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Supportive Care in Cancer

, Volume 27, Issue 5, pp 1783–1792 | Cite as

Developmentally appropriate care for adolescents and young adults with cancer: how well is Australia doing?

  • S. M. SawyerEmail author
  • R. McNeil
  • K. Thompson
  • L. M. Orme
  • M. McCarthy
Original Article
  • 112 Downloads

Abstract

Purpose

Developmentally appropriate care underpins quality cancer treatment. This study aimed to describe how well Australian cancer services deliver patient-focussed, developmentally appropriate care to adolescents and young adults (AYAs) with cancer.

Methods

In a national, cross sectional study, 196 AYAs with cancer aged between 15 and 25 years at diagnosis reported their general experiences of the cancer care team (Cancer Needs Questionnaire), access to age-appropriate treatment environments (Cancer Needs Questionnaire) and frequency of psychosocial assessment (Adolescent Friendly Hospital Survey).

Results

Very positive responses were reported around engagement and communication with staff who were reported as approachable, friendly and trustworthy; 11 of the 14 items were positively rated by over 90% of respondents. In contrast, over 70% of AYAs expressed unmet need around their physical and social environments, whether in relation to the opportunity to be nursed in wards designed for AYAs, spend time with other young people with cancer, or talk to young people their own age; less than a third reported their needs had been met on the majority of these items. The frequency that specific psychosocial assessment domains were discussed was highly variable; responses suggested that AYAs were less commonly questioned about overtly sensitive topics. AYAs who experienced private consultations with health care providers (41%) were significantly more likely to experience thorough psychosocial assessment.

Conclusion

Australian cancer services are generally communicating well with AYAs. There is room for improvement around more developmentally specific aspects of healthcare quality, such as psychosocial assessment, and around treatment environments that promote greater social interaction between AYAs.

Keywords

Adolescents Quality Risk assessment Confidentiality Patient-reported outcomes Patient experience Physical environment Health reform 

Notes

Acknowledgments

We wish to acknowledge the generosity of the Australian young people and their families who participated in this study and the contribution of Dr. Sarah Drew, deceased.

Funding information

This project was funded by a grant from Cancer Australia (APP1010977) in association with Beyondblue and Canteen through the Priority-driven Collaborative Cancer Research Scheme. Additional funding was gratefully received from Redkite, the Royal Children’s Hospital Foundation and the Victorian Adolescent & Young Adult Cancer Service, Peter MacCallum Cancer Centre and the Victorian Government Department of Health and Human Services and Operational Infrastructure Support Program. Dr. McCarthy is funded via a Murdoch Children’s Research Institute Career Development Award.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Centre for Adolescent HealthRoyal Children’s HospitalParkvilleAustralia
  2. 2.Murdoch Children’s Research InstituteParkvilleAustralia
  3. 3.Department of PaediatricsThe University of MelbourneParkvilleAustralia
  4. 4.Victorian Youth Cancer ServicePeter MacCallum HospitalParkvilleAustralia
  5. 5.Children’s Cancer CentreRoyal Children’s HospitalParkvilleAustralia

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