Evidence map›Paper›PMID 36130327›Full record

ArticleThe Journal of infectious diseases2023

Nasopharyngeal Carriage of Pneumococcus in Children in England up to 10 Years After 13-Valent Pneumococcal Conjugate Vaccine Introduction: Persistence of Serotypes 3 and 19A and Emergence of 7C.

Karen S Tiley, Helen Ratcliffe, Merryn Voysey, Kimberley Jefferies, Gemma Sinclair, Melanie Carr, Rachel Colin-Jones, David Smith, Jaclyn Bowman, Thomas Hart and 9 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03102840 (Cross-sectional Study to Establish the Point Prevalence of Serotype 19A Pneumococcal Nasopharyngeal Carriage of Fully Vaccinated Children Aged 6-48 Months 7 Years Following Introduction of PCV-13), which is not on this map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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.

NCT03102840 unknown statusnot on this map

Cross-sectional Study to Establish the Point Prevalence of Serotype 19A Pneumococcal Nasopharyngeal Carriage of Fully Vaccinated Children Aged 6-48 Months 7 Years Following Introduction of PCV-13

TypeobservationalSponsorUniversity of OxfordRan2017 to 2020Enrolled2,400ConditionsStreptococcus Pneumoniae Infection, Streptococcus Pneumoniae, Invasive Disease, Streptococcal PneumoniaArmsNasopharyngeal swab, blood sampling
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
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  3. Serotype distribution ofHuman vaccines & immunotherapeutics · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 2 countries.

Karen S TileyOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-2125-4125
Helen RatcliffeOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Merryn VoyseyOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-6324-6559
Kimberley JefferiesOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Gemma SinclairOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Melanie CarrOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Rachel Colin-JonesOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
David SmithOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Jaclyn BowmanOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Thomas HartOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Rama KandasamyOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Jason HindsInstitute for Infection and Immunity, St George's University, London, United Kingdom.
Katherine GouldInstitute for Infection and Immunity, St George's University, London, United Kingdom.
Guy BerbersImmunology, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Irina TcherniaevaImmunology, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Hannah RobinsonOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Emma PlestedOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Parvinder AleyOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Matthew D SnapeOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
University of Oxford · GBNational Institute for Health Research · GBNational Institute for Public Health and the Environment · NLSt George's, University of London · GB

Funding

Department of Health
6 · The paper itself

Abstract

backgroundMonitoring changes in pharyngeal carriage of pneumococcus in children following 13-valent pneumococcal conjugate vaccine (PCV13) introduction in the United Kingdom in 2010 informs understanding of patterns of invasive pneumococcal disease (IPD) incidence.

methodsNasopharyngeal swabs from healthy children vaccinated with PCV13 according to schedule (2, 4, and 12 months) were cultured and serotyped. Results for children aged 13-48 months were compared between 2014-2015 and 2017-2019 and with children aged 6-12 months (2017-2020). Blood was obtained from a subset of children for pneumococcal serotype-specific immunoglobulin G (IgG).

resultsTotal pneumococcal carriage at 13-48 months was 47.9% (473/988) in 2014-2015 and 51.8% (412/795) in 2017-2019 (P = .10); at age 6-12 months this value was 44.6% (274/615). In 2017-2019, 2.9% (95% confidence interval, 1.8%-4.3%) of children aged 13-48 months carried PCV13 serotypes (mainly 3 [1.5%] and 19A [0.8%]) and >20% carried the additional 20-valent PCV (PCV20) serotypes. Similar proportions of children had IgG ≥0.35 IU/mL for each serotype in 2014-2015 and 2017-2019. Serotype 7C carriage increased significantly (P < .01) between 2014-2015 and 2017-2019. Carriage of PCV20 serotypes 8 and 12F, both major causes of IPD, was rare.

conclusionsIntroduction of PCV20, if licensed for children, could significantly change the composition of pneumococcal serotypes carried in the pharynx of UK children. CLINICAL TRIALS REGISTRATION: NCT03102840.

Indexed as

Pneumococcal InfectionsStreptococcus pneumoniaeCarrier StateChildEnglandHumansImmunoglobulin GInfantNasopharynxPneumococcal VaccinesSerogroupVaccines, ConjugateImmunoglobulin GPneumococcal VaccinesVaccines, ConjugatecarriageconjugateinvasiveIPDnasopharyngealPCVpneumococcalserotypevaccine

Identifiers

PMID36130327
PMCPMC9978316
OpenAlexW4296700419

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.