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This document is used by hospitals to provide contact information for key personnel involved in the Newborn Screening Program, including directors of various departments and individuals responsible
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How to fill out Newborn Screening Program Hospital Contacts and Designees

01
Gather all relevant information about the hospital's newborn screening program.
02
Identify the primary contact person responsible for the newborn screening process.
03
Fill in the contact person's full name, position, and direct phone number.
04
Include an alternate contact person in case the primary contact is unavailable.
05
Provide the alternate contact's full name, position, and direct phone number.
06
Ensure all information is accurate and up-to-date.
07
Review the completed form for any errors or missing information before submission.
08
Submit the filled-out form to the designated authority or department handling newborn screening.

Who needs Newborn Screening Program Hospital Contacts and Designees?

01
Hospitals that conduct newborn screening tests.
02
Healthcare providers involved in the newborn screening process.
03
Public health officials monitoring newborn screening programs.
04
Administrators responsible for ensuring compliance with newborn screening laws and regulations.
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People Also Ask about

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 NBS Program takes a blood sample from a newborn's heel from 12 to 48 hours after birth to check for genetic disorders. At the same time, the newborn receives a hearing and congenital heart disease screening.
Newborn screening is a preventative public health initiative which allows detection of disorders early in life before clinical features are present.
Newborn blood spot screening is offered to parents to test their baby for one of nine rare but serious health conditions. Early diagnosis and treatment can improve the health of affected individuals, as well as prevent complications including severe disability and death.
Newborn screening is a simple procedure to find out if baby has a congenital metabolic disorder that may lead to mental retardation and even death if left untreated. Importance of Newborn Screening Newborn screening allows for early detection of disorders. If detected, treatment may be done immediately.
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.

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The Newborn Screening Program Hospital Contacts and Designees is a protocol that establishes designated individuals within hospitals who are responsible for managing and relaying information related to newborn screening tests and results.
All hospitals that perform newborn screenings or have facilities that accommodate newborn deliveries are required to file Hospital Contacts and Designees to ensure proper communication and management of screening processes.
To fill out the Hospital Contacts and Designees form, hospitals must provide accurate contact information for designated personnel, including names, roles, phone numbers, and email addresses, ensuring that the data is up-to-date.
The purpose of the Newborn Screening Program Hospital Contacts and Designees is to streamline communication between healthcare providers and public health agencies, facilitating timely follow-up on newborn screening results and ensuring compliance with public health protocols.
The information required includes the names and roles of designated contacts, their phone numbers, email addresses, and the specific responsibilities related to newborn screenings at the hospital.
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