What are the criteria for tuberculosis (TB) in ascitic fluid cell count?

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Criteria for Tuberculosis in Ascitic Fluid Cell Count

Adenosine deaminase (ADA) levels ≥39 IU/L in ascitic fluid is the most reliable diagnostic criterion for tuberculous peritonitis, with sensitivity of 100% and specificity of 97%. 1

Diagnostic Approach for Tuberculous Peritonitis

Primary Diagnostic Criteria

  • Adenosine Deaminase (ADA) Testing:

    • ADA level ≥39 IU/L is the optimal cut-off point for diagnosing tuberculous peritonitis 1
    • Sensitivity: 100%, Specificity: 97%
    • Different studies have shown similar cut-offs:
      • Values above 36-40 IU/L are highly suggestive of TB peritonitis 1
      • Some centers use a cut-off of 30 U/L (sensitivity 94%, specificity 92%) 2
  • Cell Count Characteristics:

    • Lymphocyte predominance is typical in TB peritonitis
    • PMN count may be elevated but typically not as high as in bacterial peritonitis
    • Total white cell count is often elevated but not specific for TB

Secondary Diagnostic Features

  • Ascitic Fluid Analysis:
    • Low SAAG (<1.1 g/dL) - characteristic of exudative ascites 3
    • High protein content (>2.5 g/dL) - typical of TB peritonitis
    • Acid-fast bacilli smear - rarely positive (<3% of cases)
    • Mycobacterial culture - positive in <50% of cases 3

Differential Diagnostic Considerations

  1. Spontaneous Bacterial Peritonitis (SBP):

    • PMN count ≥250 cells/mm³ is diagnostic for SBP 3
    • SBP typically has neutrophil predominance rather than lymphocyte predominance
    • ADA levels are typically lower in SBP compared to TB peritonitis 4
  2. Pancreatic Ascites:

    • Characterized by ascitic fluid amylase >1000 IU/L or >6× serum amylase 5
    • Protein level >3 g/dL in ascitic fluid 5
    • May also have elevated PMN count, but amylase levels differentiate it from TB
  3. Malignant Ascites:

    • Cytology may be positive (variable yield)
    • ADA levels typically lower than in TB peritonitis 4

Clinical Algorithm for Diagnosing TB Peritonitis

  1. Perform diagnostic paracentesis (strongly recommended for all patients with new-onset ascites) 3
  2. Initial ascitic fluid analysis:
    • Total protein concentration and SAAG calculation
    • Cell count with differential
    • ADA level
    • Acid-fast bacilli smear and mycobacterial culture
  3. Interpret results:
    • If ADA ≥39 IU/L: High probability of TB peritonitis
    • If ADA 30-39 IU/L: Moderate probability, consider additional testing
    • If ADA <30 IU/L: Low probability, consider alternative diagnoses

Important Caveats and Pitfalls

  • False Positive ADA Results: Can occur in some cases of malignancy and empyema, though less common
  • Culture Limitations: Mycobacterial culture has low sensitivity (<50%) but remains important for drug susceptibility testing 3
  • Delayed Diagnosis: TB peritonitis often has an insidious onset; high clinical suspicion is needed
  • Sampling Technique: Ensure adequate fluid volume (50-100 mL) for comprehensive testing including culture
  • Interpretation in Cirrhosis: ADA remains useful even in the presence of underlying cirrhosis 2

Practical Recommendations

  • Always send ascitic fluid for ADA testing when TB peritonitis is in the differential diagnosis
  • Use flow cytometry for cell counting when available, as it provides higher specificity (100%) compared to automated cell counters (65%) for detecting elevated PMN counts 6
  • Consider peritoneal biopsy if ADA results are borderline and clinical suspicion remains high
  • In high TB prevalence areas, routine ADA testing should be considered for all unexplained exudative ascites 2

By following this approach, clinicians can accurately diagnose tuberculous peritonitis and initiate appropriate treatment promptly, reducing morbidity and mortality associated with delayed diagnosis.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Pancreatic Ascites Management

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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