Abstract
Good end of life care always requires preparation, but this is especially so in neurological disease, where the signs of impending death can be unclear and there may be a substantial period of mental incapacity. A sensitive process of advance care planning can enable both patient and family to face what lies ahead and makes choices about what style of care would be preferred. It also facilitates both psychological and spiritual preparedness and also an awareness of what symptoms are likely to occur and how they can be managed. Achieving all this needs cooperation and mutual learning between neurology, palliative care, and rehabilitation, in addition to support for long-term care staff who may be involved. Symptoms, which will center around issues of breathing, restlessness, hydration, and pain, have to be anticipated and appropriate drugs made available for their management. Ventilation, whether noninvasive or via tracheostomy, deserves careful consideration with respect both to starting it and to when and how it may be withdrawn. The importance of good care at the end of life cannot be overestimated, as this phase of the illness leaves a powerful impression in the minds of those who were close to the patient and is influential in shaping their attitudes both to illness and to healthcare.
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References
Bromberg MN, Liow M, Forshew DA, Swenson M. A time line for predicting durable medical equipment needs for ALS/MND patients. Proceedings of the 9th international symposium on ALS/MND. Munich: International Alliance of ALS/MND Associations; 1998.
O’Brien T, Kelly M, Saunders C. Motor neurone disease: a hospice perspective. BMJ. 1992;304:471–3.
Aboussouan LS, Khan SU, Meeker DP, Stehnach K, Mitsumoto H. Effect of non-invasive positive pressure ventilation on survival in ALS. Ann Intern Med. 1997;127:450–3.
Henry C, Seymour JE. Advance care planning: a guide for health and social care professionals. Leicester: National End of Life Care Programme; 2008.
Fries JF, Everett Koop C, Sokolov J, Beadle CE, Wright D. Beyond health promotion: reducing need and demand for medical care. Health care reforms to improve health while reducing costs. Health Aff (Millwood). 1998;17:70–84.
Wilkinson AM. Advance directives and advance care planning: the US experience. In: Thomas K, Lobo B, editors. Advance care planning in end of life care. Oxford: University Press; 2011. p. 189–204.
Hinton J. Which patients with terminal cancer are admitted from home care? Palliat Med. 1994;8:197–210.
Davison SN, Simpson C. Hope and advance care planning in patients with end stage renal disease: qualitative interview study. BMJ. 2006;333:886–90.
Calman KC. Quality of life in cancer patients – an hypothesis. J Med Ethics. 1984;10:124–7.
McCoubrie RC, Davies AN. Is there a correlation between spirituality and anxiety and depression in patients with advanced cancer? Support Care Cancer. 2006;14:379–85.
Neudert C, Oliver D, Wasner M, Borasio GD. The course of the terminal phase in patients with amyotrophic lateral sclerosis. J Neurol. 2001;248:612–6.
Thomas K, Sawkins N. The gold standards framework in care homes training programme: good practice guide. Walsall: Gold Standards Framework Programme; 2008.
The Liverpool Care Pathway for the Dying Patient. Liverpool: Marie Curie Palliative Care Institute. http://www.liv.ac.uk/mcpcil/liverpool-care-pathway/. Accessed 8 Sept 2012.
Hockley J, Watson J, Oxenham D, Murray SA. The integrated implementation of two end-of-life care tools in nursing care homes in the UK: an in-depth evaluation. Palliat Med. 2010;24:828–38.
Turner-Stokes L, Sykes N, Silber E, Khatri A, Sutton L, Young E. From diagnosis to death: exploring the interface between neurology, rehabilitation and palliative care in the management of people with long-term neurological conditions. Clin Med. 2007;7:129–36.
Edmonds P, Hart S, Wei G, Vivat B, Burman R, Silber E, Higginson IJ. Palliative care for people severely affected by multiple sclerosis: evaluation of a novel palliative care service. Multiple Sclerosis. 2010;16:627–36.
Dalal S, Del Fabbro E, Bruera E. Is there a role for hydration at the end of life? Curr Opin Support Palliat Care. 2009;3:72–8.
Dy SM. Enteral and parenteral nutrition in terminally ill cancer patients: a review of the literature. Am J Hosp Palliat Care. 2006;23:369–77.
Wee B, Hillier R. Interventions for noisy breathing in patients near to death. Cochrane Database Syst Rev 2008; 1:CD005177. doi: 10.1002/14651858.CD005177.pub2.
LeBon B, Fisher S. Case report: maintaining and withdrawing long-term invasive ventilation in a patient with MND/ALS in a home setting. Palliat Med. 2010;25:262–5.
Jennings AL, Davies AN, Higgins JPT, Anzures-Cabrera J, Broadley KE. Opioids for the palliation of breathlessness in advanced disease and terminal illness. Cochrane Database Syst Rev 2001; 4: CD002066. doi: 10.1002/14651858.CD002066.
Simon ST, Higginson IJ, Booth S, Harding R, Bausewein C. Benzodiazepines for the relief of breathlessness in advanced malignant and non-malignant diseases in adults. Cochrane Database Syst Rev 2010; 1:CD007354. doi: 10.1002/14651858.CD007354.pub2.
Ventafridda V, Spoldi E, De Conno F. Control of dyspnoea in advanced cancer patients. Chest. 1990;6:1544–5.
Latimer EJ. Ethical decision-making in the care of the dying and its applications to clinical practice. J Pain Symptom Manage. 1991;6:329–36.
Cherny N, Radbruch L. European Association for Palliative Care (EAPC) recommended framework for the use of sedation in palliative care. Palliat Med. 2009;23:581–93.
Sykes NP, Thorns A. The use of opioids and sedatives at the end of life. Lancet Oncol. 2003;4:312–8.
Oliver D. Opioid medication in the palliative care of motor neurone disease. Palliat Med. 1998;12:113–5.
Healthcare Commission. Spotlight on complaints. London: Healthcare Commission; 2007.
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Sykes, N.P. (2013). Care at the End of Life. In: Oliver, D. (eds) End of Life Care in Neurological Disease. Springer, London. https://doi.org/10.1007/978-0-85729-682-5_8
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