Informed refusal: Difference between revisions
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Latest revision as of 15:03, 17 March 2025
Informed refusal is a term used in the field of medicine and healthcare to describe a situation where a patient has been fully informed about the details of a needed medical treatment, including the potential risks and benefits, and has chosen to refuse the treatment.
Definition[edit]
Informed refusal is a legal and ethical term that refers to the patient's right to refuse recommended medical treatments. It is based on the principle of patient autonomy and the belief that patients should have the final say in decisions about their own healthcare.
Process[edit]
The process of informed refusal involves several steps. First, the healthcare provider must inform the patient about the nature of their illness or condition, the proposed treatment, the potential benefits and risks of the treatment, and any alternative treatments that may be available. This information must be presented in a way that the patient can understand.
Once the patient has been fully informed, they have the right to refuse the treatment if they wish. This refusal must be voluntary and not coerced. The healthcare provider must respect the patient's decision, even if they believe it is not in the patient's best interest.
Legal implications[edit]
Informed refusal has important legal implications. If a healthcare provider fails to fully inform a patient about a treatment and the patient subsequently suffers harm as a result, the provider could be held legally liable for medical malpractice.
Ethical considerations[edit]
From an ethical perspective, informed refusal is seen as a way to respect patient autonomy and promote shared decision-making in healthcare. However, it can also raise ethical dilemmas when a patient's refusal of treatment could lead to serious harm or death.


