What is the recommended treatment for Staphylococcus lugdunensis infections?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 12, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Treatment of Staphylococcus lugdunensis Infections

Staphylococcus lugdunensis should be treated like Staphylococcus aureus rather than other coagulase-negative staphylococci, using oxacillin or nafcillin as first-line therapy for susceptible strains, with treatment duration and surgical approach determined by the specific infection type. 1

Key Clinical Recognition

S. lugdunensis is an unusually virulent coagulase-negative staphylococcus that behaves clinically like S. aureus, causing aggressive infections with high rates of complications including valve destruction, perivalvular extension, and metastatic spread. 1 This organism requires species-level identification through specialized biochemical assays or matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry, as standard coagulase-negative staphylococcus identification is insufficient. 1, 2

Antibiotic Selection by Infection Type

Infective Endocarditis (Native Valve)

  • First-line for oxacillin-susceptible strains: Oxacillin or (flu)cloxacillin 12 g/day IV in 4-6 divided doses for 4-6 weeks 1
  • Add gentamicin 3 mg/kg/day IV in 2-3 doses for the first 3-5 days (though clinical benefit not formally demonstrated and associated with increased toxicity) 1
  • For penicillin allergy or methicillin resistance: Vancomycin 30 mg/kg/day IV in 2 doses for 4-6 weeks, with trough levels of 10-15 mg/L 1

Prosthetic Valve Endocarditis

  • Oxacillin-susceptible strains: Oxacillin 12 g/day IV in 4-6 doses PLUS rifampin 1200 mg/day IV or orally in 2 doses PLUS gentamicin 3 mg/kg/day IV in 2-3 doses, all for 6 weeks minimum 1
  • Methicillin-resistant strains: Vancomycin 30 mg/kg/day IV in 2 doses PLUS rifampin 1200 mg/day PLUS gentamicin 3 mg/kg/day, all for 6 weeks, with vancomycin trough levels of 25-30 mg/L 1
  • Rifampin is critical for prosthetic device infections as it eradicates bacteria attached to foreign material, but must always be combined with another effective antistaphylococcal agent to prevent resistance. 1

Prosthetic Joint Infections

  • Two-stage revision is strongly recommended as it achieves 85% cure rate compared to 33% for other treatment modalities (P=0.009) 3
  • Debridement alone results in 44% relapse rate, while no surgical intervention or one-stage revision results in 100% relapse regardless of antibiotic regimen 3
  • Antibiotic therapy: Oxacillin-based regimen for susceptible strains (all isolates except one were oxacillin-susceptible in the largest series) 3
  • Prolonged antibiotic course is required in conjunction with aggressive surgical management 3

Skin and Soft Tissue Infections

  • For oxacillin-susceptible strains (which represent the vast majority): Oxacillin, dicloxacillin, or cephalexin for 5-21 days depending on severity 4, 5
  • Penicillin G may be superior to oxacillin when susceptible, as MIC50 and MIC90 values for penicillin G are threefold lower than oxacillin among penicillin-susceptible isolates 6
  • Most infections resolve with appropriate oral antibiotics, with or without surgical drainage 4, 5
  • Common presentations include folliculitis/pustulosis (55%), abscesses, surgical wound infections, and secondary infection of hidradenitis suppurativa 4, 5

Antimicrobial Susceptibility Profile

  • Penicillin resistance varies widely (15-87% worldwide), but methicillin resistance remains rare 6, 2
  • S. lugdunensis remains highly susceptible to most antibiotics, which is uncharacteristic of other coagulase-negative staphylococci 6, 2
  • Breakpoints for S. lugdunensis are higher than other coagulase-negative staphylococci and similar to S. aureus breakpoints 2
  • Among 540 Swedish isolates, 74.6% were susceptible to penicillin G, with only 2 isolates carrying mecA gene (SCCmec type IVa) 6

Critical Clinical Pitfalls

Do not treat S. lugdunensis like other coagulase-negative staphylococci. The European Society of Cardiology explicitly excludes S. lugdunensis from standard coagulase-negative staphylococcus treatment protocols due to its aggressive behavior. 1 This organism causes IE with a protracted course associated with higher rates of complications and treatment failure (up to 40%). 1

Early surgical intervention is often necessary due to high rates of perivalvular extension, valve destruction, and metastatic infection. 1 The ESC guidelines list S. lugdunensis as a microorganism with "high potential for rapid destruction of cardiac structures" warranting consideration of early surgery. 1

Monitor closely for complications including abscess formation, pseudoaneurysms, fistulas, conduction disturbances, and extracardiac spread, as these occur more frequently than with other coagulase-negative staphylococci. 1

Monitoring Parameters

  • Gentamicin levels (when used): Pre-dose (trough) <1 mg/L, post-dose (peak at 1 hour) 10-12 mg/L, with renal function and levels monitored weekly 1
  • Vancomycin levels: Trough 10-15 mg/L for native valve IE, 25-30 mg/L for prosthetic valve IE 1
  • Clinical response: Continue therapy at least 48 hours after patient becomes afebrile, asymptomatic, and cultures are negative 7, 8

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.