Evidence map›Paper›PMID 24653231›Full record

ArticleBMJ supportive & palliative care2011

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

Hilary Pinnock, Marilyn Kendall, Scott A Murray, Allison Worth, Pamela Levack, Mike Porter, William MacNee, Aziz Sheikh

Registry-linked trialAbstract read
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In one paragraph

Article in BMJ supportive & palliative care, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03355677 (A Clinical Interventional Study Into Airways Disease Case Finding and Complex Case Management), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03355677 nacompletednot on this mapstarted 2017, after this paper: background citation

A Clinical Interventional Study Into Airways Disease Case Finding and Complex Case Management

TypeinterventionalSponsorUniversity of SouthamptonRan2017 to 2019Enrolled327ConditionsCOPD, AsthmaArmsCase finding Clinic, At Risk Case Clinics, Usual Care
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  11. Do patients and carers agree on symptom burden in advanced COPD?International journal of chronic obstructive pulmonary disease · 2018
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  14. Observational
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  18. Enhancing the diagnosis and management of COPD in Primary care.Multidisciplinary respiratory medicine · 2014
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  19. Article
  20. Attitudes of COPD patients towards tele-rehabilitation: a cross-sector case study.International journal of environmental research and public health · 2013
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Hilary PinnockAllergy and Respiratory Research Group, Centre for Population Health Sciences: GP Section, University of Edinburgh, Edinburgh, UK.
Marilyn Kendall
Scott A Murray
Allison Worth
Pamela Levack
Mike Porter
William MacNee
Aziz Sheikh

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo 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.

designUp 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.

participants21 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.

settingPrimary and secondary care in Lothian, Tayside, and Forth Valley, Scotland, during 2007-9.

resultsEleven 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.

conclusionsOur 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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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.