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The Patient Self-Determination Act (PSDA) was passed by the United States Congress in 1990 as an amendment to the Omnibus Budget Reconciliation Act of 1990.Effective on December 1, 1991, this legislation required many hospitals, nursing homes, home health agencies, hospice providers, health maintenance organizations (HMOs), and other health care institutions to provide information about ...
The public's response was to press for further legislative support. The most recent result was the Patient Self-Determination Act of 1990, [21] which attempted to address this awareness problem by requiring health care institutions to better promote and support the use of advance directives. [22] [23]
The Federal Patient Self-Determination Act (PSDA) requires health care institutions to provide newly admitted adult patients with information regarding advance health care directives. [6] The intent of this law is to make patients aware of their rights with regard to end-of-life care .
An advance directive allows an individual to state what treatments he or she would want in a medical crisis, but it is not a medical order. [4] Advance directives are not portable in a sense that it is not accessible across medical systems, so it is the individual's responsibility to have the form on them at all times. [ 4 ]
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A person will typically have these conversations with their doctor and ultimately record their preferences in an advance healthcare directive. [9] An advance healthcare directive is a legal document that either documents a person's decisions about desired treatment or indicates who a person has entrusted to make their care decisions for them ...
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