Abstract

BackgroundSepsis is a major health issue in preterm infants. Biomarkers are used to diagnose and monitor patients with sepsis, but C-reactive protein (CRP) is proven not predictive at onset of late onset neonatal sepsis (LONS) diagnosis. The aim of this study was to evaluate the association of interleukin-6(IL-6), procalcitonin (PCT) and CRP with subsequent sepsis severity and mortality in preterm infants suspected of late onset neonatal sepsis.MethodsThe study was conducted at the Erasmus University Medical Center–Sophia Children’s Hospital Rotterdam. Patient data from January 2018 until October 2019 were reviewed for all preterm neonates born with a gestational age below 32 weeks with signs and symptoms suggestive of systemic infection, in whom blood was taken for blood culture and for inflammatory biomarkers determinations. Plasma IL-6 and PCT were assessed next to CRP at the moment of suspicion. We assessed the association with 7-day mortality and sepsis severity (neonatal sequential organ failure assessment (nSOFA) score, need for inotropic support, invasive ventilation and thrombocytopenia).ResultsA total of 480 suspected late onset neonatal sepsis episodes in 208 preterm neonates (gestational age < 32 weeks) were retrospectively analyzed, of which 143 episodes were classified as sepsis (29.8%), with 56 (11.7%) cases of culture negative, 63 (13.1%) cases of gram-positive and 24(5.0%) cases of gram-negative sepsis. A total of 24 (5.0%) sepsis episodes resulted in death within 7 days after suspicion of LONS. Both IL-6 (adjusted hazard ratio (aHR): 2.28; 95% CI 1.64–3.16; p < 0.001) and PCT (aHR: 2.91; 95% CI 1.70–5.00; p < 0.001) levels were associated with 7-day mortality; however, CRP levels were not significantly correlated with 7-day mortality (aHR: 1.16; 95% CI (0.68–2.00; p = 0.56). Log IL-6, log PCT and log CRP levels were all significantly correlated with the need for inotropic support.ConclusionsOur findings show that serum IL-6 and PCT levels at moment of suspected late onset neonatal sepsis offer valuable information about sepsis severity and mortality risk in infants born below 32 weeks of gestation. The discriminative value was superior to that of CRP. Determining these biomarkers in suspected sepsis may help identify patients with imminent severe sepsis, who may require more intensive monitoring and therapy.

Highlights

  • Neonatal sepsis is a major health issue, in the preterm neonatal population, where low birth weight, immature immune system and other compromising factors make it a primary cause of morbidity and death [1,2,3,4,5]

  • Log IL-6 levels were associated with 7-day mortality (adjusted hazard ratio: 2.28; 95% CI (1.64–3.16; p < 0.001), in a model corrected for birth weight, gestational age and sex

  • Inotropic and respiratory support and thrombocytopenia Inotropic support Log IL-6, log PCT and log C-reactive protein (CRP) levels were all significantly correlated with the need for inotropic support with an aHR of 2.41; 4.24 and 2.0, respectively)

Read more

Summary

Introduction

Neonatal sepsis is a major health issue, in the preterm neonatal population, where low birth weight, immature immune system and other compromising factors make it a primary cause of morbidity and death [1,2,3,4,5]. Late onset neonatal sepsis (LONS) occurs after three days of life and may be caused by pathogens. Several chemical biomarkers are used to diagnose and monitor disease progression in patients suspected of sepsis. Three commonly used biomarkers are: C-reactive protein (CRP), procalcitonin (PCT) and interleukin-6 (IL-6) [9]. CRP level at onset is proven not predictive of LONS diagnosis [11]. Biomarkers are used to diagnose and monitor patients with sepsis, but C-reactive protein (CRP) is proven not predictive at onset of late onset neonatal sepsis (LONS) diagnosis. The aim of this study was to evaluate the association of interleukin-6(IL-6), procalcitonin (PCT) and CRP with subsequent sepsis severity and mortality in preterm infants suspected of late onset neonatal sepsis

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

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