This book is a printed edition of the Special Issue "Pediatric Palliative Care" that was published in Children

The first volume in the "What Do I Do Now?: Palliative Care" series, Pediatric Palliative Care uses a case-based palliative care approach to cover common and important topics in the examination, investigation, and management of children with serious illness. Each chapter provides a discussion of the diagnosis, key points to remember, and selected references for further reading. The book addresses a wide range of topics, including the goals of care, symptom management, care for neonatal and adolescent populations, and the emotional, social, cultural and spiritual needs of ill children and their families. Written by authors from a variety of fields such as nursing, chaplaincy, social work, and psychology, this book is suited for pediatricians, palliative care and hospice providers, nurses, and allied health practitioners. Pediatric Palliative Care is an engaging collection of thought-provoking cases which clinicians can utilize when they encounter difficult patients. The volume is also a self-assessment tool that tests the reader's ability to answer the question, "What do I do now?"

Pediatric Palliative Care Consultant (PPCC) was designed to provide practical recommendations for palliative symptom management in pediatric patients. The aim of this guide is to equip all practitioners who care for pediatric patients with chronic life-limiting conditions, whether they have pediatric-specific training, or rarely see a pediatric patient. For those experienced in treating pediatric patients, this book may be used as a resource for support of current practice and a quick reference guide. For those who only occasionally treat pediatric patients, this book may be used as a learning guide and a resource to ensure symptoms are appropriately treated. For educators, this book may be used as a training guide to address the basics of pediatric palliative care and assist learners in developing a comprehensive plan for symptom management.

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.

This ebook is a practical guide to all of the issues relating to the care of a child or young person with a life limiting condition. It aims to empower clinicians to care for children at home or as close to home as possible. It is a national resource and a major contribution towards supporting dying children and their families to have the best quality of life. Sections include psychosocial considerations, symptom management, the dying process, bereavement and ethics. New sections for this edition include perinatal palliative care and quality improvement in paediatric palliative care. The booklet includes a number of appendices including commonly used drugs and doses. The booklet where possible tries to be evidence based, and reflects best practice guidelines for the Australian and New Zealand context.