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PROPOSAL FOR EXPANDED NEWBORN SCREENING IN ARKANSASOctober 2006DIVISION OF HEALTH ARKANSAS DEPARTMENT OF HEALTH AND HUMAN SERVICESNBS9.0 101806 Final RN 071507 TABLE OF CONTENTS EXECUTIVE SUMMARY
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How to fill out expanded newborn screening

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Here is how to fill out expanded newborn screening:
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Obtain the expanded newborn screening kit from a healthcare provider or hospital.
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Follow the instructions provided in the kit carefully.
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Use the lancets provided to prick the baby's heel and collect a small blood sample on the designated filter paper.
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Allow the blood sample to dry completely before placing it in the envelope provided.
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Fill out the required information on the envelope, including the baby's name, date of birth, and any other necessary details.
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Seal the envelope securely.
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Return the completed kit to the healthcare provider or hospital as instructed.
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Wait for the results to be sent to you, which usually takes a few weeks.
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Please note that it is essential to follow the instructions carefully to ensure accurate results.

Who needs expanded newborn screening?

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Expanded newborn screening is recommended for:
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- All newborns, regardless of birth weight or gestational age.
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- Babies born prematurely or with low birth weight.
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- Babies born to parents with a history of hereditary metabolic disorders or previous affected children.
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- Babies born to parents who are carriers of certain genetic conditions.
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- Babies with a family history of hereditary disorders.
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It is best to consult with a healthcare provider to determine if expanded newborn screening is necessary for a specific baby.
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Expanded newborn screening is a screening test that includes additional genetic disorders beyond the standard newborn screening test.
Healthcare providers are required to file expanded newborn screening for newborn babies.
Healthcare providers can fill out expanded newborn screening by collecting blood samples from newborn babies and sending them to a laboratory for analysis.
The purpose of expanded newborn screening is to detect potential genetic disorders in newborn babies early on so that treatment can be started promptly.
Expanded newborn screening requires reporting on a wide range of genetic disorders and conditions that may not be detected in a standard newborn screening.
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