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

被引:215
作者
Pinnock, Hilary [1 ]
Kendall, Marilyn [2 ]
Murray, Scott A. [2 ]
Worth, Allison
Levack, Pamela [3 ]
Porter, Mike
MacNee, William [4 ]
Sheikh, Aziz
机构
[1] Univ Edinburgh, Allergy & Resp Res Grp, Ctr Populat Hlth Sci, GP Sect,Med Sch, Edinburgh EH8 9AG, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Populat Hlth Sci, Primary Palliat Care Res Grp, GP Sect, Edinburgh EH8 9AG, Midlothian, Scotland
[3] Ninewells Hosp, NHS Tayside, Dundee DD1 9SY, Scotland
[4] Univ Edinburgh, Queens Med Res Inst, MRC Ctr Inflammat Res, Edinburgh EH8 9AG, Midlothian, Scotland
来源
BMJ-BRITISH MEDICAL JOURNAL | 2011年 / 342卷
关键词
END-STAGE COPD; PALLIATIVE CARE; CHRONIC ILLNESS; BIOGRAPHICAL DISRUPTION; LUNG-CANCER; OLDER AGE; OF-LIFE; COMMUNITY;
D O I
10.1136/bmj.d142
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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页数:10
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