Meeting for Software Developers on the Common Formats for Patient Safety Data Collection and Event Reporting, 4301-4302 [2016-01353]
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Federal Register / Vol. 81, No. 16 / Tuesday, January 26, 2016 / Notices
meeting will commence in open session
before closing to the public for the
duration of the meeting. The
subcommittee meetings will be closed to
the public in accordance with the
provisions set forth in 5 U.S.C. App. 2
section 10(d), 5 U.S.C. 552b(c)(4), and 5
U.S.C. 552b(c)(6) The grant applications
and the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Agenda items for these meetings are
subject to change as priorities dictate.
Sharon B. Arnold,
AHRQ Deputy Director.
[FR Doc. 2016–01354 Filed 1–25–16; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Meeting for Software Developers on
the Common Formats for Patient
Safety Data Collection and Event
Reporting
Agency for Healthcare Research
and Quality (AHRQ), Department of
Health and Human Services (HHS).
ACTION: Notice of public meeting.
AGENCY:
AHRQ coordinates the
development of sets of common
definitions and reporting formats
(Common Formats) for reporting on
health care quality and patient safety. In
order to support the Common Formats,
AHRQ has provided technical
specifications to promote
standardization by ensuring that data
collected by Patient Safety
Organizations (PSOs) and other entities
are clinically and electronically
comparable. More information on the
Common Formats, including the
technical specifications, can be obtained
through AHRQ’s PSO Web site: https://
www.pso.ahrq.gov/.
The purpose of this notice is to
announce a meeting to discuss the
Common Formats. This meeting is
designed as an interactive forum where
software developers and PSOs can
provide input on the formats. AHRQ
especially requests participation by and
input from those entities which have
used AHRQ’s technical specifications
and implemented, or plan to implement,
the formats electronically.
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
21:57 Jan 25, 2016
Jkt 238001
The meeting will be held from
8:00 a.m.–2:30 p.m. on Friday, April 15,
2016.
ADDRESSES: The meeting will be held at
5600 Fishers Lane, Rockville, MD
20857.
FOR FURTHER INFORMATION CONTACT: A.
Gretchen Buckler, MD MPH, CDR,
USPHS Commissioned Corps, Medical
Officer, Center for Quality Improvement
and Patient Safety, AHRQ, 5600 Fishers
Lane, Rockville, MD 20857; Telephone
(toll free): (866) 403–3697; Telephone
(local): (301) 427–1111; TTY (toll free):
(866) 438–7231; TTY (local): (301) 427–
1130; Email: PSO@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
DATES:
Background
The Patient Safety and Quality
Improvement Act of 2005, 42 U.S.C.
299b-21 to b-26, (Patient Safety Act) and
the related Patient Safety and Quality
Improvement Final Rule, 42 CFR part 3
(Patient Safety Rule), published in the
Federal Register on November 21, 2008,
(73 FR 70732–70814), provide for the
formation of PSOs, which collect,
aggregate, and analyze confidential
information regarding the quality and
safety of health care delivery. The
collection of patient safety work product
allows the aggregation of data that help
to identify and address underlying
causal factors of patient quality and
safety problems.
The Patient Safety Act and Patient
Safety Rule establish a framework by
which doctors, hospitals, skilled
nursing facilities, and other healthcare
providers may assemble information
regarding patient safety events and
quality of care. Information that is
assembled and developed by providers
for reporting to PSOs and the
information received and analyzed by
PSOs—called ‘‘patient safety work
product’’—is privileged and
confidential. Patient safety work
product is used to conduct patient
safety activities, which may include
identifying events, patterns of care, and
unsafe conditions that increase risks
and hazards to patients. Definitions and
other details about PSOs and patient
safety work product are included in the
Patient Safety Act and Patient Safety
Rule which can be accessed
electronically at: https://www.pso.ahrq.
gov/legislation/.
Definition of Common Formats
The term ‘‘Common Formats’’ refers
to the common definitions and reporting
formats, specified by AHRQ, that allow
health care providers to collect and
submit standardized information
regarding patient quality and safety to
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
4301
PSOs and other entities. The Common
Formats are not intended to replace any
current mandatory reporting system,
collaborative/voluntary reporting
system, research-related reporting
system, or other reporting/recording
system; rather the formats are intended
to enhance the ability of health care
providers to report information that is
standardized both clinically and
electronically.
In collaboration with the interagency
Federal Patient Safety Workgroup
(PSWG), the National Quality Forum
(NQF), and the public, AHRQ has
developed Common Formats for three
settings of care — acute care hospitals,
skilled nursing facilities, and retail
pharmacies — in order to facilitate
standardized data collection and
analysis. The scope of Common Formats
applies to all patient safety concerns
including: incidents—patient safety
events that reached the patient, whether
or not there was harm; near misses or
close calls—patient safety events that
did not reach the patient; and unsafe
conditions—circumstances that increase
the probability of a patient safety event.
AHRQ’s Common Formats include:
• Event descriptions (descriptions of
patient safety events and unsafe
conditions to be reported),
• Specifications for patient safety
aggregate reports and individual event
summaries,
• Delineation of data elements to be
collected for different types of events to
populate the reports,
• A user’s guide and quick guide, and
• Technical specifications for
electronic data collection and reporting.
Common Formats Development
In anticipation of the need for
Common Formats, AHRQ began their
development by creating an inventory of
functioning private and public sector
patient safety reporting systems. This
inventory provided an evidence base to
inform construction of the Common
Formats. The inventory included many
systems from the private sector,
including prominent academic settings,
hospital systems, and international
reporting systems (e.g., from the United
Kingdom and the Commonwealth of
Australia). In addition, virtually all
major Federal patient safety reporting
systems were included, such as those
from the Centers for Disease Control and
Prevention (CDC), the Food and Drug
Administration (FDA), the Department
of Defense (DoD), and the Department of
Veterans Affairs (VA).
Since February 2005, AHRQ has
convened the PSWG to assist AHRQ
with developing and maintaining the
Common Formats. The PSWG includes
E:\FR\FM\26JAN1.SGM
26JAN1
mstockstill on DSK4VPTVN1PROD with NOTICES
4302
Federal Register / Vol. 81, No. 16 / Tuesday, January 26, 2016 / Notices
major health agencies within HHS—
CDC, Centers for Medicare & Medicaid
Services, FDA, Health Resources and
Services Administration, Indian Health
Service, National Institutes of Health,
National Library of Medicine, Office of
the National Coordinator for Health
Information Technology, Office of
Public Health and Science, and
Substance Abuse and Mental Health
Services Administration—as well as the
DoD and VA.
When developing Common Formats,
AHRQ first reviews existing patient
safety practices and event reporting
systems. In collaboration with the
PSWG and Federal subject matter
experts, AHRQ drafts and releases beta
versions of the Common Formats for
public review and comment. The PSWG
assists AHRQ with assuring the
consistency of definitions/formats with
those of relevant government agencies
as refinement of the Common Formats
continues.
Since the initial release of the
Common Formats in August 2008,
AHRQ has regularly revised the formats
based upon public comment. AHRQ
solicits feedback on beta (and
subsequent) versions of Common
Formats from private sector
organizations and individuals. Based
upon the feedback received, AHRQ
further revises the Common Formats. To
the extent practicable, the Common
Formats are also aligned with World
Health Organization (WHO) concepts,
frameworks, and definitions.
Participation by the private sector in
the development and subsequent
revision of the Common Formats is
achieved through working with the
NQF. The Agency engages the NQF, a
non-profit organization focused on
health care quality, to solicit comments
and advice regarding proposed versions
of the Common Formats. AHRQ began
this process with the NQF in 2008,
receiving feedback on AHRQ’s 0.1 Beta
release of the Common Formats for
Event Reporting—Hospital. After
receiving public comment, the NQF
solicits the review and advice of its
Common Formats Expert Panel and
subsequently provides feedback to
AHRQ. The Agency then revises and
refines the Common Formats and issues
them as a production version. AHRQ
has continued to employ this process for
all subsequent versions of the Common
Formats.
The technical specifications promote
standardization of collected patient
safety event information by specifying
rules for data collection and submission,
as well as by providing guidance for
how and when to create data elements,
their valid values, conditional and go-to
VerDate Sep<11>2014
21:57 Jan 25, 2016
Jkt 238001
logic, and reports. These specifications
will ensure that data collected by PSOs
and other entities have comparable
clinical meaning.
The technical specifications also
provide direction to software
developers, so that the Common
Formats can be implemented
electronically, and to PSOs, so that the
Common Formats can be submitted
electronically to the Patient Safety
Organization Privacy Protection Center
(PSOPPC) for data de-identification and
transmission to the NPSD.
Common Formats technical
specifications consist of the following:
• Data dictionary—defines data
elements and their attributes (data
element name, answer values, field
length, guide for use, etc.) included in
Common Formats;
• Clinical document architecture
(CDA) implementation guide—provides
instructions for developing a file to
transmit the Common Formats Patient
Safety data from the PSO to the PSOPPC
using the Common Formats;
• Validation rules and errors
document—specifies and defines the
validation rules that will be applied to
the Common Formats data elements
submitted to the PSOPPC;
• Common Formats flow charts—
diagrams the valid paths to complete
generic and event specific formats (a
complete event report);
• Local specifications—provides
specifications for processing, linking
and reporting on events and details
specifications for reports; and
• Metadata registry—includes
descriptive facts about information
contained in the data dictionary to
illustrate how such data corresponds
with similar data elements used by
other Federal agencies and standards
development organizations [e.g., HL—7,
International Standards Organization
(ISO)].
Agenda, Registration, and Other
Information about the Meeting
The 2016 meeting will be an
interactive forum designed to allow
meeting participants not only to provide
input but also to respond to the input
provided by others. The meeting agenda
will include: an update of Federal
efforts related to the Common Formats,
including development of formats for
new settings; Common Formats software
products demonstrations; a discussion
of data integrity related to submission of
patient safety adverse events; and a
question and answer session.
AHRQ requests that interested
persons send an email to the PSOPPC at
support@psoppc.org for registration
information. Before the meeting, a
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
detailed agenda and logistical
information will be provided to
registrants. Prior to the meeting, AHRQ
invites review of the technical
specifications for Common Formats
which can be accessed through AHRQ’s
PSO Web site at https://www.psoppc.
org/psoppc_web/publicpages/common
FormatsOverview.
Sharon B. Arnold,
AHRQ Deputy Director.
[FR Doc. 2016–01353 Filed 1–25–16; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Request for Nominations of
Candidates To Serve on the Advisory
Committee on Immunization Practices
(ACIP)
The Centers for Disease Control and
Prevention (CDC) is soliciting
nominations for membership on ACIP.
The ACIP consists of 15 experts in fields
associated with immunization, who are
selected by the Secretary of the U.S.
Department of Health and Human
Services (HHS) to provide advice and
guidance to the Secretary, the Assistant
Secretary for Health, and the CDC on the
control of vaccine-preventable diseases.
The role of the ACIP is to provide
advice that will lead to a reduction in
the incidence of vaccine preventable
diseases in the United States, and an
increase in the safe use of vaccines and
related biological products. The
committee also establishes, reviews, and
as appropriate, revises the list of
vaccines for administration to children
eligible to receive vaccines through the
Vaccines for Children (VFC) Program.
Nominations are being sought for
individuals who have expertise and
qualifications necessary to contribute to
the accomplishments of the committee’s
objectives. Nominees will be selected
based on expertise in the field of
immunization practices; multidisciplinary expertise in public health;
expertise in the use of vaccines and
immunologic agents in both clinical and
preventive medicine; knowledge of
vaccine development, evaluation, and
vaccine delivery; or knowledge about
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employees will not be considered for
membership. Members may be invited
to serve for four-year terms.
The next cycle of selection of
candidates will begin in the fall of 2016,
E:\FR\FM\26JAN1.SGM
26JAN1
Agencies
[Federal Register Volume 81, Number 16 (Tuesday, January 26, 2016)]
[Notices]
[Pages 4301-4302]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-01353]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Meeting for Software Developers on the Common Formats for Patient
Safety Data Collection and Event Reporting
AGENCY: Agency for Healthcare Research and Quality (AHRQ), Department
of Health and Human Services (HHS).
ACTION: Notice of public meeting.
-----------------------------------------------------------------------
SUMMARY: AHRQ coordinates the development of sets of common definitions
and reporting formats (Common Formats) for reporting on health care
quality and patient safety. In order to support the Common Formats,
AHRQ has provided technical specifications to promote standardization
by ensuring that data collected by Patient Safety Organizations (PSOs)
and other entities are clinically and electronically comparable. More
information on the Common Formats, including the technical
specifications, can be obtained through AHRQ's PSO Web site: https://www.pso.ahrq.gov/.
The purpose of this notice is to announce a meeting to discuss the
Common Formats. This meeting is designed as an interactive forum where
software developers and PSOs can provide input on the formats. AHRQ
especially requests participation by and input from those entities
which have used AHRQ's technical specifications and implemented, or
plan to implement, the formats electronically.
DATES: The meeting will be held from 8:00 a.m.-2:30 p.m. on Friday,
April 15, 2016.
ADDRESSES: The meeting will be held at 5600 Fishers Lane, Rockville, MD
20857.
FOR FURTHER INFORMATION CONTACT: A. Gretchen Buckler, MD MPH, CDR,
USPHS Commissioned Corps, Medical Officer, Center for Quality
Improvement and Patient Safety, AHRQ, 5600 Fishers Lane, Rockville, MD
20857; Telephone (toll free): (866) 403-3697; Telephone (local): (301)
427-1111; TTY (toll free): (866) 438-7231; TTY (local): (301) 427-1130;
Email: PSO@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Background
The Patient Safety and Quality Improvement Act of 2005, 42 U.S.C.
299b-21 to b-26, (Patient Safety Act) and the related Patient Safety
and Quality Improvement Final Rule, 42 CFR part 3 (Patient Safety
Rule), published in the Federal Register on November 21, 2008, (73 FR
70732-70814), provide for the formation of PSOs, which collect,
aggregate, and analyze confidential information regarding the quality
and safety of health care delivery. The collection of patient safety
work product allows the aggregation of data that help to identify and
address underlying causal factors of patient quality and safety
problems.
The Patient Safety Act and Patient Safety Rule establish a
framework by which doctors, hospitals, skilled nursing facilities, and
other healthcare providers may assemble information regarding patient
safety events and quality of care. Information that is assembled and
developed by providers for reporting to PSOs and the information
received and analyzed by PSOs--called ``patient safety work product''--
is privileged and confidential. Patient safety work product is used to
conduct patient safety activities, which may include identifying
events, patterns of care, and unsafe conditions that increase risks and
hazards to patients. Definitions and other details about PSOs and
patient safety work product are included in the Patient Safety Act and
Patient Safety Rule which can be accessed electronically at: https://www.pso.ahrq.gov/legislation/.
Definition of Common Formats
The term ``Common Formats'' refers to the common definitions and
reporting formats, specified by AHRQ, that allow health care providers
to collect and submit standardized information regarding patient
quality and safety to PSOs and other entities. The Common Formats are
not intended to replace any current mandatory reporting system,
collaborative/voluntary reporting system, research-related reporting
system, or other reporting/recording system; rather the formats are
intended to enhance the ability of health care providers to report
information that is standardized both clinically and electronically.
In collaboration with the interagency Federal Patient Safety
Workgroup (PSWG), the National Quality Forum (NQF), and the public,
AHRQ has developed Common Formats for three settings of care -- acute
care hospitals, skilled nursing facilities, and retail pharmacies -- in
order to facilitate standardized data collection and analysis. The
scope of Common Formats applies to all patient safety concerns
including: incidents--patient safety events that reached the patient,
whether or not there was harm; near misses or close calls--patient
safety events that did not reach the patient; and unsafe conditions--
circumstances that increase the probability of a patient safety event.
AHRQ's Common Formats include:
Event descriptions (descriptions of patient safety events
and unsafe conditions to be reported),
Specifications for patient safety aggregate reports and
individual event summaries,
Delineation of data elements to be collected for different
types of events to populate the reports,
A user's guide and quick guide, and
Technical specifications for electronic data collection
and reporting.
Common Formats Development
In anticipation of the need for Common Formats, AHRQ began their
development by creating an inventory of functioning private and public
sector patient safety reporting systems. This inventory provided an
evidence base to inform construction of the Common Formats. The
inventory included many systems from the private sector, including
prominent academic settings, hospital systems, and international
reporting systems (e.g., from the United Kingdom and the Commonwealth
of Australia). In addition, virtually all major Federal patient safety
reporting systems were included, such as those from the Centers for
Disease Control and Prevention (CDC), the Food and Drug Administration
(FDA), the Department of Defense (DoD), and the Department of Veterans
Affairs (VA).
Since February 2005, AHRQ has convened the PSWG to assist AHRQ with
developing and maintaining the Common Formats. The PSWG includes
[[Page 4302]]
major health agencies within HHS--CDC, Centers for Medicare & Medicaid
Services, FDA, Health Resources and Services Administration, Indian
Health Service, National Institutes of Health, National Library of
Medicine, Office of the National Coordinator for Health Information
Technology, Office of Public Health and Science, and Substance Abuse
and Mental Health Services Administration--as well as the DoD and VA.
When developing Common Formats, AHRQ first reviews existing patient
safety practices and event reporting systems. In collaboration with the
PSWG and Federal subject matter experts, AHRQ drafts and releases beta
versions of the Common Formats for public review and comment. The PSWG
assists AHRQ with assuring the consistency of definitions/formats with
those of relevant government agencies as refinement of the Common
Formats continues.
Since the initial release of the Common Formats in August 2008,
AHRQ has regularly revised the formats based upon public comment. AHRQ
solicits feedback on beta (and subsequent) versions of Common Formats
from private sector organizations and individuals. Based upon the
feedback received, AHRQ further revises the Common Formats. To the
extent practicable, the Common Formats are also aligned with World
Health Organization (WHO) concepts, frameworks, and definitions.
Participation by the private sector in the development and
subsequent revision of the Common Formats is achieved through working
with the NQF. The Agency engages the NQF, a non-profit organization
focused on health care quality, to solicit comments and advice
regarding proposed versions of the Common Formats. AHRQ began this
process with the NQF in 2008, receiving feedback on AHRQ's 0.1 Beta
release of the Common Formats for Event Reporting--Hospital. After
receiving public comment, the NQF solicits the review and advice of its
Common Formats Expert Panel and subsequently provides feedback to AHRQ.
The Agency then revises and refines the Common Formats and issues them
as a production version. AHRQ has continued to employ this process for
all subsequent versions of the Common Formats.
The technical specifications promote standardization of collected
patient safety event information by specifying rules for data
collection and submission, as well as by providing guidance for how and
when to create data elements, their valid values, conditional and go-to
logic, and reports. These specifications will ensure that data
collected by PSOs and other entities have comparable clinical meaning.
The technical specifications also provide direction to software
developers, so that the Common Formats can be implemented
electronically, and to PSOs, so that the Common Formats can be
submitted electronically to the Patient Safety Organization Privacy
Protection Center (PSOPPC) for data de-identification and transmission
to the NPSD.
Common Formats technical specifications consist of the following:
Data dictionary--defines data elements and their
attributes (data element name, answer values, field length, guide for
use, etc.) included in Common Formats;
Clinical document architecture (CDA) implementation
guide--provides instructions for developing a file to transmit the
Common Formats Patient Safety data from the PSO to the PSOPPC using the
Common Formats;
Validation rules and errors document--specifies and
defines the validation rules that will be applied to the Common Formats
data elements submitted to the PSOPPC;
Common Formats flow charts--diagrams the valid paths to
complete generic and event specific formats (a complete event report);
Local specifications--provides specifications for
processing, linking and reporting on events and details specifications
for reports; and
Metadata registry--includes descriptive facts about
information contained in the data dictionary to illustrate how such
data corresponds with similar data elements used by other Federal
agencies and standards development organizations [e.g., HL--7,
International Standards Organization (ISO)].
Agenda, Registration, and Other Information about the Meeting
The 2016 meeting will be an interactive forum designed to allow
meeting participants not only to provide input but also to respond to
the input provided by others. The meeting agenda will include: an
update of Federal efforts related to the Common Formats, including
development of formats for new settings; Common Formats software
products demonstrations; a discussion of data integrity related to
submission of patient safety adverse events; and a question and answer
session.
AHRQ requests that interested persons send an email to the PSOPPC
at support@psoppc.org for registration information. Before the meeting,
a detailed agenda and logistical information will be provided to
registrants. Prior to the meeting, AHRQ invites review of the technical
specifications for Common Formats which can be accessed through AHRQ's
PSO Web site at https://www.psoppc.org/psoppc_web/publicpages/commonFormatsOverview.
Sharon B. Arnold,
AHRQ Deputy Director.
[FR Doc. 2016-01353 Filed 1-25-16; 8:45 am]
BILLING CODE 4160-90-P