图书简介
Comprehensive in scope, exhaustive in detail, and definitive in authority, this third edition has been thoroughly updated to cover new practices, current epidemiological data, and the evolving models that support the delivery of palliative medicine to children. This book is an essential resource for anyone who works with children worldwide.
Section I: Foundations of care; 1 Lorna Fraser, Stephen Connor, and Joan Marston: History and epidemiology; 2 Jennifer Mack and Bryan Sisk: Communication; 3 Robert MacAuley and Richard Hain: Children are not little adults the distinctiveness of ethics in children; 4 Myra Bluebond-Langner and Richard Langner: Decision making with children, young people and parents; 5 Erica Brown, Mary Ann Muckaden, and Nokuzola Mndende: Culture, spirituality, religion, and ritual; Section II: Child and family care; 6 Nancy Contro and Jane Zimmerman: Assessment of the child and family; 7 Myra Bluebond Langner and Ignasi Clemente: Children s views of death; 8 Jan Aldridge and Barbara M Sourkes: The psychological impact of life-limiting conditions on the child; 9 Chana Korenblum and Finella Craig: Adolescents and young adults; 10 Amy Volans and Emma Brown: Children expressing themselves; 11 Sue Boucher: Education and school; 12 Veronica Dussell and Barbara Jones: Impact on the family; 13 Sara Portnoy and Lori Ives Bain: Bereavement; Section III: Symptom care; 14 Dilini Rajapakse and Maggie Comac: Overview of symptoms and their assessment in life-limiting illness; 15 Andy Gray, Jane Ridden, Richard Hain: Using medication in children s palliative care; 16 Antoine Bioy and Chantal Wood: Introduction to pain; 17 Stefan J. Friedrichsdorf: Multimodal analgesia in pediatric palliative care; 18 Manuel Rigal, Ricardo Martino, and Richard Hain: Opioids and the WHO pain ladder; 19 Renee McCulloch and Charles Berde: Difficult pain: adjuvants or co-analgesics; 20 David Steinhorn: Integrative approach to pain and other symptoms; 21 Jo Laddie, Alta Terblanche, and Michelle Meiring: Gastrointestinal and liver related symptoms in paediatric palliative care; 22 Adam Rapoport,Sanjay Mahant and Michelle Meiring: Feeding, cachexia and malnutrition in children s palliative care; 23 Julie M. Hauer and Jori Bogetz: Neurological and neuromuscular conditions and symptoms; 24 Pamela J. Mosher and Anna C. Muriel: Depression, anxiety, and delirium; 25 Emily Harrop and Roxanne Kirsch: Cardiorespiratory symptoms; 26 Carol Hlela, Rene Albertyn, and Michelle Meiring: Skin symptoms; 27 Mei-Yoke Chan and Kevin Weingarten: Haematological symptoms; 28 Michelle Meiring and Tonya Arscott-Mills: Palliative care for children with communicable illnesses; Section IV: Delivery of care; 29 Aine Ni Laoire, Daniel Nuzum, Maeve O’Reilly, Marie Twomey, Keelin O Donoghue, and Mary Devins: Perinatal palliative care; 30 Brian Carter: Intensive-care units; 31 Michelle Grunauer and Jenny Hynson: Planning care; 32 Dawn Davies and Justin Baker: Care in the final hours and days; 33 Julia Downing and Joan Marston: Delivering care around the world; 34 Danai Papadatou: Healthcare providers responses to the death of a child; 35 Jan Aldridge and Pat Carragher: Teamwork; 36 Fiona Rawlinson and Michelle Meiring: Education; 37 Susan Blacker and Rachel Thienprayoon: Quality improvement in paediatric hospice and palliative care; 38 Harold Siden and Kimberly Widger: Research in paediatric palliative care; Appendix 1 The Association of Paediatric Palliative Medicine Master Formulary, Fifth Edition, 2020
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