Health Insurance Reform; Announcement of Maintenance Changes to Electronic Data Transaction Standards Adopted Under the Health Insurance Portability and Accountability Act of 1996, 62684-62686 [2010-25684]
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62684
Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Rules and Regulations
§ 416.1002
Definitions.
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Compassionate allowance means a
determination or decision we make
under a process that identifies for
expedited handling claims that involve
impairments that invariably qualify
under the Listing of Impairments in
appendix 1 to subpart P of part 404 of
this chapter based on minimal, but
sufficient, objective medical evidence.
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■ 19. Amend § 416.1015 by revising the
introductory text of paragraph (c),
removing the word ‘‘or’’ at the end of
paragraph (c)(2), redesignating
paragraph (c)(3) as paragraph (c)(4), and
adding a new paragraph (c)(3) to read as
follows:
§ 416.1015 Making disability
determinations.
medical and nonmedical evidence in
the file.
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(c) If the quick disability
determination examiner cannot make a
determination that is fully favorable, or
if there is an unresolved disagreement
between the disability examiner and the
medical or psychological consultant
(except when a disability examiner
makes the determination alone under
§ 416.1015(c)(3)), the State agency will
adjudicate the claim using the regularly
applicable procedures in this subpart.
[FR Doc. 2010–25502 Filed 10–12–10; 8:45 am]
BILLING CODE 4191–02–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
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(c) Disability determinations will be
made by:
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(3) A State agency disability examiner
alone if you are not a child (a person
who has not attained age 18), and the
claim is adjudicated under the quick
disability determination process (see
§ 416.1019) or as a compassionate
allowance (see § 416.1002), and the
initial or reconsidered determination is
fully favorable to you. This paragraph
will no longer be effective on November
12, 2013 unless we terminate it earlier
or extend it beyond that date by
publication of a final rule in the Federal
Register; or
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■ 20. Amend § 416.1019 by revising
paragraphs (b) introductory text, (b)(1),
(b)(2), and (c) to read as follows:
§ 416.1019
process.
Quick disability determination
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(b) If we refer a claim to the State
agency for a quick disability
determination, a designated quick
disability determination examiner must
do all of the following:
(1) Subject to the provisions in
paragraph (c) of this section, make the
disability determination after consulting
with a State agency medical or
psychological consultant if the State
agency disability examiner determines
consultation is appropriate or if
consultation is required under
§ 416.926(c). The State agency may
certify the disability determination
forms to us without the signature of the
medical or psychological consultant.
(2) Make the quick disability
determination based only on the
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45 CFR Part 162
[CMS–0009–N]
RIN 0938–AM50
Health Insurance Reform;
Announcement of Maintenance
Changes to Electronic Data
Transaction Standards Adopted Under
the Health Insurance Portability and
Accountability Act of 1996
Office of the Secretary, HHS.
Notification.
AGENCY:
ACTION:
This document announces
maintenance changes to some of the
Health Insurance Portability and
Accountability Act of 1996 standards
made by the Designated Standard
Maintenance Organizations. The
maintenance changes are nonsubstantive changes to correct minor
errors, such as typographical errors, or
to provide clarifications of the standards
adopted in our regulations entitled
‘‘Health Insurance Reform;
Modifications to the Health Insurance
Portability and Accountability Act
(HIPAA) Electronic Transaction
Standards,’’ published in the Federal
Register on January 16, 2009. This
document also instructs interested
persons on how to obtain the
corrections.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Denise Buenning, (410) 786–6711
Gladys Wheeler, (410) 786–0273
SUPPLEMENTARY INFORMATION:
I. Background
The Health Insurance Portability and
Accountability Act of 1996 (HIPAA)
mandated the adoption of standards for
electronically conducting certain health
PO 00000
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Fmt 4700
Sfmt 4700
care administrative transactions
between certain entities. Through
subtitle F of title II of HIPAA, the
Congress added to title XI of the Social
Security Act (the Act) a new Part C,
entitled ‘‘Administrative
Simplification.’’ Part C of title XI of the
Act consists of sections 1171 through
1180. These sections define various
terms and impose several requirements
on the Department of Health & Human
Services (HHS), health plans, health
care clearinghouses, and certain health
care providers concerning the electronic
transmission of health information.
On August 17, 2000, we published a
final rule in the Federal Register (65 FR
50312) entitled ‘‘Health Insurance
Reform: Standards for Electronic
Transactions’’ (hereinafter referred to as
the Transactions and Code Sets rule).
That rule implemented some of the
HIPAA Administrative Simplification
requirements by adopting standards
developed by standard setting
organizations (SSOs) for eight electronic
transactions, and code sets to be used in
those transactions. The SSOs are
organizations that are accredited by the
American National Standards Institute
(ANSI), and that develop industry
standards for, among others, the HIPAA
transactions. We adopted standards
developed by the Accredited Standards
Committee X12 (hereinafter referred to
as ASC X12) and the National Council
for Prescription Drug Programs
(NCPDP). We defined those transactions
and specified the adopted standards at
45 CFR part 162, subparts I and K
through R. Designated Standard
Maintenance Organizations (DSMOs)
receive, manage, and process requested
changes to the adopted standards in
accordance with the process identified
in the HIPAA regulations at § 162.900.
A description of the DSMO process can
be found in the May 31, 2002 proposed
rule (67 FR 38050). Both ASC X12 and
NCPDP are DSMOs.
On August 22, 2008, we published a
proposed rule in the Federal Register
(73 FR 49742) entitled ‘‘Health
Insurance Reform: Modifications to
Electronic Data Transactions Standards
and Code Sets’’ (hereinafter referred to
as the Modifications proposed rule)
proposing to modify the HIPAA
transaction standards by adopting
updated versions of the standards. On
January 16, 2009, we published a final
rule in the Federal Register (74 FR
3296) entitled Health Insurance Reform;
Modifications to the Health Insurance
Portability and Accountability Act
(HIPAA) Electronic Transaction
Standards (hereinafter referred to as the
Modifications final rule), that adopted
updated versions of the standards for
E:\FR\FM\13OCR1.SGM
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Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Rules and Regulations
the electronic transactions originally
adopted under HIPAA. We refer readers
to the regulations cited above for a
detailed discussion of the standards for
electronic transactions and information
about electronic data interchange, the
statutory background, and the regulatory
history.
In the Transactions and Code Sets
rule, we defined the terms
‘‘modification’’ and ‘‘maintenance of
standards.’’ We explained that, when a
change is substantial enough to justify
publication of a new version of an
implementation specification, such
change is considered a modification,
and must be adopted by the Secretary
through regulation (65 FR 50322).
Maintenance, on the other hand,
describes the activities necessary to
support the use of a standard, including
technical corrections to an
implementation specification.
Maintenance changes are typically
changes that are obvious to readers of
the implementation guides, are not
controversial, and are essential to
implementation (68 FR 8388, (February
20, 2003)). We note that regulatory
action is not required to make
maintenance type changes to the HIPAA
adopted standards (65 FR 50322).
II. Provisions of the Notification
A. ASC X12 Version 5010 HIPAA
Transaction Standards
We adopted ASC X12 standards for
the following eight HIPAA
administrative transactions: (1) Health
care claims or equivalent encounter
information; (2) health care payment
and remittance advice; (3) coordination
of benefits; (4) eligibility for a health
plan; (5) health care claim status;
(6) enrollment and disenrollment in a
health plan; (7) referral certification and
authorization; and (8) health plan
premium payments. In the January 16,
2009 Modifications final rule, we
adopted the ASC X12 Technical Reports
Type 3, Version 005010 (hereinafter
referred to as Version 5010) to replace
the currently adopted Version 4010/
4010A1 standard for the eight HIPAA
transactions (74 FR 3296).
jdjones on DSK8KYBLC1PROD with RULES
1. Errata Notification
Following publication of the
Modifications final rule, ASC X12
notified HHS that they were receiving
feedback from the industry regarding
errors that had been overlooked during
ASC X12 standards review process.
These errors were not identified in the
comments submitted during the public
comment period for the Modifications
proposed rule, and therefore are not
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14:59 Oct 12, 2010
Jkt 223001
reflected in the Version 5010 standards
adopted in the Modifications final rule.
After the industry reported these
errors, ASC X12 compiled a summary
and in February 2010 as required under
the DSMO process, initiated
consultations with HHS and the
National Committee on Vital and Health
Statistics (NCVHS), an advisory body to
HHS on health data, statistics and
national health information policy. (For
a complete discussion of this NCVHS
process, we refer readers to the August
22, 2008 proposed rule (73 FR 49742).
ASC X12 then balloted and completed
approval for these changes to the
Version 5010 standards in accordance
with the established ASC X12 approval
process, in July 2010.
2. Errata Classification
ASC X12 issued errata to Version
5010 in July 2010. It has categorized the
errata as both Type 1 and Type 2. These
errata constitute maintenance changes
under the HIPAA regulations, not
modifications. The ASC X12 defines
errata as: (1) Publication variances from
approved X12 Committee actions
(publication errors); or (2) editorial
corrections such as spelling,
punctuation, spelling out abbreviations
or acronyms.
ASC X12 further defines Type 1 and
Type 2 errata as follows:
• Type 1 Errata change the
constraints of the base standard, but do
not change the base standard itself. The
sender and receiver must implement the
Type I Errata in order to conduct a
successful interchange.
• Type 2 Errata supplement a
published Technical Report Type 3
(TR3) with minor changes that clarify or
correct the TR3 Report. Implementation
Guide constraints are not changed, and
the sender and the receiver do not have
to implement the errata to conduct a
successful interchange.
Neither Type 1 or Type 2 Errata can
change the underlying base ASC X12
transaction standard or associated
internal code sets (https://www.x12.org/
newsletters/tr/index.cfm).
3. Errata Distribution
The errors that were identified by the
industry, and ASC X12’s balloted and
approved response that was completed
July 2010, are contained in the errata
posted to the ASC X12 Web site, at
https://www.x12.org, and are available
free of charge for purchasers of Version
5010. In the interest of broad
stakeholder outreach, CMS also posted
a link for the ASC X12 errata to its Web
site, at https://cms.gov/ICD10.
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62685
B. NCPDP Telecommunication Standard
D.0
We adopted NCPDP standards for the
following retail pharmacy drug
transactions: Health care claims or
equivalent encounter information;
eligibility for a health plan; referral
certification and authorization,
coordination of benefits; and Medicaid
pharmacy subrogation. In the
Modifications final rule, we adopted the
NCPDP Telecommunications Standard
Implementation Guide, Version D,
Release 0 (Version D.0) and equivalent
NCPDP Batch Standard Implementation
Guide, Version 1, Release 2 (Version
1.2) in place of the NCPDP
Telecommunication Standard
Implementation Guide, Version 5,
Release 1 (Version 5.1) and equivalent
NCPDP Batch Standard Implementation
Guide, Version 1, Release 1 (Version
1.1), for the HIPAA retail pharmacy
drug transactions.
1. Change Notification
Following publication of the
Modifications final rule, NCPDP and
industry stakeholders notified HHS that
corrections were needed for errors in
Version D.0 that had been either
unintended mistakes or overlooked
during the NCPDP standards review
process. Those errors were not
identified in the comments submitted
during the public comment period for
the Modifications proposed rule, and
therefore are not reflected in the
standards adopted in the Modifications
final rule.
After the industry reported these
errors, NCPDP compiled a summary of
the needed corrections and their
proposed remedies, and in April 2010
initiated consultations with HHS and
the NCVHS. NCPDP balloted the
changes and approved them, in
accordance with the established NCPDP
approval process, in August 2010. Each
of the error corrections to Version D.0
are maintenance changes, as that term is
defined under the HIPAA regulations.
2. NCPDP Change Distribution
The errors that were identified by the
industry, and NCPDP’s balloted and
approved response that was completed
in August 2010, are contained in the
August 2010 publication of NCPDP
Editorial Document posted to the
NCPDP Web site, at https://
www.ncpdp.org. The publication of the
changes is available free of charge for
purchasers of Version D.0. In the
interest of broad stakeholder outreach,
CMS also posted a link for the NCPDP
August 2010 Editorial Document to its
Web site, at https://cms.gov/ICD10.
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Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Rules and Regulations
It is important that HIPAA covered
entities, vendors, and third party billers
obtain the ASC X12 Version 5010 and
the NCPDP Version D.0 error corrections
and include them in their
implementation of Version 5010 and
Version D.0 standards. It should be
noted that the HIPAA compliant
versions include the error corrections.
The Version 5010 and Version D.0
HIPAA compliant standards should be
incorporated into systems as soon as
possible. There is urgency for entities to
do so quickly in light of the HHSspecified Version 5010 and Version D.0
January 1, 2011 testing date and the
January 2012 implementation date. In
addition, adhering to these time frames
is critical for meeting the requirements
to implement Version 5010 and Version
D.0 prior to the October 2013
implementation date for the ICD–10
code set.
The ASC X12 Standards for Electronic
Data Interchange Technical Report Type
3 and Errata may be obtained from the
ASC X12, 7600 Leesburg Pike, Suite
430, Falls Church, VA 22043; Telephone
(703) 970–4480; Fax: (703) 970 4488.
They also are available through the
Internet at https://www.X12.org.
The implementation specifications
and the NCPDP D.0 Editorial Document
may be obtained from the National
Council for Prescription Drug programs,
9240 East Raintree Drive, Scottsdale, AZ
85260; Telephone (480) 477–1000; Fax:
(480) 767–1042. They are also available
through the Internet at https://
www.ncpdp.org.
III. Collection of Information
Requirements
This document does not impose
information collection and
recordkeeping requirements.
Consequently, it need not be reviewed
by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995.
jdjones on DSK8KYBLC1PROD with RULES
(Catalog of Federal Domestic Assistance
Program No. 93.778, Medical Assistance
Program; No. 93.773 Medicare—Hospital
Insurance Program; and No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Approved: October 6, 2010.
Kathleen Sebelius,
Secretary.
[FR Doc. 2010–25684 Filed 10–8–10; 11:15 am]
BILLING CODE 4150–29–P
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
45 CFR Part 170
RIN 0991–AB76
Health Information Technology:
Revisions to Initial Set of Standards,
Implementation Specifications, and
Certification Criteria for Electronic
Health Record Technology
Office of the National
Coordinator for Health Information
Technology (ONC), Department of
Health and Human Services.
ACTION: Interim final rule with request
for comments.
AGENCY:
The Department of Health and
Human Services (HHS) is issuing this
interim final rule with a request for
comment to remove the implementation
specifications related to public health
surveillance.
SUMMARY:
Effective Date: This interim final
rule is effective October 13, 2010.
Comment Date: To be assured
consideration, written or electronic
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on November 12, 2010.
ADDRESSES: Because of staff and
resource limitations, we cannot accept
comments by facsimile (FAX)
transmission. You may submit
comments, identified by RIN 0991–
AB76, by any of the following methods
(please do not submit duplicate
comments).
• Federal eRulemaking Portal: Follow
the instructions for submitting
comments. Attachments should be in
Microsoft Word, WordPerfect, or Excel;
however, we prefer Microsoft Word.
https://www.regulations.gov.
• Regular, Express, or Overnight Mail:
Department of Health and Human
Services, Office of the National
Coordinator for Health Information
Technology, Attention: Steven Posnack,
Hubert H. Humphrey Building, Suite
729D, 200 Independence Ave., SW.,
Washington, DC 20201. Please submit
one original and two copies.
• Hand Delivery or Courier: Office of
the National Coordinator for Health
Information Technology, Attention:
Steven Posnack, Hubert H. Humphrey
Building, Suite 729D, 200 Independence
Ave., SW., Washington, DC 20201.
Please submit one original and two
copies. (Because access to the interior of
the Hubert H. Humphrey Building is not
readily available to persons without
federal government identification,
DATES:
PO 00000
Frm 00012
Fmt 4700
Sfmt 4700
commenters are encouraged to leave
their comments in the mail drop slots
located in the main lobby of the
building.)
Inspection of Public Comments: All
comments received before the close of
the comment period will be available for
public inspection, including any
personally identifiable or confidential
business information that is included in
a comment. Please do not include
anything in your comment submission
that you do not wish to share with the
general public. Such information
includes, but is not limited to: A
person’s social security number; date of
birth; driver’s license number; state
identification number or foreign country
equivalent; passport number; financial
account number; credit or debit card
number; any personal health
information; or any business
information that could be considered to
be proprietary. We will post all
comments received before the close of
the comment period at https://
www.regulations.gov.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.regulations.gov or U.S. Department
of Health and Human Services, Office of
the National Coordinator for Health
Information Technology, Hubert H.
Humphrey Building, Suite 729D, 200
Independence Ave., SW., Washington,
DC 20201 (call ahead to the contact
listed below to arrange for inspection).
FOR FURTHER INFORMATION CONTACT:
Steven Posnack, Director, Federal Policy
Division, Office of Policy and Planning,
Office of the National Coordinator for
Health Information Technology, 202–
690–7151.
SUPPLEMENTARY INFORMATION:
Acronyms
ARRA American Recovery and
Reinvestment Act of 2009
CDC Centers for Disease Control and
Prevention
CFR Code of Federal Regulations
EHR Electronic Health Record
HHS Department of Health and Human
Services
HIT Health Information Technology
HITECH Health Information Technology for
Economic and Clinical Health
HL7 Health Level Seven
NAICS North American Industry
Classification System
OMB Office of Management and Budget
ONC Office of the National Coordinator for
Health Information Technology
ONC–ATCB ONC-Authorized Testing and
Certification Body
PHSA Public Health Service Act
RFA Regulatory Flexibility Act
RIA Regulatory Impact Analysis
UMRA Unfunded Mandates Reform Act of
1995
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Agencies
[Federal Register Volume 75, Number 197 (Wednesday, October 13, 2010)]
[Rules and Regulations]
[Pages 62684-62686]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-25684]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
45 CFR Part 162
[CMS-0009-N]
RIN 0938-AM50
Health Insurance Reform; Announcement of Maintenance Changes to
Electronic Data Transaction Standards Adopted Under the Health
Insurance Portability and Accountability Act of 1996
AGENCY: Office of the Secretary, HHS.
ACTION: Notification.
-----------------------------------------------------------------------
SUMMARY: This document announces maintenance changes to some of the
Health Insurance Portability and Accountability Act of 1996 standards
made by the Designated Standard Maintenance Organizations. The
maintenance changes are non-substantive changes to correct minor
errors, such as typographical errors, or to provide clarifications of
the standards adopted in our regulations entitled ``Health Insurance
Reform; Modifications to the Health Insurance Portability and
Accountability Act (HIPAA) Electronic Transaction Standards,''
published in the Federal Register on January 16, 2009. This document
also instructs interested persons on how to obtain the corrections.
FOR FURTHER INFORMATION CONTACT:
Denise Buenning, (410) 786-6711
Gladys Wheeler, (410) 786-0273
SUPPLEMENTARY INFORMATION:
I. Background
The Health Insurance Portability and Accountability Act of 1996
(HIPAA) mandated the adoption of standards for electronically
conducting certain health care administrative transactions between
certain entities. Through subtitle F of title II of HIPAA, the Congress
added to title XI of the Social Security Act (the Act) a new Part C,
entitled ``Administrative Simplification.'' Part C of title XI of the
Act consists of sections 1171 through 1180. These sections define
various terms and impose several requirements on the Department of
Health & Human Services (HHS), health plans, health care
clearinghouses, and certain health care providers concerning the
electronic transmission of health information.
On August 17, 2000, we published a final rule in the Federal
Register (65 FR 50312) entitled ``Health Insurance Reform: Standards
for Electronic Transactions'' (hereinafter referred to as the
Transactions and Code Sets rule). That rule implemented some of the
HIPAA Administrative Simplification requirements by adopting standards
developed by standard setting organizations (SSOs) for eight electronic
transactions, and code sets to be used in those transactions. The SSOs
are organizations that are accredited by the American National
Standards Institute (ANSI), and that develop industry standards for,
among others, the HIPAA transactions. We adopted standards developed by
the Accredited Standards Committee X12 (hereinafter referred to as ASC
X12) and the National Council for Prescription Drug Programs (NCPDP).
We defined those transactions and specified the adopted standards at 45
CFR part 162, subparts I and K through R. Designated Standard
Maintenance Organizations (DSMOs) receive, manage, and process
requested changes to the adopted standards in accordance with the
process identified in the HIPAA regulations at Sec. 162.900. A
description of the DSMO process can be found in the May 31, 2002
proposed rule (67 FR 38050). Both ASC X12 and NCPDP are DSMOs.
On August 22, 2008, we published a proposed rule in the Federal
Register (73 FR 49742) entitled ``Health Insurance Reform:
Modifications to Electronic Data Transactions Standards and Code Sets''
(hereinafter referred to as the Modifications proposed rule) proposing
to modify the HIPAA transaction standards by adopting updated versions
of the standards. On January 16, 2009, we published a final rule in the
Federal Register (74 FR 3296) entitled Health Insurance Reform;
Modifications to the Health Insurance Portability and Accountability
Act (HIPAA) Electronic Transaction Standards (hereinafter referred to
as the Modifications final rule), that adopted updated versions of the
standards for
[[Page 62685]]
the electronic transactions originally adopted under HIPAA. We refer
readers to the regulations cited above for a detailed discussion of the
standards for electronic transactions and information about electronic
data interchange, the statutory background, and the regulatory history.
In the Transactions and Code Sets rule, we defined the terms
``modification'' and ``maintenance of standards.'' We explained that,
when a change is substantial enough to justify publication of a new
version of an implementation specification, such change is considered a
modification, and must be adopted by the Secretary through regulation
(65 FR 50322). Maintenance, on the other hand, describes the activities
necessary to support the use of a standard, including technical
corrections to an implementation specification. Maintenance changes are
typically changes that are obvious to readers of the implementation
guides, are not controversial, and are essential to implementation (68
FR 8388, (February 20, 2003)). We note that regulatory action is not
required to make maintenance type changes to the HIPAA adopted
standards (65 FR 50322).
II. Provisions of the Notification
A. ASC X12 Version 5010 HIPAA Transaction Standards
We adopted ASC X12 standards for the following eight HIPAA
administrative transactions: (1) Health care claims or equivalent
encounter information; (2) health care payment and remittance advice;
(3) coordination of benefits; (4) eligibility for a health plan; (5)
health care claim status; (6) enrollment and disenrollment in a health
plan; (7) referral certification and authorization; and (8) health plan
premium payments. In the January 16, 2009 Modifications final rule, we
adopted the ASC X12 Technical Reports Type 3, Version 005010
(hereinafter referred to as Version 5010) to replace the currently
adopted Version 4010/4010A1 standard for the eight HIPAA transactions
(74 FR 3296).
1. Errata Notification
Following publication of the Modifications final rule, ASC X12
notified HHS that they were receiving feedback from the industry
regarding errors that had been overlooked during ASC X12 standards
review process. These errors were not identified in the comments
submitted during the public comment period for the Modifications
proposed rule, and therefore are not reflected in the Version 5010
standards adopted in the Modifications final rule.
After the industry reported these errors, ASC X12 compiled a
summary and in February 2010 as required under the DSMO process,
initiated consultations with HHS and the National Committee on Vital
and Health Statistics (NCVHS), an advisory body to HHS on health data,
statistics and national health information policy. (For a complete
discussion of this NCVHS process, we refer readers to the August 22,
2008 proposed rule (73 FR 49742). ASC X12 then balloted and completed
approval for these changes to the Version 5010 standards in accordance
with the established ASC X12 approval process, in July 2010.
2. Errata Classification
ASC X12 issued errata to Version 5010 in July 2010. It has
categorized the errata as both Type 1 and Type 2. These errata
constitute maintenance changes under the HIPAA regulations, not
modifications. The ASC X12 defines errata as: (1) Publication variances
from approved X12 Committee actions (publication errors); or (2)
editorial corrections such as spelling, punctuation, spelling out
abbreviations or acronyms.
ASC X12 further defines Type 1 and Type 2 errata as follows:
Type 1 Errata change the constraints of the base standard,
but do not change the base standard itself. The sender and receiver
must implement the Type I Errata in order to conduct a successful
interchange.
Type 2 Errata supplement a published Technical Report Type
3 (TR3) with minor changes that clarify or correct the TR3 Report.
Implementation Guide constraints are not changed, and the sender and
the receiver do not have to implement the errata to conduct a
successful interchange.
Neither Type 1 or Type 2 Errata can change the underlying base ASC
X12 transaction standard or associated internal code sets (https://www.x12.org/newsletters/tr/index.cfm).
3. Errata Distribution
The errors that were identified by the industry, and ASC X12's
balloted and approved response that was completed July 2010, are
contained in the errata posted to the ASC X12 Web site, at https://www.x12.org, and are available free of charge for purchasers of Version
5010. In the interest of broad stakeholder outreach, CMS also posted a
link for the ASC X12 errata to its Web site, at https://cms.gov/ICD10.
B. NCPDP Telecommunication Standard D.0
We adopted NCPDP standards for the following retail pharmacy drug
transactions: Health care claims or equivalent encounter information;
eligibility for a health plan; referral certification and
authorization, coordination of benefits; and Medicaid pharmacy
subrogation. In the Modifications final rule, we adopted the NCPDP
Telecommunications Standard Implementation Guide, Version D, Release 0
(Version D.0) and equivalent NCPDP Batch Standard Implementation Guide,
Version 1, Release 2 (Version 1.2) in place of the NCPDP
Telecommunication Standard Implementation Guide, Version 5, Release 1
(Version 5.1) and equivalent NCPDP Batch Standard Implementation Guide,
Version 1, Release 1 (Version 1.1), for the HIPAA retail pharmacy drug
transactions.
1. Change Notification
Following publication of the Modifications final rule, NCPDP and
industry stakeholders notified HHS that corrections were needed for
errors in Version D.0 that had been either unintended mistakes or
overlooked during the NCPDP standards review process. Those errors were
not identified in the comments submitted during the public comment
period for the Modifications proposed rule, and therefore are not
reflected in the standards adopted in the Modifications final rule.
After the industry reported these errors, NCPDP compiled a summary
of the needed corrections and their proposed remedies, and in April
2010 initiated consultations with HHS and the NCVHS. NCPDP balloted the
changes and approved them, in accordance with the established NCPDP
approval process, in August 2010. Each of the error corrections to
Version D.0 are maintenance changes, as that term is defined under the
HIPAA regulations.
2. NCPDP Change Distribution
The errors that were identified by the industry, and NCPDP's
balloted and approved response that was completed in August 2010, are
contained in the August 2010 publication of NCPDP Editorial Document
posted to the NCPDP Web site, at https://www.ncpdp.org. The publication
of the changes is available free of charge for purchasers of Version
D.0. In the interest of broad stakeholder outreach, CMS also posted a
link for the NCPDP August 2010 Editorial Document to its Web site, at
https://cms.gov/ICD10.
[[Page 62686]]
It is important that HIPAA covered entities, vendors, and third
party billers obtain the ASC X12 Version 5010 and the NCPDP Version D.0
error corrections and include them in their implementation of Version
5010 and Version D.0 standards. It should be noted that the HIPAA
compliant versions include the error corrections. The Version 5010 and
Version D.0 HIPAA compliant standards should be incorporated into
systems as soon as possible. There is urgency for entities to do so
quickly in light of the HHS-specified Version 5010 and Version D.0
January 1, 2011 testing date and the January 2012 implementation date.
In addition, adhering to these time frames is critical for meeting the
requirements to implement Version 5010 and Version D.0 prior to the
October 2013 implementation date for the ICD-10 code set.
The ASC X12 Standards for Electronic Data Interchange Technical
Report Type 3 and Errata may be obtained from the ASC X12, 7600
Leesburg Pike, Suite 430, Falls Church, VA 22043; Telephone (703) 970-
4480; Fax: (703) 970 4488. They also are available through the Internet
at https://www.X12.org.
The implementation specifications and the NCPDP D.0 Editorial
Document may be obtained from the National Council for Prescription
Drug programs, 9240 East Raintree Drive, Scottsdale, AZ 85260;
Telephone (480) 477-1000; Fax: (480) 767-1042. They are also available
through the Internet at https://www.ncpdp.org.
III. Collection of Information Requirements
This document does not impose information collection and
recordkeeping requirements. Consequently, it need not be reviewed by
the Office of Management and Budget under the authority of the
Paperwork Reduction Act of 1995.
(Catalog of Federal Domestic Assistance Program No. 93.778, Medical
Assistance Program; No. 93.773 Medicare--Hospital Insurance Program;
and No. 93.774, Medicare--Supplementary Medical Insurance Program)
Approved: October 6, 2010.
Kathleen Sebelius,
Secretary.
[FR Doc. 2010-25684 Filed 10-8-10; 11:15 am]
BILLING CODE 4150-29-P