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10 Asia Pacific J. Health L. & Ethics 5 (2016-2017)

handle is hein.journals/aspjhle10 and id is 1 raw text is: 



Asia Pacific Journal of Health Law & Ethics
Vol.10 No.1, December 2016,  pp.5-26




   Vulnerable Patients and End-of-Life Decision-Making




                            Leslie   E.  Wolf*,   Sylvia   Caley**



 Abstract

 Over several decades, U.S. physicians, medical ethicists, and policy-makers have worked to enhance
 patient decision-making at the end-of-life. States have passed laws allowing patients to express their
 preferences through advance directives and to appoint a surrogate to make decisions if they are unable
 to do so. Both the federal and state governments have provided incentives to encourage patients to
 complete advance directives and discuss their care preferences with their physicians. Despite these efforts,
 for a variety of reasons, few people actually complete an advance directive or appoint a health care
 surrogate. However, real world medical decision-making frequently deviates from the ideal of the
 empowered patient with capacity exercising her autonomy over what happens to her body. In this paper,
 we explore how the legal and ethical frameworks that have developed around end-of-life decision-making
 in the United States may fail in the case of the most vulnerable patients. We argue that it is time to
 shift the focus from patients to providers and the health care system to achieve the goal of improved
 end-of-life decision-making, and suggest specific ways toward making this transition.



Keywords  : Advance Directives, Decision Making, RVdnerable Populations, United States





   Over  several decades,  U.S. physicians, medical  ethicists, and policy-makers  have  worked
to  enhance  patient  decision-making   at the  end-of-life. States have  passed  laws  allowing
patients to express  their preferences  through  advance  directives, which  are usually written
but  may  be  oral, and to  appoint  a surrogate  to make  decisions  if they are unable  to  do
so. Both  the federal and  state governments   have  provided  incentives to encourage  patients
to  complete  advance   directives and discuss  their care preferences  with  their physicians.
   Despite  these efforts, for a variety of reasons, few  people  actually complete  an advance
directive or appoint  a health  care surrogate. Even  when   they do,  medical  decision-making


    JD,  MPH,  Professor of Law, Director, Center for Law, Medicine & Ethics, luwolf@gsu.edu
      Clinical Professor, Director of Health Law Partnership (HeLP), Co-director of HeLP Legal Services Clinic,
sbcaleyggsu.edu


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