What are the diagnostic criteria and treatment for Spontaneous Bacterial Peritonitis (SBP)?

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Diagnosis of Spontaneous Bacterial Peritonitis (SBP)

SBP is diagnosed when ascitic fluid polymorphonuclear (PMN) leukocyte count exceeds 250/mm³, and diagnostic paracentesis must be performed in all hospitalized cirrhotic patients with ascites, even without symptoms of infection. 1, 2, 3

When to Perform Diagnostic Paracentesis

Perform diagnostic paracentesis immediately in the following scenarios:

  • All cirrhotic patients with ascites upon hospital admission, regardless of symptoms 1, 2
  • Patients with gastrointestinal bleeding 2
  • Shock or hemodynamic instability 2
  • Fever or signs of systemic inflammation 2
  • Abdominal pain or gastrointestinal symptoms 2
  • Worsening liver and/or renal function 2
  • Hepatic encephalopathy 2

Critical pitfall: SBP is asymptomatic in approximately 7% of cases, making clinical criteria unreliable for diagnosis. 4 You cannot exclude SBP based on absence of symptoms—paracentesis is mandatory. 4

Diagnostic Criteria

The definitive diagnostic threshold is:

  • Ascitic fluid PMN count >250/mm³ 1, 2, 3

This applies regardless of culture results. Culture-negative neutrocytic ascites (PMN ≥250/mm³ with negative culture) should be treated identically to culture-positive SBP. 3

Key characteristics of SBP:

  • Typically monomicrobial infection (single organism) 3
  • Most commonly gram-negative bacteria (~60%), particularly E. coli and Klebsiella pneumoniae 1
  • Increasing prevalence of gram-positive organisms and multidrug-resistant organisms (MDROs), especially in nosocomial infections (35% of overall infections) 1

Proper Specimen Collection

Culture technique is critical for diagnostic yield:

  • Inoculate at least 10 mL of ascitic fluid into blood culture bottles at the bedside (aerobic and anaerobic) before administering antibiotics 1, 2
  • This bedside inoculation technique increases culture sensitivity to >90% 1
  • Obtain simultaneous blood cultures before starting antibiotics 1, 5

Important caveat: Ascitic fluid culture is positive in only 50-80% of SBP cases, even with optimal technique. 3 Never delay treatment waiting for culture results.

Rapid Bedside Diagnosis

Leukocyte esterase reagent strips (Multistix, Combur test, Nephur-Test) can provide immediate bedside diagnosis while awaiting formal cell count:

  • Sensitivity: 83-100%, Specificity: 92.5-100% 6, 7
  • Positive predictive value: 75-100%, Negative predictive value: 96-100% 6, 7
  • Allows immediate initiation of empirical antibiotics 6

Distinguishing SBP from Secondary Bacterial Peritonitis

Secondary bacterial peritonitis requires surgical intervention and has different characteristics:

  • Localized abdominal symptoms or signs 3
  • Multiple organisms on Gram stain or culture (polymicrobial) 3
  • Higher ascitic PMN count (often >1,000/mm³) 3
  • Requires prompt surgical consultation 3

If secondary peritonitis is suspected (e.g., diverticulitis, cholecystitis, perforation), do not treat as SBP—obtain surgical consultation and treat the underlying condition. 1

Treatment Initiation

Start empirical IV antibiotics immediately upon diagnosis (PMN >250/mm³) without waiting for culture results. 1, 2, 3

Delaying antibiotics increases mortality by 10% for every hour's delay in patients with septic shock. 2, 3

First-Line Antibiotic Therapy

For community-acquired SBP in settings without high MDRO prevalence:

  • Cefotaxime 2g IV every 6-8 hours for 5 days (third-generation cephalosporin) 1, 2, 5
  • Alternative: Ceftriaxone 1
  • Resolution rate approximately 90% 1

For nosocomial SBP, recent hospitalization, or critically ill patients (high MDRO risk):

  • Consider initial carbapenem therapy 1
  • Inappropriate initial antimicrobial therapy in septic shock increases death risk 10-fold 1

Do not use quinolones if:

  • Patient already on quinolone prophylaxis 2
  • High quinolone resistance in your area 2
  • Nosocomial SBP 2

Albumin Therapy

Administer IV albumin concurrently with antibiotics:

  • 1.5 g/kg at diagnosis 2, 3, 5
  • 1.0 g/kg on day 3 2, 3, 5

This significantly reduces hepatorenal syndrome risk and mortality. 2, 3, 5

Monitoring Treatment Response

Perform repeat paracentesis after 48 hours of treatment. 5

Treatment success is defined as:

  • Ascitic neutrophil count decrease by at least 25% of pre-treatment value 2, 5
  • Improvement in clinical signs and symptoms 2, 5

Treatment failure indicators:

  • Failure of PMN count to decrease by ≥25% 2, 5
  • Worsening clinical status 2, 5
  • Consider resistant bacteria requiring antibiotic change or secondary bacterial peritonitis requiring surgical evaluation 5

Antibiotic Stewardship

Narrow antibiotic coverage as soon as culture results are available. 1 The emerging threat of MDROs makes stewardship critical—use broad-spectrum antibiotics for the shortest duration necessary. 1

Five-day therapy is as effective as 10-day treatment. 5

Prognosis

Despite appropriate treatment, SBP carries approximately 20% hospital mortality rate. 2, 5 However, early appropriate antibiotic treatment combined with albumin therapy significantly improves survival. 2, 5

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Diagnosis and Treatment of Spontaneous Bacterial Peritonitis (SBP)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Spontaneous Bacterial Peritonitis and Secondary Bacterial Peritonitis Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Spontaneous Bacterial Peritonitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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