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Published on: August 19, 2020
Clinical study of Presepsin and Pentraxin3 in critically ill children
Fady M El Gendy1, Muhammad S El-Mekkawy1, Nagwan Y Saleh1
1Department of Pediatrics, Faculty of Medicine, Menoufia University, Egypt.
Insights
Biomarkers Presepsin and Pentraxin3 show potential in monitoring critically ill children and diagnosing sepsis. Pentraxin3 levels correlate with mortality, while Presepsin indicates disease severity in pediatric intensive care.
Area of Science:
- Pediatric Critical Care Medicine
- Biomarker Discovery
- Sepsis Diagnostics
Background:
- Sepsis diagnosis and monitoring in critically ill children remain challenging.
- Identifying reliable biomarkers is crucial for improving patient outcomes.
- Acute phase proteins are potential candidates for sepsis assessment.
Purpose of the Study:
- To evaluate the diagnostic and prognostic value of Presepsin and Pentraxin3 in critically ill children.
- To compare biomarker levels between septic and non-septic patients.
- To assess the association of these biomarkers with disease severity and mortality.
Main Methods:
- Prospective observational study involving 80 critically ill children and 80 healthy controls.
- Measurement of serum Presepsin and Pentraxin3 levels within 24 hours of PICU admission.
- Calculation of Pediatric Risk of Mortality (PRISM) and Pediatric Index of Mortality (PIM2) scores.
Main Results:
- Presepsin and Pentraxin3 were significantly elevated in the patient cohort compared to controls.
- Pentraxin3 levels were higher in non-survivors and correlated with PIM2, showing moderate mortality prediction (AUC 0.631).
- Presepsin was associated with increased mechanical ventilation use and longer PICU stays.
Conclusions:
- Presepsin and Pentraxin3 are useful acute phase proteins for monitoring critically ill children and sepsis diagnosis.
- Pentraxin3 shows association with mortality, though with modest discriminatory power.
- Presepsin correlates with indicators of disease severity, suggesting its role in monitoring illness progression. Further large-scale studies are warranted.
Purpose:
To assess the value of Presepsin and Pentraxin3 measurement in critically ill children.
Materials And Methods:
Prospective observational study conducted on 80 children admitted into Pediatric Intensive Care Unit (PICU) and 80 healthy controls. Patients were evaluated for presence of sepsis. Pediatric Risk of Mortality (PRISM) and Pediatric Index of Mortality (PIM2) were calculated. Serum Presepsin and Pentraxin3 were measured within 24 h of admission.
Results:
Presepsin and Pentraxin3 were significantly higher among the whole patient cohort and among septic patients compared with controls (p < 0.001) but no difference was found between septic and non-septic patients. Pentraxin3, but not Presepsin, was significantly higher among non-survivors compared with survivors (p = 0.048) and was correlated with PIM2. Receiver operating characteristic (ROC) curve analysis revealed that Pentraxin3 had an AUC of 0.631 for prediction of mortality which was comparable to that of PRISM and PIM2. Presepsin was associated with a higher rate of mechanical ventilation and longer PICU stay.
Conclusions:
Presepsin and Pentraxin3 are acute phase proteins potentially useful for monitoring critically ill children and diagnosing sepsis. Pentraxin3 is associated with mortality but modestly discriminates survivors from non-survivors. Presepsin is associated with certain indicators of disease severity. Larger studies are certainly required.
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