Abstract

Objectives: Neonatal late-onset sepsis work-up is a frequent occurrence in every neonatal department. Blood cultures are the diagnostic gold standard, however, a negative culture prior to 48–72 h is often considered insufficient to exclude sepsis. We aimed to develop a decision tree which would enable exclusion of late-onset sepsis within 24 h using clinical and laboratory variables.Study Design: Infants evaluated for late-onset sepsis during the years 2016–2019, without major malformations, in a tertiary neonatal center were eligible for inclusion. Blood cultures and clinical and laboratory data were extracted at 0 and 24 h after sepsis work-up. Infants with bacteriologically confirmed late-onset sepsis were compared to matched control infants. Univariate logistic regression identified potential risk factors. A decision tree based on Chi-square automatic interaction detection methodology was developed and validated.Results: The study cohort was divided to a development cohort (105 patients) and a validation cohort (60 patients). At 24 h after initial evaluation, the best variables to identify sepsis were C-reactive protein > 0.75 mg/dl, neutrophil-to-lymphocyte ratio > 1.5 and sick-appearance at 24 h. Use of these 3 variables together with blood culture status at 24 h, enabled identification of all infants that eventually developed sepsis through the decision tree model. Our decision tree has an area under the receiver operating characteristic curve of 0.94 (95% CI: 0.90–0.98).Conclusions: In non-sick appearing infants with a negative blood culture at 24 h and normal laboratory values, sepsis is highly unlikely and discontinuing antibiotics after 24 h is a viable option.

Highlights

  • Neonatal late-onset sepsis (LOS) is an important worldwide health care issue commonly occurring in Neonatal Intensive Care Units (NICU’s) [1,2,3]

  • Culture positive LOS was identified in 140 of 3263 infants (4.3%) that were admitted to our NICU, representing 145 episodes

  • The entire study cohort was divided in a 2:1 ratio, to a development cohort (33 infants with LOS, 72 control infants) and a temporal validation cohort (20 infants with LOS, 40 control infants)

Read more

Summary

Introduction

Neonatal late-onset sepsis (LOS) is an important worldwide health care issue commonly occurring in Neonatal Intensive Care Units (NICU’s) [1,2,3]. Infants suspected of having sepsis often receive antibiotics for 48–72 h until sepsis is excluded. Many infants at risk of LOS are treated with antibiotics as the consequences of untreated sepsis are severe compared to the side effects of short-term antibiotic therapy [2]. Physicians often prefer to err on the side of caution and to continue antibiotics until there is virtually no risk of sepsis. Short-term effects have been shown in preterm infants and result in an increase in adverse outcomes such as necrotizing enterocolitis and sepsis [4]. Training cohort (n = 105) All. No sepsis (n = 72) Sepsis (n = 33) P-value.

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.