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Pediatric Management of S. aureus Bacteremia

Infectious diseases consultation for Staphylococcus aureus bacteremia (SAB) has been associated with significant improvement in patient outcomes and mortality. However, as evidenced by several recent EIN posts, there exists substantial variation in provider practice with respect to certain aspects of this condition, particularly in areas where there are limited data to guide management. Moreover, there are key differences in epidemiology, pathogenesis, and treatment between pediatric SAB and adult SAB.

The main purpose of this survey is to assess provider opinion and practice habits regarding areas in the management of SAB where data are inconclusive and clinical management is most likely to vary between providers.

Our hope is that the responses can help to identify areas of consensus in practice, guide future directions in SAB research, as well as inform development of future IDSA and PIDS guidelines on the management of SAB.



    Name:                                                                    EIN ID:

    If you do not manage children with S. aureus bacteremia, check here:    [Stop here & submit]

    Case 1: A previously healthy 4 y/o is diagnosed by MRI with distal femoral osteomyelitis. On admission, blood cultures grow MRSA (MIC: clindamycin 0.125, vancomycin MIC 1). Cultures on hospital day 2 (after 3 doses of vancomycin) are also positive for MRSA. By hospital day 4, the child has clinically improved (improved clinical exam, afebrile, CRP is substantially decreased from admission).

  1. What diagnostic evaluation do you routinely perform when treating a patient like this (osteomyelitis) with S. aureus bacteremia?
      Rarely     Sometimes     Usually    Almost always 
    Repeat blood cultures q24-48hrs until negative
    Echocardiogram
    Abdominal imaging (U/S or CT)
    Ophthalmologic exam
    Doppler U/S for evaluation of DVT
    Other, specify:

  2. Which of the following statements best describes your typical approach to therapy for children with osteomyelitis and concomitant S. aureus bacteremia?
    --I treat nearly all children with culture-proven S. aureus bacteremia with parenteral therapy for the first 10-14 days.
    --The presence of bacteremia does not prevent me from an early transition to oral therapy, but if bacteremia is persistent (e.g., >48-72 hours of bacteremia on effective therapy) I typically treat with parenteral therapy for the first 10-14 days.
    --Even in the setting of persistent bacteremia (>48-72 hours while on effective therapy), I almost always treat with oral antimicrobials once they have clinically improved (i.e., no minimum duration of parenteral therapy).


  3. Case 2: A 10-month-old child with severe eczema is seen in the emergency department for 103°F fever and gastrointestinal symptoms (diarrhea, vomiting). He is moderately dehydrated but otherwise well appearing, and is admitted for observation. Peripheral WBC is normal. A blood culture obtained in the ED grows S. aureus within 24 hours. Vancomycin is begun empirically, and a second blood culture obtained prior to initiation of vancomycin is negative.

  4. Which of the following best describes your approach to this child?
    Stop antibiotics as initial cultures likely a contaminant
    Transition to oral antibiotics to complete:   [select one duration] 7 or 14 days
    Continue IV antibiotics to complete:           [select one duration] 7 or 14 days
    I would choose an alternative management strategy:


  5. A patient has persistent MRSA bacteremia (MIC: vancomycin 0.5, daptomycin 0.5, linezolid 0.5, ceftaroline 1, TMP-SMX 1) on day 6 of vancomycin (trough 18). Liver and renal function are normal. In addition to source control, what is your most likely treatment strategy?
    Continue vancomycin alone
    Continue vancomycin and ADD another MRSA active agent, specify:
    Change to daptomycin
    Change to ceftaroline
    Other, specify:

  6. A 7-year-old develops a PICC-associated deep venous thrombus in the setting of MSSA bacteremia. The PICC is removed and bacteremia resolves promptly. What is your general management strategy regarding treatment duration and anticoagulation?
      Anticoagulation
    Antibiotic/InterventionYes     No    [Select a single choice below]
    Two weeks of effective IV antibioticsYes    No
    Four weeks of effective IV antibioticsYes    No
    Six weeks of effective IV antibioticsYes    No
    Other strategy:        Yes    No

  7. You are consulted on a child with MSSA osteomyelitis (tibia) with three positive blood cultures for MSSA. While receiving parenteral therapy, what is your treatment of choice?
    Cefazolin
    Nafcillin/oxacillin every 4-6 hours
    Nafcillin by continuous infusion
    Other, specify:

  8. The IDSA and PIDS are developing guidelines for S. aureus bacteremia. What topics would you like to ensure that the guidelines address?