Pinnock Hilary, Kendall Marilyn, Murray Scott A, Worth Allison, Levack Pamela, Porter Mike, MacNee William, Sheikh Aziz
Allergy and Respiratory Research Group, Centre for Population Health Sciences: GP Section, University of Edinburgh, Edinburgh, UK.
BMJ Support Palliat Care. 2011 Sep;1(2):174-83. doi: 10.1136/bmjspcare.d142rep.
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.
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.
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.
Primary and secondary care in Lothian, Tayside, and Forth Valley, Scotland, during 2007-9.
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.
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.
了解重度慢性阻塞性肺疾病(COPD)患者病情进展过程中的观点,以及他们的非正式和专业护理人员的观点,为COPD患者的生存及临终护理提供参考。
在18个月内,对每位患者及其指定的护理人员进行多达四次的系列定性访谈。访谈内容进行转录,并进行主题分析和叙事分析。
21名患者、13名非正式护理人员(家庭成员、朋友或邻居)以及患者指定的18名专业护理人员(主要的健康或社会护理专业人员)。
2007年至2009年期间,苏格兰洛锡安、泰赛德和福斯谷的初级和二级护理机构。
在研究期间,11名患者死亡。我们的最终数据集包括92次访谈(其中23次是患者和非正式护理人员一起进行的)。患者描述了严重症状对正常生活造成的重大干扰,通常暗示将这种情况视为一种“生活方式”而非“疾病”来接受。患者及其非正式护理人员适应并接受了这种终身疾病带来的衰弱症状。专业护理人员对患者病情的熟悉程度(通常长达数年)以及预后的不确定性,导致难以识别和积极管理终末期疾病。总体而言,患者讲述了他们疾病的“混乱叙事”,这与他们的生活故事难以区分,没有明确的开端,结局也出乎意料,其描述方式与正常老年人群对死亡的态度相似。
我们的研究结果对当前为COPD患者提供临终护理的假设提出了挑战。政策侧重于确定向姑息治疗过渡的时间点,这对COPD患者或其临床医生来说几乎没有共鸣,如果它分散了对早期逐步引入支持性护理的注意力,反而会适得其反。在COPD患者一生的病程中,特别是在因病情加重住院后,应在关键疾病节点触发对可能的支持性和姑息性护理需求的仔细评估。