Evidence map›Paper›PMID 30375054›Full record

ArticleActa paediatrica (Oslo, Norway : 1992)2019

Increased surfactant protein-D levels in the airways of preterm neonates with sepsis indicated responses to infectious challenges.

Rose-Marie A Mackay, J Paul Townsend, Jennifer Calvert, Mark Anthony, Andrew R Wilkinson, Anthony D Postle, Howard W Clark, David A Todd

Open access · hybridAbstract read
In one paragraph

Article in Acta paediatrica (Oslo, Norway : 1992), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Observational
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
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

8 authors at 5 institutions in 2 countries.

Rose-Marie A MackayFaculty of Medicine, Child Health, Academic Unit of Clinical and Experimental Sciences, University of Southampton, Southampton, UK.ORCID 0000-0002-9493-9654
J Paul TownsendRespiratory Biomedical Research Unit, Southampton NIHR, Southampton, UK.
Jennifer CalvertNeonatal Intensive Care Unit, Cardiff and Vale University Health Board, University Hospital of Wales, Cardiff, Wales, UK.
Mark AnthonyNeonatal Intensive Care Unit, Department of Paediatrics, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Andrew R WilkinsonNeonatal Intensive Care Unit, Department of Paediatrics, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Anthony D PostleFaculty of Medicine, Child Health, Academic Unit of Clinical and Experimental Sciences, University of Southampton, Southampton, UK.
Howard W ClarkFaculty of Medicine, Child Health, Academic Unit of Clinical and Experimental Sciences, University of Southampton, Southampton, UK.
David A ToddFaculty of Medicine, Child Health, Academic Unit of Clinical and Experimental Sciences, University of Southampton, Southampton, UK.
Princess Anne Hospital · GBJohn Radcliffe Hospital · GBCardiff and Vale University Health Board · GBCentenary Institute · AUUniversity of Southampton · GB

Funding

Medical Research Council MR/P026907/1Southampton National Institute for Health Research Respiratory BiomedicalThe MRC Immunochemistry Unit
6 · The paper itself

Abstract

aimSepsis is multifactorial and potentially devastating for preterm neonates. Changes in surfactant protein-D (SP-D), phosphatidylcholine (PC) and PC molecular species during infection may indicate innate immunity or inflammation during sepsis. We aimed to compare these important pulmonary molecules in ventilated neonates without or with sepsis.

methodsEndotracheal aspirates were collected from preterm neonates born at 23-35 weeks and admitted to the neonatal intensive care unit at the John Radcliffe Hospital, Oxford, UK, from October 2000 to March 2002. Samples were collected at one day to 30 days and analysed for SP-D, total PC and PC molecular species concentrations using enzyme-linked immunosorbent assay and mass spectrometry.

resultsWe found that 8/54 (14.8%) neonates developed sepsis. SP-D (p < 0.0001), mono- and di-unsaturated PC were significantly increased (p = 0.05), and polyunsaturated PC was significantly decreased (p < 0.01) during sepsis compared to controls. SP-D:PC ratios were significantly increased during sepsis (p < 0.001), and SP-D concentrations were directly related to gestational age in neonates with sepsis (r

conclusionIncreased SP-D levels and changes in PC molecular species during sepsis were consistent with direct or indirect pulmonary inflammatory processes. Very preterm neonates we able to mount an acute inflammatory innate immune response to infectious challenges, despite low levels of surfactant proteins at birth.

Indexed as

Case-Control StudiesFemaleGestational AgeHumansInfant, NewbornInfant, PrematureMaleNeonatal SepsisPhosphatidylcholinesPulmonary Surfactant-Associated Protein DPhosphatidylcholinesPulmonary Surfactant-Associated Protein DPhosphatidylcholinePreterm neonatesSepsisSurfactant protein-DVentilation

Identifiers

PMID30375054
PMCPMC6492096
OpenAlexW2898742180

What OpenQuestion holds

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Registered trials

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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.