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Get the free Newborn Screening Quality Assurance Program Data Report Form - cdc

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This document serves as a data report form for the Newborn Screening Quality Assurance Program, collecting quality control data related to various analytes in newborns.
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How to fill out newborn screening quality assurance

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How to fill out Newborn Screening Quality Assurance Program Data Report Form

01
Obtain the Newborn Screening Quality Assurance Program Data Report Form from the official website or request from the relevant authority.
02
Fill out the 'Facility Information' section with the name and address of the hospital or clinic.
03
Enter the date of the report and the reporting period.
04
Complete the 'Newborn Screening Tests Conducted' section, indicating the number of tests performed.
05
Provide data on the number of positive screening results and the follow-up actions taken.
06
Fill in the 'Outcomes' section, detailing the results of follow-up screening and any confirmed diagnoses.
07
Review all entries for accuracy and completeness.
08
Sign and date the form to certify the information is correct.
09
Submit the form according to the provided submission guidelines (online or by mail).

Who needs Newborn Screening Quality Assurance Program Data Report Form?

01
Hospitals and clinics that conduct newborn screenings.
02
Healthcare providers involved in neonatal care.
03
State public health departments monitoring newborn screening performance.
04
Quality assurance teams focused on improving newborn screening outcomes.
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0:22 1:47 Identification band matches the information on the newborn screening specimen collection. DeviceMoreIdentification band matches the information on the newborn screening specimen collection. Device select the safest area for puncturing the newborn's.
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 can get all the newborn screening test results from the baby's doctor. The Department of State Health Services (DSHS) will send the results to the doctor in seven to 14 days.
Newborn screening programs may screen for up to 50 diseases, including phenylketonuria (PKU), sickle cell disease, and hypothyroidism.
Results of newborn screening for hearing loss and heart disease are available as soon as the test is done. Blood test results usually are ready by the time a baby is 5–7 days old. Often, parents won't hear about results if screening tests were normal. They are contacted if a test was positive for a condition.
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.
Expanded Newborn Screening allows the detection of more genetic disorders which includes the following: Glucose-6 Phosphate Dehydrogenase Deficiency. Congenital Hypothyroidism. Congenital Adrenal Hyperplasia. Galactosemia. Phenylketonuria. Maple Syrup Disease. Cystic Fibrosis. Biotinidase Deficiency.
The newborn blood spot test checks for: cystic fibrosis (CF) sickle cell disease (SCD) congenital hypothyroidism (CHT) phenylketonuria (PKU) medium-chain acyl-CoA dehydrogenase deficiency (MCADD) maple syrup disease (MSUD) isovaleric acidaemia (IVA) glutaric aciduria type 1 (GA1)

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The Newborn Screening Quality Assurance Program Data Report Form is a standardized document used to collect and analyze data related to newborn screening processes, outcomes, and quality assurance measures.
Healthcare providers, hospitals, and laboratories that conduct newborn screening tests are required to file the Newborn Screening Quality Assurance Program Data Report Form to ensure compliance and monitor the quality of screening processes.
To fill out the form, users should follow the provided instructions, input relevant patient data, screening results, and any follow-up actions taken. It's important to ensure accuracy in all entries to maintain the integrity of the data.
The purpose of the form is to enhance the quality of newborn screening programs by systematically collecting data that can be used for quality monitoring, improvement initiatives, and ensuring the timely identification of congenital conditions.
The form requires reporting of information such as newborn's identification details, screening test results, follow-up actions taken, any diagnoses made, and outcomes related to the screening process.
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