Summary
Australian Genomics will conduct a post-implementation evaluation of the usage of different MBS item numbers for genomic testing in rare disease (e.g. childhood syndromes, renal, cardiac, mitochondrial, deafness) to understand laboratory implementation, uptake among different professional groups, jurisdictional variations and costs. We will systematically identify barriers and enablers to adoption. This work will inform strategies to support implementation of existing MBS item numbers as well as the development and assessment of future applications, including associated reanalysis items.
Project Leads
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Professor Zornitza Stark
Victorian Clinical Genetic Services
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A/Professor Ilias Goranitis
University of Melbourne
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Dr Stephanie Best
Murdoch Children’s Research Institute
Project Coordinators
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Michael Quinn
Contact
michael.quinn3@health.qld.gov.au
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Matilda Jackson
Contact
matilda.jackson@sa.gov.au