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 thoroughpresentation 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 andtheir families through the treatment, recovery and grieving process.
I Introduction; Why a Comprehensive Handbook on Paediatric Psychosocial Oncology/Hematology; Cancer and Blood Disorders in Childhood: Biopsychosocial-Developmental Issues in Assessment and Treatment; II The Cancer Experience On Treatment; Stress and Coping in the Pediatric Cancer Experience; Family Issues When a Child Is on Treatment for Cancer; Psychosocial and Behavioral Issues in Stem Cell Transplantation; Peer, Friendship Issues and Emotional Well-Being; Pain and Procedure Management; Adherence to Treatment Demands; Quality of Life in Childhood Cancer: Meaning, Methods, and Missing Pieces; Spirituality and Complementary and Alternative Medicine; A Goodness-of-Fit Ethic for Informed Consent to Pediatric Cancer Research; Problem-Solving Skills for Mothers of Children With Newly Diagnosed Cancer; III Cancer Late Effects Off Treatment; Psychological and Social Effects of Surviving Childhood Cancer; Neuropsychological Late Effects; Posttraumatic Stress and Posttraumatic Growth in Childhood Cancer Survivors and Their Parents; Interventions for Cancer Late Effects and Survivorship; Maximizing School, Academic and Social Outcomes in Children and Adolescents with Cancer; IV Palliative Care and End-of-Life Issues; Issues in Palliative Care; Loss and Grief; V Prevention of Primary and Secondary Malignancies; Genetic Issues; Prevention and Cessation of Tobacco Use and Exposure to Environmental Tobacco Smoke; Health Promotion and Primary Prevention of Cancer; VI Sickle Cell Disease; Biopsychosocial and Developmental Issues Related to Sickle Cell Disease; Neuropsychological Aspects of Sickle Cell Disease; Psychosocial Adaption of Children and Adolescents with Sickle Cell Disease; Family Systems in Paediatric Sickle Cell Disease; Pain Management of Sickle Cell Disease; VII Training, Funding and Collaborative Endevours; Training in Pediatric Hematology/Oncology; Research Opportunities and Collaborative Multisite Studies in Psychosocial Hemotology/Oncology; VIII Prospective and Retrospective View of Pediatric Hematology/Oncology; A Prospective and Retrospective View of Pediatric Hematology/Oncology;
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