Treatment of Serratia marcescens Infections
For Serratia marcescens infections, initiate treatment with piperacillin-tazobactam 4.5g IV every 6 hours or a third/fourth-generation cephalosporin (ceftazidime or cefepime) plus an aminoglycoside, with therapy duration of at least 6 weeks for serious infections such as endocarditis. 1
First-Line Antibiotic Selection
Standard Therapy
- Piperacillin-tazobactam 4.5g IV every 6 hours is the preferred first-line agent for susceptible Serratia isolates, though combination therapy is strongly recommended for serious infections 1
- Combination therapy with a third or fourth-generation cephalosporin (ceftazidime or cefepime) plus an aminoglycoside (gentamicin or amikacin) is recommended for severe infections including bacteremia and sepsis 1
- An extended-spectrum cephalosporin (ceftazidime, ceftriaxone, or cefotaxime) combined with an aminoglycoside provides effective coverage for Gram-negative bacteria including Serratia 1
Alternative Agents
- Carbapenems (meropenem, imipenem-cilastatin, or doripenem) should be used in settings with high local prevalence of ESBL-producing Enterobacteriaceae or for necrotizing soft tissue infections 1
- Fluoroquinolones (ciprofloxacin or levofloxacin) may be used for less severe infections or as step-down oral therapy, but resistance concerns limit their use as first-line agents 1
Site-Specific Treatment Recommendations
Endocarditis
- Cardiac surgery combined with prolonged antibiotic therapy is the cornerstone of treatment, with valve replacement recommended after 7-10 days of antibiotic therapy, as mortality rates can reach 70% 1
- A combination of a third-generation cephalosporin and an aminoglycoside (gentamicin or amikacin) is specifically recommended for Gram-negative bacillary endocarditis 1
- Therapy must be administered for a minimum of 6 weeks 1
Necrotizing Soft Tissue Infections
- Broad-spectrum coverage should be urgently commenced with carbapenems (meropenem, imipenem-cilastatin, or doripenem) in settings with high ESBL prevalence 1
- Antimicrobial therapy should continue until further debridement is no longer necessary, the patient has improved clinically, and fever has been resolved for 48-72 hours 1
Intra-abdominal Infections
- Fluoroquinolones (ciprofloxacin or levofloxacin) combined with metronidazole are appropriate options 1
- Ceftolozane/tazobactam plus metronidazole may be valuable for treating infections caused by gram-negative MDROs to preserve carbapenems 1
- Metronidazole should be added to fluoroquinolone or cephalosporin regimens for anaerobic coverage 1
Central Nervous System Infections
- Meropenem is preferred over imipenem due to lower seizure risk and better CSF penetration 1
Healthcare-Associated Pneumonia
- For ventilator-associated pneumonia, use antipseudomonal agents including cefepime, ceftazidime, piperacillin-tazobactam, imipenem, or meropenem, combined with either an aminoglycoside or fluoroquinolone 1
Critical Resistance Considerations
ESBL and Resistance Patterns
- Serratia species may develop resistance during therapy, and meropenem-containing regimens are preferred for hyperproducing lactamases 1
- Significant ceftriaxone resistance (22.7%) and ceftazidime resistance (19.6%) have been documented, with 36% of isolates showing possible or confirmed ESBL production 2, 3
- Serratia is intrinsically resistant to colistin, which should never be used 1
- Cefotaxime and gentamicin show very low resistance rates (0.6%) and may be suitable alternatives 3
Empiric Therapy Recommendations
- For bloodstream isolates, empiric treatment with cefepime or carbapenem therapy is suggested pending full susceptibility data, given significant ceftriaxone resistance and ESBL activity 2
- Imipenem and ciprofloxacin demonstrate good activity against S. marcescens with MIC90 of 1.0 mcg/mL and 0.19 mcg/mL, respectively 4
Special Populations
Neutropenic/Immunocompromised Patients
- Broad-spectrum coverage with vancomycin plus an antipseudomonal agent (cefepime, carbapenem, or piperacillin-tazobactam) is recommended empirically 1
- S. marcescens is recognized as a potential pathogen in neutropenic patients with cancer 1
Intravenous Drug Users
- IV drug users represent a high-risk population for Serratia bacteremia, often with HCV co-infection 2
- These patients are younger (median age 40 years) and have high rates of complications including endocarditis (12%) and osteomyelitis (10%) 2
Vascular Catheter-Related Infections
- Catheter removal may be required if response to antibiotics is not apparent after 2-3 days of therapy 1
Treatment Duration and Monitoring
Duration
- Minimum of 6 weeks of therapy for endocarditis and other serious infections 1
- For uncomplicated infections, 5-10 days may be adequate 1
- Continue therapy until debridement is no longer necessary, clinical improvement occurs, and fever resolves for 48-72 hours 1
Monitoring
- Blood cultures should be obtained if systemic symptoms are present to rule out concurrent bacteremia, which requires more aggressive management 1
- Follow-up cultures should be obtained to document clearance of infection, especially in persistent or recurrent cases 1
- Clinical reassessment within 48-72 hours is essential 1
- Procalcitonin monitoring may be useful to guide antimicrobial discontinuation in necrotizing infections 1
Common Pitfalls and Caveats
- Do not use ceftriaxone as monotherapy given documented resistance rates of 22.7% and only 32% susceptibility in some series 2, 4
- Never use colistin for Serratia infections due to intrinsic resistance 1
- Always obtain cultures before initiating antibiotics to guide definitive therapy and detect resistance patterns 1
- Be aware that portal of entry is unknown in up to 64% of cases, and concurrent polymicrobial bacteremia occurs in 23% of patients 4
- The overall mortality rate for Serratia bacteremia can reach 50%, with 32% directly attributable to the infection 4
- High readmission rates (21%) and prolonged length of stay (median 7 days) are common 2