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Palliative Care for Infants, Children, and Adolescents

A Practical Handbook
Buch | Softcover
560 Seiten
2011 | second edition
Johns Hopkins University Press (Verlag)
978-1-4214-0149-2 (ISBN)
CHF 56,75 inkl. MwSt
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There are few things requiring more expertise, delicacy, and compassion than caring for an infant, child, or young adult with a life-limiting condition. Written by leading researchers, clinicians from relevant disciplines, family members, and advocates, this practical guide provides professionals involved in pediatric palliative and end-of-life care with comprehensive information in a single volume. Thoroughly updated and expanded, this edition includes chapters addressing the unique challenges facing children with HIV/AIDS and their families, care in home and ICU settings, difficult decision-making processes, and the importance of communication with the child and family, as well as completely new chapters on spiritual dimensions of care and educational and advocacy initiatives. Intended for primary care physicians, pediatric practitioners and specialists, home care and hospice personnel, pastoral counselors, and affected families, the book includes useful resource and reference material and practical, hands-on tips.
With contributions from an international group of expert educators, clinicians, and parents, this book takes a truly interdisciplinary approach to pediatric palliative care, presenting best practices, clear instruction, and the latest information and research for anyone involved in pediatric palliative and end-of-life care.

Brian S. Carter, M.D., is a professor in the Department of Pediatrics, Division of Neonatology, at Vanderbilt University Medical Center. Marcia Levetown, M.D., is Principal, HealthCare Communication Associates in Houston, past chair of the American Academy of Pediatrics' Section on Hospice and Palliative Medicine, and a Soros Faculty Scholar Alumna of the Project on Death in America. Sarah E. Friebert, M.D., is Director of Palliative Care at Akron Children's Hospital, associate professor of pediatrics at Northeast Ohio Universities Colleges of Medicine and Pharmacy, and chair of the American Academy of Pediatrics' Section on Hospice and Palliative Medicine.

List of Contributors
Preface
Part I: Societal and Institutional Issues
Chapter 1. Epidemiology and Health Services Research
Chapter 2. Goals, Values, and Confl ict Resolution
Chapter 3. Barriers to Integrating Palliative Care and Potential Solutions
Chapter 4. Educational Initiatives
Chapter 5. The Art of Advocacy
Part II: The Cycle of Care
Chapter 6. Decision Making
Chapter 7. Communication Skills and Relational Abilities
Chapter 8. Psychosocial Needs of the Child and Family
Chapter 9. Spiritual Dimensions
Chapter 10. Holistic Management of Symptoms
Chapter 11. Bereavement
Chapter 12. The Other Side of Caring: Caregiver Suffering
Part III: Special Care Environments and Patient Populations
Chapter 13. Palliative Care in the Neonatal-Perinatal Period
Chapter 14. Palliative Care in the Pediatric Intensive Care Setting
Chapter 15. Palliative Care in the Home, School, and Community
Chapter 16. Palliative Care for the Child Who Has a Genetic Condition
Chapter 17. Integrating Palliative Care with HIV Care and Treatment
Chapter 18. Integrating Palliative Care with Pediatric Hematology/Oncology
Index

Erscheint lt. Verlag 10.12.2011
Zusatzinfo 11 Line drawings, black and white
Verlagsort Baltimore, MD
Sprache englisch
Maße 152 x 229 mm
Gewicht 748 g
Themenwelt Medizin / Pharmazie Gesundheitswesen
Medizin / Pharmazie Medizinische Fachgebiete Pädiatrie
Medizin / Pharmazie Medizinische Fachgebiete Palliativmedizin
Medizin / Pharmazie Pflege Palliativpflege / Sterbebegleitung
Studium Querschnittsbereiche Geschichte / Ethik der Medizin
ISBN-10 1-4214-0149-5 / 1421401495
ISBN-13 978-1-4214-0149-2 / 9781421401492
Zustand Neuware
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