Cody Loveland MPH Surveillance Epidemiologist Wyoming Department of Health Learning Objectives Upon completion of this presentation attendees will be able to 1 Understand the clinical significance of CRE and its modes of ID: 913482
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Slide1
CRE Surveillance and Prevention
Cody Loveland, MPH
Surveillance Epidemiologist
Wyoming Department of Health
Slide2Learning Objectives
Upon completion of this presentation, attendees will be able to:
1
.
Understand the clinical significance of CRE and its modes of
transmission
2
.
Identify and describe the WDH CRE definition
3
.
Describe 12 facility-level CRE prevention strategies
4
.
Evaluate your facility’s readiness for detecting, reporting, and
containing CRE
Slide3CRE Basics
Slide4CRE =
C
arbapenem
-
R
esistant
Enterobacteriaceae
Family of bacteria -
Enterobacteriaceae
Normal part of human gut flora
Carbapenems are broad spectrum antibacterial drugs
Imipenem,
meropenem
,
doripenem
,
ertapenem
Often treatment of last choice for gram-negative bacteria
CRE are bacteria that have developed resistance to carbapenems
Either through susceptibility testing or through the production of carbapenemase
Slide5Family of
Enterobacteriaceae
Medically Important CRE
Klebsiella
pneumoniae
Enterobacter
species
Escherichia coli
Klebsiella
oxytoca
Salmonella
entericaSerratia marcescensCitrobacter freundii
https://www.livingoceansfoundation.org/education/portal/course/classification/
Slide6Why are CRE Important?
Slide7Mortality in CRE Bacteremia
p
<0.001
Patel et al. Infect Control
Hosp
Epidemiol
2008;29:1099-1106
Slide8Not just a hospital problem
Matters for whole healthcare system
Shared healthcare providers
Patient and resident transfers
Mode of transmission
Person-to-person
Especially contact with wounds or stool
Contaminated medical equipment
Slide9Mechanisms of Resistance
Carbapenemase Producing (CP-CRE)
enzyme that breaks down Carbapenems
KPC (most common)
NDM
OXA-48
VIM
IMP
Others??
These are an infection control emergency!
Non-Carbapenemase Producing, but resistant (Non-CP-CRE)
Slide10WDH CRE Definition
The Wyoming Department of Health defines CRE as any
Enterobacteriaceae
that:
A
re
resistant to at least one carbapenem (including imipenem
1
, meropenem, doripenem, or ertapenem) using the current M100-S25 CLSI
breakpoints
2
; OR
Test positive for carbapenemase production by the Carba NP test; ORTest positive for a known carbapenemase gene by nucleic acid amplification testing.
1, 2
See WDH CRE Toolkit p. 3.
Available at https://health.wyo.gov/publichealth/infectious-disease-epidemiology-unit/disease/cre/
Slide11Sample CRE Lab Result
Susceptibility Results (WDH Def. part 1)
Whether sample produces carbapenemase (WDH Def. Part 2)
Results of NAAT Testing (WDH Def. Part 3)
Genus and species
This is a non-CP-CRE
Slide12Other
Carbapenem
-Resistant Organisms
Pseudomonas aeruginosa
and
Acinetobacter
baumannii
species
are not part of the
Enterobacteriaceae
family and therefore are not technically considered CRE.HOWEVER, still medically important and drug resistant!Often contain same carbapenemase genes as CRESend CR-PA and CR-AB samples to WPHL for confirmation testing! Only send non-mucoid CR-PA samples Follow same prevention principles as CRE, but also consult with WDH
Slide13Colonization vs. Infection
Colonization
– The presence of bacteria on a body surface (like on the skin, mouth, intestines or airway) without causing disease in the person
.
CRE colonization can be prolonged (>6 months)
Can lead to unidentified transmission
Infection
– The presence of bacteria on the body that is associated with an immune response.
Both statuses have different implications in the healthcare setting and impact your response
Created
by Uwe
Kils
(iceberg) and User:Wiska Bodo (sky). [GFDL (http://www.gnu.org/copyleft/fdl.html) or CC-BY-SA-3.0 (http://creativecommons.org/licenses/by-sa/3.0/)], via Wikimedia Commons
ColonizedPatients
Infected Patients
Slide14Measure
CP-CRE Infection
CP-CRE Colonization
Non-CP-CRE Infection
Non-CP-CRE Colonization
††
Notify Receiving facility
Yes
Yes
Yes
Yes
Notify WDH upon transfer or death
Yes
Yes
No
No
Standard Precautions
Yes
Yes
Yes
Yes
Contact Precautions
†
Gown/gloves
for in-room resident care
Yes
Yes
Yes
For residents at higher risk of CRE transmission
Door Signage
Yes
Yes
Yes
For residents at higher risk of CRE transmission
Private Room
Yes (strongly encouraged)
Yes (strongly encouraged)
Yes
No
Restricted to room
Yes
No**
No**
No**
Enhanced Environmental Cleaning
Yes
Yes
Yes
No
Designated or disposable equipment
Yes
Yes
Yes
No
If >1 case, cohort staff if feasible
Yes
Yes
Optional
Optional
If >1 case, cohort residents if feasible
Yes
Yes
Optional
Optional
Consult with WDH regarding screening cultures
Yes
Yes
No
No
Visitor recommendations
:
Perform hand hygiene often, particularly after leaving the resident’s room
.
Gown/gloves if contact with body fluids is anticipated
.
Gown/gloves if no contact with body fluids is anticipated.
Yes
Yes
No
Yes
Yes
No
Yes
Yes
No
Yes
Yes
No
Slide15Facility-Level Prevention Strategies
Slide16Facility-Level Prevention Strategies
1.
Hand Hygiene
Single most important aspect of preventing CRE transmission!
Reminders, education, audits
http://www.glasbergen.com/diet-health-fitness-medical/hand-washing-hygiene/
Slide17Facility-Level Prevention Strategies
2. Contact Precautions
In acute care and ventilator units of skilled nursing facilities:
Perform hand hygiene
Donning gown and gloves before entering
patient’s
room
Removing the gown and gloves and performing hand hygiene
before
exiting the affected patient’s room
Lower-acuity post-acute setting:
Depends on procedures and perceived
riskhttps://www.compliancesigns.com/NHE-18543.shtml
Slide18Facility-Level Prevention Strategies
3. Education
Need to educate HCP about preventing transmission of CRE
At minimum, education should include reviews of proper use of contact precautions and proper donning and doffing of PPE so HCP don’t expose
themselves
Consider giving in-service to staff on CRE and other gram-negative
MDRO
MDR-
Klebsiella pneumoniae
Photo credit:
David
Dorward
; Ph.D.; National Institute of Allergy and Infectious Diseases (NIAID)
Slide19Facility-Level Prevention
Strategies
4. Use of Devices
Device use has been associated with CRE
Minimizing device use should be part of effort to prevent all MDROs
Regularly review device use to ensure it’s still required and promptly discontinue use when no longer needed
5. Laboratory Notification
Need protocol in place to notify proper clinical and IP staff in a timely manner (i.e. within 4 to 6 hours)
True for facilities with both on-site and off-site laboratories
Slide20Facility-Level Prevention
Strategies
6. Inter-facility Communication
CRE infection/colonization shouldn’t preclude transfers
Facilities transferring patients colonized or infected with CRE
must
notify the receiving facility of the patient’s CRE status
Notify about invasive devices the patient has and the duration of any ongoing antimicrobial therapy
Identification of CRE Patients at
admission
Need a mechanism to identify patients colonized or infected with CRE at re-admission so the appropriate infection control precautions can be initiated
Slide21Facility-Level Prevention
Strategies
7. Antimicrobial stewardship
Multiple antimicrobial classes have been shown to be a risk for CRE colonization and/or infection
Active antimicrobial stewardship program
8. Environmental Cleaning
Once CRE patients are discharged, terminal cleaning of CRE patient rooms should be performed.
Slide22Facility-Level Prevention
Strategies
9. Patient and Staff
Cohorting
Patients colonized
or
infected with CP-CRE should be housed in single patient rooms.
If insufficient numbers of rooms, give preference to patients at highest risk of transmission (incontinent, uncontrolled draining wounds, medical devices
)
Consider a dedicated staff that provide the bulk of patient’s care. The specific staff that are dedicated may vary depending on the healthcare setting.
Not generally recommended for single patients, but in high prevalence areas and during outbreaks
.
CRE
Patient w/o CRE
Slide23Facility-Level Prevention
Strategies
10. Screening Contacts of CRE Patients
Screening process for CRE is rectal or
peri
-rectal swabs
Screen
patient with epidemiologic links to unrecognized
CP-CRE
colonized or infected patients
Should be done even if patient has been discharged – consult with WDH!
Slide24Facility-Level Prevention
Strategies
11. Active Surveillance Testing
Clinical cultures identify only a minority of patients colonized with CRE and unrecognized colonized patients who are not on contact precautions may be a source of CRE transmission.
Screen
high-risk patients at admission or at admission and periodically during their facility stay for
CRE (during outbreaks)
Consider surveillance cultures for patients admitted overnight to healthcare setting in foreign country within last 6-12 months, or within the US in an area with high CP-CRE prevalence.
Slide25Facility-Level
Prevention Strategies
12. Chlorhexidine Bathing
Used successfully to prevent certain types of HAIs and to decrease MDRO colonization in ICUs.
Bathe patients daily with 2% liquid chlorhexidine or 2% chlorhexidine wipes
Usually high risk settings (ICUs)
Do not use above the jaw line or on open wounds
In LTC, may be used on targeted high-risk residents or high-risk settings (i.e. ventilator unit).
Slide26Facility CRE Readiness Evaluation
Slide27CRE Readiness Questions to Ask in Your Facility
Does your lab and/or reference lab test for CRE?
What CLSI standards are they using
?
Can they test for Carbapenemase production?
What
indicators prompt them to suspect a CRE? Positive ESBL? Ceftazidime or Ceftriaxone resistance
?
If my lab cannot perform carbapenemase testing, what will be the infection control response protocol while we wait for confirmatory results?
Slide28CRE Readiness Questions to Ask in Your Facility
What is the timeframe in which you want to be notified for a CRE?
How will the lab notify the IP staff and clinicians of a positive?
Will they notify you if they
suspect
a positive before it’s identified?
Make sure they still notify you and report to public health if the sample is Carbapenem resistant, but susceptible to a more first-line drug!
Are
our
notification systems and protocol
set up in a way that everything can be implemented properly (i.e. initiating precautions,
communicating
CRE status at transfers) if you (the IP) are gone?
Slide29CRE Readiness Questions to Ask in Your Facility
Do we have a system in place to flag patients with CRE at re-admission?
Is
this something our EMR can handle?
D
o
I need to talk to IT staff about setting this up?
Will our administration support this as a priority? Who can be a champion to help administration understand this should be a priority
?
Do we have a procedure upon intake to identify potentially infectious people (especially nursing homes
)?
If the patient is transferred, how will you notify the receiving facility?
Do NOT assume that just because it is in the chart, they have read it.Who will be responsible for making sure this notification is clear?Don’t forget to notify medical transport
Slide30CRE Readiness Questions to Ask in Your Facility
What is my system for tracking CRE in my facility?
Line list? EMR? MS Access Database? NHSN?
Is my system capable of tracking patient risk factors?
Can I come back and review former cases to identify trends?
Slide31Resources
https://health.wyo.gov/publichealth/infectious-disease-epidemiology-unit/disease/
cre
/
https
://
www.cdc.gov/hai/organisms/cre/cre-toolkit/index.html
Slide32Questions?
cody.Loveland@wyo.gov
307-777-8634