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Preventing False Positive Blood Cultures

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Preventing False Positive Blood Cultures. Lisa L. Steed, Ph.D., D(ABMM) Diagnostic Microbiology ... State the consequences of false positive blood cultures ... – PowerPoint PPT presentation

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Title: Preventing False Positive Blood Cultures


1
Preventing False Positive Blood Cultures
  • Lisa L. Steed, Ph.D., D(ABMM)
  • Diagnostic Microbiology
  • Wanda Beardsley, BSN, RN, ICP
  • June 2008

2
Objectives
  • After viewing the presentation the viewer will be
    able to
  • Define false positive blood culture
  • State the consequences of false positive blood
    cultures
  • List proper techniques to prevent a false
    positive blood culture
  • Describe importance of timing and amount in
    obtaining blood culture specimens
  • Select the appropriate blood culture bottles

3
Blood culture definitions
  • Blood culture or Blood culture set volume of
    blood obtained under aseptic conditions that is
    inoculated into one or more bottles of broth
    culture medium
  • Positive culture one or more bottles of a blood
    culture set demonstrate(s) growth

4
What is the Problem?
  • The problem is numbers of false positive blood
    cultures obtained at MUHA
  • A false positive means that a specimen contains
    an organism that is from a source other than the
    patients blood i.e. skin organisms
  • When this occurs a patient may be treated
    unnecessarily for the skin organism when there is
    NO bloodstream infection.

5
Occurrence of False Positive Blood Cultures
(Trash)
6
Question 1
  • What is considered a false positive blood
    culture?
  • a. Aerobic growth in specimen when anaerobic is
    expected
  • b. The specimen is contaminated with an
    organism that is from a source other than the
    patients blood.
  • c. Specimen positive for MRSA
  • d. Specimen positive for VRE

7
Why should we care about properly collected blood
cultures?
  • 1. Inaccurate reimbursement
  • 2. Questionable contaminants require obtaining
    more blood cultures to determine true infection.
    This means more work for nursing/ phlebotomy.
  • 3. Inappropriate antimicrobial therapy
  • Unnecessary drug levels, drug administration
  • May lead to C difficile associated diarrhea
    (isolation)

8
Timing is Crucial in Drawing Blood Culture Sets
  • Blood culture sets must be drawn within two hours
    of each other.
  • Two or more positive cultures growing an organism
    usually considered a contaminant will not be
    considered a blood stream infection if the
    cultures were collected more than 2 hrs apart
  • Sensitivities will NOT be done unless otherwise
    specified by the physician.

9
Blood culture collection issues
  • Volume
  • THE MOST IMPORTANT variable in detecting
    bacteremia and fungemia
  • Collect MAXIMUM volume for pt weight bottle
    type
  • Timing (within 2 hours of the first set)
  • Antiseptic site prep
  • Site of collection
  • Venipuncture (one set must be peripheral site)
  • Line draws (avoid if possible)
  • Site must be documented on lab requisition

10
How much blood to draw per set?
(ml)
11
Getting blood from a turnip
  • If less than the recommended volume of blood is
    collected for culture, the blood should be
    inoculated into the AEROBIC bottle first,
    maximizing the volume, then into the anaerobic
    bottle
  • Most bacteremias are caused by aerobic bacteria
  • Yeast are aerobes and grow almost exclusively in
    aerobic bottles

12
Question 2
  • To prevent false positives, sets of blood
    cultures must be drawn
  • Within 3 hours of each other
  • Within 4 hours of each other
  • Within 5 hours of each other
  • Within 2 hours of each other

13
Question 3
  • The most important variable in detecting
  • bacteremia and fungemia is the volume of blood
  • collected
  • T
  • F

14
Question 4
  • Which of the following are consequences of
  • false positive blood cultures?
  • a. Inaccurate reimbursement
  • b. Repeat blood cultures to determine true
    infection.
  • c. Inappropriate antimicrobial therapy
  • d. All of the above

15
Antipseptic Preparation
  • Venipuncture blood culture
  • Disinfect the tops of the blood culture bottles
    by wiping with an alcohol pad prior to collection
    (do not use iodine/iodophor)
  • Disinfect the site with ChloraPrep using
    friction for 30 seconds dry for 30 seconds
  • Do not re-palpate the site to relocate vessel

Infection Control policy 3-002 Collection of
Blood Samples
16
Antiseptic Preparation
  • Intravascular line blood culture
  • Use SmartSite valve closest to insertion site
  • ChloraPrep SmartSite valve using friction for
    30 seconds
  • Allow to air dry for 30 seconds
  • Collect blood
  • Do not discard initial blood draw. This specimen
    should be used for culture.

17
Antiseptic Preparation
  • Tops of blood culture bottles do not come sterile
    from the factory!
  • Disinfect the tops of the blood culture bottles
    by wiping with an alcohol pad for 1-2 seconds
  • Allow to air dry for one minute prior to
    collection
  • Do not use iodine/iodophor or ChloraPrep as
    this may kill organisms from the patients blood

18
Why Let ChloraPrep and Alcohol Dry?
  • Drying Time is Dying Time!
  • Microorganisms are killed only when the
    antiseptic has dried.
  • Hurrying is not an option!

19
Blood Culture Reminders
  • Higher contamination from ports/lines
  • Disinfect ports/lines with ChloraPrep
  • ALWAYS SEND A VENIPUNCTURE blood culture when a
    line blood culture is sent
  • 2 line draws is not equivalent to a
    venipuncture
  • Why can we use the initial blood draw for blood
    cultures?
  • Bacteria may be dwelling in the catheter
  • Maximize the volume of blood in the bottles

20
Question 5
  • Proper techniques for preventing false positive
    blood cultures when drawing from a venipuncture
  • Prep skin with ChloraPrep for 30 seconds
  • Allow ChloraPrep to dry for 30 seconds
  • Prep top of culture bottle for 1-2 seconds with
    alcohol and allow to dry for 1 minute
  • All of the above

21
Question 6
  • Proper techniques for preventing false positive
    blood cultures when drawing from an IV line
    include
  • Use SmartSite valve closest to insertion site
  • ChloraPrep blue portion of SmartSite valve
    using friction for 30 seconds allow to air dry
    for 30 seconds
  • Do not discard initial blood draw. This specimen
    should be used for culture.
  • All of the above

22
Selecting Blood Culture Bottles
  • Blue Standard Aerobic
  • Purple Standard Anaerobic

23
Selecting Blood Culture Bottles
  • FAN (Activated charcoal) bottles only to be used
    for special situations and must be ordered by
    practitioner
  • Orange
  • Green
  • Yellow (pediatric)

24
Question 7
  • A physician order is required to use a FAN
    culture bottle
  • T
  • F
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