Staphylococci

Gram positive cocci that:

Staphylococcus Aureus

Common skin commensal that:

  • Causes illness by local infection and toxin production
  • Generally requires host compromise to cause infection:
    • Skin breaks
    • Foreign body
    • Immunosuppression
  • May lead to infection in:
    • B
      • HAP
        Classically necrotising.
    • C
      • Infective endocarditis
        May be associated with local abscesses if related to injection.
      • Invasive vascular devices
        • CLABSI
        • Pacemaker
    • D
      • Osteomyelitis
      • Discitis
      • Epidural abscess
    • E
      • Skin
      • Soft tissue infections
      • Joint prostheses

Staphylococcal toxic shock is a complication of S. Aureus colonisation, and is covered under Toxic Shock Syndrome.

Methicillin-Resistant Staphylococcus Aureus

MRSA is a common mutation of S. Aureus that:

  • Alters the Penicillin Binding Protein
  • Significantly ↓ affinity of β-lactams for the cell wall so they become non-responsive
  • Require treatment with a much more limited arsenal of antimicrobials

Coagulase Negative Staphylococcus

Coagulase-negative Staphylococcus:

  • Include several strains, the most common which are:
    • S. Epidermidis
      IE, line infections.
    • S. Saprophyticus
      UTIs.
    • S. lugdunensis
      IE.
    • S. haemolyticus
      IE.
    • S. schleiferi
      IE.
    • S. warneri
    • S. hominis
    • S. capitis
  • Usually exist as skin and nares commensals
    Common cause of false-positive blood cultures. True infection can be distinguished on:
    • Clinical suspicion
    • Number of positive cultures
    • Differential time to positivity
      Time between the bottle from an infected line (classically a CVC) flagging positive, and a peripheral culture taken at the same time; if the CVC culture becomes positive earlier it is more likely to be the source.
    • Positive in aerobic and anaerobic bottles
      85% of “true” infections, compared to ~35% of potentially contaminated specimens.
    • Culture positive in <16 hours
  • Cause infections in:
    • Areas obscured from the immune system:
      • Septic arthritis
      • Endocarditis
      • Invasive devices
        • Lines
        • Pacemakers
        • Prosthetics
          • Valves
          • Joints
          • VP shunts
    • Immunocompromised host
    • Disrupted integumentary barriers
      • Burns
  • Are generally multiresistant, and sensitive to glycopeptides and linezolid

Investigations

Bedside:

  • TTE
    For vegetations. Does not exclude IE, but can rule-in.
  • TOE
    Should be performed if TTE is negative.

Management

Specific therapy:

  • Pharmacological
    • MSSA
      • β-lactams
        • Flucloxacillin
        • Cefazolin
      • Clindamycin
      • Moxifloxacin
      • Vancomycin
        Failure rates ~4× that of β-lactams.
    • MRSA
      • Glycopeptides
        • Vancomycin
        • Teicoplanin
      • Linezolid 600mg IV Q12H
        No dose adjustments required for renal or hepatic impairment.
      • 5th generation cephalosporins:
        • Ceftaroline 600mg IV Q8H
        • Ceftobiprole 500mg Q8H
      • Daptomycin
      • Rifampicin/fusidic acid
      • Trimethoprim/sulfamethoxazole
    • Coagulase-negative
      • Vancomycin as empiric therapy
      • Flucloxacillin/Cephalosporin
        May be appropriate de-escalation once sensitivity testing completed.
  • Procedural
    • Source Control

Desensitisation for β-lactam allergic patients is preferable - these are by far and away the best agents.

Prognosis

Mortality varies on site of origin, but can reach 50% with:

  • Lung
  • CLABSI
  • Infective endocarditis

References

  1. Harvey RA, Cornelissen CN, Fisher BD. Lippincott Illustrated Reviews: Microbiology (Lippincott Illustrated Reviews Series). 3rd Ed. LWW.