The significant disparities in cancer outcomes between Aboriginal and Torres Strait Islander cancer patients and non-Aboriginal people, are well documented. These disparities in part are a result of factors relating to the accessibility, acceptability, and effectiveness of health services. In addition, concepts and understandings of health and wellbeing, and the importance of connection to family, community and Country are factors that are priorities for Aboriginal and Torres Strait Islander people and these must be considered in improving cancer outcomes.
PROs are used to and guide policies, programs and service delivery. Systematically identifying and addressing patient reported outcomes and experiences of Aboriginal and Torres Strait Islander cancer patients and their carers, a critical component in improving cancer care and outcomes. There is growing recognition that different approaches are needed to adequately capture and understand the experiences and perspectives of Aboriginal and Torres Strait Islander cancer patients.
This presentation will provide discrete examples of PROs development, and establishing partnerships to systematically include PROs implementation in cancer care to ensure equity for Aboriginal and Torres Strait Islander people.