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Introduction
On September 18, 2008 the
Centers for Medicare & Medicaid Services (CMS), issued Interim Final
Regulations, with a comment period, implementing certain aspects of
the Medicare Improvements for Patients and Providers Act of 2008 (MIPPA)
concerning Medicare Parts C and D. The primary, though not
exclusive, matters addressed in this Interim Final Rule are Medicare
Advantage Special Needs Plans and marketing rules relating to
Medicare Advantage Plans and Prescription Drug Plans.
In a somewhat confusing
preamble, CMS distinguishes these regulations from others that it
intends to release "in the near future" that will respond to public
comments made on a proposed rule it issued on May 16, 2008. The
confusion arises from the contents of the May proposed rule, which
included specific provisions that were subsequently addressed by
MIPPA as well as other provisions.
This Weekly Alert will
discuss the regulations governing Medicare Advantage Special Needs
Plans (SNPs), which address only some of the MIPPA provisions
concerning SNPs and only some of the SNP provisions addressed in the
May proposed rule. A future Weekly Alert will address marketing
provisions, both of this regulation and of a final rule also
released on September 18.
The regulations governing
Medicare Advantage Special Needs Plans address four key areas:
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Models of Care for SNPs;
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Contracts with State Medicaid agencies for Dual-Eligible SNPs;
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Disclosure of certain information for Dual-Eligible SNPs;
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Data collection, analysis and reporting.
Background
Created by the Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA),
SNPs are conceptually related to government-supported
demonstrations, such as On Lok, the Program of All Inclusive Care
for the Elderly (PACE), and the dual eligible integration
demonstrations that have, for decades, delivered focused services to
those Medicare beneficiaries who generally need more intense health
care services than the average Medicare beneficiary.
The MMA laid out three
specific categories of SNPs:
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Dual SNPs for those beneficiaries who are dually eligible for
Medicare and Medicaid;
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Chronic SNPs for those beneficiaries who have a specific severe
or disabling chronic condition identified by the SNP;
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Institutional SNPs for those beneficiaries residing in specified
institutions for extended periods of time.
SNPs have proliferated
since 2004, the first year of operation, due in part to the revenue
they generate for plans. In 2004, 11 SNPs were approved by CMS. As
of January 2008, CMS had approved 787 SNPs, comprising 442
dual-eligible SNPs, 256 chronic care SNPs, and 89 institutional
SNPs. In September 2008, SNPs enrolled more than 1.2 million
people.
In marked contrast with
"regular" Medicare Advantage (MA) plans, which are prohibited from
discriminating among Medicare beneficiaries in their enrollment,
SNPs are designed to serve, either exclusively or
disproportionately, specific Medicare subpopulations. SNPs must be
coordinated care plans and they must offer a Part D (prescription
drug) benefit in addition to all benefits under Parts A and B.
Aside from these two conditions, SNPs have operated with few
requirements from either the law or implementing regulations and
with little oversight of how or whether they deliver what they
promise.
Additionally, SNPs are
not subject to the same enrollment periods as other Medicare
Advantage plans. Dual eligible beneficiaries and beneficiaries who
reside in an institution are not subject to the "lock-in rules" for
all MA plans, including SNPs, so they may enroll in or disenroll
from an MA plan at any time. CMS created a special enrollment
period (SEP) to allow beneficiaries to enroll in a chronic care SNP
at any time. However, these beneficiaries can only disenroll from
the chronic care SNP during the Annual Enrollment Period (November
15 – December 31) or the open enrollment period (January 1- March
31).
Interim Final Rule
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Models of
Care/Care Management. Each SNP must implement an
evidence-based model of care with networks of providers and
specialists designed to meet the needs of the specific
population the plan is serving. The preamble to the regulations
makes clear that CMS will not prescribe a particular model of
care; rather, CMS directs plans to the website of the Agency for
health care Research and Quality (www.ahrq.gov)
where various models of care are identified and evaluated.
In addition to the
model of care, MIPPA and the regulation require care management
comprising, essentially, three elements:
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A comprehensive
initial assessment (and annual reassessments) of the
individual's physical, psychosocial and functional needs
using a tool that CMS will review through oversight;
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A care plan
developed by an interdisciplinary care team and in
consultation with the individual, identifying goals and
objectives as well as specific services and benefits to be
provided;
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An
interdisciplinary team to manage the care.
The regulatory
language for this provision closely tracks MIPPA language.
Although the preamble says the provision is effective January 1,
2010 (as it is under MIPPA), the regulatory language is silent
on effective date and the overall effective date of the rule is
September 18, 2008. Model of care requirements were actually
included in CMS's Call Letter for 2009 for SNPs, so SNPs
being offered during the upcoming Annual Enrollment Period
starting November 15, 2008, are required to have designed a
model of care.
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Contracts for
State Medicaid Agencies for Dual SNPs. This regulatory
provision implements the MIPPA provision requiring that by
January 1, 2010, a Dual SNP plan will have a contract with the
State Medicaid agency in the state in which it operates that
assures that the plan will provide, or arrange for the provision
of, Medicaid benefits available to the dual eligible enrollee of
the plan.
The regulation
includes greater detail than the statute, requiring that the
contract document:
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The plan's responsibility with respect to Medicaid benefits;
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The categories of dual eligibles served by the plan;
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The Medicaid benefits covered by the SNP;
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Cost-sharing protections covered under the SNP;
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Identification and sharing of information on Medicaid
provider participation;
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Verification of the enrollee's eligibility for both Medicare
and Medicaid;
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The service area of the SNP; and
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The contract period.
Plans newly operating
in 2010 must have such a contract; existing plans without a
contract can continue to operate but cannot expand their service
areas.
While much might be
said of these requirements, two elements stand out for comment.
CMS does not specify the parameters of cost-sharing protections,
suggesting in its regulatory language that the contract must
merely specify what they are. MIPPA, however, is more
prescriptive: it prohibits plan cost-sharing for those in Dual
SNPs from being greater than it would be if the individual were
not in a Medicare Advantage plan, thus incorporating protections
that pre-date MIPPA. Element five of the contract, regarding
Medicaid provider participation raises the question of how a SNP
could possibly be providing Medicaid services, as required under
the contract, without an extensive Medicaid provider network.
Yet again, CMS is silent on the particulars of this requirement.
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Disclosure
Requirements for Dual SNPs. MIPPA requires that Dual SNPs
provide to each prospective enrollee a written statement, using
standardized content and format established by the Secretary,
describing the benefits and cost-sharing protections the
individual is entitled to under Medicaid and which of those are
provided under the plan. It should be noted that this language
suggests that the contract between the state Medicaid agency and
the Dual SNP does not necessarily include having the SNP provide
all Medicaid benefits available to the individual.
The regulatory provision changes this statutory requirement to
say that the plan must provide a statement of benefits the
individual is entitled to under Medicare and Medicaid. It makes
no mention of the standardized content and format required by
MIPPA, nor of any statement of benefits provided by the plan.
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Quality
Improvement Program. MIPPA required that all SNPs, as part
of their Quality Improvement Program, collect, analyze and
report data related to their model of care. The data are
required to be collected at the plan, rather than the sponsor,
level and must permit the measurement of health outcomes and
other indices of quality related to the model of care.
The regulation
elaborates on the statutory provision by requiring that the data
demonstrate:
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Access to care;
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Improvement in beneficiary health status;
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Staff implementation of the model of care;
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Comprehensive health risk assessment;
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Implementation of an individualized plan of care;
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A provider network with targeted clinical expertise;
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Delivery of services across the continuum of care;
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Delivery of extra services that meet the specialized needs
of enrollees;
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Use of evidence-based practices; and
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Use of integrated systems of communication.
For many of these ten
indicators, the regulation provides examples of data that would
support the element. For access to care, CMS suggests data on
service and benefit utilization rates, or timeliness of
referrals or treatment.
Again, much might be
said of each of these requirements, but one stands out:
improvement in beneficiary health status. CMS suggests "quality
of life indicators, depression scales, or chronic disease
outcomes" as measures of this element. But the very requirement
to report on improvement in health status raises the concern
that plans would be cautious about whom they enroll, to ensure
they can demonstrate that they are improving the health status
of their enrollees.
Conclusion
The Center for Medicare
Advocacy has developed recommendations (see
http://www.medicareadvocacy.org/MA_08_01.31.SNPConference.htm)
with respect to federal requirements and oversight for SNPs. While
the MIPPA and regulatory requirements are first steps toward making
SNPs different from, and potentially better than, other forms of
health care delivery for this population, more is left to do. The
Center will continue to report on SNP developments.
Although some of these
rules are already in effect (though, as noted, the preamble suggests
effective dates for some provisions different from what appears in
the provisions themselves), CMS invites comment on them. Comments
are due no later than 5 p.m. EST on November 17, 2008. For the
regulations and details about filing comments, go to
http://www.access.gpo.gov/su_docs/fedreg/a080918c.html and
scroll down to Centers for Medicare & Medicaid Services, then
Revisions to the Medicare Advantage and Prescription Drug Benefit
Programs, 54226-54254 [E8-21686]. The Center for Medicare Advocacy
hopes to make its comments available for others in advance of the
due date. |