Management of Spontaneous Bacterial Peritonitis in Cirrhotic Patients
Immediately perform diagnostic paracentesis and start empirical cefotaxime 2g IV every 8 hours plus intravenous albumin (1.5 g/kg within 6 hours, then 1 g/kg on day 3) without waiting for culture results when ascitic fluid neutrophil count exceeds 250/mm³. 1, 2
Diagnostic Approach
When to Perform Paracentesis
- Perform diagnostic paracentesis immediately in all hospitalized cirrhotic patients with ascites at admission, even without symptoms, as 16% of SBP cases are completely asymptomatic 3, 2
- Urgent paracentesis is mandatory in patients presenting with:
Diagnostic Criteria
- SBP is diagnosed when ascitic fluid polymorphonuclear (PMN) neutrophil count >250/mm³, regardless of culture results 3, 4
- Obtain at least 10 mL of ascitic fluid and inoculate blood culture bottles at bedside before starting antibiotics to increase culture sensitivity to >90% 4, 2
- Simultaneously obtain blood cultures before antibiotic initiation 3, 4
- Do not wait for culture results to initiate treatment—the PMN count alone is sufficient 1, 4
Critical Diagnostic Pitfall: Secondary Bacterial Peritonitis
- Suspect secondary bacterial peritonitis (requiring surgical intervention) when patients have:
- Perform prompt CT scanning and early surgical consultation in suspected secondary peritonitis 3
Immediate Treatment Protocol
First-Line Antibiotic Therapy
- Initiate cefotaxime 2g IV every 8 hours (or every 6-8 hours) for 5 days immediately upon diagnosis 1, 4, 2
- A 5-day course is as effective as 10 days of treatment 1, 4
- Cefotaxime achieves 77-98% resolution rates and is the most extensively studied regimen 4, 2
- Alternative for uncomplicated community-acquired SBP: oral ofloxacin 400mg twice daily 4
Important caveat: Third-generation cephalosporins are appropriate for community-acquired SBP, but nosocomial or healthcare-associated SBP (onset >48 hours after admission) requires broader coverage due to multidrug-resistant organisms 3, 5, 6. Consider piperacillin-tazobactam or carbapenems for nosocomial cases 5, 6.
Albumin Therapy (Essential for Mortality Reduction)
- Administer IV albumin 1.5 g/kg body weight within 6 hours of diagnosis, followed by 1.0 g/kg on day 3 1, 4, 2
- This regimen reduces mortality from 29% to 10% and decreases type 1 hepatorenal syndrome from 30% to 10% 4, 2
- Albumin therapy significantly reduces the risk of hepatorenal syndrome and mortality 1, 4
Monitoring Treatment Response
48-Hour Reassessment
- Perform repeat paracentesis at 48 hours to assess treatment efficacy 3, 1, 4, 2
- Treatment success is defined as:
Management of Treatment Failure
- If PMN count fails to decrease by at least 25% or clinical signs worsen, suspect: 3, 1, 4
- Resistant bacteria requiring antibiotic modification based on culture sensitivities 1, 4
- Secondary bacterial peritonitis requiring CT imaging and surgical consultation 1, 4
- Consider broader-spectrum antibiotics (piperacillin-tazobactam or carbapenems) 5, 6
- In patients with septic shock or failure of aggressive antibiotic regimen, consider empiric antifungal coverage for spontaneous fungal peritonitis 6
Special Considerations
Bacterascites Management
- Patients with bacterascites (positive culture but PMN <250/mm³) exhibiting signs of systemic inflammation should be treated with antibiotics 3
- If asymptomatic, perform a second paracentesis 3
- If culture remains positive on repeat tap regardless of neutrophil count, treat as SBP 3
Nosocomial vs. Community-Acquired SBP
- Distinguish between community-acquired and nosocomial SBP (>48 hours after admission) as this determines antibiotic choice 3, 6
- Nosocomial SBP has higher likelihood of multidrug-resistant organisms including gram-positive cocci (Staphylococcus, Enterococcus) 5, 7, 6
- Do not use quinolones in patients already on quinolone prophylaxis, in areas with high quinolone resistance, or in nosocomial SBP 4
Fungal Peritonitis Consideration
- Spontaneous fungal peritonitis occurs in <5% of cases but carries >50% mortality 3
- Consider empiric antifungal therapy in patients with septic shock or those failing aggressive antibiotic regimens 6