Primary palliative care: Onwards and upwards!

Peeler et al. present a scoping review to explore how palliative care is integrated in community settings in low and middle-income countries where it is most urgently needed. They very helpfully lay out five models of how people can access palliative care in primary care.¹ Pereira et al.,² in contrast, describe models of integrated palliative care in Canada and other higher-income countries. They also highlight the need for some new more nuanced indicators to monitor primary palliative care, such as how many months before death this approach was started.

Leng et al.³ conducted consecutive rapid participatory appraisals to develop and evaluate palliative care integration in a refugee setting in Uganda. They demonstrate the utility of this method to foster palliative care with community involvement under challenging circumstances. Mitchell et al.⁴ examined how the integration of primary and palliative care services can improve cultural competency and equity in the UK. Realist stakeholder workshops found that inequalities in access to palliative care can be addressed through integrated partnerships, emphasising, as Leng et al.³ also found, the importance of trust, communication and patient-centred care.

Education is an essential aspect in developing palliative care in primary care. The study by Seiça Cardoso et al.⁵ in Portugal explores a two-tiered complex intervention involving General Practitioner training combined with a new consultation model for patients with palliative care needs in primary care settings. They demonstrate the feasibility and effectiveness of empowering General Practitioners in this way. Ambulance services also daily face patients with life-threatening diseases. So Juhrmann et al.⁶ employed a Delphi study to develop a framework for national implementation in Australia to enhance palliative care delivery by paramedics. This framework will help improve the integration of palliative care in urgent and emergency care out-of-hours.

Cao et al.⁷ conduct a systematic review of electronic symptom monitoring in home-based palliative care. This shows promise in enhancing patient-provider communication and extend specialist and generalist palliative care into the community. Technological advances can be used for reaching those living in rural areas. A further qualitative study by Lion et al.⁸ investigated the experiences of family caregivers of people with brain cancer. Caregivers want timely access to coordinated support and information throughout the illness trajectory. This study finds that support needs could be provided by primary care providers such as general practitioners and community nurses, who typically have established relationships with patients and caregivers.

Finally, two studies explore that less may be more at the end of life. Davies et al.⁹ conduct a systematic review of hospital admissions at the end of life in people who are frail to explore the complex factors influencing clinical decision-making in primary care. They emphasise the need for a balanced approach and continuity of care. van der Waal et al.¹⁰ explore factors influencing deprescribing in the last phase of life in primary care settings. They identify barriers and facilitators to deprescribing, emphasising the importance of patient-centred care and systematic identification of patients with limited life expectancy.

These above papers add to the body of evidence that primary care workers, supported by specialists and more experienced generalists can and actually do provide integrated palliative care for people with all diseases, at all times from diagnosis to death and can deal with all dimensions of need, in all settings and all countries (see Figure 1).

Over twenty years of longitudinal qualitative and quantitative research on illness trajectories has helped us understand the multidimensional experiences and needs of patients as their health declines. This has brought a new vocabulary and an understanding of the concept of ‘illness trajectories of decline’ which clearly indicates that dying is a process that can take months or years rather than an isolated event.¹¹ Understanding these dynamic patterns allows researchers and clinicians to pro-actively identify when patients might benefit from a palliative care approach. Subsequently tools were developed and validated across many patient groups and countries so that intervention studies could proceed (GSF¹² and SPICT¹³). The development and testing of tools for assessment and care planning has also been proven useful to routinise in clinical practice and guide future care planning discussions in people with all illnesses including multimorbidity.¹⁴ Our EAPC toolkit to help advocate for and operationalise palliative care in primary care is now available in English, French, German, Spanish, Portuguese and Italian.¹⁵

Primary care can also bring continuity of care and compassion, and communication and co-ordination skills to patients (adults and children) and their carers. See Figure 2.

We were disappointed that we did not receive any papers about the following topics which we had indicated as relevant: people with multimorbidity; people living in care homes; when to trigger palliative care in various illnesses to provide optimal benefit; cost-effectiveness outcomes of care provided in primary care; interventions to provide urgent care; or studies using a systems-based approach where palliative care is considered within a wider health and social and community context.

To promote universal access, we present a framework based on the ‘5 Alls’ listed above to overview the potential and scope of future primary palliative care research.

‘Primary palliative care’ was initially defined in the UK as palliative care delivered by the primary care team. However, it is now interpreted in different ways in different countries. As many policymakers, clinicians, educators and planers find this confusing and studies hard to interpret, we have included a further editorial in this issue to redefine this term to allow this field to progress clearly.²² We believe that palliative care by primary care workers is vital, so that ‘Health for all’ includes ‘Palliative care for all’.