Literature DB >> 9116444

Using research to develop care for patients with Huntington's disease.

H Skirton1, N Glendinning.   

Abstract

Huntington's disease (HD) is a progressive neurodegenerative disorder affecting approximately 5-10 per 100,000 people in the UK (Harper, 1992). This dominantly inherited genetic condition causes movement disturbance (especially chorea), depression and dementia. The complex physical, mental, psychological and social problems caused by HD can result in particular difficulties in care. The course of the disease may span 15-20 years from diagnosis to death, necessitating long-term nursing care. The NHS and Community Care Act 1990 has made statutory provision for patients to be cared for at home if they so wish, placing a greater onus of care on the primary healthcare team. A survey of 25 patients in Somerset who had been diagnosed with HD was recently undertaken to ascertain the health and social care needs of patients and their carers. Of a possible 300 care needs in 12 categories (e.g. housing, dietary advice, carer support), 73 unmet needs were identified in this group. Using the survey as a basis, this article describes the steps taken in Somerset to ensure that the future needs of this group of patients are fulfilled. This model may be appropriate for the care of patients with other complex long-term diseases.

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Year:  1997        PMID: 9116444     DOI: 10.12968/bjon.1997.6.2.83

Source DB:  PubMed          Journal:  Br J Nurs        ISSN: 0966-0461


  10 in total

Review 1.  State of the science: social, psychological, and ethical nursing research in genetics.

Authors:  G Anderson
Journal:  Biol Res Nurs       Date:  1999-10       Impact factor: 2.522

2.  Huntington disease: families' experiences of healthcare services.

Authors:  Heather Skirton; Janet K Williams; J Jackson Barnette; Jane S Paulsen
Journal:  J Adv Nurs       Date:  2010-03       Impact factor: 3.187

3.  Further evidence of reliability and validity of the Huntington's disease quality of life battery for carers: Italian and French translations.

Authors:  Aimee Aubeeluck; Julie Dorey; Ferdinando Squitieri; Emilie Clay; Edward J N Stupple; Annunziata De Nicola; Heather Buchanan; Tiziana Martino; Mondher Toumi
Journal:  Qual Life Res       Date:  2012-07-21       Impact factor: 4.147

4.  'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.

Authors:  Aimee Victoria Aubeeluck; Heather Buchanan; Edward J N Stupple
Journal:  Qual Life Res       Date:  2011-11-13       Impact factor: 4.147

5.  The emotional experiences of family carers in Huntington disease.

Authors:  Janet K Williams; Heather Skirton; Jane S Paulsen; Toni Tripp-Reimer; Lori Jarmon; Meghan McGonigal Kenney; Emily Birrer; Bonnie L Hennig; Joann Honeyford
Journal:  J Adv Nurs       Date:  2009-02-09       Impact factor: 3.187

6.  How do partners find out about the risk of Huntington's disease in couple relationships?

Authors:  Karen Forrest Keenan; Sheila A Simpson; Zosia Miedzybrodzka; David A Alexander; June Semper
Journal:  J Genet Couns       Date:  2013-01-09       Impact factor: 2.537

7.  Utilisation of Healthcare and Associated Services in Huntington's disease: a data mining study.

Authors:  Monica Busse; Dr Hasan Al-Madfai; Joyce Kenkre; G Bernhard Landwehrmeyer; Annarita Bentivoglio; Anne Rosser
Journal:  PLoS Curr       Date:  2011-01-21

8.  Avoidance as a strategy of (not) coping: qualitative interviews with carers of Huntington's Disease patients.

Authors:  Alison Lowit; Edwin R van Teijlingen
Journal:  BMC Fam Pract       Date:  2005-09-14       Impact factor: 2.497

9.  Exploring the Reliability and Validity of the Huntington's Disease Quality of Life Battery for Carers (HDQoL-C) within A Polish Population.

Authors:  Agnieszka Bartoszek; Aimee Aubeeluck; Edward Stupple; Adrian Bartoszek; Katarzyna Kocka; Barbara Ślusarska
Journal:  Int J Environ Res Public Health       Date:  2019-06-30       Impact factor: 3.390

10.  Unmet needs for healthcare and social support services in patients with Huntington's disease: a cross-sectional population-based study.

Authors:  Marleen R van Walsem; Emilie I Howe; Kristin Iversen; Jan C Frich; Nada Andelic
Journal:  Orphanet J Rare Dis       Date:  2015-09-28       Impact factor: 4.123

  10 in total

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