Literature DB >> 32152037

The dying parent and dependent children: a nationwide survey of hospice and community palliative care support services.

Jane Cockle-Hearne1, Elizabeth Reed2, Jennifer Todd2, Emma Ream3.   

Abstract

BACKGROUND: Annually, across the world a substantial number of dependent children experience the death of a parent through life-limiting illness. Without support, this has long-term implications for children's emotional, social and physical well-being, impacting on health and social care services globally. Limited information exists on how service providers are meeting family needs when a parent with dependent children is dying. AIM: To determine the bereavement support provided to families with dependent children by UK hospices before and after a parent's death.
DESIGN: A 23-item, cross-sectional, web-based survey of adult UK hospices. Closed and open-ended questions were asked about the features of support provided; open-ended response was sought to a question about the challenges faced by hospices in delivering support. Descriptive and non-parametric statistics and framework analysis were used to analyse the data.
RESULTS: 197 hospices were invited to participate. Response rate was 66% (130/197). More types of support were provided after, than before, parental death (mean 6.36/5.64, z=-5.767, p<0001). Twenty-two per cent of hospices reported no formal processes for asking or documenting the presence of dependent children. Volunteers were an underused resource before parental death. Four themes characterised challenges in delivering support for families: emotional difficulties for families; practical and social difficulties for families; funding/resources; and staff training/numbers.
CONCLUSIONS: Family needs are not consistently being met when a parent is dying. Areas for development include: enhanced systems to record when patients have dependent children; flexible approaches to support vulnerable families; staff training to help communication with families and management of their own fears of making the situation worse. Effective educational interventions and service developments to better support staff, parents and children are needed. © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Entities:  

Keywords:  bereavement support; children; family; hospices; palliative care; parental death

Year:  2020        PMID: 32152037     DOI: 10.1136/bmjspcare-2019-001947

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   4.633


  2 in total

1.  Communicating with young children who have a parent dying of a life-limiting illness: a qualitative systematic review of the experiences and impact on healthcare, social and spiritual care professionals.

Authors:  Lasitha M Wickramasinghe; Zhi Zheng Yeo; Poh Heng Chong; Bridget Johnston
Journal:  BMC Palliat Care       Date:  2022-07-12       Impact factor: 3.113

2.  'Don't forget the children': a qualitative study when a parent is at end of life from cancer.

Authors:  Eilís McCaughan; Cherith J Semple; Jeffrey R Hanna
Journal:  Support Care Cancer       Date:  2021-06-18       Impact factor: 3.603

  2 in total

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