Treatment of Citrobacter Bacteremia
For Citrobacter bacteremia, the recommended treatment is a carbapenem such as imipenem-cilastatin or meropenem, with consideration for combination therapy in severe cases or multidrug-resistant strains. 1, 2
Initial Assessment and Management
- Obtain blood cultures from both the central line (if present) and peripheral vein before starting antibiotics 3
- Assess for hemodynamic stability, source of infection, and risk factors for multidrug resistance
- Remove central venous catheters if present, especially for Citrobacter-related CLABSI 3, 4
Empiric Antibiotic Therapy
First-line options:
- Carbapenems: Imipenem-cilastatin or meropenem 1, 2
- Imipenem-cilastatin has demonstrated consistent efficacy against Citrobacter species, including multidrug-resistant strains
- Dosing: 500mg IV every 6 hours (adjust based on renal function)
Alternative options (based on susceptibility):
- Third-generation cephalosporins: Cefotaxime or ceftazidime 5
- Fluoroquinolones: Ciprofloxacin or levofloxacin 4, 2
- Piperacillin-tazobactam: Consider for non-resistant strains 2
Special Considerations
For multidrug-resistant Citrobacter:
- Consider combination therapy with:
Source control:
- Identify and address the primary source of infection
- Most common sources: intra-abdominal (51%), urinary tract (20%), respiratory (11-20%) 5, 6
- Surgical drainage of abscesses or removal of infected devices is essential
Duration of Treatment
- Uncomplicated bacteremia: 10-14 days 3
- Complicated bacteremia (endovascular infection, metastatic foci): 4-6 weeks 3
- Continue treatment until:
- Resolution of fever for at least 48-72 hours
- Clearance of blood cultures
- Clinical improvement
Monitoring and Follow-up
- Repeat blood cultures 48-72 hours after initiating antibiotics to document clearance 3
- Monitor for clinical response (resolution of fever, hemodynamic stability)
- Assess for complications (endocarditis, metastatic infections)
- Adjust antibiotics based on susceptibility results
Pitfalls and Caveats
- Citrobacter species, especially C. freundii, frequently develop resistance to third-generation cephalosporins during therapy due to inducible AmpC β-lactamases 2
- Prior treatment with third-generation cephalosporins is significantly associated with development of multidrug resistance 6
- Polymicrobial bacteremia is common with Citrobacter (33-46% of cases), particularly with intra-abdominal sources 5, 6
- Mortality rates are high (18-56%), especially in immunocompromised patients 5, 6
Risk Factors for Poor Outcomes
- Immunocompromised status (malignancy, transplant recipients)
- Pneumonia as source
- Septic shock
- Delayed appropriate antimicrobial therapy
- Multidrug-resistant isolates