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希望的坚韧与脆弱:当孩子癌症预后不佳时,父母对希望的体验。

The tenacity and tenuousness of hope: parental experiences of hope when their child has a poor cancer prognosis.

机构信息

Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Cancer Nurs. 2013 Sep-Oct;36(5):408-16. doi: 10.1097/NCC.0b013e318291ba7d.

DOI:10.1097/NCC.0b013e318291ba7d
PMID:23640272
Abstract

BACKGROUND

The meaning and role of hope in parents of children with life-threatening illnesses remain relatively unstudied.

OBJECTIVE

The objectives of this study were to explore parental hope when a child is being treated for a malignancy resistant to treatment and to identify facilitators and barriers to maintaining hope in this context.

METHODS

Thirty-five parents of children with difficult-to-treat cancer were interviewed 3 months after diagnosis. Line-by-line coding of transcripts was used to establish categories and themes. Constant comparison was used to examine relationships within and across codes and categories.

RESULTS

Parental hope was related to the child's cure and future. The concept, however, oscillated between being tenacious and robust, and tenuous and elusive, depending on how the child was responding to treatment and the psychosocial context. Focusing on positive outcomes and experiences, spirituality, and social support facilitated being hopeful. Awareness of negative outcomes, information overload, physical and emotional depletion, and fear and uncertainty challenged parental hope.

CONCLUSIONS

Developing a model that identifies the nature of parental hope as well as barriers and facilitators to maintaining hope shortly after childhood cancer diagnosis may assist healthcare professionals in supporting parents.

IMPLICATIONS FOR PRACTICE

Understanding parental hope may assist healthcare professionals to avoid overloading parents with too much information at once. Healthcare professionals can also ensure that social support from family, community, and the medical center is available for parents and that their physical and emotional needs are being met to ensure that they maintain hope to best care for their child with cancer.

摘要

背景

在患有危及生命的疾病的儿童的父母中,希望的意义和作用仍相对未得到充分研究。

目的

本研究旨在探讨在儿童接受难治性恶性肿瘤治疗时父母的希望,并确定在这种情况下维持希望的促进因素和障碍。

方法

在诊断后 3 个月,对 35 名患有难治性癌症的儿童的父母进行了访谈。对转录本进行逐行编码,以建立类别和主题。使用恒比比较来检查代码和类别内部以及跨代码和类别的关系。

结果

父母的希望与孩子的治愈和未来有关。但是,这种观念在孩子对治疗的反应和心理社会背景的影响下,在坚韧和稳健与脆弱和难以捉摸之间摇摆不定。关注积极的结果和体验、精神性和社会支持有助于保持希望。对负面结果的认识、信息过载、身体和情绪枯竭以及恐惧和不确定性挑战了父母的希望。

结论

在儿童癌症诊断后不久,制定一种识别父母希望的性质以及维持希望的障碍和促进因素的模型,可能有助于医疗保健专业人员为父母提供支持。

实践意义

了解父母的希望可能有助于医疗保健专业人员避免一次向父母提供过多的信息。医疗保健专业人员还可以确保为父母提供来自家庭、社区和医疗中心的社会支持,并满足他们的身体和情感需求,以确保他们保持希望,从而更好地照顾患有癌症的孩子。

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