BD BACTEC Blood Culture Media Shortage

Authored by: Kristina Bryant, MD, Larry K. Kociolek, MD, MSCI, Andi L. Shane, MD, MPH, MSc, and Danielle M. Zerr, MD, MPH

This communication is to inform pediatric clinicians about a critical supply shortage of blood culture media bottles (both aerobic and anaerobic bottles) for the Becton Dickinson (BD) BACTEC blood culture system. According to the US Centers for Disease Control and Prevention (CDC), “this shortage has the potential to disrupt patient care by leading to delays in diagnosis, misdiagnosis, or other challenges in the clinical management of patients with certain infectious diseases.” This shortage has an unclear timeline for resolution at this time, although it is expected to continue at least into September 2024.

Current blood culture supply is limited nationally, and alternative blood culture media are unavailable for this BD BACTEC blood culture system. For this reason, clinicians must be judicious and avoid unnecessary blood culture utilization. This can be done safely by following best practices. Below are some recommendations for optimizing blood culture use in children.

General Guidance

Inform local stakeholders: Work with your local clinical microbiology laboratory on situational awareness, developing and implementing a strategy for educating local pediatric clinicians, and process for monitoring blood culture usage, media availability, and opportunities for improvements in utilization. Your clinical microbiology laboratory may be able to additionally validate recently expired blood culture media to extend shelf life during the shortage.

Guidance may vary by clinical condition and/or specialty: Clinicians should familiarize themselves with local clinical care guidelines and/or published guidelines for their specialty, when available, to avoid inappropriate blood culture utilization. A sample clinical care guideline from Johns Hopkins Medicine is available.

Familiarize yourself with literature and resources: See references at the end for additional information. Pay considerable attention to the safe, evidence-based, and pediatric-focused principles proposed by the BrighT STAR research group. Although this guidance was developed for children receiving care in the PICU, many of the presented principles are broadly applicable to pediatric care.

Evaluate patients for clinical likelihood of bloodstream infection: Before reflexively ordering a blood culture for a non-specific symptom (e.g., fever), review patient’s history/risk factors, clinical signs/symptoms, and lab and imaging results, and perform a physical examination, to determine if there is a clinical indication for a blood culture.

Eliminate blood culture “draw and hold” by nursing staff: Blood cultures should not be collected and held (just in case one is needed later) prior to a clinician evaluating the patient and ordering a blood culture.

Avoid blood culture contamination: Educate on CDC best practices to prevent blood culture contamination.

Limit repeat blood cultures: Repeat blood cultures should be based on clinical suspicion of true bloodstream infection (vs contamination) and a planned intervention based on the result (e.g., escalation or de-escalation of antimicrobial therapy). Confirming bloodstream infection clearance for true bloodstream infection is necessary in specific situations (more specific information below).

Limit number of blood cultures collected: A single blood culture collected aseptically with appropriate weight-based volume is sufficient to detect bacteremia in most clinical situations. More than one blood culture may be indicated for some conditions such as endocarditis or those where more than one blood culture result is needed to support a suspected diagnosis. In general, a single appropriate weight-based volume blood culture from a vascular access device collected simultaneously with an appropriate weight-based volume peripheral blood culture, should be adequate to guide management of patients with a vascular access device. Follow local practice for collection of cultures from multi-lumen vascular access devices if local practice differs from this guidance.

Utilize pediatric infectious diseases consultants: Please consult the local pediatric infectious diseases team, if available, when guidance is needed regarding blood culture utility.

Leverage your electronic medical record: Consider eliminating the option to order blood cultures more frequently than a one-time order and incorporation of clinical decision support tools for optimal blood culture utilization.

Optimize blood culture yield: To optimize the yield of pathogen recovery by blood culture, manufacturer-recommended blood culture volumes* should be collected.

  • BACTEC Peds Plus
    • Pediatric-sized bottles for recovery of aerobic pathogens (including Candida species)
    • Manufacturer allowable range: 0.5-5.0 ml (1.0-3.0 ml is optimal)
  • BACTEC Lytic Anaerobic
    • For recovery of anaerobic pathogens in children and adults
    • Manufacturer allowable range: 3.0-7.0 ml (5.0-7.0 ml is optimal)
  • BACTEC Plus Aerobic
    • For recovery of aerobic pathogens in adults (including Candida species)
    • Manufacturer allowable range: 3.0-10.0 ml (8.0-10.0 ml is optimal)
  • BACTEC Myco/f Lytic
    • For recovery of fungal pathogens in children and adults
    • Manufacturer allowable range: 1.0-5.0 ml (3.0-5.0 ml is optimal)

* In children with low blood volumes and/or frequent blood draws, such as infants neonates, follow local guidance for safe blood volume collection. Johns Hopins provides additional guidance for weight-based dosing for blood culture media other than BACTEC Peds Plus, for which lower blood volumes are required.

Specific Scenarios

In general, scenarios when a blood culture is likely beneficial for patient management includes, but not limited to:

  • Febrile neonate when meeting criteria per recently updated AAP recommendations
  • Sepsis
  • Meningitis
  • Septic arthritis and acute osteomyelitis
  • Endocarditis
  • Document bacteremia/fungemia clearance with repeat blood culture* in the following scenarios:
    • Staphylococcus aureus bacteremia
    • Candidemia
    • Endovascular infection (including central venous catheter-related bloodstream infections and endocarditis)
    • Known bacteremia/fungemia and not clinically improving

* In general, repeat blood cultures are not needed more frequently than every 48 hours.

In general, scenarios when a blood culture is unlikely beneficial for patient management includes, but not limited to:

  • Repeat blood cultures in a well-appearing patient with a likely blood culture contaminant
  • Repeat blood cultures in a febrile patient who is otherwise stable or slowly improving on effective antibiotic therapy with known focus of infection
  • Repeat blood cultures in a patient with known bloodstream infection who is clinically improving unless they meet criteria listed above (i.e., endovascular/catheter-related bloodstream infection, S. aureus bacteremia, Candidemia)
  • Non-severe community-acquired pneumonia
  • Symptoms compatible with a viral syndrome
  • Cellulitis, including pre-septal and orbital cellulitis
  • >12 months of age with uncomplicated urinary tract infection, irrespective of presence of fever

Pathogen-Specific Media Alternatives

  • Decisions regarding use of alternative culture media in the specific situations below should be based on local relative availability of various culture media and consultation with your local clinical microbiology laboratory.
  • Candidemia
    • For patients with confirmed isolated candidemia (i.e., Candida species identified in the blood without a concomitant pathogen), BACTEC Myco/F Lytic culture media can be used to document clearance
    • Infectious disease consult is strongly recommended for patients with candidemia
  • Staphylococcus aureus bacteremia
    • For patients with confirmed isolated S. aureus (i.e., S. aureus identified in the blood without a concomitant pathogen), BACTEC Lytic Anaerobic culture media can be used to document clearance
    • Infectious disease consult is strongly recommended for patients with S. aureus bacteremia

Additional Resources