Immediate Treatment for Spontaneous Bacterial Peritonitis (SBP)
Start intravenous cefotaxime 2g every 8-12 hours (or ceftriaxone 1-2g every 12-24 hours) immediately upon diagnosis without waiting for culture results, and administer IV albumin 1.5 g/kg within 6 hours followed by 1.0 g/kg on day 3. 1, 2
Empirical Antibiotic Therapy
First-Line Treatment for Community-Acquired SBP
- Third-generation cephalosporins are the drugs of choice for immediate empirical treatment, with cefotaxime achieving infection resolution rates of 77-98% 3, 1
- Cefotaxime 2g IV every 8-12 hours for 5-7 days is the standard regimen (4g/day is as effective as 8g/day) 3, 1, 4
- Ceftriaxone 1-2g IV every 12-24 hours is an equally effective alternative with resolution rates of 73-100% 1, 2
- Never delay antibiotics waiting for culture results—empirical therapy must begin immediately after diagnostic paracentesis shows ascitic neutrophil count ≥250/mm³ 3, 1
Alternative Antibiotic Options for Community-Acquired SBP
- Amoxicillin/clavulanic acid (1g/0.2g IV every 8 hours, then switch to 0.5g/0.125g PO every 8 hours) achieves 87% resolution rates, similar to cefotaxime 3, 1
- Oral ofloxacin 400mg every 12 hours can be used only in uncomplicated SBP (no renal failure, hepatic encephalopathy, GI bleeding, ileus, or shock) with 84% resolution rates 3, 1
- Oral ciprofloxacin 500mg every 12 hours for 5-7 days is acceptable for clinically stable patients with community-acquired SBP as step-down therapy 1
Nosocomial or Healthcare-Associated SBP
- Broader-spectrum coverage is critical for patients with recent hospitalization, ICU admission, or septic shock due to 35% multidrug-resistant organism (MDRO) rates 1
- Meropenem 1g IV every 8 hours plus daptomycin 6mg/kg/day should be considered in high MDRO prevalence settings 1
- In critically ill patients (CLIF-SOFA scores ≥7), empirical carbapenem treatment significantly reduces in-hospital mortality compared to third-generation cephalosporins 5
Critical Adjunctive Therapy: IV Albumin
Albumin administration is mandatory, not optional—it reduces hepatorenal syndrome from 30% to 10% and mortality from 29% to 10% 3, 1, 2
Albumin Dosing Protocol
- 1.5 g/kg body weight within 6 hours of diagnosis 1, 2
- Followed by 1.0 g/kg on day 3 1, 2
- This applies to all patients with SBP, particularly those with serum creatinine ≥1 mg/dL, BUN ≥30 mg/dL, or total bilirubin ≥4 mg/dL 2
Monitoring Treatment Response
48-Hour Reassessment
- Perform repeat paracentesis at 48 hours to assess treatment efficacy 3, 1, 2
- Treatment failure is suspected if ascitic neutrophil count fails to decrease to <25% of pre-treatment value 3, 1
- If no clinical improvement by 48-72 hours, suspect resistant organisms or secondary bacterial peritonitis and broaden antibiotic coverage 1, 2
Treatment Duration
- 5 days of therapy is as effective as 10 days for uncomplicated SBP 3, 2
- Extend beyond 5 days if clinical response is inadequate or cultures reveal resistant organisms 2
Critical Pitfalls to Avoid
Antibiotic Selection Errors
- Never use aminoglycosides (e.g., tobramycin) as empirical therapy due to nephrotoxicity 3, 1
- Do not use quinolones as first-line if the patient has been on quinolone prophylaxis—resistance rates are high 2
- Avoid cefotaxime/ceftriaxone alone for nosocomial SBP without considering MDRO coverage 1
Albumin Administration Errors
- Do not omit albumin—it is evidence-based therapy that significantly reduces mortality 3, 1
- Ensure albumin is given within 6 hours of diagnosis for maximum benefit 1, 2
Diagnostic Delays
- Do not wait for culture results to start antibiotics—cultures are positive in only 40-59% of cases 3, 4
- Inoculate ascitic fluid into blood culture bottles at bedside to improve culture yield 6
Special Considerations
Patients on Norfloxacin Prophylaxis
- Cefotaxime or amoxicillin/clavulanic acid remain effective in patients who develop SBP while on norfloxacin prophylaxis 3
Renal Impairment
- Adjust cefotaxime dose in patients with creatinine clearance <20 mL/min/1.73 m²—halve the total daily dose 7
- Monitor renal function carefully, especially if combining with other potentially nephrotoxic agents 7