Civilian Health and Medical Program of the Uniformed Services (CHAMPUS); TRICARE: Implementation of Changes to the Pharmacy Benefits Program; Double Coverage With Medicare Part D, 78110-78115 [E6-22258]
Download as PDF
78110
Federal Register / Vol. 71, No. 249 / Thursday, December 28, 2006 / Proposed Rules
after submitting comments
electronically. Anyone is able to search
the electronic form of all comments in
any one of our dockets by the name of
the individual submitting the comment
(or signing the comment, if submitted
on behalf of an association, business, or
labor union). You may review DOT’s
complete Privacy Act Statement in the
Federal Register published on April 11,
2000 (Volume 65, Number 70, Pages
19477–78) or you may visit https://
dms.dot.gov.
FOR FURTHER INFORMATION CONTACT:
Mr.
Edward Strocko, Office of Freight
Management and Operations, (202) 366–
2997; or Ms. Alla Shaw, Office of the
Chief Counsel, (202) 366–0764, U.S.
Department of Transportation, Federal
Highway Administration, 400 Seventh
Street, SW., Washington, DC 20590.
Office hours are from 7:45 a.m. to 4:15
p.m., e.t., Monday through Friday,
except Federal holidays.
SUPPLEMENTARY INFORMATION:
cprice-sewell on PROD1PC66 with PROPOSALS
Electronic Access and Filing
You may submit or retrieve comments
online through the Document
Management System (DMS) at: https://
dmses.dot.gov/submit. Electronic
submission and retrieval help and
guidelines are available under the help
section of the Web site. Alternatively,
internet users may access all comments
received by the DOT Docket Facility by
using the universal resource locator
(URL) https://dms.dot.gov. It is available
24 hours each day, 365 days each year.
Please follow the instructions. An
electronic copy of this document may
also be downloaded by accessing the
Office of the Federal Register’s home
page at: https://www.archives.gov or the
Government Printing Office’s Web page
at: https://www.gpoaccess.gov/nara.
Background
The Projects of National and Regional
Significance program established under
section 1301 of the Safe, Accountable,
Flexible, Efficient Transportation Equity
Act: A Legacy for Users (Pub. L. 109–59)
is intended to finance critical, high-cost
transportation infrastructure facilities
that address critical national economic
and transportation needs. These projects
often involve multiple levels of
government, agencies, modes of
transportation, and transportation goals
and planning processes that are not
easily addressed or funded within
existing surface transportation program
categories. Projects of National and
Regional Significance would have
national and regional benefits, including
improving economic productivity by
facilitating international trade, relieving
VerDate Aug<31>2005
15:22 Dec 27, 2006
Jkt 211001
congestion, and improving
transportation safety by facilitating
passenger and freight movement.
Additionally, this program would
further the goals of the Secretary’s
Congestion Initiative.1
The benefits of PNRS would accrue
beyond local areas and States to the
Nation as a whole. A program dedicated
to constructing PNRS would improve
the safe, secure, and efficient movement
of people and goods throughout the
United States as well as improve the
health and welfare of the national
economy.
On July 24, 2006, at 71 FR 41748, the
FHWA published a NPRM proposing
the establishment of regulations for 23
CFR 505, the evaluation and rating
guidelines for projects proposed for
funding under the PNRS program. The
FHWA is looking for specific and
detailed comments that contribute to the
definition of grant criteria, project
eligibility, project ratings, and the
nature and form of full funding grant
agreements. The FHWA specifically
invites comments that contribute to an
understanding and a quantification of
criteria related to congestion, system
throughput, safety, technology, private
contributions and national and/or
regional economic benefits.
The original comment period for the
NPRM closed on September 22, 2006.
The FHWA recognizes that additional
time will allow interested parties a
broader and more comprehensive
review and discussion of the proposed
regulations; and then, allow the
development and submission of
complete responses to the docket. To
allow time for interested parties to
submit comprehensive comments, the
comment period is being reopened until
February 9, 2007.
Authority: 23 U.S.C. 101(a), 104, 109(d),
114(a), 217, 315, and 402(a); 23 CFR 1.32 and
49 CFR 1.48(b).
Issued on: December 21, 2006.
J. Richard Capka,
Federal Highway Administrator.
[FR Doc. E6–22322 Filed 12–27–06; 8:45 am]
BILLING CODE 4910–22–P
1 Speaking before the National Retail
Foundation’s annual conference on May 16, 2006,
in Washington, DC, former U.S. Transportation
Secretary Norman Mineta unveiled a new plan to
reduce congestion plaguing America’s roads, rail
and airports. The National Strategy to Reduce
Congestion on America’s Transportation Network
includes a number of initiatives designed to reduce
transportation congestion and is available at the
following URL: https://isddc.dot.gov/OLPFiles/OST/
012988.pdf.
PO 00000
Frm 00015
Fmt 4702
Sfmt 4702
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD–2006–HA–0149; RIN 0720-AB01]
Civilian Health and Medical Program of
the Uniformed Services (CHAMPUS);
TRICARE: Implementation of Changes
to the Pharmacy Benefits Program;
Double Coverage With Medicare Part D
Department of Defense.
Proposed rule.
AGENCY:
ACTION:
SUMMARY: TRICARE eligible
beneficiaries, who are entitled to
Medicare Part A on the basis of age,
disability, or end-stage renal disease,
maintain their TRICARE eligibility
when they are enrolled in the
supplementary medical insurance
program under Part B of Medicare. In
general, in the case of medical or dental
care provided to these individuals for
which payment may be made under
both Medicare and TRICARE, Medicare
is the primary payer and TRICARE will
normally pay the actual out-of-pocket
costs incurred by the person. This
proposed rule prescribes double
coverage payment procedures and
makes revisions to TRICARE rules to
accommodate beneficiaries who are
eligible under both Medicare and
TRICARE, and who participate in
Medicare’s outpatient prescription drug
program under Medicare Part D. These
revisions are necessary because of the
requirements contained in the Centers
for Medicare and Medicaid Services
(CMS) final rule for the Medicare
Prescription Drug Benefit, Part D Plans
with Other Prescription Drug Coverage.
This proposed rule also establishes
requirements and procedures for
implementation of the improvements to
the TRICARE Pharmacy Benefits
Program directed by section 714 of the
Ronald W. Reagan National Defense
Authorization Act for Fiscal Year 2005
(NDAA FY 05) (Public Law 108–365).
The rule clarifies that the cost-sharing
requirements for Medicare-eligible
beneficiaries may not be in excess of the
cost-sharing requirements applicable to
other retirees, their dependents, former
spouses and survivors. Additionally, the
rule authorizes the DoD Pharmacy and
Therapeutics Committee to make a
separate and additional determination
of the relative clinical and cost
effectiveness of pharmaceutical agents
to assure pharmacies of the uniformed
services have on their formularies
pharmaceutical agents that provide
greater value than other uniform
formulary agents in that therapeutic
E:\FR\FM\28DEP1.SGM
28DEP1
Federal Register / Vol. 71, No. 249 / Thursday, December 28, 2006 / Proposed Rules
cprice-sewell on PROD1PC66 with PROPOSALS
class. This rule also describes the
transition process that will occur as the
uniform formulary is developed and
uniform service facilities move to a
uniform formulary, consistent with their
scope of practice.
DATES: Comments on this proposed rule
will be accepted until February 26,
2007.
ADDRESSES: You may submit comments,
identified by docket number and/or RIN
number and title, by any of the
following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Federal Docket Management
System Office, 1160 Defense Pentagon,
Washington, DC 20301–1160.
Instructions: All submissions received
must include the agency name and
docket number or Regulatory
Information Number (RIN) for this
Federal Register document. The general
policy for comments and other
submissions from members of the public
is to make these submissions available
for public viewing on the Internet at
https://regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
FOR FURTHER INFORMATION CONTACT: MAJ
Travis Watson, TRICARE Management
Activity, Pharmacy Directorate,
telephone (703) 681–2890 x6707.
SUPPLEMENTARY INFORMATION:
I. Double Coverage With Medicare
Part D
Section 101 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA),
(Pub. L. 108–173), amended Title XVIII
of the Social Security Act by
establishing a new Part D: the Voluntary
Prescription Drug Benefit Program
(henceforth, Medicare Part D). The
Department of Health and Human
Services, Centers for Medicare and
Medicaid Services (CMS), published
their Final Rule on January 28, 2005 (70
FR 4193—4585). The addition of a
prescription drug benefit to Medicare
represents a landmark change to the
Medicare program, and became
available to beneficiaries beginning on
January 1, 2006.
The Floyd D. Spence National
Defense Authorization Act for Fiscal
Year 2001 (Pub. L. 106–398), established
the TRICARE Senior Pharmacy Program
under section 711 (which was effective
April 1, 2001). The Act also under
section 712 (which was effective
October 1, 2001) continued TRICARE
eligibility for beneficiaries entitled to
Medicare Part A on the basis of age,
VerDate Aug<31>2005
15:22 Dec 27, 2006
Jkt 211001
provided they also are enrolled in
Medicare Part B. This program has come
to be known as TRICARE for Life. Under
section 701 of the National Defense
Authorization Act for Fiscal Year 2000
(Public Law 106–65), codified at Title
10, United States Code, Section 1074g,
the Department established its new
pharmacy benefits program for all
TRICARE beneficiaries (as implemented
by 32 CFR 199.21). The full
implementation of the pharmacy
benefits program was not effective until
May 3, 2004, however, changes in
pharmacy cost shares were effective
with the implementation of TRICARE
Senior Pharmacy on April 1, 2001.
In implementing TRICARE Senior
Pharmacy, DoD stated that the double
coverage rules in 32 CFR 199.8 are
applicable to services provided to all
beneficiaries under the retail pharmacy
network, retail pharmacy non-network,
or TRICARE Mail Order programs. In
implementing TRICARE for Life, DoD
explained the double coverage rules
under 10 U.S.C. 1086(d)(3). The statute
states that if a TRICARE-Medicare dualeligible beneficiary receives medical or
dental care for which payment may be
made under Medicare and TRICARE,
the amount payable for that care by
TRICARE shall be the amount of the
actual out-of-pocket costs incurred by
the person for that care over the sum of
(i) the amount paid for that care under
Medicare; and (ii) the total of all
amounts paid or payable by third party
payers other than Medicare. The amount
payable by TRICARE may not exceed
the total amount that would be paid
under TRICARE if payment for the care
were made solely under TRICARE.
TRICARE for Life did not expand the
scope of benefits available to this group
of beneficiaries beyond the scope of
TRICARE benefits available to other
retirees and their families. The critical
fact is whether the service or supply is
payable by both Medicare and
TRICARE. For health care services for
which payment may be made under
both Medicare and TRICARE, TRICARE
will pay up to the beneficiary’s legal
liability the actual out-of-pocket costs
incurred by the beneficiary, less any
payments made by Medicare or other
sources of insurance). Actual out-ofpocket costs incurred by the beneficiary
include the initial deductible, which are
for services payable by Medicare and
TRICARE, but for the fact that the
beneficiary has not met the deductible
amount, and any subsequent beneficiary
cost shares. However, if a health care
service or supply is a benefit payable
only by Medicare, but not TRICARE,
then Medicare has sole responsibility
PO 00000
Frm 00016
Fmt 4702
Sfmt 4702
78111
for payment of the health care service or
supply, as defined by Medicare, and the
beneficiary has the responsibility to pay
any corresponding Medicare cost-share
or deductible. Likewise, if a health care
service or supply is a benefit payable
only by TRICARE, but not Medicare,
then TRICARE has sole responsibility
for payment of the health care service
and supply, and the beneficiary has the
responsibility to pay any corresponding
TRICARE cost-shares or deductible.
Finally, if a health care service or
supply is neither a benefit payable by
Medicare or TRICARE, the beneficiary
pays the total cost.
TRICARE has applied the double
coverage rules of 32 CFR 199.8 to the
Pharmacy Benefits Program under
section 199.21(m), and said to the extent
they provide a prescription drug benefit,
Medicare supplemental insurance plans
or Medicare HMO plans are double
coverage plans and will be primary
payer. This rule was written prior to
Medicare providing a prescription drug
benefit under Medicare Part D, and
CMS’s final rule on the Medicare
Prescription Drug Benefit. Under 42
CFR part 423, Subpart J, Coordination of
Part D Plans With Other Prescription
Drug Coverage, section 423.464(f)(1)(iv),
military coverage, including TRICARE
coverage under chapter 55 of title 10,
United States Code, qualifies as other
prescription drug coverage with which
a Part D plan must coordinate benefits.
Medicare Part D plans are offered by
private insurance companies that
contract with CMS. Part D benefits may
be offered by a stand-alone prescription
drug plan sponsor, a Medicare
Advantage Organization offering
qualified prescription drug coverage, a
Program for All-Inclusive Care for the
Elderly (PACE) organization offering
qualified prescription drug coverage, or
a cost plan offering qualified
prescription drug coverage (collectively
referred to as a ‘‘Part D plan sponsor’’).
Each Part D plan sponsor submits a bid
to CMS for plan benefit packages, which
results in, among other things, the
offering of Part D plans with varying
monthly premiums and benefits
designs. Part D plan sponsors may offer
a defined standard benefit, which is the
type of benefit used as an example in
this preamble, or an actuarially
equivalent standard benefit. Part D plan
sponsors may also offer alternative
prescription drug coverage, which may
consist of basic alternative coverage or
enhanced alternative coverage.
Therefore depending on the Part D plan
that a beneficiary chooses, monthly
premiums, coinsurances, co-pays,
deductibles and benefit design may vary
from plan to plan. Under the MMA,
E:\FR\FM\28DEP1.SGM
28DEP1
cprice-sewell on PROD1PC66 with PROPOSALS
78112
Federal Register / Vol. 71, No. 249 / Thursday, December 28, 2006 / Proposed Rules
certain low-income beneficiaries may be
eligible for reduced premiums and costsharing for their drug coverage. In some
cases, beneficiaries pay no premium and
nominal cost-sharing. Other
beneficiaries have a reduced premium
and lower cost-sharing.
The standard Part D benefit includes
several phases of beneficiary spending,
as described below.
Premiums. Statute requires a
beneficiary to pay a monthly premium
to participate in the plan. A beneficiary
who wants to participate in a standard
Medicare Part D plan is solely
responsible for payment of any
premium that is not otherwise
subsidized under the program.
Beneficiary premiums do not count
toward any required beneficiary costsharing to reach the deductible,
coverage gap, or catastrophic limit
(described below).
Deductible. Under the Medicare Part
D defined standard benefit, the
beneficiary is responsible for paying an
out-of-pocket deductible ($265 in 2007)
that adjusts annually according to the
annual percentage increase in spending
on covered Part D drugs. For purposes
of meeting the deductible, both
spending by the beneficiary and
spending by TRICARE on behalf of the
beneficiary (i.e., the TRICARE
wraparound coverage) qualify.
Cost-sharing between deductible and
coverage gap. After the deductible is
met, the standard Part D plan sponsors
are responsible for 75% of the actual
cost of the covered Part D drug, and the
beneficiary is responsible for 25% of the
actual cost of the covered Part D drug,
until the beneficiary reaches the
coverage gap. TRICARE wraparound
coverage qualifies as beneficiary costsharing between the deductible and
coverage gap.
Coverage gap. To reach the coverage
gap, the beneficiary must reach a
statutorily-specified amount of total
drug spending. Total beneficiary
spending needed to meet the coverage
gap is defined as beneficiary out-ofpocket spending, or TRICARE spending
on behalf of the beneficiary, and
spending by the Part D plan sponsor. In
2007, a beneficiary reaches the coverage
gap when he has incurred $2,400 in
total drug spending and remains in the
gap until he has incurred $3,850 in
beneficiary out-of-pocket spending.
Individuals who qualify for the lowincome subsidies pay lower cost-sharing
amounts before they reach the coverage
gap. In the coverage gap, the beneficiary
is responsible for 100% of the cost of
the drug, although the beneficiary by
law is entitled to receive the plan’s
negotiated price. Individuals who
VerDate Aug<31>2005
15:22 Dec 27, 2006
Jkt 211001
qualify for low-income subsidies do not
have a coverage gap.
Catastrophic threshold. To reach the
catastrophic threshold defined in the
standard benefit, the beneficiary must
have incurred total spending defined in
statute as true out-of-pocket spending
(TrOOP) ($3,850 in 2007). In the
catastrophic phase, the beneficiary is
responsible for the greater of 5% of the
cost of the drug, or, in 2007, $2.15 for
a generic/preferred multi-source drug or
$5.35 for other drugs. In the catastrophic
phase of the defined standard benefit,
the Part D plan sponsor and Medicare
are responsible for what is not paid by
the beneficiary up to the Part D plan
sponsor’s negotiated price.
Under 42 CFR 423.100, incurred costs
means costs incurred by the Part D
enrollee for covered Part D drugs—(1)
That are not paid for under the Part D
plan as a result of application of any
annual deductible or other cost-sharing
rules for covered Part D drugs prior to
the Part D enrollee satisfying annual
out-of-pocket threshold amount under
section 423.104(d)(5)(iii); and (2) That
are paid for by the Part D enrollee or on
behalf of the enrollee by another person,
and the enrollee or other person is not
reimbursed through insurance or
otherwise, a group health plan or other
third party arrangement. Because
TRICARE falls under the definition of
‘‘or otherwise,’’ which refers to
‘‘government-funded health programs,’’
wraparound payments made by
TRICARE for covered Part D drugs on
behalf of an enrollee eligible for both
Part D and TRICARE do not count
towards beneficiary incurred costs.
Therefore, for purposes of reaching the
catastrophic limit, only true beneficiary
out-of-pocket spending (TrOOP) counts
as beneficiary spending. Although
TRICARE supplementary coverage
counts toward meeting the deductible
and the initial coverage limit, it does not
count toward meeting the catastrophic
threshold.
Generally, a Part D plan is primary
payer under 42 CFR 423.464,
coordination of benefits with other
providers of prescription drug coverage,
which includes military coverage
(including TRICARE) under chapter 55
of title 10, United States Code. A Part
D plan under section 423.464(f)(2) must
exclude expenditures for covered Part D
drugs made by TRICARE for purposes of
determining whether a Part D enrollee
has satisfied the out-of-pocket
threshold, which for 2007 is $3,850.
As a result of these provisions
implementing Medicare Part D,
TRICARE double coverage rules must be
modified. If a TRICARE-Medicare
beneficiary enrolls in a Part D plan that
PO 00000
Frm 00017
Fmt 4702
Sfmt 4702
adds prescription coverage to their
Medicare plan, the Medicare Part D plan
is generally primary payer and
TRICARE is secondary payer. TRICARE
will pay the beneficiary’s out-of-pocket
costs for Medicare and TRICARE
covered medications, including the
initial deductible and Medicare Part D
cost-share. TRICARE will not pay the
beneficiary’s out-of-pocket cost
associated with any monthly premium
required to enroll in and participate in
the Medicare Part D plan.
In the coverage gap, the Part D plan
is generally still the primary payer.
Thus, assuming the beneficiary is
accessing a pharmacy under contract
with his or her Part D plan, the
pharmacy would bill the Part D plan,
which would respond by indicating that
it is responsible for $0, at which point
the pharmacy would bill TRICARE.
When the beneficiary becomes
responsible for 100% of the drug costs
in the coverage gap, the beneficiary may
use the TRICARE pharmacy benefit as
the secondary payer. TRICARE will cost
share during the coverage gap to the
same extent as it does under section
199.21 for beneficiaries not enrolled in
a Medicare Part D plan. The beneficiary
is responsible for the applicable
TRICARE pharmacy cost-sharing
amounts (and deductible if using a retail
non-network pharmacy). During the
coverage gap, TRICARE is incurring the
cost of the drugs during the Medicare
Part D coverage gap and not the
beneficiary. Thus none of the costs of
the drugs borne by TRICARE will be
applied to meeting the beneficiary’s
annual Medicare Part D true out-ofpocket (TrOOP) threshold. Generally,
however, the beneficiary’s own
TRICARE pharmacy benefit cost-share
will accrue to meeting his/her annual
Medicare Part D TrOOP spending
because this cost-sharing is an actual
out-of-pocket expense incurred by the
beneficiary. Any actual out-of-pocket
expense incurred by the beneficiary also
will apply toward the TRICARE fiscal
year catastrophic cap.
Similarly, if the TRICARE-Medicare
dual-eligible beneficiary enrolls in a
Medicare Advantage drug plan, the
beneficiary has to pay the plan’s
monthly premiums and obtain all
medical care and prescription drugs
through the Medicare Advantage plan.
The Medicare Advantage plan will
generally be the primary payer, and
TRICARE will be the secondary payer.
If the Medicare Advantage plan has a
Part D drug benefit, TRICARE will pay
secondary as described above.
E:\FR\FM\28DEP1.SGM
28DEP1
cprice-sewell on PROD1PC66 with PROPOSALS
Federal Register / Vol. 71, No. 249 / Thursday, December 28, 2006 / Proposed Rules
II. Legislative Changes for TRICAREMedicare Dual-Eligible Beneficiaries
Section 701 of the National Defense
Authorization Act for Fiscal Year 2000
(Public Law 106–65), codified at Title
10, United States Code, Section 1074g,
directs the Department to establish an
effective, efficient, integrated pharmacy
benefits program. The Department
published the final rule on the
Pharmacy Benefits Program on April 1,
2004 (69 FR 17035–17052)
implementing the pharmacy benefits
program, effective May 3, 2004.
Congress in section 714 of the Ronald
W. Reagan NDAA for FY 05 has directed
certain improvements to the TRICARE
pharmacy benefits program.
Section 714(a) directs that for a
TRICARE-Medicare dual-eligible
beneficiary, the cost-sharing
requirements under the pharmacy
benefits program may not be greater
than the cost-sharing requirements
applicable to all other beneficiaries
covered by 10 U.S.C. 1086, which are
beneficiaries who are retirees, their
authorized dependents, survivors, and
certain former spouses. Under 10 U.S.C.
1074g(a)(6), the Department may
establish cost-sharing requirements for
the pharmacy benefits program, which
may be established as a percentage or
fixed dollar amount, for generic,
formulary, and non-formulary
pharmaceutical agents. For nonformulary agents, cost-sharing shall be
consistent with common industry
practice and not in excess of amounts
generally comparable to 20 percent for
beneficiaries who are dependents of
active duty members of the uniformed
services, and 25 percent for
beneficiaries who are retirees, their
authorized dependents, survivors, and
certain former spouses.
In the TRICARE Pharmacy Benefits
Program final rule, the Department
published the cost share amounts for
pharmaceutical agents based upon two
factors: (1) The agent’s status as generic,
formulary, or non-formulary; and (2) the
venue in which the agent was obtained,
that is, military treatment facility (MTF),
TRICARE Mail Order Program (TMOP),
retail network pharmacy, or retail nonnetwork pharmacy. The Department is
authorized under 10 U.S.C. 1074g(a)(6)
to have two non-formulary cost-shares
based upon the status of the beneficiary,
no more than 20 percent for active duty
family members and no more than 25
percent for all others (other than active
duty members who have no cost share).
The Department chose to have one nonformulary cost-share equal to no more
than 20 percent of the anticipated
aggregated cost of non-formulary agents
VerDate Aug<31>2005
15:22 Dec 27, 2006
Jkt 211001
that is $22 for non-formulary agents
obtained in the TMOP or retail network
pharmacies, and $22 or 20 percent
(whichever is greater) for non-formulary
agents obtained in retail non-network
pharmacies. (For more information on
TRICARE Pharmacy Benefit Program
cost shares, see Section 199.21(i)).
Section 714(a) emphasizes that if the
Department were to move to a two-tier
non-formulary cost-share based upon
the status of the beneficiary, the
Department may not have a higher costshare for TRICARE-Medicare dualeligible beneficiaries than for other
retirees, their authorized dependents,
survivors, and certain former spouses.
The Department has no intention at this
time of establishing two separate nonformulary cost-shares based upon the
status of the beneficiary as an active
duty family member or other category of
beneficiary.
This proposed rule adds to § 199.21 a
provision incorporating into the
regulation the new statutory
requirement.
III. Legislative Changes To Improve the
Uniform Formulary Process
Under 10 U.S.C. 1074g(a)(2)(E)(i),
pharmaceutical agents included on the
uniform formulary on the basis of
relative clinical effectiveness and cost
effectiveness are required to be available
to beneficiaries through facilities of the
uniformed services, consistent with the
scope of health care services offered in
such facilities. Section 714(b) of the
Ronald W. Reagan NDAA for FY 05
directs the Department to allow the DoD
Pharmacy and Therapeutics Committee
(P&T Committee) to make additional
relative clinical and cost effectiveness
determinations for military treatment
facilities (MTFs). This change in the law
means that MTFs are not required to
include on their formularies every
pharmaceutical agent in a therapeutic
class that is on the uniform formulary
that is consistent with the scope of
health care services offered in the MTF.
This proposed rule incorporates into
section 199.21 a provision reflecting the
change in statute.
IV. Transition to the Uniform
Formulary
The DoD P&T Committee is required
under section 199.21 to make
recommendations concerning which
pharmaceutical agents should be on the
uniform formulary and the Basic Core
Formulary (BCF), and may now make
recommendations concerning which
agents should be on the Extended Core
Formulary (ECF). The BCF contains the
minimum set of pharmaceutical agents
that each MTF pharmacy must have on
PO 00000
Frm 00018
Fmt 4702
Sfmt 4702
78113
its formulary to support the primary
care scope of practice for Primary Care
Manager enrollment sites. The ECF
contains the minimum set of
pharmaceutical agents that each MTF
pharmacy must have on its formulary to
support an extended care scope of
practice if the MTF Pharmacy and
Therapeutics Committee has authorized
agents in that class based upon the
scope of practice at that facility.
The DoD Pharmacy and Therapeutics
Committee will review the classes in a
methodical but expeditious manner,
taking into consideration circumstances
that may include but are not limited to:
DoD national contracting, or DoD and
Veterans Affairs national joint
contracting or other agreements with
pharmaceutical manufacturers; approval
of a new drug by FDA; approval of a
new indication for an existing drug;
changes in the clinical use of existing
drugs; new information concerning the
safety, effectiveness or clinical
outcomes of existing drugs; price
changes; shifts in market share;
scheduled review of a therapeutic class;
and requests from DoD P&T Committee
members, military treatment facilities,
or other Military Health System
officials. During the transition period
from the previous methodology of
formulary management involving only
the MTFs and the TRICARE Mail Order
Program, previous decisions by the DoD
P&T Committee or committed use
requirements contracts executed by
DoD, or jointly by DoD and VA, shall
continue in effect. This is necessary to
comply with the statutory requirements
of 38 U.S.C. 8111 and 10 U.S.C. 1104
relating to resource sharing between
DoD and VA, and allow time to
incorporate the impact of uniform
formulary management into those
agreements. As therapeutic classes are
reviewed under the new formulary
management process and
pharmaceutical agents are designated
for formulary or non-formulary status,
this transition methodology shall apply.
The P&T Committee will meet at least
quarterly to review new and existing
drugs and drug classes, and recommend
pharmaceutical agents for inclusion on
or exclusion from the uniform formulary
after evaluating their relative clinical
and cost effectiveness. Pending review
of a pharmaceutical agent or class,
previous decisions by the predecessor to
the P&T Committee regarding national
contracts, agreements, formulary status,
BCF status, pre-authorization
requirements and quantity limits shall
remain in effect. The P&T Committee
will eventually evaluate all applicable
drug classes at which time the transition
period will be complete.
E:\FR\FM\28DEP1.SGM
28DEP1
78114
Federal Register / Vol. 71, No. 249 / Thursday, December 28, 2006 / Proposed Rules
cprice-sewell on PROD1PC66 with PROPOSALS
During this transition period,
pharmaceutical agents in drug classes
not yet evaluated by the P&T Committee
will continue to be available from the
TRICARE Mail Order Pharmacy (TMOP)
and the TRICARE Retail Pharmacy
network at either the generic or
formulary (brand) cost share. MTFs may
evaluate for inclusion on the MTF
formulary pharmaceutical agents in
drug classes that do not already have
BCF status, or have not yet been
evaluated by the P&T Committee. BCF
listed agents must be on the formulary
at all full-service MTF pharmacies at all
times.
V. Regulatory Procedures
Executive Order 12866 directs
agencies to assess all costs and benefits
available, regulatory alternatives and,
when regulation is necessary, to select
regulatory approaches that maximize
net benefits (including potential
economic, environmental, public health
and safety, and other advantages;
distributive impacts; and equity). The
Order classifies a rule as a significant
regulatory action requiring review by
the Office of Management and Budget if
it meets any one of a number of
specified conditions, including: having
an annual effect on the national
economy of $100 million or more,
creating a serious inconsistency or
interfering with an action of another
agency, materially altering the
budgetary impact of entitlements or the
rights of entitlement recipients, or
raising novel legal or policy issues. DoD
has examined the economic, legal, and
policy implications of this proposed
rule and has concluded that it is a
significant regulatory action as it
addresses novel policy issues relating to
implementation of coordination of
medical benefits programs for covered
beneficiaries of the uniformed services
under TRICARE and the Medicare
Prescription Drug Benefit. Thus, this
rule has been reviewed by the Office of
Management and Budget under E.O.
12866. The Regulatory Flexibility Act
(RFA) requires that each Federal Agency
prepare, and make available for public
comment, a regulatory flexibility
analysis when the agency issues
regulations which would have a
significant impact on a substantial
number of small entities.
This proposed rule is not a major rule
under the Congressional Review Act,
because its economic impact will be less
than $100 million. There are
approximately 1.9 million TRICAREMedicare dual-eligible beneficiaries,
and approximately 7% have enrolled in
Medicare Part D plans. For those who
have Medicare Part D coverage, the cost
VerDate Aug<31>2005
15:22 Dec 27, 2006
Jkt 211001
of their pharmacy benefit to DoD is less,
as Medicare Part D Plans are the first
payer as opposed to DoD, resulting in a
cost avoidance for DoD. The amount of
the cost avoidance is directly related to
the number and cost of prescriptions
filled by beneficiaries for which
Medicare is first payer. Under the
standard benefit package, there is a
potential of about $1,601.25 in DoD cost
avoidance (in 2007) for Medicare/
TRICARE Part D enrollees whose drug
spending is high enough to enter the
Medicare coverage gap. For beneficiaries
with lower drug spending, DoD’s cost
avoidance would also be lower. In
addition, this rule will have minor
impact and will not significantly affect
a substantial number of small entities.
In light of the above, no regulatory
impact analysis is required.
This proposed rule will not impose
additional information collection
requirements on the public under the
Paperwork Reduction Act of 1995 (44
U.S.C. 55). In order to determine which
dual-eligible beneficiaries are
participating in Medicare Part D,
TRICARE will rely on the Defense
Eligibility Enrollment Reporting System
(DEERS) to identify which beneficiaries
are enrolled in Medicare Part D through
existing data sharing agreements with
CMS and will not need to collect
additional information from them.
We have examined the impact(s) of
the proposed rule under Executive
Order 13132 and it does not have
policies that have federalism
implications that would have
substantial direct effects on the States,
on the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government, therefore,
consultation with State and local
officials is not required.
List of Subjects in 32 CFR Part 199
Claims, Health care, Health insurance,
Military personnel, Pharmacy benefits.
Accordingly, 32 CFR part 199 is
proposed to be amended as follows:
PART 199—[AMENDED]
1. The authority citation for Part 199
continues to read as follows:
Authority: 5 U.S.C. 301; 10 U.S.C. chapter
55.
2. Section 199.8 is amended by
adding paragraph (d)(1)(iii)(C) and
revising paragraph (d)(1)(vi) to read as
follows:
§ 199.8
*
Double coverage.
*
*
(d) * * *
PO 00000
Frm 00019
*
Fmt 4702
*
Sfmt 4702
(1) * * *
(iii) * * *
(C) For Medicare beneficiaries who
enroll in Medicare Part D, the Part D
plan is primary and TRICARE is
secondary payer. TRICARE will pay the
beneficiary’s out-of-pocket costs for
Medicare and TRICARE covered
medications, including the initial
deductible and Medicare Part D cost
sharing amounts up to the initial
coverage limit of the Medicare Part D
plan. The Medicare Part D plan,
although the primary plan pays nothing
during any coverage gap period. When
the beneficiary becomes responsible for
100 percent of the drug costs under a
Part D coverage gap period, the
beneficiary may use the TRICARE
pharmacy benefit as the secondary
payer. TRICARE will cost share during
the coverage gap to the same extent as
it does under § 199.21 for beneficiaries
not enrolled in a Medicare Part D plan.
The beneficiary is responsible for the
applicable TRICARE pharmacy costsharing amounts (and deductible if
using a retail non-network pharmacy).
Part D plan sponsors may offer a defined
standard benefit, or an actuarially
equivalent standard benefit. Part D plan
sponsors may also offer alternative
prescription drug coverage, which may
consist of basic alternative coverage or
enhanced alternative coverage.
Therefore depending on the Part D plan
that a beneficiary chooses, monthly
premiums, coinsurances, co-pays,
deductibles and benefit design may vary
from plan to plan. TRICARE payment of
the beneficiary’s initial deductible, if
any, along with payment of any
beneficiary cost share count towards
total spending on drugs, and may have
the effect of moving the beneficiary
more quickly through the initial phase
of coverage to the coverage gap.
Irrespective of the phase of the benefit
in which a beneficiary may be, if a
beneficiary is accessing a pharmacy
under contract with his or her Part D
plan, the provider will bill the Part D
plan first, then TRICARE. If the
beneficiary chooses to use his or her
TRICARE pharmacy benefit during a
coverage gap under Part D, the
beneficiary may do so, but the
beneficiary is responsible for the
TRICARE cost-shares.
*
*
*
*
*
(vi) Effect of enrollment in Medicare
Advantage Prescription Drug (MA–PD)
plan. In the case of a beneficiary
enrolled in a MA–PD plan who receives
items or services for which payment
may be made under both the MA–PD
plan and CHAMPUS/TRICARE, a claim
for the beneficiary’s normal out-of-
E:\FR\FM\28DEP1.SGM
28DEP1
Federal Register / Vol. 71, No. 249 / Thursday, December 28, 2006 / Proposed Rules
pocket costs under the MA–PD plan
may be submitted for CHAMPUS/
TRICARE payment. However, consistent
with paragraph (c)(4) of this section,
out-of-pocket costs do not include costs
associated with unauthorized out-ofsystem care or care otherwise obtained
under circumstances that result in a
denial or limitation of coverage for care
that would have been covered or fully
covered had the beneficiary met
applicable requirements and
procedures. In such cases, the
CHAMPUS/TRICARE amount payable is
limited to the amount that would have
been paid if the beneficiary had
received care covered by the Medicare
Advantage plan. If the TRICAREMedicare beneficiary enrolls in a MA–
PD drug plan, it will be governed by
Medicare Part C, although plans that
offer a prescription drug benefit also
must comply with Medicare Part D
rules. The beneficiary has to pay the
plan’s monthly premiums and obtain all
medical care and prescription drugs
through the Medicare Advantage plan
before seeking CHAMPUS/TRICARE
payment. CHAMPUS/TRICARE
payment for such beneficiaries may not
exceed that which would be payable for
a beneficiary under paragraph
(d)(1)(iii)(C) of this section.
3. Section 199.21 is amended by
adding new paragraphs (g)(4) and
(i)(2)(xi), and by revising paragraphs
(h)(2)(ii) and (m), to read as follows:
§ 199.21
Pharmacy benefits program.
cprice-sewell on PROD1PC66 with PROPOSALS
*
*
*
*
*
(g) * * *
(4) Transition to the uniform
formulary. Beginning in Fiscal Year
2005, under an updated charter for the
DoD P&T Committee, the committee
shall meet at least quarterly to review
therapeutic classes of pharmaceutical
agents and make recommendations
concerning which pharmaceutical
agents should be on the Uniform
Formulary, Basic Core Formulary, and
Extended Core Formulary. The P&T
Committee will review the classes in a
methodical, but expeditious manner.
During the transition period from the
previous methodology of formulary
management involving only the MTFs
and the TRICARE Mail Order Pharmacy
Program, previous decisions by the
predecessor DoD P&T Committee
concerning MTF and Mail Order
Pharmacy Program formularies shall
continue in effect. As therapeutic
classes are reviewed under the new
formulary management process, the
processes established by this section
shall apply.
*
*
*
*
*
(h) * * *
VerDate Aug<31>2005
15:22 Dec 27, 2006
Jkt 211001
(2) * * *
(ii) Availability of formulary
pharmaceutical agents at military
treatment facilities. Pharmaceutical
agents included on the uniform
formulary are available through
facilities of uniformed services,
consistent with the scope of health care
services offered in such facilities and
additional determinations by the
Pharmacy and Therapeutics Committee
of the relative clinical effectiveness and
cost effectiveness, based on costs to the
Program associated with providing the
agents to beneficiaries. The Basic Core
Formulary (BCF) is a subset of the
uniform formulary and is a mandatory
component of formularies at all fullservice MTF pharmacies. The BCF
contains the minimum set of
pharmaceutical agents that each fullservice MTF pharmacy must have on its
formulary to support the primary care
scope of practice for Primary Care
Manager enrollment sites. Limitedservice MTF pharmacies (e.g., specialty
pharmacies within an MTF or
pharmacies servicing only active duty
military members) are not required to
include the entire BCF on their
formularies, but may limit their
formularies to those BCF agents
appropriate to the needs of the patients
they serve. An Extended Core
Formulary (ECF) may list preferred
agents in drug classes other than those
covered by the BCF. Among BCF and
ECF agents, individual MTF formularies
are determined by local Pharmacy and
Therapeutics Committees based on the
scope of health care services provided at
the respective MTFs. All
pharmaceutical agents on the local
formulary of full-service MTF
pharmacies must be available to all
categories of beneficiaries.
*
*
*
*
*
(i) * * *
(2) * * *
(xi) For a Medicare-eligible
beneficiary, the cost sharing
requirements may not be in excess of
the cost-sharing requirements applicable
to all other beneficiaries covered by 10
U.S.C. 1086.
*
*
*
*
*
(m) Effect of other health insurance.
The double coverage rules of section
199.8 of this part are applicable to
services provided under the pharmacy
benefits program. For this purpose, the
Medicare prescription drug benefit
under Medicare Part D, prescription
drug benefits provided under Medicare
Part D plans are double coverage plans
and such plans will be the primary
payer, to the extent described in section
199.8 of this part. Beneficiaries who
PO 00000
Frm 00020
Fmt 4702
Sfmt 4702
78115
elect to use these pharmacy benefits
shall provide DoD with other health
insurance information.
Dated: December 21, 2006.
L.M. Bynum,
Alternate OSD Federal Register Liaison
Officer, DoD.
[FR Doc. E6–22258 Filed 12–27–06; 8:45 am]
BILLING CODE 5001–06–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R09–OAR–2005–AZ–0009; FRL–8262–
5]
Approval and Promulgation of
Implementation Plans; Arizona; Motor
Vehicle Inspection and Maintenance
Programs
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
SUMMARY: EPA is proposing to approve
two revisions to the Arizona State
Implementation Plan submitted by the
Arizona Department of Environmental
Quality. These revisions consist of
changes to Arizona’s Basic and
Enhanced Vehicle Emissions Inspection
Programs that would exempt collectible
vehicles in the Phoenix metropolitan
area, and collectible vehicles and
motorcycles in the Tucson metropolitan
area, from emissions testing
requirements; an updated performance
standard evaluation for the vehicle
emissions inspection program in the
Phoenix area; and new contingency
measures. EPA is proposing approval of
these two state implementation plan
revisions because they meet all
applicable requirements of the Clean Air
Act and EPA’s regulations and because
the exemptions would not interfere with
attainment or maintenance of the
national ambient air quality standards
in the two affected areas. EPA is
proposing this action under the Clean
Air Act obligation to take action on
State submittals of revisions to state
implementation plans. The intended
effect is to exempt these vehicle
categories from the emissions testing
requirements of the State’s vehicle
emissions inspection programs as
approved for the Phoenix and Tucson
areas.
Written comments must be
received at the address below on or
before January 29, 2007.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–R09–
DATES:
E:\FR\FM\28DEP1.SGM
28DEP1
Agencies
[Federal Register Volume 71, Number 249 (Thursday, December 28, 2006)]
[Proposed Rules]
[Pages 78110-78115]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-22258]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD-2006-HA-0149; RIN 0720-AB01]
Civilian Health and Medical Program of the Uniformed Services
(CHAMPUS); TRICARE: Implementation of Changes to the Pharmacy Benefits
Program; Double Coverage With Medicare Part D
AGENCY: Department of Defense.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: TRICARE eligible beneficiaries, who are entitled to Medicare
Part A on the basis of age, disability, or end-stage renal disease,
maintain their TRICARE eligibility when they are enrolled in the
supplementary medical insurance program under Part B of Medicare. In
general, in the case of medical or dental care provided to these
individuals for which payment may be made under both Medicare and
TRICARE, Medicare is the primary payer and TRICARE will normally pay
the actual out-of-pocket costs incurred by the person. This proposed
rule prescribes double coverage payment procedures and makes revisions
to TRICARE rules to accommodate beneficiaries who are eligible under
both Medicare and TRICARE, and who participate in Medicare's outpatient
prescription drug program under Medicare Part D. These revisions are
necessary because of the requirements contained in the Centers for
Medicare and Medicaid Services (CMS) final rule for the Medicare
Prescription Drug Benefit, Part D Plans with Other Prescription Drug
Coverage.
This proposed rule also establishes requirements and procedures for
implementation of the improvements to the TRICARE Pharmacy Benefits
Program directed by section 714 of the Ronald W. Reagan National
Defense Authorization Act for Fiscal Year 2005 (NDAA FY 05) (Public Law
108-365). The rule clarifies that the cost-sharing requirements for
Medicare-eligible beneficiaries may not be in excess of the cost-
sharing requirements applicable to other retirees, their dependents,
former spouses and survivors. Additionally, the rule authorizes the DoD
Pharmacy and Therapeutics Committee to make a separate and additional
determination of the relative clinical and cost effectiveness of
pharmaceutical agents to assure pharmacies of the uniformed services
have on their formularies pharmaceutical agents that provide greater
value than other uniform formulary agents in that therapeutic
[[Page 78111]]
class. This rule also describes the transition process that will occur
as the uniform formulary is developed and uniform service facilities
move to a uniform formulary, consistent with their scope of practice.
DATES: Comments on this proposed rule will be accepted until February
26, 2007.
ADDRESSES: You may submit comments, identified by docket number and/or
RIN number and title, by any of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: Federal Docket Management System Office, 1160
Defense Pentagon, Washington, DC 20301-1160.
Instructions: All submissions received must include the agency name
and docket number or Regulatory Information Number (RIN) for this
Federal Register document. The general policy for comments and other
submissions from members of the public is to make these submissions
available for public viewing on the Internet at https://regulations.gov
as they are received without change, including any personal identifiers
or contact information.
FOR FURTHER INFORMATION CONTACT: MAJ Travis Watson, TRICARE Management
Activity, Pharmacy Directorate, telephone (703) 681-2890 x6707.
SUPPLEMENTARY INFORMATION:
I. Double Coverage With Medicare Part D
Section 101 of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), (Pub. L. 108-173), amended Title XVIII
of the Social Security Act by establishing a new Part D: the Voluntary
Prescription Drug Benefit Program (henceforth, Medicare Part D). The
Department of Health and Human Services, Centers for Medicare and
Medicaid Services (CMS), published their Final Rule on January 28, 2005
(70 FR 4193--4585). The addition of a prescription drug benefit to
Medicare represents a landmark change to the Medicare program, and
became available to beneficiaries beginning on January 1, 2006.
The Floyd D. Spence National Defense Authorization Act for Fiscal
Year 2001 (Pub. L. 106-398), established the TRICARE Senior Pharmacy
Program under section 711 (which was effective April 1, 2001). The Act
also under section 712 (which was effective October 1, 2001) continued
TRICARE eligibility for beneficiaries entitled to Medicare Part A on
the basis of age, provided they also are enrolled in Medicare Part B.
This program has come to be known as TRICARE for Life. Under section
701 of the National Defense Authorization Act for Fiscal Year 2000
(Public Law 106-65), codified at Title 10, United States Code, Section
1074g, the Department established its new pharmacy benefits program for
all TRICARE beneficiaries (as implemented by 32 CFR 199.21). The full
implementation of the pharmacy benefits program was not effective until
May 3, 2004, however, changes in pharmacy cost shares were effective
with the implementation of TRICARE Senior Pharmacy on April 1, 2001.
In implementing TRICARE Senior Pharmacy, DoD stated that the double
coverage rules in 32 CFR 199.8 are applicable to services provided to
all beneficiaries under the retail pharmacy network, retail pharmacy
non-network, or TRICARE Mail Order programs. In implementing TRICARE
for Life, DoD explained the double coverage rules under 10 U.S.C.
1086(d)(3). The statute states that if a TRICARE-Medicare dual-eligible
beneficiary receives medical or dental care for which payment may be
made under Medicare and TRICARE, the amount payable for that care by
TRICARE shall be the amount of the actual out-of-pocket costs incurred
by the person for that care over the sum of (i) the amount paid for
that care under Medicare; and (ii) the total of all amounts paid or
payable by third party payers other than Medicare. The amount payable
by TRICARE may not exceed the total amount that would be paid under
TRICARE if payment for the care were made solely under TRICARE. TRICARE
for Life did not expand the scope of benefits available to this group
of beneficiaries beyond the scope of TRICARE benefits available to
other retirees and their families. The critical fact is whether the
service or supply is payable by both Medicare and TRICARE. For health
care services for which payment may be made under both Medicare and
TRICARE, TRICARE will pay up to the beneficiary's legal liability the
actual out-of-pocket costs incurred by the beneficiary, less any
payments made by Medicare or other sources of insurance). Actual out-
of-pocket costs incurred by the beneficiary include the initial
deductible, which are for services payable by Medicare and TRICARE, but
for the fact that the beneficiary has not met the deductible amount,
and any subsequent beneficiary cost shares. However, if a health care
service or supply is a benefit payable only by Medicare, but not
TRICARE, then Medicare has sole responsibility for payment of the
health care service or supply, as defined by Medicare, and the
beneficiary has the responsibility to pay any corresponding Medicare
cost-share or deductible. Likewise, if a health care service or supply
is a benefit payable only by TRICARE, but not Medicare, then TRICARE
has sole responsibility for payment of the health care service and
supply, and the beneficiary has the responsibility to pay any
corresponding TRICARE cost-shares or deductible. Finally, if a health
care service or supply is neither a benefit payable by Medicare or
TRICARE, the beneficiary pays the total cost.
TRICARE has applied the double coverage rules of 32 CFR 199.8 to
the Pharmacy Benefits Program under section 199.21(m), and said to the
extent they provide a prescription drug benefit, Medicare supplemental
insurance plans or Medicare HMO plans are double coverage plans and
will be primary payer. This rule was written prior to Medicare
providing a prescription drug benefit under Medicare Part D, and CMS's
final rule on the Medicare Prescription Drug Benefit. Under 42 CFR part
423, Subpart J, Coordination of Part D Plans With Other Prescription
Drug Coverage, section 423.464(f)(1)(iv), military coverage, including
TRICARE coverage under chapter 55 of title 10, United States Code,
qualifies as other prescription drug coverage with which a Part D plan
must coordinate benefits.
Medicare Part D plans are offered by private insurance companies
that contract with CMS. Part D benefits may be offered by a stand-alone
prescription drug plan sponsor, a Medicare Advantage Organization
offering qualified prescription drug coverage, a Program for All-
Inclusive Care for the Elderly (PACE) organization offering qualified
prescription drug coverage, or a cost plan offering qualified
prescription drug coverage (collectively referred to as a ``Part D plan
sponsor''). Each Part D plan sponsor submits a bid to CMS for plan
benefit packages, which results in, among other things, the offering of
Part D plans with varying monthly premiums and benefits designs. Part D
plan sponsors may offer a defined standard benefit, which is the type
of benefit used as an example in this preamble, or an actuarially
equivalent standard benefit. Part D plan sponsors may also offer
alternative prescription drug coverage, which may consist of basic
alternative coverage or enhanced alternative coverage. Therefore
depending on the Part D plan that a beneficiary chooses, monthly
premiums, coinsurances, co-pays, deductibles and benefit design may
vary from plan to plan. Under the MMA,
[[Page 78112]]
certain low-income beneficiaries may be eligible for reduced premiums
and cost-sharing for their drug coverage. In some cases, beneficiaries
pay no premium and nominal cost-sharing. Other beneficiaries have a
reduced premium and lower cost-sharing.
The standard Part D benefit includes several phases of beneficiary
spending, as described below.
Premiums. Statute requires a beneficiary to pay a monthly premium
to participate in the plan. A beneficiary who wants to participate in a
standard Medicare Part D plan is solely responsible for payment of any
premium that is not otherwise subsidized under the program. Beneficiary
premiums do not count toward any required beneficiary cost-sharing to
reach the deductible, coverage gap, or catastrophic limit (described
below).
Deductible. Under the Medicare Part D defined standard benefit, the
beneficiary is responsible for paying an out-of-pocket deductible ($265
in 2007) that adjusts annually according to the annual percentage
increase in spending on covered Part D drugs. For purposes of meeting
the deductible, both spending by the beneficiary and spending by
TRICARE on behalf of the beneficiary (i.e., the TRICARE wraparound
coverage) qualify.
Cost-sharing between deductible and coverage gap. After the
deductible is met, the standard Part D plan sponsors are responsible
for 75% of the actual cost of the covered Part D drug, and the
beneficiary is responsible for 25% of the actual cost of the covered
Part D drug, until the beneficiary reaches the coverage gap. TRICARE
wraparound coverage qualifies as beneficiary cost-sharing between the
deductible and coverage gap.
Coverage gap. To reach the coverage gap, the beneficiary must reach
a statutorily-specified amount of total drug spending. Total
beneficiary spending needed to meet the coverage gap is defined as
beneficiary out-of-pocket spending, or TRICARE spending on behalf of
the beneficiary, and spending by the Part D plan sponsor. In 2007, a
beneficiary reaches the coverage gap when he has incurred $2,400 in
total drug spending and remains in the gap until he has incurred $3,850
in beneficiary out-of-pocket spending. Individuals who qualify for the
low-income subsidies pay lower cost-sharing amounts before they reach
the coverage gap. In the coverage gap, the beneficiary is responsible
for 100% of the cost of the drug, although the beneficiary by law is
entitled to receive the plan's negotiated price. Individuals who
qualify for low-income subsidies do not have a coverage gap.
Catastrophic threshold. To reach the catastrophic threshold defined
in the standard benefit, the beneficiary must have incurred total
spending defined in statute as true out-of-pocket spending (TrOOP)
($3,850 in 2007). In the catastrophic phase, the beneficiary is
responsible for the greater of 5% of the cost of the drug, or, in 2007,
$2.15 for a generic/preferred multi-source drug or $5.35 for other
drugs. In the catastrophic phase of the defined standard benefit, the
Part D plan sponsor and Medicare are responsible for what is not paid
by the beneficiary up to the Part D plan sponsor's negotiated price.
Under 42 CFR 423.100, incurred costs means costs incurred by the
Part D enrollee for covered Part D drugs--(1) That are not paid for
under the Part D plan as a result of application of any annual
deductible or other cost-sharing rules for covered Part D drugs prior
to the Part D enrollee satisfying annual out-of-pocket threshold amount
under section 423.104(d)(5)(iii); and (2) That are paid for by the Part
D enrollee or on behalf of the enrollee by another person, and the
enrollee or other person is not reimbursed through insurance or
otherwise, a group health plan or other third party arrangement.
Because TRICARE falls under the definition of ``or otherwise,'' which
refers to ``government-funded health programs,'' wraparound payments
made by TRICARE for covered Part D drugs on behalf of an enrollee
eligible for both Part D and TRICARE do not count towards beneficiary
incurred costs. Therefore, for purposes of reaching the catastrophic
limit, only true beneficiary out-of-pocket spending (TrOOP) counts as
beneficiary spending. Although TRICARE supplementary coverage counts
toward meeting the deductible and the initial coverage limit, it does
not count toward meeting the catastrophic threshold.
Generally, a Part D plan is primary payer under 42 CFR 423.464,
coordination of benefits with other providers of prescription drug
coverage, which includes military coverage (including TRICARE) under
chapter 55 of title 10, United States Code. A Part D plan under section
423.464(f)(2) must exclude expenditures for covered Part D drugs made
by TRICARE for purposes of determining whether a Part D enrollee has
satisfied the out-of-pocket threshold, which for 2007 is $3,850.
As a result of these provisions implementing Medicare Part D,
TRICARE double coverage rules must be modified. If a TRICARE-Medicare
beneficiary enrolls in a Part D plan that adds prescription coverage to
their Medicare plan, the Medicare Part D plan is generally primary
payer and TRICARE is secondary payer. TRICARE will pay the
beneficiary's out-of-pocket costs for Medicare and TRICARE covered
medications, including the initial deductible and Medicare Part D cost-
share. TRICARE will not pay the beneficiary's out-of-pocket cost
associated with any monthly premium required to enroll in and
participate in the Medicare Part D plan.
In the coverage gap, the Part D plan is generally still the primary
payer. Thus, assuming the beneficiary is accessing a pharmacy under
contract with his or her Part D plan, the pharmacy would bill the Part
D plan, which would respond by indicating that it is responsible for
$0, at which point the pharmacy would bill TRICARE. When the
beneficiary becomes responsible for 100% of the drug costs in the
coverage gap, the beneficiary may use the TRICARE pharmacy benefit as
the secondary payer. TRICARE will cost share during the coverage gap to
the same extent as it does under section 199.21 for beneficiaries not
enrolled in a Medicare Part D plan. The beneficiary is responsible for
the applicable TRICARE pharmacy cost-sharing amounts (and deductible if
using a retail non-network pharmacy). During the coverage gap, TRICARE
is incurring the cost of the drugs during the Medicare Part D coverage
gap and not the beneficiary. Thus none of the costs of the drugs borne
by TRICARE will be applied to meeting the beneficiary's annual Medicare
Part D true out-of-pocket (TrOOP) threshold. Generally, however, the
beneficiary's own TRICARE pharmacy benefit cost-share will accrue to
meeting his/her annual Medicare Part D TrOOP spending because this
cost-sharing is an actual out-of-pocket expense incurred by the
beneficiary. Any actual out-of-pocket expense incurred by the
beneficiary also will apply toward the TRICARE fiscal year catastrophic
cap.
Similarly, if the TRICARE-Medicare dual-eligible beneficiary
enrolls in a Medicare Advantage drug plan, the beneficiary has to pay
the plan's monthly premiums and obtain all medical care and
prescription drugs through the Medicare Advantage plan. The Medicare
Advantage plan will generally be the primary payer, and TRICARE will be
the secondary payer. If the Medicare Advantage plan has a Part D drug
benefit, TRICARE will pay secondary as described above.
[[Page 78113]]
II. Legislative Changes for TRICARE-Medicare Dual-Eligible
Beneficiaries
Section 701 of the National Defense Authorization Act for Fiscal
Year 2000 (Public Law 106-65), codified at Title 10, United States
Code, Section 1074g, directs the Department to establish an effective,
efficient, integrated pharmacy benefits program. The Department
published the final rule on the Pharmacy Benefits Program on April 1,
2004 (69 FR 17035-17052) implementing the pharmacy benefits program,
effective May 3, 2004. Congress in section 714 of the Ronald W. Reagan
NDAA for FY 05 has directed certain improvements to the TRICARE
pharmacy benefits program.
Section 714(a) directs that for a TRICARE-Medicare dual-eligible
beneficiary, the cost-sharing requirements under the pharmacy benefits
program may not be greater than the cost-sharing requirements
applicable to all other beneficiaries covered by 10 U.S.C. 1086, which
are beneficiaries who are retirees, their authorized dependents,
survivors, and certain former spouses. Under 10 U.S.C. 1074g(a)(6), the
Department may establish cost-sharing requirements for the pharmacy
benefits program, which may be established as a percentage or fixed
dollar amount, for generic, formulary, and non-formulary pharmaceutical
agents. For non-formulary agents, cost-sharing shall be consistent with
common industry practice and not in excess of amounts generally
comparable to 20 percent for beneficiaries who are dependents of active
duty members of the uniformed services, and 25 percent for
beneficiaries who are retirees, their authorized dependents, survivors,
and certain former spouses.
In the TRICARE Pharmacy Benefits Program final rule, the Department
published the cost share amounts for pharmaceutical agents based upon
two factors: (1) The agent's status as generic, formulary, or non-
formulary; and (2) the venue in which the agent was obtained, that is,
military treatment facility (MTF), TRICARE Mail Order Program (TMOP),
retail network pharmacy, or retail non-network pharmacy. The Department
is authorized under 10 U.S.C. 1074g(a)(6) to have two non-formulary
cost-shares based upon the status of the beneficiary, no more than 20
percent for active duty family members and no more than 25 percent for
all others (other than active duty members who have no cost share). The
Department chose to have one non-formulary cost-share equal to no more
than 20 percent of the anticipated aggregated cost of non-formulary
agents that is $22 for non-formulary agents obtained in the TMOP or
retail network pharmacies, and $22 or 20 percent (whichever is greater)
for non-formulary agents obtained in retail non-network pharmacies.
(For more information on TRICARE Pharmacy Benefit Program cost shares,
see Section 199.21(i)). Section 714(a) emphasizes that if the
Department were to move to a two-tier non-formulary cost-share based
upon the status of the beneficiary, the Department may not have a
higher cost-share for TRICARE-Medicare dual-eligible beneficiaries than
for other retirees, their authorized dependents, survivors, and certain
former spouses. The Department has no intention at this time of
establishing two separate non-formulary cost-shares based upon the
status of the beneficiary as an active duty family member or other
category of beneficiary.
This proposed rule adds to Sec. 199.21 a provision incorporating
into the regulation the new statutory requirement.
III. Legislative Changes To Improve the Uniform Formulary Process
Under 10 U.S.C. 1074g(a)(2)(E)(i), pharmaceutical agents included
on the uniform formulary on the basis of relative clinical
effectiveness and cost effectiveness are required to be available to
beneficiaries through facilities of the uniformed services, consistent
with the scope of health care services offered in such facilities.
Section 714(b) of the Ronald W. Reagan NDAA for FY 05 directs the
Department to allow the DoD Pharmacy and Therapeutics Committee (P&T
Committee) to make additional relative clinical and cost effectiveness
determinations for military treatment facilities (MTFs). This change in
the law means that MTFs are not required to include on their
formularies every pharmaceutical agent in a therapeutic class that is
on the uniform formulary that is consistent with the scope of health
care services offered in the MTF. This proposed rule incorporates into
section 199.21 a provision reflecting the change in statute.
IV. Transition to the Uniform Formulary
The DoD P&T Committee is required under section 199.21 to make
recommendations concerning which pharmaceutical agents should be on the
uniform formulary and the Basic Core Formulary (BCF), and may now make
recommendations concerning which agents should be on the Extended Core
Formulary (ECF). The BCF contains the minimum set of pharmaceutical
agents that each MTF pharmacy must have on its formulary to support the
primary care scope of practice for Primary Care Manager enrollment
sites. The ECF contains the minimum set of pharmaceutical agents that
each MTF pharmacy must have on its formulary to support an extended
care scope of practice if the MTF Pharmacy and Therapeutics Committee
has authorized agents in that class based upon the scope of practice at
that facility.
The DoD Pharmacy and Therapeutics Committee will review the classes
in a methodical but expeditious manner, taking into consideration
circumstances that may include but are not limited to: DoD national
contracting, or DoD and Veterans Affairs national joint contracting or
other agreements with pharmaceutical manufacturers; approval of a new
drug by FDA; approval of a new indication for an existing drug; changes
in the clinical use of existing drugs; new information concerning the
safety, effectiveness or clinical outcomes of existing drugs; price
changes; shifts in market share; scheduled review of a therapeutic
class; and requests from DoD P&T Committee members, military treatment
facilities, or other Military Health System officials. During the
transition period from the previous methodology of formulary management
involving only the MTFs and the TRICARE Mail Order Program, previous
decisions by the DoD P&T Committee or committed use requirements
contracts executed by DoD, or jointly by DoD and VA, shall continue in
effect. This is necessary to comply with the statutory requirements of
38 U.S.C. 8111 and 10 U.S.C. 1104 relating to resource sharing between
DoD and VA, and allow time to incorporate the impact of uniform
formulary management into those agreements. As therapeutic classes are
reviewed under the new formulary management process and pharmaceutical
agents are designated for formulary or non-formulary status, this
transition methodology shall apply.
The P&T Committee will meet at least quarterly to review new and
existing drugs and drug classes, and recommend pharmaceutical agents
for inclusion on or exclusion from the uniform formulary after
evaluating their relative clinical and cost effectiveness. Pending
review of a pharmaceutical agent or class, previous decisions by the
predecessor to the P&T Committee regarding national contracts,
agreements, formulary status, BCF status, pre-authorization
requirements and quantity limits shall remain in effect. The P&T
Committee will eventually evaluate all applicable drug classes at which
time the transition period will be complete.
[[Page 78114]]
During this transition period, pharmaceutical agents in drug
classes not yet evaluated by the P&T Committee will continue to be
available from the TRICARE Mail Order Pharmacy (TMOP) and the TRICARE
Retail Pharmacy network at either the generic or formulary (brand) cost
share. MTFs may evaluate for inclusion on the MTF formulary
pharmaceutical agents in drug classes that do not already have BCF
status, or have not yet been evaluated by the P&T Committee. BCF listed
agents must be on the formulary at all full-service MTF pharmacies at
all times.
V. Regulatory Procedures
Executive Order 12866 directs agencies to assess all costs and
benefits available, regulatory alternatives and, when regulation is
necessary, to select regulatory approaches that maximize net benefits
(including potential economic, environmental, public health and safety,
and other advantages; distributive impacts; and equity). The Order
classifies a rule as a significant regulatory action requiring review
by the Office of Management and Budget if it meets any one of a number
of specified conditions, including: having an annual effect on the
national economy of $100 million or more, creating a serious
inconsistency or interfering with an action of another agency,
materially altering the budgetary impact of entitlements or the rights
of entitlement recipients, or raising novel legal or policy issues. DoD
has examined the economic, legal, and policy implications of this
proposed rule and has concluded that it is a significant regulatory
action as it addresses novel policy issues relating to implementation
of coordination of medical benefits programs for covered beneficiaries
of the uniformed services under TRICARE and the Medicare Prescription
Drug Benefit. Thus, this rule has been reviewed by the Office of
Management and Budget under E.O. 12866. The Regulatory Flexibility Act
(RFA) requires that each Federal Agency prepare, and make available for
public comment, a regulatory flexibility analysis when the agency
issues regulations which would have a significant impact on a
substantial number of small entities.
This proposed rule is not a major rule under the Congressional
Review Act, because its economic impact will be less than $100 million.
There are approximately 1.9 million TRICARE-Medicare dual-eligible
beneficiaries, and approximately 7% have enrolled in Medicare Part D
plans. For those who have Medicare Part D coverage, the cost of their
pharmacy benefit to DoD is less, as Medicare Part D Plans are the first
payer as opposed to DoD, resulting in a cost avoidance for DoD. The
amount of the cost avoidance is directly related to the number and cost
of prescriptions filled by beneficiaries for which Medicare is first
payer. Under the standard benefit package, there is a potential of
about $1,601.25 in DoD cost avoidance (in 2007) for Medicare/TRICARE
Part D enrollees whose drug spending is high enough to enter the
Medicare coverage gap. For beneficiaries with lower drug spending,
DoD's cost avoidance would also be lower. In addition, this rule will
have minor impact and will not significantly affect a substantial
number of small entities. In light of the above, no regulatory impact
analysis is required.
This proposed rule will not impose additional information
collection requirements on the public under the Paperwork Reduction Act
of 1995 (44 U.S.C. 55). In order to determine which dual-eligible
beneficiaries are participating in Medicare Part D, TRICARE will rely
on the Defense Eligibility Enrollment Reporting System (DEERS) to
identify which beneficiaries are enrolled in Medicare Part D through
existing data sharing agreements with CMS and will not need to collect
additional information from them.
We have examined the impact(s) of the proposed rule under Executive
Order 13132 and it does not have policies that have federalism
implications that would have substantial direct effects on the States,
on the relationship between the national government and the States, or
on the distribution of power and responsibilities among the various
levels of government, therefore, consultation with State and local
officials is not required.
List of Subjects in 32 CFR Part 199
Claims, Health care, Health insurance, Military personnel, Pharmacy
benefits.
Accordingly, 32 CFR part 199 is proposed to be amended as follows:
PART 199--[AMENDED]
1. The authority citation for Part 199 continues to read as
follows:
Authority: 5 U.S.C. 301; 10 U.S.C. chapter 55.
2. Section 199.8 is amended by adding paragraph (d)(1)(iii)(C) and
revising paragraph (d)(1)(vi) to read as follows:
Sec. 199.8 Double coverage.
* * * * *
(d) * * *
(1) * * *
(iii) * * *
(C) For Medicare beneficiaries who enroll in Medicare Part D, the
Part D plan is primary and TRICARE is secondary payer. TRICARE will pay
the beneficiary's out-of-pocket costs for Medicare and TRICARE covered
medications, including the initial deductible and Medicare Part D cost
sharing amounts up to the initial coverage limit of the Medicare Part D
plan. The Medicare Part D plan, although the primary plan pays nothing
during any coverage gap period. When the beneficiary becomes
responsible for 100 percent of the drug costs under a Part D coverage
gap period, the beneficiary may use the TRICARE pharmacy benefit as the
secondary payer. TRICARE will cost share during the coverage gap to the
same extent as it does under Sec. 199.21 for beneficiaries not
enrolled in a Medicare Part D plan. The beneficiary is responsible for
the applicable TRICARE pharmacy cost-sharing amounts (and deductible if
using a retail non-network pharmacy). Part D plan sponsors may offer a
defined standard benefit, or an actuarially equivalent standard
benefit. Part D plan sponsors may also offer alternative prescription
drug coverage, which may consist of basic alternative coverage or
enhanced alternative coverage. Therefore depending on the Part D plan
that a beneficiary chooses, monthly premiums, coinsurances, co-pays,
deductibles and benefit design may vary from plan to plan. TRICARE
payment of the beneficiary's initial deductible, if any, along with
payment of any beneficiary cost share count towards total spending on
drugs, and may have the effect of moving the beneficiary more quickly
through the initial phase of coverage to the coverage gap. Irrespective
of the phase of the benefit in which a beneficiary may be, if a
beneficiary is accessing a pharmacy under contract with his or her Part
D plan, the provider will bill the Part D plan first, then TRICARE. If
the beneficiary chooses to use his or her TRICARE pharmacy benefit
during a coverage gap under Part D, the beneficiary may do so, but the
beneficiary is responsible for the TRICARE cost-shares.
* * * * *
(vi) Effect of enrollment in Medicare Advantage Prescription Drug
(MA-PD) plan. In the case of a beneficiary enrolled in a MA-PD plan who
receives items or services for which payment may be made under both the
MA-PD plan and CHAMPUS/TRICARE, a claim for the beneficiary's normal
out-of-
[[Page 78115]]
pocket costs under the MA-PD plan may be submitted for CHAMPUS/TRICARE
payment. However, consistent with paragraph (c)(4) of this section,
out-of-pocket costs do not include costs associated with unauthorized
out-of-system care or care otherwise obtained under circumstances that
result in a denial or limitation of coverage for care that would have
been covered or fully covered had the beneficiary met applicable
requirements and procedures. In such cases, the CHAMPUS/TRICARE amount
payable is limited to the amount that would have been paid if the
beneficiary had received care covered by the Medicare Advantage plan.
If the TRICARE-Medicare beneficiary enrolls in a MA-PD drug plan, it
will be governed by Medicare Part C, although plans that offer a
prescription drug benefit also must comply with Medicare Part D rules.
The beneficiary has to pay the plan's monthly premiums and obtain all
medical care and prescription drugs through the Medicare Advantage plan
before seeking CHAMPUS/TRICARE payment. CHAMPUS/TRICARE payment for
such beneficiaries may not exceed that which would be payable for a
beneficiary under paragraph (d)(1)(iii)(C) of this section.
3. Section 199.21 is amended by adding new paragraphs (g)(4) and
(i)(2)(xi), and by revising paragraphs (h)(2)(ii) and (m), to read as
follows:
Sec. 199.21 Pharmacy benefits program.
* * * * *
(g) * * *
(4) Transition to the uniform formulary. Beginning in Fiscal Year
2005, under an updated charter for the DoD P&T Committee, the committee
shall meet at least quarterly to review therapeutic classes of
pharmaceutical agents and make recommendations concerning which
pharmaceutical agents should be on the Uniform Formulary, Basic Core
Formulary, and Extended Core Formulary. The P&T Committee will review
the classes in a methodical, but expeditious manner. During the
transition period from the previous methodology of formulary management
involving only the MTFs and the TRICARE Mail Order Pharmacy Program,
previous decisions by the predecessor DoD P&T Committee concerning MTF
and Mail Order Pharmacy Program formularies shall continue in effect.
As therapeutic classes are reviewed under the new formulary management
process, the processes established by this section shall apply.
* * * * *
(h) * * *
(2) * * *
(ii) Availability of formulary pharmaceutical agents at military
treatment facilities. Pharmaceutical agents included on the uniform
formulary are available through facilities of uniformed services,
consistent with the scope of health care services offered in such
facilities and additional determinations by the Pharmacy and
Therapeutics Committee of the relative clinical effectiveness and cost
effectiveness, based on costs to the Program associated with providing
the agents to beneficiaries. The Basic Core Formulary (BCF) is a subset
of the uniform formulary and is a mandatory component of formularies at
all full-service MTF pharmacies. The BCF contains the minimum set of
pharmaceutical agents that each full-service MTF pharmacy must have on
its formulary to support the primary care scope of practice for Primary
Care Manager enrollment sites. Limited-service MTF pharmacies (e.g.,
specialty pharmacies within an MTF or pharmacies servicing only active
duty military members) are not required to include the entire BCF on
their formularies, but may limit their formularies to those BCF agents
appropriate to the needs of the patients they serve. An Extended Core
Formulary (ECF) may list preferred agents in drug classes other than
those covered by the BCF. Among BCF and ECF agents, individual MTF
formularies are determined by local Pharmacy and Therapeutics
Committees based on the scope of health care services provided at the
respective MTFs. All pharmaceutical agents on the local formulary of
full-service MTF pharmacies must be available to all categories of
beneficiaries.
* * * * *
(i) * * *
(2) * * *
(xi) For a Medicare-eligible beneficiary, the cost sharing
requirements may not be in excess of the cost-sharing requirements
applicable to all other beneficiaries covered by 10 U.S.C. 1086.
* * * * *
(m) Effect of other health insurance. The double coverage rules of
section 199.8 of this part are applicable to services provided under
the pharmacy benefits program. For this purpose, the Medicare
prescription drug benefit under Medicare Part D, prescription drug
benefits provided under Medicare Part D plans are double coverage plans
and such plans will be the primary payer, to the extent described in
section 199.8 of this part. Beneficiaries who elect to use these
pharmacy benefits shall provide DoD with other health insurance
information.
Dated: December 21, 2006.
L.M. Bynum,
Alternate OSD Federal Register Liaison Officer, DoD.
[FR Doc. E6-22258 Filed 12-27-06; 8:45 am]
BILLING CODE 5001-06-P