Ceftriaxone for Spontaneous Bacterial Peritonitis in Cirrhosis
Ceftriaxone is sufficient as first-line therapy for community-acquired SBP in cirrhotic patients with ascites, and should be given at 2 grams intravenously once daily (or 1 gram every 12 hours) for 5 days in uncomplicated cases. 1, 2
Antibiotic Selection and Dosing
First-Line Therapy
- Ceftriaxone 2 grams IV once daily is the recommended dose, achieving resolution rates of 73-100% in clinical trials 2
- Alternative dosing of 1 gram IV every 12 hours is equally effective 2, 3
- Both regimens achieve adequate ascitic fluid concentrations to cover the most common pathogens (E. coli, Klebsiella pneumoniae, Streptococcus species) 2
When Ceftriaxone May NOT Be Sufficient
- Nosocomial (hospital-acquired) SBP requires broader coverage due to multidrug-resistant organisms (MDROs), particularly extended-spectrum beta-lactamase (ESBL)-producing bacteria 1, 2
- Patients with recent hospitalization, critically ill patients in the ICU, or those with septic shock should receive carbapenems (meropenem, imipenem) as initial therapy 1
- Do not use ceftriaxone if the patient is on quinolone prophylaxis - resistance rates are high and broader coverage is needed 2
Treatment Duration
Standard Duration
- 5 days of treatment is sufficient for uncomplicated SBP 1, 2
- This is as effective as 10-day therapy based on randomized controlled trials 1
- Resolution rates after 5 days range from 73-95% 4, 5
When to Extend Beyond 5 Days
- Extend therapy to 10 days if clinical response is inadequate 2
- Continue treatment if culture results indicate resistant organisms 2
- Perform repeat paracentesis at 48 hours - if ascitic neutrophil count fails to decrease to <25% of pre-treatment value, suspect treatment failure 1, 2
Critical Adjunctive Therapy
Albumin Administration
- Give IV albumin 1.5 g/kg within 6 hours of diagnosis, followed by 1.0 g/kg on day 3 for patients with high-risk features 2
- High-risk features include: serum creatinine ≥1 mg/dL, blood urea nitrogen ≥30 mg/dL, or total bilirubin ≥4 mg/dL 2
- This reduces mortality from 29% to 10% 2
- Albumin should be given to patients with signs of developing renal impairment 1
Monitoring Treatment Response
48-Hour Assessment
- Repeat diagnostic paracentesis at 48 hours to assess treatment efficacy 1, 2
- Expect ascitic PMN count to decrease to <25% of pre-treatment value 1
- If no clinical improvement by 48-72 hours, suspect resistant organisms or secondary bacterial peritonitis 2
Resolution Rates
- Cytological cure (PMN <250 cells/mm³) occurs in 65% of patients after 48 hours 4
- Total resolution after 5 days occurs in 73-95% of cases 4, 5
Common Pitfalls and Caveats
Dosing Errors
- Many clinicians use 1 gram daily instead of the recommended 2 grams daily - this may result in worse outcomes 6
- Patients receiving 2 grams daily may have improved survival and fewer ICU days compared to 1 gram daily, though this difference becomes non-significant after adjusting for disease severity 6
Antibiotic Stewardship
- Narrow coverage as soon as culture results are available 1, 2
- Over 70% of patients receive multiple unnecessary antibiotics - avoid polypharmacy 6
- Inappropriate initial antimicrobial therapy in septic shock increases mortality risk 10-fold 1
Resistance Patterns
- There is a shift toward gram-positive and MDRO infections, particularly in nosocomial SBP (35% of overall infections) 1
- Increasing quinolone resistance makes empiric ciprofloxacin problematic 2
- Long-term quinolone prophylaxis leads to more gram-positive infections (79%) including MRSA 1
Secondary Prophylaxis After SBP
- All patients who survive SBP should receive indefinite prophylaxis with norfloxacin 400 mg daily or ciprofloxacin 500 mg daily until liver transplantation 1, 2
- Recurrence rate without prophylaxis is 70% at one year 1, 2
- All patients with SBP should be evaluated for liver transplantation - one-year survival is only 30-50% 1