MN Patients’ Bill of Rights

Rev. 07/01/2007
Minnesota Patients’ Bill of Rights
Legislative Intent
It is the intent of the Legislature and the purpose of this statement to promote the interests
and well-being of the patients of health care facilities. No health care facility may require a
patient to waive these rights as a condition of admission to the facility. Any guardian or
conservator of a patient or, in the absence of a guardian or conservator, an interested person,
may seek enforcement of these rights on behalf of a patient. An interested person may also
seek enforcement of these rights on behalf of a patient who has a guardian or conservator
through administrative agencies or in probate court or county court having jurisdiction over
guardianships and conservatorships. Pending the outcome of an enforcement proceeding the
health care facility may, in good faith, comply with the instructions of a guardian or
conservator. It is the intent of this section that every patient’s civil and religious liberties,
including the right to independent personal decisions and knowledge of available choices, shall
not be infringed and that the facility shall encourage and assist in the fullest possible exercise of
these rights.

Definitions
For the purposes of this statement, “patient” means a person who is admitted to an acute care
inpatient facility for a continuous period longer than 24 hours, for the purpose of diagnosis or
treatment bearing on the physical or mental health of that person. “Patient” also means a
minor who is admitted to a residential program as defined in Section 7, Laws of Minnesota
1986, Chapter 326. For purposes of this statement, “patient” also means any person who is
receiving mental health treatment on an out-patient basis or in a community support program
or other community-based program.

Public Policy Declaration
It is declared to be the public policy of this state that the interests of each patient be protected
by a declaration of a patient’s bill of rights which shall include but not be limited to the rights
specified in this statement.

1. Information about Rights
Patients shall, at admission, be told that there are legal rights for their protection during
their stay at the facility or throughout their course of treatment and maintenance in the
community and that these are described in an accompanying written statement of the
applicable rights and responsibilities set forth in this section. In the case of patients
admitted to residential programs as defined in Section 7, the written statement shall also describe the right of a person 16 years old or older to request release as provided in Section
253B.04, Subdivision 2, and shall list the names and telephone numbers of individuals and
organizations that provide advocacy and legal services for patients in residential programs.
Reasonable accommodations shall be made for those with communication impairments,
and those who speak a language other than English. Current facilities policies, inspection
findings of state and local health authorities, and further explanation of the written
statement of rights shall be available to patients, their guardians or their chosen
representatives upon reasonable request to the administrator or other designated staff
person, consistent with chapter 13, the Data Practices Act, and Section 626.557, relating to
vulnerable adults.

2. Courteous Treatment
Patients have the right to be treated with courtesy and respect for their individuality by
employees of or persons providing service in a health care facility.

3. Appropriate Health Care
Patients shall have the right to appropriate medical and personal care based on individual
needs. This right is limited where the service is not reimbursable by public or private
resources.

4. Physician’s Identity
Patients shall have or be given, in writing, the name, business address, telephone number,
and specialty, of any, of the physician responsible for coordination of their care. In cases
where it is medically inadvisable, as documented by the attending physician in a patient’s
care record, the information shall be given to the patient’s guardian or other person
designated by the patient as his or her representative.

5. Relationship with Other Health Services
Patients who receive services from an outside provider are entitled, upon request, to be
told the identity of the provider. Information shall include the name of the outside provider,
the address, and a description of the service which may be rendered. In cases where it is
medically inadvisable, as documented by the attending physician in a patient’s care record,
the information shall be given to the patient’s guardian or other person designated by the
patient as his or her representative.

6. Information about Treatment
Patients shall be given by their physicians complete and current information concerning
their diagnosis, treatment, alternatives, risks and prognosis as required by the physician’s
legal duty to disclose. This information shall be in terms and language the patients can
reasonably be expected to understand. Patients may be accompanied by a family member
or other chosen representative, or both. This information shall include the likely medical or
major psychological results of the treatment and its alternatives. In cases where it is
medically inadvisable, as documented by the attending physician in a patient’s medical
record, the information shall be given to the patient’s guardian or other person designated
by the patient as his or her representative. Individuals have the right to refuse this
information.

Every patient suffering from any form of breast cancer shall be fully informed, prior to or at
the time of admission and during her stay, of all alternative effective methods of treatment
of which the treating physician is knowledgeable, including surgical, radiological, or
chemotherapeutic treatments or combinations of treatments and the risks associated with
each of those methods.

7. Participation in Planning Treatment
Notification of Family Members:

(a.) Patients shall have the right to participate in the planning of their health care. This
right includes the opportunity to discuss treatment and alternatives with individual
caregivers, the opportunity to request and participate in formal care conferences,
and the right to include a family member or other chosen representative, or both.
In the event that the patient cannot be present, a family member or other
representative chosen by the patient may be included in such conferences. A
chosen representative may include a doula of the patient’s choice.

(b.) If a patient who enters a facility is unconscious or comatose or is unable to
communicate, the facility shall make reasonable efforts as required under
paragraph (c) to notify either a family member or a person designated in writing by
the patient as the person to contact in an emergency that the patient has been
admitted to the facility. The facility shall allow the family member to participate in
treatment planning, unless the facility knows or has reason to believe the patient
has an effective advance directive to the contrary or knows the patient has
specified in writing that they do not want a family member included in treatment
planning. After notifying a family member but prior to allowing a family member to
participate in treatment planning, the facility must make reasonable efforts,
consistent with reasonable medical practice, to determine if the patient has
executed an advance directive relative to the patient’s health care decisions. For
purposes of this paragraph, “reasonable efforts” include:
(1.) examining the personal effects of the patient;
(2.) examining the medical records of the patient in the possession of the facility;
(3.) inquiring of any emergency contact or family member contacted whether the
patient has executed an advance directive and whether the patient has a
physician to whom the patient normally goes for care; and
(4.) inquiring of the physician to whom the patient normally goes for care, if
known, whether the patient has executed an advance directive. If a facility
notifies a family member or designated emergency contact or allows a family
member to participate in treatment planning in accordance with this
paragraph, the facility is not liable to the patient for damages on the grounds
that the notification of the family member or emergency contact or the
participation of the family member was improper or violated the patient’s
privacy rights.

(c.) In making reasonable efforts to notify a family member or designated emergency
contact, the facility shall attempt to identify family members or a designated
emergency contact by examining the personal effects of the patient and the
medical records of the patient in the possession of the facility. If the facility is
unable to notify a family member or designated emergency contact within 24 hours
after the admission, the facility shall notify the county social service agency or local
law enforcement agency that the patient has been admitted and the facility has
been unable to notify a family member or designated emergency contact. The
county social service agency and local law enforcement agency shall assist the
facility in identifying and notifying a family member or designated emergency
contact. A county social service agency or local law enforcement agency that assists
a facility is not liable to the patient for damages on the grounds that the notification
of the family member or emergency contact or the participation of the family
member was improper or violated the patient’s privacy rights.

8. Continuity of Care
Patients shall have the right to be cared for with reasonable regularity and continuity of
staff assignment as far as facility policy allows.

9. Right to Refuse Care
Competent patients shall have the right to refuse treatment based on the information
required in Right No. 6. In cases where a patient is incapable of understanding the
circumstances but has not been adjudicated incompetent, or when legal requirements limit
the right to refuse treatment, the conditions and circumstances shall be fully documented
by the attending physician in the patient’s medical record.

10. Experimental Research
Written, informed consent must be obtained prior to patient’s participation in
experimental research. Patients have the right to refuse participation. Both consent and
refusal shall be documented in the individual care record.

11. Freedom from Maltreatment
Patients shall be free from maltreatment as defined in the Vulnerable Adults Protection
Act. “Maltreatment” means conduct described in Section 626.5572, Subdivision 15, or the
intentional and nontherapeutic infliction of physical pain or injury, or any persistent course of conduct intended to produce mental or emotional distress. Every patient shall
also be free from nontherapeutic chemical and physical restraints, except in fully
documented emergencies, or as authorized in writing after examination by a patients’
physician for a specified and limited period of time, and only when necessary to protect
the patient from self-injury or injury to others.

12. Treatment Privacy
Patients shall have the right to respectfulness and privacy as it relates to their medical and
personal care program. Case discussion, consultation, examination, and treatment are
confidential and shall be conducted discreetly. Privacy shall be respected during toileting,
bathing, and other activities of personal hygiene, except as needed for patient safety or
assistance.

13. Confidentiality of Records
Patients shall be assured confidential treatment of their personal and medical records,
and may approve or refuse their release to any individual outside the facility. Copies of
records and written information from the records shall be made available in accordance
with this subdivision and Section 144.335. This right does not apply to complaint
investigations and inspections by the department of health, where required by third party
payment contracts, or where otherwise provided by law.

14. Disclosure of Services Available
Patients shall be informed, prior to or at the time of admission and during their stay, of
services which are included in the facility’s basic per diem or daily room rate and that
other services are available at additional charges. Facilities shall make every effort to
assist patients in obtaining information regarding whether the Medicare or Medical
Assistance program will pay for any or all of the aforementioned services.

15. Responsive Service
Patients shall have the right to a prompt and reasonable response to their questions and
requests.

16. Personal Privacy
Patients shall have the right to every consideration of their privacy, individuality, and
cultural identity as related to their social, religious, and psychological well-being.

17. Grievances
Patients shall be encouraged and assisted, throughout their stay in a facility or their
course of treatment, to understand and exercise their rights as patients and citizens.
Patients may voice grievances and recommend changes in policies and services to facility
staff and others of their choice, free from restraint, interference, coercion, discrimination,
or reprisal, including threat of discharge. Notice of the grievance procedure of the facility
or program, as well as addresses and telephone numbers for the Office of Health Facility
Complaints and the area nursing home ombudsman pursuant to the Older Americans Act,
Section 307 (a)(12) shall be posted in a conspicuous place.
Every acute care in-patient facility, every residential program as defined in Section 7, and
every facility employing more than two people that provides out-patient mental health
services shall have a written internal grievance procedure that, at a minimum, sets forth
the process to be followed; specifies time limits, including time limits for facility response;
provides for the patient to have the assistance of an advocate; requires a written
response to written grievances; and provides for a timely decision by an impartial
decision-maker if the grievance is not otherwise resolved. Compliance by hospitals,
residential programs as defined in Section 7 which are hospital-based primary treatment
programs, and outpatient surgery centers with Section 144.691 and compliance by health
maintenance organizations with Section 62D.11 is deemed to be in compliance with the
requirement for a written internal grievance procedure.

18. Communication Privacy
Patients may associate and communicate privately with persons of their choice and enter
and, except as provided by the Minnesota Commitment Act, leave the facility as they
choose. Patients shall have access, at their expense, to writing instruments, stationery,
and postage. Personal mail shall be sent without interference and received unopened
unless medically or programmatically contraindicated and documented by the physician in
the medical record. There shall be access to a telephone where patients can make and
receive calls as well as speak privately. Facilities which are unable to provide a private
area shall make reasonable arrangements to accommodate the privacy of patients’ calls.
This right is limited where medically inadvisable, as documented by the attending
physician in a patient’s care record. Where programmatically limited by a facility abuse
prevention plan pursuant to the Vulnerable Adults Protection Act, Section 626.557,
Subdivision 14, Paragraph (b), this right shall also be limited accordingly.

19. Personal Property
Patients may retain and use their personal clothing and possessions as space permits,
unless to do so would infringe upon rights of other patients, and unless medically or
programmatically contraindicated for documented medical, safely, or programmatic
reasons. The facility may, but is not required to, provide compensation for or replacement
of lost or stolen items.

20. Services for the Facility
Patients shall not perform labor or services for the facility unless those activities are
included for therapeutic purposes and appropriately goal-related in their individual
medical record.

21. Protection and Advocacy Services
Patients shall have the right of reasonable access at reasonable times to any available
rights protection services and advocacy services so that the patient may receive assistance
in understanding, exercising, and protecting the rights described in this Section and in
other law. This right shall include the opportunity for private communication between the
patient and a representative of the rights protection service or advocacy service.

22. Right to Communication Disclosure and Right to Associate
Upon admission to a facility, where federal law prohibits unauthorized disclosure of
patient identifying information to callers and visitors, the patient, or the legal guardian or
conservator of the patient, shall be given the opportunity to authorize disclosure of the
patient’s presence in the facility to callers and visitors who may seek to communicate with
the patient. To the extent possible, the legal guardian or conservator of the patient shall
consider the opinions of the patient regarding the disclosure of the patient’s presence in
the facility

The patient has the right to visitation by an individual the patient has appointed as the
patient’s health care agent under chapter 145C and the right to visitation and health care
decision making by an individual designated by the patient under paragraph 22.
Upon admission to a facility, the patient or the legal guardian or conservator of the
patient, must be given the opportunity to designate a person who is not related who will
have the status of the patient’s next of kin with respect to visitation and making a health
care decision. A designation must be included in the patient’s health record. With respect
to making a health care decision, a health care directive or appointment of a health care
agent under chapter 145C prevails over a designation made under this paragraph. The
unrelated person may also be identified as such by the patient or by the patient’s family.

ADDITIONAL RIGHTS IN RESIDENTIAL PROGRAMS THAT PROVIDE TREATMENT TO CHEMICALLY DEPENDENT OR MENTALLY ILL MINORS OR IN FACILITIES PROVIDING SERVICES FOR EMOTIONALLY DISTURBED MINORS ON A 24-HOUR BASIS:

23. Isolation and Restraints
A minor patient who has been admitted to a residential program as defined in Section 7
has the right to be free from physical restraint and isolation except in emergency
situations involving likelihood that the patient will physically harm the patient’s self or
others. These procedures may not be used for disciplinary purposes, to enforce program
rules, or for the convenience of staff. Isolation or restraint may be used only upon the
prior authorization of a physician, psychiatrist, or licensed consulting psychologist, only
when less restrictive measures are ineffective or not feasible and only for the shortest
time necessary.

24. Treatment Plan
A minor patient who has been admitted to a residential program as defined in Section 7
has the right to a written treatment plan that describes in behavioral terms the case
problems, the precise goals of the plan, and the procedures that will be utilized to
minimize the length of time that the minor requires inpatient treatment. The plan shall
also state goals for release to a less restrictive facility and follow-up treatment measures
and services, if appropriate. To the degree possible, the minor patient and his or her
parents or guardian shall be involved in the development of the treatment and discharge
plan.

Inquiries or complaints regarding medical treatment or the Patients’ Bill of Rights may be
directed to:
Minnesota Board of Medical Practice
2829 University Ave. SE, Suite 400
Minneapolis, MN 55414-3246
612-617-2130
800-657-3709
Office of Health Facility Complaints
P.O. Box 64970 St. Paul, MN 55164-0970
651-201-4201
800-369-7994
Inquiries regarding access to care or possible premature discharge may be directed to:
Ombudsman for Long-Term Care
PO Box 64971
St. Paul, MN 55164-0971
800-657-3591
651-431-2555 (metro)
Minnesota Department of Health
Health Regulation Division
P.O. Box 64900
St. Paul, Minnesota 55164-0900
651-201-4101
health.fpc-licensing@state.mn.us
To obtain this information in a different format, call: 651-201-4101.