Developing a creative alliance with the 'person' beyond the 'patient' is a core tenet of effective palliative care. The need for a better understanding of how to develop active partnerships between service users and professionals has never been greater. This book examines progress thus far and attemts to delineate future challenges by bringing together a leading group of physicians, nurses, social workers, chaplains and psychologists who stress the importance of patient participation in palliative care. Recent developments are covered as well as bereavement issues and cultural differences.…mehr
Developing a creative alliance with the 'person' beyond the 'patient' is a core tenet of effective palliative care. The need for a better understanding of how to develop active partnerships between service users and professionals has never been greater. This book examines progress thus far and attemts to delineate future challenges by bringing together a leading group of physicians, nurses, social workers, chaplains and psychologists who stress the importance of patient participation in palliative care. Recent developments are covered as well as bereavement issues and cultural differences. There is also material from the patients themselves. Most importantly, this book highlights the difficulties in involving patients in their own care due to poor life expectancy, debilitating illness and severe pain. More knowledge and insight is needed to see how far these patients can realistically be expected to be involved in improving the services they need. The book will be of interest to a multi-professional audience in palliative care particularly practitioners in general and specialist palliative care, specialist nurses, bereavement counsellors, and social workers. audienceHinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Edited by BARBARA MONROE, Chief Executive, St Christopher's Hospice, Sydenham, London, UK, and DAVID OLIVIERE, Director of Education and Training, St Christopher's Hospice, Sydenham, London, UK
Inhaltsangabe
* Part 1: The Role of the Patient in Palliative Care * 1: Cicely Saunders: A voice for the voiceless * 2: Neil Small: The changing National Health Service, user involvement and palliative care * 3: Jane Bradburn: Developments in user organisations * 4: Sam Ahmedzai and John Hunt: Quality issues in palliative and supportive care * 5: Emma Davie and Bill Noble: Education in palliative care * 6: Juan M. Nunez Olarte: Cultural difference and palliative care * 7: Marilyn Relf: Bereavement care * Part 2: Multi-professional perspectives * 8: Pam Firth: Multi-professional teamwork * 9: James Gilbert: Palliative medicine * 10: Mandy Stratford: Palliative nursing * 11: Lindsey Napier: Palliative care social work * 12: Peter Speck: Palliative care and chaplaincy * 13: Christine Kalus: Palliative care and psychology * 14: Alywyn Lishman: Conclusions * 15: Fiona Broughton: Conclusions: thoughts of a palliative care user
* Part 1: The Role of the Patient in Palliative Care * 1: Cicely Saunders: A voice for the voiceless * 2: Neil Small: The changing National Health Service, user involvement and palliative care * 3: Jane Bradburn: Developments in user organisations * 4: Sam Ahmedzai and John Hunt: Quality issues in palliative and supportive care * 5: Emma Davie and Bill Noble: Education in palliative care * 6: Juan M. Nunez Olarte: Cultural difference and palliative care * 7: Marilyn Relf: Bereavement care * Part 2: Multi-professional perspectives * 8: Pam Firth: Multi-professional teamwork * 9: James Gilbert: Palliative medicine * 10: Mandy Stratford: Palliative nursing * 11: Lindsey Napier: Palliative care social work * 12: Peter Speck: Palliative care and chaplaincy * 13: Christine Kalus: Palliative care and psychology * 14: Alywyn Lishman: Conclusions * 15: Fiona Broughton: Conclusions: thoughts of a palliative care user
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