Privacy Act of 1974; Report of a Modified or Altered System of Records, 11643-11646 [E8-4070]
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Federal Register / Vol. 73, No. 43 / Tuesday, March 4, 2008 / Notices
may make searching for a record easier
and prevent delay.
RECORD ACCESS PROCEDURE:
For purpose of access, use the same
procedures outlined in Notification
Procedures above. Requestors should
also specify the record contents being
sought. (These procedures are in
accordance with department regulation
45 CFR 5b.5(a)(2)).
CONTESTING RECORDS PROCEDURES:
The subject individual should contact
the system manager named above, and
reasonably identify the records and
specify the information to be contested.
State the corrective action sought and
the reasons for the correction with
supporting justification. (These
Procedures are in accordance with
Department regulation 45 CFR 5b.7).
RECORDS SOURCE CATEGORIES:
CMS obtains the identifying
information contained in this system
from state Medicaid agencies, or
Medicaid Management Information
Systems maintained by the individual
states, and information contained on
CMS Form 2082.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
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BILLING CODE 4120–03–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
Privacy Act of 1974; Report of a
Modified or Altered System of Records
Department of Health and
Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
ACTION: Notice of a Modified or Altered
System of Records (SOR).
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AGENCY:
SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
we are proposing to modify or alter an
existing system of records titled ‘‘Links
of Social Security Administration (SSA)
and Health Care Financing
Administration (HCFA) Data (LOD),
System No. 09–70–0069, established at
65 Federal Register 50544 (August 18,
2000). The system name reflects the
former name of the Agency—the Health
Care Financing Administration. For this
reason, we propose to change the name
of the system to read: the ‘‘Links of
Social Security Administration (SSA)
and the Centers for Medicare &
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Medicaid Services Data (LOD).’’ We
propose to assign a new CMS
identification number to this system to
simplify the obsolete and confusing
numbering system originally designed
to identify the Bureau, Office, or Center
that maintained information in the
Health Care Financing Administration
systems of records. The new assigned
identifying number for this system
should read: System No. 09–70–0512.
We propose to modify existing routine
use number 2 that permits disclosure to
agency contractors and consultants to
include disclosure to CMS grantees who
perform a task for the agency. CMS
grantees, charged with completing
projects or activities that require CMS
data to carry out that activity, are
classified separate from CMS
contractors and/or consultants. The
modified routine use will be
renumbered as routine use number 1.
We will delete routine use number 3
authorizing disclosure to support
constituent requests made to a
congressional representative. If an
authorization for the disclosure has
been obtained from the data subject,
then no routine use is needed. We
propose to broaden the scope of the
disclosure provisions of this system by
adding a routine use to permit the
release of information to another
Federal and state agencies to: (1) Allow
such agency to comply with Title XI,
Part C of the Act; (2) enable such agency
to administer a Federal health benefits
program, and/or as necessary to enable
such agency to fulfill a requirement of
a Federal statute or regulation that
implements a health benefits program
funded in whole or in part with Federal
funds; and (3) support data exchanges
between the cooperating agencies. The
new routine use will be numbered as
routine use number 2.
We will broaden the scope of this
system by including the section titled
‘‘Additional Circumstances Affecting
Routine Use Disclosures,’’ that
addresses ‘‘Protected Health Information
(PHI)’’ and ‘‘small cell size.’’ The
requirement for compliance with HHS
regulation ‘‘Standards for Privacy of
Individually Identifiable Health
Information’’ apply whenever the
system collects or maintains PHI. This
system may contain PHI. In addition,
our policy to prohibit release if there is
a possibility that an individual can be
identified through ‘‘small cell size’’ will
apply to the data disclosed from this
system.
We are modifying the language in the
remaining routine uses to provide a
proper explanation as to the need for the
routine use and to provide clarity to
CMS’s intention to disclose individual-
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specific information contained in this
system. The routine uses will then be
prioritized and reordered according to
their usage. We will also take the
opportunity to update any sections of
the system that were affected by the
recent reorganization or because of the
impact of the Medicare Prescription
Drug, Improvement, and Modernization
Act of 2003 (MMA) (Pub. L. 108–173)
provisions and to update language in
the administrative sections to
correspond with language used in other
CMS SORs.
The primary purpose of the LOD is to
collect and maintain information that
will be used to conduct research,
perform policy analysis, and improve
program management for populations
served by both SSA and CMS.
Information maintained in this system
will also be disclosed to: (1) Support
regulatory, reimbursement, and policy
functions performed within the Agency
or by a contractor, consultant or grantee;
(2) assist another Federal or state
agency, agency of a state government, an
agency established by state law, or its
fiscal agent; (3) facilitate research on the
quality and effectiveness of care
provided, as well as epidemiological
projects; and (4) support litigation
involving the Agency. We have
provided background information about
the new system in the ‘‘Supplementary
Information’’ section below. Although
the Privacy Act requires only that CMS
provide an opportunity for interested
persons to comment on the proposed
routine uses, CMS invites comments on
all portions of this notice. See ‘‘Effective
Dates’’ section for comment period.
Effective Dates: CMS filed a modified
or altered system report with the Chair
of the House Committee on Government
Reform and Oversight, the Chair of the
Senate Committee on Homeland
Security & Governmental Affairs, and
the Administrator, Office of Information
and Regulatory Affairs, Office of
Management and Budget (OMB) on
February 26, 2008. To ensure that all
parties have adequate time in which to
comment, the modified system,
including routine uses, will become
effective 30 days from the publication of
the notice, or 40 days from the date it
was submitted to OMB and Congress,
whichever is later, unless CMS receives
comments that require alterations to this
notice.
ADDRESSES: The public should address
comments to: CMS Privacy Officer,
Division of Privacy Compliance,
Enterprise Architecture and Strategy
Group, Office of Information Services,
CMS, Room N2–04–27, 7500 Security
Boulevard, Baltimore, Maryland 21244–
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1850. Comments received will be
available for review at this location, by
appointment, during regular business
hours, Monday through Friday from 9
a.m.–3 p.m., Eastern Time zone.
FOR FURTHER INFORMATION CONTACT:
Dave Baugh, Senior Technical Advisor,
Research and Evaluation Group, Office
of Research, Development and
Information, CMS, Mail Stop Room C3–
20–17, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850. He
can be reached by telephone at 410–
786–7716, or via e-mail at
David.Baugh@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Description of the Modified or
Altered System of Records
A. Statutory and Regulatory Basis for
SOR
Authority for maintenance of this
system is given under Section 1875(a)
[42 U.S.C. 1395II(a)] and 1110 of the
Social Security Act [42 U.S.C. 1310].
B. Collection and Maintenance of Data
in the System
Information maintained in this system
contains samples of the United States
population served by programs
administered by CMS and SSA. The
system includes the following
information for each: Name, social
security number, Medicaid
identification number, health insurance
claim number, eligibility for SSA and
CMS programs, and benefit record
information.
II. Agency Policies, Procedures, and
Restrictions on the Routine Use
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A. Agency Policies, Procedures, and
Restrictions on the Routine Use
The Privacy Act permits us to disclose
information without an individual’s
consent if the information is to be used
for a purpose that is compatible with the
purpose(s) for which the information
was collected. Any such disclosure of
data is known as a ‘‘routine use.’’ The
government will only release LOD
information that can be associated with
an individual as provided for under
‘‘Section III. Proposed Routine Use
Disclosures of Data in the System.’’ Both
individually identifiable and nonindividually-identifiable data may be
disclosed under a routine use.
We will only disclose the minimum
personal data necessary to achieve the
purpose of LOD. CMS has the following
policies and procedures concerning
disclosures of information that will be
maintained in the system. Disclosure of
information from the system will be
approved only to the extent necessary to
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accomplish the purpose of the
disclosure and only after CMS:
1. Determines that the use or
disclosure is consistent with the reason
that the data is being collected; e.g., to
collect and maintain information that
will be used to conduct research,
perform policy analysis, and improve
program management for populations
served by both SSA and CMS.
2. Determines that:
a. The purpose for which the
disclosure is to be made can only be
accomplished if the record is provided
in individually identifiable form;
b. The purpose for which the
disclosure is to be made is of sufficient
importance to warrant the effect and/or
risk on the privacy of the individual that
additional exposure of the record might
bring; and
c. There is a strong probability that
the proposed use of the data would in
fact accomplish the stated purpose(s).
3. Requires the information recipient
to:
a. Establish administrative, technical,
and physical safeguards to prevent
unauthorized use or disclosure of the
record;
b. Remove or destroy at the earliest
time all individually-identifiable
information; and
c. Agree to not use or disclose the
information for any purpose other than
the stated purpose under which the
information was disclosed.
4. Determines that the data are valid
and reliable.
III. Proposed Routine Use Disclosures
of Data in the System
A. The Privacy Act allows us to
disclose information without an
individual’s consent if the information
is to be used for a purpose that is
compatible with the purpose(s) for
which the information was collected.
Any such compatible use of data is
known as a ‘‘routine use.’’ The proposed
routine uses in this system meet the
compatibility requirement of the Privacy
Act. We are proposing to establish the
following routine use disclosures of
information maintained in the system:
1. To support Agency contractors,
consultants, or grantees that have been
contracted by the Agency to assist in
accomplishment of a CMS function
relating to the purposes for this system
and who need access to the records in
order to assist CMS.
We contemplate disclosing
information under this routine use only
in situations in which CMS may enter
into a contractual or similar agreement
with a third party to assist in
accomplishing a CMS function relating
to purposes for this system.
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CMS occasionally contracts out
certain of its functions when doing so
would contribute to effective and
efficient operations. CMS must be able
to give a contractor, consultant, or
grantee whatever information is
necessary for the contractor, consultant,
or grantee to fulfill its duties. In these
situations, safeguards are provided in
the contract prohibiting the contractor,
consultant, or grantee from using or
disclosing the information for any
purpose other than that described in the
contract and requires the contractor,
consultant, or grantee to return or
destroy all information at the
completion of the contract.
2. To assist another Federal or state
agency, agency of a state government, an
agency established by state law, or its
fiscal agent to:
a. Allow such agency to comply with
Title XI, Part C of the Act,
b. Enable such agency to administer a
Federal health benefits program, or as
necessary to enable such agency to
fulfill a requirement of a Federal statute
or regulation that implements a health
benefits program funded in whole or in
part with Federal funds, and/or
c. Support data exchanges between
the cooperating agencies.
In addition, other state agencies in
their administration of a Federal health
program may require LOD information
for the purposes of determining,
evaluating and/or assessing cost,
effectiveness, and /or the quality of
health care services provided in the
state.
Disclosure under this routine use
shall be used by state Medicaid agencies
pursuant to agreements with the HHS
for administration of Titles IV, XVIII,
and XIX of the Act, and for the
administration of the Medicaid program.
3. To support an individual or
organization for a research, evaluation,
or epidemiological project related to the
prevention of disease or disability or the
restoration or maintenance of health.
LOD data may be able to provide for
research, evaluation, and
epidemiological projects a broader
longitudinal national perspective of the
status of health care patients. CMS
anticipates that many researchers will
have legitimate requests to use these
data in projects that could ultimately
improve the care provided to patients
and the policy that governs the care.
4. To assist the Department of Justice
(DOJ), court or adjudicatory body when:
a. The Agency or any component
thereof, or
b. Any employee of the Agency in his
or her official capacity, or
c. Any employee of the Agency in his
or her individual capacity where the
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DOJ has agreed to represent the
employee, or
d. The United States Government is a
party to litigation or has an interest in
such litigation, and by careful review,
CMS determines that the records are
both relevant and necessary to the
litigation and that the use of such
records by the DOJ, court or
adjudicatory body is compatible with
the purpose for which the agency
collected the records.
Whenever CMS is involved in
litigation, or occasionally when another
party is involved in litigation and CMS’s
policies or operations could be affected
by the outcome of the litigation, CMS
would be able to disclose information to
the DOJ, court, or adjudicatory body
involved.
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B. Additional Provisions Affecting
Routine Use Disclosures
To the extent this system contains
Protected Health Information (PHI) as
defined by HHS regulation ‘‘Standards
for Privacy of Individually Identifiable
Health Information’’ (45 CFR parts 160
and 164, subparts A and E) 65 FR 82462
(12–28–00). Disclosures of such PHI that
are otherwise authorized by these
routine uses may only be made if, and
as, permitted or required by the
‘‘Standards for Privacy of Individually
Identifiable Health Information.’’ (See
45 CFR 164–512 (a)(1)).
In addition, our policy will be to
prohibit release even of data not directly
identifiable, except pursuant to one of
the routine uses or if required by law,
if we determine there is a possibility
that an individual can be identified
through implicit deduction based on
small cell sizes (instances where the
patient population is so small that
individuals could, because of the small
size, use this information to deduce the
identity of the beneficiary).
IV. Safeguards
CMS has safeguards in place for
authorized users and monitors such
users to ensure against unauthorized
use. Personnel having access to the
system have been trained in the Privacy
Act and information security
requirements. Employees who maintain
records in this system are instructed not
to release data until the intended
recipient agrees to implement
appropriate management, operational
and technical safeguards sufficient to
protect the confidentiality, integrity and
availability of the information and
information systems and to prevent
unauthorized access.
This system will conform to all
applicable Federal laws and regulations
and Federal, HHS, and CMS policies
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and standards as they relate to
information security and data privacy.
These laws and regulations may apply
but are not limited to: the Privacy Act
of 1974; the Federal Information
Security Management Act of 2002; the
Computer Fraud and Abuse Act of 1986;
the Health Insurance Portability and
Accountability Act of 1996; the
E-Government Act of 2002, the ClingerCohen Act of 1996; the Medicare
Modernization Act of 2003, and the
corresponding implementing
regulations. OMB Circular A–130,
Management of Federal Resources,
Appendix III, Security of Federal
Automated Information Resources also
applies. Federal, HHS, and CMS
policies and standards include but are
not limited to: All pertinent National
Institute of Standards and Technology
publications; the HHS Information
Systems Program Handbook and the
CMS Information Security Handbook.
V. Effects of the Modified System of
Records on Individual Rights
CMS proposes to modify this system
in accordance with the principles and
requirements of the Privacy Act and will
collect, use, and disseminate
information only as prescribed therein.
Data in this system will be subject to the
authorized releases in accordance with
the routine uses identified in this
system of records.
CMS will take precautionary
measures to minimize the risks of
unauthorized access to the records and
the potential harm to individual privacy
or other personal or property rights of
patients whose data are maintained in
the system. CMS will collect only that
information necessary to perform the
system’s functions. In addition, CMS
will make disclosure from the proposed
system only with consent of the subject
individual, or his/her legal
representative, or in accordance with an
applicable exception provision of the
Privacy Act. CMS, therefore, does not
anticipate an unfavorable effect on
individual privacy as a result of
information relating to individuals.
Dated: February 25, 2008.
Charlene Frizzera,
Chief Operating Officer, Centers for Medicare
& Medicaid Services.
SYSTEM NO. 09–70–0512
SYSTEM NAME:
‘‘Links To Social Security
Administration and Centers For
Medicare & Medicaid Services Data
(LOD),’’ HHS/CMS/ORDI
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11645
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive
Data
SYSTEM LOCATION:
Centers for Medicare & Medicaid
Services (CMS) Data Center, 7500
Security Boulevard, North Building,
First Floor, Baltimore, Maryland 21244–
1850 and at various other locations.
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
The system includes samples of the
United States population served by
Social Security Administration (SSA)
and CMS programs.
CATEGORIES OF RECORDS IN THE SYSTEM:
The collected information will
include, but is not limited to name,
social security number (SSN), Medicaid
identification number, health insurance
claim number (HICN), eligibility for
SSA and CMS programs, and benefit
record information.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for maintenance of this
system is given under Section 1875(a)
[42 U.S.C. 1395II(a)] and 1110 of the
Social Security Act [42 U.S.C. 1310].
PURPOSE(S) OF THE SYSTEM:
The primary purpose of the LOD is to
collect and maintain information that
will be used to conduct research,
perform policy analysis, and improve
program management for populations
served by both SSA and CMS.
Information maintained in this system
will also be disclosed to: (1) Support
regulatory, reimbursement, and policy
functions performed within the Agency
or by a contractor, consultant or grantee;
(2) assist another Federal or state
agency, agency of a state government, an
agency established by state law, or its
fiscal agent; (3) facilitate research on the
quality and effectiveness of care
provided, as well as epidemiological
projects; and (4) support litigation
involving the Agency.
ROUTINE USES OF RECORDS MAINTAINED IN THE
SYSTEM, INCLUDING CATEGORIES OR USERS AND
THE PURPOSES OF SUCH USES:
A. The Privacy Act allows us to
disclose information without an
individual’s consent if the information
is to be used for a purpose that is
compatible with the purpose(s) for
which the information was collected.
Any such compatible use of data is
known as a ‘‘routine use.’’ The proposed
routine uses in this system meet the
compatibility requirement of the Privacy
Act. We are proposing to establish the
following routine use disclosures of
information maintained in the system:
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1. To agency contractors, consultants
or grantees, who have been engaged by
the agency to assist in the performance
of a service related to this collection and
who need to have access to the records
in order to perform the activity.
2. To assist another Federal or state
agency, agency of a state government, an
agency established by state law, or its
fiscal agent to:
a. Allow such agency to comply with
Title XI, Part C of the Act,
b. Enable such agency to administer a
Federal health benefits program, or as
necessary to enable such agency to
fulfill a requirement of a Federal statute
or regulation that implements a health
benefits program funded in whole or in
part with Federal funds, and/or
c. Support data exchanges between
the cooperating agencies.
3. To an individual or organization for
a research project or in support of an
evaluation project related to the
prevention of disease, disability, or
quality care projects, the restoration or
maintenance of health, and payment
related projects.
4. To the Department of Justice (DOJ),
court or adjudicatory body when:
a. The agency or any component
thereof, or
b. Any employee of the agency in his
or her official capacity, or
c. Any employee of the agency in his
or her individual capacity where the
DOJ has agreed to represent the
employee, or
d. The United States Government, is
a party to litigation or has an interest in
such litigation, and, by careful review,
CMS determines that the records are
both relevant and necessary to the
litigation and that the use of such
records by the DOJ, court or
adjudicatory body is compatible with
the purpose for which the agency
collected the records.
B. Additional Provisions Affecting
Routine Use Disclosures
To the extent this system contains
Protected Health Information (PHI) as
defined by HHS regulation ‘‘Standards
for Privacy of Individually Identifiable
Health Information’’ (45 CFR Parts 160
and 164, Subparts A and E) 65 FR 82462
(12–28–00). Disclosures of such PHI that
are otherwise authorized by these
routine uses may only be made if, and
as, permitted or required by the
‘‘Standards for Privacy of Individually
Identifiable Health Information.’’ (See
45 CFR 164–512 (a) (1).)
In addition, our policy will be to
prohibit release even of data not directly
identifiable, except pursuant to one of
the routine uses or if required by law,
if we determine there is a possibility
that an individual can be identified
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through implicit deduction based on
small cell sizes (instances where the
patient population is so small that
individuals could, because of the small
size, use this information to deduce the
identity of the beneficiary).
POLICIES AND PRACTICES FOR STORING,
RETRIEVING, ACCESSING, RETAINING, AND
DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on electronic
media.
RETRIEVABILITY:
The collected data are retrieved by an
individual identifier; e.g., beneficiary
name, health insurance claim number,
State assigned personal identifier, or
social security number.
SAFEGUARDS:
CMS has safeguards in place for
authorized users and monitors such
users to ensure against unauthorized
use. Personnel having access to the
system have been trained in the Privacy
Act and information security
requirements. Employees who maintain
records in this system are instructed not
to release data until the intended
recipient agrees to implement
appropriate management, operational
and technical safeguards sufficient to
protect the confidentiality, integrity and
availability of the information and
information systems and to prevent
unauthorized access.
This system will conform to all
applicable Federal laws and regulations
and Federal, HHS, and CMS policies
and standards as they relate to
information security and data privacy.
These laws and regulations may apply
but are not limited to: The Privacy Act
of 1974; the Federal Information
Security Management Act of 2002; the
Computer Fraud and Abuse Act of 1986;
the Health Insurance Portability and
Accountability Act of 1996; the EGovernment Act of 2002; the ClingerCohen Act of 1996; the Medicare
Modernization Act of 2003; and the
corresponding implementing
regulations. OMB Circular A–130,
Management of Federal Resources,
Appendix III, Security of Federal
Automated Information Resources also
applies. Federal, HHS, and CMS
policies and standards include but are
not limited to: All pertinent National
Institute of Standards and Technology
publications; the HHS Information
Systems Program Handbook and the
CMS Information Security Handbook.
CMS will retain information for a total
period not to exceed 25 years. All
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SYSTEM MANAGER AND ADDRESS:
Director, Information and Methods
Group, Office of Research, Development
& Information, Mail Stop C3–16–07,
Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, MD 21244–1849.
NOTIFICATION PROCEDURE:
For purpose of access, the subject
individual should write to the system
manager who will require the system
name, employee identification number,
tax identification number, national
provider number, and for verification
purposes, the subject individual’s name
(woman’s maiden name, if applicable),
HICN, and/or SSN (furnishing the SSN
is voluntary, but it may make searching
for a record easier and prevent delay).
RECORD ACCESS PROCEDURE:
For purpose of access, use the same
procedures outlined in Notification
Procedures above. Requestors should
also reasonably specify the record
contents being sought. (These
procedures are in accordance with
Department regulation 45 CFR
5b.5(a)(2).)
CONTESTING RECORD PROCEDURES:
The subject individual should contact
the system manager named above, and
reasonably identify the record and
specify the information to be contested.
State the corrective action sought and
the reasons for the correction with
supporting justification. (These
procedures are in accordance with
Department regulation 45 CFR 5b.7.)
RECORDS SOURCE CATEGORIES:
Sources of information contained in
this records system include data
collected from SSA systems of records,
e.g., Supplemental Security Record (09–
60–0103), Master Beneficiary Record
(09–60–0090), Disability Determination
Files (09–60–0044), and Social Security
Account Number Identification File
(09–60–0058) and LOD systems of
records, e.g., Medicaid Statistical
Information System (09–70–0541),
Current Beneficiary Survey (09–70–
0519), Common Working Files (09–70–
0526), National Claims History Files
(09–70–0558) and Enrollment Data Base
(09–70–0502).
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
RETENTION AND DISPOSAL:
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claims-related records are encompassed
by the document preservation order and
will be retained until notification is
received from DOJ.
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Agencies
[Federal Register Volume 73, Number 43 (Tuesday, March 4, 2008)]
[Notices]
[Pages 11643-11646]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-4070]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
Privacy Act of 1974; Report of a Modified or Altered System of
Records
AGENCY: Department of Health and Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
ACTION: Notice of a Modified or Altered System of Records (SOR).
-----------------------------------------------------------------------
SUMMARY: In accordance with the requirements of the Privacy Act of
1974, we are proposing to modify or alter an existing system of records
titled ``Links of Social Security Administration (SSA) and Health Care
Financing Administration (HCFA) Data (LOD), System No. 09-70-0069,
established at 65 Federal Register 50544 (August 18, 2000). The system
name reflects the former name of the Agency--the Health Care Financing
Administration. For this reason, we propose to change the name of the
system to read: the ``Links of Social Security Administration (SSA) and
the Centers for Medicare & Medicaid Services Data (LOD).'' We propose
to assign a new CMS identification number to this system to simplify
the obsolete and confusing numbering system originally designed to
identify the Bureau, Office, or Center that maintained information in
the Health Care Financing Administration systems of records. The new
assigned identifying number for this system should read: System No. 09-
70-0512.
We propose to modify existing routine use number 2 that permits
disclosure to agency contractors and consultants to include disclosure
to CMS grantees who perform a task for the agency. CMS grantees,
charged with completing projects or activities that require CMS data to
carry out that activity, are classified separate from CMS contractors
and/or consultants. The modified routine use will be renumbered as
routine use number 1. We will delete routine use number 3 authorizing
disclosure to support constituent requests made to a congressional
representative. If an authorization for the disclosure has been
obtained from the data subject, then no routine use is needed. We
propose to broaden the scope of the disclosure provisions of this
system by adding a routine use to permit the release of information to
another Federal and state agencies to: (1) Allow such agency to comply
with Title XI, Part C of the Act; (2) enable such agency to administer
a Federal health benefits program, and/or as necessary to enable such
agency to fulfill a requirement of a Federal statute or regulation that
implements a health benefits program funded in whole or in part with
Federal funds; and (3) support data exchanges between the cooperating
agencies. The new routine use will be numbered as routine use number 2.
We will broaden the scope of this system by including the section
titled ``Additional Circumstances Affecting Routine Use Disclosures,''
that addresses ``Protected Health Information (PHI)'' and ``small cell
size.'' The requirement for compliance with HHS regulation ``Standards
for Privacy of Individually Identifiable Health Information'' apply
whenever the system collects or maintains PHI. This system may contain
PHI. In addition, our policy to prohibit release if there is a
possibility that an individual can be identified through ``small cell
size'' will apply to the data disclosed from this system.
We are modifying the language in the remaining routine uses to
provide a proper explanation as to the need for the routine use and to
provide clarity to CMS's intention to disclose individual-specific
information contained in this system. The routine uses will then be
prioritized and reordered according to their usage. We will also take
the opportunity to update any sections of the system that were affected
by the recent reorganization or because of the impact of the Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA)
(Pub. L. 108-173) provisions and to update language in the
administrative sections to correspond with language used in other CMS
SORs.
The primary purpose of the LOD is to collect and maintain
information that will be used to conduct research, perform policy
analysis, and improve program management for populations served by both
SSA and CMS. Information maintained in this system will also be
disclosed to: (1) Support regulatory, reimbursement, and policy
functions performed within the Agency or by a contractor, consultant or
grantee; (2) assist another Federal or state agency, agency of a state
government, an agency established by state law, or its fiscal agent;
(3) facilitate research on the quality and effectiveness of care
provided, as well as epidemiological projects; and (4) support
litigation involving the Agency. We have provided background
information about the new system in the ``Supplementary Information''
section below. Although the Privacy Act requires only that CMS provide
an opportunity for interested persons to comment on the proposed
routine uses, CMS invites comments on all portions of this notice. See
``Effective Dates'' section for comment period.
Effective Dates: CMS filed a modified or altered system report with
the Chair of the House Committee on Government Reform and Oversight,
the Chair of the Senate Committee on Homeland Security & Governmental
Affairs, and the Administrator, Office of Information and Regulatory
Affairs, Office of Management and Budget (OMB) on February 26, 2008. To
ensure that all parties have adequate time in which to comment, the
modified system, including routine uses, will become effective 30 days
from the publication of the notice, or 40 days from the date it was
submitted to OMB and Congress, whichever is later, unless CMS receives
comments that require alterations to this notice.
ADDRESSES: The public should address comments to: CMS Privacy Officer,
Division of Privacy Compliance, Enterprise Architecture and Strategy
Group, Office of Information Services, CMS, Room N2-04-27, 7500
Security Boulevard, Baltimore, Maryland 21244-
[[Page 11644]]
1850. Comments received will be available for review at this location,
by appointment, during regular business hours, Monday through Friday
from 9 a.m.-3 p.m., Eastern Time zone.
FOR FURTHER INFORMATION CONTACT: Dave Baugh, Senior Technical Advisor,
Research and Evaluation Group, Office of Research, Development and
Information, CMS, Mail Stop Room C3-20-17, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850. He can be reached by telephone at 410-
786-7716, or via e-mail at David.Baugh@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Description of the Modified or Altered System of Records
A. Statutory and Regulatory Basis for SOR
Authority for maintenance of this system is given under Section
1875(a) [42 U.S.C. 1395II(a)] and 1110 of the Social Security Act [42
U.S.C. 1310].
B. Collection and Maintenance of Data in the System
Information maintained in this system contains samples of the
United States population served by programs administered by CMS and
SSA. The system includes the following information for each: Name,
social security number, Medicaid identification number, health
insurance claim number, eligibility for SSA and CMS programs, and
benefit record information.
II. Agency Policies, Procedures, and Restrictions on the Routine Use
A. Agency Policies, Procedures, and Restrictions on the Routine Use
The Privacy Act permits us to disclose information without an
individual's consent if the information is to be used for a purpose
that is compatible with the purpose(s) for which the information was
collected. Any such disclosure of data is known as a ``routine use.''
The government will only release LOD information that can be associated
with an individual as provided for under ``Section III. Proposed
Routine Use Disclosures of Data in the System.'' Both individually
identifiable and non-individually-identifiable data may be disclosed
under a routine use.
We will only disclose the minimum personal data necessary to
achieve the purpose of LOD. CMS has the following policies and
procedures concerning disclosures of information that will be
maintained in the system. Disclosure of information from the system
will be approved only to the extent necessary to accomplish the purpose
of the disclosure and only after CMS:
1. Determines that the use or disclosure is consistent with the
reason that the data is being collected; e.g., to collect and maintain
information that will be used to conduct research, perform policy
analysis, and improve program management for populations served by both
SSA and CMS.
2. Determines that:
a. The purpose for which the disclosure is to be made can only be
accomplished if the record is provided in individually identifiable
form;
b. The purpose for which the disclosure is to be made is of
sufficient importance to warrant the effect and/or risk on the privacy
of the individual that additional exposure of the record might bring;
and
c. There is a strong probability that the proposed use of the data
would in fact accomplish the stated purpose(s).
3. Requires the information recipient to:
a. Establish administrative, technical, and physical safeguards to
prevent unauthorized use or disclosure of the record;
b. Remove or destroy at the earliest time all individually-
identifiable information; and
c. Agree to not use or disclose the information for any purpose
other than the stated purpose under which the information was
disclosed.
4. Determines that the data are valid and reliable.
III. Proposed Routine Use Disclosures of Data in the System
A. The Privacy Act allows us to disclose information without an
individual's consent if the information is to be used for a purpose
that is compatible with the purpose(s) for which the information was
collected. Any such compatible use of data is known as a ``routine
use.'' The proposed routine uses in this system meet the compatibility
requirement of the Privacy Act. We are proposing to establish the
following routine use disclosures of information maintained in the
system:
1. To support Agency contractors, consultants, or grantees that
have been contracted by the Agency to assist in accomplishment of a CMS
function relating to the purposes for this system and who need access
to the records in order to assist CMS.
We contemplate disclosing information under this routine use only
in situations in which CMS may enter into a contractual or similar
agreement with a third party to assist in accomplishing a CMS function
relating to purposes for this system.
CMS occasionally contracts out certain of its functions when doing
so would contribute to effective and efficient operations. CMS must be
able to give a contractor, consultant, or grantee whatever information
is necessary for the contractor, consultant, or grantee to fulfill its
duties. In these situations, safeguards are provided in the contract
prohibiting the contractor, consultant, or grantee from using or
disclosing the information for any purpose other than that described in
the contract and requires the contractor, consultant, or grantee to
return or destroy all information at the completion of the contract.
2. To assist another Federal or state agency, agency of a state
government, an agency established by state law, or its fiscal agent to:
a. Allow such agency to comply with Title XI, Part C of the Act,
b. Enable such agency to administer a Federal health benefits
program, or as necessary to enable such agency to fulfill a requirement
of a Federal statute or regulation that implements a health benefits
program funded in whole or in part with Federal funds, and/or
c. Support data exchanges between the cooperating agencies.
In addition, other state agencies in their administration of a
Federal health program may require LOD information for the purposes of
determining, evaluating and/or assessing cost, effectiveness, and /or
the quality of health care services provided in the state.
Disclosure under this routine use shall be used by state Medicaid
agencies pursuant to agreements with the HHS for administration of
Titles IV, XVIII, and XIX of the Act, and for the administration of the
Medicaid program.
3. To support an individual or organization for a research,
evaluation, or epidemiological project related to the prevention of
disease or disability or the restoration or maintenance of health.
LOD data may be able to provide for research, evaluation, and
epidemiological projects a broader longitudinal national perspective of
the status of health care patients. CMS anticipates that many
researchers will have legitimate requests to use these data in projects
that could ultimately improve the care provided to patients and the
policy that governs the care.
4. To assist the Department of Justice (DOJ), court or adjudicatory
body when:
a. The Agency or any component thereof, or
b. Any employee of the Agency in his or her official capacity, or
c. Any employee of the Agency in his or her individual capacity
where the
[[Page 11645]]
DOJ has agreed to represent the employee, or
d. The United States Government is a party to litigation or has an
interest in such litigation, and by careful review, CMS determines that
the records are both relevant and necessary to the litigation and that
the use of such records by the DOJ, court or adjudicatory body is
compatible with the purpose for which the agency collected the records.
Whenever CMS is involved in litigation, or occasionally when
another party is involved in litigation and CMS's policies or
operations could be affected by the outcome of the litigation, CMS
would be able to disclose information to the DOJ, court, or
adjudicatory body involved.
B. Additional Provisions Affecting Routine Use Disclosures
To the extent this system contains Protected Health Information
(PHI) as defined by HHS regulation ``Standards for Privacy of
Individually Identifiable Health Information'' (45 CFR parts 160 and
164, subparts A and E) 65 FR 82462 (12-28-00). Disclosures of such PHI
that are otherwise authorized by these routine uses may only be made
if, and as, permitted or required by the ``Standards for Privacy of
Individually Identifiable Health Information.'' (See 45 CFR 164-512
(a)(1)).
In addition, our policy will be to prohibit release even of data
not directly identifiable, except pursuant to one of the routine uses
or if required by law, if we determine there is a possibility that an
individual can be identified through implicit deduction based on small
cell sizes (instances where the patient population is so small that
individuals could, because of the small size, use this information to
deduce the identity of the beneficiary).
IV. Safeguards
CMS has safeguards in place for authorized users and monitors such
users to ensure against unauthorized use. Personnel having access to
the system have been trained in the Privacy Act and information
security requirements. Employees who maintain records in this system
are instructed not to release data until the intended recipient agrees
to implement appropriate management, operational and technical
safeguards sufficient to protect the confidentiality, integrity and
availability of the information and information systems and to prevent
unauthorized access.
This system will conform to all applicable Federal laws and
regulations and Federal, HHS, and CMS policies and standards as they
relate to information security and data privacy. These laws and
regulations may apply but are not limited to: the Privacy Act of 1974;
the Federal Information Security Management Act of 2002; the Computer
Fraud and Abuse Act of 1986; the Health Insurance Portability and
Accountability Act of 1996; the E-Government Act of 2002, the Clinger-
Cohen Act of 1996; the Medicare Modernization Act of 2003, and the
corresponding implementing regulations. OMB Circular A-130, Management
of Federal Resources, Appendix III, Security of Federal Automated
Information Resources also applies. Federal, HHS, and CMS policies and
standards include but are not limited to: All pertinent National
Institute of Standards and Technology publications; the HHS Information
Systems Program Handbook and the CMS Information Security Handbook.
V. Effects of the Modified System of Records on Individual Rights
CMS proposes to modify this system in accordance with the
principles and requirements of the Privacy Act and will collect, use,
and disseminate information only as prescribed therein. Data in this
system will be subject to the authorized releases in accordance with
the routine uses identified in this system of records.
CMS will take precautionary measures to minimize the risks of
unauthorized access to the records and the potential harm to individual
privacy or other personal or property rights of patients whose data are
maintained in the system. CMS will collect only that information
necessary to perform the system's functions. In addition, CMS will make
disclosure from the proposed system only with consent of the subject
individual, or his/her legal representative, or in accordance with an
applicable exception provision of the Privacy Act. CMS, therefore, does
not anticipate an unfavorable effect on individual privacy as a result
of information relating to individuals.
Dated: February 25, 2008.
Charlene Frizzera,
Chief Operating Officer, Centers for Medicare & Medicaid Services.
SYSTEM NO. 09-70-0512
SYSTEM NAME:
``Links To Social Security Administration and Centers For Medicare
& Medicaid Services Data (LOD),'' HHS/CMS/ORDI
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive Data
SYSTEM LOCATION:
Centers for Medicare & Medicaid Services (CMS) Data Center, 7500
Security Boulevard, North Building, First Floor, Baltimore, Maryland
21244-1850 and at various other locations.
CATEGORIES OF INDIVIDUALS COVERED BY THE SYSTEM:
The system includes samples of the United States population served
by Social Security Administration (SSA) and CMS programs.
CATEGORIES OF RECORDS IN THE SYSTEM:
The collected information will include, but is not limited to name,
social security number (SSN), Medicaid identification number, health
insurance claim number (HICN), eligibility for SSA and CMS programs,
and benefit record information.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for maintenance of this system is given under Section
1875(a) [42 U.S.C. 1395II(a)] and 1110 of the Social Security Act [42
U.S.C. 1310].
PURPOSE(S) OF THE SYSTEM:
The primary purpose of the LOD is to collect and maintain
information that will be used to conduct research, perform policy
analysis, and improve program management for populations served by both
SSA and CMS. Information maintained in this system will also be
disclosed to: (1) Support regulatory, reimbursement, and policy
functions performed within the Agency or by a contractor, consultant or
grantee; (2) assist another Federal or state agency, agency of a state
government, an agency established by state law, or its fiscal agent;
(3) facilitate research on the quality and effectiveness of care
provided, as well as epidemiological projects; and (4) support
litigation involving the Agency.
ROUTINE USES OF RECORDS MAINTAINED IN THE SYSTEM, INCLUDING CATEGORIES
OR USERS AND THE PURPOSES OF SUCH USES:
A. The Privacy Act allows us to disclose information without an
individual's consent if the information is to be used for a purpose
that is compatible with the purpose(s) for which the information was
collected. Any such compatible use of data is known as a ``routine
use.'' The proposed routine uses in this system meet the compatibility
requirement of the Privacy Act. We are proposing to establish the
following routine use disclosures of information maintained in the
system:
[[Page 11646]]
1. To agency contractors, consultants or grantees, who have been
engaged by the agency to assist in the performance of a service related
to this collection and who need to have access to the records in order
to perform the activity.
2. To assist another Federal or state agency, agency of a state
government, an agency established by state law, or its fiscal agent to:
a. Allow such agency to comply with Title XI, Part C of the Act,
b. Enable such agency to administer a Federal health benefits
program, or as necessary to enable such agency to fulfill a requirement
of a Federal statute or regulation that implements a health benefits
program funded in whole or in part with Federal funds, and/or
c. Support data exchanges between the cooperating agencies.
3. To an individual or organization for a research project or in
support of an evaluation project related to the prevention of disease,
disability, or quality care projects, the restoration or maintenance of
health, and payment related projects.
4. To the Department of Justice (DOJ), court or adjudicatory body
when:
a. The agency or any component thereof, or
b. Any employee of the agency in his or her official capacity, or
c. Any employee of the agency in his or her individual capacity
where the DOJ has agreed to represent the employee, or
d. The United States Government, is a party to litigation or has
an interest in such litigation, and, by careful review, CMS determines
that the records are both relevant and necessary to the litigation and
that the use of such records by the DOJ, court or adjudicatory body is
compatible with the purpose for which the agency collected the records.
B. Additional Provisions Affecting Routine Use Disclosures
To the extent this system contains Protected Health Information
(PHI) as defined by HHS regulation ``Standards for Privacy of
Individually Identifiable Health Information'' (45 CFR Parts 160 and
164, Subparts A and E) 65 FR 82462 (12-28-00). Disclosures of such PHI
that are otherwise authorized by these routine uses may only be made
if, and as, permitted or required by the ``Standards for Privacy of
Individually Identifiable Health Information.'' (See 45 CFR 164-512 (a)
(1).)
In addition, our policy will be to prohibit release even of data
not directly identifiable, except pursuant to one of the routine uses
or if required by law, if we determine there is a possibility that an
individual can be identified through implicit deduction based on small
cell sizes (instances where the patient population is so small that
individuals could, because of the small size, use this information to
deduce the identity of the beneficiary).
POLICIES AND PRACTICES FOR STORING, RETRIEVING, ACCESSING, RETAINING,
AND DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on electronic media.
RETRIEVABILITY:
The collected data are retrieved by an individual identifier; e.g.,
beneficiary name, health insurance claim number, State assigned
personal identifier, or social security number.
SAFEGUARDS:
CMS has safeguards in place for authorized users and monitors such
users to ensure against unauthorized use. Personnel having access to
the system have been trained in the Privacy Act and information
security requirements. Employees who maintain records in this system
are instructed not to release data until the intended recipient agrees
to implement appropriate management, operational and technical
safeguards sufficient to protect the confidentiality, integrity and
availability of the information and information systems and to prevent
unauthorized access.
This system will conform to all applicable Federal laws and
regulations and Federal, HHS, and CMS policies and standards as they
relate to information security and data privacy. These laws and
regulations may apply but are not limited to: The Privacy Act of 1974;
the Federal Information Security Management Act of 2002; the Computer
Fraud and Abuse Act of 1986; the Health Insurance Portability and
Accountability Act of 1996; the E-Government Act of 2002; the Clinger-
Cohen Act of 1996; the Medicare Modernization Act of 2003; and the
corresponding implementing regulations. OMB Circular A-130, Management
of Federal Resources, Appendix III, Security of Federal Automated
Information Resources also applies. Federal, HHS, and CMS policies and
standards include but are not limited to: All pertinent National
Institute of Standards and Technology publications; the HHS Information
Systems Program Handbook and the CMS Information Security Handbook.
RETENTION AND DISPOSAL:
CMS will retain information for a total period not to exceed 25
years. All claims-related records are encompassed by the document
preservation order and will be retained until notification is received
from DOJ.
SYSTEM MANAGER AND ADDRESS:
Director, Information and Methods Group, Office of Research,
Development & Information, Mail Stop C3-16-07, Centers for Medicare &
Medicaid Services, 7500 Security Boulevard, Baltimore, MD 21244-1849.
NOTIFICATION PROCEDURE:
For purpose of access, the subject individual should write to the
system manager who will require the system name, employee
identification number, tax identification number, national provider
number, and for verification purposes, the subject individual's name
(woman's maiden name, if applicable), HICN, and/or SSN (furnishing the
SSN is voluntary, but it may make searching for a record easier and
prevent delay).
RECORD ACCESS PROCEDURE:
For purpose of access, use the same procedures outlined in
Notification Procedures above. Requestors should also reasonably
specify the record contents being sought. (These procedures are in
accordance with Department regulation 45 CFR 5b.5(a)(2).)
CONTESTING RECORD PROCEDURES:
The subject individual should contact the system manager named
above, and reasonably identify the record and specify the information
to be contested. State the corrective action sought and the reasons for
the correction with supporting justification. (These procedures are in
accordance with Department regulation 45 CFR 5b.7.)
RECORDS SOURCE CATEGORIES:
Sources of information contained in this records system include
data collected from SSA systems of records, e.g., Supplemental Security
Record (09-60-0103), Master Beneficiary Record (09-60-0090), Disability
Determination Files (09-60-0044), and Social Security Account Number
Identification File (09-60-0058) and LOD systems of records, e.g.,
Medicaid Statistical Information System (09-70-0541), Current
Beneficiary Survey (09-70-0519), Common Working Files (09-70-0526),
National Claims History Files (09-70-0558) and Enrollment Data Base
(09-70-0502).
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS OF THE ACT:
None.
[FR Doc. E8-4070 Filed 3-3-08; 8:45 am]
BILLING CODE 4120-03-P