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Sen. Julie A. Morrison
Filed: 3/8/2024
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1 | | AMENDMENT TO SENATE BILL 3414
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2 | | AMENDMENT NO. ______. Amend Senate Bill 3414 by replacing |
3 | | everything after the enacting clause with the following: |
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) A group or individual policy of accident and health |
9 | | insurance or a managed care plan that is amended, delivered, |
10 | | issued, or renewed before January 1, 2026 on or after January |
11 | | 1, 2024 shall provide coverage for medically necessary |
12 | | continuous glucose monitors for individuals who are diagnosed |
13 | | with any form of diabetes mellitus type 1 or type 2 diabetes |
14 | | and require insulin for the management of their diabetes. A |
15 | | group or individual policy of accident and health insurance or |
16 | | a managed care plan that is amended, delivered, issued, or |
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1 | | renewed on or after January 1, 2026 shall provide coverage for |
2 | | continuous glucose monitors, related supplies, and training in |
3 | | the use of continuous glucose monitors for any individual if |
4 | | the policy is in full alignment with Medicare and the |
5 | | following 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 use by individuals, and the choice of |
7 | | device shall be made based upon the individual's circumstances |
8 | | and medical needs in consultation with the individual's |
9 | | medical provider, subject to the terms of the policy. |
10 | | (b) 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 | | (c) 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, 2026 shall not impose |
18 | | a deductible, coinsurance, copayment, or any other |
19 | | cost-sharing requirement on the coverage of one continuous |
20 | | glucose monitor, as provided under this Section. The |
21 | | provisions of this subsection do not apply to coverage under |
22 | | this Section to the extent such coverage would disqualify a |
23 | | high-deductible health plan from eligibility for a health |
24 | | savings account pursuant to the federal Internal Revenue Code, |
25 | | 26 U.S.C. 23. |
26 | | (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 glu |
| | cose 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 |
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1 | | beneficiary is not required to have suboptimal glycemic |
2 | | control that is likely to harm the beneficiary or the |
3 | | fetus; |
4 | | (6) if a beneficiary has diabetes mellitus and the |
5 | | beneficiary does not meet the coverage requirements or if |
6 | | the beneficiary is in a population in which continuous |
7 | | glucose monitor usage has not been well-studied, requests |
8 | | shall be reviewed, on a case-by-case basis, for medical |
9 | | necessity and approved if appropriate; and |
10 | | (7) the beneficiary is not required to obtain prior |
11 | | authorization for coverage for a continuous glucose |
12 | | monitor, and that coverage is continuous once the |
13 | | continuous glucose monitor is prescribed. |
14 | | Section 99. Effective date. This Act takes effect July 1, |
15 | | 2024.". |