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Get the free Newborn Screening Report - dshs state tx

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This document is a report of newborn screening results indicating normal outcomes for various disorders screened by the Texas Department of State Health Services.
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How to fill out newborn screening report

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How to fill out Newborn Screening Report

01
Start by gathering the required information including the baby's name, date of birth, and parent's contact details.
02
Fill out the baby's medical history, including any known health issues or family health history.
03
Ensure that you have the correct screening collection date and time.
04
Collect the necessary blood samples using a heel prick method.
05
Apply the blood samples to the designated filter paper as per the guidelines.
06
Label the sample correctly with the baby's information and ensure all details are legible.
07
Complete the newborn screening report form by entering all the collected data accurately.
08
Review the report for accuracy and completeness before submission.
09
Submit the report along with the blood samples to the designated health authority or laboratory.

Who needs Newborn Screening Report?

01
All newborns typically need a Newborn Screening Report to identify potential health issues early.
02
Parents and caregivers who want to ensure their baby's health and development.
03
Healthcare providers who are responsible for monitoring the baby's health post-delivery.
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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.
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 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 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.
Specifications Test CodeNBS004 Test Summary Newborn Screening is a process where infants arescreened shortly after birth for a list of conditions thatare treatable, but are often not seen at birth.This panel screens for TSH, 17OHP, G6PD, IRT, TGAL, Biotinidase, Phenylalanine Turn Around Time 3 days3 more rows
The fastest way to obtain your child's NBS results is to contact the facility where the baby was born. If there is a result that needs follow-up, you will be contacted by phone to let you know what other testing is needed.
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.
There are four possible results in newborn blood spot screening: Within Normal Limits/Negative, Trait, Borderline, and Positive/Abnormal. A Within Normal Limits or Negative result means that the screen was normal for the disorder and no additional follow-up is required.

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The Newborn Screening Report is a document that contains the results of tests performed on newborns to identify any potential health conditions or disorders that may require early intervention.
Healthcare providers and hospitals are responsible for filing the Newborn Screening Report for each newborn shortly after birth.
To fill out the Newborn Screening Report, healthcare providers must collect necessary information about the newborn, including demographics, medical history, and the results of the screening tests performed.
The purpose of the Newborn Screening Report is to detect genetic, metabolic, and other congenital disorders in newborns early, allowing for timely treatment and better health outcomes.
The Newborn Screening Report must include the newborn's name, date of birth, specimen collection date, results of the screening tests, and any follow-up actions or recommendations.
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