Patient Protection and Affordable Care Act; Exchange Program Integrity, 56015-56031 [2018-24504]
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Federal Register / Vol. 83, No. 218 / Friday, November 9, 2018 / Proposed Rules
Technology Transfer and Advancement
Act of 1995 (15 U.S.C. 272 note) because
application of those requirements would
be inconsistent with the CAA; and
• Does not provide EPA with the
discretionary authority to address, as
appropriate, disproportionate human
health or environmental effects, using
practicable and legally permissible
methods, under Executive Order 12898
(59 FR 7629, February 16, 1994).
The SIP is not approved to apply on
any Indian reservation land or in any
other area where EPA or an Indian tribe
has demonstrated that a tribe has
jurisdiction. In those areas of Indian
country, the rule does not have tribal
implications as specified by Executive
Order 13175 (65 FR 67249, November 9,
2000), nor will it impose substantial
direct costs on tribal governments or
preempt tribal law.
List of Subjects in 40 CFR Part 52
Environmental protection, Air
pollution control, Incorporation by
Reference, Intergovernmental relations,
Reporting and recordkeeping
requirements, Sulfur oxides.
Authority: 42 U.S.C. 7401 et seq.
Dated: November 1, 2018.
Onis ‘‘Trey’’ Glenn, III,
Regional Administrator, Region 4.
[FR Doc. 2018–24582 Filed 11–8–18; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 60
[EPA–HQ–OAR–2018–0696; FRL–9986–28–
OAR]
RIN 2060–AU33
Adopting Subpart Ba Requirements in
Emission Guidelines for Municipal
Solid Waste Landfills; Correction
Environmental Protection
Agency (EPA).
ACTION: Proposed rule; correction.
AGENCY:
This document corrects the
preamble to a proposed rule published
in the Federal Register on October 30,
2018, regarding the implementing
regulations that govern the Emission
Guidelines for Municipal Solid Waste
(MSW) Landfills. The listed docket
number in that preamble was incorrect.
Any comments received prior to this
correction have been redirected to the
correct docket.
DATES: Comments. Comments must be
received on or before December 14,
2018.
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SUMMARY:
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For
questions about this proposed action,
contact Andrew Sheppard, Sector
Policies and Programs Division (E143–
03), Office of Air Quality Planning and
Standards, U.S. Environmental
Protection Agency, Research Triangle
Park, North Carolina 27711; telephone
number: (919) 541–4161; fax number:
(919) 541–0516; and email address:
sheppard.andrew@epa.gov.
SUPPLEMENTARY INFORMATION: In
proposed rule FR 2018–23700, in the
issue of Tuesday, October 30, 2018, on
page 54527, in the third column, correct
the docket numbers listed in the
ADDRESSES section to read:
‘‘ADDRESSES: Comments. Submit your
comments, identified by Docket ID No.
EPA–HQ–OAR–2018–0696 at https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Once submitted, comments cannot be
edited or removed from Regulations.gov.
See SUPPLEMENTARY INFORMATION for
detail about how the EPA treats
submitted comments. Regulations.gov is
our preferred method of receiving
comments. However, the following
other submission methods are also
accepted:
• Email: a-and-r-docket@epa.gov.
Include Docket ID No. EPA–HQ–OAR–
2018–0696 in the subject line of the
message.
• Fax: (202) 566–9744. Attention
Docket ID No. EPA–HQ–OAR–2018–
0696.
• Mail: To ship or send mail via the
United States Postal Service, use the
following address: U.S. Environmental
Protection Agency, EPA Docket Center,
Docket ID No. EPA–HQ–OAR–2018–
0696, Mail Code 28221T, 1200
Pennsylvania Avenue NW, Washington,
DC 20460.
• Hand/Courier Delivery: Use the
following Docket Center address if you
are using express mail, commercial
delivery, hand delivery, or courier: EPA
Docket Center, EPA WJC West Building,
Room 3334, 1301 Constitution Avenue
NW, Washington, DC 20004. Delivery
verification signatures will be available
only during regular business hours.’’
In proposed rule FR 2018–23700, in
the issue of Tuesday, October 30, 2018,
on page 54528, make the following
correction to the docket numbers listed
in the SUPPLEMENTARY INFORMATION
section. In the second paragraph of the
section, in the first column, revise the
docket number in the first sentence to
say, ‘‘Docket. The EPA has established
a docket for this rulemaking under
Docket ID No. EPA–HQ–OAR–2018–
0696.’’
In the third paragraph of the section,
in the first column, revise the docket
FOR FURTHER INFORMATION CONTACT:
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number in the first sentence to say,
‘‘Instructions. Direct your comments to
Docket ID No. EPA–HQ–OAR–2018–
0696.’’
In the sixth paragraph of the section,
in the third column, revise the docket
number in the last sentence to say,
‘‘Send or deliver information identified
as CBI only to the following address:
OAQPS Document Control Officer
(C404–02), OAQPS, U.S. Environmental
Protection Agency, Research Triangle
Park, North Carolina 27711, Attention
Docket ID No. EPA–HQ–OAR–2018–
0696.’’
Dated: November 2, 2018.
William L. Wehrum,
Assistant Administrator, Office of Air and
Radiation.
[FR Doc. 2018–24581 Filed 11–8–18; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
45 CFR Parts 155 and 156
[CMS–9922–P]
RIN 0938–AT53
Patient Protection and Affordable Care
Act; Exchange Program Integrity
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
AGENCY:
This proposed rule would
revise standards relating to oversight of
Exchanges established by states,
periodic data matching frequency and
authority, and the length of a
consumer’s authorization for the
Exchange to obtain updated tax
information. This proposed rule would
also propose new requirements for
certain issuers related to the collection
of a separate payment for the premium
portion attributable to coverage for
certain abortion services. Many of these
proposed changes would help
strengthen Exchange program integrity.
DATES: Comments: To be assured
consideration, comments must be
received at one of the addresses
provided below, no later than 5 p.m. on
January 8, 2019.
ADDRESSES: In commenting, please refer
to file code CMS–9922–P. Because of
staff and resource limitations, we cannot
accept comments by facsimile (FAX)
transmission.
Comments, including mass comment
submissions, must be submitted in one
of the following three ways (please
choose only one of the ways listed):
1. Electronically. You may submit
electronic comments on this regulation
SUMMARY:
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Federal Register / Vol. 83, No. 218 / Friday, November 9, 2018 / Proposed Rules
to https://www.regulations.gov. Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–9922–P, P.O. Box 8016, Baltimore,
MD 21244–8010.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–9922–P, Mail
Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT:
Emily Ames, (301) 492–4246, or
Christine Hammer, (202) 260–6089, for
general information.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following
website as soon as possible after they
have been received: https://
www.regulations.gov. Follow the search
instructions on that website to view
public comments.
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I. Executive Summary
American Health Benefit Exchanges,
or ‘‘Exchanges’’ (also called
‘‘Marketplaces’’) are entities established
under the Patient Protection and
Affordable Care Act (Pub. L. 111–148),
as amended by the Heath Care and
Education Reconciliation Act of 2010
(Pub. L. 111–152) (collectively referred
to as PPACA) through which qualified
individuals and qualified employers can
purchase health insurance coverage.
Exchanges that were established by
states (State Exchanges) include Statebased Exchanges (SBEs) which perform
eligibility and enrollment functions, as
well as State-based Exchanges on the
Federal platform (SBE–FPs) that utilize
the Federally-facilitated Exchange’s
infrastructure to perform eligibility and
enrollment functions. Many individuals
who enroll in qualified health plans
(QHPs) through individual market
Exchanges are eligible to receive a
premium tax credit (PTC) to reduce
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their costs for health insurance
premiums, and receive reductions in
required cost-sharing payments to
reduce out-of-pocket expenses for health
care services. Eligible individuals can
receive the estimated amount of the PTC
on an advance basis, known as advance
payments of the premium tax credit
(APTC), in accordance with section
1412 of the PPACA.
Strengthening program integrity with
respect to subsidy payments in the
individual market is a top priority of
this Administration. Key areas of focus
include—(1) ensuring that eligible
enrollees receive the correct amount of
APTC and cost-sharing reduction (CSR)
(as applicable), and do not receive
APTC or CSRs for abortion coverage
and/or services for which such
payments are not available under
section 1303 of the PPACA; (2)
conducting effective and efficient
monitoring and oversight of State
Exchanges to ensure that consumers are
receiving the correct amount of APTC
and CSRs in SBEs, and that State
Exchanges are meeting the standards of
federal law in a transparent manner; and
(3) protecting the interests of taxpayers,
and consumers, and the financial
integrity of Federally-facilitated
Exchanges (FFEs) through oversight of
health insurance issuers, including
ensuring compliance with Exchange
requirements, such as maintenance of
records and participation in
investigations and compliance reviews,
and with the requirements of section
1303 of the PPACA.
The Department of Health and Human
Services (HHS) has recently made
significant strides in these areas. For
example, we have implemented policybased payments in the FFEs and almost
all of the SBEs, a critical system change
across Exchanges and issuers that
ensures the data used to generate APTC
and CSR payments to issuers are
verified and associated with particular
enrollees.
We also recently implemented preenrollment verification of eligibility for
applicable individual market special
enrollment periods for all Exchanges
served by the federal eligibility and
enrollment platform (the HealthCare.gov
platform), ensuring that only those who
qualify for special enrollment periods
receive them. In the HHS Notice of
Benefit and Payment Parameters for
2019 Final Rule (83 FR 16930) (April 17,
2018), we established a policy to require
documentary evidence for certain
consumers who attest to income that is
significantly higher than the amount
found in the Exchange’s income data.
This new check will be conducted for
applicants for whom trusted data
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sources (such as the Internal Revenue
Service, the Social Security
Administration, the Department of
Homeland Security, Veterans Health
Administration, Peace Corps, the
Department of Defense, Experian, and
Carahsoft).1 This new check will not be
performed with respect to non-citizen
applicants who are ineligible for
Medicaid based on their immigration
status, as these applicants may be
statutorily eligible for APTC with
annual household income below 100
percent of the FPL. An accurate
eligibility determination is critical for
consumers near this threshold to ensure
APTC is not paid on behalf of
consumers who are statutorily ineligible
for APTC.
In late 2017, we developed an
innovative approach to provide
additional notification to tax filers who,
based on Internal Revenue Service (IRS)
data, had received APTC for a prior
benefit year but failed to reconcile these
payments on their tax returns. The
notices explained that the tax filer was
required to take action to reconcile these
prior APTC payments, or APTC
associated with all enrollees for whom
the individual is the tax filer would be
terminated. While HHS was already
contacting these affected households
through its standard annual notification
processes, this supplemental notice
provided further clarification and
instruction for the tax filer, while
adhering to IRS’ protocols regarding the
safe disclosure of protected federal tax
information.
We continue to explore opportunities
to improve program integrity. We work
on an ongoing basis on improving
program oversight and procedures to
conduct comprehensive audits of FFE
processes to verify their integrity. These
efforts further our goal of protecting
consumers enrolled in FFEs and
safeguarding taxpayer dollars. We
review consumer complaints and
allegations of fraud and abuse received
by the FFE call center from insurers, as
well as law enforcement and states.
Additionally, we analyze data to
identify issues and vulnerabilities, share
relevant information with issuers, and
identify administrative actions to stop
bad actors and protect consumers.
We are proposing several changes
targeting these priorities. First, we are
planning changes to the current periodic
data matching (PDM) processes, which
are the processes through which
Exchanges periodically examine
1 One criterion for eligibility for APTC is an
income equal to or greater than 100 percent but not
greater than 400 percent of an amount equal to the
poverty line based on family size.
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available data sources to identify
changes that would affect enrollees’
eligibility for subsidies. Second, we are
planning to add an optional
authorization to the Exchange
application that would allow an
individual to authorize the FFE to
receive Medicare eligibility and
enrollment information about the
enrollee. If an applicant provides this
authorization and elects to have the
Exchange automatically terminate QHP
coverage if the applicant is found to be
dually enrolled, then the FFE will end
enrollees’ QHP coverage on their behalf
in such a circumstance, even if the
enrollee is not receiving APTC or CSRs.
Third, we propose to specify that
Exchanges must conduct PDM for
Medicare, Medicaid, the Children’s
Health Insurance Program (CHIP), and
the Basic Health Program (BHP), if
applicable, at least twice a year,
beginning with the 2020 calendar year,
to ensure that Exchanges make adequate
efforts to discontinue APTC and CSR for
those who are eligible for or enrolled in
other minimum essential coverage
(MEC) and, therefore, are ineligible for
APTC or CSRs.
We are also proposing changes to
improve program integrity related to
State Exchanges. To strengthen the
mechanisms and tools HHS uses in its
oversight of compliance by State
Exchanges with federal requirements,
including eligibility and enrollment
requirements under 45 CFR part 155,
subparts D and E, we are proposing
changes that provide further specificity
to their program reporting requirements.
In addition, to ensure proper eligibility
determinations and enrollments in
SBEs, we are proposing to clarify the
scope of the annual programmatic
audits that SBEs are required to conduct
and submit results of annually to HHS,
and include testing of SBE eligibility
and enrollment transactions in the
annual programmatic audits.
Lastly, we are proposing changes
related to the separate payment
requirement in section 1303 of the
PPACA. To align the regulatory
requirements for issuer billing of the
portion of the enrollee’s premium
attributable to certain abortion services
with the separate payment requirement
applicable to issuers offering coverage of
these services, we are proposing
changes to the billing and payment
collection requirements for QHP issuers
in connection with their plans offered
through an individual market Exchange
that include coverage for abortion
services for which federal funding is
prohibited.
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II. Background
A. Legislative and Regulatory Overview
Sections 1311(b) and 1321(b) of the
PPACA provide that each state has the
opportunity to establish an Exchange.
Section 1311(b)(1) of the PPACA gives
each state the opportunity to establish
an Exchange that both facilitates the
purchase of QHPs by individuals and
families, and provides for the
establishment of a Small Business
Health Options Program (SHOP) that is
designed to assist qualified employers
in the state who are small employers in
facilitating the enrollment of their
employees in QHPs offered in the small
group market in the state.
Section 1313 of the PPACA describes
the steps the Secretary of Health and
Human Services (the Secretary) may
take to oversee Exchanges’ compliance
with HHS standards related to Title I of
the PPACA and ensure their financial
integrity, including conducting
investigations and annual audits.
Section 1321(a) of the PPACA
provides broad authority for the
Secretary to establish standards and
regulations to implement the statutory
standards related to Exchanges, QHPs,
and other standards of title I of the
PPACA.
Section 1321(c)(2) of the PPACA
authorizes the Secretary to enforce the
Exchange standards using civil money
penalties (CMPs) on the same basis as
detailed in section 2723(b) of the Public
Health Service Act (PHS Act). Section
2723(b) of the PHS Act authorizes the
Secretary to impose CMPs as a means of
enforcing the individual and group
market reforms contained in Part A of
title XXVII of the PHS Act when a state
fails to substantially enforce these
provisions.
Section 1411(c) of the PPACA
requires the Secretary to submit certain
information provided by applicants
under section 1411(b) of the PPACA to
other federal officials for verification,
including income and family size
information to the Secretary of the
Treasury.
Section 1411(d) of the PPACA
provides that the Secretary must verify
the accuracy of information provided by
applicants under section 1411(b) of the
PPACA for which section 1411(c) does
not prescribe a specific verification
procedure, in such manner as the
Secretary determines appropriate.
Section 1411(f)(1)(B) of the PPACA
requires the Secretary to establish
procedures to redetermine eligibility on
a periodic basis, in appropriate
circumstances, including for eligibility
to purchase a QHP through the
Exchange and for APTC and CSRs.
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Section 1411(g) of the PPACA allows
the exchange of applicant information
only for the limited purposes of, and to
the extent necessary to, ensure the
efficient operation of the Exchange,
including by verifying eligibility to
enroll through the Exchange and for
APTC and CSRs.
On October 30, 2013, we published a
final rule entitled, ‘‘Patient Protection
and Affordable Care Act; Program
Integrity: Exchange, Premium
Stabilization Programs, and Market
Standards; Amendments to the HHS
Notice of Benefit and Payment
Parameters for 2014,’’ (78 FR 65046), to
implement certain program integrity
standards and oversight requirements
for State Exchanges.
Section 1303 of the PPACA, as
implemented in 45 CFR 156.280,
specifies standards for issuers of QHPs
through the Exchanges that cover
abortion services for which public
funding is prohibited (also referred to as
non-Hyde abortion services). The statute
and regulations establish that, unless
otherwise prohibited by state law, a
QHP issuer may elect to cover such nonHyde abortion services. If an issuer
elects to cover such services under a
QHP sold through an individual market
Exchange, the issuer must take certain
steps to ensure that no PTC or CSR
funds are used to pay for abortion
services for which public funding is
prohibited. One such step is that
individual market Exchange issuers
must determine the amount of, and
collect, from each enrollee, a ‘‘separate
payment’’ for an amount equal to the
actuarial value of the coverage for
abortions for which public funding is
prohibited,2 which must be no less than
$1 per enrollee per month. QHP issuers
must also segregate funds for non-Hyde
abortion services collected through this
payment into a separate allocation
account used exclusively to pay for nonHyde abortion services.
In the 2012 Exchange Establishment
Rule, we codified the statutory
provisions of section 1303 of the PPACA
in regulation at 45 CFR 156.280. On
February 27, 2015, we published the
Patient Protection and Affordable Care
Act; HHS Notice of Benefit and Payment
Parameters for 2016, (80 FR 10750)
(herein after referred to as the 2016
Payment Notice) providing guidance
regarding acceptable billing and
premium collection methods for the
portion of the consumer’s total premium
attributable to non-Hyde abortion
coverage for purposes of satisfying the
statutory separate payment requirement.
2 Section 1303 also specifies how such actuarial
value is to be calculated.
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B. Stakeholder Consultation and Input
HHS has consulted with stakeholders
on policies related to the operation of
Exchanges. We have held a number of
listening sessions with consumers,
providers, employers, health plans, the
actuarial community, and state
representatives to gather public input,
with a particular focus on risks to the
individual and small group markets,
and how we can alleviate burdens
facing patients and issuers. We
consulted with stakeholders through
regular meetings with the National
Association of Insurance
Commissioners, regular contact with
State Exchanges through the Exchange
Blueprint process and ongoing oversight
and technical assistance engagements,
and meetings with Tribal leaders and
representatives, health insurance
issuers, trade groups, consumer
advocates, employers, and other
interested parties.
III. Provisions of the Proposed
Regulations
A. Exchange Establishment Standards
and Other Related Standards Under the
Affordable Care Act
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1. Functions of an Exchange (§ 155.200)
Section 155.200 of the PPACA
establishes the functions that an
Exchange must perform. Section
155.200(c) of the PPACA specifies that
the Exchange must perform oversight
and financial integrity functions,
specifically that the Exchange must
perform required functions related to
oversight and financial integrity
requirements in accordance with section
1313 of the PPACA. HHS interprets this
requirement broadly to include program
integrity functions related to protecting
against fraud, waste, and abuse,
including functions not explicitly
identified in section 1313 of the PPACA.
We believe SBEs have generally
interpreted this requirement broadly as
well, as evidenced by their engagement
in activities designed to combat fraud
and abuse related to the Exchange.
However, questions about the breadth
of this function have arisen when
Exchanges have sought to understand
what uses and disclosures of personally
identifiable information (PII) are
permitted under § 155.260.3
3 Section 155.260 limits an Exchange’s use and
disclosure of PII when an Exchange creates or
collects personally identifiable information for the
purposes of determining eligibility for enrollment
in a qualified health plan; determining eligibility
for other insurance affordability programs, as
defined in § 155.300; or determining eligibility for
exemptions from the individual shared
responsibility provisions in section 5000A of the
Code. One of the permitted uses and disclosures is
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Specifically, we have received questions
about whether Exchanges are permitted
under § 155.260 to disclose applicant PII
to certain entities, such as the state
departments of insurance, when
investigating fraudulent behavior
related to Exchange enrollments on the
part of agents and brokers. We believe
that use and disclosure related to
Exchange program integrity efforts, like
combatting fraud, currently fall under
§ 155.200(c), but believe the regulation
is not as clear as it could be. Therefore,
we propose to revise § 155.200(c) to
clarify that the Exchanges must perform
oversight functions generally, and
cooperate with oversight activities, in
accordance with section 1313 of the
PPACA and as required under 45 CFR
part 155, including overseeing its
Exchange programs, Navigators, agents,
brokers, and other non-Exchange
entities as defined in § 155.260(b).
Because this change is a clarification
and not a new function, we do not
believe it would impose additional
burdens on State Exchanges, but instead
would help resolve questions about
whether states have the necessary tools
and authority to enable them to
effectively oversee and combat
potentially fraudulent behavior. We
seek comment on this proposal,
including with respect to our
understanding of the potential
imposition of additional burden on
State Exchanges.
2. Verification Process Related to
Eligibility for Insurance Affordability
Programs (§ 155.320)
Currently, under § 155.330, Exchanges
are required to periodically examine
available data sources to identify, with
respect to enrollees on whose behalf
APTC or CSRs are being paid, eligibility
or enrollment determinations for
Medicare, Medicaid, CHIP, or the BHP,
if a BHP is operating in the service area
of the Exchange. Individuals identified
as enrolled both in Exchange coverage
with or without APTC or CSRs and one
of these other forms of coverage are
referred to as dually enrolled
consumers.
If a consumer is eligible for premiumfree Medicare Part A or enrolled in
Medicare Part A or Part C (also known
as Medicare Advantage), all of which
qualify as MEC, he or she is not eligible
to receive APTC or CSRs to help pay for
an Exchange plan or covered services.
The Secretary has broad authority
under section 1321(a) of the PPACA to
establish regulations setting standards to
implement the statutory requirements
for the Exchange to carry out the functions
described in § 155.200.
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under title I of the PPACA, including
with respect to the establishment and
operation of Exchanges, the offering of
QHPs through the Exchanges, the
establishment of statutory reinsurance
and risk adjustment programs, and such
other requirements as the Secretary
determines appropriate. Additionally,
section 1411(g) of the PPACA allows the
exchange of certain applicant
information as necessary to ensure the
efficient operation of the Exchange,
including verifying eligibility to enroll
in coverage through the Exchange and to
receive APTC or CSRs.
Section 155.320(b)(2) specifies that
the disclosure to HHS of information
regarding eligibility for and enrollment
in a health plan that is a government
program, which may be considered
protected health information (PHI), is
expressly authorized for the purposes of
verification of applicant eligibility for
MEC as part of the eligibility
determination process for APTC or
CSRs. Section 155.430(b)(1)(ii) requires
an Exchange to provide an opportunity
at the time of plan selection for an
enrollee to choose to remain enrolled in
a QHP if he or she becomes eligible for
other MEC, or to terminate QHP
coverage if the enrollee does not choose
to remain enrolled in the QHP upon
completion of the redetermination
process. As such, we added language to
the existing single, streamlined
application used by Exchanges using the
federal eligibility and enrollment
platform to allow consumers to
authorize the Exchange to obtain
eligibility and enrollment data and, if
desired, to end their QHP coverage if the
Exchange finds that the consumer has
become eligible for or enrolled in other
qualifying coverage, such as Medicare,
Medicaid/CHIP, or BHP, during periodic
checks.
In addition, for plan years beginning
with the 2020 plan year, we also plan
to add a new authorization to the single,
streamlined application used by
Exchanges using the federal eligibility
and enrollment platform, which will
meet Health Insurance Portability and
Accountability Act of 1996 (HIPAA)
(Pub. L. 104–191) standards regarding
how one’s PHI is collected and used.
This new authorization will expand the
current scope of Medicare PDM to
individuals in the Exchange population
not receiving financial assistance who
authorize the FFE to conduct certain
PDM for them. Specifically, this new
authorization will allow applicants or
QHP enrollees, whether or not they have
applied for or are receiving APTC or
CSRs, to authorize the Exchange, when
conducting Medicare PDM, to request
PHI from HHS such as their name,
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Social Security Number, Medicare
eligibility or enrollment status, and
other data elements the Exchange may
determine necessary, to allow the
Exchange to determine whether the
consumer is simultaneously enrolled in
Medicare and, if requested, to act on the
enrollee’s behalf to terminate QHP
coverage in cases of dual enrollment.
We note that, because entitlement to
premium-free Medicare Part A is based
on age and information held by the
Social Security Administration (that is,
the number of quarters of coverage
toward a Social Security benefit under
Title II of the Act), the Exchange will
not be able to identify through this
process any consumer who is eligible
for premium-free Part A; we encourage
all consumers who are age 65 and older
to apply with the Social Security
Administration to receive an eligibility
determination with respect to Medicare.
Our adoption of this new optional
authorization to access Medicare
enrollment information does not extend
to access to Medicaid, CHIP, or BHP
information for applicants who are not
receiving APTC or CSRs, because these
programs are targeted to relatively lower
income consumers and we would not
expect to identify a significant number
of enrollees dually enrolled in one of
these programs and an unsubsidized
QHP through the Exchange.
For consumers who request voluntary
termination upon a finding of dual
enrollment, the Exchange would
terminate coverage after following the
current PDM process outlined in
§ 155.330(e)(2)(i), which requires the
Exchange to provide notice of the
updated information the Exchange has
found and a 30-day period for the
enrollee to respond. For example, upon
receiving the required notice, the
enrollee could (1) return to the
Exchange and terminate his or her QHP
coverage, (2) revoke the prior
authorization for the Exchange to
terminate his or her QHP coverage in
the event dual enrollment is found, so
that he or she would remain enrolled
both in the QHP and in Medicare, or (3)
notify the Exchange that he or she is not
eligible for, or enrolled in, Medicare.
For consumers who revoke their prior
authorization for the Exchange to
terminate their QHP enrollment where
the Exchange finds the enrollee is
eligible for or enrolled in Medicare, or
who disagree that they are eligible for or
enrolled in Medicare, the Exchange
would only proceed to terminate the
enrollee’s APTC and CSRs, and not his
or her enrollment in QHP coverage
through the Exchange, using the process
specified in § 155.330(e)(2)(i). Again, as
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the Exchange cannot identify through
this process those consumers who are
eligible for but not enrolled in premiumfree Part A, we encourage all consumers
who are 65 and older to apply with the
Social Security Administration to
receive an eligibility determination with
respect to Medicare.
Based on our experience performing
Medicare PDM, we believe that many
consumers are inadvertently enrolled in
Medicare and QHP coverage at the same
time, and that their dual enrollment
does not represent an informed
decision. For example, we have found
that, once consumers are informed of
the consequences of their dual
enrollment, such as paying full price for
a QHP and risk for financial penalties
for delaying Medicare Part B
enrollment, the majority of consumers
end their QHP coverage shortly
thereafter. Furthermore, our own
internal analyses show that the majority
of QHP enrollees who become dually
enrolled do so by aging into Medicare
and failing to terminate the APTC or
CSRs they are receiving through the
Exchange (and, if desired, their
Exchange coverage itself) during their
Medicare initial enrollment period. We
believe that Exchanges should play an
important role in helping to ensure that
consumers, regardless of whether the
consumer has applied for, or is
receiving, APTC or CSRs through the
Exchange, are aware of their dual
enrollment, the fact that their QHP
coverage may duplicate coverage
available to them through Medicare at
potentially lower expense, and their
potential risk for tax liability for APTC
received during months of overlapping
coverage (for consumers receiving
APTC) or financial penalties (such as
the Medicare Part B late enrollment
penalty if they delay enrolling in
Medicare during their initial eligibility
period).
We believe these changes will support
HHS’s program integrity efforts
regarding the Exchanges by helping
promote a balanced risk pool for the
individual market as Medicare and
Medicaid/CHIP beneficiaries tend to be
higher utilizers of medical services,
ensuring that consumers are accurately
determined eligible for APTC and
income-based CSRs, and safeguarding
consumers against enrollment in
unnecessary or duplicative coverage.
Such unnecessary or duplicative
coverage, coupled with typically higher
utilization, generally results in higher
premiums across the individual market,
leading to unnecessarily inflated
expenditures of federal funds on PTC
for taxpayers eligible for PTC in the
individual market. We also encourage
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SBEs and enhanced direct enrollment
partners to adopt these changes if they
are not already using the single,
streamlined application. We seek
comment on these plans.
3. Eligibility Redetermination During a
Benefit Year (§ 155.330)
In accordance with § 155.330(d),
Exchanges must periodically examine
available data sources to determine
whether enrollees in a QHP through an
Exchange with APTC or CSRs have been
determined eligible for or enrolled in
other qualifying coverage through
Medicare, Medicaid, CHIP, or the BHP,
if applicable. HHS has not previously
defined ‘‘periodically.’’ Currently, FFEs
conduct Medicare PDM and Medicaid/
CHIP PDM twice a year. To ensure that
all Exchanges are taking adequate steps
to check for enrollees who have become
eligible for or enrolled in these other
forms of MEC, and to terminate APTC
and CSRs if so, we propose to add a
clearer requirement to conduct
Medicare, Medicaid/CHIP, and BHP, if
applicable, periodic data matching with
regular frequency. Specifically, we
propose to add paragraph (d)(3) to
specify that Exchanges conduct
Medicare, Medicaid/CHIP, and BHP, if
applicable, PDM at least twice a year,
beginning with the 2020 calendar year.
We believe this timeframe will give
Exchanges that are not already
performing these PDM checks twice a
year sufficient time to implement any
business, operational, and information
technology changes needed to comply
with the proposed new requirement.
Based on HHS’s experience, Exchanges
should consider spacing Medicare,
Medicaid/CHIP, and BHP, if applicable,
PDM checks evenly throughout the year,
which we believe would help ensure the
greatest number of potentially affected
enrollees are identified and notified.
Further, we do not anticipate that the
proposal—to apply Medicare PDM to
those enrollees who are not receiving
APTC/CSRs but authorize the Exchange
to receive Medicare enrollment
information—would add significant
costs to performing Medicare PDM.
Based on HHS’s experience, the dually
enrolled unsubsidized population is
significantly smaller than the
population receiving APTC/CSRs. We
believe this policy would likely reduce
QHP premiums and improve program
integrity for all Exchanges, since
Medicare and Medicaid/CHIP
beneficiaries tend to have a higher risk
profile than a typical Exchange enrollee
and, therefore, may have negative
impacts on the risk pool because of the
typically increased utilization of
services expected for these populations,
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which include significant numbers of
older and disabled beneficiaries or
poorer health outcomes associated with
lower income statuses.4 As noted above,
this negative effect on the risk pool
likely results in higher premiums across
the individual market, leading to
increased expenditures of federal funds
on PTC for taxpayers eligible for PTC
resulting from unnecessary or
duplicative coverage. So that the FFEs
and SBEs may prioritize the
implementation of the proposed
requirement to conduct PDM for
Medicare, Medicaid, CHIP, and BHP (if
applicable) eligibility or enrollment at
least twice yearly, we are not proposing
to require Exchanges to perform PDM
for death at least twice in a calendar
year. We will consider whether to
require this check to be performed at a
particular frequency through future
rulemaking.
Since most SBEs have shared,
integrated eligibility systems with their
respective Medicaid programs,
Medicaid/CHIP and BHP, if applicable,
PDM requirements may be met
differently for SBEs than for the FFEs.
While there is some variation among
SBEs in their Medicaid/CHIP and BHP,
if applicable, PDM processes, most SBEs
have implemented fully integrated
eligibility systems where the design of
the system mitigates risk of dual
enrollment in, or inconsistent eligibility
results regarding, APTC/CSRs and
Medicaid/CHIP and BHP, if applicable,
coverage by having one eligibility rules
engine for eligibility determinations for
all these programs. In these SBEs, an
individual cannot be enrolled in both a
QHP through the Exchange with APTC/
CSRs, and Medicaid/CHIP or BHP, if
applicable, coverage, at any given time.
At paragraph (d)(3), we propose to
specify that we will deem these SBEs to
be in compliance with the requirement
to perform Medicaid/CHIP PDM or BHP
PDM, if applicable. SBEs that do not
have fully integrated eligibility systems
for APTC/CSRs and Medicaid/CHIP
would be required to perform Medicaid/
CHIP PDM at least twice a year.
Similarly, SBEs in states that have
implemented the BHP, but where the
BHP is not integrated into the state’s
shared eligibility system, would be
required to perform BHP PDM at least
twice a year. We anticipate most SBEs
will meet or exceed the proposed
requirements for Medicaid/CHIP PDM
and BHP PDM, if applicable, based on
current or planned operations for
calendar year 2018, as reported to us
through the State-based Marketplace
Annual Reporting Tool and through
technical assistance engagements.
Therefore, we anticipate that the
proposed requirement to conduct
Medicaid/CHIP PDM and BHP PDM, if
applicable, at least twice a year would
not result in a significant administrative
burden for SBEs that are not deemed to
be in compliance (and no administrative
burden for those that are so deemed).
Although we believe that compliance
by SBEs with these proposed
requirements is critically important for
program integrity, we are not proposing
specific penalties if SBEs do not
comply. However, we note that under
current authority HHS requires a SBE to
take corrective action if it is not
complying with federal guidance and
regulations. We utilize specific
oversight tools (SMART, programmatic
audits, etc. as described in the preamble
to § 155.1200) to identify issues with,
and place corrective actions on
Exchanges, and provide technical
assistance and ongoing monitoring to
track those actions until the Exchange
comes into compliance.
Additionally, under section 1313(a)(4)
PPACA, if HHS determines that an
Exchange has engaged in serious
misconduct with respect to compliance
with Exchange requirements, it has the
option to rescind up to 1 percent of
payments due a state under any program
administered by HHS until it is
resolved. These existing authorities
would apply to the proposed periodic
data matching requirements in
§ 155.330(d). If HHS determines it is
necessary to apply this authority due to
non-compliance by an Exchange with
§ 155.330(d), HHS would also determine
the HHS-administered program from
which it will rescind payments that are
due to that state.
Lastly, we propose to make a
technical correction in § 155.330(d)(1)
by adding an additional reference to the
process and authority in § 155.320(b).
This reference was omitted previously,
but the requirements in § 155.320(b),
specifying that Exchanges must verify
whether an applicant is eligible for MEC
other than through an eligible employersponsored plan using information
obtained by transmitting identifying
information specified by HHS to HHS
for verification purposes, apply to the
PDM process in § 155.330.
4 For example, see Urban Institute and Center on
Society and Health, How Are Income and Wealth
Linked to Health and Longevity? (April 2015),
available at https://www.urban.org/sites/default/
files/publication/49116/2000178-How-are-Incomeand-Wealth-Linked-to-Health-and-Longevity.pdf.
4. General Program Integrity and
Oversight Requirements (§ 155.1200)
As section 1311 of the PPACA
Exchange Establishment grant program
has come to a conclusion and State
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Exchanges are financially selfsustaining, HHS has a need for
strengthening the mechanisms and tools
for overseeing SBE and SBE–FP ongoing
compliance with federal requirements
for Exchanges, including eligibility and
enrollment requirements under 45 CFR
part 155.
HHS approves or conditionally
approves a state to establish a State
Exchange (either an SBE or SBE–FP)
based on an assessment of a state’s
attested compliance with statutory and
regulatory rules. Once approved or
conditionally approved, State
Exchanges must meet specific program
integrity and oversight requirements
specified at section 1313(a) of the
PPACA, §§ 155.1200 and 155.1210.
These requirements provide HHS with
the authority to oversee the Exchanges
after their establishment. Currently,
annual reporting requirements for State
Exchanges at § 155.1200(b) include the
annual submission of: (1) A financial
statement in accordance with generally
accepted accounting principles (GAAP);
(2) eligibility and enrollment reports;
and (3) performance monitoring data.
Additionally, under § 155.1200(c),
each State Exchange is required to
contract with an independent external
auditing entity that follows generally
accepted governmental auditing
standards (GAGAS) to perform annual
independent external financial and
programmatic audits. State Exchanges
are required to provide HHS with the
results of the annual external audits,
including corrective action plans to
address any material weaknesses or
significant deficiencies identified by the
auditor. All corrective action plans are
monitored by HHS until closed.
Currently, the audits must address
compliance with all Exchange
requirements under 45 CFR part 155.
HHS designed and developed the
State-based Marketplace Annual
Reporting Tool (SMART) in 2014 to
assist Exchanges in conducting a
defined set of oversight activities. The
SMART was designed to facilitate State
Exchanges’ reporting to HHS on how
they are meeting federal program
requirements and operational
requirements set forth in statute,
regulations, and applicable guidance
that implements the statutory and
regulatory requirements, including
reporting compliance with Federal
eligibility and enrollment program
requirements under 45 CFR 155
subparts D and E. The SMART, thus,
enables HHS to evaluate and monitor
State Exchange progress in coming into
compliance with federal requirements
where needed. Since then, HHS has
come to utilize the SMART, along with
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the annual programmatic and financial
audit reports, as primary oversight tools
for identifying and addressing State
Exchange non-compliance issues. HHS
requires State Exchanges to take
corrective actions to address issues that
are identified through the SMART and
annual programmatic and financial
audits, and HHS monitors the
implementation of the corrective
actions. We propose to modify
§ 155.1200(b)(2) to reflect that HHS
requires State Exchanges to submit
annual compliance reports (such as the
SMART), that encompass eligibility and
enrollment reporting, but also include
reporting on compliance across other
Exchange program requirements under
45 CFR part 155. We also propose to
modify § 155.1200(b)(1) to eliminate the
April 1st date in which states must
provide a financial statement to HHS, to
provide HHS the flexibility to align the
financial statement deadline with the
SMART deadline, which is set annually
by HHS. Because we are proposing to
remove the April 1st date, but intend to
maintain the requirement that State
Exchanges submit the required reports
by a deadline, we also propose to
modify the introductory text to
§ 155.1200(b) to specify that State
Exchanges must provide the required
annual reporting by deadlines to be set
by HHS.
We propose to retain the requirement
at § 155.1200(c) that an annual
programmatic audit be conducted by
SBEs and SBE–FPs, but make a minor
change from ‘‘state’’ to ‘‘State
Exchanges’’ to be consistent and clear
on the entities to which this rule
applies. We also propose to add
specificity to the annual programmatic
audit requirement by proposing a
clarification of § 155.1200(d)(2) to make
clear that HHS may specify or target the
scope of a programmatic audit to
address compliance with particular
Exchange program areas or
requirements. This would provide HHS
with the ability to specify those
Exchange functions that are most
pertinent to a particular State Exchange
model (SBE or SBE–FP) and need to be
regularly included in the audit; target
those Exchange functions most likely to
impact program integrity, such as
eligibility verifications; and reduce
burden on State Exchanges where
possible. In addition, we propose to
modify § 155.1200(d) by replacing
existing paragraph (d)(4) with new
paragraphs (d)(4) and (5). These
requirements specify that SBEs must
ensure that the independent audits
implement testing procedures or other
auditing procedures that assess whether
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an SBE is conducting accurate eligibility
determinations and enrollment
transactions under 45 CFR 155 subparts
D and E. Such auditing procedures
include the use of statistically valid
sampling methods in the testing or
auditing procedures.
We believe these proposed changes
will strengthen our programmatic
oversight and the program integrity of
State Exchanges, while providing
flexibility for HHS in the collection of
information. Through the Paperwork
Reduction Act (PRA) process, we are
able to make updates and refinements to
the SMART reporting tool to align with
our oversight and program integrity
priorities for Exchanges as they evolve.
In addition, allowing HHS to specify the
scope of the programmatic audit at
§ 155.1200(d)(2) would provide us the
ability to target our oversight to specific
Exchange program requirements based
on the particular State Exchange model,
our program integrity priorities, and the
goal of reducing burden on State
Exchanges where possible. For instance,
this would allow the audits to focus on
SBE compliance with Exchange
eligibility and enrollment requirements
in 45 CFR 155 subparts D and E, and
SBE–FP compliance with Exchange
requirements in 45 CFR 155 subpart C.
We believe this approach will provide
HHS and states with greater insight into
SBE and SBE–FP compliance with
federal standards in a more costeffective manner. We believe these two
tools, state reporting and independent
testing, coupled with our ongoing
oversight activities would strengthen
program integrity in State Exchanges.
We believe this approach would allow
HHS to identify State Exchange noncompliance issues with more precision
and efficacy. It would also allow HHS
to provide more effective, targeted
technical assistance to State Exchanges
in developing corrective action plans to
address issues that are identified, thus
mitigating the need for more drastic or
severe enforcement actions against a
State Exchange. We believe this
approach can reduce administrative
burden on State Exchanges while
maintaining the traditional role of State
Exchanges in managing and operating
their Exchanges, with HHS maintaining
its role of overseeing State Exchange
compliance with federal requirements
through structured reporting processes.
We seek comment on these proposals.
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B. Health Insurance Issuer Standards
Under the Affordable Care Act,
Including Standards Related to
Exchanges
Segregation of Funds for Abortion
Services (§ 156.280)
Since 1976, the Congress has included
language, commonly known as the Hyde
Amendment, in the Labor, Health and
Human Services, Education and Related
Agencies appropriations legislation.5
The Hyde Amendment as currently in
effect permits federal funds to be used
for abortion services only in the limited
cases of rape, incest, or if a woman
suffers from a life-threatening physical
disorder, physical injury, or physical
illness, including a life-endangering
physical condition caused by or arising
from the pregnancy itself, that would, as
certified by a physician, place the
woman in danger of death unless an
abortion is performed (Hyde abortion
coverage). The Hyde Amendment
prohibits the use of federal funds for
abortion coverage in instances beyond
those limited circumstances (non-Hyde
abortion coverage). Consistent with the
Hyde Amendment, section 1303(b)(2) of
the PPACA prohibits the issuer of a
QHP that includes non-Hyde abortion
coverage from using any amount
attributable to PTC (including APTC) or
CSRs (including advance payments of
those funds to the issuer, if any) for
abortions for which federal funds
appropriated for HHS are prohibited,
‘‘based on the law as in effect as of the
date that is 6 months before the
beginning of the plan year involved.’’ 6
Section 1303 of the PPACA outlines
specific accounting and notice
requirements that QHPs covering nonHyde abortion services on the
Exchanges must follow to ensure that no
federal funding is used to pay for those
services. Under section 1303(b)(2)(B) of
the PPACA, as implemented in
§ 156.280(e)(2)(i), QHP issuers must
collect a ‘‘separate payment,’’ from each
enrollee in a plan ‘‘without regard to the
enrollee’s age, sex, or family status,’’ for
an amount equal to the greater of the
actuarial value of the coverage for
abortions for which public funding is
prohibited or $1 per enrollee per month.
Section 1303(b)(2)(D) of the PPACA,
implemented in § 156.280(e)(4),
provides that the estimation is to be
determined on an average actuarial basis
and that QHP issuers may take into
account the impact on overall costs of
the inclusion of such coverage, but may
5 Accordingly, the Hyde Amendment is not
permanent Federal law, but applies only to the
extent reenacted by Congress from time to time in
appropriations legislation.
6 Section 1303(b)(1)(B)(I) of the PPACA.
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not take into account any cost reduction
estimated to result from such services,
including prenatal care, delivery, or
postnatal care. Section 1303(b)(2)(D) of
the PPACA as implemented in
§ 156.280(e)(4) further states that QHP
issuers are to estimate these costs as if
the coverage were included for the
entire population covered. With respect
to the ‘‘separate payment’’ requirement,
if an enrollee’s premium for coverage
under the plan is paid through
employee payroll deposit (or deduction)
under section 1303(b)(2)(B), the separate
payments ‘‘shall each be paid by a
separate deposit.’’
As mentioned above, QHP issuers that
offer coverage for non-Hyde abortion
may not use APTC to pay for such
coverage, or use CSR funds to pay for
such services. Pursuant to section
1303(b)(2)(D)(ii)(III) of the PPACA, these
QHP issuers may not estimate the
premium attributable to the benefit to be
less than $1 per enrollee per month,
regardless of the actual cost of the
benefit. Currently, in certain rare
scenarios, the FFE system allocates an
amount of APTC to a policy such that
the share of the aggregate premium for
which the consumer is responsible is
too low to meet this minimum standard.
We intend to make system changes for
open enrollment for plan year 2019 to
ensure that the minimum premium
amount of $1 per enrollee per month is
assigned to all enrollments into plans
offering coverage of non-Hyde abortion,
so that issuers may separately collect
this amount directly from consumers for
the portion of the total premium
attributable to coverage of non-Hyde
abortion services.
Under section 1303(b)(3)(A) of the
PPACA as implemented in § 156.280(f),
QHP issuers must provide notice to
enrollees as part of the Summary of
Benefits and Coverage (SBC) at the time
of enrollment if non-Hyde abortion
services are covered by the QHP. As
required under § 155.205(b)(1)(ii), each
Exchange must maintain an up-to-date
website that provides the SBCs. Section
147.200(a)(4) requires that individual
market QHP issuers that provide the
SBC electronically must place it in a
prominent and readily accessible
location on the QHP issuer’s internet
website. Additionally, pursuant to
section 1303(b)(2)(C) of the PPACA, as
implemented at § 156.280(e)(3), QHP
issuers must segregate funds for nonHyde abortion services collected from
consumers into a separate allocation
account that is to be used exclusively to
pay for non-Hyde abortion services.
Thus, if a QHP issuer disburses funds
for a non-Hyde abortion on behalf of a
consumer, it must draw those funds
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from the segregated allocation account.
The account cannot be used for any
other purpose.
Section 1303 of the PPACA and
regulations at § 156.280 do not specify
the method a QHP issuer must use to
comply with the separate payment
requirement under section
1303(b)(2)(B)(i) of the PPACA and
§ 156.280(e)(2)(i). In the 2016 Payment
Notice, we provided guidance with
respect to acceptable methods that a
QHP issuer offering non-Hyde abortion
coverage on the individual market
Exchange may use to comply with the
separate payment requirement. We
stated that the QHP issuer could satisfy
the separate payment requirement in
one of several ways, including by
sending the enrollee a single monthly
invoice or bill that separately itemizes
the premium amount for non-Hyde
abortion services; sending the enrollee a
separate monthly bill for these services;
or sending the enrollee a notice at or
soon after the time of enrollment that
the monthly invoice or bill will include
a separate charge for such services and
specify the charge. In the 2016 Payment
Notice, we also stated that a consumer
may make the payment for non-Hyde
abortion services and the separate
payment for all other services in a single
transaction. On October 6, 2017, we
released a bulletin that discussed the
statutory requirements for separate
payment, as well as this previous
guidance with respect to the separate
payment requirement.7
HHS now believes that some of the
methods for billing and collection of the
separate payment for non-Hyde abortion
services noted as permissible in the
preamble to the 2016 Payment Notice do
not adequately reflect what we see as
Congressional intent that the QHP issuer
bill separately for two distinct (that is,
‘‘separate’’) payments, one for the nonHyde abortion services, and one for all
other services covered under the policy,
rather than simply itemizing these two
components of a single total billed
amount or notifying the enrollee, at or
soon after the time of enrollment, that
the monthly invoice or bill will include
a separate charge for these services.
Although we recognize that itemizing or
providing advance notice about the
amounts arguably identifies two
‘‘separate’’ amounts for two separate
purposes, we believe that the statute
contemplates issuers billing for two
separate ‘‘payments’’ of these two
7 CMS Bulletin Addressing Enforcement of
Section 1303 of the Patient Protection and
Affordable Care Act (October 6, 2017), available at
https://www.cms.gov/CCIIO/Resources/Regulationsand-Guidance/Downloads/Section-1303-Bulletin10-6-2017-FINAL-508.pdf.
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amounts (for example, two different
checks or two distinct transactions),
consistent with the requirement on
issuers in section 1303(b)(2)(B)(i) of the
PPACA to collect two separate
payments. HHS, thus, believes that
requiring QHP issuers to separately bill
the portion of the consumer’s premium
attributable to non-Hyde abortion
services and instruct consumers to make
a separate payment for this amount is a
better implementation of the statutory
requirement for issuers to collect a
separate payment for these services.
As such, we are proposing an
amendment at § 156.280(e)(2) relating to
billing and payment of the consumer’s
portion of the premium attributable to
non-Hyde abortion services to reflect
this interpretation of the statute.
Specifically, we are proposing that, if
these policies are finalized, as of the
effective date of the final rule, QHP
issuers (1) send an entirely separate
monthly bill to the policy subscriber for
only the portion of premium attributable
to non-Hyde abortion coverage, and (2)
instruct the policy subscriber to pay the
portion of their premium attributable to
non-Hyde abortion coverage in a
separate transaction from any payment
the policy subscriber makes for the
portion of their premium not
attributable to non-Hyde abortion
coverage. We believe that these
proposals would better align the
regulatory requirements for QHP issuer
billing of enrollee premiums with the
separate payment requirement in
section 1303 of the PPACA. If these
proposals are finalized, QHP issuers
would no longer be permitted to send
the enrollee a single monthly invoice or
bill that separately itemizes the
premium amount for non-Hyde abortion
services, or send the enrollee a notice at
or soon after the time of enrollment that
the monthly invoice or bill will include
a separate charge for such services and
specify the charge in order to meet the
separate payment requirement. Instead,
QHP issuers would have to send a
separate bill and instruct enrollees to
send a separate payment in the manner
specified by the final rule.8 We invite
comment on these proposals.
To better align the regulatory
requirements for issuer billing of
enrollee premiums with the separate
payment requirement in section 1303 of
the PPACA, our proposal would require
8 We noted above the situation where, as a result
of APTCs, the out-of-pocket premium payable by
the consumer is less than $1 per enrollee per
month. Under this proposed rule, and to ensure
compliance with section 1303, if the QHP includes
non-Hyde abortion coverage, the QHP issuer would
be required to bill the consumer at least $1 per
enrollee per month.
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the QHP issuer to send this separate bill
in a separate mailing with separate
postage. If a QHP issuer sends bills
electronically, we propose that it
provide consumers with the two bills in
separate emails or other electronic
communications. We believe this
approach will help reduce consumer
confusion about receiving two separate
bills in a single envelope. For example,
consumers may inadvertently miss or
discard a second paper bill included in
a single envelope, increasing
terminations of coverage for failure to
pay premiums. The QHP issuer would
also be required to produce an invoice
or bill that is distinctly separate from
the invoice or bill for the other portion
of the consumer’s premium that is not
attributable to non-Hyde abortion
coverage, whether in paper or electronic
format. We solicit comment on any
operational issues that may arise from
this aspect of the proposed rule.
We also seek comment on ways to
mitigate any possible confusion, for
example through an annual notice or
standard explanatory language on each
of the two monthly bills. To meet the
requirements of this new proposal, QHP
issuers would be required to instruct
policy subscribers to pay the separately
billed or invoiced portion of the
premium for non-Hyde abortion
coverage in a transaction separate from
the transaction for payment of the other
portion of the premium that is not
attributable to non-Hyde abortion
coverage and make reasonable efforts to
collect the payment separately, such as
by including a separate payment stub on
each of the separately mailed bills or
invoices (if sent on paper) or providing
a separate payment link in the separate
email or electronic communication with
a separate payment field on the payment
web page for each separate payment to
be collected (if sending an electronic
bill, or accepting electronic payments
regardless of how the bills were
transmitted). Under this proposal,
consumer non-payment of any premium
due (including non-payment of the
portion of the consumer’s premium
attributable to non-Hyde abortion
coverage) would continue to be subject
to state and federal rules regarding grace
periods. In the event that a policy
subscriber does not follow the separate
payment instructions, however, and
pays the entire premium in a single
transaction (both the portion
attributable to non-Hyde abortion
coverage, as well as the portion
attributable to coverage for other
services), the QHP issuer would not be
permitted to refuse to accept such a
combined payment on the basis that the
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17:11 Nov 08, 2018
Jkt 247001
policy subscriber did not send two
checks as requested by the QHP issuer,
and to then terminate the policy, subject
to any applicable grace period, for nonpayment of premiums. We believe that
potential loss of coverage would be an
unreasonable result of a consumer
paying in full but failing to adhere to the
QHP issuer’s requested payment
procedure. Under our new
interpretation, a QHP issuer would thus
be required to accept a combined
payment, to the extent necessary to
avoid this result.
QHP issuers that do receive combined
consumer premiums covering the
portion attributable to non-Hyde
abortion coverage as well as the portion
attributable to coverage for other
services in one single payment would
treat the portion of the premium
attributable to non-Hyde abortion
services as a separate payment for
which the QHP issuer would be
expected to disaggregate into the
separate allocation account used solely
for these services. We would expect the
QHP issuer in this scenario to again
explain to the consumer the separate
payment requirement in the law, and
take steps to inform the consumer not
complying with this policy that he or
she should do so in future months,
including documentation of such
outreach and educational efforts. Again,
if the consumer still declines to do so,
however, the combined payment must
be accepted to avoid a loss of coverage.
Likewise, QHP issuers would not be
permitted to refuse to accept separate
premium payments paid to the issuer in
a single return envelope (for example,
two separate checks returned to the
issuer in a single return envelope) on
the basis that the consumer did not
separately return each premium
payment in a separate mailing. We seek
comment on these proposals.
We are also proposing a technical
change, to Section 156.280(e)(2)(iii) as
redesignated, to insert appropriate cross
reference to the explanation of the
separate payments.
Consistent with § 156.715, HHS has
broad authority to perform compliance
reviews to monitor FFE issuer
compliance. HHS conducts compliance
reviews throughout the year, and issuer
notification of selection for a review
may occur at any time during the year.
Detailed examples of regulatory and
operational areas that will be reviewed
are included in the Key Priorities for
FFM Compliance Review, which is
updated each year with new key
oversight priorities.9 Consistent with
9 CCIIO Examinations, Audits and Reviews of
Issuers: Issuer Resources, available at https://
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56023
this authority, we propose updating our
compliance reviews governing QHP
certification to include new reviews of
FFE issuer compliance with § 156.280,
including the segregation of funds
requirement and the new proposals for
separate billing of the portion of the
consumer’s premium attributable to
coverage of non-Hyde abortion services
as specified in this rule. FFE issuers
subject to these compliance reviews
should maintain all documents and
records of compliance with section 1303
of the PPACA and these requirements in
accordance with § 156.705, and should
anticipate making available to HHS the
types of records specified at § 156.715(b)
that would be necessary to establish
their compliance with these
requirements. For example, FFE issuers
subject to compliance reviews for
§ 156.280 should anticipate supplying
HHS with documentation of their
estimate of the basic per enrollee per
month cost, determined on an average
actuarial basis, for coverage of non-Hyde
abortion services; detailed invoice and
billing records demonstrating they are
separately billing in a separate mailing
or separate electronic communication
and collecting the portion of the
premium attributable to coverage of
non-Hyde abortion services as specified
in this rule; and appropriately
segregating the funds collected from
consumers into a separate allocation
account that is used exclusively to pay
for non-Hyde abortion services. We
believe the addition of these compliance
reviews will help to address remaining
issuer compliance issues, if any,
previously identified by the 2014 U.S.
Government Accountability Office
report.10 We seek comment on this
proposal.
As is the case with many provisions
in the PPACA, states are the entities
primarily responsible for implementing
and enforcing the provisions in section
1303 of the PPACA related to individual
market QHP coverage of non-Hyde
abortion services. Section
1303(b)(2)(E)(i) of the PPACA, as
implemented at § 156.280(e)(5),
designates the state insurance
commissioners as the entities
responsible for monitoring, overseeing,
and enforcing the provisions in section
1303 of the PPACA related to QHP
segregation of funds for non-Hyde
abortion services. However, as stated in
www.cms.gov/CCIIO/Resources/Forms-Reports-andOther-Resources/Exams_Audits_Reviews_Issuer_
Resources-.html.
10 U.S. Government Accountability Office,
‘‘Health Insurance Exchanges: Coverage of Nonexcepted Abortion Services by Qualified Health
Plans,’’ (Sept. 15, 2014), available at https://
www.gao.gov/products/GAO-14-742R.
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2017 guidance,11 where we are charged
with directly enforcing these statutory
requirements in the FFEs, we intend to
do so fully in instances of issuer noncompliance. We call upon states that
operate their own Exchanges to fully
enforce these requirements as codified
in the federal regulations governing the
Exchanges. To the extent such a state
operating its own Exchange fails to
substantially enforce these
requirements, HHS would expect to
enforce them in the state’s place.
However, as states remain the primary
enforcers of these requirements, we
propose that HHS involvement in
enforcement would be limited to
ensuring that federal funds are
appropriately managed. For example,
HHS enforcement would be limited to
instances where it becomes clear that
the state department of insurance is not
overseeing the requirement for the QHP
issuer to determine the actuarial value
of the coverage of non-Hyde abortions,
to separately bill (and collect) premium
of at least $1 per enrollee per month for
such coverage, or to segregate funds
effectively; a state department of
insurance or other entity notifies HHS of
suspected misuse of federal funding for
coverage of non-Hyde abortion services;
or the state’s enforcement actions are
inadequate and fail to result in
compliance from the QHP issuer. The
Office of Personnel Management may
issue guidance related to these
provisions for multi-state plan issuers.12
We remind issuers that pursuant to
§ 156.280(e)(5)(ii), any issuer offering
coverage of non-Hyde abortions services
on the Exchange must submit a plan to
its state department of insurance that
details the issuer’s process and
methodology for meeting the
requirements of section 1303(b)(2)(C),
(D), and (E) of the PPACA (hereinafter,
‘‘separation plan’’) to the state health
insurance commissioner. The separation
plan should describe the QHP issuer’s
financial accounting systems, including
appropriate accounting documentation
and internal controls, that would ensure
the segregation of funds required by
section 1303(b)(2)(C), (D), and (E) of the
11 CMS Bulletin Addressing Enforcement of
Section 1303 of the Patient Protection and
Affordable Care Act (October 6, 2017), available at
https://www.cms.gov/CCIIO/Resources/Regulationsand-Guidance/Downloads/Section-1303-Bulletin10-6-2017-FINAL-508.pdf.
12 Section 1334(a)(6) of the PPACA requires that
at least one multi-state plan in each Exchange
excludes coverage of non-Hyde abortion services.
Currently, no multi-state plan options cover nonHyde abortion services. See OPM’s Frequently
Asked Questions: Insurance, available at https://
www.opm.gov/faqs/QA.aspx?fid=fd635746-de0a4dd7-997d-b5706a0fd8d2&pid=8313a65b-c5b84d58-a58f-9d81f26856a2.
VerDate Sep<11>2014
17:11 Nov 08, 2018
Jkt 247001
PPACA. Issuers should refer to
§ 156.280(e)(5)(ii) for more information
on precisely what issuers should
include in their separation plans to
demonstrate compliance with these
requirements.
As mentioned previously, consistent
with HHS’s authority under § 156.715,
we propose monitoring FFE issuer
compliance with the requirements
under § 156.280 by requiring QHP
issuers in FFEs to show documentation
of compliance with the requirement to
estimate the basic per enrollee per
month cost, determined on an average
actuarial basis, for coverage of non-Hyde
abortion services and charge at least $1
per enrollee per month for such
coverage, as well as with the segregation
of funds requirements when undergoing
compliance reviews, including detailed
records and documentation
demonstrating compliance with the
separate billing (including mailing, as
applicable) and collection requirements
proposed in this rule, as well as the
segregation of funds requirements. We
also remind issuers offering medical
QHPs in the FFEs that they must already
attest to adhering to all applicable
requirements of 45 CFR part 156 as part
of the QHP certification application,
including those requirements related to
the segregation of funds for abortion
services implemented in § 156.280.13 If
the separate billing and premium
collection proposals at § 156.280(e)(2)
are finalized as proposed, issuers in the
FFE completing this attestation would
also attest to adhering to these new
separate billing and collection
requirements. As part of the QHP
certification process, issuers in states
with FFEs where the States perform
plan management functions must also
complete similar program attestations
attesting to adherence with § 156.280.14
Issuers in states with SBEs that offer
QHPs including non-Hyde abortion
coverage should contact their state for
attestation requirements as part of the
QHP certification process.
We seek comment on these proposals.
IV. Collection of Information
Requirements
Under the Paperwork Reduction Act
of 1995 (PRA), we are required to
provide 60-day notice in the Federal
Register and solicit public comment
before a collection of information
13 2019 Qualified Health Plan Issuer Application
Instructions, available at: https://
www.qhpcertification.cms.gov/s/
2019QHPInstructionsVersion1.pdf?v=1.
14 State Partnership Exchange Issuer Program
Attestation Response Form, available at: https://
www.qhpcertification.cms.gov/s/SuppDoc_SPE_
Attestationsed._revised_508.pdf?v=1.
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Frm 00048
Fmt 4702
Sfmt 4702
requirement is submitted to the Office of
Management and Budget (OMB) for
review and approval. This proposed
rule contains information collection
requirements (ICRs) that are subject to
review by OMB. A description of these
provisions is given in the following
paragraphs.
In order to fairly evaluate whether an
information collection should be
approved by OMB, section 3506(c)(2)(A)
of the PRA requires that we solicit
comment on the following issues:
• The need for the information
collection and its usefulness in carrying
out the proper functions of our agency.
• The accuracy of our estimate of the
information collection burden.
• The quality, utility, and clarity of
the information to be collected.
• Recommendations to minimize the
information collection burden on the
affected public, including automated
collection techniques.
We are soliciting public comment on
each of these issues for the following
sections of this document that contain
ICRs:
A. ICRs Regarding General Program
Integrity and Oversight Requirements
(§ 155.1200)
The burden associated with State
Exchanges meeting the proposed
program integrity reporting
requirements in § 155.1200 have already
been assessed and encompassed through
SMART currently approved under OMB
control number: 0938–1244 (CMS–
10507). This proposed rule does not
impose any new burden or add any
additional requirements to the existing
collection.
B. ICRs Regarding Segregation of Funds
for Abortion Services (§ 156.280)
In the preamble to § 156.280, we
explain that the proposals to require
separate issuer billing for, and
collection of, the portion of the
premium attributable to non-Hyde
abortion coverage would be subject to
future HHS compliance reviews of FFE
issuers, requiring issuers in the FFE to
maintain and submit records showing
compliance with these requirements to
HHS. We have determined that the
requirements associated with
compliance reviews have already been
assessed and encompassed by the
Program Integrity: Exchange, Premium
Stabilization Programs, and Market
Standards; Amendments to the HHS
Notice of Benefit and Payment
Parameters for 2014; Final Rule II ICR
currently approved under OMB control
number: 0938–1277 (CMS–10516).
To show compliance with FFE
standards and program requirements, all
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issuers seeking QHP certification in FFE
states are required to submit responses
to program attestations as part of their
QHP application. This response already
includes an attestation that the issuer
agrees to adhere to the requirements
related to the segregation of funds for
abortion services implemented in
§ 156.280. We have determined that the
requirements associated with QHP
certification have already been assessed
and encompassed by the Establishment
of Exchanges and Qualified Health
Plans; Exchange Standard for Employers
approved under OMB control number
0938–1187 (CMS–10433). Therefore,
proposed § 156.280(e)(2) adds no new
ICRs as it relates to program attestations.
In § 156.280(e)(2), we propose that
QHP issuers must send an entirely
separate monthly bill in a separate
mailing or separate electronic
communication to the policy subscriber
for only the portion of premium
attributable to non-Hyde abortion
coverage, and instruct the policy
subscriber to pay the portion of their
premium attributable to non-Hyde
abortion coverage in a separate
transaction from any payment the policy
subscriber makes for the portion of their
premium not attributable to non-Hyde
abortion coverage. Based on 2018 QHP
certification data in the FFEs and SBE–
FPs, we estimate that 15 QHP issuers
khammond on DSK30JT082PROD with PROPOSAL
Labor category
Respondents
offered a total of 111 plans with
coverage of non-Hyde abortion services
in 7 States. In SBEs, we estimate that 60
QHP issuers offered a total of
approximately 1,000 plans offering this
coverage across 10 SBEs. In total, this
leads to an estimated 75 QHP issuers
offering a total of 1,111 plans covering
non-Hyde abortion services across 17
states. As such, the ICRs associated with
these proposals would create a new
burden on QHP issuers and plans and
are subject to the Paperwork Reduction
Act. Salaries for the positions cited
below were taken from the May 2017
National Occupational Employment and
Wage Estimates United States
Department of Labor’s Bureau of Labor
Statistics (BLS) (https://www.bls.gov/oes/
current/oes_nat.htm) based on the listed
national median hourly wage. All wages
on the following pages are inflated by
100 percent to account for the cost of
fringe benefits and overhead costs.
We anticipate that populating the
enrollee information on the separate
electronic or paper bill, transmitting the
separate electronic or paper bill in a
separate mailing or separate electronic
communication, and processing the
enrollee’s separate electronic or mailed
payment, will be an automated process
that occurs monthly after a computer
programmer adds this functionality to
the QHP issuer’s billing and payment
Responses
Wage rate
(p/hr) including
100% fringe
benefits
Burden per
response
(hours)
56025
operating system. We estimate that, on
a one-time basis, a computer
programmer will require 10 hours to
add this functionality to an affected
QHP issuer’s systems (at a rate of $84.16
per hour) for a total burden of 10 hours.
We estimate that this will result in a
one-time cost of $841.60 per QHP issuer
that offers plans that cover non-Hyde
abortion services to meet this reporting
requirement. This would be a one-time
cost, such that the overall burden for all
75 QHP issuers would be 750 hours,
with an associated total cost of $63,120.
Because an estimated 75 QHP issuers
offered a total of 1,111 plans with
coverage of non-Hyde abortion services
across 17 states, we estimate that the
total number of QHP issuers that offer
plans with coverage of non-Hyde
abortion, for which they would be
required to send separate bills in a
separate mailing or separate electronic
communication and collect separate
payments as proposed at § 156.280(e)(2),
would be 75 per year, for a total onetime burden of 750 hours. Below is the
estimate of the burden imposed on a
single QHP issuer subject to the
reporting requirements of this rule. The
aggregate burden for 3 years will be
same as for 1 year: $841.60 per
respondent and $63,120 for all
respondents.
Total annual
burden per
response
(hours)
Labor cost
of one-time
reporting
($)
Total one-time
cost for all
respondents
($)
Computer programmer
to add automated billing & payment processing functionality ...
75
75
10
$42.08
10
$841.60
$63,120
Total ......................
75
75
10
42.08
10
841.60
63,120
Although we anticipate that
populating the enrollee information on
the separate electronic or paper bill and
transmitting that bill in a separate
mailing or separate electronic
communication would be an automated
process, we estimate that a general
office clerk working for an affected QHP
issuer would require 2 hours monthly
(at a rate of $30.28 per hour) per plan
to determine which enrollees are
enrolled in plans that cover non-Hyde
abortion and to oversee the process of
sending a separately packaged complete
and accurate bill in a separate mailing
or separate electronic communication to
these enrollees for the portion of their
premium attributable to that coverage,
for an annual burden of 24 hours. This
estimate includes the amount of time
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17:11 Nov 08, 2018
Jkt 247001
the office clerk would spend
determining which enrollees prefer
paper billing versus electronic billing,
and ensuring that the bills are complete
and accurate and are being sent in a
separate mailing or separate electronic
communication. We estimate that it
would cost $726.72 annually per plan
that covers non-Hyde abortion services
to meet the reporting requirement, with
a total annual burden for all 1,111 plans
of 26,664 hours and an associated total
annual cost of $807,385.92.
We similarly anticipate that
processing the payment made by
enrollees for this portion of their
premium would be an automated
process. However, we estimate that a
general office clerk working for an
affected QHP issuer would require 2
hours monthly (at a rate of $30.28 per
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Frm 00049
Fmt 4702
Sfmt 4702
hour) per plan to review for accuracy
the separate payment an enrollee in a
plan covering non-Hyde abortion
services sends for the portion of their
premium attributable to that coverage
and to process any payments or paper
checks made by enrollees through the
mail, for an annual burden of 24 hours.
This estimate includes the amount of
additional time the office clerk would
need to spend reviewing for accuracy
the separate payments returned in
separate mailings from the payments
received for the portion of the policy
subscriber’s premium not attributable to
non-Hyde abortion. We estimate that it
would cost $726.72 annually per plan
that covers non-Hyde abortion services
to meet the reporting requirement, with
a total annual burden for all 1,111 plans
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Labor category
Respondents
General office clerk for
preparing and sending the bill .................
General office clerk for
receiving and processing the separate
payment ....................
Total ......................
Responses
Labor cost
of reporting
annually
($)
Total annual
cost for all
respondents
($)
2
24
$30.28
$726.72
$807,385.92
1,111
1,111
2
24
30.28
726.72
807,385.92
2,222
2,222
4
48
60.56
1,453.44
1,614,771.84
V. Response to Comments
khammond on DSK30JT082PROD with PROPOSAL
Wage rate
(p/hr) including
100% fringe
benefits
1,111
We have submitted a copy of this
proposed rule to OMB for its review of
the rule’s information collection and
recordkeeping requirements. The
requirements are not effective until they
have been approved by OMB.
We invite public comments on these
information collection requirements. If
you wish to comment, please identify
the rule (CMS–9922–P) and, where
applicable, the ICR’s CFR citation, CMS
ID number, and OMB control number.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’s website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
See this rule’s DATES and ADDRESSES
sections for the comment due date and
for additional instructions.
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
able to acknowledge or respond to them
individually. We will consider all
comments we receive by the date and
time specified in the DATES section of
this preamble, and, when we proceed
with a subsequent document, we will
respond to the comments in the
preamble to that document.
17:11 Nov 08, 2018
Total annual
burden per
response
(hours)
Burden per
response
(hours)
1,111
C. Submission of PRA-Related
Comments
VerDate Sep<11>2014
on a single plan subject to the reporting
requirements of this rule. The aggregate
burden for 3 years will be $4,360.32 per
respondent and $4,844,315.52 for all
respondents.
communication and collect separate
payments as proposed at § 156.280(e)(2)
would be 1,111 per year, for a total
burden of 53,328 hours to meet these
reporting requirements per year. Below
is the estimate of the burden imposed
of 26,664 hours and an associated total
cost of $807,385.92.
As such, we estimate that the total
number of plans for which QHP issuers
would need to send separate bills in a
separate mailing or separate electronic
Jkt 247001
VI. Regulatory Impact Statement
We have examined the impact of this
rule as required by Executive Order
12866 on Regulatory Planning and
Review (September 30, 1993), Executive
Order 13563 on Improving Regulation
and Regulatory Review (January 18,
2011), the Regulatory Flexibility Act
(RFA) (September 19, 1980, Pub. L. 96–
354), section 1102(b) of the Social
Security Act, section 202 of the
Unfunded Mandates Reform Act of 1995
(March 22, 1995; Pub. L. 104–4),
Executive Order 13132 on Federalism
(August 4, 1999), the Congressional
Review Act (5 U.S.C. 804(2)), and
Executive Order 13771 on Reducing
Regulation and Controlling Regulatory
Costs (January 30, 2017).
Executive Orders 12866 and 13563
direct agencies to assess all costs and
benefits of available regulatory
alternatives and, if regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, distributive impacts, and
equity).
Section 3(f) of Executive Order 12866
defines a ‘‘significant regulatory action’’
as an action that is likely to result in a
regulation: (1) Having an annual effect
on the economy of $100 million or more
in any 1 year, or adversely and
materially affecting a sector of the
economy, productivity, competition,
jobs, the environment, public health or
safety, or state, local, or tribal
governments or communities (also
referred to as ‘‘economically
significant’’); (2) creating a serious
inconsistency or otherwise interfering
with an action taken or planned by
another agency; (3) materially altering
the budgetary impacts of entitlement
grants, user fees, or loan programs or the
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Frm 00050
Fmt 4702
Sfmt 4702
rights and obligations of recipients
thereof; or (4) raising novel legal or
policy issues arising out of legal
mandates, the President’s priorities, or
the principles set forth in the Executive
Order.
A regulatory impact analysis must be
prepared for major rules with
economically significant effects ($100
million or more in any 1 year), and an
‘‘economically significant’’ regulatory
action is subject to review by the Office
of Management and Budget (OMB). As
discussed below regarding their
anticipated effects, these proposals are
not likely to have economic impacts of
$100 million or more in any 1 year, and
therefore do not meet the definition of
‘‘economically significant’’ under
Executive Order 12866. However, OMB
has determined that the actions are
significant within the meaning of
section 3(f)(4) of the Executive Order.
Therefore, OMB has reviewed these
final rules and the Departments have
provided the following assessment of
their impact.
A. Need for Regulatory Action
HHS is committed to promoting
program integrity throughout its
programs to ensure that federal statutory
requirements are met and federal
monies are not being inappropriately
spent. Ensuring that consumers receive
the correct amount of APTC and CSRs
at the time of enrollment or reenrollment is a top priority for us, and
necessitates regulatory action. Accurate
and up-to-date eligibility determinations
help reduce the possibility that an
individual or family is paying a
premium amount that is either higher or
lower than they should have to, the
latter of which could result in the
individual or family needing to pay a
large amount back to the federal
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Treasury on their federal income tax
returns. We propose a number of
changes in this rule to help mitigate the
risk of federal dollars incorrectly leaving
the federal Treasury in the form of
APTC during the year. To further
improve program integrity and ensure
that individuals receiving APTC/CSRs
are appropriately enrolled in insurance
affordability programs, we are also
proposing to specify that Exchanges
must conduct Medicare PDM, Medicaid/
CHIP PDM, and BHP PDM, if applicable,
pursuant to § 155.330(d)(1)(ii), at least
twice a year beginning with the 2020
calendar year. We also believe this
policy would likely reduce QHP
premiums and improve program
integrity for all Exchanges, since
Medicare and Medicaid/CHIP
beneficiaries tend to have a higher risk
profile than a typical Exchange enrollee
and, therefore, may have negative
impacts on the risk pool because of the
typically increased utilization of
services expected for these populations,
which include significant numbers of
older and disabled beneficiaries or
poorer health outcomes associated with
lower income statuses.15 As noted
above, this negative effect on the risk
pool results in higher premiums across
the individual market, leading to
increased expenditures of federal funds
on PTC for taxpayers eligible for PTC
resulting from duplicative coverage.
As part of our efforts to strengthen
program integrity with respect to
subsidy payments in the individual
market, we also believe improvements
should be made to our ability to conduct
effective and efficient oversight of State
Exchanges to ensure consumers receive
the correct amount of APTC and CSRs
(as applicable). As section 1311 of the
PPACA Exchange Establishment grant
program has come to a conclusion and
State Exchanges are financially selfsustaining, HHS has a need to
strengthen the mechanisms and tools for
overseeing ongoing compliance by State
Exchanges with federal program
requirements, including eligibility and
enrollment requirements under 45 CFR
part 155. For these reasons, we are
proposing to add specificity to the
reporting requirements for State
Exchanges at § 155.1200 to focus on
activities that speak to compliance with
Exchange program requirements,
including eligibility and enrollment
requirements. We are also proposing
changes at § 155.1200 to clarify the
15 For example, see Urban Institute and Center on
Society and Health, How Are Income and Wealth
Linked to Health and Longevity? (April 2015),
available at https://www.urban.org/sites/default/
files/publication/49116/2000178-How-are-Incomeand-Wealth-Linked-to-Health-and-Longevity.pdf.
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scope of annual programmatic audits
that State Exchanges are required to
conduct, and include new requirements
that focus on ensuring proper eligibility
determinations and enrollments in
SBEs. It is our intent that these changes
would enable us to better identify and
address State Exchange non-compliance
issues.
HHS believes that some of the
methods for billing and collection of the
separate payment for non-Hyde abortion
services noted as permissible in the
preamble to the 2016 Payment Notice do
not adequately reflect what we see as
Congressional intent that the QHP issuer
bill separately for two distinct (that is,
‘‘separate’’) payments as required by
section 1303 of the PPACA. To remedy
this, we are proposing at § 156.280(e)(2)
that: (1) QHP issuers send an entirely
separate monthly bill to the policy
subscriber for only the portion of
premium attributable to non-Hyde
abortion coverage, and (2) instruct the
policy subscriber to pay the portion of
their premium attributable to non-Hyde
abortion coverage in a separate
transaction from any payment the policy
subscriber makes for the portion of their
premium not attributable to non-Hyde
abortion coverage. We believe that these
proposals are necessary to better align
the regulatory requirements for QHP
issuer billing of enrollee premiums with
the separate payment requirement in
section 1303 of the PPACA. HHS
believes that requiring QHP issuers to
separately bill the portion of the policy
subscriber’s premium attributable to
non-Hyde abortion services and instruct
policy subscribers to make a separate
payment for this amount is a better
interpretation of, and would result in
greater compliance with this
interpretation of, the statutory
requirement for QHP issuers to collect a
separate payment for these services.
B. Anticipated Effects
Revising § 155.200(c) to clarify that
the Exchanges must perform oversight
functions or cooperate with activities
related to oversight and financial
integrity requirements is a clarification
and not a new function. Therefore, it
would not impose additional burdens
on State Exchanges.
Our proposal that Exchanges conduct
Medicare PDM, Medicaid/CHIP PDM,
and BHP PDM, if applicable, at least
twice a year beginning with the 2020
calendar year, merely adds specificity to
the existing requirement that Exchanges
must periodically examine available
data sources to determine whether
Exchange enrollees have been
determined eligible for or enrolled in
other qualifying coverage such as
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Medicare, Medicaid, CHIP, or the BHP,
if applicable. Therefore, we expect the
costs associated with this proposal to be
minimal. However, SBEs that are not
already conducting PDM with the
frequency proposed, or deemed in
compliance with the Medicaid, CHIP,
and BHP (where applicable) PDM
requirements, would likely be required
to engage in IT system development
activity in order to communicate with
these programs and act on enrollment
data either in a new way, or in the same
way more frequently. Thus, there may
be additional associated administrative
cost for these SBEs to implement the
proposed PDM requirements. We
anticipate a majority (about eight) of the
twelve SBEs would be exempt from the
requirement to perform Medicaid, CHIP,
and BHP (where applicable) PDM
because they have shared, integrated
eligibility systems, as they would be
deemed in compliance with this
requirement. However, at this point we
are not able to confirm the exact number
because we have not yet set specific
criteria and process to assess and
confirm which SBEs would be exempt,
and would need additional operational
information from SBEs to confirm our
assessment. We would establish and
engage in that process after finalization
of the rule. For an SBE not already
conducting Medicare, Medicaid/CHIP,
and BHP PDM at least twice a year, and
that does not already have a shared,
integrated eligibility system with its
respective Medicaid/CHIP, and BHP
(where applicable) programs, we
estimate that it would cost
approximately $1,740,000 per SBE to
build such capabilities in their system.
These costs would be incurred by the
SBE as they are required to be
financially self-sustaining and do not
receive federal funding for their
establishment or operational activities.
We believe these changes will support
HHS’s program integrity efforts
regarding the Exchanges by helping
promote a balanced risk pool for the
individual market as Medicare and
Medicaid/CHIP beneficiaries tend to be
higher utilizers of medical services,
ensuring that consumers are accurately
determined eligible for APTC and
income-based CSRs, and safeguarding
consumers against enrollment in
unnecessary or duplicative coverage.
Such unnecessary or duplicative
coverage, coupled with typically higher
utilization, generally results in higher
premiums across the individual market,
leading to unnecessarily inflated
expenditures of federal funds on PTC
for taxpayers eligible for PTC in the
individual market.
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We expect our plan to permit HHS to
verify applicant eligibility for or
enrollment in MEC in order for HHS to
perform the periodic checks required
under § 155.330(d) for those consumers
who provide consent to the Exchange to
obtain their eligibility and enrollment
data, and, if desired, to end their QHP
coverage if found dually enrolled in
other qualifying coverage, to have
minimal economic impact. Based on
HHS’s experience, the dually enrolled
unsubsidized population is significantly
smaller than those receiving APTC or
CSRs. This plan would help expand the
scope of the population that is part of
Medicare PDM, rather than adding new
Exchange requirements.
We do not anticipate the proposed
changes to § 155.1200 will result in any
additional cost for the State Exchanges
because the changes leverage an existing
reporting mechanism, the annual State
Based Marketplace Reporting Tool, for
meeting eligibility and enrollment
reporting requirements in § 155.1200(b).
Additionally, State Exchanges are
already required to annually contract
with, and budget accordingly for, an
external independent audit entity to
perform an annual financial and
programmatic audit as required under
§ 155.1200(c). We believe the proposed
requirement that HHS be able to specify
the scope of annual programmatic
audits to focus on the program areas that
are most pertinent to a State Exchange
model (SBE or SBE–FP), or have the
greatest program integrity implications,
would allow State Exchanges to utilize
the funds that they already allocate to
contracting with an external
independent audit entity in the most
cost-effective manner.
In § 156.280, we propose to amend
billing and premium collection
requirements related to the separate
payment requirement for abortions for
which public funding is prohibited
pursuant to section 1303 of the PPACA,
as implemented at § 156.280.
Specifically, the proposals described at
§ 156.280(e)(2) would require QHP
issuers offering non-Hyde abortion
coverage through an Exchange to send
an entirely separate monthly bill in a
separate mailing or separate electronic
communication to the policy subscriber
for only the portion of premium
attributable to non-Hyde abortion
coverage, and instruct the policy
subscriber to pay the portion of their
premium attributable to non-Hyde
abortion coverage in a separate
transaction from any payment the policy
subscriber makes for the portions of the
premium not attributable to coverage for
non-Hyde abortion services. These
proposals aim to better align the
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regulatory requirements for QHP issuer
billing of premiums with the separate
payment requirement in section 1303 of
the PPACA.
As reflected in the associated ICRs for
the proposals at § 156.280(e)(2), we
recognize that QHP issuers that cover
non-Hyde abortion services may
experience an increase in burden if
these proposals are finalized. We
anticipate that QHP issuers would need
to invest additional time and resources
to develop a separate invoice for nonHyde abortion services, separately mail
with separate postage the bill for the
portion of the premium attributable to
non-Hyde abortion coverage or
separately email or electronically send
the separate bill, as well as additional
time and resources for receipt and
processing of the separate payment
through a separate transaction as
proposed at § 156.280(e)(2). Specifically,
we anticipate QHP issuers would need
to invest time and resources to oversee
the process of sending in a separate
mailing or separate electronic
communication a complete and accurate
bill to these enrollees for the portion of
their premium attributable to that
coverage, to review for accuracy the
separate payment a policy subscriber in
a QHP covering non-Hyde abortion
sends for the portion of their premium
attributable to that coverage, and to
process separate payments, whether
made electronically or by mail. We also
anticipate that QHP issuers would need
to add functionality to their operating
systems to develop an automated
process to populate the enrollee
information on the separate bill,
transmit the separate bill in a separate
mailing or separate electronic
communication, and process the
separate payment.
Based on 2018 QHP certification data
in FFEs and SBE–FPs, 15 QHP issuers
offered a total of 111 plans with
coverage of non-Hyde abortion services
in 7 states. In SBEs, we estimate that 60
issuers offered a total of 1,000 QHPs
offering non-Hyde abortion coverage
across 10 SBEs. In total, this leads to an
estimated 75 QHP issuers offering a total
of 1,111 QHPs covering non-Hyde
abortion services across 17 states. This
rule could significantly increase the
administrative burden for QHP issuers
covering non-Hyde abortion services in
developing, sending, and processing the
separate invoices required under this
proposal.
Based on 2018 QHP Certification data
in FFEs and SBE–FPs, there were
approximately 300,000 enrollees across
the 111 QHPs covering non-Hyde
abortion coverage. In SBEs, we estimate
that there were approximately 1,000,000
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enrollees across the approximate 1,000
QHPs offering non-Hyde abortion
coverage. If finalized, these
requirements would also increase
burden on those 1,300,000 consumers,
related to paying the portion of the
premium attributable to non-Hyde
abortion services through a separate
paper check or electronic transaction;
that burden, however, is contemplated
by the specific language of section 1303
which requires a QHP issuer ‘‘to collect
from each enrollee in the plan . . . a
separate payment’’ for the coverage of
non-Hyde abortion services. In order to
develop a preliminary estimate of the
consumer cost of this proposed
provision, we assume that a policy
subscriber reading their separately
received paper or electronic bill and
writing out an additional paper check or
filling in the necessary information for
completion of a separate electronic
payment adds approximately ten
minutes per month to a policy
subscriber’s’ monthly payment process
for payment of their QHP premiums, for
a total of 2 hours per year. Based on the
May 2017 National Occupational
Employment and Wage Estimates
United States Department of Labor’s
Bureau of Labor Statistics (BLS) (https://
www.bls.gov/oes/current/oes_nat.htm),
using the listed national mean hourly
wage for the 25th percentile,16 it would
cost a policy subscriber $11.91 for an
additional hour of burden, or
approximately $1.98 for an additional
10 minutes of burden. As such, the 10
minute monthly estimated burden for
filling out a separate check or online
payment for a policy subscriber would
be $1.98, and the yearly added burden
for each policy subscriber would be
$23.76. We note that many consumers
are enrolled on the Exchange for an
average of 10 months. For those
enrollees, the annual consumer burden
would be $19.80 for a total annual
burden of $25,740,000. However, in
total for all affected enrollees in QHPs
covering non-Hyde abortion enrolled in
plans for 12 months, we estimate that it
would annually cost $30,888,000 for
policy subscribers to comply with these
proposals. This estimate excludes the
cost of consumer learning (which may
have significant upfront costs and could
also continue to be resource intensive
on an ongoing basis given the potential
confusion of consumers in receiving
multiple bills. In some cases, these may
entail costs not just to consumers but
16 The 25th percentile mean hourly wage most
closely resembles the group of consumers likely to
be affected by this proposal as most enrollees
enrolled in QHPs on the Exchange are between
100% and 400% of the federal poverty level.
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also to QHP issuers, such as in
increased volume of requests for
customer service assistance and follow
up needed to consumers to pay their full
bill). However, HHS believes that, if
finalized as proposed, the proposed
changes would better align the
regulatory requirements for QHP issuer
billing of premiums with the separate
payment requirement in section 1303 of
the PPACA. As such, HHS believes that
this outweighs the estimated consumer
burden. We solicit comments on the
impact of the proposed policy at
§ 156.280(e)(2) and on whether other
impacts should be considered or
quantified.
We request comment on both our
assessment of the need for the
regulatory action and an explanation of
how the regulatory action will meet that
need, as well as our assessment of the
potential costs and benefits of the
regulatory action. To be sure our
analysis is as accurate as possible with
respect to any additional costs to states,
issuers, or other entities, we encourage
robust comment in this area.
The RFA requires agencies to analyze
options for regulatory relief of small
entities. For purposes of the RFA, small
entities include small businesses,
nonprofit organizations, and small
governmental jurisdictions. Individuals
and states are not included in the
definition of a small entity. We are not
preparing an analysis for the RFA
because we have determined, and the
Secretary certifies, that this proposed
rule would not have a significant
economic impact on a substantial
number of small entities.
Section 202 of the Unfunded
Mandates Reform Act of 1995 also
requires that agencies assess anticipated
costs and benefits before issuing any
rule whose mandates require spending
in any 1 year of $100 million in 1995
dollars, updated annually for inflation.
In 2018, that threshold is approximately
$150 million. This rule will have no
consequential effect on state, local, or
tribal governments or on the private
sector.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a
proposed rule (and subsequent final
rule) that imposes substantial direct
requirement costs on state and local
governments, preempts state law, or
otherwise has Federalism implications.
This proposed rule does not impose
substantial direct costs on state and
local governments or preempt state law.
However, we believe the rule has
Federalism implications.
In HHS’s view, this regulation has
Federalism implications due to our
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proposal that Exchanges conduct
Medicare, Medicaid/CHIP, and, if
applicable, BHP PDM at least twice a
year, beginning with the 2020 calendar
year. However, HHS believes that the
Federalism implications are
substantially mitigated because the
proposed requirement sets only a
minimum frequency with which
Exchanges must conduct Medicare,
Medicaid/CHIP, and, if applicable, BHP
PDM, which is already required to be
conducted periodically; SBEs would
continue to have the flexibility to
conduct PDM with greater frequency.
Additionally, the proposed changes to
State Exchange oversight and reporting
requirements in § 155.1200 have
Federalism implications since those
rules would require State Exchanges to
submit certain reports to HHS and
require them to enter into contracts with
an external independent audit entity to
perform audits, and incur the associated
costs. However, HHS believes that the
Federalism implications are
substantially mitigated because the
proposed changes do not impose new
requirements on State Exchanges, but
rather add specificity to the existing
requirements.
This proposed rule is subject to the
Congressional Review Act (5 U.S.C. 801,
et seq.), which specifies that before a
rule can take effect, the federal agency
promulgating the rule shall submit to
each House of the Congress and to the
Comptroller General a report containing
a copy of the rule along with other
specified information, and has been
transmitted to the Congress and the
Comptroller General for review.
Executive Order 13771, titled
Reducing Regulation and Controlling
Regulatory Costs, was issued on January
30, 2017. Section 2(a) of Executive
Order 13771 requires an agency, unless
prohibited by law, to identify at least
two existing regulations to be repealed
when the agency publicly proposes for
notice and comment, or otherwise
promulgates, a new regulation. In
furtherance of this requirement, section
2(c) of Executive Order 13771 requires
that the new incremental costs
associated with new regulations shall, to
the extent permitted by law, be offset by
the elimination of existing costs
associated with at least two prior
regulations. OMB Guidance
Implementing Executive Order 13771
(April 5, 2017) defines a regulatory
action as (1) a significant regulatory
action as defined in section 3(f) of
Executive Order 12866, or (2) a
significant guidance document (for
example, significant interpretive
guidance) that has been reviewed by
OMB under the procedures of Executive
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56029
Order 12866 and that, when finalized, is
expected to impose total costs greater
than zero. This proposed rule, if
finalized as proposed, is expected to be
an E.O. 13771 regulatory action. Details
on the estimated costs appear in the
preceding analysis.
C. Regulatory Review Costs
If regulations impose administrative
costs on private entities, such as the
time needed to read and interpret this
proposed rule, we estimate the cost
associated with regulatory review. Due
to the uncertainty involved with
accurately quantifying the number of
entities that will review the rule, we
assume that the total number of unique
commenters on similar Exchangerelated CMS rules will be the number of
reviewers of this proposed rule. We
acknowledge this assumption may
understate or overstate the costs of
reviewing this rule. It is possible that
not all commenters will review the rule
in detail, and it is also possible that
some reviewers will chose not to
comment on the proposed rule. For
these reasons, we consider the number
of past commenters on similar CMS
rules will be a fair estimate of the
number of reviewers of this rule. We
welcome any comments on the
approach in estimating the number of
entities which will review this proposed
rule.
We recognize that different types of
entities may be affected by only certain
provisions of this proposed rule, and
therefore, for the purposes of our
estimate, we assume that each reviewer
reads approximately 50 percent of the
rule.
Using the wage information from the
Bureau of Labor and Statistics (BLS) for
medical and health service managers
(Code 11–9111), we estimate that the
cost of reviewing this rule is $107.38 per
hour, including overhead and fringe
benefits.17 We estimate that it would
take approximately 1 hour for the staff
to review the relevant portions of this
proposed rule. Based on previous and
similar CMS rules, we assume that 321
entities will review this proposed rule.
Therefore, we estimate that the total cost
of reviewing this regulation is
approximately $34,469 ($107.38 × 321
reviewers).
This may underestimate the review
costs, since not all reviewers may have
submitted comments. In addition,
stakeholders may need to do a detailed
analysis in order to implement the
unanticipated provisions of this rule
will need additional time and
personnel, which will vary depending
17 https://www.bls.gov/oes/current/oes_nat.htm.
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on the extent to which they are affected.
To estimate an upper bound, we assume
that on average 530 issuers and 50 states
will spend 10 hours each, 100 other
organizations will spend 5 hours each
and 100 individuals will spend 1 hour
each to review the rule. Under these
assumptions, total time spent reviewing
the rule would be 6,400 hours with an
estimated cost of approximately
$673,024.
In accordance with the provisions of
Executive Order 12866, this proposed
rule was reviewed by the Office of
Management and Budget.
List of Subjects
45 CFR Part 155
Administrative practice and
procedure, Advertising, Brokers,
Conflict of interests, Consumer
protection, Grants administration, Grant
programs—health, Health care, Health
insurance, Health maintenance
organizations (HMO), Health records,
Hospitals, Indians, Individuals with
disabilities, Intergovernmental relations,
Loan programs—health, Medicaid,
Organization and functions
(Government agencies), Public
assistance programs, Reporting and
recordkeeping requirements, Technical
assistance, Women and youth.
45 CFR Part 156
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Administrative practice and
procedure, Advertising, Advisory
committees, Brokers, Conflict of
interests, Consumer protection, Grant
programs—health, Grants
administration, Health care, Health
insurance, Health maintenance
organization (HMO), Health records,
Hospitals, Indians, Individuals with
disabilities, Loan programs—health,
Medicaid, Organization and functions
(Government agencies), Public
assistance programs, Reporting and
recordkeeping requirements, State and
local governments, Sunshine Act,
Technical assistance, Women, Youth.
For the reasons set forth in the
preamble, the Department of Health and
Human Services proposes to amend 45
CFR parts 155 and 156 as set forth
below:
PART 155—EXCHANGE
ESTABLISHMENT STANDARDS AND
OTHER RELATED STANDARDS
UNDER THE AFFORDABLE CARE ACT
Authority: 42 U.S.C. 18021–18024, 18031–
18033, 18041–18042, 18051, 18054, 18071,
and 18081–18083.
17:11 Nov 08, 2018
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§ 155.200
Functions of an Exchange.
*
*
*
*
*
(c) Oversight and financial integrity.
The Exchange must perform required
functions and cooperate with activities
related to oversight and financial
integrity requirements in accordance
with section 1313 of the Affordable Care
Act and as required under this part,
including overseeing its Exchange
programs, assisters, and other nonExchange entities as defined in
§ 155.260(b)(1).
*
*
*
*
*
■ 3. Section 155.330 is amended by
revising paragraph (d)(1) introductory
text and adding paragraph (d)(3) to read
as follows:
§ 155.330 Eligibility redetermination during
a benefit year
*
*
*
*
*
(d) * * *
(1) General requirement. Subject to
paragraph (d)(3) of this section, the
Exchange must periodically examine
available data sources described in
§§ 155.315(b)(1) and 155.320(b) to
identify the following changes:
*
*
*
*
*
(3) Definition of periodically.
Beginning with the 2020 calendar year,
the Exchange must perform the periodic
examination of data sources described
in paragraph (d)(1)(ii) of this section at
least twice in a calendar year. SBEs that
have implemented a fully integrated
eligibility system that determines
eligibility for advance payments of the
premium tax credit, cost-sharing
reductions, Medicaid, CHIP, and the
BHP, if a BHP is operating in the service
area of the Exchange, will be deemed in
compliance with paragraphs (d)(1)(ii)
and (d)(3) of this section.
*
*
*
*
*
■ 4. Section 155.1200 is amended by—
■ a. Revising paragraphs (b)
introductory text, (b)(1) and (2), (c)
introductory text, and (d)(2) and (3);
■ b. Redesignating (d)(4) as paragraph
(d)(5);
■ c. Adding a new paragraph (d)(4); and
■ d. Revising newly redesignated
paragraph (d)(5).
The revisions and addition read as
follows:
§ 155.1200 General program integrity and
oversight requirements.
*
1. The authority citation for part 155
is revised to read as follows:
■
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2. Section 155.200 is amended by
revising paragraph (c) to read as follows:
■
*
*
*
*
(b) Reporting. The State Exchange
must, at least annually, provide to HHS,
in a manner specified by HHS and by
applicable deadlines specified by HHS,
the following data and information:
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(1) A financial statement presented in
accordance with GAAP,
(2) Information showing compliance
with Exchange requirements under this
part 155 through submission of annual
reports,
*
*
*
*
*
(c) External audits. The State
Exchange must engage an independent
qualified auditing entity which follows
generally accepted governmental
auditing standards (GAGAS) to perform
an annual independent external
financial and programmatic audit and
must make such information available
to HHS for review. The State Exchange
must:
*
*
*
*
*
(d)* * *
(2) Compliance with subparts D and E
of this part 155, or other requirements
under this part 155 as specified by HHS;
(3) Processes and procedures designed
to prevent improper eligibility
determinations and enrollment
transactions, as applicable;
(4) Compliance with eligibility and
enrollment standards through sampling,
testing, or other equivalent auditing
procedures that demonstrate the
accuracy of eligibility determinations
and enrollment transactions; and
(5) Identification of errors that have
resulted in incorrect eligibility
determinations, as applicable.
PART 156—HEALTH INSURANCE
ISSUER STANDARDS UNDER THE
AFFORDABLE CARE ACT, INCLUDING
STANDARDS RELATED TO
EXCHANGES
5. The authority citation for part 156
is revised to read as follows:
■
Authority: 42 U.S.C. 18021–18024, 18031–
18032, 18041–18042, 18044, 18054, 18061,
18063, 18071, 18082, 26 U.S.C. 36B, and 31
U.S.C. 9701.
6. Section 156.280 is amended by —
a. Redesignating paragraph (e)(2)(ii) as
(e)(2)(iii);
■ b. Adding a new paragraph (e)(2)(ii);
and
■ c. Revising newly redesignated
paragraph (e)(2)(iii).
The revisions and addition read as
follows:
■
■
§ 156.280 Segregation of funds for
abortion services.
*
*
*
*
*
(e) * * *
(2) * * *
(ii) Send to each policy subscriber
(without regard to the policy
subscriber’s age, sex, or family status) in
the QHP separate monthly bills for each
of the amounts specified in paragraphs
(e)(2)(i)(A) and (B) of this section, and
E:\FR\FM\09NOP1.SGM
09NOP1
Federal Register / Vol. 83, No. 218 / Friday, November 9, 2018 / Proposed Rules
instruct the policy subscriber to pay
each of these amounts through separate
transactions. If the policy subscriber
fails to pay each of these amounts in a
separate transaction as instructed by the
issuer, the issuer may not terminate the
policy subscriber’s coverage on this
basis, provided the amount due is
otherwise paid.
(iii) Deposit all such separate
payments into separate allocation
accounts as provided in paragraph (e)(3)
of this section. In the case of an enrollee
whose premium for coverage under the
QHP is paid through employee payroll
deposit, the separate payments required
under paragraph (e)(2)(i) of this section
shall each be paid by a separate deposit.
*
*
*
*
*
Dated: October 11, 2018.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: October 18, 2018.
Alex M. Azar II,
Secretary, Department of Health and Human
Services.
[FR Doc. 2018–24504 Filed 11–7–18; 4:15 pm]
BILLING CODE 4120–01–P
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Parts 1 and 73
[AU Docket No. 17–329; DA 18–1038]
Auction of Cross-Service FM
Translator Construction Permits;
Comment Sought on Competitive
Bidding Procedures for Auction 100
Federal Communications
Commission.
ACTION: Proposed rule; proposed auction
procedures.
AGENCY:
The Wireless
Telecommunications and Media
Bureaus (Bureaus) announce an auction
of certain cross-service FM translator
construction permits. This document
also seeks comment on competitive
bidding procedures and proposed
minimum opening bids for Auction 100.
DATES: Comments are due on or before
November 15, 2018, and reply
comments are due on or before
November 28, 2018.
ADDRESSES: Interested parties may
submit comments in response to the
Auction 100 Comment Public Notice by
any of the following methods:
• FCC’s Website: Federal
Communications Commission’s
Electronic Comment Filing System
(ECFS): https://apps.fcc.gov/ecfs. Follow
khammond on DSK30JT082PROD with PROPOSAL
SUMMARY:
VerDate Sep<11>2014
17:11 Nov 08, 2018
Jkt 247001
the instructions for submitting
comments.
• Mail: FCC Headquarters, 445 12th
Street SW, Room TW–A325,
Washington, DC 20554.
• People with Disabilities: To request
materials in accessible formats for
people with disabilities (braille, large
print, electronic files, or audio format),
send an email to FCC504@fcc.gov or call
the Consumer & Governmental Affairs
Bureau at 202–418–0530 (voice), 202–
418–0432 (TTY). For detailed
instructions for submitting comments,
see the SUPPLEMENTARY INFORMATION
section of this document.
FOR FURTHER INFORMATION CONTACT: For
auction legal questions, Lynne Milne in
the Wireless Telecommunications
Bureau’s Auctions and Spectrum Access
Division at (202) 418–0660. For general
auction questions, the Auctions Hotline
at (717) 338–2868. For FM translator
service questions, James Bradshaw, Lisa
Scanlan or Tom Nessinger in the Media
Bureau’s Audio Division at (202) 418–
2700.
SUPPLEMENTARY INFORMATION: This is a
summary of the Auction 100 Comment
Public Notice in AU Docket No.17–329,
DA 18–1038, released on October 19,
2018. The complete text of this
document, including its attachment, is
available for public inspection and
copying from 8:00 a.m. to 4:30 p.m.
Eastern Time (ET) Monday through
Thursday or from 8:00 a.m. to 11:30 a.m.
ET on Fridays in the FCC Reference
Information Center, 445 12th Street SW,
Room CY–A257, Washington, DC 20554.
The Auction 100 Comment Public
Notice and related documents also are
available on the internet at the
Commission’s website: https://
www.fcc.gov/auction/100/, or by using
the search function for AU Docket No.
17–329 on the Commission’s ECFS web
page at https://www.fcc.gov/ecfs/.
All filings in response to the Auction
100 Comment Public Notice must refer
to AU Docket No. 17–329. The Bureaus
strongly encourage interested parties to
file comments electronically, and
request that an additional copy of all
comments and reply comments be
submitted electronically to the
following address: auction100@fcc.gov.
Electronic Filers: Comments may be
filed electronically using the internet by
accessing ECFS: https://apps.fcc.gov/
ecfs. Follow the instructions for
submitting comments.
Paper Filers: Parties who choose to
file by paper must file an original and
one copy of each filing. Filings can be
sent by hand or messenger delivery, by
commercial overnight courier or by firstclass or overnight U.S. Postal Service
PO 00000
Frm 00055
Fmt 4702
Sfmt 4702
56031
mail. All filings must be addressed to
the Commission’s Secretary, Office of
the Secretary, Federal Communications
Commission (FCC). All hand-delivered
or messenger-delivered paper filings for
the Commission’s Secretary must be
delivered to the FCC Headquarters at
445 12th Street SW, Room TW–A325,
Washington, DC 20554. The filing hours
are 8:00 a.m. to 7:00 p.m. Eastern Time
(ET). All hand deliveries must be held
together with rubber bands or fasteners.
Any envelope or box must be disposed
of before entering the building.
Commercial overnight mail (other than
U.S. Postal Service Express Mail and
Priority Mail) must be sent to 9050
Junction Drive, Annapolis Junction, MD
20701. U.S. Postal Service first-class,
Express, and Priority mail must be
addressed to 445 12th Street SW,
Washington, DC 20554.
I. Introduction
1. On December 4, 2017, the Bureaus
announced a second auction filing
window for AM broadcasters seeking
new cross-service FM translator station
construction permits. By this Public
Notice, the Bureaus seek comment on
the procedures to be used for Auction
100. Auction 100 will be a closed
auction: Only those entities listed in
Attachment A of the Auction 100
Comment Public Notice will be eligible
to participate further in Auction 100.
2. The Bureaus anticipate that the
bidding for Auction 100 will commence
in fiscal year 2019. The Bureaus will
announce a schedule for bidding in
Auction 100 by public notice, to provide
applicants with sufficient time to
submit upfront payments and prepare
for bidding in the auction.
II. Construction Permits in Auction 100
3. Auction 100 will resolve by
competitive bidding mutually exclusive
(MX) engineering proposals for
construction permits for up to 13 new
cross-service FM translator stations. The
locations and channels of these
proposed stations are identified in
Attachment A of the Auction 100
Comment Public Notice. Attachment A
also specifies a proposed minimum
opening bid and a proposed upfront
payment amount for each construction
permit listed.
4. An applicant listed in Attachment
A may become qualified to bid only if
it complies with the additional filing,
qualification, and payment
requirements, and otherwise complies
with applicable rules, policies, and
procedures. Each qualified bidder will
be eligible to bid on only those
construction permits specified for that
qualified bidder in Attachment A of the
E:\FR\FM\09NOP1.SGM
09NOP1
Agencies
[Federal Register Volume 83, Number 218 (Friday, November 9, 2018)]
[Proposed Rules]
[Pages 56015-56031]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-24504]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
45 CFR Parts 155 and 156
[CMS-9922-P]
RIN 0938-AT53
Patient Protection and Affordable Care Act; Exchange Program
Integrity
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule would revise standards relating to
oversight of Exchanges established by states, periodic data matching
frequency and authority, and the length of a consumer's authorization
for the Exchange to obtain updated tax information. This proposed rule
would also propose new requirements for certain issuers related to the
collection of a separate payment for the premium portion attributable
to coverage for certain abortion services. Many of these proposed
changes would help strengthen Exchange program integrity.
DATES: Comments: To be assured consideration, comments must be received
at one of the addresses provided below, no later than 5 p.m. on January
8, 2019.
ADDRESSES: In commenting, please refer to file code CMS-9922-P. Because
of staff and resource limitations, we cannot accept comments by
facsimile (FAX) transmission.
Comments, including mass comment submissions, must be submitted in
one of the following three ways (please choose only one of the ways
listed):
1. Electronically. You may submit electronic comments on this
regulation
[[Page 56016]]
to https://www.regulations.gov. Follow the ``Submit a comment''
instructions.
2. By regular mail. You may mail written comments to the following
address ONLY: Centers for Medicare & Medicaid Services, Department of
Health and Human Services, Attention: CMS-9922-P, P.O. Box 8016,
Baltimore, MD 21244-8010.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments to
the following address ONLY: Centers for Medicare & Medicaid Services,
Department of Health and Human Services, Attention: CMS-9922-P, Mail
Stop C4-26-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
For information on viewing public comments, see the beginning of
the SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: Emily Ames, (301) 492-4246, or
Christine Hammer, (202) 260-6089, for general information.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. We post all comments
received before the close of the comment period on the following
website as soon as possible after they have been received: https://www.regulations.gov. Follow the search instructions on that website to
view public comments.
I. Executive Summary
American Health Benefit Exchanges, or ``Exchanges'' (also called
``Marketplaces'') are entities established under the Patient Protection
and Affordable Care Act (Pub. L. 111-148), as amended by the Heath Care
and Education Reconciliation Act of 2010 (Pub. L. 111-152)
(collectively referred to as PPACA) through which qualified individuals
and qualified employers can purchase health insurance coverage.
Exchanges that were established by states (State Exchanges) include
State-based Exchanges (SBEs) which perform eligibility and enrollment
functions, as well as State-based Exchanges on the Federal platform
(SBE-FPs) that utilize the Federally-facilitated Exchange's
infrastructure to perform eligibility and enrollment functions. Many
individuals who enroll in qualified health plans (QHPs) through
individual market Exchanges are eligible to receive a premium tax
credit (PTC) to reduce their costs for health insurance premiums, and
receive reductions in required cost-sharing payments to reduce out-of-
pocket expenses for health care services. Eligible individuals can
receive the estimated amount of the PTC on an advance basis, known as
advance payments of the premium tax credit (APTC), in accordance with
section 1412 of the PPACA.
Strengthening program integrity with respect to subsidy payments in
the individual market is a top priority of this Administration. Key
areas of focus include--(1) ensuring that eligible enrollees receive
the correct amount of APTC and cost-sharing reduction (CSR) (as
applicable), and do not receive APTC or CSRs for abortion coverage and/
or services for which such payments are not available under section
1303 of the PPACA; (2) conducting effective and efficient monitoring
and oversight of State Exchanges to ensure that consumers are receiving
the correct amount of APTC and CSRs in SBEs, and that State Exchanges
are meeting the standards of federal law in a transparent manner; and
(3) protecting the interests of taxpayers, and consumers, and the
financial integrity of Federally-facilitated Exchanges (FFEs) through
oversight of health insurance issuers, including ensuring compliance
with Exchange requirements, such as maintenance of records and
participation in investigations and compliance reviews, and with the
requirements of section 1303 of the PPACA.
The Department of Health and Human Services (HHS) has recently made
significant strides in these areas. For example, we have implemented
policy-based payments in the FFEs and almost all of the SBEs, a
critical system change across Exchanges and issuers that ensures the
data used to generate APTC and CSR payments to issuers are verified and
associated with particular enrollees.
We also recently implemented pre-enrollment verification of
eligibility for applicable individual market special enrollment periods
for all Exchanges served by the federal eligibility and enrollment
platform (the HealthCare.gov platform), ensuring that only those who
qualify for special enrollment periods receive them. In the HHS Notice
of Benefit and Payment Parameters for 2019 Final Rule (83 FR 16930)
(April 17, 2018), we established a policy to require documentary
evidence for certain consumers who attest to income that is
significantly higher than the amount found in the Exchange's income
data. This new check will be conducted for applicants for whom trusted
data sources (such as the Internal Revenue Service, the Social Security
Administration, the Department of Homeland Security, Veterans Health
Administration, Peace Corps, the Department of Defense, Experian, and
Carahsoft).\1\ This new check will not be performed with respect to
non-citizen applicants who are ineligible for Medicaid based on their
immigration status, as these applicants may be statutorily eligible for
APTC with annual household income below 100 percent of the FPL. An
accurate eligibility determination is critical for consumers near this
threshold to ensure APTC is not paid on behalf of consumers who are
statutorily ineligible for APTC.
---------------------------------------------------------------------------
\1\ One criterion for eligibility for APTC is an income equal to
or greater than 100 percent but not greater than 400 percent of an
amount equal to the poverty line based on family size.
---------------------------------------------------------------------------
In late 2017, we developed an innovative approach to provide
additional notification to tax filers who, based on Internal Revenue
Service (IRS) data, had received APTC for a prior benefit year but
failed to reconcile these payments on their tax returns. The notices
explained that the tax filer was required to take action to reconcile
these prior APTC payments, or APTC associated with all enrollees for
whom the individual is the tax filer would be terminated. While HHS was
already contacting these affected households through its standard
annual notification processes, this supplemental notice provided
further clarification and instruction for the tax filer, while adhering
to IRS' protocols regarding the safe disclosure of protected federal
tax information.
We continue to explore opportunities to improve program integrity.
We work on an ongoing basis on improving program oversight and
procedures to conduct comprehensive audits of FFE processes to verify
their integrity. These efforts further our goal of protecting consumers
enrolled in FFEs and safeguarding taxpayer dollars. We review consumer
complaints and allegations of fraud and abuse received by the FFE call
center from insurers, as well as law enforcement and states.
Additionally, we analyze data to identify issues and vulnerabilities,
share relevant information with issuers, and identify administrative
actions to stop bad actors and protect consumers.
We are proposing several changes targeting these priorities. First,
we are planning changes to the current periodic data matching (PDM)
processes, which are the processes through which Exchanges periodically
examine
[[Page 56017]]
available data sources to identify changes that would affect enrollees'
eligibility for subsidies. Second, we are planning to add an optional
authorization to the Exchange application that would allow an
individual to authorize the FFE to receive Medicare eligibility and
enrollment information about the enrollee. If an applicant provides
this authorization and elects to have the Exchange automatically
terminate QHP coverage if the applicant is found to be dually enrolled,
then the FFE will end enrollees' QHP coverage on their behalf in such a
circumstance, even if the enrollee is not receiving APTC or CSRs.
Third, we propose to specify that Exchanges must conduct PDM for
Medicare, Medicaid, the Children's Health Insurance Program (CHIP), and
the Basic Health Program (BHP), if applicable, at least twice a year,
beginning with the 2020 calendar year, to ensure that Exchanges make
adequate efforts to discontinue APTC and CSR for those who are eligible
for or enrolled in other minimum essential coverage (MEC) and,
therefore, are ineligible for APTC or CSRs.
We are also proposing changes to improve program integrity related
to State Exchanges. To strengthen the mechanisms and tools HHS uses in
its oversight of compliance by State Exchanges with federal
requirements, including eligibility and enrollment requirements under
45 CFR part 155, subparts D and E, we are proposing changes that
provide further specificity to their program reporting requirements. In
addition, to ensure proper eligibility determinations and enrollments
in SBEs, we are proposing to clarify the scope of the annual
programmatic audits that SBEs are required to conduct and submit
results of annually to HHS, and include testing of SBE eligibility and
enrollment transactions in the annual programmatic audits.
Lastly, we are proposing changes related to the separate payment
requirement in section 1303 of the PPACA. To align the regulatory
requirements for issuer billing of the portion of the enrollee's
premium attributable to certain abortion services with the separate
payment requirement applicable to issuers offering coverage of these
services, we are proposing changes to the billing and payment
collection requirements for QHP issuers in connection with their plans
offered through an individual market Exchange that include coverage for
abortion services for which federal funding is prohibited.
II. Background
A. Legislative and Regulatory Overview
Sections 1311(b) and 1321(b) of the PPACA provide that each state
has the opportunity to establish an Exchange. Section 1311(b)(1) of the
PPACA gives each state the opportunity to establish an Exchange that
both facilitates the purchase of QHPs by individuals and families, and
provides for the establishment of a Small Business Health Options
Program (SHOP) that is designed to assist qualified employers in the
state who are small employers in facilitating the enrollment of their
employees in QHPs offered in the small group market in the state.
Section 1313 of the PPACA describes the steps the Secretary of
Health and Human Services (the Secretary) may take to oversee
Exchanges' compliance with HHS standards related to Title I of the
PPACA and ensure their financial integrity, including conducting
investigations and annual audits.
Section 1321(a) of the PPACA provides broad authority for the
Secretary to establish standards and regulations to implement the
statutory standards related to Exchanges, QHPs, and other standards of
title I of the PPACA.
Section 1321(c)(2) of the PPACA authorizes the Secretary to enforce
the Exchange standards using civil money penalties (CMPs) on the same
basis as detailed in section 2723(b) of the Public Health Service Act
(PHS Act). Section 2723(b) of the PHS Act authorizes the Secretary to
impose CMPs as a means of enforcing the individual and group market
reforms contained in Part A of title XXVII of the PHS Act when a state
fails to substantially enforce these provisions.
Section 1411(c) of the PPACA requires the Secretary to submit
certain information provided by applicants under section 1411(b) of the
PPACA to other federal officials for verification, including income and
family size information to the Secretary of the Treasury.
Section 1411(d) of the PPACA provides that the Secretary must
verify the accuracy of information provided by applicants under section
1411(b) of the PPACA for which section 1411(c) does not prescribe a
specific verification procedure, in such manner as the Secretary
determines appropriate.
Section 1411(f)(1)(B) of the PPACA requires the Secretary to
establish procedures to redetermine eligibility on a periodic basis, in
appropriate circumstances, including for eligibility to purchase a QHP
through the Exchange and for APTC and CSRs.
Section 1411(g) of the PPACA allows the exchange of applicant
information only for the limited purposes of, and to the extent
necessary to, ensure the efficient operation of the Exchange, including
by verifying eligibility to enroll through the Exchange and for APTC
and CSRs.
On October 30, 2013, we published a final rule entitled, ``Patient
Protection and Affordable Care Act; Program Integrity: Exchange,
Premium Stabilization Programs, and Market Standards; Amendments to the
HHS Notice of Benefit and Payment Parameters for 2014,'' (78 FR 65046),
to implement certain program integrity standards and oversight
requirements for State Exchanges.
Section 1303 of the PPACA, as implemented in 45 CFR 156.280,
specifies standards for issuers of QHPs through the Exchanges that
cover abortion services for which public funding is prohibited (also
referred to as non-Hyde abortion services). The statute and regulations
establish that, unless otherwise prohibited by state law, a QHP issuer
may elect to cover such non-Hyde abortion services. If an issuer elects
to cover such services under a QHP sold through an individual market
Exchange, the issuer must take certain steps to ensure that no PTC or
CSR funds are used to pay for abortion services for which public
funding is prohibited. One such step is that individual market Exchange
issuers must determine the amount of, and collect, from each enrollee,
a ``separate payment'' for an amount equal to the actuarial value of
the coverage for abortions for which public funding is prohibited,\2\
which must be no less than $1 per enrollee per month. QHP issuers must
also segregate funds for non-Hyde abortion services collected through
this payment into a separate allocation account used exclusively to pay
for non-Hyde abortion services.
---------------------------------------------------------------------------
\2\ Section 1303 also specifies how such actuarial value is to
be calculated.
---------------------------------------------------------------------------
In the 2012 Exchange Establishment Rule, we codified the statutory
provisions of section 1303 of the PPACA in regulation at 45 CFR
156.280. On February 27, 2015, we published the Patient Protection and
Affordable Care Act; HHS Notice of Benefit and Payment Parameters for
2016, (80 FR 10750) (herein after referred to as the 2016 Payment
Notice) providing guidance regarding acceptable billing and premium
collection methods for the portion of the consumer's total premium
attributable to non-Hyde abortion coverage for purposes of satisfying
the statutory separate payment requirement.
[[Page 56018]]
B. Stakeholder Consultation and Input
HHS has consulted with stakeholders on policies related to the
operation of Exchanges. We have held a number of listening sessions
with consumers, providers, employers, health plans, the actuarial
community, and state representatives to gather public input, with a
particular focus on risks to the individual and small group markets,
and how we can alleviate burdens facing patients and issuers. We
consulted with stakeholders through regular meetings with the National
Association of Insurance Commissioners, regular contact with State
Exchanges through the Exchange Blueprint process and ongoing oversight
and technical assistance engagements, and meetings with Tribal leaders
and representatives, health insurance issuers, trade groups, consumer
advocates, employers, and other interested parties.
III. Provisions of the Proposed Regulations
A. Exchange Establishment Standards and Other Related Standards Under
the Affordable Care Act
1. Functions of an Exchange (Sec. 155.200)
Section 155.200 of the PPACA establishes the functions that an
Exchange must perform. Section 155.200(c) of the PPACA specifies that
the Exchange must perform oversight and financial integrity functions,
specifically that the Exchange must perform required functions related
to oversight and financial integrity requirements in accordance with
section 1313 of the PPACA. HHS interprets this requirement broadly to
include program integrity functions related to protecting against
fraud, waste, and abuse, including functions not explicitly identified
in section 1313 of the PPACA. We believe SBEs have generally
interpreted this requirement broadly as well, as evidenced by their
engagement in activities designed to combat fraud and abuse related to
the Exchange.
However, questions about the breadth of this function have arisen
when Exchanges have sought to understand what uses and disclosures of
personally identifiable information (PII) are permitted under Sec.
155.260.\3\ Specifically, we have received questions about whether
Exchanges are permitted under Sec. 155.260 to disclose applicant PII
to certain entities, such as the state departments of insurance, when
investigating fraudulent behavior related to Exchange enrollments on
the part of agents and brokers. We believe that use and disclosure
related to Exchange program integrity efforts, like combatting fraud,
currently fall under Sec. 155.200(c), but believe the regulation is
not as clear as it could be. Therefore, we propose to revise Sec.
155.200(c) to clarify that the Exchanges must perform oversight
functions generally, and cooperate with oversight activities, in
accordance with section 1313 of the PPACA and as required under 45 CFR
part 155, including overseeing its Exchange programs, Navigators,
agents, brokers, and other non-Exchange entities as defined in Sec.
155.260(b). Because this change is a clarification and not a new
function, we do not believe it would impose additional burdens on State
Exchanges, but instead would help resolve questions about whether
states have the necessary tools and authority to enable them to
effectively oversee and combat potentially fraudulent behavior. We seek
comment on this proposal, including with respect to our understanding
of the potential imposition of additional burden on State Exchanges.
---------------------------------------------------------------------------
\3\ Section 155.260 limits an Exchange's use and disclosure of
PII when an Exchange creates or collects personally identifiable
information for the purposes of determining eligibility for
enrollment in a qualified health plan; determining eligibility for
other insurance affordability programs, as defined in Sec. 155.300;
or determining eligibility for exemptions from the individual shared
responsibility provisions in section 5000A of the Code. One of the
permitted uses and disclosures is for the Exchange to carry out the
functions described in Sec. 155.200.
---------------------------------------------------------------------------
2. Verification Process Related to Eligibility for Insurance
Affordability Programs (Sec. 155.320)
Currently, under Sec. 155.330, Exchanges are required to
periodically examine available data sources to identify, with respect
to enrollees on whose behalf APTC or CSRs are being paid, eligibility
or enrollment determinations for Medicare, Medicaid, CHIP, or the BHP,
if a BHP is operating in the service area of the Exchange. Individuals
identified as enrolled both in Exchange coverage with or without APTC
or CSRs and one of these other forms of coverage are referred to as
dually enrolled consumers.
If a consumer is eligible for premium-free Medicare Part A or
enrolled in Medicare Part A or Part C (also known as Medicare
Advantage), all of which qualify as MEC, he or she is not eligible to
receive APTC or CSRs to help pay for an Exchange plan or covered
services.
The Secretary has broad authority under section 1321(a) of the
PPACA to establish regulations setting standards to implement the
statutory requirements under title I of the PPACA, including with
respect to the establishment and operation of Exchanges, the offering
of QHPs through the Exchanges, the establishment of statutory
reinsurance and risk adjustment programs, and such other requirements
as the Secretary determines appropriate. Additionally, section 1411(g)
of the PPACA allows the exchange of certain applicant information as
necessary to ensure the efficient operation of the Exchange, including
verifying eligibility to enroll in coverage through the Exchange and to
receive APTC or CSRs.
Section 155.320(b)(2) specifies that the disclosure to HHS of
information regarding eligibility for and enrollment in a health plan
that is a government program, which may be considered protected health
information (PHI), is expressly authorized for the purposes of
verification of applicant eligibility for MEC as part of the
eligibility determination process for APTC or CSRs. Section
155.430(b)(1)(ii) requires an Exchange to provide an opportunity at the
time of plan selection for an enrollee to choose to remain enrolled in
a QHP if he or she becomes eligible for other MEC, or to terminate QHP
coverage if the enrollee does not choose to remain enrolled in the QHP
upon completion of the redetermination process. As such, we added
language to the existing single, streamlined application used by
Exchanges using the federal eligibility and enrollment platform to
allow consumers to authorize the Exchange to obtain eligibility and
enrollment data and, if desired, to end their QHP coverage if the
Exchange finds that the consumer has become eligible for or enrolled in
other qualifying coverage, such as Medicare, Medicaid/CHIP, or BHP,
during periodic checks.
In addition, for plan years beginning with the 2020 plan year, we
also plan to add a new authorization to the single, streamlined
application used by Exchanges using the federal eligibility and
enrollment platform, which will meet Health Insurance Portability and
Accountability Act of 1996 (HIPAA) (Pub. L. 104-191) standards
regarding how one's PHI is collected and used. This new authorization
will expand the current scope of Medicare PDM to individuals in the
Exchange population not receiving financial assistance who authorize
the FFE to conduct certain PDM for them. Specifically, this new
authorization will allow applicants or QHP enrollees, whether or not
they have applied for or are receiving APTC or CSRs, to authorize the
Exchange, when conducting Medicare PDM, to request PHI from HHS such as
their name,
[[Page 56019]]
Social Security Number, Medicare eligibility or enrollment status, and
other data elements the Exchange may determine necessary, to allow the
Exchange to determine whether the consumer is simultaneously enrolled
in Medicare and, if requested, to act on the enrollee's behalf to
terminate QHP coverage in cases of dual enrollment. We note that,
because entitlement to premium-free Medicare Part A is based on age and
information held by the Social Security Administration (that is, the
number of quarters of coverage toward a Social Security benefit under
Title II of the Act), the Exchange will not be able to identify through
this process any consumer who is eligible for premium-free Part A; we
encourage all consumers who are age 65 and older to apply with the
Social Security Administration to receive an eligibility determination
with respect to Medicare. Our adoption of this new optional
authorization to access Medicare enrollment information does not extend
to access to Medicaid, CHIP, or BHP information for applicants who are
not receiving APTC or CSRs, because these programs are targeted to
relatively lower income consumers and we would not expect to identify a
significant number of enrollees dually enrolled in one of these
programs and an unsubsidized QHP through the Exchange.
For consumers who request voluntary termination upon a finding of
dual enrollment, the Exchange would terminate coverage after following
the current PDM process outlined in Sec. 155.330(e)(2)(i), which
requires the Exchange to provide notice of the updated information the
Exchange has found and a 30-day period for the enrollee to respond. For
example, upon receiving the required notice, the enrollee could (1)
return to the Exchange and terminate his or her QHP coverage, (2)
revoke the prior authorization for the Exchange to terminate his or her
QHP coverage in the event dual enrollment is found, so that he or she
would remain enrolled both in the QHP and in Medicare, or (3) notify
the Exchange that he or she is not eligible for, or enrolled in,
Medicare. For consumers who revoke their prior authorization for the
Exchange to terminate their QHP enrollment where the Exchange finds the
enrollee is eligible for or enrolled in Medicare, or who disagree that
they are eligible for or enrolled in Medicare, the Exchange would only
proceed to terminate the enrollee's APTC and CSRs, and not his or her
enrollment in QHP coverage through the Exchange, using the process
specified in Sec. 155.330(e)(2)(i). Again, as the Exchange cannot
identify through this process those consumers who are eligible for but
not enrolled in premium-free Part A, we encourage all consumers who are
65 and older to apply with the Social Security Administration to
receive an eligibility determination with respect to Medicare.
Based on our experience performing Medicare PDM, we believe that
many consumers are inadvertently enrolled in Medicare and QHP coverage
at the same time, and that their dual enrollment does not represent an
informed decision. For example, we have found that, once consumers are
informed of the consequences of their dual enrollment, such as paying
full price for a QHP and risk for financial penalties for delaying
Medicare Part B enrollment, the majority of consumers end their QHP
coverage shortly thereafter. Furthermore, our own internal analyses
show that the majority of QHP enrollees who become dually enrolled do
so by aging into Medicare and failing to terminate the APTC or CSRs
they are receiving through the Exchange (and, if desired, their
Exchange coverage itself) during their Medicare initial enrollment
period. We believe that Exchanges should play an important role in
helping to ensure that consumers, regardless of whether the consumer
has applied for, or is receiving, APTC or CSRs through the Exchange,
are aware of their dual enrollment, the fact that their QHP coverage
may duplicate coverage available to them through Medicare at
potentially lower expense, and their potential risk for tax liability
for APTC received during months of overlapping coverage (for consumers
receiving APTC) or financial penalties (such as the Medicare Part B
late enrollment penalty if they delay enrolling in Medicare during
their initial eligibility period).
We believe these changes will support HHS's program integrity
efforts regarding the Exchanges by helping promote a balanced risk pool
for the individual market as Medicare and Medicaid/CHIP beneficiaries
tend to be higher utilizers of medical services, ensuring that
consumers are accurately determined eligible for APTC and income-based
CSRs, and safeguarding consumers against enrollment in unnecessary or
duplicative coverage. Such unnecessary or duplicative coverage, coupled
with typically higher utilization, generally results in higher premiums
across the individual market, leading to unnecessarily inflated
expenditures of federal funds on PTC for taxpayers eligible for PTC in
the individual market. We also encourage SBEs and enhanced direct
enrollment partners to adopt these changes if they are not already
using the single, streamlined application. We seek comment on these
plans.
3. Eligibility Redetermination During a Benefit Year (Sec. 155.330)
In accordance with Sec. 155.330(d), Exchanges must periodically
examine available data sources to determine whether enrollees in a QHP
through an Exchange with APTC or CSRs have been determined eligible for
or enrolled in other qualifying coverage through Medicare, Medicaid,
CHIP, or the BHP, if applicable. HHS has not previously defined
``periodically.'' Currently, FFEs conduct Medicare PDM and Medicaid/
CHIP PDM twice a year. To ensure that all Exchanges are taking adequate
steps to check for enrollees who have become eligible for or enrolled
in these other forms of MEC, and to terminate APTC and CSRs if so, we
propose to add a clearer requirement to conduct Medicare, Medicaid/
CHIP, and BHP, if applicable, periodic data matching with regular
frequency. Specifically, we propose to add paragraph (d)(3) to specify
that Exchanges conduct Medicare, Medicaid/CHIP, and BHP, if applicable,
PDM at least twice a year, beginning with the 2020 calendar year. We
believe this timeframe will give Exchanges that are not already
performing these PDM checks twice a year sufficient time to implement
any business, operational, and information technology changes needed to
comply with the proposed new requirement. Based on HHS's experience,
Exchanges should consider spacing Medicare, Medicaid/CHIP, and BHP, if
applicable, PDM checks evenly throughout the year, which we believe
would help ensure the greatest number of potentially affected enrollees
are identified and notified. Further, we do not anticipate that the
proposal--to apply Medicare PDM to those enrollees who are not
receiving APTC/CSRs but authorize the Exchange to receive Medicare
enrollment information--would add significant costs to performing
Medicare PDM. Based on HHS's experience, the dually enrolled
unsubsidized population is significantly smaller than the population
receiving APTC/CSRs. We believe this policy would likely reduce QHP
premiums and improve program integrity for all Exchanges, since
Medicare and Medicaid/CHIP beneficiaries tend to have a higher risk
profile than a typical Exchange enrollee and, therefore, may have
negative impacts on the risk pool because of the typically increased
utilization of services expected for these populations,
[[Page 56020]]
which include significant numbers of older and disabled beneficiaries
or poorer health outcomes associated with lower income statuses.\4\ As
noted above, this negative effect on the risk pool likely results in
higher premiums across the individual market, leading to increased
expenditures of federal funds on PTC for taxpayers eligible for PTC
resulting from unnecessary or duplicative coverage. So that the FFEs
and SBEs may prioritize the implementation of the proposed requirement
to conduct PDM for Medicare, Medicaid, CHIP, and BHP (if applicable)
eligibility or enrollment at least twice yearly, we are not proposing
to require Exchanges to perform PDM for death at least twice in a
calendar year. We will consider whether to require this check to be
performed at a particular frequency through future rulemaking.
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\4\ For example, see Urban Institute and Center on Society and
Health, How Are Income and Wealth Linked to Health and Longevity?
(April 2015), available at https://www.urban.org/sites/default/files/publication/49116/2000178-How-are-Income-and-Wealth-Linked-to-Health-and-Longevity.pdf.
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Since most SBEs have shared, integrated eligibility systems with
their respective Medicaid programs, Medicaid/CHIP and BHP, if
applicable, PDM requirements may be met differently for SBEs than for
the FFEs. While there is some variation among SBEs in their Medicaid/
CHIP and BHP, if applicable, PDM processes, most SBEs have implemented
fully integrated eligibility systems where the design of the system
mitigates risk of dual enrollment in, or inconsistent eligibility
results regarding, APTC/CSRs and Medicaid/CHIP and BHP, if applicable,
coverage by having one eligibility rules engine for eligibility
determinations for all these programs. In these SBEs, an individual
cannot be enrolled in both a QHP through the Exchange with APTC/CSRs,
and Medicaid/CHIP or BHP, if applicable, coverage, at any given time.
At paragraph (d)(3), we propose to specify that we will deem these SBEs
to be in compliance with the requirement to perform Medicaid/CHIP PDM
or BHP PDM, if applicable. SBEs that do not have fully integrated
eligibility systems for APTC/CSRs and Medicaid/CHIP would be required
to perform Medicaid/CHIP PDM at least twice a year. Similarly, SBEs in
states that have implemented the BHP, but where the BHP is not
integrated into the state's shared eligibility system, would be
required to perform BHP PDM at least twice a year. We anticipate most
SBEs will meet or exceed the proposed requirements for Medicaid/CHIP
PDM and BHP PDM, if applicable, based on current or planned operations
for calendar year 2018, as reported to us through the State-based
Marketplace Annual Reporting Tool and through technical assistance
engagements. Therefore, we anticipate that the proposed requirement to
conduct Medicaid/CHIP PDM and BHP PDM, if applicable, at least twice a
year would not result in a significant administrative burden for SBEs
that are not deemed to be in compliance (and no administrative burden
for those that are so deemed).
Although we believe that compliance by SBEs with these proposed
requirements is critically important for program integrity, we are not
proposing specific penalties if SBEs do not comply. However, we note
that under current authority HHS requires a SBE to take corrective
action if it is not complying with federal guidance and regulations. We
utilize specific oversight tools (SMART, programmatic audits, etc. as
described in the preamble to Sec. 155.1200) to identify issues with,
and place corrective actions on Exchanges, and provide technical
assistance and ongoing monitoring to track those actions until the
Exchange comes into compliance.
Additionally, under section 1313(a)(4) PPACA, if HHS determines
that an Exchange has engaged in serious misconduct with respect to
compliance with Exchange requirements, it has the option to rescind up
to 1 percent of payments due a state under any program administered by
HHS until it is resolved. These existing authorities would apply to the
proposed periodic data matching requirements in Sec. 155.330(d). If
HHS determines it is necessary to apply this authority due to non-
compliance by an Exchange with Sec. 155.330(d), HHS would also
determine the HHS-administered program from which it will rescind
payments that are due to that state.
Lastly, we propose to make a technical correction in Sec.
155.330(d)(1) by adding an additional reference to the process and
authority in Sec. 155.320(b). This reference was omitted previously,
but the requirements in Sec. 155.320(b), specifying that Exchanges
must verify whether an applicant is eligible for MEC other than through
an eligible employer-sponsored plan using information obtained by
transmitting identifying information specified by HHS to HHS for
verification purposes, apply to the PDM process in Sec. 155.330.
4. General Program Integrity and Oversight Requirements (Sec.
155.1200)
As section 1311 of the PPACA Exchange Establishment grant program
has come to a conclusion and State Exchanges are financially self-
sustaining, HHS has a need for strengthening the mechanisms and tools
for overseeing SBE and SBE-FP ongoing compliance with federal
requirements for Exchanges, including eligibility and enrollment
requirements under 45 CFR part 155.
HHS approves or conditionally approves a state to establish a State
Exchange (either an SBE or SBE-FP) based on an assessment of a state's
attested compliance with statutory and regulatory rules. Once approved
or conditionally approved, State Exchanges must meet specific program
integrity and oversight requirements specified at section 1313(a) of
the PPACA, Sec. Sec. 155.1200 and 155.1210. These requirements provide
HHS with the authority to oversee the Exchanges after their
establishment. Currently, annual reporting requirements for State
Exchanges at Sec. 155.1200(b) include the annual submission of: (1) A
financial statement in accordance with generally accepted accounting
principles (GAAP); (2) eligibility and enrollment reports; and (3)
performance monitoring data.
Additionally, under Sec. 155.1200(c), each State Exchange is
required to contract with an independent external auditing entity that
follows generally accepted governmental auditing standards (GAGAS) to
perform annual independent external financial and programmatic audits.
State Exchanges are required to provide HHS with the results of the
annual external audits, including corrective action plans to address
any material weaknesses or significant deficiencies identified by the
auditor. All corrective action plans are monitored by HHS until closed.
Currently, the audits must address compliance with all Exchange
requirements under 45 CFR part 155.
HHS designed and developed the State-based Marketplace Annual
Reporting Tool (SMART) in 2014 to assist Exchanges in conducting a
defined set of oversight activities. The SMART was designed to
facilitate State Exchanges' reporting to HHS on how they are meeting
federal program requirements and operational requirements set forth in
statute, regulations, and applicable guidance that implements the
statutory and regulatory requirements, including reporting compliance
with Federal eligibility and enrollment program requirements under 45
CFR 155 subparts D and E. The SMART, thus, enables HHS to evaluate and
monitor State Exchange progress in coming into compliance with federal
requirements where needed. Since then, HHS has come to utilize the
SMART, along with
[[Page 56021]]
the annual programmatic and financial audit reports, as primary
oversight tools for identifying and addressing State Exchange non-
compliance issues. HHS requires State Exchanges to take corrective
actions to address issues that are identified through the SMART and
annual programmatic and financial audits, and HHS monitors the
implementation of the corrective actions. We propose to modify Sec.
155.1200(b)(2) to reflect that HHS requires State Exchanges to submit
annual compliance reports (such as the SMART), that encompass
eligibility and enrollment reporting, but also include reporting on
compliance across other Exchange program requirements under 45 CFR part
155. We also propose to modify Sec. 155.1200(b)(1) to eliminate the
April 1st date in which states must provide a financial statement to
HHS, to provide HHS the flexibility to align the financial statement
deadline with the SMART deadline, which is set annually by HHS. Because
we are proposing to remove the April 1st date, but intend to maintain
the requirement that State Exchanges submit the required reports by a
deadline, we also propose to modify the introductory text to Sec.
155.1200(b) to specify that State Exchanges must provide the required
annual reporting by deadlines to be set by HHS.
We propose to retain the requirement at Sec. 155.1200(c) that an
annual programmatic audit be conducted by SBEs and SBE-FPs, but make a
minor change from ``state'' to ``State Exchanges'' to be consistent and
clear on the entities to which this rule applies. We also propose to
add specificity to the annual programmatic audit requirement by
proposing a clarification of Sec. 155.1200(d)(2) to make clear that
HHS may specify or target the scope of a programmatic audit to address
compliance with particular Exchange program areas or requirements. This
would provide HHS with the ability to specify those Exchange functions
that are most pertinent to a particular State Exchange model (SBE or
SBE-FP) and need to be regularly included in the audit; target those
Exchange functions most likely to impact program integrity, such as
eligibility verifications; and reduce burden on State Exchanges where
possible. In addition, we propose to modify Sec. 155.1200(d) by
replacing existing paragraph (d)(4) with new paragraphs (d)(4) and (5).
These requirements specify that SBEs must ensure that the independent
audits implement testing procedures or other auditing procedures that
assess whether an SBE is conducting accurate eligibility determinations
and enrollment transactions under 45 CFR 155 subparts D and E. Such
auditing procedures include the use of statistically valid sampling
methods in the testing or auditing procedures.
We believe these proposed changes will strengthen our programmatic
oversight and the program integrity of State Exchanges, while providing
flexibility for HHS in the collection of information. Through the
Paperwork Reduction Act (PRA) process, we are able to make updates and
refinements to the SMART reporting tool to align with our oversight and
program integrity priorities for Exchanges as they evolve. In addition,
allowing HHS to specify the scope of the programmatic audit at Sec.
155.1200(d)(2) would provide us the ability to target our oversight to
specific Exchange program requirements based on the particular State
Exchange model, our program integrity priorities, and the goal of
reducing burden on State Exchanges where possible. For instance, this
would allow the audits to focus on SBE compliance with Exchange
eligibility and enrollment requirements in 45 CFR 155 subparts D and E,
and SBE-FP compliance with Exchange requirements in 45 CFR 155 subpart
C. We believe this approach will provide HHS and states with greater
insight into SBE and SBE-FP compliance with federal standards in a more
cost-effective manner. We believe these two tools, state reporting and
independent testing, coupled with our ongoing oversight activities
would strengthen program integrity in State Exchanges.
We believe this approach would allow HHS to identify State Exchange
non-compliance issues with more precision and efficacy. It would also
allow HHS to provide more effective, targeted technical assistance to
State Exchanges in developing corrective action plans to address issues
that are identified, thus mitigating the need for more drastic or
severe enforcement actions against a State Exchange. We believe this
approach can reduce administrative burden on State Exchanges while
maintaining the traditional role of State Exchanges in managing and
operating their Exchanges, with HHS maintaining its role of overseeing
State Exchange compliance with federal requirements through structured
reporting processes. We seek comment on these proposals.
B. Health Insurance Issuer Standards Under the Affordable Care Act,
Including Standards Related to Exchanges
Segregation of Funds for Abortion Services (Sec. 156.280)
Since 1976, the Congress has included language, commonly known as
the Hyde Amendment, in the Labor, Health and Human Services, Education
and Related Agencies appropriations legislation.\5\ The Hyde Amendment
as currently in effect permits federal funds to be used for abortion
services only in the limited cases of rape, incest, or if a woman
suffers from a life-threatening physical disorder, physical injury, or
physical illness, including a life-endangering physical condition
caused by or arising from the pregnancy itself, that would, as
certified by a physician, place the woman in danger of death unless an
abortion is performed (Hyde abortion coverage). The Hyde Amendment
prohibits the use of federal funds for abortion coverage in instances
beyond those limited circumstances (non-Hyde abortion coverage).
Consistent with the Hyde Amendment, section 1303(b)(2) of the PPACA
prohibits the issuer of a QHP that includes non-Hyde abortion coverage
from using any amount attributable to PTC (including APTC) or CSRs
(including advance payments of those funds to the issuer, if any) for
abortions for which federal funds appropriated for HHS are prohibited,
``based on the law as in effect as of the date that is 6 months before
the beginning of the plan year involved.'' \6\
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\5\ Accordingly, the Hyde Amendment is not permanent Federal
law, but applies only to the extent reenacted by Congress from time
to time in appropriations legislation.
\6\ Section 1303(b)(1)(B)(I) of the PPACA.
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Section 1303 of the PPACA outlines specific accounting and notice
requirements that QHPs covering non-Hyde abortion services on the
Exchanges must follow to ensure that no federal funding is used to pay
for those services. Under section 1303(b)(2)(B) of the PPACA, as
implemented in Sec. 156.280(e)(2)(i), QHP issuers must collect a
``separate payment,'' from each enrollee in a plan ``without regard to
the enrollee's age, sex, or family status,'' for an amount equal to the
greater of the actuarial value of the coverage for abortions for which
public funding is prohibited or $1 per enrollee per month. Section
1303(b)(2)(D) of the PPACA, implemented in Sec. 156.280(e)(4),
provides that the estimation is to be determined on an average
actuarial basis and that QHP issuers may take into account the impact
on overall costs of the inclusion of such coverage, but may
[[Page 56022]]
not take into account any cost reduction estimated to result from such
services, including prenatal care, delivery, or postnatal care. Section
1303(b)(2)(D) of the PPACA as implemented in Sec. 156.280(e)(4)
further states that QHP issuers are to estimate these costs as if the
coverage were included for the entire population covered. With respect
to the ``separate payment'' requirement, if an enrollee's premium for
coverage under the plan is paid through employee payroll deposit (or
deduction) under section 1303(b)(2)(B), the separate payments ``shall
each be paid by a separate deposit.''
As mentioned above, QHP issuers that offer coverage for non-Hyde
abortion may not use APTC to pay for such coverage, or use CSR funds to
pay for such services. Pursuant to section 1303(b)(2)(D)(ii)(III) of
the PPACA, these QHP issuers may not estimate the premium attributable
to the benefit to be less than $1 per enrollee per month, regardless of
the actual cost of the benefit. Currently, in certain rare scenarios,
the FFE system allocates an amount of APTC to a policy such that the
share of the aggregate premium for which the consumer is responsible is
too low to meet this minimum standard. We intend to make system changes
for open enrollment for plan year 2019 to ensure that the minimum
premium amount of $1 per enrollee per month is assigned to all
enrollments into plans offering coverage of non-Hyde abortion, so that
issuers may separately collect this amount directly from consumers for
the portion of the total premium attributable to coverage of non-Hyde
abortion services.
Under section 1303(b)(3)(A) of the PPACA as implemented in Sec.
156.280(f), QHP issuers must provide notice to enrollees as part of the
Summary of Benefits and Coverage (SBC) at the time of enrollment if
non-Hyde abortion services are covered by the QHP. As required under
Sec. 155.205(b)(1)(ii), each Exchange must maintain an up-to-date
website that provides the SBCs. Section 147.200(a)(4) requires that
individual market QHP issuers that provide the SBC electronically must
place it in a prominent and readily accessible location on the QHP
issuer's internet website. Additionally, pursuant to section
1303(b)(2)(C) of the PPACA, as implemented at Sec. 156.280(e)(3), QHP
issuers must segregate funds for non-Hyde abortion services collected
from consumers into a separate allocation account that is to be used
exclusively to pay for non-Hyde abortion services. Thus, if a QHP
issuer disburses funds for a non-Hyde abortion on behalf of a consumer,
it must draw those funds from the segregated allocation account. The
account cannot be used for any other purpose.
Section 1303 of the PPACA and regulations at Sec. 156.280 do not
specify the method a QHP issuer must use to comply with the separate
payment requirement under section 1303(b)(2)(B)(i) of the PPACA and
Sec. 156.280(e)(2)(i). In the 2016 Payment Notice, we provided
guidance with respect to acceptable methods that a QHP issuer offering
non-Hyde abortion coverage on the individual market Exchange may use to
comply with the separate payment requirement. We stated that the QHP
issuer could satisfy the separate payment requirement in one of several
ways, including by sending the enrollee a single monthly invoice or
bill that separately itemizes the premium amount for non-Hyde abortion
services; sending the enrollee a separate monthly bill for these
services; or sending the enrollee a notice at or soon after the time of
enrollment that the monthly invoice or bill will include a separate
charge for such services and specify the charge. In the 2016 Payment
Notice, we also stated that a consumer may make the payment for non-
Hyde abortion services and the separate payment for all other services
in a single transaction. On October 6, 2017, we released a bulletin
that discussed the statutory requirements for separate payment, as well
as this previous guidance with respect to the separate payment
requirement.\7\
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\7\ CMS Bulletin Addressing Enforcement of Section 1303 of the
Patient Protection and Affordable Care Act (October 6, 2017),
available at https://www.cms.gov/CCIIO/Resources/Regulations-and-Guidance/Downloads/Section-1303-Bulletin-10-6-2017-FINAL-508.pdf.
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HHS now believes that some of the methods for billing and
collection of the separate payment for non-Hyde abortion services noted
as permissible in the preamble to the 2016 Payment Notice do not
adequately reflect what we see as Congressional intent that the QHP
issuer bill separately for two distinct (that is, ``separate'')
payments, one for the non-Hyde abortion services, and one for all other
services covered under the policy, rather than simply itemizing these
two components of a single total billed amount or notifying the
enrollee, at or soon after the time of enrollment, that the monthly
invoice or bill will include a separate charge for these services.
Although we recognize that itemizing or providing advance notice about
the amounts arguably identifies two ``separate'' amounts for two
separate purposes, we believe that the statute contemplates issuers
billing for two separate ``payments'' of these two amounts (for
example, two different checks or two distinct transactions), consistent
with the requirement on issuers in section 1303(b)(2)(B)(i) of the
PPACA to collect two separate payments. HHS, thus, believes that
requiring QHP issuers to separately bill the portion of the consumer's
premium attributable to non-Hyde abortion services and instruct
consumers to make a separate payment for this amount is a better
implementation of the statutory requirement for issuers to collect a
separate payment for these services.
As such, we are proposing an amendment at Sec. 156.280(e)(2)
relating to billing and payment of the consumer's portion of the
premium attributable to non-Hyde abortion services to reflect this
interpretation of the statute. Specifically, we are proposing that, if
these policies are finalized, as of the effective date of the final
rule, QHP issuers (1) send an entirely separate monthly bill to the
policy subscriber for only the portion of premium attributable to non-
Hyde abortion coverage, and (2) instruct the policy subscriber to pay
the portion of their premium attributable to non-Hyde abortion coverage
in a separate transaction from any payment the policy subscriber makes
for the portion of their premium not attributable to non-Hyde abortion
coverage. We believe that these proposals would better align the
regulatory requirements for QHP issuer billing of enrollee premiums
with the separate payment requirement in section 1303 of the PPACA. If
these proposals are finalized, QHP issuers would no longer be permitted
to send the enrollee a single monthly invoice or bill that separately
itemizes the premium amount for non-Hyde abortion services, or send the
enrollee a notice at or soon after the time of enrollment that the
monthly invoice or bill will include a separate charge for such
services and specify the charge in order to meet the separate payment
requirement. Instead, QHP issuers would have to send a separate bill
and instruct enrollees to send a separate payment in the manner
specified by the final rule.\8\ We invite comment on these proposals.
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\8\ We noted above the situation where, as a result of APTCs,
the out-of-pocket premium payable by the consumer is less than $1
per enrollee per month. Under this proposed rule, and to ensure
compliance with section 1303, if the QHP includes non-Hyde abortion
coverage, the QHP issuer would be required to bill the consumer at
least $1 per enrollee per month.
---------------------------------------------------------------------------
To better align the regulatory requirements for issuer billing of
enrollee premiums with the separate payment requirement in section 1303
of the PPACA, our proposal would require
[[Page 56023]]
the QHP issuer to send this separate bill in a separate mailing with
separate postage. If a QHP issuer sends bills electronically, we
propose that it provide consumers with the two bills in separate emails
or other electronic communications. We believe this approach will help
reduce consumer confusion about receiving two separate bills in a
single envelope. For example, consumers may inadvertently miss or
discard a second paper bill included in a single envelope, increasing
terminations of coverage for failure to pay premiums. The QHP issuer
would also be required to produce an invoice or bill that is distinctly
separate from the invoice or bill for the other portion of the
consumer's premium that is not attributable to non-Hyde abortion
coverage, whether in paper or electronic format. We solicit comment on
any operational issues that may arise from this aspect of the proposed
rule.
We also seek comment on ways to mitigate any possible confusion,
for example through an annual notice or standard explanatory language
on each of the two monthly bills. To meet the requirements of this new
proposal, QHP issuers would be required to instruct policy subscribers
to pay the separately billed or invoiced portion of the premium for
non-Hyde abortion coverage in a transaction separate from the
transaction for payment of the other portion of the premium that is not
attributable to non-Hyde abortion coverage and make reasonable efforts
to collect the payment separately, such as by including a separate
payment stub on each of the separately mailed bills or invoices (if
sent on paper) or providing a separate payment link in the separate
email or electronic communication with a separate payment field on the
payment web page for each separate payment to be collected (if sending
an electronic bill, or accepting electronic payments regardless of how
the bills were transmitted). Under this proposal, consumer non-payment
of any premium due (including non-payment of the portion of the
consumer's premium attributable to non-Hyde abortion coverage) would
continue to be subject to state and federal rules regarding grace
periods. In the event that a policy subscriber does not follow the
separate payment instructions, however, and pays the entire premium in
a single transaction (both the portion attributable to non-Hyde
abortion coverage, as well as the portion attributable to coverage for
other services), the QHP issuer would not be permitted to refuse to
accept such a combined payment on the basis that the policy subscriber
did not send two checks as requested by the QHP issuer, and to then
terminate the policy, subject to any applicable grace period, for non-
payment of premiums. We believe that potential loss of coverage would
be an unreasonable result of a consumer paying in full but failing to
adhere to the QHP issuer's requested payment procedure. Under our new
interpretation, a QHP issuer would thus be required to accept a
combined payment, to the extent necessary to avoid this result.
QHP issuers that do receive combined consumer premiums covering the
portion attributable to non-Hyde abortion coverage as well as the
portion attributable to coverage for other services in one single
payment would treat the portion of the premium attributable to non-Hyde
abortion services as a separate payment for which the QHP issuer would
be expected to disaggregate into the separate allocation account used
solely for these services. We would expect the QHP issuer in this
scenario to again explain to the consumer the separate payment
requirement in the law, and take steps to inform the consumer not
complying with this policy that he or she should do so in future
months, including documentation of such outreach and educational
efforts. Again, if the consumer still declines to do so, however, the
combined payment must be accepted to avoid a loss of coverage.
Likewise, QHP issuers would not be permitted to refuse to accept
separate premium payments paid to the issuer in a single return
envelope (for example, two separate checks returned to the issuer in a
single return envelope) on the basis that the consumer did not
separately return each premium payment in a separate mailing. We seek
comment on these proposals.
We are also proposing a technical change, to Section
156.280(e)(2)(iii) as redesignated, to insert appropriate cross
reference to the explanation of the separate payments.
Consistent with Sec. 156.715, HHS has broad authority to perform
compliance reviews to monitor FFE issuer compliance. HHS conducts
compliance reviews throughout the year, and issuer notification of
selection for a review may occur at any time during the year. Detailed
examples of regulatory and operational areas that will be reviewed are
included in the Key Priorities for FFM Compliance Review, which is
updated each year with new key oversight priorities.\9\ Consistent with
this authority, we propose updating our compliance reviews governing
QHP certification to include new reviews of FFE issuer compliance with
Sec. 156.280, including the segregation of funds requirement and the
new proposals for separate billing of the portion of the consumer's
premium attributable to coverage of non-Hyde abortion services as
specified in this rule. FFE issuers subject to these compliance reviews
should maintain all documents and records of compliance with section
1303 of the PPACA and these requirements in accordance with Sec.
156.705, and should anticipate making available to HHS the types of
records specified at Sec. 156.715(b) that would be necessary to
establish their compliance with these requirements. For example, FFE
issuers subject to compliance reviews for Sec. 156.280 should
anticipate supplying HHS with documentation of their estimate of the
basic per enrollee per month cost, determined on an average actuarial
basis, for coverage of non-Hyde abortion services; detailed invoice and
billing records demonstrating they are separately billing in a separate
mailing or separate electronic communication and collecting the portion
of the premium attributable to coverage of non-Hyde abortion services
as specified in this rule; and appropriately segregating the funds
collected from consumers into a separate allocation account that is
used exclusively to pay for non-Hyde abortion services. We believe the
addition of these compliance reviews will help to address remaining
issuer compliance issues, if any, previously identified by the 2014
U.S. Government Accountability Office report.\10\ We seek comment on
this proposal.
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\9\ CCIIO Examinations, Audits and Reviews of Issuers: Issuer
Resources, available at https://www.cms.gov/CCIIO/Resources/Forms-Reports-and-Other-Resources/Exams_Audits_Reviews_Issuer_Resources-.html.
\10\ U.S. Government Accountability Office, ``Health Insurance
Exchanges: Coverage of Non-excepted Abortion Services by Qualified
Health Plans,'' (Sept. 15, 2014), available at https://www.gao.gov/products/GAO-14-742R.
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As is the case with many provisions in the PPACA, states are the
entities primarily responsible for implementing and enforcing the
provisions in section 1303 of the PPACA related to individual market
QHP coverage of non-Hyde abortion services. Section 1303(b)(2)(E)(i) of
the PPACA, as implemented at Sec. 156.280(e)(5), designates the state
insurance commissioners as the entities responsible for monitoring,
overseeing, and enforcing the provisions in section 1303 of the PPACA
related to QHP segregation of funds for non-Hyde abortion services.
However, as stated in
[[Page 56024]]
2017 guidance,\11\ where we are charged with directly enforcing these
statutory requirements in the FFEs, we intend to do so fully in
instances of issuer non-compliance. We call upon states that operate
their own Exchanges to fully enforce these requirements as codified in
the federal regulations governing the Exchanges. To the extent such a
state operating its own Exchange fails to substantially enforce these
requirements, HHS would expect to enforce them in the state's place.
However, as states remain the primary enforcers of these requirements,
we propose that HHS involvement in enforcement would be limited to
ensuring that federal funds are appropriately managed. For example, HHS
enforcement would be limited to instances where it becomes clear that
the state department of insurance is not overseeing the requirement for
the QHP issuer to determine the actuarial value of the coverage of non-
Hyde abortions, to separately bill (and collect) premium of at least $1
per enrollee per month for such coverage, or to segregate funds
effectively; a state department of insurance or other entity notifies
HHS of suspected misuse of federal funding for coverage of non-Hyde
abortion services; or the state's enforcement actions are inadequate
and fail to result in compliance from the QHP issuer. The Office of
Personnel Management may issue guidance related to these provisions for
multi-state plan issuers.\12\
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\11\ CMS Bulletin Addressing Enforcement of Section 1303 of the
Patient Protection and Affordable Care Act (October 6, 2017),
available at https://www.cms.gov/CCIIO/Resources/Regulations-and-Guidance/Downloads/Section-1303-Bulletin-10-6-2017-FINAL-508.pdf.
\12\ Section 1334(a)(6) of the PPACA requires that at least one
multi-state plan in each Exchange excludes coverage of non-Hyde
abortion services. Currently, no multi-state plan options cover non-
Hyde abortion services. See OPM's Frequently Asked Questions:
Insurance, available at https://www.opm.gov/faqs/QA.aspx?fid=fd635746-de0a-4dd7-997d-b5706a0fd8d2&pid=8313a65b-c5b8-4d58-a58f-9d81f26856a2.
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We remind issuers that pursuant to Sec. 156.280(e)(5)(ii), any
issuer offering coverage of non-Hyde abortions services on the Exchange
must submit a plan to its state department of insurance that details
the issuer's process and methodology for meeting the requirements of
section 1303(b)(2)(C), (D), and (E) of the PPACA (hereinafter,
``separation plan'') to the state health insurance commissioner. The
separation plan should describe the QHP issuer's financial accounting
systems, including appropriate accounting documentation and internal
controls, that would ensure the segregation of funds required by
section 1303(b)(2)(C), (D), and (E) of the PPACA. Issuers should refer
to Sec. 156.280(e)(5)(ii) for more information on precisely what
issuers should include in their separation plans to demonstrate
compliance with these requirements.
As mentioned previously, consistent with HHS's authority under
Sec. 156.715, we propose monitoring FFE issuer compliance with the
requirements under Sec. 156.280 by requiring QHP issuers in FFEs to
show documentation of compliance with the requirement to estimate the
basic per enrollee per month cost, determined on an average actuarial
basis, for coverage of non-Hyde abortion services and charge at least
$1 per enrollee per month for such coverage, as well as with the
segregation of funds requirements when undergoing compliance reviews,
including detailed records and documentation demonstrating compliance
with the separate billing (including mailing, as applicable) and
collection requirements proposed in this rule, as well as the
segregation of funds requirements. We also remind issuers offering
medical QHPs in the FFEs that they must already attest to adhering to
all applicable requirements of 45 CFR part 156 as part of the QHP
certification application, including those requirements related to the
segregation of funds for abortion services implemented in Sec.
156.280.\13\ If the separate billing and premium collection proposals
at Sec. 156.280(e)(2) are finalized as proposed, issuers in the FFE
completing this attestation would also attest to adhering to these new
separate billing and collection requirements. As part of the QHP
certification process, issuers in states with FFEs where the States
perform plan management functions must also complete similar program
attestations attesting to adherence with Sec. 156.280.\14\ Issuers in
states with SBEs that offer QHPs including non-Hyde abortion coverage
should contact their state for attestation requirements as part of the
QHP certification process.
---------------------------------------------------------------------------
\13\ 2019 Qualified Health Plan Issuer Application Instructions,
available at: https://www.qhpcertification.cms.gov/s/2019QHPInstructionsVersion1.pdf?v=1.
\14\ State Partnership Exchange Issuer Program Attestation
Response Form, available at: https://www.qhpcertification.cms.gov/s/SuppDoc_SPE_Attestationsed._revised_508.pdf?v=1.
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We seek comment on these proposals.
IV. Collection of Information Requirements
Under the Paperwork Reduction Act of 1995 (PRA), we are required to
provide 60-day notice in the Federal Register and solicit public
comment before a collection of information requirement is submitted to
the Office of Management and Budget (OMB) for review and approval. This
proposed rule contains information collection requirements (ICRs) that
are subject to review by OMB. A description of these provisions is
given in the following paragraphs.
In order to fairly evaluate whether an information collection
should be approved by OMB, section 3506(c)(2)(A) of the PRA requires
that we solicit comment on the following issues:
The need for the information collection and its usefulness
in carrying out the proper functions of our agency.
The accuracy of our estimate of the information collection
burden.
The quality, utility, and clarity of the information to be
collected.
Recommendations to minimize the information collection
burden on the affected public, including automated collection
techniques.
We are soliciting public comment on each of these issues for the
following sections of this document that contain ICRs:
A. ICRs Regarding General Program Integrity and Oversight Requirements
(Sec. 155.1200)
The burden associated with State Exchanges meeting the proposed
program integrity reporting requirements in Sec. 155.1200 have already
been assessed and encompassed through SMART currently approved under
OMB control number: 0938-1244 (CMS-10507). This proposed rule does not
impose any new burden or add any additional requirements to the
existing collection.
B. ICRs Regarding Segregation of Funds for Abortion Services (Sec.
156.280)
In the preamble to Sec. 156.280, we explain that the proposals to
require separate issuer billing for, and collection of, the portion of
the premium attributable to non-Hyde abortion coverage would be subject
to future HHS compliance reviews of FFE issuers, requiring issuers in
the FFE to maintain and submit records showing compliance with these
requirements to HHS. We have determined that the requirements
associated with compliance reviews have already been assessed and
encompassed by the Program Integrity: Exchange, Premium Stabilization
Programs, and Market Standards; Amendments to the HHS Notice of Benefit
and Payment Parameters for 2014; Final Rule II ICR currently approved
under OMB control number: 0938-1277 (CMS-10516).
To show compliance with FFE standards and program requirements, all
[[Page 56025]]
issuers seeking QHP certification in FFE states are required to submit
responses to program attestations as part of their QHP application.
This response already includes an attestation that the issuer agrees to
adhere to the requirements related to the segregation of funds for
abortion services implemented in Sec. 156.280. We have determined that
the requirements associated with QHP certification have already been
assessed and encompassed by the Establishment of Exchanges and
Qualified Health Plans; Exchange Standard for Employers approved under
OMB control number 0938-1187 (CMS-10433). Therefore, proposed Sec.
156.280(e)(2) adds no new ICRs as it relates to program attestations.
In Sec. 156.280(e)(2), we propose that QHP issuers must send an
entirely separate monthly bill in a separate mailing or separate
electronic communication to the policy subscriber for only the portion
of premium attributable to non-Hyde abortion coverage, and instruct the
policy subscriber to pay the portion of their premium attributable to
non-Hyde abortion coverage in a separate transaction from any payment
the policy subscriber makes for the portion of their premium not
attributable to non-Hyde abortion coverage. Based on 2018 QHP
certification data in the FFEs and SBE-FPs, we estimate that 15 QHP
issuers offered a total of 111 plans with coverage of non-Hyde abortion
services in 7 States. In SBEs, we estimate that 60 QHP issuers offered
a total of approximately 1,000 plans offering this coverage across 10
SBEs. In total, this leads to an estimated 75 QHP issuers offering a
total of 1,111 plans covering non-Hyde abortion services across 17
states. As such, the ICRs associated with these proposals would create
a new burden on QHP issuers and plans and are subject to the Paperwork
Reduction Act. Salaries for the positions cited below were taken from
the May 2017 National Occupational Employment and Wage Estimates United
States Department of Labor's Bureau of Labor Statistics (BLS) (https://www.bls.gov/oes/current/oes_nat.htm) based on the listed national
median hourly wage. All wages on the following pages are inflated by
100 percent to account for the cost of fringe benefits and overhead
costs.
We anticipate that populating the enrollee information on the
separate electronic or paper bill, transmitting the separate electronic
or paper bill in a separate mailing or separate electronic
communication, and processing the enrollee's separate electronic or
mailed payment, will be an automated process that occurs monthly after
a computer programmer adds this functionality to the QHP issuer's
billing and payment operating system. We estimate that, on a one-time
basis, a computer programmer will require 10 hours to add this
functionality to an affected QHP issuer's systems (at a rate of $84.16
per hour) for a total burden of 10 hours. We estimate that this will
result in a one-time cost of $841.60 per QHP issuer that offers plans
that cover non-Hyde abortion services to meet this reporting
requirement. This would be a one-time cost, such that the overall
burden for all 75 QHP issuers would be 750 hours, with an associated
total cost of $63,120.
Because an estimated 75 QHP issuers offered a total of 1,111 plans
with coverage of non-Hyde abortion services across 17 states, we
estimate that the total number of QHP issuers that offer plans with
coverage of non-Hyde abortion, for which they would be required to send
separate bills in a separate mailing or separate electronic
communication and collect separate payments as proposed at Sec.
156.280(e)(2), would be 75 per year, for a total one-time burden of 750
hours. Below is the estimate of the burden imposed on a single QHP
issuer subject to the reporting requirements of this rule. The
aggregate burden for 3 years will be same as for 1 year: $841.60 per
respondent and $63,120 for all respondents.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Wage rate (p/ Total annual Total one-time
Burden per hr) including burden per Labor cost of cost for all
Labor category Respondents Responses response 100% fringe response one-time respondents
(hours) benefits (hours) reporting ($) ($)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Computer programmer to add automated 75 75 10 $42.08 10 $841.60 $63,120
billing & payment processing
functionality..........................
---------------------------------------------------------------------------------------------------------------
Total............................... 75 75 10 42.08 10 841.60 63,120
--------------------------------------------------------------------------------------------------------------------------------------------------------
Although we anticipate that populating the enrollee information on
the separate electronic or paper bill and transmitting that bill in a
separate mailing or separate electronic communication would be an
automated process, we estimate that a general office clerk working for
an affected QHP issuer would require 2 hours monthly (at a rate of
$30.28 per hour) per plan to determine which enrollees are enrolled in
plans that cover non-Hyde abortion and to oversee the process of
sending a separately packaged complete and accurate bill in a separate
mailing or separate electronic communication to these enrollees for the
portion of their premium attributable to that coverage, for an annual
burden of 24 hours. This estimate includes the amount of time the
office clerk would spend determining which enrollees prefer paper
billing versus electronic billing, and ensuring that the bills are
complete and accurate and are being sent in a separate mailing or
separate electronic communication. We estimate that it would cost
$726.72 annually per plan that covers non-Hyde abortion services to
meet the reporting requirement, with a total annual burden for all
1,111 plans of 26,664 hours and an associated total annual cost of
$807,385.92.
We similarly anticipate that processing the payment made by
enrollees for this portion of their premium would be an automated
process. However, we estimate that a general office clerk working for
an affected QHP issuer would require 2 hours monthly (at a rate of
$30.28 per hour) per plan to review for accuracy the separate payment
an enrollee in a plan covering non-Hyde abortion services sends for the
portion of their premium attributable to that coverage and to process
any payments or paper checks made by enrollees through the mail, for an
annual burden of 24 hours. This estimate includes the amount of
additional time the office clerk would need to spend reviewing for
accuracy the separate payments returned in separate mailings from the
payments received for the portion of the policy subscriber's premium
not attributable to non-Hyde abortion. We estimate that it would cost
$726.72 annually per plan that covers non-Hyde abortion services to
meet the reporting requirement, with a total annual burden for all
1,111 plans
[[Page 56026]]
of 26,664 hours and an associated total cost of $807,385.92.
As such, we estimate that the total number of plans for which QHP
issuers would need to send separate bills in a separate mailing or
separate electronic communication and collect separate payments as
proposed at Sec. 156.280(e)(2) would be 1,111 per year, for a total
burden of 53,328 hours to meet these reporting requirements per year.
Below is the estimate of the burden imposed on a single plan subject to
the reporting requirements of this rule. The aggregate burden for 3
years will be $4,360.32 per respondent and $4,844,315.52 for all
respondents.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total annual Wage rate (p/ Total annual
Burden per burden per hr) including Labor cost of cost for all
Labor category Respondents Responses response response 100% fringe reporting respondents
(hours) (hours) benefits annually ($) ($)
--------------------------------------------------------------------------------------------------------------------------------------------------------
General office clerk for preparing and 1,111 1,111 2 24 $30.28 $726.72 $807,385.92
sending the bill.......................
General office clerk for receiving and 1,111 1,111 2 24 30.28 726.72 807,385.92
processing the separate payment........
---------------------------------------------------------------------------------------------------------------
Total............................... 2,222 2,222 4 48 60.56 1,453.44 1,614,771.84
--------------------------------------------------------------------------------------------------------------------------------------------------------
C. Submission of PRA-Related Comments
We have submitted a copy of this proposed rule to OMB for its
review of the rule's information collection and recordkeeping
requirements. The requirements are not effective until they have been
approved by OMB.
We invite public comments on these information collection
requirements. If you wish to comment, please identify the rule (CMS-
9922-P) and, where applicable, the ICR's CFR citation, CMS ID number,
and OMB control number.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS's website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to [email protected].
3. Call the Reports Clearance Office at (410) 786-1326.
See this rule's DATES and ADDRESSES sections for the comment due
date and for additional instructions.
V. Response to Comments
Because of the large number of public comments we normally receive
on Federal Register documents, we are not able to acknowledge or
respond to them individually. We will consider all comments we receive
by the date and time specified in the DATES section of this preamble,
and, when we proceed with a subsequent document, we will respond to the
comments in the preamble to that document.
VI. Regulatory Impact Statement
We have examined the impact of this rule as required by Executive
Order 12866 on Regulatory Planning and Review (September 30, 1993),
Executive Order 13563 on Improving Regulation and Regulatory Review
(January 18, 2011), the Regulatory Flexibility Act (RFA) (September 19,
1980, Pub. L. 96-354), section 1102(b) of the Social Security Act,
section 202 of the Unfunded Mandates Reform Act of 1995 (March 22,
1995; Pub. L. 104-4), Executive Order 13132 on Federalism (August 4,
1999), the Congressional Review Act (5 U.S.C. 804(2)), and Executive
Order 13771 on Reducing Regulation and Controlling Regulatory Costs
(January 30, 2017).
Executive Orders 12866 and 13563 direct agencies to assess all
costs and benefits of available regulatory alternatives and, if
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, distributive impacts, and equity).
Section 3(f) of Executive Order 12866 defines a ``significant
regulatory action'' as an action that is likely to result in a
regulation: (1) Having an annual effect on the economy of $100 million
or more in any 1 year, or adversely and materially affecting a sector
of the economy, productivity, competition, jobs, the environment,
public health or safety, or state, local, or tribal governments or
communities (also referred to as ``economically significant''); (2)
creating a serious inconsistency or otherwise interfering with an
action taken or planned by another agency; (3) materially altering the
budgetary impacts of entitlement grants, user fees, or loan programs or
the rights and obligations of recipients thereof; or (4) raising novel
legal or policy issues arising out of legal mandates, the President's
priorities, or the principles set forth in the Executive Order.
A regulatory impact analysis must be prepared for major rules with
economically significant effects ($100 million or more in any 1 year),
and an ``economically significant'' regulatory action is subject to
review by the Office of Management and Budget (OMB). As discussed below
regarding their anticipated effects, these proposals are not likely to
have economic impacts of $100 million or more in any 1 year, and
therefore do not meet the definition of ``economically significant''
under Executive Order 12866. However, OMB has determined that the
actions are significant within the meaning of section 3(f)(4) of the
Executive Order. Therefore, OMB has reviewed these final rules and the
Departments have provided the following assessment of their impact.
A. Need for Regulatory Action
HHS is committed to promoting program integrity throughout its
programs to ensure that federal statutory requirements are met and
federal monies are not being inappropriately spent. Ensuring that
consumers receive the correct amount of APTC and CSRs at the time of
enrollment or re-enrollment is a top priority for us, and necessitates
regulatory action. Accurate and up-to-date eligibility determinations
help reduce the possibility that an individual or family is paying a
premium amount that is either higher or lower than they should have to,
the latter of which could result in the individual or family needing to
pay a large amount back to the federal
[[Page 56027]]
Treasury on their federal income tax returns. We propose a number of
changes in this rule to help mitigate the risk of federal dollars
incorrectly leaving the federal Treasury in the form of APTC during the
year. To further improve program integrity and ensure that individuals
receiving APTC/CSRs are appropriately enrolled in insurance
affordability programs, we are also proposing to specify that Exchanges
must conduct Medicare PDM, Medicaid/CHIP PDM, and BHP PDM, if
applicable, pursuant to Sec. 155.330(d)(1)(ii), at least twice a year
beginning with the 2020 calendar year. We also believe this policy
would likely reduce QHP premiums and improve program integrity for all
Exchanges, since Medicare and Medicaid/CHIP beneficiaries tend to have
a higher risk profile than a typical Exchange enrollee and, therefore,
may have negative impacts on the risk pool because of the typically
increased utilization of services expected for these populations, which
include significant numbers of older and disabled beneficiaries or
poorer health outcomes associated with lower income statuses.\15\ As
noted above, this negative effect on the risk pool results in higher
premiums across the individual market, leading to increased
expenditures of federal funds on PTC for taxpayers eligible for PTC
resulting from duplicative coverage.
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\15\ For example, see Urban Institute and Center on Society and
Health, How Are Income and Wealth Linked to Health and Longevity?
(April 2015), available at https://www.urban.org/sites/default/files/publication/49116/2000178-How-are-Income-and-Wealth-Linked-to-Health-and-Longevity.pdf.
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As part of our efforts to strengthen program integrity with respect
to subsidy payments in the individual market, we also believe
improvements should be made to our ability to conduct effective and
efficient oversight of State Exchanges to ensure consumers receive the
correct amount of APTC and CSRs (as applicable). As section 1311 of the
PPACA Exchange Establishment grant program has come to a conclusion and
State Exchanges are financially self-sustaining, HHS has a need to
strengthen the mechanisms and tools for overseeing ongoing compliance
by State Exchanges with federal program requirements, including
eligibility and enrollment requirements under 45 CFR part 155. For
these reasons, we are proposing to add specificity to the reporting
requirements for State Exchanges at Sec. 155.1200 to focus on
activities that speak to compliance with Exchange program requirements,
including eligibility and enrollment requirements. We are also
proposing changes at Sec. 155.1200 to clarify the scope of annual
programmatic audits that State Exchanges are required to conduct, and
include new requirements that focus on ensuring proper eligibility
determinations and enrollments in SBEs. It is our intent that these
changes would enable us to better identify and address State Exchange
non-compliance issues.
HHS believes that some of the methods for billing and collection of
the separate payment for non-Hyde abortion services noted as
permissible in the preamble to the 2016 Payment Notice do not
adequately reflect what we see as Congressional intent that the QHP
issuer bill separately for two distinct (that is, ``separate'')
payments as required by section 1303 of the PPACA. To remedy this, we
are proposing at Sec. 156.280(e)(2) that: (1) QHP issuers send an
entirely separate monthly bill to the policy subscriber for only the
portion of premium attributable to non-Hyde abortion coverage, and (2)
instruct the policy subscriber to pay the portion of their premium
attributable to non-Hyde abortion coverage in a separate transaction
from any payment the policy subscriber makes for the portion of their
premium not attributable to non-Hyde abortion coverage. We believe that
these proposals are necessary to better align the regulatory
requirements for QHP issuer billing of enrollee premiums with the
separate payment requirement in section 1303 of the PPACA. HHS believes
that requiring QHP issuers to separately bill the portion of the policy
subscriber's premium attributable to non-Hyde abortion services and
instruct policy subscribers to make a separate payment for this amount
is a better interpretation of, and would result in greater compliance
with this interpretation of, the statutory requirement for QHP issuers
to collect a separate payment for these services.
B. Anticipated Effects
Revising Sec. 155.200(c) to clarify that the Exchanges must
perform oversight functions or cooperate with activities related to
oversight and financial integrity requirements is a clarification and
not a new function. Therefore, it would not impose additional burdens
on State Exchanges.
Our proposal that Exchanges conduct Medicare PDM, Medicaid/CHIP
PDM, and BHP PDM, if applicable, at least twice a year beginning with
the 2020 calendar year, merely adds specificity to the existing
requirement that Exchanges must periodically examine available data
sources to determine whether Exchange enrollees have been determined
eligible for or enrolled in other qualifying coverage such as Medicare,
Medicaid, CHIP, or the BHP, if applicable. Therefore, we expect the
costs associated with this proposal to be minimal. However, SBEs that
are not already conducting PDM with the frequency proposed, or deemed
in compliance with the Medicaid, CHIP, and BHP (where applicable) PDM
requirements, would likely be required to engage in IT system
development activity in order to communicate with these programs and
act on enrollment data either in a new way, or in the same way more
frequently. Thus, there may be additional associated administrative
cost for these SBEs to implement the proposed PDM requirements. We
anticipate a majority (about eight) of the twelve SBEs would be exempt
from the requirement to perform Medicaid, CHIP, and BHP (where
applicable) PDM because they have shared, integrated eligibility
systems, as they would be deemed in compliance with this requirement.
However, at this point we are not able to confirm the exact number
because we have not yet set specific criteria and process to assess and
confirm which SBEs would be exempt, and would need additional
operational information from SBEs to confirm our assessment. We would
establish and engage in that process after finalization of the rule.
For an SBE not already conducting Medicare, Medicaid/CHIP, and BHP PDM
at least twice a year, and that does not already have a shared,
integrated eligibility system with its respective Medicaid/CHIP, and
BHP (where applicable) programs, we estimate that it would cost
approximately $1,740,000 per SBE to build such capabilities in their
system. These costs would be incurred by the SBE as they are required
to be financially self-sustaining and do not receive federal funding
for their establishment or operational activities.
We believe these changes will support HHS's program integrity
efforts regarding the Exchanges by helping promote a balanced risk pool
for the individual market as Medicare and Medicaid/CHIP beneficiaries
tend to be higher utilizers of medical services, ensuring that
consumers are accurately determined eligible for APTC and income-based
CSRs, and safeguarding consumers against enrollment in unnecessary or
duplicative coverage. Such unnecessary or duplicative coverage, coupled
with typically higher utilization, generally results in higher premiums
across the individual market, leading to unnecessarily inflated
expenditures of federal funds on PTC for taxpayers eligible for PTC in
the individual market.
[[Page 56028]]
We expect our plan to permit HHS to verify applicant eligibility
for or enrollment in MEC in order for HHS to perform the periodic
checks required under Sec. 155.330(d) for those consumers who provide
consent to the Exchange to obtain their eligibility and enrollment
data, and, if desired, to end their QHP coverage if found dually
enrolled in other qualifying coverage, to have minimal economic impact.
Based on HHS's experience, the dually enrolled unsubsidized population
is significantly smaller than those receiving APTC or CSRs. This plan
would help expand the scope of the population that is part of Medicare
PDM, rather than adding new Exchange requirements.
We do not anticipate the proposed changes to Sec. 155.1200 will
result in any additional cost for the State Exchanges because the
changes leverage an existing reporting mechanism, the annual State
Based Marketplace Reporting Tool, for meeting eligibility and
enrollment reporting requirements in Sec. 155.1200(b). Additionally,
State Exchanges are already required to annually contract with, and
budget accordingly for, an external independent audit entity to perform
an annual financial and programmatic audit as required under Sec.
155.1200(c). We believe the proposed requirement that HHS be able to
specify the scope of annual programmatic audits to focus on the program
areas that are most pertinent to a State Exchange model (SBE or SBE-
FP), or have the greatest program integrity implications, would allow
State Exchanges to utilize the funds that they already allocate to
contracting with an external independent audit entity in the most cost-
effective manner.
In Sec. 156.280, we propose to amend billing and premium
collection requirements related to the separate payment requirement for
abortions for which public funding is prohibited pursuant to section
1303 of the PPACA, as implemented at Sec. 156.280. Specifically, the
proposals described at Sec. 156.280(e)(2) would require QHP issuers
offering non-Hyde abortion coverage through an Exchange to send an
entirely separate monthly bill in a separate mailing or separate
electronic communication to the policy subscriber for only the portion
of premium attributable to non-Hyde abortion coverage, and instruct the
policy subscriber to pay the portion of their premium attributable to
non-Hyde abortion coverage in a separate transaction from any payment
the policy subscriber makes for the portions of the premium not
attributable to coverage for non-Hyde abortion services. These
proposals aim to better align the regulatory requirements for QHP
issuer billing of premiums with the separate payment requirement in
section 1303 of the PPACA.
As reflected in the associated ICRs for the proposals at Sec.
156.280(e)(2), we recognize that QHP issuers that cover non-Hyde
abortion services may experience an increase in burden if these
proposals are finalized. We anticipate that QHP issuers would need to
invest additional time and resources to develop a separate invoice for
non-Hyde abortion services, separately mail with separate postage the
bill for the portion of the premium attributable to non-Hyde abortion
coverage or separately email or electronically send the separate bill,
as well as additional time and resources for receipt and processing of
the separate payment through a separate transaction as proposed at
Sec. 156.280(e)(2). Specifically, we anticipate QHP issuers would need
to invest time and resources to oversee the process of sending in a
separate mailing or separate electronic communication a complete and
accurate bill to these enrollees for the portion of their premium
attributable to that coverage, to review for accuracy the separate
payment a policy subscriber in a QHP covering non-Hyde abortion sends
for the portion of their premium attributable to that coverage, and to
process separate payments, whether made electronically or by mail. We
also anticipate that QHP issuers would need to add functionality to
their operating systems to develop an automated process to populate the
enrollee information on the separate bill, transmit the separate bill
in a separate mailing or separate electronic communication, and process
the separate payment.
Based on 2018 QHP certification data in FFEs and SBE-FPs, 15 QHP
issuers offered a total of 111 plans with coverage of non-Hyde abortion
services in 7 states. In SBEs, we estimate that 60 issuers offered a
total of 1,000 QHPs offering non-Hyde abortion coverage across 10 SBEs.
In total, this leads to an estimated 75 QHP issuers offering a total of
1,111 QHPs covering non-Hyde abortion services across 17 states. This
rule could significantly increase the administrative burden for QHP
issuers covering non-Hyde abortion services in developing, sending, and
processing the separate invoices required under this proposal.
Based on 2018 QHP Certification data in FFEs and SBE-FPs, there
were approximately 300,000 enrollees across the 111 QHPs covering non-
Hyde abortion coverage. In SBEs, we estimate that there were
approximately 1,000,000 enrollees across the approximate 1,000 QHPs
offering non-Hyde abortion coverage. If finalized, these requirements
would also increase burden on those 1,300,000 consumers, related to
paying the portion of the premium attributable to non-Hyde abortion
services through a separate paper check or electronic transaction; that
burden, however, is contemplated by the specific language of section
1303 which requires a QHP issuer ``to collect from each enrollee in the
plan . . . a separate payment'' for the coverage of non-Hyde abortion
services. In order to develop a preliminary estimate of the consumer
cost of this proposed provision, we assume that a policy subscriber
reading their separately received paper or electronic bill and writing
out an additional paper check or filling in the necessary information
for completion of a separate electronic payment adds approximately ten
minutes per month to a policy subscriber's' monthly payment process for
payment of their QHP premiums, for a total of 2 hours per year. Based
on the May 2017 National Occupational Employment and Wage Estimates
United States Department of Labor's Bureau of Labor Statistics (BLS)
(https://www.bls.gov/oes/current/oes_nat.htm), using the listed national
mean hourly wage for the 25th percentile,\16\ it would cost a policy
subscriber $11.91 for an additional hour of burden, or approximately
$1.98 for an additional 10 minutes of burden. As such, the 10 minute
monthly estimated burden for filling out a separate check or online
payment for a policy subscriber would be $1.98, and the yearly added
burden for each policy subscriber would be $23.76. We note that many
consumers are enrolled on the Exchange for an average of 10 months. For
those enrollees, the annual consumer burden would be $19.80 for a total
annual burden of $25,740,000. However, in total for all affected
enrollees in QHPs covering non-Hyde abortion enrolled in plans for 12
months, we estimate that it would annually cost $30,888,000 for policy
subscribers to comply with these proposals. This estimate excludes the
cost of consumer learning (which may have significant upfront costs and
could also continue to be resource intensive on an ongoing basis given
the potential confusion of consumers in receiving multiple bills. In
some cases, these may entail costs not just to consumers but
[[Page 56029]]
also to QHP issuers, such as in increased volume of requests for
customer service assistance and follow up needed to consumers to pay
their full bill). However, HHS believes that, if finalized as proposed,
the proposed changes would better align the regulatory requirements for
QHP issuer billing of premiums with the separate payment requirement in
section 1303 of the PPACA. As such, HHS believes that this outweighs
the estimated consumer burden. We solicit comments on the impact of the
proposed policy at Sec. 156.280(e)(2) and on whether other impacts
should be considered or quantified.
---------------------------------------------------------------------------
\16\ The 25th percentile mean hourly wage most closely resembles
the group of consumers likely to be affected by this proposal as
most enrollees enrolled in QHPs on the Exchange are between 100% and
400% of the federal poverty level.
---------------------------------------------------------------------------
We request comment on both our assessment of the need for the
regulatory action and an explanation of how the regulatory action will
meet that need, as well as our assessment of the potential costs and
benefits of the regulatory action. To be sure our analysis is as
accurate as possible with respect to any additional costs to states,
issuers, or other entities, we encourage robust comment in this area.
The RFA requires agencies to analyze options for regulatory relief
of small entities. For purposes of the RFA, small entities include
small businesses, nonprofit organizations, and small governmental
jurisdictions. Individuals and states are not included in the
definition of a small entity. We are not preparing an analysis for the
RFA because we have determined, and the Secretary certifies, that this
proposed rule would not have a significant economic impact on a
substantial number of small entities.
Section 202 of the Unfunded Mandates Reform Act of 1995 also
requires that agencies assess anticipated costs and benefits before
issuing any rule whose mandates require spending in any 1 year of $100
million in 1995 dollars, updated annually for inflation. In 2018, that
threshold is approximately $150 million. This rule will have no
consequential effect on state, local, or tribal governments or on the
private sector.
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates a proposed rule (and subsequent
final rule) that imposes substantial direct requirement costs on state
and local governments, preempts state law, or otherwise has Federalism
implications. This proposed rule does not impose substantial direct
costs on state and local governments or preempt state law. However, we
believe the rule has Federalism implications.
In HHS's view, this regulation has Federalism implications due to
our proposal that Exchanges conduct Medicare, Medicaid/CHIP, and, if
applicable, BHP PDM at least twice a year, beginning with the 2020
calendar year. However, HHS believes that the Federalism implications
are substantially mitigated because the proposed requirement sets only
a minimum frequency with which Exchanges must conduct Medicare,
Medicaid/CHIP, and, if applicable, BHP PDM, which is already required
to be conducted periodically; SBEs would continue to have the
flexibility to conduct PDM with greater frequency.
Additionally, the proposed changes to State Exchange oversight and
reporting requirements in Sec. 155.1200 have Federalism implications
since those rules would require State Exchanges to submit certain
reports to HHS and require them to enter into contracts with an
external independent audit entity to perform audits, and incur the
associated costs. However, HHS believes that the Federalism
implications are substantially mitigated because the proposed changes
do not impose new requirements on State Exchanges, but rather add
specificity to the existing requirements.
This proposed rule is subject to the Congressional Review Act (5
U.S.C. 801, et seq.), which specifies that before a rule can take
effect, the federal agency promulgating the rule shall submit to each
House of the Congress and to the Comptroller General a report
containing a copy of the rule along with other specified information,
and has been transmitted to the Congress and the Comptroller General
for review.
Executive Order 13771, titled Reducing Regulation and Controlling
Regulatory Costs, was issued on January 30, 2017. Section 2(a) of
Executive Order 13771 requires an agency, unless prohibited by law, to
identify at least two existing regulations to be repealed when the
agency publicly proposes for notice and comment, or otherwise
promulgates, a new regulation. In furtherance of this requirement,
section 2(c) of Executive Order 13771 requires that the new incremental
costs associated with new regulations shall, to the extent permitted by
law, be offset by the elimination of existing costs associated with at
least two prior regulations. OMB Guidance Implementing Executive Order
13771 (April 5, 2017) defines a regulatory action as (1) a significant
regulatory action as defined in section 3(f) of Executive Order 12866,
or (2) a significant guidance document (for example, significant
interpretive guidance) that has been reviewed by OMB under the
procedures of Executive Order 12866 and that, when finalized, is
expected to impose total costs greater than zero. This proposed rule,
if finalized as proposed, is expected to be an E.O. 13771 regulatory
action. Details on the estimated costs appear in the preceding
analysis.
C. Regulatory Review Costs
If regulations impose administrative costs on private entities,
such as the time needed to read and interpret this proposed rule, we
estimate the cost associated with regulatory review. Due to the
uncertainty involved with accurately quantifying the number of entities
that will review the rule, we assume that the total number of unique
commenters on similar Exchange-related CMS rules will be the number of
reviewers of this proposed rule. We acknowledge this assumption may
understate or overstate the costs of reviewing this rule. It is
possible that not all commenters will review the rule in detail, and it
is also possible that some reviewers will chose not to comment on the
proposed rule. For these reasons, we consider the number of past
commenters on similar CMS rules will be a fair estimate of the number
of reviewers of this rule. We welcome any comments on the approach in
estimating the number of entities which will review this proposed rule.
We recognize that different types of entities may be affected by
only certain provisions of this proposed rule, and therefore, for the
purposes of our estimate, we assume that each reviewer reads
approximately 50 percent of the rule.
Using the wage information from the Bureau of Labor and Statistics
(BLS) for medical and health service managers (Code 11-9111), we
estimate that the cost of reviewing this rule is $107.38 per hour,
including overhead and fringe benefits.\17\ We estimate that it would
take approximately 1 hour for the staff to review the relevant portions
of this proposed rule. Based on previous and similar CMS rules, we
assume that 321 entities will review this proposed rule. Therefore, we
estimate that the total cost of reviewing this regulation is
approximately $34,469 ($107.38 x 321 reviewers).
---------------------------------------------------------------------------
\17\ https://www.bls.gov/oes/current/oes_nat.htm.
---------------------------------------------------------------------------
This may underestimate the review costs, since not all reviewers
may have submitted comments. In addition, stakeholders may need to do a
detailed analysis in order to implement the unanticipated provisions of
this rule will need additional time and personnel, which will vary
depending
[[Page 56030]]
on the extent to which they are affected. To estimate an upper bound,
we assume that on average 530 issuers and 50 states will spend 10 hours
each, 100 other organizations will spend 5 hours each and 100
individuals will spend 1 hour each to review the rule. Under these
assumptions, total time spent reviewing the rule would be 6,400 hours
with an estimated cost of approximately $673,024.
In accordance with the provisions of Executive Order 12866, this
proposed rule was reviewed by the Office of Management and Budget.
List of Subjects
45 CFR Part 155
Administrative practice and procedure, Advertising, Brokers,
Conflict of interests, Consumer protection, Grants administration,
Grant programs--health, Health care, Health insurance, Health
maintenance organizations (HMO), Health records, Hospitals, Indians,
Individuals with disabilities, Intergovernmental relations, Loan
programs--health, Medicaid, Organization and functions (Government
agencies), Public assistance programs, Reporting and recordkeeping
requirements, Technical assistance, Women and youth.
45 CFR Part 156
Administrative practice and procedure, Advertising, Advisory
committees, Brokers, Conflict of interests, Consumer protection, Grant
programs--health, Grants administration, Health care, Health insurance,
Health maintenance organization (HMO), Health records, Hospitals,
Indians, Individuals with disabilities, Loan programs--health,
Medicaid, Organization and functions (Government agencies), Public
assistance programs, Reporting and recordkeeping requirements, State
and local governments, Sunshine Act, Technical assistance, Women,
Youth.
For the reasons set forth in the preamble, the Department of Health
and Human Services proposes to amend 45 CFR parts 155 and 156 as set
forth below:
PART 155--EXCHANGE ESTABLISHMENT STANDARDS AND OTHER RELATED
STANDARDS UNDER THE AFFORDABLE CARE ACT
0
1. The authority citation for part 155 is revised to read as follows:
Authority: 42 U.S.C. 18021-18024, 18031-18033, 18041-18042,
18051, 18054, 18071, and 18081-18083.
0
2. Section 155.200 is amended by revising paragraph (c) to read as
follows:
Sec. 155.200 Functions of an Exchange.
* * * * *
(c) Oversight and financial integrity. The Exchange must perform
required functions and cooperate with activities related to oversight
and financial integrity requirements in accordance with section 1313 of
the Affordable Care Act and as required under this part, including
overseeing its Exchange programs, assisters, and other non-Exchange
entities as defined in Sec. 155.260(b)(1).
* * * * *
0
3. Section 155.330 is amended by revising paragraph (d)(1) introductory
text and adding paragraph (d)(3) to read as follows:
Sec. 155.330 Eligibility redetermination during a benefit year
* * * * *
(d) * * *
(1) General requirement. Subject to paragraph (d)(3) of this
section, the Exchange must periodically examine available data sources
described in Sec. Sec. 155.315(b)(1) and 155.320(b) to identify the
following changes:
* * * * *
(3) Definition of periodically. Beginning with the 2020 calendar
year, the Exchange must perform the periodic examination of data
sources described in paragraph (d)(1)(ii) of this section at least
twice in a calendar year. SBEs that have implemented a fully integrated
eligibility system that determines eligibility for advance payments of
the premium tax credit, cost-sharing reductions, Medicaid, CHIP, and
the BHP, if a BHP is operating in the service area of the Exchange,
will be deemed in compliance with paragraphs (d)(1)(ii) and (d)(3) of
this section.
* * * * *
0
4. Section 155.1200 is amended by--
0
a. Revising paragraphs (b) introductory text, (b)(1) and (2), (c)
introductory text, and (d)(2) and (3);
0
b. Redesignating (d)(4) as paragraph (d)(5);
0
c. Adding a new paragraph (d)(4); and
0
d. Revising newly redesignated paragraph (d)(5).
The revisions and addition read as follows:
Sec. 155.1200 General program integrity and oversight requirements.
* * * * *
(b) Reporting. The State Exchange must, at least annually, provide
to HHS, in a manner specified by HHS and by applicable deadlines
specified by HHS, the following data and information:
(1) A financial statement presented in accordance with GAAP,
(2) Information showing compliance with Exchange requirements under
this part 155 through submission of annual reports,
* * * * *
(c) External audits. The State Exchange must engage an independent
qualified auditing entity which follows generally accepted governmental
auditing standards (GAGAS) to perform an annual independent external
financial and programmatic audit and must make such information
available to HHS for review. The State Exchange must:
* * * * *
(d)* * *
(2) Compliance with subparts D and E of this part 155, or other
requirements under this part 155 as specified by HHS;
(3) Processes and procedures designed to prevent improper
eligibility determinations and enrollment transactions, as applicable;
(4) Compliance with eligibility and enrollment standards through
sampling, testing, or other equivalent auditing procedures that
demonstrate the accuracy of eligibility determinations and enrollment
transactions; and
(5) Identification of errors that have resulted in incorrect
eligibility determinations, as applicable.
PART 156--HEALTH INSURANCE ISSUER STANDARDS UNDER THE AFFORDABLE
CARE ACT, INCLUDING STANDARDS RELATED TO EXCHANGES
0
5. The authority citation for part 156 is revised to read as follows:
Authority: 42 U.S.C. 18021-18024, 18031-18032, 18041-18042,
18044, 18054, 18061, 18063, 18071, 18082, 26 U.S.C. 36B, and 31
U.S.C. 9701.
0
6. Section 156.280 is amended by --
0
a. Redesignating paragraph (e)(2)(ii) as (e)(2)(iii);
0
b. Adding a new paragraph (e)(2)(ii); and
0
c. Revising newly redesignated paragraph (e)(2)(iii).
The revisions and addition read as follows:
Sec. 156.280 Segregation of funds for abortion services.
* * * * *
(e) * * *
(2) * * *
(ii) Send to each policy subscriber (without regard to the policy
subscriber's age, sex, or family status) in the QHP separate monthly
bills for each of the amounts specified in paragraphs (e)(2)(i)(A) and
(B) of this section, and
[[Page 56031]]
instruct the policy subscriber to pay each of these amounts through
separate transactions. If the policy subscriber fails to pay each of
these amounts in a separate transaction as instructed by the issuer,
the issuer may not terminate the policy subscriber's coverage on this
basis, provided the amount due is otherwise paid.
(iii) Deposit all such separate payments into separate allocation
accounts as provided in paragraph (e)(3) of this section. In the case
of an enrollee whose premium for coverage under the QHP is paid through
employee payroll deposit, the separate payments required under
paragraph (e)(2)(i) of this section shall each be paid by a separate
deposit.
* * * * *
Dated: October 11, 2018.
Seema Verma,
Administrator, Centers for Medicare & Medicaid Services.
Dated: October 18, 2018.
Alex M. Azar II,
Secretary, Department of Health and Human Services.
[FR Doc. 2018-24504 Filed 11-7-18; 4:15 pm]
BILLING CODE 4120-01-P