Background Guidelines recommend open discussions between patients and healthcare professionals as the end-of-life (EOL) approaches. Much of the knowledge about the EOL is based on the needs of patients with cancer and the applicability of this to other diseases is often queried. A literature review was undertaken concerning EOL care (EOLC) conversations in chronic obstructive pulmonary disease (COPD).
Design A systematic literature review and narrative synthesis obtained papers reporting on EOLC conversations between patients with COPD and their healthcare professionals with respect to the prevalence of conversations; each party's preferences for timing and content; and the facilitators and blockers. Inclusion criteria were articles published in peer-reviewed journals, written in English, reporting studies of adult patients with COPD and/or their healthcare professionals concerning discussions of care at the EOL.
Results 30 papers were identified. Most patients reported that they have not had EOLC discussions with healthcare professionals. While many patients would like these conversations, a potentially large minority would not; the proportions varied among studies. Healthcare professionals find these discussions difficult and many prefer patients to initiate them.
Conclusions Patients' preferences for EOLC conversations vary greatly. Healthcare professionals need to respect the wishes of those not wanting to discuss EOLC and provide multiple opportunities for those who do wish to have these discussions. Recommendations on how to approach the conversation are made.
- Clinical epidemiology
- COPD epidemiology
- COPD exacerbations
- palliative care
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
What is the key question?
What is the prevalence of conversations about end-of-life care between patients with chronic obstructive pulmonary disease (COPD) and their healthcare professionals?
What are each parties' preferences for their timing and content?
What are the facilitators and blockers?
What is the bottom line?
Although a substantial minority of patients with COPD do not want end-of-life care conversations with their healthcare professionals, most do but are not being given the opportunity to have such a discussion due to a wide range of barriers.
Why read on?
COPD is a leading cause of death. This paper discusses the implications of avoidance of conversations and makes recommendations on how they might be approached.
Chronic obstructive pulmonary disease (COPD) is a progressive, incurable lung disease punctuated by acute exacerbations that are characterised by airflow obstruction caused by chronic inflammation.1 It is estimated that by 2020, COPD will be the third leading cause of death worldwide.2
Patients with advanced COPD need palliation of symptoms, such as breathlessness and anxiety, throughout the long duration of their illness. End-of-life care (EOLC) focuses more on the final stages of the illness and has been defined as care that ‘enables the supportive and palliative care needs of patient and family to be identified and met throughout the last phase of life and into bereavement.’3 Prognostication in COPD is, however, challenging: death often occurs ‘before the patient is perceived as being “terminal”’.4 Many patients die ‘with’, rather than ‘of’, COPD: causes of death include respiratory (35%), cardiovascular (26%), cancer (21%) and other (18%).5 The best current prognostic model is the BODE Index, which is better at predicting death than forced expiratory volume in 1 s (FEV1) alone.6 As with all such models, this is of some use with groups of patients but of little help with individuals. The consequence is often a ‘prognostic paralysis’; and because prognosis is so uncertain EOLC issues are not addressed.7
The palliative and EOLC needs of people living with COPD have only recently been recognised in health policy, the previous focus being on active disease management. The National Institute for Health and Clinical Excellence stated in its 2004 COPD guideline1 that ‘the full range of palliative care services should be offered to people with COPD’. The American Thoracic Society stated that palliative care should be available throughout all stages of illness.8 The National Institute for Health and Clinical Excellence highlighted the need to involve multidisciplinary palliative care teams in advanced COPD.9
The UK NHS EOLC strategy3 calls for open discussions between healthcare professionals (HPs) and patients as the end-of-life (EOL) approaches. This is the first step of the ‘EOLC pathway’,3 to ensure well planned care is delivered. Patient knowledge that death is approaching and of what can be expected is seen as a prerequisite of a ‘good death’.10 Concern has been expressed that EOLC policy and services are based on the needs of patients with cancer, which has a clearer terminal phase: uncertainty over the extent to which a cancer model for EOLC fits with the unpredictable course of COPD has stimulated this review.
EOLC conversations are not taking place as policy recommends in COPD.11 ,12 HPs are more likely to have such discussions with patients with cancer than those with COPD.13 This is despite frequent contact providing multiple opportunities for discussions: of those hospitalised with an exacerbation, 74% see their general practitioner (GP) in the month before admission, 31% three or more times.14
A 2011 BMJ editorial highlighted the need to establish how patients with COPD will respond to EOLC discussions and their appropriate timing.15 We seek to address these issues in the first systematic literature review of the attitudes of patients with COPD, and those of their HPs.
The search aimed to identify all papers reporting studies of adult patients with COPD and/or their HPs concerning EOLC discussions in Medline, PsycINFO and CINAHL that were written in English and published in peer-reviewed journals, concerning:
the prevalence of conversations;
the preferences of patients with COPD and HPs for the timing and content of conversations;
the barriers and facilitators to conversations.
The exclusion criteria and process for the literature search, search strategy (box 1 in online supplement), paper selection and the narrative synthesis are described in the online supplement to this paper.
The search strategy was complex and generated a large number of titles. After screening and discussion by reviewers (figure 1), 29 papers were found that met the inclusion criteria. One additional paper16 was found when hand-searching Chest, electronically published ahead of print. In total, 30 papers were included (see table 1 in online supplement).
A summary of the findings is presented below. The online supplement presents the results in greater detail.
Are these discussions taking place?
A minority of patients report having discussed EOLC with their HPs. HPs confirm this. They ‘very rarely initiate’ EOLC discussions as described in the NHS EOLC strategy3 ,12 and agree that prognosis and dying are infrequently discussed.17
Patient attitudes towards EOLC discussions
Studies report a range of patients to want more information about their illness and the future. Some want all available information to enable planning ahead.18 ,19 Around half of patients, however, do not want further information,20 ,21 citing the potentially distressing nature.20
Patient preference for timing of discussions
The limited literature concerning timing indicates a patient preference to wait until COPD is advanced.22 ,23
HP attitudes towards EOLC discussions
HPs face a dilemma. While the majority view these discussions as necessary,13 ,24 ,25 they believe only a minority of patients want to know their prognosis and it is difficult to recognise who these individuals are.13 ,24 HPs are concerned that such discussions may create anxiety or destroy hope.13 ,26 Many doctors find conversations initiated by patients easier25 ,26 but admit to feeling uncomfortable even when patients ask about EOLC directly.26
HP preference for timing of discussions
HPs are unsure when to initiate EOLC conversations. In practice, HPs report that discussions often take place when the patient's health has deteriorated25 and they may be too unwell to make decisions.12 While some suggest discussions should be early in the illness,25 in practice this rarely occurs; only a small minority of GPs initiate discussions early on.12
Barriers, cues and facilitators to EOLC discussions
A wide range of barriers were identified, such as the difficultly in prognostication in COPD which leads to uncertainty over when discussions should begin12 ,26 ,27; and the poor understanding of COPD among the general public.12 ,18 ,26 Additionally, many HPs do not identify EOLC discussions as their responsibility. A good rapport with the patient,12 ,28 experience in dealing with EOLC matters,28 adequate training in breaking bad news12 and specialist knowledge12 ,28 are seen as particularly important.
Conversations about EOLC are rare in COPD. Patient preference varies: some want all available information, while others wish to avoid potentially distressing conversations. HPs acknowledge the value of conversations but find them difficult, recognising that not all patients want these conversations. There are numerous barriers and each party prefers that the other initiates the discussion. Patients' preferences are mainly for discussions when disease is advanced; in practice they usually occur late in the disease course (if at all) when there is greater ‘certainty’, though patients are less able to participate. Three previous non-systematic reviews29–31 found a similar prevalence for conversations and planning.
Strengths and weaknesses of this study
Although the search strategy used only the three most pertinent databases, it appears to have been effective. Additional searches identified only one further paper, electronically published ahead of print. Only English language papers were included: most are from the UK or USA, with fewer from Canada, New Zealand or Europe. Additionally, unpublished data and the grey literature were not included.
The literature is relatively recent; only three papers were published before 2000. Studies presented a uniform picture with regards to the prevalence of conversations. The data concerning patient preferences were more diverse, partly due to studies investigating a variety of aspects of EOLC conversations, and the diversity of patient samples and disease severity.
Explanations and implications
There are many patients living with the life-limiting illness of COPD who are not being given the opportunity to discuss its progression, their future care and the EOL. A range of barriers inhibit these discussions.
Not all patients wish to have such conversations.32 Some may feel they do not have EOLC needs, preferring to focus on management of the disease and its symptoms, having lived with it for years.33 Patients not wishing to discuss EOLC preferences are often those who estimate their prognosis to be excellent, report quality of life to be good and do not desire active involvement in decision making.34 HPs are rarely able to predict individuals' EOLC preferences,30 including preferences for discussions.
Additionally, patients' understanding of COPD as a life-limiting disease is poor; when stating preferences for further information they may be unaware of the implications of such discussions. Patients often see COPD ‘not so much as an illness, more a way of life’ with attitudes to death comparable to those ‘in a normal elderly population’.27
One major barrier is the uncertainty of prognosis creating difficulty in providing patients with information on the likely future course of their illness. Discussions might usefully cover explanation of the functional decline common in COPD, the possibility of fatal exacerbations and the potential for cardiovascular and other causes of death, including sudden death.29
No single group of HPs felt that their roles, relationships with patients or work settings made them the most appropriate HPs to have EOLC conversations. The NHS EOLC strategy emphasises the importance of multidisciplinary involvement3: while these conversations are a ‘collective responsibility’,28 held on multiple occasions, the danger remains that no HP takes the responsibility.
Ensuring that patients who wish to discuss EOLC have the opportunity to do so is challenging. Practitioners and healthcare systems need to address the wide range of barriers that exist, for example, more time is required for consultations or training of healthcare professionals to have these difficult conversations. However, discomfort around the subject of EOL and the uncertainty and difficulties in prognostication are likely to remain.
HPs frequently worry that EOLC discussions may remove hope,13 ,16 ,26 ,31 however avoidance of discussions may give false hope and deny patients the opportunity to prepare and plan. A balance needs to be struck between optimism and realism: ‘I encourage you to hope for and expect the best, but it is also wise to prepare for the worst’.35 To maintain hope, HPs need to give patients time to get used to their poor prognosis, ‘redirecting’ them from hope for recovery to hope for quality time and a comfortable death.19
How to do that in practice remains a considerable challenge (box 1). As Sir William Osler wrote, ‘If it were not for the great variability among individuals, medicine might as well be a science and not an art’.
Suggested approach to end-of-life care conversations in chronic obstructive pulmonary disease
Respect autonomy: allow the patient to decide whether to have an end-of-life care conversation, when and with whom.
Patient centred: content, timing and pace set by the patient.
Multiple opportunities: for the patient to explore issues if they wish.
Maintain balance: combine realistic hope with practical planning.
Honest information: including acknowledgement of uncertainty.
Document discussion: enable other healthcare professionals to be aware of the patient's preferences for care.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Files in this Data Supplement:
- Data supplement 1 - Online Box 1
- Data supplement 2 - Online Supplement
Linked article 201581.
Funding This study was funded by the NIHR CLAHRC (Collaborations for Leadership in Applied Health Research and Care) for Cambridgeshire and Peterborough and Macmillan Cancer Support: their support is gratefully acknowledged. The opinions expressed are those of the authors not the funders.
Competing interests None.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement We would be prepared to share data extraction sheets.