Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 May 17:9:623043.
doi: 10.3389/fped.2021.623043. eCollection 2021.

Procalcitonin in Preterm Neonates: A Different Threshold and Prolonged Interpretation

Affiliations

Procalcitonin in Preterm Neonates: A Different Threshold and Prolonged Interpretation

Blandine Bianco et al. Front Pediatr. .

Abstract

Objectives: To evaluate the positive threshold of PCT for neonates of <32 weeks of gestation for the diagnosis of early-onset sepsis and to determine if the level of PCT collected within 6 h of life could be used. Design: Retrospective and bicentric study from May 2016 to April 2018. Setting: Two groups were established, neonates evaluated for PCT at birth (CordPCT) and within 6 h of life (delPCT). Patients: Two hundred and sixty neonates of <32 weeks of gestation born in Nice and South Paris (Bicêtre) University Hospitals, had been evaluated for PCT level. Main Outcomes Measures: The value of the PCT positive threshold was determined for the total population and each groups thanks ROC curves. Results: The threshold level of PCT for the total population was 0.98 ng/mL. The threshold value of cordPCT group was 1.00 vs. 0.98 ng/mL for delPCT group. The area under the Receiver Operating Characteristics curve for PCT sampled in delPCT group was significantly higher than in cordPCT group (0.94 compared to 0.75). Conclusions: The threshold level of PCT was higher in this cohort of neonates of <32 weeks of gestation compared to the value generally described for term neonates. The secondary sampling PCT level seems to be usable in screening algorithm for early-onset neonatal sepsis.

Keywords: biomarker; early-onset sepsis; preterm; procalcitonin; threshold.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Study flow diagram. PCT, procalcitonin.
Figure 2
Figure 2
(A) Receiver operating characteristic (ROC) curves of cord blood procalcitonin (PCT) and PCT of 4th h of life for the whole population. (B) Areas under the ROC curve of cord blood PCT and PCT of the first few hours of life for the whole population with a confident interval of 95% (CI 95%).

Similar articles

Cited by

References

    1. Stoll BJ, Gordon T, Korones SB, Shankaran S, Tyson JE, Bauer CR, et al. . Early-onset sepsis in very low birth weight neonates: a report from the National Institute of Child Health and Human Development Neonatal Research Network. J Pediatr. (1996) 129:72–80. 10.1016/S0022-3476(96)70192-0 - DOI - PubMed
    1. Simonsen KA, Anderson-Berry AL, Delair SF, Davies HD. Early-onset neonatal sepsis. Clin Microbiol Rev. (2014) 27:21–47. 10.1128/CMR.00031-13 - DOI - PMC - PubMed
    1. Hornik CP, Fort P, Clark RH, Watt K, Benjamin DK, Jr, Smith PB, et al. . Early and late onset sepsis in very-low-birth-weight infants from a large group of neonatal intensive care units. Early Hum Dev. (2012) 88(Suppl. 2):S69–74. 10.1016/S0378-3782(12)70019-1 - DOI - PMC - PubMed
    1. Sharma AA, Jen R, Butler A, Lavoie PM. The developing human preterm neonatal immune system: a case for more research in this area. Clin Immunol Orlando Fla. (2012) 145:61–8. 10.1016/j.clim.2012.08.006 - DOI - PMC - PubMed
    1. Cottineau M, Launay E, Branger B, Caillon J, Muller JB, Boscher C, et al. . Diagnostic value of suspicion criteria for early-onset neonatal bacterial infection: report ten years after the Anaes recommendations. Arch Pediatr Organe Off Soc Francaise Pediatr. (2014) 21:187–93. 10.1016/j.arcped.2013.11.011 - DOI - PubMed