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Procalcitonin for the diagnosis of early-onset neonatal sepsis: a multilevel probabilistic approach.

Authors :
Santuz P
Soffiati M
Dorizzi RM
Benedetti M
Zaglia F
Biban P
Source :
Clinical biochemistry [Clin Biochem] 2008 Oct; Vol. 41 (14-15), pp. 1150-5. Date of Electronic Publication: 2008 Jun 20.
Publication Year :
2008

Abstract

Objectives: To compare the accuracy of procalcitonin (PCT) in early-onset neonatal sepsis (EOS) using standard cut-off values and a multilevel probabilistic approach.<br />Design and Methods: A retrospective study of PCT was performed in 149 newborns at risk of EOS, including preterm or prolonged rupture of membranes, chorioamnionitis or maternal infection, GBS colonization and signs of fetal distress. PCT values were analysed according to time of assay, i.e. at birth and at 24 and 48 h. We estimated sensitivity, specificity, positive (LR+) and negative likelihood ratio (LR-), diagnostic odds ratio (DOR) and number needed to diagnose (NND) using traditional and optimal (derived from ROC analysis) PCT cut-off values.<br />Results: Using optimal cut-off, the LR+, DOR and NND at birth were 10, 18.9 and 2.2, at 24 h they were 5.3, 11.2 and 2.1, and at 48 h they were 5.6, 18.1 and 1.7, respectively. The multilevel analysis generated three post-test probabilities for each time of assay. At 24 h post-test probabilities of EOS were 78% for PCT >90, 11% for PCT 10.1-90 and 3% for PCT <10.1 mg/L, respectively. Similar results were found in the other time points, with a wide range of intermediate PCT concentrations that did not change the post-test probability.<br />Conclusions: The multilevel probabilistic approach was more effective in assessing the diagnostic power of PCT in EOS, showing that a wide range of intermediate PCT values was not able to discriminate between presence and absence of infection.

Details

Language :
English
ISSN :
1873-2933
Volume :
41
Issue :
14-15
Database :
MEDLINE
Journal :
Clinical biochemistry
Publication Type :
Academic Journal
Accession number :
18606160
Full Text :
https://doi.org/10.1016/j.clinbiochem.2008.05.015