Place and Provision of Palliative Care for Children With Progressive Cancer: A Study by the Paediatric Oncology Nurses’ Forum/United Kingdom Children's Cancer Study Group Palliative Care Working Group [Новость добавлена - 02.10.2007]

Journal of Clinical Oncology, Vol 25, No 28 (October 1), 2007: pp. 4472-4476 © 2007 American Society of Clinical Oncology. DOI: 10.1200/JCO.2007.12.0493

Jan Vickers, Anne Thompson, Gary S. Collins, Margaret Childs, Richard Hain

From Oncology Outreach and Palliative Care, Oncology Unit, Royal Liverpool Children's Hospital, Liverpool; Paediatric Macmillan Unit, Children & Young Peoples Cancer Unit, Royal Victoria Infirmary, Newcastle; UK Children's Cancer Study Group, University of Leicester, Leicester; and the Paediatric Palliative Medicine, Department of Child Health, Cardiff University School of Medicine, Wales, United Kingdom

Address reprint requests to Richard Hain, MBBS, MSc, MD, MRCP (UK), FRCPCH, Dip Pall Med, Senior Lecturer in Paediatric Palliative Medicine and Oncology, Department of Child Health, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, United Kingdom; e-mail: hainrd@cardiff.ac.uk

Purpose: The purpose of this study was to describe and show effectiveness of the outreach team model of palliative care (PC) in allowing home death for children with incurable cancer. 

Patients and Methods: Over 7 months, 185 children from 22 United Kingdom oncology centers were recruited to a prospective questionnaire survey. 

Results: One hundred sixty-four children from 22 centers died (median age, 8.7 years; 88 boys, 76 girls). One hundred twenty-six families completed two or more questionnaires. One hundred twenty (77%) of 155 with complete data died at home. Preference for home death was recorded in 90 (68%) of 164 and 132 (80%) 164 at study entry and last month of life, respectively. Death occurred in preferred place for 84 (80%) of 105 with recorded preference at entry. Forty-one (25%) of 164 and 68 (41.5%) of 164 needed no outpatient or inpatient hospital visits, respectively. A named individual provided on-call PC advice by phone or home visit in 22 (100%) and 18 (82%) of 22 oncology centers, respectively. As PC progressed, involvement of oncologist and social worker appeared less, whereas pediatric oncology outreach nurse specialists (POONSs) remained prominent. 

Conclusion: Preference for home death expressed by families in our study is similar to others, but the proportion of children actually able to die there is higher. Home death is facilitated by this model. Key components are POONSs, pediatric palliative and/or oncology specialist, and general practitioner. Professional roles change during PC and after death. An ongoing role for the oncology team in bereavement support is highlighted. 

The UKCCSG is now known as the Children's Cancer and Leukaemia Group. 

Authors’ disclosures of potential conflicts of interest and author contributions are found at the end of this article. 

^{Original abstract at: http://jco.ascopubs.org/cgi/content/abstract/25/28/4472}