Smallpox Vaccine Injury Compensation Program: Smallpox (Vaccinia) Vaccine Injury Table, 29805-29808 [06-4761]
Download as PDF
Federal Register / Vol. 71, No. 100 / Wednesday, May 24, 2006 / Rules and Regulations
t0.975
1 or 2 ........................
3 ................................
4 ................................
5 ................................
6 ................................
7 ................................
8 ................................
9 ................................
10 ..............................
11 ..............................
12 ..............................
13 ..............................
14 ..............................
15 ..............................
16 ..............................
17 ..............................
18 ..............................
19 ..............................
20 ..............................
21 ..............................
t0.90
N/A
4.303
3.182
2.776
2.571
2.447
2.365
2.306
2.262
2.228
2.201
2.179
2.160
2.145
2.131
2.120
2.110
2.101
2.093
2.086
N/A
1.886
1.638
1.533
1.476
1.440
1.415
1.397
1.383
1.372
1.363
1.356
1.350
1.345
1.341
1.337
1.333
1.330
1.328
1.325
*
*
*
*
*
4.8 The LCL is calculated at an 80
percent (two-sided) confidence level as
follows using Equation 11:
LC1 = x avg −
t 0.90 s
n
Eq. 11
Where:
LC1 = LCL at an 80-percent (two-sided)
confidence level.
n = Number of valid test runs.
s = Sample standard deviation.
t0.90 = t-value at the 80-percent (twosided) confidence level (see Table
A–1).
xavg = Average measured CE value
(calculated from all valid test runs).
*
*
*
*
*
Subpart JJJJ—[Amended]
12. Section 63.3300 is amended by
revising paragraph (a) to read as follows:
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I
§ 63.3300 Which of my emission sources
are affected by this subpart?
*
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*
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*
(a) Any web coating line that is standalone equipment under subpart KK of
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16:41 May 23, 2006
Subpart OOOO—[Amended]
13. Section 63.4281 is amended by:
a. Revising paragraph (d) introductory
text.
I b. Adding paragraphs (d)(4) to read as
follows:
I
I
§ 63.4281
Am I subject to this subpart?
*
TABLE A–1.—t-VALUES
Number of valid test
runs, n
this part (National Emission Standards
for the Printing and Publishing
Industry) which the owner or operator
includes in the affected source under
subpart KK.
*
*
*
*
*
Jkt 208001
*
*
*
*
(d) Web coating lines specified in
paragraphs (d)(1) through (4) of this
section are not part of the affected
source of this subpart.
*
*
*
*
*
(4) Any web coating line that coats or
prints fabric or other textiles for use in
flexible packaging and that is included
in an affected source under subpart KK
of this part (National Emission
Standards for the Printing and
Publishing Industry).
*
*
*
*
*
[FR Doc. 06–4821 Filed 5–23–06; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
42 CFR Part 102
RIN 0906—AA60
Smallpox Vaccine Injury
Compensation Program: Smallpox
(Vaccinia) Vaccine Injury Table
Health Resources and Services
Administration (HRSA), HHS.
ACTION: Adoption of interim final rule as
final rule with an amendment.
AGENCY:
SUMMARY: This document adopts the
Smallpox (Vaccinia) Vaccine Injury
Table (the Table) Interim Final Rule as
the Final Rule with an amendment, as
follows: the Final Rule clarifies that, in
order for the presumption of causation
to apply, the time intervals listed on the
Table refer specifically to the period in
which the first symptom or
manifestation of onset of injury must
appear following administration of the
smallpox vaccine or exposure to
vaccinia, and that the time intervals
listed have no relevance to time of
diagnosis of the injury.
DATES: The Interim Final Rule,
published on August 27, 2003, was
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Fmt 4700
Sfmt 4700
effective on that date, and is adopted as
the Final Rule with an amendment
effective May 24, 2006.
FOR FURTHER INFORMATION CONTACT: Paul
T. Clark, Director, Smallpox Vaccine
Injury Compensation Program,
Healthcare Systems Bureau, Health
Resources and Services Administration,
(301) 443–2330.
SUPPLEMENTARY INFORMATION:
Background
The Smallpox Emergency Personnel
Protection Act of 2003 (SEPPA), Pub. L.
108–20, 117 Stat. 638, directed the
Secretary of Health and Human Services
(the Secretary) to establish the Smallpox
Vaccine Injury Compensation Program
(the Program). Secondary to other
payers, the Program provides medical,
lost employment income, and death
benefits for eligible individuals who
sustained covered injuries as a result of
receiving smallpox vaccine or other
covered countermeasures, or as a result
of accidental exposure to vaccinia.
Congress appropriated $42 million in
fiscal year (FY) 2003 for the
administration of, and payment of
benefits under, the Program. The
Consolidated Appropriations Act of
2005 reduced this appropriation to $22
million. The Departments of Labor,
Health and Human Services, and
Education, and Related Agencies
Appropriations Act, 2006 (Pub. L. 109–
149) further reduced the Program’s
appropriation by $10 million to a total
of $12 million.
Individuals who receive a smallpox
vaccination under a Department of
Health and Human Services (HHS),
State, or local emergency response plan
approved by HHS within the period
described in the Secretary’s Declaration,
and who sustain a covered injury may
be eligible for benefits under SEPPA.
Individuals who contracted vaccinia
through contact with such individuals
or other eligible vaccinia contacts and
who sustain a covered injury may also
be eligible for benefits. In the case of
death resulting directly from receipt of
the smallpox vaccine or exposure to
vaccinia by eligible individuals, certain
of their survivors may be considered for
death benefits. If an eligible individual
who sustained a covered injury dies
from another cause before payment of
benefits has been made under the
Program, the estate may qualify for
payment of unreimbursed medical
expenses incurred and employment
income lost as a result of the covered
injury, secondary to other payers.
SEPPA directed the Secretary to
establish a table identifying adverse
effects (including injuries, disabilities,
E:\FR\FM\24MYR1.SGM
24MYR1
ER24MY06.006
n = Number of valid test runs.
P = DQO indicator statistic, distance
from the average measured CE value
to the endpoints of the 95-percent
(two-sided) confidence interval,
expressed as a percent of the
average measured CE value.
s = Sample standard deviation.
t0.975 = t-value at the 95-percent (twosided) confidence level (see Table
A–1).
xavg = Average measured CE value
(calculated from all valid test runs).
xi = The CE value calculated from the
ith test run.
29805
29806
Federal Register / Vol. 71, No. 100 / Wednesday, May 24, 2006 / Rules and Regulations
conditions, and deaths) that shall be
presumed to result from the
administration of, or exposure to, the
smallpox vaccine, and the time interval
in which the first symptom or
manifestation of each listed injury must
appear in order for such presumption to
apply. An Interim Final Rule for the
Table was published in the Federal
Register on August 27, 2003 (68 FR
51492), with public comments sought
on these provisions.
Based on the comments received, this
Final Rule clarifies that the Table is not
the sole standard for determining
medical eligibility for benefits under the
Program. Therefore, an individual who
sustains an injury that is not on the
Table or not within the timeframes on
the Table, and believes it was caused by
a smallpox vaccination, is encouraged to
submit a Request Package to the
Program. This Final Rule makes it clear
that the time intervals on the Table refer
specifically to the first symptom or
manifestation of onset of illness or
injury, not to the date of the diagnosis.
It also clarifies that any component of a
smallpox vaccine, not only the vaccinia,
could be the possible cause of a covered
injury. Further, this regulation updates
the Interim Final Rule to reflect that the
Secretary has extended the effective
period of the Declaration Regarding
Administration of Smallpox
Countermeasures (the Declaration).
Finally, this Final Rule also updates the
change in name of the Special Programs
Bureau to the Healthcare Systems
Bureau; and provides the new address
of the Program Office.
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Discussion of Comments
The public comment period ended on
October 27, 2003. HHS received a total
of 11 public comments. Four were from
professional associations; three were
from medical professionals; two were
from the general public; one was from
a State health department; and one was
from a nonprofit community health
organization. The issues raised and
HHS’s responses appear below.
A. Time Intervals for the First Symptom
or Manifestation of Onset of Injury
The Secretary received two comments
suggesting that the time intervals listed
on the Table be lengthened. One
commenter requested that the Secretary
extend the time limit for the onset of
myocarditis and pericarditis from 21
days to 60 days. The other commenter
indicated concern that the time intervals
listed on the Table seem potentially
short, and should be determined in
consultation with the Centers for
Disease Control and Prevention (CDC)
and the military regarding all the Table
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16:41 May 23, 2006
Jkt 208001
time intervals, independent of how long
it takes for a scab to fall off. The
Secretary received a third comment
related to the time intervals on the Table
requesting an appeal process to the
Table time intervals.
The Secretary does not concur with
changing the time intervals on the
Table, whether it be for the onset of
myocarditis or pericarditis from 21 to 60
days, or any other seemingly short time
intervals. The Secretary did consult
with the Department of Defense (DoD)
and CDC, as well as with other HHS
components and the private sector.
Their scientific data support the time
intervals as specified on the Table. The
commenters did not provide evidence to
support lengthening the time intervals
beyond that which the Secretary had
already considered and, therefore, they
remain as currently listed. However, as
discussed below, if any individual has
symptoms that manifest outside of those
time intervals, he or she may still be
considered for benefits under the
Program.
The third commenter expressed the
hope that the Table permits adequate
time for injured individuals to seek
compensation, and recommended that
language be added to the regulations to
provide an avenue for appeal to the
timeframes established in the Table,
should an individual become ill or
exhibit symptoms related to the vaccine
beyond the established Table
timeframes.
The Secretary wishes to emphasize
that an injury that manifests itself
outside of the timeframe listed on the
Table may still be a covered injury. The
Secretary recognizes that symptoms can
occur subsequent to the Table
timeframes in some cases. In this event,
the individual may be found medically
eligible if he or she submits evidence to
show that it is more likely than not that
the smallpox vaccine or other covered
countermeasure, or the vaccinia
contracted from accidental vaccinia
exposure, actually caused the injury.
SEPPA does not provide an avenue for
appeal of the timeframes established in
the Table. Thus, the Secretary disagrees
with the commenter that there is a need
for an appeal process for the time
intervals. However, the Secretary has
established a reconsideration process for
re-review of the Program’s
determinations on medical/program and
financial eligibility requirements
through the Administrative Regulations
for this Program published in the
Federal Register on December 16, 2003.
If a requester is not satisfied with the
Program’s decisions, the requester has
the right to seek reconsideration of any
adverse determination.
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There were two additional comments
regarding time intervals. One
commenter wanted to make sure that
HHS clarifies that the time intervals
relate to the timeframe of the first
symptom or manifestation of onset of
injury, not to the timeframe of the
diagnosis. The Secretary agrees with
this comment and has clarified this
issue by inserting appropriate language
into this Final Rule.
The other commenter requested that
the time intervals of 21 days be
extended because it may take 6 to 8
weeks for the scab at the vaccination
site to fall off. The Secretary does not
agree to change the time intervals on the
Table because these timeframes are not
related to the time it takes for the scab
to fall off spontaneously.
B. Additions of Injuries to the Table
There were three comments
pertaining to the injuries listed on the
Table. Two comments suggested that the
Table should be amended to include
myocardial infarction and tremors,
respectively. The other commenter
indicated that the list of injuries limited
to those published in the August 27,
2003, Interim Final Rule, was
incomplete.
The Secretary does not concur with
these comments. At this time, there is
no clear scientific evidence to support
the inclusion of myocardial infarction,
tremors, or other conditions as
additional Table injuries, and the
commenters did not provide additional
evidence showing it would be
appropriate to add more Table injuries.
Should an individual have any injury
believed to have resulted from the
administration of, or exposure to, the
smallpox vaccine that is not listed on
the Table, he or she may nevertheless be
eligible for benefits and should submit
a request to the Program.
C. The Documentation Requirements
One commenter raised the issue that
the Table regulations exceed the
statute’s requirements in terms of
medical injury documentation burden
and related cost. The commenter
believes that these regulations are far
more onerous than SEPPA requires,
specifying that the issues of
documenting method of treatment,
identification of injury, etc., are not
even referenced in the statute. The
commenter stated that the burdensome
and costly requirements for first
responders should immediately be
rescinded.
The Secretary disagrees with the
commenter that the documentation
requirement is onerous and exceeds
legislative intent. The specific comment
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24MYR1
Federal Register / Vol. 71, No. 100 / Wednesday, May 24, 2006 / Rules and Regulations
relates to the requirement for a
treatment plan in order to be considered
for a Table injury. This language
appears in five of the twelve Table
injuries. The requirement for a
treatment plan is case-specific and
applies only in certain circumstances
where there is an issue of needed longterm medical/surgical care. Requesters
do not need to provide one in order to
be considered for a Table injury.
The commenter also wrote that first
responders are obligated to pay out of
their own pockets for immediate
treatment and again for a detailed
surgical treatment plan. Section 264(b)
of the Smallpox Emergency Personnel
Protection Act of 2003 establishes that
the government is the payer of last
resort after all other payments have been
or will be made to an individual for
medical care directly resulting from an
injury caused by the smallpox
vaccination. Individuals are reimbursed
for their out-of-pocket medical expenses
in accordance with the Act.
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D. Other Issues Raised by Commenters
One commenter raised the concern
that the Table regulations cover only
those injuries caused by the vaccinia
virus and not all components of the
smallpox vaccine. Another commenter
was concerned about the scope of the
Program and if it would cover the
general population.
In reference to the issue of the
components in the smallpox vaccine,
the Secretary concurs that the
components of a smallpox vaccine may
cause a covered injury. Therefore, the
Secretary has clarified in this final
regulation that a covered injury can be
caused not only by vaccinia, but by any
component or constituent of the
smallpox vaccine.
In response to the concern about the
scope of the legislation, SEPPA only
covers individuals who are members of
HHS-approved smallpox emergency
response plans and individuals who
contracted vaccinia from them or from
other eligible contacts. SEPPA is not
designed to provide benefits to the
general population.
Explanation of Provisions
Some of the comments received
indicate to the Secretary that there may
be confusion as to the significance of the
Table. Therefore, this Final Rule
clarifies that having an injury listed on
the Table is only one of the ways that
an individual can show medical
eligibility for Program benefits. The
Secretary emphasizes that the purpose
of the Table is merely to provide
potential requesters who can
demonstrate that they sustained a Table
VerDate Aug<31>2005
16:41 May 23, 2006
Jkt 208001
injury within the specified time interval
with the presumption that the smallpox
vaccine caused the injury. However,
sustaining an injury not listed on the
Table (including an injury resulting
from administration of another covered
countermeasure), or manifesting a Table
injury outside of the time interval listed,
simply means that the presumption
does not apply. In those cases, the
individual must show that it is more
likely than not (i.e., by a preponderance
of the evidence), that administration of
the smallpox vaccine (or other covered
countermeasure), or exposure to the
vaccine in the case of contacts, was the
cause of the injury. The Secretary
encourages such individuals to file a
request for benefits. The Program has
found individuals with Table or nonTable injuries to be medically eligible.
As previously mentioned, this Final
Rule also clarifies that the time intervals
listed on the Table refer specifically to
the period in which the first symptom
or manifestation of onset of injury must
appear following administration of the
smallpox vaccine or exposure to
vaccinia, in order for the presumption of
causation to apply. The time intervals
listed have no relevance whatsoever to
when the injury is diagnosed.
Thus, the Secretary herein amends
§ 102.21(a) of the Interim Final Rule by
adding language to the subheading of
the Table that lists the time intervals.
This additional language makes it clear
that these time intervals refer only to the
first symptom or manifestation of onset
of the injury, not to the time interval
within which a diagnosis of the injury
must be made.
The Secretary also wishes to make it
clear that a covered injury can be caused
not only by the vaccinia component of
the smallpox vaccine, but by any
component or constituent of the
vaccine.
Further, this Final Rule updates the
effective period of the Secretary’s
Declaration. The Secretary has amended
the effective period of the Declaration
by extending it each year. The Secretary
will continue to publish a Notice in the
Federal Register as needed to update
any further amendments to the effective
period. These amendments to the
Declaration are made pursuant to the
Secretary’s authority under section
261(a)(5) of SEPPA (section 224(p)(2)(A)
of the Public Health Service Act).
Additionally, this Final Rule reflects
the change in name of the Special
Programs Bureau, which has been
renamed the Healthcare Systems
Bureau. Finally, this regulation updates
the address of the Program Office. The
new address, to which all mail to the
Program should be sent, whether by
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29807
U.S. Postal Service, commercial carrier,
or private courier service, is: Parklawn
Building, Room 11C–06, 5600 Fishers
Lane, Rockville, Maryland 20857.
Justification of Waiver of Delay of
Effective Date
The Secretary has found that a delay
in the effective date of this Final Rule
with an amendment is unnecessary and
contrary to the public interest. The
adoption of the Interim Final Rule as a
Final Rule reflects an amendment and
clarifications that are a result of
comments received on the Interim Final
Rule and, therefore, will be helpful to
requesters without imposing additional
burdens. It has no effect on any
individual’s rights or responsibilities.
Economic and Regulatory Impact
Executive Order 12866 directs
agencies to assess all costs and benefits
of available regulatory alternatives and,
when rulemaking is necessary, to select
regulatory approaches that provide the
greatest net benefits (including potential
economic, environmental, public health,
safety distributive and equity effects). In
addition, under the Regulatory
Flexibility Act of 1980 (RFA), if a rule
has a significant economic effect on a
substantial number of small entities, the
Secretary must specifically consider the
economic effect of a rule on small
entities and analyze regulatory options
that could lessen the impact of the rule.
Executive Order 12866 requires that
all regulations reflect consideration of
alternatives, of costs, of benefits, of
incentives, of equity, and of available
information. Regulations must meet
certain standards, such as avoiding an
unnecessary burden. Regulations that
are ‘‘significant’’ because of cost,
adverse effects on the economy,
inconsistency with other agency actions,
effects on the budget, or novel legal or
policy issues, require special analysis.
The Secretary has determined that
minimal resources are required to
implement the provisions included in
this regulation. Therefore, in accordance
with the RFA, and the Small Business
Regulatory Enforcement Fairness Act of
1996, which amended the RFA, the
Secretary certifies that this Final Rule
will not have a significant impact on a
substantial number of small entities.
The Secretary has also determined
that this rule does not meet the criteria
for a major rule as defined by Executive
Order 12866 and would have no major
effect on the economy or Federal
expenditures. This rule is not a ‘‘major
rule’’ within the meaning of the statute
providing for Congressional Review of
Agency Rulemaking, 5 U.S.C. 801.
E:\FR\FM\24MYR1.SGM
24MYR1
29808
Federal Register / Vol. 71, No. 100 / Wednesday, May 24, 2006 / Rules and Regulations
Unfunded Mandates Reform Act of
1995
The Secretary has determined that
this Final Rule will not have effects on
State, local, or tribal governments or on
the private sector such as to require
consultation under the Unfunded
Mandates Reform Act of 1995.
Federalism Impact Statement
The Secretary has also reviewed this
rule in accordance with Executive Order
13132 regarding federalism, and has
determined that it does not have
‘‘federalism implications.’’ The rule
does not ‘‘have substantial direct effects
on the States, or on the relationship
between the national government and
the States, or on the distribution of
power and responsibilities among the
various levels of government.’’
Impact on Family Well-Being
This rule will not adversely affect the
following elements of family well-being:
Family safety, family stability, marital
commitment; parental rights in the
education, nurture and supervision of
their children; family functioning,
disposable income or poverty; or the
behavior and personal responsibility of
youth, as determined under section
654(c) of the Treasury and General
Government Appropriations Act of
1999. In fact, this Final Rule may have
a positive impact on the disposable
income and poverty elements of family
well-being to the extent that injured
persons (or their survivors who are
eligible to receive compensation)
receive benefits without a
corresponding burden being imposed on
them.
Paperwork Reduction Act
The information collection
requirements remain unchanged.
List of Subjects in 42 CFR Part 102
Benefits, Biologics, Compensation,
Immunization, Public health, Smallpox,
Vaccinia.
Dated: November 14, 2005.
Elizabeth M. Duke,
Administrator.
Approved: December 22, 2005.
Michael O. Leavitt,
Secretary.
Editorial Note: This document was
received at the Office of the Federal Register
on May 18, 2006.
For the reasons stated above, the
Secretary is adopting the Interim Final
Rule adding 42 CFR part 102, published
at 68 FR 51492 on Wednesday, August
27, 2003, as a Final Rule with the
following amendment:
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I
VerDate Aug<31>2005
17:22 May 23, 2006
Jkt 208001
PART 102—SMALLPOX
COMPENSATION PROGRAM
1. The authority citation for part 102
continues to read as follows:
I
Authority: 42 U.S.C. 216, 42 U.S.C. 239–
239h.
2. In section 102.21, the table in
paragraph (a) is amended by adding the
following sentence at the end of the
time interval description subheading:
I
§ 102.21 Smallpox (Vaccinia) Vaccine
Injury Table.
(a) * * *
Please note that these time intervals
do not refer to time periods for the date
of diagnosis of the injury.
*
*
*
*
*
[FR Doc. 06–4761 Filed 5–23–06; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
42 CFR Part 102
RIN 0906—AA61
Smallpox Vaccine Injury
Compensation Program:
Administrative Implementation
Health Resources and Services
Administration (HRSA), HHS.
ACTION: Adoption of interim final rule as
final rule with amendments.
AGENCY:
SUMMARY: This document adopts the
Smallpox Vaccine Injury Compensation
Program (the Program) Administrative
Implementation Interim Final Rule as
the Final Rule with amendments, as
follows: explains how the term ‘‘child’’
survivor is defined; updates the
effective period of the Secretary’s
Declaration Regarding Administration of
Smallpox Countermeasures (the
Declaration); corrects an error in
§ 102.20(d) to clarify that one of the
Smallpox (Vaccinia) Vaccine Injury
Table requirements to establish a
covered Table injury is the first
symptom or manifestation of onset of
the injury in the Table time period
specified; reflects the change in name
from the Special Programs Bureau to the
Healthcare Systems Bureau; provides
the new address of the Bureau’s
Associate Administrator, and the new
address of the Program Office; clarifies
that no payments are authorized for fees
or costs of personal representatives,
including those of attorneys; and
corrects a typographical error in
§ 102.83(c) to make clear that the
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Sfmt 4700
Secretary determines the timeframe for
submission of required documentation.
DATES: The interim final rule, published
on December 16, 2003, was effective on
that date, and is adopted as the final
rule with an amendment effective May
24, 2006.
FOR FURTHER INFORMATION CONTACT: Paul
T. Clark, Director, Smallpox Vaccine
Injury Compensation Program,
Healthcare Systems Bureau, Health
Resources and Services Administration,
(301) 443–2330.
SUPPLEMENTARY INFORMATION:
Background
The Smallpox Emergency Personnel
Protection Act of 2003 (SEPPA), Pub. L.
108–20, 117 Stat. 638, directed the
Secretary of Health and Human Services
(the Secretary) to establish the Program.
Secondary to other payers, the Program
provides medical, lost employment
income, and death benefits for eligible
individuals who sustained covered
injuries as a result of receiving smallpox
vaccine or other covered
countermeasures, or as a result of
accidental exposure to vaccinia.
Congress appropriated $42 million in
fiscal year (FY) 2003 for the
administration of, and payment of
benefits under, the Program. The
Consolidated Appropriations Act of
2005 reduced this amount by $20
million. The Departments of Labor,
Health and Human Services and
Education and Related Agencies
Appropriations Act, 2006 (Pub. L. 109–
149) further reduced the Program’s
appropriation by $10 million to a total
of $12 million. Section 220 of the
Appropriations Act of 2006 (Pub. L.
109–149) further reduced the Program’s
appropriation by $10 million to a total
of $12 million.
Individuals who receive a smallpox
vaccination under a Department of
Health and Human Services (HHS),
State, or local emergency response plan
approved by HHS within the time
period described in the Secretary’s
Declaration, and who sustain a covered
injury, may be eligible for benefits
under SEPPA. Individuals who
contracted vaccinia through contact
with such individuals or other eligible
vaccinia contacts and who sustain a
covered injury may also be eligible for
benefits. In the case of death resulting
directly from receipt of the smallpox
vaccine or exposure to vaccinia by
eligible individuals, certain of their
survivors may be considered for death
benefits. If an eligible individual who
sustained a covered injury dies from
another cause before payment of
benefits has been made under the
E:\FR\FM\24MYR1.SGM
24MYR1
Agencies
[Federal Register Volume 71, Number 100 (Wednesday, May 24, 2006)]
[Rules and Regulations]
[Pages 29805-29808]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-4761]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
42 CFR Part 102
RIN 0906--AA60
Smallpox Vaccine Injury Compensation Program: Smallpox (Vaccinia)
Vaccine Injury Table
AGENCY: Health Resources and Services Administration (HRSA), HHS.
ACTION: Adoption of interim final rule as final rule with an amendment.
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SUMMARY: This document adopts the Smallpox (Vaccinia) Vaccine Injury
Table (the Table) Interim Final Rule as the Final Rule with an
amendment, as follows: the Final Rule clarifies that, in order for the
presumption of causation to apply, the time intervals listed on the
Table refer specifically to the period in which the first symptom or
manifestation of onset of injury must appear following administration
of the smallpox vaccine or exposure to vaccinia, and that the time
intervals listed have no relevance to time of diagnosis of the injury.
DATES: The Interim Final Rule, published on August 27, 2003, was
effective on that date, and is adopted as the Final Rule with an
amendment effective May 24, 2006.
FOR FURTHER INFORMATION CONTACT: Paul T. Clark, Director, Smallpox
Vaccine Injury Compensation Program, Healthcare Systems Bureau, Health
Resources and Services Administration, (301) 443-2330.
SUPPLEMENTARY INFORMATION:
Background
The Smallpox Emergency Personnel Protection Act of 2003 (SEPPA),
Pub. L. 108-20, 117 Stat. 638, directed the Secretary of Health and
Human Services (the Secretary) to establish the Smallpox Vaccine Injury
Compensation Program (the Program). Secondary to other payers, the
Program provides medical, lost employment income, and death benefits
for eligible individuals who sustained covered injuries as a result of
receiving smallpox vaccine or other covered countermeasures, or as a
result of accidental exposure to vaccinia. Congress appropriated $42
million in fiscal year (FY) 2003 for the administration of, and payment
of benefits under, the Program. The Consolidated Appropriations Act of
2005 reduced this appropriation to $22 million. The Departments of
Labor, Health and Human Services, and Education, and Related Agencies
Appropriations Act, 2006 (Pub. L. 109-149) further reduced the
Program's appropriation by $10 million to a total of $12 million.
Individuals who receive a smallpox vaccination under a Department
of Health and Human Services (HHS), State, or local emergency response
plan approved by HHS within the period described in the Secretary's
Declaration, and who sustain a covered injury may be eligible for
benefits under SEPPA. Individuals who contracted vaccinia through
contact with such individuals or other eligible vaccinia contacts and
who sustain a covered injury may also be eligible for benefits. In the
case of death resulting directly from receipt of the smallpox vaccine
or exposure to vaccinia by eligible individuals, certain of their
survivors may be considered for death benefits. If an eligible
individual who sustained a covered injury dies from another cause
before payment of benefits has been made under the Program, the estate
may qualify for payment of unreimbursed medical expenses incurred and
employment income lost as a result of the covered injury, secondary to
other payers. SEPPA directed the Secretary to establish a table
identifying adverse effects (including injuries, disabilities,
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conditions, and deaths) that shall be presumed to result from the
administration of, or exposure to, the smallpox vaccine, and the time
interval in which the first symptom or manifestation of each listed
injury must appear in order for such presumption to apply. An Interim
Final Rule for the Table was published in the Federal Register on
August 27, 2003 (68 FR 51492), with public comments sought on these
provisions.
Based on the comments received, this Final Rule clarifies that the
Table is not the sole standard for determining medical eligibility for
benefits under the Program. Therefore, an individual who sustains an
injury that is not on the Table or not within the timeframes on the
Table, and believes it was caused by a smallpox vaccination, is
encouraged to submit a Request Package to the Program. This Final Rule
makes it clear that the time intervals on the Table refer specifically
to the first symptom or manifestation of onset of illness or injury,
not to the date of the diagnosis. It also clarifies that any component
of a smallpox vaccine, not only the vaccinia, could be the possible
cause of a covered injury. Further, this regulation updates the Interim
Final Rule to reflect that the Secretary has extended the effective
period of the Declaration Regarding Administration of Smallpox
Countermeasures (the Declaration). Finally, this Final Rule also
updates the change in name of the Special Programs Bureau to the
Healthcare Systems Bureau; and provides the new address of the Program
Office.
Discussion of Comments
The public comment period ended on October 27, 2003. HHS received a
total of 11 public comments. Four were from professional associations;
three were from medical professionals; two were from the general
public; one was from a State health department; and one was from a
nonprofit community health organization. The issues raised and HHS's
responses appear below.
A. Time Intervals for the First Symptom or Manifestation of Onset of
Injury
The Secretary received two comments suggesting that the time
intervals listed on the Table be lengthened. One commenter requested
that the Secretary extend the time limit for the onset of myocarditis
and pericarditis from 21 days to 60 days. The other commenter indicated
concern that the time intervals listed on the Table seem potentially
short, and should be determined in consultation with the Centers for
Disease Control and Prevention (CDC) and the military regarding all the
Table time intervals, independent of how long it takes for a scab to
fall off. The Secretary received a third comment related to the time
intervals on the Table requesting an appeal process to the Table time
intervals.
The Secretary does not concur with changing the time intervals on
the Table, whether it be for the onset of myocarditis or pericarditis
from 21 to 60 days, or any other seemingly short time intervals. The
Secretary did consult with the Department of Defense (DoD) and CDC, as
well as with other HHS components and the private sector. Their
scientific data support the time intervals as specified on the Table.
The commenters did not provide evidence to support lengthening the time
intervals beyond that which the Secretary had already considered and,
therefore, they remain as currently listed. However, as discussed
below, if any individual has symptoms that manifest outside of those
time intervals, he or she may still be considered for benefits under
the Program.
The third commenter expressed the hope that the Table permits
adequate time for injured individuals to seek compensation, and
recommended that language be added to the regulations to provide an
avenue for appeal to the timeframes established in the Table, should an
individual become ill or exhibit symptoms related to the vaccine beyond
the established Table timeframes.
The Secretary wishes to emphasize that an injury that manifests
itself outside of the timeframe listed on the Table may still be a
covered injury. The Secretary recognizes that symptoms can occur
subsequent to the Table timeframes in some cases. In this event, the
individual may be found medically eligible if he or she submits
evidence to show that it is more likely than not that the smallpox
vaccine or other covered countermeasure, or the vaccinia contracted
from accidental vaccinia exposure, actually caused the injury. SEPPA
does not provide an avenue for appeal of the timeframes established in
the Table. Thus, the Secretary disagrees with the commenter that there
is a need for an appeal process for the time intervals. However, the
Secretary has established a reconsideration process for re-review of
the Program's determinations on medical/program and financial
eligibility requirements through the Administrative Regulations for
this Program published in the Federal Register on December 16, 2003. If
a requester is not satisfied with the Program's decisions, the
requester has the right to seek reconsideration of any adverse
determination.
There were two additional comments regarding time intervals. One
commenter wanted to make sure that HHS clarifies that the time
intervals relate to the timeframe of the first symptom or manifestation
of onset of injury, not to the timeframe of the diagnosis. The
Secretary agrees with this comment and has clarified this issue by
inserting appropriate language into this Final Rule.
The other commenter requested that the time intervals of 21 days be
extended because it may take 6 to 8 weeks for the scab at the
vaccination site to fall off. The Secretary does not agree to change
the time intervals on the Table because these timeframes are not
related to the time it takes for the scab to fall off spontaneously.
B. Additions of Injuries to the Table
There were three comments pertaining to the injuries listed on the
Table. Two comments suggested that the Table should be amended to
include myocardial infarction and tremors, respectively. The other
commenter indicated that the list of injuries limited to those
published in the August 27, 2003, Interim Final Rule, was incomplete.
The Secretary does not concur with these comments. At this time,
there is no clear scientific evidence to support the inclusion of
myocardial infarction, tremors, or other conditions as additional Table
injuries, and the commenters did not provide additional evidence
showing it would be appropriate to add more Table injuries. Should an
individual have any injury believed to have resulted from the
administration of, or exposure to, the smallpox vaccine that is not
listed on the Table, he or she may nevertheless be eligible for
benefits and should submit a request to the Program.
C. The Documentation Requirements
One commenter raised the issue that the Table regulations exceed
the statute's requirements in terms of medical injury documentation
burden and related cost. The commenter believes that these regulations
are far more onerous than SEPPA requires, specifying that the issues of
documenting method of treatment, identification of injury, etc., are
not even referenced in the statute. The commenter stated that the
burdensome and costly requirements for first responders should
immediately be rescinded.
The Secretary disagrees with the commenter that the documentation
requirement is onerous and exceeds legislative intent. The specific
comment
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relates to the requirement for a treatment plan in order to be
considered for a Table injury. This language appears in five of the
twelve Table injuries. The requirement for a treatment plan is case-
specific and applies only in certain circumstances where there is an
issue of needed long-term medical/surgical care. Requesters do not need
to provide one in order to be considered for a Table injury.
The commenter also wrote that first responders are obligated to pay
out of their own pockets for immediate treatment and again for a
detailed surgical treatment plan. Section 264(b) of the Smallpox
Emergency Personnel Protection Act of 2003 establishes that the
government is the payer of last resort after all other payments have
been or will be made to an individual for medical care directly
resulting from an injury caused by the smallpox vaccination.
Individuals are reimbursed for their out-of-pocket medical expenses in
accordance with the Act.
D. Other Issues Raised by Commenters
One commenter raised the concern that the Table regulations cover
only those injuries caused by the vaccinia virus and not all components
of the smallpox vaccine. Another commenter was concerned about the
scope of the Program and if it would cover the general population.
In reference to the issue of the components in the smallpox
vaccine, the Secretary concurs that the components of a smallpox
vaccine may cause a covered injury. Therefore, the Secretary has
clarified in this final regulation that a covered injury can be caused
not only by vaccinia, but by any component or constituent of the
smallpox vaccine.
In response to the concern about the scope of the legislation,
SEPPA only covers individuals who are members of HHS-approved smallpox
emergency response plans and individuals who contracted vaccinia from
them or from other eligible contacts. SEPPA is not designed to provide
benefits to the general population.
Explanation of Provisions
Some of the comments received indicate to the Secretary that there
may be confusion as to the significance of the Table. Therefore, this
Final Rule clarifies that having an injury listed on the Table is only
one of the ways that an individual can show medical eligibility for
Program benefits. The Secretary emphasizes that the purpose of the
Table is merely to provide potential requesters who can demonstrate
that they sustained a Table injury within the specified time interval
with the presumption that the smallpox vaccine caused the injury.
However, sustaining an injury not listed on the Table (including an
injury resulting from administration of another covered
countermeasure), or manifesting a Table injury outside of the time
interval listed, simply means that the presumption does not apply. In
those cases, the individual must show that it is more likely than not
(i.e., by a preponderance of the evidence), that administration of the
smallpox vaccine (or other covered countermeasure), or exposure to the
vaccine in the case of contacts, was the cause of the injury. The
Secretary encourages such individuals to file a request for benefits.
The Program has found individuals with Table or non-Table injuries to
be medically eligible.
As previously mentioned, this Final Rule also clarifies that the
time intervals listed on the Table refer specifically to the period in
which the first symptom or manifestation of onset of injury must appear
following administration of the smallpox vaccine or exposure to
vaccinia, in order for the presumption of causation to apply. The time
intervals listed have no relevance whatsoever to when the injury is
diagnosed.
Thus, the Secretary herein amends Sec. 102.21(a) of the Interim
Final Rule by adding language to the subheading of the Table that lists
the time intervals. This additional language makes it clear that these
time intervals refer only to the first symptom or manifestation of
onset of the injury, not to the time interval within which a diagnosis
of the injury must be made.
The Secretary also wishes to make it clear that a covered injury
can be caused not only by the vaccinia component of the smallpox
vaccine, but by any component or constituent of the vaccine.
Further, this Final Rule updates the effective period of the
Secretary's Declaration. The Secretary has amended the effective period
of the Declaration by extending it each year. The Secretary will
continue to publish a Notice in the Federal Register as needed to
update any further amendments to the effective period. These amendments
to the Declaration are made pursuant to the Secretary's authority under
section 261(a)(5) of SEPPA (section 224(p)(2)(A) of the Public Health
Service Act).
Additionally, this Final Rule reflects the change in name of the
Special Programs Bureau, which has been renamed the Healthcare Systems
Bureau. Finally, this regulation updates the address of the Program
Office. The new address, to which all mail to the Program should be
sent, whether by U.S. Postal Service, commercial carrier, or private
courier service, is: Parklawn Building, Room 11C-06, 5600 Fishers Lane,
Rockville, Maryland 20857.
Justification of Waiver of Delay of Effective Date
The Secretary has found that a delay in the effective date of this
Final Rule with an amendment is unnecessary and contrary to the public
interest. The adoption of the Interim Final Rule as a Final Rule
reflects an amendment and clarifications that are a result of comments
received on the Interim Final Rule and, therefore, will be helpful to
requesters without imposing additional burdens. It has no effect on any
individual's rights or responsibilities.
Economic and Regulatory Impact
Executive Order 12866 directs agencies to assess all costs and
benefits of available regulatory alternatives and, when rulemaking is
necessary, to select regulatory approaches that provide the greatest
net benefits (including potential economic, environmental, public
health, safety distributive and equity effects). In addition, under the
Regulatory Flexibility Act of 1980 (RFA), if a rule has a significant
economic effect on a substantial number of small entities, the
Secretary must specifically consider the economic effect of a rule on
small entities and analyze regulatory options that could lessen the
impact of the rule.
Executive Order 12866 requires that all regulations reflect
consideration of alternatives, of costs, of benefits, of incentives, of
equity, and of available information. Regulations must meet certain
standards, such as avoiding an unnecessary burden. Regulations that are
``significant'' because of cost, adverse effects on the economy,
inconsistency with other agency actions, effects on the budget, or
novel legal or policy issues, require special analysis.
The Secretary has determined that minimal resources are required to
implement the provisions included in this regulation. Therefore, in
accordance with the RFA, and the Small Business Regulatory Enforcement
Fairness Act of 1996, which amended the RFA, the Secretary certifies
that this Final Rule will not have a significant impact on a
substantial number of small entities.
The Secretary has also determined that this rule does not meet the
criteria for a major rule as defined by Executive Order 12866 and would
have no major effect on the economy or Federal expenditures. This rule
is not a ``major rule'' within the meaning of the statute providing for
Congressional Review of Agency Rulemaking, 5 U.S.C. 801.
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Unfunded Mandates Reform Act of 1995
The Secretary has determined that this Final Rule will not have
effects on State, local, or tribal governments or on the private sector
such as to require consultation under the Unfunded Mandates Reform Act
of 1995.
Federalism Impact Statement
The Secretary has also reviewed this rule in accordance with
Executive Order 13132 regarding federalism, and has determined that it
does not have ``federalism implications.'' The rule does not ``have
substantial direct effects on the States, or on the relationship
between the national government and the States, or on the distribution
of power and responsibilities among the various levels of government.''
Impact on Family Well-Being
This rule will not adversely affect the following elements of
family well-being: Family safety, family stability, marital commitment;
parental rights in the education, nurture and supervision of their
children; family functioning, disposable income or poverty; or the
behavior and personal responsibility of youth, as determined under
section 654(c) of the Treasury and General Government Appropriations
Act of 1999. In fact, this Final Rule may have a positive impact on the
disposable income and poverty elements of family well-being to the
extent that injured persons (or their survivors who are eligible to
receive compensation) receive benefits without a corresponding burden
being imposed on them.
Paperwork Reduction Act
The information collection requirements remain unchanged.
List of Subjects in 42 CFR Part 102
Benefits, Biologics, Compensation, Immunization, Public health,
Smallpox, Vaccinia.
Dated: November 14, 2005.
Elizabeth M. Duke,
Administrator.
Approved: December 22, 2005.
Michael O. Leavitt,
Secretary.
Editorial Note: This document was received at the Office of the
Federal Register on May 18, 2006.
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For the reasons stated above, the Secretary is adopting the Interim
Final Rule adding 42 CFR part 102, published at 68 FR 51492 on
Wednesday, August 27, 2003, as a Final Rule with the following
amendment:
PART 102--SMALLPOX COMPENSATION PROGRAM
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1. The authority citation for part 102 continues to read as follows:
Authority: 42 U.S.C. 216, 42 U.S.C. 239-239h.
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2. In section 102.21, the table in paragraph (a) is amended by adding
the following sentence at the end of the time interval description
subheading:
Sec. 102.21 Smallpox (Vaccinia) Vaccine Injury Table.
(a) * * *
Please note that these time intervals do not refer to time periods
for the date of diagnosis of the injury.
* * * * *
[FR Doc. 06-4761 Filed 5-23-06; 8:45 am]
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