Millions of people worldwide are affected by life-threatening illnesses such as cancer, organ failure, neurological diseases and HIV/Aids, which cause them and their families great suffering and economic hardship1. In the developing world, there is often limited accessibility to prompt and effective treatment for these diseases. Palliative care services in this type of resource-restricted environment are usually effective and are able to apply low-cost approaches that respond to the urgent needs of those affected, or requiring care and improve their quality of life by:
The word ‘palliative’ is derived from the Latin word ‘pallium’ meaning ’a cloak’. Patients are cloaked in care. The primary aim of this approach is to promote comfort and provide relief from pain and suffering which are key components in palliative care2.
The link between primary health care and palliative care is… potential and quality of life.
The current scope of palliative care in South Africa is a broad one, where any disease that is life-limiting qualifies, where multi-disciplinary teams work together, where it’s recognised that palliative care should be introduced early on in the course of illness, that families and caregivers are involved and that physical, cognitive, emotional, social and spiritual needs are all considered.
The ‘Total Pain’ concept is an example of the importance of an approach that bears emotional, cognitive, social and spiritual needs in mind. A term coined by Dame Cicely Saunders, ‘Total Pain’ recognises the effect or impact of pain on an individual’s overall wellbeing. A person’s experience of physical pain can be made worse by some of the following:
The ‘Total Pain’ concept sketches out what a patient might be experiencing, and goes some way towards explaining why psychosocial care is so important in palliative care.
Psychosocial practitioners form an integral part of the multidisciplinary team where they provide skilled consultations between professionals, the patient and family members, in which each draw on the expertise and knowledge of the other to assist with the physical, psychosocial or spiritual issues facing the patient and family. Psychosocial professionals usually receive a referral from the professional nurse who has already made contact with the patient and family and has done an initial assessment.
At the assessment, the nursing sister identifies key areas of psychosocial needs, and refers these to the appropriate psychosocial professional. Depending upon the urgency of the care required, this referral may be immediately after the initial assessment or at a report back at the interdisciplinary patient rounds.
The professional will then arrange to do a visit and explains their involvement in the patient’s care. Depending on the reasons for referral, the identified needs will then be explored with the patient and his/her family and a discussion had on how these might be addressed. A comprehensive psychosocial assessment will also be undertaken, which may include the following areas:
During the working phase, within the context of a counselling relationship, the psychosocial professional will spend time exploring the feelings, thoughts, and expectations of the patient and family in relation to the illness, as well as addressing practical issues that may arise, such as finances and future care planning. Mutually agreed upon goals are then acted upon, or facilitated, with the intention of achieving the desired care.
In summary, psychosocial palliative care is integral to the provision of quality palliative care in bringing care and comfort to patients and their families as they journey through a life-threatening or life-limiting illness.
This series contains information from the Hospice Palliative Care Association (HPCA) Psychosocial Palliative Care Course manual. Online courses take place regularly, with the next courses planned for 9 May, 24 July and 11 September 2023. For more details, visit https://bit.ly/3nSpN1X.
1(Sepulveda et al. 2002).