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This document serves as a statement of need and reasonableness for proposed amendments to the Newborn Screening Rules by the Minnesota Department of Health, detailing the need for updated practices
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How to fill out newborn screening rule

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How to fill out Newborn Screening Rule

01
Obtain the Newborn Screening Rule form from your healthcare provider.
02
Ensure that the form includes all necessary information, such as the baby's name, date of birth, and parent's contact information.
03
Follow the instructions on the form to collect the required biological samples, usually from a heel prick.
04
Label the samples accurately as per the guidelines provided.
05
Submit the completed form and samples to the designated laboratory within the specified timeframe.

Who needs Newborn Screening Rule?

01
All newborns, typically within the first few days after birth, as mandated by state laws.
02
Parents or guardians of newborns should ensure screening takes place to detect potential health issues early.
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About Newborn Screening Within the first 24 to 48 hours after birth, babies undergo a simple heel stick and a few drops of blood are collected on a special paper card. Health care providers then test those blood spots for a number of congenital disorders (conditions that are present at birth).
Newborn screening usually starts with a blood test, followed by a hearing test and possibly other tests. First, hospital staff fill out a newborn screening card with the infant's vital information — name, sex, weight, and date and time of birth — and the date and time of the blood collection.
Blood spots are best collected between 24 and 48 hours of age. Blood spots collected before 24 hours of age cannot be fully interpreted, which means some test results will be marked “unsatisfactory” on the newborn screening report. An unsatisfactory result will require another blood spot collection.
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.
Blood spots are best collected between 24 and 48 hours of age. Blood spots collected before 24 hours of age cannot be fully interpreted, which means some test results will be marked “unsatisfactory” on the newborn screening report.
Newborn Screening Tests 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.
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.

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The Newborn Screening Rule is a set of guidelines and regulations designed to ensure that all newborns are screened for certain genetic, metabolic, hormonal, and functional conditions that can affect their long-term health.
Healthcare providers, hospitals, and birthing facilities that conduct births and provide care to newborns are required to file the Newborn Screening Rule.
To fill out the Newborn Screening Rule, healthcare providers must accurately complete the specified forms with information about the newborn, including parental details, birth details, and results from the screening tests.
The purpose of the Newborn Screening Rule is to identify infants with certain serious conditions early, so they can receive timely treatment and support, thus improving health outcomes and reducing the risk of severe complications.
The information that must be reported includes the newborn's name, date of birth, mother's details, screening test results, and any follow-up actions that may be necessary.
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