Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/26968
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles
Peer Review Status: Refereed
Title: Palliative and end-of-life care conversations in COPD: A systematic literature review
Author(s): Tavares, Nuno
Jarrett, Nikki
Hunt, Kate
Wilkinson, Tom
Issue Date: 27-Apr-2017
Date Deposited: 11-Apr-2018
Citation: Tavares N, Jarrett N, Hunt K & Wilkinson T (2017) Palliative and end-of-life care conversations in COPD: A systematic literature review. ERS Monograph, 3 (2), Art. No.: 00068-2016. https://doi.org/10.1183/23120541.00068-2016
Abstract: Chronic obstructive pulmonary disease (COPD) is a chronic life-limiting disorder characterised by persistent airflow obstruction and progressive breathlessness. Discussions/conversations between patients and clinicians ensure palliative care plans are grounded in patients’ preferences. This systematic review aimed to explore what is known about palliative care conversations between clinicians and COPD patients.  A comprehensive search of all major healthcare-related databases and websites was performed following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Studies were quality assessed, employing widely used quality-assessment tools, with only papers scoring moderate-to-high quality included. All relevant data were extracted. A narrative synthesis was used to analyse, process and present the final data.  The findings indicated that the frequency and quality of palliative care conversations is generally poor. Patients and physicians identified many barriers and important topics were not discussed. Patients and clinicians reported tension between remaining hopeful and the reality of the patients’ condition. When discussions did happen, they often occurred at an advanced stage of illness and in respiratory wards and intensive care units.  In conclusion, current care practices do not facilitate satisfactory conversations about palliative care between COPD patients and clinicians. This impacts upon the fulfilment of patients’ preferences at the end of life.
DOI Link: 10.1183/23120541.00068-2016
Rights: opyright ©ERS 2017 This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
Licence URL(s): http://creativecommons.org/licenses/by-nc/4.0/

Files in This Item:
File Description SizeFormat 
00068-2016.full.pdfFulltext - Published Version433.72 kBAdobe PDFView/Open



This item is protected by original copyright



A file in this item is licensed under a Creative Commons License Creative Commons

Items in the Repository are protected by copyright, with all rights reserved, unless otherwise indicated.

The metadata of the records in the Repository are available under the CC0 public domain dedication: No Rights Reserved https://creativecommons.org/publicdomain/zero/1.0/

If you believe that any material held in STORRE infringes copyright, please contact library@stir.ac.uk providing details and we will remove the Work from public display in STORRE and investigate your claim.