Treatment of Spontaneous Bacterial Peritonitis
Third-generation cephalosporins, particularly cefotaxime 2g IV every 8 hours for 5-7 days, are the first-line treatment for spontaneous bacterial peritonitis (SBP), with intravenous albumin supplementation recommended for high-risk patients. 1, 2
First-Line Antibiotic Therapy
Third-generation cephalosporins: The European Association for the Study of the Liver (EASL) recommends third-generation cephalosporins as first-line treatment 1
Alternative antibiotic options:
- Amoxicillin/clavulanic acid: 1/0.2g IV every 8 hours, followed by 0.5/0.125g PO every 8 hours 1, 2
- Ciprofloxacin: Only for uncomplicated SBP (no renal failure, hepatic encephalopathy, GI bleeding, ileus, or shock) 2, 4
- Important caveat: Quinolones should be avoided in patients already on quinolone prophylaxis, in areas with high quinolone resistance, or in nosocomial SBP 1
Albumin Supplementation
- High-risk patients (serum bilirubin ≥4 mg/dL or serum creatinine ≥1 mg/dL) should receive IV albumin 1, 2:
- 1.5 g/kg at diagnosis
- 1 g/kg on day 3
- This reduces the incidence of hepatorenal syndrome and decreases mortality from 29% to 10% 1
Monitoring Treatment Response
- Follow-up paracentesis should be performed after 48 hours of antibiotic therapy 1, 2
- Treatment success is defined as:
- Decrease in ascitic fluid neutrophil count to <250/mm³
- Decrease of at least 25% from pre-treatment value
- Sterile cultures (if positive at diagnosis)
- Clinical improvement 1
Treatment Failure Management
Suspect treatment failure if:
Management of treatment failure:
- Rule out secondary bacterial peritonitis
- Adjust antibiotics based on culture results
- Consider broader spectrum antibiotics for resistant organisms 1
Special Considerations
Resistant organisms: More common in:
Spontaneous bacterial empyema should be managed similarly to SBP 1
Common Pitfalls to Avoid
- Delayed treatment initiation: Antibiotics should be started immediately after diagnosis 1
- Inadequate dosing: Using 1g instead of 2g cefotaxime may lead to worse outcomes 6
- Failing to administer albumin to high-risk patients (bilirubin ≥4 mg/dL or creatinine ≥1 mg/dL) 1
- Not performing follow-up paracentesis to confirm treatment response 1, 2
- Using quinolones in patients already on quinolone prophylaxis 1, 2
- Missing secondary peritonitis: Consider this if treatment fails 1
Despite appropriate antibiotic therapy and resolution of infection, SBP still carries a high in-hospital mortality rate (approximately 20%) due to complications such as renal failure and hepatic decompensation 1, 3.