Evidence map›Paper›PMID 35240934›Full record

ArticleHuman vaccines & immunotherapeutics2022

Rotavirus genotypes and clinical outcome of natural infection based on vaccination status in the post-vaccine era.

Kei Kozawa, Yuki Higashimoto, Yoshiki Kawamura, Hiroki Miura, Takumi Negishi, Fumihiko Hattori, Masaru Ihira, Satoshi Komoto, Koki Taniguchi, Tetsushi Yoshikawa

Open access · goldAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Kei KozawaDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Yuki HigashimotoFaculty of Medical Technology, Fujita Health University School of Health Sciences, Toyoake, Japan.
Yoshiki KawamuraDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.ORCID 0000-0003-3942-7098
Hiroki MiuraDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Takumi NegishiDepartment of Clinical Laboratory, Fujita Health University Hospital, Toyoake, Japan.
Fumihiko HattoriDepartment of Pediatrics, Kariya Toyota General Hospital, Kariya, Japan.
Masaru IhiraFaculty of Clinical Engineering, Fujita Health University School of Medical Sciences, Toyoake, Japan.
Satoshi KomotoDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Japan.
Koki TaniguchiDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Japan.
Tetsushi YoshikawaDepartment of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
Fujita Health University · JPFujita Health University Hospital · JPKariya Toyota General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rotavirus (RV) is a leading cause of gastroenteritis in children. In Japan, Rotarix (RV1; GlaxoSmithKline), which is a monovalent vaccine derived from human RV (G1P[8]), has been introduced since November 2011, and RotaTeq (RV5; MSD) which is an pentavalent, human-bovine mono-reassortant vaccine (G1, G2, G3, G4, and P1A[8]), has been introduced since July 2012. Long-term follow-up on vaccine efficacy and RV genotypical change should be carried out in order to control RV infection. The RV gastroenteritis (RVGE) outbreak occurred during the 2018/2019 season in Aichi prefecture, Japan. Therefore, the molecular epidemiology of RV among three different groups of RVGE, which were outpatients who received RV1, those who received RV5, and those without vaccination, was explored. Clinical features of RVGE patients were compared among the three patient groups. Children less than 15 years of age with gastroenteritis who visited any of seven pediatric practices between January and June 2019 were enrolled in the study. G, P, and E genotypes were determined by direct sequencing of reverse transcription-polymerase chain reaction products amplified from stool samples. Among 110 patients, there were 27, 28, and 55 in the RV1-vaccinated, RV5-vaccinated, and unvaccinated groups, respectively. The most frequent genotype was G8P[8] (92/110 patients, 83.6%). Genotype distributions did not significantly differ among the three patient groups (

Indexed as

GastroenteritisRotavirusRotavirus InfectionsRotavirus VaccinesAnimalsCattleChildGenotypeHumansInfantVaccinationVaccines, AttenuatedVaccines, CombinedRotavirus VaccinesVaccines, AttenuatedVaccines, Combinedacute gastroenteritisgenotypeRotavirussurveillancevaccine

Identifiers

PMID35240934
PMCPMC9009920
OpenAlexW4214825745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.