A qualitative study of health care professionals' views and experiences of paediatric advance care planning

被引:25
作者
Jack, Barbara A. [1 ,2 ]
Mitchell, Tracy K. [3 ]
O'Brien, Mary R. [3 ]
Silverio, Sergio A. [1 ,4 ]
Knighting, Katherine [1 ]
机构
[1] Edge Hill Univ, Evidence Based Practice Res Ctr, Fac Hlth & Social Care, St Helens Rd, Ormskirk L39 4QP, Lancs, England
[2] Edge Hill Univ, Postgrad Med Inst, St Helens Rd, Ormskirk L39 4QP, Lancs, England
[3] Fac Hlth & Social Care, St Helens Rd, Ormskirk L39 4QP, Lancs, England
[4] UCL, Elizabeth Garrett Anderson Inst Womens Hlth, Res Dept Reprod Hlth, 74 Huntley St, London WC1E 6AU, England
来源
BMC PALLIATIVE CARE | 2018年 / 17卷
关键词
Advance care planning; End-of-life care; Interviews; Paediatrics; Palliative care; Qualitative research; Terminal care; Thematic analysis; FAMILY-MEMBERS; INTERVIEWS;
D O I
10.1186/s12904-018-0347-8
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Good end-of-life care planning is vital to ensure optimal care is provided for patients and their families. Two key factors are open and honest advance care planning conversations between the patient (where possible), family, and health care professionals, focusing on exploring what their future wishes are; and the development of an advance care plan document However, in paediatric and neonatal settings, there has been little research to demonstrate how advance care planning conversations take place. This study explored health care professionals' views and experiences of paediatric advance care planning in hospitals, community settings and hospices. Methods: A qualitative methodology was employed using purposive sampling of health care professionals involved in the end-of-life care for children aged 0-18 years known to the hospital palliative care team, and had died at least three months before, but less than 18 months prior to the study. Ethics committee approval was obtained for the study. Located in the North of England, the study involved three hospitals, a children's hospice, and community services. Data were collected using semi-structured, digitally recorded, telephone interviews. All interviews were transcribed verbatim and subjected to thematic analysis. Results: Twenty-one health care professionals participated, including generalist paediatric staff as well as specialist palliative care staff. Two themes were generated from the study: The timing of planning conversations, including waiting for the relationship with the family to form; the introduction of parallel planning; avoiding a crisis situation. Secondly, supporting effective conversations around advance care planning, including where to have the conversation; introducing the conversation; and how to approach the topic encompassing the value of advance care planning and documentation for families. Conclusion: The timing of when to start the advance care planning conversations remains an issue for health care professionals. The value of doing it in stages and considering the environment where the conversations are held was noted. Timely planning was seen as vital to avoid difficult conversations at a crisis point and for co-ordination of care. Good advance care planning is to provide the best person-centred care for the child and experience for the family.
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页数:9
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