Both medical and psychiatric advance directives relate to medical decisions for patients. While psychiatric advance directives cover psychiatric care, medical advance directives relate to general healthcare decisions.
According to the American Psychiatric Association, “Psychiatric advance directives (PADs) provide an opportunity for patients to outline their preferences about their mental health treatment if they become unable to make such decisions for themselves in the future.” They provide patients with autonomy and dignity even in the face of incapacitation. It can cover medication handling, future hospitalizations, emergency care planning, and the nomination of proxies (trusted decision-makers).
A medical advance directive is a way for patients to express their preferences for medical care in case if they can’t make decisions themselves. These decisions are generally placed in a patient's living will and can vary. Some may specify treatment and interventions or end-of-life care.
Legislation has advanced over the last four decades. A study from the Journal of the American Geriatrics Society stated, “The Patient Self-Determination Act (PSDA) was passed in 1991 and requires hospitals, skilled nursing facilities, home healthcare agencies, and providers of home health care to provide patients with a written summary of patients’ healthcare decision-making rights and the facilities’ policies concerning advance directives.”
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Informed consent is when a patient is given all the necessary information about a treatment or procedure.
EHRs can be used to track consent and store patients' approval.
A medical directive outlines a person's preferences related to general medical care.