Robert M. Freedom is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley.
Shi-joon Yoo is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley.
Haverj Mikailian is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley.
William G. Williams is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley.
Exhaustive in its scope, this book provides a comprehensive study of the natural and modified history of congenital heart disease. Focusing particularly on the discussion of fetal and post-natal outcomes, the contributors seek to place developments in historical perspective. Virtually all surgical and catheter-based strategies to enhance outcomes of all forms of congenitally malformed heart are analysed, covering the morphology and genetic basis of each particular abnormality, and issues that were germane to evolving different therapeutic strategies. Using data from the records of the Toronto Hospital for Sick Children, contributors highlight the complications of the various forms of therapies and identifies particular risk factors for mortality and morbidity.
Robert M. Freedom is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley. Shi-joon Yoo is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley. Haverj Mikailian is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley. William G. Williams is the editor of The Natural and Modified History of Congenital Heart Disease, published by Wiley.
The Natural and Modified History of Congenital Heart Disease 1
Contents 19
Foreword 9
Preface 11
Acknowledgements 13
Contributors 15
1 Historical Overview: a Brief Narrative of the Modern Era of Congenital Heart Disease 22
2 The Prevalence of Congenital Cardiac Lesions 29
3 Ventricular Septal Defect 37
4 Atrial Septal Defect 52
5 Atrioventricular Septal Defect 65
6 Common Arterial Trunk 77
7 Anomalous Origin of One Pulmonary Artery from the Ascending Aorta 85
8 Distal Ductal or Ligamental Origin of the Pulmonary Artery 89
9 The Patent Arterial Duct 93
10 Anomalous Left Coronary Artery from the Pulmonary Artery 104
11A Ebstein’s Malformation of the Tricuspid Valve 112
11B Uhl’s Anomaly of the Right Ventricle 118
12 Congenital Abnormalities of the Mitral Valve 120
13A Congenital Pulmonary Stenosis and Isolated Congenital Pulmonary Insufficiency 128
13B Peripheral Pulmonary Artery Stenosis 140
13C Pulmonary Artery Sling 156
14A Congenital Aortic Valve Stenosis or Regurgitation 159
14B Supravalvular Aortic Stenosis 190
14C Fixed, Short-segment Subaortic Stenosis 195
15A Aortocameral Communications 202
15B Sinus of Valsalva Aneurysm 204
16 Tetralogy of Fallot 207
17 Tetralogy of Fallot with Absent Pulmonary Valve 233
18 Tetralogy of Fallot with Pulmonary Atresia (Pulmonary Atresia and Ventricular Septal Defect) 238
19A The Divided Right Ventricle 253
19B Isolated Right Ventricular Hypoplasia 257
20 Aortopulmonary Window 258
21 Hypertrophic Cardiomyopathy 262
22 Coarctation of the Aorta 272
23 Interruption of the Aortic Arch 297
24A Total Anomalous Pulmonary Venous Connections 303
24B The Scimitar Syndrome or Hypogenetic Right Lung Complex 311
24C The Divided Left Atrium (Cor Triatriatum) 316
24D Partial Anomalous Pulmonary Venous Connections 320
24E Congenital Stenosis of the Individual Pulmonary Veins 323
25A Complete Transposition of the Great Arteries: History of Palliation and Atrial Repair 327
25B Transposition of the Great Arteries: Arterial Repair 344
25C The Rastelli and Other Procedures for Complex Transposition of the Great Arteries 369
26A Conditions with Double Discordance (Congenitally Corrected Transposition of the Great Arteries) 377
26B Isolated Atrioventricular Discordance 387
27 Anatomically Corrected Malposition of the Great Arteries 389
28 Double-Outlet Ventricle 391
29 Tricuspid Atresia 402
30 Pulmonary Atresia and Intact Ventricular Septum 407
31 Hypoplastic Left Heart Syndrome 418
32 Double-Inlet Ventricle 429
33 The Syndrome of Isomeric Right Atrial Appendages and Visceroatrial Heterotaxy, Often Associated with Congenital Asplenia 444
34 The Syndrome of Isomeric Left Atrial Appendages, Often Associated with Polysplenia 451
35 The Cavopulmonary Shunt 456
36 The Fontan–Kreutzer Procedure 470
37 Complications of the Fontan Procedure 481
38 Coronary Arteriovenous Fistula 492
39 Cardiac Diverticulum and Aneurysm 496
40 Cardiac Tumors 500
41A Conjoined Twins 505
41B Ectopia Cordis (Exteriorization of the Heart) 507
41C Idiopathic Arterial Calcification of Infancy 508
41D Persistent Fifth Aortic Arch 509
41E Superoinferior Ventricles and Hearts with Twisted Atrioventricular Connections 513
41F Kartagener’s Syndrome 516
41G Myocardial Noncompaction 518
41H Systemic Venous Anomalies Including Divided Right Atrium 522
41I Isolation of the Subclavian, Innominate, or Left Common Carotid Artery 527
42 Pulmonary Ventricle to Pulmonary Artery Conduits 529
43 Pulmonary Veno-Occlusive Disease 534
44 Pulmonary Vascular Disease 539
45 Outcomes of Extracorporeal Membrane Oxygenation and Ventricular Assist for Congenital Heart Disease 549
46 Dilated Cardiomyopathy 558
47 Heart Transplantation 571
48 Congenital Heart Block 583
49 Long QT Syndrome 590
50 Supraventricular Arrhythmias 596
51 Ventricular Tachycardia 608
52 Epilogue 618
References 622
Index 890
| Erscheint lt. Verlag | 15.4.2008 |
|---|---|
| Sprache | englisch |
| Themenwelt | Medizin / Pharmazie ► Allgemeines / Lexika |
| Medizinische Fachgebiete ► Innere Medizin ► Kardiologie / Angiologie | |
| Naturwissenschaften ► Biologie ► Humanbiologie | |
| Schlagworte | Adult • Analyses • Book • Congenital • Congenital Heart Disease • congenitally • Different • discussion • Disease • enhance • ERA • Exhaustive • Fetus • forms • Germane • Hearts • historical perspective • History • Kongenitale Herzkrankheit • Medical Science • Medizin • NATURAL • outcomes • Strategies • Study • surgical |
| ISBN-13 | 9780470986899 / 9780470986899 |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
| Haben Sie eine Frage zum Produkt? |
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