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This document provides instructions for completing a newborn screening lab slip, including the necessary information to be filled out for the newborn's screening tests, including infant and mother's
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How to fill out newborn screening lab slip

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How to fill out Newborn Screening Lab Slip

01
Start by filling in the baby's full name.
02
Include the baby's date of birth and time of birth.
03
Write the baby's gender.
04
Fill in the parent's or guardian's name.
05
Provide the contact information for the parents or guardians.
06
Record the place of birth, including facility name and address.
07
Enter the Medicaid or insurance information, if applicable.
08
Check that all information is accurate and complete.
09
Sign and date the form as required.

Who needs Newborn Screening Lab Slip?

01
All newborns should have a Newborn Screening Lab Slip filled out shortly after birth to screen for various health conditions.
02
Parents or guardians of newborns should ensure that the lab slip is filled out and submitted.
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Newborn screening has three different parts: Blood spot screening, which determines if a baby might have one of many serious conditions. Pulse oximetry screening, which determines if a newborn might have certain heart conditions. Hearing screening, which determines if a newborn might be deaf or hard of hearing.
Every state in the U.S. has a newborn screening program that screens newborns for many serious but treatable congenital diseases. Many of these conditions are detected by testing a small sample of blood taken from a newborn's heel.
For each state, a small blood sample (“heel stick”) is collected from each newborn within 48 hours of birth and sent to a laboratory for testing for a panel of genetic disorders. Newborn screening programs may screen for up to 50 diseases, including phenylketonuria (PKU), sickle cell disease, and hypothyroidism.
Screening tests are offered during pregnancy to try to find any health problems that could affect you or the baby. The tests – ultrasound scans, blood tests and a questionnaire – can help you make choices about care or treatment during pregnancy or after your baby is born.
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.
Every newborn is tested for a group of health disorders that aren't otherwise found at birth. With a simple blood test, doctors can check for rare genetic, hormone-related, and metabolic conditions that can cause serious health problems.
Every newborn is tested for a group of health disorders that aren't otherwise found at birth. With a simple blood test, doctors can check for rare genetic, hormone-related, and metabolic conditions that can cause serious health problems.

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A Newborn Screening Lab Slip is a document used to collect and submit samples for testing metabolic and genetic disorders in newborns.
Healthcare providers who deliver or care for newborns are required to file the Newborn Screening Lab Slip.
To fill out the Newborn Screening Lab Slip, provide the newborn's identification information, the date of collection, the healthcare provider's details, and any other required medical information.
The purpose of the Newborn Screening Lab Slip is to ensure that newborns are tested for specific disorders early in life to promote timely interventions and treatment.
The information that must be reported includes the newborn's name, date of birth, mother's name, test date, and any relevant clinical information.
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