Medicare Program; E-Prescribing and the Prescription Drug Program; Correction, 76198-76199 [05-24445]
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76198
Federal Register / Vol. 70, No. 246 / Friday, December 23, 2005 / Rules and Regulations
particular category of health care
providers are met solely through
§ 422.114(a)(2)(ii) and the MA
organization imposes higher beneficiary
copayments as permitted under
§ 422.114(c).
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(i) Provider credential requirements.
Contracts with providers must provide
that, in order to be paid to provide
services to plan enrollees, providers
must meet the requirements specified in
§§ 422.204(b)(1)(i) and (b)(3).
I 6. Amend § 422.256, by revising
paragraph (b)(3) introductory text to
read as follows:
Dated: December 20, 2005.
Ann C. Agnew,
Executive Secretary to the Department.
[FR Doc. 05–24446 Filed 12–22–05; 8:45 am]
§ 422.256 Review, negotiation and
approval of bid.
Medicare Program; E-Prescribing and
the Prescription Drug Program;
Correction
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(b) * * *
(2) * * *
(3) Limitation on enrollee cost
sharing. For coordinated care plans
(including regional MA plans and
specialized MA plans) and private feefor-service plans:
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I 7. Amend § 422.316 by revising
paragraph (a) to read as follows:
§ 422.316 Special rules for payouts to
Federally qualified health centers.
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(a) CMS will pay the amount
determined under section 1833(a)(3)(B)
of the Act directly to the FQHC at a
minimum on a quarterly basis, less the
amount the FQHC would receive for the
MA enrollee from the MA organization
(which includes the cost sharing
amount the FQHC may charge an
enrollee, as established in the contract
between the FQHC and the MA
organization); and
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I 8. Amend § 422.503 by revising
paragraph (b)(4)(ii) to read as follows:
§ 422.503
General provisions.
erjones on PROD1PC68 with RULES
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(b) * * *
(4) * * *
(ii) Personnel and systems sufficient
for the MA organization to organize,
implement, control, and evaluate
financial and marketing activities, the
furnishing of services, the quality
improvement program, and the
administrative and management aspects
of the organization.
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(Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare—Hospital
Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
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15:34 Dec 22, 2005
Jkt 208001
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 423
[CMS–0011–CN]
RIN 0938–AN49
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final rule; Correction.
AGENCY:
This document corrects
technical errors that appeared in the
final rule published in the Federal
Register on November 7, 2005, entitled
‘‘Medicare Program; E-Prescribing and
the Prescription Drug Program.’’
EFFECTIVE DATE: November 7, 2005.
FOR FURTHER INFORMATION CONTACT:
Gladys Wheeler, (410) 786–0273.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
FR Doc. 05–22026, entitled ‘‘Medicare
Program E-Prescribing and the
Prescription Drug Program,’’ which was
published November 7, 2005 (70 FR
67568), adopted several final standards
for an electronic prescription drug
program under Title I of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA). We
have identified several technical errors
in that final rule. We are correcting
those errors in the Correction of Errors
section below. Because these technical
corrections are not substantive in
nature, the effective date of the
November 7, 2005, final rule is
unaffected by this notice.
II. Summary of Errors
On page 67571, in the second
‘‘Response’’ of the first column, we are
revising the reference to the https://
www.cms.hhs.gov/hipaa/hipaa2 Web
site because, in the near future, the
Frequently Asked Questions (FAQs)
will be available through a link on the
general CMS Web site.
On page 67571, in the last paragraph
of the second column, the word
‘‘direction’’ should be replaced with the
more appropriate word ‘‘discretion.’’
PO 00000
Frm 00070
Fmt 4700
Sfmt 4700
Also, in that same paragraph the word
‘‘is’’ should be added to the phrase ‘‘and
designed’’ to improve clarity.
On page 67574, in the fourth full
paragraph of the second column, the
singular word ‘‘criterion’’ should have
been in the plural form. Therefore,
‘‘criterion,’’, needs to be replaced with
‘‘criteria’’.
On page 67581, in the first full
paragraph of the second column, the
word ‘‘may’’ was inadvertently omitted.
On page 67592, in the first response
of the second column, we inadvertently
left language related to an initial plan to
include computer-generated
prescription facsimiles in the definition
of electronic media after a phase-in
period. We explicitly exempted
computer-generated facsimiles from the
requirements to use the NCPDP SCRIPT
standard in the final regulatory text.
Therefore, the preamble discussion of a
phase-in should be deleted.
III. Correction of Errors
FR Doc. 05–22026, entitled ‘‘Medicare
Program E-Prescribing and the
Prescription Drug Program,’’ which was
published November 7, 2005 (70 FR
67568), is corrected as follows:
1. On page 67571,
a. In the first column, fourth full
paragraph, lines 9 and 10, the CMS Web
site address ‘‘(https://www.cms.hhs.gov/
hippa/hippa2)’’ is corrected to read
‘‘(https://www.cms.hhs.gov).’’
b. In the second column, last
paragraph, first sentence,—
(1) Line 2, the word ‘‘direction’’ is
corrected to read ‘‘discretion’’;
(2) Line 6, the phrase ‘‘and designed’’
is corrected to read ‘‘and is designed.’’
2. On page 67574, in the second
column, in the fourth full paragraph,
line 6, the word ‘‘criterion’’ is corrected
to read ‘‘criteria.’’
3. On page 67581, in the second
column, in the first full paragraph, line
3, the phrase ‘‘PDPs continue’’ is
corrected to read ‘‘PDPs may continue.’’
4. On page 67592, in the second
column, the second full paragraph, lines
11 through 23, the sentences beginning
with the phrase ‘‘We also believe that
our’’ and ending with the phrase ‘‘costs
associated with e-prescribing adoption’’
are deleted.
IV. Waiver of Proposed Rulemaking
We ordinarily publish a notice of
proposed rulemaking in the Federal
Register to provide a period for public
comment before the provisions of a
notice take effect. We can waive this
procedure, however, if we find good
cause that notice and comment
procedure is impracticable,
unnecessary, or contrary to the public
E:\FR\FM\23DER1.SGM
23DER1
Federal Register / Vol. 70, No. 246 / Friday, December 23, 2005 / Rules and Regulations
interest and incorporate a statement of
the finding and the reasons for it into
the notice issued.
We find it unnecessary to undertake
notice and comment rulemaking
because this notice merely provides
technical corrections to the regulations.
Therefore, we find good cause to waive
notice and comment procedures.
(Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare—Hospital
Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: December 20, 2005.
Ann C. Agnew,
Executive Secretary to the Department.
[FR Doc. 05–24445 Filed 12–22–05; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare and Medicaid
Services
42 CFR Part 484
[CMS–3006–F]
RIN 0938–AJ10
Medicare and Medicaid Programs:
Reporting Outcome and Assessment
Information Set Data as Part of the
Conditions of Participation for Home
Health Agencies
Centers for Medicare and
Medicaid Services (CMS), HHS.
ACTION: Final rule.
AGENCY:
SUMMARY: This final rule makes
revisions in response to public
comments received on the January 25,
1999 interim final rule with comment
period (64 FR 3748). The interim final
rule requires electronic reporting of data
from the Outcome and Assessment
Information Set as a Condition of
Participation for home health agencies.
DATES: Effective Dates: This final rule is
effective on June 21, 2006.
FOR FURTHER INFORMATION CONTACT:
Rebecca Donnay (410) 786–1428,
Patricia Sevast (410) 786–8135, Steve
Miller (410) 786–6656.
SUPPLEMENTARY INFORMATION:
I. Background
erjones on PROD1PC68 with RULES
A. General Legislative Background
Home health services are furnished to
Medicare beneficiaries under the
Hospital Insurance (Part A) and
Supplemental Medical Insurance (Part
B) benefits of the Medicare program,
and are described in section 1861(m) of
the Social Security Act (the Act). These
VerDate Aug<31>2005
15:34 Dec 22, 2005
Jkt 208001
services must be furnished by, or under
arrangement with, a home health agency
(HHA) that participates in the Medicare
program, and must be provided on a
visiting basis in the beneficiary’s home.
Section 1861(o) of the Act specifies
certain requirements that an HHA must
meet to participate in the Medicare
program. In particular, section
1861(o)(6) of the Act provides that an
HHA must meet the Conditions of
Participation (CoPs) specified in section
1891(a) of the Act, and any other CoPs
that we find necessary in the interest of
the health and safety of HHA patients.
Section 1861(o)(8) of the Act provides
that an HHA must meet additional
requirements that the Secretary finds
necessary for the effective and efficient
operation of the home health program.
Section 1891 of the Act sets forth
many of the conditions that HHAs must
meet to participate in the Medicare
program. Specifically, section 1891(a) of
the Act establishes requirements for
HHAs with respect to patient rights,
home health aide training and
competency, and compliance with
applicable Federal, State, and local
laws. Under section 1891 of the Act, we
are responsible for assuring that the
CoPs, and their enforcement, are
adequate to protect the health and safety
of all individuals under the care of an
HHA and to promote the effective and
efficient use of Medicare funds.
Under the authority of sections
1861(o), 1871, and 1891 of the Act, we
have established in regulations the
requirements that an HHA must meet to
participate in Medicare. These
requirements are set forth at 42 CFR part
484, Home Health Services. The CoPs
apply to an HHA as an entity and the
services furnished to all individuals
under the care of the HHA, unless a
condition is specifically limited to
Medicare beneficiaries. Existing
regulations in § 440.70(d) specify that
HHAs participating in the Medicaid
program must also meet the Medicare
CoPs.
In accordance with sections 1864 and
1891(c) of the Act, State agencies
generally conduct surveys of HHAs to
determine whether they are complying
with the CoPs. Section 1864 of the Act
authorizes the use of State agencies to
determine providers’ compliance with
the CoPs. Responsibilities of States in
ensuring compliance with the CoPs are
set forth at 42 CFR part 488, Survey,
Certification, and Enforcement
Procedures.
B. Legislation and Related Regulations
Section 1861(o) of the Act, as
amended by section 4603 of the
Balanced Budget Act of 1997 (BBA)
PO 00000
Frm 00071
Fmt 4700
Sfmt 4700
76199
(Pub. L. 105–33), enacted on August 5,
1997, requires us to establish a Home
Health Prospective Payment System
(HHPPS) for services on or after October
1, 1999. Section 5101 of the Omnibus
Consolidated and Emergency
Supplemental Appropriations Act for
1999 (OCESAA) (Pub. L. 105–277),
enacted on October 21, 1998, delayed
the implementation date of the HHPPS
until October 1, 2000.
In order to implement the prospective
payment system, it was necessary that
we have data from HHAs to develop a
reliable case-mix adjustor system.
Section 4602 of the BBA provided that,
for cost reporting periods beginning on
or after October 1, 1997, we may require
HHAs to submit additional information
that we consider necessary for the
development of a reliable case-mix
system. The Outcome and Assessment
Information Set (OASIS), the assessment
instrument developed to measure
patient health care outcomes in HHAs,
is also a vehicle through which
information is collected and used for the
case-mix system.
Thus, to facilitate the implementation
of the prospective payment system and
to gather data to be used to evaluate and
develop plans to improve outcomes of
care in HHAs, we published two
regulations in the Federal Register on
January 25, 1999. The final rule,
Comprehensive Assessment and Use of
the OASIS as Part of the Conditions of
Participation for Home Health Agencies
(64 FR 3764), requires that HHAs
complete a comprehensive assessment
for each patient, and that they
incorporate the OASIS into their current
patient assessment process. In addition,
we published an interim final rule with
comment period to require HHAs to
electronically report data from the
OASIS to the State survey agency, or
other entity designated by us (64 FR
3748).
The June 18, 1999, notice (64 FR
32984) in the Federal Register entitled
‘‘Mandatory Use, Collection, Encoding,
and Transmission of Outcome and
Assessment Information Set (OASIS) for
Home Health Agencies (HHAs)’’,
announced the effective dates for the
mandatory use, collection, encoding,
and transmission of OASIS data for all
Medicare/Medicaid patients receiving
skilled services. This notice also
described the development of a new
OASIS System of Records (SOR). We
indicated that for patients receiving
only personal care services, regardless
of payer source, requirements for OASIS
and the transmission of those data
would be delayed until further notice.
In addition, the notice announced that
for non-Medicare/non-Medicaid
E:\FR\FM\23DER1.SGM
23DER1
Agencies
[Federal Register Volume 70, Number 246 (Friday, December 23, 2005)]
[Rules and Regulations]
[Pages 76198-76199]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-24445]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 423
[CMS-0011-CN]
RIN 0938-AN49
Medicare Program; E-Prescribing and the Prescription Drug
Program; Correction
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule; Correction.
-----------------------------------------------------------------------
SUMMARY: This document corrects technical errors that appeared in the
final rule published in the Federal Register on November 7, 2005,
entitled ``Medicare Program; E-Prescribing and the Prescription Drug
Program.''
EFFECTIVE DATE: November 7, 2005.
FOR FURTHER INFORMATION CONTACT: Gladys Wheeler, (410) 786-0273.
SUPPLEMENTARY INFORMATION:
I. Background
FR Doc. 05-22026, entitled ``Medicare Program E-Prescribing and the
Prescription Drug Program,'' which was published November 7, 2005 (70
FR 67568), adopted several final standards for an electronic
prescription drug program under Title I of the Medicare Prescription
Drug, Improvement, and Modernization Act of 2003 (MMA). We have
identified several technical errors in that final rule. We are
correcting those errors in the Correction of Errors section below.
Because these technical corrections are not substantive in nature, the
effective date of the November 7, 2005, final rule is unaffected by
this notice.
II. Summary of Errors
On page 67571, in the second ``Response'' of the first column, we
are revising the reference to the https://www.cms.hhs.gov/hipaa/hipaa2
Web site because, in the near future, the Frequently Asked Questions
(FAQs) will be available through a link on the general CMS Web site.
On page 67571, in the last paragraph of the second column, the word
``direction'' should be replaced with the more appropriate word
``discretion.'' Also, in that same paragraph the word ``is'' should be
added to the phrase ``and designed'' to improve clarity.
On page 67574, in the fourth full paragraph of the second column,
the singular word ``criterion'' should have been in the plural form.
Therefore, ``criterion,'', needs to be replaced with ``criteria''.
On page 67581, in the first full paragraph of the second column,
the word ``may'' was inadvertently omitted.
On page 67592, in the first response of the second column, we
inadvertently left language related to an initial plan to include
computer-generated prescription facsimiles in the definition of
electronic media after a phase-in period. We explicitly exempted
computer-generated facsimiles from the requirements to use the NCPDP
SCRIPT standard in the final regulatory text. Therefore, the preamble
discussion of a phase-in should be deleted.
III. Correction of Errors
FR Doc. 05-22026, entitled ``Medicare Program E-Prescribing and the
Prescription Drug Program,'' which was published November 7, 2005 (70
FR 67568), is corrected as follows:
1. On page 67571,
a. In the first column, fourth full paragraph, lines 9 and 10, the
CMS Web site address ``(https://www.cms.hhs.gov/hippa/hippa2)'' is
corrected to read ``(https://www.cms.hhs.gov).''
b. In the second column, last paragraph, first sentence,--
(1) Line 2, the word ``direction'' is corrected to read
``discretion'';
(2) Line 6, the phrase ``and designed'' is corrected to read ``and
is designed.''
2. On page 67574, in the second column, in the fourth full
paragraph, line 6, the word ``criterion'' is corrected to read
``criteria.''
3. On page 67581, in the second column, in the first full
paragraph, line 3, the phrase ``PDPs continue'' is corrected to read
``PDPs may continue.''
4. On page 67592, in the second column, the second full paragraph,
lines 11 through 23, the sentences beginning with the phrase ``We also
believe that our'' and ending with the phrase ``costs associated with
e-prescribing adoption'' are deleted.
IV. Waiver of Proposed Rulemaking
We ordinarily publish a notice of proposed rulemaking in the
Federal Register to provide a period for public comment before the
provisions of a notice take effect. We can waive this procedure,
however, if we find good cause that notice and comment procedure is
impracticable, unnecessary, or contrary to the public
[[Page 76199]]
interest and incorporate a statement of the finding and the reasons for
it into the notice issued.
We find it unnecessary to undertake notice and comment rulemaking
because this notice merely provides technical corrections to the
regulations. Therefore, we find good cause to waive notice and comment
procedures.
(Catalog of Federal Domestic Assistance Program No. 93.773,
Medicare--Hospital Insurance; and Program No. 93.774, Medicare--
Supplementary Medical Insurance Program)
Dated: December 20, 2005.
Ann C. Agnew,
Executive Secretary to the Department.
[FR Doc. 05-24445 Filed 12-22-05; 8:45 am]
BILLING CODE 4120-01-P