Medicare Program; Approval of Request for an Exception to the Prohibition on Expansion of Facility Capacity Under the Hospital Ownership and Rural Provider Exceptions to the Physician Self-Referral Prohibition, 77844-77847 [2022-27566]
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Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
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Georgia 30329. Email: cdc-roybalgaseis@cdc.gov. Telephone: 770–488–
8170.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
SUPPLEMENTARY INFORMATION:
[CMS–1774–FN]
Correction
In the Decision section of the Federal
Register notice of November 17, 2022
(87 FR 69023), center column, the
description of the incinerator was
labeled as a Hazardous/Medical/
Infectious Waste Incinerator. The
correct description is a Hospital/
Medical/Infectious Waste Incinerator.
The correct Decision section to read:
Decision
Dated: December 15, 2022.
Angela K. Oliver,
Executive Secretary, Centers for Disease
Control and Prevention.
lotter on DSK11XQN23PROD with NOTICES1
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces our
decision to approve the request from
Doctors Hospital at Renaissance, Ltd.’s
for an exception to the prohibition on
expansion of facility capacity.
DATES: The decision announced in this
notice is applicable on December 16,
2022.
SUMMARY:
Based on the Final SEIS, CDC has
decided to implement Alternative 1
(Preferred Alternative) as the selected
alternative. This Alternative includes
the construction and operation of a new
Hospital/Medical/Infectious Waste
Incinerator in a new laboratory building,
the operation of two proposed
emergency standby power diesel
generators to support that laboratory,
and annual testing of the generators.
According to the analysis, no potential
significant impacts were identified for
the selected alternative.
CDC’s decision is based on an
analysis of the potential impacts of the
alternatives considered in the SEIS
weighed against CDC’s continuing need
to fulfill its unique and critical public
health mission and its ability to mitigate
in whole or in part the adverse impacts.
CDC also considered the input from the
public and agencies, such as the U.S.
Fish and Wildlife Service, Georgia
Department of Natural Resources,
Georgia Environmental Protection
Division, and Georgia Historic
Preservation Division.
Availability of the ROD: The ROD is
available in the Supplemental Materials
tab of the docket found on the Federal
eRulemaking Portal at https://
www.regulations.gov, identified by
Docket No. CDC–2022–0014.
[FR Doc. 2022–27584 Filed 12–19–22; 8:45 am]
BILLING CODE 4163–18–P
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Medicare Program; Approval of
Request for an Exception to the
Prohibition on Expansion of Facility
Capacity Under the Hospital
Ownership and Rural Provider
Exceptions to the Physician SelfReferral Prohibition
18:41 Dec 19, 2022
Jkt 259001
POH-ExceptionRequests@
cms.hhs.gov.
ADDRESSES:
I. Background
Section 1877 of the Social Security
Act (the Act), also known as the
physician self-referral law: (1) prohibits
a physician from making referrals for
certain designated health services
payable by Medicare to an entity with
which he or she (or an immediate family
member) has a financial relationship
unless the requirements of an applicable
exception are satisfied; and (2) prohibits
the entity from filing claims with
Medicare (or billing another individual,
entity, or third party payer) for any
improperly referred designated health
services. A financial relationship may
be an ownership or investment interest
in the entity or a compensation
arrangement with the entity. The statute
establishes a number of specific
exceptions and grants the Secretary of
the Department of Health and Human
Services (the Secretary) the authority to
create regulatory exceptions for
financial relationships that do not pose
a risk of program or patient abuse.
Section 1877(d) of the Act sets forth
exceptions related to ownership or
investment interests held by a physician
(or an immediate family member of a
physician) in an entity that furnishes
designated health services. Section
1877(d)(2) of the Act provides an
exception for ownership or investment
interests in rural providers (the ‘‘rural
provider exception’’). In order to qualify
for the rural provider exception, the
designated health services must be
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furnished in a rural area (as defined in
section 1886(d)(2) of the Act) and
substantially all the designated health
services furnished by the entity must be
furnished to individuals residing in a
rural area. In addition, in the case where
the entity is a hospital, the hospital
must meet the requirements of section
1877(i)(1) of the Act no later than
September 23, 2011. Section 1877(d)(3)
of the Act provides an exception for
ownership or investment interests in a
hospital located outside of Puerto Rico
(the ‘‘whole hospital exception’’). In
order to qualify for the whole hospital
exception, the referring physician must
be authorized to perform services at the
hospital, the ownership or investment
interest must be in the hospital itself
(and not merely in a subdivision of the
hospital), and the hospital must meet
the requirements of section 1877(i)(1) of
the Act no later than September 23,
2011.
II. Prohibition on Facility Expansion
Section 6001(a)(3) of the Patient
Protection and Affordable Care Act
(Affordable Care Act) (Pub. L. 111–148)
amended the rural provider and whole
hospital exceptions to provide that a
hospital may not increase the number of
operating rooms, procedure rooms, and
beds beyond that for which the hospital
was licensed on March 23, 2010 (or, in
the case of a hospital that did not have
a provider agreement in effect as of this
date, but did have a provider agreement
in effect on December 31, 2010, the
effective date of such provider
agreement) (the hospital’s ‘‘baseline
number of operating rooms, procedure
rooms, and beds’’). Thus, since March
23, 2010, a physician-owned hospital
that seeks to avail itself of either
exception is prohibited from expanding
the number of operating rooms,
procedure rooms, and beds (‘‘facility
capacity’’) unless it has been granted an
exception to the prohibition by the
Secretary.
Section 6001(a)(3) of the Affordable
Care Act added new section
1877(i)(3)(A)(i) of the Act, which
required the Secretary to establish and
implement a process for granting
exceptions to the prohibition on
expansion of facility capacity for
hospitals that qualify as an ‘‘applicable
hospital.’’ Section 1106 of the Health
Care and Education Reconciliation Act
of 2010 (Pub. L. 111–152) amended
section 1877(i)(3)(A)(i) of the Act to
require the Secretary to establish and
implement a process for granting
exceptions to the prohibition on
expansion of facility capacity for
hospitals that qualify as either an
‘‘applicable hospital’’ or a ‘‘high
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Federal Register / Vol. 87, No. 243 / Tuesday, December 20, 2022 / Notices
Medicaid facility.’’ These terms are
defined at sections 1877(i)(3)(E) and
1877(i)(3)(F) of the Act. The process for
requesting an exception to the
prohibition on expansion of facility
capacity is discussed in section III of
this notice.
The requirements for qualifying as an
applicable hospital are set forth at
§ 411.362(c)(2), and the requirements for
qualifying as a high Medicaid facility
are set forth at § 411.362(c)(3). An
‘‘applicable hospital’’ means a hospital:
(1) that is located in a county in which
the percentage increase in the
population during the most recent 5year period (as of the date that the
hospital submits its request for an
exception to the prohibition on
expansion of facility capacity) is at least
150 percent of the percentage increase
in the population growth of the State in
which the hospital is located during that
period, as estimated by the Bureau of
the Census; (2) whose annual percent of
total inpatient admissions under
Medicaid is equal to or greater than the
average percent with respect to such
admissions for all hospitals in the
county in which the hospital is located
during the most recent 12-month period
for which data are available (as of the
date that the hospital submits its request
for an exception to the prohibition on
expansion of facility capacity); (3) that
does not discriminate against
beneficiaries of Federal health care
programs and does not permit
physicians practicing at the hospital to
discriminate against such beneficiaries;
(4) that is located in a State in which the
average bed capacity in the State is less
than the national average bed capacity;
and (5) that has an average bed
occupancy rate that is greater than the
average bed occupancy rate in the State
in which the hospital is located. A
‘‘high Medicaid facility’’ means a
hospital that: (1) is not the sole hospital
in a county; (2) with respect to each of
the three most recent 12-month periods
for which data are available, has an
annual percent of total inpatient
admissions under Medicaid that is
estimated to be greater than such
percent with respect to such admissions
for any other hospital located in the
county in which the hospital is located;
and (3) does not discriminate against
beneficiaries of Federal health care
programs and does not permit
physicians practicing at the hospital to
discriminate against such beneficiaries.
The regulation at § 411.362(c)(2)(ii)
specifies the acceptable data sources for
determining whether a hospital qualifies
as an applicable hospital, and the
regulation at § 411.362(c)(3)(ii) specifies
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the acceptable data sources for
determining whether a hospital qualifies
as a high Medicaid facility.
III. Exception Approval Process
In the Calendar Year (CY) 2012
Outpatient Prospective Payment
System/Ambulatory Surgical Centers
(OPPS/ASC) final rule (76 FR 74121),
we published regulations establishing
the process for a hospital to request an
exception from the prohibition on
facility expansion (the ‘‘exception
process’’) at § 411.362(c)(4), the process
for obtaining community input related
to a hospital’s request at § 411.362(c)(5),
and related definitions at § 411.362(a).
In the CY 2015 OPPS/ASC final rule
(79 FR 66770), we expanded the
permissible data sources on which a
hospital may rely to show that it is
qualified to request an exception to the
prohibition on expansion of facility
capacity (that is, that the hospital
qualifies as either an applicable hospital
or a high Medicaid facility). We also
amended the exception process
established in the CY 2012 OPPS/ASC
final rule to increase the period of time
after which an exception request will be
deemed complete when an external data
source is used by a requesting hospital
or in the public comments to determine
whether a hospital qualifies as either an
applicable hospital or high Medicaid
facility. In the CY 2015 OPPS/ASC final
rule, we stated that it is possible (if not
likely) that, when reviewing an
expansion exception request, the
Centers for Medicare & Medicaid
Services (CMS) would need to verify the
data (and other information, if any)
provided by the requesting hospital and
any commenters, as well as consider the
data in light of the information
otherwise available to CMS (79 FR
66995).
In the CY 2021 OPPS/ASC final rule
(85 FR 85866), we revised the
regulations that set forth the exception
process with respect to high Medicaid
facilities to remove certain regulatory
restrictions that are not included in the
Act. As of January 1, 2021, a high
Medicaid facility may request an
exception to the prohibition on
expansion of facility capacity more
frequently than once every 2 years; may
request to expand its facility capacity
beyond 200 percent of the hospital’s
baseline number of operating rooms,
procedure rooms, and beds; and, if its
request is granted, is not restricted to
locating approved expansion capacity
on the hospital’s main campus. An
applicable hospital remains subject to
the statutory limitation on the frequency
of requests for an exception to the
prohibition on expansion of facility
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capacity (no more than once every 2
years); may not request to expand its
facility capacity beyond 200 percent of
the hospital’s baseline number of
operating rooms, procedure rooms, and
beds; and, if its request is granted, is
restricted to locating approved
expansion capacity on the hospital’s
main campus.
Our regulations at § 411.362(c)(5)
require us to solicit community input on
the request for an exception by
publishing a notice of the request in the
Federal Register. Individuals and
entities in the hospital’s community
will have 30 days to submit comments
on the request. Community input must
take the form of written comments and
may include documentation
demonstrating that the hospital
requesting the exception does or does
not qualify as an applicable hospital or
high Medicaid facility as defined at
§ 411.362(c)(2) and (3), respectively. In
the November 30, 2011 final rule (76 FR
74522), we gave examples of community
input, such as documentation
demonstrating that the hospital does not
satisfy one or more of the data criteria
or that the hospital discriminates
against beneficiaries of Federal health
programs; however, we noted that these
were examples only and that we do not
restrict the type of community input
that may be submitted. If we receive
timely comments from the community,
we notify the requesting hospital, and
the hospital has 30 days after such
notice to submit a rebuttal statement
(§ 411.362(c)(5)).
A request for an exception to the
facility expansion prohibition is
considered complete as follows:
• If the request, any written
comments, and any rebuttal statement
include only Healthcare Provider Cost
Reporting Information System (HCRIS)
data, the request is considered complete
as of: (1) the end of the 30-day comment
period if CMS receives no written
comments from the community; or (2)
the end of the 30-day rebuttal period if
CMS receives written comments from
the community, regardless of whether
the hospital submitting the request
submits a rebuttal statement
(§ 411.362(c)(5)(i)).
• If the request, any written
comments, or any rebuttal statement
include data from an external data
source, the request is considered
complete no later than: (1) 180 days
after the end of the 30-day comment
period if CMS receives no written
comments from the community; or (2)
180 days after the end of the 30-day
rebuttal period if CMS receives written
comments from the community,
regardless of whether the hospital
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submitting the request submits a
rebuttal statement (§ 411.362(c)(5)(ii)).
If we grant the request for an
exception to the prohibition on
expansion of facility capacity for a
hospital that qualifies as an applicable
hospital, the expansion may occur only
in facilities on the hospital’s main
campus and may not result in the
number of operating rooms, procedure
rooms, and beds for which the hospital
is licensed exceeding 200 percent of the
hospital’s baseline number of operating
rooms, procedure rooms, and beds
(§ 411.362(c)(6)). If we grant the request
for an exception to the prohibition on
expansion of facility capacity for a
hospital that qualifies as a high
Medicaid facility, these limitations do
not apply. The CMS decision to grant or
deny a hospital’s request for an
exception to the prohibition on
expansion of facility capacity must be
published in the Federal Register in
accordance with our regulations at
§ 411.362(c)(7).
IV. Public Response to Notice With
Comment Period
On February 9, 2022, we published a
notice in the Federal Register entitled
‘‘Announcement of Request for an
Exception to the Prohibition on
Expansion of Facility Capacity under
the Hospital Ownership and Rural
Provider Exceptions to the Physician
Self-Referral Prohibition’’ (87 FR 7471).
In the February 9, 2022 notice, we stated
that, as permitted by section 1877(i)(3)
of the Act and our regulations at
§ 411.362(c), the following physicianowned hospital requested an exception
to the prohibition on expansion of
facility capacity:
Name of Facility: Doctors Hospital at
Renaissance, Ltd.
Location: 5501 South McColl Road,
Edinburg, Texas 78539.
Basis for Exception Request: High
Medicaid Facility.
The request that is the subject of this
notice is the second request for an
exception to the prohibition against
expansion of facility capacity that
Doctors Hospital at Renaissance, Ltd.
(DHR) has submitted to CMS. In the
September 17, 2015 Federal Register
notice (80 FR 55851), we published our
decision granting DHR’s request to add
a total of 551 operating rooms,
procedure rooms, and beds for which it
is licensed, permitting an increase in
DHR’s facility capacity to 200 percent of
its baseline number of operating rooms,
procedure rooms, and beds (the 2014
Request). DHR qualified as an
applicable hospital at the time it
submitted its 2014 Request, which
occurred prior to the regulatory
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18:41 Dec 19, 2022
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revisions that became effective on
January 1, 2021. As stated above, the
January 1, 2021 regulatory revisions
permit a hospital that qualifies as a high
Medicaid facility to: (1) request an
exception to the prohibition on
expansion of facility capacity more
frequently than once every 2 years; and
(2) request to expand its facility capacity
beyond 200 percent of the hospital’s
baseline number of operating rooms,
procedure rooms, and beds. From
September 11, 2015 (the effective date of
our decision to grant the 2014 Request)
until January 1, 2021, DHR was
prohibited from submitting a second
request for an exception to the
prohibition against expansion of facility
capacity under section 1877(i)(3)(B) of
the Act and § 411.362(c)(1) (as then in
effect). DHR submitted the request that
is the subject of this notice (the 2021
Request) on July 21, 2021.
During the 30-day public comment
period, we received 14 public comments
through www.regulations.gov. Twelve
comments supported CMS approving
DHR’s 2021 Request for an exception to
the prohibition against expansion of
facility capacity; two comments
opposed CMS approving the request.
The comments in opposition to CMS
approving the 2021 Request did not
challenge DHR’s qualification as a high
Medicaid facility in Hidalgo County,
Texas. Rather, the commenters asserted
that, even if DHR qualifies as a high
Medicaid facility, CMS has authority to
deny the request and, to be consistent
with the statutory purpose of allowing
limited expansion of grandfathered
physician-owned hospitals, which
focuses on the need for additional
facility capacity and beneficiary
interests in the community in which the
requesting hospital is located, CMS
should deny the request. One of these
commenters asserted that, given DHR’s
publicly-stated plans to expand outside
Hidalgo County, Texas, granting the
2021 Request would result in the
establishment of a new physicianowned hospital in contravention of
section 1877(i) of the Act.
On April 22, 2022, DHR filed a
rebuttal statement in response to the
comments that opposed CMS granting
its 2021 Request for an exception to the
prohibition against expansion of facility
capacity. Among other things, DHR
asserted that, because it qualifies as a
high Medicaid facility, CMS must grant
its 2021 Request for an exception to the
prohibition against expansion of facility
capacity.
V. Decision
DHR submitted the information, data,
and certifications specified at
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§ 411.362(c)(4). This notice announces
our decision with respect to DHR’s 2021
Request for an exception to the
prohibition against expansion of facility
capacity.
A. Qualification as a High Medicaid
Facility
In order to make a request with
respect to which CMS may issue a
decision, a hospital must qualify as an
applicable hospital or a high Medicaid
facility. As of the date of its 2021
Request, DHR was located in Hidalgo
County, Texas. We determined that, on
the date the 2021 Request was
submitted, DHR qualified as a high
Medicaid facility in Hidalgo County,
Texas, for the following reasons:
• DHR is not the sole hospital in
Hidalgo County, Texas;
• With respect to each of the three
most recent 12-month periods for which
data were available as of the date the
hospital submitted its 2021 Request,
DHR had an annual percent of total
inpatient admissions under Medicaid
that was estimated to be greater than
such percent with respect to such
admissions for any other hospital
located in Hidalgo County, Texas; and
• DHR certified that it does not
discriminate against beneficiaries of
Federal health care programs and does
not permit physicians practicing at the
hospital to discriminate against such
beneficiaries.
B. Decision Regarding the 2021 Request
for an Exception to the Prohibition on
Facility Expansion
After reviewing DHR’s 2021 Request,
the public comments, and DHR’s
rebuttal statement, we are granting
DHR’s 2021 Request for an exception to
the prohibition against expansion of
facility capacity. Our decision grants
DHR’s 2021 Request to add a total of 551
operating rooms, procedure rooms, and
beds. Under the regulations in effect as
of the date that the 2021 Request was
submitted, the location of the expansion
is not limited to facilities on the
hospital’s main campus, and may result
in the number of operating rooms,
procedure rooms, and beds for which
DHR is licensed exceeding 200 percent
of its baseline number of operating
rooms, procedure rooms, and beds.
CMS makes no determination as to
whether, following expansion, any
financial relationships between DHR
and its physician owners would satisfy
any other requirement of the whole
hospital or rural hospital exceptions.
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VI. Collection of Information
Requirements
This document does not impose
information collection requirements,
that is, reporting, recordkeeping or
third-party disclosure requirements.
Consequently, there is no need for
review by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.).
The Administrator of the Centers for
Medicare & Medicaid Services (CMS),
Chiquita Brooks-LaSure, having
reviewed and approved this document,
authorizes Lynette Wilson, who is the
Federal Register Liaison, to
electronically sign this document for
purposes of publication in the Federal
Register.
Dated: December 15, 2022.
Lynette Wilson,
Federal Register Liaison, Center for Medicare
& Medicaid Services.
[FR Doc. 2022–27566 Filed 12–16–22; 4:15 pm]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[OMB No. 0970–0545]
Proposed Information Collection
Activity; Next Generation of Enhanced
Employment Strategies Project
Office of Planning, Research,
and Evaluation, Administration for
Children and Families, U.S. Department
of Health and Human Services.
ACTION: Request for public comments.
AGENCY:
The Office of Planning,
Research, and Evaluation (OPRE) within
SUMMARY:
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Baseline survey and identifying and contact information—participants ...
Baseline survey and identifying and contact information—staff ...............
First follow-up survey—participants ..........................................................
Second follow-up survey—participants .....................................................
Service receipt tracking—program staff ....................................................
Staff characteristics survey—staff .............................................................
Program leadership survey—program leaders .........................................
Semi-structured program discussion guide—program leaders ................
Semi-structured program discussion guide—program supervisors and
partners ..................................................................................................
Semi-structured program discussion guide—program staff and providers .....................................................................................................
Semi-structured program discussion guide—employers ..........................
In-depth participant interviews—participants ............................................
Cost workbook—program staff .................................................................
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This extension request does not
change the average burden per response
for any of the data collections. The
annual burden estimates under this
request are for an additional 3 years of
data collection. The number of
respondents has been updated to reflect
the estimated number over the next 3
years.
Average
burden per
response
(in hours)
Total
burden
(in hours)
Annual
burden
(in hours)
3,000
120
3,100
3,360
80
20
5
4
1
25
1
1
150
1
1
1
0.42
0.42
0.83
0.83
0.08
0.42
0.25
1.5
1,260
1,260
2,573
2,789
960
8
1
6
420
420
858
930
320
3
1
2
8
1
1.0
8
3
8
8
20
28
1
1
1
1
1.0
1.0
2.0
32.0
8
8
40
896
3
3
13
299
Comments: The Department
specifically requests comments on (a)
PO 00000
Annual Burden Estimates
Number of
responses per
respondent
(total over
request period)
Number of
respondents
(total over
request period)
Instrument
Estimated Total Annual Burden
Hours: 3,275.
interventions for people with current or
foreseeable disabilities who have
limited work history and are potential
applicants for Supplemental Security
Income.
We seek approval for an extension
without change for the currently
approved data collection activities. For
the impact study, this includes: (1)
Baseline survey and identifying and
contact information data collection, (2)
a first follow-up survey, and (3) a
second follow-up survey. For the
descriptive study, this includes (1)
service receipt tracking, (2) a staff
characteristics survey, (3) a program
leadership survey, (4) semi-structured
program discussions (conducted with
program leaders, supervisors, partners,
staff, and providers), (5) semi-structured
employer discussions, and (6) in-depth
participant interviews. For the cost
study, this includes an Excel-based cost
workbook.
Respondents: Program staff, program
partners, employer staff, and
individuals enrolled in the NextGen
Project. Program staff and partners may
include case managers, health
professionals, workshop instructors, job
developers, supervisors, managers, and
administrators. Employers may include
administrators, human resources staff,
and worksite supervisors.
the Administration for Children and
Families (ACF) is proposing an
extension to the data collection
activities conducted for the Next
Generation of Enhanced Employment
Strategies (NextGen) Project (Office of
Management and Budget (OMB) #0970–
0545). The project is rigorously
evaluating innovative interventions to
promote employment and economic
security among low-income individuals
with complex challenges. The project
includes an experimental impact study,
descriptive study, and cost study. This
extension will allow additional time to
conduct study intake, collect data from
NextGen programs and staff, and to
conduct participant data collections. No
changes are proposed to the data
collection instruments.
DATES: Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act (PRA) of 1995, ACF is
soliciting public comment on the
specific aspects of the information
collection described above.
ADDRESSES: You can obtain copies of the
proposed collection of information and
submit comments by emailing
opreinfocollection@acf.hhs.gov. Identify
all requests by the title of the
information collection.
SUPPLEMENTARY INFORMATION:
Description: OPRE is conducting the
NextGen Project to build the evidence
around effective strategies for helping
low-income individuals find and
sustain employment. This project will
identify and test innovative
employment programs designed to help
people facing complex challenges
secure economic independence. The
project is partnering with the Social
Security Administration to incorporate a
focus on employment-related early
Sfmt 4703
whether the proposed collection of
information is necessary for the proper
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Agencies
[Federal Register Volume 87, Number 243 (Tuesday, December 20, 2022)]
[Notices]
[Pages 77844-77847]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27566]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-1774-FN]
Medicare Program; Approval of Request for an Exception to the
Prohibition on Expansion of Facility Capacity Under the Hospital
Ownership and Rural Provider Exceptions to the Physician Self-Referral
Prohibition
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces our decision to approve the request from
Doctors Hospital at Renaissance, Ltd.'s for an exception to the
prohibition on expansion of facility capacity.
DATES: The decision announced in this notice is applicable on December
16, 2022.
ADDRESSES: [email protected].
I. Background
Section 1877 of the Social Security Act (the Act), also known as
the physician self-referral law: (1) prohibits a physician from making
referrals for certain designated health services payable by Medicare to
an entity with which he or she (or an immediate family member) has a
financial relationship unless the requirements of an applicable
exception are satisfied; and (2) prohibits the entity from filing
claims with Medicare (or billing another individual, entity, or third
party payer) for any improperly referred designated health services. A
financial relationship may be an ownership or investment interest in
the entity or a compensation arrangement with the entity. The statute
establishes a number of specific exceptions and grants the Secretary of
the Department of Health and Human Services (the Secretary) the
authority to create regulatory exceptions for financial relationships
that do not pose a risk of program or patient abuse.
Section 1877(d) of the Act sets forth exceptions related to
ownership or investment interests held by a physician (or an immediate
family member of a physician) in an entity that furnishes designated
health services. Section 1877(d)(2) of the Act provides an exception
for ownership or investment interests in rural providers (the ``rural
provider exception''). In order to qualify for the rural provider
exception, the designated health services must be furnished in a rural
area (as defined in section 1886(d)(2) of the Act) and substantially
all the designated health services furnished by the entity must be
furnished to individuals residing in a rural area. In addition, in the
case where the entity is a hospital, the hospital must meet the
requirements of section 1877(i)(1) of the Act no later than September
23, 2011. Section 1877(d)(3) of the Act provides an exception for
ownership or investment interests in a hospital located outside of
Puerto Rico (the ``whole hospital exception''). In order to qualify for
the whole hospital exception, the referring physician must be
authorized to perform services at the hospital, the ownership or
investment interest must be in the hospital itself (and not merely in a
subdivision of the hospital), and the hospital must meet the
requirements of section 1877(i)(1) of the Act no later than September
23, 2011.
II. Prohibition on Facility Expansion
Section 6001(a)(3) of the Patient Protection and Affordable Care
Act (Affordable Care Act) (Pub. L. 111-148) amended the rural provider
and whole hospital exceptions to provide that a hospital may not
increase the number of operating rooms, procedure rooms, and beds
beyond that for which the hospital was licensed on March 23, 2010 (or,
in the case of a hospital that did not have a provider agreement in
effect as of this date, but did have a provider agreement in effect on
December 31, 2010, the effective date of such provider agreement) (the
hospital's ``baseline number of operating rooms, procedure rooms, and
beds''). Thus, since March 23, 2010, a physician-owned hospital that
seeks to avail itself of either exception is prohibited from expanding
the number of operating rooms, procedure rooms, and beds (``facility
capacity'') unless it has been granted an exception to the prohibition
by the Secretary.
Section 6001(a)(3) of the Affordable Care Act added new section
1877(i)(3)(A)(i) of the Act, which required the Secretary to establish
and implement a process for granting exceptions to the prohibition on
expansion of facility capacity for hospitals that qualify as an
``applicable hospital.'' Section 1106 of the Health Care and Education
Reconciliation Act of 2010 (Pub. L. 111-152) amended section
1877(i)(3)(A)(i) of the Act to require the Secretary to establish and
implement a process for granting exceptions to the prohibition on
expansion of facility capacity for hospitals that qualify as either an
``applicable hospital'' or a ``high
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Medicaid facility.'' These terms are defined at sections 1877(i)(3)(E)
and 1877(i)(3)(F) of the Act. The process for requesting an exception
to the prohibition on expansion of facility capacity is discussed in
section III of this notice.
The requirements for qualifying as an applicable hospital are set
forth at Sec. 411.362(c)(2), and the requirements for qualifying as a
high Medicaid facility are set forth at Sec. 411.362(c)(3). An
``applicable hospital'' means a hospital: (1) that is located in a
county in which the percentage increase in the population during the
most recent 5-year period (as of the date that the hospital submits its
request for an exception to the prohibition on expansion of facility
capacity) is at least 150 percent of the percentage increase in the
population growth of the State in which the hospital is located during
that period, as estimated by the Bureau of the Census; (2) whose annual
percent of total inpatient admissions under Medicaid is equal to or
greater than the average percent with respect to such admissions for
all hospitals in the county in which the hospital is located during the
most recent 12-month period for which data are available (as of the
date that the hospital submits its request for an exception to the
prohibition on expansion of facility capacity); (3) that does not
discriminate against beneficiaries of Federal health care programs and
does not permit physicians practicing at the hospital to discriminate
against such beneficiaries; (4) that is located in a State in which the
average bed capacity in the State is less than the national average bed
capacity; and (5) that has an average bed occupancy rate that is
greater than the average bed occupancy rate in the State in which the
hospital is located. A ``high Medicaid facility'' means a hospital
that: (1) is not the sole hospital in a county; (2) with respect to
each of the three most recent 12-month periods for which data are
available, has an annual percent of total inpatient admissions under
Medicaid that is estimated to be greater than such percent with respect
to such admissions for any other hospital located in the county in
which the hospital is located; and (3) does not discriminate against
beneficiaries of Federal health care programs and does not permit
physicians practicing at the hospital to discriminate against such
beneficiaries. The regulation at Sec. 411.362(c)(2)(ii) specifies the
acceptable data sources for determining whether a hospital qualifies as
an applicable hospital, and the regulation at Sec. 411.362(c)(3)(ii)
specifies the acceptable data sources for determining whether a
hospital qualifies as a high Medicaid facility.
III. Exception Approval Process
In the Calendar Year (CY) 2012 Outpatient Prospective Payment
System/Ambulatory Surgical Centers (OPPS/ASC) final rule (76 FR 74121),
we published regulations establishing the process for a hospital to
request an exception from the prohibition on facility expansion (the
``exception process'') at Sec. 411.362(c)(4), the process for
obtaining community input related to a hospital's request at Sec.
411.362(c)(5), and related definitions at Sec. 411.362(a).
In the CY 2015 OPPS/ASC final rule (79 FR 66770), we expanded the
permissible data sources on which a hospital may rely to show that it
is qualified to request an exception to the prohibition on expansion of
facility capacity (that is, that the hospital qualifies as either an
applicable hospital or a high Medicaid facility). We also amended the
exception process established in the CY 2012 OPPS/ASC final rule to
increase the period of time after which an exception request will be
deemed complete when an external data source is used by a requesting
hospital or in the public comments to determine whether a hospital
qualifies as either an applicable hospital or high Medicaid facility.
In the CY 2015 OPPS/ASC final rule, we stated that it is possible (if
not likely) that, when reviewing an expansion exception request, the
Centers for Medicare & Medicaid Services (CMS) would need to verify the
data (and other information, if any) provided by the requesting
hospital and any commenters, as well as consider the data in light of
the information otherwise available to CMS (79 FR 66995).
In the CY 2021 OPPS/ASC final rule (85 FR 85866), we revised the
regulations that set forth the exception process with respect to high
Medicaid facilities to remove certain regulatory restrictions that are
not included in the Act. As of January 1, 2021, a high Medicaid
facility may request an exception to the prohibition on expansion of
facility capacity more frequently than once every 2 years; may request
to expand its facility capacity beyond 200 percent of the hospital's
baseline number of operating rooms, procedure rooms, and beds; and, if
its request is granted, is not restricted to locating approved
expansion capacity on the hospital's main campus. An applicable
hospital remains subject to the statutory limitation on the frequency
of requests for an exception to the prohibition on expansion of
facility capacity (no more than once every 2 years); may not request to
expand its facility capacity beyond 200 percent of the hospital's
baseline number of operating rooms, procedure rooms, and beds; and, if
its request is granted, is restricted to locating approved expansion
capacity on the hospital's main campus.
Our regulations at Sec. 411.362(c)(5) require us to solicit
community input on the request for an exception by publishing a notice
of the request in the Federal Register. Individuals and entities in the
hospital's community will have 30 days to submit comments on the
request. Community input must take the form of written comments and may
include documentation demonstrating that the hospital requesting the
exception does or does not qualify as an applicable hospital or high
Medicaid facility as defined at Sec. 411.362(c)(2) and (3),
respectively. In the November 30, 2011 final rule (76 FR 74522), we
gave examples of community input, such as documentation demonstrating
that the hospital does not satisfy one or more of the data criteria or
that the hospital discriminates against beneficiaries of Federal health
programs; however, we noted that these were examples only and that we
do not restrict the type of community input that may be submitted. If
we receive timely comments from the community, we notify the requesting
hospital, and the hospital has 30 days after such notice to submit a
rebuttal statement (Sec. 411.362(c)(5)).
A request for an exception to the facility expansion prohibition is
considered complete as follows:
If the request, any written comments, and any rebuttal
statement include only Healthcare Provider Cost Reporting Information
System (HCRIS) data, the request is considered complete as of: (1) the
end of the 30-day comment period if CMS receives no written comments
from the community; or (2) the end of the 30-day rebuttal period if CMS
receives written comments from the community, regardless of whether the
hospital submitting the request submits a rebuttal statement (Sec.
411.362(c)(5)(i)).
If the request, any written comments, or any rebuttal
statement include data from an external data source, the request is
considered complete no later than: (1) 180 days after the end of the
30-day comment period if CMS receives no written comments from the
community; or (2) 180 days after the end of the 30-day rebuttal period
if CMS receives written comments from the community, regardless of
whether the hospital
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submitting the request submits a rebuttal statement (Sec.
411.362(c)(5)(ii)).
If we grant the request for an exception to the prohibition on
expansion of facility capacity for a hospital that qualifies as an
applicable hospital, the expansion may occur only in facilities on the
hospital's main campus and may not result in the number of operating
rooms, procedure rooms, and beds for which the hospital is licensed
exceeding 200 percent of the hospital's baseline number of operating
rooms, procedure rooms, and beds (Sec. 411.362(c)(6)). If we grant the
request for an exception to the prohibition on expansion of facility
capacity for a hospital that qualifies as a high Medicaid facility,
these limitations do not apply. The CMS decision to grant or deny a
hospital's request for an exception to the prohibition on expansion of
facility capacity must be published in the Federal Register in
accordance with our regulations at Sec. 411.362(c)(7).
IV. Public Response to Notice With Comment Period
On February 9, 2022, we published a notice in the Federal Register
entitled ``Announcement of Request for an Exception to the Prohibition
on Expansion of Facility Capacity under the Hospital Ownership and
Rural Provider Exceptions to the Physician Self-Referral Prohibition''
(87 FR 7471). In the February 9, 2022 notice, we stated that, as
permitted by section 1877(i)(3) of the Act and our regulations at Sec.
411.362(c), the following physician-owned hospital requested an
exception to the prohibition on expansion of facility capacity:
Name of Facility: Doctors Hospital at Renaissance, Ltd.
Location: 5501 South McColl Road, Edinburg, Texas 78539.
Basis for Exception Request: High Medicaid Facility.
The request that is the subject of this notice is the second
request for an exception to the prohibition against expansion of
facility capacity that Doctors Hospital at Renaissance, Ltd. (DHR) has
submitted to CMS. In the September 17, 2015 Federal Register notice (80
FR 55851), we published our decision granting DHR's request to add a
total of 551 operating rooms, procedure rooms, and beds for which it is
licensed, permitting an increase in DHR's facility capacity to 200
percent of its baseline number of operating rooms, procedure rooms, and
beds (the 2014 Request). DHR qualified as an applicable hospital at the
time it submitted its 2014 Request, which occurred prior to the
regulatory revisions that became effective on January 1, 2021. As
stated above, the January 1, 2021 regulatory revisions permit a
hospital that qualifies as a high Medicaid facility to: (1) request an
exception to the prohibition on expansion of facility capacity more
frequently than once every 2 years; and (2) request to expand its
facility capacity beyond 200 percent of the hospital's baseline number
of operating rooms, procedure rooms, and beds. From September 11, 2015
(the effective date of our decision to grant the 2014 Request) until
January 1, 2021, DHR was prohibited from submitting a second request
for an exception to the prohibition against expansion of facility
capacity under section 1877(i)(3)(B) of the Act and Sec. 411.362(c)(1)
(as then in effect). DHR submitted the request that is the subject of
this notice (the 2021 Request) on July 21, 2021.
During the 30-day public comment period, we received 14 public
comments through www.regulations.gov. Twelve comments supported CMS
approving DHR's 2021 Request for an exception to the prohibition
against expansion of facility capacity; two comments opposed CMS
approving the request. The comments in opposition to CMS approving the
2021 Request did not challenge DHR's qualification as a high Medicaid
facility in Hidalgo County, Texas. Rather, the commenters asserted
that, even if DHR qualifies as a high Medicaid facility, CMS has
authority to deny the request and, to be consistent with the statutory
purpose of allowing limited expansion of grandfathered physician-owned
hospitals, which focuses on the need for additional facility capacity
and beneficiary interests in the community in which the requesting
hospital is located, CMS should deny the request. One of these
commenters asserted that, given DHR's publicly-stated plans to expand
outside Hidalgo County, Texas, granting the 2021 Request would result
in the establishment of a new physician-owned hospital in contravention
of section 1877(i) of the Act.
On April 22, 2022, DHR filed a rebuttal statement in response to
the comments that opposed CMS granting its 2021 Request for an
exception to the prohibition against expansion of facility capacity.
Among other things, DHR asserted that, because it qualifies as a high
Medicaid facility, CMS must grant its 2021 Request for an exception to
the prohibition against expansion of facility capacity.
V. Decision
DHR submitted the information, data, and certifications specified
at Sec. 411.362(c)(4). This notice announces our decision with respect
to DHR's 2021 Request for an exception to the prohibition against
expansion of facility capacity.
A. Qualification as a High Medicaid Facility
In order to make a request with respect to which CMS may issue a
decision, a hospital must qualify as an applicable hospital or a high
Medicaid facility. As of the date of its 2021 Request, DHR was located
in Hidalgo County, Texas. We determined that, on the date the 2021
Request was submitted, DHR qualified as a high Medicaid facility in
Hidalgo County, Texas, for the following reasons:
DHR is not the sole hospital in Hidalgo County, Texas;
With respect to each of the three most recent 12-month
periods for which data were available as of the date the hospital
submitted its 2021 Request, DHR had an annual percent of total
inpatient admissions under Medicaid that was estimated to be greater
than such percent with respect to such admissions for any other
hospital located in Hidalgo County, Texas; and
DHR certified that it does not discriminate against
beneficiaries of Federal health care programs and does not permit
physicians practicing at the hospital to discriminate against such
beneficiaries.
B. Decision Regarding the 2021 Request for an Exception to the
Prohibition on Facility Expansion
After reviewing DHR's 2021 Request, the public comments, and DHR's
rebuttal statement, we are granting DHR's 2021 Request for an exception
to the prohibition against expansion of facility capacity. Our decision
grants DHR's 2021 Request to add a total of 551 operating rooms,
procedure rooms, and beds. Under the regulations in effect as of the
date that the 2021 Request was submitted, the location of the expansion
is not limited to facilities on the hospital's main campus, and may
result in the number of operating rooms, procedure rooms, and beds for
which DHR is licensed exceeding 200 percent of its baseline number of
operating rooms, procedure rooms, and beds.
CMS makes no determination as to whether, following expansion, any
financial relationships between DHR and its physician owners would
satisfy any other requirement of the whole hospital or rural hospital
exceptions.
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VI. Collection of Information Requirements
This document does not impose information collection requirements,
that is, reporting, recordkeeping or third-party disclosure
requirements. Consequently, there is no need for review by the Office
of Management and Budget under the authority of the Paperwork Reduction
Act of 1995 (44 U.S.C. 3501 et seq.).
The Administrator of the Centers for Medicare & Medicaid Services
(CMS), Chiquita Brooks-LaSure, having reviewed and approved this
document, authorizes Lynette Wilson, who is the Federal Register
Liaison, to electronically sign this document for purposes of
publication in the Federal Register.
Dated: December 15, 2022.
Lynette Wilson,
Federal Register Liaison, Center for Medicare & Medicaid Services.
[FR Doc. 2022-27566 Filed 12-16-22; 4:15 pm]
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