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This document outlines the procedures, requirements, and guidelines for newborn blood screening in Oklahoma, including the tests required, conditions screened for, follow-up procedures, treatment
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How to fill out newborn blood screening
How to fill out Newborn Blood Screening
01
Prepare for the screening by ensuring that all necessary materials are available.
02
Wash hands thoroughly and put on gloves.
03
Identify the newborn and ensure consent is obtained from the parents or guardians.
04
Use a heel lancet to prick the baby's heel to obtain a blood sample.
05
Collect the blood onto a special blotting card, ensuring the blood soaks through to the other side.
06
Allow the sample to dry completely at room temperature.
07
Fill out the necessary information on the form attached to the blood spot card, including the baby's name, date of birth, and other identifying details.
08
Package the dried blood sample according to the guidelines provided by the testing laboratory.
09
Send the sample to the designated laboratory within the timeframe specified.
Who needs Newborn Blood Screening?
01
All newborns should receive newborn blood screening.
02
It is particularly important for premature infants and those with a family history of genetic disorders.
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How is baby screening done?
A midwife or nurse will your baby's heel with a lancet (a special needle) and will collect a few drops of blood onto a screening card. Then, the card is sent to a central laboratory for processing. Newborn bloodspot screening involves a combination of biochemical and genetic testing.
What is the routine newborn screening test?
Nearly all babies will have a simple blood test to check for disorders that are not apparent immediately after delivery. Some of these disorders are genetic, metabolic, blood, or hormone-related. Each state in the United States requires screening tests, but the specific tests performed vary among the states.
What are the guidelines for newborn screening?
Parents should take babies not born in a hospital or not screened before hospital discharge to a clinic (or back to the hospital) to be checked. Babies need to be screened within 24-48 hours after birth. A few drops of blood from the baby's heel provide the blood sample sent to a lab for screening.
What are the steps in newborn screening?
There are three parts to newborn screening: the blood test (or heel stickWhen the baby's heel is pricked to collect a sample of blood for newborn screening); the hearing screen; and pulse oximetry.
What is included in newborn blood screening?
Within 48 hours of a child's birth, a sample of blood is obtained from a “heel stick,” and the blood is analyzed for up to 50 diseases, including phenylketonuria (PKU), sickle cell disease, and hypothyroidism. The sample, called a “blood spot,” is tested at a state public health or other participating laboratory.
What is the blood test for a newborn?
The newborn blood spot test might find your baby is, or may be, a genetic carrier of cystic fibrosis, sickle cell disease or another red blood cell condition. Babies who are genetic carriers do not have the condition themselves and will usually be healthy. But they could pass the condition on to any children they have.
What are the steps for newborn screening?
There are three parts to newborn screening: the blood test (or heel stickWhen the baby's heel is pricked to collect a sample of blood for newborn screening); the hearing screen; and pulse oximetry.
What are the 7 conditions for a newborn screening test?
Newborn screening tests may include: Phenylketonuria (PKU). PKU is an inherited disease in which the body cannot metabolize a protein called phenylalanine. Congenital hypothyroidism. Galactosemia. Sickle cell disease. Maple syrup disease. Homocystinuria. Biotinidase deficiency. Congenital adrenal hyperplasia.
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What is Newborn Blood Screening?
Newborn Blood Screening is a public health program that tests newborns for certain genetic, endocrine, and metabolic conditions that may not be apparent at birth.
Who is required to file Newborn Blood Screening?
The healthcare provider or hospital that delivers the baby is responsible for filing the Newborn Blood Screening.
How to fill out Newborn Blood Screening?
To fill out Newborn Blood Screening, healthcare providers should complete the designated form with the newborn's information, including their name, date of birth, and any relevant clinical history.
What is the purpose of Newborn Blood Screening?
The purpose of Newborn Blood Screening is to identify infants who may have serious health conditions early on, allowing for timely intervention and treatment to prevent severe health issues or developmental delays.
What information must be reported on Newborn Blood Screening?
The information that must be reported on Newborn Blood Screening includes the newborn's name, date of birth, the tests performed, and results, as well as any other relevant clinical information.
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