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1 Accordingly, the patient may refuse to be informed about their medical condition and make a decision. An example would be the statement, \u201cI don't want to hear anything from you. I'm not going to the hospital.\u201d They may be informed and then refuse to make a decision. \u201cWow, that sounds bad either way.
3) In order for a patient to refuse treatment and/or transportation two events must occur to protect both the patient and yourself: 1) You must give the patient enough information about the decision Page 2 2 they are making so that there is an informed consent, and; 2) You must be satisfied that the patient has ...
3) In order for a patient to refuse treatment and/or transportation two events must occur to protect both the patient and yourself: 1) You must give the patient enough information about the decision Page 2 2 they are making so that there is an informed consent, and; 2) You must be satisfied that the patient has ...
The right to refuse treatment applies to those who cannot make medical decisions for themselves, as well as to those who can; the only difference is how we protect the rights of people who cannot make decisions for themselves (see VEN's free handbook Making Medical Decisions for Someone Else).
But to avoid legal and ethical ramifications, you must document such refusals properly. If your patient refuses treatment or medication, your first responsibility is to make sure that he's been informed about the possible consequences of his decision in terms he can understand.
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Explore Reasons Behind Refusal Patients may refuse treatments for many reasons, including financial concerns, fear, misinformation, and personal values and beliefs. Exploring these reasons with the patient may reveal a solution or a different approach.
Informed refusal is where a person has refused a recommended medical treatment based upon an understanding of the facts and implications of not following the treatment. Informed refusal is linked to the informed consent process, as a patient has a right to consent, but also may choose to refuse.
An adult patient with capacity has the right to refuse any medical treatment, even where that decision may lead to their death or the death of their unborn baby. This right exists even where the reasons for making the choice seem irrational, are unknown or even non-existent.
Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision. US federal regulations require a full, detailed explanation of the study and its potential risks.
The right to refuse treatment applies to those who cannot make medical decisions for themselves, as well as to those who can; the only difference is how we protect the rights of people who cannot make decisions for themselves (see VEN's free handbook Making Medical Decisions for Someone Else).

refusal medical treatment form