Department of Pediatrics, Maastricht Universtity Medical Centre, P. Debyelaan 25, 6229 HX, Maastricht, The Netherlands.
Department of Medical Humanities, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA, Utrecht, The Netherlands.
Eur J Pediatr. 2019 Jul;178(7):1075-1085. doi: 10.1007/s00431-019-03393-w. Epub 2019 May 19.
Parenting and providing extensive care to a child with a life-limiting or life-threatening disease while being aware of the future loss of the child are among the most stressful parental experiences. Due to technical and medical improvements, children are living longer and are increasingly cared for at home. To align healthcare professionals' support with the needs of parents, a clear understanding of prominent experiences and main coping strategies of parents caring for a child in need of palliative care is needed. An interpretative qualitative study using thematic analysis was performed. Single or repeated interviews were undertaken with 42 parents of 24 children with malignant or non-malignant diseases receiving palliative care. Prominent reported parental experiences were daily anxiety of child loss, confrontation with loss and related grief, ambiguity towards uncertainty, preservation of a meaningful relationship with their child, tension regarding end-of-life decisions and engagement with professionals. Four closely related coping strategies were identified: suppressing emotions by keeping the loss of their child at bay, seeking support, taking control to arrange optimal childcare and adapting to and accepting the ongoing change(s).Conclusion: Parents need healthcare professionals who understand and carefully handle their worries, losses, parent-child relationship and coping strategies. What is Known: • In paediatric palliative care, parents have a daunting task in fulfilling all caregiving tasks while striving for control of their child's symptoms, a life worth living and a family balance. What is New: • Prominent experiences were: continuous management of anxiety of child loss, feelings of uncertainty, tension with end-of-life decision making and engagement with professionals. Parents experienced unique significance to their child, reinforcing a meaningful parent-child relationship. • Relevant coping strategies were: suppressing emotions, seeking support, taking control to arrange optimal care and adapting to the ongoing changes. • To provide tailored support, professionals need to understand parents' perceptions, relationship with their child and coping strategies.
养育患有危及生命疾病的孩子并为其提供全面的照顾,同时意识到孩子未来的丧失,这是父母最紧张的经历之一。由于技术和医疗的进步,孩子们的寿命更长,并且越来越多地在家中接受护理。为了使医疗保健专业人员的支持与父母的需求保持一致,需要清楚地了解照顾需要姑息治疗的孩子的父母的主要经历和主要应对策略。本研究采用解释性定性研究方法,通过主题分析进行。对 24 名患有恶性或非恶性疾病并接受姑息治疗的儿童的 42 名父母进行了一次或多次访谈。报告的主要父母经历是对孩子丧失的日常焦虑,面对丧失和相关的悲伤,对不确定性的模糊认识,与孩子保持有意义的关系,对临终决策的紧张以及与专业人员的接触。确定了四种密切相关的应对策略:通过将孩子的丧失拒之门外来抑制情绪,寻求支持,控制以安排最佳的育儿方式,以及适应和接受正在进行的变化。结论:父母需要理解和谨慎处理他们的担忧、损失、亲子关系和应对策略的医疗保健专业人员。已知内容:• 在儿科姑息治疗中,父母在履行所有照顾任务的同时,需要努力控制孩子的症状、有价值的生活和家庭平衡,这是一项艰巨的任务。新内容:• 主要经历包括:持续管理对孩子丧失的焦虑、不确定感、与临终决策制定相关的紧张感以及与专业人员的接触。父母对孩子有独特的意义,加强了有意义的亲子关系。• 相关的应对策略包括:抑制情绪、寻求支持、控制以安排最佳护理以及适应正在进行的变化。• 为了提供量身定制的支持,专业人员需要了解父母的看法、与孩子的关系和应对策略。