Platelet indices and inflammatory markers as diagnostic predictors for ascitic fluid infection

Ahmed Abdel-Razik1, Waleed Eldars, Ehsan Rizk

  • 1aTropical Medicine Department bMedical Microbiology and Immunology Department cClinical Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.

Abstract

Insights

Mean platelet volume (MPV) can accurately predict ascitic fluid infection (AFI) in cirrhosis patients. Increased MPV and platelet distribution width (PDW) indicate inflammation, making them valuable diagnostic markers for AFI.

Area of Science:

  • Hepatology
  • Internal Medicine
  • Clinical Diagnostics

Background:

  • Ascitic fluid infection (AFI) is a frequent complication in patients with cirrhosis and ascites.
  • Platelet indices, such as mean platelet volume (MPV) and platelet distribution width (PDW), are potential indicators of inflammation.

Purpose of the Study:

  • To evaluate the utility of platelet size alterations and platelet indices in predicting AFI in cirrhotic patients.
  • To determine if MPV and PDW can serve as simple, inexpensive markers for AFI diagnosis.

Main Methods:

  • A study involving 150 cirrhotic patients with ascites and 70 healthy controls.
  • Patients were categorized into AFI and non-AFI groups based on ascitic fluid analysis.
  • MPV, PDW, and inflammatory markers were measured; receiver operating characteristic (ROC) curve analysis was used to assess predictive ability.

Main Results:

  • Cirrhotic patients with AFI showed significantly higher MPV levels compared to those without AFI and healthy controls.
  • Elevated MPV, PDW, C-reactive protein, and white blood cell counts were observed in the AFI group.
  • ROC analysis indicated MPV has high sensitivity (95.9%) and specificity (91.7%) for detecting AFI at a cutoff of 8.77.

Conclusions:

  • Platelet indices (MPV, PDW) and C-reactive protein are elevated in cirrhotic patients with AFI.
  • MPV measurement is a highly accurate diagnostic tool for predicting AFI, likely reflecting ongoing systemic inflammation.

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