Literature DB >> 26818373

Undefined and unpredictable responsibility: a focus group study of the experiences of informal caregiver spouses of patients with severe COPD.

Dorthe Gaby Bove1, Ann-Britt Zakrisson2,3, Julie Midtgaard4,5, Kirsten Lomborg6, Dorthe Overgaard7.   

Abstract

AIMS AND
OBJECTIVES: To explore how spouses of patients with severe chronic obstructive pulmonary disease experience their role as informal caregiver.
BACKGROUND: Informal caregiver spouses are of pivotal importance in the way that patients with chronic obstructive pulmonary disease cope with their daily life, including their opportunity to stay at home and avoid hospitalisations in the last stages of the disease. However, caregiving is associated with increased morbidity and mortality among caregivers. Further understanding of the role as an informal caregiver spouse of patients with severe chronic obstructive pulmonary disease is needed to develop supportive interventions aimed at reducing the caregiver burden.
DESIGN: The study had a qualitative exploratory design. The data collection and analysis were based on framework method. Framework method is a thematic methodology and consists of five key stages: familiarisation, identifying a thematic framework, indexing, charting and mapping & interpretation.
METHODS: Three focus groups were conducted in November 2013 with 22 spouses of patients with severe chronic obstructive pulmonary disease.
RESULTS: Undefined and unpredictable responsibility was found to be the overarching theme describing the informal caregiver role. Underlying themes were: being constantly in a state of alertness, social life modified, maintaining normality, ambivalence in the relationship and a willingness to be involved.
CONCLUSIONS: The informal caregiver spouses experienced ambiguity about expectations from their private and the health professionals' surroundings. The informal caregiver spouses wanted to provide meaningful care for their partners, but sought knowledge and support from the health professionals. RELEVANCE TO CLINICAL PRACTICE: We recommend that nurses take on the responsibility for including the informal caregiver spouses in those aspects of decision-making that involve the common life of the patients and their spouses.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  caregiver burden; chronic obstructive pulmonary disease; decision-making; focus group; framework method; nursing; spouses

Mesh:

Year:  2016        PMID: 26818373     DOI: 10.1111/jocn.13076

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  11 in total

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2.  Next of kin's protracted challenges with access to relevant information and involvement opportunities.

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Journal:  J Multidiscip Healthc       Date:  2018-12-18

3.  Support to informal caregivers of patients with severe chronic obstructive pulmonary disease: a qualitative study of caregivers' and professionals' experiences in Swedish hospitals.

Authors:  Susann Strang; Josefin Fährn; Peter Strang; Agneta Ronstad; Louise Danielsson
Journal:  BMJ Open       Date:  2019-08-10       Impact factor: 2.692

4.  The partner's perspective of the impact of pituitary disease: Looking beyond the patient.

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Journal:  J Health Psychol       Date:  2017-03-01

5.  Frustrated Caring: Family Members' Experience of Motivating COPD Patients Towards Self-Management.

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6.  Does the carer support needs assessment tool cover the established support needs of carers of patients with chronic obstructive pulmonary disease? A systematic literature search and narrative review.

Authors:  Kerry Micklewright; Morag Farquhar
Journal:  Palliat Med       Date:  2020-07-16       Impact factor: 4.762

7.  Sexual health communication in COPD: The role, contents and design of patient information leaflets.

Authors:  Sandra Esperanza Rubio-Rask; Ingeborg Farver-Vestergaard; Ole Hilberg; Anders Løkke
Journal:  Chron Respir Dis       Date:  2021 Jan-Dec       Impact factor: 2.444

8.  Caregiver Experiences and Roles in Care Seeking During COPD Exacerbations: A Qualitative Study.

Authors:  Madhuvanthi Suresh; Jessica Young; Vincent Fan; Carol Simons; Catherine Battaglia; Tracy L Simpson; John C Fortney; Emily R Locke; Ranak Trivedi
Journal:  Ann Behav Med       Date:  2022-03-01

9.  Two faces of the same coin: a qualitative study of patients' and carers' coexistence with chronic breathlessness associated with chronic obstructive pulmonary disease (COPD).

Authors:  Diana H Ferreira; Slavica Kochovska; Aaron Honson; Jane L Phillips; David C Currow
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10.  'Who Cares?' The experiences of caregivers of adults living with heart failure, chronic obstructive pulmonary disease and coronary artery disease: a mixed methods systematic review.

Authors:  Miriam Catherine Noonan; Jennifer Wingham; Rod S Taylor
Journal:  BMJ Open       Date:  2018-07-11       Impact factor: 2.692

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