Privacy Act of 1974; Report of a Modified or Altered System of Records, 26121-26126 [E7-8757]
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Federal Register / Vol. 72, No. 88 / Tuesday, May 8, 2007 / Notices
Nebraska
Arsenic in Soil in East Omaha,
Nebraska; March 20, 2007.
New Jersey
Celotex Corporation; January 10, 2007.
North Carolina
APAC Carolina Inc. and Associated
Asphalt Inc., Jake Alexander
Boulevard; February 14, 2007.
Weyerhaeuser Pulp and Paper Mill—
Exposure Investigation Report; March
22, 2007.
Pennsylvania
Ivy Industrial Park Site—Public Health
Evaluation of Residential Indoor Air
and Well Water Sample Results;
March 5, 2007.
Remacor Site; January 10, 2007.
Tennessee
Mr. Zip Convenience Store; March 14,
2007.
Texas
Former Delroc Oil Refinery/Woodwind
Lakes Subdivision; February 23, 2007.
Utah
Vermiculite Intermountain and
Intermountain Products, Inc.—
Epidemiological Investigation of
Human Exposure to a Contaminated
Vermiculite Ore Processing Site in
Utah; March 1, 2007.
Washington
Home Heating Oil Release, Technical
Review of the Site Hazard
Assessment; March 29, 2007.
Wisconsin
Amery-Dresser Trail; January 23, 2007.
Dated: May 2, 2007.
Kenneth Rose,
Acting Director, Office of Policy, Planning,
and Evaluation, National Center for
Environmental Health/Agency for Toxic
Substances and Disease Registry.
[FR Doc. E7–8758 Filed 5–7–07; 8:45 am]
BILLING CODE 4163–70–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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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).
AGENCY:
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SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
CMS is proposing to modify or alter
existing system of records titled
‘‘Complaints Against Health Insurance
Issuers and Health Plans (CAHII),’’
System No. 09–70–9005, established at
66 FR 9858, (February 12, 2001). 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. 09–70–0516.
We propose to modify existing routine
use number 1 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 remain as
routine use number 1. We will delete
routine use number 2 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. The Privacy Act allows for
disclosures with the ‘‘prior written
consent’’ of the data subject.
We propose to add 2 new routine uses
authorizing disclosure to support a CMS
contractor, consultant, or a grantee of a
CMS-administered grant program, when
disclosure is deemed reasonably
necessary by CMS to combat fraud,
waste, and abuse in certain health care
programs. The new routine use will be
published as routine use number 6. We
will add a second new routine use to
support another Federal agency or to an
instrumentality of any governmental
jurisdiction within or under the control
of the United States, when disclosure is
deemed reasonably necessary by CMS to
combat fraud, waste, and abuse in
certain health care programs. This new
routine use will be published as routine
use number 7. 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
when ever the system collects or
maintain PHI. This system may contain
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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 individualspecific 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 this system is
to collect and maintain information
initiated by consumers complaints/
reports to CMS that their health
insurance issuers and/or non-Federal
governmental health plans are in
violation of one or more of the following
statutes: §§ 2722 and 2761 of the Public
Health Service (PHS) Act; the Mental
Health Parity Act of 1996 (MHPA); the
Newborns’ and Mothers’ Health
Protection Act of 1996 (NMHPA); and,
the Women’s Health and Cancer Rights
Act of 1998 (WHCRA). 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) assist third party contacts in
situations where the party to be
contacted has, or is expected to have
information relating to the individual’s
capacity to manage his or her affairs or
to his or her eligibility for, or an
entitlement to benefits under the
Medicare program; (4) inform a health
insurance issuer and/or health plan who
has been named in a complaint/inquiry
and is believed to be potentially in
violation of relevant portions of the
PHS; (5) support litigation involving the
Agency; and (6) combat fraud, waste,
and abuse in certain health benefits
programs. We have provided
background information about this 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
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all portions of this notice. See ‘‘Effective
Dates’’ section for comment period.
DATES: Effective Dates: CMS filed a new
system report with the Chair of the
House Committee on Government
Reform and Oversight, the Chair of the
Senate Committee on Homeland
Security and Governmental Affairs, and
the Administrator, Office of Information
and Regulatory Affairs, Office of
Management and Budget (OMB) on
April 12, 2007. To ensure that all parties
have adequate time in which to
comment, the new SOR, including
routine uses, will become effective 40
days from the publication of the notice,
or from the date it was submitted to
OMB and the 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–
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 Mlawsky, Health Insurance
Specialist, Division of Employer
Operations, Employer Policy and
Operations Group, Center for
Beneficiary Choices, CMS, 7500
Security Boulevard, Mail Stop S3–16–
26, Baltimore, Maryland 21244–1850.
The telephone number is 410–786–6851
or e-mail david.mlawsky@cms.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Description of the Modified or
Altered System of Records
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A. Statutory and Regulatory Basis for
SOR
Authority for maintenance of this
system is given under §§ 2722 and 2761
of the Public Health Service (PHS) Act;
the Mental Health Parity Act of 1996
(MHPA); the Newborns’ and Mothers’
Health Protection Act of 1996
(NMHPA); and the Women’s Health and
Cancer Rights Act of 1998 (WHCRA)
with respect to non-Federal
governmental plans.
B. Collection and Maintenance of Data
in the System
This system will collect and maintain
individually identifiable and other data
collected on individuals/consumers
who make complaints/inquiries to CMS
that their health insurance issuers and/
or non-Federal governmental health
plans are in violation of the PHS.
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The system contains information such
as consumer’s name, address, phone
number, the name and address of their
health plan or health insurance issuer,
their plan ID number or social security
number, the nature of their complaint/
inquiry against their health plan or
issuer, and any medical and other
additional information that is necessary
for CAHII to help resolve the
consumer’s complaint.
II. Agency Policies, Procedures, and
Restrictions on the Routine Use
A. 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 CAHII information that can
be associated with an individual as
provided for under ‘‘Section III.
Proposed Routine Use Disclosures of
Data in the System.’’ Both identifiable
and non-identifiable data may be
disclosed under a routine use.
We will only collect the minimum
personal data necessary to achieve the
purpose of CAHII. CMS has the
following policies and procedures
concerning disclosures of information
that will be maintained in the system.
Disclosure of information from the SOR
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
data is being collected; e.g., to collect
and maintain information initiated by
consumers complaints/reports to CMS
that their health insurance issuers and/
or non-Federal governmental health
plans are in violation of the PHS;
2. Determines that the purpose for
which the disclosure is to be made can
only be accomplished if the record is
provided in individually identifiable
form;
a. 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
b. 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 of disclosure of the
record;
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b. Remove or destroy at the earliest
time all patient-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. Modified 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 or
consultant 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. Contribute to the accuracy of CMS’s
proper payment of Medicare benefits,
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
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c. Refer a complaint or inquiry with
respect to Title I of the Health Insurance
Portability and Accountability Act of
1996 (HIPAA), the Mental Health Parity
Act of 1996 (MHPA), the Newborns’ and
Mothers’ Health Protection Act of 1996
(NMHPA), and the Women’s Health and
Cancer Rights Act of 1998 (WHCRA).
CAHII shares enforcement
responsibilities with the U.S.
Department of Labor, the U.S.
Department of Treasury and State
regulatory bodies with respect to Title I
of HIPAA, MHPA, NMHPA and
WHCRA. CAHII’s enforcement
responsibilities are discussed in the
‘‘Description of the New System of
Records’’ section above. The
Department of Labor enforces Title I of
HIPAA, MHPA, NMHPA and WHCRA
with respect to private group health
plans. The Department of Treasury may
levy excise taxes against private group
health plans that do not comply with
these Acts, except for WHCRA. In States
that are substantially enforcing Title I of
PHS, MHPA, NMHPA and WHCRA, the
appropriate State agency enforces these
provisions with respect to health
insurance issuers.
Occasionally, CAHII will receive an
inquiry or complaint related to one of
these four Acts in situations where it is
within Labor’s or Treasury’s or a State’s,
and not CAHII’s, jurisdiction to resolve.
In such cases, CAHII must disclose
information from the system of records
to the appropriate agency so they can
perform their enforcement function.
Other Federal or state agencies in
their administration of a Federal health
program may require CAHII information
in order to support evaluations and
monitoring of Medicare claims
information of beneficiaries, including
proper reimbursement for services
provided.
In addition, other state agencies in
their administration of a Federal health
program may require CAHII information
for the purposes of determining,
evaluating and/or assessing cost,
effectiveness, and /or the quality of
health care services provided in the
state.
3. To assist third party contacts in
situations where the party to be
contacted has, or is expected to have
information relating to the individual’s
capacity to manage his or her affairs or
to his or her eligibility for, or an
entitlement to, benefits under the
Medicare program and,
a. The individual is unable to provide
the information being sought (an
individual is considered to be unable to
provide certain types of information
when any of the following conditions
exists: The individual is confined to a
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mental institution, a court of competent
jurisdiction has appointed a guardian to
manage the affairs of that individual, a
court of competent jurisdiction has
declared the individual to be mentally
incompetent, or the individual’s
attending physician has certified that
the individual is not sufficiently
mentally competent to manage his or
her own affairs or to provide the
information being sought, the individual
cannot read or write, cannot afford the
cost of obtaining the information, a
language barrier exist, or the custodian
of the information will not, as a matter
of policy, provide it to the individual),
or
b. The data are needed to establish the
validity of evidence or to verify the
accuracy of information presented by
the individual, and it concerns one or
more of the following: The individual’s
entitlement to benefits under the
Medicare program, the amount of
reimbursement, and in cases in which
the evidence is being reviewed as a
result of suspected fraud and abuse,
program integrity, quality appraisal, or
evaluation and measurement of
activities.
Third parties contacts require CAHII
information in order to provide support
for the individual’s entitlement to
benefits under the Medicare program; to
establish the validity of evidence or to
verify the accuracy of information
presented by the individual, and assist
in the monitoring of Medicare claims
information of beneficiaries, including
proper reimbursement of services
provided.
4. To inform a health insurance issuer
and/or health plan, who has been
named in a complaint and is believed to
be potentially in violation of relevant
portions of the PHS Act.
When individuals file complaints or
inquiries asking CAHII to clarify or
enforce their rights under Title I of the
Health Insurance Portability and
Accountability Act of 1996 (HIPAA), the
Mental Health Parity Act of 1996
(MHPA), the Newborns’ and Mothers’
Health Protection Act of 1996
(NMHPA), and the Women’s Health and
Cancer Rights Act of 1998 (WHCRA),
CAHII often must disclose information
maintained in this system of records to
the individual’s health insurance issuer
or health plan in order for CAHII to
satisfy its statutory charge to enforce
these Federal Acts with respect to nonFederal governmental health plans in all
States and health insurance issuers in
some States.
5. To assist the Department of Justice
(DOJ), court or adjudicatory body when:
a. The Agency or any component
thereof, or
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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.
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.
6. To support a CMS contractor that
assists in the administration of a CMSadministered health benefits program,
or to a grantee of a CMS-administered
grant program, when disclosure is
deemed reasonably necessary by CMS to
prevent, deter, discover, detect,
investigate, examine, prosecute, sue
with respect to, defend against, correct,
remedy, or otherwise combat fraud,
waste or abuse in such programs.
We contemplate disclosing
information under this routine use only
in situations in which CMS may enter
into a contract or grant with a third
party to assist in accomplishing CMS
functions relating to the purpose of
combating fraud, waste or abuse.
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 or grantee whatever
information is necessary for the
contractor or grantee to fulfill its duties.
In these situations, safeguards are
provided in the contract prohibiting the
contractor or grantee from using or
disclosing the information for any
purpose other than that described in the
contract and requiring the contractor or
grantee to return or destroy all
information.
7. To support another Federal agency
or to an instrumentality of any
governmental jurisdiction within or
under the control of the United States
(including any state or local
governmental agency), that administers,
or that has the authority to investigate
potential fraud, waste, or abuse in a
program funded in whole or in part by
Federal funds, when disclosure is
deemed reasonably necessary by CMS to
prevent, deter, discover, detect,
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investigate, examine, prosecute, sue
with respect to, defend against, correct,
remedy, or otherwise combat fraud,
waste or abuse in such programs.
Other agencies may require CAHII
information for the purpose of
combating fraud, waste or abuse in such
Federally-funded programs.
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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
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
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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 or Altered
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: April 12, 2007.
Charlene Frizzera,
Acting Chief Operating Officer Centers for
Medicare & Medicaid Services.
System No. 09–70–0516.
SYSTEM NAME:
• Complaints Against Health
Insurance Issuers and Health Plans
(CAHII),’’ HHS/CMS/CBC.
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive
Data.
SYSTEM LOCATION:
CMS Data Center, 7500 Security
Boulevard, North Building, First Floor,
Baltimore, Maryland 21244–1850 and at
various other contractor locations.
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
This system will collect and maintain
individually identifiable and other data
collected on individuals/consumers
who make complaints/inquiries to CMS
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that their health insurance issuers and/
or non-Federal governmental health
plans are in violation of the PHS ACT.
CATEGORIES OF RECORDS IN THE SYSTEM:
The system contains information such
as consumer’s name, address, phone
number, the name and address of their
health plan or health insurance issuer,
their plan ID number or social security
number, the nature of their complaint/
inquiry against their health plan or
issuer, and any medical and other
additional information that is necessary
for CAHII to help resolve the
consumer’s complaint.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for maintenance of this
system is given under §§ 2722 and 2761
of the Public Health Service (PHS) Act;
the Mental Health Parity Act of 1996
(MHPA); the Newborns’ and Mothers’
Health Protection Act of 1996
(NMHPA); and the Women’s Health and
Cancer Rights Act of 1998 (WHCRA)
with respect to non-Federal
governmental plans.
PURPOSE(S) OF THE SYSTEM:
The primary purpose of this system is
to collect and maintain information
initiated by consumers complaints/
reports to CMS that their health
insurance issuers and/or non-Federal
governmental health plans are in
violation of one or more of the following
statutes: §§ 2722 and 2761 of the Public
Health Service (PHS) Act; the Mental
Health Parity Act of 1996 (MHPA); the
Newborns’ and Mothers’ Health
Protection Act of 1996 (NMHPA); and ,
the Women’s Health and Cancer Rights
Act of 1998 (WHCRA). 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) assist third party contacts in
situations where the party to be
contacted has, or is expected to have
information relating to the individual’s
capacity to manage his or her affairs or
to his or her eligibility for, or an
entitlement to benefits under the
Medicare program; (4) inform a health
insurance issuer and/or health plan who
has been named in a complaint/inquiry
and is believed to be potentially in
violation of relevant portions of the PHS
ACT; (5) support litigation involving the
Agency; and (6) combat fraud, waste,
and abuse in certain health benefits
programs.
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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:
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.
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. Contribute to the accuracy of CMS’s
payment of Medicare benefits,
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. Refer a complaint or with respect to
Title I of the Health Insurance
Portability and Accountability Act of
1996 (HIPAA), the Mental Health Parity
Act of 1996 (MHPA), the Newborns’ and
Mothers’ Health Protection Act of 1996
(NMHPA), and the Women’s Health and
Cancer Rights Act of 1998 (WHCRA).
3. To assist third party contacts in
situations where the party to be
contacted has, or is expected to have
information relating to the individual’s
capacity to manage his or her affairs or
to his or her eligibility for, or an
entitlement to, benefits under the
Medicare program and,
a. The individual is unable to provide
the information being sought (an
individual is considered to be unable to
provide certain types of information
when any of the following conditions
exists: The individual is confined to a
mental institution, a court of competent
jurisdiction has appointed a guardian to
manage the affairs of that individual, a
court of competent jurisdiction has
declared the individual to be mentally
incompetent, or the individual’s
attending physician has certified that
the individual is not sufficiently
mentally competent to manage his or
her own affairs or to provide the
information being sought, the individual
VerDate Aug<31>2005
15:36 May 07, 2007
Jkt 211001
cannot read or write, cannot afford the
cost of obtaining the information, a
language barrier exists, or the custodian
of the information will not, as a matter
of policy, provide it to the individual),
or
b. The data are needed to establish the
validity of evidence or to verify the
accuracy of information presented by
the individual, and it concerns one or
more of the following: The individual’s
entitlement to benefits under the
Medicare program, the amount of
reimbursement, and in cases in which
the evidence is being reviewed as a
result of suspected fraud and abuse,
program integrity, quality appraisal, or
evaluation and measurement of
activities.
4. To inform a health insurance issuer
and/or health plan, who has been
named in a complaint and is believed to
be potentially in violation of relevant
portions of the PHS Act.
5. 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
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.
6. To support a CMS contractor that
assists in the administration of a CMSadministered health benefits program,
or to a grantee of a CMS-administered
grant program, when disclosure is
deemed reasonably necessary by CMS to
prevent, deter, discover, detect,
investigate, examine, prosecute, sue
with respect to, defend against, correct,
remedy, or otherwise combat fraud or
abuse in such programs.
7. To support another Federal agency
or to an instrumentality of any
governmental jurisdiction within or
under the control of the United States
(including any state or local
governmental agency), that administers,
or that has the authority to investigate
potential fraud or abuse in a program
funded in whole or in part by Federal
funds, when disclosure is deemed
reasonably necessary by CMS to
prevent, deter, discover, detect,
investigate, examine, prosecute, sue
with respect to, defend against, correct,
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
26125
remedy, or otherwise combat fraud or
abuse in such programs.
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., consumer’s
name or health insurance claims
number, if, applicable.
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
E:\FR\FM\08MYN1.SGM
08MYN1
26126
Federal Register / Vol. 72, No. 88 / Tuesday, May 8, 2007 / Notices
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 6 years. All claimsrelated records are encompassed by the
document preservation order and will
be retained until notification is received
from DOJ.
SYSTEM MANAGER AND ADDRESS:
Director, Division of Policy, Employer
Policy and Operations Group, Center for
Beneficiary Choices, CMS, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
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)).
cprice-sewell on PROD1PC66 with NOTICES
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).
15:36 May 07, 2007
The data collected and maintained in
this system are retrieved from
individuals/consumers who file
complaints/reports to CMS that their
health insurance issuers and/or nonFederal governmental health plans are
in violation of the PHS ACT.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
[FR Doc. E7–8757 Filed 5–7–07; 8:45 am]
BILLING CODE 4120–03–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
RETENTION AND DISPOSAL:
VerDate Aug<31>2005
RECORDS SOURCE CATEGORIES:
Jkt 211001
Privacy Act of 1974; Report of a
Modified System of Records
Department of Health and
Human Services (HHS), Center for
Medicare & Medicaid Services (CMS).
ACTION: Notice of a Modified System of
Records (SOR).
AGENCY:
SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
we are proposing to modify or alter a
system titled, ‘‘End Stage Renal Disease
(ESRD) Program Management and
Medical Information System (PMMIS),
System No. 09–70–0520,’’ and last
modified at 67 Fed. Reg. 41244 (June 17,
2002). This system contains records on
individuals with ESRD who are entitled
to receive Medicare benefits or who are
treated by Department of Veteran Affairs
(DVA) health care facilities. We propose
to modify existing routine use number
1 that permits disclosure to agency
contractors and consultants to include
disclosure to CMS grantees who perform
a task for the agency. The modified
routine use will remain as routine use
number 1. For further clarity, we
propose to separate existing routine use
number 3 that permit disclosures to
ESRD Network Organizations and to
Quality Improvement Organizations into
separate routine uses. The activities
performed by the 2 different type
organizations are not so closely related
that they should be combined in one
routine use. The modified routine use
will be republished as routine use
number 3 for ESRD Network
Organizations and routine use number 4
for Quality Improvement Organizations.
We will delete routine use number 5
authorizing disclosure to support
constituent requests made to a
congressional representative. If an
authorization for the disclosure has
been obtained from the data subject,
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
then no routine use is needed. The
Privacy Act allows for disclosures with
the ‘‘prior written consent’’ of the data
subject.
We propose to broaden the scope of
the disclosure provisions of this system
by adding a routine use to permit the
release of priority personal information
to complete a transfer out event from a
losing ESRD facility and/or a transfer-in
event to a gaining ESRD facility to: (1)
Contribute to the accuracy of CMS’
proper payment of Medicare benefits;
and (2) enable such facilities to ensure
the proper transfer of health records,
and/or as necessary to enable such a
facility 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; (3) assist ESRD programs which
may require PMMIS information for
purposes related to this system.
Information will be released to these
organizations upon specific request, and
only for those organizations if they meet
the following requirements: (1) Provide
an attestation or other qualifying
information that they are providing
assistance to qualified ESRD
beneficiaries; (2) submit a report of the
transfer-in or transfer-out event; (3)
safeguard the confidentiality of the data
and prevent unauthorized access; and
(4) complete a written statement
attesting to the information recipient’s
understanding of and willingness to
abide by these provisions. The PMMIS
data will provide the ESRD facility with
information regarding its enrollees’
enrollment status, transplant activities,
dialysis activities, and Medicare
utilization; facilitate the facility’s
required utilization reviews and
medication management program
activities; and assist in quality of care
issues as they relate to the beneficiary.
The added routine use will be
numbered as routine use number 6.
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 individualspecific 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.
E:\FR\FM\08MYN1.SGM
08MYN1
Agencies
[Federal Register Volume 72, Number 88 (Tuesday, May 8, 2007)]
[Notices]
[Pages 26121-26126]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-8757]
-----------------------------------------------------------------------
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, CMS is proposing to modify or alter existing system of records
titled ``Complaints Against Health Insurance Issuers and Health Plans
(CAHII),'' System No. 09-70-9005, established at 66 FR 9858, (February
12, 2001). 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. 09-70-0516.
We propose to modify existing routine use number 1 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 remain as routine use
number 1. We will delete routine use number 2 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. The Privacy Act allows for
disclosures with the ``prior written consent'' of the data subject.
We propose to add 2 new routine uses authorizing disclosure to
support a CMS contractor, consultant, or a grantee of a CMS-
administered grant program, when disclosure is deemed reasonably
necessary by CMS to combat fraud, waste, and abuse in certain health
care programs. The new routine use will be published as routine use
number 6. We will add a second new routine use to support another
Federal agency or to an instrumentality of any governmental
jurisdiction within or under the control of the United States, when
disclosure is deemed reasonably necessary by CMS to combat fraud,
waste, and abuse in certain health care programs. This new routine use
will be published as routine use number 7. 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 when ever the system collects
or maintain 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 this system is to collect and maintain
information initiated by consumers complaints/reports to CMS that their
health insurance issuers and/or non-Federal governmental health plans
are in violation of one or more of the following statutes: Sec. Sec.
2722 and 2761 of the Public Health Service (PHS) Act; the Mental Health
Parity Act of 1996 (MHPA); the Newborns' and Mothers' Health Protection
Act of 1996 (NMHPA); and, the Women's Health and Cancer Rights Act of
1998 (WHCRA). 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) assist third party contacts in situations where the party to be
contacted has, or is expected to have information relating to the
individual's capacity to manage his or her affairs or to his or her
eligibility for, or an entitlement to benefits under the Medicare
program; (4) inform a health insurance issuer and/or health plan who
has been named in a complaint/inquiry and is believed to be potentially
in violation of relevant portions of the PHS; (5) support litigation
involving the Agency; and (6) combat fraud, waste, and abuse in certain
health benefits programs. We have provided background information about
this 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
[[Page 26122]]
all portions of this notice. See ``Effective Dates'' section for
comment period.
DATES: Effective Dates: CMS filed a new system report with the Chair of
the House Committee on Government Reform and Oversight, the Chair of
the Senate Committee on Homeland Security and Governmental Affairs, and
the Administrator, Office of Information and Regulatory Affairs, Office
of Management and Budget (OMB) on April 12, 2007. To ensure that all
parties have adequate time in which to comment, the new SOR, including
routine uses, will become effective 40 days from the publication of the
notice, or from the date it was submitted to OMB and the 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 21244-1850. 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 Mlawsky, Health Insurance
Specialist, Division of Employer Operations, Employer Policy and
Operations Group, Center for Beneficiary Choices, CMS, 7500 Security
Boulevard, Mail Stop S3-16-26, Baltimore, Maryland 21244-1850. The
telephone number is 410-786-6851 or e-mail david.mlawsky@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 Sec. Sec.
2722 and 2761 of the Public Health Service (PHS) Act; the Mental Health
Parity Act of 1996 (MHPA); the Newborns' and Mothers' Health Protection
Act of 1996 (NMHPA); and the Women's Health and Cancer Rights Act of
1998 (WHCRA) with respect to non-Federal governmental plans.
B. Collection and Maintenance of Data in the System
This system will collect and maintain individually identifiable and
other data collected on individuals/consumers who make complaints/
inquiries to CMS that their health insurance issuers and/or non-Federal
governmental health plans are in violation of the PHS.
The system contains information such as consumer's name, address,
phone number, the name and address of their health plan or health
insurance issuer, their plan ID number or social security number, the
nature of their complaint/inquiry against their health plan or issuer,
and any medical and other additional information that is necessary for
CAHII to help resolve the consumer's complaint.
II. Agency Policies, Procedures, and Restrictions on the Routine Use
A. 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 CAHII information that can be
associated with an individual as provided for under ``Section III.
Proposed Routine Use Disclosures of Data in the System.'' Both
identifiable and non-identifiable data may be disclosed under a routine
use.
We will only collect the minimum personal data necessary to achieve
the purpose of CAHII. CMS has the following policies and procedures
concerning disclosures of information that will be maintained in the
system. Disclosure of information from the SOR 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 data is being collected; e.g., to collect and maintain
information initiated by consumers complaints/reports to CMS that their
health insurance issuers and/or non-Federal governmental health plans
are in violation of the PHS;
2. Determines that the purpose for which the disclosure is to be
made can only be accomplished if the record is provided in individually
identifiable form;
a. 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
b. 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 of disclosure of the record;
b. Remove or destroy at the earliest time all patient-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. Modified 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 or consultant 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. Contribute to the accuracy of CMS's proper payment of Medicare
benefits,
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
[[Page 26123]]
c. Refer a complaint or inquiry with respect to Title I of the
Health Insurance Portability and Accountability Act of 1996 (HIPAA),
the Mental Health Parity Act of 1996 (MHPA), the Newborns' and Mothers'
Health Protection Act of 1996 (NMHPA), and the Women's Health and
Cancer Rights Act of 1998 (WHCRA).
CAHII shares enforcement responsibilities with the U.S. Department
of Labor, the U.S. Department of Treasury and State regulatory bodies
with respect to Title I of HIPAA, MHPA, NMHPA and WHCRA. CAHII's
enforcement responsibilities are discussed in the ``Description of the
New System of Records'' section above. The Department of Labor enforces
Title I of HIPAA, MHPA, NMHPA and WHCRA with respect to private group
health plans. The Department of Treasury may levy excise taxes against
private group health plans that do not comply with these Acts, except
for WHCRA. In States that are substantially enforcing Title I of PHS,
MHPA, NMHPA and WHCRA, the appropriate State agency enforces these
provisions with respect to health insurance issuers.
Occasionally, CAHII will receive an inquiry or complaint related to
one of these four Acts in situations where it is within Labor's or
Treasury's or a State's, and not CAHII's, jurisdiction to resolve. In
such cases, CAHII must disclose information from the system of records
to the appropriate agency so they can perform their enforcement
function.
Other Federal or state agencies in their administration of a
Federal health program may require CAHII information in order to
support evaluations and monitoring of Medicare claims information of
beneficiaries, including proper reimbursement for services provided.
In addition, other state agencies in their administration of a
Federal health program may require CAHII information for the purposes
of determining, evaluating and/or assessing cost, effectiveness, and /
or the quality of health care services provided in the state.
3. To assist third party contacts in situations where the party to
be contacted has, or is expected to have information relating to the
individual's capacity to manage his or her affairs or to his or her
eligibility for, or an entitlement to, benefits under the Medicare
program and,
a. The individual is unable to provide the information being sought
(an individual is considered to be unable to provide certain types of
information when any of the following conditions exists: The individual
is confined to a mental institution, a court of competent jurisdiction
has appointed a guardian to manage the affairs of that individual, a
court of competent jurisdiction has declared the individual to be
mentally incompetent, or the individual's attending physician has
certified that the individual is not sufficiently mentally competent to
manage his or her own affairs or to provide the information being
sought, the individual cannot read or write, cannot afford the cost of
obtaining the information, a language barrier exist, or the custodian
of the information will not, as a matter of policy, provide it to the
individual), or
b. The data are needed to establish the validity of evidence or to
verify the accuracy of information presented by the individual, and it
concerns one or more of the following: The individual's entitlement to
benefits under the Medicare program, the amount of reimbursement, and
in cases in which the evidence is being reviewed as a result of
suspected fraud and abuse, program integrity, quality appraisal, or
evaluation and measurement of activities.
Third parties contacts require CAHII information in order to
provide support for the individual's entitlement to benefits under the
Medicare program; to establish the validity of evidence or to verify
the accuracy of information presented by the individual, and assist in
the monitoring of Medicare claims information of beneficiaries,
including proper reimbursement of services provided.
4. To inform a health insurance issuer and/or health plan, who has
been named in a complaint and is believed to be potentially in
violation of relevant portions of the PHS Act.
When individuals file complaints or inquiries asking CAHII to
clarify or enforce their rights under Title I of the Health Insurance
Portability and Accountability Act of 1996 (HIPAA), the Mental Health
Parity Act of 1996 (MHPA), the Newborns' and Mothers' Health Protection
Act of 1996 (NMHPA), and the Women's Health and Cancer Rights Act of
1998 (WHCRA), CAHII often must disclose information maintained in this
system of records to the individual's health insurance issuer or health
plan in order for CAHII to satisfy its statutory charge to enforce
these Federal Acts with respect to non-Federal governmental health
plans in all States and health insurance issuers in some States.
5. 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 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.
6. To support a CMS contractor that assists in the administration
of a CMS-administered health benefits program, or to a grantee of a
CMS-administered grant program, when disclosure is deemed reasonably
necessary by CMS to prevent, deter, discover, detect, investigate,
examine, prosecute, sue with respect to, defend against, correct,
remedy, or otherwise combat fraud, waste or abuse in such programs.
We contemplate disclosing information under this routine use only
in situations in which CMS may enter into a contract or grant with a
third party to assist in accomplishing CMS functions relating to the
purpose of combating fraud, waste or abuse.
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 or grantee whatever information is necessary
for the contractor or grantee to fulfill its duties. In these
situations, safeguards are provided in the contract prohibiting the
contractor or grantee from using or disclosing the information for any
purpose other than that described in the contract and requiring the
contractor or grantee to return or destroy all information.
7. To support another Federal agency or to an instrumentality of
any governmental jurisdiction within or under the control of the United
States (including any state or local governmental agency), that
administers, or that has the authority to investigate potential fraud,
waste, or abuse in a program funded in whole or in part by Federal
funds, when disclosure is deemed reasonably necessary by CMS to
prevent, deter, discover, detect,
[[Page 26124]]
investigate, examine, prosecute, sue with respect to, defend against,
correct, remedy, or otherwise combat fraud, waste or abuse in such
programs.
Other agencies may require CAHII information for the purpose of
combating fraud, waste or abuse in such Federally-funded programs.
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 or Altered 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: April 12, 2007.
Charlene Frizzera,
Acting Chief Operating Officer Centers for Medicare & Medicaid
Services.
System No. 09-70-0516.
System Name:
Complaints Against Health Insurance Issuers and Health
Plans (CAHII),'' HHS/CMS/CBC.
Security Classification:
Level Three Privacy Act Sensitive Data.
System Location:
CMS Data Center, 7500 Security Boulevard, North Building, First
Floor, Baltimore, Maryland 21244-1850 and at various other contractor
locations.
Categories of Individuals Covered by the System:
This system will collect and maintain individually identifiable and
other data collected on individuals/consumers who make complaints/
inquiries to CMS that their health insurance issuers and/or non-Federal
governmental health plans are in violation of the PHS ACT.
Categories of Records in the System:
The system contains information such as consumer's name, address,
phone number, the name and address of their health plan or health
insurance issuer, their plan ID number or social security number, the
nature of their complaint/inquiry against their health plan or issuer,
and any medical and other additional information that is necessary for
CAHII to help resolve the consumer's complaint.
Authority for Maintenance of the System:
Authority for maintenance of this system is given under Sec. Sec.
2722 and 2761 of the Public Health Service (PHS) Act; the Mental Health
Parity Act of 1996 (MHPA); the Newborns' and Mothers' Health Protection
Act of 1996 (NMHPA); and the Women's Health and Cancer Rights Act of
1998 (WHCRA) with respect to non-Federal governmental plans.
Purpose(s) of the System:
The primary purpose of this system is to collect and maintain
information initiated by consumers complaints/reports to CMS that their
health insurance issuers and/or non-Federal governmental health plans
are in violation of one or more of the following statutes: Sec. Sec.
2722 and 2761 of the Public Health Service (PHS) Act; the Mental Health
Parity Act of 1996 (MHPA); the Newborns' and Mothers' Health Protection
Act of 1996 (NMHPA); and , the Women's Health and Cancer Rights Act of
1998 (WHCRA). 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) assist third party contacts in situations where the party to be
contacted has, or is expected to have information relating to the
individual's capacity to manage his or her affairs or to his or her
eligibility for, or an entitlement to benefits under the Medicare
program; (4) inform a health insurance issuer and/or health plan who
has been named in a complaint/inquiry and is believed to be potentially
in violation of relevant portions of the PHS ACT; (5) support
litigation involving the Agency; and (6) combat fraud, waste, and abuse
in certain health benefits programs.
[[Page 26125]]
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:
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.
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. Contribute to the accuracy of CMS's payment of Medicare
benefits,
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. Refer a complaint or with respect to Title I of the Health
Insurance Portability and Accountability Act of 1996 (HIPAA), the
Mental Health Parity Act of 1996 (MHPA), the Newborns' and Mothers'
Health Protection Act of 1996 (NMHPA), and the Women's Health and
Cancer Rights Act of 1998 (WHCRA).
3. To assist third party contacts in situations where the party to
be contacted has, or is expected to have information relating to the
individual's capacity to manage his or her affairs or to his or her
eligibility for, or an entitlement to, benefits under the Medicare
program and,
a. The individual is unable to provide the information being sought
(an individual is considered to be unable to provide certain types of
information when any of the following conditions exists: The individual
is confined to a mental institution, a court of competent jurisdiction
has appointed a guardian to manage the affairs of that individual, a
court of competent jurisdiction has declared the individual to be
mentally incompetent, or the individual's attending physician has
certified that the individual is not sufficiently mentally competent to
manage his or her own affairs or to provide the information being
sought, the individual cannot read or write, cannot afford the cost of
obtaining the information, a language barrier exists, or the custodian
of the information will not, as a matter of policy, provide it to the
individual), or
b. The data are needed to establish the validity of evidence or to
verify the accuracy of information presented by the individual, and it
concerns one or more of the following: The individual's entitlement to
benefits under the Medicare program, the amount of reimbursement, and
in cases in which the evidence is being reviewed as a result of
suspected fraud and abuse, program integrity, quality appraisal, or
evaluation and measurement of activities.
4. To inform a health insurance issuer and/or health plan, who has
been named in a complaint and is believed to be potentially in
violation of relevant portions of the PHS Act.
5. 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 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.
6. To support a CMS contractor that assists in the administration
of a CMS-administered health benefits program, or to a grantee of a
CMS-administered grant program, when disclosure is deemed reasonably
necessary by CMS to prevent, deter, discover, detect, investigate,
examine, prosecute, sue with respect to, defend against, correct,
remedy, or otherwise combat fraud or abuse in such programs.
7. To support another Federal agency or to an instrumentality of
any governmental jurisdiction within or under the control of the United
States (including any state or local governmental agency), that
administers, or that has the authority to investigate potential fraud
or abuse in a program funded in whole or in part by Federal funds, when
disclosure is deemed reasonably necessary by CMS to prevent, deter,
discover, detect, investigate, examine, prosecute, sue with respect to,
defend against, correct, remedy, or otherwise combat fraud or abuse in
such programs.
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.,
consumer's name or health insurance claims number, if, applicable.
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
[[Page 26126]]
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 6
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, Division of Policy, Employer Policy and Operations Group,
Center for Beneficiary Choices, CMS, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
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:
The data collected and maintained in this system are retrieved from
individuals/consumers who file complaints/reports to CMS that their
health insurance issuers and/or non-Federal governmental health plans
are in violation of the PHS ACT.
Systems Exempted from Certain Provisions of the Act:
None.
[FR Doc. E7-8757 Filed 5-7-07; 8:45 am]
BILLING CODE 4120-03-P