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    Palliare: A Handbook for Palliative Care Volunteers in NSW
    Palliare: A Handbook for Palliative Care Volunteers in NSW
    Palliare: A Handbook for Palliative Care Volunteers in NSW
    Ebook146 pages2 hours

    Palliare: A Handbook for Palliative Care Volunteers in NSW

    By Alex Huntir

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    About this ebook

    “Palliare: A Handbook for Palliative Care Volunteers in NSW” offers background and practical guidance for people who volunteer in palliative care settings.
    Chapters include Introduction to Palliative Care, The Volunteer's Role, Boundaries and Self-Care, Communication Skills, Home and Community Visiting, Advance Care Directives, Young People in Palliative Care, Spirituality and Palliative Care, Grief and Bereavement, Palliative Care, Multiculturalism and Families, The Volunteer and Comfort Care and About Dying. The information is specific to the state of NSW (Australia) but will be of interest to hospice and palliative care volunteers everywhere.
    Palliare was developed in 2015 as a learning resource for palliative care volunteers in NSW as part of the Volunteer Support Services Program hosted by Palliative Care NSW and funded by the NSW Ministry of Health.

    LanguageEnglish
    PublisherAlex Huntir
    Release dateDec 17, 2015
    ISBN9780994438713
    Palliare: A Handbook for Palliative Care Volunteers in NSW

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      Book preview

      Palliare - Alex Huntir

      Chapter 1 Introduction to Palliative Care

      What is Palliative Care?

      ‘Palliate’ means ‘to cloak’ or to ease symptoms without curing the underlying disease. The primary goal of palliative care is to provide quality of life for the patient and family, achieved through an team-based approach that includes symptom control and support for the patient and family –whatever the diagnosis.

      Palliative Care is both a medical specialty and a philosophy of care. Both are discussed in this chapter.

      Palliative Care is also known as Hospice Care in some countries. In Australia the word ‘hospice’ generally refers to a facility rather than a model of care.

      The word ‘hospice’ has the same derivation as ‘hospital’ and ‘hospitality’, and dates back to the 4th century when pilgrims were cared for at an inn or hostel¹.

      World Health Organisation (WHO) Definition of Palliative Care²

      "Palliative care is an approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial and spiritual. Palliative care:

      •

      provides relief from pain and other distressing symptoms;

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      affirms life and regards dying as a normal process;

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      intends neither to hasten or postpone death;

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      integrates the psychological and spiritual aspects of patient care;

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      offers a support system to help patients live as actively as possible until death;

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      offers a support system to help the family cope during the patients illness and in their own bereavement;

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      uses a team approach to address the needs of patients and their families, including bereavement counselling, if indicated;

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      will enhance quality of life, and may also positively influence the course of illness;

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      is applicable early in the course of illness, in conjunction with other therapies that are intended to prolong life, such as chemotherapy or radiation therapy, and includes those investigations needed to better understand and manage distressing clinical complications."

      You will find that different organisations, states and countries may have different definitions of Palliative Care.

      NSW Health endorses the WHO definitions of palliative care, and this forms the basis of the NSW Government’s Plan to increase access to Palliative Care 2012–2016³

      Specialist Palliative Care services

      Most volunteer services are attached to, or have a close working relationship with, a specialist Palliative Care service.

      People seeking the help of specialist palliative care can be referred by any doctor, including their own General Practitioner (GP). The referral will take into account the prognosis for the person, and the support from their loved ones.

      In Paediatric Palliative Care the referral will usually come through the primary care team associated with the child. The focus broadens to include the siblings of the patient, carers and grandparents.

      A list of Palliative Care Services in NSW can be found on the Palliative Care NSW website at www.palliativecarensw.org.au.

      Once a person is seen by Palliative Care they will receive support according to their need and prognosis. Assistance may be needed for short term symptom control, or they may be involved throughout their illness journey.

      Not everyone will require specialist Palliative Care in hospital at end of life, but those that do may have repeat admissions.

      Curative vs Palliative Approaches

      Curative (Traditional) Approach

      The curative approach is the approach taken when all treatment and care is focused on ensuring the person will recover. In this approach the decision maker is usually the medical practitioner.

      One of the challenges of clinical treatment is to find the greatest benefit for the person. Not all treatments result in beneficial outcomes for them – such treatment is described as ‘futile’⁴.

      On the other hand treatment may bring benefit, but be very burdensome for the patient, and therefore decisions about treatment has to consider the person’s distress and suffering which may result from the treatment⁵.

      This approach differs from the palliative approach in that the palliative approach focuses on the holistic care of the person, and does not include futile treatments which may be considered where the curative approach is used⁶.

      Palliative (Integrated) Approach

      The contemporary approach to Palliative Care is to integrate Palliative Care into the ‘curative’ treatment of the person as it becomes necessary. One of the guiding questions used by clinicians is ‘would I be surprised if this person died within the next 12 months?’ If the answer is no, then Palliative Care may become involved.

      Underlying the philosophy of a palliative approach is a positive and open attitude toward death and dying. The promotion of a more open approach to discussions of death and dying between the Palliative Care team, clients, and their families, facilitates identification of their wishes regarding end-of-life care.

      A palliative approach is not confined to the end stages. Instead, a palliative approach provides a focus on active comfort care, and a positive approach to reducing an individual’s symptoms and distress. This assists clients and their families in understanding they are being actively supported through this process⁷.

      In Paediatric Palliative Care the ‘12 month’ question may not apply to children in Palliative Care. Children with life-threatening illnesses (such as of a genetic and chronic nature) may be involved with Palliative Care for many years.

      For more information see Chapter 7 Young People in Palliative Care.

      Standards for Providing Quality Palliative Care for all Australians (The National Palliative Care Standards)

      Since the first edition in 1994 the National Palliative Care Standards have been guiding the delivery of specialist Palliative Care services⁸.

      These standards are set-out below.

      Standard 1 – Care, decision making and care planning are each based on a respect for the uniqueness of the patient, their caregiver/s and family. The patients, their caregiver/s and families’ needs and wishes are acknowledged and guide decision making and care planning.

      Standard 2 – The holistic needs of the patient, their caregiver/s and family are acknowledged in the assessment and care planning processes, and strategies are developed to address those needs, in line with their wishes.

      Standard 3 – Ongoing and comprehensive assessment and care planning are undertaken to meet the needs and wishes of the patient, their caregiver/s and family.

      Standard 4 – Care is coordinated to minimise the burden on the patient, their caregiver/s and family.

      Standard 5 – The primary caregiver/s is provided with information, support and guidance about their role according to their needs and wishes.

      Standard 6 – The unique needs of dying patients are considered, their comfort maximised and their dignity preserved.

      Standard 7 – The service has an appropriate philosophy, values, culture, structure and environment for the provision of competent and compassionate palliative care.

      Standard 8 – Formal mechanisms are in place to ensure that the patient, their caregiver/s and family have access to bereavement care, information and support services.

      Standard 9 – Community capacity to respond to the needs of people who have a life limiting illness, their caregiver/s and family is built through effective collaboration and partnerships.

      Standard 10 – Access to palliative care is available for all people based on clinical need and is independent of diagnosis, age, cultural background or geography.

      Standard 11 – The service is committed to quality improvement and research in clinical and management practices.

      Standard 12 – Staff and volunteers are appropriately qualified for the level of service offered and demonstrate ongoing participation in continuing professional development.

      Standard 13 – Staff and volunteers reflect on practice and initiate and maintain effective self-care strategies.

      The standards are under review as at the time of writing.

      National Standards Assessment Program (NSAP)

      NSAP is a program hosted by Palliative Care Australia that enables services to engage in continuous quality improvement through self-assessment against the National Palliative Care Standards.

      The volunteer and the Palliative Care team

      The ‘team’ is made up of everyone who is involved in the person’s care. This includes specialist Palliative Care staff, physicians, GP, nursing, pharmacy, counselling and social work, clergy, nutritionists, occupational therapy, physiotherapy, speech pathology, home support workers, volunteers and volunteer managers, music and complementary therapy.

      Not all teams will have a representative from each discipline. Some may involve staff from outside of their service in a ‘consultant’ role.

      At the heart of the team is the group of clinicians who have regular or ‘as needed’ contact. This group will communicate regularly about the person’s situation and revise and adapt the plan of care accordingly.

      The team may decide to ask others to be involved by ‘making a referral’ on behalf of the person.

      This is the formal way in which volunteers become involved in the

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