Sepsis treatment options identified by 10-year study of microbial isolates and antibiotic susceptibility in a level-four neonatal intensive care unit
- PMID: 34787905
- DOI: 10.1111/apa.16189
Sepsis treatment options identified by 10-year study of microbial isolates and antibiotic susceptibility in a level-four neonatal intensive care unit
Abstract
Aim: This observational study investigated the microbiology of blood culture-positive sepsis episodes and susceptibility to empiric antibiotics in early-onset sepsis (EOS) and late-onset sepsis (LOS) in a level-four neonatal intensive care unit (NICU) from 2010 to 2019.
Methods: It was based on patient records and data that Oslo University Hospital, Norway, routinely submitted to the Norwegian Neonatal Network database. Clinical data were merged with blood culture results, including antibiotic susceptibility.
Results: We studied 5249 infants admitted to the NICU 6321 times and identified 324 positive blood cultures from 287 infants, with 30 EOS and 305 LOS episodes. Frequent causative agents for EOS were group B streptococci (33.3%), Escherichia coli (20.0%) and Staphylococcus aureus (16.7%). All were susceptible to empiric ampicillin and gentamicin. LOS was most frequently caused by coagulase-negative staphylococci (CONS) (73.8%), Staphylococcus aureus (15.7%) and Enterococci (6.9%). CONS, Staphylococcus aureus, Enterococci, Escherichia coli, Klebsiella and Enterobacter represented 91.9% of LOS episodes and were susceptible to vancomycin and cefotaxime (96.1%), vancomycin and gentamicin (97.0%) and cloxacillin and gentamicin (38.1%).
Conclusion: Empiric treatment with ampicillin and gentamicin was adequate for EOS. Combining vancomycin and gentamicin may be a safer alternative to cefotaxime for LOS, as this reduces exposure to broad-spectrum antibiotics.
Keywords: antibiotic susceptibility; early-onset sepsis; late-onset sepsis; neonatal intensive care unit; neonatal sepsis.
© 2021 The Authors. Acta Paediatrica published by John Wiley & Sons Ltd on behalf of Foundation Acta Paediatrica.
Similar articles
-
Neonatal bloodstream infections in a Ghanaian Tertiary Hospital: Are the current antibiotic recommendations adequate?BMC Infect Dis. 2016 Oct 24;16(1):598. doi: 10.1186/s12879-016-1913-4. BMC Infect Dis. 2016. PMID: 27776490 Free PMC article.
-
Bacteriological profile and antibiotic susceptibility of neonatal sepsis in neonatal intensive care unit of a tertiary hospital in Nepal.BMC Pediatr. 2018 Jun 27;18(1):208. doi: 10.1186/s12887-018-1176-x. BMC Pediatr. 2018. PMID: 29950162 Free PMC article.
-
Cloxacillin versus vancomycin for presumed late-onset sepsis in the Neonatal Intensive Care Unit and the impact upon outcome of coagulase negative staphylococcal bacteremia: a retrospective cohort study.BMC Pediatr. 2005 Dec 23;5:49. doi: 10.1186/1471-2431-5-49. BMC Pediatr. 2005. PMID: 16375769 Free PMC article.
-
Neonatal early onset sepsis in Middle Eastern countries: a systematic review.Arch Dis Child. 2020 Jul;105(7):639-647. doi: 10.1136/archdischild-2019-317110. Epub 2020 Jan 22. Arch Dis Child. 2020. PMID: 31969351
-
Antibiotic use in neonatal sepsis.Turk J Pediatr. 1998 Jan-Mar;40(1):17-33. Turk J Pediatr. 1998. PMID: 9722468 Review.
Cited by
-
Staphylococcus capitis Central-Line-Associated Bloodstream Infections in the Neonatal Intensive Care Unit: A Single-Center, Four-Year Experience in Central-Line Management during Sepsis Treatment.Pathogens. 2024 Mar 7;13(3):234. doi: 10.3390/pathogens13030234. Pathogens. 2024. PMID: 38535577 Free PMC article.
-
Trends in Causative Organisms and Antimicrobial Resistance in Late-onset Neonatal Sepsis.Turk Arch Pediatr. 2024 Jun 17;59(4):375-382. doi: 10.5152/TurkArchPediatr.2024.24006. Turk Arch Pediatr. 2024. PMID: 39140990 Free PMC article.
-
Prevalence of Multidrug-Resistant Pathogens Causing Neonatal Early and Late Onset Sepsis, a Retrospective Study from the Tertiary Referral Children's Hospital.Infect Drug Resist. 2023 Jun 29;16:4213-4225. doi: 10.2147/IDR.S416020. eCollection 2023. Infect Drug Resist. 2023. PMID: 37404253 Free PMC article.
-
Global patterns of antibiotic resistance in group B Streptococcus: a systematic review and meta-analysis.Front Microbiol. 2025 Apr 16;16:1541524. doi: 10.3389/fmicb.2025.1541524. eCollection 2025. Front Microbiol. 2025. PMID: 40342597 Free PMC article.
-
Antimicrobial Resistance Pattern and Empirical Antibiotic Treatments in Neonatal Sepsis: A Retrospective, Single-Center, 12-Year Study.Antibiotics (Basel). 2023 Sep 27;12(10):1488. doi: 10.3390/antibiotics12101488. Antibiotics (Basel). 2023. PMID: 37887188 Free PMC article.
References
REFERENCES
-
- Liu L, Johnson HL, Cousens S, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet. 2012;379(9832):2151-2161.
-
- Hsieh EM, Hornik CP, Clark RH, et al. Medication use in the neonatal intensive care unit. Am J Perinatol. 2014;31(9):811-821.
-
- Esaiassen E, Fjalstad JW, Klingenberg C, Juvet LK, van den Anker JN. Antibiotic exposure in neonates and early adverse outcomes: a systematic review and meta-analysis. J Antimicrob Chemother. 2017;72(7):1858-1870.
-
- Fjalstad JW, Esaiassen E, Juvet LK, van den Anker JN, Klingenberg C. Antibiotic therapy in neonates and impact on gut microbiota and antibiotic resistance development: a systematic review. J Antimicrob Chemother. 2018;73(3):569-580.
-
- Fjalstad JW, Stensvold HJ, Bergseng H, et al. Early-onset sepsis and antibiotic exposure in term infants: a Nationwide Population-based study in Norway. Pediatr Infect Dis J. 2016;35(1):1-6.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical