Optimal Care Pathway domain

Models of care

The National Pancreatic Cancer Roadmap identifies key priority areas and strategies which focus on developing evidence-based, culturally competent models of care

Evidence summary and stakeholder input

The following is a summary of the findings from the evidence gathering activities and stakeholder consultations undertaken to inform development of the Roadmap. For more information on the development of the Roadmap see the About page.

Key priority areas

Models of care

Improve the provision of culturally appropriate models of care for Aboriginal and Torres Strait Islander people and people from CALD backgrounds affected by pancreatic cancer and their carers

Learn more about strategies and associated activities for implementation for this key priority area

Models of care

Improve integrated care coordination models, including telehealth, for people from regional and remote areas to minimise delayed treatment

Learn more about strategies and associated activities for implementation for this key priority area

Models of care

Improve evidence-based care coordination models for people affected by metastatic pancreatic cancer, including those living in regional and remote areas

Learn more about strategies and associated activities for implementation for this key priority area

Models of care

Improve the capacity and capability of the workforce in rural and remote areas to support pancreatic cancer care

Learn more about strategies and associated activities for implementation for this key priority area

Models of care

Improve capacity and capability of palliative care nurses and GPs in the provision of pancreatic cancer care particularly in regional areas

Learn more about strategies and associated activities for implementation for this key priority area

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Data and reporting

Next step

Optimal Care Pathway domain

Models of care

Evidence summary and stakeholder input

Key priority areas

Improve the provision of culturally appropriate models of care for Aboriginal and Torres Strait Islander people and people from CALD backgrounds affected by pancreatic cancer and their carers

Improve integrated care coordination models, including telehealth, for people from regional and remote areas to minimise delayed treatment

Improve evidence-based care coordination models for people affected by metastatic pancreatic cancer, including those living in regional and remote areas

Improve the capacity and capability of the workforce in rural and remote areas to support pancreatic cancer care

Improve capacity and capability of palliative care nurses and GPs in the provision of pancreatic cancer care particularly in regional areas

Data and reporting

Prevention and early detection