Page 102 - HA Convention 2015
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Special Topics

                                    ST8.3 Palliative Care in Non-cancer Patients  14:30  Room 228

Monday, 18 May                      Empowerment for Patients with Advanced Illnesses and Their Family Caregivers
                                    Lai TTK
                                    Palliative Medical Unit, Grantham Hospital, Hong Kong

                                    Patients with advanced illnesses have a substantial symptom burden that lowers their quality of life. Palliative care is
                                    specialised medical care that focuses on improving the quality of life of patients by relieving their symptoms, pain, and
                                    stresses from serious illnesses, including heart, liver, kidney, neurological diseases, as well as cancer. Palliative care
                                    provides extra support and improves the well-being of patients and their family caregivers. However, most people are often
                                    not prepared to live with an incurable illness. Most families do not know their information needs until a crisis occurs.

                                    The concept of patient empowerment has become an integral part of palliative care and one of the major attributes of
                                    healthcare professionals who provide palliative care services (Ciemins et al., 2014). Embracing empowerment means making
                                    a paradigm shift, which is often difficult. Empowerment occurs when patients are actually making autonomous, informed
                                    decisions about their preferred care and way of life. Apart from patients, caregivers may also look for help and support
                                    themselves or other family members. Extended families and communities may have questions and require information on
                                    palliative care.

                                    Information transmission and communication among patients, families, and caregivers is a major issue of providing care
                                    to people who are reaching the end of their lives. Patients and their family members commonly express the importance of
                                    adequate information, attitudes of professionals, and quality of communication in the context of palliative care (Andershed,
                                    2006; McIlfatrick et al., 2007). The appropriate and timely delivery of information can make the difference between a positive
                                    care-giving experience and a distressing one (Dunbrack, 2005).

                                    Providing effective counselling with high quality information can help patients and caregivers cope with their situation and
                                    make expert decisions. A series of booklets and workbooks for patients and caregivers has been developed by the palliative
                                    care team of the Grantham Hospital to help them understand their situation and to inform them about other care options.

HOSPITAL AUTHORITY CONVENTION 2015

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