The Role of Primary Care Physicians in Childhood Cancer Survivorship Care: Multiperspective Interviews

Author:

Signorelli Christina12,Wakefield Claire E.12,Fardell Joanna E.12,Foreman Tali12,Johnston Karen A.12,Emery Jon3,Thornton-Benko Elysia45,Girgis Afaf6,Lie Hanne C.78,Cohn Richard J.12,

Affiliation:

1. Kids Cancer Centre, Sydney Children's Hospital, Randwick, New South Wales, Australia

2. School of Women's & Children's Health, UNSW Sydney, New South Wales, Australia

3. Centre for Cancer Research and Department of General Practice, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Victorian Comprehensive Cancer Centre, Victoria, Australia

4. Bondi Road Doctors, Bondi Junction, New South Wales, Australia

5. Wellac Lifestyle: Wellness After, And during Cancer, New South Wales, Australia

6. Centre for Oncology Education and Research Translation, Ingham Institute for Applied Medical Research, South Western Sydney Clinical School, University of New South Wales, New South Wales, Australia

7. Department of Behavioural Sciences in Medicine, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Norway

8. Department of Paediatric Medicine, Children's and Adolescents Division, Oslo University Hospital, Norway

Abstract

Abstract Background Primary care physicians (PCPs) are well placed to provide holistic care to survivors of childhood cancer and may relieve growing pressures on specialist-led follow-up. We evaluated PCPs' role and confidence in providing follow-up care to survivors of childhood cancer. Subjects, Materials, and Methods In Stage 1, survivors and parents (of young survivors) from 11 Australian and New Zealand hospitals completed interviews about their PCPs' role in their follow-up. Participants nominated their PCP for an interview for Stage 2. In Stage 2, PCPs completed interviews about their confidence and preparedness in delivering childhood cancer survivorship care. Results Stage 1: One hundred twenty survivors (36% male, mean age: 25.6 years) and parents of young survivors (58% male survivors, survivors' mean age: 12.7 years) completed interviews. Few survivors (23%) and parents (10%) visited their PCP for cancer-related care and reported similar reasons for not seeking PCP-led follow-up including low confidence in PCPs (48%), low perceived PCP cancer knowledge (38%), and difficulty finding good/regular PCPs (31%). Participants indicated feeling "disconnected" from their PCP during their cancer treatment phase. Stage 2: Fifty-one PCPs (57% male, mean years practicing: 28.3) completed interviews. Fifty percent of PCPs reported feeling confident providing care to childhood cancer survivors. PCPs had high unmet information needs relating to survivors' late effects risks (94%) and preferred a highly prescriptive approach to improve their confidence delivering survivorship care. Conclusion Improved communication and greater PCP involvement during treatment/early survivorship may help overcome survivors' and parents' low confidence in PCPs. PCPs are willing but require clear guidance from tertiary providers.

Funder

Cancer Council NSW

Cancer Institute NSW

Kids Cancer Alliance

Kids with Cancer Foundation

National Health and Medical Research Council of Australia

The Kids' Cancer Project

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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