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Newborn screening programs initially used screening criteria based largely on criteria established by JMG Wilson and F. Jungner in 1968. [6] Although not specifically about newborn population screening programs, their publication, Principles and practice of screening for disease proposed ten criteria that screening programs should meet before being used as a public health measure.
A newborn infant undergoes a hearing screening. Universal neonatal hearing screening ( UNHS ), which is part of early hearing detection and intervention ( EHDI) programmes, refer to those services aimed at screening hearing of all newborns, regardless of the presence of a risk factor for hearing loss. UNHS is the first step in the EHDI program ...
Early-onset neonatal sepsis is found to be 0.77 to 1 per 100,000 live births in the U.S. In premature babies, the incidence and mortality rates are higher due to the weakness of their immune system. For infants with low birth weight, cases of early-onset sepsis is found to be about 26 per 1,000 and 8 per 1,000 live births.
Neonatology is a subspecialty of pediatrics that consists of the medical care of newborn infants, especially the ill or premature newborn. It is a hospital -based specialty and is usually practised in neonatal intensive care units (NICUs). The principal patients of neonatologists are newborn infants who are ill or require special medical care ...
Marion Downs (January 26, 1914 – November 13, 2014) [1] was an American audiologist and professor emerita at the University of Colorado Health Sciences Center in Denver. She pioneered universal newborn hearing screening in the early 1960s and spent over 30 years advocating for its adoption in hospitals, as well as for the provision of hearing aids to infants displaying hearing loss. [2]
The Apgar score is a quick way for health professionals to evaluate the health of all newborns at 1 and 5 minutes after birth and in response to resuscitation. [1] It was originally developed in 1952 by an anesthesiologist at Columbia University, Virginia Apgar, to address the need for a standardized way to evaluate infants shortly after birth. [2]
Cystic fibrosis (CF) > 1 in 5,000. Congenital hypothyroidism (CH) > 1 in 5,000. Biotinidase deficiency (BIOT) > 1 in 75,000. Congenital adrenal hyperplasia (CAH) > 1 in 25,000. Classical galactosemia (GALT) > 1 in 50,000. Newborn screening by other methods than blood testing. Congenital deafness (HEAR) > 1 in 5,000.
Newborn Screening Saves Lives Reauthorization Act of 2013; P. Pediatrix Medical Group; Phenylketonuria This page was last edited on 14 January 2019, at 04:50 (UTC). ...