Office of the National Coordinator for Health Information Technology; American Health Information Community Consumer Empowerment Workgroup Meeting, 8319 [08-625]

Download as PDF Federal Register / Vol. 73, No. 30 / Wednesday, February 13, 2008 / Notices Office of the National Coordinator for Health Information Technology; American Health Information Community Personalized Healthcare Workgroup Meeting ACTION: Announcement of meeting. SUMMARY: This notice announces the 13th meeting of the American Health Information Community Personalized Healthcare Workgroup in accordance with the Federal Advisory Committee Act (Pub. L. No. 92–463, 5 U.S.C., App.). DATES: March 17, 2008, from 1 p.m. to 4 p.m. [Eastern Time]. ADDRESSES: Mary C. Switzer Building (330 C Street, SW., Washington, DC 20201), Conference Room 4090. Please bring photo ID for entry to a Federal building. FOR FURTHER INFORMATION CONTACT: https://www.hhs.gov/healthit/ahic/ healthcare/. SUPPLEMENTARY INFORMATION: The Workgroup will discuss possible common data standards to incorporate interoperable, clinically useful genetic/ genomic information and analytical tools into Electronic Health Records (EHRs) to support clinical decisionmaking for clinician and consumer. The meeting will be available via Web cast. For additional information, go to: https://www.hhs.gov/healthit/ahic/ healthcare/phc_instruct.html. BILLING CODE 4150–45–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the National Coordinator for Health Information Technology; American Health Information Community Consumer Empowerment Workgroup Meeting rwilkins on PROD1PC63 with NOTICES Announcement of meeting. SUMMARY: This notice announces the 24th meeting of the American Health Information Community Consumer Empowerment Workgroup in accordance with the Federal Advisory Committee Act (Pub. L. No. 92–463, 5 U.S.C., App.). VerDate Aug<31>2005 17:45 Feb 12, 2008 Jkt 214001 Dated: January 30, 2008. Judith Sparrow, Director, American Health Information Community, Office of Programs and Coordination, Office of the National Coordinator for Health Information Technology. [FR Doc. 08–625 Filed 2–12–08; 8:45 am] BILLING CODE 4150–45–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–08–08AO] Proposed Data Collections Submitted for Public Comment and Recommendations Dated: January 30, 2008. Judith Sparrow, Director, American Health Information Community, Office of Programs and Coordination, Office of the National Coordinator for Health Information Technology. [FR Doc. 08–624 Filed 2–12–08; 8:45 am] ACTION: March 18, 2008, from 1 p.m. to 4 p.m. [Eastern]. ADDRESSES: Mary C. Switzer Building (330 C Street, SW., Washington, DC 20201), Conference Room 4090. Please bring photo ID for entry to a Federal building. FOR FURTHER INFORMATION CONTACT: https://www.hhs.gov/healthit/ahic/ consumer/. SUPPLEMENTARY INFORMATION: The Workgroup will continue its discussion on how to encourage the widespread adoption of a personal health record that is easy-to-use, portable, longitudinal, affordable, and consumercentered. The meeting will be available via Web cast. For additional information, go to: https://www.hhs.gov/healthit/ahic/ consumer/ce_instruct.html. DATES: DEPARTMENT OF HEALTH AND HUMAN SERVICES In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 for opportunity for public comment on proposed data collection projects, the Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a copy of the data collection plans and instruments, call 404–639–5960 and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance Officer, 1600 Clifton Road, MS–D74, Atlanta, GA 30333 or send an e-mail to omb@cdc.gov. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 8319 ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Written comments should be received within 60 days of this notice. Proposed Project Children’s Peer Relations and the Risk for Injury at School—New—National Center for Injury Prevention and Control (NCIPC), Coordinating Center for Environmental Health and Injury Prevention (CCEHIP), Centers for Disease Control and Prevention (CDC). Background and Brief Description Injuries are responsible for more deaths than all other causes combined for people under 19. In 2003, the Centers for Disease Control and Prevention (CDC) estimated that, annually, one in four children sustain an injury severe enough to warrant medical care, school absence, or bed rest. An investigation of modifiable risk factors for childhood injuries is necessary to improve the health of children. The Division of Unintentional Injury Prevention at the CDC will investigate the relation between children’s social behaviors and experiences at school and school injuries. Peer nominated and teacher rated social behaviors will be collected and compared to injury rates measured in the school health room of 3rd-5th graders at one public elementary school with an ethnically diverse and lower socioeconomic status student body. From this data, a behavioral risk profile for injury will be derived. By learning which children are at risk based on various behavioral characteristics, successful secondary injury prevention strategies may be targeted when resources do not allow universal prevention. The main hypothesis of the study is that children with maladaptive behaviors and social experiences (e.g., aggression, bullying, social withdrawal, peer rejection) will be more at risk for injury than their well-adapted peers. Information collected will include one-time peer nominations of social behaviors and peer relationships and one-time teacher report data of children’s behavior that will reflect children’s behavior across a school year as well as injury event reports from that school year as determined by school health room visits for injury. Injury event reports will be compiled by the school health room aide. By learning E:\FR\FM\13FEN1.SGM 13FEN1

Agencies

DEPARTMENT OF HEALTH AND HUMAN SERVICES

[Federal Register Volume 73, Number 30 (Wednesday, February 13, 2008)]
[Notices]
[Page 8319]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 08-625]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES


Office of the National Coordinator for Health Information 
Technology; American Health Information Community Consumer Empowerment 
Workgroup Meeting

ACTION: Announcement of meeting.

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

SUMMARY: This notice announces the 24th meeting of the American Health 
Information Community Consumer Empowerment Workgroup in accordance with 
the Federal Advisory Committee Act (Pub. L. No. 92-463, 5 U.S.C., 
App.).

DATES: March 18, 2008, from 1 p.m. to 4 p.m. [Eastern].

ADDRESSES: Mary C. Switzer Building (330 C Street, SW., Washington, DC 
20201), Conference Room 4090. Please bring photo ID for entry to a 
Federal building.

FOR FURTHER INFORMATION CONTACT: https://www.hhs.gov/healthit/ahic/
consumer/.

SUPPLEMENTARY INFORMATION: The Workgroup will continue its discussion 
on how to encourage the widespread adoption of a personal health record 
that is easy-to-use, portable, longitudinal, affordable, and consumer-
centered.
    The meeting will be available via Web cast. For additional 
information, go to: https://www.hhs.gov/healthit/ahic/consumer/ce_
instruct.html.

    Dated: January 30, 2008.
Judith Sparrow,
Director, American Health Information Community, Office of Programs and 
Coordination, Office of the National Coordinator for Health Information 
Technology.
[FR Doc. 08-625 Filed 2-12-08; 8:45 am]
BILLING CODE 4150-45-M

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