All 50 states
require newborn screening tests.
Not exact matches
Save Babies Through
Screening Foundation educates parents, pediatric healthcare providers, and policy makers about available comprehensive newborn screening, the importance of obtaining positive or other test results requiring follow - up actions within 5 days of birth, and the importance of prompt confirmatory testing and treatment / management whe
Screening Foundation educates parents, pediatric healthcare providers, and policy makers about available comprehensive
newborn screening, the importance of obtaining positive or other test results requiring follow - up actions within 5 days of birth, and the importance of prompt confirmatory testing and treatment / management whe
screening, the importance of obtaining positive or other
test results
requiring follow - up actions within 5 days of birth, and the importance of prompt confirmatory
testing and treatment / management when needed.
Although most states
require only a handful of
tests, a panel of experts convened by the U.S. Department of Health and Human Services and the March of Dimes recommends
newborns be
screened for 30 genetic disorders, including hypothyroidism, cystic fibrosis, and sickle cell anemia.
More than 40 states
require screening at birth for sickle cell anemia, along with other routine
newborn screening tests.
All states
require certain
screening tests to be performed on
newborns, even if they appear healthy.
For example, a new policy was recently passed that
requires an oxygen saturation
test be performed at the time of the
newborn screening to help prevent against congenital heart disease.
Universal
newborn screening: Every
newborn infant should undergo universal
newborn screening, including blood
testing, as
required by state laws.
All states
require at least some
newborn testing, like
screening for PKU, sickle cell anemia, and other inherited conditions.
Newborn Screen / Metabolic Panel: A blood
test done by a small prick to the heel, this
test checks baby for a number of potential diseases and disorders that
require fast treatment to ensure normal development.
California had begun an experimental program to
screen newborns for two dozen genetic disorders, a great leap from the four
tests required.
«Our study demonstrates that policy changes such as the one in Utah that
required CMV
testing after failed
newborn hearing
screening can improve the identification of infants with hearing loss, even those without congenital CMV,» said Marissa Diener, lead author and associate professor at the University of Utah's Department of Family and Consumer Studies.
Other recommendations include
requiring parental permission for the
screening of
newborn patients, adding genetic information to health records, and how genetic
testing should be used regarding adoption and paternity issues.