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1 | HOUSE RESOLUTION
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2 | WHEREAS, The Department of Health and Human Services (HHS) | ||||||
3 | has announced proposed changes to the federal regulations | ||||||
4 | governing the confidentiality of patient records created by | ||||||
5 | federally-assisted substance use disorder treatment programs, | ||||||
6 | known as 42 CFR part 2; and
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7 | WHEREAS, The 42 CFR part 2 regulations serve to protect | ||||||
8 | patient records created by federally-funded programs for the | ||||||
9 | treatment of substance abuse disorder (SUD); SAMHSA is | ||||||
10 | currently proposing to revise part 2 to facilitate better | ||||||
11 | coordination of care for substance use disorders, which will | ||||||
12 | also enhance care for opioid use disorder (OUD); these | ||||||
13 | provisions will be an important part of the Federal response to | ||||||
14 | the opioid epidemic, while maintaining part 2 confidentiality | ||||||
15 | protections; and
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16 | WHEREAS, In these proposed federal regulation changes, | ||||||
17 | "non-OTP (opioid treatment program) providers will become | ||||||
18 | eligible to query a central registry, in order to determine | ||||||
19 | whether their patients are already receiving opioid treatment | ||||||
20 | through a member program," and "OTPs will be permitted to | ||||||
21 | enroll in a state prescription drug monitoring program (PDMP), | ||||||
22 | and permitted to report data into the PDMP when prescribing or | ||||||
23 | dispensing medications on Schedules II to V, consistent with |
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1 | applicable state law"; and
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2 | WHEREAS, These changes could improve the care of persons | ||||||
3 | with opioid use disorder because primary care providers could | ||||||
4 | more easily receive treatment information from other treatment | ||||||
5 | programs and could utilize the Illinois Prescription Drug | ||||||
6 | Monitoring Program to see if a patient is receiving methadone | ||||||
7 | or other controlled substances from an opioid treatment program | ||||||
8 | (OTP); these changes will help to prevent duplicative | ||||||
9 | enrollments in SUD care, duplicative prescriptions in SUD | ||||||
10 | treatment, and adverse drug events related to SUD treatment; | ||||||
11 | and
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12 | WHEREAS, The proposed rule will not alter the basic | ||||||
13 | framework for confidentiality protection of SUD patient | ||||||
14 | records created by federally-funded treatment programs; part 2 | ||||||
15 | will continue to prohibit law enforcement use of SUD patient | ||||||
16 | records in criminal prosecution against the patient; part 2 | ||||||
17 | will also continue to restrict the disclosure of SUD treatment | ||||||
18 | records without patient consent, other than as statutorily | ||||||
19 | authorized in the context of a bona fide medical emergency, or | ||||||
20 | for the purpose of scientific research, audit, or program | ||||||
21 | evaluation, or based on an appropriate court order for good | ||||||
22 | cause; therefore, be it
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23 | RESOLVED, BY THE HOUSE OF REPRESENTATIVES OF THE ONE |
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1 | HUNDRED FIRST GENERAL ASSEMBLY OF THE STATE OF ILLINOIS, that | ||||||
2 | we urge the support of the proposed changes to 42 CFR part 2 to | ||||||
3 | improve communication and exchange of information between all | ||||||
4 | providers of care for people with substance abuse disorder; and | ||||||
5 | be it further
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6 | RESOLVED, That suitable copies of this resolution be | ||||||
7 | presented to the members of the Illinois Congressional | ||||||
8 | Delegation.
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