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Modified Glasgow prognostic score and APRI predict ICU admission in Crimean-Congo hemorrhagic fever

Nazan Cinislioğlu1, Ayten Yanık1

  • 1Department of Infectious Diseases and Clinical Microbiology, Erzurum Regional Training and Research Hospital, Erzurum, Turkey.

Acta Tropica
|July 29, 2026
PubMed

Insights

The Modified Glasgow Prognostic Score (mGPS) and Aspartate Aminotransferase-to-Platelet Ratio Index (APRI) effectively predict intensive care unit (ICU) needs in Crimean-Congo hemorrhagic fever (CCHF) patients. These scores aid in early risk stratification for CCHF cases requiring critical care.

Area of Science:

  • Infectious Diseases
  • Clinical Medicine
  • Prognostic Biomarkers

Background:

  • Crimean-Congo hemorrhagic fever (CCHF) poses a significant public health threat.
  • Effective prognostic tools are crucial for managing CCHF patients and anticipating intensive care unit (ICU) needs.

Purpose of the Study:

  • To evaluate the prognostic value of the Modified Glasgow Prognostic Score (mGPS) and the Aspartate Aminotransferase-to-Platelet Ratio Index (APRI).
  • To determine the predictive accuracy of mGPS and APRI for ICU admission in CCHF patients.

Main Methods:

  • Retrospective analysis of 181 CCHF patients diagnosed between January 2023 and January 2026.
  • Calculation of mGPS and APRI scores.
  • Logistic regression and Receiver Operating Characteristic (ROC) curve analysis to assess associations with ICU requirement.

Main Results:

  • mGPS score of 2 increased ICU admission likelihood by 10-fold (OR=10.041).
  • Each unit increase in APRI correlated with a 3.9% rise in ICU risk (OR=1.039).
  • mGPS (AUC=0.738) and APRI (AUC=0.715) demonstrated strong discriminative power for predicting ICU admission.

Conclusions:

  • mGPS and APRI are independent and significant prognostic indicators for ICU requirement in CCHF.
  • These scores offer a simple and practical method for early risk stratification in CCHF patients.
  • Utilizing mGPS and APRI can enhance clinical decision-making for critical care allocation.
Abstract

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