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Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?

Background: The palliative and supportive care needs of children with cancer and their families are unique and require special attention. Children and their families in Africa facing lifethreatening/ life-limiting diseases have unique needs and have the right to achieve effective and evidence-based...

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Main Author: du Plessis, Johannes
Other Authors: Stones, D K
Format: Thesis
Language:English
Published: Department of Public Health and Family Medicine 2017
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access_status_str Open Access
author du Plessis, Johannes
author2 Stones, D K
author_browse Stones, D K
du Plessis, Johannes
author_facet Stones, D K
du Plessis, Johannes
author_sort du Plessis, Johannes
collection Thesis
description Background: The palliative and supportive care needs of children with cancer and their families are unique and require special attention. Children and their families in Africa facing lifethreatening/ life-limiting diseases have unique needs and have the right to achieve effective and evidence-based care. Development of appropriate services sensitive to the needs of families and based on observed evidence has become more and more recognized. As an introduction to develop and improve supportive and palliative care services for children with cancer, families were questioned regarding their experiences and suggestions for improvements. Methods: Sixteen family members of children with cancer and treated at Universitas Academic Hospital, Bloemfontein, South Africa, were questioned regarding their children's standard oncology and supportive/palliative care. Their responses were studied and repeating themes were identified. Results: A number of areas of need were identified: erratic psychosocial support, minimal financial support, poor parental access to basic needs and food provision, preventable errors in procedures and lack of sibling support. Staff were also not always sufficiently equipped to attend to palliative care patients. Conclusions: Supportive and palliative care for children with cancer needs to be improved. Family members are a valuable resource and the interviews identified a number of themes, valuable to consider in the expansion of a supportive/palliative care service. The intension of the study was to create the awareness that by making small and affordable changes, the quality of care that children and families receive can be improved.
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language eng
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provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2017
publishDateRange 2017
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spelling oai:open.uct.ac.za:11427/25066 Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better? du Plessis, Johannes Stones, D K Meiring, Michelle Palliative Medicine Background: The palliative and supportive care needs of children with cancer and their families are unique and require special attention. Children and their families in Africa facing lifethreatening/ life-limiting diseases have unique needs and have the right to achieve effective and evidence-based care. Development of appropriate services sensitive to the needs of families and based on observed evidence has become more and more recognized. As an introduction to develop and improve supportive and palliative care services for children with cancer, families were questioned regarding their experiences and suggestions for improvements. Methods: Sixteen family members of children with cancer and treated at Universitas Academic Hospital, Bloemfontein, South Africa, were questioned regarding their children's standard oncology and supportive/palliative care. Their responses were studied and repeating themes were identified. Results: A number of areas of need were identified: erratic psychosocial support, minimal financial support, poor parental access to basic needs and food provision, preventable errors in procedures and lack of sibling support. Staff were also not always sufficiently equipped to attend to palliative care patients. Conclusions: Supportive and palliative care for children with cancer needs to be improved. Family members are a valuable resource and the interviews identified a number of themes, valuable to consider in the expansion of a supportive/palliative care service. The intension of the study was to create the awareness that by making small and affordable changes, the quality of care that children and families receive can be improved. 2017-09-06T07:07:08Z 2017-09-06T07:07:08Z 2017 Master Thesis Masters MPhil http://hdl.handle.net/11427/25066 eng application/pdf Department of Public Health and Family Medicine Faculty of Health Sciences University of Cape Town
spellingShingle Palliative Medicine
du Plessis, Johannes
Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
thesis_degree_str Master's
title Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
title_full Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
title_fullStr Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
title_full_unstemmed Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
title_short Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
title_sort family experiences and viewpoints of palliative and supportive care for children with cancer can we do better
topic Palliative Medicine
url http://hdl.handle.net/11427/25066
work_keys_str_mv AT duplessisjohannes familyexperiencesandviewpointsofpalliativeandsupportivecareforchildrenwithcancercanwedobetter