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How Should Physicians Care for Dying Patients with Amyotrophic Lateral Sclerosis

Bibliographic Data

ID15744308
AuthorsAlexander Craig (0000-0003-1720-8687, University of California San Francisco Medical Center, corresponding author), Elizabeth Dzeng (0000-0001-5235-8053, University of California San Francisco Medical Center)
Year2018
Volume20
Issue8
PagesE690-698
Publication date2018-08-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueThe AMA Journal of Ethic (JOURNAL)
Journal identifiersISSN: 2376-6980 • E-ISSN: 2376-6980
PublisherAmerican Medical Association (PUBLISHER • US)
DOI10.1001/amajethics.2018.690
PMID30118418
OpenAlexW2887949085
LanguageEN
Citations received3
References cited2

We discuss physician aid in dying, euthanasia, and other dimensions of palliative care decision making and define relevant terms raised by this case of a dying patient with amyotrophic lateral sclerosis in Washington State who is unable to self-administer a lethal prescription. We then present a concrete framework that clinicians can directly apply when faced with difficult cases such as this one. We outline how exploring motivations, obtaining informed consent, defining goals, and examining alternatives can help guide physicians like the one in this case. We conclude by summarizing one way in which physicians might balance these issues while still remaining within the constraints of the law

Amyotrophic lateral sclerosis · Disease · Family medicine · Medical prescription · Palliative care · Ethics in medical practice · Healthcare Decision-Making and Restraints · Medicine · Nursing · Palliative Care and End-of-Life Issues · Psychology

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Unique citing works3
Citations per year0,38
Citation span2018 - 2026 (9)
Citation velocitycurrent
Highly citedNo
Citation typesNeutral: 3

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