Evidence map›Paper›PMID 33833072›Full record

ArticlePediatrics2021

Intrapartum Group B Streptococcal Prophylaxis and Childhood Allergic Disorders.

Miren B Dhudasia, Jonathan M Spergel, Karen M Puopolo, Corinna Koebnick, Matthew Bryan, Robert W Grundmeier, Jeffrey S Gerber, Scott A Lorch, William O Quarshie, Theoklis Zaoutis and 1 more

Abstract read
In one paragraph

Article in Pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Effect of antibiotics in the first week of life on faecal microbiota development.Archives of disease in childhood. Fetal and neonatal edition · 2022
    Article
  13. Group B Streptococcal Neonatal Meningitis.Clinical microbiology reviews · 2022
    Review
  14. Article
  15. Article
  16. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Miren B DhudasiaDivisions of Neonatology.
Jonathan M SpergelDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania Philadelphia, Pennsylvania.
Karen M PuopoloDivisions of Neonatology.
Corinna KoebnickDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, California; and.
Matthew BryanIndependent Statistician.
Robert W GrundmeierDepartment of Pediatrics, Perelman School of Medicine, University of Pennsylvania Philadelphia, Pennsylvania.
Jeffrey S GerberCenter for Pediatric Clinical Effectiveness, and.
Scott A LorchDivisions of Neonatology.
William O QuarshieDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Theoklis ZaoutisCenter for Pediatric Clinical Effectiveness, and.
Sagori MukhopadhyayDivisions of Neonatology, mukhopadhs@chop.edu.

Funding

Incidence of atopy and childhood infections in uninfected term newborns with perinatal antibiotic exposureK23HD088753 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI MUKHOPADHYAY, SAGORI · 2017 to 2021
$790k
NICHD NIH HHS K23 HD088753
6 · The paper itself

Abstract

objectivesTo determine if maternal intrapartum group B

methodsRetrospective cohort study of 14 046 children. GBS prophylaxis was defined as administration of intravenous penicillin, ampicillin, cefazolin, clindamycin, or vancomycin to the mother, ≥4 hours before delivery. Composite primary outcome was asthma, eczema, or food allergy diagnosis within 5 years of age, identified by diagnosis codes and appropriate medication prescription. Allergic rhinitis was defined by using diagnostic codes only and analyzed as a separate outcome. Analysis was a priori stratified by delivery mode and conducted by using Cox proportional hazards model adjusted for multiple confounders and covariates. Secondary analyses, restricted to children retained in cohort at 5 years' age, were conducted by using multivariate logistic regression.

resultsGBS prophylaxis was not associated with increased incidence of composite outcome among infants delivered vaginally (hazard ratio: 1.13, 95% confidence interval [CI]: 0.95-1.33) or by cesarean delivery (hazard ratio: 1.08, 95% CI: 0.88-1.32). At 5 years of age, among 10 404 children retained in the study, GBS prophylaxis was not associated with the composite outcome in vaginal (odds ratio: 1.21, 95% CI: 0.96-1.52) or cesarean delivery (odds ratio: 1.17, 95% CI: 0.88-1.56) cohorts. Outcomes of asthma, eczema, food allergy, separately, and allergic rhinitis were also not associated with GBS prophylaxis.

conclusionsIntrapartum GBS prophylaxis was not associated with subsequent diagnosis of asthma, eczema, food allergy, or allergic rhinitis in the first 5 years of age.

Indexed as

ParturitionStreptococcus agalactiaeAnti-Bacterial AgentsAntibiotic ProphylaxisAsthmaChild, PreschoolCohort StudiesEczemaFemaleFood HypersensitivityHumansHypersensitivityInfantInfant, NewbornMalePregnancyAnti-Bacterial Agents

Identifiers

PMID33833072
PMCPMC8085997

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.