# Increased Mortality with Intermediate Ascitic Polymorphonuclear Cell Counts Amongst Patients with Cirrhosis: Time to Redefine the Care Approach

**Authors:** Shahid Habib, Michael Ball, Chris Thomas, Traci Murakami, Nehali Patel, Sandeep Yarlagadda, Sarah Patel, Courtney Walker, Varun Takyar, Krunal Patel, Christian Domingues, Chiu-Hsieh Hsu

PMC · DOI: 10.3390/pathophysiology32040062 · Pathophysiology · 2025-11-11

## TL;DR

Patients with cirrhosis and intermediate levels of certain cells in their abdominal fluid have higher mortality rates, suggesting current diagnostic thresholds may need reevaluation.

## Contribution

The study identifies intermediate ascitic polymorphonuclear cell counts as a significant mortality risk factor, challenging current SBP diagnostic criteria.

## Key findings

- Intermediate A-PMN counts (51–249 cells/HPF) were linked to higher 90- and 365-day mortality risks.
- Low ascitic albumin levels independently increased 365-day mortality risk.
- Binary thresholds for diagnosing SBP may not fully capture mortality risk in cirrhotic patients.

## Abstract

Background: Spontaneous bacterial peritonitis (SBP) is a serious complication in patients with decompensated cirrhosis and ascites. Diagnosis typically relies on an ascitic polymorphonuclear (A-PMN) cell count ≥ 250 cells/high-power field (HPF). Methods: In this retrospective cohort study, 117 hospitalized patients with acute decompensation of chronic liver disease and a diagnostic paracentesis were evaluated. Clinical, laboratory, and imaging data were collected. Patients were stratified by A-PMN counts of ≤50, 51–249, or ≥250 cells/HPF. Additional analysis was performed with patients stratified by ascitic white blood cell (WBC) count and albumin. Mortality risk was assessed at 28, 90, and 365 days. Results: Patients with A-PMN ≤ 50 cells/HPF had the lowest 28-day mortality (8%). At 90 and 365 days, mortality risk was significantly higher for the A-PMN 51–249 cells/HPF group (90-day hazard ratio (HR) 3.55, p = 0.01; 365-day HR 2.43, p = 0.02), but not A-PMN ≥ 250 cells/HPF group (90-day HR 2.95, p = 0.1; 365-day HR 2.95, p = 0.2). Ascitic WBC count did not significantly predict mortality, though higher counts were associated with extraperitoneal infections. Ascitic fluid albumin ≤ 1.0 g/dL was independently associated with increased 365-day mortality (HR 3.53, p = 0.03). Conclusions: Binary SBP A-PMN thresholds may not adequately capture mortality risk in cirrhotic patients with ascites. Low ascitic albumin and intermediate A-PMN counts are associated with increased long-term mortality, suggesting the need for more nuanced diagnostic and prognostic criteria in SBP evaluation.

## Linked entities

- **Diseases:** cirrhosis (MONDO:0005155)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** cirrhotic (MESH:D000094724), bacterial peritonitis (MESH:D010538), extraperitoneal infections (MESH:D007239), Cirrhosis (MESH:D005355), ascites (MESH:D001201), SBP (MESH:D010534), chronic liver disease (MESH:D008107)
- **Chemicals:** HPF (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12641635/full.md

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Source: https://tomesphere.com/paper/PMC12641635