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Public Act 103-0639 Public Act 0639 103RD GENERAL ASSEMBLY | Public Act 103-0639 | SB3414 Enrolled | LRB103 38590 RPS 68726 b |
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| AN ACT concerning regulation. | Be it enacted by the People of the State of Illinois, | represented in the General Assembly: | Section 5. The Illinois Insurance Code is amended by | changing Section 356z.59 as follows: | (215 ILCS 5/356z.59) | Sec. 356z.59. Coverage for continuous glucose monitors. | (a) A group or individual policy of accident and health | insurance or a managed care plan that is amended, delivered, | issued, or renewed before January 1, 2026 on or after January | 1, 2024 shall provide coverage for medically necessary | continuous glucose monitors for individuals who are diagnosed | with any form of diabetes mellitus type 1 or type 2 diabetes | and require insulin for the management of their diabetes. 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, 2026 shall provide coverage for | continuous glucose monitors, related supplies, and training in | the use of continuous glucose monitors for any individual if | the following requirements are met: | (1) the individual is diagnosed with diabetes | mellitus; | (2) the continuous glucose monitor has been prescribed |
| by a physician licensed under the Medical Practice Act of | 1987 or a certified nurse practitioner or physician | assistant with a collaborative agreement with the | physician; | (3) the continuous glucose monitor has been prescribed | in accordance with the Food and Drug Administration's | indications for use; | (4) the prescriber has concluded that the individual | or individual's caregiver has sufficient training in using | the continuous glucose monitor, which may be evidenced by | the prescriber having prescribed a continuous glucose | monitor, and has attested that the patient will be | provided with that training; | (5) the individual either: | (A) uses insulin for treatment via one or more | injections or infusions of insulin per day, and only | one injection or infusion of one type of insulin shall | be sufficient utilization of insulin to qualify for a | continuous glucose monitor under this Section; or | (B) has reported a history of problematic | hypoglycemia with documentation to the individual's | medical provider showing at least one of the | following: | (i) recurrent hypoglycemic events | characterized by an altered mental or physical | state, despite multiple attempts to adjust |
| medications or modify the diabetes treatment plan, | as documented by a medical provider; or | (ii) a history of at least one hypoglycemic | event characterized by an altered mental or | physical state requiring third-party assistance | for treatment of hypoglycemia, as documented by | the individual's medical provider, which may be | self-reported by the individual; third-party | assistance shall not, in any event, be deemed to | require that the individual had been admitted to a | hospital or visited an emergency department; and | (6) within 6 months prior to prescribing a continuous | glucose monitor, the medical provider prescribing the | continuous glucose monitor had an in-person or covered | telehealth visit with the individual to evaluate the | individual's diabetes control and has determined that the | criteria of paragraphs (1) through (5) are met. | Notwithstanding any other provision of this Section, to | qualify for a continuous glucose monitor under this Section, | an individual is not required to have a diagnosis of | uncontrolled diabetes; have a history of emergency room visits | or hospitalizations; or show improved glycemic control. | All continuous glucose monitors covered under this Section | shall be approved for use by individuals, and the choice of | device shall be made based upon the individual's circumstances | and medical needs in consultation with the individual's |
| medical provider, subject to the terms of the policy. | (b) Any individual who is diagnosed with diabetes mellitus | and meets the requirements of this Section shall not be | required to obtain prior authorization for coverage for a | continuous glucose monitor, and coverage shall be continuous | once the continuous glucose monitor is prescribed. | (c) 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, 2026 shall not impose | a deductible, coinsurance, copayment, or any other | cost-sharing requirement on the coverage of a one-month supply | of continuous glucose monitors, including one transmitter if | necessary, as provided under this Section. The provisions of | this subsection do not apply to coverage under this Section to | the extent such coverage would disqualify a high-deductible | health plan from eligibility for a health savings account | pursuant to the federal Internal Revenue Code, 26 U.S.C. 23. | (Source: P.A. 102-1093, eff. 1-1-23; 103-154, eff. 6-30-23.) | Section 10. The Illinois Public Aid Code is amended by | adding Section 5-16.8a as follows: | (305 ILCS 5/5-16.8a new) | Sec. 5-16.8a. Rules concerning continuous glucose monitor | coverage. The Department shall adopt rules to implement the | changes made to Section 356z.59 of the Illinois Insurance |
| Code, as applied to the medical assistance program. The rules | shall, at a minimum, provide that: | (1) the ordering provider must be a physician licensed | under the Medical Practice Act of 1987 or a certified | nurse practitioner or physician assistant with a | collaborative agreement with the physician; the ordering | provider is not required to obtain continuing medical | education in order to prescribe a continuous glucose | monitor; | (2) continuous glucose monitors are not required to | have an alarm when glucose levels are outside the | pre-determined range; the capacity to generate predictive | alerts in case of impending hypoglycemia; or the ability | to transmit real-time glucose values and alerts to the | patient and designated other persons; | (3) the beneficiary is not required to need intensive | insulin therapy; | (4) the beneficiary is not required to have a recent | history of emergency room visits or hospitalizations | related to hypoglycemia, hyperglycemia, or ketoacidosis; | (5) if the beneficiary has gestational diabetes, the | beneficiary is not required to have suboptimal glycemic | control that is likely to harm the beneficiary or the | fetus; | (6) if a beneficiary has diabetes mellitus and the | beneficiary does not meet the coverage requirements or if |
| the beneficiary is in a population in which continuous | glucose monitor usage has not been well-studied, requests | shall be reviewed, on a case-by-case basis, for medical | necessity and approved if appropriate; and | (7) prior authorization is required for a prescription | of a continuous glucose monitor; once a continuous glucose | monitor is prescribed, the prior authorization shall be | approved for a 12-month period. | Section 99. Effective date. This Act takes effect July 1, | 2024. |
Effective Date: 7/1/2024
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