How can end of life care excellence be normalized in hospitals? Lessons from a qualitative framework study
BMC Palliative Care volume 17, Article number: 100 (2018)
There is a pressing need to improve end-of-life care in acute settings. This requires meeting the learning needs of all acute care healthcare professionals to develop broader clinical expertise and bring about positive change. The UK experience with the Liverpool Care of the Dying Pathway (LCP), also demonstrates a greater focus on implementation processes and daily working practices is necessary.
This qualitative study, informed by Normalisation Process Theory (NPT), investigates how a tool for end-of-life care was embedded in a large Australian teaching hospital. The study identified contextual barriers and facilitators captured in real time, as the ‘Clinical Guidelines for Dying Patients’ (CgDp) were implemented. A purposive sample of 28 acute ward (allied health 7 [including occupational therapist, pharmacists, physiotherapist, psychologist, speech pathologist], nursing 10, medical 8) and palliative care (medical 2, nursing 1) staff participated. Interviews (n = 18) and focus groups (n = 2), were audio-recorded and transcribed verbatim. Data were analysed using an a priori framework of NPT constructs; coherence, cognitive participation, collective action and reflexive monitoring.
The CgDp afforded staff support, but the reality of the clinical process was invariably perceived as more complex than the guidelines suggested. The CgDp ‘made sense’ to nursing and medical staff, but, because allied health staff were not ward-based, they were not as engaged (coherence). Implementation was challenged by competing concerns in the acute setting where most patients required a different care approach (cognitive participation). The CgDp is designed to start when a patient is dying, yet staff found it difficult to diagnose dying. Staff were concerned that they lacked ready access to experts (collective action) to support this. Participants believed using CgDp improved patient care, but there was an absence of participation in real time monitoring or quality improvement activity.
We propose a model, which addresses the risks and barriers identified, to guide implementation of end-of-life care tools in acute settings. The model promotes interprofessional and interdisciplinary working and learning strategies to develop capabilities for embedding end of life (EOL) care excellence whilst guided by experienced palliative care teams. Further research is needed to determine if this model can be prospectively applied to positively influence EOL practices.
Providing high-quality care for dying patients in acute settings is essential to meet changing population needs and societal expectations . Increasingly people live with chronic, potentially life limiting conditions; prognosis is uncertain and inevitably some will spend their final days of life in acute hospital care [2, 3]. In Australia, despite 70% of people wanting to die at home only about 14% do [3, 4]. While healthcare organisations are adopting care pathways to ensure appropriate end of life care, globally, studies report suboptimal care quality in hospitals [5,6,7].
For many years, the Liverpool Care Pathway (LCP) was considered as a gold standard for care for dying patients, yet it has been withdrawn in the United Kingdom (UK). Significant gaps were identified between the goals of the LCP and its enactment in practice, with criticism focused on failure to have studied the process of implementation, lack of available expertise embedded in acute settings and not addressing the learning needs of non-specialist healthcare professionals . As a result five priorities for improving care for a dying person  were identified: a) recognising the possibility of dying; b) sensitive communication with the dying person and loved ones; c) involve dying person and loved ones in treatment and care decision making; d) explore and respect the need of the dying person’s loved ones and e) agree and deliver an individualised care plan with compassion . Contrasting with the UK experience, Italian studies suggest that the quality of end of life (EOL) care can be improved using the LCP when implemented with a structured program and clear goals [5,6,7,8,9,10,11]. These findings align with emerging evidence suggesting that effective LCP implementation can be aided by a comprehensive understanding of the local context including appreciating and valuing differing professional perspectives and work structures [10, 11].
Achieving high-quality end-of-life care in acute settings is challenging.  Acute settings are orientated towards interventional treatment of reversible conditions. Institutions are designed to ensure rapid provision of immediate and urgent care with finite specialist palliative care resources, staff turnover is often high and staff not necessarily experienced in recognising dying, or determining likelihood of reversible causes versus irreversible deterioration  despite multiple attempts to educate and improve . Enabling excellence in EOL care in acute care settings is a significant concern, with both national  and international  strategies being developed to support these provisions of EOL care excellence.
This study aimed to investigate if and how EOL care excellence can be embedded or normalised in acute healthcare settings. Our objectives were to: 1) generate a rich description of individual and contextual barriers and enablers surrounding implementation of the Clinical Guidelines for Dying Patients (CgDp), in an acute setting; 2) identify learning strategies to mitigate barriers and strengthen enablers; 3) integrate our data analysis, using normalization process theory (NPT) (see below), to generate a conceptual model to inform further implementation research.
We adopted a social constructionist research approach  to understand the meanings participants generated through interactions when enacting practices related to the CgDp. Normalisation Process Theory (NPT) [14, 15] was used as our theoretical lens as it offers an explanation of processes for implementing, embedding and integrating practices in everyday work . Individual and contextual factors promoting or inhibiting normalisation of practices include coherence, cognitive participation, collective action and reflexive monitoring (see Table 1 for further explanation of each construct). This approach enabled us to develop in-depth descriptions and interpretative explanations for how learning strategies can facilitate the CgDp becoming integrated in practice.
Given the need to understand local contextual factors for effective implementation [8, 14], an explanatory qualitative interview study, using the framework analytic approach , was conducted that aligned to our theoretical stance. Our design facilitated in-depth exploration into the health care professionals’ perspective of individual and contextual barriers and enablers to implementing the CgDp. NPT as a sensitising tool for embedding practices  enabled us to generate a programme theory and model  to inform the development of a complex intervention to normalise end of life care excellence in acute care settings. The study was approved by Gold Coast Health Ethics Committee (HREC/14/QGC/185). To ensure the anonymity of the participants and the practices where they work, all identifiers have been removed. Written consent was obtained.
This study was conducted in a large acute care tertiary hospital, located in Queensland, Australia with 750 inpatient beds. The study focussed on a 24-bed acute care medical ward, where there were 48 deaths in 2015. In 2009, an EOL care pathway, CgDp, based on LCP was endorsed by Queensland Health for state-wide use within its acute hospitals.  (The current version of the CgDp can be found here: https://www.health.qld.gov.au/clinical-practice/guidelines-procedures/patient-safety/end-of-life/guidelines along with further information about the documents and implementation strategy of Queensland Health plus their contact details. The document has undergone minor revisions since the study was conducted). In 2013, acute care providers were charged with providing local education and audits to support implementation of the pathway. However, acute ward hospital staff reported that, from their perspective, the CgDp had ‘appeared’ on the wards with limited formal training provision. Efforts to address this need provided the opportunity for this study to capture ‘real world’ acute care clinician challenges as they integrated the CgDp into acute practice settings. Moreover, it offered an opportunity to systematically identify strategies to normalise EOL care excellence in a typical acute care setting.
Purposive sampling  was used to ensure recruitment of a range of perspectives within professional stakeholders, including the nursing, medical and allied health professionals and the palliative care team. Staff were identified through discussion with nursing, medical and allied health staff leaders and participants were recruited in the following ways. For allied health staff, the Directors of each professional group were emailed and asked for the details of the clinician working in the study ward. Seven clinicians were identified and contacted by the study team via email and all agreed to participate in the study. For the medical staff, the researchers presented an overview of the study at their team meeting (n = 17) and 8 agreed to participate. For nursing staff, because of shift work, the research team attended two nursing handovers to present an overview of the study and placed posters in the tea room. It is not known how many nursing staff viewed the poster or missed the handover meeting. For palliative care staff consulting to the study ward, we directly contacted, via email and follow up phone call, the consultant, advanced trainee and clinical nurse consultant and all agreed to participate.
Qualitative, semi-structured interviews, individual or group, depending on participant availability, were conducted. The interviews, conducted from June to August 2015, explored perceptions, views and experiences of caring for dying patients and how the CgDp was used. Interviews were conducted by the authors who did not work in the study (ward) setting. The interviews occurred face to face in private rooms and were planned so that there was no conflict of interest or perceived hierarchy between interviewer and interviewee. All interviews were audio recorded, transcribed verbatim and rechecked for accuracy. Data collection continued until the research team agreed that theoretical saturation was reached; that is, additional data was not anticipated to produce new perspectives or insights .
Data were analysed using a five phase framework method: 1) familiarisation, 2) identifying a thematic framework, 3) indexing, 4) charting and mapping and 5) interpretation . Research team members who conducted the interviews (CN, LG, BS, JM), and led on the analysis (SY, AT) familiarised themselves with raw data and discussed their impressions of the dataset. The NPT constructs provided the a priori thematic framework (See Table 1). Next, the transcripts were divided amongst members of the research team (CN, LG, JM, BS and BH), and each transcript was independently coded or indexed, using the framework, by two researchers who then discussed the coding in pairs and to negotiate agreement. Once the transcripts were coded and the data were charted and mapped in Excel®, themes were agreed upon. This coding and theming was independently reviewed and confirmed by AT and SY. The key themes were presented to the participants, who verified these themes, as part of two usual ward meetings. Patterns and associations between themes were interpreted and used to develop a mid-range theory model to inform further implementation strategies.
Twenty-eight professionals were interviewed, in 18 individual and two group interviews, including allied health (7) (occupational therapist, pharmacists, physiotherapist, psychologist, speech pathologist), nursing (10), medical (8) and palliative care (medical, 2; nursing, 1). The average time for the interviews was 36 min (range: 18–55 min). The results are presented in two parts: 1) based on the NPT constructs, the key barriers and enablers identified (Table 2) 2) implementation and learning model, including accompanying learning strategies (Table 3). A mid-range programme theory, based on these findings, to inform strategies for augmenting EOL care excellence in acute care settings is developed from analysis of the findings (See Fig. 1).
Coherence – Making sense of the CgDp
Participants agreed the CgDp’s purpose made sense as a support for effective EOL care, yet they experienced tensions when attempting to integrate EOL practice into their daily work. For example, participants indicated that using the CgDp provided evidence to legitimise EOL care provision in acute settings and increased confidence to take action. This was described in the following extract by a nurse who explained:
… That [the pathway] gives us a bit more reassurance that we can do less [acute care] and focus more on comfort and quality… They just want to cover themselves legally I think. (Nurse-3).
Hence it appeared that the pathway ‘gives permission’ to shift the focus of care from a more traditional biomedical model to a more holistic approach. Despite this permission, based on their understanding of their role in acute care, other people felt that EOL care lacked alignment with this role:
I don’t want to use them [CgDp]…we are an acute ward…our patients are meant to recover… (Nurse-5).
In this extract, the nurse suggests that using the CgDp is somewhat at odds with her role identity which defines success as cure.
The CgDp did not account for the uncertainties and complexities participants experienced when engaging in EOL care. Participants found recognising dying a particularly challenging aspect. Reasons were multifactorial including a lack of experience and/or guidance; not understanding palliative care principles; experiencing diagnostic uncertainty and avoiding EOL care decision making and/or worrying the wrong decision has been made; wanting to exhaust all treatment options before commencing CgDP and finding the process personally uncomfortable. This is captured in the next extract by an allied health professional:
I didn’t pick up the signs of that last patient that I had that was actually passing away. Ahh! They weren’t on a care of the dying pathway, so I still treated them actively, which I felt at the time was appropriate. On reflection…maybe I didn’t add any benefit to it. I don’t think I made it any worse, at least I hope I didn’t. (Allied Health-2).
While the CgDp increased awareness of the need for EOL care in acute settings, this was perceived as a challenge rather than empowerment. The CgDp as an artefact introduced into the setting created disruption in routines and consequently staff had to consider the possibility of dying and decide if this might be the case but they found it challenging to do make such a decision. This is reflected in the next extract when two nurses within a focus group outline the difficulty, experienced by doctors, in deciding when a patient is at the point to need transfer to the CgDp:
Nurse-1: It’s like they’re [doctors] are scared of it.
Nurse-2: …as doctors they’re taught to save lives and then when they’ve got to do this thing [CgDp] where they’re basically withdrawing treatment to let somebody die, they worry that they are doing the wrong thing. I think they need to be told that it’s okay to do this. This is a good thing for them. (Group interview 1-nursing).
Participants described uncertainty with the duality of aiming to ‘reverse the reversible’ while holding the possibility of dying and appropriate CgDp care alongside this. In contrast, participants felt much more comfortable when they could focus solely on one form of practice e.g. active treatment or EOL care:
So to give you an idea, we have had elderly patients who come in with bad pneumonia and are possibly dying, not responding to treatment, and the question is do you continue with full measures, such as antibiotics, fluids et cetera or do you just focus on comfort care? (Medical officer-10).
Participants agreed that the CgDp provided guidance on priorities when caring for dying patients. This was reassuring to staff, especially to novice practitioners:
So, it’s more like a guideline. So, it’s more of a checklist for everyone making sure that we don’t miss things you know. So, it’s a cross multidisciplinary thing. (Medical officer-5).
Overall, participants understanding of the purpose of the CgDp in acute care, was that it was to systematise EOL care. However, the key challenges to EOL care excellence were uncertainty when diagnosing dying, appropriately individualising patient care, and difficulties experienced integrating EOL care practices with acute care practices. These findings are presented in Table 2.
Cognitive participation – Getting involved in CgDp
Contrary to the CgDp goal, of providing uniformly good, albeit individualised, care to dying patients, using the guidelines did not disrupt parallel working between professions to achieve fully the integrated multidisciplinary and interprofessional working required. Working in parallel, profession-specific lines meant that some professional groups lacked certainty regarding the legitimacy of their engagement. For example, the decision to commence the CgDp was consultant (senior physician) led, with prompting from nursing staff but little to no engagement from allied health practitioners (AHP). The following extract outlines how AHPs perceived they were potentially excluded from these processes:
I don’t know if I should be doing it [CgDp]. I know there’s an allied health section, but I was never really told to or asked to write in the forms, so I never have. (Allied Health-7).
However, using the CgDp promoted certain staff to reflect on and change their existing ways of working. Some nursing staff felt empowered to prompt the medical team to make decisions about EOL care and played a role in reassuring medical staff about their EOL care decision. However, they were often frustrated when waiting for the CgDp paperwork to be completed by medical staff as illustrated in the following extract:
Interviewee 3: The doctors not filling stuff out.
Interviewee 4: Sometimes it could take 24 h for a doctor to do it.
(Group interview 1-nursing)
Nursing staff were concerned this delayed multiprofessional provision of holistic EOL care.
Moreover, some senior nursing staff noted that because patients infrequently died on the ward, they needed to reorient themselves to the practices associated with the CgDp:
Yes I’m probably a bit shaky on it for myself because I haven’t actually used it for quite a long time. (Nurse-3).
This meant usual patterns of co-working e.g. seeking guidance from more senior staff differed for practices associated with the CgDp from usual acute care practices.
The perceptions of medical staff, recognising their need for decision-making reassurance sometimes sought guidance from the palliative care team, usually via telephone consults. Despite this, aspects of EOL care, including completing the CgDp paperwork, were delegated by senior medical staff to their juniors. Thus, some consultants (senior physician) avoided direct engagement with practical complexities required for effective enactment of the CgDp, and did not always appear to have insight into these, as described by a consultant (senior physician):
I know about it [CgDp] but I don’t know …the details… probably because I’m confident that I know when a patient is near reaching their end stage I don’t need to look for any guidelines to help me. (Medical officer-6).
Additional care strategies were sometimes triggered and adopted instead of the CgDp when complexities became explicit, such as a so-called, ‘trial of life’ where full treatments were applied for 24 to 48 h to determine if patients might improve. This is described by a consultant below:
If there’s anything that you felt like, oh look, you know, he’s not - we’ll give him a trial of 24 to 48 h, for example, and there’s still no progression and still no improvement and having a chat with the family and things you know say, look if that’s not improving I think it’s for comfort measures and then that’s the time that we’ll be looking at the realm of like the Care of the Dying Pathway. (Medical Officer-5).
This suggests an ‘either or’ conceptualisation of active disease treatment versus palliation remained suggesting that further opportunities for learning about palliative care principles are necessary for effective enactment. In particular, education should include individualised decision-making and the appropriateness of multifaceted approaches when situations are uncertain i.e. using CgDp alongside interventional treatments.
Lastly, the strength of medical and nursing dyad created a barrier to AHP engagement and decision making when the CgDp commenced. All AH participants indicated that they were willing and able to contribute to EOL care. Moreover, they noted that the CgDp specifies the AHP contributions (as above), however, they expressed concern that medical and nursing teams did not understand how they might contribute to EOL care:
Just someone say, we [nursing and medical staff] want you to do it, because at the moment no one is saying that we need to do it or want us to do it, so we’re not going to do something that is going to probably take up more time if we’ve never been asked to do it…if we sat down and it was said that – a ward says we want everyone to be involved in this, in using this pathway [CgDp], so we work together, then for sure, I wouldn’t mind. I’d be more than happy to be involved. (Allied Health-1).
Collective action – Implementing CgDp
Effectively enacting the CgDp in a busy acute setting was challenging and barriers to effective EOL care provision included: 1) an over reactive response to EOL care rather than proactive or long-term i.e. advance care planning and 2) privileging of acute care practices and work. Combined, these two factors created a sense of being overwhelmed faced with the work associated with attending to dying patients’ needs as exemplified in the following extract by a medical officer:
But our days are busy, so I figure there’d almost be a bit of a delay sometimes, because for instance we did one ward round this morning, we finished at 11:00. Then the senior doctors had to go to the radiology meeting until about 12:00. Then comes the next consultant for the next ward round. So, at what point do you have that time to throw that paperwork [CgDp] together as well. It can be quite difficult. (Medical officer 9).
The reactive response, as opposed to proactive (i.e. advance care planning), and lack of prioritisation related to perceptions that CgDp required a complex cascade of actions, many of which fell outside of participants’ comfort zone e.g. family meetings, completion of paperwork. This response could also be attributed to complex and busy work practices, staff resourcing and lack of palliative care training. For example, the medical team needing to attend to patients on other wards; allied health work scheduling meant they were not ward-based and therefore not fully integrated into ward practices. Thus, missed opportunities, because some allied health staff were reactively rather than collaboratively invited to participate, existed for appropriate skill mix and building relationship with patients and family members:
…it depends on how much rapport you’ve built with the family I think. I’ve been thrown in a few where there’s such - on the ward with the nursing staff and the doctors it’s, he or she is going to pass away, quick, get in there, and the moment you get in there the family is like, who are you. (Allied health-5).
Several system-level issues created barriers to EOL care including: 1) organisational pressure for patient discharges; 2) lack of opportunity for meaningful palliative care team guidance and 3) paper-based CgDp guidelines in the context of electronic medical records. Each of these barriers are explored below. Firstly, the organisational pressures being experienced are described here:
There is always someone from the top calling you to discharge the patients…and there is not time to go through [the dying conversation] when they are not dying…for example, with chronic obstructive airways disease exacerbation, come in, get steroids and antibiotics, go home… there is no time to talk about dying then. When they come back with acute illness and are dying… all of a sudden someone will ask, where is their resuscitation plan…there’s no plan so you press the panic button …it’s a big mess. (Medical officer-2).
Secondly, participants appreciated palliative care guidance, however, obtaining this guidance was a challenging endeavour due to both teams’ busy workloads. Thus, often resorting to telephone conversations rather than face to face collaborations. Palliative care staff were also uncertain if their advice was always sought when needed:
I think some consultants must have their own views on how the care should be given for a dying patient and I guess they must think that they know. You can’t be an expert in every area and I think it’s important enough not to think that you could do everything and then blind yourself to the mistakes that you’re making. (Palliative care medical officer-4).
Thus, in terms of collective action, some palliative care team members perceived that their contributions were not being acted on.
Thirdly, a further crucial contextual factor was that the hospital uses electronic medical records and the CgDp was paper based. This meant that staff who defaulted to the electronic medical records were not always aware of the decision to commence the CgDp or its progress. Moreover, the CgDp was a large document, which combined with infrequent use became perceived as challenging to complete. These views contrasted with palliative care staff who indicated that despite its size, with practice, the document was relatively easy to engage with.
Reflexive monitoring –embedding and improving CgDp
Embedding EOL care in acute settings requires staff reflection on the implementation of the CgDp and where necessary amending of practices to ensure best outcomes. Despite having the CgDp as a practice guide, the participants indicated further improvements in EOL care were required. Barriers to effective staff reflection and improvement were identified and these included firstly, a lack of structured and meaningful team debriefing to improve EOL care. Secondly, a lack of knowledge and skills to meaningfully appraise EOL care and its outcomes. Finally, a lack of systematic audit and feedback processes to inform and improve EOL care outcomes.
While some staff indicated that they informally debrief after a patient death with peers, there was an absence of interprofessional and structured debriefing. Attempts at changing EOL practices seemed to be largely speculative and participants were not able to describe ways that they were changing or had changed their EOL practices as a team. This meant that important ways to improve EOL care were left unresolved:
I guess the one thing we don’t do more of, or I don’t do more of, is to actually talk about dying much earlier on. So, we don’t have a lot of that. So that discussion sort of comes about in context of Care of the Dying Pathway, which may not be ideal. I’m not sure if it is the right thing to be discussing these things early on. I mean, there’s some evidence to say that that’s what patients want to know and we probably should do that. But we haven’t been, mainly because we don’t have a structure for that; who does it and when, do you do it in hospital or clinic? (Medical officer-10).
In these ways, this medical officer recognises the reactive responsive EOL care whilst acknowledging that integrative of EOL care planning had not been addressed.
A key factor hampering staff ability to meaningfully reflect on and improve EOL care was a lack of expertise and experience in palliative care. This meant it was challenging to recognise the features and enact EOL care excellence as evidenced by the next extract:
But we don’t know what to compare it [EOL care] to. I don’t know if anybody else has worked in a hospice or palliative care where would it be just - could it be not as busy but it could be a lot of noise and trolleys and things trundling up and down and bells going off you know. (Nurse-5).
Since comprehensive audit and feedback processes to inform and improve outcomes related to effective implementation of CgDp were absent, the effectiveness of EOL care was not apparent to participants. As such they were not receiving individualised feedback on the quality of their care nor were they aware of the quality standards to be achieved. Many participants noted that quality EOL care is not being wholly addressed through audit processes:
I mean, we do have deaths in hospital but the kind of deaths we have on our ward are ones that are fairly catastrophic, so where people have had MET calls and had cardiac arrests and gone to ICU [intensive care unit] and then died in ICU. They are few and far between and we review them in our morbidity and mortality meetings and almost always there is nothing that could have prevented that outcome that we can pick up and it’s just the natural course of the illness. Then occasionally we have the patients who have come in, not improved with treatment and have just deteriorated and in those situations they are often patients that we know have severe illness and for them that would seem very appropriate. In fact, you could even argue not starting Care of the Dying Pathway was probably inappropriate and we’re just continuing their agony and misery. (Medical officer-10).
Development of a theoretical model for education and implementation
Figure 1, presents a proposed implementation model for augmenting EOL care excellence in acute care settings. The model, presents the key barriers to effectively embedding EOL care in acute settings. In response to these barriers, learning and implementations strategies have been identified which are likely to contribute to EOL care excellence and to sustain these practices [21, 22]. Recognising the complexity of EOL practice, guidance and support from palliative care is recommended . However, as the acute teams’ EOL capability is augmented and the key learning outcomes are achieved, guidance is likely to be limited to the most complex cases. This model provides lessons for implementation for acute care settings who are implementing and/or revising their EOL care practices. Additionally, this model presents an EOL learning curriculum for HCP working in acute setting using a range of practice-based pedagogic strategies.
This study sought to generate a conceptual model of the realities of embedding an end-of-life-care tool into an Australian acute hospital. Our research team were cognisant of the challenges this presented from international experience. Using the normalisation process theory provided an opportunity to study mechanisms of ‘real world’ acute care clinician challenges as they integrated the CgDp into acute practice settings and consider if and how these led to desired improvements in end-of-life care. NPT constructs informed the analysis of empirical data collected during the implementation period. NPT was chosen for its resonance with the desired outcomes: behaviour change needs to be normalised to become routine practice. The tensions identified with this ideal and the realities of practice allowed us to generate a model to guide further implementation while drawing attention to barriers and facilitators of success.
The principal findings are that while staff described the CgDp as being intrinsically coherent its use was not in keeping with what they considered to be their primary focus of work, that is, getting patients to recovery. Participants found it challenging to hold the tension created by uncertainty of whether a patient might recover or not in mind, preferring to focus solely on so called ‘active management’ which they defined as disease focused treatment. The findings confirm other studies for example in intensive care  and other areas of the UK health service , including hospital doctors  and Italian general medicine settings . Additionally, some participants had insight into their difficulties in recognising a dying patient (which is not surprising given the challenges all clinicians experience accurately predicting prognosis ). Taken together these factors meant the CgDp would be used late, if at all, as it was only of use once agreement was reached that a person was dying. However, if this point was reached the CgDp was praised for offering a more systematic (and in fact, active) approach to care for the dying patient.
There was evidence of the tool being used as a prompt for collaborative working and in some cases junior medical and nursing staff reported being empowered to raise concerns that a patient might be dying with senior medical staff. In turn, however, senior staff would seek advice and reassurance from the palliative care team and sometimes redelegated the completion and hands-on application of the tool back to junior staff. An unintended consequence of the implementation was that closer working between nursing and medical staff left AHPs to feel excluded and their contributions to EOL care unrecognised. This finding demonstrates a need to further foster effective interprofessional collaboration .
Perceptions of extensive paperwork and an expansion of roles, including increased activity outwith professionals’ comfort zones, acted as barriers to prospective planning for end of life care and use of the tool was often delayed or incomplete for these reasons. Whilst everyone could contribute, it was possible to opt out from doing so by choosing to focus on other activities and respond to different pressures when prioritising workload. System factors also prevented close working relationships with the palliative care team, and the tool was not integrated into the electronic notes system meaning its use could easily be overlooked. These challenges, the importance of integration of palliative and medical care team working and lack of integration of care of the dying plans with electronic notes, are in keeping with the findings of McConnell et al.  and Raijmakers et al. , respectively. Thus, for effective implementation and normalisation of EOL care excellence to be achieved, these organisational and systems barriers need to be addressed.
Crucial to the implementation success was the potential for staff to learn from their experiences. Time, opportunities, and lack of skilled facilitation for reflection and case review meant this was not capitalised upon. These experiences need to move beyond provision of education and training, which can be challenging for practitioners to attend , towards generating embedded real time practice-based learning experiences .
In summary, implementation occurred but with risks such as the lack of recognition of dying leading to unmet needs, and staff experiences leading to unintended learning. As identified in the UK, there is a risk of the tool taking on a life of its own without professionals learning the foundational principles of good palliative care alongside treating potentially reversible conditions.
Strengths and limitations
This study investigated the real-time perceptions and experiences of interprofessional team members working in an acute medical ward concerning embedding of high quality palliative care. Use of NPT as an analytic framework enabled an understanding of how care of the dying practices were or were not becoming normalized within an acute setting, identification of barriers and enablers to provisions of care excellence and recommendations for learning strategies to support EOL care excellence (see implications section and Table 3). However, the study took place in a single acute care setting within a tertiary hospital which limits the broader applicability of its findings. Potential transferability is enhanced by rich descriptions, using purposive sampling and the findings resonance with existing literature from other settings [20, 31]. The study relied on individual accounts of EOL care practices and engagement with CgDp rather than observations. To increase the study’s dependability , data were collected until saturation, no new themes, and data were analysed iteratively by an interprofessional team. Further strategies to enhance study credibility included seeking feedback from participants on our data analysis. There would have been value in also having the middle range programme theory model confirmed by further professional validation. This was not practical; however, the model has been informed by NPT and generated through extensive, reflexive discussions within the research team. Finally, to quantify outcomes, there may have been value in conducting a chart audit to determine when the CgDp had been used, and with what effects, however, our goal in the present study was to primarily explore the process of implementation.
Implications for practice and further research
This study provides important empirical evidence from healthcare practitioners working in acute care settings on their experiences of providing EOL care. It is an example of patient focussed theoretically informed medical education research that extends into clinical practice . The findings and conceptual model, could inform and optimise interventions to support practitioners’ effective normalisation of EOL care excellence in acute care settings. EOL care excellence requires meaningful collaboration with and specialist support from the palliative care team combined with effective interprofessional co-working . As the acute care team’s coherence, collective action, cognitive participation and reflective monitoring are enhanced, the reliance on specialist palliative care may be limited to complex cases.
To achieve these goals in practice, we propose the following learning strategies informed by the NPT constructs and our findings (See Table 3 and Fig. 1). To address coherence, acute care staff need support to develop their palliative care knowledge and skills to recognise dying and the point at which to initiate the pathway whilst developing the ability to hold two approaches to care at the same time during transition . This must also relate to understanding of the importance of integrating care practices and promoting the CgDp as a positive aspect of care rather than a failing (See Fig. 1). Expert and accessible guidance (See Fig. 1) e.g. from palliative care specialist or champions is required to assist acute care staff to navigate such situations of clinical uncertainty e.g. case-based interprofessional and interdisciplinary team learning sessions.
Learning strategies to increase cognitive participation might include harnessing genuine interprofessional working (See Fig. 1) to promote shared understanding of each other’s roles (see Table 2) . Furthermore, learning strategies might include creating meaningful interprofessional learning experiences where collaboratively the team work through genuine cases to make decisions on EOL care and to identify team members’ roles and responsibilities (See Fig. 1); or learning sessions with palliative care team members who provide guidance on collaborative approaches EOL care (See Table 3).
To address collective action, consideration needs to be given to reviewing work structures, rostering and processes to support the prioritisation of EOL care e.g. prioritising dying patients on ward rounds; ward-based AHPs (See Table 3 and Fig. 1) . In this regard rearranging key documents and pathways within the hospital care processes can help facilitate delivering high quality end of life care. By such so called “textual regulation” , the institution can demonstrate that it values end of life care and support workers. Moreover, creation of learning programs challenging assumptions about work practices facilitated by the palliative care team to role model effective interprofessional co-working (See Fig. 1) may further help . A key system factor to support change would be integration of the CgDP into the routine electronic records.
Finally, strategies (also see Table 2) likely to augment acute care staff’s ability to reflexively monitor EOL care and recognise EOL care excellence include: 1) local quality improvement processes to assist staff understanding of EOL care and provide local solutions to specific barriers and gaps; 2) foster feedback processes [21, 36] to increase practitioners’ ability to self-evaluate EOL care performance and 3) create opportunities for staff to debrief as a team e.g. ‘after death’ care reviews with support from the palliative care team (See Fig. 1).
Our findings emphasise the importance of in-depth examination of implementation processes and offers strategies for normalising EOL care excellence in acute care setting using guidelines. Further exploration into these experiences will provide insights to how these tensions might be reconciled and/or held to ensure holistic EOL in acute care settings. Finally, research to test and refine our programme theory model is required.
Allied health practitioners
Clinical Guidelines for Dying Patients
End of life
Liverpool Care of the Dying Pathway
Normalisation Process Theory
Virdun C, et al. Dying in the hospital setting: a systematic review of quantitative studies identifying the elements of end-of-life care that patients and their families rank as being most important. Palliat Med. 2015;29(9):774–96.
Gomes B, Higginson IJ. Where people die (1974—2030): past trends, future projections and implications for care. Palliat Med. 2008;22(1):33–41.
Broad JB, et al. Where do people die? An international comparison of the percentage of deaths occurring in hospital and residential aged care settings in 45 populations, using published and available statistics. Int J Public Health. 2013;58(2):257–67.
Swerissen, H. and S. Duckett, Dying Well, G. Institute, Editor. 2014, Grattan Institute: Carlton, Victoria p 37.
Costantini M, Alquati S, Di Leo S. End-of-life care: pathways and evidence. Curr Opin Support Palliat Care. 2014;8(4):399–404.
Australian Commission on Safety and Quality in Health Care, National Consensus Statement: essential elements for safe and high-quality end-of-life care in acute hospitals. 2015, Australian Commission on Safety and Quality in Health Care: Sydney, NSW, Australia.
Robinson J, Gott M, Ingleton C. Patient and family experiences of palliative care in hospital: what do we know? An integrative review. Palliat Med. 2014;28(1):18–33.
Department of Health, More care less pathway: a review of the Liverpool Care Pathway. 2013, Crown Copyright.
Leadership Alliance for the Care of Dying People. One chance to get it right: improving people’s experience of care in the last few days and hours of life. London: Leadership Alliance for the Care of Dying People; 2014. https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/323188/One_chance_to_get_it_right.pdf
McConnell T, et al. Factors affecting the successful implementation and sustainability of the Liverpool care pathway for dying patients: a realist evaluation. BMJ Support Palliat Care. 2014;
McConnell T, et al. Systematic realist review of key factors affecting the successful implementation and sustainability of the Liverpool care pathway for the dying patient. Worldviews Evid-Based Nurs. 2013;10(4):218–37.
Palliative Care Australia, Standards for Providing Quality Palliative Care for all Australians. 2005, Palliative Care Australia: Deakin West, ACT.
Crotty M. The foundations of social research. London: SAGE Publications Ltd.; 1998.
May C, Finch T. Implementing, embedding, and integrating practices: an outline of normalization process theory. Sociology. 2009;43(3):535–54.
May C, et al. Understanding the implementation of complex interventions in health care: the normalization process model. BMC Health Serv Res. 2007;7(1):148.
Ritchie, J. and L. Spencer, Qualitative data analysis for applied policy research, in Analyzing Qualitative Data, A. Bryman and R. Burgess, editors. 1994, RoutledgeFalmer: London.
Murray E, et al. Normalisation process theory: a framework for developing, evaluating and implementing complex interventions. BMC Med. 2010;8(1):1–11.
Davidoff F, Dixon-Woods M, Leviton L, Michie S. Demystifying theory and its use in improvement. BMJ Qual Saf. 2015;24:228–38. https://doi.org/10.1136/bmjqs-2014-003627.
Queensland Health. Queensland Health clinical guidelines. 2018 [cited 2018 26/6/18]; Available from: https://www.health.qld.gov.au/clinical-practice/guidelines-procedures/patient-safety/end-of-life/guidelines
Creswell JW. Qualitative inquiry and research design: choosing among five approaches. London: SAGE Publications Ltd.; 2013.
Johnson MJ, May CR. Promoting professional behaviour change in healthcare: what interventions work, and why? A theory-led overview of systematic reviews. BMJ Open. 2015;5(9):1–13.
Cummings A, et al. Implementing communication and decision-making interventions directed at goals of care: a theory-led scoping review. BMJ Open. 2017;7(10):1–17.
Billett S, Choy S. Learning through work: emerging perspectives and new challenges. J Work Learn. 2013;25(4):264–76.
Sleeman KE, et al. ‘It doesn't do the care for you’: a qualitative study of health care professionals' perceptions of the benefits and harms of integrated care pathways for end of life care. BMJ Open. 2015;5(9):1–7.
Twigger S, Yardley SJ. Hospital doctors’ understanding of use and withdrawal of the Liverpool care pathway: a qualitative study of practice-based experiences during times of change. Palliat Med. 2017;31(9):833–41.
Di Leo S, et al. ‘Less ticking the boxes, more providing support’: a qualitative study on health professionals’ concerns towards the Liverpool Care of the Dying Pathway. Palliat Med. 2015;29(6):529–37.
White N, et al. How accurate is the ‘surprise question’ at identifying patients at the end of life? A systematic review and meta-analysis. BMC Med. 2017;15(1):139.
Edwards A, Daniels H, Gallagher T, Leadbetter J, Warmington P. Improving inter-professional collaborations: Multi-agency working for children's wellbeing. Oxon: Routledge; 2009.
Raijmakers N, et al. Barriers and facilitators to implementation of the Liverpool care pathway in the Netherlands: a qualitative study. BMJ Support Palliat Care. 2015;5(3):259–65.
Billett S. Learning through work: workplace affordances and individual engagement. J Work Learn. 2001;13(5/6):209–14.
Lincoln, Y. and E. Guba, Naturalistic Inquiry. 1985, Newbury Park, CA: Sage Publications.
Teodorczuk A, et al. Medical education research should extend further into clinical practice. Med Educ. 2017;51(11):1098–100.
Kilbertus FMDM, Ajjawi RP, Archibald DBP. "You're Not Trying to Save Somebody From Death": Learning as "Becoming" in Palliative Care. Acad Med. 2018;93(6):929–36.
Billett S. Securing intersubjectivity through interprofessional workplace learning experiences. J Interprofessional Care. 2014;28(3):206–11.
Smith D. Institutional ethnography as practice. Oxford: Rowan and Littlefield; 2006.
Boud, D. and E. Molloy, Feedback in Higher and Professional Education: Understanding it and doing it well. 2013, New York: Routledge.
May C, et al. Development of a theory of implementation and integration: normalization process theory. Implement Sci. 2009;4(1):29.
The authors would like to thank the study participants and Adele Blissett for her administration support.
This research was funded by the Gold Cold Hospital Foundation. The views expressed are those of the authors.
Availability of data and materials
The datasets generated and/or analysed during the current study are not publicly available due the risk of compromising individual privacy but are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
Ethical approval was obtained from the Gold Coast Health Human Research Committee. The approval number is HREC/14/QGC/185. Comprehensive information sheets were given to all participants in the research, written informed consent was taken from all interviewees.
Consent for publication
A full information sheet was given to all participants in the study including information regarding the intention to publish findings from the research and consent given for use of anonymized data.
The authors declare that they have no competing interests.
About this article
Cite this article
Noble, C., Grealish, L., Teodorczuk, A. et al. How can end of life care excellence be normalized in hospitals? Lessons from a qualitative framework study. BMC Palliat Care 17, 100 (2018). https://doi.org/10.1186/s12904-018-0353-x