Literature DB >> 24681558

Family carer perspectives of acute hospital care following a diagnosis of motor neuron disease: a qualitative secondary analysis.

Mary R O'Brien1, Harriet Preston2.   

Abstract

OBJECTIVES: The multifaceted nature of the problems faced by someone with motor neuron disease requires a knowledgeable multidisciplinary team approach. Where available, generally, such services are only provided on an outpatient basis, meaning that hospitalised patients are frequently admitted to non-specialist wards where understanding of their needs is limited. Little is known regarding the inpatient care received by patients. Our objective was to address this by exploring the experience of hospitalisation following a diagnosis of motor neuron disease from the perspective of family carers of those diagnosed with the illness.
METHOD: This was a qualitative secondary analysis of pre-existing data from two previously published, separately conducted, qualitative studies. The study involved interview data from 18 bereaved carers and 3 current carers of family members diagnosed with motor neuron disease in Northwest England.
RESULTS: The findings reveal dissatisfaction with the inpatient care received, which impacted negatively not only on patient and carer enthusiasm for future hospital admissions but also on carer bereavement.
CONCLUSIONS: Patients with motor neuron disease have specialist needs that are not always met during hospital admission, particularly to non-specialist units. The inpatient care provided for these patients must be improved as must the knowledge and understanding of the illness among healthcare professionals who treat them. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Entities:  

Keywords:  Acute Hospital; Carers; Motor Neurone Disease; Qualitative Research; Secondary Analysis

Mesh:

Year:  2014        PMID: 24681558     DOI: 10.1136/bmjspcare-2013-000627

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   3.568


  3 in total

Review 1.  End of life care for long-term neurological conditions: A meta-ethnographic review of the experiences of informal carers.

Authors:  Michael Toze; Mo Ray; Thomas George; Kelly Sisson; David Nelson
Journal:  Palliat Med       Date:  2020-11-25       Impact factor: 4.762

2.  Supportive needs of informal caregivers of people with amyotrophic lateral sclerosis in Switzerland: a qualitative study.

Authors:  Christopher Poppe; Kathi Schweikert; Tanja Krones; Tenzin Wangmo
Journal:  Palliat Care Soc Pract       Date:  2022-02-28

3.  The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review.

Authors:  Kate Flemming; Victoria Turner; Samantha Bolsher; Bill Hulme; Elizabeth McHugh; Ian Watt
Journal:  Palliat Med       Date:  2020-04-14       Impact factor: 4.762

  3 in total

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