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

Journal of Law, Medicine and Ethics 21 (1):102-107 (1993)
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Abstract

As of December 1991, the Patient Self-Determination Act 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 concerning advance directives that would be distributed by providers or organizations under the requirements of [the Act].

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The Patient Self-Determination Act.Elizabeth Leibold McCloskey - 1991 - Kennedy Institute of Ethics Journal 1 (2):163-169.

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