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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 ...
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 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.
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 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 ...
The Case Management process encompasses communication and facilitates care along a continuum through effective resource coordination. The goals of Case Management include the achievement of optimal health, access to care and appropriate utilization of resources, balanced with the patient's right to self determination.
The Charter of Patients' Rights lists seventeen rights that patients are entitled to: [6] Right to information: Every patient has the right to know what is the illness that they are suffering, its causes, the status of the diagnosis (provisional or confirmed), expected costs of treatment. Furthermore, service providers should communicate this ...
Both legal and ethical issues are important in considering patient-based research. The American Nurses Association (ANA) has set up five basic rights for patient protection: Right to self-determination; Right to privacy and dignity; Right to anonymity and confidentiality; Right to fair treatment; Right to protection from discomfort and harm.