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Public Act 104-0762 |
| HB3454 Enrolled | LRB104 09749 BDA 19815 b |
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AN ACT concerning health. |
Be it enacted by the People of the State of Illinois, |
represented in the General Assembly: |
Section 5. The Illinois State Police Act is amended by |
changing Section 40 as follows: |
(20 ILCS 2610/40) |
Sec. 40. Administration of epinephrine. |
(a) This Section, along with Section 10.19 of the Illinois |
Police Training Act, may be referred to as the Annie LeGere |
Law. |
(b) For the purposes of this Section, "epinephrine |
delivery system" "epinephrine auto-injector" means a |
single-use device used for the automatic injection of a |
pre-measured dose of epinephrine into the human body |
prescribed in the name of the Illinois State Police. |
(c) The Illinois State Police may conduct or approve a |
training program for State Police officers to recognize and |
respond to anaphylaxis, including, but not limited to: |
(1) how to recognize symptoms of an allergic reaction; |
(2) how to respond to an emergency involving an |
allergic reaction; |
(3) how to administer an epinephrine delivery system |
epinephrine auto-injector; |
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(4) how to respond to an individual with a known |
allergy as well as an individual with a previously unknown |
allergy; |
(5) a test demonstrating competency of the knowledge |
required to recognize anaphylaxis and administer an |
epinephrine delivery system epinephrine auto-injector; and |
(6) other criteria as determined in rules adopted by |
the Illinois State Police. |
(d) The Illinois State Police may authorize a State Police |
officer who has completed the training program under |
subsection (c) to carry, administer, or assist with the |
administration of epinephrine delivery systems epinephrine |
auto-injectors whenever he or she is performing official |
duties. |
(e) The Illinois State Police must establish a written |
policy to control the acquisition, storage, transportation, |
administration, and disposal of epinephrine delivery systems |
epinephrine auto-injectors before it allows any State Police |
officer to carry and administer epinephrine delivery systems |
epinephrine auto-injectors. |
(f) A physician, physician assistant with prescriptive |
authority, or advanced practice registered nurse with |
prescriptive authority may provide a standing protocol or |
prescription for epinephrine delivery systems epinephrine |
auto-injectors in the name of the Illinois State Police to be |
maintained for use when necessary. |
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(g) When a State Police officer administers an epinephrine |
delivery system epinephrine auto-injector in good faith, the |
officer and the Illinois State Police, and its employees and |
agents, including a physician, physician assistant with |
prescriptive authority, or advanced practice registered nurse |
with prescriptive authority who provides a standing order or |
prescription for an epinephrine delivery system epinephrine |
auto-injector, incur no civil or professional liability, |
except for willful and wanton conduct, as a result of any |
injury or death arising from the use of an epinephrine |
delivery system epinephrine auto-injector. |
(Source: P.A. 104-24, eff. 1-1-26.) |
Section 10. The Illinois Police Training Act is amended by |
changing Section 10.19 as follows: |
(50 ILCS 705/10.19) |
Sec. 10.19. Training; administration of epinephrine. |
(a) This Section, along with Section 40 of the Illinois |
State Police Act, may be referred to as the Annie LeGere Law. |
(b) For purposes of this Section, "epinephrine delivery |
system" "epinephrine auto-injector" means a single-use device |
used for the automatic injection of a pre-measured dose of |
epinephrine into the human body prescribed in the name of a |
local law enforcement agency. |
(c) The Board shall conduct or approve an optional |
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advanced training program for law enforcement officers to |
recognize and respond to anaphylaxis, including the |
administration of an epinephrine delivery system epinephrine |
auto-injector. The training must include, but is not limited |
to: |
(1) how to recognize symptoms of an allergic reaction; |
(2) how to respond to an emergency involving an |
allergic reaction; |
(3) how to administer an epinephrine delivery system |
epinephrine auto-injector; |
(4) how to respond to an individual with a known |
allergy as well as an individual with a previously unknown |
allergy; |
(5) a test demonstrating competency of the knowledge |
required to recognize anaphylaxis and administer an |
epinephrine delivery system epinephrine auto-injector; and |
(6) other criteria as determined in rules adopted by |
the Board. |
(d) A local law enforcement agency may authorize a law |
enforcement officer who has completed an optional advanced |
training program under subsection (c) to carry, administer, or |
assist with the administration of epinephrine delivery systems |
epinephrine auto-injectors provided by the local law |
enforcement agency whenever the officer is performing official |
duties. |
(e) A local law enforcement agency that authorizes its |
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officers to carry and administer epinephrine delivery systems |
epinephrine auto-injectors under subsection (d) must establish |
a policy to control the acquisition, storage, transportation, |
administration, and disposal of epinephrine delivery systems |
epinephrine auto-injectors and to provide continued training |
in the administration of epinephrine delivery systems |
epinephrine auto-injectors. |
(f) A physician, physician assistant with prescriptive |
authority, or advanced practice registered nurse with |
prescriptive authority may provide a standing protocol or |
prescription for epinephrine delivery systems epinephrine |
auto-injectors in the name of a local law enforcement agency |
to be maintained for use when necessary. |
(g) When a law enforcement officer administers an |
epinephrine delivery system epinephrine auto-injector in good |
faith, the law enforcement officer and local law enforcement |
agency, and its employees and agents, including a physician, |
physician assistant with prescriptive authority, or advanced |
practice registered nurse with prescriptive authority who |
provides a standing order or prescription for an epinephrine |
delivery system epinephrine auto-injector, incur no civil or |
professional liability, except for willful and wanton conduct, |
or as a result of any injury or death arising from the use of |
an epinephrine delivery system epinephrine auto-injector. |
(Source: P.A. 102-538, eff. 8-20-21; 102-694, eff. 1-7-22; |
103-154, eff. 6-30-23.) |
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Section 15. The School Code is amended by changing Section |
22-30 as follows: |
(105 ILCS 5/22-30) |
Sec. 22-30. Self-administration and self-carry of asthma |
medication and epinephrine delivery systems injectors; |
administration of undesignated epinephrine delivery systems |
injectors; administration of an opioid antagonist; |
administration of undesignated asthma medication; supply of |
undesignated oxygen tanks; asthma episode emergency response |
protocol. |
(a) For the purpose of this Section only, the following |
terms shall have the meanings set forth below: |
"Asthma action plan" means a written plan developed with a |
pupil's medical provider to help control the pupil's asthma. |
The goal of an asthma action plan is to reduce or prevent |
flare-ups and emergency department visits through day-to-day |
management and to serve as a student-specific document to be |
referenced in the event of an asthma episode. |
"Asthma episode emergency response protocol" means a |
procedure to provide assistance to a pupil experiencing |
symptoms of wheezing, coughing, shortness of breath, chest |
tightness, or breathing difficulty. |
"Epinephrine delivery system" means any form of |
epinephrine that is approved by the United States Food and |
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Drug Administration, including any device that contains a dose |
of epinephrine, and that is used to administer epinephrine |
into the human body to prevent or treat a life-threatening |
allergic reaction injector" includes an auto-injector approved |
by the United States Food and Drug Administration for the |
administration of epinephrine and a pre-filled syringe |
approved by the United States Food and Drug Administration and |
used for the administration of epinephrine that contains a |
pre-measured dose of epinephrine that is equivalent to the |
dosages used in an auto-injector. |
"Asthma medication" means quick-relief asthma medication, |
including albuterol or other short-acting bronchodilators, |
that is approved by the United States Food and Drug |
Administration for the treatment of respiratory distress. |
"Asthma medication" includes medication delivered through a |
device, including a metered dose inhaler with a reusable or |
disposable spacer or a nebulizer with a mouthpiece or mask. |
"Opioid antagonist" means a drug that binds to opioid |
receptors and blocks or inhibits the effect of opioids acting |
on those receptors, including, but not limited to, naloxone |
hydrochloride or any other similarly acting drug approved by |
the U.S. Food and Drug Administration. |
"Respiratory distress" means the perceived or actual |
presence of wheezing, coughing, shortness of breath, chest |
tightness, breathing difficulty, or any other symptoms |
consistent with asthma. Respiratory distress may be |
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categorized as "mild-to-moderate" or "severe". |
"School nurse" means a registered nurse working in a |
school with or without licensure endorsed in school nursing. |
"Self-administration" means a pupil's discretionary use of |
his or her prescribed asthma medication or epinephrine |
delivery system injector. |
"Self-carry" means a pupil's ability to carry his or her |
prescribed asthma medication or epinephrine delivery system |
injector. |
"Standing protocol" may be issued by (i) a physician |
licensed to practice medicine in all its branches, (ii) a |
licensed physician assistant with prescriptive authority, or |
(iii) a licensed advanced practice registered nurse with |
prescriptive authority. |
"Trained personnel" means any school employee or volunteer |
personnel authorized in Sections 10-22.34, 10-22.34a, and |
10-22.34b of this Code who has completed training under |
subsection (g) of this Section to recognize and respond to |
anaphylaxis, an opioid overdose, or respiratory distress. |
"Undesignated asthma medication" means asthma medication |
prescribed in the name of a school district, public school, |
charter school, or nonpublic school. |
"Undesignated epinephrine delivery system injector" means |
an epinephrine delivery system injector prescribed in the name |
of a school district, public school, charter school, or |
nonpublic school. |
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(b) A school, whether public, charter, or nonpublic, must |
permit the self-administration and self-carry of asthma |
medication by a pupil with asthma or the self-administration |
and self-carry of an epinephrine delivery system injector by a |
pupil, provided that: |
(1) the parents or guardians of the pupil provide to |
the school (i) written authorization from the parents or |
guardians for (A) the self-administration and self-carry |
of asthma medication or (B) the self-carry of asthma |
medication or (ii) for (A) the self-administration and |
self-carry of an epinephrine delivery system injector or |
(B) the self-carry of an epinephrine delivery system |
injector, written authorization from the pupil's |
physician, physician assistant, or advanced practice |
registered nurse; and |
(2) the parents or guardians of the pupil provide to |
the school (i) the prescription label, which must contain |
the name of the asthma medication, the prescribed dosage, |
and the time at which or circumstances under which the |
asthma medication is to be administered, or (ii) for the |
self-administration or self-carry of an epinephrine |
delivery system injector, a written statement from the |
pupil's physician, physician assistant, or advanced |
practice registered nurse containing the following |
information: |
(A) the name and purpose of the epinephrine |
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delivery system injector; |
(B) the prescribed dosage; and |
(C) the time or times at which or the special |
circumstances under which the epinephrine delivery |
system injector is to be administered. |
The information provided shall be kept on file in the office of |
the school nurse or, in the absence of a school nurse, the |
school's administrator. |
(b-5) A school district, public school, charter school, or |
nonpublic school may authorize the provision of a |
student-specific or undesignated epinephrine delivery system |
injector to a student or any personnel authorized under a |
student's Individual Health Care Action Plan, allergy |
emergency action plan, or plan pursuant to Section 504 of the |
federal Rehabilitation Act of 1973 to administer an |
epinephrine delivery system injector to the student, that |
meets the student's prescription on file. |
(b-10) The school district, public school, charter school, |
or nonpublic school may authorize a school nurse or trained |
personnel to do the following: (i) provide an undesignated |
epinephrine delivery system injector to a student for |
self-administration only or any personnel authorized under a |
student's Individual Health Care Action Plan, allergy |
emergency action plan, plan pursuant to Section 504 of the |
federal Rehabilitation Act of 1973, or individualized |
education program plan to administer to the student that meets |
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the student's prescription on file; (ii) administer an |
undesignated epinephrine delivery system injector that meets |
the prescription on file to any student who has an Individual |
Health Care Action Plan, allergy emergency action plan, plan |
pursuant to Section 504 of the federal Rehabilitation Act of |
1973, or individualized education program plan that authorizes |
the use of an epinephrine delivery system injector; (iii) |
administer an undesignated epinephrine delivery system |
injector to any person that the school nurse or trained |
personnel in good faith believes is having an anaphylactic |
reaction; (iv) administer an opioid antagonist to any person |
that the school nurse or trained personnel in good faith |
believes is having an opioid overdose; (v) provide |
undesignated asthma medication to a student for |
self-administration only or to any personnel authorized under |
a student's Individual Health Care Action Plan or asthma |
action plan, plan pursuant to Section 504 of the federal |
Rehabilitation Act of 1973, or individualized education |
program plan to administer to the student that meets the |
student's prescription on file; (vi) administer undesignated |
asthma medication that meets the prescription on file to any |
student who has an Individual Health Care Action Plan or |
asthma action plan, plan pursuant to Section 504 of the |
federal Rehabilitation Act of 1973, or individualized |
education program plan that authorizes the use of asthma |
medication; and (vii) administer undesignated asthma |
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medication to any person that the school nurse or trained |
personnel believes in good faith is having respiratory |
distress. |
(c) The school district, public school, charter school, or |
nonpublic school must inform the parents or guardians of the |
pupil, in writing, that the school district, public school, |
charter school, or nonpublic school and its employees and |
agents, including a physician, physician assistant, or |
advanced practice registered nurse providing standing protocol |
and a prescription for school epinephrine delivery systems |
injectors, an opioid antagonist, or undesignated asthma |
medication, are to incur no liability or professional |
discipline, except for willful and wanton conduct, as a result |
of any injury arising from the administration of asthma |
medication, an epinephrine delivery system injector, or an |
opioid antagonist regardless of whether authorization was |
given by the pupil's parents or guardians or by the pupil's |
physician, physician assistant, or advanced practice |
registered nurse. The parents or guardians of the pupil must |
sign a statement acknowledging that the school district, |
public school, charter school, or nonpublic school and its |
employees and agents are to incur no liability, except for |
willful and wanton conduct, as a result of any injury arising |
from the administration of asthma medication, an epinephrine |
delivery system injector, or an opioid antagonist regardless |
of whether authorization was given by the pupil's parents or |
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guardians or by the pupil's physician, physician assistant, or |
advanced practice registered nurse and that the parents or |
guardians must indemnify and hold harmless the school |
district, public school, charter school, or nonpublic school |
and its employees and agents against any claims, except a |
claim based on willful and wanton conduct, arising out of the |
administration of asthma medication, an epinephrine delivery |
system injector, or an opioid antagonist regardless of whether |
authorization was given by the pupil's parents or guardians or |
by the pupil's physician, physician assistant, or advanced |
practice registered nurse. |
(c-5) When a school nurse or trained personnel administers |
an undesignated epinephrine delivery system injector to a |
person whom the school nurse or trained personnel in good |
faith believes is having an anaphylactic reaction, administers |
an opioid antagonist to a person whom the school nurse or |
trained personnel in good faith believes is having an opioid |
overdose, or administers undesignated asthma medication to a |
person whom the school nurse or trained personnel in good |
faith believes is having respiratory distress, notwithstanding |
the lack of notice to the parents or guardians of the pupil or |
the absence of the parents or guardians signed statement |
acknowledging no liability, except for willful and wanton |
conduct, the school district, public school, charter school, |
or nonpublic school and its employees and agents, and a |
physician, a physician assistant, or an advanced practice |
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registered nurse providing standing protocol and a |
prescription for undesignated epinephrine delivery systems |
injectors, an opioid antagonist, or undesignated asthma |
medication, are to incur no liability or professional |
discipline, except for willful and wanton conduct, as a result |
of any injury arising from the use of an undesignated |
epinephrine delivery system injector, the use of an opioid |
antagonist, or the use of undesignated asthma medication, |
regardless of whether authorization was given by the pupil's |
parents or guardians or by the pupil's physician, physician |
assistant, or advanced practice registered nurse. |
(d) The permission for self-administration and self-carry |
of asthma medication or the self-administration and self-carry |
of an epinephrine delivery system injector is effective for |
the school year for which it is granted and shall be renewed |
each subsequent school year upon fulfillment of the |
requirements of this Section. |
(e) Provided that the requirements of this Section are |
fulfilled, a pupil with asthma may self-administer and |
self-carry his or her asthma medication or a pupil may |
self-administer and self-carry an epinephrine delivery system |
injector (i) while in school, (ii) while at a school-sponsored |
activity, (iii) while under the supervision of school |
personnel, or (iv) before or after normal school activities, |
such as while in before-school or after-school care on |
school-operated property or while being transported on a |
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school bus. |
(e-5) Provided that the requirements of this Section are |
fulfilled, a school nurse or trained personnel may administer |
an undesignated epinephrine delivery system injector to any |
person whom the school nurse or trained personnel in good |
faith believes to be having an anaphylactic reaction (i) while |
in school, (ii) while at a school-sponsored activity, (iii) |
while under the supervision of school personnel, or (iv) |
before or after normal school activities, such as while in |
before-school or after-school care on school-operated property |
or while being transported on a school bus. A school nurse or |
trained personnel may carry undesignated epinephrine delivery |
systems injectors on his or her person while in school or at a |
school-sponsored activity. |
(e-10) Provided that the requirements of this Section are |
fulfilled, a school nurse or trained personnel may administer |
an opioid antagonist to any person whom the school nurse or |
trained personnel in good faith believes to be having an |
opioid overdose (i) while in school, (ii) while at a |
school-sponsored activity, (iii) while under the supervision |
of school personnel, or (iv) before or after normal school |
activities, such as while in before-school or after-school |
care on school-operated property. A school nurse or trained |
personnel may carry an opioid antagonist on his or her person |
while in school or at a school-sponsored activity. |
(e-15) If the requirements of this Section are met, a |
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school nurse or trained personnel may administer undesignated |
asthma medication to any person whom the school nurse or |
trained personnel in good faith believes to be experiencing |
respiratory distress (i) while in school, (ii) while at a |
school-sponsored activity, (iii) while under the supervision |
of school personnel, or (iv) before or after normal school |
activities, including before-school or after-school care on |
school-operated property. A school nurse or trained personnel |
may carry undesignated asthma medication on his or her person |
while in school or at a school-sponsored activity. |
(f) The school district, public school, charter school, or |
nonpublic school may maintain a supply of undesignated |
epinephrine delivery systems injectors in any secure location |
that is accessible before, during, and after school where an |
allergic person is most at risk, including, but not limited |
to, classrooms and lunchrooms. A physician, a physician |
assistant who has prescriptive authority in accordance with |
Section 7.5 of the Physician Assistant Practice Act of 1987, |
or an advanced practice registered nurse who has prescriptive |
authority in accordance with Section 65-40 of the Nurse |
Practice Act may prescribe undesignated epinephrine delivery |
systems injectors in the name of the school district, public |
school, charter school, or nonpublic school to be maintained |
for use when necessary. Any supply of epinephrine delivery |
systems injectors shall be maintained in accordance with the |
manufacturer's instructions. |
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The school district, public school, charter school, or |
nonpublic school shall maintain a supply of an opioid |
antagonist in any secure location where an individual may have |
an opioid overdose, unless there is a shortage of opioid |
antagonists, in which case the school district, public school, |
charter school, or nonpublic school shall make a reasonable |
effort to maintain a supply of an opioid antagonist. Unless |
the school district, public school, charter school, or |
nonpublic school is able to obtain opioid antagonists without |
a prescription, a health care professional who has been |
delegated prescriptive authority for opioid antagonists in |
accordance with Section 5-23 of the Substance Use Disorder Act |
shall prescribe opioid antagonists in the name of the school |
district, public school, charter school, or nonpublic school, |
to be maintained for use when necessary. Any supply of opioid |
antagonists shall be maintained in accordance with the |
manufacturer's instructions. |
The school district, public school, charter school, or |
nonpublic school may maintain a supply of asthma medication in |
any secure location that is accessible before, during, or |
after school where a person is most at risk, including, but not |
limited to, a classroom or the nurse's office. A physician, a |
physician assistant who has prescriptive authority under |
Section 7.5 of the Physician Assistant Practice Act of 1987, |
or an advanced practice registered nurse who has prescriptive |
authority under Section 65-40 of the Nurse Practice Act may |
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prescribe undesignated asthma medication in the name of the |
school district, public school, charter school, or nonpublic |
school to be maintained for use when necessary. Any supply of |
undesignated asthma medication must be maintained in |
accordance with the manufacturer's instructions. |
A school district that provides special educational |
facilities for children with disabilities under Section |
14-4.01 of this Code may maintain a supply of undesignated |
oxygen tanks in any secure location that is accessible before, |
during, and after school where a person with developmental |
disabilities is most at risk, including, but not limited to, |
classrooms and lunchrooms. A physician, a physician assistant |
who has prescriptive authority in accordance with Section 7.5 |
of the Physician Assistant Practice Act of 1987, or an |
advanced practice registered nurse who has prescriptive |
authority in accordance with Section 65-40 of the Nurse |
Practice Act may prescribe undesignated oxygen tanks in the |
name of the school district that provides special educational |
facilities for children with disabilities under Section |
14-4.01 of this Code to be maintained for use when necessary. |
Any supply of oxygen tanks shall be maintained in accordance |
with the manufacturer's instructions and with the local fire |
department's rules. |
(f-3) Whichever entity initiates the process of obtaining |
undesignated epinephrine delivery systems injectors and |
providing training to personnel for carrying and administering |
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undesignated epinephrine delivery systems injectors shall pay |
for the costs of the undesignated epinephrine delivery systems |
injectors. |
(f-5) Upon any administration of an epinephrine delivery |
system injector, a school district, public school, charter |
school, or nonpublic school must immediately activate the EMS |
system and notify the student's parent, guardian, or emergency |
contact, if known. |
Upon any administration of an opioid antagonist, a school |
district, public school, charter school, or nonpublic school |
must immediately activate the EMS system and notify the |
student's parent, guardian, or emergency contact, if known. |
(f-10) Within 24 hours of the administration of an |
undesignated epinephrine delivery system injector, a school |
district, public school, charter school, or nonpublic school |
must notify the physician, physician assistant, or advanced |
practice registered nurse who provided the standing protocol |
and a prescription for the undesignated epinephrine delivery |
system injector of its use. |
Within 24 hours after the administration of an opioid |
antagonist, a school district, public school, charter school, |
or nonpublic school must notify the health care professional |
who provided the prescription for the opioid antagonist of its |
use. |
Within 24 hours after the administration of undesignated |
asthma medication, a school district, public school, charter |
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school, or nonpublic school must notify the student's parent |
or guardian or emergency contact, if known, and the physician, |
physician assistant, or advanced practice registered nurse who |
provided the standing protocol and a prescription for the |
undesignated asthma medication of its use. The district or |
school must follow up with the school nurse, if available, and |
may, with the consent of the child's parent or guardian, |
notify the child's health care provider of record, as |
determined under this Section, of its use. |
(g) Prior to the administration of an undesignated |
epinephrine delivery system injector, trained personnel must |
submit to the school's administration proof of completion of a |
training curriculum to recognize and respond to anaphylaxis |
that meets the requirements of subsection (h) of this Section. |
Training must be completed annually. The school district, |
public school, charter school, or nonpublic school must |
maintain records related to the training curriculum and |
trained personnel. |
Prior to the administration of an opioid antagonist, |
trained personnel must submit to the school's administration |
proof of completion of a training curriculum to recognize and |
respond to an opioid overdose, which curriculum must meet the |
requirements of subsection (h-5) of this Section. The school |
district, public school, charter school, or nonpublic school |
must maintain records relating to the training curriculum and |
the trained personnel. |
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Prior to the administration of undesignated asthma |
medication, trained personnel must submit to the school's |
administration proof of completion of a training curriculum to |
recognize and respond to respiratory distress, which must meet |
the requirements of subsection (h-10) of this Section. |
Training must be completed annually, and the school district, |
public school, charter school, or nonpublic school must |
maintain records relating to the training curriculum and the |
trained personnel. |
(h) A training curriculum to recognize and respond to |
anaphylaxis, including the administration of an undesignated |
epinephrine delivery system injector, may be conducted online |
or in person. |
Training shall include, but is not limited to: |
(1) how to recognize signs and symptoms of an allergic |
reaction, including anaphylaxis; |
(2) how to administer an epinephrine delivery system |
injector; and |
(3) a test demonstrating competency of the knowledge |
required to recognize anaphylaxis and administer an |
epinephrine delivery system injector. |
Training may also include, but is not limited to: |
(A) a review of high-risk areas within a school and |
its related facilities; |
(B) steps to take to prevent exposure to allergens; |
(C) emergency follow-up procedures, including the |
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importance of calling 9-1-1 or, if 9-1-1 is not available, |
other local emergency medical services; |
(D) how to respond to a student with a known allergy, |
as well as a student with a previously unknown allergy; |
(E) other criteria as determined in rules adopted |
pursuant to this Section; and |
(F) any policy developed by the State Board of |
Education under Section 2-3.190. |
In consultation with statewide professional organizations |
representing physicians licensed to practice medicine in all |
of its branches, registered nurses, and school nurses, the |
State Board of Education shall make available resource |
materials consistent with criteria in this subsection (h) for |
educating trained personnel to recognize and respond to |
anaphylaxis. The State Board may take into consideration the |
curriculum on this subject developed by other states, as well |
as any other curricular materials suggested by medical experts |
and other groups that work on life-threatening allergy issues. |
The State Board is not required to create new resource |
materials. The State Board shall make these resource materials |
available on its Internet website. |
(h-5) A training curriculum to recognize and respond to an |
opioid overdose, including the administration of an opioid |
antagonist, may be conducted online or in person. The training |
must comply with any training requirements under Section 5-23 |
of the Substance Use Disorder Act and the corresponding rules. |
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It must include, but is not limited to: |
(1) how to recognize symptoms of an opioid overdose; |
(2) information on drug overdose prevention and |
recognition; |
(3) how to perform rescue breathing and resuscitation; |
(4) how to respond to an emergency involving an opioid |
overdose; |
(5) opioid antagonist dosage and administration; |
(6) the importance of calling 9-1-1 or, if 9-1-1 is |
not available, other local emergency medical services; |
(7) care for the overdose victim after administration |
of the overdose antagonist; |
(8) a test demonstrating competency of the knowledge |
required to recognize an opioid overdose and administer a |
dose of an opioid antagonist; and |
(9) other criteria as determined in rules adopted |
pursuant to this Section. |
(h-10) A training curriculum to recognize and respond to |
respiratory distress, including the administration of |
undesignated asthma medication, may be conducted online or in |
person. The training must include, but is not limited to: |
(1) how to recognize symptoms of respiratory distress |
and how to distinguish respiratory distress from |
anaphylaxis; |
(2) how to respond to an emergency involving |
respiratory distress; |
|
(3) asthma medication dosage and administration; |
(4) the importance of calling 9-1-1 or, if 9-1-1 is |
not available, other local emergency medical services; |
(5) a test demonstrating competency of the knowledge |
required to recognize respiratory distress and administer |
asthma medication; and |
(6) other criteria as determined in rules adopted |
under this Section. |
(i) Within 3 days after the administration of an |
undesignated epinephrine delivery system injector by a school |
nurse, trained personnel, or a student at a school or |
school-sponsored activity, the school must report to the State |
Board of Education in a form and manner prescribed by the State |
Board the following information: |
(1) age and type of person receiving epinephrine |
(student, staff, visitor); |
(2) any previously known diagnosis of a severe |
allergy; |
(3) trigger that precipitated allergic episode; |
(4) location where symptoms developed; |
(5) number of doses administered; |
(6) type of person administering epinephrine (school |
nurse, trained personnel, student); and |
(7) any other information required by the State Board. |
If a school district, public school, charter school, or |
nonpublic school maintains or has an independent contractor |
|
providing transportation to students who maintains a supply of |
undesignated epinephrine delivery systems injectors, then the |
school district, public school, charter school, or nonpublic |
school must report that information to the State Board of |
Education upon adoption or change of the policy of the school |
district, public school, charter school, nonpublic school, or |
independent contractor, in a manner as prescribed by the State |
Board. The report must include the number of undesignated |
epinephrine delivery systems injectors in supply. |
(i-5) Within 3 days after the administration of an opioid |
antagonist by a school nurse or trained personnel, the school |
must report to the State Board of Education, in a form and |
manner prescribed by the State Board, the following |
information: |
(1) the age and type of person receiving the opioid |
antagonist (student, staff, or visitor); |
(2) the location where symptoms developed; |
(3) the type of person administering the opioid |
antagonist (school nurse or trained personnel); and |
(4) any other information required by the State Board. |
(i-10) Within 3 days after the administration of |
undesignated asthma medication by a school nurse, trained |
personnel, or a student at a school or school-sponsored |
activity, the school must report to the State Board of |
Education, on a form and in a manner prescribed by the State |
Board of Education, the following information: |
|
(1) the age and type of person receiving the asthma |
medication (student, staff, or visitor); |
(2) any previously known diagnosis of asthma for the |
person; |
(3) the trigger that precipitated respiratory |
distress, if identifiable; |
(4) the location of where the symptoms developed; |
(5) the number of doses administered; |
(6) the type of person administering the asthma |
medication (school nurse, trained personnel, or student); |
(7) the outcome of the asthma medication |
administration; and |
(8) any other information required by the State Board. |
(j) By October 1, 2015 and every year thereafter, the |
State Board of Education shall submit a report to the General |
Assembly identifying the frequency and circumstances of |
undesignated epinephrine and undesignated asthma medication |
administration during the preceding academic year. Beginning |
with the 2017 report, the report shall also contain |
information on which school districts, public schools, charter |
schools, and nonpublic schools maintain or have independent |
contractors providing transportation to students who maintain |
a supply of undesignated epinephrine delivery systems |
injectors. This report shall be published on the State Board's |
Internet website on the date the report is delivered to the |
General Assembly. |
|
(j-5) Annually, each school district, public school, |
charter school, or nonpublic school shall request an asthma |
action plan from the parents or guardians of a pupil with |
asthma. If provided, the asthma action plan must be kept on |
file in the office of the school nurse or, in the absence of a |
school nurse, the school administrator. Copies of the asthma |
action plan may be distributed to appropriate school staff who |
interact with the pupil on a regular basis, and, if |
applicable, may be attached to the pupil's federal Section 504 |
plan or individualized education program plan. |
(j-10) To assist schools with emergency response |
procedures for asthma, the State Board of Education, in |
consultation with statewide professional organizations with |
expertise in asthma management and a statewide organization |
representing school administrators, shall develop a model |
asthma episode emergency response protocol before September 1, |
2016. Each school district, charter school, and nonpublic |
school shall adopt an asthma episode emergency response |
protocol before January 1, 2017 that includes all of the |
components of the State Board's model protocol. |
(j-15) (Blank). |
(j-20) On or before October 1, 2016 and every year |
thereafter, the State Board of Education shall submit a report |
to the General Assembly and the Department of Public Health |
identifying the frequency and circumstances of opioid |
antagonist administration during the preceding academic year. |
|
This report shall be published on the State Board's Internet |
website on the date the report is delivered to the General |
Assembly. |
(k) The State Board of Education may adopt rules necessary |
to implement this Section. |
(l) Nothing in this Section shall limit the amount of |
epinephrine delivery systems injectors that any type of school |
or student may carry or maintain a supply of. |
(Source: P.A. 102-413, eff. 8-20-21; 102-813, eff. 5-13-22; |
103-175, eff. 6-30-23; 103-196, eff. 1-1-24; 103-348, eff. |
1-1-24; 103-542, eff. 7-1-24 (see Section 905 of P.A. 103-563 |
for effective date of P.A. 103-542); 103-605, eff. 7-1-24.) |
Section 20. The Illinois Insurance Code is amended by |
changing Section 356z.33 as follows: |
(215 ILCS 5/356z.33) |
Sec. 356z.33. Coverage for epinephrine delivery systems |
epinephrine injectors. |
(a) A group or individual policy of accident and health |
insurance or a managed care plan that is amended, delivered, |
issued, or renewed on or after January 1, 2020 (the effective |
date of Public Act 101-281) shall provide coverage for |
medically necessary epinephrine delivery systems epinephrine |
injectors for persons 18 years of age or under. As used in this |
Section, "epinephrine delivery system" "epinephrine injector" |
|
has the meaning given to that term in Section 5 of the |
Epinephrine Delivery System Epinephrine Injector Act. |
(b) An insurer that provides coverage for medically |
necessary epinephrine delivery systems epinephrine injectors |
shall limit the total amount that an insured is required to pay |
for a twin-pack of medically necessary epinephrine delivery |
systems epinephrine injectors at an amount not to exceed $60, |
regardless of the type of epinephrine delivery system |
epinephrine injector; except that this provision does not |
apply to the extent such coverage would disqualify a |
high-deductible health plan from eligibility for a health |
savings account pursuant to Section 223 of the Internal |
Revenue Code (26 U.S.C. 223). |
(c) Nothing in this Section prevents an insurer from |
reducing an insured's cost sharing by an amount greater than |
the amount specified in subsection (b). |
(d) The Department may adopt rules as necessary to |
implement and administer this Section. |
(Source: P.A. 102-558, eff. 8-20-21; 103-454, eff. 1-1-25; |
103-718, eff. 7-19-24.) |
Section 25. The Medical Practice Act of 1987 is amended by |
changing Section 65 as follows: |
(225 ILCS 60/65) |
(Section scheduled to be repealed on January 1, 2027) |
|
Sec. 65. Annie LeGere Law; epinephrine delivery system |
epinephrine auto-injector. A licensee under this Act may not |
be subject to discipline for providing a standing order or |
prescription for an epinephrine delivery system epinephrine |
auto-injector in accordance with Section 40 of the Illinois |
State Police Act or Section 10.19 of the Illinois Police |
Training Act. |
(Source: P.A. 102-538, eff. 8-20-21.) |
Section 30. The Epinephrine Injector Act is amended by |
changing Sections 1, 5, 10, 15, and 20 as follows: |
(410 ILCS 27/1) |
Sec. 1. Short title. This Act may be cited as the |
Epinephrine Delivery System Epinephrine Injector Act. |
(Source: P.A. 99-711, eff. 1-1-17; 100-799, eff. 1-1-19.) |
(410 ILCS 27/5) |
Sec. 5. Definitions. As used in this Act: |
"Administer" means to directly apply an epinephrine |
delivery system to the body of an individual. |
"Authorized entity" means any entity or organization, |
other than a school covered under Section 22-30 of the School |
Code, in connection with or at which allergens capable of |
causing anaphylaxis may be present, including, but not limited |
to, independent contractors who provide student transportation |
|
to schools, recreation camps, colleges and universities, day |
care facilities, youth sports leagues, amusement parks, |
restaurants, sports arenas, and places of employment. The |
Department shall, by rule, determine what constitutes a day |
care facility under this definition. |
"Authorized individual" means an individual who has |
successfully completed the training program under Section 10 |
of this Act. |
"Department" means the Department of Public Health. |
"Epinephrine delivery system" means any form of |
epinephrine that is approved by the United States Food and |
Drug Administration, including any device that contains a dose |
of epinephrine, and that is used to administer epinephrine |
into the human body to prevent or treat a life-threatening |
allergic reaction. |
"Health care practitioner" means a physician licensed to |
practice medicine in all its branches under the Medical |
Practice Act of 1987, a physician assistant under the |
Physician Assistant Practice Act of 1987 with prescriptive |
authority, or an advanced practice registered nurse with |
prescribing authority under Article 65 of the Nurse Practice |
Act. |
"Pharmacist" has the meaning given to that term under |
subsection (k-5) of Section 3 of the Pharmacy Practice Act. |
"Undesignated epinephrine delivery system injector" means |
an epinephrine delivery system injector prescribed in the name |
|
of an authorized entity. |
(Source: P.A. 104-229, eff. 1-1-26.) |
(410 ILCS 27/10) |
Sec. 10. Prescription to authorized entity; use; training. |
(a) A health care practitioner may prescribe epinephrine |
delivery systems injectors in the name of an authorized entity |
or authorized individual for use in accordance with this Act, |
and pharmacists and health care practitioners may dispense |
epinephrine delivery systems pursuant to a prescription issued |
in the name of an authorized entity or authorized individual. |
Such prescriptions shall be valid for a period of 2 years. |
(a-1) A health care provider with prescribing authority |
who is employed by or under contract with the Department may |
issue a statewide standing order for the dispensing of |
epinephrine delivery systems for use under subsection (c) by |
authorized individuals or by employees or agents of authorized |
entities who have completed the training required by |
subsection (d). |
(b) An authorized entity or authorized individual may |
acquire and stock a supply of undesignated epinephrine |
delivery systems pursuant to a prescription issued under |
subsection (a) of this Section. Such undesignated epinephrine |
delivery systems shall be stored in a location readily |
accessible in an emergency and in accordance with the |
instructions for use of the epinephrine delivery systems. The |
|
Department may establish any additional requirements an |
authorized entity or authorized individual must follow under |
this Act. |
(c) An employee or agent of an authorized entity who is an |
authorized individual or any other individual who is an |
authorized individual may: |
(1) anywhere allergens capable of causing anaphylaxis |
may be present provide an epinephrine delivery system to |
any individual whom the employee, agent, or other |
individual believes in good faith is experiencing |
anaphylaxis, or to the parent, guardian, or caregiver of |
such individual, for immediate administration, regardless |
of whether the individual has a prescription for an |
epinephrine delivery system or has previously been |
diagnosed with an allergy; or |
(2) anywhere allergens capable of causing anaphylaxis |
may be present administer an epinephrine delivery system |
to any individual whom the employee, agent, or other |
individual believes in good faith is experiencing |
anaphylaxis, regardless of whether the individual has a |
prescription for an epinephrine delivery system or has |
previously been diagnosed with an allergy. |
(d) An employee, agent, or other individual authorized |
must complete an anaphylaxis training program before he or she |
is able to provide or administer an epinephrine delivery |
system under this Section. Such training shall be valid for a |
|
period of 2 years and shall be conducted by a nationally |
recognized organization experienced in training laypersons in |
emergency health treatment. The Department shall include links |
to training providers' websites on its website. |
Training shall include, but is not limited to: |
(1) how to recognize signs and symptoms of an allergic |
reaction, including anaphylaxis; |
(2) how to administer an epinephrine delivery system; |
and |
(3) a test demonstrating competency of the knowledge |
required to recognize anaphylaxis and administer an |
epinephrine delivery system. |
Training may also include, but is not limited to: |
(A) a review of high-risk areas on the authorized |
entity's property and its related facilities; |
(B) steps to take to prevent exposure to allergens; |
(C) emergency follow-up procedures; and |
(D) other criteria as determined in rules adopted |
pursuant to this Act. |
Training may be conducted either online or in person. The |
entity or individual conducting the training shall issue a |
certificate to each person who successfully completes the |
anaphylaxis training program. The Department shall approve |
training programs and list permitted training programs on the |
Department's Internet website. |
(Source: P.A. 104-229, eff. 1-1-26.) |
|
(410 ILCS 27/15) |
Sec. 15. Costs. Whichever entity initiates the process of |
obtaining undesignated epinephrine delivery systems and |
providing training to personnel for carrying and administering |
undesignated epinephrine delivery systems shall pay for the |
costs of the undesignated epinephrine delivery systems. |
(Source: P.A. 104-229, eff. 1-1-26.) |
(410 ILCS 27/20) |
Sec. 20. Limitations. The use of an undesignated |
epinephrine delivery system in accordance with the |
requirements of this Act does not constitute the practice of |
medicine or any other profession that requires medical |
licensure. |
Nothing in this Act shall limit the amount of epinephrine |
delivery systems that an authorized entity or individual may |
carry or maintain a supply of. |
(Source: P.A. 104-229, eff. 1-1-26.) |
Section 35. The Emergency Asthma Inhalers and Allergy |
Treatment for Children Act is amended by changing Section 10 |
as follows: |
(410 ILCS 607/10) |
Sec. 10. Possession, self-administration, and use of |
|
epinephrine delivery systems epinephrine auto-injectors or |
inhalers at recreation camps and after-school care programs. |
(a) A recreation camp or an after-school care program |
shall permit a child with severe, potentially life-threatening |
allergies to possess, self-administer, and use an epinephrine |
delivery system epinephrine auto-injector or inhaler, if the |
following conditions are satisfied: |
(1) The child has the written approval of his or her |
parent or guardian. |
(2) The recreational camp or after-school care program |
administrator or, if a nurse is assigned to the camp or |
program, the nurse shall receive copies of the written |
approvals required under paragraph (1) of subsection (a) |
of this Section. |
(3) The child's parent or guardian shall submit |
written verification confirming that the child has the |
knowledge and skills to safely possess, self-administer, |
and use an epinephrine delivery system epinephrine |
auto-injector or inhaler in a camp or an after-school care |
program setting. |
(b) The child's parent or guardian shall provide the camp |
or program with the following information: |
(1) the child's name; |
(2) the name, route, and dosage of medication; |
(3) the frequency and time of medication |
administration or assistance; |
|
(4) the date of the order; |
(5) a diagnosis and any other medical conditions |
requiring medications, if not a violation of |
confidentiality or if not contrary to the request of the |
parent or guardian to keep confidential; |
(6) specific recommendations for administration; |
(7) any special side effects, contraindications, and |
adverse reactions to be observed; |
(8) the name of each required medication; and |
(9) any severe adverse reactions that may occur to |
another child, for whom the epinephrine delivery system |
epinephrine auto-injector or inhaler is not prescribed, |
should the other child receive a dose of the medication. |
(c) If the conditions of this Act are satisfied, the child |
may possess, self-administer, and use an epinephrine delivery |
system epinephrine auto-injector or inhaler at the camp or |
after-school care program or at any camp-sponsored or |
program-sponsored activity, event, or program. |
(d) The recreational camp or after-school care program |
must inform the parents or guardians of the child, in writing, |
that the recreational camp or after-school care program and |
its employees and agents are to incur no liability, as |
applicable, except for willful and wanton conduct, as a result |
of any injury arising from the self-administration of |
medication to the child. The parents or guardians of the child |
must sign a statement acknowledging that the recreational camp |
|
or after-school care program is to incur no liability, except |
for willful and wanton conduct, as a result of any injury |
arising from the self-administration of medication by the |
child and that the parents or guardians must indemnify and |
hold harmless the recreational camp or after-school care |
program and its employees and agents, as applicable, against |
any claims, except a claim based on willful and wanton |
conduct, arising out of the self-administration of medication |
by the child. |
(e) After-school care program personnel who have completed |
an anaphylaxis training program as identified under the |
Epinephrine Delivery System Epinephrine Injector Act may |
administer an undesignated epinephrine injection to any child |
if the after-school care program personnel believe in good |
faith that the child is having an anaphylactic reaction while |
in the after-school care program. After-school care program |
personnel may carry undesignated epinephrine delivery systems |
epinephrine injectors on their person while in the |
after-school care program. |
(f) After-school care program personnel may administer |
undesignated asthma medication to any child if the |
after-school care program personnel believe in good faith that |
the child is experiencing respiratory distress while in the |
after-school care program. After-school care program personnel |
may carry undesignated asthma medication on their person while |
in the after-school care program. |
|
(g) If after-school care program personnel are to |
administer an undesignated epinephrine injection or an |
undesignated asthma medication to a child, the after-school |
care program personnel must inform the parents or guardians of |
the child, in writing, that the after-school care program and |
its employees and agents, acting in accordance with standard |
protocols and the prescription for the injection or |
medication, shall incur no liability, except for willful and |
wanton conduct, as a result of any injury arising from the |
administration of the injection or medication, notwithstanding |
whether authorization was given by the child's parents or |
guardians or by the child's physician, physician assistant, or |
advanced practice registered nurse. A parent or guardian of |
the child must sign a statement acknowledging that the |
after-school care program and its employees and agents are to |
incur no liability, except for willful and wanton conduct, as |
a result of any injury arising from the administration of the |
medication or injection, regardless of whether authorization |
was given by a parent or guardian of the child or by the |
child's physician, physician assistant, or advanced practice |
registered nurse, and that the parent or guardian must also |
indemnify and hold harmless the after-school care program and |
its employees and agents against any claims, except a claim |
based on willful and wanton conduct, arising out of the |
administration of the medication or injection, regardless of |
whether authorization was given by the child's parent or |
|
guardian or by the child's physician, physician assistant, or |
advanced practice registered nurse. |
(h) If after-school care program personnel administer an |
undesignated epinephrine injection to a person and the |
after-school care program personnel believe in good faith the |
person is having an anaphylactic reaction or administer |
undesignated asthma medication to a person and believe in good |
faith the person is experiencing respiratory distress, then |
the after-school care program and its employees and agents, |
acting in accordance with standard protocols and the |
prescription for the injection or medication, shall not incur |
any liability or be subject to professional discipline, except |
for willful and wanton conduct, as a result of any injury |
arising from the use of the injection or medication, |
notwithstanding whether notice was given to or authorization |
was given by the child's parent or guardian or by the child's |
physician, physician assistant, or advanced practice |
registered nurse and notwithstanding the absence of the |
parent's or guardian's signed statement acknowledging release |
from liability. |
(i) The changes made to this Section by this amendatory |
Act of the 103rd General Assembly apply to actions filed on or |
after the effective date of this amendatory Act of the 103rd |
General Assembly. |
(Source: P.A. 103-438, eff. 8-4-23.) |
|
Section 40. The Illinois Food, Drug and Cosmetic Act is |
amended by changing Section 3.21 as follows: |
(410 ILCS 620/3.21) (from Ch. 56 1/2, par. 503.21) |
Sec. 3.21. Except as authorized by this Act, the Illinois |
Controlled Substances Act, the Pharmacy Practice Act, the |
Dental Practice Act, the Medical Practice Act of 1987, the |
Veterinary Medicine and Surgery Practice Act of 2004, the |
Podiatric Medical Practice Act of 1987, Section 22-30 of the |
School Code, Section 40 of the Illinois State Police Act, |
Section 10.19 of the Illinois Police Training Act, or the |
Epinephrine Delivery System Epinephrine Injector Act, to sell |
or dispense a prescription drug without a prescription. |
(Source: P.A. 102-538, eff. 8-20-21.) |