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II
116TH CONGRESS
1ST SESSION
S. 3067
To amend title XVIII of the Social Security Act to combat the opioid crisis
by promoting access to non-opioid treatments in the hospital outpatient
setting.
IN THE SENATE OF THE UNITED STATES
DECEMBER 17, 2019
Mrs. CAPITO (for herself, Mr. JONES, Ms. ERNST, Mrs. SHAHEEN, and Mr.
MANCHIN) introduced the following bill; which was read twice and re-
ferred to the Committee on Finance
A BILL
To amend title XVIII of the Social Security Act to combat
the opioid crisis by promoting access to non-opioid treat-
ments in the hospital outpatient setting.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Non-Opioids Prevent
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Addiction In the Nation Act’’ or the ‘‘NOPAIN Act’’.
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SEC. 2. ACCESS TO NON-OPIOID TREATMENTS FOR PAIN.
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(a) IN GENERAL.—Section 1833(t) of the Social Se-
7
curity Act (42 U.S.C. 1395l(t)) is amended—
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(1) in paragraph (2)(E), by inserting ‘‘and sep-
1
arate payments for non-opioid treatments under
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paragraph (16)(G),’’ after ‘‘payments under para-
3
graph (6)’’; and
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(2) in paragraph (16), by adding at the end the
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following new subparagraph:
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‘‘(G) ACCESS TO NON-OPIOID TREATMENTS
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FOR PAIN.—
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‘‘(i) IN
GENERAL.—Notwithstanding
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any other provision of this subsection, with
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respect to a covered OPD service (or group
11
of services) furnished on or after January
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1, 2020, and before January 1, 2025, the
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Secretary shall not package, and shall
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make a separate payment as specified in
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clause (ii) for, a non-opioid treatment (as
16
defined in clause (iii)) furnished as part of
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such service (or group of services).
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‘‘(ii) AMOUNT
OF
PAYMENT.—The
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amount of the payment specified in this
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clause is, with respect to a non-opioid
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treatment that is—
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‘‘(I) a drug or biological product,
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the amount of payment for such drug
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•S 3067 IS
or biological determined under section
1
1847A; or
2
‘‘(II)
a
medical
device,
the
3
amount of the hospital’s charges for
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the device, adjusted to cost.
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‘‘(iii) DEFINITION
OF
NON-OPIOID
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TREATMENT.—A
‘non-opioid
treatment’
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means—
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‘‘(I) a drug or biological product
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that is indicated to produce analgesia
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without acting upon the body’s opioid
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receptors; or
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‘‘(II) an implantable, reusable, or
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disposable medical device cleared or
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approved by the Administrator for
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Food and Drugs for the intended use
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of managing or treating pain,
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that has demonstrated the ability to re-
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place or reduce opioid consumption in a
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clinical trial or through clinical data pub-
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lished in a peer-reviewed journal.’’.
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(b) AMBULATORY SURGICAL CENTER PAYMENT SYS-
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TEM.—Section 1833(i)(2)(D) of the Social Security Act
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(42 U.S.C. 1395l(i)(2)(D)) is amended—
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(1) by aligning the margins of clause (v) with
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the margins of clause (iv);
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(2) by redesignating clause (vi) as clause (vii);
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and
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(3) by inserting after clause (v) the following
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new clause:
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‘‘(vi) In the case of surgical services
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furnished on or after January 1, 2020, and
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before January 1, 2025, the payment sys-
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tem described in clause (i) shall provide for
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a separate payment for a non-opioid treat-
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ment (as defined in clause (iii) of sub-
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section (t)(16)(G)) furnished as part of
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such services in the amount specified in
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clause (ii) of such subsection.’’.
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(c) EVALUATION OF THERAPEUTIC SERVICES FOR
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PAIN MANAGEMENT.—
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(1) REPORT TO CONGRESS.—Not later than 1
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year after the date of the enactment of this Act, the
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Secretary of Health and Human Services (in this
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subsection referred to as the ‘‘Secretary’’), acting
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through the Administrator of the Centers for Medi-
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care & Medicaid Services, shall submit to Congress
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a report identifying—
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(A) limitations, gaps, barriers to access, or
1
deficits in Medicare coverage or reimbursement
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for restorative therapies, behavioral approaches,
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and complementary and integrative health serv-
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ices that are identified in the Pain Management
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Best Practices Inter-Agency Task Force Report
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and that have demonstrated the ability to re-
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place or reduce opioid consumption; and
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(B) recommendations to address the limi-
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tations, gaps, barriers to access, or deficits
10
identified under subparagraph (A) to improve
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Medicare coverage and reimbursement for such
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therapies, approaches, and services.
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(2) PUBLIC CONSULTATION.—In developing the
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report described in paragraph (1), the Secretary
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shall consult with relevant stakeholders as deter-
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mined appropriate by the Secretary.
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(3) EXCLUSIVE TREATMENT.—Any drug, bio-
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logical product, or medical device that is a non-
19
opioid
treatment
(as
defined
in
section
20
1833(t)(16)(G)(iii) of the Social Security Act, as
21
added by subsection (a)) shall not be considered a
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therapeutic service for the purpose of the report de-
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scribed in paragraph (1).
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Æ
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