This is intended for Health Care Professionals only


Beacons of excellence

On Saturday 11th October 2008, people in more than 70 countries around the world took part in a series of events to mark World Hospice and Palliative Care Day. Everybody concerned had the same message - that access to hospice and palliative care must be considered a basic human right.

By Jonathan Ellis

Everyone affected by terminal and life-limiting illnesses should be able to live their lives free from pain and with dignity. Yet, around the world millions of people endure unbearable and unnecessary suffering and are left to die without any pain relief, symptom control or emotional, physical and spiritual support.


Thanks to Dame Cicely Saunders and the hospice movement, the UK has led way in the provision of hospice and palliative care and indeed hospices were described as ‘beacons of excellence’ in the Department of Health’s recently published End of Life Care Strategy for England, which promotes high quality care for all adults at the end of life.

 

The Strategy, which was warmly welcomed by Help the Hospices, sets out to raise awareness and improve access to good quality end of life care, including where people are cared for. While its intentions are honourable, delivery will no doubt prove a formidable challenge.

 

Of course limits on, and competing priorities, for resources will have an impact on delivery. And access to provision varies greatly across the country and across the many different types of care settings. One thing is certain – there is a real need to improve the knowledge, competence and skills around supporting people at the end of their lives right across the health and social care system. What is needed, and what the UK hospice movement is already delivering, is a greater sharing of information and expertise among professionals across all community settings.

 

It is worth remembering that hospices are not just another provider of services but contribute funding to the delivery of palliative care through the fundraising efforts of their local communities.  In this respect, voluntary hospices are effectively ‘co-commissioners’ as well as providers of palliative care, offering individuals appropriate support within the community and preventing avoidable admission to hospitals. Their key role in the provision of palliative care extends to sharing specialist knowledge, providing training and development and supporting their local health and social care colleagues.

 

Strong local partnerships between hospices and Primary Care Trusts are vital if the ambitious aims of the End of Life Care Strategy are to be met. PCTs will need to ensure that all staff are equipped and skilled in the provision of supportive end of life care and many are already benefiting from strong relationships with hospices, accessing quality training and education and tapping into the expertise and specialist palliative care knowledge that exists both on a local and national level.

 

October 2008 not only marked World Hospice and Palliative Care Day. It also saw the results of a research study into the relationships between hospices and PCTs published by the Commission for the Compact in partnership with Help the Hospices. Entitled Positive Engagement, Future Practice: Learning for End of Life Care, the study found that the Compact with the Third Sector (the agreement between the government and the voluntary sector in England drawn up in 1998) has the potential to deepen good practice and help strengthen relationships.

 

Through a series of case studies, the research focussed on how well the Compact is being implemented in relation to supportive and palliative care and examined some of the different local relationships between PCTs and charitable hospices. There were several key findings, not least the fact that the success of relationships between hospices and PCTs relies upon constructive and effective personal relationships between key players.

 

Close and effective working relationships are essential if the UK is to continue to lead the way in the provision of palliative care. The aims of the End of Life Care Strategy while ambitious, should be welcomed by everyone working within a health and social care setting and hospices are ideally placed to take a lead role in sharing knowledge and expertise, delivering training and promoting best practice. The challenges are great but the long term effects will be greater still.

 

For so many people around the world, hospice and palliative care is simply non-existent. As we remember that, let us continue to work together to ensure that we not only meet the aims of the End of Life Care Strategy but also that we continue to set standards on a global level.

 

Jonathan Ellis is Director of Public Policy and Parliamentary Affairs at

Help the Hospices: www.helpthehospices.org.uk

 

 


This is intended for Health Care Professionals only