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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 mature minor doctrine is a rule of law found in the United States and Canada accepting that an unemancipated minor patient may possess the maturity to choose or reject a particular health care treatment, sometimes without the knowledge or agreement of parents, and should be permitted to do so. [1]
Self-determination is a ... of children by analyzing ... way of promoting patient autonomy. For example, self-testing medical procedures which have become ...
The Patient Self-Determination Act guarantees a patient's right to formally designate a surrogate to make treatment decisions for the patient if the patient becomes unable to make their own decisions. A surrogate decision-maker, or durable power of attorney for health care (DPA/HC), must be documented.
Edozien challenges the widely accepted method of securing a patient's self-determination: securing their consent. He argues against it while presenting an alternative property model, where a patient's body and its integrity must be protected from invasions, and where the right of a patient's to access to comprehensible information upon which a rational decision can be made is considered a ...
The 1991 Patient Self-Determination Act passed by the US Congress at the request of the financial arm of Medicare does permit elderly Medicare/Medicaid patients (and by implication, all "terminal" patients) to prepare an advance directive in which they elect or choose to refuse life-extending and/or life-saving treatments as a means of ...
Dignity of risk is the idea that self-determination and the right to take reasonable risks are essential for dignity and self esteem and so should not be impeded by excessively-cautious caregivers, concerned about their duty of care.
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]