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Palliative care to support the needs of adults with neurological disease.

Kluger, Benzi M, Hudson, Peter, Hanson, Laura C, Bužgovà, Radka, Creutzfeldt, Claire J, Gursahani, Roop, Sumrall, Malenna, White, Charles, Oliver, David J., Pantilat, Steven Z, and others. (2023) Palliative care to support the needs of adults with neurological disease. The Lancet. Neurology, 22 (7). pp. 619-631. ISSN 1474-4465. (doi:10.1016/S1474-4422(23)00129-1) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:101982)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. (Contact us about this Publication)
Official URL:
https://doi.org/10.1016/S1474-4422(23)00129-1

Abstract

Neurological diseases cause physical, psychosocial, and spiritual or existential suffering from the time of their diagnosis. Palliative care focuses on improving quality of life for people with serious illness and their families by addressing this multidimensional suffering. Evidence from clinical trials supports the ability of palliative care to improve patient and caregiver outcomes by the use of outpatient or home-based palliative care interventions for people with motor neuron disease, multiple sclerosis, or Parkinson's disease; inpatient palliative care consultations for people with advanced dementia; telephone-based case management for people with dementia in the community; and nurse-led discussions with decision aids for people with advanced dementia in long-term care. Unfortunately, most people with neurological diseases do not get the support that they need for their palliative care under current standards of healthcare. Improving this situation requires the deployment of routine screening to identify individual palliative care needs, the integration of palliative care approaches into routine neurological care, and collaboration between neurologists and palliative care specialists. Research, education, and advocacy are also needed to raise standards of care. [Abstract copyright: Copyright © 2023 Elsevier Ltd. All rights reserved.]

Item Type: Article
DOI/Identification number: 10.1016/S1474-4422(23)00129-1
Uncontrolled keywords: Long-Term Care, Palliative Care, Quality of Life, Adult, Dementia, Humans, Caregivers
Subjects: H Social Sciences
Divisions: Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research > Tizard
Funders: University of Kent (https://ror.org/00xkeyj56)
SWORD Depositor: JISC Publications Router
Depositing User: JISC Publications Router
Date Deposited: 09 Aug 2023 15:26 UTC
Last Modified: 31 Aug 2023 10:14 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/101982 (The current URI for this page, for reference purposes)

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