Agency Information Collection Activities: Proposed Collection; Comment Request, 731-734 [2019-00433]
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Federal Register / Vol. 84, No. 21 / Thursday, January 31, 2019 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Medicare & Medicaid
Services
[CDC–2018–0085, Docket Number NIOSH–
319]
[Document Identifier: CMS–10330, CMS–
10673, CMS–906, CMS–10433, CMS–276 and
CMS–10694 and CMS–P–0015A]
Partnership Opportunity To Identify
Products for Fentanyl Exposure in
Personal Protective Equipment
Information Database; Reopening of
the Comment Period
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice and reopening of
comment period.
AGENCY:
On October 18, 2018 the
National Institute for Occupational
Safety and Health (NIOSH) of the
Centers for Disease Control and
Prevention (CDC), published a notice in
the Federal Register [83 FR 52834]
announcing the availability of a
Partnership Opportunity to Identify
Products for Fentanyl Exposure in
Personal Protective Equipment
Information Database. Written
comments were to be received by
November 19, 2018. In response to
requests from interested parties, NIOSH
is announcing the reopening of the
comment period.
DATES: Electronic or written comments
must be received by April 1, 2019.
FOR FURTHER INFORMATION CONTACT:
ppeconcerns@cdc.gov, NIOSH, National
Personal Protective Technology
Laboratory, Office of the Director, 626
Cochrans Mill Road, Pittsburgh PA
15236, 1–888–654–2294 (a toll free
number).
SUMMARY:
You may submit comments,
identified by CDC–2018–0085 and
Docket Number NIOSH–319, by either
of the following two methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
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ADDRESSES:
Dated: January 23, 2019.
Frank J. Hearl,
Chief of Staff, National Institute for
Occupational Safety and Health, Centers for
Disease Control and Prevention.
[FR Doc. 2019–00229 Filed 1–30–19; 8:45 am]
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The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
April 1, 2019.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lll, Room C4–26–
SUMMARY:
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731
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10330 Enrollment Opportunity
Notice Relating to Lifetime Limits;
Required Notice of Rescission of
Coverage; and Disclosure
Requirements for Patient Protection
under the Affordable Care Act
CMS–10379 Rate Increase Disclosure
and Review Requirements (45 CFR
part 154)
CMS–10673 Medicare Advantage
Qualifying Payment Arrangement
Incentive (MAQI) Demonstration
CMS–906 The Fiscal Soundness
Reporting Requirements
CMS–276 Prepaid Health Plan Cost
Report
CMS–10694 Testing of Web Survey
Design and Administration for CMS
Experience of Care Surveys
CMS–P–0015A Medicare Current
Beneficiary Survey
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
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collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Extension; Title of Information
Collection: Enrollment Opportunity
Notice Relating to Lifetime Limits;
Required Notice of Rescission of
Coverage; and Disclosure Requirements
for Patient Protection under the
Affordable Care Act; Use: Sections 2712
and 2719A of the Public Health Service
Act, as added by the Affordable Care
Act, and the interim final regulations
titled ‘‘Patient Protection and Affordable
Care Act: Preexisting Condition
Exclusions, Lifetime and Annual Limits,
Rescissions, and Patient Protections’’
(75 FR 37188, June 28, 2010) contain
rescission notice, and patient protection
disclosure requirements that are subject
to the Paperwork Reduction Act of 1995.
The rescission notice will be used by
health plans to provide advance notice
to certain individuals that their coverage
may be rescinded as a result of fraud or
intentional misrepresentation of
material fact. The patient protection
notification will be used by health plans
to inform certain individuals of their
right to choose a primary care provider
or pediatrician and to use obstetrical/
gynecological services without prior
authorization.
The related provisions are finalized in
the final regulations titled ‘‘Final Rules
under the Affordable Care Act for
Grandfathered Plans, Preexisting
Condition Exclusions, Lifetime and
Annual Limits, Rescissions, Dependent
Coverage, Appeals, and Patient
Protections’’. The final regulations also
require that, if State law prohibits
balance billing, or a plan or issuer is
contractually responsible for any
amounts balanced billed by an out-ofnetwork emergency services provider, a
plan or issuer must provide a
participant, beneficiary or enrollee
adequate and prominent notice of their
lack of financial responsibility with
respect to amounts balanced billed in
order to prevent inadvertent payment by
the individual. Form Number: CMS–
10330 (OMB control number: 0938–
1094); Frequency: Occasionally;
Affected Public: Private Sector, State,
Local, or Tribal Governments; Number
of Respondents: 920; Total Annual
Responses: 71,268; Total Annual Hours:
524. (For policy questions regarding this
collection contact Usree
Bandyopadhyay at 410–786–6650.)
2. Type of Information Collection
Request: Revision of a currently
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approved collection; Title of
Information Collection: Medicare
Advantage Qualifying Payment
Arrangement Incentive (MAQI)
Demonstration; Use: The Centers for
Medicare & Medicaid Services (CMS) is
testing a demonstration, under Section
402 of the Social Security Amendments
of 1967 (as amended), entitled the
Medicare Advantage Qualifying
Payment Arrangement Incentive (MAQI)
Demonstration (‘‘the Demonstration’’).
The MAQI demonstration tests whether
providing exclusions from the Meritbased Incentive Payment System (MIPS)
reporting requirements, payment
adjustments, and performance feedback
(collectively, the ‘‘MIPS exclusions’’) for
eligible clinicians who participate to a
sufficient degree in certain payment
arrangements with Medicare Advantage
Organizations (MAOs) (combined with
participation, if any, in Advanced
Alternative Payment Models (APMs)
with Medicare Fee-for-Service (FFS))
will increase or maintain participation
in payment arrangements with MAOs
similar to Advanced APMs and change
the manner in which clinicians deliver
care.
Clinicians may currently participate
in one of two paths of the Quality
Payment Program (QPP): (1) MIPS,
which adjusts Medicare payments based
on combined performance on measures
of quality, cost, improvement activities,
and advancing care information, or (2)
Advanced Alternative Payment Models
with Medicare (Advanced APMs), under
which eligible clinicians may earn an
incentive payment for sufficient
participation in certain payment
arrangements with Medicare fee-forservice (FFS) and other payers, and
starting in the 2019 performance period,
with other payers such as Medicare
Advantage, commercial payers, and
Medicaid managed care. To participate
in the Advanced APM path of QPP for
a given year and earn an incentive
payment, eligible clinicians must meet
the criteria of Qualifying APM
Participants (QPs); in addition to
earning an APM incentive payment, QPs
are excluded from the MIPS reporting
requirements and payment adjustment.
An eligible clinician that does not
meet the criteria to be a QP for a given
year will be subject to MIPS for that year
unless the clinician meets certain other
MIPS exclusion criteria, such as being
newly enrolled in Medicare or meeting
the low volume threshold for Medicare
FFS patients, payments and services.
The MAQI Demonstration allows
participating eligible clinicians to have
the opportunity to receive the MIPS
exclusions for a given year if they
participate to a sufficient degree in
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certain Qualifying Payment
Arrangements with MAOs (and
Advanced APMs with Medicare FFS)
during the performance period for that
year, without requiring them to be QPs
or otherwise meet the MIPS exclusion
criteria of QPP. Under this
Demonstration, clinicians are not
required to have a minimum amount of
participation in an Advanced APM with
Medicare FFS in order to receive the
MIPS exclusions for a year, but if they
did have participation in Advanced
APMs with Medicare FFS, that
participation will also be counted
towards the thresholds that trigger the
provision of MIPS exclusions under the
demonstration.
The first performance period for the
Demonstration was 2018 and the
Demonstration will last up to five years.
Clinicians who meet the definition of an
eligible clinician under QPP, as defined
under 42 CFR 414.1305, are eligible to
participate in the MAQI Demonstration.
Participation will last the duration of
the Demonstration, unless participation
is voluntarily or involuntarily
terminated under the terms and
conditions of the Demonstration.
Demonstration participants will have
the opportunity to submit the required
documentation and be evaluated for the
MIPS exclusions each year. If
Demonstration participants submit
information, but do not meet the
conditions of the Demonstration, their
participation in the Demonstration will
not be terminated, but they will not
receive the MIPS exclusions. Therefore,
unless they become QPs or are excluded
from MIPS for other reasons, the
participating clinicians will be subject
to MIPS and will face the MIPS payment
adjustments for the applicable year.
In order to conduct an evaluation and
effectively implement the MAQI
Demonstration, CMS must collect
information from Demonstration
participants on (a) payment
arrangements with MAOs and (b)
Medicare Advantage (MA) payments
and patient counts. CMS requires a new
collection of this information as this
information is not already available
through other sources. The information
collected in these forms will allow CMS
to evaluate whether the payment
arrangement(s) that clinicians have with
MAOs meet the Qualifying Payment
Arrangement criteria, and determine
whether a clinician’s MAO and FFS
APM patient population or payments
meet demonstration thresholds. Both of
these areas are also requirements for
review and data collection under QPP
(i.e. the Eligible Clinician-Initiated
Other Payer Advanced APM
Determination form and All-Payer QP
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Submission form), and therefore similar
forms have been prepared and reviewed
under the QPP.
Given these similarities in forms,
burden estimates for the MAQI
Demonstration PRA package were
derived from burden analyses and
formulation done in conjunction with
the QPP forms; more specifically the
estimated burden associated with the
submission of payment arrangement
information for Other Payer Advanced
APM Determinations. CMS estimates
the total hour burden per respondent for
the MAQI demonstration to be 15 hours
or less, to match the hours listed in the
equivalent QPP forms. Full detail of
how these estimates were derived can
be found in the published (83 FR
59452).
Based on public comments, we have
revised the collection instruments to
include modifications to allow Taxpayer
Identification Numbers (TIN) level
participation and greater functionality
for organization/authorized
representatives to submit on behalf of
their clinicians. Form Number: CMS–
10673 (OMB control number: 0938–
1354; Frequency: Annually; Affected
Public: Business or other for-profit and
Not-for-profit institutions; Number of
Respondents: 100,000; Total Annual
Responses: 100,000; Total Annual
Hours: 1,500,000. (For policy questions
regarding this collection contact John
Amoh at john.amoh@cms.hhs.gov.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: The Fiscal
Soundness Reporting Requirements;
Use: All contracting organizations must
submit audited annual financial
statements one time per year. In
addition, to the audited annual
submission, Health Plans with a
negative net worth and/or a net loss and
the amount of that loss is greater than
one-half of the organization’s total net
worth must file quarterly financial
statements for fiscal soundness
monitoring. Part D organizations are
required to submit three (3) quarterly
financial statements. Lastly, PACE
organizations are required to file four (4)
quarterly financial statements for the
first three (3) years in the program. After
the first three (3) years, PACE
organizations with a negative net worth
and/or a net loss and the amount of that
loss is greater than one-half of the
organization’s total net worth must
submit quarterly financial statements for
fiscal soundness monitoring. CMS is
responsible for overseeing the ongoing
financial performance for all Medicare
Health Plans, PDPs, and PACE
organizations. Specifically, CMS needs
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the requested information collected in
order to establish that contracting
entities within those programs maintain
fiscally sound operations. Form
Number: CMS–906 (OMB control
number: 0938–0469); Frequency: Yearly;
Affected Public: Business or other forprofits, Not-for profits institutions;
Number of Respondents: 767; Total
Annual Responses: 1589; Total Annual
Hours: 530. (For policy questions
regarding this collection contact Christa
Zalewski at 410–786–1971.)
4. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Information
Collection Requirements for Compliance
with Individual and Group Market
Reforms under Title XXVII of the Public
Health Service Act; Use: Sections 2723
and 2761 of the Public Health Service
Act (PHS Act) direct the Centers for
Medicare and Medicaid Services (CMS)
to enforce a provision (or provisions) of
title XXVII of the PHS Act (including
the implementing regulations in parts
144, 146, 147, and 148 of title 45 of the
Code of Federal Regulations) with
respect to health insurance issuers when
a state has notified CMS that it has not
enacted legislation to enforce or that it
is not otherwise enforcing a provision
(or provisions) of the group and
individual market reforms with respect
to health insurance issuers, or when
CMS has determined that a state is not
substantially enforcing one or more of
those provisions. Section 2723 of the
PHS Act directs CMS to enforce an
applicable provision (or applicable
provisions) of title XXVII of the PHS Act
(including the implementing regulations
in parts 146 and 147 of title 45 of the
Code of Federal Regulations) with
respect to group health plans that are
non-Federal governmental plans. This
collection of information includes
requirements that are necessary for CMS
to conduct compliance review activities.
The Department of the Treasury, the
Department of Labor, and the
Department of Health and Human
Services (collectively, the Departments)
issued proposed regulations titled
‘‘Health Reimbursement Arrangements
and Other Account-Based Group Health
Plans’’ under section 2711 of the PHS
Act and the health nondiscrimination
provisions of HIPAA, Public Law 104–
191 (HIPAA nondiscrimination
provisions.) The proposed regulations
are intended to expand the usability of
health reimbursement arrangements and
other account-based group health plans
(collectively referred to as HRAs). In
general, the proposed regulations would
expand the usability of HRAs by
eliminating the current prohibition on
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integrating HRAs with individual health
insurance coverage, thereby permitting
employers to offer HRAs to employees
enrolled in individual health insurance
coverage. Under the proposed
regulations employees would be
permitted to use amounts in an HRA
integrated with individual health
insurance coverage to pay expenses for
medical care (including premiums for
individual health insurance coverage),
subject to certain requirements. This
collection includes the requirements
related to substantiation of individual
health insurance coverage by an HRA
prior to making reimbursements and the
notice that HRAs would be required to
provide to each participant. Form
Number: CMS–10430 (OMB control
number: 0938–0702); Frequency:
Annually; Affected Public: State
Governments, Private Sector, State or
local governments; Number of
Respondents: 2,785; Total Annual
Responses: 298,175; Total Annual
Hours: 7,737. (For policy questions
regarding this collection contact Usree
Bandyopadhyay at 410–786–6650.)
5. Type of Information Collection
Request: Revision of a currently
approved information collection; Title
of Information Collection: Prepaid
Health Plan Cost Report; Use: Health
Maintenance Organizations and
Competitive Medical Plans (HMO/
CMPs) contracting with the Secretary
under Section 1876 of the Social
Security Act are required to submit a
budget and enrollment forecast, semiannual interim report, 4th Quarter
interim report (CMS has waived this
annual submission), and a final certified
cost report in accordance with 42 CFR
417.572–417.576. The submission,
receipt and processing of the cost
reports is imperative to determine if
MCOs are paid on a reasonable basis for
the covered services furnished to
Medicare enrollees. CMS reviews the
data submitted within the cost reports to
establish monthly payment rates,
monitor interim rates, and determine
the final reimbursement. Health Care
Prepayment Plans (HCPPs) contracting
with the Secretary under Section 1833
of the Social Security Act are required
to submit a budget and enrollment
forecast, semi-annual interim report,
and final cost report in accordance with
42 CFR 417.808 and 42 CFR 417.810.
Form Number: CMS–276 (OMB control
number: 0938–0165); Frequency:
Quarterly; Affected Public: Businesses
or other for-profits, Not-for-profit
institutions; Number of Respondents:
57; Total Annual Responses: 67; Total
Annual Hours: 1,800. (For policy
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questions regarding this collection,
contact Bilal Farrakh at 410–786–4456.)
6. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Testing of Web
Survey Design and Administration for
CMS Experience of Care Surveys; Use:
This collection is a new generic
clearance request which encompasses
an array of research activities to add
web administration protocols to a series
of surveys conducted by the Centers for
Medicare & Medicaid Services (CMS).
This request seeks burden hours to
allow CMS and its contractors to
conduct cognitive in-depth interviews,
focus groups, pilot tests, and usability
studies to support a variety of
methodological studies around web
modes of data collection for programs
such as the Emergency Department
Experience of Care (EDPEC), Fee-forService (FFS) Consumer Assessment of
Healthcare Providers and Systems
(CAHPS), Hospital CAHPS (HCAHPS),
Medicare Advantage and Prescription
Drug (MA & PDP) CAHPS, Home Health
(HH) CAHPS, Hospice CAHPS, InCenter Hemodialysis (ICH) CAHPS, the
Health Outcomes Survey (HOS), and the
Medicare Advantage and Part D Plan
Disenrollment Reasons surveys.
Providers. Form Number: CMS–10694
(OMB control number: 0938-New);
Frequency: Yearly; Affected Public:
Business or other for-profits, Not-forProfit Institutions; Number of
Respondents: 75,250; Total Annual
Responses: 75,250; Total Annual Hours:
17,000. (For policy, questions regarding
this collection contact Elizabeth H.
Goldstein at 410–786–6665.)
7. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare
Current Beneficiary Survey; Use: CMS is
the largest single payer of health care in
the United States. The agency plays a
direct or indirect role in administering
health insurance coverage for more than
120 million people across the Medicare,
Medicaid, CHIP, and Exchange
populations. A critical aim for CMS is
to be an effective steward, major force,
and trustworthy partner in supporting
innovative approaches to improving
quality, accessibility, and affordability
in healthcare. CMS also aims to put
patients first in the delivery of their
health care needs.
The Medicare Current Beneficiary
Survey (MCBS) is the most
comprehensive and complete survey
available on the Medicare population
and is essential in capturing data not
otherwise collected through our
operations. The MCBS is an in-person,
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nationally-representative, longitudinal
survey of Medicare beneficiaries that we
sponsor and is directed by the Office of
Enterprise Data and Analytics (OEDA).
The survey captures beneficiary
information whether aged or disabled,
living in the community or facility, or
serviced by managed care or fee-forservice. Data produced as part of the
MCBS are enhanced with our
administrative data (e.g. fee-for-service
claims, prescription drug event data,
enrollment, etc.) to provide users with
more accurate and complete estimates of
total health care costs and utilization.
The MCBS has been continuously
fielded for more than 26 years,
encompassing over 1 million interviews
and more than 100,000 survey
participants. Respondents participate in
up to 11 interviews over a four year
period. This gives a comprehensive
picture of health care costs and
utilization over a period of time.
The MCBS continues to provide
unique insight into the Medicare
program and helps CMS and our
external stakeholders better understand
and evaluate the impact of existing
programs and significant new policy
initiatives. In the past, MCBS data have
been used to assess potential changes to
the Medicare program. For example, the
MCBS was instrumental in supporting
the development and implementation of
the Medicare prescription drug benefit
by providing a means to evaluate
prescription drug costs and out-ofpocket burden for these drugs to
Medicare beneficiaries. Beginning in
2020, this proposed revision to the
clearance will add a few new measures
to existing questionnaire sections. The
revisions will result in a slight decrease
in respondent burden of 4%, due to
fewer projected completed cases each
round. Form Number: CMS–P–0015A
(OMB control number: 0938–0568);
Frequency: Occasionally; Affected
Public: Business or other for-profits and
Not-for-profit institutions; Number of
Respondents: 13,656; Total Annual
Responses: 35,998; Total Annual Hours:
42,610. (For policy questions regarding
this collection contact William Long at
410–786–7927.)
Dated: January 28, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2019–00433 Filed 1–30–19; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–R–262, CMS–
224–14, CMS–R–240, CMS–10164, CMS–
2552–10, CMS–R–306, CMS–10684, CMS–
10237, CMS–10524 and CMS–10511]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by March 4, 2019.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 OR, Email:
OIRA_submission@omb.eop.gov.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
SUMMARY:
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Agencies
[Federal Register Volume 84, Number 21 (Thursday, January 31, 2019)]
[Notices]
[Pages 731-734]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-00433]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10330, CMS-10673, CMS-906, CMS-10433, CMS-276
and CMS-10694 and CMS-P-0015A]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Department of Health
and Human Services.
ACTION: Notice.
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SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (the PRA), federal agencies are required to publish notice
in the Federal Register concerning each proposed collection of
information (including each proposed extension or reinstatement of an
existing collection of information) and to allow 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility, and clarity of the information to be
collected, and the use of automated collection techniques or other
forms of information technology to minimize the information collection
burden.
DATES: Comments must be received by April 1, 2019.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ___, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' website address at website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: William N. Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-10330 Enrollment Opportunity Notice Relating to Lifetime Limits;
Required Notice of Rescission of Coverage; and Disclosure Requirements
for Patient Protection under the Affordable Care Act
CMS-10379 Rate Increase Disclosure and Review Requirements (45 CFR part
154)
CMS-10673 Medicare Advantage Qualifying Payment Arrangement Incentive
(MAQI) Demonstration
CMS-906 The Fiscal Soundness Reporting Requirements
CMS-276 Prepaid Health Plan Cost Report
CMS-10694 Testing of Web Survey Design and Administration for CMS
Experience of Care Surveys
CMS-P-0015A Medicare Current Beneficiary Survey
Under the PRA (44 U.S.C. 3501-3520), federal agencies must obtain
approval from the Office of Management and Budget (OMB) for each
collection of information they conduct or sponsor. The term
``collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA requires federal agencies
to publish a 60-day notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
or reinstatement of an existing
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collection of information, before submitting the collection to OMB for
approval. To comply with this requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection Request: Extension; Title of
Information Collection: Enrollment Opportunity Notice Relating to
Lifetime Limits; Required Notice of Rescission of Coverage; and
Disclosure Requirements for Patient Protection under the Affordable
Care Act; Use: Sections 2712 and 2719A of the Public Health Service
Act, as added by the Affordable Care Act, and the interim final
regulations titled ``Patient Protection and Affordable Care Act:
Preexisting Condition Exclusions, Lifetime and Annual Limits,
Rescissions, and Patient Protections'' (75 FR 37188, June 28, 2010)
contain rescission notice, and patient protection disclosure
requirements that are subject to the Paperwork Reduction Act of 1995.
The rescission notice will be used by health plans to provide advance
notice to certain individuals that their coverage may be rescinded as a
result of fraud or intentional misrepresentation of material fact. The
patient protection notification will be used by health plans to inform
certain individuals of their right to choose a primary care provider or
pediatrician and to use obstetrical/gynecological services without
prior authorization.
The related provisions are finalized in the final regulations
titled ``Final Rules under the Affordable Care Act for Grandfathered
Plans, Preexisting Condition Exclusions, Lifetime and Annual Limits,
Rescissions, Dependent Coverage, Appeals, and Patient Protections''.
The final regulations also require that, if State law prohibits balance
billing, or a plan or issuer is contractually responsible for any
amounts balanced billed by an out-of-network emergency services
provider, a plan or issuer must provide a participant, beneficiary or
enrollee adequate and prominent notice of their lack of financial
responsibility with respect to amounts balanced billed in order to
prevent inadvertent payment by the individual. Form Number: CMS-10330
(OMB control number: 0938-1094); Frequency: Occasionally; Affected
Public: Private Sector, State, Local, or Tribal Governments; Number of
Respondents: 920; Total Annual Responses: 71,268; Total Annual Hours:
524. (For policy questions regarding this collection contact Usree
Bandyopadhyay at 410-786-6650.)
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicare
Advantage Qualifying Payment Arrangement Incentive (MAQI)
Demonstration; Use: The Centers for Medicare & Medicaid Services (CMS)
is testing a demonstration, under Section 402 of the Social Security
Amendments of 1967 (as amended), entitled the Medicare Advantage
Qualifying Payment Arrangement Incentive (MAQI) Demonstration (``the
Demonstration''). The MAQI demonstration tests whether providing
exclusions from the Merit-based Incentive Payment System (MIPS)
reporting requirements, payment adjustments, and performance feedback
(collectively, the ``MIPS exclusions'') for eligible clinicians who
participate to a sufficient degree in certain payment arrangements with
Medicare Advantage Organizations (MAOs) (combined with participation,
if any, in Advanced Alternative Payment Models (APMs) with Medicare
Fee-for-Service (FFS)) will increase or maintain participation in
payment arrangements with MAOs similar to Advanced APMs and change the
manner in which clinicians deliver care.
Clinicians may currently participate in one of two paths of the
Quality Payment Program (QPP): (1) MIPS, which adjusts Medicare
payments based on combined performance on measures of quality, cost,
improvement activities, and advancing care information, or (2) Advanced
Alternative Payment Models with Medicare (Advanced APMs), under which
eligible clinicians may earn an incentive payment for sufficient
participation in certain payment arrangements with Medicare fee-for-
service (FFS) and other payers, and starting in the 2019 performance
period, with other payers such as Medicare Advantage, commercial
payers, and Medicaid managed care. To participate in the Advanced APM
path of QPP for a given year and earn an incentive payment, eligible
clinicians must meet the criteria of Qualifying APM Participants (QPs);
in addition to earning an APM incentive payment, QPs are excluded from
the MIPS reporting requirements and payment adjustment.
An eligible clinician that does not meet the criteria to be a QP
for a given year will be subject to MIPS for that year unless the
clinician meets certain other MIPS exclusion criteria, such as being
newly enrolled in Medicare or meeting the low volume threshold for
Medicare FFS patients, payments and services. The MAQI Demonstration
allows participating eligible clinicians to have the opportunity to
receive the MIPS exclusions for a given year if they participate to a
sufficient degree in certain Qualifying Payment Arrangements with MAOs
(and Advanced APMs with Medicare FFS) during the performance period for
that year, without requiring them to be QPs or otherwise meet the MIPS
exclusion criteria of QPP. Under this Demonstration, clinicians are not
required to have a minimum amount of participation in an Advanced APM
with Medicare FFS in order to receive the MIPS exclusions for a year,
but if they did have participation in Advanced APMs with Medicare FFS,
that participation will also be counted towards the thresholds that
trigger the provision of MIPS exclusions under the demonstration.
The first performance period for the Demonstration was 2018 and the
Demonstration will last up to five years. Clinicians who meet the
definition of an eligible clinician under QPP, as defined under 42 CFR
414.1305, are eligible to participate in the MAQI Demonstration.
Participation will last the duration of the Demonstration, unless
participation is voluntarily or involuntarily terminated under the
terms and conditions of the Demonstration. Demonstration participants
will have the opportunity to submit the required documentation and be
evaluated for the MIPS exclusions each year. If Demonstration
participants submit information, but do not meet the conditions of the
Demonstration, their participation in the Demonstration will not be
terminated, but they will not receive the MIPS exclusions. Therefore,
unless they become QPs or are excluded from MIPS for other reasons, the
participating clinicians will be subject to MIPS and will face the MIPS
payment adjustments for the applicable year.
In order to conduct an evaluation and effectively implement the
MAQI Demonstration, CMS must collect information from Demonstration
participants on (a) payment arrangements with MAOs and (b) Medicare
Advantage (MA) payments and patient counts. CMS requires a new
collection of this information as this information is not already
available through other sources. The information collected in these
forms will allow CMS to evaluate whether the payment arrangement(s)
that clinicians have with MAOs meet the Qualifying Payment Arrangement
criteria, and determine whether a clinician's MAO and FFS APM patient
population or payments meet demonstration thresholds. Both of these
areas are also requirements for review and data collection under QPP
(i.e. the Eligible Clinician-Initiated Other Payer Advanced APM
Determination form and All-Payer QP
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Submission form), and therefore similar forms have been prepared and
reviewed under the QPP.
Given these similarities in forms, burden estimates for the MAQI
Demonstration PRA package were derived from burden analyses and
formulation done in conjunction with the QPP forms; more specifically
the estimated burden associated with the submission of payment
arrangement information for Other Payer Advanced APM Determinations.
CMS estimates the total hour burden per respondent for the MAQI
demonstration to be 15 hours or less, to match the hours listed in the
equivalent QPP forms. Full detail of how these estimates were derived
can be found in the published (83 FR 59452).
Based on public comments, we have revised the collection
instruments to include modifications to allow Taxpayer Identification
Numbers (TIN) level participation and greater functionality for
organization/authorized representatives to submit on behalf of their
clinicians. Form Number: CMS-10673 (OMB control number: 0938-1354;
Frequency: Annually; Affected Public: Business or other for-profit and
Not-for-profit institutions; Number of Respondents: 100,000; Total
Annual Responses: 100,000; Total Annual Hours: 1,500,000. (For policy
questions regarding this collection contact John Amoh at
john.amoh@cms.hhs.gov.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: The Fiscal
Soundness Reporting Requirements; Use: All contracting organizations
must submit audited annual financial statements one time per year. In
addition, to the audited annual submission, Health Plans with a
negative net worth and/or a net loss and the amount of that loss is
greater than one-half of the organization's total net worth must file
quarterly financial statements for fiscal soundness monitoring. Part D
organizations are required to submit three (3) quarterly financial
statements. Lastly, PACE organizations are required to file four (4)
quarterly financial statements for the first three (3) years in the
program. After the first three (3) years, PACE organizations with a
negative net worth and/or a net loss and the amount of that loss is
greater than one-half of the organization's total net worth must submit
quarterly financial statements for fiscal soundness monitoring. CMS is
responsible for overseeing the ongoing financial performance for all
Medicare Health Plans, PDPs, and PACE organizations. Specifically, CMS
needs the requested information collected in order to establish that
contracting entities within those programs maintain fiscally sound
operations. Form Number: CMS-906 (OMB control number: 0938-0469);
Frequency: Yearly; Affected Public: Business or other for-profits, Not-
for profits institutions; Number of Respondents: 767; Total Annual
Responses: 1589; Total Annual Hours: 530. (For policy questions
regarding this collection contact Christa Zalewski at 410-786-1971.)
4. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Information
Collection Requirements for Compliance with Individual and Group Market
Reforms under Title XXVII of the Public Health Service Act; Use:
Sections 2723 and 2761 of the Public Health Service Act (PHS Act)
direct the Centers for Medicare and Medicaid Services (CMS) to enforce
a provision (or provisions) of title XXVII of the PHS Act (including
the implementing regulations in parts 144, 146, 147, and 148 of title
45 of the Code of Federal Regulations) with respect to health insurance
issuers when a state has notified CMS that it has not enacted
legislation to enforce or that it is not otherwise enforcing a
provision (or provisions) of the group and individual market reforms
with respect to health insurance issuers, or when CMS has determined
that a state is not substantially enforcing one or more of those
provisions. Section 2723 of the PHS Act directs CMS to enforce an
applicable provision (or applicable provisions) of title XXVII of the
PHS Act (including the implementing regulations in parts 146 and 147 of
title 45 of the Code of Federal Regulations) with respect to group
health plans that are non-Federal governmental plans. This collection
of information includes requirements that are necessary for CMS to
conduct compliance review activities.
The Department of the Treasury, the Department of Labor, and the
Department of Health and Human Services (collectively, the Departments)
issued proposed regulations titled ``Health Reimbursement Arrangements
and Other Account-Based Group Health Plans'' under section 2711 of the
PHS Act and the health nondiscrimination provisions of HIPAA, Public
Law 104-191 (HIPAA nondiscrimination provisions.) The proposed
regulations are intended to expand the usability of health
reimbursement arrangements and other account-based group health plans
(collectively referred to as HRAs). In general, the proposed
regulations would expand the usability of HRAs by eliminating the
current prohibition on integrating HRAs with individual health
insurance coverage, thereby permitting employers to offer HRAs to
employees enrolled in individual health insurance coverage. Under the
proposed regulations employees would be permitted to use amounts in an
HRA integrated with individual health insurance coverage to pay
expenses for medical care (including premiums for individual health
insurance coverage), subject to certain requirements. This collection
includes the requirements related to substantiation of individual
health insurance coverage by an HRA prior to making reimbursements and
the notice that HRAs would be required to provide to each participant.
Form Number: CMS-10430 (OMB control number: 0938-0702); Frequency:
Annually; Affected Public: State Governments, Private Sector, State or
local governments; Number of Respondents: 2,785; Total Annual
Responses: 298,175; Total Annual Hours: 7,737. (For policy questions
regarding this collection contact Usree Bandyopadhyay at 410-786-6650.)
5. Type of Information Collection Request: Revision of a currently
approved information collection; Title of Information Collection:
Prepaid Health Plan Cost Report; Use: Health Maintenance Organizations
and Competitive Medical Plans (HMO/CMPs) contracting with the Secretary
under Section 1876 of the Social Security Act are required to submit a
budget and enrollment forecast, semi-annual interim report, 4th Quarter
interim report (CMS has waived this annual submission), and a final
certified cost report in accordance with 42 CFR 417.572-417.576. The
submission, receipt and processing of the cost reports is imperative to
determine if MCOs are paid on a reasonable basis for the covered
services furnished to Medicare enrollees. CMS reviews the data
submitted within the cost reports to establish monthly payment rates,
monitor interim rates, and determine the final reimbursement. Health
Care Prepayment Plans (HCPPs) contracting with the Secretary under
Section 1833 of the Social Security Act are required to submit a budget
and enrollment forecast, semi-annual interim report, and final cost
report in accordance with 42 CFR 417.808 and 42 CFR 417.810. Form
Number: CMS-276 (OMB control number: 0938-0165); Frequency: Quarterly;
Affected Public: Businesses or other for-profits, Not-for-profit
institutions; Number of Respondents: 57; Total Annual Responses: 67;
Total Annual Hours: 1,800. (For policy
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questions regarding this collection, contact Bilal Farrakh at 410-786-
4456.)
6. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection: Testing
of Web Survey Design and Administration for CMS Experience of Care
Surveys; Use: This collection is a new generic clearance request which
encompasses an array of research activities to add web administration
protocols to a series of surveys conducted by the Centers for Medicare
& Medicaid Services (CMS). This request seeks burden hours to allow CMS
and its contractors to conduct cognitive in-depth interviews, focus
groups, pilot tests, and usability studies to support a variety of
methodological studies around web modes of data collection for programs
such as the Emergency Department Experience of Care (EDPEC), Fee-for-
Service (FFS) Consumer Assessment of Healthcare Providers and Systems
(CAHPS), Hospital CAHPS (HCAHPS), Medicare Advantage and Prescription
Drug (MA & PDP) CAHPS, Home Health (HH) CAHPS, Hospice CAHPS, In-Center
Hemodialysis (ICH) CAHPS, the Health Outcomes Survey (HOS), and the
Medicare Advantage and Part D Plan Disenrollment Reasons surveys.
Providers. Form Number: CMS-10694 (OMB control number: 0938-New);
Frequency: Yearly; Affected Public: Business or other for-profits, Not-
for-Profit Institutions; Number of Respondents: 75,250; Total Annual
Responses: 75,250; Total Annual Hours: 17,000. (For policy, questions
regarding this collection contact Elizabeth H. Goldstein at 410-786-
6665.)
7. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicare Current
Beneficiary Survey; Use: CMS is the largest single payer of health care
in the United States. The agency plays a direct or indirect role in
administering health insurance coverage for more than 120 million
people across the Medicare, Medicaid, CHIP, and Exchange populations. A
critical aim for CMS is to be an effective steward, major force, and
trustworthy partner in supporting innovative approaches to improving
quality, accessibility, and affordability in healthcare. CMS also aims
to put patients first in the delivery of their health care needs.
The Medicare Current Beneficiary Survey (MCBS) is the most
comprehensive and complete survey available on the Medicare population
and is essential in capturing data not otherwise collected through our
operations. The MCBS is an in-person, nationally-representative,
longitudinal survey of Medicare beneficiaries that we sponsor and is
directed by the Office of Enterprise Data and Analytics (OEDA). The
survey captures beneficiary information whether aged or disabled,
living in the community or facility, or serviced by managed care or
fee-for-service. Data produced as part of the MCBS are enhanced with
our administrative data (e.g. fee-for-service claims, prescription drug
event data, enrollment, etc.) to provide users with more accurate and
complete estimates of total health care costs and utilization. The MCBS
has been continuously fielded for more than 26 years, encompassing over
1 million interviews and more than 100,000 survey participants.
Respondents participate in up to 11 interviews over a four year period.
This gives a comprehensive picture of health care costs and utilization
over a period of time.
The MCBS continues to provide unique insight into the Medicare
program and helps CMS and our external stakeholders better understand
and evaluate the impact of existing programs and significant new policy
initiatives. In the past, MCBS data have been used to assess potential
changes to the Medicare program. For example, the MCBS was instrumental
in supporting the development and implementation of the Medicare
prescription drug benefit by providing a means to evaluate prescription
drug costs and out-of-pocket burden for these drugs to Medicare
beneficiaries. Beginning in 2020, this proposed revision to the
clearance will add a few new measures to existing questionnaire
sections. The revisions will result in a slight decrease in respondent
burden of 4%, due to fewer projected completed cases each round. Form
Number: CMS-P-0015A (OMB control number: 0938-0568); Frequency:
Occasionally; Affected Public: Business or other for-profits and Not-
for-profit institutions; Number of Respondents: 13,656; Total Annual
Responses: 35,998; Total Annual Hours: 42,610. (For policy questions
regarding this collection contact William Long at 410-786-7927.)
Dated: January 28, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2019-00433 Filed 1-30-19; 8:45 am]
BILLING CODE 4120-01-P