Comprehensive handbook of childhood cancer and sickle cell disease : a biopsychosocial approach

著者

    • Brown, Ronald T.

書誌事項

Comprehensive handbook of childhood cancer and sickle cell disease : a biopsychosocial approach

edited by Ronald T. Brown

Oxford University Press, 2006

タイトル別名

Childhood cancer and sickle cell disease

大学図書館所蔵 件 / 全6件

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注記

Includes bibliographical references and index

HTTP:URL=http://www.loc.gov/catdir/toc/ecip0516/2005020559.html Information=Table of contents

HTTP:URL=http://www.loc.gov/catdir/enhancements/fy0636/2005020559-d.html Information=Publisher description

HTTP:URL=http://www.loc.gov/catdir/enhancements/fy0723/2005020559-b.html Information=Contributor biographical information

内容説明・目次

内容説明

Over recent decades, tremendous advances in the prevention, medical treatment, and quality of life issues in children and adolescents surviving cancer have spawned a host of research on paediatric psychosocial oncology. This important volume fulfills the clear need for an up-to-date, comprehensive handbook for practitioners that delineates the most recent research in the field - the first of its kind in a decade. Over 60 renowned authors have been assembled to provide a thorough presentation of state-of-the-art research and literature, with topics including: *Neuropsychological effects of chemotherapy and radiation therapy *Bone marrow transplant *Important issues about quality of life during and following treatment *Collaborative research among child-focused psychologists *Standards of psychological care for children and adolescents *Stress and coping in the paediatric cancer experience *The role of family and peer relationships The Comprehensive Handbook of Childhood Cancer and Sickle Cell Disease represents both multidisciplinary and international efforts, an alliance between physicians and parents, and a combination of research and service. With a wealth of information of great interest to patients and their families, this volume will also be a welcome resource to the psychologists, psychiatrists, paediatricians, oncologists, nurses, and social workers who confront these issues as they help children and their families through the treatment, recovery and grieving process.

目次

  • I INTRODUCTION
  • 1. Why a Comprehensive Handbook on Paediatric Psychosocial Oncology/Hematology
  • 2. Cancer and Blood Disorders in Childhood: Biopsychosocial-Developmental Issues in Assessment and Treatment
  • II THE CANCER EXPERIENCE "ON TREATMENT"
  • 3. Stress and Coping in the Pediatric Cancer Experience
  • 4. Family Issues When a Child Is on Treatment for Cancer
  • 5. Psychosocial and Behavioral Issues in Stem Cell Transplantation
  • 6. Peer, Friendship Issues and Emotional Well-Being
  • 7. Pain and Procedure Management
  • 8. Adherence to Treatment Demands
  • 9. Quality of Life in Childhood Cancer: Meaning, Methods, and Missing Pieces
  • 10. Spirituality and Complementary and Alternative Medicine
  • 11. A Goodness-of-Fit Ethic for Informed Consent to Pediatric Cancer Research
  • 12. Problem-Solving Skills for Mothers of Children With Newly Diagnosed Cancer
  • III CANCER LATE EFFECTS "OFF TREATMENT"
  • 13. Psychological and Social Effects of Surviving Childhood Cancer
  • 14. Neuropsychological Late Effects
  • 15. Posttraumatic Stress and Posttraumatic Growth in Childhood Cancer Survivors and Their Parents
  • 16. Interventions for Cancer Late Effects and Survivorship
  • 17. Maximizing School, Academic and Social Outcomes in Children and Adolescents with Cancer
  • IV PALLIATIVE CARE AND END-OF-LIFE ISSUES
  • 18. Issues in Palliative Care
  • 19. Loss and Grief
  • V PREVENTION OF PRIMARY AND SECONDARY MALIGNANCIES
  • 20. Genetic Issues
  • 21. Prevention and Cessation of Tobacco Use and Exposure to Environmental Tobacco Smoke
  • 22. Health Promotion and Primary Prevention of Cancer
  • VI SICKLE CELL DISEASE
  • 23. Biopsychosocial and Developmental Issues Related to Sickle Cell Disease
  • 24. Neuropsychological Aspects of Sickle Cell Disease
  • 25. Psychosocial Adaption of Children and Adolescents with Sickle Cell Disease
  • 26. Family Systems in Paediatric Sickle Cell Disease
  • 27. Pain Management of Sickle Cell Disease
  • VII TRAINING, FUNDING AND COLLABORATIVE ENDEVOURS
  • 28. Training in Pediatric Hematology/Oncology
  • 29. Research Opportunities and Collaborative Multisite Studies in Psychosocial Hemotology/Oncology
  • VIII PROSPECTIVE AND RETROSPECTIVE VIEW OF PEDIATRIC HEMATOLOGY/ONCOLOGY
  • 30. A Prospective and Retrospective View of Pediatric Hematology/Oncology

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