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Tools and resources

This section provides tools and resources to support the delivery of shared follow-up and survivorship care for women with early breast cancer.

Shared cancer follow-up and survivorship care resources

Shared care plan for early breast cancer follow-up and survivorship care template

This individualised care plan template is a tool developed to assist the GP, specialist and patient to manage follow-up and survivorship care for early breast cancer and DCIS together. It aims to facilitate effective communication, define responsibilities for care providers, and support the delivery of best-practice care  

The shared care plan is developed within the specialist setting at the initial follow-up appointment three months post completion of active treatment. It contains all the key elements required for follow-up care including a record of diagnosis and treatment summaries, appointment schedule, follow-up actions required and contact details of all involved.

Access:  Shared care plan for early breast cancer follow-up and survivorship care template

Rapid Access Request template 

The rapid access request is a template designed to be used by the GP when follow-up raises a clinical issue requiring urgent specialist consultation or advice. It is an integral part of the shared follow-up care model and helps facilitate effective communication between the GP and specialist.

Access: Rapid Access Request template

Continuing professional development - Online Education

Cancer Australia breast cancer online learning series

Cancer Australia has developed six accredited online courses for general practitioners, practice nurses and other health professionals to support learning and improved practice of evidence-based breast cancer treatment and care. The courses are hosted on the Australian College of Rural and Remote Medicine’s online learning platform. The course titled ‘Follow-up and survivorship care for early breast cancer’ addresses best practice follow-up care for women who have completed active treatment for early breast cancer, including shared follow-up care arrangements.

Registration to the courses is free through Cancer Australia, by clicking on Register at the bottom of the page and entering a few demographic details.

Other available online education:

Optimal care pathway

Optimal care pathway for women with breast cancer

This optimal cancer care pathway for women with breast cancer aims to foster an understanding of the whole cancer pathway and its distinct components through mapping the patient journey, to promote quality cancer care and patient experiences.

Cancer Council Victoria was commissioned by the Victorian Department of Health to develop the Optimal Cancer Care Pathways through consultation with a wide range of expert multidisciplinary teams, peak health organisations, consumers and carers. They are nationally endorsed by the National Cancer Expert Reference Group (NCERG) (includes representation from each jurisdiction and nationally), Cancer Australia and Cancer Council Australia.

An online patient version is also available.

Access: Optimal care pathway for women with breast cancer
 

Supportive care resources

  • The Australian Cancer Survivorship Centre - My Care Plan - an online tool that can be used to create a personalised survivorship care plan following treatment for early breast cancer. The personalised survivorship care plan can be used in conjunction with the Shared care plan for early breast cancer follow-up and survivorship care. It helps patients to better understand their personal health risks depending on the type and combination of cancer treatments they received.
  • Breast Cancer Network Australia (BCNA) – Fear of Cancer Recurrence - This BCNA fact sheet provides information on fear of cancer recurrence for people who have been diagnosed with early breast cancer; their partners, families, friends, and colleagues; and others who support people with early breast cancer.
  • National Comprehensive Cancer Network distress thermometer and problem list – a tool that measures distress in a similar way to pain – on a scale of zero to ten (ten being the worst). This tool makes it easier for people to talk to their doctors about the emotional effects caused by the diagnosis, symptoms, and treatment of cancer.
     

Clinical practice guidelines 

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