Journal article
Determinants of access to chronic illness care – a mixed-methods evaluation of a national multifaceted chronic disease package for Indigenous Australians
Objectives: Indigenous Australians have a disproportionately high burden of chronic illness, and relatively poor access to healthcare. This paper examines how a national multicomponent programme aimed at improving prevention and management of chronic disease among Australian Indigenous people addressed various dimensions of access.
Report
ABCD national research partnership: impact and research findings
The ABCD National Research Partnership works across states and territories in Australia to improve the quality of primary health care available to Indigenous people. Using participatory action research approaches, The partnership aims to: investigate the variation in quality of care in Indigenous primary health care (PHC) centres explore the underlying factors associated with variation at...
Report
Chronic illness care for Aboriginal and Torres Strait Islander people: final report
This project engage a range of stakeholders across different levels of the primary health care system, including service providers, management, policy-makers and researchers and capture their knowledge on the barriers and enablers to addressing the identified priority-evidence practice gaps and their suggestions on strategies for improvement. Overview
Report
Primary health care for Aboriginal and Torres Strait Islander children
This final report presents the findings from each of the phases of the Engaging Stakeholders in Identifying Priority Evidence-Practice Gaps and Strategies for Improvement in Primary Health Care (ESP) Project.
Journal article
Consistency of denominator data in electronic health records in Australian primary healthcare services: enhancing data quality
This paper examines the consistency of denominator data extracted from electronic health records (EHRs) for monitoring of access and quality of primary health care.