QOL-32. THE PROMOTE STUDY: HEALTH-RELATED QUALITY OF LIFE COMMUNICATION NEEDS OF CHILDREN, ADOLESCENTS, AND THEIR FAMILIES ATTENDING OUTPATIENT CONSULTATIONS AFTER TREATMENT FOR A BRAIN TUMOUR
QOL-32. THE PROMOTE STUDY: HEALTH-RELATED QUALITY OF LIFE COMMUNICATION NEEDS OF CHILDREN, ADOLESCENTS, AND THEIR FAMILIES ATTENDING OUTPATIENT CONSULTATIONS AFTER TREATMENT FOR A BRAIN TUMOUR
BACKGROUND: Childhood brain tumours and their treatment can reduce health-related quality of life (HRQoL) and cause anxiety and depression, withdrawal, and social isolation. Improved communication within outpatient consultations may allow early identification and treatment of these issues. We explored family communication needs in survivors of childhood brain tumours receiving six-monthly follow-up outpatient review within the English NHS. METHODS: Semi-structured interviews were conducted with 18 families whose child aged 8–17 years had finished treatment for a brain tumour within the preceding five years. Thematic analysis used the Framework Method. RESULTS: Adjusting to change and finding a “new normal” was the overarching theme to emerge. HRQoL issues included fatigue, coping with physical changes, challenges at school, isolation, and adjusting to changes in abilities. Survivors described a need for greater knowledge about and more support with changes in cognitive functioning. Parents spoke about the impact on the wider family and their changed role in supporting the child’s HRQoL. Communication barriers included short-term memory loss, shyness, and the need to suppress or regulate emotions evoked by these issues. Communication needs included more information regarding recovery and rehabilitation and/or help managing anxiety or emotional health.
CONCLUSION: The above communication needs and barriers should be addressed. Having a digital record to document and monitor this information systematically could improve service planning and provide patients and their families with the resources to reach their full potential and experience a better HRQoL.
437-437
Stubley, Shelly
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Freeman, Anita
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Liossi, Christina
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Darlington, Anne-Sophie
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Grootenhuis, Martha A.
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Hargrave, Darren R.
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Morris, Christopher
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Walker, David
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Kennedy, Colin
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Bull, Kim
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4 December 2020
Stubley, Shelly
c0f620a1-5888-4481-85a8-b7f11a483c12
Freeman, Anita
ebc69b0b-4721-4d04-b54f-ee9e9d3ca004
Liossi, Christina
fd401ad6-581a-4a31-a60b-f8671ffd3558
Darlington, Anne-Sophie
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Grootenhuis, Martha A.
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Hargrave, Darren R.
ffb8f016-db32-44c7-9c66-f05b84431164
Morris, Christopher
a5dc6cdc-49e0-4fbb-92e0-7f57811c5dc4
Walker, David
305b146b-bd74-4aec-9dfc-030439b07105
Kennedy, Colin
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Bull, Kim
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Stubley, Shelly, Freeman, Anita, Liossi, Christina, Darlington, Anne-Sophie, Grootenhuis, Martha A., Hargrave, Darren R., Morris, Christopher, Walker, David, Kennedy, Colin and Bull, Kim
(2020)
QOL-32. THE PROMOTE STUDY: HEALTH-RELATED QUALITY OF LIFE COMMUNICATION NEEDS OF CHILDREN, ADOLESCENTS, AND THEIR FAMILIES ATTENDING OUTPATIENT CONSULTATIONS AFTER TREATMENT FOR A BRAIN TUMOUR.
Neuro-Oncology, 22 (Supplement_3), .
(doi:10.1093/neuonc/noaa222.692).
Record type:
Meeting abstract
Abstract
BACKGROUND: Childhood brain tumours and their treatment can reduce health-related quality of life (HRQoL) and cause anxiety and depression, withdrawal, and social isolation. Improved communication within outpatient consultations may allow early identification and treatment of these issues. We explored family communication needs in survivors of childhood brain tumours receiving six-monthly follow-up outpatient review within the English NHS. METHODS: Semi-structured interviews were conducted with 18 families whose child aged 8–17 years had finished treatment for a brain tumour within the preceding five years. Thematic analysis used the Framework Method. RESULTS: Adjusting to change and finding a “new normal” was the overarching theme to emerge. HRQoL issues included fatigue, coping with physical changes, challenges at school, isolation, and adjusting to changes in abilities. Survivors described a need for greater knowledge about and more support with changes in cognitive functioning. Parents spoke about the impact on the wider family and their changed role in supporting the child’s HRQoL. Communication barriers included short-term memory loss, shyness, and the need to suppress or regulate emotions evoked by these issues. Communication needs included more information regarding recovery and rehabilitation and/or help managing anxiety or emotional health.
CONCLUSION: The above communication needs and barriers should be addressed. Having a digital record to document and monitor this information systematically could improve service planning and provide patients and their families with the resources to reach their full potential and experience a better HRQoL.
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Published date: 4 December 2020
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© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.
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Local EPrints ID: 467739
URI: http://eprints.soton.ac.uk/id/eprint/467739
ISSN: 1522-8517
PURE UUID: aba46d0c-d6cb-4fbc-8e28-39c8f965c82e
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Date deposited: 21 Jul 2022 16:56
Last modified: 17 Mar 2024 03:04
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Author:
Shelly Stubley
Author:
Anita Freeman
Author:
Martha A. Grootenhuis
Author:
Darren R. Hargrave
Author:
Christopher Morris
Author:
David Walker
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