Newborn Screenings And A Systematic Framework - 1499 Words

Newborn Screenings and a Systematic Framework William Anderson MPH 603 Assignment #6 August 15,2016 Abstract Newborn genome screening is an issue that will becoming increasingly important in the coming decades. It has the potential to bring about many early diagnoses which could have a large impact on healthcare. This will only occur though if states can uniformly adopt a standard set of tests to be screened for. Equally important is the subject of uniformed consent. When we apply these variables to the 6 steps process we can fully compare the benefits and risks. This gives insight into taking the most appropriate actions in the future. Introduction The subject of newborn genome screening is one that is highly controversial. Everyone would agree though that newborn children should be protected, and given every opportunity to grow up to become healthy and strong. Screenings are a testing procedure which is done when a baby is first born, or within a couple days of birth. A small blood sample is collected from the baby’s heel; it is then sent to a lab for processing. The baby’s blood is then tested (screened)for a variety of diseases and medical conditions. 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