摘要
Little is known about the psychosocial process of parental decisions on 'drop out' from cancer treatment for paediatric patients in Taiwan. This study, based on structured in-depth interviews, attempted to document the determinants of parental decisions on drop out. A total of 19 parents of paediatric cancer patients who dropped out from a cancer treatment for at least a month within 3 years since first treatment were interviewed. Content analysis of qualitative data revealed six categories of determinants associated with parental decisions: suffering severe pain from medical treatments and adverse side-effects; desire for better and less painful treatments; adverse effect of other patients' experiences; searching for possible explanations for disease after prolonged denial of diagnosis; lack of empathy from health care professionals; and misinterpretation of improved prognostics. These findings reflected the deficiency of psychological and emotional support for parents from health care professionals prior to and during cancer treatment.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 193-199 |
| 頁數 | 7 |
| 期刊 | Journal of Advanced Nursing |
| 卷 | 30 |
| 發行號 | 1 |
| DOIs | |
| 出版狀態 | 已出版 - 07 1999 |
UN SDG
此研究成果有助於以下永續發展目標
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SDG3 健康與福祉
指紋
深入研究「Determinants of parental decisions on 'drop out' from cancer treatment for childhood cancer patients」主題。共同形成了獨特的指紋。引用此
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