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Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study

Objectives To understand the perspectives of people with severe chronic obstructive pulmonary disease (COPD) as their illness progresses, and of their informal and professional carers, to inform provision of care for people living and dying with COPD. Design Up to four serial qualitative interviews...

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Autores principales: Pinnock, Hilary, Kendall, Marilyn, Murray, Scott A, Worth, Allison, Levack, Pamela, Porter, Mike, MacNee, William, Sheikh, Aziz
Formato: Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025692/
https://www.ncbi.nlm.nih.gov/pubmed/21262897
http://dx.doi.org/10.1136/bmj.d142
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author Pinnock, Hilary
Kendall, Marilyn
Murray, Scott A
Worth, Allison
Levack, Pamela
Porter, Mike
MacNee, William
Sheikh, Aziz
author_facet Pinnock, Hilary
Kendall, Marilyn
Murray, Scott A
Worth, Allison
Levack, Pamela
Porter, Mike
MacNee, William
Sheikh, Aziz
author_sort Pinnock, Hilary
collection PubMed
description Objectives To understand the perspectives of people with severe chronic obstructive pulmonary disease (COPD) as their illness progresses, and of their informal and professional carers, to inform provision of care for people living and dying with COPD. Design Up to four serial qualitative interviews were conducted with each patient and nominated carer over 18 months. Interviews were transcribed and analysed both thematically and as narratives. Participants 21 patients, and 13 informal carers (a family member, friend, or neighbour) and 18 professional carers (a key health or social care professional) nominated by the patients. Setting Primary and secondary care in Lothian, Tayside, and Forth Valley, Scotland, during 2007-9. Results Eleven patients died during the study period. Our final dataset comprised 92 interviews (23 conducted with patient and informal carer together). Severe symptoms that caused major disruption to normal life were described, often in terms implying acceptance of the situation as a “way of life” rather than an “illness.” Patients and their informal carers adapted to and accepted the debilitating symptoms of a lifelong condition. Professional carers’ familiarity with the patients’ condition, typically over many years, and prognostic uncertainty contributed to the difficulty of recognising and actively managing end stage disease. Overall, patients told a “chaos narrative” of their illness that was indistinguishable from their life story, with no clear beginning and an unanticipated end described in terms comparable with attitudes to death in a normal elderly population. Conclusions Our findings challenge current assumptions underpinning provision of end of life care for people with COPD. The policy focus on identifying a time point for transition to palliative care has little resonance for people with COPD or their clinicians and is counter productive if it distracts from early phased introduction of supportive care. Careful assessment of possible supportive and palliative care needs should be triggered at key disease milestones along a lifetime journey with COPD, in particular after hospital admission for an exacerbation.
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spelling pubmed-30256922011-01-25 Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study Pinnock, Hilary Kendall, Marilyn Murray, Scott A Worth, Allison Levack, Pamela Porter, Mike MacNee, William Sheikh, Aziz BMJ Research Objectives To understand the perspectives of people with severe chronic obstructive pulmonary disease (COPD) as their illness progresses, and of their informal and professional carers, to inform provision of care for people living and dying with COPD. Design Up to four serial qualitative interviews were conducted with each patient and nominated carer over 18 months. Interviews were transcribed and analysed both thematically and as narratives. Participants 21 patients, and 13 informal carers (a family member, friend, or neighbour) and 18 professional carers (a key health or social care professional) nominated by the patients. Setting Primary and secondary care in Lothian, Tayside, and Forth Valley, Scotland, during 2007-9. Results Eleven patients died during the study period. Our final dataset comprised 92 interviews (23 conducted with patient and informal carer together). Severe symptoms that caused major disruption to normal life were described, often in terms implying acceptance of the situation as a “way of life” rather than an “illness.” Patients and their informal carers adapted to and accepted the debilitating symptoms of a lifelong condition. Professional carers’ familiarity with the patients’ condition, typically over many years, and prognostic uncertainty contributed to the difficulty of recognising and actively managing end stage disease. Overall, patients told a “chaos narrative” of their illness that was indistinguishable from their life story, with no clear beginning and an unanticipated end described in terms comparable with attitudes to death in a normal elderly population. Conclusions Our findings challenge current assumptions underpinning provision of end of life care for people with COPD. The policy focus on identifying a time point for transition to palliative care has little resonance for people with COPD or their clinicians and is counter productive if it distracts from early phased introduction of supportive care. Careful assessment of possible supportive and palliative care needs should be triggered at key disease milestones along a lifetime journey with COPD, in particular after hospital admission for an exacerbation. BMJ Publishing Group Ltd. 2011-01-24 /pmc/articles/PMC3025692/ /pubmed/21262897 http://dx.doi.org/10.1136/bmj.d142 Text en © Pinnock et al 2011 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Research
Pinnock, Hilary
Kendall, Marilyn
Murray, Scott A
Worth, Allison
Levack, Pamela
Porter, Mike
MacNee, William
Sheikh, Aziz
Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
title Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
title_full Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
title_fullStr Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
title_full_unstemmed Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
title_short Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
title_sort living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025692/
https://www.ncbi.nlm.nih.gov/pubmed/21262897
http://dx.doi.org/10.1136/bmj.d142
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