Evidence map›Paper›PMID 38889701›Full record

ArticleNeonatology2024

Epidemiology and Outcomes of Neonatal Sepsis: Experience from a Tertiary Australian NICU.

Cheryl Anne Mackay, Elizabeth A Nathan, Michelle Claire Porter, Damber Shrestha, Rolland Kohan, Tobias Strunk

Registry-linked trialAbstract read
In one paragraph

Article in Neonatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07670624 (T6A Biomarker for Detection of Bacterial Infection in Newborn Infants), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07670624 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

T6A Biomarker for Detection of Bacterial Infection in Newborn Infants

Typeobservational_patient_registrySponsorSalzburger LandesklinikenRan2026 to 2029Enrolled210ConditionsSepsis, Newborn Sepsis, Biomarker Discovery
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Cheryl Anne MackayNeonatal Directorate, Child and Adolescent Health Service, King Edward Memorial Hospital, Subiaco, Washington, Australia.
Elizabeth A NathanSchool of Medicine, University of Western Australia, Crawley, Washington, Australia.
Michelle Claire PorterMicrobiology Department, PathWest Laboratory Services, Nedlands, Perth, Washington, Australia.
Damber ShresthaNeonatal Directorate, Child and Adolescent Health Service, King Edward Memorial Hospital, Subiaco, Washington, Australia.
Rolland KohanNeonatal Directorate, Child and Adolescent Health Service, King Edward Memorial Hospital, Subiaco, Washington, Australia.
Tobias StrunkNeonatal Directorate, Child and Adolescent Health Service, King Edward Memorial Hospital, Subiaco, Washington, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeonatal sepsis is associated with significant mortality and morbidity. Low-middle-income countries are disproportionately affected, but late-onset sepsis (LOS) still occurs in up to 20% of infants <28 weeks in high-income countries. Understanding site-specific data is vital to guide management.

methodsA retrospective cohort study was conducted at King Edward Memorial Hospital (KEMH), Perth. Infants admitted between January 2012 and June 2022 were included. Data were extracted from routine electronic databases. Incidence and aetiology of sepsis were determined and the association of sepsis with neonatal outcomes analysed.

resultsDuring the study period, 23,395 newborns were admitted with a median gestation of 37 weeks and birth weight of 2,800 g. There were 370 sepsis episodes in 350 infants; 102 were early-onset sepsis (EOS) (1.6 per 1,000 live births), predominantly Streptococcus agalactiae (35, 34.3%) and Escherichia coli (27, 26.5%); 268 were LOS (0.9 per 1,000 inpatient days), predominantly coagulase-negative staphylococci (CONS) (156, 57.6%) and E. coli (30, 11.1%). The incidence of LOS declined from 2012 to 2022 (p = 0.002). Infants with EOS had increased brain injury (25.7% vs. 4.1%; p = 0.002) and mortality (18.8% vs. 1.6%; p < 0.001). Those with LOS had increased hospital stay (median 95 vs. 15 days; p < 0.001), mortality (15.3% vs. 1.6%; p = 0.018), necrotising enterocolitis (NEC) (7.4% vs. 0.5%; p < 0.001), and chronic lung disease (CLD) (58.1% vs. 5.9%; p = 0.005). Infants <28 weeks with sepsis were at increased risk of neurodevelopmental impairment compared to those without infection (43.2% vs. 30.9%, p = 0.027).

conclusionsWhile we observed a reduction in LOS incidence, sepsis remains associated with higher mortality, and in survivors with longer hospital stay and increased risk of brain injury, NEC, CLD, and neurodevelopmental impairment.

Indexed as

Intensive Care Units, NeonatalNeonatal SepsisTertiary Care CentersAustraliaBirth WeightFemaleGestational AgeHospital MortalityHumansIncidenceInfant, NewbornLength of StayMaleRetrospective StudiesEarly-onset sepsisLate-onset sepsisNeonateOutcomes

Identifiers

PMID38889701
PMCPMC11633889

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.