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Informed Consent: A Patient's Right to
Know
Your health care provider is responsible for providing enough information
for you to make an informed decision about your treatment options. The
information sharing process prior to making a treatment decision is called
informed consent. Before performing any non-emergency procedure or
treatment, your health care provider must have a signed consent form
reflecting that:
you
understand the nature of the treatment and the treatment process
you understand the
possible benefits and risks
you give your permission
to proceed with the treatment
Your health care provider is required to
provide the following information to you about any treatment or procedure.
the
treatment to be given, or procedure to be performed
the possible risks and
benefits that are likely to occur
the reasons for giving
the treatment or performing the procedure
the expected outcome
with and without the treatment or procedure
the alternatives to
receiving the treatment or having the procedure
It is important to read the consent form
carefully. Ask questions about anything you do not understand. If you do
not agree with something on the form, discuss the changes you wish to make
with your health care provider. Keep in mind, you always have the right to
refuse a treatment or procedure if you so desire.
The informed consent process is standard procedure in most hospitals,
clinics, and doctors' offices. However, it may not be as routine in other
environments. Although informed consent is your right as a patient, you
and your health care providers share responsibility for making sure you
are adequately informed. It is important to ask questions and learn what
you can before you proceed with any form of treatment.
Patients' Bill of Rights and Responsibilities
President William Clinton established the Advisory Commission on Consumer
Protection and Quality on the Health Care Industry in November 1997. As
part of its work, the Commission issued the Patients' Bill of Rights and
Responsibilities in 1998. The document has three goals:
to
strengthen consumer confidence that the health care system is fair and
responsive to consumer needs
to reaffirm the
importance of a strong relationship between patients and their health
care providers
to reaffirm the critical
role consumers play in safeguarding their own health
While the Commissions' recommendations are not legally
binding, they express the beliefs of some of the nation's leading health
care experts and patient advocates. The Patients' Bill of Rights and
Responsibilities outlines seven sets of rights and one set of
responsibilities.
The Right to Information
- Patients have the right to receive accurate, easily understood
information to assist them in making informed decisions about their
health plans, facilities, and [health care] professionals.
The Right to Choose
- Patients have the right to a choice of health care providers that is
sufficient to assure access to appropriate high-quality health care
including … giving patients with serious medical conditions and chronic
illnesses access to specialists.
Access to Emergency Services
- Patients have the right to access emergency health services when and
where the need arises.
Being a Full Partner in
Health Care Decisions - Patients have the right to fully
participate in all decisions related to their health care. Consumers who
are unable to fully participate in treatment decisions have the right to
be represented by parents, guardians, family members, or other
conservators.
Care Without Discrimination
- Patients have the right to considerate, respectful care
from all members of the health care industry at all times and under all
circumstances. Patients must not be discriminated against in the
marketing or enrollment or in the provision of health care services,
consistent with the benefits covered in their policy and/or as required
by law, based on race, ethnicity, national origin, religion, sex, age,
current or anticipated mental or physical disability, sexual
orientation, genetic information, or source of payment.
The Right to Privacy
- Patients have the right to communicate with health care providers in
confidence and to have the confidentiality of their individually
identifiable health care information protected. Patients also have the
right to review and copy their own medical records and request
amendments to their records.
The Right to Speedy Complaint
Resolution - Patients have the right to a fair and efficient
process for resolving differences with their health plans, health care
providers, and the institutions that serve them, including a rigorous
system of internal review and an independent system of external review.
Taking on New
Responsibilities - In a health care system that affords
patients rights and protections, patients must also take greater
responsibility for maintaining good health.
In recent years, most states have passed legislation
addressing specific aspects of patients' rights, especially with respect
to members of health maintenance organizations. Several national patients'
rights bills have been introduced. However to date, the bills have failed
to pass both Houses of Congress. Many health care professional
organizations and patient advocacy groups continue to push for a national
Patients' Bill of Rights to establish minimum standards for all health
care insurance plans.
Despite the absence of a national Patients' Bill of
Rights, most hospitals and large clinics have already developed their own
list of Patients' Rights. Clients are usually provided with a copy of an
institution's list of Patients' Rights when they are receiving care at
that facility. If you have not been given such a document, ask if one
exists. These documents often provide helpful information about whom to
contact during the course of your care if you have questions or concerns.
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