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II
116TH CONGRESS
1ST SESSION
S. 3049
To amend title XVIII of the Social Security Act to provide for certain
amendments relating to reporting requirements with respect to clinical
diagnostic laboratory tests, and for other purposes.
IN THE SENATE OF THE UNITED STATES
DECEMBER 12, 2019
Mr. BROWN (for himself and Mr. BURR) introduced the following bill; which
was read twice and referred to the Committee on Finance
A BILL
To amend title XVIII of the Social Security Act to provide
for certain amendments relating to reporting require-
ments with respect to clinical diagnostic laboratory tests,
and for other purposes.
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 ‘‘Laboratory Access for
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Beneficiaries Act’’ or the ‘‘LAB Act’’.
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•S 3049 IS
SEC. 2. AMENDMENTS RELATING TO REPORTING REQUIRE-
1
MENTS WITH RESPECT TO CLINICAL DIAG-
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NOSTIC LABORATORY TESTS.
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(a) REVISED REPORTING PERIOD FOR REPORTING
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OF PRIVATE SECTOR PAYMENT RATES FOR ESTABLISH-
5
MENT
OF
MEDICARE
PAYMENT
RATES.—Section
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1834A(a) of the Social Security Act (42 U.S.C. 1395m–
7
1(a)) is amended—
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(1) in paragraph (1)—
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(A) by striking ‘‘Beginning January 1,
10
2016’’ and inserting the following:
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‘‘(A)
GENERAL
REPORTING
REQUIRE-
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MENTS.—Subject to subparagraph (B), begin-
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ning January 1, 2016’’;
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(B) in subparagraph (A), as added by sub-
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paragraph (A) of this paragraph, by inserting
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‘‘(referred to in this subsection as the ‘reporting
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period’)’’ after ‘‘at a time specified by the Sec-
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retary’’; and
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(C) by adding at the end the following:
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‘‘(B) REVISED
REPORTING
PERIOD.—In
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the case of reporting with respect to clinical di-
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agnostic laboratory tests that are not advanced
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diagnostic laboratory tests, the Secretary shall
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revise the reporting period under subparagraph
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(A) such that—
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•S 3049 IS
‘‘(i) no reporting is required during
1
the period beginning January 1, 2020, and
2
ending December 31, 2020;
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‘‘(ii) reporting is required during the
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period beginning January 1, 2021, and
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ending March 31, 2021; and
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‘‘(iii) reporting is required every three
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years after the period described in clause
8
(ii).’’; and
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(2) in paragraph (4)—
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(A) by striking ‘‘In this section’’ and in-
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serting the following:
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‘‘(A) IN
GENERAL.—Subject to subpara-
13
graph (B), in this section’’; and
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(B) by adding at the end the following:
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‘‘(B) EXCEPTION.—In the case of the re-
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porting period described in paragraph (1)(B)(ii)
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with respect to clinical diagnostic laboratory
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tests that are not advanced diagnostic labora-
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tory tests, the term ‘data collection period’
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means the period beginning January 1, 2019,
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and ending June 30, 2019.’’.
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(b) CORRECTIONS RELATING TO PHASE-IN OF RE-
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DUCTIONS FROM PRIVATE PAYOR RATE IMPLEMENTA-
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TION.—Section 1834A(b)(3) of the Social Security Act
1
(42 U.S.C. 1395m–1(b)(3)) is amended—
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(1) in subparagraph (A), by striking ‘‘through
3
2022’’ and inserting ‘‘through 2023’’; and
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(2) in subparagraph (B)—
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(A) in clause (i), by striking ‘‘through
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2019’’ and inserting ‘‘through 2020’’; and
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(B) in clause (ii), by striking ‘‘2020
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through 2022’’ and inserting ‘‘2021 through
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2023’’.
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SEC. 3. STUDY AND REPORT BY MEDPAC.
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(a) IN GENERAL.—The Medicare Payment Advisory
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Commission (in this section referred to as the ‘‘Commis-
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sion’’) shall conduct a study to review the methodology
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the Administrator of the Centers for Medicare & Medicaid
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Services has implemented for the private payor rate-based
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clinical laboratory fee schedule under the Medicare pro-
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gram under title XVIII of the Social Security Act (42
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U.S.C. 1395 et seq.).
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(b) SCOPE OF STUDY.—In carrying out the study de-
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scribed in subsection (a), the Commission shall consider
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the following:
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(1) How best to implement the least burden-
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some data collection process required under section
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1834A(a)(1) of such Act (42 U.S.C. 1395m–1(a)(1))
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that would—
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(A) result in a representative and statis-
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tically valid data sample of private market rates
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from all laboratory market segments, including
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hospital outreach laboratories, physician office
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laboratories, and independent laboratories; and
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(B) consider the variability of private
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payor payment rates across market segments
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and laboratory setttings.
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(2) Appropriate statistical methods for esti-
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mating rates that are representative of the market.
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(c) REPORT
TO CONGRESS.—Not later than 18
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months after the date of the enactment of this Act, the
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Commission shall submit to the Administrator, the Com-
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mittee on Finance of the Senate, and the Committees on
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Ways and Means and Energy and Commerce of the House
17
of Representatives a report that includes—
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(1) conclusions about the methodology de-
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scribed in such subsection; and
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(2) any recommendations the Commission
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deems appropriate.
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Æ
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