Evidence map›Paper›PMID 35235604›Full record

Observational studyPloS one2022

Composition of early life leukocyte populations in preterm infants with and without late-onset sepsis.

Julie Hibbert, Tobias Strunk, Elizabeth Nathan, Amy Prosser, Dorota Doherty, Karen Simmer, Peter Richmond, David Burgner, Andrew Currie

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. IL-18-associated basophil and mast cell activation in sepsis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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

9 authors at 3 institutions in 1 country.

Julie HibbertNeonatal Directorate, Child and Adolescent Health Service, Perth, Western Australia, Australia.ORCID 0000-0002-8839-3966
Tobias StrunkNeonatal Directorate, Child and Adolescent Health Service, Perth, Western Australia, Australia.
Elizabeth NathanMedical School, University of Western Australia, Perth, Western Australia, Australia.
Amy ProsserMedical School, University of Western Australia, Perth, Western Australia, Australia.
Dorota DohertyMedical School, University of Western Australia, Perth, Western Australia, Australia.ORCID 0000-0002-5507-9065
Karen SimmerMedical School, University of Western Australia, Perth, Western Australia, Australia.
Peter RichmondMedical School, University of Western Australia, Perth, Western Australia, Australia.
David BurgnerMurdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.ORCID 0000-0002-8304-4302
Andrew CurrieWesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, Western Australia, Australia.ORCID 0000-0002-5193-3404
The Kids Research Institute Australia · AUThe University of Western Australia · AURoyal Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComposition of leukocyte populations in the first month of life remains incompletely characterised, particularly in preterm infants who go on to develop late-onset sepsis (LOS).

aimTo characterise and compare leukocyte populations in preterm infants with and without LOS during the first month of life. STUDY

designSingle-centre prospective observational cohort study.

participantsInfants born <30 weeks gestational age (GA). OUTCOME MEASURES: Peripheral blood samples were collected at 1, 7, 14, 21 and 28 days of life. Leukocyte populations were characterised using 5-fluorophore-6-marker flow cytometry. Absolute leukocyte counts and frequency of total CD45+ leukocytes of each population were adjusted for GA, birth weight z-scores, sex and total leukocyte count.

resultsOf 119 preterm infants enrolled, 43 (36%) had confirmed or clinical LOS, with a median onset at 13 days (range 6-26). Compared to infants without LOS, the adjusted counts and frequency of neutrophils, basophils and non-cytotoxic T lymphocytes were generally lower and immature granulocytes were higher over the first month of life in infants who developed LOS. Specific time point comparisons identified lower adjusted neutrophil counts on the first day of life in those infants who developed LOS more than a week later, compared to those without LOS, albeit levels were within the normal age-adjusted range. Non-cytotoxic T lymphocyte counts and/or frequencies were lower in infants following LOS on days 21 and 28 when compared to those who did not develop LOS.

conclusionChanges in non-cytotoxic T lymphocytes occurred following LOS suggesting sepsis-induced immune suppression.

Indexed as

Infant, PrematureSepsisGestational AgeHumansInfantInfant, NewbornLeukocytesProspective Studies

Identifiers

PMID35235604
PMCPMC8890632
OpenAlexW4214873872

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.