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Get the free Newborn Screening ACT Sheet - ncbi nlm nih

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This guideline provides information on the diagnosis and management of tyrosinemia, a genetic condition affecting the metabolism of tyrosine in newborns, and outlines actions for clinicians to take
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How to fill out newborn screening act sheet

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How to fill out Newborn Screening ACT Sheet

01
Start by gathering all necessary information about the newborn, including full name, date of birth, and mother's details.
02
Complete the identification section of the ACT Sheet accurately.
03
Fill in the 'Screening Test Results' section, ensuring that all relevant tests have been performed.
04
If applicable, indicate any follow-up actions required based on screening results.
05
Review all entered information for accuracy and completeness.
06
Sign and date the form, and submit it to the relevant health department or authority.

Who needs Newborn Screening ACT Sheet?

01
All newborns should undergo newborn screening, so the Newborn Screening ACT Sheet is needed for each infant after birth.
02
Parents or guardians of the newborn must complete this sheet to ensure appropriate screening and follow-up.
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Recommended Specimen Collection Technique Place baby's limb in dependent position. Cleanse skin with alcohol, DRY, and puncture with disposable heel lancet (<2.0mm length). Wipe off first drop of blood. Allow a drop of blood to form and apply DIRECTLY to filter paper.
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.
The blood test or heel stick determines if a newborn might have one of many serious health conditions, including severe combined immunodeficiency (SCID). A small blood sample is taken from a baby's heel, or sometimes through a vein, and placed on a newborn screening card.
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.
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.
The conditions screened for include spinal muscular atrophy, cystic fibrosis, sickle cell disease and other hemoglobinopathies, endocrine diseases, inborn errors of metabolism, lysosomal storage diseases, severe combined immunodeficiencies, critical congential heart defects, and hearing loss.
This test panel checks for thyroid disease, deficiency of important enzymes namely G6PD & Biotinidase and for evidence of other diseases like Galactosemia, Phenylketonuria (PKU), Cystic fibrosis & Congenital adrenal hyperplasia (CAH) .
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.

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The Newborn Screening ACT Sheet is a document used to report the results of newborn screening tests, which are conducted to identify certain genetic, metabolic, hormonal, and functional conditions in newborns.
Health care providers, such as hospitals and birthing centers, that perform newborn screenings are responsible for filling out and filing the Newborn Screening ACT Sheet.
To fill out the Newborn Screening ACT Sheet, providers need to enter patient information, screening results, any follow-up actions needed, and contact information for the responsible health care professional.
The purpose of the Newborn Screening ACT Sheet is to ensure timely reporting and follow-up for newborn screening tests, facilitating early detection and management of potential health issues in newborns.
The information that must be reported includes the newborn's demographic information, screening results, any abnormal findings, actions taken, and the health care provider's contact details.
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