Children’s Medical Services
Publications
Provides a comprehensive list of risk factors that are associated with permanent congenital, delayed onset or progressive hearing loss in childhood.
Describes the competencies and skills required by all newborn hearing screeners.
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 helpful brochure explains how genetic tests could save your baby’s life. It covers why babies need newborn screening tests, how the testing is performed, how you will get the results, why some babies need more testing, where you can ask questions, and more.
This procedure explains how to pack and ship blood spots to the newborn screening program.