Informed consent for teaching patient in california

WHAT IS INFORMED CONSENT?

Informed consent is more than merely your agreement to a particular treatment or procedure. Informed consent is your agreement to a proposed course of treatment based on receiving clear, understandable information about the treatment's potential benefits and risks. 1 You must also be informed about all treatments available for your health condition, and the risks of receiving no treatment.

WHY IS INFORMED CONSENT IMPORTANT TO ME?

You must take an active role in order to receive high quality health care. The first step is having the appropriate information about your medical condition. Once you know about all the risks, benefits and treatment alternatives, you may decide the risks are too great or the benefits too few to justify undergoing the treatment. With this kind of information, you may choose to refuse the treatment by withholding your consent.

IS MY INFORMED CONSENT ALWAYS REQUIRED FOR ALL MEDICAL TESTS OR PROCEDURES?

Most of the time, yes. While your informed consent is usually required, there are two exceptions where your doctor does not need to have your informed consent before beginning treatment.

Simple and Common Exception:
The first occurs when a "simple and common" procedure, such as a typical blood screening is performed. When risks from such procedures are commonly understood to be remote, your doctor need not discuss the risks, benefits or alternatives to the procedure with you. 2 You must still agree to the procedure, however, before it is done.

Emergency Exception:
The second situation is in a life-threatening emergency. This is known as the Emergency Exception. 3

An "emergency" is defined for purposes of this exception as a situation requiring immediate treatment of a medical condition that would otherwise lead to serious disability or death. 4

Yes. Your doctor has a duty to fully inform you about all of the risks and benefits of suggested treatments in terms you can understand.

HOW DO I GIVE THE DOCTOR INFORMED CONSENT?

Informally
Often, your informed consent comes informally in the course of discussion with your doctor during a routine office visit or similar situation.

Formally
Informed consent can also be given formally, by signing a document that states your doctor has fully discussed a treatment or procedure with you and that you have acknowledged and agreed to the risks. In a formal consent, you are usually asked to sign a form titled "Informed Consent to Treatment," or something similar. This is especially true in situations involving hospitalization, surgery or invasive testing.

Another circumstance in which specific disclosures and obligation of physicians to you are mandated by law is the area of human experimentation and research. 15 Federal law has established extensive regulations governing federally funded biomedical and behavioral research. 16

WHEN SHOULD MY DOCTOR DISCUSS THE RISKS AND BENEFITS OF A PROPOSED COURSE OF TREATMENT AND ANY TREATMENT ALTERNATIVES WITH ME?

Any discussion of a proposed course of treatment must take place BEFORE the treatment is given. 17

You are sometimes asked, as a routine part of filling out medical history and personal information forms, to sign an informed consent document. This sometimes happens before you see the doctor or care provider and before you have had the treatment and/or any alternatives explained and before there has been any chance to ask any questions.

Never sign any such document until AFTER there has been a full opportunity to have all of your questions answered and concerns discussed.

WHAT KINDS OF QUESTIONS SHOULD I ASK SO I CAN GIVE "INFORMED CONSENT?"