World Health Organisation (WHO) says that global demand for care for people with life threatening illnesses will continue to grow as populations, age and the burden of non-communicable diseases rise.
According to the UN health agency, by 2060, the need for palliative care is expected to nearly double.
To address this need, the agency released two new resources to support countries in assessing the development of palliative care and improving the quality of services.
The resources are being released in advance of World Hospice and Palliative Care Day, marked on October 9, 2021.
One of the resources is a technical report with indicators that can be used by countries to monitor the provision of services. The goal is to create a global consensus on indicators, providing data that supports decision-making.
The second is a technical brief, that includes practical approaches and resources to support policy, strategy, and practice. The brief guides action at the national, district level, and point of care.
To date, the monitoring of palliative care services has been most often done by assessing the consumption of opioid analgesics. For WHO, though, opioids are only one component.
The agency believes that shared data across countries will provide a clearer picture of global needs and challenges, such as inequity. Measurement will also help identify success stories and best practices from other countries.
Each year, it is estimated over 56.8 million people, including 25.7 million in the last year of life, need palliative care. Around 78 per cent of those people live in low and middle-income countries.
For WHO, the COVID-19 pandemic has highlighted the need for this type of care to relieve suffering at the end of life, such as the physical suffering caused by breathlessness, or mental pain.
The pandemic also reminded of the need for all health professionals to have some training in this area.
The agency argues that optimal care requires a supportive policy environment, empowered communities, palliative care research, access to essential palliative care medicines, strong education and training systems.
For WHO, “palliative care is a human right and a moral imperative of all health systems.”
