Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/138695
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorArchibald, A.D.-
dc.contributor.authorMcClaren, B.J.-
dc.contributor.authorCaruana, J.-
dc.contributor.authorTutty, E.-
dc.contributor.authorKing, E.A.-
dc.contributor.authorHalliday, J.L.-
dc.contributor.authorBest, S.-
dc.contributor.authorKanga-Parabia, A.-
dc.contributor.authorBennetts, B.H.-
dc.contributor.authorCliffe, C.C.-
dc.contributor.authorMadelli, E.O.-
dc.contributor.authorHo, G.-
dc.contributor.authorLiebelt, J.-
dc.contributor.authorLong, J.C.-
dc.contributor.authorBraithwaite, J.-
dc.contributor.authorKennedy, J.-
dc.contributor.authorMassie, J.-
dc.contributor.authorEmery, J.D.-
dc.contributor.authorMcGaughran, J.-
dc.contributor.authorMarum, J.E.-
dc.contributor.authoret al.-
dc.date.issued2022-
dc.identifier.citationJournal of Personalized Medicine, 2022; 12(11):1781-1-1781-25-
dc.identifier.issn2075-4426-
dc.identifier.issn2075-4426-
dc.identifier.urihttps://hdl.handle.net/2440/138695-
dc.descriptionPublished: 28 October 2022-
dc.description.abstractReproductive genetic carrier screening (RGCS) provides people with information about their chance of having children with autosomal recessive or X-linked genetic conditions, enabling informed reproductive decision-making. RGCS is recommended to be offered to all couples during preconception or in early pregnancy. However, cost and a lack of awareness may prevent access. To address this, the Australian Government funded Mackenzie’s Mission—the Australian Reproductive Genetic Carrier Screening Project. Mackenzie’s Mission aims to assess the acceptability and feasibility of an easily accessible RGCS program, provided free of charge to the participant. In study Phase 1, implementation needs were mapped, and key study elements were developed. In Phase 2, RGCS is being offered by healthcare providers educated by the study team. Reproductive couples who provide consent are screened for over 1200 genes associated with >750 serious, childhood-onset genetic conditions. Those with an increased chance result are provided comprehensive genetic counseling support. Reproductive couples, recruiting healthcare providers, and study team members are also invited to complete surveys and/or interviews. In Phase 3, a mixed-methods analysis will be undertaken to assess the program outcomes, psychosocial implications and implementation considerations alongside an ongoing bioethical analysis and a health economic evaluation. Findings will inform the implementation of an ethically robust RGCS program.-
dc.description.statementofresponsibilityAlison D. Archibald ... Tristan Hardy ... et al. and The Mackenzie’s Mission Study Team-
dc.language.isoen-
dc.publisherMDPI AG-
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).-
dc.source.urihttp://dx.doi.org/10.3390/jpm12111781-
dc.subjectreproductive genetic carrier screening; implementation science; bioethics; health economics; psychosocial outcomes-
dc.titleThe Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation-
dc.typeJournal article-
dc.identifier.doi10.3390/jpm12111781-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/GNT1113531-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/GNT2000001-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1117510-
pubs.publication-statusPublished-
dc.identifier.orcidHardy, T. [0000-0002-5878-0340]-
Appears in Collections:Pathology publications

Files in This Item:
File Description SizeFormat 
hdl_138695.pdfPublished version2.34 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.