1
A WHO
guide for planners, implementers
and managers
Introduction
Inequality of access to palliative care and symptom relief is one of the greatest disparities in global health
care (
1). Currently, there is avoidable suffering on a massive scale due to lack of access to palliative care
and symptom relief in low- and middle-income countries (LMICs)
(1). Yet basic palliative care that can
prevent or relieve most suffering due to serious or life-threatening health conditions
can be taught easily
to generalist clinicians, can be provided in the community and requires only simple, inexpensive medicines
and equipment. For these reasons, the World Health Assembly (WHA) resolved that palliative care is “an
ethical responsibility of health systems”
(2). Further, most patients who need
palliative care are at home
and prefer to remain there. Thus, it is imperative that palliative care be provided in the community as part of
primary care (Annex 1). This document was written to assist ministries of health and health care planners,
implementers and managers to integrate palliative care and symptom control into primary health care
(PHC).
This second in a series of World Health Organization (WHO) guides on palliative care follows a general one
entitled Planning and implementing palliative care services: a
guide for programme managers, published
in 2016
(3). The current document may be used by itself for integrating palliative care into primary care or
in combination with the earlier guide by those working to integrate palliative care into multiple levels of a
health care system.
This document is not a clinical manual, and does not provide clinical guidelines. Rather, it contains
detailed information about what palliative
care is and should be, the rationale for it being a medical and
moral imperative, an Essential Package of Palliative Care for Primary Health Care (EP PHC) and a method
for implementing palliative care within primary care in a way that strengthens health care systems
(Annex 2). It represents
the collective knowledge, experience and recommendations of a group of experienced
palliative care clinicians, all of whom either are also primary care clinicians or work in LMICs, or both.