59 Ill. Adm. Code 112.90
Administration of Psychotropic Medications and ECT
Section 112
Section 112.90Â
Administration of
Psychotropic Medications and ECT
This Section addresses the use
of psychotropic medications or electroconvulsive therapy (ECT) in the treatment
of patients receiving services within Department programs.
Definitions
"Authorized
involuntary treatment" means psychotropic medication or electroconvulsive
therapy, including those tests and related procedures that are essential for
the safe and effective administration of the treatment
. [405 ILCS
5/1-121.5]
"Capable"
means the ability of the recipient to make reasoned decisions regarding treatment/habilitation
alternatives.
"Code"
means the Mental Health and Developmental Disabilities Code [405 ILCS 5].
"Electroconvulsive
therapy (ECT)" means the use of electrical stimulation, for therapeutic
ends, to induce a generalized seizure.
"Guardianship"
refers to the legal relationship between an adult recipient or ward and a court
appointed guardian, including a public guardian such as the Office of State
Guardian. Illinois guardians may make legally binding decisions on behalf of
wards in personal or financial affairs, or both. For the purposes of this
Part, the guardian must have court authority to make personal decisions for the
ward. Guardians with personal decision-making authority will typically act
under a plenary guardianship. A plenary guardian is one who has full
decision-making authority over the person without restrictions. However, a
guardian may also legitimately act under a temporary or a limited guardianship
in which the guardian has clearly defined medical decision-making authority. A
parent of an adult recipient without guardianship is not legally authorized to
make binding decisions on behalf of a recipient. When doubt exists as to the
decision-making authority of a guardian, the guardian shall supply either
letters of office or a copy of a court order documenting legal authority to
act on behalf of the ward.
"Informed
consent" means the voluntary and knowing choice by a recipient or his/her
legal guardian.
"Lack of
capacity" means the inability, due to mental impairment, to make reasoned
decisions regarding treatment/habilitation alternatives, including the taking
of medication, by evaluating, among other factors, information about the
likelihood of therapeutic benefits and the risk of side effects.
"Legally
and clinically competent recipient" means an individual who is not under
guardianship and has the capacity to make reasoned decisions and give informed
consent.
"Legally
and clinically incompetent recipient" means an individual under
guardianship or who lacks the capacity to make reasoned decisions and give
informed consent.
"Long-acting
psychotropic medication" means psychotropic medications, including but not
limited to Haldol Decanoate and Prolixin Decanoate, that are designed so that a
single dose will have an intended clinical effect for a period of at least 48
hours
. [405 ILCS 5/1-113.5]
"Medical
Coordinator" means the Medical Coordinator for Mental Health (if the
recipient resides in a mental health facility) or the Medical Coordinator for
Developmental Disabilities (if the recipient resides in a developmental
disabilities facility).
"Medication",
as used in this Section, means psychotropic medication.
"Psychotropic
medication" means medication used for antipsychotic, antidepressant,
antimanic, antianxiety, behavioral modification or behavioral management
purposes, as listed in the Physician's Desk Reference (PDR), Drug Information
Manual and Drug Facts and Comparisons, as incorporated by Section 112.80(a), or
where there is a body of peer reviewed medical literature supporting its use.
"Substitute
decision maker" means a person who possesses the authority to make
decisions under the Powers of Attorney for Health Care Law
[755 ILCS
45/Art. IV]
or under the Mental Health Treatment Preference Declaration Act
[755 ILCS 43]. [405 ILCS 5/1-110.5]
Procedures
a)Â Â Â Â Â Â Â Â Evaluation
1)Â Â Â Â Â Â Â Â No psychotropic medication or electroconvulsive therapy (ECT)
shall be prescribed for a recipient unless examinations have been conducted in
accordance with Section 112.30. The prescribing physician shall conduct the
examinations personally, or shall review the record of the examinations. The
prescribing physician shall record, sign, and date (with time) the
prescription. The prescribing physician shall also document in the recipient's
clinical record any appropriate clinical information.
2)Â Â Â Â Â Â Â Â With regard to psychotropic medication on an emergency basis,
the requirements of subsection (a)(1) need not be met when the prescribing
physician has determined by personal observation or from information supplied
by another clinician with thorough knowledge of the recipient's current
clinical condition that the recipient is in need of immediate medication in
order to prevent the recipient from causing serious and imminent physical harm
to self or others.
b)Â Â Â Â Â Â Â Â Informed Consent
Prior to
prescribing psychotropic medications or ECT in non-emergency situations, a
physician shall ascertain and document whether the recipient is capable of
giving informed consent.
1)Â Â Â Â Â Â Â Â Legally and Clinically Competent Recipients
A)Â Â Â Â Â Â Â If the recipient is able to give informed consent, the
physician shall advise the recipient, in writing, of the following:
i)Â Â Â Â Â Â Â Â Â nature and purpose of the proposed treatment;
ii)Â Â Â Â Â Â Â Â whether the proposed treatment requires periodic
testing/procedures to ensure safety/efficacy;
iii)Â Â Â Â Â Â Â side effects, risks and benefits of the proposed treatment;
iv)Â Â Â Â Â Â Â prognosis and risks without the proposed treatment;
v)Â Â Â Â Â Â Â Â alternative treatments and their risks, side effects, benefits
and efficacy; and
vi)Â Â Â Â Â Â Â the right to refuse the proposed treatment.
B)Â Â Â Â Â Â Â The required information shall be given to the recipient in a
manner consistent with his/her ability to understand, including regular use of
sign language for any deaf or hard of hearing individual for whom sign language
is a primary mode of communication.
C)Â Â Â Â Â Â Â Informed written consent shall be obtained from the recipient.
D)Â Â Â Â Â Â Â If the recipient has previously executed a declaration for
mental health treatment under the Mental Health Treatment Preference
Declaration Act or a health care power of attorney under the Power of Attorney
for Health Care Law, the facility is required to act in accordance with that
declaration or power of attorney.
2)Â Â Â Â Â Â Â Â Legally and Clinically Incompetent Recipients
A)Â Â Â Â Â Â Â Prior to prescribing psychotropic medications or ECT in
non-emergency situations, a physician shall advise the recipient and the
recipient's guardian or substitute decision maker, in writing, of the
following:
i)Â Â Â Â Â Â Â Â Â nature and purpose of the proposed treatment;
ii)Â Â Â Â Â Â Â Â whether the proposed treatment requires periodic
testing/procedures to ensure safety/efficacy;
iii)Â Â Â Â Â Â Â side effects and risks of the proposed treatment;
iv)Â Â Â Â Â Â Â prognosis and risks without the proposed treatment;
v)Â Â Â Â Â Â Â Â alternative treatments and their risks, side effects, benefits
and efficacy; and
vi)Â Â Â Â Â Â Â the right to refuse the proposed treatment.
B)Â Â Â Â Â Â Â The required information shall be given to the recipient and
the recipient's guardian or substitute decision maker in a manner consistent
with his/her ability to understand, including regular use of sign language for
any deaf or hard of hearing individual for whom sign language is a primary mode
of communication.
C)Â Â Â Â Â Â Â The recipient shall be asked if he/she agrees to receive the
proposed treatment. If the recipient does not object, informed written consent
shall be obtained from the recipient's guardian or substitute decision maker
and shall be documented in the recipient's medical record. If the recipient
has no guardian or substitute decision maker or if the guardian or substitute
decision maker does not provide such informed written consent, any treatment
must proceed in accordance with subsection (c) (Refusal of Treatment).
D)Â Â Â Â Â Â Â If the recipient objects to the proposed treatment, any
treatment must proceed in accordance with subsection (c) (Refusal of
Treatment).
E)Â Â Â Â Â Â Â If the recipient has previously executed a declaration for
mental health treatment under the Mental Health Treatment Preference
Declaration Act or a health care power of attorney under the Power of Attorney
for Health Care Law, the facility is required to act in accordance with that
declaration or power of attorney.
c)Â Â Â Â Â Â Â Â Refusal of Treatment
A recipient's
refusal to receive psychotropic medication or ECT does not in itself constitute
an emergency. Such refusal, as documented in the clinical record, shall be
honored except in the following circumstances:
1)Â Â Â Â Â Â Â Â Emergencies
In an
emergency, when treatment is necessary to prevent a recipient from causing
serious and imminent physical harm to self or others.
A)Â Â Â Â Â Â Â In such an emergency, a member of the treatment/habilitation
team shall document in the recipient's clinical record that the staff have
explored alternative treatment options to contain the emergency. The
documentation shall include a written explanation of the reasons why
alternative treatments are not appropriate.
B)Â Â Â Â Â Â Â For administration of psychotropic medications the prescribing
physician or a nurse in consultation with a physician shall document his/her
determination that an emergency exists based on a personal examination of the
individual. Administration of the medication shall be accompanied by a
physician's order.
C)Â Â Â Â Â Â Â In prescribing psychotropic medications on an emergency basis
the prescribing physician shall examine the recipient and document his/her
determination of the initial emergency and response, including the
circumstances leading up to the need for emergency treatment, in the recipient's
clinical record as soon as possible, but within 24 hours. Psychotropic
medication may not be continued unless the need for such medication is
redetermined at least every 24 hours and the circumstances demonstrating that
need are set forth in the recipient's clinical record. A redetermination is
based on a personal examination of the recipient by a physician or a nurse with
the consultation of a physician.
D)Â Â Â Â Â Â Â Treatment shall not be administered over a recipient's refusal
under Section 2-107 of the Mental Health and Developmental Disabilities Code
for a period in excess of 72 hours, excluding Saturdays, Sundays and holidays,
unless the treating physician with the support of the treatment/habilitation
team files a petition for a court order under Section 2-107.1 of the Code and
the treatment continues to be necessary in order to prevent the recipient from
causing serious and imminent physical harm to self or others. If no such
petition is filed, treatment must be discontinued.
E)Â Â Â Â Â Â Â A restriction of rights form shall be completed for each
administration of emergency treatment.
F)Â Â Â Â Â Â Â Â ECT may be administered over a patient's refusal only with a
court order and prior written physician's order or in emergency situations as
defined in Section 2-107 of the Code.
G)
Upon commencement of services, or as soon thereafter as the
condition of the recipient permits, the facility shall advise the recipient as
to the circumstances under which the use of emergency forced medication is
permitted under Section 2-107(a) of the Mental Health and Developmental
Disabilities Code
[405 ILCS 5/2-200(d)].
Concurrently,
the facility shall ask the recipient which form of intervention he/she would
prefer if any of these circumstances arise. The recipient's preference shall
be documented in the clinical record and communicated by the facility to the
recipient's guardian or substitute decision maker, if any. If any such
circumstances arise, the facility shall give due consideration to the
preferences of the recipient regarding which form of intervention to use as
communicated to the facility by the recipient or as stated in the recipient's
advance directive.
H)Â Â Â Â Â Â Â Under no circumstances may long-acting psychotropic medications
be administered under Section 2-107 of the Code.
I)Â Â Â Â Â Â Â Â Under no circumstances may ECT be administered to a minor
recipient without a court order.
2)Â Â Â Â Â Â Â Â Administration of Treatment on Court Order
A)Â Â Â Â Â Â Â If the treating physician, with the support of the
treatment/habilitation team, determines that psychotropic medication or ECT is
clinically indicated for a recipient who does not at the time pose an imminent
risk of serious physical harm to self or others, and the situation described in
subsections (b)(2)(c) or (b)(2)(D) of this Part applies, the facility may file
a petition in the circuit court under Section 2-107.1 of the Code for
court-ordered treatment.
B)Â Â Â Â Â Â Â If the treating physician, with the support of the
treatment/habilitation team, files a petition under Section 2-107.1 of the
Code, a physician shall examine the recipient and address the following issues
for the court:
i)Â Â Â Â Â Â Â Â Â whether the recipient has a serious mental illness or
developmental disability;
ii)        whether, because of the mental illness or developmental
disability, the recipient exhibits any one the following: deterioration of
his/her ability to function, suffering, or threatening behavior;
iii)Â Â Â Â Â Â Â whether the illness or disability has existed for a period
marked by the continuing presence of the symptoms set forth in subsection
(c)(2)(B)(ii) or the repeated episodic occurrence of such symptoms;
iv)Â Â Â Â Â Â Â whether the predicted benefits of the treatment will outweigh
any possible harm;
v)Â Â Â Â Â Â Â Â whether the recipient lacks the capacity to make a reasoned
decision about the treatment;
vi)Â Â Â Â Â Â Â whether other less restrictive treatment methods have been
explored and found to be inappropriate;
vii)Â Â Â Â Â Â the specific treatments proposed, including dosage range
and/or frequency of administration, as applicable; and
viii)Â Â Â Â Â if the petition seeks authorization for testing and other
procedures, the physician shall include a statement that such testing and
procedures are essential for the safe and effective administration of the
treatment.
C)Â Â Â Â Â Â Â If the court grants the petition for involuntary treatment
pursuant to Section 2-107.1 of the Code, the recipient may be administered
treatment over his/her refusal (or the guardian's or substitute decision
maker's refusal if the recipient was legally incompetent but did not object)
within the constraints and for the duration of the court order.
d)Â Â Â Â Â Â Â Â Monitoring of Treatment
1)Â Â Â Â Â Â Â Â Documentation
A)Â Â Â Â Â Â Â The attending physician shall examine and document the status
of the recipient's condition in the recipient's clinical record as often as the
recipient's clinical condition warrants but no less often than every 30
calendar days. Documentation of the rationale for treatment, including type,
dosage or frequency of the proposed treatment as applicable, shall be included.
Beneficial effects and significant side effects as well as their treatment
and/or management or the absence of treatment and/or management shall also be
noted.
B)Â Â Â Â Â Â Â Facility staff shall document in the recipient's clinical
record additional clinical information such as assessments, evaluations or
laboratory results as they become available.
2)Â Â Â Â Â Â Â Â Treatment Review
A)Â Â Â Â Â Â Â When a recipient at a State-operated mental health facility has
been receiving psychotropic medications and/or ECT continuously or regularly
for a period of three months, and if such treatment is continued, every six
months thereafter for so long as the treatment shall continue, the facility
medical director, or other physician designated by the facility director,
shall convene a treatment review panel.
B)Â Â Â Â Â Â Â The panel shall consist of representatives from at least two of
the following clinical disciplines: psychiatry, medicine, clinical pharmacy and
nursing. At least one panel member shall be a physician with expertise in the
use of psychotropic medication (for example, psychiatrist or behavioral
neurologist).
C)Â Â Â Â Â Â Â At least 7 days prior to the date of the treatment review panel
meeting, the recipient, guardian or substitute decision maker, if any, and any
person designated under Section 2-200(b) of the Mental Health and Developmental
Disabilities Code shall be given written notification of the time and place of the
treatment review panel meeting. The notice shall also advise the recipient of
his/her right to designate some person to attend the meeting and assist the
recipient in accordance with Section 2-107.2 of the Mental Health and
Developmental Disabilities Code.
D)Â Â Â Â Â Â Â The panel shall provide a recommendation concerning the
suitability of continued treatment.
E)Â Â Â Â Â Â Â If, during the course of the treatment review panel meeting,
the recipient advises the committee that he/she no longer agrees to continue
receiving medication or ECT, or if the recipient has a guardian or substitute
decision maker and the guardian or substitute decision maker refuses medication
or ECT for the recipient, the treatment shall be discontinued, except when the
recipient is receiving treatment pursuant to subsections (c)(1) and (c)(2) of
this Section.
i)Â Â Â Â Â Â Â Â Â If the panel determines that the recipient is receiving
appropriate treatment and that the benefit to the recipient outweighs the risk
of harm to the recipient, treatment shall be continued, provided that the
recipient does not object (and the guardian or substitute decision maker, if
any, does not refuse). (See Section 2-107.2 of the Code.)
ii)Â Â Â Â Â Â Â Â If the findings of the treatment review panel are not in
agreement with the current treatment plan, revision shall be considered by the
treatment/habilitation team.
iii)Â Â Â Â Â Â Â If there is disagreement on the implementation of the panel
recommendations, the facility medical director or lead physician (designated by
the facility director) shall review the case and make a final decision. The
facility medical director (or lead physician) may consult with the appropriate
Medical Coordinator in making a final determination.
F)Â Â Â Â Â Â Â Â The participation of the recipient and guardian or substitute
decision maker if any, and the recommendations of the treatment review panel
shall be recorded in the recipient's clinical record.
3)Â Â Â Â Â Â Â Â Annual ECT Report
The Department
of Human Services shall summarize on an annual basis all quarterly reports
(prepared in accordance with Section 2-110.1 of the Mental Health and
Developmental Disabilities Code) from State-operated hospitals or facilities at
which ECT is performed.