Abstract
AbstractNewborn screening (NBS) programmes are highly successful, trusted, public health interventions. Genomic sequencing offers the opportunity to increase the benefits of NBS by screening infants for a greater number and variety of childhood-onset conditions. This study aimed to describe who needs to do what, when, and for whom to deliver genomic newborn screening (gNBS) and capture perceived implementation barriers and enablers. ‘Key informants’ (individuals involved in the delivery of NBS) were interviewed. The Actor, Action, Context, Time and Target framework guided data collection and analysis. Participants (N = 20) identified new Actions required to deliver gNBS (educating healthcare providers, longitudinal psychosocial support), NBS Actions needing modification (obtaining consent) and NBS Actions that could be adopted for gNBS (prompt referral pathways). Obtaining consent in a prenatal Context was a source of some disagreement. The Time to disclose high chance results was raised as a key consideration in gNBS programme design. Genetic counsellors were identified as key Actors in results management, but workforce limitations may be a barrier. Online decision support tools were an enabler to offering gNBS. The implementation of gNBS will require behaviour changes from HCPs delivering NBS. Findings can inform how to deliver gNBS at population-scale.
Publisher
Springer Science and Business Media LLC
Reference35 articles.
1. Centers for Disease Control and Prevention. Ten great public health achievements worldwide, 2001-2010. Morb Mortal Wkly Rep. 2011;60:814–8.
2. Stark Z, Scott RH. Genomic newborn screening for rare diseases. Nat Rev Genet. 2023;24:755–66.
3. Friedman JM, Cornel MC, Goldenberg AJ, Lister KJ, Senecal K, Vears DF. Genomic newborn screening: public health policy considerations and recommendations. BMC Med Genomics 2017;10:9.
4. Department of Health, Victorian State Government. Newborn bloodspot screening. 2024. https://www2.health.vic.gov.au/public-health/population-screening/newborn-bloodspot-screening.
5. Remec ZI, Trebusak Podkrajsek K, Repic Lampret B, Kovac J, Groselj U, Tesovnik T, et al. Next-generation sequencing in newborn screening: a review of current state. Front Genet. 2021;12:662254.
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