
Amytrophic Lateral Sclerosis (or motor neurone disease) is a rare disease but one that can cause profound suffering for both the patient and their family. Whilst new treatments for ALS are being developed, these are not curative and offer only the potential to slow its progression. Palliative care must therefore be integral to the clinical approach to the disease. Palliative Care in Amyotrophic Lateral Sclerosis: From diagnosis to bereavement reflects the wide scope of this care; it must cover not just the terminal phase, but support the patient and their family from the onset of the disease. Both the multidisciplinary palliative care team and the neurology team are essential in providing a high standard of care and allowing quality of life (both patient and carer) to be maintained. Clear guidelines are provided to address care throughout the disease process. Control of symptoms is covered alongside the psychosocial care of patients and their families, culminating in discussion of bereavement. The experience of patients and families is considered and case studies are provided to show the practical application of the theoretical knowledge. Different models of care are explored, and this new edition utilises the increase in both the evidence-base and available literature on the subject. Additional chapters on nursing, spiritual care, decision making, and ethical issues surrounding end of life care ensure that this new edition remains the essential guide to palliative care in ALS.
This text investigates the necessity of integrating comprehensive palliative care into the clinical management of Amyotrophic Lateral Sclerosis (ALS) from the moment of diagnosis through to bereavement. The authors, experts in neurology and palliative medicine, argue that because current treatments for ALS are not curative, the focus must shift toward maintaining quality of life for both patients and their families. By synthesizing clinical guidelines with psychosocial support strategies, the book provides a framework for multidisciplinary teams to address the physical, ethical, and spiritual challenges inherent in the disease process.
What You Will Find
Experts recognize this work as a foundational resource for clinicians seeking to improve the standard of care for ALS patients. Readers frequently note the practical utility of the case studies and the comprehensive nature of the updated clinical guidelines provided in this edition.
Page Count:
364
Publication Date:
2006-11-09
Publisher:
OUP Oxford
ISBN-10:
0199212937
ISBN-13:
9780199212934
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