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Procalcitonin use in febrile children attending European emergency departments: a prospective multicenter study
Dorine M Borensztajn1,2, Joany M Zachariasse3, Enitan D Carrol4
1Department of General Pediatrics, Erasmus MC-Sophia Children's Hospital, Wytemaweg 80, Rotterdam, 3015 CN, the Netherlands. dm.borensztajn@nwz.nl.
Insights
Procalcitonin (PCT) use in European pediatric emergency departments is limited and highly variable, despite its proven benefits in diagnosing sepsis. Further research is needed to understand and overcome barriers to its wider clinical adoption.
Area of Science:
- Biomarkers in pediatric emergency medicine
- Infectious disease diagnostics
- Clinical practice variations
Background:
- Procalcitonin (PCT) has been studied for sepsis identification since 1993, with over 8,500 publications.
- Studies indicate PCT is superior to C-reactive protein (CRP) in differentiating invasive infections from viral infections, particularly early in disease.
- Actual clinical utilization of PCT remains poorly documented.
Purpose of the Study:
- To investigate the utilization of PCT in febrile children presenting to European emergency departments (EDs).
- To compare PCT usage with C-reactive protein (CRP) in this pediatric population.
- To identify patterns of PCT use based on patient age, fever duration, and clinical signs.
Main Methods:
- A secondary analysis of the prospective, multicenter MOFICHE/PERFORM study involving 12 European EDs.
- Inclusion of febrile children under 18 years old across eight countries.
- Descriptive analysis of PCT use in nine participating EDs, examining variations by age, fever characteristics, and clinical presentation.
Main Results:
- Out of 31,612 febrile episodes, blood tests were performed in 50.0%.
- CRP was used in 98.3% of blood tests, while PCT was used in only 3.9% of cases.
- PCT was most frequently used in infants under 3 months (12.0%), children with fever <24h (4.9%), and those with meningeal signs (7.0%) or non-blanching rash (10.9%).
Conclusions:
- Actual PCT use in European EDs for febrile children is limited and shows significant inter-hospital variability.
- Potential reasons for low PCT adoption include a lack of guidelines, restricted availability, higher costs, and resistance to new clinical strategies.
Background:
Studies on procalcitonin (PCT) for identifying sepsis were published as early as 1993 and since then, PCT has been the topic of over 8,500 studies. Several studies show PCT to be superior to CRP in differentiating invasive infections such as sepsis from viral infections, especially early in the disease course. However, its actual use in clinical practice is poorly documented. Our aim was to study the use of PCT in febrile children attending the ED across Europe and compare this to the use of CRP.
Methods:
The MOFICHE/PERFORM study, a prospective multicenter study, took place at 12 European EDs in eight countries and included febrile children < 18 years. In this secondary analysis of nine participating EDs that used PCT, descriptive analyses were performed, describing the use of PCT in all febrile children and for different age groups, foci of fever and fever duration.
Results:
In total, 31,612 pediatric febrile episodes were available for analyses. Blood tests were performed in 15,812 (50.0%, range 9.6-92.6%)) febrile episodes. CRP was included in 98.3% of blood tests (range between hospitals 80-100%), while PCT was included in only 3.9% (range 0.1-86%). PCT was most often performed in children below 3 months (12.0% versus 3.6% in older children, p < 0.001). PCT was used slightly more often in children with fever less than 24 h in comparison to children with a duration of fever ≥ 24 h (4.9% versus 3.4%, p < 0.001). Regarding clinical alarming signs, PCT was used most often in children with meningeal signs (7.0%) or a non-blanching rash (10.9%).
Conclusion:
Actual PCT use in febrile children at European EDs is limited and varies largely between hospitals. Possible explanations include lack of guidelines, limited availability, higher costs and lack of readiness to adapt new clinical strategies.
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