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MRSA Prevention Strategies for Healthcare and Community Settings

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Title: MRSA Prevention Strategies for Healthcare and Community Settings


1
MRSA Prevention Strategies for Healthcare and
Community Settings
  • Pam Webb, RN, CIC
  • Infection Control Coordinator
  • Benefis Healthcare

2
Objectives
  • At the end of this session you will be able to
  • Describe what MRSA is and how it is spread from
    person to person
  • Explain the difference between healthcare
    associated MRSA and community acquired MRSA
  • Describe the impact of MRSA in healthcare and
    community settings
  • Identify measures to prevent the spread of MRSA
    in the healthcare or community setting

3
What is Staphylococcus aureus?
  • Staph
  • MSSA (methicillin susceptible Staph aureus)
  • Bacteria commonly carried on the skin or in the
    nose of healthy people
  • 25 30 colonized with Staph
  • Major cause of
  • Invasive systemic infections
  • Skin and soft tissue infections

4
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5
What is MRSA?
  • Type of Staph aureus that is resistant to an
    antibiotic class called beta-lactams (includes
    methicillin, oxacillin, penicillin, amoxicillin)
  • Resistant Staph emerged in 1961
  • First associated with hospitals
  • Widespread use of antibiotics results in
    resistance

6
What is MRSA?
  • Commonly found on human skin, nose, perineal and
    rectal areas of the body
  • Can cause serious infections
  • Spread primarily via contact with contaminated
    hands, skin or fomites
  • Antibiotic resistance limits treatment options
    for infections

7
Factors Promoting Resistance
  • Antibiotic selective pressure
  • Prolonged antibiotic courses
  • Inadequate dose of antibiotic
  • Protected sites/foreign bodies
  • Hospitalized patients with weakened immune
    systems
  • Inadequate infection prevention and control
    practices

8
Whats the difference between HA-MRSA and CA-MRSA?
9
HA-MRSA vs. CA-MRSA
  • Community Associated
  • No recent healthcare exposure
  • Contact sports, military recruits, prisoners, IV
    drug users
  • PVL toxin gene common
  • Susceptible to more antibiotics than HA- MRSA
  • Healthcare Associated
  • Recent healthcare exposure
  • 59 community onset disease
  • PVL toxin gene rare
  • Resistant to more antibiotics than CA-MRSA

10
HA-MRSA vs. CA-MRSAAntibiotic Susceptibilities
11
CA-MRSA
  • Environmental Conditions
  • Living in crowded or unsanitary conditions
  • Close contact with someone known to be infected
    or colonized with MRSA
  • Contact with a colonized pet
  • High incidence of MRSA in the community

12
What types of infections does MRSA cause?
13
Sites of MRSA InfectionsHealth Care vs.
Community
Median age 68 years 4 were PVL-positive
Median age 23 years 77 were PVL-positive
14
CA-MRSA Predominantly Causes Skin Disease
Disease Syndrome () Skin/soft tissue
(SSTI) 1,266 (77) Wound (Traumatic) 157
(10) Urinary Tract Infection 64
(4) Sinusitis 61 (4) Bacteremia 43
(3) Pneumonia 31 (2)
15
CA-MRSA Skin and Soft Tissue Infections
  • Skin and soft tissue infections can be of many
    types
  • Most common presentations are soft tissue
    infections such as boils, abscesses, furuncles,
    carbuncles etc.

16
Dont be too quick to blame spiders for those
spider bite wounds!
  • Misdiagnosis of MRSA infections as spider bites
    has been occurring throughout the United States
  • This misdiagnosis impedes the proper treatment of
    the infection and facilitates the spread of the
    infection.

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18
What is the impact of MRSA?
19
Implications for Antimicrobial Resistance
  • Limited treatment options, treatment failure
  • Increased morbidity and mortality
  • MRSA are transmissible
  • Increased healthcare costs
  • Decreased patient satisfaction
  • Can negatively impact quality of life

20
Impact of MRSA
PHC4 Research Brief MRSA in Pennsylvania
Hospitals Issue 10 August 2006
21
Burden of Disease
  • Nationally 59 of SSTIs in ERs attributed to
    MRSA
  • Varied geographically from 15-74
  • Recent APIC study estimated 1.2 million
    infections in hospitalized patients per year 10
    times previous estimate
  • Total prevalence of 46/1000 patients either
    infected or colonized
  • Last estimate was 3.9/1000
  • Two-thirds of MRSA patients were found on medical
    floors
  • 77 admitted to hospital already colonized or
    infected

22
Burden of DiseaseTrends in MRSA for Montana
Based on results from state-wide antimicrobial
susceptibility testing survey of laboratories
conducted by Montana DPHHS 1 Preliminary
analysis of 2006 data For more information,
contact the Montana Antibiotic Resistance
Awareness Program at (406) 444-0273
(www.mara.mt.gov)
23
U.S. Federal and State Policy Actions
  • 5 states discussing legislation of MRSA
    eradication program, including Active
    Surveillance IL, NJ, NY, PA and MD SHEA/APIC
    in opposition
  • Legislation passed May 25th in Minnesota
  • CMS Deficit Reduction Act (DRA) proposals for
    non-reimbursement of certain HAIs starting Oct
    08
  • Catheter-associated UTIs - Vascular catheter HAIs
  • Staph aureus septicemia - Vent Associated
    Pneumonias
  • MRSA infections -Surgical site infections
  • Clostridium difficile associated disease
  • SELECTING 6 CONDITIONS FOR IMPLEMENTATION OCT 08

24
Reporting MRSA Infections in Montana
  • Individual cases of MRSA are not specifically
    reportable conditions in Montana.
  • Some states require selective reporting of only
    invasive infections
  • Some states are considering legislation to
    require reporting of all MRSA infections
    (Tennessee, Texas)
  • Clusters of 4 or more culture confirmed MRSA
    infections within a common setting/venue within a
    month long period are reportable
  • http//arm.sos.mt.gov/37137-28771.htm

25
How can MRSA transmission be prevented?
26
Modes of transmission
  • Primarily person-to-person via hands
  • Environmental Contact w/ contaminated items

27
Infection Control- Healthcare Setting
28
Active Surveillance (ASC)
  • Colonization usually precedes infection
  • Purpose of ASC is to find unrecognized MRSA
    reservoirs to prevent spread
  • Nares (culture or PCR test) most common site
  • Groin, perineum, rectal, open wounds (culture)

29
Colonization vs. Infection
  • Colonization
  • No signs and symptoms
  • Sites differ
  • CA-MRSA groin, axilla, vagina, rectum
  • HA-MRSA nares and invasive device sites
  • Infection
  • Clinical signs and symptoms, e.g., skin wound
  • Usually requires medical intervention

30
Reservoir for the Spread of Antibiotic Resistant
Pathogens
clinical infections
colonized (asymptomatic)
31
BHC Active Surveillance
  • Identify surveillance groups based on facility
    risk assessment
  • Traditional groups new clinical cultures, admit
    from nursing home, readmit with previous history
    of infection or colonization
  • Additional groups Critical Care Total Joint
    Surgery

32
Active Surveillance- Communication
  • Flag chart for readmission so that contact
    isolation can be implemented immediately
  • Keep a patient/resident line listing
  • Communicate MRSA status to receiving facility

33
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34
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35
Contact Isolation
  • Patient/Resident Placement
  • Private room preferable
  • If need to cohort avoid placing MRSA patient or
    resident with roommate who
  • Has open wound, nonintact skin, surgical
    incision, ostomy
  • Has trach, or uncontrolled respiratory secretions
  • Has invasive devices such Foley catheter, JP
    tubes. chest tubes
  • Is on a ventilator
  • Is culture positive for another multi-drug
    resistant organism such as VRE (Vancomycin
    resistant Enterococcus)
  • Is incontinent of urine or feces or has drainage
    from a site that cant be contained

36
Decolonization Strategies
  • Not necessary for every case of MRSA colonization
    (ex. chronic colonization)
  • Used for control of outbreak situation
  • Decolonization regimens may include
  • Mupirocin ointment to nares bid x 5 days
  • Oral antibiotics
  • Chlorhexidine showers

37
Decolonization _at_ BHC
  • Mupirocin ointment to nares bid x 5 days for
    positive nares PCR
  • Repeat nares screen (culture) at least 24 hours
    after last dose
  • Goal is to discontinue isolation though
    decolonization might be transient
  • DC isolation when nares and clinical culture
    negative nares negative consider whether
    patient has non-intact skin before discontinuing
    isolation

38
Interim Guidelines for the Control and
Prevention ofMethicillin-Resistant
Staphylococcus aureus (MRSA) Skin and Soft Tissue
Infectionsin Non-Healthcare SettingsAugust,
2007
39
CA-MRSA GuidelinesPrevention - Four Simple Steps
  • Hand hygiene
  • Keep wounds clean and covered
  • Dont share personal items
  • Clean environmental surfaces regularly

40
Hand Hygiene
41
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42
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43
Example of an EPA Registered Disinfectant
  • LYSOL ? Brand ICTM Ready to Use Disinfectant
    Cleaner
  • Kills 99.9 of bacteria in 30 seconds on hard
    nonporous surfaces
  • Meets the requirements of the OSHA Bloodborne
    Pathogens Standard
  • Effective against Tuberculosis (TB), Poliovirus,
    and
  • Human Immunodeficiency Virus Type 1 (HIV-1)
    (Aids-Virus)
  • Contains no bleach, phenol, alcohol, or harsh
    abrasives
  • EPA Registration No. 675-55

44
Mixing Bleach Solutions for Disinfection
  • For routine disinfection of non-porous surfaces
  • 1100 dilution of household chlorine bleach
    (5.25)
  • 2 ½ tablespoons of bleach in a gallon of water
  • Open bottles of bleach lose effectiveness after
    30 days change bleach every 30 days for accurate
    concentrations.
  • Chlorine solutions are most effective if mixed on
    a daily basis.
  • Leave on surface for 5-10 minutes to achieve
    maximum disinfection
  • ALWAYS make sure surface/item is compatible with
    bleach
  • NEVER use bleach to clean a persons skin

45
Dealing with Skin Infections in the Community
  • Prevent Transmission
  • The 4 Steps!
  • Evaluate and Refer

46
Evaluate and Refer
  • Any unusual skin lesion or draining wound is
    potentially infectious to others and should be
    evaluated by a health care provider.
  • Encourage persons with skin and soft tissue
    infections to see their health care provider
    promptly for evaluation and treatment.

47
Use Antibiotics Appropriately
  • If you have a virus, dont demand antibiotics
    they wont work!
  • The presence of yellow/green mucus does not mean
    the infection is bacterial
  • If antibiotics are prescribed, take as directed
    and finish them
  • Dont save or share antibiotics

48
Where can you get more information?
49
Centers for Disease Control and
Prevention http//www.cdc.gov/ncidod/dhqp/ar_mrsa_
ca.html
50
Montana Antimicrobial Resistance
Awareness www.mara.mt.gov
51
Montana Antibiotic Resistance Awareness Program
Antibiotic Resistance Awareness Program MT
DPHHS- Communicable Disease Control and
Prevention BureauCogswell Building, RM
C-2161400 Broadway PO Box 202951Helena, MT
59620Phone (406) 444-0273Fax (406)
444-0272Email hhsmara_at_mt.gov or
www.mara.mt.gov
52
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53
Resources
  • www.apic.org
  • MRSA webinars
  • Guide to the Elimination of Methicillin-Resistant
    Staphylococcus aureus (MRSA) Transmission in
    Hospital Settings, March 2007
  • Dispelling the Myths The True Costs of
    Healthcare-Associated Infections, February 2007
  • www.cdc.gov
  • Management of Multidrug-Resistant Organisms in
  • Healthcare Settings, 2006
  • Living with MRSA booklet and handouts
  • www.doh.wa.gov/Topics/Antibiotics/MRSA.htm

54
Resources
  • www.ihi.org/IHI/Programs/Campaign
  • Getting Started Kit Reduce Methicillin-Resistant
    Staphylococcus aureus Infection How to Guide
  • www.dphhs.mt.gov/PHSD/MARA/documents/MT-DPHHSMRSAG
    uidelinesFINAL090507.pdf
  • Muto, C., Jernigan, J., Ostrowsky, B., Richet,
    H., Jarvis, W., Boyce, J., Farr, B., SHEA
    Guideline for Preventing Nosocomial Transmission
    of Multidrug-Resistant Strains of Staphylococcus
    aureus and Enterococcus, Infection Control and
    Hospital Epidemiology, May 2003

55
Questions?
  • Pam Webb, IC Coordinator, Benefis Health System
  • 406.455.4292
  • webbpama_at_benefis.org
  • Bonnie Barnard, Epidemiologist, MTDPHHS
  • 406.444.0274
  • bbarnard_at_mt.gov
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