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Public Act 103-0980 Public Act 0980 103RD GENERAL ASSEMBLY | Public Act 103-0980 | SB3350 Enrolled | LRB103 38262 CES 68397 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 Substance Use Disorder Act is amended by | changing Section 5-23 as follows: | (20 ILCS 301/5-23) | Sec. 5-23. Drug Overdose Prevention Program. | (a) Reports. | (1) The Department may publish annually a report on | drug overdose trends statewide that reviews State death | rates from available data to ascertain changes in the | causes or rates of fatal and nonfatal drug overdose. The | report shall also provide information on interventions | that would be effective in reducing the rate of fatal or | nonfatal drug overdose and on the current substance use | disorder treatment capacity within the State. The report | shall include an analysis of drug overdose information | reported to the Department of Public Health pursuant to | subsection (e) of Section 3-3013 of the Counties Code, | Section 6.14g of the Hospital Licensing Act, and | subsection (j) of Section 22-30 of the School Code. | (2) The report may include: | (A) Trends in drug overdose death rates. |
| (B) Trends in emergency room utilization related | to drug overdose and the cost impact of emergency room | utilization. | (C) Trends in utilization of pre-hospital and | emergency services and the cost impact of emergency | services utilization. | (D) Suggested improvements in data collection. | (E) A description of other interventions effective | in reducing the rate of fatal or nonfatal drug | overdose. | (F) A description of efforts undertaken to educate | the public about unused medication and about how to | properly dispose of unused medication, including the | number of registered collection receptacles in this | State, mail-back programs, and drug take-back events. | (G) An inventory of the State's substance use | disorder treatment capacity, including, but not | limited to: | (i) The number and type of licensed treatment | programs in each geographic area of the State. | (ii) The availability of medication-assisted | treatment at each licensed program and which types | of medication-assisted treatment are available. | (iii) The number of recovery homes that accept | individuals using medication-assisted treatment in | their recovery. |
| (iv) The number of medical professionals | currently authorized to prescribe buprenorphine | and the number of individuals who fill | prescriptions for that medication at retail | pharmacies as prescribed. | (v) Any partnerships between programs licensed | by the Department and other providers of | medication-assisted treatment. | (vi) Any challenges in providing | medication-assisted treatment reported by programs | licensed by the Department and any potential | solutions. | (b) Programs; drug overdose prevention. | (1) The Department may establish a program to provide | for the production and publication, in electronic and | other formats, of drug overdose prevention, recognition, | and response literature. The Department may develop and | disseminate curricula for use by professionals, | organizations, individuals, or committees interested in | the prevention of fatal and nonfatal drug overdose, | including, but not limited to, drug users, jail and prison | personnel, jail and prison inmates, drug treatment | professionals, emergency medical personnel, hospital | staff, families and associates of drug users, peace | officers, firefighters, public safety officers, needle | exchange program staff, and other persons. In addition to |
| information regarding drug overdose prevention, | recognition, and response, literature produced by the | Department shall stress that drug use remains illegal and | highly dangerous and that complete abstinence from illegal | drug use is the healthiest choice. The literature shall | provide information and resources for substance use | disorder treatment. | The Department may establish or authorize programs for | prescribing, dispensing, or distributing opioid | antagonists for the treatment of drug overdose and for | dispensing and distributing fentanyl test strips to | further promote harm reduction efforts and prevent an | overdose . Such programs may include the prescribing of | opioid antagonists for the treatment of drug overdose to a | person who is not at risk of opioid overdose but who, in | the judgment of the health care professional, may be in a | position to assist another individual during an | opioid-related drug overdose and who has received basic | instruction on how to administer an opioid antagonist. | (2) The Department may provide advice to State and | local officials on the growing drug overdose crisis, | including the prevalence of drug overdose incidents, | programs promoting the disposal of unused prescription | drugs, trends in drug overdose incidents, and solutions to | the drug overdose crisis. | (3) The Department may support drug overdose |
| prevention, recognition, and response projects by | facilitating the acquisition of opioid antagonist | medication approved for opioid overdose reversal, | facilitating the acquisition of opioid antagonist | medication approved for opioid overdose reversal, | providing trainings in overdose prevention best practices, | facilitating the acquisition of fentanyl test strips to | test for the presence of fentanyl, a fentanyl analog, or a | drug adulterant within a controlled substance, connecting | programs to medical resources, establishing a statewide | standing order for the acquisition of needed medication, | establishing learning collaboratives between localities | and programs, and assisting programs in navigating any | regulatory requirements for establishing or expanding such | programs. | (4) In supporting best practices in drug overdose | prevention programming, the Department may promote the | following programmatic elements: | (A) Training individuals who currently use drugs | in the administration of opioid antagonists approved | for the reversal of an opioid overdose and in the use | of fentanyl test strips to test for the presence of | fentanyl, a fentanyl analog, or a drug adulterant | within a controlled substance . | (B) Directly distributing opioid antagonists | approved for the reversal of an opioid overdose rather |
| than providing prescriptions to be filled at a | pharmacy. | (B-1) Directly distributing fentanyl test strips | to test for the presence of fentanyl, a fentanyl | analog, or a drug adulterant within a controlled | substance. | (C) Conducting street and community outreach to | work directly with individuals who are using drugs. | (D) Employing community health workers or peer | recovery specialists who are familiar with the | communities served and can provide culturally | competent services. | (E) Collaborating with other community-based | organizations, substance use disorder treatment | centers, or other health care providers engaged in | treating individuals who are using drugs. | (F) Providing linkages for individuals to obtain | evidence-based substance use disorder treatment. | (G) Engaging individuals exiting jails or prisons | who are at a high risk of overdose. | (H) Providing education and training to | community-based organizations who work directly with | individuals who are using drugs and those individuals' | families and communities. | (I) Providing education and training on drug | overdose prevention and response to emergency |
| personnel and law enforcement. | (J) Informing communities of the important role | emergency personnel play in responding to accidental | overdose. | (K) Producing and distributing targeted mass media | materials on drug overdose prevention and response, | the potential dangers of leaving unused prescription | drugs in the home, and the proper methods for | disposing of unused prescription drugs. | (c) Grants. | (1) The Department may award grants, in accordance | with this subsection, to create or support local drug | overdose prevention, recognition, and response projects. | Local health departments, correctional institutions, | hospitals, universities, community-based organizations, | and faith-based organizations may apply to the Department | for a grant under this subsection at the time and in the | manner the Department prescribes. Eligible grant | activities include, but are not limited to, purchasing and | distributing opioid antagonists and fentanyl test strips , | hiring peer recovery specialists or other community | members to conduct community outreach, and hosting public | health fairs or events to distribute opioid antagonists | and fentanyl test strips , promote harm reduction | activities, and provide linkages to community partners. | (2) In awarding grants, the Department shall consider |
| the overall rate of opioid overdose, the rate of increase | in opioid overdose, and racial disparities in opioid | overdose experienced by the communities to be served by | grantees. The Department shall encourage all grant | applicants to develop interventions that will be effective | and viable in their local areas. | (3) (Blank). | (3.5) Any hospital licensed under the Hospital | Licensing Act or organized under the University of | Illinois Hospital Act shall be deemed to have met the | standards and requirements set forth in this Section to | enroll in the drug overdose prevention program upon | completion of the enrollment process except that proof of | a standing order and attestation of programmatic | requirements shall be waived for enrollment purposes. | Reporting mandated by enrollment shall be necessary to | carry out or attain eligibility for associated resources | under this Section for drug overdose prevention projects | operated on the licensed premises of the hospital and | operated by the hospital or its designated agent. The | Department shall streamline hospital enrollment for drug | overdose prevention programs by accepting such deemed | status under this Section in order to reduce barriers to | hospital participation in drug overdose prevention, | recognition, or response projects. Subject to | appropriation, any hospital under this paragraph and any |
| other organization deemed eligible by the Department shall | be enrolled to receive fentanyl test strips from the | Department and distribute fentanyl test strips upon | enrollment in the Drug Overdose Prevention Program. | (4) In addition to moneys appropriated by the General | Assembly, the Department may seek grants from private | foundations, the federal government, and other sources to | fund the grants under this Section and to fund an | evaluation of the programs supported by the grants. | (d) Health care professional prescription of opioid | antagonists. | (1) A health care professional who, acting in good | faith, directly or by standing order, prescribes or | dispenses an opioid antagonist to: (a) a patient who, in | the judgment of the health care professional, is capable | of administering the drug in an emergency, or (b) a person | who is not at risk of opioid overdose but who, in the | judgment of the health care professional, may be in a | position to assist another individual during an | opioid-related drug overdose and who has received basic | instruction on how to administer an opioid antagonist | shall not, as a result of his or her acts or omissions, be | subject to: (i) any disciplinary or other adverse action | under the Medical Practice Act of 1987, the Physician | Assistant Practice Act of 1987, the Nurse Practice Act, | the Pharmacy Practice Act, or any other professional |
| licensing statute or (ii) any criminal liability, except | for willful and wanton misconduct. | (1.5) Notwithstanding any provision of or requirement | otherwise imposed by the Pharmacy Practice Act, the | Medical Practice Act of 1987, or any other law or rule, | including, but not limited to, any requirement related to | labeling, storage, or recordkeeping, a health care | professional or other person acting under the direction of | a health care professional may, directly or by standing | order, obtain, store, and dispense an opioid antagonist to | a patient in a facility that includes, but is not limited | to, a hospital, a hospital affiliate, or a federally | qualified health center if the patient information | specified in paragraph (4) of this subsection is provided | to the patient. A person acting in accordance with this | paragraph shall not, as a result of his or her acts or | omissions, be subject to: (i) any disciplinary or other | adverse action under the Medical Practice Act of 1987, the | Physician Assistant Practice Act of 1987, the Nurse | Practice Act, the Pharmacy Practice Act, or any other | professional licensing statute; or (ii) any criminal | liability, except for willful and wanton misconduct. | (2) A person who is not otherwise licensed to | administer an opioid antagonist may in an emergency | administer without fee an opioid antagonist if the person | has received the patient information specified in |
| paragraph (4) of this subsection and believes in good | faith that another person is experiencing a drug overdose. | The person shall not, as a result of his or her acts or | omissions, be (i) liable for any violation of the Medical | Practice Act of 1987, the Physician Assistant Practice Act | of 1987, the Nurse Practice Act, the Pharmacy Practice | Act, or any other professional licensing statute, or (ii) | subject to any criminal prosecution or civil liability, | except for willful and wanton misconduct. | (3) A health care professional prescribing an opioid | antagonist to a patient shall ensure that the patient | receives the patient information specified in paragraph | (4) of this subsection. Patient information may be | provided by the health care professional or a | community-based organization, substance use disorder | program, or other organization with which the health care | professional establishes a written agreement that includes | a description of how the organization will provide patient | information, how employees or volunteers providing | information will be trained, and standards for documenting | the provision of patient information to patients. | Provision of patient information shall be documented in | the patient's medical record or through similar means as | determined by agreement between the health care | professional and the organization. The Department, in | consultation with statewide organizations representing |
| physicians, pharmacists, advanced practice registered | nurses, physician assistants, substance use disorder | programs, and other interested groups, shall develop and | disseminate to health care professionals, community-based | organizations, substance use disorder programs, and other | organizations training materials in video, electronic, or | other formats to facilitate the provision of such patient | information. | (4) For the purposes of this subsection: | "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. | "Health care professional" means a physician licensed | to practice medicine in all its branches, a licensed | physician assistant with prescriptive authority, a | licensed advanced practice registered nurse with | prescriptive authority, an advanced practice registered | nurse or physician assistant who practices in a hospital, | hospital affiliate, or ambulatory surgical treatment | center and possesses appropriate clinical privileges in | accordance with the Nurse Practice Act, or a pharmacist | licensed to practice pharmacy under the Pharmacy Practice | Act. | "Patient" includes a person who is not at risk of |
| opioid overdose but who, in the judgment of the physician, | advanced practice registered nurse, or physician | assistant, may be in a position to assist another | individual during an overdose and who has received patient | information as required in paragraph (2) of this | subsection on the indications for and administration of an | opioid antagonist. | "Patient information" includes information provided to | the patient on drug overdose prevention and recognition; | how to perform rescue breathing and resuscitation; opioid | antagonist dosage and administration; the importance of | calling 911; care for the overdose victim after | administration of the overdose antagonist; and other | issues as necessary. | (e) Drug overdose response policy. | (1) Every State and local government agency that | employs a law enforcement officer or fireman as those | terms are defined in the Line of Duty Compensation Act | must possess opioid antagonists and must establish a | policy to control the acquisition, storage, | transportation, and administration of such opioid | antagonists and to provide training in the administration | of opioid antagonists. A State or local government agency | that employs a fireman as defined in the Line of Duty | Compensation Act but does not respond to emergency medical | calls or provide medical services shall be exempt from |
| this subsection. | (2) Every publicly or privately owned ambulance, | special emergency medical services vehicle, non-transport | vehicle, or ambulance assist vehicle, as described in the | Emergency Medical Services (EMS) Systems Act, that | responds to requests for emergency services or transports | patients between hospitals in emergency situations must | possess opioid antagonists. | (3) Entities that are required under paragraphs (1) | and (2) to possess opioid antagonists may also apply to | the Department for a grant to fund the acquisition of | opioid antagonists and training programs on the | administration of opioid antagonists. | (Source: P.A. 101-356, eff. 8-9-19; 102-598, eff. 1-1-22 .) | Section 10. The Overdose Prevention and Harm Reduction Act | is amended by changing Section 5 as follows: | (410 ILCS 710/5) | Sec. 5. Needle and hypodermic syringe access program. | (a) Any governmental or nongovernmental organization, | including a local health department, community-based | organization, or a person or entity, that promotes | scientifically proven ways of mitigating health risks | associated with drug use and other high-risk behaviors may | establish and operate a needle and hypodermic syringe access |
| program. The objective of the program shall be accomplishing | all of the following: | (1) reducing the spread of HIV, AIDS, viral hepatitis, | and other bloodborne diseases; | (2) reducing the potential for needle stick injuries | from discarded contaminated equipment; and | (3) facilitating connections or linkages to | evidence-based treatment. | (b) Programs established under this Act shall provide all | of the following: | (1) Disposal of used needles and hypodermic syringes. | (2) Needles, hypodermic syringes, and other safer drug | consumption supplies, at no cost and in quantities | sufficient to ensure that needles, hypodermic syringes, or | other supplies are not shared or reused. | (3) Educational materials or training on: | (A) overdose prevention and intervention; and | (B) the prevention of HIV, AIDS, viral hepatitis, | and other common bloodborne diseases resulting from | shared drug consumption equipment and supplies. | (4) Access to opioid antagonists approved for the | reversal of an opioid overdose, or referrals to programs | that provide access to opioid antagonists approved for the | reversal of an opioid overdose. | (5) Linkages to needed services, including mental | health treatment, housing programs, substance use disorder |
| treatment, and other relevant community services. | (6) Individual consultations from a trained employee | tailored to individual needs. | (7) If feasible, a hygienic, separate space for | individuals who need to administer a prescribed injectable | medication that can also be used as a quiet space to gather | composure in the event of an adverse on-site incident, | such as a nonfatal overdose. | (8) If feasible, access to on-site drug adulterant | testing supplies. | (9) If feasible, access to fentanyl test strips to | test for the presence of fentanyl, a fentanyl analog, or a | drug adulterant within a controlled substance. | (c) Notwithstanding any provision of the Illinois | Controlled Substances Act, the Drug Paraphernalia Control Act, | or any other law, no employee or volunteer of or participant in | a program established under this Act shall be charged with or | prosecuted for possession of any of the following: | (1) Needles, hypodermic syringes, or other drug | consumption paraphernalia obtained from or returned, | directly or indirectly, to a program established under | this Act. | (2) Residual amounts of a controlled substance | contained in used needles, used hypodermic syringes, or | other used drug consumption paraphernalia obtained from or | returned, directly or indirectly, to a program established |
| under this Act. | (3) Drug adulterant testing supplies obtained from or | returned, directly or indirectly, to a program established | under this Act or a pharmacy, hospital, clinic, or other | health care facility or medical office dispensing drug | adulterant testing supplies in accordance with Section 10. | This paragraph also applies to any employee or customer of | a pharmacy, hospital, clinic, or other health care | facility or medical office dispensing drug adulterant | testing supplies in accordance with Section 10. | (4) Any residual amounts of controlled substances used | in the course of testing the controlled substance to | determine the chemical composition and potential threat of | the substances obtained for consumption that are obtained | from or returned, directly or indirectly, to a program | established under this Act. This paragraph also applies to | any person using drug adulterant testing supplies procured | in accordance with Section 10 of this Act. | In addition to any other applicable immunity or limitation | on civil liability, a law enforcement officer who, acting on | good faith, arrests or charges a person who is thereafter | determined to be entitled to immunity from prosecution under | this subsection (c) shall not be subject to civil liability | for the arrest or filing of charges. | (d) Prior to the commencing of operations of a program | established under this Act, the governmental or |
| nongovernmental organization shall submit to the Illinois | Department of Public Health all of the following information: | (1) the name of the organization, agency, group, | person, or entity operating the program; | (2) the areas and populations to be served by the | program; and | (3) the methods by which the program will meet the | requirements of subsection (b) of this Section. | The Department of Public Health may adopt rules to | implement this subsection. | (Source: P.A. 101-356, eff. 8-9-19; 102-1039, eff. 6-2-22.) | Section 5. The Overdose Prevention and Harm Reduction Act | is amended by changing Section 15 as follows: | (410 ILCS 710/15) | Sec. 15. Fentanyl test strips. To further promote harm | reduction efforts, a pharmacist or retailer may sell fentanyl | test strips over-the-counter to the public to test for the | presence of fentanyl, a fentanyl analog, or a drug adulterant | within a controlled substance. A county health department may | distribute fentanyl test strips at the county health | department facility for no fee. | (Source: P.A. 103-336, eff. 1-1-24 .) |
Effective Date: 1/1/2025
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