Abstract

The aim of this study is to evaluate the diagnostic ability of multiplex real-time polymerase chain reaction (PCR) in very preterm infants assessed for risk of early onset neonatal sepsis (EOS). Prospective observational cohort study. Blood samples of preterm neonates≤32weeks of gestation were evaluated by commercial multiplex real-time PCR within 2h after delivery. The definition of EOS was based on positive blood culture and clinical signs of infection or negative blood culture, clinical signs of infection and abnormal neonatal blood count and serum biomarkers. Among 82 subjects analyzed in the study, 15 had clinical or confirmed EOS. PCR was positive in four of these infants (including the only one with a positive blood culture), as well as in 15 of the 67 infants without sepsis (sensitivity 27%, specificity 78%). Out of 19 PCR positive subjects, Escherichia coli was detected in 12 infants (63%). Statistically significant association was found between vaginal E.coli colonization of the mother and E.coli PCR positivity of the neonate (p=0.001). No relationship was found between neonatal E.coli swab results and assessment findings of bacterial DNA in neonatal blood stream. Multiplex real-time PCR had insufficient diagnostic capability for EOS in high risk very preterm infants. The study revealed no significant association between PCR results and the diagnosis of clinical EOS. Correlation between maternal vaginal swab results and positive PCR in the newborn needs further investigation to fully understand the role of bacterial DNA analysis in preterm infants.

Highlights

  • Onset neonatal sepsis (EOS) remains a challenging issue accompanied by alarmingly high mortality and adverse outcomes [1, 2]

  • Twenty-nine infants were assessed by BactoPlex Real-Time polymerase chain reaction (PCR) Kit, 53 by FTD Neonatal sepsis

  • Seven positive results were assessed by BactoPlex Real-Time PCR Kit, 12 by FTD Neonatal sepsis

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Summary

Introduction

Onset neonatal sepsis (EOS) remains a challenging issue accompanied by alarmingly high mortality and adverse outcomes [1, 2]. The diagnosis is based on a positive blood culture and the time of onset within 72 h after delivery [3]. It is considered to be the result of a vertical pathogen transmission [4]. A high risk of EOS is seen in the case of prolonged premature rupture of membranes, clinical and/or laboratory signs of chorioamnionitis and presence of maternal urinary tract infection [4]. Gestational age of

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