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1 | | (3) the continuous glucose monitor has been prescribed |
2 | | in accordance with the Food and Drug Administration's |
3 | | indications for use; |
4 | | (4) the prescriber has concluded that the individual |
5 | | or individual's caregiver has sufficient training in using |
6 | | the continuous glucose monitor, which may be evidenced by |
7 | | the prescriber having prescribed a continuous glucose |
8 | | monitor, and has attested that the patient will be |
9 | | provided with that training; |
10 | | (5) the individual either: |
11 | | (A) uses insulin for treatment via one or more |
12 | | injections or infusions of insulin per day, and only |
13 | | one injection or infusion of one type of insulin shall |
14 | | be sufficient utilization of insulin to qualify for a |
15 | | continuous glucose monitor under this Section; or |
16 | | (B) has reported a history of problematic |
17 | | hypoglycemia with documentation to the individual's |
18 | | medical provider showing at least one of the |
19 | | following: |
20 | | (i) recurrent hypoglycemic events |
21 | | characterized by an altered mental or physical |
22 | | state, despite multiple attempts to adjust |
23 | | medications or modify the diabetes treatment plan, |
24 | | as documented by a medical provider; or |
25 | | (ii) a history of at least one hypoglycemic |
26 | | event characterized by an altered mental or |
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1 | | physical state requiring third-party assistance |
2 | | for treatment of hypoglycemia, as documented by |
3 | | the individual's medical provider, which may be |
4 | | self-reported by the individual; third-party |
5 | | assistance shall not, in any event, be deemed to |
6 | | require that the individual had been admitted to a |
7 | | hospital or visited an emergency department; and |
8 | | (6) within 6 months prior to prescribing a continuous |
9 | | glucose monitor, the medical provider prescribing the |
10 | | continuous glucose monitor had an in-person or covered |
11 | | telehealth visit with the individual to evaluate the |
12 | | individual's diabetes control and has determined that the |
13 | | criteria of paragraphs (1) through (5) are met. |
14 | | Notwithstanding any other provision of this Section, to |
15 | | qualify for a continuous glucose monitor under this Section, |
16 | | an individual is not required to have a diagnosis of |
17 | | uncontrolled diabetes; have a history of emergency room visits |
18 | | or hospitalizations; or show improved glycemic control. |
19 | | All continuous glucose monitors covered under this Section |
20 | | shall be approved for use by individuals, and the choice of |
21 | | device shall be made based upon the individual's |
22 | | circumstances, preferences, and needs in consultation with the |
23 | | individual's medical provider. |
24 | | (b) Any individual who is diagnosed with diabetes mellitus |
25 | | and meets the requirements of this Section shall not be |
26 | | required to obtain prior authorization for coverage for a |
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1 | | continuous glucose monitor, and coverage shall be continuous |
2 | | once the continuous glucose monitor is prescribed. |
3 | | (c) A group or individual policy of accident and health |
4 | | insurance or a managed care plan that is amended, delivered, |
5 | | issued, or renewed on or after January 1, 2026 shall not impose |
6 | | a deductible, coinsurance, copayment, or any other |
7 | | cost-sharing requirement on the coverage provided under this |
8 | | Section. The provisions of this subsection do not apply to |
9 | | coverage under this Section to the extent such coverage would |
10 | | disqualify a high-deductible health plan from eligibility for |
11 | | a health savings account pursuant to the federal Internal |
12 | | Revenue Code, 26 U.S.C. 23. |
13 | | Section 10. The Illinois Public Aid Code is amended by |
14 | | adding Section 5-16.8a as follows: |
15 | | (305 ILCS 5/5-16.8a new) |
16 | | Sec. 5-16.8a. Rules concerning continuous glucose monitor |
17 | | coverage. The Department shall adopt rules to implement the |
18 | | changes made to Section 356z.59 of the Illinois Insurance |
19 | | Code, as applied to the medical assistance program. The rules |
20 | | shall, at a minimum, provide that: |
21 | | (1) the ordering provider must be a physician licensed |
22 | | under the Medical Practice Act of 1987 or a certified |
23 | | nurse practitioner or physician assistant with a |
24 | | collaborative agreement with the physician; |
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1 | | (2) continuous glucose monitors are not required to |
2 | | have an alarm when glucose levels are outside the |
3 | | pre-determined range; the capacity to generate predictive |
4 | | alerts in case of impending hypoglycemia; or the ability |
5 | | to transmit real-time glucose values and alerts to the |
6 | | patient and designated other persons; |
7 | | (3) the beneficiary is not required to need intensive |
8 | | insulin therapy; |
9 | | (4) the beneficiary is not required to have a recent |
10 | | history of emergency room visits or hospitalizations |
11 | | related to hypoglycemia, hyperglycemia, or ketoacidosis; |
12 | | (5) if the beneficiary has gestational diabetes, the |
13 | | beneficiary is not required to have suboptimal glycemic |
14 | | control that is likely to harm the beneficiary or the |
15 | | fetus; |
16 | | (6) if a beneficiary has diabetes mellitus and the |
17 | | beneficiary does not meet the coverage requirements or if |
18 | | the beneficiary is in a population in which continuous |
19 | | glucose monitor usage has not been well-studied, requests |
20 | | shall be reviewed, on a case-by-case basis, for medical |
21 | | necessity and approved if appropriate; and |
22 | | (7) the beneficiary is not required to obtain prior |
23 | | authorization for coverage for a continuous glucose |
24 | | monitor, and that coverage is continuous once the |
25 | | continuous glucose monitor is prescribed. ". |