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PapaHappyStar
I did some looking around in online journals and in the library before my surgery:
- Papers and notes ( Contact me if you need copies )
AVR -- Ross Procedure- Claudia Schmidtke,Matthias Bechtel,Michael Hueppe,Hans-H. Sievers Time Course of Aortic Valve Function and Root Dimensions After Subcoronary Ross Procedure for Bicuspid Versus Tricuspid Aortic Valve Disease Circulation. 2001;104:I-21
- Phillips, John R. Long-term outcomes of the Ross operation in children and adults Prog. in Ped. Card. 2003;16:149-154
- Schmid et al. Structural and biomolecular changes in aorta and pulmonary trunk of patients with aortic aneurysm and valve disease: implications for the Ross procedure Eur J Cardiothorac Surg.2004; 25: 748-753.
- Shahzad G. Raja Dilation of the pulmonary autograft: much more than just histopathological and biomolecular mechanisms Eur J Cardiothorac Surg 2004;26:661-662
- Solowiejczyk DE, Bourlon F, Apfel HD, Hordof AJ, Hsu DT, Crabtree G, Galantowicz M, Gersony WM, Quaegebeur JM Serial echocardiographic measurements of the pulmonary autograft in the aortic valve position after the Ross operation in a pediatric population using normal pulmonary artery dimensions as the reference standard. Am J Cardiol. 2000 May 1;85(9):1119-23.
- Tirone E. David, Ahmad Omran, Joan Ivanov, Susan Armstrong, Mauro P.L. de Sa, Brian Sonnenberg, Gary Webb DILATION OF THE PULMONARY AUTOGRAFT AFTER THE ROSS PROCEDURE J Thorac Cardiovasc Surg 2000;119:210-220
- Ward, C Clinical significance of bicuspic aortic valve Heart 2000;83:81-85
- Fedak,Verma,David,Leask,Weisel,Butany Clinical and Pathophysiological Implications of a Bicuspid Aortic Valve Circulation 2002;106:900-904
- Cripe L, Andelfinger G, Martin LJ, Shooner K, Benson DW Bicuspid aortic valve is heritable. J Am Coll Cardiol. 2004 Jul 7;44(1):138-43.
- L Wallby, B Janerot-Sjöberg, T Steffensen and M Broqvist T lymphocyte infiltration in non-rheumatic aortic stenosis: a comparative descriptive study between tricuspid and bicuspid aortic valves Heart 2002;88:348-351
- Sondergaard,Stahlberg,Thomsen Magnetic Resonance Imaging of Valvular Heart Disease Journal of Magnetic Resonance Imaging 1999;10:627
- Arai,Epstein,Bove,WolffVisualization of Aortic Valve Leaflets using Black Blood MRI Journal of Magnetic Resonance Imaging 1999;10:771
- Books
Adults with Congenital Heart Disease- Congenital Heart Disease in Adults
Joseph K. Perloff, MD and John S. Child, MD. 406 pp.Philadelphia, Pa: WB Saunders; 1997. ISBN 0-7216-2998-9.
Circulation. 1998;98:1039-1040 said:The organization of the book highlights the multisystem, problem-oriented approach to healthcare delivery in this group of patients. Complete and careful indexing allows identification of issues pertinent to specific anatomic lesions, whether treated by surgery or not. The book is amply illustrated. A unique collection of high-quality prints exemplifies specific physical findings, pathological and histological specimens, x-rays, and angiographic and echocardiographic views in addition to ECGs, surgical drawings, and historical photographs.
Learning from this book is a pleasurable experience for the student of adult congenital heart disease at any level. The wealth of information ranges from the basic to the complex. The end product is luxuriously assembled as can only be done when knowledge meets experience. Perloff and Child have provided us with a classic textbook. - Diagnosis and Management of Adult Congenital Heart Disease
Edited by Michael A. Gatzoulis, Gary D. Webb, and Piers E.F. Daubeney. 517 pp., illustrated. Philadelphia, Churchill Livingstone, 2003. ISBN 0-443-07103-9.
NEJM said:The book has several sections. The first, entitled "General Principles," is an extensive discussion of cardiac morphology, genetics, procedures (both percutaneous and surgical) for the treatment of congenital abnormalities, arrhythmias, and heart and lung transplantation. Subsequent sections concisely discuss septal defects, valvular disorders, abnormalities of left and right ventricular outflow, and cyanotic conditions, the most important of which are tetralogy of Fallot and Eisenmenger's syndrome. The final sections deal with uncommon and obscure abnormalities, such as univentricular hearts and coronary arterial anomalies. Within each chapter that is devoted to a specific abnormality, the discussion focuses on long-term management, prognosis, and the risks associated with pregnancy, noncardiac surgery, and infective endocarditis. Each chapter contains an abundance of illustrative diagrams as well as numerous morphologic, radiographic, and echocardiographic images. In addition, much of the most important information is highlighted in carefully constructed tables.
This book should serve very effectively as an accessible resource for the internist or cardiologist who does not have extensive training in congenital heart disease. Its organization and highly focused discussions should allow the reader to locate needed information easily and efficiently. - Congenital Heart Disease in the Adult
By Welton M. Gersony and Marlon S. Rosenbaum. 304 pp., illustrated. New York, McGraw-Hill, 2001. ISBN 0-07-032909-5.
NEJM said:This monograph does not contain all the information that one might conceivably desire about a specific congenital cardiac abnormality. It is precisely designed not to be exhaustive. Rather, it is intended to be an easily accessible resource for the general internist (in training or practice) or the cardiologist without extensive training in congenital heart disease. It is undoubtedly successful in these terms. For such physicians, the patient with congenital heart disease can be intimidating and anxiety provoking. The design, style, and content of the book ensure that it will succeed in alleviating much of that intimidation and anxiety.
- Congenital Heart Disease in Adults