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Requiring Newborn Screening of Critical Congenital Heart Disease

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Requiring Newborn Screening of Critical Congenital Heart Disease

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With the numerous technological advances that have occurred in today’s health care system, one would think newborn screening would be required in Maryland for the most common birth defect in the United States, critical congenital heart disease (CCHD), but only just this year has the state considered the requirement (Department of Legislative Services, Office of Information Systems [DLSOIS], 2011). Critical congenital heart disease, a disorder in which an infant’s heart or blood vessels near the heart develop abnormally before birth, affects approximately 8 out of every 1,000 infants each year in the US, amounting to around 36,000 infants (DLSOIS, 2011). CCHD is the leading cause of death among infants within the first year of life, amounting to nearly 40% of deaths, often due to the fact that a large number of infants with this disease go undetected (Martin, Bradshaw, & Wright, n.d.). Although some babies are diagnosed with congenital heart disease shortly before or after birth, many diagnoses are not made until days, weeks, or months later; sometimes not at all. Many benefits are associated with implementing CCHD screening, many treatment options are available for those diagnosed with CCHD, and a bill is being proposed to the State of Maryland’s General Assembly about including this screening in the Department of Health and Mental Hygiene’s Newborn Screening Program (DLSOIS, 2011). The benefits outweigh the concerns when referring to implementing CCHD screening in today’s hospitals. An effective screening mechanism for newborns which could accurately detect CCHD constitutes a great reduction in infant mortality (DLSOIS, 2011). If diagnosed early, most infants can undergo surgery to effectively remove the abnormalities before complications occur (Chang, Gurvitz, & Rodriguez,

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