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AntimicrobialResistant Organisms: An Update

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Title: AntimicrobialResistant Organisms: An Update


1
Antimicrobial-Resistant Organisms An Update
  • Bruce Gamage
  • Infection Control Consultant
  • BC Centre for Disease Control

2
Outline
  • Background
  • MRSA
  • VRE
  • VISA/VRSA
  • Current guidelines and recommendations
  • Prevention and control

3
The Antibiotic Era
  • 1928 Fleming discovers penicillin (PCN)
  • 1940s PCN becomes widely used
  • Present 235 million doses of antibiotics
    consumed in the US annually

4
Antimicrobial-Resistant Organism (ARO)
  • Definition
  • An organism that is resistant to two or more
    unrelated antibiotics to which the organism is
    normally considered susceptible.
  • Bennett and Brachman, 4th edition.

5
Why Is Antimicrobial Resistance a Problem?
  • Fewer drug choices
  • Increased costs
  • Increased morbidity and mortality

6
Costs Associated With AROs
  • Costs associated with AROs in Canadian
    Hospitals is estimated to be 42 million to 59
    million annually.

7
How Resistance Develops
  • Previously silent (unexpressed) genes can be
    inherited
  • Genetic mutations can spontaneously produce a
    resistance trait (hypermutation)
  • Genes can be transferred between organisms

8
Emergence of AROs
9
Factors That Promote Resistance
  • Resistance genes are prevalent in nature
  • Rapid multiplication of organisms favors genetic
    mutations
  • Selective pressure from antimicrobial use in
    humans and animals allows resistant organisms to
    predominate
  • Biofilms?

10
Practices That Promote Resistance
  • Overuse of antimicrobials in outpatient settings
  • Overuse of broad-spectrum antimicrobials in
    hospital settings
  • Poor compliance with regimens
  • Use of antimicrobials in animals

11
Colonization vs. Infection
  • Colonization
  • Organism is present in a normally nonsterile body
    site
  • No clinical symptoms are present
  • Infection
  • Organism present in a normally sterile body site
  • Clinical signs and symptoms of infection are
    present
  • Fever
  • Purulence
  • Pneumonia
  • Inflammation

12
MRSA
  • Gram-positive cocci in clusters
  • Causes variety of infections (cellulitis,
    abscess, wound infection, osteomyelitis,
    arthritis, endocarditis, pneumonia, bacteremia)
  • MRSA and MSSA appear to be equally virulent
    (capable of causing infection)

13
MRSA Reservoir
  • The major reservoir for MRSA is humans
  • S aureus (whether sensitive to methicillin or
    not) can be normal flora
  • Nares
  • Wounds
  • Skin

14
MRSA Epidemiology
  • In the US MRSA is endemic in majority of
    hospitals (35 of all S. aureus isolates)
  • In Canada (CNISP)
  • 1995 0.9 of S. aureus isolates and 0.3 cases
    per 1000 admissions
  • 1999 6 of S. aureus isolates and 4.12 cases per
    1000 admissions

15
BCCAMM Surveillance Project
16
MRSA Transmission
  • Patient-to-patient via transient carriage on the
    hands of HCWs
  • Via devices or environmental surfaces

17
MRSA Risk Factors
  • Exposure in the healthcare setting
  • Dialysis
  • Injecting drug use
  • Burn unit exposure
  • Diabetes
  • Chronic skin conditions
  • ICU

18
MRSA Treatment
  • Vancomycin is indicated for the treatment of
    serious MRSA infections (bacteremia, meningitis)
  • May use combination of other antibiotics if
    organism is susceptible
  • Linezolid
  • New class of antimicrobial

19
VRE
  • Gram-positive coccus
  • Causes a variety of infections
  • Bacteremia
  • Endocarditis
  • Wound infections
  • Urinary tract infections
  • Intra-abdominal infections

20
Enterococcus Species
  • Most enterococcal infections are caused by
  • E faecalis 85-90
  • E faecium 5-15

21
Vancomycin Resistance carried on Genes
  • vanA High-level resistance to vancomycin most
    common in E faecium
  • vanB Variable level of resistance to vancomycin
  • vanC Low-level resistance to vancomycin

22
VRE Reservoir
  • Enterococci are part of the normal flora of the
    GI tract and the female genital tract
  • The GI tract is the most important reservoir

23
VRE Epidemiology
  • In US 1995 gt 10 of enterococcal strains VRE
  • In Canada
  • First VRE reported in 1993
  • 411 cases reported in 23 hospitals between
    October 1998-September 2000
  • 95 are colonization picked up on screening

24
BCCAMM Surveillance Project
25
VRE Transmission
  • Patient-to-patient via transient carriage on
    hands of HCW
  • Devices, equipment, or environmental surfaces
    contaminated with VRE from a patient

26
VRE Risk Factors
  • Critical illness, severe underlying disease, or
    immunosuppression
  • Prolonged hospital stay
  • Indwelling urinary catheters or central venous
    catheters
  • Prior exposure to vancomycin, cephalosporins, or
    other antibiotics

27
VRE Treatment
  • Linezolid (Zyvox)
  • Quinupristin/dalfopristin (Synercid)
  • Indicated for life-threatening infections with
    VRE

28
Decolonization?
  • Controversial
  • Not recommended unless there is evidence that
    colonized person is spreading the organism
  • 40 of attempts fail and repeated attempts result
    in further resistance
  • There is no proven regimen for VRE

29
Transfer of Vancomycin Resistance From VRE to
MRSA
  • vanA and vanB genes can be transferred between
    bacteria
  • In vitro studies demonstrate that vancomycin
    resistance can be transferred from VRE to MRSA

30
VISA and VRSA
  • VISA first recognized in 1996 in Japan
  • Additional cases reported from Europe, Asia, and
    the US
  • Resistance has not been caused by the vanA, vanB,
    or vanC genes
  • VRSA seen in US in 2002
  • Resistance gene vanA was detected in the isolate
  • No detected transmission to others

31
Guidelines and Recommendations
  • 1999 APIC/CHICA/ICNA Global Consensus
    Conference Final Recommendations
  • 2001 BC Guidelines for the Control of Antibiotic
    Resistant Organisms
  • Available at www.bccdc.org

32
Contact PrecautionsHand Hygiene
  • Hands must be washed after any direct contact
    with a patient and before contact with the next
    patient
  • Use of and alcohol-based hand sanitizer may be
    substituted if hands not visibly soiled

33
Contact PrecautionsGloves
  • Wear gloves when having direct contact with the
    patient
  • Change gloves between dirty and clean procedures
    on the same patient
  • Change gloves between patients
  • Wash hands after removal of gloves

34
Contact Precautions Gowns/Face Masks
  • Gown if clothing may contact the patient or
    environmental surfaces
  • Insufficient evidence to support the use of
    masks/eye protection use if patient is coughing
    in your face or anticipate splashes of body
    fluids

35
Environmental Cleaning
  • Routine daily
  • Standard cleaning
  • Emphasis on touched
  • surfaces in room (bed
  • rails, door knobs)

36
Environmental Cleaning (cont.)
  • No need to use special disinfectants/detergents
  • Disinfect patient-care equipment that are used on
    multiple patients
  • Dedicate patient equipment if possible

37
Conclusions
  • Antimicrobial-resistant organisms are here to
    stay
  • We can make a difference by
  • Educating HCWs
  • Using antibiotics wisely
  • Identifying the organisms accurately
  • Putting infection control measures into place and
    following them!
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