This proposed rule is no longer the most current information.
It will continue to be available for reference, but the
final rule has been published. View
the final rule.
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Under the Paperwork Reduction Act of 1995 (PRA), we are required
to provide 60-day notice in the Federal Register and solicit
public comment before a collection of information requirement is
submitted to the Office of Management and Budget (OMB) for review
and approval. In order to fairly evaluate whether an information
collection should be approved by OMB, section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 requires that we solicit comment
on the following issues:
- The need for the information collection and its usefulness
in carrying out the proper functions of our agency.
- The accuracy of our estimate of the information collection
burden.
- The quality, utility, and clarity of the information to be
collected.
- Recommendations to minimize the information collection burden
on the affected public, including automated collection techniques.
Subpart K - Health Claims or Equivalent Encounter Information
Standard
142.1104 Requirements: Health plans.
142.1108 Requirements: Health care providers.
Subpart L - Health Care Payment and Remittance Advice
142.1204 Requirements: Health plans.
Subpart M - Coordination of Benefits
142.1304 Requirements: Health plans.
Subpart N - Health Claims Status
142.1404 Requirements: Health plans.
142.1408 Requirements: Health care providers.
Subpart O - Enrollment and Disenrollment in a Health Plan
142.1504 Requirements: Health plans.
Subpart P -Eligibility for a Health Plan
142.1604 Requirements: Health plans.
142.1608 Requirements: Health care providers.
Subpart Q - Health Plan Premium Payments
142.1704 Requirements: Health plans.
Subpart R - Referral Certification and Authorization
142.1804 Requirements: Health plans.
142.1808 Requirements: Health care providers.
Discussion: In summary, each of the sections identified
above require health care plans, and/or health care providers to
use any given standard proposed in this regulation for all electronically
transmitted standard transactions that require it on and after the
effective date given to it.
The emerging and increasing use of health care EDI standards and
transactions raises the issue of the applicability of the PRA. The
question arises whether a regulation that adopts an EDI standard
used to exchange certain information constitutes an information
collection subject to the PRA. However, for the purpose of soliciting
useful public comment we provide the following burden estimates.
In particular, the initial burden on the estimated 4 million health
plans and 1.2 million health care providers to modify their current
computer systems software would be 10 hours/$300 per entity,
for a total burden of 52 million hours/$1.56 billion. While
this burden estimate may appear low, on average, we believe it to
be accurate. This is based on the assumption that these and the
other burden calculations associated with the HIPAA administrative
simplification systems modifications may overlap. This average also
takes into consideration that: (1) one or more of these standards
may not be used; (2) some of the these standards may already be
in use by several of the estimated entities; (3) modifications may
be performed in an aggregate manner during the course of routine
business and/or; (4) modifications may be made by contractors such
as practice management vendors, in a single effort for a multitude
of affected entities.
We solicit comment on whether the requirements to which we refer
above constitute a one-time or an ongoing, usual and customary business
practice as defined 5 CFR 1320.3(b)(2), the Paperwork Reduction
regulations.
We invite public comment on the issues discussed above. If you
comment on these information collection and recordkeeping requirements,
please e-mail comments to JBurke1@hcfa.gov (Attn:HCFA-0149) or mail
copies directly to the following:
Health Care Financing Administration,
Office of Information Services,
Information Technology Investment Management Group,
Division of HCFA Enterprise Standards,
Room C2-26-17, 7500 Security Boulevard,
Baltimore, MD 21244-1850.
Attn: John Burke HCFA-0149.
And,
Office of Information and Regulatory Affairs,
Office of Management and Budget,
Room 10235, New Executive Office Building,
Washington, DC 20503,
Attn: Allison Herron Eydt, HCFA Desk Officer.
VI. Response to Comments
Because of the large number of items of correspondence we normally
receive on Federal Register documents published for comment, we
are not able to acknowledge or respond to them individually. We
will consider all comments we receive by the date and time specified
in the "DATES" section of this preamble, and, if we proceed
with a subsequent document, we will respond to comments in the preamble
to that document.
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