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J Thorac Cardiovasc Surg 2007;134:1410-1412
© 2007 The American Association for Thoracic Surgery
Surgery for Congenital Heart Disease |
| The first 300 words of the full text of this article appear below. |
Dr V. Mohan Reddy. (Stanford, Calif). I would like to thank the association for the privilege of discussing this manuscript. I would also like to thank the authors for providing me with the manuscript early enough and congratulate them for an elegant presentation and study.
Dr Reemtsen and colleagues report on a 15-year single-institution experience of neonatal Ebsteins anomaly with an overall mortality of 25% but none since 1996. This approach commits all patients to single—ventricle circulation. Probably some of these could have been a 2-ventricle or a 1
-ventricle type of repair based on our experience and review of the literature on neonatal Ebsteins anomaly. It might be that although this approach yields very good survival, a more balanced individualized approach might yield similar results without committing all patients to single-ventricle repairs.
In your manuscript, at least, I would say that 50% of the patients have a GOS ratio of less than 1. Perhaps in these patients a 2-ventricle or a 1
-ventricle type of repair could be attempted as a first option.
Also, by means of right atrial reduction and RV plication, with or without, the GOS ratio immediately decreases if you do a postoperative study. But what is more important in your manuscript is the long-term follow-up and continued remodeling of the ventricle and the septum. This is, I think, the strength of your study.
The authors state that these patients were all catheterized but do not present any data on the catheterization. I have 4 or 5 questions for you, and I would appreciate if you could answer each one of them before I move on to the next.
Do you currently adopt this approach in all neonates or consider 2-ventricle repair in some? If so, what criteria do you use?
Dr Reemtsen. Our goal,
Related Article
J. Thorac. Cardiovasc. Surg. 2007 134: 1406-1412.
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