Federal
To amend title XVIII of the Social Security Act to provide for additional requirements with respect to electrodiagnostic services under the Medicare program.
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I
116TH CONGRESS
2D SESSION
H. R. 8780
To amend title XVIII of the Social Security Act to provide for additional
requirements with respect to electrodiagnostic services under the Medi-
care program.
IN THE HOUSE OF REPRESENTATIVES
NOVEMBER 18, 2020
Mr. WALDEN (for himself and Ms. BLUNT ROCHESTER) introduced the fol-
lowing bill; which was referred to the Committee on Energy and Com-
merce, and in addition to the Committee on Ways and Means, for a pe-
riod to be subsequently determined by the Speaker, in each case for con-
sideration of such provisions as fall within the jurisdiction of the com-
mittee concerned
A BILL
To amend title XVIII of the Social Security Act to provide
for additional requirements with respect to electrodiag-
nostic services under the Medicare program.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. ADDITIONAL REQUIREMENTS FOR ELECTRODI-
3
AGNOSTIC SERVICES.
4
Section 1834 of the Social Security Act (42 U.S.C.
5
1395m) is amended by adding at the end the following
6
new subsection:
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•HR 8780 IH
‘‘(x) PAYMENT
FOR
ELECTRODIAGNOSTIC
SERV-
1
ICES.—
2
‘‘(1) IN GENERAL.—No payment may be made
3
under this part for electrodiagnostic services de-
4
scribed in paragraph (2) furnished on or after a date
5
determined appropriate by the Secretary that is not
6
less than 3 years after the date of the enactment of
7
this subsection and not later than 4 years after such
8
date of enactment that are not furnished at a quali-
9
fied facility.
10
‘‘(2)
ELECTRODIAGNOSTIC
SERVICES.—The
11
services described in this paragraph are the fol-
12
lowing:
13
‘‘(A) Nerve conduction studies.
14
‘‘(B) Needle electromyography tests.
15
‘‘(3) QUALIFIED FACILITY.—In this subsection,
16
the term ‘qualified facility’ means a facility accred-
17
ited by an organization specified by the Secretary
18
pursuant to paragraph (4).
19
‘‘(4) ACCREDITATION ORGANIZATIONS.—
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‘‘(A) IN GENERAL.—Not later than 2 years
21
after the date of the enactment of this sub-
22
section, the Secretary shall specify one or more
23
accrediting organizations, in consultation with
24
the advisory committee described in paragraph
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•HR 8780 IH
(5), for purposes determining whether a facility
1
is a qualified facility. The Secretary may speci-
2
fy an organization pursuant to the preceding
3
sentence only if such organization requires, as
4
a condition of accreditation of a facility by such
5
organization, that such facility meet the re-
6
quirements described in subparagraph (B).
7
‘‘(B) FACILITY REQUIREMENTS.—The re-
8
quirements described in this subparagraph are,
9
with respect to a facility and electrodiagnostic
10
services furnished at such facility, the following:
11
‘‘(i) The facility establishes and main-
12
tains a quality assurance and control pro-
13
gram to ensure the reliability, safety, and
14
accuracy of such service.
15
‘‘(ii) The facility ensures that such
16
service is conducted using a device capable
17
of performing both nerve conduction stud-
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ies that record amplitude and latency and
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needle electromyography tests capable of
20
real-time waveform display and analysis.
21
‘‘(iii) In the case that such service is
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a needle electromyography test, the facility
23
ensures that the physician furnishing such
24
test has completed not less than three
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•HR 8780 IH
months
of
training
in
furnishing
1
electrodiagnostic services through a resi-
2
dency or fellowship program accredited by
3
the Accreditation Council for Graduate
4
Medical Education or the Royal College of
5
Physicians and Surgeons of Canada.
6
‘‘(iv) The facility ensures that the re-
7
sults are interpreted on-site and at the
8
time of the procedure—
9
‘‘(I) in the case of a needle
10
electromyography test, by the physi-
11
cian who performed such test; and
12
‘‘(II) in the case of a nerve con-
13
duction study, by the physician who
14
performed or supervised such study.
15
‘‘(v) Any other requirement deter-
16
mined appropriate by the Secretary.
17
‘‘(C) REGULATIONS.—Not later than 1
18
year after the date of the enactment of this
19
subsection, the Secretary shall finalize regula-
20
tions that outline—
21
‘‘(i) the process by which an accred-
22
iting organization may be specified under
23
subparagraph (A);
24
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‘‘(ii) the duration and the minimum
1
time period between reviews for reaccredi-
2
tation an organization so specified must
3
provide for with respect to an accreditation
4
of a facility made by such organization;
5
‘‘(iii) the process by which the Sec-
6
retary may withdraw approval of an ac-
7
crediting organization so specified if the
8
Secretary determines that such organiza-
9
tion no longer requires, as a condition of
10
accreditation of a facility by such organiza-
11
tion, that such facility meet the require-
12
ments described in subparagraph (B); and
13
‘‘(iv) the effect such a withdrawal will
14
have on facilities accredited by such orga-
15
nization as of the date of such withdrawal.
16
‘‘(5) ADVISORY COMMITTEE.—
17
‘‘(A) IN GENERAL.—Not later than 2 years
18
after the date of the enactment of this sub-
19
section, the Secretary shall establish an advi-
20
sory committee to be known as the ‘National
21
Electrodiagnostic Services Advisory Committee’
22
(in this subsection referred to as the ‘com-
23
mittee’) for purposes of carrying out the duties
24
specified in subparagraph (B).
25
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‘‘(B) DUTIES.—The duties of the com-
1
mittee are the following:
2
‘‘(i) To provide to the Secretary rec-
3
ommendations with respect to require-
4
ments that may be determined appropriate
5
by the Secretary pursuant to paragraph
6
(4)(B)(v), including any proposed additions
7
to such requirements or modifications of
8
such requirements. In developing such rec-
9
ommendations,
the
committee
shall
10
prioritize—
11
‘‘(I) reducing unnecessary treat-
12
ments and surgeries;
13
‘‘(II) decreasing the need for re-
14
testing of individuals;
15
‘‘(III) enhancing the reliability of
16
diagnoses
and
promoting
positive
17
health outcomes for individuals;
18
‘‘(IV) addressing emerging waste,
19
fraud, and abuse schemes; and
20
‘‘(V) otherwise improving the
21
quality of care for individuals.
22
‘‘(ii) To provide to the Secretary rec-
23
ommendations regarding the regulations
24
described in paragraph (4)(C).
25
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‘‘(iii) To provide to the Secretary rec-
1
ommendations with respect to whether ac-
2
crediting organizations seeking to be speci-
3
fied pursuant to paragraph (4)(A) should
4
be so specified.
5
‘‘(C) COMPOSITION.—The committee shall
6
be composed of not fewer than 9 and not more
7
than 11 individuals selected by the Secretary.
8
Such individuals shall not be officers or employ-
9
ees of the Federal Government and shall in-
10
clude—
11
‘‘(i) physicians;
12
‘‘(ii) other health care practitioners;
13
and
14
‘‘(iii) other individuals determined ap-
15
propriate by the Secretary.
16
‘‘(D) MEETINGS.—The committee shall
17
convene not less than twice each year.’’.
18
Æ
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