Abstract
In the Ross procedure, the normal pulmonary valve with part of the pulmonary artery is moved to the aortic position to replace a diseased aortic valve and the native pulmonary artery and valve are replaced with a pulmonary homograft. The coronary arteries are transplanted into the neoaorta (native pulmonary artery). This procedure is the operation of choice in infants and children, since it allows the valve replacement to grow as the patient matures thus eliminating the need for anticoagulation to prevent thromboembolism. Its use in adults remains controversial.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Fukuma A, Moritake K, Fukuda M, Kuwabara S. Experimental study on the difference of ischemic threshold between cerebral cortex and thalamus with middle latency auditory evoked potentials. No To Shinkei. 1990;42:481–8.
Gaca A, Jaggers JJ, Dudley T, Bisset GS. Repair of congenital heart disease: a primer-part 1. Radiology. 2008;247:617–31.
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer-Verlag London
About this chapter
Cite this chapter
Mazur, W., Siegel, M.J., Miszalski-Jamka, T., Pelberg, R. (2013). Ross Procedure. In: CT Atlas of Adult Congenital Heart Disease. Springer, London. https://doi.org/10.1007/978-1-4471-5088-6_30
Download citation
DOI: https://doi.org/10.1007/978-1-4471-5088-6_30
Published:
Publisher Name: Springer, London
Print ISBN: 978-1-4471-5087-9
Online ISBN: 978-1-4471-5088-6
eBook Packages: MedicineMedicine (R0)