Evidence map›Paper›PMID 24836781›Full record

ArticlePloS one2014

Prevalence of bloodstream pathogens is higher in neonatal encephalopathy cases vs. controls using a novel panel of real-time PCR assays.

Cally J Tann, Peter Nkurunziza, Margaret Nakakeeto, James Oweka, Jennifer J Kurinczuk, Jackson Were, Natasha Nyombi, Peter Hughes, Barbara A Willey, Alison M Elliott and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
3.4field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Neonatal Encephalopathy With Group B Streptococcal Disease Worldwide: Systematic Review, Investigator Group Datasets, and Meta-analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2017
    Pooled it
  3. Trial
  4. Trial
  5. Infection and neonatal encephalopathy.Pediatric research · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Group B Streptococcal Neonatal Meningitis.Clinical microbiology reviews · 2022
    Review
  13. The association between early-onset sepsis and neonatal encephalopathy.Journal of perinatology : official journal of the California Perinatal Association · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Inflammatory Phenotypes Predict Changes in Arterial Stiffness Following Antiretroviral Therapy Initiation.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  19. Article
  20. 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

13 authors at 6 institutions in 2 countries.

Cally J TannClinical Research Department, Faculty of Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine, London, United Kingdom; Mulago University Hospital, Kampala, Uganda.
Peter NkurunzizaMRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda.
Margaret NakakeetoMulago University Hospital, Kampala, Uganda.
James OwekaMRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda.
Jennifer J KurinczukNational Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
Jackson WereMRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda.
Natasha NyombiMulago University Hospital, Kampala, Uganda.
Peter HughesInstitute for Women's Health, University College London, Medical School Building, London, United Kingdom.
Barbara A WilleyClinical Research Department, Faculty of Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Alison M ElliottClinical Research Department, Faculty of Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine, London, United Kingdom; MRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda.
Nicola J RobertsonInstitute for Women's Health, University College London, Medical School Building, London, United Kingdom.
Nigel KleinInstitute for Child Health, University College London, London, United Kingdom; Department of Microbiology, Virology and Infection Control, Great Ormond Street Hospital for Children, London, United Kingdom.
Kathryn A HarrisInstitute for Child Health, University College London, London, United Kingdom; Department of Microbiology, Virology and Infection Control, Great Ormond Street Hospital for Children, London, United Kingdom.
Uganda Virus Research Institute · UGMulago Hospital · UGUniversity College London · GBGreat Ormond Street Hospital · GBLondon School of Hygiene & Tropical Medicine · GBUniversity of Oxford · GB

Funding

Medical Research Council MC_UP_1204/9Wellcome Trust 095778Wellcome Trust 100714
6 · The paper itself

Abstract

backgroundIn neonatal encephalopathy (NE), infectious co-morbidity is difficult to diagnose accurately, but may increase the vulnerability of the developing brain to hypoxia-ischemia. We developed a novel panel of species-specific real-time PCR assays to identify bloodstream pathogens amongst newborns with and without NE in Uganda. METHODOLOGY: Multiplex real-time PCR assays for important neonatal bloodstream pathogens (gram positive and gram negative bacteria, cytomegalovirus (CMV), herpes simplex virus(HSV) and P. falciparum) were performed on whole blood taken from 202 encephalopathic and 101 control infants. Automated blood culture (BACTEC) was performed for all cases and unwell controls. PRINCIPAL

findingsPrevalence of pathogenic bacterial species amongst infants with NE was 3.6%, 6.9% and 8.9%, with culture, PCR and both tests in combination, respectively. More encephalopathic infants than controls had pathogenic bacterial species detected (8.9%vs2.0%, p = 0.028) using culture and PCR in combination. PCR detected bacteremia in 11 culture negative encephalopathic infants (3 Group B Streptococcus, 1 Group A Streptococcus, 1 Staphylococcus aureus and 6 Enterobacteriacae). Coagulase negative staphylococcus, frequently detected by PCR amongst case and control infants, was considered a contaminant. Prevalence of CMV, HSV and malaria amongst cases was low (1.5%, 0.5% and 0.5%, respectively). CONCLUSION/SIGNIFICANCE: This real-time PCR panel detected more bacteremia than culture alone and provides a novel tool for detection of neonatal bloodstream pathogens that may be applied across a range of clinical situations and settings. Significantly more encephalopathic infants than controls had pathogenic bacterial species detected suggesting that infection may be an important risk factor for NE in this setting.

Indexed as

BacteremiaBase SequenceBrain DiseasesCase-Control StudiesComorbidityCytomegalovirusDNA PrimersEnterobacteriaceaeHumansInfant, NewbornMolecular Sequence DataPlasmodium falciparumPrevalenceReal-Time Polymerase Chain ReactionSequence Analysis, DNASimplexvirusDNA Primers

Identifiers

PMID24836781
PMCPMC4023955
OpenAlexW2100453906

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.