Evidence map›Paper›PMID 29509833›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2018

Serial Clustering of Late-Onset Group B Streptococcal Infections in the Neonatal Unit: A Genomic Re-evaluation of Causality.

Elita Jauneikaite, Georgia Kapatai, Frances Davies, Ioana Gozar, Juliana Coelho, Kathleen B Bamford, Benedetto Simone, Lipi Begum, Shannon Katiyo, Bharat Patel and 12 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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.

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

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

  1. Pooled it
  2. Article
  3. Population genetics of group BFrontiers in microbiology · 2023
    Article
  4. Article
  5. Frontiers in cellular and infection microbiology · 2022
    Article
  6. Review
  7. Article
  8. Enhanced Postnatal Acquisition of Hypervirulent Group B Streptococcus.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Article
  9. Uncertainties in Screening and Prevention of Group B Streptococcus Disease.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Article
  10. Review
  11. 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

22 authors.

Elita JauneikaiteHealth Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, Imperial College London, United Kingdom.
Georgia KapataiNational Infection Service, Public Health England, United Kingdom.
Frances DaviesImperial College Healthcare NHS Trust, United Kingdom.
Ioana GozarImperial College Healthcare NHS Trust, United Kingdom.
Juliana CoelhoNational Infection Service, Public Health England, United Kingdom.
Kathleen B BamfordImperial College Healthcare NHS Trust, United Kingdom.
Benedetto SimoneLondon and South East Field Epidemiology Services, United Kingdom.
Lipi BegumNorth West London Health Protection Team, Public Health England, United Kingdom.
Shannon KatiyoLondon and South East Field Epidemiology Services, United Kingdom.
Bharat PatelNational Infection Service, Public Health England, United Kingdom.
Peter HoffmanNational Infection Service, Public Health England, United Kingdom.
Theresa LamagniNational Infection Service, Public Health England, United Kingdom.
Eimear T BranniganImperial College Healthcare NHS Trust, United Kingdom.
Alison H HolmesHealth Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, Imperial College London, United Kingdom.
Tokozani KadhaniImperial College Healthcare NHS Trust, United Kingdom.
Tracey GalletlyImperial College Healthcare NHS Trust, United Kingdom.
Kate MartinImperial College Healthcare NHS Trust, United Kingdom.
Hermione LyallImperial College Healthcare NHS Trust, United Kingdom.
Yimmy ChowNorth West London Health Protection Team, Public Health England, United Kingdom.
Sunit GodambeImperial College Healthcare NHS Trust, United Kingdom.
Victoria ChalkerNational Infection Service, Public Health England, United Kingdom.
Shiranee SriskandanHealth Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, Imperial College London, United Kingdom.

Funding

Department of HealthMedical Research Council G0800777Medical Research Council MR/R015600/1
6 · The paper itself

Abstract

Background: Invasive Group B streptococcus (GBS) is a major cause of serious neonatal infection. Current strategies to reduce early-onset GBS disease have no impact on late-onset disease (LOD). Although GBS LOD is viewed as a sporadic event in the community, LOD arising within the neonatal intensive care unit (ICU) raises questions about mode of acquisition. Methods: Following a cluster of 4 GBS LOD cases, enhanced surveillance for all GBS LOD was undertaken over 2 years in the neonatal ICU supported by neonatal rectal screening. GBS isolates were serotyped and genome-sequenced. Results: Twelve late -onset invasive GBS episodes were identified (incidence 0.6/1000 live births). Genomic analysis revealed that 11/12 GBS isolates (92%) were linked to at least one other LOD isolate. Isolates from the first cluster were serotype V, resistant to macrolides and lincosamides, and sequencing confirmed isolates were indistinguishable, or distinguishable by only one SNP difference, from each other. Rectal carriage was rare. Prospective surveillance identified three further clusters of LOD due to serotypes Ia (3 cases), Ib (2 cases), and III (2 cases), that would not have been identified without surveillance and genome sequencing, leading to a re-evaluation of interventions required to prevent GBS LOD. Conclusion: Acquisition routes for LOD GBS in the neonatal ICU are poorly understood; cases may not necessarily be sporadic. Within this neonatal ICU, our data suggest that a single case of LOD GBS sepsis should be considered a potential nosocomial transmission event warranting prompt investigation, heightened infection prevention vigilance and action where required.

Indexed as

Intensive Care Units, NeonatalBacteremiaCluster AnalysisGenomicsHumansIncidenceInfant, NewbornNeonatal ScreeningPhylogenyProspective StudiesRisk FactorsSerogroupStreptococcal InfectionsStreptococcus agalactiaeUnited KingdomWhole Genome Sequencing

Identifiers

PMID29509833
PMCPMC6117446

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.