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Ann Thorac Surg 2002;74:973-974
© 2002 The Society of Thoracic Surgeons
a Cardiovascular Surgery Program, Advanced Cardiology Center, Centro Medico Ramon Emeterio Betances, PO Box 1838, Mayaguzz, PR 00681 USA
e-mail: garciarinald{at}prtc.net
To the Editor
I was very surprised to read the article on pulmonary artery translocation by Rodefeld and associates [1]. Right coronary arteries that arise from the left sinus, of which four variants exist [2], have a slit orifice and an intramural segment [3]. The anomalous right coronary artery has a common wall with the aorta. In cases where the anomalous trunk passes under the left-right commissure, additional compression is applied by the aortic valve [3].
In 1994, my colleagues and I [3] reported our experience with the surgical treatment of coronary arteries with anomalous origin and slit ostium. Right coronary arteries that arise ectopically from the right sinus also have a slit ostium and an intramural segment [4, 5]. These right coronary arteries physiologically behave like those that arise in an anomalous manner [3]. The rationale for surgical therapy is to convert the slit orifice into an opening of 4 to 5 mm that alleviates compression of the trunk in the intramural segment.
We recently reviewed our data and, to date, have operated on 19 patients without any operative deaths. The mean follow-up is 6.2 years (range, 0.3 year to 12.3 years), and the 18 surviving patients are in New York Heart Association class I or II.
Creating a new orifice for the takeoff of the right coronary artery is a very simple procedure and is certainly easier than performing a pulmonary artery translocation. I encourage Rodefeld and colleagues to try this simple approach to a complex clinical problem.
References
This article has been cited by other articles:
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B. G. Vasseur, P. Lerch, and M. L. Sage Statue with clubbed feet: another reading Ann. Thorac. Surg., February 1, 2004; 77(2): 756 - 756. [Full Text] [PDF] |
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