European Heart Journal Advance Access published online on July 3, 2009
European Heart Journal, doi:10.1093/eurheartj/ehp283
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Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org
Doing the right thing at the right time: is there more to pulmonary valve replacement than meets the eye?
Division of Cardiology, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5g1X8
* Corresponding author. Tel: +1 416 813 6132, Fax: +1 416 813 7547, Email: andrew.redington@sickkids.ca
This editorial refers to Quantitative assessment of homograft function 1 year after insertion into the pulmonary position: impact of in situ homograft geometry on valve competence, by J. Nordmeyer et al. doi:10.1093/eurheartj/ehp204
| The first 10% of the full text of this article appears below. |
Prior to Lillehei's first intracardiac repair, a child born with tetralogy of Fallot had a 50% chance of being alive at the age of 2 years.1 In the modern era, >90% of patients reach the age of 40.2 This dramatic increase in survival is primarily a reflection of the improvements in surgical technique and peri-operative care at the time of primary repair. Indeed, the overall late mortality and morbidity have not changed substantially during the last decades.2 Consequently there are a growing number of teenage and adult survivors after right ventricular outflow tract (RVOT) surgery, many of whom are destined to become symptomatic as a result of decades of free pulmonary incompetence. Previously thought to be the innocent
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Related articles in EHJ:
- Quantitative assessment of homograft function 1 year after insertion into the pulmonary position: impact of in situ homograft geometry on valve competence
- Johannes Nordmeyer, Victor Tsang, Régis Gaudin, Philipp Lurz, Alessandra Frigiola, Alexander Jones, Silvia Schievano, Carin van Doorn, Philipp Bonhoeffer, and Andrew M. Taylor
EHJ 2009 30: 2147-2154.[Abstract] [Full Text]