Evidence map›Paper›PMID 21262897›Full record

ArticleBMJ (Clinical research ed.)2011

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

Open access · hybridAbstract read
In one paragraph

Article in BMJ (Clinical research ed.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 8 pooled it
35.5field-weighted citation impact, top 1% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

137 citing papers in PubMed, 8 syntheses or guidelines pooled it, 340 citations in OpenAlex.

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  3. Support needs of patients with COPD: a systematic literature search and narrative review.International journal of chronic obstructive pulmonary disease · 2018
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77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Hilary PinnockCentre for Population Health Sciences: GP Section, University of Edinburgh, UK. hilary.pinnock@ed.ac.uk
Marilyn Kendall
Scott A Murray
Allison Worth
Pamela Levack
Mike Porter
William MacNee
Aziz Sheikh
University of Edinburgh · GBCentre for Inflammation Research · GBGlasgow Centre for Population Health · GBNHS Tayside · GB

Funding

Chief Scientist Office
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.

Indexed as

Adaptation, PsychologicalAgedAged, 80 and overAttitude to HealthFemaleHumansMaleMiddle AgedProspective StudiesPulmonary Disease, Chronic ObstructiveScotlandTerminal Care

Identifiers

PMID21262897
PMCPMC3025692
OpenAlexW2125262290

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.