Epidemiology and Control of MethicillinResistant Staphylococcus aureus in hospitals Maria Kapi,MD Re - PowerPoint PPT Presentation

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Epidemiology and Control of MethicillinResistant Staphylococcus aureus in hospitals Maria Kapi,MD Re

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Title: Epidemiology and Control of MethicillinResistant Staphylococcus aureus in hospitals Maria Kapi,MD Re


1
Epidemiology and Control of Methicillin-Resistant
Staphylococcus aureusin hospitalsMaria
Kapi,MDRegistrar of Medical MicrobiologyLaiko
General Hospital of Athens, GreeceReadings MRSA
2
What are MRSA?
  • If we want to understand what are MRSA, we should
    first know
  • What are Staphylococci?
  • What is Staphylococcus aureus?

3
What are MRSA?
  • 3. What are penicillin and methicillin?
  • 4. What are PBPs?
  • 5. What are beta-lactams and beta-lactames?

4
  • Staphylococci Gram positive cocci ( from
    Greek staphyle, means bunch of grapes ) that
    occur singly and in pairs, short chains and
    irregular grape-like clusters.

5
  • Staphylococcus aureus is the staphylococcus
    which has the ability to clot plasma or in other
    words, which is coagulase positive. More than 80
    of Staphylococcous aureus strains produce
    beta-lactamases.

6
  • Penicillin is the antibiotic agent that
    Alexander Fleming a Scottish physician discovered
    in 1929. In 195 only 15 of
  • S.aureus was susceptible to penicillin.
  • Approximately 5 of S.
  • aureus today are
    sensitive
  • to penicillin.

7
  • Methicillin was with oxacillin the new line of
    penicillins in 1959, which became a new hope to
    the treatment of St. aureus. In 1961 the St.
    aureus became resistant to methicillin. Strains
    that are
  • oxacillin and methicillin
  • resistant, historically termed
  • Methicillin-Resistant S.aureus
  • (MRSA)

8
  • PBPs are penicillin-binding proteins. They are
    responsible for the final stages of peptidoglycan
    synthesis of the bacterial cell wall structure.
    Inhibition of one or more of these essential
    enzymes leads to bacterial lysis.

9
  • Beta lactams are the antibiotics that contain
    the beta lactam ring. These are penicillins,
    cephamycins, cephalosporins, carbapenems
    monobactams. The ring structure is common to all
    beta-lactams and must be intact for antibacterial
    action. They are cell
  • wall synthesis inhibitors.

10
  • Beta lactamases are enzymes that catalyse the
    hydrolysis of the beta-lactam ring and inactivate
    these group of antibiotics. Genes encoding these
    enzymes are widespread in the bacteria.

11
What MRSA are doing?
  • Methicillin Resistant Staphylococcus aureus,
    when its cell is exposed to ß-lactam antibiotics,
    a supernumerary ß-lactam-resistant PBP (PBP2a),
    takes over the the biosynthetic functions of the
    normal PBPs. This protein is responsible for the
    methicillin resistance.

12
Heteroresistance of MRSA
  • All the cell in the population may have the
    genetic information for resistance , which is
    encoded by the mecA gene. Only a small number of
    cells can actually express the resistant
    phenotype under in vitro testing conditions. This
    phenomenon is termed heteroresistance.

13
Why are MRSA important?
  • Hospital acquired infections. MRSA are common
    nosocomial pathogens around the world.
  • The treatment is very difficult. Vancomycin often
    is the only drug of choice for severe infections.

14
Why are MRSA important?
  • MRSA with reduced susceptibility to
    glycopeptides. Since 1996 has been identified in
    Europe, Asia and United States. That increases
    the possibility some strains became fully
    resistant to glycopeptides.
  • MRSA are easily transmissible between patients.

15
MRSA in Europe.
  • In England and Wales, from
  • January to December 1999
  • methicillin resistance was
  • 37 of the S.aureus reports.
  • Except Scandinavia and
  • Netherlands most countries
  • have high rates of MRSA.

16
MRSA in the United States
  • From January till December 1999, 52,3 MRSA are
    associated with nosocomial infections in
    intensive care unit patients.

  • The increase

  • in resistance

  • is 37 from

  • 1994-98.

17
Epidemiology of MRSA
  • Mode of Transmission. Is transmitted by
    contact with a person who has MRSA infection or
    is colonized with the organism.Hands of the
    health care workers is the most common mode of
    transmission from patient to patient.

18
Epidemiology of MRSA
  • Reservoirs .Colonized and infected
    patients are the major reservoir of MRSA.
    Although has been isolated from environmental
    surfaces, these are not the most likely source of
    spread.

19
Epidemiology of MRSA.
  • Risk factors. The factors that have been
    identified as increasing the risk of MRSA
    infection are
  • Increased length of hospital stay
  • Multiple hospitalizations
  • Wounds

20
Epidemiology of MRSA.
  • Risk factors
  • Invasive procedures
  • Greater than 65 years old
  • Severe underlying disease.
  • Administration of broad-spectrum antibiotics.

21
Costs of MRSA
  • Directly attributable costs
  • hotel costs of extended lengths of stay
  • the cost of diagnostic procedures,
  • morbidity and mortality that can follow infection
  • glycopeptides are more expensive than other
    antibiotics e.t.c

22
Costs of MRSA
  • Costs of control
  • costs of involvement of the infection control
    team.
  • temporary closure of wards or theatres.
  • re-deployment of staff.

23
Control of MRSA in Hospitals
  • General Principles
  • Prevention of acquisition and spread of infection
    by patients and staff
  • Priorities are high risk units, such as intensive
    care units and patients who are susceptible to
    infection.

24
Control of MRSA in Hospitals
  • Handwashing. Health care workers should wash
    their hands before and after contact with all
    patients, even when gloves are worn. A written
    protocol detailing proper hand wash technique
    should be available for reference.

25
Control of MRSA in Hospitals
  • Gloves should be worn when in contact with any
    body substance. Gloves should be changed and
    hands washed immediately after contact with each
    resident.
  • Appropriate use of antimicrobials. Monitoring and
    auditing of drug use.

26
Control of MRSA in Hospitals
  • Isolation is necessary for infected patients and
    possible carriers in a single room or preferably
    in an isolation unit with designated staff.
    Isolation reduce staphylococcal cross-infection.

27
Control of MRSA in Hospitals
  • Ward Closure should be considered when new
    patients become infected with MRSA. The presence
    of strains of MRSA causing invasive infection is
    another indication.
  • Screening of patients for MRSA at the nose,
    throat and perineum.

28
Control of MRSA in Hospitals
  • Carriage of MRSA by health care workers. During
    outbreaks staff should be reminded of the
    handwashing and transient carriage of MRSA. Staff
    with infected or colonized lesions should not be
    at work especially in critical areas, as
    intensive care units, cardiothoracic words e.t.c.

29
Control of MRSA in Hospitals
  • Treatment of carriers. Nasal carriage is treated
    topical with mupirocin.
  • Systemic treatment of infections The glycopeptide
    antibiotics are currently the agents of choice
    for treatment.
  • Microbiological characterization of MRSA.

30
Antimicrobial resistance is a major threat to
public health.
  • Bacterial resistance to multiple antibiotics
    characterises the present decade. Finding
    organisms resistant to over 10 different
    antibiotics is not unusual. Globally we need to
    look at how antibiotics are used and
  • reduce their inappropriate use.
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