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This document offers a comprehensive listing all of the conditions and disorders which the newborn screening program currently tests for.
This procedure explains how to properly collect a specimen for the newborn screening program.
Families with children should create a plan for what will happen if the caregiver or caregivers in the family become ill with COVID-19. A Covid-19 Family Plan should establish a Circle of Support which includes family members, friends, and other trusted people who can help care for children.
Audiologist section of the newborn hearing screening program manual.
This glossary of terms makes understanding the terminology used when talking about newborn hearing screening much easier. It explains such terms as auditory brainstem response, audiogram, audiologist, early intervention, and dozens more.
This form makes it easy for physician’s to track a baby’s hearing screening follow-up tasks from birth to 6 months old.
Explains the many reasons why you should continue with follow-up visits if your baby does not pass newborn hearing screening.
Explains requirements for initial hearing screening, rescreening of infants who refer, infants not screened prior to discharge, infants who pass screen but have an identified risk factor, hospital documentation and communication of screening results, hospital screening requirements, and more.
Since 1999, the Joint Committee on Infant Hearing has advocated for appropriate and necessary care for the infant with hearing loss to be directed and coordinated by the child’s physician within the medical home with support from appropriate ancillary services.
Since the first universal newborn hearing screening programs were established in the early 1990s, there has been significant progress. Progress is evident in the development and implementation of protocols for newborn hearing screening, pediatric audiologic evaluation of newborns, fitting of amplification, and medical management of children who are deaf or hard of hearing.
When a hearing loss is first diagnosed, the test results may seem confusing. Although hearing loss is often described as a percentage, it is too complex to describe with one number. Remember, also, that determining how your child uses, or will use, his or her residual hearing is a process.
This document explains why physicians check newborn hearing screen status and provide needed follow-up.
This script helps healthcare providers to talk to parents in English and Spanish about a variety of situations including informing parents of the screen, explaining passing and not passing, inconclusive results or could not screen, passing and not passing with risk factors for hearing loss, and does not pass.
This manual provides a wealth of information for the newborn screening practitioner including screening essentials, conditions included in the screening panel, summary of conditions, criteria for requesting follow-up specimens, screening practices, recommendations for specimen collection, unsatisfactory specimens, reporting results, problems in screening practice, educational services, fees and screening kit information, exemptions, and more.
This procedure explains how to pack and ship blood spots to the newborn screening program.