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    De 2 a 3 Semanas

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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.

1. Historical Overview: A Brief Narrative of the Modern Era of Congenital Heart Disease.
2. The Prevalence of Congenital Cardiac Lesions.
3. Ventricular Septal Defect.
4. Atrial Septal Defect.
5. Atrioventricular Septal Defect.
6. Common Arterial Trunk.
7. Anomalous Origin of One Pulmonary Artery from the Ascending Aorta.
8. Distal Ductal or Ligamental Origin of the Pulmonary Artery.
9. The Patent Arterial Duct.
10. Anomalous Left Coronary Artery from the Pulmonary Artery.
11A. Ebstein""s Malformation of the Tricuspid Valve.
11B. Uhl""s Anomaly of the Right Ventricle.
12. Congenital Abnormalities of the Mitral Valve.
13A. Congenital Pulmonary Stenosis and Isolated Congenital Pulmonary Insufficiency.
13B. Peripheral Pulmonary Artery Stenosis.
14A. Congenital Aortic Valve Stenosis or Regurgitation.
14B. Supravalvular Aortic Stenosis.
14C. Fixed, Short-Segment Subaortic Stenosis.
15A. Aorto-Cameral Communications.
15B. Sinus of Valsalva Aneurysm.
16. Tetralogy of Fallot.
17. Tetralogy of Fallot with Absent Pulmonary Valve.
18. Tetralogy of Fallot with Pulmonary Atresia (Pulmonary Atresia and Ventricular Septal Defect).
19A. The Divided Right Ventricle.
19B. Isolated Right Ventricular Hypoplasia.
20. Aortopulmonary Window.
21. Hypertrophic Cardiomyopathy.
22. Coarctation of the Aorta.
23. Interruption of the Aortic Arch.
24A. Total Anomalous Pulmonary Venous Connections.
24B. The Scimitar Syndrome or Hypogenetic Right Lung Complex.
24C. The Divided left Atrium (Cor Triatriatum).
24D. Partial Anomalous Pulmonary Venous Connections.
24E. Congenital Stenosis of the Individual Pulmonary Veins.
25A. Complete Transposition of the Great Arteries: History of Palliation and Atrial Repair.
25B. Transposition of the Great Arteries: Arterial Repair.
25C. The Rastelli and Other Procedures for Complex Transposition of the Great Arteries.
26A. Conditions with Double Discordance (Congenitally Corrected Transposition of the Great Arteries).
26B. Isolated Atrioventricular Discordance.
27. Anatomically Corrected Malposition of the Great Arteries.
28. Double-Outlet Ventricle.
29. Tricuspid Atresia.
30. Pulmonary Atresia and Intact Ventricular Septum.
31. Hypoplastic Left Heart Syndrome.
32. Double-Inlet Ventricle.
33. The Syndrome of Isomeric Right Atrial Appendages and Visceroatrial Heterotaxy, Often Associated with Congenital Asplenia.
34. The Syndrome of Isomeric Left Atrial Appendages and Visceroatrial Heterotaxy, Often Associated with Polysplenia.
35. The Cavopulmonary Shunt.
36. The Fontan-Kreutzer Procedure.
37. Complications of the Fontan Procedure.
38. Coronary Arteriovenous Fistula.
39. Cardiac Diverticulum and Aneurysm.
40. Cardiac Tumors.
41A. Conjoined Twins.
41B. Ectopia Cordis.
41C. Idiopathic Arterial Calcification of Infancy.
41D. Persistent Fifth Aortic Arch.
41E. Supero-Inferior Ventricles and Hearts with Twisted Atrioventricular Connections.
41F. Kartagener""s Syndrome.
41G. Myocardial Non-Compaction.
41H. Systemic Venous Anomalies Including Divided Right Atrium.
41I. Isolation of the Subclavian, Innominate, or Left Common Carotid Artery.
42. Pulmonary Ventricle to Pulmonary Artery Conduits.
43. Pulmonary Veno-Occlusive Disease.
44. Pulmonary Vascular Disease.
45. Outcomes of Extracorporeal Membrane Oxygenation and Ventricular Assist for Congenital Heart Disease.
46. Dilated Cardiomyopathy.
47. Heart Transplantation.
48. Congenital Heart Block.
49. Long QT Syndrome.
50. Supraventricular Arrhythmias.
51. Ventricular Tachycardia.
52. Epilogue.

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