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Nomenclature, Classification, and Risk Score Assessment of the Adult with Congenital Heart Disease

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Intensive Care of the Adult with Congenital Heart Disease

Part of the book series: Congenital Heart Disease in Adolescents and Adults ((CHDAA))

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Abstract

More adults than children are alive with congenital heart disease, and many of these require cardiac surgery. Notwithstanding this fact, data about the outcomes of adults undergoing congenital heart surgery are limited. Multi-institutional databases are used for outcomes analysis, quality assessment, and quality improvement. The Society of Thoracic Surgeons (STS) Congenital Heart Surgery Database (CHSD) is the largest database of pediatric and congenital cardiac operations in the world. STS CHSD contains preoperative, operative, and outcomes data for all patients undergoing congenital and pediatric cardiovascular operations at participating hospitals. The nomenclature, classification, and risk score assessment provided by this platform is standardized across all participants. These tools facilitate multi-institutional initiatives to analyze outcomes and assess and ultimately improve the quality of care provided to adults with congenial heart disease who undergo cardiac surgery. The purpose of this chapter is to review nomenclature, classification, and risk scores for adults with congenital heart disease.

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Jacobs, J.P. (2019). Nomenclature, Classification, and Risk Score Assessment of the Adult with Congenital Heart Disease. In: da Cruz, E., Macrae, D., Webb, G. (eds) Intensive Care of the Adult with Congenital Heart Disease. Congenital Heart Disease in Adolescents and Adults. Springer, Cham. https://doi.org/10.1007/978-3-319-94171-4_3

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  • DOI: https://doi.org/10.1007/978-3-319-94171-4_3

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  • Publisher Name: Springer, Cham

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  • Online ISBN: 978-3-319-94171-4

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