European Palliative Care Research Centre (PRC), Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), 4. etg. Kunnskapssenteret vest, St. Olavs hospital, 7006, Trondheim, Norway.
St. Olavs hospital HF, Trondheim University Hospital, 4. etg. Kunnskapssenteret vest, St. Olavs hospital, 7006, Trondheim, Norway.
BMC Palliat Care. 2019 Jul 16;18(1):58. doi: 10.1186/s12904-019-0444-3.
Health care professionals should prevent and relieve suffering in carers of patients with advanced cancer. Despite known positive effects of systematic carer support, carers still do not receive sufficient support. Carers have reported to be less satisfied with coordination of care and involvement of the family in treatment and care decisions than patients. In a rural district of Mid-Norway, cancer palliative care services across specialist and community care were developed. Participants' experiences and opinions were investigated as part of this development process.
The aim of this qualitative study was to explore and describe health care professionals' experiences with carer support from their own perspective. Data were collected in focus groups. Purposeful sampling guided the inclusion. Six groups were formed with 21 professionals. The discussions were audio-recorded, transcribed, and analyzed using systematic text condensation.
In the analyzis of the focus group discussions, ten categories emerged from the exploration of health care professionals' carer support, assessment of needs, and factors hampering carer support: 1) dependent on profession, role, and context, 2) personal relationship, 3) personal skills and competence, 4) adjusted to the stage of the disease, 5) informal assessment of carers' needs, 6) lack of education 7) lack of systems for carer consultations, 8) lack of systems for documentation, 9) lack of systems for involving GPs, and 10) lack of systematic spiritual care.
Health care professionals built a personal relationship with the carers as early as possible, to facilitate carer support throughout the disease trajectory. Systematic carer support was hampered by lack of education and system insufficiencies. Organizational changes were needed, including 1) education in carer support, communication, and spiritual care, 2) use of standardized care pathways, including systematic carer needs assessment, 3) systematic involvement of general practitioners, and 4) a system for documentation of clinical work with carers.
医疗保健专业人员应预防和减轻晚期癌症患者照顾者的痛苦。尽管系统的照顾者支持具有已知的积极影响,但照顾者仍未得到足够的支持。照顾者报告说,他们对护理协调以及家庭参与治疗和护理决策的满意度低于患者。在挪威中北部的一个农村地区,跨专科和社区护理的癌症姑息治疗服务得到了发展。作为这一发展过程的一部分,调查了参与者的经验和意见。
本定性研究的目的是从自身角度探讨和描述医疗保健专业人员对照顾者支持的经验。数据是通过焦点小组收集的。有目的的抽样指导纳入。共形成了 6 个小组,共 21 名专业人员。讨论内容进行了录音、转录,并使用系统文本浓缩进行了分析。
在对焦点小组讨论的分析中,从医疗保健专业人员对照顾者支持、需求评估以及阻碍照顾者支持的因素的探索中得出了十个类别:1)依赖于专业、角色和背景,2)个人关系,3)个人技能和能力,4)适应疾病阶段,5)对照顾者需求的非正式评估,6)缺乏教育,7)缺乏照顾者咨询系统,8)缺乏文档系统,9)缺乏全科医生参与系统,10)缺乏系统的精神关怀。
医疗保健专业人员尽早与照顾者建立个人关系,以便在整个疾病过程中为照顾者提供支持。系统的照顾者支持受到缺乏教育和系统不足的阻碍。需要进行组织变革,包括 1)照顾者支持、沟通和精神关怀方面的教育,2)使用包括系统的照顾者需求评估在内的标准化护理途径,3)系统地纳入全科医生,以及 4)照顾者临床工作记录系统。