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Public Act 103-1040
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SB3741 Enrolled | LRB103 37781 RPS 67910 b |
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AN ACT concerning regulation.
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Be it enacted by the People of the State of Illinois, |
represented in the General Assembly:
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Section 5. The Illinois Insurance Code is amended by |
changing Section 370c as follows:
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(215 ILCS 5/370c) (from Ch. 73, par. 982c) |
Sec. 370c. Mental and emotional disorders. |
(a)(1) On and after January 1, 2022 (the effective date of |
Public Act 102-579), every insurer that amends, delivers, |
issues, or renews group accident and health policies providing |
coverage for hospital or medical treatment or services for |
illness on an expense-incurred basis shall provide coverage |
for the medically necessary treatment of mental, emotional, |
nervous, or substance use disorders or conditions consistent |
with the parity requirements of Section 370c.1 of this Code. |
(2) Each insured that is covered for mental, emotional, |
nervous, or substance use disorders or conditions shall be |
free to select the physician licensed to practice medicine in |
all its branches, licensed clinical psychologist, licensed |
clinical social worker, licensed clinical professional |
counselor, licensed marriage and family therapist, licensed |
speech-language pathologist, or other licensed or certified |
professional at a program licensed pursuant to the Substance |
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Use Disorder Act of his or her choice to treat such disorders, |
and the insurer shall pay the covered charges of such |
physician licensed to practice medicine in all its branches, |
licensed clinical psychologist, licensed clinical social |
worker, licensed clinical professional counselor, licensed |
marriage and family therapist, licensed speech-language |
pathologist, or other licensed or certified professional at a |
program licensed pursuant to the Substance Use Disorder Act up |
to the limits of coverage, provided (i) the disorder or |
condition treated is covered by the policy, and (ii) the |
physician, licensed psychologist, licensed clinical social |
worker, licensed clinical professional counselor, licensed |
marriage and family therapist, licensed speech-language |
pathologist, or other licensed or certified professional at a |
program licensed pursuant to the Substance Use Disorder Act is |
authorized to provide said services under the statutes of this |
State and in accordance with accepted principles of his or her |
profession. |
(3) Insofar as this Section applies solely to licensed |
clinical social workers, licensed clinical professional |
counselors, licensed marriage and family therapists, licensed |
speech-language pathologists, and other licensed or certified |
professionals at programs licensed pursuant to the Substance |
Use Disorder Act, those persons who may provide services to |
individuals shall do so after the licensed clinical social |
worker, licensed clinical professional counselor, licensed |
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marriage and family therapist, licensed speech-language |
pathologist, or other licensed or certified professional at a |
program licensed pursuant to the Substance Use Disorder Act |
has informed the patient of the desirability of the patient |
conferring with the patient's primary care physician. |
(4) "Mental, emotional, nervous, or substance use disorder |
or condition" means a condition or disorder that involves a |
mental health condition or substance use disorder that falls |
under any of the diagnostic categories listed in the mental |
and behavioral disorders chapter of the current edition of the |
World Health Organization's International Classification of |
Disease or that is listed in the most recent version of the |
American Psychiatric Association's Diagnostic and Statistical |
Manual of Mental Disorders. "Mental, emotional, nervous, or |
substance use disorder or condition" includes any mental |
health condition that occurs during pregnancy or during the |
postpartum period and includes, but is not limited to, |
postpartum depression. |
(5) Medically necessary treatment and medical necessity |
determinations shall be interpreted and made in a manner that |
is consistent with and pursuant to subsections (h) through |
(t). |
(b)(1) (Blank). |
(2) (Blank). |
(2.5) (Blank). |
(3) Unless otherwise prohibited by federal law and |
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consistent with the parity requirements of Section 370c.1 of |
this Code, the reimbursing insurer that amends, delivers, |
issues, or renews a group or individual policy of accident and |
health insurance, a qualified health plan offered through the |
health insurance marketplace, or a provider of treatment of |
mental, emotional, nervous, or substance use disorders or |
conditions shall furnish medical records or other necessary |
data that substantiate that initial or continued treatment is |
at all times medically necessary. An insurer shall provide a |
mechanism for the timely review by a provider holding the same |
license and practicing in the same specialty as the patient's |
provider, who is unaffiliated with the insurer, jointly |
selected by the patient (or the patient's next of kin or legal |
representative if the patient is unable to act for himself or |
herself), the patient's provider, and the insurer in the event |
of a dispute between the insurer and patient's provider |
regarding the medical necessity of a treatment proposed by a |
patient's provider. If the reviewing provider determines the |
treatment to be medically necessary, the insurer shall provide |
reimbursement for the treatment. Future contractual or |
employment actions by the insurer regarding the patient's |
provider may not be based on the provider's participation in |
this procedure. Nothing prevents the insured from agreeing in |
writing to continue treatment at his or her expense. When |
making a determination of the medical necessity for a |
treatment modality for mental, emotional, nervous, or |
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substance use disorders or conditions, an insurer must make |
the determination in a manner that is consistent with the |
manner used to make that determination with respect to other |
diseases or illnesses covered under the policy, including an |
appeals process. Medical necessity determinations for |
substance use disorders shall be made in accordance with |
appropriate patient placement criteria established by the |
American Society of Addiction Medicine. No additional criteria |
may be used to make medical necessity determinations for |
substance use disorders. |
(4) A group health benefit plan amended, delivered, |
issued, or renewed on or after January 1, 2019 (the effective |
date of Public Act 100-1024) or an individual policy of |
accident and health insurance or a qualified health plan |
offered through the health insurance marketplace amended, |
delivered, issued, or renewed on or after January 1, 2019 (the |
effective date of Public Act 100-1024): |
(A) shall provide coverage based upon medical |
necessity for the treatment of a mental, emotional, |
nervous, or substance use disorder or condition consistent |
with the parity requirements of Section 370c.1 of this |
Code; provided, however, that in each calendar year |
coverage shall not be less than the following: |
(i) 45 days of inpatient treatment; and |
(ii) beginning on June 26, 2006 (the effective |
date of Public Act 94-921), 60 visits for outpatient |
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treatment including group and individual outpatient |
treatment; and |
(iii) for plans or policies delivered, issued for |
delivery, renewed, or modified after January 1, 2007 |
(the effective date of Public Act 94-906), 20 |
additional outpatient visits for speech therapy for |
treatment of pervasive developmental disorders that |
will be in addition to speech therapy provided |
pursuant to item (ii) of this subparagraph (A); and |
(B) may not include a lifetime limit on the number of |
days of inpatient treatment or the number of outpatient |
visits covered under the plan. |
(C) (Blank). |
(5) An issuer of a group health benefit plan or an |
individual policy of accident and health insurance or a |
qualified health plan offered through the health insurance |
marketplace may not count toward the number of outpatient |
visits required to be covered under this Section an outpatient |
visit for the purpose of medication management and shall cover |
the outpatient visits under the same terms and conditions as |
it covers outpatient visits for the treatment of physical |
illness. |
(5.5) An individual or group health benefit plan amended, |
delivered, issued, or renewed on or after September 9, 2015 |
(the effective date of Public Act 99-480) shall offer coverage |
for medically necessary acute treatment services and medically |
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necessary clinical stabilization services. The treating |
provider shall base all treatment recommendations and the |
health benefit plan shall base all medical necessity |
determinations for substance use disorders in accordance with |
the most current edition of the Treatment Criteria for |
Addictive, Substance-Related, and Co-Occurring Conditions |
established by the American Society of Addiction Medicine. The |
treating provider shall base all treatment recommendations and |
the health benefit plan shall base all medical necessity |
determinations for medication-assisted treatment in accordance |
with the most current Treatment Criteria for Addictive, |
Substance-Related, and Co-Occurring Conditions established by |
the American Society of Addiction Medicine. |
As used in this subsection: |
"Acute treatment services" means 24-hour medically |
supervised addiction treatment that provides evaluation and |
withdrawal management and may include biopsychosocial |
assessment, individual and group counseling, psychoeducational |
groups, and discharge planning. |
"Clinical stabilization services" means 24-hour treatment, |
usually following acute treatment services for substance |
abuse, which may include intensive education and counseling |
regarding the nature of addiction and its consequences, |
relapse prevention, outreach to families and significant |
others, and aftercare planning for individuals beginning to |
engage in recovery from addiction. |
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(6) An issuer of a group health benefit plan may provide or |
offer coverage required under this Section through a managed |
care plan. |
(6.5) An individual or group health benefit plan amended, |
delivered, issued, or renewed on or after January 1, 2019 (the |
effective date of Public Act 100-1024): |
(A) shall not impose prior authorization requirements, |
including limitations on dosage, other than those |
established under the Treatment Criteria for Addictive, |
Substance-Related, and Co-Occurring Conditions |
established by the American Society of Addiction Medicine, |
on a prescription medication approved by the United States |
Food and Drug Administration that is prescribed or |
administered for the treatment of substance use disorders; |
(B) shall not impose any step therapy requirements, |
other than those established under the Treatment Criteria |
for Addictive, Substance-Related, and Co-Occurring |
Conditions established by the American Society of |
Addiction Medicine, before authorizing coverage for a |
prescription medication approved by the United States Food |
and Drug Administration that is prescribed or administered |
for the treatment of substance use disorders; |
(C) shall place all prescription medications approved |
by the United States Food and Drug Administration |
prescribed or administered for the treatment of substance |
use disorders on, for brand medications, the lowest tier |
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of the drug formulary developed and maintained by the |
individual or group health benefit plan that covers brand |
medications and, for generic medications, the lowest tier |
of the drug formulary developed and maintained by the |
individual or group health benefit plan that covers |
generic medications; and |
(D) shall not exclude coverage for a prescription |
medication approved by the United States Food and Drug |
Administration for the treatment of substance use |
disorders and any associated counseling or wraparound |
services on the grounds that such medications and services |
were court ordered. |
(7) (Blank). |
(8) (Blank). |
(9) With respect to all mental, emotional, nervous, or |
substance use disorders or conditions, coverage for inpatient |
treatment shall include coverage for treatment in a |
residential treatment center certified or licensed by the |
Department of Public Health or the Department of Human |
Services. |
(c) This Section shall not be interpreted to require |
coverage for speech therapy or other habilitative services for |
those individuals covered under Section 356z.15 of this Code. |
(d) With respect to a group or individual policy of |
accident and health insurance or a qualified health plan |
offered through the health insurance marketplace, the |
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Department and, with respect to medical assistance, the |
Department of Healthcare and Family Services shall each |
enforce the requirements of this Section and Sections 356z.23 |
and 370c.1 of this Code, the Paul Wellstone and Pete Domenici |
Mental Health Parity and Addiction Equity Act of 2008, 42 |
U.S.C. 18031(j), and any amendments to, and federal guidance |
or regulations issued under, those Acts, including, but not |
limited to, final regulations issued under the Paul Wellstone |
and Pete Domenici Mental Health Parity and Addiction Equity |
Act of 2008 and final regulations applying the Paul Wellstone |
and Pete Domenici Mental Health Parity and Addiction Equity |
Act of 2008 to Medicaid managed care organizations, the |
Children's Health Insurance Program, and alternative benefit |
plans. Specifically, the Department and the Department of |
Healthcare and Family Services shall take action: |
(1) proactively ensuring compliance by individual and |
group policies, including by requiring that insurers |
submit comparative analyses, as set forth in paragraph (6) |
of subsection (k) of Section 370c.1, demonstrating how |
they design and apply nonquantitative treatment |
limitations, both as written and in operation, for mental, |
emotional, nervous, or substance use disorder or condition |
benefits as compared to how they design and apply |
nonquantitative treatment limitations, as written and in |
operation, for medical and surgical benefits; |
(2) evaluating all consumer or provider complaints |
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regarding mental, emotional, nervous, or substance use |
disorder or condition coverage for possible parity |
violations; |
(3) performing parity compliance market conduct |
examinations or, in the case of the Department of |
Healthcare and Family Services, parity compliance audits |
of individual and group plans and policies, including, but |
not limited to, reviews of: |
(A) nonquantitative treatment limitations, |
including, but not limited to, prior authorization |
requirements, concurrent review, retrospective review, |
step therapy, network admission standards, |
reimbursement rates, and geographic restrictions; |
(B) denials of authorization, payment, and |
coverage; and |
(C) other specific criteria as may be determined |
by the Department. |
The findings and the conclusions of the parity compliance |
market conduct examinations and audits shall be made public. |
The Director may adopt rules to effectuate any provisions |
of the Paul Wellstone and Pete Domenici Mental Health Parity |
and Addiction Equity Act of 2008 that relate to the business of |
insurance. |
(e) Availability of plan information. |
(1) The criteria for medical necessity determinations |
made under a group health plan, an individual policy of |
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accident and health insurance, or a qualified health plan |
offered through the health insurance marketplace with |
respect to mental health or substance use disorder |
benefits (or health insurance coverage offered in |
connection with the plan with respect to such benefits) |
must be made available by the plan administrator (or the |
health insurance issuer offering such coverage) to any |
current or potential participant, beneficiary, or |
contracting provider upon request. |
(2) The reason for any denial under a group health |
benefit plan, an individual policy of accident and health |
insurance, or a qualified health plan offered through the |
health insurance marketplace (or health insurance coverage |
offered in connection with such plan or policy) of |
reimbursement or payment for services with respect to |
mental, emotional, nervous, or substance use disorders or |
conditions benefits in the case of any participant or |
beneficiary must be made available within a reasonable |
time and in a reasonable manner and in readily |
understandable language by the plan administrator (or the |
health insurance issuer offering such coverage) to the |
participant or beneficiary upon request. |
(f) As used in this Section, "group policy of accident and |
health insurance" and "group health benefit plan" includes (1) |
State-regulated employer-sponsored group health insurance |
plans written in Illinois or which purport to provide coverage |
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for a resident of this State; and (2) State employee health |
plans. |
(g) (1) As used in this subsection: |
"Benefits", with respect to insurers, means the benefits |
provided for treatment services for inpatient and outpatient |
treatment of substance use disorders or conditions at American |
Society of Addiction Medicine levels of treatment 2.1 |
(Intensive Outpatient), 2.5 (Partial Hospitalization), 3.1 |
(Clinically Managed Low-Intensity Residential), 3.3 |
(Clinically Managed Population-Specific High-Intensity |
Residential), 3.5 (Clinically Managed High-Intensity |
Residential), and 3.7 (Medically Monitored Intensive |
Inpatient) and OMT (Opioid Maintenance Therapy) services. |
"Benefits", with respect to managed care organizations, |
means the benefits provided for treatment services for |
inpatient and outpatient treatment of substance use disorders |
or conditions at American Society of Addiction Medicine levels |
of treatment 2.1 (Intensive Outpatient), 2.5 (Partial |
Hospitalization), 3.5 (Clinically Managed High-Intensity |
Residential), and 3.7 (Medically Monitored Intensive |
Inpatient) and OMT (Opioid Maintenance Therapy) services. |
"Substance use disorder treatment provider or facility" |
means a licensed physician, licensed psychologist, licensed |
psychiatrist, licensed advanced practice registered nurse, or |
licensed, certified, or otherwise State-approved facility or |
provider of substance use disorder treatment. |
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(2) A group health insurance policy, an individual health |
benefit plan, or qualified health plan that is offered through |
the health insurance marketplace, small employer group health |
plan, and large employer group health plan that is amended, |
delivered, issued, executed, or renewed in this State, or |
approved for issuance or renewal in this State, on or after |
January 1, 2019 (the effective date of Public Act 100-1023) |
shall comply with the requirements of this Section and Section |
370c.1. The services for the treatment and the ongoing |
assessment of the patient's progress in treatment shall follow |
the requirements of 77 Ill. Adm. Code 2060. |
(3) Prior authorization shall not be utilized for the |
benefits under this subsection. The substance use disorder |
treatment provider or facility shall notify the insurer of the |
initiation of treatment. For an insurer that is not a managed |
care organization, the substance use disorder treatment |
provider or facility notification shall occur for the |
initiation of treatment of the covered person within 2 |
business days. For managed care organizations, the substance |
use disorder treatment provider or facility notification shall |
occur in accordance with the protocol set forth in the |
provider agreement for initiation of treatment within 24 |
hours. If the managed care organization is not capable of |
accepting the notification in accordance with the contractual |
protocol during the 24-hour period following admission, the |
substance use disorder treatment provider or facility shall |
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have one additional business day to provide the notification |
to the appropriate managed care organization. Treatment plans |
shall be developed in accordance with the requirements and |
timeframes established in 77 Ill. Adm. Code 2060. If the |
substance use disorder treatment provider or facility fails to |
notify the insurer of the initiation of treatment in |
accordance with these provisions, the insurer may follow its |
normal prior authorization processes. |
(4) For an insurer that is not a managed care |
organization, if an insurer determines that benefits are no |
longer medically necessary, the insurer shall notify the |
covered person, the covered person's authorized |
representative, if any, and the covered person's health care |
provider in writing of the covered person's right to request |
an external review pursuant to the Health Carrier External |
Review Act. The notification shall occur within 24 hours |
following the adverse determination. |
Pursuant to the requirements of the Health Carrier |
External Review Act, the covered person or the covered |
person's authorized representative may request an expedited |
external review. An expedited external review may not occur if |
the substance use disorder treatment provider or facility |
determines that continued treatment is no longer medically |
necessary. |
If an expedited external review request meets the criteria |
of the Health Carrier External Review Act, an independent |
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review organization shall make a final determination of |
medical necessity within 72 hours. If an independent review |
organization upholds an adverse determination, an insurer |
shall remain responsible to provide coverage of benefits |
through the day following the determination of the independent |
review organization. A decision to reverse an adverse |
determination shall comply with the Health Carrier External |
Review Act. |
(5) The substance use disorder treatment provider or |
facility shall provide the insurer with 7 business days' |
advance notice of the planned discharge of the patient from |
the substance use disorder treatment provider or facility and |
notice on the day that the patient is discharged from the |
substance use disorder treatment provider or facility. |
(6) The benefits required by this subsection shall be |
provided to all covered persons with a diagnosis of substance |
use disorder or conditions. The presence of additional related |
or unrelated diagnoses shall not be a basis to reduce or deny |
the benefits required by this subsection. |
(7) Nothing in this subsection shall be construed to |
require an insurer to provide coverage for any of the benefits |
in this subsection. |
(h) As used in this Section: |
"Generally accepted standards of mental, emotional, |
nervous, or substance use disorder or condition care" means |
standards of care and clinical practice that are generally |
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recognized by health care providers practicing in relevant |
clinical specialties such as psychiatry, psychology, clinical |
sociology, social work, addiction medicine and counseling, and |
behavioral health treatment. Valid, evidence-based sources |
reflecting generally accepted standards of mental, emotional, |
nervous, or substance use disorder or condition care include |
peer-reviewed scientific studies and medical literature, |
recommendations of nonprofit health care provider professional |
associations and specialty societies, including, but not |
limited to, patient placement criteria and clinical practice |
guidelines, recommendations of federal government agencies, |
and drug labeling approved by the United States Food and Drug |
Administration. |
"Medically necessary treatment of mental, emotional, |
nervous, or substance use disorders or conditions" means a |
service or product addressing the specific needs of that |
patient, for the purpose of screening, preventing, diagnosing, |
managing, or treating an illness, injury, or condition or its |
symptoms and comorbidities, including minimizing the |
progression of an illness, injury, or condition or its |
symptoms and comorbidities in a manner that is all of the |
following: |
(1) in accordance with the generally accepted |
standards of mental, emotional, nervous, or substance use |
disorder or condition care; |
(2) clinically appropriate in terms of type, |
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frequency, extent, site, and duration; and |
(3) not primarily for the economic benefit of the |
insurer, purchaser, or for the convenience of the patient, |
treating physician, or other health care provider. |
"Utilization review" means either of the following: |
(1) prospectively, retrospectively, or concurrently |
reviewing and approving, modifying, delaying, or denying, |
based in whole or in part on medical necessity, requests |
by health care providers, insureds, or their authorized |
representatives for coverage of health care services |
before, retrospectively, or concurrently with the |
provision of health care services to insureds. |
(2) evaluating the medical necessity, appropriateness, |
level of care, service intensity, efficacy, or efficiency |
of health care services, benefits, procedures, or |
settings, under any circumstances, to determine whether a |
health care service or benefit subject to a medical |
necessity coverage requirement in an insurance policy is |
covered as medically necessary for an insured. |
"Utilization review criteria" means patient placement |
criteria or any criteria, standards, protocols, or guidelines |
used by an insurer to conduct utilization review. |
(i)(1) Every insurer that amends, delivers, issues, or |
renews a group or individual policy of accident and health |
insurance or a qualified health plan offered through the |
health insurance marketplace in this State and Medicaid |
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managed care organizations providing coverage for hospital or |
medical treatment on or after January 1, 2023 shall, pursuant |
to subsections (h) through (s), provide coverage for medically |
necessary treatment of mental, emotional, nervous, or |
substance use disorders or conditions. |
(2) An insurer shall not set a specific limit on the |
duration of benefits or coverage of medically necessary |
treatment of mental, emotional, nervous, or substance use |
disorders or conditions or limit coverage only to alleviation |
of the insured's current symptoms. |
(3) All medical necessity determinations made by the |
insurer concerning service intensity, level of care placement, |
continued stay, and transfer or discharge of insureds |
diagnosed with mental, emotional, nervous, or substance use |
disorders or conditions shall be conducted in accordance with |
the requirements of subsections (k) through (u). |
(4) An insurer that authorizes a specific type of |
treatment by a provider pursuant to this Section shall not |
rescind or modify the authorization after that provider |
renders the health care service in good faith and pursuant to |
this authorization for any reason, including, but not limited |
to, the insurer's subsequent cancellation or modification of |
the insured's or policyholder's contract, or the insured's or |
policyholder's eligibility. Nothing in this Section shall |
require the insurer to cover a treatment when the |
authorization was granted based on a material |
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misrepresentation by the insured, the policyholder, or the |
provider. Nothing in this Section shall require Medicaid |
managed care organizations to pay for services if the |
individual was not eligible for Medicaid at the time the |
service was rendered. Nothing in this Section shall require an |
insurer to pay for services if the individual was not the |
insurer's enrollee at the time services were rendered. As used |
in this paragraph, "material" means a fact or situation that |
is not merely technical in nature and results in or could |
result in a substantial change in the situation. |
(j) An insurer shall not limit benefits or coverage for |
medically necessary services on the basis that those services |
should be or could be covered by a public entitlement program, |
including, but not limited to, special education or an |
individualized education program, Medicaid, Medicare, |
Supplemental Security Income, or Social Security Disability |
Insurance, and shall not include or enforce a contract term |
that excludes otherwise covered benefits on the basis that |
those services should be or could be covered by a public |
entitlement program. Nothing in this subsection shall be |
construed to require an insurer to cover benefits that have |
been authorized and provided for a covered person by a public |
entitlement program. Medicaid managed care organizations are |
not subject to this subsection. |
(k) An insurer shall base any medical necessity |
determination or the utilization review criteria that the |
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insurer, and any entity acting on the insurer's behalf, |
applies to determine the medical necessity of health care |
services and benefits for the diagnosis, prevention, and |
treatment of mental, emotional, nervous, or substance use |
disorders or conditions on current generally accepted |
standards of mental, emotional, nervous, or substance use |
disorder or condition care. All denials and appeals shall be |
reviewed by a professional with experience or expertise |
comparable to the provider requesting the authorization. |
(l) For medical necessity determinations relating to level |
of care placement, continued stay, and transfer or discharge |
of insureds diagnosed with mental, emotional, and nervous |
disorders or conditions, an insurer shall apply the patient |
placement criteria set forth in the most recent version of the |
treatment criteria developed by an unaffiliated nonprofit |
professional association for the relevant clinical specialty |
or, for Medicaid managed care organizations, patient placement |
criteria determined by the Department of Healthcare and Family |
Services that are consistent with generally accepted standards |
of mental, emotional, nervous or substance use disorder or |
condition care. Pursuant to subsection (b), in conducting |
utilization review of all covered services and benefits for |
the diagnosis, prevention, and treatment of substance use |
disorders an insurer shall use the most recent edition of the |
patient placement criteria established by the American Society |
of Addiction Medicine. |
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(m) For medical necessity determinations relating to level |
of care placement, continued stay, and transfer or discharge |
that are within the scope of the sources specified in |
subsection (l), an insurer shall not apply different, |
additional, conflicting, or more restrictive utilization |
review criteria than the criteria set forth in those sources. |
For all level of care placement decisions, the insurer shall |
authorize placement at the level of care consistent with the |
assessment of the insured using the relevant patient placement |
criteria as specified in subsection (l). If that level of |
placement is not available, the insurer shall authorize the |
next higher level of care. In the event of disagreement, the |
insurer shall provide full detail of its assessment using the |
relevant criteria as specified in subsection (l) to the |
provider of the service and the patient. |
Nothing in this subsection or subsection (l) prohibits an |
insurer from applying utilization review criteria that were |
developed in accordance with subsection (k) to health care |
services and benefits for mental, emotional, and nervous |
disorders or conditions that are not related to medical |
necessity determinations for level of care placement, |
continued stay, and transfer or discharge. If an insurer |
purchases or licenses utilization review criteria pursuant to |
this subsection, the insurer shall verify and document before |
use that the criteria were developed in accordance with |
subsection (k). |
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(n) In conducting utilization review that is outside the |
scope of the criteria as specified in subsection (l) or |
relates to the advancements in technology or in the types or |
levels of care that are not addressed in the most recent |
versions of the sources specified in subsection (l), an |
insurer shall conduct utilization review in accordance with |
subsection (k). |
(o) This Section does not in any way limit the rights of a |
patient under the Medical Patient Rights Act. |
(p) This Section does not in any way limit early and |
periodic screening, diagnostic, and treatment benefits as |
defined under 42 U.S.C. 1396d(r). |
(q) To ensure the proper use of the criteria described in |
subsection (l), every insurer shall do all of the following: |
(1) Educate the insurer's staff, including any third |
parties contracted with the insurer to review claims, |
conduct utilization reviews, or make medical necessity |
determinations about the utilization review criteria. |
(2) Make the educational program available to other |
stakeholders, including the insurer's participating or |
contracted providers and potential participants, |
beneficiaries, or covered lives. The education program |
must be provided at least once a year, in-person or |
digitally, or recordings of the education program must be |
made available to the aforementioned stakeholders. |
(3) Provide, at no cost, the utilization review |
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criteria and any training material or resources to |
providers and insured patients upon request. For |
utilization review criteria not concerning level of care |
placement, continued stay, and transfer or discharge used |
by the insurer pursuant to subsection (m), the insurer may |
place the criteria on a secure, password-protected website |
so long as the access requirements of the website do not |
unreasonably restrict access to insureds or their |
providers. No restrictions shall be placed upon the |
insured's or treating provider's access right to |
utilization review criteria obtained under this paragraph |
at any point in time, including before an initial request |
for authorization. |
(4) Track, identify, and analyze how the utilization |
review criteria are used to certify care, deny care, and |
support the appeals process. |
(5) Conduct interrater reliability testing to ensure |
consistency in utilization review decision making that |
covers how medical necessity decisions are made; this |
assessment shall cover all aspects of utilization review |
as defined in subsection (h). |
(6) Run interrater reliability reports about how the |
clinical guidelines are used in conjunction with the |
utilization review process and parity compliance |
activities. |
(7) Achieve interrater reliability pass rates of at |
|
least 90% and, if this threshold is not met, immediately |
provide for the remediation of poor interrater reliability |
and interrater reliability testing for all new staff |
before they can conduct utilization review without |
supervision. |
(8) Maintain documentation of interrater reliability |
testing and the remediation actions taken for those with |
pass rates lower than 90% and submit to the Department of |
Insurance or, in the case of Medicaid managed care |
organizations, the Department of Healthcare and Family |
Services the testing results and a summary of remedial |
actions as part of parity compliance reporting set forth |
in subsection (k) of Section 370c.1. |
(r) This Section applies to all health care services and |
benefits for the diagnosis, prevention, and treatment of |
mental, emotional, nervous, or substance use disorders or |
conditions covered by an insurance policy, including |
prescription drugs. |
(s) This Section applies to an insurer that amends, |
delivers, issues, or renews a group or individual policy of |
accident and health insurance or a qualified health plan |
offered through the health insurance marketplace in this State |
providing coverage for hospital or medical treatment and |
conducts utilization review as defined in this Section, |
including Medicaid managed care organizations, and any entity |
or contracting provider that performs utilization review or |
|
utilization management functions on an insurer's behalf. |
(t) If the Director determines that an insurer has |
violated this Section, the Director may, after appropriate |
notice and opportunity for hearing, by order, assess a civil |
penalty between $1,000 and $5,000 for each violation. Moneys |
collected from penalties shall be deposited into the Parity |
Advancement Fund established in subsection (i) of Section |
370c.1. |
(u) An insurer shall not adopt, impose, or enforce terms |
in its policies or provider agreements, in writing or in |
operation, that undermine, alter, or conflict with the |
requirements of this Section. |
(v) The provisions of this Section are severable. If any |
provision of this Section or its application is held invalid, |
that invalidity shall not affect other provisions or |
applications that can be given effect without the invalid |
provision or application. |
(Source: P.A. 102-558, eff. 8-20-21; 102-579, eff. 1-1-22; |
102-813, eff. 5-13-22; 103-426, eff. 8-4-23.)
|
Section 10. The Illinois Public Aid Code is amended by |
changing Section 5-5 as follows:
|
(305 ILCS 5/5-5) |
Sec. 5-5. Medical services. The Illinois Department, by |
rule, shall determine the quantity and quality of and the rate |
|
of reimbursement for the medical assistance for which payment |
will be authorized, and the medical services to be provided, |
which may include all or part of the following: (1) inpatient |
hospital services; (2) outpatient hospital services; (3) other |
laboratory and X-ray services; (4) skilled nursing home |
services; (5) physicians' services whether furnished in the |
office, the patient's home, a hospital, a skilled nursing |
home, or elsewhere; (6) medical care, or any other type of |
remedial care furnished by licensed practitioners; (7) home |
health care services; (8) private duty nursing service; (9) |
clinic services; (10) dental services, including prevention |
and treatment of periodontal disease and dental caries disease |
for pregnant individuals, provided by an individual licensed |
to practice dentistry or dental surgery; for purposes of this |
item (10), "dental services" means diagnostic, preventive, or |
corrective procedures provided by or under the supervision of |
a dentist in the practice of his or her profession; (11) |
physical therapy and related services; (12) prescribed drugs, |
dentures, and prosthetic devices; and eyeglasses prescribed by |
a physician skilled in the diseases of the eye, or by an |
optometrist, whichever the person may select; (13) other |
diagnostic, screening, preventive, and rehabilitative |
services, including to ensure that the individual's need for |
intervention or treatment of mental disorders or substance use |
disorders or co-occurring mental health and substance use |
disorders is determined using a uniform screening, assessment, |
|
and evaluation process inclusive of criteria, for children and |
adults; for purposes of this item (13), a uniform screening, |
assessment, and evaluation process refers to a process that |
includes an appropriate evaluation and, as warranted, a |
referral; "uniform" does not mean the use of a singular |
instrument, tool, or process that all must utilize; (14) |
transportation and such other expenses as may be necessary; |
(15) medical treatment of sexual assault survivors, as defined |
in Section 1a of the Sexual Assault Survivors Emergency |
Treatment Act, for injuries sustained as a result of the |
sexual assault, including examinations and laboratory tests to |
discover evidence which may be used in criminal proceedings |
arising from the sexual assault; (16) the diagnosis and |
treatment of sickle cell anemia; (16.5) services performed by |
a chiropractic physician licensed under the Medical Practice |
Act of 1987 and acting within the scope of his or her license, |
including, but not limited to, chiropractic manipulative |
treatment; and (17) any other medical care, and any other type |
of remedial care recognized under the laws of this State. The |
term "any other type of remedial care" shall include nursing |
care and nursing home service for persons who rely on |
treatment by spiritual means alone through prayer for healing. |
Notwithstanding any other provision of this Section, a |
comprehensive tobacco use cessation program that includes |
purchasing prescription drugs or prescription medical devices |
approved by the Food and Drug Administration shall be covered |
|
under the medical assistance program under this Article for |
persons who are otherwise eligible for assistance under this |
Article. |
Notwithstanding any other provision of this Code, |
reproductive health care that is otherwise legal in Illinois |
shall be covered under the medical assistance program for |
persons who are otherwise eligible for medical assistance |
under this Article. |
Notwithstanding any other provision of this Section, all |
tobacco cessation medications approved by the United States |
Food and Drug Administration and all individual and group |
tobacco cessation counseling services and telephone-based |
counseling services and tobacco cessation medications provided |
through the Illinois Tobacco Quitline shall be covered under |
the medical assistance program for persons who are otherwise |
eligible for assistance under this Article. The Department |
shall comply with all federal requirements necessary to obtain |
federal financial participation, as specified in 42 CFR |
433.15(b)(7), for telephone-based counseling services provided |
through the Illinois Tobacco Quitline, including, but not |
limited to: (i) entering into a memorandum of understanding or |
interagency agreement with the Department of Public Health, as |
administrator of the Illinois Tobacco Quitline; and (ii) |
developing a cost allocation plan for Medicaid-allowable |
Illinois Tobacco Quitline services in accordance with 45 CFR |
95.507. The Department shall submit the memorandum of |
|
understanding or interagency agreement, the cost allocation |
plan, and all other necessary documentation to the Centers for |
Medicare and Medicaid Services for review and approval. |
Coverage under this paragraph shall be contingent upon federal |
approval. |
Notwithstanding any other provision of this Code, the |
Illinois Department may not require, as a condition of payment |
for any laboratory test authorized under this Article, that a |
physician's handwritten signature appear on the laboratory |
test order form. The Illinois Department may, however, impose |
other appropriate requirements regarding laboratory test order |
documentation. |
Upon receipt of federal approval of an amendment to the |
Illinois Title XIX State Plan for this purpose, the Department |
shall authorize the Chicago Public Schools (CPS) to procure a |
vendor or vendors to manufacture eyeglasses for individuals |
enrolled in a school within the CPS system. CPS shall ensure |
that its vendor or vendors are enrolled as providers in the |
medical assistance program and in any capitated Medicaid |
managed care entity (MCE) serving individuals enrolled in a |
school within the CPS system. Under any contract procured |
under this provision, the vendor or vendors must serve only |
individuals enrolled in a school within the CPS system. Claims |
for services provided by CPS's vendor or vendors to recipients |
of benefits in the medical assistance program under this Code, |
the Children's Health Insurance Program, or the Covering ALL |
|
KIDS Health Insurance Program shall be submitted to the |
Department or the MCE in which the individual is enrolled for |
payment and shall be reimbursed at the Department's or the |
MCE's established rates or rate methodologies for eyeglasses. |
On and after July 1, 2012, the Department of Healthcare |
and Family Services may provide the following services to |
persons eligible for assistance under this Article who are |
participating in education, training or employment programs |
operated by the Department of Human Services as successor to |
the Department of Public Aid: |
(1) dental services provided by or under the |
supervision of a dentist; and |
(2) eyeglasses prescribed by a physician skilled in |
the diseases of the eye, or by an optometrist, whichever |
the person may select. |
On and after July 1, 2018, the Department of Healthcare |
and Family Services shall provide dental services to any adult |
who is otherwise eligible for assistance under the medical |
assistance program. As used in this paragraph, "dental |
services" means diagnostic, preventative, restorative, or |
corrective procedures, including procedures and services for |
the prevention and treatment of periodontal disease and dental |
caries disease, provided by an individual who is licensed to |
practice dentistry or dental surgery or who is under the |
supervision of a dentist in the practice of his or her |
profession. |
|
On and after July 1, 2018, targeted dental services, as |
set forth in Exhibit D of the Consent Decree entered by the |
United States District Court for the Northern District of |
Illinois, Eastern Division, in the matter of Memisovski v. |
Maram, Case No. 92 C 1982, that are provided to adults under |
the medical assistance program shall be established at no less |
than the rates set forth in the "New Rate" column in Exhibit D |
of the Consent Decree for targeted dental services that are |
provided to persons under the age of 18 under the medical |
assistance program. |
Notwithstanding any other provision of this Code and |
subject to federal approval, the Department may adopt rules to |
allow a dentist who is volunteering his or her service at no |
cost to render dental services through an enrolled |
not-for-profit health clinic without the dentist personally |
enrolling as a participating provider in the medical |
assistance program. A not-for-profit health clinic shall |
include a public health clinic or Federally Qualified Health |
Center or other enrolled provider, as determined by the |
Department, through which dental services covered under this |
Section are performed. The Department shall establish a |
process for payment of claims for reimbursement for covered |
dental services rendered under this provision. |
On and after January 1, 2022, the Department of Healthcare |
and Family Services shall administer and regulate a |
school-based dental program that allows for the out-of-office |
|
delivery of preventative dental services in a school setting |
to children under 19 years of age. The Department shall |
establish, by rule, guidelines for participation by providers |
and set requirements for follow-up referral care based on the |
requirements established in the Dental Office Reference Manual |
published by the Department that establishes the requirements |
for dentists participating in the All Kids Dental School |
Program. Every effort shall be made by the Department when |
developing the program requirements to consider the different |
geographic differences of both urban and rural areas of the |
State for initial treatment and necessary follow-up care. No |
provider shall be charged a fee by any unit of local government |
to participate in the school-based dental program administered |
by the Department. Nothing in this paragraph shall be |
construed to limit or preempt a home rule unit's or school |
district's authority to establish, change, or administer a |
school-based dental program in addition to, or independent of, |
the school-based dental program administered by the |
Department. |
The Illinois Department, by rule, may distinguish and |
classify the medical services to be provided only in |
accordance with the classes of persons designated in Section |
5-2. |
The Department of Healthcare and Family Services must |
provide coverage and reimbursement for amino acid-based |
elemental formulas, regardless of delivery method, for the |
|
diagnosis and treatment of (i) eosinophilic disorders and (ii) |
short bowel syndrome when the prescribing physician has issued |
a written order stating that the amino acid-based elemental |
formula is medically necessary. |
The Illinois Department shall authorize the provision of, |
and shall authorize payment for, screening by low-dose |
mammography for the presence of occult breast cancer for |
individuals 35 years of age or older who are eligible for |
medical assistance under this Article, as follows: |
(A) A baseline mammogram for individuals 35 to 39 |
years of age. |
(B) An annual mammogram for individuals 40 years of |
age or older. |
(C) A mammogram at the age and intervals considered |
medically necessary by the individual's health care |
provider for individuals under 40 years of age and having |
a family history of breast cancer, prior personal history |
of breast cancer, positive genetic testing, or other risk |
factors. |
(D) A comprehensive ultrasound screening and MRI of an |
entire breast or breasts if a mammogram demonstrates |
heterogeneous or dense breast tissue or when medically |
necessary as determined by a physician licensed to |
practice medicine in all of its branches. |
(E) A screening MRI when medically necessary, as |
determined by a physician licensed to practice medicine in |
|
all of its branches. |
(F) A diagnostic mammogram when medically necessary, |
as determined by a physician licensed to practice medicine |
in all its branches, advanced practice registered nurse, |
or physician assistant. |
The Department shall not impose a deductible, coinsurance, |
copayment, or any other cost-sharing requirement on the |
coverage provided under this paragraph; except that this |
sentence does not apply to coverage of diagnostic mammograms |
to the extent such coverage would disqualify a high-deductible |
health plan from eligibility for a health savings account |
pursuant to Section 223 of the Internal Revenue Code (26 |
U.S.C. 223). |
All screenings shall include a physical breast exam, |
instruction on self-examination and information regarding the |
frequency of self-examination and its value as a preventative |
tool. |
For purposes of this Section: |
"Diagnostic mammogram" means a mammogram obtained using |
diagnostic mammography. |
"Diagnostic mammography" means a method of screening that |
is designed to evaluate an abnormality in a breast, including |
an abnormality seen or suspected on a screening mammogram or a |
subjective or objective abnormality otherwise detected in the |
breast. |
"Low-dose mammography" means the x-ray examination of the |
|
breast using equipment dedicated specifically for mammography, |
including the x-ray tube, filter, compression device, and |
image receptor, with an average radiation exposure delivery of |
less than one rad per breast for 2 views of an average size |
breast. The term also includes digital mammography and |
includes breast tomosynthesis. |
"Breast tomosynthesis" means a radiologic procedure that |
involves the acquisition of projection images over the |
stationary breast to produce cross-sectional digital |
three-dimensional images of the breast. |
If, at any time, the Secretary of the United States |
Department of Health and Human Services, or its successor |
agency, promulgates rules or regulations to be published in |
the Federal Register or publishes a comment in the Federal |
Register or issues an opinion, guidance, or other action that |
would require the State, pursuant to any provision of the |
Patient Protection and Affordable Care Act (Public Law |
111-148), including, but not limited to, 42 U.S.C. |
18031(d)(3)(B) or any successor provision, to defray the cost |
of any coverage for breast tomosynthesis outlined in this |
paragraph, then the requirement that an insurer cover breast |
tomosynthesis is inoperative other than any such coverage |
authorized under Section 1902 of the Social Security Act, 42 |
U.S.C. 1396a, and the State shall not assume any obligation |
for the cost of coverage for breast tomosynthesis set forth in |
this paragraph. |
|
On and after January 1, 2016, the Department shall ensure |
that all networks of care for adult clients of the Department |
include access to at least one breast imaging Center of |
Imaging Excellence as certified by the American College of |
Radiology. |
On and after January 1, 2012, providers participating in a |
quality improvement program approved by the Department shall |
be reimbursed for screening and diagnostic mammography at the |
same rate as the Medicare program's rates, including the |
increased reimbursement for digital mammography and, after |
January 1, 2023 (the effective date of Public Act 102-1018), |
breast tomosynthesis. |
The Department shall convene an expert panel including |
representatives of hospitals, free-standing mammography |
facilities, and doctors, including radiologists, to establish |
quality standards for mammography. |
On and after January 1, 2017, providers participating in a |
breast cancer treatment quality improvement program approved |
by the Department shall be reimbursed for breast cancer |
treatment at a rate that is no lower than 95% of the Medicare |
program's rates for the data elements included in the breast |
cancer treatment quality program. |
The Department shall convene an expert panel, including |
representatives of hospitals, free-standing breast cancer |
treatment centers, breast cancer quality organizations, and |
doctors, including breast surgeons, reconstructive breast |
|
surgeons, oncologists, and primary care providers to establish |
quality standards for breast cancer treatment. |
Subject to federal approval, the Department shall |
establish a rate methodology for mammography at federally |
qualified health centers and other encounter-rate clinics. |
These clinics or centers may also collaborate with other |
hospital-based mammography facilities. By January 1, 2016, the |
Department shall report to the General Assembly on the status |
of the provision set forth in this paragraph. |
The Department shall establish a methodology to remind |
individuals who are age-appropriate for screening mammography, |
but who have not received a mammogram within the previous 18 |
months, of the importance and benefit of screening |
mammography. The Department shall work with experts in breast |
cancer outreach and patient navigation to optimize these |
reminders and shall establish a methodology for evaluating |
their effectiveness and modifying the methodology based on the |
evaluation. |
The Department shall establish a performance goal for |
primary care providers with respect to their female patients |
over age 40 receiving an annual mammogram. This performance |
goal shall be used to provide additional reimbursement in the |
form of a quality performance bonus to primary care providers |
who meet that goal. |
The Department shall devise a means of case-managing or |
patient navigation for beneficiaries diagnosed with breast |
|
cancer. This program shall initially operate as a pilot |
program in areas of the State with the highest incidence of |
mortality related to breast cancer. At least one pilot program |
site shall be in the metropolitan Chicago area and at least one |
site shall be outside the metropolitan Chicago area. On or |
after July 1, 2016, the pilot program shall be expanded to |
include one site in western Illinois, one site in southern |
Illinois, one site in central Illinois, and 4 sites within |
metropolitan Chicago. An evaluation of the pilot program shall |
be carried out measuring health outcomes and cost of care for |
those served by the pilot program compared to similarly |
situated patients who are not served by the pilot program. |
The Department shall require all networks of care to |
develop a means either internally or by contract with experts |
in navigation and community outreach to navigate cancer |
patients to comprehensive care in a timely fashion. The |
Department shall require all networks of care to include |
access for patients diagnosed with cancer to at least one |
academic commission on cancer-accredited cancer program as an |
in-network covered benefit. |
The Department shall provide coverage and reimbursement |
for a human papillomavirus (HPV) vaccine that is approved for |
marketing by the federal Food and Drug Administration for all |
persons between the ages of 9 and 45. Subject to federal |
approval, the Department shall provide coverage and |
reimbursement for a human papillomavirus (HPV) vaccine for |
|
persons of the age of 46 and above who have been diagnosed with |
cervical dysplasia with a high risk of recurrence or |
progression. The Department shall disallow any |
preauthorization requirements for the administration of the |
human papillomavirus (HPV) vaccine. |
On or after July 1, 2022, individuals who are otherwise |
eligible for medical assistance under this Article shall |
receive coverage for perinatal depression screenings for the |
12-month period beginning on the last day of their pregnancy. |
Medical assistance coverage under this paragraph shall be |
conditioned on the use of a screening instrument approved by |
the Department. |
Any medical or health care provider shall immediately |
recommend, to any pregnant individual who is being provided |
prenatal services and is suspected of having a substance use |
disorder as defined in the Substance Use Disorder Act, |
referral to a local substance use disorder treatment program |
licensed by the Department of Human Services or to a licensed |
hospital which provides substance abuse treatment services. |
The Department of Healthcare and Family Services shall assure |
coverage for the cost of treatment of the drug abuse or |
addiction for pregnant recipients in accordance with the |
Illinois Medicaid Program in conjunction with the Department |
of Human Services. |
All medical providers providing medical assistance to |
pregnant individuals under this Code shall receive information |
|
from the Department on the availability of services under any |
program providing case management services for addicted |
individuals, including information on appropriate referrals |
for other social services that may be needed by addicted |
individuals in addition to treatment for addiction. |
The Illinois Department, in cooperation with the |
Departments of Human Services (as successor to the Department |
of Alcoholism and Substance Abuse) and Public Health, through |
a public awareness campaign, may provide information |
concerning treatment for alcoholism and drug abuse and |
addiction, prenatal health care, and other pertinent programs |
directed at reducing the number of drug-affected infants born |
to recipients of medical assistance. |
Neither the Department of Healthcare and Family Services |
nor the Department of Human Services shall sanction the |
recipient solely on the basis of the recipient's substance |
abuse. |
The Illinois Department shall establish such regulations |
governing the dispensing of health services under this Article |
as it shall deem appropriate. The Department should seek the |
advice of formal professional advisory committees appointed by |
the Director of the Illinois Department for the purpose of |
providing regular advice on policy and administrative matters, |
information dissemination and educational activities for |
medical and health care providers, and consistency in |
procedures to the Illinois Department. |
|
The Illinois Department may develop and contract with |
Partnerships of medical providers to arrange medical services |
for persons eligible under Section 5-2 of this Code. |
Implementation of this Section may be by demonstration |
projects in certain geographic areas. The Partnership shall be |
represented by a sponsor organization. The Department, by |
rule, shall develop qualifications for sponsors of |
Partnerships. Nothing in this Section shall be construed to |
require that the sponsor organization be a medical |
organization. |
The sponsor must negotiate formal written contracts with |
medical providers for physician services, inpatient and |
outpatient hospital care, home health services, treatment for |
alcoholism and substance abuse, and other services determined |
necessary by the Illinois Department by rule for delivery by |
Partnerships. Physician services must include prenatal and |
obstetrical care. The Illinois Department shall reimburse |
medical services delivered by Partnership providers to clients |
in target areas according to provisions of this Article and |
the Illinois Health Finance Reform Act, except that: |
(1) Physicians participating in a Partnership and |
providing certain services, which shall be determined by |
the Illinois Department, to persons in areas covered by |
the Partnership may receive an additional surcharge for |
such services. |
(2) The Department may elect to consider and negotiate |
|
financial incentives to encourage the development of |
Partnerships and the efficient delivery of medical care. |
(3) Persons receiving medical services through |
Partnerships may receive medical and case management |
services above the level usually offered through the |
medical assistance program. |
Medical providers shall be required to meet certain |
qualifications to participate in Partnerships to ensure the |
delivery of high quality medical services. These |
qualifications shall be determined by rule of the Illinois |
Department and may be higher than qualifications for |
participation in the medical assistance program. Partnership |
sponsors may prescribe reasonable additional qualifications |
for participation by medical providers, only with the prior |
written approval of the Illinois Department. |
Nothing in this Section shall limit the free choice of |
practitioners, hospitals, and other providers of medical |
services by clients. In order to ensure patient freedom of |
choice, the Illinois Department shall immediately promulgate |
all rules and take all other necessary actions so that |
provided services may be accessed from therapeutically |
certified optometrists to the full extent of the Illinois |
Optometric Practice Act of 1987 without discriminating between |
service providers. |
The Department shall apply for a waiver from the United |
States Health Care Financing Administration to allow for the |
|
implementation of Partnerships under this Section. |
The Illinois Department shall require health care |
providers to maintain records that document the medical care |
and services provided to recipients of Medical Assistance |
under this Article. Such records must be retained for a period |
of not less than 6 years from the date of service or as |
provided by applicable State law, whichever period is longer, |
except that if an audit is initiated within the required |
retention period then the records must be retained until the |
audit is completed and every exception is resolved. The |
Illinois Department shall require health care providers to |
make available, when authorized by the patient, in writing, |
the medical records in a timely fashion to other health care |
providers who are treating or serving persons eligible for |
Medical Assistance under this Article. All dispensers of |
medical services shall be required to maintain and retain |
business and professional records sufficient to fully and |
accurately document the nature, scope, details and receipt of |
the health care provided to persons eligible for medical |
assistance under this Code, in accordance with regulations |
promulgated by the Illinois Department. The rules and |
regulations shall require that proof of the receipt of |
prescription drugs, dentures, prosthetic devices and |
eyeglasses by eligible persons under this Section accompany |
each claim for reimbursement submitted by the dispenser of |
such medical services. No such claims for reimbursement shall |
|
be approved for payment by the Illinois Department without |
such proof of receipt, unless the Illinois Department shall |
have put into effect and shall be operating a system of |
post-payment audit and review which shall, on a sampling |
basis, be deemed adequate by the Illinois Department to assure |
that such drugs, dentures, prosthetic devices and eyeglasses |
for which payment is being made are actually being received by |
eligible recipients. Within 90 days after September 16, 1984 |
(the effective date of Public Act 83-1439), the Illinois |
Department shall establish a current list of acquisition costs |
for all prosthetic devices and any other items recognized as |
medical equipment and supplies reimbursable under this Article |
and shall update such list on a quarterly basis, except that |
the acquisition costs of all prescription drugs shall be |
updated no less frequently than every 30 days as required by |
Section 5-5.12. |
Notwithstanding any other law to the contrary, the |
Illinois Department shall, within 365 days after July 22, 2013 |
(the effective date of Public Act 98-104), establish |
procedures to permit skilled care facilities licensed under |
the Nursing Home Care Act to submit monthly billing claims for |
reimbursement purposes. Following development of these |
procedures, the Department shall, by July 1, 2016, test the |
viability of the new system and implement any necessary |
operational or structural changes to its information |
technology platforms in order to allow for the direct |
|
acceptance and payment of nursing home claims. |
Notwithstanding any other law to the contrary, the |
Illinois Department shall, within 365 days after August 15, |
2014 (the effective date of Public Act 98-963), establish |
procedures to permit ID/DD facilities licensed under the ID/DD |
Community Care Act and MC/DD facilities licensed under the |
MC/DD Act to submit monthly billing claims for reimbursement |
purposes. Following development of these procedures, the |
Department shall have an additional 365 days to test the |
viability of the new system and to ensure that any necessary |
operational or structural changes to its information |
technology platforms are implemented. |
The Illinois Department shall require all dispensers of |
medical services, other than an individual practitioner or |
group of practitioners, desiring to participate in the Medical |
Assistance program established under this Article to disclose |
all financial, beneficial, ownership, equity, surety or other |
interests in any and all firms, corporations, partnerships, |
associations, business enterprises, joint ventures, agencies, |
institutions or other legal entities providing any form of |
health care services in this State under this Article. |
The Illinois Department may require that all dispensers of |
medical services desiring to participate in the medical |
assistance program established under this Article disclose, |
under such terms and conditions as the Illinois Department may |
by rule establish, all inquiries from clients and attorneys |
|
regarding medical bills paid by the Illinois Department, which |
inquiries could indicate potential existence of claims or |
liens for the Illinois Department. |
Enrollment of a vendor shall be subject to a provisional |
period and shall be conditional for one year. During the |
period of conditional enrollment, the Department may terminate |
the vendor's eligibility to participate in, or may disenroll |
the vendor from, the medical assistance program without cause. |
Unless otherwise specified, such termination of eligibility or |
disenrollment is not subject to the Department's hearing |
process. However, a disenrolled vendor may reapply without |
penalty. |
The Department has the discretion to limit the conditional |
enrollment period for vendors based upon the category of risk |
of the vendor. |
Prior to enrollment and during the conditional enrollment |
period in the medical assistance program, all vendors shall be |
subject to enhanced oversight, screening, and review based on |
the risk of fraud, waste, and abuse that is posed by the |
category of risk of the vendor. The Illinois Department shall |
establish the procedures for oversight, screening, and review, |
which may include, but need not be limited to: criminal and |
financial background checks; fingerprinting; license, |
certification, and authorization verifications; unscheduled or |
unannounced site visits; database checks; prepayment audit |
reviews; audits; payment caps; payment suspensions; and other |
|
screening as required by federal or State law. |
The Department shall define or specify the following: (i) |
by provider notice, the "category of risk of the vendor" for |
each type of vendor, which shall take into account the level of |
screening applicable to a particular category of vendor under |
federal law and regulations; (ii) by rule or provider notice, |
the maximum length of the conditional enrollment period for |
each category of risk of the vendor; and (iii) by rule, the |
hearing rights, if any, afforded to a vendor in each category |
of risk of the vendor that is terminated or disenrolled during |
the conditional enrollment period. |
To be eligible for payment consideration, a vendor's |
payment claim or bill, either as an initial claim or as a |
resubmitted claim following prior rejection, must be received |
by the Illinois Department, or its fiscal intermediary, no |
later than 180 days after the latest date on the claim on which |
medical goods or services were provided, with the following |
exceptions: |
(1) In the case of a provider whose enrollment is in |
process by the Illinois Department, the 180-day period |
shall not begin until the date on the written notice from |
the Illinois Department that the provider enrollment is |
complete. |
(2) In the case of errors attributable to the Illinois |
Department or any of its claims processing intermediaries |
which result in an inability to receive, process, or |
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adjudicate a claim, the 180-day period shall not begin |
until the provider has been notified of the error. |
(3) In the case of a provider for whom the Illinois |
Department initiates the monthly billing process. |
(4) In the case of a provider operated by a unit of |
local government with a population exceeding 3,000,000 |
when local government funds finance federal participation |
for claims payments. |
For claims for services rendered during a period for which |
a recipient received retroactive eligibility, claims must be |
filed within 180 days after the Department determines the |
applicant is eligible. For claims for which the Illinois |
Department is not the primary payer, claims must be submitted |
to the Illinois Department within 180 days after the final |
adjudication by the primary payer. |
In the case of long term care facilities, within 120 |
calendar days of receipt by the facility of required |
prescreening information, new admissions with associated |
admission documents shall be submitted through the Medical |
Electronic Data Interchange (MEDI) or the Recipient |
Eligibility Verification (REV) System or shall be submitted |
directly to the Department of Human Services using required |
admission forms. Effective September 1, 2014, admission |
documents, including all prescreening information, must be |
submitted through MEDI or REV. Confirmation numbers assigned |
to an accepted transaction shall be retained by a facility to |
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verify timely submittal. Once an admission transaction has |
been completed, all resubmitted claims following prior |
rejection are subject to receipt no later than 180 days after |
the admission transaction has been completed. |
Claims that are not submitted and received in compliance |
with the foregoing requirements shall not be eligible for |
payment under the medical assistance program, and the State |
shall have no liability for payment of those claims. |
To the extent consistent with applicable information and |
privacy, security, and disclosure laws, State and federal |
agencies and departments shall provide the Illinois Department |
access to confidential and other information and data |
necessary to perform eligibility and payment verifications and |
other Illinois Department functions. This includes, but is not |
limited to: information pertaining to licensure; |
certification; earnings; immigration status; citizenship; wage |
reporting; unearned and earned income; pension income; |
employment; supplemental security income; social security |
numbers; National Provider Identifier (NPI) numbers; the |
National Practitioner Data Bank (NPDB); program and agency |
exclusions; taxpayer identification numbers; tax delinquency; |
corporate information; and death records. |
The Illinois Department shall enter into agreements with |
State agencies and departments, and is authorized to enter |
into agreements with federal agencies and departments, under |
which such agencies and departments shall share data necessary |
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for medical assistance program integrity functions and |
oversight. The Illinois Department shall develop, in |
cooperation with other State departments and agencies, and in |
compliance with applicable federal laws and regulations, |
appropriate and effective methods to share such data. At a |
minimum, and to the extent necessary to provide data sharing, |
the Illinois Department shall enter into agreements with State |
agencies and departments, and is authorized to enter into |
agreements with federal agencies and departments, including, |
but not limited to: the Secretary of State; the Department of |
Revenue; the Department of Public Health; the Department of |
Human Services; and the Department of Financial and |
Professional Regulation. |
Beginning in fiscal year 2013, the Illinois Department |
shall set forth a request for information to identify the |
benefits of a pre-payment, post-adjudication, and post-edit |
claims system with the goals of streamlining claims processing |
and provider reimbursement, reducing the number of pending or |
rejected claims, and helping to ensure a more transparent |
adjudication process through the utilization of: (i) provider |
data verification and provider screening technology; and (ii) |
clinical code editing; and (iii) pre-pay, pre-adjudicated , or |
post-adjudicated predictive modeling with an integrated case |
management system with link analysis. Such a request for |
information shall not be considered as a request for proposal |
or as an obligation on the part of the Illinois Department to |
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take any action or acquire any products or services. |
The Illinois Department shall establish policies, |
procedures, standards and criteria by rule for the |
acquisition, repair and replacement of orthotic and prosthetic |
devices and durable medical equipment. Such rules shall |
provide, but not be limited to, the following services: (1) |
immediate repair or replacement of such devices by recipients; |
and (2) rental, lease, purchase or lease-purchase of durable |
medical equipment in a cost-effective manner, taking into |
consideration the recipient's medical prognosis, the extent of |
the recipient's needs, and the requirements and costs for |
maintaining such equipment. Subject to prior approval, such |
rules shall enable a recipient to temporarily acquire and use |
alternative or substitute devices or equipment pending repairs |
or replacements of any device or equipment previously |
authorized for such recipient by the Department. |
Notwithstanding any provision of Section 5-5f to the contrary, |
the Department may, by rule, exempt certain replacement |
wheelchair parts from prior approval and, for wheelchairs, |
wheelchair parts, wheelchair accessories, and related seating |
and positioning items, determine the wholesale price by |
methods other than actual acquisition costs. |
The Department shall require, by rule, all providers of |
durable medical equipment to be accredited by an accreditation |
organization approved by the federal Centers for Medicare and |
Medicaid Services and recognized by the Department in order to |
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bill the Department for providing durable medical equipment to |
recipients. No later than 15 months after the effective date |
of the rule adopted pursuant to this paragraph, all providers |
must meet the accreditation requirement. |
In order to promote environmental responsibility, meet the |
needs of recipients and enrollees, and achieve significant |
cost savings, the Department, or a managed care organization |
under contract with the Department, may provide recipients or |
managed care enrollees who have a prescription or Certificate |
of Medical Necessity access to refurbished durable medical |
equipment under this Section (excluding prosthetic and |
orthotic devices as defined in the Orthotics, Prosthetics, and |
Pedorthics Practice Act and complex rehabilitation technology |
products and associated services) through the State's |
assistive technology program's reutilization program, using |
staff with the Assistive Technology Professional (ATP) |
Certification if the refurbished durable medical equipment: |
(i) is available; (ii) is less expensive, including shipping |
costs, than new durable medical equipment of the same type; |
(iii) is able to withstand at least 3 years of use; (iv) is |
cleaned, disinfected, sterilized, and safe in accordance with |
federal Food and Drug Administration regulations and guidance |
governing the reprocessing of medical devices in health care |
settings; and (v) equally meets the needs of the recipient or |
enrollee. The reutilization program shall confirm that the |
recipient or enrollee is not already in receipt of the same or |
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similar equipment from another service provider, and that the |
refurbished durable medical equipment equally meets the needs |
of the recipient or enrollee. Nothing in this paragraph shall |
be construed to limit recipient or enrollee choice to obtain |
new durable medical equipment or place any additional prior |
authorization conditions on enrollees of managed care |
organizations. |
The Department shall execute, relative to the nursing home |
prescreening project, written inter-agency agreements with the |
Department of Human Services and the Department on Aging, to |
effect the following: (i) intake procedures and common |
eligibility criteria for those persons who are receiving |
non-institutional services; and (ii) the establishment and |
development of non-institutional services in areas of the |
State where they are not currently available or are |
undeveloped; and (iii) notwithstanding any other provision of |
law, subject to federal approval, on and after July 1, 2012, an |
increase in the determination of need (DON) scores from 29 to |
37 for applicants for institutional and home and |
community-based long term care; if and only if federal |
approval is not granted, the Department may, in conjunction |
with other affected agencies, implement utilization controls |
or changes in benefit packages to effectuate a similar savings |
amount for this population; and (iv) no later than July 1, |
2013, minimum level of care eligibility criteria for |
institutional and home and community-based long term care; and |
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(v) no later than October 1, 2013, establish procedures to |
permit long term care providers access to eligibility scores |
for individuals with an admission date who are seeking or |
receiving services from the long term care provider. In order |
to select the minimum level of care eligibility criteria, the |
Governor shall establish a workgroup that includes affected |
agency representatives and stakeholders representing the |
institutional and home and community-based long term care |
interests. This Section shall not restrict the Department from |
implementing lower level of care eligibility criteria for |
community-based services in circumstances where federal |
approval has been granted. |
The Illinois Department shall develop and operate, in |
cooperation with other State Departments and agencies and in |
compliance with applicable federal laws and regulations, |
appropriate and effective systems of health care evaluation |
and programs for monitoring of utilization of health care |
services and facilities, as it affects persons eligible for |
medical assistance under this Code. |
The Illinois Department shall report annually to the |
General Assembly, no later than the second Friday in April of |
1979 and each year thereafter, in regard to: |
(a) actual statistics and trends in utilization of |
medical services by public aid recipients; |
(b) actual statistics and trends in the provision of |
the various medical services by medical vendors; |
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(c) current rate structures and proposed changes in |
those rate structures for the various medical vendors; and |
(d) efforts at utilization review and control by the |
Illinois Department. |
The period covered by each report shall be the 3 years |
ending on the June 30 prior to the report. The report shall |
include suggested legislation for consideration by the General |
Assembly. The requirement for reporting to the General |
Assembly shall be satisfied by filing copies of the report as |
required by Section 3.1 of the General Assembly Organization |
Act, and filing such additional copies with the State |
Government Report Distribution Center for the General Assembly |
as is required under paragraph (t) of Section 7 of the State |
Library Act. |
Rulemaking authority to implement Public Act 95-1045, if |
any, is conditioned on the rules being adopted in accordance |
with all provisions of the Illinois Administrative Procedure |
Act and all rules and procedures of the Joint Committee on |
Administrative Rules; any purported rule not so adopted, for |
whatever reason, is unauthorized. |
On and after July 1, 2012, the Department shall reduce any |
rate of reimbursement for services or other payments or alter |
any methodologies authorized by this Code to reduce any rate |
of reimbursement for services or other payments in accordance |
with Section 5-5e. |
Because kidney transplantation can be an appropriate, |
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cost-effective alternative to renal dialysis when medically |
necessary and notwithstanding the provisions of Section 1-11 |
of this Code, beginning October 1, 2014, the Department shall |
cover kidney transplantation for noncitizens with end-stage |
renal disease who are not eligible for comprehensive medical |
benefits, who meet the residency requirements of Section 5-3 |
of this Code, and who would otherwise meet the financial |
requirements of the appropriate class of eligible persons |
under Section 5-2 of this Code. To qualify for coverage of |
kidney transplantation, such person must be receiving |
emergency renal dialysis services covered by the Department. |
Providers under this Section shall be prior approved and |
certified by the Department to perform kidney transplantation |
and the services under this Section shall be limited to |
services associated with kidney transplantation. |
Notwithstanding any other provision of this Code to the |
contrary, on or after July 1, 2015, all FDA approved forms of |
medication assisted treatment prescribed for the treatment of |
alcohol dependence or treatment of opioid dependence shall be |
covered under both fee-for-service fee for service and managed |
care medical assistance programs for persons who are otherwise |
eligible for medical assistance under this Article and shall |
not be subject to any (1) utilization control, other than |
those established under the American Society of Addiction |
Medicine patient placement criteria, (2) prior authorization |
mandate, or (3) lifetime restriction limit mandate , or (4) |
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limitations on dosage . |
On or after July 1, 2015, opioid antagonists prescribed |
for the treatment of an opioid overdose, including the |
medication product, administration devices, and any pharmacy |
fees or hospital fees related to the dispensing, distribution, |
and administration of the opioid antagonist, shall be covered |
under the medical assistance program for persons who are |
otherwise eligible for medical assistance under this Article. |
As used in this Section, "opioid antagonist" means a drug that |
binds to opioid receptors and blocks or inhibits the effect of |
opioids acting on those receptors, including, but not limited |
to, naloxone hydrochloride or any other similarly acting drug |
approved by the U.S. Food and Drug Administration. The |
Department shall not impose a copayment on the coverage |
provided for naloxone hydrochloride under the medical |
assistance program. |
Upon federal approval, the Department shall provide |
coverage and reimbursement for all drugs that are approved for |
marketing by the federal Food and Drug Administration and that |
are recommended by the federal Public Health Service or the |
United States Centers for Disease Control and Prevention for |
pre-exposure prophylaxis and related pre-exposure prophylaxis |
services, including, but not limited to, HIV and sexually |
transmitted infection screening, treatment for sexually |
transmitted infections, medical monitoring, assorted labs, and |
counseling to reduce the likelihood of HIV infection among |
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individuals who are not infected with HIV but who are at high |
risk of HIV infection. |
A federally qualified health center, as defined in Section |
1905(l)(2)(B) of the federal Social Security Act, shall be |
reimbursed by the Department in accordance with the federally |
qualified health center's encounter rate for services provided |
to medical assistance recipients that are performed by a |
dental hygienist, as defined under the Illinois Dental |
Practice Act, working under the general supervision of a |
dentist and employed by a federally qualified health center. |
Within 90 days after October 8, 2021 (the effective date |
of Public Act 102-665), the Department shall seek federal |
approval of a State Plan amendment to expand coverage for |
family planning services that includes presumptive eligibility |
to individuals whose income is at or below 208% of the federal |
poverty level. Coverage under this Section shall be effective |
beginning no later than December 1, 2022. |
Subject to approval by the federal Centers for Medicare |
and Medicaid Services of a Title XIX State Plan amendment |
electing the Program of All-Inclusive Care for the Elderly |
(PACE) as a State Medicaid option, as provided for by Subtitle |
I (commencing with Section 4801) of Title IV of the Balanced |
Budget Act of 1997 (Public Law 105-33) and Part 460 |
(commencing with Section 460.2) of Subchapter E of Title 42 of |
the Code of Federal Regulations, PACE program services shall |
become a covered benefit of the medical assistance program, |
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subject to criteria established in accordance with all |
applicable laws. |
Notwithstanding any other provision of this Code, |
community-based pediatric palliative care from a trained |
interdisciplinary team shall be covered under the medical |
assistance program as provided in Section 15 of the Pediatric |
Palliative Care Act. |
Notwithstanding any other provision of this Code, within |
12 months after June 2, 2022 (the effective date of Public Act |
102-1037) and subject to federal approval, acupuncture |
services performed by an acupuncturist licensed under the |
Acupuncture Practice Act who is acting within the scope of his |
or her license shall be covered under the medical assistance |
program. The Department shall apply for any federal waiver or |
State Plan amendment, if required, to implement this |
paragraph. The Department may adopt any rules, including |
standards and criteria, necessary to implement this paragraph. |
Notwithstanding any other provision of this Code, the |
medical assistance program shall, subject to appropriation and |
federal approval, reimburse hospitals for costs associated |
with a newborn screening test for the presence of |
metachromatic leukodystrophy, as required under the Newborn |
Metabolic Screening Act, at a rate not less than the fee |
charged by the Department of Public Health. The Department |
shall seek federal approval before the implementation of the |
newborn screening test fees by the Department of Public |
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Health. |
Notwithstanding any other provision of this Code, |
beginning on January 1, 2024, subject to federal approval, |
cognitive assessment and care planning services provided to a |
person who experiences signs or symptoms of cognitive |
impairment, as defined by the Diagnostic and Statistical |
Manual of Mental Disorders, Fifth Edition, shall be covered |
under the medical assistance program for persons who are |
otherwise eligible for medical assistance under this Article. |
Notwithstanding any other provision of this Code, |
medically necessary reconstructive services that are intended |
to restore physical appearance shall be covered under the |
medical assistance program for persons who are otherwise |
eligible for medical assistance under this Article. As used in |
this paragraph, "reconstructive services" means treatments |
performed on structures of the body damaged by trauma to |
restore physical appearance. |
(Source: P.A. 102-43, Article 30, Section 30-5, eff. 7-6-21; |
102-43, Article 35, Section 35-5, eff. 7-6-21; 102-43, Article |
55, Section 55-5, eff. 7-6-21; 102-95, eff. 1-1-22; 102-123, |
eff. 1-1-22; 102-558, eff. 8-20-21; 102-598, eff. 1-1-22; |
102-655, eff. 1-1-22; 102-665, eff. 10-8-21; 102-813, eff. |
5-13-22; 102-1018, eff. 1-1-23; 102-1037, eff. 6-2-22; |
102-1038, eff. 1-1-23; 103-102, Article 15, Section 15-5, eff. |
1-1-24; 103-102, Article 95, Section 95-15, eff. 1-1-24; |
103-123, eff. 1-1-24; 103-154, eff. 6-30-23; 103-368, eff. |