Evidence map›Paper›PMID 31175819›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Impact of 13-Valent Pneumococcal Conjugate Vaccine on Colonization and Invasive Disease in Cambodian Children.

Paul Turner, Phana Leab, Sokeng Ly, Sena Sao, Thyl Miliya, James D Heffelfinger, Nyambat Batmunkh, Fernanda C Lessa, Jenny A Walldorf, Terri B Hyde and 8 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

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

  1. Pooled it
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  13. Molecular characterization ofMicrobial genomics · 2023
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  17. Microbial genomics · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Paul TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
Phana LeabCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
Sokeng LyCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
Sena SaoCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
Thyl MiliyaCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
James D HeffelfingerRegional Office for the Western Pacific, World Health Organization, Manila, Philippines.
Nyambat BatmunkhRegional Office for the Western Pacific, World Health Organization, Manila, Philippines.
Fernanda C LessaCenters for Disease Control and Prevention, Atlanta, Georgia.
Jenny A WalldorfCenters for Disease Control and Prevention, Atlanta, Georgia.
Terri B HydeCenters for Disease Control and Prevention, Atlanta, Georgia.
Vichit OrkNational Immunisation Program, Ministry of Health, Cambodia.
Md Shafiqul HossainWorld Health Organization, Phnom Penh, Cambodia.
Katherine A GouldInstitute for Infection and Immunity, St George's, University of London, United Kingdom.
Jason HindsInstitute for Infection and Immunity, St George's, University of London, United Kingdom.
Ben S CooperCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, United Kingdom.
Chanpheaktra NgounCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
Claudia TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap.
Nicholas P J DayCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, United Kingdom.

Funding

Medical Research Council MR/K006924/1Wellcome Trust 106698/Z/14/ZWorld Health Organization 001
6 · The paper itself

Abstract

backgroundCambodia introduced the 13-valent pneumococcal conjugate vaccine (PCV13) in January 2015 using a 3 + 0 dosing schedule and no catch-up campaign. We investigated the effects of this introduction on pneumococcal colonization and invasive disease in children aged <5 years.

methodsThere were 6 colonization surveys done between January 2014 and January 2018 in children attending the outpatient department of a nongovernmental pediatric hospital in Siem Reap. Nasopharyngeal swabs were analyzed by phenotypic and genotypic methods to detect pneumococcal serotypes and antimicrobial resistance. Invasive pneumococcal disease (IPD) data for January 2012-December 2018 were retrieved from hospital databases. Pre-PCV IPD data and pre-/post-PCV colonization data were modelled to estimate vaccine effectiveness (VE).

resultsComparing 2014 with 2016-2018, and using adjusted prevalence ratios, VE estimates for colonization were 16.6% (95% confidence interval [CI] 10.6-21.8) for all pneumococci and 39.2% (95% CI 26.7-46.1) for vaccine serotype (VT) pneumococci. There was a 26.0% (95% CI 17.7-33.0) decrease in multidrug-resistant pneumococcal colonization. The IPD incidence was estimated to have declined by 26.4% (95% CI 14.4-35.8) by 2018, with a decrease of 36.3% (95% CI 23.8-46.9) for VT IPD and an increase of 101.4% (95% CI 62.0-145.4) for non-VT IPD.

conclusionsFollowing PCV13 introduction into the Cambodian immunization schedule, there have been declines in VT pneumococcal colonization and disease in children aged <5 years. Modelling of dominant serotype colonization data produced plausible VE estimates.

Indexed as

Pneumococcal InfectionsPneumococcal VaccinesAsian PeopleCambodiaChildChild, PreschoolHeptavalent Pneumococcal Conjugate VaccineHumansInfantSerogroupVaccines, ConjugateHeptavalent Pneumococcal Conjugate VaccinePneumococcal VaccinesVaccines, ConjugateCambodiachildrencolonizationStreptococcus pneumoniaevaccine

Identifiers

PMID31175819
PMCPMC7145996

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Registered trials

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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.