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The Impact of the Patient Self-Determination Act's Requirement That States Describe Law concerning Patients' Rights

Published online by Cambridge University Press:  01 January 2021

Joan M. Teno ,
Charles Sabatino ,
Lauren Parisier ,
Fenella Rouse  and
Joanne Lynn
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Extract

As of December 1991, the Patient Self-Determination Act (PSDA) mandated that health care institutions which receive funding from Medicare or Medicaid provide written information about persons rights to participate in medical decision-making and formulate advance directives. The PSDA required each state

…acting through a State agency, association, or other private nonprofit entity develop a written description of the law of the State (whether statutory or as recognized by the courts of the State) concerning advance directives that would be distributed by providers or organizations under the requirements of [the Act].

Type
Article
Information
Journal of Law, Medicine & Ethics , Volume 21 , Issue 1 , Spring 1993 , pp. 102 - 108
Copyright
Copyright © American Society of Law, Medicine and Ethics 1993

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References

Patient Self-Determination Act, in the Omnibus Budget Reconciliation Act of 1990, P.L. 101–508, sections 4206, 4751, enacted November 5, 1990.Google Scholar
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