منابع مشابه
Improving early audiological intervention via newborn hearing screening in Belgium
BACKGROUND Newborn hearing screening programs aim to lower the ages at audiological intervention among hearing-impaired children. In Wallonia and Brussels (Belgium), audiological intervention data are not collected in the screening program, and the ages at initiating audiological care have never been assessed. This study aimed to assess the evolution in the ages at initiating audiological inter...
متن کاملLevels of evidence: universal newborn hearing screening (UNHS) and early hearing detection and intervention systems (EHDI).
UNLABELLED Levels of evidence differ according to the audience addressed. Implementation of universal newborn hearing screening requires responses to a complex myriad of diverse groups: the general public, families with children who are deaf or hard of hearing, the deaf and hard of hearing communities, hospital administrators, physicians (pediatricians, general practitioners, ear nose and throa...
متن کاملEvaluation of the universal newborn hearing screening and intervention program.
During the last 20 years, the number of infants evaluated for permanent hearing loss at birth has increased dramatically with universal newborn hearing screening and intervention (UNHSI) programs operating in all US states and many territories. One of the most urgent challenges of UNHSI programs involves loss to follow-up among families whose infants screen positive for hearing loss. We surveye...
متن کاملScreening, Early Detection, and Early Intervention Strategies for Lung Cancer.
Screening for lung cancer has been utilized for several decades without demonstrating overall survival benefit. However, recent advances in treatment of lung cancer, improvements in our biologic understanding of lung cancer development, and an increasing population of healthy ex-smokers provide cause for optimism. Several chemoprevention trials suggest that it may be possible to intervene in th...
متن کاملNewborn , Carrier , and Early Childhood Screening Recommendations for Fragile
Fragile X syndrome, diagnosed by Fragile X Mental Retardation 1 (FMR1) DNA testing, is the most common single-gene cause of inherited intellectual disability. The expanded CGG mutation in the FMR1 gene, once thought to have clinical significance limited to fragile X syndrome, is now well established as the cause for other fragile X–associated disorders including fragile X–associated primary ova...
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ژورنال
عنوان ژورنال: Infants & Young Children
سال: 2021
ISSN: 0896-3746
DOI: 10.1097/iyc.0000000000000181