Division of Bioethics and Palliative Care, Department of Pediatrics (J.B.), University of Washington School of Medicine; Palliative Care and Resilience Lab, Center for Clinical and Translational Research, Seattle Children's Research Institute, Seattle, Washington.
Divisions of Bioethics and Palliative Care/Hospital Medicine, Department of Pediatrics (A.T.), University of Washington School of Medicine; Palliative Care and Resilience Lab, Center for Clinical and Translational Research, Seattle Children's Research Institute, Seattle, Washington.
J Pain Symptom Manage. 2021 Oct;62(4):709-719. doi: 10.1016/j.jpainsymman.2021.03.015. Epub 2021 Mar 26.
With advances in treatments that have resulted in children living longer with serious illness, it is essential to understand how parents adapt to changes during the final stages of their child's life or after their child's death.
To examine the process by which parents adapt to their child's serious illness and death among a group of non-bereaved and bereaved parents of adolescents and young adults (AYAs) with advanced cancer.
Qualitative study exploring the experiences of parents of AYAs who were being treated for recurrent or refractory advanced cancer (nonbereaved parents) or had died from their disease (bereaved parents) at one large academic center. Participants completed demographic surveys and semi-structured interviews to better understand parent adaptation. Data were analyzed using content and thematic approaches.
Of the 37 participating parents; 22 (59%) were non-bereaved and 15 (41%) were bereaved. The AYAs predominantly had hematologic malignancies (n = 18/34, 53%). Across both cohorts, parents described the process of adapting to their child's worsening health or death as moments of feeling stuck and moments of gratitude and meaning.
Adaptation to a child's serious illness and death likely occurs on a dynamic spectrum and parents may oscillate both cognitively and emotionally. This has important implications for how clinicians and communities support parents. Greater comfort with and normalization of the adaptation process may enable parents to more openly share both the unimaginable hardships and unexpected silver-linings that are part of their parenting experiences during their child's illness and death.
随着治疗方法的进步,患有严重疾病的儿童能够存活更长时间,因此了解父母如何适应孩子生命末期或孩子去世后的变化至关重要。
在一组未经历丧亲之痛和经历丧亲之痛的青少年和年轻成人(AYA)晚期癌症患儿的父母中,研究父母如何适应孩子的严重疾病和死亡。
这是一项定性研究,探索了在一家大型学术中心接受复发性或难治性晚期癌症治疗的 AYA 未经历丧亲之痛的父母(非丧亲之痛父母)或因疾病去世的父母(丧亲之痛父母)的父母的经历。参与者完成了人口统计学调查和半结构化访谈,以更好地了解父母的适应情况。使用内容分析和主题分析方法对数据进行分析。
37 名参与的父母中,22 名(59%)是非丧亲之痛父母,15 名(41%)是丧亲之痛父母。AYA 主要患有血液系统恶性肿瘤(n=18/34,53%)。在两个队列中,父母都将适应孩子健康状况恶化或死亡的过程描述为感到被困和感恩有意义的时刻。
适应孩子的严重疾病和死亡可能发生在一个动态的范围内,父母可能在认知和情感上都存在波动。这对临床医生和社区如何支持父母具有重要意义。对适应过程的更大的舒适感和正常化可能使父母能够更公开地分享他们在孩子患病和死亡期间育儿经历中所面临的难以想象的困难和意想不到的一线希望。