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Point-of-care procalcitonin trends in suspected neonatal late-onset infection: a prospective observational study | Pediatric Research

Oct 26, 2024Oct 26, 2024

Pediatric Research (2024)Cite this article

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Procalcitonin-guided antimicrobial decision-making has been shown to be safe in adult intensive care settings. Most antimicrobial exposure in neonatal units is in culture-negative conditions. We hypothesise that Procalcitonin aids antimicrobial stewardship efforts in suspected Late-Onset Neonatal Sepsis.

Neonates were enrolled if they were aged over 72 h and were placed on antibiotics for a suspected infection. Procalcitonin levels were taken at set timepoints for the duration of antimicrobial exposure. Three subgroups were created: non-infectious episodes, blood culture-negative infectious episodes, and bloodstream infections.

Eighty-five suspected infectious episodes were recruited across two tertiary neonatal and paediatric intensive care units. There was a significant difference between the median PCT in bloodstream infections (BSI) compared to non-infectious episodes (2.13 versus 0.26 µg/L, p < 0.001). A cut-off of 0.5 µg/L had sensitivity 92.9% and specificity 68% for bloodstream infections at 24 h. The difference between median PCT values at 24 h was significant (0.27 vs 7.08; p < 0.001) for feed intolerance vs. NEC Grade IIIa-IIIb subgroups.

Procalcitonin levels taken 24 h following evaluation for late-onset neonatal infection are useful in out ruling BSI or severe Necrotising Enterocolitis. Up to 30% of antimicrobial exposure could be avoided with the use of Procalcitonin levels in low-risk neonates.

This study demonstrates the utility of serial Procalcitonin measurements in antimicrobial stewardship efforts in the Neonatal Unit.

Procalcitonin can be used to aid in antimicrobial decision making in suspected Late-Onset neonatal infection.

Procalcitonin testing at twenty-four hours in episodes of Gastrointestinal deterioration can out rule Bells Grade III Necrotising Enterocolitis.

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The datasets generated during and/or analysed during the current study are not publicly available due GDPR restrictions but are available from the corresponding author on reasonable request.

Eschborn, S. & Weitkamp, J. H. Procalcitonin versus C-reactive protein: review of kinetics and performance for diagnosis of neonatal sepsis. J. Perinatol. 39, 893–903 (2019).

Article PubMed Google Scholar

Prkno A., Wacker C., Brunkhorst F. M., Schlattmann P. Procalcitonin-guided therapy in intensive care unit patients with severe sepsis and septic shock - a systematic review and meta-analysis. Crit. Care. 2013;17. https://doi.org/10.1186/cc13157

Vouloumanou, E. K., Plessa, E., Karageorgopoulos, D. E., Mantadakis, E. & Falagas, M. E. Serum procalcitonin as a diagnostic marker for neonatal sepsis: a systematic review and meta-analysis. Intensive Care Med. 37, 747–762 (2011).

Article CAS PubMed Google Scholar

Simon L., Gauvin F., Amre D. K., Saint-Louis P., Lacroix J. Serum procalcitonin and C-reactive protein levels as markers of bacterial infection: a systematic review and meta-analysis. Clin. Infect. Dis. 2004;39. http://cid.oxfordjournals.org/.

van Rossum, A., Wulkan, R. & Oudesluys-Murphy, A. Procalcitonin as an early marker of infection inneonates and children. Lancet Infect. Dis. 4, 620–630, http://infection.thelancet.com (2004).

Article PubMed Google Scholar

Milcent, K. et al. Use of procalcitonin assays to predict serious bacterial infection in young febrile infants. JAMA Pediatr. 170, 62–69 (2016).

Article PubMed Google Scholar

Isidor, B. et al. The use of procalcitonin in the diagnosis of late-onset infection in neonatal intensive care unit patients. Scand. J. Infect. Dis. 39, 1063–1066 (2007).

Article CAS PubMed Google Scholar

So-Ngern, A. et al. Prognostic value of serum procalcitonin level for the diagnosis of bacterial infections in critically-ill patients. Infect. Chemother. 51, 263–273 (2019).

Article CAS PubMed PubMed Central Google Scholar

Schuetz, P. et al. Serial procalcitonin predicts mortality in severe sepsis patients: results from the multicenter procalcitonin monitoring SEpsis (MOSES) Study. Crit. Care Med 45, 781–789 (2017).

Article CAS PubMed PubMed Central Google Scholar

Pantell, R. H. et al. Evaluation and management of well-appearing febrile infants 8 to 60 days old. Pediatrics 148, e2021052228 (2021).

Article PubMed Google Scholar

Schuetz, P., Albrich, W., Christ-Crain, M., Chastre, J. & Mueller, B. Procalcitonin for guidance of antibiotic therapy. Expert Rev. Anti Infect. Ther. 8, 575–587 (2010).

Article CAS PubMed Google Scholar

Bouadma, L. et al. Use of procalcitonin to reduce patients’ exposure to antibiotics in intensive care units (PRORATA trial): a multicentre randomised controlled trial. Lancet 375, 463–474 (2010).

Article CAS PubMed Google Scholar

de Jong, E. et al. Efficacy and safety of procalcitonin guidance in reducing the duration of antibiotic treatment in critically ill patients: A randomised, controlled, open-label trial. Lancet Infect. Dis. 16, 819–827 (2016).

Article PubMed Google Scholar

Mewes J. C. et al. The cost impact of PCT-guided antibiotic stewardship versus usual care for hospitalised patients with suspected sepsis or lower respiratory tract infections in the US: A health economic model analysis. PLoS ONE. 2019;14. https://doi.org/10.1371/journal.pone.0214222

Stocker, M. et al. Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis: a multicentre, randomised controlled trial (NeoPIns). Lancet 390, 871–881 (2017).

Article CAS PubMed Google Scholar

Prusakov P. et al. A global point prevalence survey of antimicrobial use in neonatal intensive care units: The no-more-antibiotics and resistance (NO-MAS-R) study. eClinicalMedicine. 2021;32. https://doi.org/10.1016/j.eclinm.2021.100727

Schulman J., Dimand R. J., Lee H. C., Duenas G. V., Bennett M. V. Neonatal intensive care unit antibiotic use. Pediatrics. 2015;135. https://doi.org/10.1542/peds.2014-3409

Mukhopadhyay, S. et al. Neurodevelopmental outcomes following neonatal late-onset sepsis and blood culture-negative conditions. Arch. Dis. Child Fetal Neonatal Ed. 106, 467–473 (2021).

Article PubMed Google Scholar

Wirtschafter, D. D. et al. Antibiotic use for presumed neonatally acquired infections far exceeds that for central line-associated blood stream infections: an exploratory critique. J. Perinatol. 31, 514–518 (2011).

Article CAS PubMed Google Scholar

Patel, S. & Saiman, L. Principles and strategies of antimicrobial stewardship in the neonatal intensive care unit. Semin. Perinatol. 36, 431–436 (2012).

Article PubMed PubMed Central Google Scholar

Gkentzi, D. & Dimitriou, G. Antimicrobial stewardship in the neonatal intensive care unit: an update. Curr. Pediatr. Rev. 15, 47–52 (2019).

Article PubMed PubMed Central Google Scholar

NICE. Antimicrobial Stewardship: Systems and Processes for Effective Antimicrobial Medicine Use. 2015. http://www.nice.org.uk/guidance/NG15.

Barlam, T. F. et al. Implementing an antibiotic stewardship program: guidelines by the Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America. Clin. Infect. Dis. 62, e51–e77 (2016).

Article PubMed PubMed Central Google Scholar

Araujo Da Silva, A. R. et al. Effectiveness of antimicrobial stewardship programmes in neonatology: A systematic review. Arch. Dis. Child 105, 563–568 (2020).

Article PubMed Google Scholar

ThermoFisher. B · R · A · H · M · S PCT Direct Reader Datasheet. 2018. https://doi.org/10.1016/j.clinmicnews.2017.08.004

Velly L. et al. Validation of B·R·A·H·M·S PCT direct, a new sensitive point-of-care device for rapid measurement of procalcitonin. In Proc. International Symposium of SICEM. 2019;9. https://isicem.esn.eu/posters_listing/see_poster/372/2019/page_2.

WHO Collaborating Centre for Drug Statistics Methodology. Guidelinesfor ATC Classification and DDD Assignment. (Norwegian Institute for Public Health, 2023).

CDC. Core Elements of Hospital Antibiotic Stewardship Programs. (US Department of Health and Human Services, CDC, 2014). http://www.cdc.gov/getsmart/healthcare/.

Benić, M. S. et al. Metrics for quantifying antibiotic use in the hospital setting: Results from a systematic review and international multidisciplinary consensus procedure. J. Antimicrob. Chemother. 73, vi50–vi58 (2018).

Article Google Scholar

Widness, J. A. et al. Reduction in red blood cell transfusions among preterm infants: results of a randomized trial with an in-line blood gas and chemistry monitor. Pediatrics 115, 1299–1306 (2005).

Article PubMed Google Scholar

Madan, A. et al. Reduction in red blood cell transfusions using a bedside analyzer in extremely low birth weight infants. J. Perinatol. 25, 21–25 (2005).

Article PubMed Google Scholar

Roberts, J. K. et al. Pharmacokinetics and pharmacodynamics of antibacterials, antifungals, and antivirals used most frequently in neonates and infants. Clin. Pharmacokinet. 53, 581–610 (2014).

Article CAS PubMed Google Scholar

Fuchs, A et al. GentamicinExposure and Sensorineural Hearing Loss in Preterm Infants. PLoS One 11, 1–11 (2016).

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This research was enabled by a researcher salary grant from the Rotunda Foundation. (RF/NICU/2020/01)

Rotunda Hospital, Dublin, Ireland

Sean J. Armstrong & Adrienne Foran

Department of Clinical Biochemistry, Children’s Health Ireland, Dublin, Ireland

Jennifer J. Brady

University College Dublin School of Medicine, Dublin, Ireland

Jennifer J. Brady

Irish Meningitis and Sepsis Reference Laboratory, Children’s Health Ireland, Dublin, Ireland

Richard J. Drew

Clinical Innovation Unit, Rotunda Hospital, Dublin, Ireland

Richard J. Drew

Department of Clinical Microbiology, Royal College of Surgeons in Ireland, Dublin, Ireland

Richard J. Drew

Department of Paediatrics, Royal College of Surgeons in Ireland, Dublin, Ireland

Adrienne Foran

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Sean Armstrong, Jennifer Brady, Richard Drew, and Adrienne Foran all made substantial contributions to conception, design, analysis, and interpretation of data. Sean Armstrong also acquired all data for the study, drafted the article and takes responsibility for final approval of the published version. Jennifer Brady, Richard Drew, and Adrienne Foran all critically reviewed the article and have taken responsibility for final approval of the published version.

Correspondence to Sean J. Armstrong.

The authors declare no competing interests.

Written information leaflets were presented to caregivers of all infants approached for study recruitment. Written consent was obtained prior to recruitment in the study.

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Armstrong, S.J., Brady, J.J., Drew, R.J. et al. Point-of-care procalcitonin trends in suspected neonatal late-onset infection: a prospective observational study. Pediatr Res (2024). https://doi.org/10.1038/s41390-024-03670-x

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Received: 14 June 2024

Revised: 23 September 2024

Accepted: 04 October 2024

Published: 25 October 2024

DOI: https://doi.org/10.1038/s41390-024-03670-x

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