Use of pharmacogenomic testing in aged care
Feasibility and clinical utility of implementation of pharmacogenomic testing in aged care
The University of Sydney
200 participants
Mar 11, 2025
Interventional
Conditions
Summary
In this project we will implement a genetic testing service in the residential aged care setting, looking specifically at genes involved in the processing of medications (i.e. pharmacogenomics). The aim of the project is to evaluate the feasibility of implementing this service using the RE-AIM framework. DNA samples of aged care residents will be collected via cheek swabs and sent to a commercial genotyping provider (myDNA) to generate a pharmacogenomic report. The report will be sent to the resident's pharmacist who will interpret it and make a recommendation regarding the resident's medication to their prescriber. Barriers and facilitators to implementing pharmacogenomics will be identified by interviewing stakeholders including residents, clinical staff, pharmacists and prescribers. A cost-benefit analysis will be conducted comparing medication-related harm in residents the did/did not partake in pharmacogenomic testing. We expect to understand the feasibility, clinical and financial utility of implementing pharmacogenomic testing in aged care.
Eligibility
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Interventions
In this project we will implement a genetic testing service in the residential aged care setting, looking specifically at genes involved in the processing of medications (i.e. pharmacogenomics). The intervention is a pharmacogenomic test using a buccal swab. The results of the pharmacogenomic test will be reviewed by the participants’ pharmacist, who upon reviewing the clinical pharmacogenomic report, will make prescribing considerations (e.g. dose adjustments or alternative medication use) to the participants’ prescriber. It is at the prescriber's discretion to follow the recommendation or not. Approximate turnaround time between the pharmacogenomic test and the prescribing considerations being delivered to the prescriber is 3-4 weeks. Changes to medication will be monitored via resident medical records and through data linkage to the Pharmaceutical Benefits Scheme.
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ACTRN12624001073594