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How to Lower MRSA Risk with Nasal Decolonization
Reduce Isolation Days
Disclosures
Speaker provides consulting services to Global Life Technologies Corp.
1. S. aureus / MRSA facts
2. MRSA nasal colonization risks
3. Limitations in current strategies for MRSA risk mitigation
4. Benefits of universal nasal decolonization
• Nasal decolonization options
Contents
1. Understand the role of the nares in MRSA/MSSA infections.
2. Describe the risks MRSA/MSSA nasal carriage represents to
patients and others.
3. List three limitations of current MRSA risk mitigation programs.
4. Understand the benefits of universal decolonization versus
screen and isolate and targeted decolonization programs.
Learning Objectives
S. aureus/MRSA
Facts
CDC—March 2019 Vital Signs Data Overview
CDC—March 2019 Vital Signs Data Overview
Decolonization:
• Bathe with an antiseptic on skin
• Apply antibiotic or antiseptic in the nose, because staph tends to live in the nose
CDC: Decolonization is a key way to prevent Staph aureus infections:
• Helps prevent colonized patient from getting an infection
• Reduces bacterial bioburden and likelihood of transmission so HCPs in contact with colonized patients are less likely to get bacteria on their skin and clothes and pass it on to the next person
“Decolonization prevents spread of pathogens and prevents the infection in the first place”
CDC—March 2019 Vital Signs Data Overview
• The most common pathogen causing VAP and SSI
• Of all S. aureus causing VAP and SSI, 44% were MRSA
• The second most common pathogen causing CLABSI
• Of all S. aureus causing CLABSI, 56% were MRSA
S. aureus / MRSA Facts
CDC Antimicrobial Resistance NHSN 2011-2014 Report
Staphylococcus aureus
* Zimlichman E et al.. JAMA Intern Med. 2013;173(22):2039-2046.
Cost to treat MRSA Infection*
SSI:$42,000
CLABSI:$58,500
Excess LOS days due to MRSA Infection*
SSI:23
CLABSI:15.7
MRSA HAI Facts
The primary reservoir
for S. aureus/MRSA
colonization is
the Nose.
S. aureus / MRSA Nasal Colonization Facts
* Wertheim HF, Lancet 2004; 364: 703–05 **Honda H, ICHE 2010 Jun; 31(6): 584–591
• ~13% of ICU patients are MRSA carriers on admission**
Patient S. aureus / MRSA Nasal Colonized
* Wertheim HF, Lancet 2004; 364: 703–05 **Honda H, ICHE 2010 Jun; 31(6): 584–591
• 8% - 10% of patients acquire MRSA colonization in the surgical ICU***
*** Warren DK, ICHE. 2006; 27(10):1032–1040
S. aureus / MRSA Nasal Colonization Facts
• 25% to 30% of healthy adults are carriers S. aureus at any given time*
MSSA/MRSA
Risks
14 - 20 times higher *
Risk of infection
MRSA non-carrierscarriers
The #1 Risk Factor for MRSA infection is MRSA nasal colonization!
MRSA Nasal Colonization Risk
vs
*Marzec et al.AJIC (2016) 405-8
MRSA ColonizationMRSA Infection
80%
** Kalmeijer, ICHE 2000;21:319-323* Von Eiff, NEJM, Vol. 344, No. 1 · January 4, 2001 * Wertheim HF, Lancet 2004; 364: 703–05
Correlation between nasal carriage and S. aureus / MRSA infections
~80% of S. aureus and MRSA BSI* and SSI** infection is endogenous and traced to the patient’s nasal flora.
MRSA BSI >20% mortality rate****
MRSA carriers 20 times higher risk for MRSA BSI***
~15 - 25% of carriers develop MRSA infection during hospitalization
or within 18 months***
• 13% ICU MRSA carriers are detected on admission*
• 8% become MRSA carriers – undetected**
MRSA Infection
Mortality
BSI
MRSA Nasal Colonization
MRSA Nasal Colonization Cascade in the ICU
MRSA BSI >20% mortality rate*****
MRSA carriers ~20 times higher risk for MRSA BSI****
~15 - 25% of carriers develop MRSA infection during hospitalization
or within 18 months***
• ~13% ICU MRSA carriers – identified on admission*
• ~8% become MRSA carriers – unidentified**
** Warren DK, ICHE. 2006; 27(10):1032–1040
MRSA Nasal Colonization Cascade in the ICU
***Huang SS et al, CID, Feb 2003, 36 (3): 281–285* Honda H, ICHE 2010 Jun; 31(6): 584–591. **** Marzec et al, AJIC (2016) 405-8 ***** Blot et al, Arch Int Med Oct 2002 (162) 2229-35
Treating a Sepsis Infection
FluidsSeveral liters initiallyColloidsCrystalloidAlbuminStarchesHigh chloride
AntibioticsEarly administration
EGDTEarly goal directed therapy
Goal-oriented therapy
Vasopressors1-6 hours after onsetNorepinephrineEpinephrineVasopressinDopaminePhenylephrine
Parenteral feeding Sedatives Enteral feeding
Molecular targeted-therapies
CorticosteroidsTNF-a
Insulin therapy
Lung Protective Ventilation
Urinary catheterDiagram by: Will Stahi Timmins©2016 BMJ Published group ltdIllustration: ©2019 Global Life Technologies Corp.
MRSA Nasal Colonization Risk of Infection
Patients with MRSA nasal colonization
pose a risk of transmission
are at risk of infecting themselves
and
• Nasal carriers are 7x more likely to have contaminated hands*
• We touch our nose over 100 times a day**
• S. aureus is transferred to the nose primarily by the hands***
*Tammelin, ICHE. 2010 Jun; 31(6): 584–591 ***Wertheim, Lancet Infect Dis 2005; 5: 751-762**Kwok YL, AJIC. 2015 Feb;43(2):112-4.
Nasal Colonization and Hand Contamination
Nasal Colonization and Transmission
Takeaways
• MSSA/MRSA continue to be major contributors to HAIs nationwide
• The nose is the primary reservoir for MSSA/MRSA and the most reliable predictor of colonization
• Nasal colonization is the #1 risk factor for subsequent infection
• 80% of MSSA/MRSA BSI and SSI infections are endogenous and traced to the patient’s nasal flora
Current MRSA Risk Mitigation Strategies
Objective
To reduce MRSA
transmission and
infection risk posed
by patients who are
MRSA colonized.
Risk Mitigation Strategy – Screen and Isolate
2. Screen high risk patients for MRSA colonization (MRSA surveillance practice)
3. Contact Isolation Precautions (CP) for detected MRSA colonized patients for length of stay
1. Identify patients with high risk of MRSA nasal carriage• Critical care patients (ICU)• ALF/Nursing home residents• Prior history of MRSA• Diabetics, oncology patients, etc.
???
Risk Mitigation Strategy – Screen and Isolate
MRSA Colonized
If identified positive, CP
Swab sent tolaboratory
Screen high risk patient
Current MRSA Surveillance Practice
Chromagar Culture5 - 15% False Negatives
PCR Amplification2 - 16% False Negatives2 - 4% False Positives
Turn around time from screen to results
Screening sensitivity and specificity
Improper swab collection *
Chromagar Culture **5 - 15% False Negatives
PCR Amplification**2 - 16% False Negatives2 - 4% False Positives
Time from Collection to
Results
Chromagar***
30 – 79 hours
PCR***
4 – 21 hours
*** Polisena. BMC Infectious Diseases2011;11:336** Lutejin. Clinical Microbiology and Infection 2011: 17(2); 46-154
Limitations of Screening for MRSA Colonization
*BD Diagnostics. 2013. BD Max MRSA XT package insert, vol 443461, P0167(01).
ICU patients screened1,000
Screened MRSA(-)870
Remains MRSA(-)800
Becomes MRSA(+)70
Screened MRSA(+)130
100%
~87%
~92% ~8%**
~13%*
* Honda H, ICHE 2010 Jun; 31(6): 584–591. ** Warren DK, ICHE. 2006; 27(10):1032–1040
MRSA(-)MRSA(+) IdentifiedMRSA(+) Not Identified
Key
Screening in the ICU
All patients screened on admission Screened for MRSA
Screening in the ICU
~13% screened MRSA (+) identified and isolated
~8% acquire MRSA (+)
All ICU Patients screened on admission Screened MRSA (-)
Screening in the ICU
~65% of MRSA (+) nasal carriers identified and isolated on admission
* Honda et al ICHE 2010 Jun; 31(6): 584–591.
Limitations with MRSA Surveillance practice in the ICU
~35% of MRSA (+) nasal carriers are not detected and not isolated • Carriage acquisition in ICU• Screening accuracy
KEY TAKEAWAY:~35% of the colonized patients are undetected and, thus, the risk represented by this undetected population is NOT addressed
Total MRSA colonized patients
Do I really know who is colonized and who is not?
Do I know in a useful timeframe?
How effective is CP?
Current Practice
Patient colonizedwith MRSA
Unidentified MRSA colonized
patient
Contamination ofenvironmental
surfaces
Transmission on HCP hands or shared
equipment
Transmission Risk of Unidentified MRSA Colonized Patient
• Does not reduce the risk of the patient contaminating the environment, which can be transmitted by HCPs to other patients.
• Does not prevent colonized patients from touching their nose and contaminating their hands.
• Does not reduce the greatest risk of endogenous infection [patient infecting themselves, via lines, tubes, incisions, airways]
Wertheim HF et al. Lancet Infect Dis. 2005 Dec;5(12):751-62. Worby C. et al. American Journal of Epidemiology, June 2013, pp 1306–1313.
Limitations with Contact Isolation Precautions
Isolation for MRSA Carriers
Isolation has adverse effects on:
• Patient
• Staff
• Facility
Isolation for MRSA Carriers
Detrimental to patients*
• Isolated patients get less care (quality & quantity)
• Isolated patients have worse outcomes
• Isolated patients have lower satisfaction scores
A hindrance to staff**
• Deterrent to frequent patient contact
• “Isolation fatigue”
• Results in lack of compliance with CP
A burden for the facility***
• Does not optimize patient flow
• Reduces throughput – utilization
• High costs of screening and isolation
* Morgan et al, AJIC. 2009 March ; 37(2): 85–93 *** Huang SS et al. ICHE, 2014; 35 (53); S23-31.** Dhar, ICHE March 2014, vol. 35, no. 3
Discontinuing CP
and using stepped up Standard Precautions
A responsible alternative?
Another Option?
• No amount of hand washing will prevent colonized patients from touching their nose and re-contaminating their hands.
• Does not address the primary reservoir of the pathogen you are trying to control (MSSA/MRSA).
*Wertheim HF et al. Lancet Infect Dis. 2005 Dec;5(12):751-62. **Worby C. et al. American Journal of Epidemiology, June 2013, pp 1306–1313.
Limitations of Standard Precautions
• Does not reduce the greatest risk—endogenous infection (~80%).
MRSA Nasal Colonization
How can we directly address
risk factors?
Is there a better way?
• 43 hospitals, 74 ICUs, 16 states
• 74,000 patients, 283,000 ICU patient days
• 18-month intervention (Apr 2010 – Sep 2011)
Huang SS et al. NEJM 2013; 368 (24):2255-65
2013 REDUCE MRSA Study:
REDUCE MRSA Study
Arm 1: Screen and Isolate
– Screened all ICU patients and isolated known MRSA (+)
Arm 2: Targeted Decolonization– Screened all ICU patients
– Targeted nasal decolonization/CHG bathing only for known MRSA (+)
Arm 3: Universal Decolonization– No screening
– Universal nasal decolonization/CHG bathing for all ICU patients
* Huang SS et al. N Engl J Med 2013; 368 (24) 2255-65.
REDUCE MRSA Study
ICU Universal Decolonization Arm
** Huang SS et al ICHE, 2014; 35 (53); S23-31.
Huang SS et al. NEJM 2013; 368 (24):2255-65
ARM 3- Universal Decolonization:- Superior to Screen & Isolate - Superior to Targeted decolonization*
Results: 37% decrease in MRSA clinical cultures28% decrease in MRSA blood stream infections44% decrease in all blood stream infections
Prevented: 9 BSIs per 1,000 ICU admissions
Cost-Savings: $171 per patient**
* Huang SS et al. N Engl J Med 2013; 368 (24) 2255-65.
Universal Decolonization Works
-0.5
0
0.5
1
1.5
2
2.5
3
Oct-12 May-13 Nov-13 Jun-14 Dec-14 Jul-15 Jan-16 Aug-16 Mar-17
MRSA bacteremia rate with & withoutUniversal Decolonization
UniversalDecolonization
(re-introduced)
* Bradley et al. ICHE 2017:1-6
Demonstrated effectiveness
Targeted Decolonization
(universal withdrawn)
UniversalDecolonization
Benefits of Universal Decolonization
Universal decolonizationTreat all patients regardless of colonization status
• eliminates MRSA surveillance tests and the associated contact precautions, which interfere with care
• begins on the first ICU day, avoiding the delay in decolonization pending results of screening tests.
• protects patients in the ICU from their own microbiota during a period of heightened vulnerability to infection.
• reduces the environmental pathogen burden, reducing opportunities for patient-to-patient transmission.
• lowers ICU costs—cost-effectiveness studies show cessation of screening, reduced contact precautions, and reduced infections offset product costs, resulting in savings
Advantages of Universal Decolonization
Reduce transmission and directly address infection risk — Improve patient safety —
Improving patient safety and satisfaction
Advantages of Universal Decolonization
MRSA/MSSA Risk FactorsContact
Precautions
Standard Precautions(without CP)
UniversalDecolonization
Patient MRSA/MSSA nasal carriage NO NO YES
Nose to hand to nose contamination NO NO YES
Risk of MRSA/MSSA transmission Limited NO YES
Endogenous/patient infection risk NO NO YES
Bioburden in environment/community Limited Limited YES
Risk Mitigation Program Comparison
ICU Universal Decolonization Protocol
On Admission
• Decolonize nares
• Decolonize body with CHG wipe/bath
Daily Protocol for LOS
Morning Protocol - Decolonize
• Nares
• Body with CHG wipe/bath
Evening Protocol - Decolonize
• Nares
Program Comparison
Screen & Isolate vs Universal Decolonization
ProgramColonized patients in isolation
Colonized patients not in Isolation
Total Colonized patients
Total Colonized
Patient days
Screen and Isolate 345 185 530 1748
Universal Decolonization* 0 0 0 0
Program Comparison
*For the purpose of this presentation, “decolonization” is defined as reducing MRSA pathogen burden significantly
Screen & Isolate vs Universal Decolonization in 30 Bed ICU, per year
MRSA (+) unidentified
screened MRSA (+) identified and isolated
Screened MRSA (-)
Screen and Isolate Universal Decolonization
~ %100 decolonized
Screen & Isolate vs Universal Decolonization
vs
Nurse hours spent gowning in and out
Gown in/out events
Nurse exposed to colonized patient
events
Screen and Isolate 1,000 68,000 36,000
Universal Decolonization 0 0 0
Program Comparison
Impact
Screen & Isolate vs Universal Decolonization in 30 Bed ICU, per year
Gown in / out events
VS
UniversalDecolonization
Gown in / out events
MRSAScreen & Isolate
68,000~ 0
Program Comparison*
*In a 30 bed ICU, per year
30 bed ICU Cost / Operating Impact
Typical Costs
Screen and Isolate program = ~$290K
Universal Decolonization program = ~$50-70K
Protocol Comparison - Cost Overview
+ +
+
decolonize
1. Topical antibiotic (mupirocin)
2. Povidone iodine based antiseptic
3. Alcohol based antiseptic
Nasal Decolonization Options
Antibiotic - Mupirocin (Bactroban®)• Was the only tool for many years – and is still used today
Limitations to consider:
• Selective mechanism of action (gram +)
• 5 day BID course – limited effectiveness until day 3*
• Does not comport with antibiotic stewardship*
• 60% - 93% effective*
• Resistance concerns**
* Anderson 2015 Antimicrobial Agents and Chemotherapy 59 (5), pp. 2765-2773. ** Miller MA et al. ICHE 1996;17:811 **Peterson LR et al. Open Forum Infect Dis 2017;4:ofx093
Antibiotic - Mupirocin
Antiseptic – Povidone iodine• Long history as a pre-op and wound antiseptic
• Effective against both gram (+) and (-) organisms
• Comports with antibiotic stewardship
Limitations to consider:
• Nasal application developed for one time, pre-op use only
• 12 hr persistence – requires daily use to prevent recolonization • Cannot be used on patients with renal or hepatic failure, those with
thyroid disfunction nor patients with hyper sensitivities/allergies to iodine• FDA warning notice of potentially severe reactions
Antiseptic - Povidone Iodine
Antiseptic – Ethanol• Long history as a pre-op, wound and skin antiseptic
• Effective against both gram (+) and (-) organisms
• Comports with antibiotic stewardship
Limitations to consider:
• 12 hr persistence – requires daily use to prevent recolonization
Antiseptic Universal Nasal Decolonization
Benefits Antibiotic (mupirocin)
Povidone-Iodine antiseptic
Alcohol-basedantiseptic
Effective against MRSA/MSSA ✔ ✔ ✔
Non-antibiotic ✖ ✔ ✔
Effective day 1 ✖ ✔ ✔
Easy to use / Pleasant ✖ ✖ ✔
Suitable for daily use ✖ ✖ ✔
All-inclusive: HCP/Caregiver use ✖ ✖ ✔
Comports with antibiotic stewardship ✖ ✔ ✔* Steed L, et al.AJIC, 2014:42(8):841-846.
Nasal Decolonization Options
Conclusions
1. Nasal carriage poses a substantial infection risk.
2. Limitations of current MRSA risk mitigation programs do not address the primary reservoir – the nose.
3. Universal ICU decolonization strategies replacing screen and isolate and targeted decolonization are feasible, cost effective and widely accepted.
4. Nasal decolonization antiseptics (which overcome the limitations of mupirocin) improve HAI outcomes, quality of care and patient/staff satisfaction.
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