Treatment of Bacterial Infections
For most bacterial infections, targeted antibiotic therapy based on culture and susceptibility testing is the gold standard, but empirical broad-spectrum coverage must be initiated immediately in critically ill patients or those with suspected resistant organisms. 1, 2
General Principles of Bacterial Infection Management
Diagnostic Approach
- Obtain cultures before initiating antibiotics from blood, urine, sputum, or fecal sources depending on the infection site to identify the causative organism and guide targeted therapy 1
- Use imaging (CT or PET-CT scans) when further confirmation is needed, particularly for pneumonia, abdominal abscesses, or deep tissue infections 1
- Microbiologic cultures with susceptibility testing are critical because antimicrobial resistance patterns vary significantly by geographic location and healthcare setting 1
Initial Empirical Therapy Selection
The choice of empirical antibiotics depends on three key factors: infection severity, patient immune status, and likelihood of resistant pathogens. 1
For Community-Acquired Infections (Mild-to-Moderate Severity)
- Use narrow-spectrum agents: ampicillin/sulbactam, cefazolin or cefuroxime plus metronidazole, or ticarcillin/clavulanate 1
- Avoid fluoroquinolones as first-line therapy due to increasing resistance and adverse effect risks 3, 4
- For uncomplicated urinary tract infections, use nitrofurantoin, fosfomycin, or trimethoprim-sulfamethoxazole (only if local E. coli resistance <20%) 3, 5
For Severe Infections or Immunocompromised Patients
- Initiate broad-spectrum coverage immediately with agents active against resistant gram-positive bacteria (MRSA) and gram-negative organisms including Pseudomonas 1
- Recommended regimens include: meropenem, imipenem/cilastatin, piperacillin/tazobactam, or fourth-generation cephalosporins (cefepime) plus metronidazole 1
- For suspected MRSA, add vancomycin, linezolid, or daptomycin 1
For Gram-Negative Bacteremia in Critically Ill Patients
- Use combination therapy with two different antimicrobial classes if recent colonization or infection with multidrug-resistant organisms is suspected 2
- Options include: carbapenem plus aminoglycoside, or antipseudomonal cephalosporin plus fluoroquinolone 2
- De-escalate to single-agent therapy once culture results confirm susceptibility 2
Site-Specific Treatment Algorithms
Complicated Skin and Soft Tissue Infections
- Prompt surgical intervention plus appropriate antibiotics targeting likely pathogens including MRSA and anaerobes 1
- Adjust therapy after culture results become available 1
- Higher-risk patients (APACHE II score >15, advanced age, nosocomial infection) require potent broad-spectrum therapy 1
Intra-Abdominal Infections
- Community-acquired: Use ertapenem, ticarcillin/clavulanate, or cefuroxime plus metronidazole 1
- Healthcare-associated (postoperative): Complex multidrug regimens are required due to more resistant flora including Pseudomonas, Enterobacter, and MRSA 1
- Local nosocomial resistance patterns should dictate empirical treatment 1
Pyelonephritis
- Oral ciprofloxacin 500mg twice daily for 7 days if local resistance <10% 3
- Trimethoprim-sulfamethoxazole 160/800mg twice daily for 14 days only if susceptibility confirmed 3
- If using oral β-lactams, start with initial IV ceftriaxone 1g or aminoglycoside 3
Bloodstream Infections
- Treatment duration should be 7-14 days for uncomplicated bacteremia, with longer courses for complicated infections 2
- Remove intravascular devices if persistent bacteremia occurs despite appropriate therapy 2
Special Populations
Neutropenic Patients
- Broad-spectrum antibiotics with reliable gram-negative coverage are essential 2, 4
- For febrile neutropenia, use anti-pseudomonal beta-lactam (piperacillin/tazobactam) as first-line therapy 4
- Prophylaxis with levofloxacin is recommended for prolonged neutropenia 1
Patients with Recurrent Infections
- Do not use the same antibiotic class if recent exposure occurred within 3-6 months due to increased resistance risk 3
- Prophylactic strategies may be considered, but treating asymptomatic bacteriuria is not recommended as it fosters resistance 3
Critical Management Principles
De-escalation Strategy
- Once culture and susceptibility results are available, narrow antibiotic spectrum to the most appropriate single agent 1, 2
- This approach reduces toxicity, cost, and selective pressure for resistance 1
Duration of Therapy
- Do not subject patients to prolonged antimicrobial therapy or arbitrary changes if persistent signs of infection occur; instead, investigate the underlying cause 1
- Treatment should continue until symptoms resolve 1
Resistance Considerations
- Current resistance trends frequently require multiple agents due to polymicrobial nature of infections 1
- MRSA, ESBL-producing Enterobacteriaceae, and resistant anaerobes (B. fragilis group) are increasingly common 1
- Review local antibiograms before selecting empirical therapy 1
Common Pitfalls to Avoid
- Never delay appropriate broad-spectrum therapy in critically ill patients with suspected bacterial infection, as this increases mortality 2
- Avoid using antibiotics with known high local resistance rates (>20%) for empirical therapy 3
- Do not fail to obtain pre-treatment cultures in patients with serious infections or recurrent disease 3
- Inadequate treatment duration (particularly for pyelonephritis requiring 7-14 days) leads to treatment failure 3
- Do not continue empirical broad-spectrum coverage once susceptibility results allow for targeted therapy 1, 2
- Underestimating infection severity in neutropenic patients can lead to delayed treatment and increased mortality 4