Literature DB >> 15810753

Palliative care in children in Wales: a study of provision and need.

Richard D W Hain1.   

Abstract

AIM: To establish incidence and prevalence of children needing palliative care in Wales. PATIENTS AND METHODS: Children were identified in three ways: (1) from paediatricians using the Welsh Paediatric Surveillance Unit (WPSU); (2) referrals to the specialist palliative medicine service based in Cardiff; and (3) children under the care of the two principal children's hospices serving Wales. All children referred or reported between January 2001 and December 2002 were included.
RESULTS: A total of 226 children were identified. Fifty (22%) were identified by paediatricians, 58 (26%) were referred to the specialist paediatric palliative medicine service, 158 (70%) had been under the care of a children's hospice, and 34 (15%) were identified by more than one source. This study identified approximately 3.75 per 10000 children. This is about half the prevalence figures quoted in the ACT/ RCPCH document in 1997.
CONCLUSIONS: The study may underestimate prevalence. Children needing palliative medicine are still under-recognized in Wales. The overlap between children's hospice care and specialist paediatric palliative medicine is relatively small.

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Year:  2005        PMID: 15810753     DOI: 10.1191/0269216305pm967oa

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  7 in total

Review 1.  Pediatric palliative care-when quality of life becomes the main focus of treatment.

Authors:  Eva Bergstraesser
Journal:  Eur J Pediatr       Date:  2012-04-03       Impact factor: 3.183

2.  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

3.  The development of an instrument that can identify children with palliative care needs: the Paediatric Palliative Screening Scale (PaPaS Scale): a qualitative study approach.

Authors:  Eva Bergstraesser; Richard D Hain; José L Pereira
Journal:  BMC Palliat Care       Date:  2013-05-08       Impact factor: 3.234

4.  Paediatric palliative care: development and pilot study of a 'Directory' of life-limiting conditions.

Authors:  Richard Hain; Mary Devins; Richard Hastings; Jayne Noyes
Journal:  BMC Palliat Care       Date:  2013-12-11       Impact factor: 3.234

5.  The journey through care: study protocol for a longitudinal qualitative interview study to investigate the healthcare experiences and preferences of children and young people with life-limiting and life-threatening conditions and their families in the West Midlands, UK.

Authors:  Sarah Mitchell; Anne-Marie Slowther; Jane Coad; Jeremy Dale
Journal:  BMJ Open       Date:  2018-01-21       Impact factor: 2.692

6.  Planning ahead with children with life-limiting conditions and their families: development, implementation and evaluation of 'My Choices'.

Authors:  Jane Noyes; Richard P Hastings; Mary Lewis; Richard Hain; Virginia Bennett; Lucie Hobson; Llinos Haf Spencer
Journal:  BMC Palliat Care       Date:  2013-02-05       Impact factor: 3.234

7.  Evidence-based planning and costing palliative care services for children: novel multi-method epidemiological and economic exemplar.

Authors:  Jane Noyes; Rhiannon Tudor Edwards; Richard P Hastings; Richard Hain; Vasiliki Totsika; Virginia Bennett; Lucie Hobson; Gareth R Davies; Ciarán Humphreys; Mary Devins; Llinos Haf Spencer; Mary Lewis
Journal:  BMC Palliat Care       Date:  2013-04-25       Impact factor: 3.234

  7 in total

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