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| | HB3549 Engrossed | | LRB099 09324 MLM 29529 b |
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1 | | AN ACT concerning regulation.
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2 | | Be it enacted by the People of the State of Illinois,
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3 | | represented in the General Assembly:
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4 | | Section 5. The Managed Care Reform and Patient Rights Act |
5 | | is amended by changing Section 45.1 as follows: |
6 | | (215 ILCS 134/45.1) |
7 | | Sec. 45.1. Medical exceptions procedures required. |
8 | | (a) Notwithstanding any other provision of law, on or after |
9 | | the effective date of this amendatory Act of the 99th General |
10 | | Assembly, every insurer licensed in this State to sell a policy |
11 | | of group or individual accident and health insurance or a |
12 | | health benefits plan shall Every health carrier that offers a |
13 | | qualified health plan, as defined in the federal Patient |
14 | | Protection and Affordable Care Act of 2010 (Public Law |
15 | | 111-148), as amended by the federal Health Care and Education |
16 | | Reconciliation Act of 2010 (Public Law 111-152), and any |
17 | | amendments thereto, or regulations or guidance issued under |
18 | | those Acts (collectively, "the Federal Act"), directly to |
19 | | consumers in this State shall establish and maintain a medical |
20 | | exceptions process that allows covered persons or their |
21 | | authorized representatives to request any clinically |
22 | | appropriate prescription drug when (1) the drug is not covered |
23 | | based on the health benefit plan's formulary; (2) the health |
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1 | | benefit plan is discontinuing coverage of the drug on the |
2 | | plan's formulary for reasons other than safety or other than |
3 | | because the prescription drug has been withdrawn from the |
4 | | market by the drug's manufacturer; (3) the prescription drug |
5 | | alternatives required to be used in accordance with a step |
6 | | therapy requirement (A) has been ineffective in the treatment |
7 | | of the enrollee's disease or medical condition or, based on |
8 | | both sound clinical evidence and medical and scientific |
9 | | evidence, the known relevant physical or mental |
10 | | characteristics of the enrollee, and the known characteristics |
11 | | of the drug regimen, is likely to be ineffective or adversely |
12 | | affect the drug's effectiveness or patient compliance or (B) |
13 | | has caused or, based on sound medical evidence, is likely to |
14 | | cause an adverse reaction or harm to the enrollee; or (4) the |
15 | | number of doses available under a dose restriction for the |
16 | | prescription drug (A) has been ineffective in the treatment of |
17 | | the enrollee's disease or medical condition or (B) based on |
18 | | both sound clinical evidence and medical and scientific |
19 | | evidence, the known relevant physical and mental |
20 | | characteristics of the enrollee, and known characteristics of |
21 | | the drug regimen, is likely to be ineffective or adversely |
22 | | affect the drug's effective or patient compliance. |
23 | | (b) The health carrier's established medical exceptions |
24 | | procedures must require, at a minimum, the following: |
25 | | (1) Any request for approval of coverage made verbally |
26 | | or in writing (regardless of whether made using a paper or |
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1 | | electronic form or some other writing) at any time shall be |
2 | | reviewed by appropriate health care professionals. |
3 | | (2) The health carrier must, within 72 hours after |
4 | | receipt of a request made under subsection (a) of this |
5 | | Section, either approve or deny the request. In the case of |
6 | | a denial, the health carrier shall provide the covered |
7 | | person or the covered person's authorized representative |
8 | | and the covered person's prescribing provider with the |
9 | | reason for the denial, an alternative covered medication, |
10 | | if applicable, and information regarding the procedure for |
11 | | submitting an appeal to the denial. |
12 | | (3) In the case of an expedited coverage determination, |
13 | | the health carrier must either approve or deny the request |
14 | | within 24 hours after receipt of the request. In the case |
15 | | of a denial, the health carrier shall provide the covered |
16 | | person or the covered person's authorized representative |
17 | | and the covered person's prescribing provider with the |
18 | | reason for the denial, an alternative covered medication, |
19 | | if applicable, and information regarding the procedure for |
20 | | submitting an appeal to the denial. |
21 | | (c) Notwithstanding any other provision of this Section, |
22 | | nothing in this Section shall be interpreted or implemented in |
23 | | a manner not consistent with the Federal Act.
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24 | | (Source: P.A. 98-1035, eff. 8-25-14.)
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