnosed in utero by fetal ultrasound. CHTDs are usually defined as malformations of the cardiac outflow tracts and presumably result in disturbance in the development of the cono-truncal apparatus of the embryonic heart, as well as of the primitive aortic arches. CTHDs include the following: truncus arteriosus, tetralogy of Fallot, double outlet right (or left) ventricle, transposition of the arteries, corrected transposition of the great arteries, interrupted aortic arch. The outcomes of CHTD surgery has considerably improved in the past 20 years, with quite fascinating innovations. Seller Inventory # 9783319230566
Book Description Condition: New. Seller Inventory # 24714286-n
Book Description Condition: New. New! This book is in the same immaculate condition as when it was published 3.02. Seller Inventory # 353-3319230565-new
Book Description Condition: New. Buy with confidence! Book is in new, never-used condition 3.02. Seller Inventory # bk3319230565xvz189zvxnew
Book Description Condition: New. Seller Inventory # I-9783319230566
Book Description Hardcover. Condition: Brand New. har/psc edition. 627 pages. 10.98x8.27x1.60 inches. In Stock. Seller Inventory # x-3319230565
Book Description Condition: New. Seller Inventory # 24714286-n
Book Description Hardcover. Condition: new. Hardcover. This book addresses the most technically demanding but life-changing techniques in the treatment of conotruncal heart defects, as many repairs are performed on small infants. Each chapter reviews surgical anatomy (the anatomical classification that the surgeon is using), preoperative evaluation (the surgeon's check list before doing the surgery), and surgical techniques (clear drawings and videos, minimal text). It is an essential reference book for newly qualified surgeons when performing these complex cases. Conotruncal heart defects (CTHDs) are a group of complex congenital anomalies of the cardiovascular system that are a major cause of symptomatic cardiac disease at birth. They may account for up to 30% of all congenital cardiac anomalies. In many instances, patients with CTHD are symptomatic in the first days or weeks of life, with severe cyanosis or heart failure, requiring surgery in the neonatal period or in infancy. Most CHTD are today diagnosed in utero by fetal ultrasound. CHTDs are usually defined as malformations of the cardiac outflow tracts and presumably result in disturbance in the development of the cono-truncal apparatus of the embryonic heart, as well as of the primitive aortic arches. CTHDs include the following: truncus arteriosus, tetralogy of Fallot, double outlet right (or left) ventricle, transposition of the arteries, corrected transposition of the great arteries, interrupted aortic arch. The outcomes of CHTD surgery has considerably improved in the past 20 years, with quite fascinating innovations. This book addresses the most technically demanding but life-changing techniques in the treatment of conotruncal heart defects, as many repairs are performed on small infants. Conotruncal heart defects (CTHDs) are a group of complex congenital anomalies of the cardiovascular system that are a major cause of symptomatic cardiac disease at birth. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Seller Inventory # 9783319230566