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1 | AN ACT concerning regulation. | |||||||||||||||||||||
2 | Be it enacted by the People of the State of Illinois, | |||||||||||||||||||||
3 | represented in the General Assembly: | |||||||||||||||||||||
4 | Section 5. The Illinois Insurance Code is amended by | |||||||||||||||||||||
5 | changing Section 356z.59 as follows: | |||||||||||||||||||||
6 | (215 ILCS 5/356z.59) | |||||||||||||||||||||
7 | Sec. 356z.59. Coverage for continuous glucose monitors. | |||||||||||||||||||||
8 | (a) In this Section, "diabetes mellitus" includes, but is | |||||||||||||||||||||
9 | not limited to: type 1 diabetes; type 1.5 diabetes; type 2 | |||||||||||||||||||||
10 | diabetes; type 3c diabetes; maturity-onset diabetes of the | |||||||||||||||||||||
11 | young; neonatal diabetes; latent autoimmune diabetes of | |||||||||||||||||||||
12 | adults; Wolfram Syndrome; Alstrom Syndrome; cystic fibrosis | |||||||||||||||||||||
13 | diabetes; gestational diabetes; diabetes caused by the loss | |||||||||||||||||||||
14 | of, or permanent damage to, the pancreas; or | |||||||||||||||||||||
15 | medication-induced diabetes. | |||||||||||||||||||||
16 | (b) A group or individual policy of accident and health | |||||||||||||||||||||
17 | insurance or a managed care plan that is amended, delivered, | |||||||||||||||||||||
18 | issued, or renewed on or after January 1, 2024 and before | |||||||||||||||||||||
19 | January 1, 2025 shall provide coverage for medically necessary | |||||||||||||||||||||
20 | continuous glucose monitors for individuals who are diagnosed | |||||||||||||||||||||
21 | with type 1 or type 2 diabetes and require insulin for the | |||||||||||||||||||||
22 | management of their diabetes. A group or individual policy of | |||||||||||||||||||||
23 | accident and health insurance or a managed care plan that is |
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1 | amended, delivered, issued, or renewed on or after January 1, | ||||||
2 | 2025 shall provide coverage for continuous glucose monitors, | ||||||
3 | related supplies, and training in the use of continuous | ||||||
4 | glucose monitors for any individual if the following | ||||||
5 | requirements are met: | ||||||
6 | (1) the individual is diagnosed with diabetes | ||||||
7 | mellitus; | ||||||
8 | (2) the continuous glucose monitor has been prescribed | ||||||
9 | by a physician licensed under the Medical Practice Act of | ||||||
10 | 1987 or a certified nurse practitioner or physician | ||||||
11 | assistant with a collaborative agreement with the | ||||||
12 | physician; | ||||||
13 | (3) the continuous glucose monitor has been prescribed | ||||||
14 | in accordance with the Food and Drug Administration's | ||||||
15 | indications for use; | ||||||
16 | (4) the prescriber has concluded that the individual | ||||||
17 | or individual's caregiver has sufficient training in using | ||||||
18 | the continuous glucose monitor, which may be evidenced by | ||||||
19 | the prescriber having prescribed a continuous glucose | ||||||
20 | monitor, and has attested that the patient will be | ||||||
21 | provided with that training; | ||||||
22 | (5) the individual either: | ||||||
23 | (A) uses insulin for treatment via one or more | ||||||
24 | injections or infusions of insulin per day, and only | ||||||
25 | one injection or infusion of one type of insulin shall | ||||||
26 | be sufficient utilization of insulin to qualify for a |
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1 | continuous glucose monitor under this Section; or | ||||||
2 | (B) has reported a history of problematic | ||||||
3 | hypoglycemia with documentation to the individual's | ||||||
4 | medical provider showing at least one of the | ||||||
5 | following: | ||||||
6 | (i) recurrent hypoglycemic events | ||||||
7 | characterized by an altered mental or physical | ||||||
8 | state, despite multiple attempts to adjust | ||||||
9 | medications or modify the diabetes treatment plan, | ||||||
10 | as documented by a medical provider; or | ||||||
11 | (ii) a history of at least one hypoglycemic | ||||||
12 | event characterized by an altered mental or | ||||||
13 | physical state requiring third-party assistance | ||||||
14 | for treatment of hypoglycemia, as documented by | ||||||
15 | the individual's medical provider, which may be | ||||||
16 | self-reported by the individual; third-party | ||||||
17 | assistance shall not, in any event, be deemed to | ||||||
18 | require that the individual had been admitted to a | ||||||
19 | hospital or visited an emergency department; and | ||||||
20 | (6) within 6 months prior to prescribing a continuous | ||||||
21 | glucose monitor, the medical provider prescribing the | ||||||
22 | continuous glucose monitor had an in-person or covered | ||||||
23 | telehealth visit with the individual to evaluate the | ||||||
24 | individual's diabetes control and has determined that the | ||||||
25 | criteria of paragraphs (1) through (5) are met. | ||||||
26 | Notwithstanding any other provision of this Section, to |
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1 | qualify for a continuous glucose monitor under this Section, | ||||||
2 | an individual is not required to have a diagnosis of | ||||||
3 | uncontrolled diabetes; have a history of emergency room visits | ||||||
4 | or hospitalizations; or show improved glycemic control. | ||||||
5 | All continuous glucose monitors covered under this Section | ||||||
6 | shall be approved for usage by individuals, and the choice of | ||||||
7 | device shall be made based upon the individual's | ||||||
8 | circumstances, preferences, and needs in consultation with the | ||||||
9 | individual's medical provider. | ||||||
10 | (c) Any individual who is diagnosed with diabetes mellitus | ||||||
11 | and meets the requirements of this Section shall not be | ||||||
12 | required to obtain prior authorization for coverage for a | ||||||
13 | continuous glucose monitor, and coverage shall be continuous | ||||||
14 | once the continuous glucose monitor is prescribed. | ||||||
15 | (d) A group or individual policy of accident and health | ||||||
16 | insurance or a managed care plan that is amended, delivered, | ||||||
17 | issued, or renewed on or after January 1, 2025 shall not impose | ||||||
18 | a deductible, coinsurance, copayment, or any other | ||||||
19 | cost-sharing requirement on the coverage provided under this | ||||||
20 | Section. The provisions of this subsection do not apply to | ||||||
21 | coverage under this Section to the extent such coverage would | ||||||
22 | disqualify a high-deductible health plan from eligibility for | ||||||
23 | a health savings account pursuant to the federal Internal | ||||||
24 | Revenue Code, 26 U.S.C. 23. | ||||||
25 | (Source: P.A. 102-1093, eff. 1-1-23; 103-154, eff. 6-30-23.) |
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1 | Section 10. The Illinois Public Aid Code is amended by | ||||||
2 | adding Section 5-16.8a as follows: | ||||||
3 | (305 ILCS 5/5-16.8a new) | ||||||
4 | Sec. 5-16.8a. Rules concerning continuous glucose monitor | ||||||
5 | coverage. The Department shall adopt rules to implement the | ||||||
6 | changes made to Section 356z.59 of the Illinois Insurance | ||||||
7 | Code, as applied to the medical assistance program. The rules | ||||||
8 | shall, at a minimum, provide that: | ||||||
9 | (1) the ordering provider must be a physician licensed | ||||||
10 | under the Medical Practice Act of 1987 or a certified | ||||||
11 | nurse practitioner or physician assistant with a | ||||||
12 | collaborative agreement with the physician; | ||||||
13 | (2) continuous glucose monitors are not required to | ||||||
14 | have an alarm when glucose levels are outside the | ||||||
15 | pre-determined range; the capacity to generate predictive | ||||||
16 | alerts in case of impending hypoglycemia; or the ability | ||||||
17 | to transmit real-time glucose values and alerts to the | ||||||
18 | patient and designated other persons; | ||||||
19 | (3) the beneficiary is not required to need intensive | ||||||
20 | insulin therapy; | ||||||
21 | (4) the beneficiary is not required to have a recent | ||||||
22 | history of emergency room visits or hospitalizations | ||||||
23 | related to hypoglycemia, hyperglycemia, or ketoacidosis; | ||||||
24 | (5) if the beneficiary has gestational diabetes, the | ||||||
25 | beneficiary is not required to have suboptimal glycemic |
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1 | control that is likely to harm the beneficiary or the | ||||||
2 | fetus; | ||||||
3 | (6) if a beneficiary has diabetes mellitus and the | ||||||
4 | beneficiary does not meet the coverage requirements or if | ||||||
5 | the beneficiary is in a population in which continuous | ||||||
6 | glucose monitor usage has not been well-studied, requests | ||||||
7 | shall be reviewed, on a case-by-case basis, for medical | ||||||
8 | necessity and approved if appropriate; and | ||||||
9 | (7) the beneficiary is not required to obtain prior | ||||||
10 | authorization for coverage for a continuous glucose | ||||||
11 | monitor, and that coverage is continuous once the | ||||||
12 | continuous glucose monitor is prescribed. | ||||||
13 | Section 99. Effective date. This Act takes effect July 1, | ||||||
14 | 2024. |