Ontology highlight
ABSTRACT: Background
Newborn bloodspot screening is a well-established population health initiative that detects serious, childhood-onset, treatable conditions to improve health outcomes. With genomic technologies advancing rapidly, many countries are actively discussing the introduction of genomic assays into newborn screening programs. While adding genomic testing to Australia's newborn screening program could improve outcomes for infants and families, it must be considered against potential harms, ethical, legal, equity and social implications, and economic and health system impacts. We must ask not only 'can' we use genomics to screen newborns?' but 'should we'?' and 'how much should health systems invest in genomic newborn screening?'.Methods
This study will use qualitative meth
SUBMITTER: Kariyawasam DS
PROVIDER: S-EPMC10962853 | biostudies-literature | 2024
REPOSITORIES: biostudies-literature