Literature DB >> 17906208

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.

Jan Vickers1, Anne Thompson, Gary S Collins, Margaret Childs, Richard Hain.   

Abstract

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.

Entities:  

Mesh:

Year:  2007        PMID: 17906208     DOI: 10.1200/JCO.2007.12.0493

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  29 in total

1.  Palliative care in children with cancer: implications for general practice.

Authors:  Ivana Mm van der Geest; Patrick Je Bindels; Saskia Mf Pluijm; Erna Mc Michiels; Agnes van der Heide; Rob Pieters; Anne-Sophie E Darlington; Marry M van den Heuvel-Eibrink
Journal:  Br J Gen Pract       Date:  2016-12       Impact factor: 5.386

2.  Trends in End-of-Life Care in Pediatric Hematology, Oncology, and Stem Cell Transplant Patients.

Authors:  Katharine E Brock; Angela Steineck; Clare J Twist
Journal:  Pediatr Blood Cancer       Date:  2015-10-29       Impact factor: 3.167

3.  The Madison Clinic: Evaluation of a collaborative outpatient paediatric palliative care clinic.

Authors:  Harold Siden; Lynn Straatman; Tanice Miller; Jennifer Ham
Journal:  Paediatr Child Health       Date:  2009-07       Impact factor: 2.253

Review 4.  Palliative Care Models for Cancer Patients: Learning for Planning in Nursing (Review).

Authors:  Hadi Hassankhani; Azad Rahmani; Fariba Taleghani; Zohreh Sanaat; Javad Dehghannezhad
Journal:  J Cancer Educ       Date:  2020-02       Impact factor: 2.037

Review 5.  Challenging issues in pediatric oncology.

Authors:  Ching-Hon Pui; Amar J Gajjar; Javier R Kane; Ibrahim A Qaddoumi; Alberto S Pappo
Journal:  Nat Rev Clin Oncol       Date:  2011-06-28       Impact factor: 66.675

6.  Patterns of End-of-Life Care in Children With Advanced Solid Tumor Malignancies Enrolled on a Palliative Care Service.

Authors:  Tamara Z Vern-Gross; Catherine G Lam; Zachary Graff; Sara Singhal; Deena R Levine; Deborah Gibson; April Sykes; Doralina L Anghelescu; Ying Yuan; Justin N Baker
Journal:  J Pain Symptom Manage       Date:  2015-04-16       Impact factor: 3.612

Review 7.  Pediatric Oncology: Managing Pain at the End of Life.

Authors:  Jennifer M Snaman; Justin N Baker; Jennifer H Ehrentraut; Doralina L Anghelescu
Journal:  Paediatr Drugs       Date:  2016-06       Impact factor: 3.022

8.  Perceptions of the Pediatric Hospice Experience among English- and Spanish-Speaking Families.

Authors:  Rachel Thienprayoon; Emily Marks; Maria Funes; Louizza Maria Martinez-Puente; Naomi Winick; Simon Craddock Lee
Journal:  J Palliat Med       Date:  2015-11-30       Impact factor: 2.947

9.  Barriers and needs in paediatric palliative home care in Germany: a qualitative interview study with professional experts.

Authors:  Saskia Jünger; Tania Pastrana; Martina Pestinger; Martina Kern; Boris Zernikow; Lukas Radbruch
Journal:  BMC Palliat Care       Date:  2010-06-02       Impact factor: 3.234

10.  The needs of professionals in the palliative care of children and adolescents.

Authors:  Eva Bergstraesser; Susanne Inglin; Rosanna Abbruzzese; Katrin Marfurt-Russenberger; Martin Hošek; Rainer Hornung
Journal:  Eur J Pediatr       Date:  2012-12-04       Impact factor: 3.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.