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Newborn screening has been identified as one of the most effective means of disease prevention in the United States by testing every newborn baby for potentially fatal conditions that may not be immediately obvious. By testing babies before symptoms begin, newborn screening programs help prevent disabilities and decrease the newborn mortality rate.
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.
[135] [136] A GBS-effective maternal vaccine could have a great effect on newborn morbidity and mortality. It has been estimated that this vaccine could prevent about 127,000 cases of GBS-EOD, 87,000 of GBS-LOD, 31,000 deaths, and 18,000 cases of neuro-developmental impairment. [137]
The blood of a two-week-old infant is collected for a Phenylketonuria, or PKU, screening. The neonatal heel prick is a blood collection procedure done on newborns. It consists of making a pinprick puncture in one heel of the newborn to collect their blood. This technique is used frequently as the main way to collect blood from neonates.
The following disorders are additional conditions that may be detected by screening. Many are listed as "secondary targets" by the 2005 ACMG report. [1] Some states are now screening for more than 50 congenital conditions. Many of these are rare and unfamiliar to pediatricians and other primary health care professionals. [1] Blood cell disorders
U.S. Department of Health and Human Services, Baby2Baby and Huggies are distributing 10,000 Newborn Supply Kits to families in high poverty areas. ‘Baby boxes’ popular in Finland are coming to ...
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