Exploring parent treatment decision-making in relapsed and refractory neuroblastoma: A qualitative study

IF 1.8 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH SSM. Qualitative research in health Pub Date : 2024-09-27 DOI:10.1016/j.ssmqr.2024.100487
Helen Pearson , Faith Gibson , Michelle Myall , Anne-Sophie Darlington
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Abstract

Parents often become involved in making treatment decisions for their child with cancer when there is no standard treatment protocol, typically seen in poor-prognosis cancers. Advances in scientific medicine has led to more treatment options being available for children resulting in parents making repeated treatment decisions depending on their child's response to treatment. The emotional turmoil of their child's cancer diagnosis can be exacerbated when combined with making decisions that have uncertain outcomes. This study aimed to identify, describe, explore, and explain how parents made repeated treatment decisions and the role of emotion in decision-making when their child had relapsed or refractory neuroblastoma, a poor-prognosis cancer.
Data were collected using qualitative interviews between 2020 and 2022 with parents of children with relapsed or refractory neuroblastoma in the United Kingdom. Data were analysed using Reflexive Thematic Analysis.
Eighteen parents who made between one to six treatment decisions participated. Decision-making incorporated four themes which enabled, influenced, and informed how parents made treatment decisions: 1) time as a structure within decision-making; 2) uncertainty and its relationships with treatment risk, side effects and outcomes; 3) parent oscillation of their cognitive and emotional adjustment; 4) parent responsibility and involvement in decision-making. Time was the central organising concept which structured and organised parent decision-making. We adopted Orlikowski and Yates’s (2002) temporal structures to characterise the experience of time and Stroebe and Schut’s (1999) dual-processing theory to explore the oscillation of parent adjustment of their situation cognitively and emotionally. A conceptual framework showed the interrelationships of these themes.
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探索复发和难治性神经母细胞瘤患者父母的治疗决策:一项定性研究
在没有标准治疗方案的情况下,家长往往会参与为患癌儿童做出治疗决定,这种情况通常发生在预后较差的癌症患者身上。科学医学的进步为儿童提供了更多的治疗选择,这导致家长需要根据孩子对治疗的反应反复做出治疗决定。孩子被确诊为癌症后,家长的情绪波动会更大,同时还要做出结果不确定的决定。本研究旨在识别、描述、探索和解释当父母的孩子患有复发或难治性神经母细胞瘤(一种预后较差的癌症)时,父母是如何做出反复治疗决定的,以及情绪在决策中的作用。研究人员在 2020 年至 2022 年期间通过定性访谈收集了英国复发或难治性神经母细胞瘤患儿父母的数据。18位做出1至6项治疗决定的家长参与了数据分析。决策包含四个主题,这些主题促成、影响并指导家长如何做出治疗决定:1)作为决策结构的时间;2)不确定性及其与治疗风险、副作用和结果的关系;3)家长在认知和情绪调整方面的摇摆;4)家长在决策中的责任和参与。时间是核心的组织概念,它构建并组织了家长的决策。我们采用 Orlikowski 和 Yates(2002 年)的时间结构来描述对时间的体验,并采用 Stroebe 和 Schut(1999 年)的双重处理理论来探讨家长在认知和情感上对自身情况的调整。一个概念框架显示了这些主题之间的相互关系。
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来源期刊
CiteScore
1.60
自引率
0.00%
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0
审稿时长
163 days
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