Effect of Viral Illness on Procalcitonin as a Predictor of Bacterial Infection in Febrile Infants
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Updated: Jul 15, 2025

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Jared Kusma1,2, Quinney Fu1,2, Maheshwor Kafle1,2
1Phoenix Children's Hospital, Phoenix, Arizona.
Insights
Confirmed viral infections (CVI) in febrile infants reduce the sensitivity of procalcitonin (PCT) tests for detecting bacterial illness (BI). However, PCT specificity remains high, meaning it is still a reliable indicator when positive for BI in infants.
Area of Science:
- Pediatrics
- Infectious Diseases
- Clinical Chemistry
Background:
- Febrile infants require accurate diagnosis of bacterial illness (BI).
- Procalcitonin (PCT) is a biomarker used to assess bacterial infections.
- The influence of concurrent viral infections (CVI) on PCT in infants with BI is not well understood.
Purpose of the Study:
- To investigate the association between CVI and PCT levels in febrile infants with and without BI.
- To evaluate PCT's effectiveness in predicting BI in infants who also have a CVI.
Main Methods:
- Retrospective cohort study of febrile infants aged 8-60 days.
- Comparison of PCT levels based on bacterial and viral test results.
- Logistic regression analysis to assess PCT's predictive ability for BI.
Main Results:
- Infants with both BI and CVI had lower PCT levels than those with BI alone.
- The presence of CVI decreased PCT sensitivity for BI detection (44% vs. 68%).
- PCT specificity for BI detection remained high (96% vs. 93%) even with CVI.
Conclusions:
- CVI in febrile infants lowers PCT sensitivity for detecting bacterial illness.
- PCT specificity for bacterial illness is minimally affected by concurrent viral infections.
- Clinical interpretation of PCT in febrile infants should consider the potential impact of viral infections.
Objective:
The impact of confirmed viral infections (CVI) on procalcitonin (PCT) levels in febrile infants aged 8-60 days with a bacterial illness (BI) is unknown. The objectives of the study were to (1) examine the association of CVI with PCT levels in patients with/without a concurrent BI, defined as bacteremia, meningitis, or urinary tract infection, and (2) assess PCT as a predictor of BI in infants with a concurrent CVI.
Methods:
In this single-center, retrospective cohort study, we examined febrile infants aged 8-60 days presenting between January 1, 2018 and December 31, 2020. PCT levels were compared between groups, according to results of bacterial cultures and viral tests, using the Wilcoxon rank test. The prediction ability of PCT to detect BI with/without concurrent CVI was assessed by using area under the curve from logistic regression.
Results:
Patients included: 404 BI-/CVI+, 73 BI+/CVI-, 48 BI+/CVI+, and 138 BI-/CVI-. Median PCT level in the BI+/CVI+ group was significantly lower when compared to BI+/CVI- (0.36 ng/mL vs 0.89 ng/mL), but significantly higher than the BI-/CVI- group (0.36 ng/mL vs 0.1 ng/mL). The presence of a CVI reduced the sensitivity of PCT in BI detection (68% vs 44%), with minimal impact specificity (93% vs 96%).
Conclusions:
In previously healthy febrile infants 8-60 days old, the presence of a CVI reduces the sensitivity of PCT BI detection without impacting its specificity. The impact of a CVI on PCT levels in febrile infants has implications for how this marker of infection should be considered when assessing risk of BI in infants.
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