Literature DB >> 30155569

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

S M Sawyer1,2,3, R McNeil4,5, K Thompson6, L M Orme6,7, M McCarthy5,8,7.   

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.

Entities:  

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

Mesh:

Year:  2018        PMID: 30155569     DOI: 10.1007/s00520-018-4420-x

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  29 in total

1.  Fulfilling the Vision of Youth-Friendly Cancer Care: A Study Protocol.

Authors:  Susan M Sawyer; Maria C McCarthy; David Dunt; Robyn McNeil; Kate Thompson; Lisa Orme; Sarah E Drew
Journal:  J Adolesc Young Adult Oncol       Date:  2016-02-26       Impact factor: 2.223

2.  Information needs of adolescent and young adult cancer patients and their parent-carers.

Authors:  Maria C McCarthy; Robyn McNeil; Sarah Drew; Lisa Orme; Susan M Sawyer
Journal:  Support Care Cancer       Date:  2017-12-08       Impact factor: 3.603

3.  Cancer Patient Experience in the Teenage Young Adult Population- Key Issues and Trends Over Time: An Analysis of the United Kingdom National Cancer Patient Experience Surveys 2010-2014.

Authors:  Caroline L Furness; Lesley Smith; Eva Morris; Caroline Brocklehurst; Sasha Daly; Rachael E Hough
Journal:  J Adolesc Young Adult Oncol       Date:  2017-05-19       Impact factor: 2.223

Review 4.  What Are the Unmet Needs and Care Experiences of Adolescents and Young Adults with Cancer? A Systematic Review.

Authors:  Helen Bibby; Victoria White; Kate Thompson; Antoinette Anazodo
Journal:  J Adolesc Young Adult Oncol       Date:  2016-07-25       Impact factor: 2.223

5.  Assessing information and service needs of young adults with cancer at a single institution: the importance of information on cancer diagnosis, fertility preservation, diet, and exercise.

Authors:  Abha A Gupta; Kim Edelstein; Alisha Albert-Green; Norma D'Agostino
Journal:  Support Care Cancer       Date:  2013-04-21       Impact factor: 3.603

Review 6.  Adolescents with a chronic condition: challenges living, challenges treating.

Authors:  Susan M Sawyer; Sarah Drew; Michele S Yeo; Maria T Britto
Journal:  Lancet       Date:  2007-04-28       Impact factor: 79.321

7.  Associations Between Patient Perceptions of Communication, Cure, and Other Patient-Related Factors Regarding Patient-Reported Quality of Care Following Surgical Resection of Lung and Colorectal Cancer.

Authors:  Aslam Ejaz; Yuhree Kim; Megan Winner; Andrew Page; Diana Tisnado; Sydney E Morss Dy; Timothy M Pawlik
Journal:  J Gastrointest Surg       Date:  2015-11-25       Impact factor: 3.452

8.  The biographical impact of teenage and adolescent cancer.

Authors:  Anne Grinyer
Journal:  Chronic Illn       Date:  2007-12

9.  Identifying the supportive care needs of adolescent and young adult survivors of cancer: a qualitative analysis and systematic literature review.

Authors:  Elena Tsangaris; Jessica Johnson; Rachel Taylor; Lorna Fern; Denise Bryant-Lukosius; Ronald Barr; Graeme Fraser; Anne Klassen
Journal:  Support Care Cancer       Date:  2013-11-24       Impact factor: 3.603

10.  Health and supportive care needs of young adult cancer patients and survivors.

Authors:  Brad J Zebrack; Jennifer Mills; Tammy S Weitzman
Journal:  J Cancer Surviv       Date:  2007-06       Impact factor: 4.062

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  1 in total

Review 1.  Long-term care for people treated for cancer during childhood and adolescence.

Authors:  Emily S Tonorezos; Richard J Cohn; Adam W Glaser; Jeremy Lewin; Eileen Poon; Claire E Wakefield; Kevin C Oeffinger
Journal:  Lancet       Date:  2022-04-16       Impact factor: 202.731

  1 in total

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