Department of Pediatric Hematology and Oncology, University Hospital Motol, V Uvalu 84, Prague, 5,150 06, Czech Republic.
Pediatric Supportive Care Team, University Hospital Motol, Prague, Czech Republic.
BMC Palliat Care. 2023 Oct 10;22(1):152. doi: 10.1186/s12904-023-01269-3.
Effective cooperation between a pediatric palliative care team (PPCT), primary treating specialists, patients and families is crucial for high quality care of children with complex life-limiting conditions. Several barriers among patients, families and treating specialists have been identified in the context of initializing pediatric palliative care. The aim of the study was to assess the experience with initial pediatric palliative care consultations from perspectives of family caregivers and treating physicians with a special focus on two innovative approaches: attendance of the treating specialist and the opportunity for parents to give feedback on the written report from the consultation.
This was a qualitative study using semi-structured interviews with family caregivers of children with malignant and non-malignant disease and their treating specialists. Framework analysis was used to guide the data collection and data analysis.
In total, 12 family caregivers and 17 treating specialists were interviewed. Four main thematic categories were identified: (1) expectations, (2) content and evaluation, (3) respect and support from the team and (4) consultation outcomes. Parents viewed the consultation as a unique opportunity to discuss difficult topics. They perceived the attendance of the treating specialist at the initial consultation as very important for facilitating communication. Treating specialists valued the possibility to learn more about psychosocial issues of the child and the family while attending the initial palliative care consultation. All participants perceived the written report from the consultation as useful for further medical decisions. Family members appreciated the chance to give feedback on the consultation report.
Our study identified several clinically relevant issues that can help initialize pediatric palliative care and establish effective collaboration between families and PPCT and treating specialists. Supporting treating specialists in their ability to explain the role of palliative care is important in order to reduce the risk of misunderstanding or unrealistic expectations. Developing more specific expectations seems to be one of the ways to further increase the effectiveness of initial consultations. The results of the study can be especially helpful for the initial phase of implementing pediatric palliative care and initializing the process of setting up a collaborative relationship with palliative care teams in the hospital.
儿科姑息治疗团队(PPCT)、初级治疗专家、患者和家庭之间的有效合作对于患有复杂生命终末期疾病的儿童的高质量护理至关重要。在启动儿科姑息治疗的背景下,已经确定了患者、家庭和治疗专家之间的几个障碍。本研究的目的是评估家庭照顾者和治疗医生对初始儿科姑息治疗咨询的体验,特别关注两种创新方法:治疗专家的参与和父母对咨询书面报告反馈的机会。
这是一项使用半结构化访谈对患有恶性和非恶性疾病的儿童的家庭照顾者及其治疗专家进行的定性研究。框架分析用于指导数据收集和数据分析。
共采访了 12 名家庭照顾者和 17 名治疗专家。确定了四个主要主题类别:(1)期望,(2)内容和评估,(3)团队的尊重和支持,(4)咨询结果。父母认为咨询是讨论困难话题的独特机会。他们认为治疗专家在初始姑息治疗咨询中出席非常重要,有助于促进沟通。治疗专家重视在参加初始姑息治疗咨询时了解更多关于儿童和家庭的心理社会问题的可能性。所有参与者都认为咨询报告对进一步的医疗决策很有用。家属赞赏有机会对咨询报告发表意见。
我们的研究确定了一些临床上相关的问题,这些问题可以帮助启动儿科姑息治疗,并在家庭和姑息治疗团队与治疗专家之间建立有效的合作。支持治疗专家解释姑息治疗作用的能力很重要,以降低误解或不切实际的期望的风险。制定更具体的期望似乎是提高初始咨询效果的一种方法。研究结果对于实施儿科姑息治疗的初始阶段和在医院启动姑息治疗团队合作过程特别有帮助。