McVeigh, C., Reid, J., Larkin, P., Porter, S. and Hudson, P., 2018. The experience of palliative care service provision for people with non-malignant respiratory disease and their family carers: an all-Ireland qualitative study. Journal of Advanced Nursing, 74 (2), 383-394.
Full text available as:
|
PDF
Veigh_et_al-2017-Journal_of_Advanced_Nursing.pdf - Accepted Version Available under License Creative Commons Attribution Non-commercial No Derivatives. 773kB | |
Copyright to original material in this document is with the original owner(s). Access to this content through BURO is granted on condition that you use it only for research, scholarly or other non-commercial purposes. If you wish to use it for any other purposes, you must contact BU via BURO@bournemouth.ac.uk. Any third party copyright material in this document remains the property of its respective owner(s). BU grants no licence for further use of that third party material. |
DOI: 10.1111/jan.13453
Abstract
AIM: To explore specialist and generalist palliative care provision for people with non-malignant respiratory disease, in rural and urban areas in the North and Republic of Ireland. BACKGROUND: Globally, palliative care is recommended as an appropriate healthcare option for people with advanced non- malignant lung disease. Yet, there is limited evidence regarding the integration of palliative care for this client group. DESIGN: Qualitative study. METHODS: Convenience sample of 17 bereaved carers and 18 healthcare professionals recruited from two rural and two urban sites on the Island of Ireland. Data were collected throughout 2012 and 2013 through semi-structured interviews with carers of patients with Chronic Obstructive Pulmonary Disease (N=12), interstitial lung disease (N=4) or bronchiectasis (N=1) who had died 3-18 months previously; and 4 focus groups with healthcare professionals. Data were analysed using a thematic analysis framework. RESULTS: Carers' interviews yielded three overarching themes:1) Lack of preparedness for death, due to ambiguity regarding disease trajectory; 2) Lack of consistency in palliative care delivery, in relation to the receipt of generalist and specialist palliative care; and 3) Role ambiguity, related to their caregiving role. Focus groups identified two overarching themes:1) Barriers to appropriate palliative care; and 2) The future direction of palliative care for patient with non-malignant respiratory disease. CONCLUSION: The uncertain disease trajectory was not only experienced by carers but also healthcare professionals. Although referral to specialist palliative care services was perceived as increasing, the availability and coordination of generalist and specialist palliative care services were fragmented and varied dependent on geographical location. This article is protected by copyright. All rights reserved.
Item Type: | Article |
---|---|
ISSN: | 0309-2402 |
Additional Information: | This research received funding from the Department of Employment and Learning, Northern Ireland. |
Uncontrolled Keywords: | COPD; bronchiectasis; chronic obstructive pulmonary disease; family carers; interstitial lung disease; non-malignant respiratory disease ; nursing and healthcare professionals; palliative care; qualitative research |
Group: | Faculty of Science & Technology |
ID Code: | 30073 |
Deposited By: | Symplectic RT2 |
Deposited On: | 05 Dec 2017 12:31 |
Last Modified: | 14 Mar 2022 14:08 |
Downloads
Downloads per month over past year
Repository Staff Only - |