Evidence map›Paper›PMID 26149186›Full record

Observational studyThe Journal of infection2015

Nasopharyngeal bacterial burden and antibiotics: Influence on inflammatory markers and disease severity in infants with respiratory syncytial virus bronchiolitis.

M Carmen Suárez-Arrabal, Cesar Mella, Santiago M Lopez, Nicole V Brown, Mark W Hall, Sue Hammond, William Shiels, Judith Groner, Mario Marcon, Octavio Ramilo and 1 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in The Journal of infection, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

  1. Pooled it
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  11. Clinical Disease Severity Scores and Viral Loads in Children With Respiratory Syncytial Virus Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
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  14. Observational
  15. Article
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  17. Review
  18. Article
  19. Lung Microbiome in Asthma: Current Perspectives.Journal of clinical medicine · 2019
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

M Carmen Suárez-ArrabalCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA. Electronic address: mcarmen1981@yahoo.com.
Cesar MellaCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA; Division of Critical Care Medicine, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA. Electronic address: cfmella@texaschildrens.org.
Santiago M LopezCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Nicole V BrownCenter for Biostatistics, The Ohio State University, Columbus, OH, USA.
Mark W HallDivision of Critical Care Medicine, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA.
Sue HammondDepartment of Pathology, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA.
William ShielsDepartment of Radiology, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA.
Judith GronerSection of Ambulatory Pediatrics, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA.
Mario MarconDepartment of Microbiology and Laboratory Medicine, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA.
Octavio RamiloCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA; Division of Infectious Diseases, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA.
Asuncion MejiasCenter for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA; Division of Infectious Diseases, Nationwide Children's Hospital and The Ohio State University School of Medicine, Columbus, OH, USA. Electronic address: Asuncion.Mejias@nationwidechildrens.org.
Nationwide Children's Hospital · USThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAnimal studies suggest that RSV increases nasopharyngeal (NP) bacterial colonization facilitating bacterial infections. We investigated the influence of antibiotic treatment and colonization with potentially pathogenic bacteria on inflammatory markers and disease severity in RSV-infected in infants.

methodsHealthy young infants hospitalized with RSV bronchiolitis (n = 136) and age-matched healthy controls (n = 23) were enrolled and NP samples cultured for potentially pathogenic bacteria including: Gram-positive bacteria (GPB): Staphylococcus aureus, Streptococcus pneumoniae, β-hemolytic Streptococcus; and Gram-negative bacteria (GNB): Moraxella catarrhalis and Haemophilus influenzae. Clinical parameters and plasma IL-8, IL-6 and TNF-α concentrations were compared according to the bacterial class and antibiotic treatment.

resultsAntibiotic treatment decreased by 10-fold NP bacterial recovery. Eighty-one percent of RSV infants who did not receive antibiotics before sample collection were colonized with pathogenic bacteria. Overall, GNB were identified in 21% of patients versus 4% of controls who were mostly colonized with GPB. Additionally, in RSV patients NP white blood cell counts (p = 0.026), and blood neutrophils (p = 0.02) were higher in those colonized with potentially pathogenic bacteria versus respiratory flora. RSV patients colonized with GNB had higher plasma IL-8 (p = 0.01) and IL-6 (p < 0.01) concentrations than controls, and required longer duration of oxygen (p = 0.049).

conclusionsInfants with RSV bronchiolitis colonized with potentially pathogenic bacteria had increased numbers of mucosal and systemic inflammatory cells. Specifically, colonization with GNB was associated with higher concentrations of proinflammatory cytokines and a trend towards increased disease severity.

Indexed as

Anti-Bacterial AgentsBacterial LoadBiomarkersBronchiolitis, ViralCytokinesFemaleGram-Negative BacteriaGram-Positive BacteriaHaemophilus influenzaeHospitalizationHumansInfantMaleMoraxella catarrhalisNasopharynxProspective StudiesAnti-Bacterial AgentsBiomarkersCytokinesAntibioticsBronchiolitisDisease severityGram-negative bacteriaNasopharyngeal bacterial colonizationRSV

Identifiers

PMID26149186
OpenAlexW1898603130

What OpenQuestion holds

Textmetadata
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.