Proposed Data Collection Submitted for Public Comment and Recommendations, 12610-12612 [2019-06305]
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12610
Federal Register / Vol. 84, No. 63 / Tuesday, April 2, 2019 / Notices
Proposed Project
Assessment of Clinical and
Microbiologic Outcomes in Patients
Infected with Shigella with Decreased
Susceptibility to Ciprofloxacin and
Azithromycin through a Prospective
Case-Control Study in California—
New—National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
A broad 60-day notice for this project
entitled ‘‘Applied Research to Address
Emerging Public Health priorities’’ was
published on May 29, 2018. This project
is part of a series of CDC research
projects funded under that Broad
Agency Announcement.
Multidrug-resistant Shigella is a
public health problem in the U.S,
including California. Resistance to first
line drugs (azithromycin and
ciprofloxacin) limits treatment options
and may be associated with worse
patient outcomes. In 2017, the Centers
for Disease Control and Prevention
(CDC) reported an increase in Shigella
isolates with ciprofloxacin minimum
inhibitory concentration (MIC)
range=0.12–1.0 mg/mL. In 2018, this was
updated (https://emergency.cdc.gov/
han/han00411.asp) and confirmed a
continued increase in such isolates.
While current Clinical and Laboratory
Standards Institute (CLSI) criteria
categorize Shigella isolates that fall
within this range as susceptible, these
strains often harbor a quinolone
resistance gene, which may be
associated with decreased susceptibility
to ciprofloxacin. Little is known about
the clinical implications of infection
with Shigella with ciprofloxacin MICs
in the range of 0.12–1 mg/mL; including
whether treatment with a
fluoroquinolone is associated with a
worse clinical outcome for the patient,
or will result in prolonged shedding and
further reduction in ciprofloxacin
susceptibility. In addition, CLSI has not
established clinical breakpoints for
azithromycin, making treatment
decisions challenging for clinicians
when managing patients with
multidrug-resistant Shigella infections.
Systematically collected data regarding
the clinical and microbiologic outcomes
of patients infected with Shigella with
ciprofloxacin MIC 0.12–1 mg/mL or that
fall above the epidemiologic cutoffs for
azithromycin (≥16 mg/mL for S. flexneri,
≥32 mg/mL for S. sonnei) are needed to
inform clinical breakpoints.
The primary objectives of the study
are to: (1) Estimate the proportion of
California Shigella isolates with a
ciprofloxacin MIC range of 0.12–1.0 mg/
mL and the proportion of Shigella
isolates that fall above the
epidemiologic cutoffs for azithromycin;
(2) determine whether patients who
were infected with Shigella with a
ciprofloxacin MIC range of 0.12–1.0 mg/
mL and treated with a fluoroquinolone
(and thus have decreased susceptibility
to ciprofloxacin, or DSC Shigella) have
worse clinical and microbiologic
outcomes than patients who were
infected with Shigella with a
ciprofloxacin MIC <0.12 mg/mL and
were also treated with a
fluoroquinolone; (3) systematically
describe the clinical outcomes of
patients infected with Shigella that fall
above the epidemiologic cutoffs for
azithromycin (referred to as decreased
susceptibility to azithromycin, DSA
Shigella); and (4) explore microbiologic
features including antimicrobial
susceptibility testing (AST) patterns and
WGS of Shigella isolates with DSC and
DSA. Results of this investigation will
provide data that may inform CLSI
breakpoints and shape public health
recommendations on management and
prevention of DSC and DSA Shigella
infections.
CDC is seeking one year of OMB
approval. There is no cost to
respondents other than the time to
participate. Total estimated annual
burden is 878 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Shigella cases and controls ...........
Case Interview Form Initial ............
Case Interview Form Second ........
Symptom Log Form .......................
Stool collection and submission initial.
Stool collection and submission
second.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–06303 Filed 4–1–19; 8:45 am]
230
230
230
230
1
1
1
1
45/60
45/60
30/60
90/60
144 .................................................
1
30/60
Centers for Disease Control and
Prevention
BILLING CODE 4163–18–P
amozie on DSK9F9SC42PROD with NOTICES
[60 Day–19–19ACB; Docket No. CDC–2019–
0021]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
VerDate Sep<11>2014
18:45 Apr 01, 2019
Jkt 247001
PO 00000
Notice with comment period.
Frm 00036
Fmt 4703
Average
burden per
response
(in hours)
.................................................
.................................................
.................................................
.................................................
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ACTION:
Number of
responses per
respondent
Number of
respondents
Type of respondents
Sfmt 4703
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled ‘‘Drug Overdose Surveillance and
Epidemiology (DOSE).’’ This new data
collection effort is an essential
component toward reducing the opioid
crisis, one of HHS Department’s top
priorities. DOSE data is critical to our
SUMMARY:
E:\FR\FM\02APN1.SGM
02APN1
Federal Register / Vol. 84, No. 63 / Tuesday, April 2, 2019 / Notices
ability to rapidly identify outbreaks and
provide situational awareness of
changes in emergency department (ED)
visits involving suspected drug, opioid,
heroin and stimulant overdoses at the
local, state, and regional level.
DATES: CDC must receive written
comments on or before June 3, 2019.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0021 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffery M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments through
the Federal eRulemaking portal
(Regulations.gov) or by U.S. mail to the
address listed above.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act
of 1995 (PRA) (44 U.S.C. 3501–3520),
Federal agencies must obtain approval
from the Office of Management and
Budget (OMB) for each collection of
information they conduct or sponsor. In
addition, the PRA also requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each new proposed
collection, each proposed extension of
existing collection of information, and
each reinstatement of previously
approved information collection before
submitting the collection to the OMB for
approval. To comply with this
requirement, we are publishing this
notice of a proposed data collection as
described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
amozie on DSK9F9SC42PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
VerDate Sep<11>2014
18:45 Apr 01, 2019
Jkt 247001
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Drug Overdose Surveillance and
Epidemiology (DOSE)—New—National
Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The rapid increase in opioid overdose
deaths since 2013, numerous severe
fentanyl and fentanyl analog outbreaks
occurring since 2015 across the United
States, and the declaration of the opioid
overdose epidemic as a national public
health emergency on October 26, 2017
have highlighted the urgent need to
rapidly establish and enhance timely
surveillance of suspected drug, opioid,
heroin, and stimulant overdoses. These
data are critical to inform timely local,
state, and regional responses, especially
to acute and/or widespread multi-state
outbreaks.
This new data collection effort is an
essential component toward reducing
the opioid crisis, one of DHHS’s top
priorities. DOSE data is critical to our
ability to rapidly identify outbreaks and
provide situational awareness of
changes in emergency department (ED)
visits involving suspected drug, opioid,
heroin and stimulant overdoses at the
local, state, and regional level. This will
be accomplished by standardizing and
enhancing sharing of existing ED data
locally collected by 52 health
departments (all 50 state health
departments, the health department of
Puerto Rico, and the health department
of the District of Columbia) with CDC.
In addition, CDC leadership
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
12611
communicates with HHS on an ongoing
basis, and this data is part of its request
to better monitor, plan, and implement
programs to prevent overdose and
reduce subsequent harms.
DOSE proposes to fund 52 health
departments (50 state health
departments, the health department of
Puerto Rico and the health department
of the District of Columbia) to rapidly
share existing ED data on counts of ED
visits involving suspected drug, opioid,
heroin, and stimulant overdoses using
two standard data forms (i.e., the Rapid
ED overdose data form and the ED
discharge overdose data form) and
standard CDC case definitions.
The system will leverage ED
syndromic data and hospital discharge
data on ED visits already routinely
collected by state and territorial health
departments. No new data will be
systematically collected from EDs, and
health departments will be reimbursed
by CDC for the burden related to sharing
ED data with CDC. The 52 funded
health departments will rapidly share
existing ED data with CDC on a monthly
basis using the Rapid ED overdose data
form and standard CDC case definitions.
Data may come from different local ED
data systems, but is expected to cover at
least 75% of ED visits in the jurisdiction
(e.g., state).
CDC will require all participating
health departments to provide counts of
ED visits involving suspected drug,
opioid, heroin, and stimulant overdoses
by county, age group, sex, and time (i.e.,
month and year) in a standardized
manner using the Rapid ED overdose
data form, which is an Excel data
template. This form also collects data
quality indicators such as percent of ED
visits missing data on key variables (i.e.,
metadata). In order to assess and
improve rapid ED data sharing, all 52
participating health departments will
also be asked to share counts of ED
visits involving suspected drug, opioid,
heroin and stimulant overdoses by
county, age group, sex, and time (i.e.,
month and year) from more finalized
hospital discharge files, the current
surveillance standard. The data will be
shared with CDC on a quarterly or
yearly basis using a standardized Excel
data form, the ED discharge overdose
data form, and standard CDC case
definitions. There are no costs to the
respondents other than their time.
E:\FR\FM\02APN1.SGM
02APN1
12612
Federal Register / Vol. 84, No. 63 / Tuesday, April 2, 2019 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(hours)
Total annual
burden
(hours)
Form name
State health departments, the DC
health department and PR health
department.
Jurisdictions sharing case-level ED
data with CDC through the NSSP
BioSense (OMB #0920–0824).
State health departments, the DC
health department and PR health
department.
State health departments, the DC
health department and PR health
department.
Rapid ED overdose data form .........
28
12
3
1,088
Rapid ED overdose data form .........
24
12
0.5
144
ED discharge overdose data form ...
26
4
3
312
ED discharge overdose data form ...
26
1
3
78
Total ...........................................
...........................................................
........................
........................
........................
1,542
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–06305 Filed 4–1–19; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–19ABV; Docket No. CDC–2019–
0019]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
ACTION:
Notice with comment period.
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Information
Collection on Soil-transmitted Helminth
Infections in Alabama and Mississippi.
CDC requests OMB approval to collect
information on prevalence and
distribution of soil-transmitted helminth
infections and potential risk factors.
SUMMARY:
amozie on DSK9F9SC42PROD with NOTICES
Total no. of
responses per
respondent
No. of
respondents
Type of respondent
CDC must receive written
comments on or before June 3, 2019.
DATES:
VerDate Sep<11>2014
18:45 Apr 01, 2019
Jkt 247001
You may submit comments,
identified by Docket No. CDC–2019–
0019 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Lead,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7118. Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
ADDRESSES:
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Investigation on soil-transmitted
helminth infections in Alabama and
Mississippi—New—Center for Global
Health (CGH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Soil-transmitted helminths (STH) are
intestinal worms transmitted through
contaminated soil. They include
roundworms (Ascaris lumbricoides),
whipworms (Trichuris trichiura),
hookworms (Ancylostoma duodenale
and Necator americanus) and the worm
Strongyloides stercoralis. These
infections were widespread across the
American South through the early 20th
E:\FR\FM\02APN1.SGM
02APN1
Agencies
[Federal Register Volume 84, Number 63 (Tuesday, April 2, 2019)]
[Notices]
[Pages 12610-12612]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-06305]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-19-19ACB; Docket No. CDC-2019-0021]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled ``Drug Overdose Surveillance and
Epidemiology (DOSE).'' This new data collection effort is an essential
component toward reducing the opioid crisis, one of HHS Department's
top priorities. DOSE data is critical to our
[[Page 12611]]
ability to rapidly identify outbreaks and provide situational awareness
of changes in emergency department (ED) visits involving suspected
drug, opioid, heroin and stimulant overdoses at the local, state, and
regional level.
DATES: CDC must receive written comments on or before June 3, 2019.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2019-
0021 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffery M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal
eRulemaking portal (Regulations.gov) or by U.S. mail to the address
listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-
3520), Federal agencies must obtain approval from the Office of
Management and Budget (OMB) for each collection of information they
conduct or sponsor. In addition, the PRA also requires Federal agencies
to provide a 60-day notice in the Federal Register concerning each
proposed collection of information, including each new proposed
collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
Drug Overdose Surveillance and Epidemiology (DOSE)--New--National
Center for Injury Prevention and Control (NCIPC), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The rapid increase in opioid overdose deaths since 2013, numerous
severe fentanyl and fentanyl analog outbreaks occurring since 2015
across the United States, and the declaration of the opioid overdose
epidemic as a national public health emergency on October 26, 2017 have
highlighted the urgent need to rapidly establish and enhance timely
surveillance of suspected drug, opioid, heroin, and stimulant
overdoses. These data are critical to inform timely local, state, and
regional responses, especially to acute and/or widespread multi-state
outbreaks.
This new data collection effort is an essential component toward
reducing the opioid crisis, one of DHHS's top priorities. DOSE data is
critical to our ability to rapidly identify outbreaks and provide
situational awareness of changes in emergency department (ED) visits
involving suspected drug, opioid, heroin and stimulant overdoses at the
local, state, and regional level. This will be accomplished by
standardizing and enhancing sharing of existing ED data locally
collected by 52 health departments (all 50 state health departments,
the health department of Puerto Rico, and the health department of the
District of Columbia) with CDC. In addition, CDC leadership
communicates with HHS on an ongoing basis, and this data is part of its
request to better monitor, plan, and implement programs to prevent
overdose and reduce subsequent harms.
DOSE proposes to fund 52 health departments (50 state health
departments, the health department of Puerto Rico and the health
department of the District of Columbia) to rapidly share existing ED
data on counts of ED visits involving suspected drug, opioid, heroin,
and stimulant overdoses using two standard data forms (i.e., the Rapid
ED overdose data form and the ED discharge overdose data form) and
standard CDC case definitions.
The system will leverage ED syndromic data and hospital discharge
data on ED visits already routinely collected by state and territorial
health departments. No new data will be systematically collected from
EDs, and health departments will be reimbursed by CDC for the burden
related to sharing ED data with CDC. The 52 funded health departments
will rapidly share existing ED data with CDC on a monthly basis using
the Rapid ED overdose data form and standard CDC case definitions. Data
may come from different local ED data systems, but is expected to cover
at least 75% of ED visits in the jurisdiction (e.g., state).
CDC will require all participating health departments to provide
counts of ED visits involving suspected drug, opioid, heroin, and
stimulant overdoses by county, age group, sex, and time (i.e., month
and year) in a standardized manner using the Rapid ED overdose data
form, which is an Excel data template. This form also collects data
quality indicators such as percent of ED visits missing data on key
variables (i.e., metadata). In order to assess and improve rapid ED
data sharing, all 52 participating health departments will also be
asked to share counts of ED visits involving suspected drug, opioid,
heroin and stimulant overdoses by county, age group, sex, and time
(i.e., month and year) from more finalized hospital discharge files,
the current surveillance standard. The data will be shared with CDC on
a quarterly or yearly basis using a standardized Excel data form, the
ED discharge overdose data form, and standard CDC case definitions.
There are no costs to the respondents other than their time.
[[Page 12612]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Total no. of Average burden Total annual
Type of respondent Form name No. of responses per per response burden
respondents respondent (hours) (hours)
----------------------------------------------------------------------------------------------------------------
State health departments, the Rapid ED 28 12 3 1,088
DC health department and PR overdose data
health department. form.
Jurisdictions sharing case- Rapid ED 24 12 0.5 144
level ED data with CDC overdose data
through the NSSP BioSense form.
(OMB #0920-0824).
State health departments, the ED discharge 26 4 3 312
DC health department and PR overdose data
health department. form.
State health departments, the ED discharge 26 1 3 78
DC health department and PR overdose data
health department. form.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,542
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-06305 Filed 4-1-19; 8:45 am]
BILLING CODE 4163-19-P