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Antimicrobial Stewardship Training

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Antimicrobial Stewardship Training Part 1: Review of Basic Principles and Selected Antimicrobials By Keith Teelucksingh, PharmD – PowerPoint PPT presentation

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Title: Antimicrobial Stewardship Training


1
Antimicrobial Stewardship Training
Part 1 Review of
Basic Principles and Selected
Antimicrobials By Keith Teelucksingh, PharmD
Infectious Disease Pharmacist, Kaiser Permanente
Vallejo With contributions by Linh Van,
PharmD Infectious Disease Pharmacist, Kaiser
Permanente Oakland
This course is accepted by the California State
Board of Pharmacy for 2.0 hours of credit.
Provider 127 Accredited by CAPE Coursework
expires 1/1/2011
2
Antimicrobial Stewardship Training
  • An Antimicrobial Stewardship program is a an
    overarching program to change and direct
    antimicrobial use at a heath care institution.1
  • A series of training programs have been developed
    to enhance pharmacists knowledge and expertise
    in providing antimicrobial stewardship at Kaiser
    Permanente hospitals.
  • 1 MacDougall C, Polk R. Antimicrobial Stewardship
    Programs in Health Care Systems. Clin. Microbiol.
    Rev. Vol. 18 Oct 2005, p. 638-656

3
Antimicrobial Stewardship Training
  • Part 1 Review of Basic Principles and Selected
    Antimicrobials
  • Provides core background information in three
    modules
  • Microbiology Lab review
  • Antibiotic review
  • Allergy review

?See Notes
4
Module 1 (of 3) Microbiology Lab Review
  • Goal
  • The goal of the Microbiology Lab Review module is
    to review and enhance pharmacists basic
    understanding of microbiology in the clinical
    setting.

? See Notes
5
Objectives
  • Upon completion of this module, the participant
    will be able to
  • Differentiate between gram-positive and
    gram-negative bacteria and name pertinent species
    from each group.
  • Be able to interpret blood, urine, tissue and
    sputum culture results.
  • Define contamination and colonization.
  • Explain the purpose of urinalysis.
  • Be able to name some species of
    Coagulase-negative Staphylococcus (CoNS) and
    explain the significance of isolating CoNS from
    blood cultures.

6
Definitions
  • Infectious Disease an interaction with a
    microbe that causes damage to the host.1
  • Pathogen any microorganism that has the
    capacity to cause disease.1
  • Virulence properties that enable a microorganism
    to establish itself on or within a host of a
    particular species and enhance its potential to
    cause disease.

1. Mandell, Bennett, Dolin Principles and
Practice of Infectious Diseases, 6th Ed.
?See Notes
7
Definitions
  • Microbiology results will be reported similar to
    this

Organism Staphylococcus aureus Organism Staphylococcus aureus Organism Staphylococcus aureus
Drug MIC Result
Penicillin gt8 R
Ampicillin gt8 R
Oxacillin lt0.25 S
Clindamycin lt1 S
Tetracycline lt1 S
Trimeth/sulfa lt0.5/9.5 S
?See Notes
8
Definitions
  • Susceptible (S) implies that an infection due to
    the isolate may be appropriately treated with the
    dosage of antimicrobial agent recommended for
    that type of infection.
  • Only use an antibiotic that is reported as
    susceptible.
  • Intermediate (I) implies that an infection due
    to the isolate may be appropriately treated in
    body sites where the drugs are physiologically
    concentrated or when a high dosage of drug can be
    used (i.e., urinary tract).

9
Definitions
  • Resistant (R) isolates that are not inhibited by
    the usually achievable concentrations of the
    agent with normal dosage schedules and/or fall in
    the range where specific microbial resistance
    mechanisms are likely (e.g., ß-lactamases).
  • Minimum inhibitory concentration (MIC) the
    lowest concentration of the antimicrobial agent
    that prevents visible growth after an incubation
    period.
  • Breakpoint discriminatory antimicrobial
    concentration used in the interpretation of
    results of susceptibility testing to define
    isolates as susceptible, intermediate or
    resistant. That is, the MIC where a bacteria goes
    from S to either I or R.

10
Gram Stain
  • Provides for rapid identification of presumed
    pathogen
  • Gram Positive () versus Gram negative (-)
  • Gives idea of morphology or arrangement of
    bacteria
  • cocci vs. rod
  • cluster, pairs, chain
  • Aids in selecting appropriate empiric antibiotic
    choices
  • Can be performed on any body fluid
  • Only useful as preliminary guide NOT definitive

?See Notes
11
Gram Stain
  • Application of series of dyes that affix to the
    peptidoglycan in bacterial cell wall
  • Purple
  • Gram Positive
  • Pink
  • Gram Negative

Bacteria isolated and colored with Gram stain.
Gram-positive cocci, Staphylococcus aureus, from
a lab culture.
Gram-negative bacilli with a capsule, Klebsiella
pneumoniae, from a pneumonia lung abscess
(magnified 1,000).
?See Notes
12
Bacterial Morphology
  • Shapes
  • cocci round
  • bacilli rods
  • coccobacilli ovoid
  • fusiform pointed-end
  • Arrangements
  • single
  • pairs
  • clusters
  • chains

?See Notes
13
Microbiology Common Pathogens
  • Gram-Positive Cocci
  • Clusters
  • Staphylococcus spp.
  • Pairs or chains
  • Streptococcus spp. including
    S. pneumoniae, S. viridans
  • Enterococcus spp.
  • Other species
  • Micrococcus spp.

Staphylococcus aureus
?See Notes
14
Microbiology Common Pathogens
  • Gram-Positive Bacilli (Rods)
  • Diphtheroids
  • Corynebacterium spp.
  • Proprionibacterium acnes
  • Large, with spores
  • Clostridium spp (anaerobic)
  • Bacillus spp
  • Branching, beaded, rods
  • Nocardia spp.
  • Actinomyces spp.
  • Other
  • Listeria spp.
  • Lactobacillus spp. (vaginal flora)

Clostridium difficile
15
Common Bacteria and Classifications
Adapted from Jeff Kuper, Pharm.D., BCPS
?See Notes
16
Microbiology Common Pathogens
  • Gram-Negative Cocci
  • Diplococci
  • Pairs
  • Neisseria meningitidis
  • Neisseria gonorrhea
  • Other
  • Acinetobacter spp. (technically a rod but can
    appear as cocci or bacilli)

Neisseria gonorrhoeae
Acinetobacter baumannii
17
Microbiology Common Pathogens
  • Gram-Negative Bacilli (Rods)
  • Lactose fermenters
  • Enterobacteriaceae (enteric Gm -)
  • Serratia spp.
  • Proteus spp.
  • Enterobacter spp.
  • Escherichia coli
  • Citrobacter spp.
  • Klebsiella spp.
  • Nonfermenters
  • Acinetobacter baumannii
  • Pseudomonas aeruginosa
  • Stenotrophomonas maltophilia

Pseudomonas aeruginosa
?See Notes
18
Microbiology Common Pathogens
  • Anaerobes
  • Gm
  • Clostridium spp. (rods/bacilli)
  • Peptostreptococcus (cocci)
  • Gm -
  • Bacteroides spp. (rods/bacilli)
  • e.g. B. fragilis
  • Prevotella spp. (rods/bacilli)

Clostridium difficile adhering to microvilli in
the gut
19
Microbiology Common Pathogens
  • Atypical bacteria
  • Mycoplasma pneumoniae
  • Legionella pneumophilia
  • Chlamydia pneumoniae
  • These bacteria are hard to culture on standard
    media, hence the name atypical.
  • Commonly implicated in infections like
    community-acquired pneumonia (CAP).

Legionella pneumophilia
20
Program Learning
  1. What type of bacteria is Bacteroides fragilis?
  2. How does the group of Enterobacteriaciae appear
    on gram stain?
  3. Name some atypical bacteria. What types of
    infections do atypical bacterial cause?

21
Program Learning Answers
  • What type of bacteria is Bacteroides fragilis?
    An anaerobic gram-negative rod.
  • How does the group of Enterobacteraciae appear on
    gram stain?
    Gram-negative and appear
    pink.
  • Name some atypical bacteria. What types of
    infections do atypical bacterial cause?
    Legionella pneumophilia,
    Chlamydia pneumoniae, Mycoplasma pneumoniae.
    These are mostly associated with
    community-acquired pneumonia.

22
Colonization
  • The presence of bacteria on a body surface or
    mucous membrance without causing
    disease/infection.
  • Upper respiratory tract (URT) Strep.
    viridans, Candida spp
  • Skin S. epidermidis, Corynebacterium spp., S.
    aureus
  • GI tract E. coli, K. pneumoniae, Candida spp.,
    Bacteroides spp.
  • Urogential Lactobacillus (vaginal flora)

S. epidermidis. CDC.
?See Notes
23
Colonization
  • The presence of bacteria/organisms in a culture
    does not necessarily mean they are pathogenic.
  • It is up to the clinician to interpret the
    culture result and clinically correlate to the
    patients signs and symptoms.

?See Notes
24
Colonization
  • The following are considered sterile sites and
    are not prone to colonization
  • Blood
  • Brain
  • Muscle
  • CSF
  • Synovial fluid

25
Contamination
  • An organism that is introduced at some point
    during the culturing process not related to or
    causing an infectious process.
  • Examples Improperly prepped skin prior to
    venipuncture, drawn from dirty IV line, poor
    lab technique ? contamination on Petri dish).
  • Example skin flora (S. epidermidis) being
    isolated in blood cultures.

26
Blood Cultures
  • Definitive means of identifying most likely
    pathogens.
  • Most pathogens will grow within first 1224 hours
    of collection (Candida, anaerobes may take
    longer).
  • Incubated for five days by laboratory.
  • Should be taken PRIOR to initiation of
    antibiotics.
  • Growth may be inhibited by antibiotics.

?See Notes
27
Blood Cultures
  • Common contaminants
  • Gm cocci Coagulase neg Staph (CoNS)
    S. epidermidis, S. hominis, S.capitis, S.
    warneri
  • Gm rods Corynebacterium spp., Micrococcus
    spp., Bacillus spp. (not anthracis)

?See Notes
28
Adapted from Jeff Kuper, Pharm.D., BCPS
?See Notes
29
Blood Cultures
  • The following should NEVER be considered
    contaminants
  • Staphylococcus aureus
  • Gram rods/bacilli
  • Candida spp.

30
Blood Cultures
  • So whats the significance of isolating a
    Coagulase negative Staphylococcus spp. (CoNS)
    species from blood cultures?

?See Notes
31
Blood Cultures Significance of CoNS
  • Assess how many blood cultures are positive vs.
    how many were drawn.
  • There should be a low suspicion for true
    infection if only one blood culture from multiple
    sets drawn around the same time period are
    positive for CoNS
  • There should be a low suspicion if only one
    culture is positive and cultures were drawn from
    separate sites (e.g., one from IV line, one from
    peripheral site). See next slide for more
    information.

32
Blood Cultures Significance of CoNS
  • What disease state/infection being treated?
  • Patients with an indwelling central line,
    hemodialysis catheter may be more at risk of
    infection.
  • Patients with foreign material (especially
    cardiac), bone/joint infections may have positive
    blood cultures for CoNS.

?See Notes
33
Blood Cultures Significance of CoNS
  • What constitutional symptoms does the patient
    have?
  • Fever, leukocytosis
  • What type of patient?
  • Immunocompetent
  • Immunocompromised
  • Chemotherapy/meds
  • Disease state (advanced HIV)
  • Transplant
  • Neutropenic

?See Notes
34
Blood Cultures Significance of CoNS
  • In general, a solitary peripheral blood culture
    positive for CoNS in an immunocompetent patient
    should be regarded as a contaminant if
  • No other blood cultures drawn in a reasonable
    time frame are also growing CoNS.
  • The patient does not have prosthetic material
    present or does not have a central line/catheter.
  • If another source of infection is identified to
    account for the patients constitutional
    symptoms.
  • If patient has no signs or symptoms of infection.

35
Blood Cultures Significance of CoNS
Just as in any clinical situation where the case
is not straightforward or there are questions
  • If ever in doubt, present case to ID physician.

36
Urine Culture
  • Urine samples are held for 24 hours by
    microbiology lab.
  • Bacterial growth expressed as colony counts,
    i.e., gt100,000 colony forming units (CFU).
  • Should always have a corresponding urinalysis
    (UA) performed for microscopy.
  • If gt2 bacteria are isolated from a urine culture,
    the lab will not perform any further work-up on
    the specimen.

?See Notes
37
Urine Culture
  • Why perform a UA?
  • The examination of fluid microscopy allows for
    some differentiation between infection vs.
    colonization vs. contamination.
  • Infected fluid should have WBC, neutrophils or
    other inflammatory markers.
  • Uninfected fluids generally are devoid of these
    markers.
  • Keep in mind that immunocompromised patients may
    not be able to mount a strong enough immune
    response to produce these markers.

38
Urine Culture Interpreting the UA
  • How many WBCs in urine?
  • How many epithelial/squamous cells present?
  • The lower the number, the cleaner the sample
    (i.e., you can probably trust culture result).
  • The higher the number increases risk of
    contamination with colonizing flora (i.e., sample
    taken too early in the urine stream)
  • What amount of leukocyte esterase present?
  • Given as trace, small, moderate and large.
  • Found in certain WBC, sign of inflammation.

39
Tissue Culture
  • Preliminary report available at 24 hours,
    incubated for 72 hours total.
  • Lab will quantify growth of organism rare,
    light, moderate and heavy.
  • Tissue sample is plated onto agar plate.
  • Quantification of growth on plate gives some idea
    of the bacterial burden of a sample.

40
Tissue Culture
  • These cultures can vary in quality
  • Some may be superficial samples (i.e., more prone
    to contamination or colonization) others may be
    deep tissue samples or cultures from an operation
    (i.e., less likely to be contaminated or
    colonized).
  • The presence of cellulitis, pus, exposed bone can
    help distinguish true infection from
    contamination or colonization.
  • Read the MD note carefully and get some idea of
    what the area looks like, whether the MD thinks
    the area looks clinically infected or not.

41
Sputum Culture
  • Gram stain done initially by lab to assess
    quality of specimen.
  • If gt 10 epithelial cells, sample is not worked
    up
  • Sample not indicative of lower airway secretion.
  • May be prone to contamination.
  • Patients with pulmonary infection should have
    purulent sputum.
  • Presence of WBC on gram stain.

42
Program Learning
  1. Name some organisms that are commonly found on
    the skin.
  2. True or False Coagulase positive Staphylococci
    growing from a blood culture should be considered
    a contaminant.
  3. Which microbes may take longer to grow out in
    blood cultures?
  4. True or False It is common for CSF and synovial
    fluid to be colonized with bacteria.

43
Program Learning Answers
  1. Name some organisms that are commonly found on
    the skin
    S. epidermidis, S.
    aureus, Corynebacterium spp.
  2. True or False Coagulase positive Staphylococci
    growing from a blood culture should be considered
    a contaminant.
    False CoNS are usually
    contaminants. Staphylococcus aureus is coagulase
    and should never be considered a contaminant
    when isolated from the blood.

44
Program Learning Answers
  1. Which microbes may take longer to grow out in
    blood cultures?
    Anaerobes and Candida spp. take
    longer to grow out in blood cultures.
  2. True or False It is common for CSF and synovial
    fluid to be colonized with bacteria.
    CSF and synovial fluid
    are considered sterile sites and are not commonly
    colonized.

45
References
  • Mandell, Bennett Dolin. Principles and Practice
    of Infectious Disease. 7th ed. http//cl.kp.org
    (accessed Oct. 14, 2009).
  • Kaiser Permanente Laboratory Manual Information
    - Northern California. http//cl.kp.org (accessed
    Oct. 14, 2009).
  • Mermel, L. et al. Clinical Practice Guidelines
    for the Diagnosis and Management of Intravascular
    catheter-related infection 2009 Update by the
    Infectious Diseases Society of America. Clin
    Infect Dis. 2009491-45.

This concludes Module 1, the Microbiology Lab
Review. Please proceed to Modules 2 and 3.
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