Equitable access to care is a core principle of Medicare and Australia's broader health policy frameworks, yet access to specialist care remains marked by persistent inequities. People with disability experience longer waits, face greater affordability pressures due to lower incomes and encounter greater administrative burden. These disparities undermine progress towards Australia's commitments to equitable and accessible healthcare set out in national and international policy agreements. Addressing them requires understanding the structural barriers that shape specialist access.
This article synthesises evidence on inequities in specialist access and fees for people with disability and identifies policy settings that shape these outcomes. It draws on existing literature, policy documents, and emerging evidence from linked administrative data, including the Person Level Integrated Data Asset (PLIDA).
Key barriers include the geographic distribution of specialists, wide variation in out-of-pocket fees, fragmented referral pathways and limited care coordination, which may contribute to delayed or foregone care. These inequities are exacerbated by gaps in monitoring healthcare system performance. Australia has no system for tracking specialist wait times, limiting policymakers’ ability to identify disparities. Advances in linked administrative data, particularly PLIDA, provide a foundation for improved monitoring.
Improved wait time monitoring, greater fee transparency, targeted incentives for equitable care and strengthened navigation support are needed to improve access to specialist care for people with disability.



