- To raise public awareness and influence public policy regarding the need for better urgent palliative care in the community
- To provide information and advice about choosing where to receive end-of-life care, and to enable those who prefer to die at home to achieve the best available care there
- To support those providing emergency care at home for people seriously ill with Covid-19 (or other conditions) by identifying exemplary and poor practice
- To identify and encourage areas of research
- Open letters to government and newspapers
- Radio broadcasts
- Blogs and evidence reviews on Oxford University’s Centre for Evidence-Based Medicine’s website
- Contacts with palliative care providers and other campaigners
- Talks and presentations
- Development of decision tools and checklists
- Links to relevant resources
PALLIATIVE CARE AND COVID-19
Palliative care, the alleviation of symptoms, has been an important aspect of medical practice since time immemorial.
The last fifty years have seen the development of palliative care specifically to manage end-of-life situations. We celebrate this and applaud the palliative care community’s continuing work to improve the quality of, and access to, this service in all settings – hospitals, homes (both domestic and institutional) and hospices.
However, providing palliative care in the community during a pandemic of a new virus is extremely challenging. The Covid-19 pandemic has highlighted difficulties in getting access to timely, sometimes urgent, palliative care for those people who, for whatever reason, are obliged or prefer to stay at home. Patients need to be diagnosed in their home, then provided with the necessary medication, equipment, care and reliable advice, while avoiding transmission of the disease.
In drawing attention to these challenges and pressing for effective responses to the current crisis, we hope that palliative care services in the community will be better prepared for the future, both in more normal times and in times of further possible pandemics.