Ill. Admin. Code tit. 89, § 325.40 - Medication Approval Standards
a)
Centralized Consent Unit and Emergency Reception Center staff may provide
consent for the administration of a psychotropic medication only after the
Department's Psychiatric Consultant has provided clinical consultation and
deemed the requested medication as appropriate. If a request for administration
of any psychotropic medication that does not meet the criteria listed in this
subsection is deemed appropriate by the Department's Psychiatric Consultant and
the Centralized Consent Unit or ERC staff consents, the staff shall note this
fact on the consent form. If all requested information has been provided to the
Centralized Consent Unit or ERC staff and consultation has occurred, the staff
must provide consent or denial of psychotropic medication within 24 hours for
inpatient requests and 48 hours for all other requests. If approval or denial
of the request for medication is not provided within specified time frames, the
requesting party may contact the Office of the Guardianship Administrator or
designee for assistance in obtaining a response.
b) Additionally, whenever the Centralized
Consent Unit or ERC staff is advised that a child for whom the Department is
legally responsible objects to the administration of psychotropic medication,
Centralized Consent Unit or ERC staff may consult with both the licensed
prescriber who is recommending the medication and the Department's psychiatric
consultant prior to approving or denying the medication. Centralized Consent
Unit or ERC staff shall assess the basis for the child's objection to the
psychotropic medication. This assessment may include asking the child's
caseworker to interview the child to determine the basis for his/her objection.
The reason for the child's objection must be fully documented on the
Psychotropic Medication Request Form. Although the Guardianship Administrator
may give consent notwithstanding the child's objection, the licensed prescriber
must follow all provisions of the Illinois Mental Health and Developmental
Disabilities Code [405 ILCS 5 ].
c)
Every consent for the administration of psychotropic medication shall be
limited in time. Under no circumstance may psychotropic medication be
authorized for a period exceeding 180 days. At the expiration of the period set
forth in the authorization, psychotropic medication may be reauthorized
pursuant to the standards and procedures contained in this Part. The duration
of consent may be less than 180 days if deemed clinically appropriate by the
Department's psychiatric consultant.
d) When the Department grants consent for the
administration of a psychotropic medication to a foster child, it is granting
consent to all prescribers who subsequently care for the child in other
treatment settings until the consent expires.
e) Psychotropic Medication Monitoring. The
licensed prescriber and facility shall monitor a child's response to
medications according to the Guidelines for the Utilization of Psychotropic
Medications for Children in Foster Care and the DCFS Psychotropic Medications
List to determine if the psychotropic medications being administered are safe
and effective based on criteria identified in the treatment plan and are being
prescribed at the appropriate dosage. Means of monitoring safety, effectiveness
and appropriateness of dosage include but are not limited to:
1) Clinical observations of symptoms and/or
side effects documented in the patient's chart;
2) Vital signs (blood pressure, pulse and
temperature);
3) Weight and
height;
4) Symptom severity
scales;
5) Adverse effects
scales;
6) Blood tests to assess
the medications' effects on the body, such as a complete blood count, metabolic
panel, and thyroid function tests; and
7) Blood levels of specific medications such
as lithium and various anticonvulsant mood stabilizers.
f) Continued use of medications that appear
not to have the desired clinical effects or that are associated with
problematic adverse effects must be re-evaluated by the licensed prescriber to
determine the appropriateness of continuing the medication.
g) At least every 90 days, the licensed
prescriber shall assess and document the status of the child/youth for any
adverse reactions and document the presence or absence of tardive dyskinesia in
a child/youth on antipsychotic medications. The licensed prescriber shall
assess the continued need for the medication at least annually. The caseworker
shall document this assessment in the child's case record.
h) Centralized Consent Unit and ERC staff may
deny consent to the administration of psychotropic medications, whether the
medications are among those listed in the Guidelines for the Utilization of
Psychotropic Medications for Children in Foster Care and the DCFS Psychotropic
Medications List or have been approved by the psychiatric consultant. However,
Centralized Consent Unit and ERC staff may only deny consent after consulting
both the licensed prescriber and the Department's psychiatric consultant. The
Guidelines for the Utilization of Psychotropic Medications for Children in
Foster Care and the DCFS Psychotropic Medications List shall contain a
statement setting forth this authority. In the event of a denial of a
medication request, the specific reasons for the denial shall be set forth on
the Psychotropic Medication Consent Form.
i) Whenever a licensed prescriber recommends
the administration of one or more psychotropic medications to a child for whom
the Department is legally responsible, the child shall be advised of the
purposes and effects of the medication and of the potential side effects of the
medication to the extent that such advice is consistent with the nature and
frequency of the side effects and the child's ability to understand the
information communicated. The child shall also be provided written information
concerning the medication and its side effects, unless it has been determined
that such information could not be understood by the child. This written
information shall be provided in the child's primary language.
Notes
Amended at 36 Ill. Reg. 3846, effective February 24, 2012
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