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Eur J Cardiothorac Surg 2006;30:414
© 2006 Elsevier Science NL
Letter to the Editor |
Cardiothoracic Centre, All India Institute of Medical Sciences, New Delhi 110029, India
Received 2 April 2006; accepted 5 May 2006.
* Corresponding author. Address: Department of Cardiothoracic and Vascular Surgery, All India Institute of Medical Sciences, New Delhi 110029, India. Tel.: +91 11 26588500; fax: +91 11 26588663. (Email: shivchoudhary{at}hotmail.com).
Key Words: Prosthetic graft Innominate vein Cavopulmonary shunt
We read with interest the case report "A Gore-Tex new-innominate vein: a surgical option for complicated bilateral cavopulmonary shunts" by Vida et al. [1]. We congratulate the authors for their innovative strategy in tiding over a troublesome situation following the bilateral cavopulmonary shunt (BCPS). However, certain reservations can be expressed over the initial management strategy planned for this patient. In the initial stage alone, considering a right pulmonary artery of only 3 mm size for a 14-month-old child (weight not specified), a left-sided systemic to pulmonary artery shunt would have provided an adequate initial palliation and considering that the pulmonary arteries were confluent, it would have probably led to the growth of the right pulmonary artery [2]. Previous experience has shown adequate growth of the pulmonary arteries after a systemic to pulmonary artery shunt [2], whereas their growth following a cavopulmonary shunt procedure is only a probability, particularly if the pulmonary arteries are not adequate in size [35]. Although the systemic to pulmonary artery shunt would have resulted in the volume overload of the systemic ventricle, the subsequent growth of the pulmonary arteries would probably have been better and avoided the unfortunate situation encountered by the authors. The risk of occlusion of the prosthetic graft when used as a systemic to pulmonary artery shunt would also have been less than its risk of occlusion between the two cavae, which the authors were forced to perform. Considering that the child was 14 months old, he could have then returned in the ensuing year for the BCPS with a more favourable pulmonary artery anatomy.
References
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