Population-based surveillance of congenital heart defects among adolescents and adults: surveillance methodology.
Jill GlidewellWendy BookCheryl Raskind-HoodCarol HogueJulie E DunnMichelle GurvitzAl OzonoffClaire McGarryAlissa Van ZutphenGeorge LuiKarrie F DowningTiffany Riehle-ColarussoPublished in: Birth defects research (2018)
To our knowledge, this is the first population-based, multi-site CHD surveillance among adolescents and adults in the U.S. Identification of people living with CHDs through healthcare encounters using multiple data sources was feasible, though data quality varied and linkage/de-duplication was labor-intensive.