Medicare Program; Hospital Inpatient Prospective Payment Systems for Acute Care Hospitals and the Long-Term Care Hospital Prospective Payment System and Policy Changes and Fiscal Year 2022 Rates; Quality Programs and Medicare Promoting Interoperability Program Requirements for Eligible Hospitals and Critical Access Hospitals; Changes to Medicaid Provider Enrollment; and Changes to the Medicare Shared Savings Program; Correction, 67874-67876 [2021-26069]

Download as PDF 67874 Federal Register / Vol. 86, No. 227 / Tuesday, November 30, 2021 / Rules and Regulations TEXAS—2015 8-HOUR OZONE NAAQS [Primary and secondary] Designation Classification Designated area 1 * * * * El Paso-Las Cruces, TX–NM ............................................................................................. El Paso County ........................................................................................................... * * * Date 2 Type * .............................. December 30, 2021 3. * Nonattainment ...... * * Date 2 * Type * Marginal. * 1 Includes any Indian country in each county or area, unless otherwise specified. EPA is not determining the boundaries of any area of Indian country in this table, including any area of Indian country located in the larger designation area. The inclusion of any Indian country in the designation area is not a determination that the state has regulatory authority under the Clean Air Act for such Indian country. 2 This date is August 3, 2018, unless otherwise noted. 3 EPA revised the nonattainment boundary in response to a court decision, which did not vacate any designations for the 2015 ozone NAAQS, but which remanded the designation for the identified county. Because this additional area is part of a previously designated nonattainment area, the associated August 3, 2021 attainment date remains unchanged regardless of this later designation date. EPA established a later state implementation plan submission date for El Paso County. * * * * Hospitals and Critical Access Hospitals; Changes to Medicaid Provider Enrollment; and Changes to the Medicare Shared Savings Program’’. DATES: Effective date: This correcting document is effective on November 29, 2021. Applicability date: This correcting document is applicable for discharges beginning October 1, 2021. FOR FURTHER INFORMATION CONTACT: Allison Pompey, (410) 786–2348, New Technology Add-On Payment Issues. SUPPLEMENTARY INFORMATION: * [FR Doc. 2021–25451 Filed 11–29–21; 8:45 am] BILLING CODE 6560–50–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services 42 CFR Part 413 [CMS–1752–CN2 and CMS–1762–CN2] RINs 0938–AU44 and 0938–AU56 Medicare Program; Hospital Inpatient Prospective Payment Systems for Acute Care Hospitals and the LongTerm Care Hospital Prospective Payment System and Policy Changes and Fiscal Year 2022 Rates; Quality Programs and Medicare Promoting Interoperability Program Requirements for Eligible Hospitals and Critical Access Hospitals; Changes to Medicaid Provider Enrollment; and Changes to the Medicare Shared Savings Program; Correction Centers for Medicare & Medicaid Services (CMS), Department of Health and Human Services (HHS). ACTION: Final rule; correction. AGENCY: This document corrects typographical errors in the final rule that appeared in the August 13, 2021, Federal Register as well as additional typographical errors in a related correcting amendment that appeared in the October 20, 2021, Federal Register. The final rule was titled ‘‘Medicare Program; Hospital Inpatient Prospective Payment Systems for Acute Care Hospitals and the Long Term Care Hospital Prospective Payment System and Policy Changes and Fiscal Year 2022 Rates; Quality Programs and Medicare Promoting Interoperability Program Requirements for Eligible lotter on DSK11XQN23PROD with RULES1 SUMMARY: VerDate Sep<11>2014 15:56 Nov 29, 2021 Jkt 256001 I. Background In the final rule which appeared in the August 13, 2021, Federal Register (86 FR 44774) entitled ‘‘Medicare Program; Hospital Inpatient Prospective Payment Systems for Acute Care Hospitals and the Long Term Care Hospital Prospective Payment System and Policy Changes and Fiscal Year 2022 Rates; Quality Programs and Medicare Promoting Interoperability Program Requirements for Eligible Hospitals and Critical Access Hospitals; Changes to Medicaid Provider Enrollment; and Changes to the Medicare Shared Savings Program’’ (hereinafter referred to as the FY 2022 IPPS/LTCH PPS final rule), there were a number of technical and typographical errors. To correct the typographical and technical errors in the FY 2022 IPPS/ LTCH PPS final rule, we published a correcting document that appeared in the October 20, 2021, Federal Register (86 FR 58019) (hereinafter referred to as the FY 2022 IPPS/LTCH PPS correcting amendment). In FR Doc. 2021–22724 of October 20, 2021 (86 FR 58019), there was an inadvertent omission and typographical error that are identified and corrected in this correcting document. This document also corrects additional typographical errors in FR Doc. 2021– PO 00000 Frm 00044 Fmt 4700 Sfmt 4700 16519 of August 13, 2021 (86 FR 44774). The corrections in this correcting document are applicable to discharges occurring on or after October 1, 2021, as if they had been included in the document that appeared in the August 13, 2021, Federal Register . II. Summary of Errors A. Summary of Errors in the FY 2022 IPPS/LTCH PPS Final Rule On page 44974, in the table displaying the continuation of technologies approved for FY 2021 new technology add-on payments and still considered new for FY 2022, we are correcting inadvertent typographical errors in the coding used to identify cases involving the use of the BAROSTIM NEOTM System that are eligible for new technology add-on payments. B. Summary of Errors in the FY 2022 IPPS/LTCH PPS Correcting Document On page 58023 in section IV.A. of the FY 2022 IPPS/LTCH PPS correcting amendment, we inadvertently omitted corrections to pages 45133, 45150, and 45157 of the FY 2022 IPPS/LTCH PPS final rule, as summarized on page 58019 in section II.A. of the FY 2022 IPPS/ LTCH PPS correcting amendment. We are also correcting an inadvertent typographical error in the coding used to identify cases involving the use of RECARBRIOTM that are eligible for new technology add-on payments. III. Waiver of Proposed Rulemaking and Delay in Effective Date Under 5 U.S.C. 553(b) of the Administrative Procedure Act (APA), the agency is required to publish a notice of the proposed rulemaking in the Federal Register before the provisions of a rule take effect. Similarly, section 1871(b)(1) of the Act requires the Secretary to provide for notice of the proposed rulemaking in the Federal Register and provide a E:\FR\FM\30NOR1.SGM 30NOR1 Federal Register / Vol. 86, No. 227 / Tuesday, November 30, 2021 / Rules and Regulations period of not less than 60 days for public comment. In addition, section 553(d) of the APA, and section 1871(e)(1)(B)(i) of the Act mandate a 30day delay in effective date after issuance or publication of a rule. Sections 553(b)(B) and 553(d)(3) of the APA provide for exceptions from the notice and comment and delay in effective date APA requirements; in cases in which these exceptions apply, sections 1871(b)(2)(C) and 1871(e)(1)(B)(ii) of the Act provide exceptions from the notice and 60-day comment period and delay in effective date requirements of the Act as well. Section 553(b)(B) of the APA and section 1871(b)(2)(C) of the Act authorize an agency to dispense with normal rulemaking requirements for good cause if the agency makes a finding that the notice and comment process are impracticable, unnecessary, or contrary to the public interest. In addition, both section 553(d)(3) of the APA and section 1871(e)(1)(B)(ii) of the Act allow the agency to avoid the 30day delay in effective date where such delay is contrary to the public interest and an agency includes a statement of support. We believe that this final rule correction does not constitute a rule that would be subject to the notice and comment or delayed effective date requirements. This document corrects typographical errors in the FY 2022 Technology FDA Newness/Start Date IPPS/LTCH PPS final rule and the FY 2022 IPPS/LTCH PPS final rule correcting amendment, but does not make substantive changes to the policies or payment methodologies that were adopted in the final rule. As a result, this final rule correction is intended to ensure that the information in the FY 2022 IPPS/LTCH PPS final rule accurately reflects the policies adopted in that document. In addition, even if this were a rule to which the notice and comment procedures and delayed effective date requirements applied, we find that there is good cause to waive such requirements. Undertaking further notice and comment procedures to incorporate the corrections in this document into the final rule or delaying the effective date would be contrary to the public interest because it is in the public’s interest for providers to receive appropriate payments in as timely a manner as possible, and to ensure that the FY 2022 IPPS/LTCH PPS final rule accurately reflects our policies. Furthermore, such procedures would be unnecessary, as we are not altering our payment methodologies or policies, but rather, we are simply implementing correctly the methodologies and policies that we previously proposed, requested comment on, and subsequently finalized. This final rule correction is intended solely to ensure that the FY NTAP Start Date NTAP Status for FY 2022 67875 2022 IPPS/LTCH PPS final rule accurately reflects these payment methodologies and policies. Therefore, we believe we have good cause to waive the notice and comment and effective date requirements. Moreover, even if these corrections were considered to be retroactive rulemaking, they would be authorized under section 1871(e)(1)(A)(ii) of the Act, which permits the Secretary to issue a rule for the Medicare program with retroactive effect if the failure to do so would be contrary to the public interest. As we have explained previously, we believe it would be contrary to the public interest not to implement the corrections in this final rule correction because it is in the public’s interest for providers to receive appropriate payments in as timely a manner as possible, and to ensure that the FY 2022 IPPS/LTCH PPS final rule accurately reflects our policies. IV. Correction of Errors A. Correction of Errors in the Final Rule In FR Doc. 2021–16519 of August 13, 2021(86 FR 44774), we are making the following corrections: 1. On page 44974, in the table titled ‘‘Continuation of Technologies Approved for FY 2021 New Technology Add-On Payments and Still Considered New for FY 2022, the entry in row 3 is corrected to read as follows: Previous Final Rule Citations Maximum NTAP Amount for FY2022 Coding Used to Identify Cases Eligible for NTAP (85 FR 58716 through 58717) $22,750 0JH60MZ in combination with 03HK3MZ or 03HL3MZ ******* 3. BAROSTIM NED™ System 08/16/2019 10/01/2020 Continue because 3-year anniversary date (8/16/2022) will occur in the second half ofFY2022 lotter on DSK11XQN23PROD with RULES1 B. Correction of Errors in the Correcting Document In FR Doc. 2021–22724 of October 20, 2021 (86 FR 58019), we are making the following corrections: 1. On page 58023, lower half of the page (following the table), third column: a. Preceding the beginning of the partial paragraph (before item 10), the paragraph is corrected by adding items 7 through 9 to read as follows: ‘‘7. On page 45133, top of the page, VerDate Sep<11>2014 15:56 Nov 29, 2021 Jkt 256001 a. First column, partial paragraph, (1) Line 4, the figure ‘‘$31,500’’ is corrected to read ‘‘$63,000’’. (2) Line 5, the figure ‘‘$10,500’’ is corrected to read ‘‘$21,000’’. b. Second column, partial paragraph, last line, the figure ‘‘$20,475’’ is corrected to read ‘‘$40,950’’. 8. On page 45150, second column, last full paragraph, lines 27 through 31, the phrase ‘‘in combination with one of the following ICD–10–CM codes: D65 PO 00000 Frm 00045 Fmt 4700 Sfmt 4700 (Disseminated intravascular coagulation) or D68.2 (Hereditary deficiency of other clotting factors).’’ is corrected to read ‘‘in combination with one of the following ICD–10–CM codes: D62 (Acute posthemorrhagic anemia), D65 (Disseminated intravascular coagulation), D68.2 (Hereditary deficiency of other clotting factors), D68.4 (Acquired coagulation factor deficiency) or D68.9 (Coagulation defect, unspecified).’’. E:\FR\FM\30NOR1.SGM 30NOR1 ER30NO21.045</GPH> ******* 67876 Federal Register / Vol. 86, No. 227 / Tuesday, November 30, 2021 / Rules and Regulations 9. On page 45157, top third of the page, first column, first partial paragraph, last line, the phrase, ‘‘technology group 6).’’ is corrected to read ‘‘technology group 6) in combination with the following ICD– 10–CM codes: Y95 (Nosocomial condition) and one of the following: J14 (Pneumonia due to Hemophilus influenzae) J15.0 (Pneumonia due to Klebsiella pneumoniae), J15.1 (Pneumonia due to Pseudomonas), J15.5 (Pneumonia due to Escherichia coli), J15.6 (Pneumonia due to other Gramnegative bacteria), J15.8 (Pneumonia due to other specified bacteria), or J95.851 (Ventilator associated pneumonia) and one of the following: B96.1 (Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified elsewhere), B96.20 (Unspecified Escherichia coli [E. coli] as the cause of diseases classified elsewhere), B96.21 (Shiga toxinproducing Escherichia coli [E. coli] [STEC] O157 as the cause of diseases classified elsewhere), B96.22 (Other specified Shiga toxin-producing Escherichia coli [E. coli] [STEC] as the cause of diseases classified elsewhere), B96.23 (Unspecified Shiga toxinproducing Escherichia coli [E. coli] [STEC] as the cause of diseases classified elsewhere, B96.29 (Other Escherichia coli [E. coli] as the cause of diseases classified elsewhere), B96.3 (Hemophilus influenzae [H. influenzae] as the cause of diseases classified elsewhere, B96.5 (Pseudomonas (aeruginosa) (mallei) (pseudomallei) as the cause of diseases classified elsewhere), or B96.89 (Other specified bacterial agents as the cause of diseases classified elsewhere).’’ b. Within the partial paragraph (item 10), line 8, the code number ‘‘J14.0’’ is corrected to read ‘‘J14’’. Karuna Seshasai, Executive Secretary to the Department, Department of Health and Human Services. [FR Doc. 2021–26069 Filed 11–29–21; 8:45 am] lotter on DSK11XQN23PROD with RULES1 BILLING CODE 4120–01–P VerDate Sep<11>2014 15:56 Nov 29, 2021 Jkt 256001 DEPARTMENT OF DEFENSE Defense Acquisition Regulations System 48 CFR Parts 201 and 237 [Docket DARS–2021–0023] RIN 0750–AK77 Defense Federal Acquisition Regulation Supplement: Peer Reviews of Contracts for Supplies and Services (DFARS Case 2019–D037) Defense Acquisition Regulations System, Department of Defense (DoD). ACTION: Final rule. AGENCY: DoD is issuing a final rule amending the Defense Federal Acquisition Regulation Supplement (DFARS) to modify internal processes for the conduct of peer reviews. DATES: Effective November 30, 2021. FOR FURTHER INFORMATION CONTACT: Ms. Barbara J. Trujillo, telephone 571–372– 6102. SUPPLEMENTARY INFORMATION: SUMMARY: I. Background DoD is amending the DFARS to revise the policies at DFARS 201.170 for the conduct of peer reviews by the Office of the Principal Director, Defense Pricing and Contracting (DPC). The rule removes the requirement for DPC-led, preaward peer reviews of competitive procurements valued at $1 billion or more unless the Under Secretary of Defense for Acquisition and Sustainment (USD(A&S)) is the milestone decision authority or unless USD(A&S) designates a competitive procurement as requiring a peer review, regardless of dollar value. Additionally, DoD components may request DPC-led peer reviews for competitive acquisitions valued below the $1 billion threshold. DPC will conduct the reviews upon approval by the Director, DPC (Contract Policy). The threshold for DPC-led, preaward peer reviews of noncompetitive procurements is increased from $500 million to $1 billion. Additionally, the requirement for DPC-led peer reviews of noncompetitive procurements will include any other contract actions USD(A&S) designates as requiring a peer review, regardless of dollar value. DoD components may request DPC-led peer reviews for noncompetitive acquisitions valued below the $1 billion threshold. DPC will conduct the reviews upon approval by the Director, DPC (Price, Cost and Finance). PO 00000 Frm 00046 Fmt 4700 Sfmt 4700 The rule includes clarification of the types of contract actions included in preaward peer reviews for noncompetitive procurements and guidance on how to identify the contract actions that are subject to preaward peer reviews for competitive and noncompetitive procurements. DoD components establish procedures to conduct preaward peer reviews of competitive and noncompetitive procurements that do not meet the criteria for a DPC-led review. The rule also removes DPC-led, postaward peer reviews of acquisitions for services from the DFARS, and the cross-reference at DFARS 237.102–76 has been removed. II. Publication of This Final Rule for Public Comment Is Not Required by Statute The statute that applies to the publication of the Federal Acquisition Regulation (FAR) is 41 U.S.C. 1707, Publication of Proposed Regulations. Subsection (a)(1) of the statute requires that a procurement policy, regulation, procedure or form (including an amendment or modification thereof) must be published for public comment if it relates to the expenditure of appropriated funds, and has either a significant effect beyond the internal operating procedures of the agency issuing the policy, regulation, procedure or form, or has a significant cost or administrative impact on contractors or offerors. This final rule is not required to be published for public comment, because the rule concerns DoD’s internal review processes and does not have a significant cost or administrative impact on contractors or offerors. III. Applicability to Contracts at or Below the Simplified Acquisition Threshold and for Commercial Items, Including Commercially Available Offthe-Shelf Items This rule does not create or revise any solicitation provisions or contract clauses. It does not impact any existing solicitation provisions or contract clauses or their applicability to contracts valued at or below the simplified acquisition threshold or for commercial items, including commercially available off-the-shelf items. IV. Executive Orders 12866 and 13563 Executive Orders (E.O.) 12866 and E.O. 13563 direct agencies to assess all costs and benefits of available regulatory alternatives and, if regulation is necessary, to select regulatory approaches that maximize net benefits (including potential economic, environmental, public health and safety E:\FR\FM\30NOR1.SGM 30NOR1

Agencies

[Federal Register Volume 86, Number 227 (Tuesday, November 30, 2021)]
[Rules and Regulations]
[Pages 67874-67876]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-26069]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

42 CFR Part 413

[CMS-1752-CN2 and CMS-1762-CN2]
RINs 0938-AU44 and 0938-AU56


Medicare Program; Hospital Inpatient Prospective Payment Systems 
for Acute Care Hospitals and the Long-Term Care Hospital Prospective 
Payment System and Policy Changes and Fiscal Year 2022 Rates; Quality 
Programs and Medicare Promoting Interoperability Program Requirements 
for Eligible Hospitals and Critical Access Hospitals; Changes to 
Medicaid Provider Enrollment; and Changes to the Medicare Shared 
Savings Program; Correction

AGENCY: Centers for Medicare & Medicaid Services (CMS), Department of 
Health and Human Services (HHS).

ACTION: Final rule; correction.

-----------------------------------------------------------------------

SUMMARY: This document corrects typographical errors in the final rule 
that appeared in the August 13, 2021, Federal Register as well as 
additional typographical errors in a related correcting amendment that 
appeared in the October 20, 2021, Federal Register. The final rule was 
titled ``Medicare Program; Hospital Inpatient Prospective Payment 
Systems for Acute Care Hospitals and the Long Term Care Hospital 
Prospective Payment System and Policy Changes and Fiscal Year 2022 
Rates; Quality Programs and Medicare Promoting Interoperability Program 
Requirements for Eligible Hospitals and Critical Access Hospitals; 
Changes to Medicaid Provider Enrollment; and Changes to the Medicare 
Shared Savings Program''.

DATES: 
    Effective date: This correcting document is effective on November 
29, 2021.
    Applicability date: This correcting document is applicable for 
discharges beginning October 1, 2021.

FOR FURTHER INFORMATION CONTACT: Allison Pompey, (410) 786-2348, New 
Technology Add-On Payment Issues.

SUPPLEMENTARY INFORMATION:

I. Background

    In the final rule which appeared in the August 13, 2021, Federal 
Register (86 FR 44774) entitled ``Medicare Program; Hospital Inpatient 
Prospective Payment Systems for Acute Care Hospitals and the Long Term 
Care Hospital Prospective Payment System and Policy Changes and Fiscal 
Year 2022 Rates; Quality Programs and Medicare Promoting 
Interoperability Program Requirements for Eligible Hospitals and 
Critical Access Hospitals; Changes to Medicaid Provider Enrollment; and 
Changes to the Medicare Shared Savings Program'' (hereinafter referred 
to as the FY 2022 IPPS/LTCH PPS final rule), there were a number of 
technical and typographical errors. To correct the typographical and 
technical errors in the FY 2022 IPPS/LTCH PPS final rule, we published 
a correcting document that appeared in the October 20, 2021, Federal 
Register (86 FR 58019) (hereinafter referred to as the FY 2022 IPPS/
LTCH PPS correcting amendment).
    In FR Doc. 2021-22724 of October 20, 2021 (86 FR 58019), there was 
an inadvertent omission and typographical error that are identified and 
corrected in this correcting document. This document also corrects 
additional typographical errors in FR Doc. 2021-16519 of August 13, 
2021 (86 FR 44774). The corrections in this correcting document are 
applicable to discharges occurring on or after October 1, 2021, as if 
they had been included in the document that appeared in the August 13, 
2021, Federal Register .

II. Summary of Errors

A. Summary of Errors in the FY 2022 IPPS/LTCH PPS Final Rule

    On page 44974, in the table displaying the continuation of 
technologies approved for FY 2021 new technology add-on payments and 
still considered new for FY 2022, we are correcting inadvertent 
typographical errors in the coding used to identify cases involving the 
use of the BAROSTIM NEO\TM\ System that are eligible for new technology 
add-on payments.

B. Summary of Errors in the FY 2022 IPPS/LTCH PPS Correcting Document

    On page 58023 in section IV.A. of the FY 2022 IPPS/LTCH PPS 
correcting amendment, we inadvertently omitted corrections to pages 
45133, 45150, and 45157 of the FY 2022 IPPS/LTCH PPS final rule, as 
summarized on page 58019 in section II.A. of the FY 2022 IPPS/LTCH PPS 
correcting amendment. We are also correcting an inadvertent 
typographical error in the coding used to identify cases involving the 
use of RECARBRIO\TM\ that are eligible for new technology add-on 
payments.

III. Waiver of Proposed Rulemaking and Delay in Effective Date

    Under 5 U.S.C. 553(b) of the Administrative Procedure Act (APA), 
the agency is required to publish a notice of the proposed rulemaking 
in the Federal Register before the provisions of a rule take effect. 
Similarly, section 1871(b)(1) of the Act requires the Secretary to 
provide for notice of the proposed rulemaking in the Federal Register 
and provide a

[[Page 67875]]

period of not less than 60 days for public comment. In addition, 
section 553(d) of the APA, and section 1871(e)(1)(B)(i) of the Act 
mandate a 30-day delay in effective date after issuance or publication 
of a rule. Sections 553(b)(B) and 553(d)(3) of the APA provide for 
exceptions from the notice and comment and delay in effective date APA 
requirements; in cases in which these exceptions apply, sections 
1871(b)(2)(C) and 1871(e)(1)(B)(ii) of the Act provide exceptions from 
the notice and 60-day comment period and delay in effective date 
requirements of the Act as well. Section 553(b)(B) of the APA and 
section 1871(b)(2)(C) of the Act authorize an agency to dispense with 
normal rulemaking requirements for good cause if the agency makes a 
finding that the notice and comment process are impracticable, 
unnecessary, or contrary to the public interest. In addition, both 
section 553(d)(3) of the APA and section 1871(e)(1)(B)(ii) of the Act 
allow the agency to avoid the 30-day delay in effective date where such 
delay is contrary to the public interest and an agency includes a 
statement of support.
    We believe that this final rule correction does not constitute a 
rule that would be subject to the notice and comment or delayed 
effective date requirements. This document corrects typographical 
errors in the FY 2022 IPPS/LTCH PPS final rule and the FY 2022 IPPS/
LTCH PPS final rule correcting amendment, but does not make substantive 
changes to the policies or payment methodologies that were adopted in 
the final rule. As a result, this final rule correction is intended to 
ensure that the information in the FY 2022 IPPS/LTCH PPS final rule 
accurately reflects the policies adopted in that document.
    In addition, even if this were a rule to which the notice and 
comment procedures and delayed effective date requirements applied, we 
find that there is good cause to waive such requirements. Undertaking 
further notice and comment procedures to incorporate the corrections in 
this document into the final rule or delaying the effective date would 
be contrary to the public interest because it is in the public's 
interest for providers to receive appropriate payments in as timely a 
manner as possible, and to ensure that the FY 2022 IPPS/LTCH PPS final 
rule accurately reflects our policies. Furthermore, such procedures 
would be unnecessary, as we are not altering our payment methodologies 
or policies, but rather, we are simply implementing correctly the 
methodologies and policies that we previously proposed, requested 
comment on, and subsequently finalized. This final rule correction is 
intended solely to ensure that the FY 2022 IPPS/LTCH PPS final rule 
accurately reflects these payment methodologies and policies. 
Therefore, we believe we have good cause to waive the notice and 
comment and effective date requirements. Moreover, even if these 
corrections were considered to be retroactive rulemaking, they would be 
authorized under section 1871(e)(1)(A)(ii) of the Act, which permits 
the Secretary to issue a rule for the Medicare program with retroactive 
effect if the failure to do so would be contrary to the public 
interest. As we have explained previously, we believe it would be 
contrary to the public interest not to implement the corrections in 
this final rule correction because it is in the public's interest for 
providers to receive appropriate payments in as timely a manner as 
possible, and to ensure that the FY 2022 IPPS/LTCH PPS final rule 
accurately reflects our policies.

IV. Correction of Errors

A. Correction of Errors in the Final Rule

    In FR Doc. 2021-16519 of August 13, 2021(86 FR 44774), we are 
making the following corrections:
    1. On page 44974, in the table titled ``Continuation of 
Technologies Approved for FY 2021 New Technology Add-On Payments and 
Still Considered New for FY 2022, the entry in row 3 is corrected to 
read as follows:
[GRAPHIC] [TIFF OMITTED] TR30NO21.045

B. Correction of Errors in the Correcting Document

    In FR Doc. 2021-22724 of October 20, 2021 (86 FR 58019), we are 
making the following corrections:
    1. On page 58023, lower half of the page (following the table), 
third column:
    a. Preceding the beginning of the partial paragraph (before item 
10), the paragraph is corrected by adding items 7 through 9 to read as 
follows:
    ``7. On page 45133, top of the page,
    a. First column, partial paragraph,
    (1) Line 4, the figure ``$31,500'' is corrected to read 
``$63,000''.
    (2) Line 5, the figure ``$10,500'' is corrected to read 
``$21,000''.
    b. Second column, partial paragraph, last line, the figure 
``$20,475'' is corrected to read ``$40,950''.
    8. On page 45150, second column, last full paragraph, lines 27 
through 31, the phrase ``in combination with one of the following ICD-
10-CM codes: D65 (Disseminated intravascular coagulation) or D68.2 
(Hereditary deficiency of other clotting factors).'' is corrected to 
read ``in combination with one of the following ICD-10-CM codes: D62 
(Acute posthemorrhagic anemia), D65 (Disseminated intravascular 
coagulation), D68.2 (Hereditary deficiency of other clotting factors), 
D68.4 (Acquired coagulation factor deficiency) or D68.9 (Coagulation 
defect, unspecified).''.

[[Page 67876]]

    9. On page 45157, top third of the page, first column, first 
partial paragraph, last line, the phrase, ``technology group 6).'' is 
corrected to read ``technology group 6) in combination with the 
following ICD-10-CM codes: Y95 (Nosocomial condition) and one of the 
following: J14 (Pneumonia due to Hemophilus influenzae) J15.0 
(Pneumonia due to Klebsiella pneumoniae), J15.1 (Pneumonia due to 
Pseudomonas), J15.5 (Pneumonia due to Escherichia coli), J15.6 
(Pneumonia due to other Gram-negative bacteria), J15.8 (Pneumonia due 
to other specified bacteria), or J95.851 (Ventilator associated 
pneumonia) and one of the following: B96.1 (Klebsiella pneumoniae [K. 
pneumoniae] as the cause of diseases classified elsewhere), B96.20 
(Unspecified Escherichia coli [E. coli] as the cause of diseases 
classified elsewhere), B96.21 (Shiga toxin-producing Escherichia coli 
[E. coli] [STEC] O157 as the cause of diseases classified elsewhere), 
B96.22 (Other specified Shiga toxin-producing Escherichia coli [E. 
coli] [STEC] as the cause of diseases classified elsewhere), B96.23 
(Unspecified Shiga toxin-producing Escherichia coli [E. coli] [STEC] as 
the cause of diseases classified elsewhere, B96.29 (Other Escherichia 
coli [E. coli] as the cause of diseases classified elsewhere), B96.3 
(Hemophilus influenzae [H. influenzae] as the cause of diseases 
classified elsewhere, B96.5 (Pseudomonas (aeruginosa) (mallei) 
(pseudomallei) as the cause of diseases classified elsewhere), or 
B96.89 (Other specified bacterial agents as the cause of diseases 
classified elsewhere).''
    b. Within the partial paragraph (item 10), line 8, the code number 
``J14.0'' is corrected to read ``J14''.

Karuna Seshasai,
Executive Secretary to the Department, Department of Health and Human 
Services.
 [FR Doc. 2021-26069 Filed 11-29-21; 8:45 am]
 BILLING CODE 4120-01-P
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