Agency Information Collection Activities: Proposed Collection; Comment Request, 13337-13338 [2012-5439]

Download as PDF Federal Register / Vol. 77, No. 44 / Tuesday, March 6, 2012 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration on Aging Centers for Medicare & Medicaid Services Agency Information Collection Activities; Proposed Collection; Comment Request; Annual Reporting Requirements for the Older American Act Title VI Grant Program AGENCY: ACTION: Administration on Aging, HHS. Notice. The Administration on Aging (AoA) is announcing that the proposed collection of information listed below has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. SUMMARY: Submit written or electronic comments on the collection of information by April 5, 2012. DATES: Submit electronic comments on the collection of information to: Cynthia.LaCounte@aoa.hhs.gov. Submit written comments on the collection of information to Cynthia LaCounte, Administration on Aging, Washington, DC 20201 or by fax at 202–357–3560. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Margaret Graves at (202) 357–0148 or Cynthia.LaCounte@aoa.hhs.gov. In compliance with 44 U.S.C 3507, AoA has submitted the following proposed collection of information to OMB for review and clearance. SUPPLEMENTARY INFORMATION: pmangrum on DSK3VPTVN1PROD with NOTICES Describe Collection of Information AoA estimates the burden of this collection of information as follows: Annual submission of the Program Performance Reports are due 90 days after the end of the budget period and final project period. Respondents: Federally Recognized Tribes, Tribal and Native Hawaiian Organizations receiving grants under Title VI, Part A, Grants for Native Americans; Title VI, Part B, Native Hawaiian Program and Title VI, Part C, Native American Caregiver Support Program. Estimated Number of Responses: 256. Total Estimated Burden Hours: 640. Dated: February 28, 2012. Kathy Greenlee, Assistant Secretary for Aging. [FR Doc. 2012–5437 Filed 3–5–12; 8:45 am] BILLING CODE 4154–01–P VerDate Mar<15>2010 14:56 Mar 05, 2012 Jkt 226001 [Document Identifier: CMS–10136, CMS– 10116, CMS–10426 and CMS–10406] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services. In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid Services (CMS) is publishing the following summary of proposed collections for public comment. Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. 1. Type of Information Collection Request: Reinstatement of a previously approved collection; Title of Information Collection: Physician Group Practice Transition Demonstration (PGP–TD) Performance Assessment Tool (‘‘PAT’’); Use: The Physician Group Practice (PGP) Demonstration was mandated by section 412 of the Medicare, Medicaid, and SCHIP Benefits Improvement and Protection Act of 2000 and is the precursor to the Medicare Shared Savings Program. Section 1899(k) of the Social Security Act, as added by section 10307(k) of the Affordable Care Act (as amended by section 10307 of the Health Care and Education Reconciliation Act of 2010), states ‘‘the Secretary may enter into an agreement with an ACO under the Demonstration under section 1866A, subject to rebasing and other modifications deemed appropriate by the Secretary.’’ The Demonstration extension is entitled the PGP Transition Demonstration (PGP–TD). We are seeking reinstatement of the collection of information as it was erroneously discontinued. Only a portion of the information collection requirements previously approved under 0938–0941 should have been AGENCY: PO 00000 Frm 00081 Fmt 4703 Sfmt 4703 13337 discontinued. The collection of information is strictly voluntary in nature and was developed in conjunction with the industry and Demonstration participants. Only organizations that voluntarily respond and elect to participate in the Demonstration will be reporting the measures. Moreover, CMS will not be using this information to regulate or sanction but rather to provide financial incentives for improving the quality of care. The collection of information to be used under this extension is being used to test quality data collection systems and determine incentive payment levels to participating physician group practices participating in the PGP–TD. In addition, this data will be used to evaluate the effectiveness of these payment models and provide insight into the most appropriate way for the agency to collect clinical information. Form Number: CMS–10136 (OCN: 0938–0941); Frequency: Yearly; Affected Public: Private Sector—Business or other for-profits and not-for-profit institutions. Number of Respondents: 10. Number of Responses: 10. Total Annual Hours: 790. (For policy questions regarding this collection contact Heather Grimsley at 410–786– 1048. For all other issues call 410–786– 1326.) 2. Type of Information Collection Request: Extension of a currently approved collection; Title of Information Collection: Conditions for Payment of Power Mobility Devices, including Power Wheelchairs and Power-Operated Vehicles; Use: CMS is renewing our request for approval for the collection requirements associated with the final rule, CMS–3017–F (71 FR 17021), which was published on April 5, 2006 and became effective on June 5, 2006. The regulation CMS–3017–F finalized provisions set forth in the interim final regulation (70 FR 50940) published on August 26, 2005. This final rule conforms our regulations to section 302(a)(2)(E)(iv) of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003. This rule defines the term power mobility devices (PMDs) as power wheelchairs and power operated vehicles (POVs or scooters). It sets forth revised conditions for Medicare payment of PMDs and defines who may prescribe PMDs. This rule also requires a face-to-face examination of the beneficiary by the physician or treating practitioner, a written prescription, and receipt of pertinent parts of the medical record by the supplier within 45 days after the face-to-face examination that the durable medical equipment (DME) E:\FR\FM\06MRN1.SGM 06MRN1 pmangrum on DSK3VPTVN1PROD with NOTICES 13338 Federal Register / Vol. 77, No. 44 / Tuesday, March 6, 2012 / Notices suppliers maintain in their records and make available to CMS and its agents upon request. Finally, this rule discusses CMS’ policy on documentation that may be requested by CMS and its agents to support a Medicare claim for payment. Form Number: CMS–10116 (OCN: 0938– 0971); Frequency: Yearly; Affected Public: Private Sector—Business or other for-profits. Number of Respondents: 90,521. Number of Responses: 173,810. Total Annual Hours: 34,762. (For policy questions regarding this collection contact Susan Miller at 410–786–2118. For all other issues call 410–786–1326.) 3. Type of Information Collection Request: New collection; Title of Information Collection: End Stage Renal Disease (ESRD) System Access Request Form; Use: Within CMS, the Office of Clinical Standards and Quality is developing a new suite of systems to support the End Stage Renal Disease (ESRD) program. Due to the sensitivity of the data being collected and reported, CMS must ensure that only authorized personnel have access to data. Personnel are given access to the ESRD systems through the creation of user IDs and passwords within the QualityNet Identity Management System (QIMS); however, once within the system, the system determines the rights and privileges the personnel has over the data within the system. The sole purpose the End Stage Renal Disease System (ESRD) System Access Request Form is to identify the individual’s data access rights once within the ESRD system. This function and the associated data collection is currently being accomplished under ‘‘Part B’’ of the QualityNet Identity Management System Account Form (CMS–10267; OCN: 0938–1050). Once the ESRD System Access Form is approved, the QualityNet Identity Management System (QIMS) Account Form will be revised to remove Part B from the QIMS data collection. Form Number: CMS–10426 (OCN: 0938– New); Frequency: Yearly; Affected Public: Private Sector—Business or other for-profits. Number of Respondents: 25,000. Number of Responses: 25,000. Total Annual Hours: 6,250. (For policy questions regarding this collection contact Michelle Tucker at 410–786–0736. For all other issues call 410–786–1326.) 4. Type of Information Collection Request: New collection; Title of Information Collection: Probable Fraud Measurement Pilot; Use: The Centers for Medicare & Medicaid Services (CMS) is seeking Office of Management and Budget (OMB) approval of the VerDate Mar<15>2010 14:56 Mar 05, 2012 Jkt 226001 collections required for a probable fraud measurement pilot. The probable fraud measurement pilot would establish a baseline estimate of probable fraud in payments for home health care services in the fee-for-service Medicare program. CMS and its agents will collect information from home health agencies, the referring physicians and Medicare beneficiaries selected in a national random sample of home health claims. The pilot will rely on the information collected along with a summary of the service history of the HHA, the referring provider, and the beneficiary to estimate the percentage of total payments that are associated with probable fraud and the percentage of all claims that are associated with probable fraud for Medicare fee-for-service home health. Form Number: CMS–10406 (OCN: 0938–New); Frequency: Yearly; Affected Public: Individual and Private Sector— Business or other for-profits. Number of Respondents: 6,000. Number of Responses: 6,000. Total Annual Hours: 10,500. (For policy questions regarding this collection contact Kelly Gent at 410–786–0918. For all other issues call 410–786–1326.) To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’ Web Site address at https://www.cms.hhs.gov/ PaperworkReductionActof1995, or Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call the Reports Clearance Office on (410) 786– 1326. In commenting on the proposed information collections please reference the document identifier or OMB control number. To be assured consideration, comments and recommendations must be submitted in one of the following ways by May 7, 2012: 1. Electronically. You may submit your comments electronically to https:// www.regulations.gov. Follow the instructions for ‘‘Comment or Submission’’ or ‘‘More Search Options’’ to find the information collection document(s) accepting comments. 2. By regular mail. You may mail written comments to the following address: CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development, Attention: Document Identifier/OMB Control Number lll, Room C4–26– 05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. PO 00000 Frm 00082 Fmt 4703 Sfmt 4703 Dated: March 1, 2012. Martique Jones, Director, Regulations Development Group, Division B, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2012–5439 Filed 3–5–12; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Tribal Consultation Meetings Office of Head Start (OHS), Administration for Children and Families, HHS. ACTION: Notice of meetings. AGENCY: Pursuant to the Improving Head Start for School Readiness Act of 2007, Public Law 110–134, notice is hereby given of one-day Tribal Consultation Sessions to be held between the Department of Health and Human Services, Administration for Children and Families, Office of Head Start leadership and the leadership of Tribal Governments operating Head Start (including Early Head Start) programs. The purpose of these Consultation Sessions is to discuss ways to better meet the needs of American Indian and Alaska Native children and their families, taking into consideration funding allocations, distribution formulas, and other issues affecting the delivery of Head Start services in their geographic locations [42 U.S.C. 9835, Section 640(l)(4)]. DATES: March 22 and April 3, 2012. ADDRESSES: 2012 Office of Head Start Tribal Consultation Sessions will be held at the following locations: Thursday, March 22, 2012—Phoenix, Arizona—Sheraton Crescent Hotel, 2620 West Dunlap Avenue Phoenix, AZ 85021; Tuesday, April 3, 2012—Billings, Montana—Holiday Inn Grand Montana 5500 Midland Road, Billings, MT 59101. FOR FURTHER INFORMATION CONTACT: Camille Loya, Acting Regional Program Manager Region XI, email Camille.Loya@acf.hhs.gov or phone (202) 401–5964. Additional information and online meeting registration is available at https:// www.headstartresourcecenter.org. SUPPLEMENTARY INFORMATION: The Department of Health and Human Services (HHS) announces Office of Head Start (OHS) Tribal Consultations with leaders of Tribal Governments operating Head Start (including Early Head Start) programs for each of the nine geographic regions of Head Start SUMMARY: E:\FR\FM\06MRN1.SGM 06MRN1

Agencies

[Federal Register Volume 77, Number 44 (Tuesday, March 6, 2012)]
[Notices]
[Pages 13337-13338]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5439]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-10136, CMS-10116, CMS-10426 and CMS-10406]


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Centers for Medicare & Medicaid Services.

    In compliance with the requirement of section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid 
Services (CMS) is publishing the following summary of proposed 
collections for public comment. Interested persons are invited to send 
comments regarding this burden estimate or any other aspect of this 
collection of information, including any of the following subjects: (1) 
The necessity and utility of the proposed information collection for 
the proper performance of the agency's functions; (2) the accuracy of 
the estimated burden; (3) ways to enhance the quality, utility, and 
clarity of the information to be collected; and (4) the use of 
automated collection techniques or other forms of information 
technology to minimize the information collection burden.
    1. Type of Information Collection Request: Reinstatement of a 
previously approved collection; Title of Information Collection: 
Physician Group Practice Transition Demonstration (PGP-TD) Performance 
Assessment Tool (``PAT''); Use: The Physician Group Practice (PGP) 
Demonstration was mandated by section 412 of the Medicare, Medicaid, 
and SCHIP Benefits Improvement and Protection Act of 2000 and is the 
precursor to the Medicare Shared Savings Program. Section 1899(k) of 
the Social Security Act, as added by section 10307(k) of the Affordable 
Care Act (as amended by section 10307 of the Health Care and Education 
Reconciliation Act of 2010), states ``the Secretary may enter into an 
agreement with an ACO under the Demonstration under section 1866A, 
subject to rebasing and other modifications deemed appropriate by the 
Secretary.'' The Demonstration extension is entitled the PGP Transition 
Demonstration (PGP-TD).
    We are seeking reinstatement of the collection of information as it 
was erroneously discontinued. Only a portion of the information 
collection requirements previously approved under 0938-0941 should have 
been discontinued. The collection of information is strictly voluntary 
in nature and was developed in conjunction with the industry and 
Demonstration participants. Only organizations that voluntarily respond 
and elect to participate in the Demonstration will be reporting the 
measures. Moreover, CMS will not be using this information to regulate 
or sanction but rather to provide financial incentives for improving 
the quality of care. The collection of information to be used under 
this extension is being used to test quality data collection systems 
and determine incentive payment levels to participating physician group 
practices participating in the PGP-TD. In addition, this data will be 
used to evaluate the effectiveness of these payment models and provide 
insight into the most appropriate way for the agency to collect 
clinical information. Form Number: CMS-10136 (OCN: 0938-0941); 
Frequency: Yearly; Affected Public: Private Sector--Business or other 
for-profits and not-for-profit institutions. Number of Respondents: 10. 
Number of Responses: 10. Total Annual Hours: 790. (For policy questions 
regarding this collection contact Heather Grimsley at 410-786-1048. For 
all other issues call 410-786-1326.)
    2. Type of Information Collection Request: Extension of a currently 
approved collection;
    Title of Information Collection: Conditions for Payment of Power 
Mobility Devices, including Power Wheelchairs and Power-Operated 
Vehicles; Use: CMS is renewing our request for approval for the 
collection requirements associated with the final rule, CMS-3017-F (71 
FR 17021), which was published on April 5, 2006 and became effective on 
June 5, 2006. The regulation CMS-3017-F finalized provisions set forth 
in the interim final regulation (70 FR 50940) published on August 26, 
2005. This final rule conforms our regulations to section 
302(a)(2)(E)(iv) of the Medicare Prescription Drug, Improvement, and 
Modernization Act of 2003. This rule defines the term power mobility 
devices (PMDs) as power wheelchairs and power operated vehicles (POVs 
or scooters). It sets forth revised conditions for Medicare payment of 
PMDs and defines who may prescribe PMDs. This rule also requires a 
face-to-face examination of the beneficiary by the physician or 
treating practitioner, a written prescription, and receipt of pertinent 
parts of the medical record by the supplier within 45 days after the 
face-to-face examination that the durable medical equipment (DME)

[[Page 13338]]

suppliers maintain in their records and make available to CMS and its 
agents upon request. Finally, this rule discusses CMS' policy on 
documentation that may be requested by CMS and its agents to support a 
Medicare claim for payment. Form Number: CMS-10116 (OCN: 0938-0971); 
Frequency: Yearly; Affected Public: Private Sector--Business or other 
for-profits. Number of Respondents: 90,521. Number of Responses: 
173,810. Total Annual Hours: 34,762. (For policy questions regarding 
this collection contact Susan Miller at 410-786-2118. For all other 
issues call 410-786-1326.)
    3. Type of Information Collection Request: New collection; Title of 
Information Collection: End Stage Renal Disease (ESRD) System Access 
Request Form; Use: Within CMS, the Office of Clinical Standards and 
Quality is developing a new suite of systems to support the End Stage 
Renal Disease (ESRD) program. Due to the sensitivity of the data being 
collected and reported, CMS must ensure that only authorized personnel 
have access to data. Personnel are given access to the ESRD systems 
through the creation of user IDs and passwords within the QualityNet 
Identity Management System (QIMS); however, once within the system, the 
system determines the rights and privileges the personnel has over the 
data within the system.
    The sole purpose the End Stage Renal Disease System (ESRD) System 
Access Request Form is to identify the individual's data access rights 
once within the ESRD system. This function and the associated data 
collection is currently being accomplished under ``Part B'' of the 
QualityNet Identity Management System Account Form (CMS-10267; OCN: 
0938-1050). Once the ESRD System Access Form is approved, the 
QualityNet Identity Management System (QIMS) Account Form will be 
revised to remove Part B from the QIMS data collection. Form Number: 
CMS-10426 (OCN: 0938-New); Frequency: Yearly; Affected Public: Private 
Sector--Business or other for-profits. Number of Respondents: 25,000. 
Number of Responses: 25,000. Total Annual Hours: 6,250. (For policy 
questions regarding this collection contact Michelle Tucker at 410-786-
0736. For all other issues call 410-786-1326.)
    4. Type of Information Collection Request: New collection; Title of 
Information Collection: Probable Fraud Measurement Pilot; Use: The 
Centers for Medicare & Medicaid Services (CMS) is seeking Office of 
Management and Budget (OMB) approval of the collections required for a 
probable fraud measurement pilot. The probable fraud measurement pilot 
would establish a baseline estimate of probable fraud in payments for 
home health care services in the fee-for-service Medicare program. CMS 
and its agents will collect information from home health agencies, the 
referring physicians and Medicare beneficiaries selected in a national 
random sample of home health claims. The pilot will rely on the 
information collected along with a summary of the service history of 
the HHA, the referring provider, and the beneficiary to estimate the 
percentage of total payments that are associated with probable fraud 
and the percentage of all claims that are associated with probable 
fraud for Medicare fee-for-service home health. Form Number: CMS-10406 
(OCN: 0938-New); Frequency: Yearly; Affected Public: Individual and 
Private Sector--Business or other for-profits. Number of Respondents: 
6,000. Number of Responses: 6,000. Total Annual Hours: 10,500. (For 
policy questions regarding this collection contact Kelly Gent at 410-
786-0918. For all other issues call 410-786-1326.)
    To obtain copies of the supporting statement and any related forms 
for the proposed paperwork collections referenced above, access CMS' 
Web Site address at https://www.cms.hhs.gov/PaperworkReductionActof1995, 
or E-mail your request, including your address, phone number, OMB 
number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call 
the Reports Clearance Office on (410) 786-1326.
    In commenting on the proposed information collections please 
reference the document identifier or OMB control number. To be assured 
consideration, comments and recommendations must be submitted in one of 
the following ways by May 7, 2012:
    1. Electronically. You may submit your comments electronically to 
https://www.regulations.gov. Follow the instructions for ``Comment or 
Submission'' or ``More Search Options'' to find the information 
collection document(s) accepting comments.
    2. By regular mail. You may mail written comments to the following 
address: CMS, Office of Strategic Operations and Regulatory Affairs, 
Division of Regulations Development, Attention: Document Identifier/OMB 
Control Number ------, Room C4-26-05, 7500 Security Boulevard, 
Baltimore, Maryland 21244-1850.

    Dated: March 1, 2012.
Martique Jones,
Director, Regulations Development Group, Division B, Office of 
Strategic Operations and Regulatory Affairs.
[FR Doc. 2012-5439 Filed 3-5-12; 8:45 am]
BILLING CODE 4120-01-P
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