Federal Guidelines for Requesting, Stockpiling, Distributing Potassium Iodide (KI) From the Strategic National Stockpile (SNS), 51065-51069 [05-17223]
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Federal Register / Vol. 70, No. 166 / Monday, August 29, 2005 / Notices
Bank of Clarksville, Clarksville,
Arkansas.
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR Part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The application also will be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Additional information on all bank
holding companies may be obtained
from the National Information Center
website at www.ffiec.gov/nic/.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than September 22,
2005.
A. Federal Reserve Bank of Chicago
(Patrick M. Wilder, Assistant Vice
President) 230 South LaSalle Street,
Chicago, Illinois 60690-1414:
1. Bank of Montreal, Montreal,
Canada; Harris Bankcorp, Inc., Chicago,
Illinois, and Harris Financial Corp.,
Wilmington, Delaware; to acquire 100
percent of the voting shares of Edville
Bankcorp, Inc., Villa Park, Illinois, and
thereby indirectly acquire Villa Park
Trust and Savings Bank, Villa Park,
Illinois.
B. Federal Reserve Bank of St. Louis
(Glenda Wilson, Community Affairs
Officer) 411 Locust Street, St. Louis,
Missouri 63166-2034:
1. Jefferson Bancshares, Inc., Pine
Bluff, Arkansas; to acquire 100 percent
of the voting shares of First Security
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15:17 Aug 26, 2005
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2. Liberty Bancshares, Inc., Jonesboro,
Arkansas; to acquire an additional 21.35
percent, for total ownership of 50.15
percent, of Russellville Bancshares, Inc.,
Jonesboro, Arkansas, and thereby
indirectly acquire First Arkansas Valley
Bank, Russellville, Arkansas.
51065
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Questionnaire, in all correspondence.
SUPPLEMENTARY INFORMATION:
A. Purpose
Board of Governors of the Federal Reserve
System, August 24, 2005.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. 05–17135 Filed 8–26–05; 8:45 am]
The Market Research Questionnaire is
used to gather information that is
necessary to develop and/or revise
Federal specifications and other
purchase descriptions.
BILLING CODE 6210–01–S
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GENERAL SERVICES
ADMINISTRATION
[OMB Control No. 3090–0259]
Federal Supply Service; Information
Collection; Market Research
Questionnaire
Federal Supply Service, GSA.
Notice of request for comments
regarding a renewal to an existing OMB
clearance.
AGENCY:
ACTION:
SUMMARY: Under the provisions of the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35), the General Services
Administration has submitted to the
Office of Management and Budget
(OMB) a request to review and approve
a renewal of a currently approved
information collection requirement
regarding the market research
questionnaire. A request for public
comments was published at 70 FR
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Public comments are particularly
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will have practical utility; whether our
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DATES: Submit comments on or before:
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FOR FURTHER INFORMATION CONTACT:
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Standards Division, Federal Supply
Service, at telephone (703) 605–1824, or
via e-mail to kathleen.baden@gsa.gov.
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Respondents: 25.
Responses Per Respondent: 1.
Total Responses: 25.
Hours Per Response: 0.5.
Total Burden Hours: 12.5.
OBTAINING COPIES OF
PROPOSALS: Requesters may obtain a
copy of the information collection
documents from the General Services
Administration, Regulatory Secretariat
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Washington, DC 20405, telephone (202)
208–7312. Please cite OMB Control No.
3090–0259, Market Research
Questionnaire, in all correspondence.
Dated: August 18, 2005.
Michael W. Carleton,
Chief Information Officer.
[FR Doc. 05–17065 Filed 8–26–05; 8:45 am]
BILLING CODE 6820–PH–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Federal Guidelines for Requesting,
Stockpiling, Distributing Potassium
Iodide (KI) From the Strategic National
Stockpile (SNS)
Office of Public Health
Emergency Preparedness (OPHEP),
HHS.
SUMMARY: In accordance with the
provisions of Section 127 of the Public
Health Security and Bioterrorism
Preparedness and Response Act of 2002,
Public Law 107–188, (the Bioterrorism
Act), this document provides guidelines
for State, local, and tribal governments,
for the expanded distribution,
stockpiling, and utilization of KI in the
event of a radioactive iodine release
from a commercial nuclear power plant
incident. This program would extend
coverage from the current ten mile
radius up to twenty miles from a
commercial nuclear power plant. This
document is being published in the
Federal Register to permit public input
on this expanded coverage from a wider
AGENCY:
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range of interested entities than was
accomplished with a previous draft.
Respondents are also invited to include
comments as to whether or not
employing measures of prophylaxis
other than KI or continuing reliance
upon established preventive measures
without expanding the area of KI
coverage would render the deployment
of this expanded KI distribution
unnecessary. Further background
follows later in these draft guidelines.
If individuals inhale or ingest
radioactive iodine, administration of KI,
when given prior to or within several
hours after exposure, can reduce the risk
of thyroid cancer among certain
categories of persons. KI does not
provide protection from external
exposure or contamination with
radioactive iodine nor does it provide
general protection from other sources of
ionizing radiation. The primary
protective actions are evacuation of the
area near the source of the plume,
external decontamination of individuals
affected, and preventing potentially
contaminated food and milk from
reaching consumers. Because
radioactive iodine exposure at distances
beyond 10 miles is likely to be due to
contamination of the food and water
supply, avoiding the consumption of
food or water is expected to be the most
effective protective measure for persons
in this zone.
The Federal Government, through the
Nuclear Regulatory Commission,
presently makes KI available to States
upon their request for distribution to or
stockpiling for individuals within 10
miles of a commercial nuclear power
plant.
FOR FURTHER INFORMATION CONTACT:
Office of Mass Casualty Planning, Office
of Public Health Emergency
Preparedness, U.S. Department of
Health and Human Services, 200
Independence Avenue SW., Room 638G,
Washington, DC 20201, Tel: 202–260–
1198.
Background
Bioterrorism Act
Section 127 of the Bioterrorism Act
established new Federal requirements
for the distribution and use of KI within
20 miles of commercial nuclear power
plants. It requires that KI tablets be
made available through the Strategic
National Stockpile (SNS) to State and
local governments for stockpiling and
distribution, as appropriate, to public
facilities, such as schools and hospitals,
in quantities sufficient to provide
adequate protection for the population
within 20 miles of a commercial nuclear
power plant.
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In addition, Section 127 requires:
• Development of guidelines by the
U.S. Government for stockpiling,
distribution and utilization of KI. State,
local, and tribal governments requesting
KI under this program are required to
submit plans for local stockpiling,
distribution, and utilization of KI
accompanied by certification that
sufficient quantities of KI have not
already been provided by the U.S.
Government.
• Submission of a Report to Congress
six months after publication of
guidelines on measures taken to
implement the Act, including whether
KI has been made available.
• A National Academy of Sciences
(NAS) study on the most effective and
safe way to distribute and administer KI.
The Department of Health and Human
Services (HHS) funded the NAS KI
study and in December 2003 the NAS
released ‘‘Distribution and
Administration of Potassium Iodide in
the Event of a Nuclear Incident.’’
Although the Homeland Security Act of
2002, Public Law 107–296, established
joint management of the Strategic
National Stockpile (SNS) by the
Department of Homeland Security
(DHS) and the Department of Health and
Human Services (HHS), the SNS was
officially transferred back to HHS under
the Project BioShield Act of 2004,
Public Law 108–276. This transfer
became effective on August 13, 2004.
plant. However, KI offers protection for
only one radiation-sensitive organ, the
thyroid, under conditions of inhalation
or ingestion of radioactive iodine. It
does not protect against external
irradiation of the thyroid, as might
happen if one is exposed to external
iodine in a radioactive cloud as opposed
to iodine that is inhaled or ingested. It
is not a panacea for protection from
radiation injury.
The health effect risks to the thyroid
gland depend upon many factors,
including: (1) The radiation dose to the
thyroid, including time (hours/days/
weeks/months) required to deliver the
dose); (2) the age of the person at the
time of exposure and; (3) whether or not
the individual is deficient in dietary
iodine intake.
A review by The National Academy of
Sciences (NAS) of experience with
thyroid cancer in populations exposed
to the consequences of nuclear events
shows that:
• Exposure to external radiation or
internal radiation from radioactive
iodine is linked to a dose-dependent
increase in thyroid-cancer incidence.
• Young children are by far the most
sensitive to the carcinogenic effect of
radiation on the thyroid, especially after
exposure to radioactive iodine in
fallout.
• The risk of thyroid cancer in adults
exposed to radioactive iodine in fallout
is low for adults over 40 years of age.
Potassium Iodide
KI is the chemical symbol for the
chemical compound potassium iodide.
It is a salt, similar to table salt and, in
fact, KI is the ingredient that is routinely
added to table salt, sodium chloride
(NaCl), to make it ‘‘iodized salt.’’
Iodine is a necessary element for the
formation of thyroid hormone, and in
order to accomplish this, KI is ‘taken up’
by the thyroid gland and used in
hormone synthesis. If KI is administered
as a countermeasure just before or
within 4 hours following exposure to
inhaled or ingested radioactive iodine, it
will saturate receptor capability within
the thyroid gland so that radioactive
iodine does not become concentrated
within the thyroid, thereby minimizing
its exposure to ionizing radiation.
Significant internal exposures to
radioactive iodine can increase the risk
of thyroid diseases, notably thyroid
cancers.
The use of KI has been recognized by
the World Health Organization, the U.S.
Food and Drug Administration and the
National Academy of Sciences as a safe
and effective thyroid prophylaxis in the
event of a significant release of
radioactive iodine from a nuclear power
Radiological Emergency Preparedness
Program (REPP)
The REPP, a program managed by the
Nuclear and Chemical Hazards Branch
within DHS, is designed to assure that
off-site response organizations are
capable of protecting the public in the
event of an incident at a commercial
nuclear power plant. The primary
actions for protecting the public include
evacuation and, as indicated, sheltering.
Off-site response organizations base
their initial protective action decisions
on plant conditions, so that the people
closest to the facility are evacuated
before significant releases of radioactive
materials occur. This ensures maximum
protection of the population closest to
the facility. The use of KI as a
supplemental action to evacuation and
sheltering is also sometimes
recommended to protect the public.
However, the use of KI should not be
adopted as an alternative for the
implementation of an effective
evacuation strategy. Additional
protective actions include
decontamination of individuals that
have external contamination and
preventing potentially contaminated
food and milk from being ingested by
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consumers. Because radioactive iodine
exposure at distances beyond 10 miles
is likely to be due to contamination of
the food and water supply, avoiding the
consumption of contaminated food or
water is the most effective
countermeasure at this distance.
Emergency Planning Zones
To permit protective measures to be
taken effectively, the Nuclear Regulatory
Commission (NRC) established two
Emergency Planning Zones (EPZ)
around each commercial nuclear power
plant. The zone within 10 miles (16 km)
of the plant is designated the plume EPZ
and the region within 50 miles (80 km)
from the plant the ingestion EPZ.
Current analyses indicate that in the
event of a power plant accident, direct
exposure to the plume poses the greatest
threat for persons near the plant, and
people who had not evacuated would be
exposed to radiation from the airborne
radioactive material, material deposited
on the ground or other surfaces, and
materials taken into the body by
inhalation. Within the plume EPZ,
circumstances may result in levels,
which, if delivered in a short period of
time, may be high enough to produce
acute radiation effects in exposed
people. Farther from the power plant,
the predominant exposure threat would
come from radioactive materials taken
into the body, primarily by the
consumption of contaminated foods,
milk, and water. The planned protective
measures differ in the two zones,
however there is flexibility in the
emergency plans, and protective
measures will be adapted to the
circumstances at the time of the
incident.
The NAS report, Chapter 5,
PROTECTIVE MEASURES, page 81,
states: ‘‘Exposure to radioactive iodine
is possible through the ingestion
pathway, so it is important that plans
address this situation. Monitoring of the
environment and food products controls
this route of exposure. Removing
contaminated products from the market
and isolating contaminated products
until the radioactive iodine decays to
safe levels are the most effective way to
eliminate radiation exposure and
damage to the thyroid. That also
eliminates the need for the use of KI by
the general public as a protective action
[in the ingestion zone].’’
• The 10 mile Emergency Planning
Zone (Plume EPZ)
The 10 mile EPZ predetermined
protective actions include sheltering,
decontamination, evacuation, and the
use of KI as a supplement to sheltering
and evacuation, where appropriate.
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• The 50 mile Emergency Planning
Zone (Ingestion EPZ)
In the area beyond 10 miles and out
to approximately 50 miles, the primary
exposure to radioactive materials is
from ingestion and the protective
actions for this exposure area include a
ban on consumption of contaminated
food, milk, and water.
The 10-mile EPZ has been reviewed
and accepted by the EPA, NRC, and
FEMA as the appropriate EPZ size for
commercial nuclear power plant
licensees to use in developing
emergency plans in cooperation with
State and local governments. It is not
within the scope of these guidelines to
question the appropriateness of the 10mile EPZ under NRC regulations, and
nuclear power plant licensees will not
be expected to modify their emergency
plans.
Chernobyl
A great deal has been learned since
the accident at Chernobyl. We believe
that design and safety features of U.S.
nuclear power plants plus our emphasis
on planning through the REPP make it
unlikely that a similar scenario could
occur on U.S. soil. Persons have tried to
extrapolate a Chernobyl experience to
the U.S. However, according to the
NAS, ‘‘although the qualitative results
after Chernobyl are valuable, the
quantitative results cannot be
transposed to the United States situation
without many caveats.’’
Terrorism and Nuclear Power Plants
The rigid design features of U.S.
nuclear power plants coupled with
heightened security measures at these
facilities would present significant
challenges to terrorists who would seek
to cause radioiodine to be released from
one of our power plants as the result of
an attack. As the National Academy of
Sciences concluded, ‘‘The terrorism
threat does not appear to add
significantly to the risk, because of the
existing mechanisms and procedures.’’
Roles and Responsibilities
In order to facilitate implementation
of the requirements of Section 127 and
ensure coordination with the existing
REPP requirements, the roles and
responsibilities of HHS, DHS, and State,
local, and tribal governments are set
forth below.
A. HHS
Within HHS, the Office of Public
Health Emergency Preparedness
(OPHEP) will be responsible for
implementing the requirements of
Section 127. OPHEP will:
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1. Review and approve in writing all
requests for KI;
2. Develop the procedures and
mechanisms for distribution of KI to
State, local, or tribal governments;
3. Provide subject matter expertise on
KI and other technical support to State,
local, and tribal governments, as
requested;
4. Provide the initial approved
quantity of KI and ensure sufficient
supplies are available to replace used or
expiring stocks; and
5. Submit Reports to Congress, as
required in Section 127, for the
following:
• Measures taken by the Federal
Government to implement Section 127
• Whether KI has been made
available to State, local, and tribal
governments under Section 127 or other
programs;
• The extent to which State, local,
and tribal governments have made KI
available to their populations;
• The findings of the NAS study.
B. DHS
Although Section 127 does not
establish direct implementing
requirements for the DHS, DHS will
maintain its current activities in support
of the NRC’s current KI program.
C. NRC
Although Section 127 does not
establish direct implementing
requirements for the NRC, the NRC will
maintain its current program for KI
distribution and will approve all
requests for the initial supply of KI
within the 10 mile EPZ, consistent with
NRC regulations, after DHS has
reviewed the requests for completeness
and appropriateness.
D. State Governments Will
1. Decide whether to add KI as a
protective measure to their emergency
plans. See the NAS Study for examples
of distribution options;
2. Submit KI applications to the HHS’
Office of Public Health Emergency
Preparedness; such applications will
include a plan for stockpiling and for
distribution and use of KI in the event
of a nuclear incident;
3. Certify that the State has not
already received sufficient quantities of
KI from the Federal Government, (See
Section 127(b)(1)(B));
4. Consider FDA’s Guidance,
‘‘Potassium Iodide as a Thyroid
Blocking Agent in Radiation
Emergencies’’ in preparing emergency
KI dosing plans;
E. Local Governments Will
1. Decide whether to add KI as a
protective measure in their emergency
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plans. We recommend that local
governments review Appendix D of the
NAS Study prior to making a decision
on the use of KI;
2. Petition the State in which they are
located to modify its plan to address
their population (not to exceed a 20mile radius from the plant);
3. Submit their plans for stockpiling,
distribution, and using KI to the State
for approval and certification that the
plan is ‘‘not inconsistent’’ with the State
emergency plan;
4. Consider FDA’s Guidance,
‘‘Potassium Iodide as a Thyroid
Blocking Agent in Radiation
Emergencies’’ in preparing emergency
KI dosing plans;
5. Submit KI requests to the HHS
Office of Public Health Emergency
Preparedness, such applications will
include a plan for stockpiling KI and for
distribution and use of KI in the event
of a nuclear incident.
Note: State approval and certification must
be obtained before HHS will accept a KI
request from a local government for review
and approval.
F. Tribal Governments
1. Decide whether to add KI as a
protective measure in their emergency
plans. We recommend that tribal
governments review Appendix D of the
NAS Study prior to making a decision
on the use of KI;
2. Petition the state in which they are
located to modify its plan to address
their population (not to exceed a 20mile radius from the plant);
3. Consider FDA’s Guidance,
‘‘Potassium Iodide as a Thyroid
Blocking Agent in Radiation
Emergencies’’ in preparing emergency
KI dosing plans;
4. Submit a KI request to the HHS’
Office of Public Health Emergency
Preparedness.
Stockpiling, Distribution, Public
Education
A. Considerations for KI Utilization
Numerous issues must be considered
when making the decision whether to
utilize KI as a protective action. These
issues include, but are not limited to,
the following:
• How will incorporation of KI as a
protective measure impact existing
emergency plans, procedures, and
operations?
• What is the benefit to public health
and safety from incorporating KI into
emergency response plans?
• Who will be responsible for the KI
program? Is there an existing program
that can take on this responsibility or
must a new one be created?
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• Who has the authority to make the
recommendation that KI be taken? If the
State government is not participating in
the program, does the local government
have the authority to recommend that KI
be taken?
• How will KI be stockpiled and
distributed?
• How will incident-specific
emergency and environmental
conditions be included in the decision
to use KI?
• How will the public be notified
during an incident when to take KI? Is
there a communication system available
to notify the public of a nuclear
incident?
• How will KI be provided to
transient populations?
• What medical assistance will be
available for the individual who
experiences an adverse medical reaction
following KI administration?
• How will medical authorities advise
the population to take KI, and under
what circumstances will this advice be
given, i.e., methods for public
education, information, and instruction?
• What is the cost-benefit of the
program? Are there better uses of the
funding and resources that would result
in a greater reduction in risk?
• What is the liability associated with
establishing a KI program?
• What procedures will be used to
monitor the expiration of KI stocks and
request KI replacement from the
stockpile?
• If KI is stockpiled under controlled
conditions, will they pursue shelf-life
extension pursuant to the Food and
Drug Administration’s guidance? (See
Reference O below.)
B. Stockpiling and Distribution
The NAS’s report on KI distribution
reviewed KI distribution programs in
various countries as well as within the
United States. An extensive discussion
on these programs can be found in
Chapter 6, EXISTING DISTRIBUTION
PLANS FOR POTASSIUM IODIDE. It is
important to note that the report did not
identify a preferred method of mass
distribution of KI to the public. The
report recognized that local conditions
surrounding the commercial power
plants and existing emergency plans
vary between the countries surveyed as
well as between the States. The report
recognized that the most successful KI
plan will take into consideration
existing State/local emergency planning
as well as specific characteristics of the
location and population around the
commercial nuclear power plants. A
method for evaluation of KI distribution
plans was developed and published in
Appendix D to the KI distribution
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report. It is recommended that the
NAS’s Report on KI distribution be
reviewed by State, local, and tribal
governments for insights in
development and implementation of KI
plans and programs.
C. Public Education
Public education is a key component
to the success of a KI program. It is
important that members of the public
have a basic knowledge about the use
and side effects of KI, are aware that KI
protects only the thyroid from internal
exposure to radioactive iodine, and
understand that it is to be taken only at
the direction of authorized officials.
Several methods have been used by
States with existing KI programs. These
include: Letters to physicians and
residents, in-home visits by public
health officials, newspaper ads,
distribution through pharmacies, press
releases and a press conference, a cable
television program, KI distribution or
‘‘pick-up’’ days, and commercial
nuclear power plant public education
materials. An expanded discussion of
various public education methods is
included in chapter 6 of the NAS KI
Report.
Health and Human Services KI
Distribution Program
A. Requests for KI should be
submitted to the:
Office of Mass Casualty Planning, Office
of Public Health Emergency
Preparedness, U.S. Department of
Health and Human Services, 200
Independence Avenue SW., Room
638G, Washington, DC 20201, Tel:
202–260–1198.
B. State Government KI requests must:
• Certify that the State has not
already received sufficient quantities of
KI from the Federal Government;
• Specify the quantity and
formulation of KI needed and describe
the calculation used to make this
determination;
• Identify the location of the
commercial nuclear power plant within
the State or within a 20-mile border
strip inside an adjacent State; and
contain the State’s and Tribal
Government’s plans and procedures for
stockpiling, distributing, and
administering KI.
These plans must:
• Identify the office with the
authority to recommend the use of KI by
the general public;
• Identify the organization(s)
responsible for implementing the KI use
decision;
• Identify the single recipient
responsible for receiving the KI; provide
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a recipient address for the shipment of
KI;
• Specify the decision-making criteria
for KI administration;
• Specify the criteria for issuing KI to
the public (location, special need);
• Specify the method for making KI
available to the public; pre-distribution
or stockpiling;
• Specify the method for ensuring the
supply of KI is sufficient for the targeted
population, including the estimated
transient/seasonal population that may
be advised to take KI;
• If pre-distributing KI, specify the
procedure for the public or special
population groups to obtain KI;
• Specify the procedure for storing,
monitoring, safeguarding, dispensing (to
include, if applicable, tracking who
received the drug, when, in what
quantity, and maintenance of waivers
from liability), and disposing of KI
stocks;
• Identify the method for alerting and
notifying the general public of the
recommendation to take KI;
• Specify how the plan is integrated
into existing emergency response plans;
and
• Specify quantities of KI (tablets and
pediatric liquid oral formulation) that
will be requested.
C. Local Governments
KI requests from local governments
must certify that:
• The State in which the local
government is located does not have a
DHS-approved KI distribution plan that
includes KI as a protective measure for
populations, or a DHS approved plan
that does not address populations
located beyond 10 miles from the
commercial nuclear power plant;
• The local government has
petitioned the State in which it is
located to modify the State plan to
address populations within 20 miles of
a commercial nuclear power plant, and
60 days have elapsed without the State
modifying the plan to accommodate the
request;
• The local government KI plans have
been approved by the State and certified
to be ‘not inconsistent’ with the State
emergency plan; and
• The local government has reached
an agreement with the State that the
State will serve as the single point of
contact for receipt of KI shipments from
the stockpile and will then redistribute
the KI to the approved governments.
Funding and Resource Requirements
State, local, and tribal governments
are responsible for obtaining the
funding and resources necessary to
request and implement the KI program
VerDate Aug<18>2005
15:17 Aug 26, 2005
Jkt 205001
within their respective jurisdictions,
should they decide to request KI. Only
the provision of KI tablets/liquid will be
funded through HHS.
Dated: August 24, 2005.
Robert G. Claypool,
Deputy Assistant Secretary, Office of Public
Health Emergency Preparedness, Department
of Health and Human Services.
References
A. NUREG–0654/DHS–REP–1, Criteria for
Preparation and Evaluation of
Radiological Emergency Response Plans
and Preparedness in Support of Nuclear
Power Plants, March 1987.
B. NUREG–0396/EPA 520/1–78–016,
Planning Basis for the Development of
State and Local Government Radiological
Emergency Response Plans in Support of
Light Water Nuclear Power Plants,
December 1978.
C. National Academy of Sciences (NAS)
Study, Distribution and Administration
of Potassium Iodide in the Event of a
Nuclear Incident, January 2004.
D. Federal Emergency Management Agency,
Notice of revised Federal policy, Federal
Policy on Use of Potassium Iodide (KI),
67 FR 1355, January 10, 2002.
E. Nuclear Regulatory Commission, Final
rule, Consideration of Potassium Iodide
in Emergency Plans, 66 FR, 5427,
January 19, 2001.
F. World Health Organization, Guidelines for
Iodine Prophylaxis Following Nuclear
Accidents, 1999. https://www.who.int/
environmentalinformation/
Information_resources/documents/
Iodine/guide.pdf.
G. National Council on Radiation Protection
and Measures (NCRP) Protection of the
Thyroid Gland in the Event of Releases
of Radioiodine. NCRP Report No. 55,
August 1, 1977.
H. Food and Drug Administration
(Department of Health and Human
Services), Potassium Iodide as a ThyroidBlocking Agent in Radiation
Emergencies; 66 FR 64046, December 11,
2001. https://www.fda.gov/cder/guidance/
4825fnl.htm.
I. Report of the President’s Commission on
the Accident at Three Mile Island.
J. Federal Emergency Management Agency,
Federal Policy on Distribution of
Potassium Iodide Around Nuclear Power
Sites for Use as a Thyroidal Blocking
Agency, 50 FR, 30258, July 24, 1985.
K. Nauman, J., and Wolff, J., Iodide
Prophylaxis in Poland After the
Chernobyl Reactor Accident: Benefits
and Risks, American Journal of
Medicine, Vol. 94, p. 524, May 1993.
L. International Atomic Energy Agency,
International Basic Safety Standards for
Protection Against Ionizing Radiation
and for Safety of Radiation Sources.
Safety Series No. 115, 1996.
M. Food and Drug Administration
(Department of Health and Human
Services) Guidance for Industry KI in
Radiation Emergencies—Questions and
Answers, https://www.fda.gov/cder/
guidance/5386fnl.htm.
PO 00000
Frm 00063
Fmt 4703
Sfmt 4703
51069
N. Food and Drug Administration
(Department of Health and Human
Services) Frequently Asked Questions on
Potassium Iodide (KI). https://
www.fda.gov/cder/drugprepare/
KI_Q&A.htm.
O. Food and Drug Administration
(Department of Health and Human
Services) Guidance for Federal Agencies
and State and Local Governments:
Potassium Iodide Tablets: Shelf Life
Extension. https://www.fda.gov/cder/
guidance/5666fnl.pdf.
P. National Council on Radiation Protection
and Measures (NCRP) Report 138,
Management of Terrorist Events
Involving Radioactive Materials.
[FR Doc. 05–17223 Filed 8–25–05; 2:41 pm]
BILLING CODE 4150–37–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Statement of Organization, Functions,
and Delegations of Authority
Part C (Centers for Disease Control
and Prevention) of the Statement of
Organization, Functions, and
Delegations of Authority of the
Department of Health and Human
Services (45 FR 67772–76, dated
October 14, 1980, and corrected at 45 FR
69296, October 20, 1980, as amended
most recently at 70 FR 46527–46530,
dated August 10, 2005) is amended to
reflect the establishment of the Office of
Chief of Public Health Practice within
the Office of the Director, Centers for
Disease Control and Prevention.
After the mission statement for the
Office of Workforce and Career
Development (CAL), insert the
following:
Office of Chief of Public Health
Practice (CAR). The Office of Chief of
Public Health Practice (OCPHP) serves
as the advocate, guardian, promoter, and
conscience of public health practice
throughout CDC and in the larger public
health community; ensures coordination
and synergy of CDC’s scientific and
practice activities; and promotes and
protects the public’s health through
science-based, practice-relevant
standards, policies, and legal tools.
Activities in support of the mission are
carried out through programs and
offices focused on public health law,
public health system standards, agency
accreditation, and surveillance for
emerging issues in public health
practice. To carry out its mission,
OCPHP: (1) Develops the legal
preparedness of CDC programs and the
public health system to address
terrorism and other national public
E:\FR\FM\29AUN1.SGM
29AUN1
Agencies
[Federal Register Volume 70, Number 166 (Monday, August 29, 2005)]
[Notices]
[Pages 51065-51069]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-17223]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Federal Guidelines for Requesting, Stockpiling, Distributing
Potassium Iodide (KI) From the Strategic National Stockpile (SNS)
AGENCY: Office of Public Health Emergency Preparedness (OPHEP), HHS.
SUMMARY: In accordance with the provisions of Section 127 of the Public
Health Security and Bioterrorism Preparedness and Response Act of 2002,
Public Law 107-188, (the Bioterrorism Act), this document provides
guidelines for State, local, and tribal governments, for the expanded
distribution, stockpiling, and utilization of KI in the event of a
radioactive iodine release from a commercial nuclear power plant
incident. This program would extend coverage from the current ten mile
radius up to twenty miles from a commercial nuclear power plant. This
document is being published in the Federal Register to permit public
input on this expanded coverage from a wider
[[Page 51066]]
range of interested entities than was accomplished with a previous
draft. Respondents are also invited to include comments as to whether
or not employing measures of prophylaxis other than KI or continuing
reliance upon established preventive measures without expanding the
area of KI coverage would render the deployment of this expanded KI
distribution unnecessary. Further background follows later in these
draft guidelines.
If individuals inhale or ingest radioactive iodine, administration
of KI, when given prior to or within several hours after exposure, can
reduce the risk of thyroid cancer among certain categories of persons.
KI does not provide protection from external exposure or contamination
with radioactive iodine nor does it provide general protection from
other sources of ionizing radiation. The primary protective actions are
evacuation of the area near the source of the plume, external
decontamination of individuals affected, and preventing potentially
contaminated food and milk from reaching consumers. Because radioactive
iodine exposure at distances beyond 10 miles is likely to be due to
contamination of the food and water supply, avoiding the consumption of
food or water is expected to be the most effective protective measure
for persons in this zone.
The Federal Government, through the Nuclear Regulatory Commission,
presently makes KI available to States upon their request for
distribution to or stockpiling for individuals within 10 miles of a
commercial nuclear power plant.
FOR FURTHER INFORMATION CONTACT: Office of Mass Casualty Planning,
Office of Public Health Emergency Preparedness, U.S. Department of
Health and Human Services, 200 Independence Avenue SW., Room 638G,
Washington, DC 20201, Tel: 202-260-1198.
Background
Bioterrorism Act
Section 127 of the Bioterrorism Act established new Federal
requirements for the distribution and use of KI within 20 miles of
commercial nuclear power plants. It requires that KI tablets be made
available through the Strategic National Stockpile (SNS) to State and
local governments for stockpiling and distribution, as appropriate, to
public facilities, such as schools and hospitals, in quantities
sufficient to provide adequate protection for the population within 20
miles of a commercial nuclear power plant.
In addition, Section 127 requires:
Development of guidelines by the U.S. Government for
stockpiling, distribution and utilization of KI. State, local, and
tribal governments requesting KI under this program are required to
submit plans for local stockpiling, distribution, and utilization of KI
accompanied by certification that sufficient quantities of KI have not
already been provided by the U.S. Government.
Submission of a Report to Congress six months after
publication of guidelines on measures taken to implement the Act,
including whether KI has been made available.
A National Academy of Sciences (NAS) study on the most
effective and safe way to distribute and administer KI.
The Department of Health and Human Services (HHS) funded the NAS KI
study and in December 2003 the NAS released ``Distribution and
Administration of Potassium Iodide in the Event of a Nuclear
Incident.'' Although the Homeland Security Act of 2002, Public Law 107-
296, established joint management of the Strategic National Stockpile
(SNS) by the Department of Homeland Security (DHS) and the Department
of Health and Human Services (HHS), the SNS was officially transferred
back to HHS under the Project BioShield Act of 2004, Public Law 108-
276. This transfer became effective on August 13, 2004.
Potassium Iodide
KI is the chemical symbol for the chemical compound potassium
iodide. It is a salt, similar to table salt and, in fact, KI is the
ingredient that is routinely added to table salt, sodium chloride
(NaCl), to make it ``iodized salt.''
Iodine is a necessary element for the formation of thyroid hormone,
and in order to accomplish this, KI is `taken up' by the thyroid gland
and used in hormone synthesis. If KI is administered as a
countermeasure just before or within 4 hours following exposure to
inhaled or ingested radioactive iodine, it will saturate receptor
capability within the thyroid gland so that radioactive iodine does not
become concentrated within the thyroid, thereby minimizing its exposure
to ionizing radiation. Significant internal exposures to radioactive
iodine can increase the risk of thyroid diseases, notably thyroid
cancers.
The use of KI has been recognized by the World Health Organization,
the U.S. Food and Drug Administration and the National Academy of
Sciences as a safe and effective thyroid prophylaxis in the event of a
significant release of radioactive iodine from a nuclear power plant.
However, KI offers protection for only one radiation-sensitive organ,
the thyroid, under conditions of inhalation or ingestion of radioactive
iodine. It does not protect against external irradiation of the
thyroid, as might happen if one is exposed to external iodine in a
radioactive cloud as opposed to iodine that is inhaled or ingested. It
is not a panacea for protection from radiation injury.
The health effect risks to the thyroid gland depend upon many
factors, including: (1) The radiation dose to the thyroid, including
time (hours/days/weeks/months) required to deliver the dose); (2) the
age of the person at the time of exposure and; (3) whether or not the
individual is deficient in dietary iodine intake.
A review by The National Academy of Sciences (NAS) of experience
with thyroid cancer in populations exposed to the consequences of
nuclear events shows that:
Exposure to external radiation or internal radiation from
radioactive iodine is linked to a dose-dependent increase in thyroid-
cancer incidence.
Young children are by far the most sensitive to the
carcinogenic effect of radiation on the thyroid, especially after
exposure to radioactive iodine in fallout.
The risk of thyroid cancer in adults exposed to
radioactive iodine in fallout is low for adults over 40 years of age.
Radiological Emergency Preparedness Program (REPP)
The REPP, a program managed by the Nuclear and Chemical Hazards
Branch within DHS, is designed to assure that off-site response
organizations are capable of protecting the public in the event of an
incident at a commercial nuclear power plant. The primary actions for
protecting the public include evacuation and, as indicated, sheltering.
Off-site response organizations base their initial protective action
decisions on plant conditions, so that the people closest to the
facility are evacuated before significant releases of radioactive
materials occur. This ensures maximum protection of the population
closest to the facility. The use of KI as a supplemental action to
evacuation and sheltering is also sometimes recommended to protect the
public. However, the use of KI should not be adopted as an alternative
for the implementation of an effective evacuation strategy. Additional
protective actions include decontamination of individuals that have
external contamination and preventing potentially contaminated food and
milk from being ingested by
[[Page 51067]]
consumers. Because radioactive iodine exposure at distances beyond 10
miles is likely to be due to contamination of the food and water
supply, avoiding the consumption of contaminated food or water is the
most effective countermeasure at this distance.
Emergency Planning Zones
To permit protective measures to be taken effectively, the Nuclear
Regulatory Commission (NRC) established two Emergency Planning Zones
(EPZ) around each commercial nuclear power plant. The zone within 10
miles (16 km) of the plant is designated the plume EPZ and the region
within 50 miles (80 km) from the plant the ingestion EPZ. Current
analyses indicate that in the event of a power plant accident, direct
exposure to the plume poses the greatest threat for persons near the
plant, and people who had not evacuated would be exposed to radiation
from the airborne radioactive material, material deposited on the
ground or other surfaces, and materials taken into the body by
inhalation. Within the plume EPZ, circumstances may result in levels,
which, if delivered in a short period of time, may be high enough to
produce acute radiation effects in exposed people. Farther from the
power plant, the predominant exposure threat would come from
radioactive materials taken into the body, primarily by the consumption
of contaminated foods, milk, and water. The planned protective measures
differ in the two zones, however there is flexibility in the emergency
plans, and protective measures will be adapted to the circumstances at
the time of the incident.
The NAS report, Chapter 5, PROTECTIVE MEASURES, page 81, states:
``Exposure to radioactive iodine is possible through the ingestion
pathway, so it is important that plans address this situation.
Monitoring of the environment and food products controls this route of
exposure. Removing contaminated products from the market and isolating
contaminated products until the radioactive iodine decays to safe
levels are the most effective way to eliminate radiation exposure and
damage to the thyroid. That also eliminates the need for the use of KI
by the general public as a protective action [in the ingestion zone].''
The 10 mile Emergency Planning Zone (Plume EPZ)
The 10 mile EPZ predetermined protective actions include
sheltering, decontamination, evacuation, and the use of KI as a
supplement to sheltering and evacuation, where appropriate.
The 50 mile Emergency Planning Zone (Ingestion EPZ)
In the area beyond 10 miles and out to approximately 50 miles, the
primary exposure to radioactive materials is from ingestion and the
protective actions for this exposure area include a ban on consumption
of contaminated food, milk, and water.
The 10-mile EPZ has been reviewed and accepted by the EPA, NRC, and
FEMA as the appropriate EPZ size for commercial nuclear power plant
licensees to use in developing emergency plans in cooperation with
State and local governments. It is not within the scope of these
guidelines to question the appropriateness of the 10-mile EPZ under NRC
regulations, and nuclear power plant licensees will not be expected to
modify their emergency plans.
Chernobyl
A great deal has been learned since the accident at Chernobyl. We
believe that design and safety features of U.S. nuclear power plants
plus our emphasis on planning through the REPP make it unlikely that a
similar scenario could occur on U.S. soil. Persons have tried to
extrapolate a Chernobyl experience to the U.S. However, according to
the NAS, ``although the qualitative results after Chernobyl are
valuable, the quantitative results cannot be transposed to the United
States situation without many caveats.''
Terrorism and Nuclear Power Plants
The rigid design features of U.S. nuclear power plants coupled with
heightened security measures at these facilities would present
significant challenges to terrorists who would seek to cause
radioiodine to be released from one of our power plants as the result
of an attack. As the National Academy of Sciences concluded, ``The
terrorism threat does not appear to add significantly to the risk,
because of the existing mechanisms and procedures.''
Roles and Responsibilities
In order to facilitate implementation of the requirements of
Section 127 and ensure coordination with the existing REPP
requirements, the roles and responsibilities of HHS, DHS, and State,
local, and tribal governments are set forth below.
A. HHS
Within HHS, the Office of Public Health Emergency Preparedness
(OPHEP) will be responsible for implementing the requirements of
Section 127. OPHEP will:
1. Review and approve in writing all requests for KI;
2. Develop the procedures and mechanisms for distribution of KI to
State, local, or tribal governments;
3. Provide subject matter expertise on KI and other technical
support to State, local, and tribal governments, as requested;
4. Provide the initial approved quantity of KI and ensure
sufficient supplies are available to replace used or expiring stocks;
and
5. Submit Reports to Congress, as required in Section 127, for the
following:
Measures taken by the Federal Government to implement
Section 127
Whether KI has been made available to State, local, and
tribal governments under Section 127 or other programs;
The extent to which State, local, and tribal governments
have made KI available to their populations;
The findings of the NAS study.
B. DHS
Although Section 127 does not establish direct implementing
requirements for the DHS, DHS will maintain its current activities in
support of the NRC's current KI program.
C. NRC
Although Section 127 does not establish direct implementing
requirements for the NRC, the NRC will maintain its current program for
KI distribution and will approve all requests for the initial supply of
KI within the 10 mile EPZ, consistent with NRC regulations, after DHS
has reviewed the requests for completeness and appropriateness.
D. State Governments Will
1. Decide whether to add KI as a protective measure to their
emergency plans. See the NAS Study for examples of distribution
options;
2. Submit KI applications to the HHS' Office of Public Health
Emergency Preparedness; such applications will include a plan for
stockpiling and for distribution and use of KI in the event of a
nuclear incident;
3. Certify that the State has not already received sufficient
quantities of KI from the Federal Government, (See Section
127(b)(1)(B));
4. Consider FDA's Guidance, ``Potassium Iodide as a Thyroid
Blocking Agent in Radiation Emergencies'' in preparing emergency KI
dosing plans;
E. Local Governments Will
1. Decide whether to add KI as a protective measure in their
emergency
[[Page 51068]]
plans. We recommend that local governments review Appendix D of the NAS
Study prior to making a decision on the use of KI;
2. Petition the State in which they are located to modify its plan
to address their population (not to exceed a 20-mile radius from the
plant);
3. Submit their plans for stockpiling, distribution, and using KI
to the State for approval and certification that the plan is ``not
inconsistent'' with the State emergency plan;
4. Consider FDA's Guidance, ``Potassium Iodide as a Thyroid
Blocking Agent in Radiation Emergencies'' in preparing emergency KI
dosing plans;
5. Submit KI requests to the HHS Office of Public Health Emergency
Preparedness, such applications will include a plan for stockpiling KI
and for distribution and use of KI in the event of a nuclear incident.
Note: State approval and certification must be obtained before
HHS will accept a KI request from a local government for review and
approval.
F. Tribal Governments
1. Decide whether to add KI as a protective measure in their
emergency plans. We recommend that tribal governments review Appendix D
of the NAS Study prior to making a decision on the use of KI;
2. Petition the state in which they are located to modify its plan
to address their population (not to exceed a 20-mile radius from the
plant);
3. Consider FDA's Guidance, ``Potassium Iodide as a Thyroid
Blocking Agent in Radiation Emergencies'' in preparing emergency KI
dosing plans;
4. Submit a KI request to the HHS' Office of Public Health
Emergency Preparedness.
Stockpiling, Distribution, Public Education
A. Considerations for KI Utilization
Numerous issues must be considered when making the decision whether
to utilize KI as a protective action. These issues include, but are not
limited to, the following:
How will incorporation of KI as a protective measure
impact existing emergency plans, procedures, and operations?
What is the benefit to public health and safety from
incorporating KI into emergency response plans?
Who will be responsible for the KI program? Is there an
existing program that can take on this responsibility or must a new one
be created?
Who has the authority to make the recommendation that KI
be taken? If the State government is not participating in the program,
does the local government have the authority to recommend that KI be
taken?
How will KI be stockpiled and distributed?
How will incident-specific emergency and environmental
conditions be included in the decision to use KI?
How will the public be notified during an incident when to
take KI? Is there a communication system available to notify the public
of a nuclear incident?
How will KI be provided to transient populations?
What medical assistance will be available for the
individual who experiences an adverse medical reaction following KI
administration?
How will medical authorities advise the population to take
KI, and under what circumstances will this advice be given, i.e.,
methods for public education, information, and instruction?
What is the cost-benefit of the program? Are there better
uses of the funding and resources that would result in a greater
reduction in risk?
What is the liability associated with establishing a KI
program?
What procedures will be used to monitor the expiration of
KI stocks and request KI replacement from the stockpile?
If KI is stockpiled under controlled conditions, will they
pursue shelf-life extension pursuant to the Food and Drug
Administration's guidance? (See Reference O below.)
B. Stockpiling and Distribution
The NAS's report on KI distribution reviewed KI distribution
programs in various countries as well as within the United States. An
extensive discussion on these programs can be found in Chapter 6,
EXISTING DISTRIBUTION PLANS FOR POTASSIUM IODIDE. It is important to
note that the report did not identify a preferred method of mass
distribution of KI to the public. The report recognized that local
conditions surrounding the commercial power plants and existing
emergency plans vary between the countries surveyed as well as between
the States. The report recognized that the most successful KI plan will
take into consideration existing State/local emergency planning as well
as specific characteristics of the location and population around the
commercial nuclear power plants. A method for evaluation of KI
distribution plans was developed and published in Appendix D to the KI
distribution report. It is recommended that the NAS's Report on KI
distribution be reviewed by State, local, and tribal governments for
insights in development and implementation of KI plans and programs.
C. Public Education
Public education is a key component to the success of a KI program.
It is important that members of the public have a basic knowledge about
the use and side effects of KI, are aware that KI protects only the
thyroid from internal exposure to radioactive iodine, and understand
that it is to be taken only at the direction of authorized officials.
Several methods have been used by States with existing KI programs.
These include: Letters to physicians and residents, in-home visits by
public health officials, newspaper ads, distribution through
pharmacies, press releases and a press conference, a cable television
program, KI distribution or ``pick-up'' days, and commercial nuclear
power plant public education materials. An expanded discussion of
various public education methods is included in chapter 6 of the NAS KI
Report.
Health and Human Services KI Distribution Program
A. Requests for KI should be submitted to the:
Office of Mass Casualty Planning, Office of Public Health Emergency
Preparedness, U.S. Department of Health and Human Services, 200
Independence Avenue SW., Room 638G, Washington, DC 20201, Tel: 202-260-
1198.
B. State Government KI requests must:
Certify that the State has not already received sufficient
quantities of KI from the Federal Government;
Specify the quantity and formulation of KI needed and
describe the calculation used to make this determination;
Identify the location of the commercial nuclear power
plant within the State or within a 20-mile border strip inside an
adjacent State; and contain the State's and Tribal Government's plans
and procedures for stockpiling, distributing, and administering KI.
These plans must:
Identify the office with the authority to recommend the
use of KI by the general public;
Identify the organization(s) responsible for implementing
the KI use decision;
Identify the single recipient responsible for receiving
the KI; provide
[[Page 51069]]
a recipient address for the shipment of KI;
Specify the decision-making criteria for KI
administration;
Specify the criteria for issuing KI to the public
(location, special need);
Specify the method for making KI available to the public;
pre-distribution or stockpiling;
Specify the method for ensuring the supply of KI is
sufficient for the targeted population, including the estimated
transient/seasonal population that may be advised to take KI;
If pre-distributing KI, specify the procedure for the
public or special population groups to obtain KI;
Specify the procedure for storing, monitoring,
safeguarding, dispensing (to include, if applicable, tracking who
received the drug, when, in what quantity, and maintenance of waivers
from liability), and disposing of KI stocks;
Identify the method for alerting and notifying the general
public of the recommendation to take KI;
Specify how the plan is integrated into existing emergency
response plans; and
Specify quantities of KI (tablets and pediatric liquid
oral formulation) that will be requested.
C. Local Governments
KI requests from local governments must certify that:
The State in which the local government is located does
not have a DHS-approved KI distribution plan that includes KI as a
protective measure for populations, or a DHS approved plan that does
not address populations located beyond 10 miles from the commercial
nuclear power plant;
The local government has petitioned the State in which it
is located to modify the State plan to address populations within 20
miles of a commercial nuclear power plant, and 60 days have elapsed
without the State modifying the plan to accommodate the request;
The local government KI plans have been approved by the
State and certified to be `not inconsistent' with the State emergency
plan; and
The local government has reached an agreement with the
State that the State will serve as the single point of contact for
receipt of KI shipments from the stockpile and will then redistribute
the KI to the approved governments.
Funding and Resource Requirements
State, local, and tribal governments are responsible for obtaining
the funding and resources necessary to request and implement the KI
program within their respective jurisdictions, should they decide to
request KI. Only the provision of KI tablets/liquid will be funded
through HHS.
Dated: August 24, 2005.
Robert G. Claypool,
Deputy Assistant Secretary, Office of Public Health Emergency
Preparedness, Department of Health and Human Services.
References
A. NUREG-0654/DHS-REP-1, Criteria for Preparation and Evaluation of
Radiological Emergency Response Plans and Preparedness in Support of
Nuclear Power Plants, March 1987.
B. NUREG-0396/EPA 520/1-78-016, Planning Basis for the Development
of State and Local Government Radiological Emergency Response Plans
in Support of Light Water Nuclear Power Plants, December 1978.
C. National Academy of Sciences (NAS) Study, Distribution and
Administration of Potassium Iodide in the Event of a Nuclear
Incident, January 2004.
D. Federal Emergency Management Agency, Notice of revised Federal
policy, Federal Policy on Use of Potassium Iodide (KI), 67 FR 1355,
January 10, 2002.
E. Nuclear Regulatory Commission, Final rule, Consideration of
Potassium Iodide in Emergency Plans, 66 FR, 5427, January 19, 2001.
F. World Health Organization, Guidelines for Iodine Prophylaxis
Following Nuclear Accidents, 1999. https://www.who.int/
environmentalinformation/Information--resources/documents/Iodine/
guide.pdf.
G. National Council on Radiation Protection and Measures (NCRP)
Protection of the Thyroid Gland in the Event of Releases of
Radioiodine. NCRP Report No. 55, August 1, 1977.
H. Food and Drug Administration (Department of Health and Human
Services), Potassium Iodide as a Thyroid-Blocking Agent in Radiation
Emergencies; 66 FR 64046, December 11, 2001. https://www.fda.gov/
cder/guidance/4825fnl.htm.
I. Report of the President's Commission on the Accident at Three
Mile Island.
J. Federal Emergency Management Agency, Federal Policy on
Distribution of Potassium Iodide Around Nuclear Power Sites for Use
as a Thyroidal Blocking Agency, 50 FR, 30258, July 24, 1985.
K. Nauman, J., and Wolff, J., Iodide Prophylaxis in Poland After the
Chernobyl Reactor Accident: Benefits and Risks, American Journal of
Medicine, Vol. 94, p. 524, May 1993.
L. International Atomic Energy Agency, International Basic Safety
Standards for Protection Against Ionizing Radiation and for Safety
of Radiation Sources. Safety Series No. 115, 1996.
M. Food and Drug Administration (Department of Health and Human
Services) Guidance for Industry KI in Radiation Emergencies--
Questions and Answers, https://www.fda.gov/cder/guidance/5386fnl.htm.
N. Food and Drug Administration (Department of Health and Human
Services) Frequently Asked Questions on Potassium Iodide (KI).
https://www.fda.gov/cder/drugprepare/KI_Q&A.htm.
O. Food and Drug Administration (Department of Health and Human
Services) Guidance for Federal Agencies and State and Local
Governments: Potassium Iodide Tablets: Shelf Life Extension. https://
www.fda.gov/cder/guidance/5666fnl.pdf.
P. National Council on Radiation Protection and Measures (NCRP)
Report 138, Management of Terrorist Events Involving Radioactive
Materials.
[FR Doc. 05-17223 Filed 8-25-05; 2:41 pm]
BILLING CODE 4150-37-P