Announcement of Requirements and Registration for “Reporting Patient Safety Events Challenge”, 21776-21777 [2012-8758]

Download as PDF 21776 Federal Register / Vol. 77, No. 70 / Wednesday, April 11, 2012 / Notices Meeting Dates: May 7th from 9 a.m. to 5 p.m. and May 8th from 8:30 a.m. to 12:30 p.m. Eastern Standard Time (EST). Deadline for Meeting Registration and Comments: April 30th, 2012, 5 p.m., EST. Deadline for Requesting Special Accommodations: April 30th, 2012, 5 p.m., EST. ADDRESSES: Meeting Location: Crystal Gateway Marriott, 1700 Jefferson Davis Highway, Arlington, VA 22202. Meeting Registration: To register, visit the Resources page on the CCIIO Web site at https://cciio.cms.gov/resources/ other/#fm.Written Comments: Jeffrey Davis, Center for Consumer Information and Insurance Oversight, CMS, 200 Independence Avenue SW., Washington, DC 20201, Phone: 301–492–4270, Fax: 301–492– 4462, or contact by email at RAspringmeeting@cms.hhs.gov. Written comments must be submitted in Microsoft Word format. FOR FURTHER INFORMATION CONTACT: Please send inquiries about the logistics of the meeting to logistics@isomglobal.com and about the content of the meeting to RAspringmeeting@cms.hhs.gov. Press inquiries are handled through CCIIO’s Press Office at (202) 690–6343. SUPPLEMENTARY INFORMATION: DATES: I. Background This notice announces a meeting on the risk adjustment program required under section 1343 of the Affordable Care Act. The purpose of this meeting is to provide information to States, issuers, and interested parties about the risk adjustment program. This meeting will provide an opportunity to hear from a variety of interested parties as the Federal risk adjustment methodology is being developed and we are working through operational issues. wreier-aviles on DSK5TPTVN1PROD with NOTICES II. Meeting Agenda The Spring Risk Adjustment Meeting will provide information to States, issuers, and interested parties about the risk adjustment program. The Risk Adjustment Spring Meeting will focus on: the risk adjustment model, calculation of plan average actuarial risk, calculation of payments and charges, data collection approach, and the schedule for running risk adjustment. The Risk Adjustment Meeting will convene stakeholders including State governments, industry representatives, and other interested parties. The Risk Adjustment Meeting will provide the public with further detail about the risk VerDate Mar<15>2010 15:14 Apr 10, 2012 Jkt 226001 adjustment methodology that is currently being developed by HHS and the operational framework for risk adjustment when HHS is operating the program on behalf of a State. In addition, the Risk Adjustment Meeting will provide stakeholders with an opportunity to communicate with HHS about the risk adjustment program. The meeting is open to the public, but attendance is limited to the space available. There are capabilities for remote access. Persons wishing to attend this meeting must register by the date listed in the DATES section above, and by visiting the CCIIO Web page listed in the ADDRESSES section above. Registration will be on a first-come, first-serve basis, limited to three attendees per organization. Catalog of Federal Domestic Assistance Program No. 93.778, Medical Assistance Program; No. 93.773 Medicare—Hospital Insurance Program; and No. 93.774, Medicare—Supplementary Medical Insurance Program. Dated: April 5, 2012. Marilyn Tavenner, Acting Administrator, Centers for Medicare & Medicaid Services. [FR Doc. 2012–8771 Filed 4–10–12; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Announcement of Requirements and Registration for ‘‘Reporting Patient Safety Events Challenge’’ Office of the National Coordinator for Health Information Technology, HHS. Award Approving Official: Farzad Mostashari, National Coordinator for Health Information Technology. ACTION: Notice. AGENCY: Patient Safety Organizations (PSOs) listed by the Agency for Healthcare Research and Quality (AHRQ) create a safe environment for health care providers to collect, aggregate, and analyze data without fear of legal discovery. Hospitals struggle to increase internal incident reporting, especially by busy physicians and nurses, and to create effective systems for the quality and risk management staff to do root cause analyses and follow-up. The ‘‘Reporting Patient Safety Events Challenge’’ asks multidisciplinary teams to develop an application that facilitates the reporting of patient safety events, whether implemented in hospital or ambulatory settings. The solution needs to make it easier for any individual to file a report SUMMARY: PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 electronically, using Common Formats but allowing for additional elements and narratives. It must allow the hospital quality and risk management staff to add information from follow-up investigation, submit reports as appropriate to PSOs, the state, or the FDA (which may differ, and need to be tracked separately), and track follow-up activities. The statutory authority for this challenge competition is Section 105 of the America COMPETES Reauthorization Act of 2010 (Pub. L. 111–358). DATES: Effective on April 11, 2012. Challenge submission period ends July 23, 2012, 11:59 p.m. et. FOR FURTHER INFORMATION CONTACT: Adam Wong, 202–720–2866; Wil Yu, 202–690–5920. SUPPLEMENTARY INFORMATION: Subject of Challenge Competition The ‘‘Reporting Patient Safety Events Challenge’’ asks multi-disciplinary teams to develop an application that facilitates the reporting of patient safety events, whether implemented in hospital or ambulatory settings. This application would: • Increase the ease of reporting patient safety events to the provider or parent organization; • Enable providers to import relevant EMR, PHR, and other electronic information, including screen shots, to the patient safety report and, in turn, submit an AHRQ Common Formatscompliant report to one or more PSOs; • Capture useful demographic and other relevant information from each patient including age, gender, race, and relevant diagnoses; • Capture information about the type of organization submitting the report using AHRQ’s PSO Information format; • Reduce burden of reporting by enabling the provider or parent organization to have the option of submitting information in the patient safety report to non-PSO public health or health oversight organizations, including state or federal programs or accrediting or certifying bodies. • Be platform-agnostic; and • Leverage and extend NwHIN standards and services including, but not limited to, transport (Direct, web services), content (Transitions of Care, CCD/CCR), and standardized vocabularies. Eligibility Rules for Participating in the Competition To be eligible to win a prize under this challenge, an individual or entity— (1) Shall have registered to participate in the competition under the rules E:\FR\FM\11APN1.SGM 11APN1 Federal Register / Vol. 77, No. 70 / Wednesday, April 11, 2012 / Notices promulgated by the Office of the National Coordinator for Health Information Technology. (2) Shall have complied with all the requirements under this section. (3) In the case of a private entity, shall be incorporated in and maintain a primary place of business in the United States, and in the case of an individual, whether participating singly or in a group, shall be a citizen or permanent resident of the United States. (4) May not be a Federal entity or Federal employee acting within the scope of their employment. (5) Shall not be an HHS employee working on their applications or submissions during assigned duty hours. (6) Shall not be an employee of Office of the National Coordinator for Health IT. (7) Federal grantees may not use Federal funds to develop COMPETES Act challenge applications unless consistent with the purpose of their grant award. (8) Federal contractors may not use Federal funds from a contract to develop COMPETES Act challenge applications or to fund efforts in support of a COMPETES Act challenge submission. An individual or entity shall not be deemed ineligible because the individual or entity used Federal facilities or consulted with Federal employees during a competition if the facilities and employees are made available to all individuals and entities participating in the competition on an equitable basis. Entrants must agree to assume any and all risks and waive claims against the Federal Government and its related entities, except in the case of willful misconduct, for any injury, death, damage, or loss of property, revenue, or profits, whether direct, indirect, or consequential, arising from my participation in this prize contest, whether the injury, death, damage, or loss arises through negligence or otherwise. Entrants must also agree to indemnify the Federal Government against third party claims for damages arising from or related to competition activities. wreier-aviles on DSK5TPTVN1PROD with NOTICES Registration Process for Participants To register for this challenge participants should: D Access the www.challenge.gov Web site and search for the ‘‘Reporting Patient Safety Events Challenge’’. D Access the ONC Investing in Innovation (i2) Challenge Web site at: Æ https://www.health2challenge.org/ onc-i2-challenges/. VerDate Mar<15>2010 15:14 Apr 10, 2012 Jkt 226001 21777 Æ A registration link for the challenge can be found on the landing page under the challenge description. DEPARTMENT OF HEALTH AND HUMAN SERVICES Amount of the Prize Centers for Disease Control and Prevention D First Prize: $50,000. D Second Prize: $15,000. D Third Prize: $5,000. Awards may be subject to Federal income taxes and HHS will comply with IRS withholding and reporting requirements, where applicable. Payment of the Prize [Docket Number NIOSH–245] Expanded Charge for Peer Review of the NIOSH document Titled: ‘‘Criteria for a Recommended Standard: Occupational Exposure to Diacetyl and 2,3-pentanedione’’ National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). AGENCY: Prize will be paid by contractor. Basis Upon Which Winner Will Be Selected The ONC review panel will make selections based upon the following criteria: 1. Effectiveness of the system in facilitating patient safety event reporting including its compliance with AHRQ’s Common Formats. 2. Usability and design from the standpoint of all stakeholders. 3. Ability to integrate with electronic health records and other HIT data sources. 4. Creativity and innovation. 5. Leverage NwHIN standards including transport, content, and vocabularies. Additional Information Ownership of intellectual property is determined by the following: D Each entrant retains title and full ownership in and to their submission. Entrants expressly reserve all intellectual property rights not expressly granted under the challenge agreement. D By participating in the challenge, each entrant hereby irrevocably grants to Sponsor and Administrator a limited, non-exclusive, royalty free, worldwide, license and right to reproduce, publically perform, publically display, and use the Submission to the extent necessary to administer the challenge, and to publically perform and publically display the Submission, including, without limitation, for advertising and promotional purposes relating to the challenge. Authority: 15 U.S.C. 3719. Notice of Expanded Charge for Peer Review. ACTION: The National Institute for Occupational Safety and Health (NIOSH) of the Centers for Disease Control and Prevention (CDC) is undergoing peer review for the draft document, ‘‘Criteria for a Recommended Standard: Occupational Exposure to Diacetyl and 2,3pentanedione.’’ NIOSH held a public meeting on August 26, 2011 in Washington, DC [76 FR 44338] to discuss and obtain comments on the draft document. Public comments were accepted into the NIOSH docket from August 12, 2011- November 18, 2011 [76 FR 64353]. The draft document and all public comments received are posted on the Internet at: https://www.cdc.gov/ niosh/docket/archive/docket245.html for Docket number NIOSH–245. After consultation with the Occupational Safety and Health Administration, Department of Labor (OSHA/DOL), NIOSH has asked the peer reviewers seven additional questions for consideration which are posted here: https://www.cdc.gov/niosh/review/peer/ HISA/diacetyl-pr.html. This entry serves as notice of the expanded charge to peer reviewers for this draft document. SUMMARY: FOR FURTHER INFORMATION CONTACT: Lauralynn Taylor McKernan, ScD CIH, NIOSH, 4676 Columbia Parkway C–32, Cincinnati, OH 45226, telephone (513) 533–8542, Fax (513) 533–8230, email LMcKernan@cdc.gov. Dated: April 5, 2012. Farzad Mostashari, National Coordinator for Health Information Technology. Dated: April 2, 2012. John Howard, Director, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention. [FR Doc. 2012–8758 Filed 4–10–12; 8:45 am] [FR Doc. 2012–8685 Filed 4–10–12; 8:45 am] BILLING CODE 4150–45–P BILLING CODE 4163–19–P PO 00000 Frm 00057 Fmt 4703 Sfmt 9990 E:\FR\FM\11APN1.SGM 11APN1

Agencies

[Federal Register Volume 77, Number 70 (Wednesday, April 11, 2012)]
[Notices]
[Pages 21776-21777]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-8758]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES


Announcement of Requirements and Registration for ``Reporting 
Patient Safety Events Challenge''

AGENCY: Office of the National Coordinator for Health Information 
Technology, HHS.
    Award Approving Official: Farzad Mostashari, National Coordinator 
for Health Information Technology.

ACTION: Notice.

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

SUMMARY: Patient Safety Organizations (PSOs) listed by the Agency for 
Healthcare Research and Quality (AHRQ) create a safe environment for 
health care providers to collect, aggregate, and analyze data without 
fear of legal discovery. Hospitals struggle to increase internal 
incident reporting, especially by busy physicians and nurses, and to 
create effective systems for the quality and risk management staff to 
do root cause analyses and follow-up. The ``Reporting Patient Safety 
Events Challenge'' asks multi-disciplinary teams to develop an 
application that facilitates the reporting of patient safety events, 
whether implemented in hospital or ambulatory settings. The solution 
needs to make it easier for any individual to file a report 
electronically, using Common Formats but allowing for additional 
elements and narratives. It must allow the hospital quality and risk 
management staff to add information from follow-up investigation, 
submit reports as appropriate to PSOs, the state, or the FDA (which may 
differ, and need to be tracked separately), and track follow-up 
activities.
    The statutory authority for this challenge competition is Section 
105 of the America COMPETES Reauthorization Act of 2010 (Pub. L. 111-
358).

DATES: Effective on April 11, 2012. Challenge submission period ends 
July 23, 2012, 11:59 p.m. et.

FOR FURTHER INFORMATION CONTACT: Adam Wong, 202-720-2866; Wil Yu, 202-
690-5920.

SUPPLEMENTARY INFORMATION:

Subject of Challenge Competition

    The ``Reporting Patient Safety Events Challenge'' asks multi-
disciplinary teams to develop an application that facilitates the 
reporting of patient safety events, whether implemented in hospital or 
ambulatory settings. This application would:
     Increase the ease of reporting patient safety events to 
the provider or parent organization;
     Enable providers to import relevant EMR, PHR, and other 
electronic information, including screen shots, to the patient safety 
report and, in turn, submit an AHRQ Common Formats-compliant report to 
one or more PSOs;
     Capture useful demographic and other relevant information 
from each patient including age, gender, race, and relevant diagnoses;
     Capture information about the type of organization 
submitting the report using AHRQ's PSO Information format;
     Reduce burden of reporting by enabling the provider or 
parent organization to have the option of submitting information in the 
patient safety report to non-PSO public health or health oversight 
organizations, including state or federal programs or accrediting or 
certifying bodies.
     Be platform-agnostic; and
     Leverage and extend NwHIN standards and services 
including, but not limited to, transport (Direct, web services), 
content (Transitions of Care, CCD/CCR), and standardized vocabularies.

Eligibility Rules for Participating in the Competition

    To be eligible to win a prize under this challenge, an individual 
or entity--
    (1) Shall have registered to participate in the competition under 
the rules

[[Page 21777]]

promulgated by the Office of the National Coordinator for Health 
Information Technology.
    (2) Shall have complied with all the requirements under this 
section.
    (3) In the case of a private entity, shall be incorporated in and 
maintain a primary place of business in the United States, and in the 
case of an individual, whether participating singly or in a group, 
shall be a citizen or permanent resident of the United States.
    (4) May not be a Federal entity or Federal employee acting within 
the scope of their employment.
    (5) Shall not be an HHS employee working on their applications or 
submissions during assigned duty hours.
    (6) Shall not be an employee of Office of the National Coordinator 
for Health IT.
    (7) Federal grantees may not use Federal funds to develop COMPETES 
Act challenge applications unless consistent with the purpose of their 
grant award.
    (8) Federal contractors may not use Federal funds from a contract 
to develop COMPETES Act challenge applications or to fund efforts in 
support of a COMPETES Act challenge submission.
    An individual or entity shall not be deemed ineligible because the 
individual or entity used Federal facilities or consulted with Federal 
employees during a competition if the facilities and employees are made 
available to all individuals and entities participating in the 
competition on an equitable basis.
    Entrants must agree to assume any and all risks and waive claims 
against the Federal Government and its related entities, except in the 
case of willful misconduct, for any injury, death, damage, or loss of 
property, revenue, or profits, whether direct, indirect, or 
consequential, arising from my participation in this prize contest, 
whether the injury, death, damage, or loss arises through negligence or 
otherwise.
    Entrants must also agree to indemnify the Federal Government 
against third party claims for damages arising from or related to 
competition activities.

Registration Process for Participants

    To register for this challenge participants should:
    [ssquf] Access the www.challenge.gov Web site and search for the 
``Reporting Patient Safety Events Challenge''.
    [ssquf] Access the ONC Investing in Innovation (i2) Challenge Web 
site at:
    [cir] https://www.health2challenge.org/onc-i2-challenges/.
    [cir] A registration link for the challenge can be found on the 
landing page under the challenge description.

Amount of the Prize

    [ssquf] First Prize: $50,000.
    [ssquf] Second Prize: $15,000.
    [ssquf] Third Prize: $5,000.
    Awards may be subject to Federal income taxes and HHS will comply 
with IRS withholding and reporting requirements, where applicable.

Payment of the Prize

    Prize will be paid by contractor.

Basis Upon Which Winner Will Be Selected

    The ONC review panel will make selections based upon the following 
criteria:
    1. Effectiveness of the system in facilitating patient safety event 
reporting including its compliance with AHRQ's Common Formats.
    2. Usability and design from the standpoint of all stakeholders.
    3. Ability to integrate with electronic health records and other 
HIT data sources.
    4. Creativity and innovation.
    5. Leverage NwHIN standards including transport, content, and 
vocabularies.

Additional Information

    Ownership of intellectual property is determined by the following:
    [ssquf] Each entrant retains title and full ownership in and to 
their submission. Entrants expressly reserve all intellectual property 
rights not expressly granted under the challenge agreement.
    [ssquf] By participating in the challenge, each entrant hereby 
irrevocably grants to Sponsor and Administrator a limited, non-
exclusive, royalty free, worldwide, license and right to reproduce, 
publically perform, publically display, and use the Submission to the 
extent necessary to administer the challenge, and to publically perform 
and publically display the Submission, including, without limitation, 
for advertising and promotional purposes relating to the challenge.

    Authority:  15 U.S.C. 3719.

    Dated: April 5, 2012.
Farzad Mostashari,
National Coordinator for Health Information Technology.
[FR Doc. 2012-8758 Filed 4-10-12; 8:45 am]
BILLING CODE 4150-45-P
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