Literature DB >> 23928324

Improving the interface between informal carers and formal health and social services: a qualitative study.

K M McPherson1, N K Kayes2, N Moloczij2, C Cummins2.   

Abstract

BACKGROUND: Reports about the impact of caring vary widely, but a consistent finding is that the role is influenced (for better or worse) by how formal services respond to, and work with informal carers and of course the cared for person.
OBJECTIVE: We aimed to explore the connection between informal and formal cares and identify how a positive connection or interface might be developed and maintained.
DESIGN: We undertook a qualitative descriptive study with focus groups and individual interviews with informal carers, formal care service providers and representatives from carer advocacy groups. Content analysis was used to identify key factors impacting on the interface between informal and formal carers and propose specific recommendations for service development.
SETTING: Community setting including urban and rural areas of New Zealand. PARTICIPANTS AND METHODS: Seventy participants (the majority informal carers) took part in 13 focus groups and 22 individual interviews.
RESULTS: Four key themes were derived: Quality of care for the care recipient; Knowledge exchange (valuing carer perspectives); One size does not fit all (creating flexible services); and A constant struggle (reducing the burden services add). An optimum interface to address these key areas was proposed.
CONCLUSION: In addition to ensuring quality care for the care recipient, specific structures and processes to support a more positive interface appear warranted if informal carers and services are to work well together. An approach recognising the caring context and carer expertise may decrease the additional burden services contribute, and reduce conflicting information and resultant confusion and/or frustration many carers experience.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Carers; Delivery of health care; Disability; Qualitative research; Quality of health care

Mesh:

Year:  2013        PMID: 23928324     DOI: 10.1016/j.ijnurstu.2013.07.006

Source DB:  PubMed          Journal:  Int J Nurs Stud        ISSN: 0020-7489            Impact factor:   5.837


  5 in total

1.  Six key topics informal carers of patients with breathlessness in advanced disease want to learn about and why: MRC phase I study to inform an educational intervention.

Authors:  Morag Farquhar; Clarissa Penfold; John Benson; Roberta Lovick; Ravi Mahadeva; Sophie Howson; Julie Burkin; Sara Booth; David Gilligan; Christopher Todd; Gail Ewing
Journal:  PLoS One       Date:  2017-05-05       Impact factor: 3.240

2.  Knowledge, help-seeking and efficacy to find respite services: an exploratory study in help-seeking carers of people with dementia in the context of aged care reforms.

Authors:  L Phillipson; K Johnson; E Cridland; D Hall; C Neville; E Fielding; H Hasan
Journal:  BMC Geriatr       Date:  2019-01-07       Impact factor: 3.921

3.  Patient and informal carer experience of hip fracture: a qualitative study using interviews and observation in acute orthopaedic trauma.

Authors:  Elizabeth Tutton; Lorena Saletti-Cuesta; Debbie Langstaff; Julie Wright; Richard Grant; Keith Willett
Journal:  BMJ Open       Date:  2021-02-04       Impact factor: 2.692

4.  Qualitative focus group study investigating experiences of accessing and engaging with social care services: perspectives of carers from diverse ethnic groups caring for stroke survivors.

Authors:  Nan Greenwood; Jess Holley; Theresa Ellmers; Gill Mein; Geoffrey Cloud
Journal:  BMJ Open       Date:  2016-01-29       Impact factor: 2.692

5.  Closing the Gap: Increasing Community Mental Health Services in Rural Indiana.

Authors:  Kristi Schultz; Sara Farmer; Sam Harrell; Carol Hostetter
Journal:  Community Ment Health J       Date:  2021-01-01
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.