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PAEDIATRIC PALLIATIVE CARE – selected resources


Healthy Lives

Healthy Lives, Brighter Futures: the strategy for children and young people’s health: disabled children, and safeguarding for all.

Better Care: Better Lives

Better Care: Better Lives



children

Conquering your child’s chronic pain
by Lonnie Zeltzer and Christina Blackett Schlank

This book has been written by one of the pioneers and leading thinkers in the area of chronic pain in children. It is easy to read, and shows in a precise and scientific way , the clinical and psychological aspects of children’s chronic pain. It is written for the parents of children with chronic pain but is a very usefull tool for any healthcare worker, developping the different approaches to treatment. I highly recommend it.

Dr Chantal Wood
Unité de Traitement de la Douleur
Hôpital Robert Debré
48 Bd Serurier
75019 Paris


Oxford Handbook of PALLIATIVE CARE
by
Max S. Watson; Caroline F. Lucas; Andrew M. Hoy; Ian N. Back

Concise and succint source busy professionals need in their daily practice

Geared to specialist doctors, nurses, and healthcare professionals, the practical Oxford Handbook of Palliative Care covers all aspects of palliative care, including the historical and epidemiological background of palliative care, the growth of palliative medicine as a specialty, as well as major physical, psychological and spiritual, and symptom management issues from diagnosis to bereavement care.

In addition to adult care, this essential Handbook includes an extensive paediatric section. The oncology chapter outlines the treatment regimes of the common cancers and details the chemotherapeutic agent including their side-effects. This book will prove invaluable for doctors, nurses and professionals allied to medicine who are involved in the day-to-day care of adults, children, and families with palliative care needs.


Oxford Textbook of Palliative Care for Children
Ann Goldman, Richard Hain and Stephen Liben

This book provides a practical and informative guide which promotes a model of care that is sufficiently flexible to address the complex and multifaceted needs of children with life-threatening illnesses and their families. The editors identify the medical, psychological and practical issues of caring for terminally ill children and their families.

It is the first authoritative, systematic and comprehensive text to define the increasingly important and evolving specialty of paediatric palliative care. It explores both the clinical aspects and the multidimensional and holistic nature of care for the dying child, based on the knowledge that all human experience has a physical, emotional, psychological and spiritual impact.


Procedure related cancer pain in children
by Liossi, Christina

Research has demonstrated that children with cancer and their parents regards procedure-related pain as one of the most difficult parts of having cancer, and their distress continues years after the completion of anti-cancer treatment.

This is a practical 'how to' book that will provide readers with the knowledge, skills, structure and techniques to help young patients and their families to cope with painful medical procedures. The author has gathered together over 10 years experience in clinical paediatric oncology and palliative care to provide a concise overview of procedure-related pain.

The book describes the pharmacological and psychological methods of pain relief and how they may be combined, along with the difficulties that may be encountered in their implementation. It also encourages better integration between research work and clinical practice.

www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1279924


Making Every Moment Count
By Leora Kuttner, PhD
National Film Board of Canada

Thoughtful and evocative, this new video addresses the complex issues surrounding end-of-life care for children. Psychologist and award-winning filmmaker Leora Kuttner, PhD, profiles five children with life threatening illness, and the families and health professionals who support them. The film clearly shows that, despite popular belief, children can talk about end-of-life issues if given proper support, and that doing so can help both them and their families cope with the realities of their situation.

The film focuses on the emotional and psychological aspects of pediatric palliative care. It features deeply caring physicians, nurses, therapists and others working with families whose children range from newborns to teenagers. Their care takes place in the hospital, in hospice programs and at home. Designed for health and social service professionals and students, this program is also compelling viewing for families and anyone caring for seriously ill children, as well as for the general public.

www.fanlight.com/catalog/films/405_memc.php


• Basic symptom control in paediatric palliative care 2005

The 2005 edition of Rainbow Children’s Hospice Guidelines: Basic symptom control in paediatric palliative care (written by Dr Satbir Singh Jassal) is now available as a free download on the ACT website: http://www.act.org.uk
The What’s New section gives details of upcoming conferences and you can also enter details of your service for inclusion in the International Directory of Children’s Palliative Care and Hospice Services now under development. Please visit http://www.act.org.uk

• PaedPalCare – An international email discussion group for those working with children with life-limiting conditions. The group is hosted by ACT and currently has over 600 members across the world. To join the group send a blank email to

• Guide to the Development of Children’s Palliative Care Services – 2nd edition, a joint publication from ACT and the Royal College of Paediatrics and Child Health, reflects the many recent changes in children’s palliative care in the UK. The Guide is available to ACT members for £5 and to non-members for £10. Order via the ACT website at http://www.act.org.uk or mailto:

• Materials on paediatric palliative care.
IPPC – the Initiative for Pediatric Palliative Care – a consortium of organisations that work together to improve care and quality of life of children and families. It is an initiative of EDC’s Centre for Applied Ethics and Professional Practice (CAEP). Website offers some useful resources including quality improvement tools, videos and a curriculum which is under development. More resources are planned – you may have to register to download tools. Website: http://www.ippcweb.org

• Cancer Pain Relief and Palliative Care in Children, WHO, 1998
Available in English, French, Spanish and Italian.
To order: Email:


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