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Origins of the CLAB definition

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Endorsed National Quality and Safety Council 2004. NSW Health Infection control program quality monitoring indicators, version 1 ... – PowerPoint PPT presentation

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Title: Origins of the CLAB definition


1
Origins of the CLAB definition
  • AICA National Advisory Board 2001-2 adapted
    National Nosocomial Infection System definition
    with minor clarification
  • Endorsed National Quality and Safety Council 2004
  • NSW Health Infection control program quality
    monitoring indicators, version 1(2003) 2
    (current) all hospitals with ICUs report
  • CLAB rates in ICUs (stratified by peripherally
    and centrally-inserted) currently per 1,000
    line-days
  • Multi-resistant bacterial events in ICU (MRSA,
    MR-Acinetobacter baumannii)

2
Blood Stream Infection Detection and
Categorisation
  • Pathogenesis of central line infection
  • Contamination of line tip during insertion
    (commonest)
  • Hub contamination (occurs during line
    disconnection etc)
  • Infusate contamination (unusual)
  • Detection of bacteraemia/fungaemia
  • Blood culture collection
  • Line tips- not recommended/required
  • 3. Categorisation of positive blood culture
    events
  • Is the isolate significant?
  • Is it a new unique event?
  • Is the event ICU-associated?
  • Is the event intravascular-line associated?

3
Detection of bloodstream infection
  • Detection of bacteraemia/fungaemia in adults is
    dependent on volume of blood at least 40mLs
    recommended (2 x independently collected sets
    best practice)
  • Collection via old lines (IA or Central)
    potential for contamination from hub and/or
    infection of line- not recommended.
  • Persistently febrile patients (eg. neurosurgical)
    will require regular blood cultures (eg. every 48
    hrs) - single set acceptable
  • Collection technique
  • alcohol skin disinfection (wet site well, allow
    30 seconds for action),
  • no-touch needle insertion,
  • best to use vacutainer sleeve for blood culture
    bottle,
  • do not overfill bottles

4
Detection of line infection
  • Ensure appropriate blood culture collection
    (above)
  • Examine line exit sites daily for exudate and/or
    inflammation
  • If line sepsis suspected, submit aseptically
    collected line tip for semi-quantitative culture
  • No routine requirement for culture of line tips
    in asymptomatic patients

5
Is an isolate significant?
  • criterion 1 recognised pathogen
  • No clinical correlate required. Single blood
    culture set accepted.
  • criterion 2 common skin contaminant (criterion
    3 children lt 1 year with common skin
    contaminant)
  • Symptoms of infection
  • AND EITHER
  • 2 sets positive with the same isolate within
    48hrs (some sort of micro ID required of CNS not
    mixed CNS)
  • OR (only for potential CLAB events)
  • 1 set positive and appropriate antimicrobial
    therapy is commenced against that isolate

6
Significance accepted pathogens
  • 1 positive set acceptable
  • Primary events treatment and/or line removal
    instigated
  • Diagnosed focus events symptoms/signs of
    infection at a particular primary site
    (microbiological confirmation not required)
  • EXCLUDE
  • events where no treatment given or action taken
    and patient remained well at 7 days

7
What are common skin contaminants?
  • Coagulase negative staphylococci
  • Bacillus species
  • Corynebacterium species
  • Rarely
  • Micrococci
  • Propionobacterium species
  • Environmental Gram negative bacteria

8
Is it a unique (new) event?
  • 14 day rule repeat similar blood isolate events
    within 14 days are disregarded

9
Is the event ICU-associated?
  • Defined as a significant blood event that is
    detected more than 48 hrs after ICU admission
    where the patient was not overtly infected upon
    admission
  • Also includes events detected within 48 hrs of
    patient discharge from ICU

10
Is the event line-associated?
  • Requirements include
  • No other diagnosed/likely source of sepsis
  • Intravascular line present within 48 hr of
    detection
  • In an ICU Patient with multiple sites of
    potential active infection, do not classify as
    line-associated unless direct evidence of line
    infection and/or multiple positive blood cultures
    with CNS
  • Patient with multiple lines, in the absence of
    direct line site/tip culture evidence to
    associate one line with the event, then assume
    central line is responsible gt IA line gt
    peripheral

11
Blood culture review requirements
  • All positive cultures require careful review,
    including events in non-ICU patients within the
    hospital
  • For ICU, classify
  • Contaminant events
  • ICU-associated events due to other infective
    sites
  • ICU line-associated events
  • Community acquired events
  • Need a surveillance system that classifies events
    in the same manner over time eg. look at
    significant shifts in classification of coag neg
    staph event significance

12
Coag neg staph issues
13
Liaison possibilities with Microbiology/IC/ ID
  • Classification of blood events in d/w ICU
    clinician(s)
  • Micro/Infectious Diseases ICU Rounds antibiotic
    advice, review of microbiology
  • Routine periodic review of events that have
    occurred with ICU group
  • Capacity to complete the BSI part of the CLAB
    checklist form providing data on events post ICU
    discharge (but would require a duplicate central
    line form in order for the form to remain in the
    medical record at ICU discharge)
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