Newborn screening packing slip - Colorado - colorado 2025

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  1. Click ‘Get Form’ to open the Newborn screening packing slip in the editor.
  2. Begin by filling in the 'Ship To' section with the address of the CDPHE Laboratory Services Division, ensuring accuracy for timely processing.
  3. In the 'From' section, enter your contact details including your name, phone number, email, company name, and complete address.
  4. Specify the shipping method you will use to send the specimen. If you have a customer number, include it in the designated field.
  5. Fill in any ID numbers related to the specimen card as required.
  6. Provide the infant's information by entering their last name(s), first name, and date of birth accurately.
  7. Finally, ensure that all fields are completed before saving or printing your packing slip for submission.

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Under Colorado statute, all babies born in Colorado are required to be tested twice unless a childs parents or legal guardians refuse testing on behalf of the child. To perform newborn screening, a few drops of blood are taken from your babys heel and put on a special paper.
Today, all 50 states, the District of Columbia, and the Commonwealth of Puerto Rico have newborn screening programs. This means that nearly every child born in the United States or Puerto Rico is screened shortly after birth. All states currently require newborn screening for at least 29 health conditions.
Newborn Screening (NBS) Specimen Collection Supplies Medicaid/CHIP/Uninsured (NBS 3) or Insurance/Self-Pay (NBS 4) Newborn Screening Specimen Collection Kit. Heel Lancet. For average weight newborns, do not exceed a puncture depth of 2.0 mm. Alcohol. Sterile gauze or cotton ball. Gloves.
A midwife or nurse will your babys heel with a lancet (a special needle) and will collect a few drops of blood onto a screening card. Then, the card is sent to a central laboratory for processing. Newborn bloodspot screening involves a combination of biochemical and genetic testing.
The newborn screening panel currently includes: phenylketonuria, maple syrup disease, arginosuccinase deficiency, citrullinemia,HMG-CoA layase deficiency, isovaleric acidemia, methylmalonic acidemia, propionic acidemia, beta-ketothiolase deficiency, methylcrotonyl-CoA carboxylase deficiency, glutaric acidemia
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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.

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