Empirical treatment of neonatal sepsis: are the current guidelines adequate?
- PMID: 20584804
- DOI: 10.1136/adc.2009.178483
Empirical treatment of neonatal sepsis: are the current guidelines adequate?
Abstract
Objectives: To use national laboratory surveillance data to determine whether pathogens responsible for neonatal bacteraemia were sensitive to nationally recommended antibiotic regimens.
Design: All reports of neonatal bacteraemia received by the Health Protection Agency's voluntary surveillance scheme in England and Wales from January 2006 until March 2008, were extracted from the database. Organisms were ranked by frequency, and proportions susceptible to antimicrobials recommended for empirical treatment of neonatal sepsis were determined.
Results: There were 1516 reports of bacteraemia for neonates <48 h old (early-onset) and 3482 reports for neonates 2-28 days old (late-onset). For early-onset bacteraemia, group B streptococcus (GBS) was the most frequent pathogen (31%) followed by coagulase-negative staphylococci (CoNS; 22%), non-pyogenic streptococci (9%) and Escherichia coli (9%). For late-onset bacteraemia, CoNS were isolated most frequently (45%), followed by Staphylococcus aureus (13%), Enterobacteriaceae (9%), E coli (7%) and GBS (7%). More than 94% of organisms (early-onset) were susceptible to regimens involving combinations of penicillin with either gentamicin or amoxicillin, amoxicillin combined with cefotaxime or cefotaxime monotherapy. More than 95% of organisms (late-onset) were susceptible to gentamicin with either flucloxacillin or amoxicillin and amoxicillin with cefotaxime, but only 79% were susceptible to cefotaxime monotherapy.
Conclusions: Current guidelines for empirical therapy in neonates with sepsis are appropriate. However, gentamicin-based regimens should be used in preference to cefotaxime-based treatments, because of lower levels of susceptibility to cefotaxime and the need to avoid exerting selective pressure for resistance. Surveillance data linked to clinical data should further inform rational antibiotic prescribing in neonatal units.
Comment in
-
Choosing the right empirical antibiotics for neonates.Arch Dis Child Fetal Neonatal Ed. 2011 Jan;96(1):F2-3. doi: 10.1136/adc.2010.188938. Epub 2010 Jun 14. Arch Dis Child Fetal Neonatal Ed. 2011. PMID: 20547581 Free PMC article. No abstract available.
-
Empirical antibiotics for suspected early neonatal sepsis.Arch Dis Child Fetal Neonatal Ed. 2012 Jan;97(1):F75. doi: 10.1136/archdischild-2011-300152. Epub 2011 Aug 17. Arch Dis Child Fetal Neonatal Ed. 2012. PMID: 21849304 No abstract available.
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.
-
Neonatal septicaemia in Ilorin: bacterial pathogens and antibiotic sensitivity pattern.Afr J Med Med Sci. 2002 Jun;31(2):127-30. Afr J Med Med Sci. 2002. PMID: 12518907
-
The changing antibiotic susceptibility of bloodstream infections in the first month of life: informing antibiotic policies for early- and late-onset neonatal sepsis.Epidemiol Infect. 2014 Apr;142(4):803-11. doi: 10.1017/S0950268813001520. Epub 2013 Jul 11. Epidemiol Infect. 2014. PMID: 23842441 Free PMC article.
-
Literature review on the distribution characteristics and antimicrobial resistance of bacterial pathogens in neonatal sepsis.J Matern Fetal Neonatal Med. 2022 Mar;35(5):861-870. doi: 10.1080/14767058.2020.1732342. Epub 2020 Feb 26. J Matern Fetal Neonatal Med. 2022. PMID: 32102584 Review.
-
Antibiotic use in neonatal sepsis.Turk J Pediatr. 1998 Jan-Mar;40(1):17-33. Turk J Pediatr. 1998. PMID: 9722468 Review.
Cited by
-
Choice and duration of antimicrobial therapy for neonatal sepsis and meningitis.Int J Pediatr. 2011;2011:712150. doi: 10.1155/2011/712150. Epub 2011 Nov 20. Int J Pediatr. 2011. PMID: 22164179 Free PMC article.
-
Population Pharmacokinetics and Dosing Considerations for Gentamicin in Newborns with Suspected or Proven Sepsis Caused by Gram-Negative Bacteria.Antimicrob Agents Chemother. 2016 Dec 27;61(1):e01304-16. doi: 10.1128/AAC.01304-16. Print 2017 Jan. Antimicrob Agents Chemother. 2016. PMID: 27795373 Free PMC article.
-
Incidence of group B streptococcus early-onset sepsis in term neonates with second-line prophylaxis maternal intrapartum antibiotics: a multicenter retrospective study.Am J Obstet Gynecol. 2024 Jun;230(6):673.e1-673.e8. doi: 10.1016/j.ajog.2023.10.035. Epub 2023 Oct 25. Am J Obstet Gynecol. 2024. PMID: 37890649 Free PMC article.
-
Current management of late onset neonatal bacterial sepsis in five European countries.Eur J Pediatr. 2014 Aug;173(8):997-1004. doi: 10.1007/s00431-014-2279-5. Epub 2014 Feb 13. Eur J Pediatr. 2014. PMID: 24522326
-
Pragmatic physiologically-based pharmacokinetic modeling to support clinical implementation of optimized gentamicin dosing in term neonates and infants: proof-of-concept.Front Pediatr. 2023 Nov 21;11:1288376. doi: 10.3389/fped.2023.1288376. eCollection 2023. Front Pediatr. 2023. PMID: 38078320 Free PMC article.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical