CDC/HRSA Advisory Committee on HIV, Viral Hepatitis and STD Prevention and Treatment, 66469-66470 [2012-26478]

Download as PDF 66469 Federal Register / Vol. 77, No. 214 / Monday, November 5, 2012 / Notices DGMQ staff will search the literature and available data sources to ensure that the information of interest has not already been collected or is in the process of being collected. DGMQ will make all reasonable efforts to ensure that the information collection does not overlap with other data collection on immigrant health, such as those authorized under OMB control numbers 1405–0113, 0920–0006, 1615–0029, and 1615–0033. DGMQ staff proposes that data collection methods for this package will include but are not limited to: Interviews, focus groups, group discussions, and surveys. Depending on the specific purpose, data collection methods may be conducted either inperson, by telephone, on paper, or online. Data may be collected in quantitative and/or qualitative forms. Each proposed information collection will submit the tools used for data collection, including screenshots of web-based surveys, in the statement provided to OMB. DGMQ estimates that 18,720 respondents will be screened in order for 9485 respondents to be involved in information collection activities each year. We anticipate that the information collections undertaken within this generic will use some combination of 15 surveys, 35 focus groups, and 125 interviews, with some information collections making use of more than one method per collection. It is estimated that information collection activities will total 10,598 burden hours per year. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent Foreign-born, migrant, bile populations. Foreign-born, migrant, bile populations. Foreign-born, migrant, bile populations. Foreign-born, migrant, bile populations. refugee and other morefugee and other morefugee and other morefugee and other mo- Dated: October 30, 2012. Ron A. Otten, Director, Office of Scientific Integrity (OSI), Office of the Associate Director for Science (OADS), Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2012–26898 Filed 11–2–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Breast and Cervical Cancer Early Detection and Control Advisory Committee (BCCEDCAC) WREIER-AVILES on DSK5TPTVN1PROD with NOTICES In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), the Centers for Disease Control and Prevention (CDC) announces the following meeting of the aforementioned committee: Name: Breast and Cervical Cancer Early Detection and Control Advisory Committee. Times and Dates: 9:00 a.m.–5:00 p.m., December 6, 2012; 9:00 a.m.–12:30 p.m., December 7, 2012. Place: University Office Park, Columbia Building, 2900 Woodcock Boulevard, Atlanta, Georgia 30341. Status: Open to the public, limited only by the space available. Purpose: The committee is charged with advising the Secretary, Department of Health and Human Services, and the Director, CDC, regarding the early detection and control of VerDate Mar<15>2010 15:30 Nov 02, 2012 Number of respondents Form name Jkt 229001 Number of responses per respondent Average burden per response (in hours) Screeners for Surveys, Focus Groups, Interviews. Surveys (Approximately 15 surveys/year) ..... 18,720 1 10/60 9,000 1 45/60 Focus Groups (Approximately 35 focus groups/year). Interviews (Approximately 125 interviews/ year). 360 1 1.5 125 1 1.5 breast and cervical cancer. The committee makes recommendations regarding national program goals and objectives; implementation strategies; and program priorities including surveillance, epidemiologic investigations, education and training, information dissemination, professional interactions and collaborations, and policy. Matters To Be Discussed: The agenda will include discussion on the impact of implementation of the Affordable Care Act on the National Breast and Cervical Cancer Early Detection Program; presentations on outcomes of Care Coordination and Waiver projects; and discussions on how to expand services to impact women beyond our eligible screening population. Agenda items are subject to change as priorities dictate. Contact Person for More Information: Jameka R. Blackmon, Executive Secretary, BCCEDCAC, Division of Cancer Prevention and Control, National Center for Chronic Disease Prevention and Health Promotion, CDC, 4770 Buford Highway, Mailstop K–52, Chamblee, Georgia 30314, Telephone: 770– 488–4880. The Director, Management Analysis and Services Office, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 Dated: October 26, 2012. Elaine L. Baker, Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. 2012–26893 Filed 11–2–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention CDC/HRSA Advisory Committee on HIV, Viral Hepatitis and STD Prevention and Treatment In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), the Centers for Disease Control and Prevention (CDC) and the Health Resources and Services Administration (HRSA) announce the following meeting of the aforementioned committee: Times and Dates: 8:00 a.m.–5:45 p.m., December 11, 2012 8:00 a.m.–2:30 p.m., December 12, 2012 Place: The Hilton Rockville, 1750 Rockville Pike, Rockville, Maryland 20852, Telephone: (301) 468–1100. Status: Open to the public, limited only by the space available. The meeting room will accommodate approximately 100 people. Purpose: This Committee is charged with advising the Director, CDC and the E:\FR\FM\05NON1.SGM 05NON1 66470 Federal Register / Vol. 77, No. 214 / Monday, November 5, 2012 / Notices Administrator, HRSA, regarding activities related to prevention and control of HIV/AIDS and other STDs, the support of health care services to persons living with HIV/AIDS, and education of health professionals and the public about HIV/AIDS and other STDs. Matters To Be Discussed: Agenda items include: (1) Treatment Cascade— Linkage to Care/Retention in Care— Treatment as Prevention; (2) Ryan White HIV/AIDS Program Client Level Data Update; (3) Viral Hepatitis Action Plan and Implementation Update; (4) Update on Translation of International HIV/ AIDS Work Domestically; and (5) CHAC Workgroups Update. Agenda items are subject to change as priorities dictate. Contact Person for More Information: Margie Scott-Cseh, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, CDC, 1600 Clifton Road NE., Mailstop E–07, Atlanta, Georgia 30333, Telephone: (404) 639–8317. The Director, Management Analysis and Services Office, has been delegated the authority to sign Federal Register Notices pertaining to announcements of meetings and other committee management activities, for both the CDC and the Agency for Toxic Substances and Disease Registry. Dated: October 22, 2012. Elaine L. Baker, Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. 2012–26478 Filed 11–2–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration WREIER-AVILES on DSK5TPTVN1PROD with NOTICES Agency Information Collection Activities: Submission for OMB Review; Comment Request Periodically, the Health Resources and Services Administration (HRSA) publishes abstracts of information collection requests under review by the Office of Management and Budget (OMB), in compliance with the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request a copy of the clearance requests submitted to OMB for review, email paperwork@hrsa.gov or call the HRSA Reports Clearance Office on (301) 443– 1984. The following request has been submitted to the Office of Management VerDate Mar<15>2010 15:30 Nov 02, 2012 Jkt 229001 and Budget for review under the Paperwork Reduction Act of 1995: Proposed Project: Sickle Cell Disease Treatment Demonstration Program— Quality Improvement Data Collection for the Hemoglobinopathy Learning Collaborative (OMB No. 0915–xxxx)– [NEW] Background: In response to the growing need for resources devoted to sickle cell disease and other hemoglobinopathies, the United States Congress, under Section 712 of the American Jobs Creation Act of 2004 (Pub. L. 108–357), authorized a demonstration program for the prevention and treatment of sickle cell disease (SCD) to be administered through the Bureau of Primary Health Care and the Maternal and Child Health Bureau (MCHB) of the Health Resources and Services Administration (HRSA) in the U.S. Department of Health and Human Services. The program is known as the Sickle Cell Disease Treatment Demonstration Program (SCDTDP). The SCDTDP is designed to improve access to services for individuals with sickle cell disease, improve and expand patient and provider education, and improve and expand the continuity and coordination of service delivery for individuals with sickle cell disease and sickle cell trait. In 2006, the MCHB Genetic Services Branch (GSB) awarded funding to a National Coordinating Center (NCC). The NCC was established to: (1) Collect, coordinate, monitor, and report on best practices and findings regarding the activities of the demonstration program; (2) identify a model protocol for eligible entities with respect to the prevention and treatment of Sickle Cell Disease; (3) identify educational materials regarding the prevention and treatment of Sickle Cell Disease; and, (4) prepare a final report on the efficacy of the demonstration program based on evaluation and quality improvement (QI) findings. To achieve the goals/objectives of the NCC, the National Initiative for Children’s Healthcare Quality (NICHQ) and partners are facilitating the Hemoglobinopathy Learning Collaborative (HLC). The HLC includes grantee teams funded from the SCDTDP and the Sickle Cell Disease for Newborn Screening Program (SCDNBSP). The HLC uses a process known as the Model for Improvement, which is a widely used approach to QI in health care settings. The Model for Improvement utilizes a structured process that asks grantee teams, who hereafter will be referred to as improvement teams, to build on small tests of change in their PO 00000 Frm 00039 Fmt 4703 Sfmt 4703 health care setting, while providing monthly reporting on measurements. The proposed QI Data Collection and reporting system is an integral component of this model. Purpose: The purpose of this QI Data Collection strategy is to implement a system to monitor the progress of MCHB-funded activities in improving care and health outcomes for individuals living with sickle cell disease/trait and meeting the goals of the SCDTDP. Each improvement team will be asked to report on a core set of measures related to quality improvement for hemoglobinopathies. Through an evidence-based process, a bank of QI measures has been developed to assess health care utilization of the SCD population as well as several aspects of the system of care. The QI Data Collection strategy will provide an effective and efficient mechanism to do the following: (1) Assess the services provided by grantees under the SCDTDP and monitor and drive improvement on quality measures; (2) collect, coordinate, and distribute data, best practices, and findings from network sites; (3) refine a common model protocol regarding the prevention and treatment of sickle cell disease; (4) examine/address barriers that individuals and families living with sickle cell disease face when accessing quality health care and health education; (5) evaluate the grantees’ performance in meeting the objectives of the SCDTDP; and, (6) provide HRSA/ Congress information on the overall progress of the program. The proposed data collection and entry forms are as follows: (1) Participant Profile Form, (2) Acute Care Visit Form, and (3) Ambulatory Care Visit Form. Respondents: Grantees funded by HRSA under the SCDTDP will be the respondents for this data collection activity. Each month, SCDTDP teams will complete up to three data collection and entry forms for 20 patients with SCD or sickle cell trait who were seen in their network that month. The Participant Profile form will collect demographic and basic health information. The Acute Care Visit and Ambulatory Care Visit forms will assess care in acute and ambulatory care settings, respectively. All information will be collected via medical chart review. Data will be entered directly into a secure web-based data collection tool, Research Electronic Data Capture (REDCap). The data entered into REDCap will be analyzed via a custom measurement generator that will calculate and export the QI E:\FR\FM\05NON1.SGM 05NON1

Agencies

[Federal Register Volume 77, Number 214 (Monday, November 5, 2012)]
[Notices]
[Pages 66469-66470]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-26478]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


CDC/HRSA Advisory Committee on HIV, Viral Hepatitis and STD 
Prevention and Treatment

    In accordance with section 10(a)(2) of the Federal Advisory 
Committee Act (Pub. L. 92-463), the Centers for Disease Control and 
Prevention (CDC) and the Health Resources and Services Administration 
(HRSA) announce the following meeting of the aforementioned committee:
    Times and Dates:
8:00 a.m.-5:45 p.m., December 11, 2012
8:00 a.m.-2:30 p.m., December 12, 2012
    Place: The Hilton Rockville, 1750 Rockville Pike, Rockville, 
Maryland 20852, Telephone: (301) 468-1100.
    Status: Open to the public, limited only by the space available. 
The meeting room will accommodate approximately 100 people.
    Purpose: This Committee is charged with advising the Director, CDC 
and the

[[Page 66470]]

Administrator, HRSA, regarding activities related to prevention and 
control of HIV/AIDS and other STDs, the support of health care services 
to persons living with HIV/AIDS, and education of health professionals 
and the public about HIV/AIDS and other STDs.
    Matters To Be Discussed: Agenda items include: (1) Treatment 
Cascade--Linkage to Care/Retention in Care--Treatment as Prevention; 
(2) Ryan White HIV/AIDS Program Client Level Data Update; (3) Viral 
Hepatitis Action Plan and Implementation Update; (4) Update on 
Translation of International HIV/AIDS Work Domestically; and (5) CHAC 
Workgroups Update.
    Agenda items are subject to change as priorities dictate.
    Contact Person for More Information: Margie Scott-Cseh, National 
Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, CDC, 1600 
Clifton Road NE., Mailstop E-07, Atlanta, Georgia 30333, Telephone: 
(404) 639-8317.
    The Director, Management Analysis and Services Office, has been 
delegated the authority to sign Federal Register Notices pertaining to 
announcements of meetings and other committee management activities, 
for both the CDC and the Agency for Toxic Substances and Disease 
Registry.

    Dated: October 22, 2012.
Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease 
Control and Prevention.
[FR Doc. 2012-26478 Filed 11-2-12; 8:45 am]
BILLING CODE 4163-18-P

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