Gram-positiveCocciCatalase-positive

Staphylococcus epidermidis

Coagulase-negative, Gram-positive coccus that is a normal skin commensal and a leading cause of biofilm-associated infections on indwelling medical devices and prosthetic implants.

Organism Card

DomainMust know
Identity
  • Coagulase-negative Staphylococcus (CNS); Gram-positive cocci in clusters [1][2]
  • Catalase +ve, coagulase −ve (distinguishes from S. aureus)
  • Usually benign commensal of skin [1]
Lab discriminator
  • Coagulase −ve (tube coagulase / slide clumping factor) vs S. aureus (coagulase +ve)
  • Single blood culture isolate of CNS usually represents contamination due to improper collection technique [1]
  • Expert practice tip: whenever GPC in clusters in blood culture, always repeat ≥ 2 sets before changing antibiotics [1]
  • Novobiocin sensitive (vs S. saprophyticus = novobiocin resistant)
Reservoir / transmission
  • Normal skin flora; ubiquitous on human skin
  • Nosocomial — introduced via hands of medical personnel, diagnostic/therapeutic procedures [3]
  • Colonises prosthetic material and indwelling devices
Key virulence
  • Biofilm (glycocalyx) formation on prostheses and catheters → difficult to eradicate without device removal [2][3]
  • Polysaccharide intercellular adhesin (PIA) mediates biofilm
  • Low intrinsic virulence; pathogenic mainly in device/foreign-body setting
Clinical syndromes
  • Prosthesis / catheter-associated infections [1][2]:
  • Early prosthetic valve endocarditis ( < 12 months post-op) [4][5]
  • Central line / implanted vascular catheter infections (exit site, tunnel, line-related bacteraemia) [3]
  • Prosthetic joint infections, VP shunt infections
  • CAPD-related peritonitis: coag −ve Staph is commonest organism [6][7]
  • Infectious keratitis (contact lens–associated) [8]
  • CSOM (one of several organisms) [9]
  • CSF shunt infections in neonates/neurosurgery
Diagnosis
  • Genuine infection: consider when CNS isolated from blood culture / sterile site in patients with prostheses [1]
  • ≥ 2 separate blood culture sets growing same CNS → suggests true bacteraemia (not contaminant)
  • Modified Duke criteria: organisms more commonly skin contaminants need ≥ 3 or majority of ≥ 4 separate C/ST positive [5]
  • PD peritonitis: dialysis effluent WCC > 100/μL ( > 50% PMN) + culture [6][7]
Treatment
  • Infections difficult to eradicate without removal of device (biofilm) [3]
  • High methicillin resistance rate (≫ S. aureus); vancomycin is usual first-line for serious CNS device infection [4][5]
  • CAPD peritonitis: empirical IP cefazolin + amikacin; adjust after culture [6][7]
  • Line sepsis: re-site line if infection documented; blood culture from infected line + distant peripheral site [10]
Prevention
  • Strict aseptic technique during line insertion, PD exchanges, surgery
  • Nasal mupirocin for recurrent S. aureus ESI but general principle of exit-site care applies to all Staph [7]
  • Antibiotic-lock therapy for tunnelled catheters (salvage)
  • No vaccine available
Classic traps
  • Single blood culture growing CNS ≠ infection — most likely contamination [1]
  • S. epidermidis = prosthesis/catheter; S. saprophyticus = CA-UTI young females; S. lugdunensis = virulent, behaves like S. aureus [1][2]
  • Early ( < 12 mo) prosthetic valve IE → coagulase −ve Staph; late ( > 12 mo) → same organisms as native valve [4][5]
  • CAPD peritonitis: bile-stained effluent suggests secondary (surgical) peritonitis, not PD-related [11]

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