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Get Newborn Screening Collection Guidelines - Adph
On 8140 AUM Drive, Zip 36117-7001 P.O. Box 244018, Zip 36124-4018 Montgomery, AL Phone: 334-260-3476 FAX: 334-260-3439 Contacts: Danita Rollin, Lynn Green, Deannie Morris Newborn Screening Lab Collection Guidelines Alabama Department of Public Health Bureau of Clinical Laboratories Newborn Screening Collection Guidelines Section 22-20-3 (as amended in 1987) of the Code of Alabama states that all infants must be administered a reliable test for PKU, Cystic Fibrosis, Hypothyroidism, CAH, Galact.
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1st FAQ
Blood Spot Collection Cards The New York State Newborn Screening Program tests dried blood specimens collected via heel stick. Drops of blood from the heel stick are used to saturate the marked circles of the specimen collection form. The blood spot is often called the Guthrie spot.
Blood collection from the heel is the standard for newborn screening. The medial and lateral parts of the underfoot are preferred.
The heel-stick is always the preferred method for collection of the newborn screening. If it is not possible to perform a heel-stick, please see the Alternative Methods for Collecting a Newborn Screen page for detailed information and instructions.
Lightly touch the filter paper against a large drop of blood and allow a sufficient quantity of blood to soak through to completely fill the circle. Apply blood to one side of the filter paper only, allowing full saturation of each circle. Either side of the filter paper may be chosen. Fill all circles.
Venepuncture. Venepuncture is the preferred method of blood sampling for term neonates, and causes less pain than heel-pricks (64).
The heel-stick is always the preferred method for collection of the newborn screening. If it is not possible to perform a heel-stick, please see the Alternative Methods for Collecting a Newborn Screen page for detailed information and instructions.
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 urine disease. ... Homocystinuria. ... Biotinidase deficiency. ... Congenital adrenal hyperplasia.
A newborn screening test should be collected when the infant is 24-48 hours of age. If the infant is discharged prior to 24 hours of age, a specimen MUST be obtained before discharge, and the parent or guardian must be informed of the importance of obtaining a repeat test before one week of age.
DANITA Related content
State Newborn Screening Request Information
• A baby's doctor will be given the recommendations on diagnosis, treatment, and...
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