Medical Loss Ratio Requirements Under the Patient Protection and Affordable Care Act, 28790-28797 [2012-11753]
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28790
Federal Register / Vol. 77, No. 95 / Wednesday, May 16, 2012 / Rules and Regulations
2. On page 74884, third column, fifth
full paragraph—
A. In line 14, remove the words ‘‘then
current.’’
B. In line 15, revise the phrase
‘‘premium credit’’ to read ‘‘rebate.’’
IV. Waiver of Proposed Rulemaking
and Delay in Effective Date
List of Subjects in 45 CFR Part 158
Administrative practice and
procedure, Claims, Health care, Health
insurance, Health plans, Penalties,
Reporting and recordkeeping
requirements.
Accordingly, 45 CFR part 158 is
corrected by making the following
correcting amendments:
PART 158—ISSUER USE OF PREMIUM
REVENUE: REPORTING AND REBATE
REQUIREMENTS
1. The authority citation for part 158
continues to read as follows:
■
Authority: Sec. 2718 of the Public Health
Service Act (42 U.S.C. 300gg–18, as
amended).
2. Amend § 158.103 as follows:
A. Remove the definition for ‘‘MultiState blended rate.’’
■ B. Add a new definition for ‘‘Blended
rate’’ in alphabetical order.
The addition reads as follows:
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■
■
Definitions.
*
*
*
*
*
Blended rate means a single rate
charged for health insurance coverage
provided to a single employer through
two or more of an issuer’s affiliated
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§ 158.240 based upon prior MLR
reporting year experience.
*
*
*
*
*
3. Amend § 158.120 by revising
paragraphs (d)(1) and (d)(2) to read as
follows:
§ 158.150
■
§ 158.120
We ordinarily publish a notice of
proposed rulemaking in the Federal
Register to provide a period for public
comment before the provisions of a rule
take effect in accordance with section
553(b) of the Administrative Procedure
Act (APA) (5 U.S.C. 553(b)), and section
553(d) of the APA ordinarily requires a
30-day delay in effective date of final
rules after the date of their publication
in the Federal Register. These
requirements may be waived, however,
if an agency finds for good cause that
the delay is impracticable, unnecessary,
or contrary to the public interest, and
the agency incorporates a statement of
the findings and its reasons in the rule
issued.
In this case, we believe that it is
unnecessary to provide for a public
comment period or to delay
implementing these corrections, as they
clarify provisions of a final rule that has
been subjected to notice and comment
procedures and do not make any
substantive changes to it.
§ 158.103
companies for employees in one or more
States.
*
*
*
*
*
Aggregate reporting.
*
*
*
*
*
(d) * * *
(1) For individual market business
sold through an association or trust, the
experience of the issuer must be
included in the State report for the issue
State of the certificate of coverage.
(2) For employer business issued
through a group trust or multiple
employer welfare association (MEWA),
the experience of the issuer must be
included in the State report for the State
where the employer (if sold through a
trust) or the MEWA (if the MEWA is the
policyholder) has its principal place of
business.
*
*
*
*
*
§ 158.130
[Amended]
4. In § 158.130(b)(3) remove the words
‘‘paid or received’’ and add the word
‘‘incurred’’ in their place.
■ 5. Amend § 158.140 by revising
paragraph (a) introductory text and
paragraph (a)(5) to read as follows:
■
§ 158.140 Reimbursement for clinical
services provided to enrollees.
(a) General requirements. The report
required in § 158.110 must include
direct claims paid to or received by
providers, including under capitation
contracts with physicians, whose
services are covered by the policy for
clinical services or supplies covered by
the policy. In addition, the report must
include claim reserves associated with
claims incurred during the MLR
reporting year, the change in contract
reserves, reserves for contingent benefits
and the medical claim portion of
lawsuits, and any incurred experience
rating refunds. Reimbursement for
clinical services, as defined in this
section, is referred to as ‘‘incurred
claims.’’ All components of and
adjustments to incurred claims, with the
exception of contract reserves, must be
calculated based on claims incurred
only during the MLR reporting year and
paid through March 31st of the
following year. Contract reserves must
be calculated as of December 31st of the
applicable year.
*
*
*
*
*
(5) Incurred claims must include
incurred experience rating refunds and
exclude rebates paid as required by
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[Amended]
6. Amend § 158.150 as follows:
A. In paragraph (b)(2)(i)(A)(1), remove
‘‘section 3606’’ and add in its place
‘‘section 3502.’’
■ B. In paragraph (c)(14), remove the
reference ‘‘paragraph (c) of this section’’
and add in its place the reference
‘‘paragraph (a) or (b) of this section.’’
■ 7. Amend § 158.232 by revising
paragraph (c)(1)(i) to read as follows:
■
■
§ 158.232 Calculating the credibility
adjustment.
*
*
*
*
*
(c) * * *
(1) * * *
(i) The per person deductible for a
policy that covers a subscriber and the
subscriber’s dependents shall be the
lesser of: The sum of the deductible
applicable to each of the individual
family members; or the overall family
deductible for the subscriber and
subscriber’s family, divided by two
(regardless of the total number of
individuals covered through the
subscriber).
*
*
*
*
*
Dated: May 10, 2012.
Jennifer Cannistra,
Executive Secretary to the Department.
[FR Doc. 2012–11773 Filed 5–15–12; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
45 CFR Part 158
[CMS–9998–F]
RIN 0938–AR41
Medical Loss Ratio Requirements
Under the Patient Protection and
Affordable Care Act
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final rule.
AGENCY:
This final rule amends the
regulations implementing medical loss
ratio (MLR) standards for health
insurance issuers under the Public
Health Service Act in order to establish
notice requirements for issuers in the
group and individual markets that meet
or exceed the applicable MLR standard
in the 2011 MLR reporting year.
DATES: Effective date. This rule is
effective on June 15, 2012.
Applicability date. The amendments
to part 158 generally apply beginning
SUMMARY:
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July 1, 2012, to health insurance issuers
offering group or individual health
insurance coverage.
FOR FURTHER INFORMATION CONTACT:
Carol Jimenez, (301) 492–4457.
SUPPLEMENTARY INFORMATION:
I. Background
The Patient Protection and Affordable
Care Act (Pub. L. 111–148) was enacted
on March 23, 2010; the Health Care and
Education Reconciliation Act (Pub. L.
111–152) was enacted on March 30,
2010. In this preamble, we refer to the
two statutes collectively as the
Affordable Care Act. The Affordable
Care Act reorganizes, amends, and adds
to the provisions of Part A of title XXVII
of the Public Health Service Act (PHS
Act) relating to group health plans and
health insurance issuers in the group
and individual markets.
A request for information relating to
the medical loss ratio (MLR) provisions
of section 2718 of the PHS Act was
published in the Federal Register on
April 14, 2010 (75 FR 19297). On
December 1, 2010, the Department of
Health and Human Services (HHS)
published an interim final rule (75 FR
74864) with a 60-day public comment
period, entitled ‘‘Health Insurance
Issuers Implementing Medical Loss
Ratio (MLR) Requirements Under the
Patient Protection and Affordable Care
Act,’’ that added a new 45 CFR part 158.
A technical correction to the interim
final rule was issued on December 30,
2010 (75 FR 82277).
On December 7, 2011, the Centers for
Medicare & Medicaid Services (CMS)
published an interim final rule (76 FR
76596) with a 60-day public comment
period entitled, ‘‘Medical Loss Ratio
Rebate Requirements for Non-Federal
Governmental Plans,’’ establishing rules
governing the distribution of rebates by
health insurance issuers in group
markets for non-Federal governmental
plans. Also on December 7, 2011, CMS
published a final rule (76 FR 76574)
with a 30-day public comment period,
entitled ‘‘Medical Loss Ratio
Requirements Under the Patient
Protection and Affordable Care Act,’’
that addressed the treatment of ‘‘minimed’’ and expatriate policies under the
MLR regulations for years after 2011;
modified the way the regulations treat
International Statistical Classification of
Diseases and Related Health Problems,
10th Revision (ICD–10) conversion
costs; changed the rules on deducting
community benefit expenditures; and
revised the rules governing the
distribution of rebates by issuers in
group markets.
In the December 7, 2011 final rule
with comment period, we noted that the
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notice requirements finalized in the rule
only applied to issuers that owed
rebates as a result of not meeting the
applicable MLR standard. Consequently,
policyholders and subscribers of issuers
meeting or exceeding the MLR standard
would not receive MLR information, an
important tool to increase transparency
to consumers. In the rule, we noted that
extending a notice requirement to such
cases would serve the policy goal of
greater transparency in how premium
dollars are used, and provide an
additional incentive for issuers that
already met the minimum standard to
achieve the highest MLR possible. We
therefore solicited comments on
whether an issuer that meets or exceeds
the MLR standard for the applicable
MLR reporting year should send a
notice to policyholders and subscribers
with information about the MLR
standard and its own MLR, as a
measurement of issuer performance. We
also solicited comments on whether it
would be useful to include information
in the notices about the issuer’s prior
year MLR in addition to the current year
MLR. We noted that this approach
would allow enrollees to determine if
the issuer was doing a better or worse
job of efficiently using premium
revenue than in the prior year.
Based on the comments received and
weighing consumer transparency and
competition gains with burden on
issuers, this final rule establishes a
simple, straightforward notice
requirement for health insurance issuers
that meet or exceed the MLR standards
established by the Affordable Care Act,
but only requires the notice for the 2011
MLR reporting year, the first year that
the MLR rules are in effect, and does not
require issuers to include information
about the current or prior year MLR.
The notice will direct enrollees to the
HHS Web site for specific information
about issuers’ MLRs.
II. Analysis of and Responses to Public
Comments
We received 56 public comments on
the December 7, 2011 final rule with
comment period. Commenters included
consumer and patient advocacy
organizations, insurance regulators,
health insurance issuers, business
advocacy organizations, provider
groups, an actuarial professional group,
and others. In addition, we received 11
public comments in response to the
draft MLR Notices and Instructions
contained in the MLR Paperwork
Reduction Act (PRA) package (CMS–
10418) posted on February 16, 2012.
Commenters consisted of consumer
groups, health insurance issuers, an
issuer trade association, and a business
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trade association. Several of these
commenters recommended technical
corrections to the draft notices and
instructions. We note that their
comments will be addressed through the
PRA process. In addition, commenters
recommended several amendments to
the December 1, 2010 interim final rule
that were beyond the scope of this final
rulemaking; therefore, we are not
making changes in this final rule based
on these comments. In this final rule,
we only address the public comments
received on the following issues: (1)
Whether a notice requirement should
apply to issuers that meet or exceed the
applicable MLR standards in a
particular MLR reporting year; and (2)
whether MLR notices should include
information on an issuer’s prior year
MLR. The comments received are
summarized below with our responses.
Comments: We received comments
that both support and oppose expanding
the notice to issuers that do not owe
rebates because they meet or exceed the
MLR standards. Commenters who
opposed expanding the notice rules
generally claimed that requiring issuers
that do not owe rebates to provide an
MLR notice would impose a burden on
issuers that meet the MLR requirement
and provide little value to consumers.
Specifically, issuers, an issuer trade
association, and a business advocacy
organization stated that MLR data
would confuse or mislead consumers
who may misinterpret the information
or who may mistakenly believe they are
owed a rebate. Commenters in support
of expanding the notice rules, such as
consumer and patient advocacy
organizations, stated that expanding the
notice rules would increase health plan
transparency and ensure that every
enrollee receives information about the
meaning of the MLR, rather than only
those owed a rebate.
We also received several comments
on the question of whether all MLR
notices should include the issuer’s MLR
from the prior MLR reporting year.
Issuers and trade associations opposed
this requirement, noting that an issuer’s
MLR from the prior MLR reporting year
is not necessarily a reliable indicator of
health plan performance. These
commenters stated that numerous
factors other than health plan efficiency,
such as variation in incurred claims,
premium revenue, and adjustments,
affect issuers’ year-to-year MLRs and
that consumers may be misled when
comparing MLRs for multiple years.
Several commenters noted that MLR
information will be publicly available
on the HHS Web site and suggested that
CMS maintain historical data so that
consumers may monitor changes in
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issuers’ MLR over time. In contrast,
consumer and patient advocacy
organizations expressed support for
including an issuer’s prior year MLR,
noting that it would help consumers to
better use the MLR information when
making plan selections and better
understand how premium dollars are
spent by health insurers. They indicated
that consumers could benefit from more
detailed information and that the notice
should include specific information that
explains how premium dollars are being
spent, not just whether the MLR was
being met.
Response: Expanding the notice of
MLR information to all issuers would
further the goals of improving
transparency of health insurance
markets, supporting more informed
purchase decisions, and promoting
competition and efficiency. At the same
time, we appreciate the concerns about
administrative costs. Further, we
recognize that under the Affordable Care
Act, issuers’ MLR information will be
available on the HHS Web site,
HealthCare.gov, providing an efficient
method of public disclosure.1
In light of these considerations and
after further review and consideration of
the costs and benefits of different notice
alternatives, we are adding a new 45
CFR 158.251 that establishes a basic
notice requirement for issuers in the
group and individual markets that meet
or exceed the applicable MLR standard.
This new notice will use standard
language to inform policyholders and
subscribers of group health plans, and
subscribers in the individual market,
that the issuer has met the minimum
MLR standards established by the
Affordable Care Act, but it will not
include the issuer’s MLR for the current
or prior reporting year or other specific
measures of issuer performance. Instead,
the notice will help educate consumers
about the MLR measures and direct
them to the HHS Web site,
HealthCare.gov, for information about
issuers’ actual MLRs. Additionally,
under this final rule, issuers will only
need to produce this notice for the 2011
MLR reporting year, when consumer
knowledge of the MLR is low and the
1 Section 2718(a) of the PHS Act provides that
‘‘The Secretary shall make reports [concerning an
issuer’s MLR and its components] received under
this section available to the public on the Internet
Web site of the Department of Health and Human
Services.’’ In addition, section 1103(b) of the
Affordable Care Act provides that the Federal
health care reform insurance Web portal created by
the Secretary under section 1103 to present
information relating to affordable coverage options
shall, among other things, ‘‘require the inclusion of
information on the percentage of total premium
revenue expended on nonclinical costs (as reported
under section 2718(a) of the Public Health Service
Act).’’
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greatest benefit can be achieved by
providing enrollees with educational
information. By leveraging existing
Federal information resources while
ensuring adequate notice to enrollees in
the first year of applicability, we believe
this new notice requirement balances
issuers’ interest in administrative
efficiency and consumers’ interest in
health plan transparency.
This notice rule will ensure that all
consumers, not just those owed a rebate,
are informed whether their issuer meets
the minimum MLR standards
established by the Affordable Care Act.
It will provide greater transparency to
consumers regarding how their
premium dollars are used, promote
informed decision-making in the
purchase of health insurance, and
ensure that efficiency in the use of
premium dollars is properly valued by
consumers. Notifying consumers of the
MLR standards will also reduce
confusion as to why certain individuals
receive rebates, while others, such as
coworkers or family members with
different insurance plans, do not.
Finally, the distribution of MLR notices
to consumers with the HHS Web site,
HealthCare.gov, will promote a more
competitive market by creating an
incentive for issuers to spend as high a
percentage of premium dollars on health
care and quality improvement as
possible, rather than spending just
enough to avoid paying rebates.
III. Provisions of the Final Rule
In paragraph (a)(1) of new § 158.251 of
this final rule, we set forth the general
requirement that an issuer whose MLR
meets or exceeds the applicable MLR
standard required by § 158.210 or
§ 158.211 must provide each
policyholder and subscriber of a group
health plan, and each subscriber in the
individual market, a notice of MLR
information. The required language for
the notice is specified in paragraph
(a)(4). This notice requirement applies
only for the 2011 MLR reporting year.
In paragraph (a)(2), we generally align
the timing of this new notice with the
timing specified in § 158.240(d) for
providing any rebates that are due and
the accompanying notice of rebates. We
specify that the MLR notice must be
provided with the first plan document
(for example, open enrollment
materials) that is provided to enrollees
on or after July 1, 2012.
In paragraph (a)(3), we direct that the
notice be prominently displayed in
clear, conspicuous 14-point bold type
on the front of the plan document,
insurance policy or certificate, or as a
separate notice. The MLR notice may be
included in the same mailing as other
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mailed notices. Further, we specify that
the notice may be provided
electronically, consistent with the
policy for providing the summary of
benefits and coverage under section
2715 of the PHS Act.
In paragraph (b), we specify certain
exceptions to the MLR notice
requirement. We are not requiring
health insurance issuers that sell plans
with total annual benefit limits of
$250,000 or less (‘‘mini-med’’ plans) or
expatriate policies, as described in
§ 158.120(d)(3) and (d)(4), respectively,
to provide MLR notices to policyholders
and subscribers if they meet or exceed
the applicable MLR standard. As
discussed in the preamble to the
December 7, 2011 final rule with
comment period, issuers of mini-med
and expatriate policies will use a
separate methodology for calculating the
MLR numerator for reporting and rebate
purposes and are subject to separate
notice rules. We note that issuers of
mini-med and expatriate plans must
continue to provide notice of rebates, if
any, to current group health plan
policyholders and subscribers, and to
subscribers in the individual market, as
provided under § 158.250.
In addition, we are not requiring
issuers whose experience is noncredible, as defined in § 158.230(c)(3)
and determined in accordance with
§ 158.231, to provide MLR notices to
policyholders and subscribers. An
issuer that has fewer than 1,000 covered
life-years does not have sufficiently
credible data to determine whether the
MLR standard has been met and thus,
under § 158.230(d), is presumed to meet
or exceed the applicable minimum MLR
standard. Because non-credible issuers
do not have an MLR to report, the MLR
notice requirement in this final rule
does not apply.
Finally, we note that issuers of
student health insurance coverage are
not required to provide the MLR notices
under this final rule, because the MLR
reporting and rebate requirements of 45
CFR part 158 generally apply for such
experience beginning January 1, 2013.
IV. Collection of Information
Requirements
This final rule establishes a
notification requirement. Although
third-party disclosures (for example,
notification requirements) are generally
subject to the Paperwork Reduction Act
of 1995 (PRA), the implementing
regulations at 5 CFR 1320.3(c)(2)
include an exclusion for ‘‘information
originally supplied by the Federal
government to the recipient for the
purpose of disclosure to the public.’’
Because the notification will be
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provided by the Federal government,
and does not contain text that must be
customized, this exclusion applies.
V. Regulatory Impact Analysis
A. Summary
This final rule amends the regulations
implementing MLR standards for health
insurance issuers under section 2718 of
the Public Health Service Act in order
to establish notice requirements for
issuers in the group and individual
markets that meet or exceed the
applicable MLR standard in the 2011
MLR reporting year.
CMS developed this rule to
accomplish its intended benefits in the
most economically efficient manner
possible. We have examined the effects
of this rule as required by Executive
Order 13563 (76 FR 3821, January 21,
2011), Executive Order 12866 (58 FR
51735, September 1993, Regulatory
Planning and Review), the Regulatory
Flexibility Act (RFA) (September 19,
1980, Pub. L. 96–354), section 1102(b) of
the Social Security Act, the Unfunded
Mandates Reform Act of 1995 (Pub. L.
104–4), Executive Order 13132 on
Federalism, and the Congressional
Review Act (5 U.S.C. 804(2)). In
accordance with the Office of
Management and Budget (OMB)
Circular A–4, CMS has quantified the
benefits, costs, and transfers where
possible and provided a qualitative
discussion of some of the benefits, costs,
and transfers that may stem from this
final rule.
B. Executive Orders 13563 and 12866
Executive Order 12866 (58 FR 51735)
directs 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). Executive Order 13563 (76 FR
3821, January 21, 2011) is supplemental
to and reaffirms the principles,
structures, and definitions governing
regulatory review as established in
Executive Order 12866.
Section 3(f) of Executive Order 12866
defines a ‘‘significant regulatory action’’
as an action that is likely to result in a
final rule—(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 (RIA)
must be prepared for major rules with
economically significant effects ($100
million or more in any 1 year), and a
‘‘significant’’ regulatory action is subject
to review by OMB. As discussed below,
CMS has concluded that this rule is not
likely to have an economic impact of
$100 million or more in any 1 year, and
therefore does not meet the definition of
a ‘‘significant rule’’ under Executive
Order 12866. Nevertheless, CMS has
provided an assessment of the potential
costs, benefits, and transfers associated
with this final rule. Accordingly, OMB
has reviewed this final rule pursuant to
the Executive Order.
1. Need for Regulatory Action
On December 7, 2011, CMS published
a final rule (76 FR 76574) that invited
comment on whether the MLR notice
requirement finalized in that rule
should apply not only to issuers that
28793
owe rebates but also to issuers that meet
or exceed the applicable MLR standard
and therefore do not owe rebates. For
the reasons discussed above and in
section V.B.3.a. below, and based on
public comments we received, this final
rule establishes a basic, one-time notice
requirement for issuers in the group and
individual markets that meet or exceed
the applicable MLR standard in the
2011 MLR reporting year. This approach
is consistent with Executive Order
13563, which directs agencies to
‘‘identify and consider regulatory
approaches that reduce burdens and
maintain flexibility and freedom of
choice for the public. These approaches
include * * * disclosure requirements
as well as provision of information to
the public in a form that is clear and
intelligible.’’
2. Summary of Impacts
In accordance with OMB Circular A–
4, Table 1 below depicts an accounting
statement summarizing CMS’s
assessment of the benefits, costs, and
transfers associated with this regulatory
action. The RIA is limited to 2012 when
the notice for the 2011 MLR reporting
year will be provided.
CMS anticipates that the provisions of
this final rule will help ensure greater
transparency for consumers regarding
how their premium dollars are used,
educate consumers about the MLR
standards established by the Affordable
Care Act, and provide an incentive for
issuers to maximize the percentage of
premium dollars they spend on health
care and activities that improve health
care quality, promoting greater
efficiency in health insurance markets.
Issuers that meet or exceed the
applicable MLR standards will incur
administrative costs related to providing
the notices to policyholders and
subscribers. In accordance with
Executive Order 12866, CMS believes
that the benefits of this regulatory action
justify the costs.
TABLE 1—ACCOUNTING TABLE
Benefits
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Qualitative:
* Greater transparency regarding how premium dollars are used by issuers.
* Incentive for issuers to maximize the percentage of premium dollars they spend on health care and activities that improve health care
quality.
* Improved information to assist consumers in making plan choices.
Low
estimate
Costs and transfers
Annualized Monetized ($millions/year) ........................................................................
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Medium
estimate
High
estimate
$2.8
$2.9
$3.0
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Year
dollar
2012
Period
covered
2012
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3. Anticipated Benefits, Costs, and
Transfers
This final rule extends a notice
requirement to issuers in the group and
individual markets that meet or exceed
the applicable MLR standard in the
2011 MLR reporting year. The notice
must use standard language specified in
this final rule. Issuers may provide the
notice with other plan documents or
through electronic transmittal, as
permitted for the summary of benefits
and coverage under section 2715 of the
PHS Act.
a. Benefits
The MLR notices will ensure that
consumers are informed whether their
issuer’s coverage meets or exceeds the
applicable minimum MLR thresholds
established by the Affordable Care Act.
Accordingly, the notices will provide
greater transparency to consumers and
may help to reduce consumers’
confusion regarding why they did not
receive a rebate. The MLR notices will
also provide consumers with
educational information in the first year
of applicability when consumer
knowledge of the MLR is low.
Additionally, the notices will inform
enrollees of the HHS Web site where
they can find issuers’ actual MLRs and
compare MLR information across
issuers and over years. This will provide
an incentive to issuers to spend as high
a percentage of premium dollars on
health care and quality improvement as
possible, rather than just enough to
avoid paying rebates. Finally, notice of
MLR information will assist individuals
in comparing plans and making plan
choices. We believe that such
information disclosure will result in a
more efficient, competitive market.
pmangrum on DSK3VPTVN1PROD with RULES
b. Costs and Transfers
Issuers that meet or exceed the
applicable MLR standard will incur the
administrative cost of preparing and
mailing the notices. It is estimated that
these costs will total approximately $3
million in 2012.
4. Overview of Data Sources, Methods,
and Limitations
On December 1, 2010, we published
an interim final rule (75 FR 74864) with
a 60-day public comment period. In that
rule, we indicated that the most
complete source of data on the number
of licensed entities offering fully
insured, private comprehensive major
medical coverage in the individual and
group markets is the National
Association of Insurance
Commissioners’ (NAIC) Annual
Financial Statements and Policy
Experience Exhibits database. These
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data contain multiple years of
information on issuers’ revenues,
expenses, and enrollment, collected on
various NAIC financial exhibits
(commonly referred to as ‘‘Blanks’’)
including Supplemental Health Care
Exhibits (SHCEs) that issuers submit to
State insurance regulators through the
NAIC. The NAIC has four different
Blanks for different types of issuers:
Health; Life; Property & Casualty; and
Fraternal issuers.2
In the December 1, 2010 interim final
rule, our analysis relied on 2009 data
from the NAIC database. A total of 618
issuers offering comprehensive major
medical coverage filed annual financial
statements in 2009, with the Health and
Life Blank filers accounting for
approximately 99 percent of all
comprehensive major medical
premiums earned. For this reason, we
restricted our analysis to Health and
Life Blank companies. Comprehensive
major medical coverage 3—including
coverage offered in the individual and
group markets subject to this final
rule—accounted for approximately 47.8
percent of all Accident and Health
(A&H) premiums in 2009. Although the
NAIC data represent the best available
data source with which to estimate
impacts of the MLR rule, the data
contain certain limitations; we
developed imputation methods to
account for these limitations, and we
made several additional data edits that
led us to exclude 176 companies from
the analysis. We used the remaining 442
companies to estimate the regulatory
impacts that were discussed in the
December 1, 2010 interim final rule, as
well as the regulatory impacts that are
discussed below. We refer readers to the
regulatory impact analysis of the
December 1, 2010 interim final rule (75
FR 74892) for additional methodological
information.
5. Estimated Number of Affected
Entities
Given the combination of data
limitations and behavioral uncertainties,
2 If a company’s premiums and reserve ratios for
its health insurance products equals 95 percent or
more of their total business for both the current and
prior reporting years, a company files its annual
statement using the Health Blank. Otherwise, a
company files the annual statement associated with
the type of license held in its domiciliary State, for
example, the Life, Property & Casualty, or Fraternal
Blank.
3 Comprehensive major medical coverage sold to
associations and trusts has been included in
individual comprehensive major medical coverage
for purposes of the RIA. CMS’s estimates exclude
Medigap coverage, which in the NAIC data is
reported separately from comprehensive major
medical coverage offered in the individual and
group markets, and which is not subject to the MLR
requirements under 45 CFR part 158.
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the December 1, 2010 interim final rule
provided a range of estimates, based on
a various assumptions. For the analysis
in this final rule, the high range
estimates correspond to the low rebate
estimates in the December 1, 2010
interim final rule, while the medium
range estimates correspond to the
medium rebate estimates, and the low
range estimates correspond to the high
rebate estimates.
As discussed above in the preamble,
health insurance issuers that sell plans
with total annual benefit limits of
$250,000 or less (‘‘mini-med’’ plans) or
expatriate policies, as described in
§ 158.120(d)(3) and (d)(4), respectively,
are not required to provide notice of
MLR information to policyholders and
subscribers. The 2009 NAIC data does
not allow us to identify these types of
policies separately. Under the December
1, 2010 interim final rule, for the 2011
MLR reporting year, issuers of mini-med
and expatriate policies were required to
report MLR data on a quarterly schedule
under § 158.110(b). Based on the
quarterly reports, it was estimated that,
in 2011, there were 25 issuers of minimed policies with approximately 1
million enrollees and 8 issuers of
expatriate policies with approximately
300,000 enrollees.4 To the extent that
enrollees in mini-med and expatriate
plans were included in the 2009 NAIC
data, this analysis overestimates the
number of entities affected by these
requirements, the number of notices to
be sent by issuers of such policies, and
the administrative costs of providing
notices.
In addition, issuers whose experience
is non-credible, as defined in
§ 158.230(c)(3) and determined in
accordance with § 158.231, are not
required to provide notice of MLR
information to policyholders and
subscribers. As discussed in the
December 1, 2010 interim final rule,
based on 2009 NAIC data, it was
estimated that approximately 68 percent
of licensed entities (State/company
combinations) had less than 1,000
enrollees in at least one State in 2011
and accounted for approximately 1
percent of enrollees. The number of
issuers with less than 1,000 enrollees in
all market/State combinations is
estimated to be 45 in 2011.
Further, issuers of student health
insurance coverage are not required to
provide the MLR notice since the MLR
requirements apply beginning January 1,
2013 for such experience. In the Student
4 For details, see final rule with comment period,
entitled ‘‘Medical Loss Ratio Requirements Under
the Patient Protection and Affordable Care Act,
published on December 7, 2011 (76 FR 76574).
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Federal Register / Vol. 77, No. 95 / Wednesday, May 16, 2012 / Rules and Regulations
Health Insurance Coverage Final Rule
(77 FR 16453) published on March 21,
2012, we estimated that there are 75
issuers of student health insurance
plans with approximately 1.1 million to
1.5 million enrollees. To the extent that
enrollees in student health insurance
plans were included in the 2009 NAIC
data, this analysis overestimates the
number of entities affected by these
requirements, the number of notices to
be provided by issuers of such policies,
and the administrative costs of
providing notices.
Table 2 includes estimates of the
number of issuers that will need to
provide MLR notices pursuant to this
final rule. Issuers are required to
provide notices to group policyholders
and each of their subscribers, and to
subscribers in the individual market. If
there are multiple enrollees in the same
household enrolled in the same health
plan, issuers would need to provide
only one notice to the subscriber. It is
estimated that in the 2011 MLR
reporting year, between 278 and 337
issuers with 65.8 million to 72.2 million
enrollees will meet or exceed the
applicable MLR standard. According to
a large issuer, there are 2.2 covered lives
per family. Therefore, it is estimated
that in 2012, between 278 and 337
issuers will send MLR notices for the
2011 MLR reporting year to 29.9 million
to 32.7 million individual market and
group market subscribers.
In addition, issuers are required to
provide MLR notices to group
policyholders. In the regulatory impact
analysis for the Interim Final Rule for
Group Health Plans and Health
Insurance Coverage Relating to Status as
a Grandfathered Health Plan Under the
Patient Protection and Affordable Care
Act (75 FR 34538) published on June 17,
2010, it was estimated that there are
approximately 3 million large and small
group plans, which include self-insured
plans (self-insured experience is not
subject to the MLR requirements).
According to Medical Expenditure
Panel Survey data, in 2010, 35.8 percent
of all private sector employers that
offered health insurance self-insured at
least one plan.5 In the December 1, 2010
MLR interim final rule, it was estimated
that between 1 percent and 3 percent of
enrollees in fully insured group health
plans would receive rebates during the
2011 MLR reporting year. In the absence
of data on the number of group health
plans in the NAIC database used for this
analysis, we use the percentages of
enrollees not receiving rebates and
employers offering self-insured plans to
estimate the number of fully insured
group health plans whose enrollees
would not receive rebates for the 2011
MLR reporting year. Therefore, it is
estimated that approximately 1.9
million fully insured group
policyholders would receive MLR
notices, pursuant to this final rule, for
the 2011 MLR reporting year.
6. Estimated Costs Related to Notice
Requirement
CMS specifies in this rule standard
language to be used for the notices,
which will minimize the burden for
issuers. Issuers have the option of
providing the notices with other plan
documents or, if the requirements for
electronic disclosure under section 2715
of the PHS Act are satisfied, by using
28795
electronic methods. In the Summary of
Benefits and Coverage and Uniform
Glossary Final Rule (77 FR 8668)
published on February 14, 2012, we
estimated that electronic distribution
would account for 38 percent of all
disclosures in the group market.6 In
addition, according to a report by the
Department of Commerce, 71 percent of
homes in the U.S. had home Internet
access in 2010.7 We therefore estimate
that 38 percent of notices to subscribers
in the group market and 71 percent of
notices to subscribers in the individual
market will be sent electronically, and
the remaining notices will be sent by
mail. Further, we assume that all notices
to group policyholders or employers
will be sent electronically. We assume
that issuers will use clerical staff to
prepare the notices that are distributed
with other plan materials by mail and
will need approximately 0.25 minutes
(or 0.004 hours) to prepare each notice.
The cost of supplies is assumed to be
$0.03 per notice, and labor costs are
assumed to be $30.67 per hour (or $0.13
per notice). Since the notice may be
included with other plan documents,
we assume there will be no additional
mailing costs.
Table 2 includes the estimated total
and average administrative costs to
issuers of preparing and sending the
notices by mail. We estimate that in
2012, issuers will incur total annual
costs of about $3 million and average
costs between $9,000 and $10,000 per
issuer to provide notices for the 2011
MLR reporting year. The average cost of
preparing and sending a notice by mail
is about $0.16 (including labor and
supply costs).
TABLE 2—ESTIMATED ADMINISTRATIVE COST OF MLR NOTICES IN 2012
Estimated
number of affected issuers
MLR reporting year
Estimated
number of notices distributed by mail
Estimated total
hours for preparing notices
distributed by
mail
Estimated supplies cost per
notice distributed by mail
Estimated total
cost of distributing notices
by mail
Estimated average cost per
affected issuer
79,000
$0.03
$3,002,919
$8,911
78,000
$0.03
$2,946,544
$9,661
74,000
$0.03
$2,800,587
$10,074
High Range Estimate
2011 .........................................................
337
19,000,000
Medium Range Estimate
2011 .........................................................
305
18,700,000
Low Range Estimate
pmangrum on DSK3VPTVN1PROD with RULES
2011 .........................................................
278
5 Source: Agency for Healthcare Research and
Quality, Center for Financing, Access and Cost
Trends, 2010 Medical Expenditures Panel SurveyInsurance Component, Table I.A.2.a, ‘‘Percent of
private-sector establishments that offer health
insurance that self-insure at least one plan by firm
size and selected characteristics: United States,
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15:22 May 15, 2012
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17,700,000
2010’’, available at https://meps.ahrq.gov/mepsweb/
data_stats/summ_tables/insr/national/series_1/
2010/tia2a.pdf.
6 The estimate was based on the methodology
used to analyze the cost burden for the Department
of Labor’s claims procedure regulation (OMB
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Control Number 1210–0053), and refers to the
ERISA e-disclosure rule at 29 CFR 2520.104b–1.
7 U.S. Department of Commerce, Exploring the
Digital Nation—Computer and Internet Use at Home
(November, 2011), available at https://
www.ntia.doc.gov/report/2011/exploring-digitalnation-computer-and-internet-use-home.
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Federal Register / Vol. 77, No. 95 / Wednesday, May 16, 2012 / Rules and Regulations
C. Regulatory Alternatives
Under the Executive Order, CMS is
required to consider alternatives to
issuing rules and alternative regulatory
approaches. CMS considered the
regulatory alternative of not requiring
issuers that meet or exceed the
applicable MLR standard to provide
notices with MLR information to
policyholders and subscribers.
However, that would result in reduced
transparency for consumers regarding
the MLR of their issuer for their State
and market, and how it compares to the
applicable standard. CMS also
considered the regulatory alternatives of
requiring issuers that meet or exceed the
applicable MLR standard to provide
notices that include the issuer’s MLR
from the current and prior MLR
reporting years and of making the notice
an ongoing annual requirement.
However, this would result in increased
burden for issuers, particularly since
their MLR information will be available
on the HHS Web site and consumer
knowledge of MLR is expected to
increase after rebates and MLR notices
are provided in 2012. As discussed
earlier, we believe that the greatest
benefit can be achieved by providing
consumers with educational
information in the first year of
applicability, when consumer
knowledge of the MLR is low, and
helping to reduce consumers’ confusion
regarding why they did not receive a
rebate. CMS believes that the option
adopted in this final rule strikes the best
balance of providing valuable
information to consumers while
providing an incentive for issuers to
maximize the percentage of premium
dollars they spend on health care and
quality improving activities.
pmangrum on DSK3VPTVN1PROD with RULES
D. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA)
requires agencies that issue a rule to
analyze options for regulatory relief of
small businesses if a rule has a
significant impact on a substantial
number of small entities. The RFA
generally defines a ‘‘small entity’’ as—
(1) A proprietary firm meeting the size
standards of the Small Business
Administration (SBA), (2) a nonprofit
organization that is not dominant in its
field, or (3) a small government
jurisdiction with a population of less
than 50,000 (States and individuals are
not included in the definition of ‘‘small
entity’’). CMS uses as its measure of
significant economic impact on a
substantial number of small entities a
change in revenue of more than 3 to 5
percent.
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As discussed in the interim final rule
with comment period published on May
5, 2010 (75 FR 24470) relating to the
Federal health care reform insurance
Web Portal requirements, CMS
examined the health insurance industry
in depth in the Regulatory Impact
Analysis prepared for the proposed rule
on establishment of the Medicare
Advantage program (69 FR 46866,
August 3, 2004). In that analysis, it was
determined that there were few, if any,
insurance firms underwriting
comprehensive health insurance
policies (in contrast, for example, to
travel insurance policies or dental
discount policies) that fell below the
size thresholds for ‘‘small’’ business
established by the SBA (currently $7
million in annual receipts for health
issuers).8
For the December 1, 2010 interim
final rule (75 FR 74892), we used the
data set created from the 2009 NAIC
Health and Life Blank annual financial
statement data to develop an updated
estimate of the number of small entities
that offer comprehensive major medical
coverage in the individual and small
group markets, and are therefore subject
to the MLR reporting requirements. For
purposes of this analysis, we used total
Accident and Health (A&H) earned
premiums as a proxy for annual
receipts. These estimates may overstate
the actual number of small health
insurance issuers that would be
affected, since they do not include
receipts from these companies’ other
lines of business.
In the December 1, 2010 interim final
rule, it was estimated that there are 28
small entities with less than $7 million
in A&H earned premiums that offer
individual or group comprehensive
major medical coverage, and would
therefore be subject to the requirements
of this final rule. These small entities
accounted for 6 percent of the estimated
442 total issuers that would be affected
by the MLR requirements. It was
estimated that 86 percent of these small
issuers are subsidiaries of larger issuers,
75 percent only offer coverage in a
single State, 68 percent only offer
individual or group comprehensive
coverage in a single market, 46 percent
also offer other types of A&H coverage,
and 29 percent are Life Blank filers.
CMS estimates that in 2012, of the 28
small entities discussed above, 8 are
subject to the requirements of this final
rule and will incur approximately $100
per issuer in administrative costs related
8 ‘‘Table of Small Business Size Standards
Matched to North American Industry Classification
System Codes,’’ effective March 26, 2012, U.S.
Small Business Administration, available at
www.sba.gov.
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Fmt 4700
Sfmt 4700
to providing notices for the 2011 MLR
reporting year (accounting for less than
0.002 percent of their total A&H
premiums).
CMS believes that these estimates
overstate the number of small entities
that will be affected by the requirements
in this final rule, as well as the relative
impact of these requirements on these
entities, because CMS has based its
analysis on issuers’ total A&H earned
premiums (rather than their total annual
receipts). Therefore, the Secretary
certifies that this final rule will not have
significant impact on a substantial
number of small entities.
In addition, section 1102(b) of the
Social Security Act requires us to
prepare a regulatory impact analysis if
a final rule may have a significant
economic impact on the operations of a
substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 604 of the
RFA. This final rule would not affect
small rural hospitals. Therefore, the
Secretary has determined that this final
rule would not have a significant impact
on the operations of a substantial
number of small rural hospitals.
E. Unfunded Mandates Reform Act
Section 202 of the Unfunded
Mandates Reform Act (UMRA) of 1995
requires that agencies assess anticipated
costs and benefits before issuing any
final rule that includes a Federal
mandate that could result in
expenditures in any 1 year by State,
local or tribal governments, in the
aggregate, or by the private sector, of
$100 million in 1995 dollars, updated
annually for inflation. In 2012, that
threshold level is approximately $139
million.
UMRA does not address the total cost
of a final rule. Rather, it focuses on
certain categories of cost, mainly those
‘‘Federal mandate’’ costs resulting
from—(1) Imposing enforceable duties
on State, local, or tribal governments, or
on the private sector; or (2) increasing
the stringency of conditions in, or
decreasing the funding of, State, local,
or tribal governments under entitlement
programs.
Consistent with policy embodied in
UMRA, this final rule has been designed
to be the least burdensome alternative
for State, local and tribal governments,
and the private sector, while achieving
the objectives of the Affordable Care
Act.
This final rule contains MLR notice
requirements for private sector firms (for
example, health insurance issuers
providing coverage in the individual
and group markets), but it is estimated
that these requirements will not cost
E:\FR\FM\16MYR1.SGM
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Federal Register / Vol. 77, No. 95 / Wednesday, May 16, 2012 / Rules and Regulations
issuers more than approximately $3
million dollars in administrative costs
in 2012. The rule contains no mandates
on State, local or tribal governments.
Thus, this final rule does not impose an
unfunded mandate on State, local or
tribal governments.
F. Federalism
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a final
rule that imposes substantial direct
requirement costs on State and local
governments, preempts State law, or
otherwise has federalism implications.
The requirements specified in this final
rule would not impose substantial direct
costs on State and local governments.
Throughout the process of developing
this final rule, CMS has attempted to
balance States’ interests in regulating
health insurance issuers and the
Congress’ intent to provide uniform
protections to consumers in every State.
By doing so, it is CMS’ view that it has
complied with the requirements of
Executive Order 13132. Under the
requirements set forth in section 8(a) of
Executive Order 13132, and by the
signatures affixed to this rule, HHS
certifies that CMS has complied with
the requirements of Executive Order
13132 for the attached final rule in a
meaningful and timely manner.
G. Congressional Review Act
This final rule is subject to the
Congressional Review Act provisions of
the Small Business Regulatory
Enforcement Fairness Act of 1996 (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.
pmangrum on DSK3VPTVN1PROD with RULES
List of Subjects in 45 CFR Part 158
Administrative practice and
procedure, Claims, Health care, Health
insurance, Health plans, Penalties,
Reporting and recordkeeping
requirements.
For the reasons stated in the
preamble, the Department of Health and
Human Services amends 45 CFR part
158 as set forth below:
PART 158—ISSUER USE OF PREMIUM
REVENUE: REPORTING AND REBATE
REQUIREMENTS
1. The authority citation for part 158
continues to read as follows:
■
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Jkt 226001
Authority: Section 2718 of the Public
Health Service Act (42 U.S.C. 300gg–18), as
amended.
2. Section 158.251 is added to read as
follows:
■
§ 158.251
Notice of MLR information.
(a) Notice of MLR information when
the MLR standard is met or exceeded.—
(1) General requirement. Except as
provided in paragraph (b) of this
section, for the 2011 MLR reporting
year, an issuer whose MLR meets or
exceeds the applicable MLR standard
required by § 158.210 or § 158.211 must
provide each policyholder and
subscriber of a group health plan, and
each subscriber in the individual
market, a notice in accordance with the
requirements of this section.
(2) Timing. An issuer must provide
the notice required in this paragraph (a)
with the first plan document that the
issuer provides to enrollees on or after
July 1, 2012.
(3) Form and appearance. The notice
must be prominently displayed in clear,
conspicuous 14-point bold type on the
front of the plan document or as a
separate notice. The notice may be
provided electronically, if the
requirements for electronic disclosure
under section 2715 of the Public Health
Service Act are met.
(4) Language. The following language
must be used to satisfy the notice
requirement of this paragraph (a):
Medical Loss Ratio Information—The
Affordable Care Act requires health
insurers in the individual and small
group markets to spend at least 80
percent of the premiums they receive on
health care services and activities to
improve health care quality (in the large
group market, this amount is 85
percent). This is referred to as the
Medical Loss Ratio (MLR) rule or the
80/20 rule. If a health insurer does not
spend at least 80 percent of the
premiums it receives on health care
services and activities to improve health
care quality, the insurer must rebate the
difference.
A health insurer’s Medical Loss Ratio
is determined separately for each State’s
individual, small group and large group
markets in which the health insurer
offers health insurance. In some States,
health insurers must meet a higher or
lower Medical Loss Ratio. No later than
August 1, 2012, health insurers must
send any rebates due for 2011 and
information to employers and
individuals regarding any rebates due
for 2011.
You are receiving this notice because
your health insurer had a Medical Loss
Ratio for 2011 that met or exceeded the
required Medical Loss Ratio. For more
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28797
information on Medical Loss Ratio and
your health insurer’s Medical Loss
Ratio, visit www.HealthCare.gov.’’
(b) Exceptions. The requirements of
paragraph (a) of this section do not
apply to an issuer that reports its
experience separately under
§ 158.120(d)(3) or (d)(4), or to an issuer
whose experience is non-credible as
defined in § 158.230(c)(3) and
determined in accordance with
§ 158.231.
Dated: March 8, 2012.
Marilyn Tavenner,
Acting Administrator, Centers for Medicare
& Medicaid Services.
Approved: May 10, 2012.
Kathleen Sebelius,
Secretary, Department of Health and Human
Services.
[FR Doc. 2012–11753 Filed 5–11–12; 11:15 am]
BILLING CODE 4120–01–P
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Parts 12 and 90
[DA 11–1838]
Redundancy of Communications
Systems: Backup Power Private Land
Mobile Radio Services: Selection and
Assignment of Frequencies, and
Transition of the Upper 200 Channels
in the 800 MHz Band to EA Licensing
Federal Communications
Commission.
ACTION: Final rule.
AGENCY:
In this document the Federal
Communications Commission’s
(Commission) Public Safety and
Homeland Security Bureau (Bureau) and
Office of Managing Director (OMD)
make nonsubstantive, editorial revisions
to the Commission’s rules. The Bureau
and OMD make these revisions to delete
certain rule provisions that are without
current legal effect and obsolete. These
nonsubstantive revisions are part of the
Commission’s ongoing examination and
improvement of its processes and
procedures. The revisions and the
specific reasons for each one are set
forth below.
DATES: Effective May 16, 2012.
FOR FURTHER INFORMATION CONTACT: Eric
Ehrenreich, Policy and Licensing
Division, Public Safety and Homeland
Security Bureau, at (202) 418–1726, or
by email at Eric.Ehrenreich@fcc.gov.
SUPPLEMENTARY INFORMATION: This is a
summary of the Bureau and OMD’s
Order, DA 11–1838, adopted and
released on November 1, 2011. The full
SUMMARY:
E:\FR\FM\16MYR1.SGM
16MYR1
Agencies
[Federal Register Volume 77, Number 95 (Wednesday, May 16, 2012)]
[Rules and Regulations]
[Pages 28790-28797]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-11753]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
45 CFR Part 158
[CMS-9998-F]
RIN 0938-AR41
Medical Loss Ratio Requirements Under the Patient Protection and
Affordable Care Act
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule amends the regulations implementing medical
loss ratio (MLR) standards for health insurance issuers under the
Public Health Service Act in order to establish notice requirements for
issuers in the group and individual markets that meet or exceed the
applicable MLR standard in the 2011 MLR reporting year.
DATES: Effective date. This rule is effective on June 15, 2012.
Applicability date. The amendments to part 158 generally apply
beginning
[[Page 28791]]
July 1, 2012, to health insurance issuers offering group or individual
health insurance coverage.
FOR FURTHER INFORMATION CONTACT: Carol Jimenez, (301) 492-4457.
SUPPLEMENTARY INFORMATION:
I. Background
The Patient Protection and Affordable Care Act (Pub. L. 111-148)
was enacted on March 23, 2010; the Health Care and Education
Reconciliation Act (Pub. L. 111-152) was enacted on March 30, 2010. In
this preamble, we refer to the two statutes collectively as the
Affordable Care Act. The Affordable Care Act reorganizes, amends, and
adds to the provisions of Part A of title XXVII of the Public Health
Service Act (PHS Act) relating to group health plans and health
insurance issuers in the group and individual markets.
A request for information relating to the medical loss ratio (MLR)
provisions of section 2718 of the PHS Act was published in the Federal
Register on April 14, 2010 (75 FR 19297). On December 1, 2010, the
Department of Health and Human Services (HHS) published an interim
final rule (75 FR 74864) with a 60-day public comment period, entitled
``Health Insurance Issuers Implementing Medical Loss Ratio (MLR)
Requirements Under the Patient Protection and Affordable Care Act,''
that added a new 45 CFR part 158. A technical correction to the interim
final rule was issued on December 30, 2010 (75 FR 82277).
On December 7, 2011, the Centers for Medicare & Medicaid Services
(CMS) published an interim final rule (76 FR 76596) with a 60-day
public comment period entitled, ``Medical Loss Ratio Rebate
Requirements for Non-Federal Governmental Plans,'' establishing rules
governing the distribution of rebates by health insurance issuers in
group markets for non-Federal governmental plans. Also on December 7,
2011, CMS published a final rule (76 FR 76574) with a 30-day public
comment period, entitled ``Medical Loss Ratio Requirements Under the
Patient Protection and Affordable Care Act,'' that addressed the
treatment of ``mini-med'' and expatriate policies under the MLR
regulations for years after 2011; modified the way the regulations
treat International Statistical Classification of Diseases and Related
Health Problems, 10th Revision (ICD-10) conversion costs; changed the
rules on deducting community benefit expenditures; and revised the
rules governing the distribution of rebates by issuers in group
markets.
In the December 7, 2011 final rule with comment period, we noted
that the notice requirements finalized in the rule only applied to
issuers that owed rebates as a result of not meeting the applicable MLR
standard. Consequently, policyholders and subscribers of issuers
meeting or exceeding the MLR standard would not receive MLR
information, an important tool to increase transparency to consumers.
In the rule, we noted that extending a notice requirement to such cases
would serve the policy goal of greater transparency in how premium
dollars are used, and provide an additional incentive for issuers that
already met the minimum standard to achieve the highest MLR possible.
We therefore solicited comments on whether an issuer that meets or
exceeds the MLR standard for the applicable MLR reporting year should
send a notice to policyholders and subscribers with information about
the MLR standard and its own MLR, as a measurement of issuer
performance. We also solicited comments on whether it would be useful
to include information in the notices about the issuer's prior year MLR
in addition to the current year MLR. We noted that this approach would
allow enrollees to determine if the issuer was doing a better or worse
job of efficiently using premium revenue than in the prior year.
Based on the comments received and weighing consumer transparency
and competition gains with burden on issuers, this final rule
establishes a simple, straightforward notice requirement for health
insurance issuers that meet or exceed the MLR standards established by
the Affordable Care Act, but only requires the notice for the 2011 MLR
reporting year, the first year that the MLR rules are in effect, and
does not require issuers to include information about the current or
prior year MLR. The notice will direct enrollees to the HHS Web site
for specific information about issuers' MLRs.
II. Analysis of and Responses to Public Comments
We received 56 public comments on the December 7, 2011 final rule
with comment period. Commenters included consumer and patient advocacy
organizations, insurance regulators, health insurance issuers, business
advocacy organizations, provider groups, an actuarial professional
group, and others. In addition, we received 11 public comments in
response to the draft MLR Notices and Instructions contained in the MLR
Paperwork Reduction Act (PRA) package (CMS-10418) posted on February
16, 2012. Commenters consisted of consumer groups, health insurance
issuers, an issuer trade association, and a business trade association.
Several of these commenters recommended technical corrections to the
draft notices and instructions. We note that their comments will be
addressed through the PRA process. In addition, commenters recommended
several amendments to the December 1, 2010 interim final rule that were
beyond the scope of this final rulemaking; therefore, we are not making
changes in this final rule based on these comments. In this final rule,
we only address the public comments received on the following issues:
(1) Whether a notice requirement should apply to issuers that meet or
exceed the applicable MLR standards in a particular MLR reporting year;
and (2) whether MLR notices should include information on an issuer's
prior year MLR. The comments received are summarized below with our
responses.
Comments: We received comments that both support and oppose
expanding the notice to issuers that do not owe rebates because they
meet or exceed the MLR standards. Commenters who opposed expanding the
notice rules generally claimed that requiring issuers that do not owe
rebates to provide an MLR notice would impose a burden on issuers that
meet the MLR requirement and provide little value to consumers.
Specifically, issuers, an issuer trade association, and a business
advocacy organization stated that MLR data would confuse or mislead
consumers who may misinterpret the information or who may mistakenly
believe they are owed a rebate. Commenters in support of expanding the
notice rules, such as consumer and patient advocacy organizations,
stated that expanding the notice rules would increase health plan
transparency and ensure that every enrollee receives information about
the meaning of the MLR, rather than only those owed a rebate.
We also received several comments on the question of whether all
MLR notices should include the issuer's MLR from the prior MLR
reporting year. Issuers and trade associations opposed this
requirement, noting that an issuer's MLR from the prior MLR reporting
year is not necessarily a reliable indicator of health plan
performance. These commenters stated that numerous factors other than
health plan efficiency, such as variation in incurred claims, premium
revenue, and adjustments, affect issuers' year-to-year MLRs and that
consumers may be misled when comparing MLRs for multiple years. Several
commenters noted that MLR information will be publicly available on the
HHS Web site and suggested that CMS maintain historical data so that
consumers may monitor changes in
[[Page 28792]]
issuers' MLR over time. In contrast, consumer and patient advocacy
organizations expressed support for including an issuer's prior year
MLR, noting that it would help consumers to better use the MLR
information when making plan selections and better understand how
premium dollars are spent by health insurers. They indicated that
consumers could benefit from more detailed information and that the
notice should include specific information that explains how premium
dollars are being spent, not just whether the MLR was being met.
Response: Expanding the notice of MLR information to all issuers
would further the goals of improving transparency of health insurance
markets, supporting more informed purchase decisions, and promoting
competition and efficiency. At the same time, we appreciate the
concerns about administrative costs. Further, we recognize that under
the Affordable Care Act, issuers' MLR information will be available on
the HHS Web site, HealthCare.gov, providing an efficient method of
public disclosure.\1\
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\1\ Section 2718(a) of the PHS Act provides that ``The Secretary
shall make reports [concerning an issuer's MLR and its components]
received under this section available to the public on the Internet
Web site of the Department of Health and Human Services.'' In
addition, section 1103(b) of the Affordable Care Act provides that
the Federal health care reform insurance Web portal created by the
Secretary under section 1103 to present information relating to
affordable coverage options shall, among other things, ``require the
inclusion of information on the percentage of total premium revenue
expended on nonclinical costs (as reported under section 2718(a) of
the Public Health Service Act).''
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In light of these considerations and after further review and
consideration of the costs and benefits of different notice
alternatives, we are adding a new 45 CFR 158.251 that establishes a
basic notice requirement for issuers in the group and individual
markets that meet or exceed the applicable MLR standard. This new
notice will use standard language to inform policyholders and
subscribers of group health plans, and subscribers in the individual
market, that the issuer has met the minimum MLR standards established
by the Affordable Care Act, but it will not include the issuer's MLR
for the current or prior reporting year or other specific measures of
issuer performance. Instead, the notice will help educate consumers
about the MLR measures and direct them to the HHS Web site,
HealthCare.gov, for information about issuers' actual MLRs.
Additionally, under this final rule, issuers will only need to produce
this notice for the 2011 MLR reporting year, when consumer knowledge of
the MLR is low and the greatest benefit can be achieved by providing
enrollees with educational information. By leveraging existing Federal
information resources while ensuring adequate notice to enrollees in
the first year of applicability, we believe this new notice requirement
balances issuers' interest in administrative efficiency and consumers'
interest in health plan transparency.
This notice rule will ensure that all consumers, not just those
owed a rebate, are informed whether their issuer meets the minimum MLR
standards established by the Affordable Care Act. It will provide
greater transparency to consumers regarding how their premium dollars
are used, promote informed decision-making in the purchase of health
insurance, and ensure that efficiency in the use of premium dollars is
properly valued by consumers. Notifying consumers of the MLR standards
will also reduce confusion as to why certain individuals receive
rebates, while others, such as coworkers or family members with
different insurance plans, do not. Finally, the distribution of MLR
notices to consumers with the HHS Web site, HealthCare.gov, will
promote a more competitive market by creating an incentive for issuers
to spend as high a percentage of premium dollars on health care and
quality improvement as possible, rather than spending just enough to
avoid paying rebates.
III. Provisions of the Final Rule
In paragraph (a)(1) of new Sec. 158.251 of this final rule, we set
forth the general requirement that an issuer whose MLR meets or exceeds
the applicable MLR standard required by Sec. 158.210 or Sec. 158.211
must provide each policyholder and subscriber of a group health plan,
and each subscriber in the individual market, a notice of MLR
information. The required language for the notice is specified in
paragraph (a)(4). This notice requirement applies only for the 2011 MLR
reporting year.
In paragraph (a)(2), we generally align the timing of this new
notice with the timing specified in Sec. 158.240(d) for providing any
rebates that are due and the accompanying notice of rebates. We specify
that the MLR notice must be provided with the first plan document (for
example, open enrollment materials) that is provided to enrollees on or
after July 1, 2012.
In paragraph (a)(3), we direct that the notice be prominently
displayed in clear, conspicuous 14-point bold type on the front of the
plan document, insurance policy or certificate, or as a separate
notice. The MLR notice may be included in the same mailing as other
mailed notices. Further, we specify that the notice may be provided
electronically, consistent with the policy for providing the summary of
benefits and coverage under section 2715 of the PHS Act.
In paragraph (b), we specify certain exceptions to the MLR notice
requirement. We are not requiring health insurance issuers that sell
plans with total annual benefit limits of $250,000 or less (``mini-
med'' plans) or expatriate policies, as described in Sec.
158.120(d)(3) and (d)(4), respectively, to provide MLR notices to
policyholders and subscribers if they meet or exceed the applicable MLR
standard. As discussed in the preamble to the December 7, 2011 final
rule with comment period, issuers of mini-med and expatriate policies
will use a separate methodology for calculating the MLR numerator for
reporting and rebate purposes and are subject to separate notice rules.
We note that issuers of mini-med and expatriate plans must continue to
provide notice of rebates, if any, to current group health plan
policyholders and subscribers, and to subscribers in the individual
market, as provided under Sec. 158.250.
In addition, we are not requiring issuers whose experience is non-
credible, as defined in Sec. 158.230(c)(3) and determined in
accordance with Sec. 158.231, to provide MLR notices to policyholders
and subscribers. An issuer that has fewer than 1,000 covered life-years
does not have sufficiently credible data to determine whether the MLR
standard has been met and thus, under Sec. 158.230(d), is presumed to
meet or exceed the applicable minimum MLR standard. Because non-
credible issuers do not have an MLR to report, the MLR notice
requirement in this final rule does not apply.
Finally, we note that issuers of student health insurance coverage
are not required to provide the MLR notices under this final rule,
because the MLR reporting and rebate requirements of 45 CFR part 158
generally apply for such experience beginning January 1, 2013.
IV. Collection of Information Requirements
This final rule establishes a notification requirement. Although
third-party disclosures (for example, notification requirements) are
generally subject to the Paperwork Reduction Act of 1995 (PRA), the
implementing regulations at 5 CFR 1320.3(c)(2) include an exclusion for
``information originally supplied by the Federal government to the
recipient for the purpose of disclosure to the public.'' Because the
notification will be
[[Page 28793]]
provided by the Federal government, and does not contain text that must
be customized, this exclusion applies.
V. Regulatory Impact Analysis
A. Summary
This final rule amends the regulations implementing MLR standards
for health insurance issuers under section 2718 of the Public Health
Service Act in order to establish notice requirements for issuers in
the group and individual markets that meet or exceed the applicable MLR
standard in the 2011 MLR reporting year.
CMS developed this rule to accomplish its intended benefits in the
most economically efficient manner possible. We have examined the
effects of this rule as required by Executive Order 13563 (76 FR 3821,
January 21, 2011), Executive Order 12866 (58 FR 51735, September 1993,
Regulatory Planning and Review), the Regulatory Flexibility Act (RFA)
(September 19, 1980, Pub. L. 96-354), section 1102(b) of the Social
Security Act, the Unfunded Mandates Reform Act of 1995 (Pub. L. 104-4),
Executive Order 13132 on Federalism, and the Congressional Review Act
(5 U.S.C. 804(2)). In accordance with the Office of Management and
Budget (OMB) Circular A-4, CMS has quantified the benefits, costs, and
transfers where possible and provided a qualitative discussion of some
of the benefits, costs, and transfers that may stem from this final
rule.
B. Executive Orders 13563 and 12866
Executive Order 12866 (58 FR 51735) directs 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). Executive
Order 13563 (76 FR 3821, January 21, 2011) is supplemental to and
reaffirms the principles, structures, and definitions governing
regulatory review as established in Executive Order 12866.
Section 3(f) of Executive Order 12866 defines a ``significant
regulatory action'' as an action that is likely to result in a final
rule--(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 (RIA) must be prepared for major rules
with economically significant effects ($100 million or more in any 1
year), and a ``significant'' regulatory action is subject to review by
OMB. As discussed below, CMS has concluded that this rule is not likely
to have an economic impact of $100 million or more in any 1 year, and
therefore does not meet the definition of a ``significant rule'' under
Executive Order 12866. Nevertheless, CMS has provided an assessment of
the potential costs, benefits, and transfers associated with this final
rule. Accordingly, OMB has reviewed this final rule pursuant to the
Executive Order.
1. Need for Regulatory Action
On December 7, 2011, CMS published a final rule (76 FR 76574) that
invited comment on whether the MLR notice requirement finalized in that
rule should apply not only to issuers that owe rebates but also to
issuers that meet or exceed the applicable MLR standard and therefore
do not owe rebates. For the reasons discussed above and in section
V.B.3.a. below, and based on public comments we received, this final
rule establishes a basic, one-time notice requirement for issuers in
the group and individual markets that meet or exceed the applicable MLR
standard in the 2011 MLR reporting year. This approach is consistent
with Executive Order 13563, which directs agencies to ``identify and
consider regulatory approaches that reduce burdens and maintain
flexibility and freedom of choice for the public. These approaches
include * * * disclosure requirements as well as provision of
information to the public in a form that is clear and intelligible.''
2. Summary of Impacts
In accordance with OMB Circular A-4, Table 1 below depicts an
accounting statement summarizing CMS's assessment of the benefits,
costs, and transfers associated with this regulatory action. The RIA is
limited to 2012 when the notice for the 2011 MLR reporting year will be
provided.
CMS anticipates that the provisions of this final rule will help
ensure greater transparency for consumers regarding how their premium
dollars are used, educate consumers about the MLR standards established
by the Affordable Care Act, and provide an incentive for issuers to
maximize the percentage of premium dollars they spend on health care
and activities that improve health care quality, promoting greater
efficiency in health insurance markets. Issuers that meet or exceed the
applicable MLR standards will incur administrative costs related to
providing the notices to policyholders and subscribers. In accordance
with Executive Order 12866, CMS believes that the benefits of this
regulatory action justify the costs.
Table 1--Accounting Table
------------------------------------------------------------------------
Benefits
-------------------------------------------------------------------------
Qualitative:
* Greater transparency regarding how premium dollars are used by
issuers.
* Incentive for issuers to maximize the percentage of premium
dollars they spend on health care and activities that improve
health care quality.
* Improved information to assist consumers in making plan choices.
------------------------------------------------------------------------
Low Medium High Year Period
Costs and transfers estimate estimate estimate dollar covered
----------------------------------------------------------------------------------------------------------------
Annualized Monetized ($millions/year).................... $2.8 $2.9 $3.0 2012 2012
----------------------------------------------------------------------------------------------------------------
[[Page 28794]]
3. Anticipated Benefits, Costs, and Transfers
This final rule extends a notice requirement to issuers in the
group and individual markets that meet or exceed the applicable MLR
standard in the 2011 MLR reporting year. The notice must use standard
language specified in this final rule. Issuers may provide the notice
with other plan documents or through electronic transmittal, as
permitted for the summary of benefits and coverage under section 2715
of the PHS Act.
a. Benefits
The MLR notices will ensure that consumers are informed whether
their issuer's coverage meets or exceeds the applicable minimum MLR
thresholds established by the Affordable Care Act. Accordingly, the
notices will provide greater transparency to consumers and may help to
reduce consumers' confusion regarding why they did not receive a
rebate. The MLR notices will also provide consumers with educational
information in the first year of applicability when consumer knowledge
of the MLR is low. Additionally, the notices will inform enrollees of
the HHS Web site where they can find issuers' actual MLRs and compare
MLR information across issuers and over years. This will provide an
incentive to issuers to spend as high a percentage of premium dollars
on health care and quality improvement as possible, rather than just
enough to avoid paying rebates. Finally, notice of MLR information will
assist individuals in comparing plans and making plan choices. We
believe that such information disclosure will result in a more
efficient, competitive market.
b. Costs and Transfers
Issuers that meet or exceed the applicable MLR standard will incur
the administrative cost of preparing and mailing the notices. It is
estimated that these costs will total approximately $3 million in 2012.
4. Overview of Data Sources, Methods, and Limitations
On December 1, 2010, we published an interim final rule (75 FR
74864) with a 60-day public comment period. In that rule, we indicated
that the most complete source of data on the number of licensed
entities offering fully insured, private comprehensive major medical
coverage in the individual and group markets is the National
Association of Insurance Commissioners' (NAIC) Annual Financial
Statements and Policy Experience Exhibits database. These data contain
multiple years of information on issuers' revenues, expenses, and
enrollment, collected on various NAIC financial exhibits (commonly
referred to as ``Blanks'') including Supplemental Health Care Exhibits
(SHCEs) that issuers submit to State insurance regulators through the
NAIC. The NAIC has four different Blanks for different types of
issuers: Health; Life; Property & Casualty; and Fraternal issuers.\2\
---------------------------------------------------------------------------
\2\ If a company's premiums and reserve ratios for its health
insurance products equals 95 percent or more of their total business
for both the current and prior reporting years, a company files its
annual statement using the Health Blank. Otherwise, a company files
the annual statement associated with the type of license held in its
domiciliary State, for example, the Life, Property & Casualty, or
Fraternal Blank.
---------------------------------------------------------------------------
In the December 1, 2010 interim final rule, our analysis relied on
2009 data from the NAIC database. A total of 618 issuers offering
comprehensive major medical coverage filed annual financial statements
in 2009, with the Health and Life Blank filers accounting for
approximately 99 percent of all comprehensive major medical premiums
earned. For this reason, we restricted our analysis to Health and Life
Blank companies. Comprehensive major medical coverage \3\--including
coverage offered in the individual and group markets subject to this
final rule--accounted for approximately 47.8 percent of all Accident
and Health (A&H) premiums in 2009. Although the NAIC data represent the
best available data source with which to estimate impacts of the MLR
rule, the data contain certain limitations; we developed imputation
methods to account for these limitations, and we made several
additional data edits that led us to exclude 176 companies from the
analysis. We used the remaining 442 companies to estimate the
regulatory impacts that were discussed in the December 1, 2010 interim
final rule, as well as the regulatory impacts that are discussed below.
We refer readers to the regulatory impact analysis of the December 1,
2010 interim final rule (75 FR 74892) for additional methodological
information.
---------------------------------------------------------------------------
\3\ Comprehensive major medical coverage sold to associations
and trusts has been included in individual comprehensive major
medical coverage for purposes of the RIA. CMS's estimates exclude
Medigap coverage, which in the NAIC data is reported separately from
comprehensive major medical coverage offered in the individual and
group markets, and which is not subject to the MLR requirements
under 45 CFR part 158.
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5. Estimated Number of Affected Entities
Given the combination of data limitations and behavioral
uncertainties, the December 1, 2010 interim final rule provided a range
of estimates, based on a various assumptions. For the analysis in this
final rule, the high range estimates correspond to the low rebate
estimates in the December 1, 2010 interim final rule, while the medium
range estimates correspond to the medium rebate estimates, and the low
range estimates correspond to the high rebate estimates.
As discussed above in the preamble, health insurance issuers that
sell plans with total annual benefit limits of $250,000 or less
(``mini-med'' plans) or expatriate policies, as described in Sec.
158.120(d)(3) and (d)(4), respectively, are not required to provide
notice of MLR information to policyholders and subscribers. The 2009
NAIC data does not allow us to identify these types of policies
separately. Under the December 1, 2010 interim final rule, for the 2011
MLR reporting year, issuers of mini-med and expatriate policies were
required to report MLR data on a quarterly schedule under Sec.
158.110(b). Based on the quarterly reports, it was estimated that, in
2011, there were 25 issuers of mini-med policies with approximately 1
million enrollees and 8 issuers of expatriate policies with
approximately 300,000 enrollees.\4\ To the extent that enrollees in
mini-med and expatriate plans were included in the 2009 NAIC data, this
analysis overestimates the number of entities affected by these
requirements, the number of notices to be sent by issuers of such
policies, and the administrative costs of providing notices.
---------------------------------------------------------------------------
\4\ For details, see final rule with comment period, entitled
``Medical Loss Ratio Requirements Under the Patient Protection and
Affordable Care Act, published on December 7, 2011 (76 FR 76574).
---------------------------------------------------------------------------
In addition, issuers whose experience is non-credible, as defined
in Sec. 158.230(c)(3) and determined in accordance with Sec. 158.231,
are not required to provide notice of MLR information to policyholders
and subscribers. As discussed in the December 1, 2010 interim final
rule, based on 2009 NAIC data, it was estimated that approximately 68
percent of licensed entities (State/company combinations) had less than
1,000 enrollees in at least one State in 2011 and accounted for
approximately 1 percent of enrollees. The number of issuers with less
than 1,000 enrollees in all market/State combinations is estimated to
be 45 in 2011.
Further, issuers of student health insurance coverage are not
required to provide the MLR notice since the MLR requirements apply
beginning January 1, 2013 for such experience. In the Student
[[Page 28795]]
Health Insurance Coverage Final Rule (77 FR 16453) published on March
21, 2012, we estimated that there are 75 issuers of student health
insurance plans with approximately 1.1 million to 1.5 million
enrollees. To the extent that enrollees in student health insurance
plans were included in the 2009 NAIC data, this analysis overestimates
the number of entities affected by these requirements, the number of
notices to be provided by issuers of such policies, and the
administrative costs of providing notices.
Table 2 includes estimates of the number of issuers that will need
to provide MLR notices pursuant to this final rule. Issuers are
required to provide notices to group policyholders and each of their
subscribers, and to subscribers in the individual market. If there are
multiple enrollees in the same household enrolled in the same health
plan, issuers would need to provide only one notice to the subscriber.
It is estimated that in the 2011 MLR reporting year, between 278 and
337 issuers with 65.8 million to 72.2 million enrollees will meet or
exceed the applicable MLR standard. According to a large issuer, there
are 2.2 covered lives per family. Therefore, it is estimated that in
2012, between 278 and 337 issuers will send MLR notices for the 2011
MLR reporting year to 29.9 million to 32.7 million individual market
and group market subscribers.
In addition, issuers are required to provide MLR notices to group
policyholders. In the regulatory impact analysis for the Interim Final
Rule for Group Health Plans and Health Insurance Coverage Relating to
Status as a Grandfathered Health Plan Under the Patient Protection and
Affordable Care Act (75 FR 34538) published on June 17, 2010, it was
estimated that there are approximately 3 million large and small group
plans, which include self-insured plans (self-insured experience is not
subject to the MLR requirements). According to Medical Expenditure
Panel Survey data, in 2010, 35.8 percent of all private sector
employers that offered health insurance self-insured at least one
plan.\5\ In the December 1, 2010 MLR interim final rule, it was
estimated that between 1 percent and 3 percent of enrollees in fully
insured group health plans would receive rebates during the 2011 MLR
reporting year. In the absence of data on the number of group health
plans in the NAIC database used for this analysis, we use the
percentages of enrollees not receiving rebates and employers offering
self-insured plans to estimate the number of fully insured group health
plans whose enrollees would not receive rebates for the 2011 MLR
reporting year. Therefore, it is estimated that approximately 1.9
million fully insured group policyholders would receive MLR notices,
pursuant to this final rule, for the 2011 MLR reporting year.
---------------------------------------------------------------------------
\5\ Source: Agency for Healthcare Research and Quality, Center
for Financing, Access and Cost Trends, 2010 Medical Expenditures
Panel Survey-Insurance Component, Table I.A.2.a, ``Percent of
private-sector establishments that offer health insurance that self-
insure at least one plan by firm size and selected characteristics:
United States, 2010'', available at https://meps.ahrq.gov/mepsweb/data_stats/summ_tables/insr/national/series_1/2010/tia2a.pdf.
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6. Estimated Costs Related to Notice Requirement
CMS specifies in this rule standard language to be used for the
notices, which will minimize the burden for issuers. Issuers have the
option of providing the notices with other plan documents or, if the
requirements for electronic disclosure under section 2715 of the PHS
Act are satisfied, by using electronic methods. In the Summary of
Benefits and Coverage and Uniform Glossary Final Rule (77 FR 8668)
published on February 14, 2012, we estimated that electronic
distribution would account for 38 percent of all disclosures in the
group market.\6\ In addition, according to a report by the Department
of Commerce, 71 percent of homes in the U.S. had home Internet access
in 2010.\7\ We therefore estimate that 38 percent of notices to
subscribers in the group market and 71 percent of notices to
subscribers in the individual market will be sent electronically, and
the remaining notices will be sent by mail. Further, we assume that all
notices to group policyholders or employers will be sent
electronically. We assume that issuers will use clerical staff to
prepare the notices that are distributed with other plan materials by
mail and will need approximately 0.25 minutes (or 0.004 hours) to
prepare each notice. The cost of supplies is assumed to be $0.03 per
notice, and labor costs are assumed to be $30.67 per hour (or $0.13 per
notice). Since the notice may be included with other plan documents, we
assume there will be no additional mailing costs.
---------------------------------------------------------------------------
\6\ The estimate was based on the methodology used to analyze
the cost burden for the Department of Labor's claims procedure
regulation (OMB Control Number 1210-0053), and refers to the ERISA
e-disclosure rule at 29 CFR 2520.104b-1.
\7\ U.S. Department of Commerce, Exploring the Digital Nation--
Computer and Internet Use at Home (November, 2011), available at
https://www.ntia.doc.gov/report/2011/exploring-digital-nation-computer-and-internet-use-home.
---------------------------------------------------------------------------
Table 2 includes the estimated total and average administrative
costs to issuers of preparing and sending the notices by mail. We
estimate that in 2012, issuers will incur total annual costs of about
$3 million and average costs between $9,000 and $10,000 per issuer to
provide notices for the 2011 MLR reporting year. The average cost of
preparing and sending a notice by mail is about $0.16 (including labor
and supply costs).
Table 2--Estimated Administrative Cost of MLR Notices in 2012
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimated
Estimated Estimated total hours Estimated Estimated Estimated
number of number of for preparing supplies cost total cost of average cost
MLR reporting year affected notices notices per notice distributing per affected
issuers distributed by distributed by distributed by notices by issuer
mail mail mail mail
--------------------------------------------------------------------------------------------------------------------------------------------------------
High Range Estimate
--------------------------------------------------------------------------------------------------------------------------------------------------------
2011.................................................... 337 19,000,000 79,000 $0.03 $3,002,919 $8,911
--------------------------------------------------------------------------------------------------------------------------------------------------------
Medium Range Estimate
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2011.................................................... 305 18,700,000 78,000 $0.03 $2,946,544 $9,661
--------------------------------------------------------------------------------------------------------------------------------------------------------
Low Range Estimate
--------------------------------------------------------------------------------------------------------------------------------------------------------
2011.................................................... 278 17,700,000 74,000 $0.03 $2,800,587 $10,074
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[[Page 28796]]
C. Regulatory Alternatives
Under the Executive Order, CMS is required to consider alternatives
to issuing rules and alternative regulatory approaches. CMS considered
the regulatory alternative of not requiring issuers that meet or exceed
the applicable MLR standard to provide notices with MLR information to
policyholders and subscribers. However, that would result in reduced
transparency for consumers regarding the MLR of their issuer for their
State and market, and how it compares to the applicable standard. CMS
also considered the regulatory alternatives of requiring issuers that
meet or exceed the applicable MLR standard to provide notices that
include the issuer's MLR from the current and prior MLR reporting years
and of making the notice an ongoing annual requirement. However, this
would result in increased burden for issuers, particularly since their
MLR information will be available on the HHS Web site and consumer
knowledge of MLR is expected to increase after rebates and MLR notices
are provided in 2012. As discussed earlier, we believe that the
greatest benefit can be achieved by providing consumers with
educational information in the first year of applicability, when
consumer knowledge of the MLR is low, and helping to reduce consumers'
confusion regarding why they did not receive a rebate. CMS believes
that the option adopted in this final rule strikes the best balance of
providing valuable information to consumers while providing an
incentive for issuers to maximize the percentage of premium dollars
they spend on health care and quality improving activities.
D. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA) requires agencies that issue a
rule to analyze options for regulatory relief of small businesses if a
rule has a significant impact on a substantial number of small
entities. The RFA generally defines a ``small entity'' as--(1) A
proprietary firm meeting the size standards of the Small Business
Administration (SBA), (2) a nonprofit organization that is not dominant
in its field, or (3) a small government jurisdiction with a population
of less than 50,000 (States and individuals are not included in the
definition of ``small entity''). CMS uses as its measure of significant
economic impact on a substantial number of small entities a change in
revenue of more than 3 to 5 percent.
As discussed in the interim final rule with comment period
published on May 5, 2010 (75 FR 24470) relating to the Federal health
care reform insurance Web Portal requirements, CMS examined the health
insurance industry in depth in the Regulatory Impact Analysis prepared
for the proposed rule on establishment of the Medicare Advantage
program (69 FR 46866, August 3, 2004). In that analysis, it was
determined that there were few, if any, insurance firms underwriting
comprehensive health insurance policies (in contrast, for example, to
travel insurance policies or dental discount policies) that fell below
the size thresholds for ``small'' business established by the SBA
(currently $7 million in annual receipts for health issuers).\8\
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\8\ ``Table of Small Business Size Standards Matched to North
American Industry Classification System Codes,'' effective March 26,
2012, U.S. Small Business Administration, available at www.sba.gov.
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For the December 1, 2010 interim final rule (75 FR 74892), we used
the data set created from the 2009 NAIC Health and Life Blank annual
financial statement data to develop an updated estimate of the number
of small entities that offer comprehensive major medical coverage in
the individual and small group markets, and are therefore subject to
the MLR reporting requirements. For purposes of this analysis, we used
total Accident and Health (A&H) earned premiums as a proxy for annual
receipts. These estimates may overstate the actual number of small
health insurance issuers that would be affected, since they do not
include receipts from these companies' other lines of business.
In the December 1, 2010 interim final rule, it was estimated that
there are 28 small entities with less than $7 million in A&H earned
premiums that offer individual or group comprehensive major medical
coverage, and would therefore be subject to the requirements of this
final rule. These small entities accounted for 6 percent of the
estimated 442 total issuers that would be affected by the MLR
requirements. It was estimated that 86 percent of these small issuers
are subsidiaries of larger issuers, 75 percent only offer coverage in a
single State, 68 percent only offer individual or group comprehensive
coverage in a single market, 46 percent also offer other types of A&H
coverage, and 29 percent are Life Blank filers.
CMS estimates that in 2012, of the 28 small entities discussed
above, 8 are subject to the requirements of this final rule and will
incur approximately $100 per issuer in administrative costs related to
providing notices for the 2011 MLR reporting year (accounting for less
than 0.002 percent of their total A&H premiums).
CMS believes that these estimates overstate the number of small
entities that will be affected by the requirements in this final rule,
as well as the relative impact of these requirements on these entities,
because CMS has based its analysis on issuers' total A&H earned
premiums (rather than their total annual receipts). Therefore, the
Secretary certifies that this final rule will not have significant
impact on a substantial number of small entities.
In addition, section 1102(b) of the Social Security Act requires us
to prepare a regulatory impact analysis if a final rule may have a
significant economic impact on the operations of a substantial number
of small rural hospitals. This analysis must conform to the provisions
of section 604 of the RFA. This final rule would not affect small rural
hospitals. Therefore, the Secretary has determined that this final rule
would not have a significant impact on the operations of a substantial
number of small rural hospitals.
E. Unfunded Mandates Reform Act
Section 202 of the Unfunded Mandates Reform Act (UMRA) of 1995
requires that agencies assess anticipated costs and benefits before
issuing any final rule that includes a Federal mandate that could
result in expenditures in any 1 year by State, local or tribal
governments, in the aggregate, or by the private sector, of $100
million in 1995 dollars, updated annually for inflation. In 2012, that
threshold level is approximately $139 million.
UMRA does not address the total cost of a final rule. Rather, it
focuses on certain categories of cost, mainly those ``Federal mandate''
costs resulting from--(1) Imposing enforceable duties on State, local,
or tribal governments, or on the private sector; or (2) increasing the
stringency of conditions in, or decreasing the funding of, State,
local, or tribal governments under entitlement programs.
Consistent with policy embodied in UMRA, this final rule has been
designed to be the least burdensome alternative for State, local and
tribal governments, and the private sector, while achieving the
objectives of the Affordable Care Act.
This final rule contains MLR notice requirements for private sector
firms (for example, health insurance issuers providing coverage in the
individual and group markets), but it is estimated that these
requirements will not cost
[[Page 28797]]
issuers more than approximately $3 million dollars in administrative
costs in 2012. The rule contains no mandates on State, local or tribal
governments. Thus, this final rule does not impose an unfunded mandate
on State, local or tribal governments.
F. Federalism
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates a final rule that imposes
substantial direct requirement costs on State and local governments,
preempts State law, or otherwise has federalism implications. The
requirements specified in this final rule would not impose substantial
direct costs on State and local governments.
Throughout the process of developing this final rule, CMS has
attempted to balance States' interests in regulating health insurance
issuers and the Congress' intent to provide uniform protections to
consumers in every State. By doing so, it is CMS' view that it has
complied with the requirements of Executive Order 13132. Under the
requirements set forth in section 8(a) of Executive Order 13132, and by
the signatures affixed to this rule, HHS certifies that CMS has
complied with the requirements of Executive Order 13132 for the
attached final rule in a meaningful and timely manner.
G. Congressional Review Act
This final rule is subject to the Congressional Review Act
provisions of the Small Business Regulatory Enforcement Fairness Act of
1996 (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.
List of Subjects in 45 CFR Part 158
Administrative practice and procedure, Claims, Health care, Health
insurance, Health plans, Penalties, Reporting and recordkeeping
requirements.
For the reasons stated in the preamble, the Department of Health
and Human Services amends 45 CFR part 158 as set forth below:
PART 158--ISSUER USE OF PREMIUM REVENUE: REPORTING AND REBATE
REQUIREMENTS
0
1. The authority citation for part 158 continues to read as follows:
Authority: Section 2718 of the Public Health Service Act (42
U.S.C. 300gg-18), as amended.
0
2. Section 158.251 is added to read as follows:
Sec. 158.251 Notice of MLR information.
(a) Notice of MLR information when the MLR standard is met or
exceeded.--(1) General requirement. Except as provided in paragraph (b)
of this section, for the 2011 MLR reporting year, an issuer whose MLR
meets or exceeds the applicable MLR standard required by Sec. 158.210
or Sec. 158.211 must provide each policyholder and subscriber of a
group health plan, and each subscriber in the individual market, a
notice in accordance with the requirements of this section.
(2) Timing. An issuer must provide the notice required in this
paragraph (a) with the first plan document that the issuer provides to
enrollees on or after July 1, 2012.
(3) Form and appearance. The notice must be prominently displayed
in clear, conspicuous 14-point bold type on the front of the plan
document or as a separate notice. The notice may be provided
electronically, if the requirements for electronic disclosure under
section 2715 of the Public Health Service Act are met.
(4) Language. The following language must be used to satisfy the
notice requirement of this paragraph (a):
Medical Loss Ratio Information--The Affordable Care Act requires
health insurers in the individual and small group markets to spend at
least 80 percent of the premiums they receive on health care services
and activities to improve health care quality (in the large group
market, this amount is 85 percent). This is referred to as the Medical
Loss Ratio (MLR) rule or the 80/20 rule. If a health insurer does not
spend at least 80 percent of the premiums it receives on health care
services and activities to improve health care quality, the insurer
must rebate the difference.
A health insurer's Medical Loss Ratio is determined separately for
each State's individual, small group and large group markets in which
the health insurer offers health insurance. In some States, health
insurers must meet a higher or lower Medical Loss Ratio. No later than
August 1, 2012, health insurers must send any rebates due for 2011 and
information to employers and individuals regarding any rebates due for
2011.
You are receiving this notice because your health insurer had a
Medical Loss Ratio for 2011 that met or exceeded the required Medical
Loss Ratio. For more information on Medical Loss Ratio and your health
insurer's Medical Loss Ratio, visit www.HealthCare.gov.''
(b) Exceptions. The requirements of paragraph (a) of this section
do not apply to an issuer that reports its experience separately under
Sec. 158.120(d)(3) or (d)(4), or to an issuer whose experience is non-
credible as defined in Sec. 158.230(c)(3) and determined in accordance
with Sec. 158.231.
Dated: March 8, 2012.
Marilyn Tavenner,
Acting Administrator, Centers for Medicare & Medicaid Services.
Approved: May 10, 2012.
Kathleen Sebelius,
Secretary, Department of Health and Human Services.
[FR Doc. 2012-11753 Filed 5-11-12; 11:15 am]
BILLING CODE 4120-01-P