CONGENITAL HEART DISEASE TESTS FOR INFANTS
What changed between versions
Added 10 new genetic disease screening requirements including acid maltase deficiency, globoid cell leukodystrophy, Gaucher's disease, Niemann-Pick disease, and Fabry disease to the mandatory newborn screening panel.
Added new heart disease screening requirements requiring echocardiograms and electrocardiograms for newborns with specific family history of congenital heart disease, sudden cardiac death, or other cardiac conditions.
Added requirement for health care providers to use a standard department-developed questionnaire to evaluate whether further heart disease screening is necessary based on abnormal fetal ultrasound or diagnosed systemic/genetic disorders.
Modified heart disease screening eligibility criteria to include specific family history factors such as sudden cardiac death before age 50, implantable defibrillators, cardiomyopathies, Marfan syndrome, and heritable pulmonary arterial hypertension.