Post-market Surveillance Of Medicine-related Adverse Events
Funder
National Health and Medical Research Council
Funding Amount
$99,248.00
Summary
Observational studies using administrative data are an important complement to spontaneous reporting systems for detecting medicine-related adverse events after they go to market, as they reflect real-world use of medicines; yet, they require rigorous methodological approaches to avoid bias. This project will review the existing methodologies for detecting adverse events in administrative data and apply them to Australian data.
An Indigenous Australian Reference Genome: Indigenous Inclusion In The Benefits Of Genomic Medicine
Funder
National Health and Medical Research Council
Funding Amount
$1,428,508.00
Summary
This project will establish an Indigenous Australian reference genome (the NCIGrg) within the National Centre for Indigenous Genomics (NCIG) using advanced genome sequencing technologies and data analytics and evaluate its research and clinical utility. The NCIGrg will be cornerstone of future genomic research and its clinical application in Indigenous communities. It will underpin NCIG’s commitment to ensuring that Indigenous Australians are included in the benefits of genomic medicine.
The Australian Perinatal Mental Health Reforms: Using Population Data To Evaluate Their Impact On Service Utilisation And Related Cost-effectiveness
Funder
National Health and Medical Research Council
Funding Amount
$526,169.00
Summary
Mental health problems associated with pregnancy and the first postnatal year are a major public health problem. This unique project will use large data sets to examine whether key Australian mental health reforms have improved maternal health outcomes and if they are providing ‘value for money’. This project will put Australia at the forefront of policy planning, analysis and health service evaluation in the field of mental health.
Investigating The Application Of Population Data To Improve Maternal And Child Health Services In Two Remote Communities
Funder
National Health and Medical Research Council
Funding Amount
$83,281.00
Summary
This project will contribute to the understanding of how routinely collected population health data relate to remote Aboriginal communities and how such data can be used in two field sites. Population data are widely used, but the opportunity to investigate these matters is limited. The nesting of this study within a larger project aimed at improving health services for mothers and babies provides a unique opportunity to investigate aspects of applying macro level data at a local level.
Clinical Outcomes From High Risk Medicines In Older Australians
Funder
National Health and Medical Research Council
Funding Amount
$307,946.00
Summary
Older adults frequently take multiple medicines for multiple medical conditions. At present, there is very limited information on the trends and risks associated with medicines use in older Australians. This project will utilise large linked health datasets to determine the prevalence, risk factors and clinical consequences from high risk medicines in older adults in Australia. The findings of this project will contribute to identifying targets to improve prescribing, and health in this populati ....Older adults frequently take multiple medicines for multiple medical conditions. At present, there is very limited information on the trends and risks associated with medicines use in older Australians. This project will utilise large linked health datasets to determine the prevalence, risk factors and clinical consequences from high risk medicines in older adults in Australia. The findings of this project will contribute to identifying targets to improve prescribing, and health in this population.Read moreRead less
Whole-of-population Linked Data: Strengthening The Evidence To Drive Improvement In Health And Health Care In Australia
Funder
National Health and Medical Research Council
Funding Amount
$1,130,376.00
Summary
In partnership with the Australian Bureau of Statistics, Australian Institute of Health and Welfare and Heart Foundation, we will create a whole-of-population linked data platform to inform improvements in health and heath care. We will investigate: socioeconomic variation in disease burden, to identify opportunities to improve population health; preventive cardiovascular disease (CVD) care, to improve treatment; and end-of-life care trajectories, focusing on CVD, to inform improvements in care.