Radio frequency consent form 2025

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Ideally, the consent process should include a clear understanding of the patients health condition, explanation of the procedure, discussion of benefits, risks, and alternatives to the procedure. The purpose of this article is to describe the ideal consent process focused on an interventional radiology practice.
At a minimum, a well-designed informed consent form will address the following information: Risks and benefits of treatment. Fees and payment policies. Confidentiality and its limits. Contact information and communication. Social media policy and general boundaries. Emergency procedures.
The consent document must include the patients name, healthcare practitioners name, diagnosis, proposed treatment plan, alternatives, potential risks, complications, and benefits. Additionally, the consent document must be signed and dated by the patient (or the patients legal guardian or representative).
To be valid, consent must be voluntary, informed, specific, current, and given by a person with capacity. Unless otherwise indicated, consent can be express or implied, written or verbal.
Informed consent language should be written in the second person (you), not in the first person (I). Minimize passive voice to the extent possible. Example of passive voice: A summary of results will be sent to all study participants. Example of active voice: We will send you a summary of the results.
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If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.

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