Informed Consent (cont.)
IN THIS ARTICLE
In order for you to give your informed consent for treatment or tests, the doctor or health care provider must give (or disclose) to you enough information so that you can make an informed decision. It is not necessary or expected that you would receive every detail of the test, treatment, or procedure. You need only the information that would be expected by a reasonable person to make an intelligent decision. This information should include the risks and likelihood (or probability) of each of the risks, and the benefits, and likelihood (or probability) of benefit. Any questions you have should be fully explained, in language and terminology that you can understand.
Documentation of Consent
For many tests and procedures, such as routine blood tests, X-rays, and splints or casts, consent is implied. No written documentation of the consent process is obtained. For many invasive tests or for treatments with significant risk, you should be given a written consent form and a verbal explanation, both preferably in your native language.
The following components should be discussed and included in the written consent form. If they are not, you should request that information:
The consent form should be signed and dated both by the doctor and by you, as the patient. You would sign for your child. You may ask for a copy of the signed consent form.
Medically Reviewed by a Doctor on 12/24/2015
Richard A Wagner, MD, PhD
James E Keany, MD, FACEP
Francisco Talavera, PharmD, PhD
Jeter (Jay) Pritchard Taylor III, MD
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