Evidence map›Paper›PMID 40479933›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2025

Epidemiology and genotypic diversity of rhinovirus in school-age children with acute respiratory illnesses seeking medical care.

Dithi Banerjee, Jennifer E Schuster, Claire M Midgley, Brian Lee, Mary Moffatt, Joana Y Lively, Ariana P Toepfer, Geoffrey A Weinberg, Julie A Boom, Leila C Sahni and 14 more

Abstract read
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
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

24 authors.

Dithi BanerjeeDepartment of Pathology and Lab Medicine, Children's Mercy Hospital, Kansas City, MO, USA.
Jennifer E SchusterDepartment of Pediatrics, Children's Mercy Hospital, Kansas City, MO, USA.
Claire M MidgleyNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Brian LeeDepartment of Health Outcomes Research, Children's Mercy Hospital, Kansas City, MO, USA.
Mary MoffattDepartment of Pathology and Lab Medicine, Children's Mercy Hospital, Kansas City, MO, USA.
Joana Y LivelyNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Ariana P ToepferNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Geoffrey A WeinbergDepartment of Pediatrics, University of Rochester Medical Center, NY, USA.
Julie A BoomDepartment of Pediatrics, Texas Children's Hospital, Houston, TX, USA.
Leila C SahniDepartment of Pediatrics, Texas Children's Hospital, Houston, TX, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Vasanthi AvadhanulaDepartment of Pediatrics, Texas Children's Hospital, Houston, TX, USA.
Pedro A PiedraDepartment of Pediatrics, Texas Children's Hospital, Houston, TX, USA.
Mary Allen StaatDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, OH, USA.
Daniel C PayneDepartment of Pediatrics, Cincinnati Children's Hospital Medical Center, OH, USA.
Natasha HalasaDepartment of Pediatrics, Vanderbilt University Medical Center, TN, USA.
John V WilliamsDepartment of Pediatrics, University of Pittsburgh, PA, USA.
Robert W HickeyDepartment of Pediatrics, University of Pittsburgh, PA, USA.
Marian G MichaelsDepartment of Pediatrics, Vanderbilt University Medical Center, TN, USA.
Janet A EnglundDepartment of Pediatrics, Seattle Children's Hospital, WA, USA.
Eileen J KleinDepartment of Pediatrics, Seattle Children's Hospital, WA, USA.
A SasidharanDepartment of Pathology and Lab Medicine, Children's Mercy Hospital, Kansas City, MO, USA.
Brian RhaNational Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Christopher J HarrisonDivision of Infectious Disease, University of Missouri, Kansas City, MO, USA.
Rangaraj SelvaranganDepartment of Pathology and Lab Medicine, Children's Mercy Hospital, Kansas City, MO, USA. Electronic address: rselvarangan@cmh.edu.

Funding

Intramural CDC HHS CC999999NCIRD CDC HHS U01 IP000460NCIRD CDC HHS U01 IP001049NCIRD CDC HHS U01 IP001057NCIRD CDC HHS U01 IP001059NCIRD CDC HHS U01 IP001154NCIRD CDC HHS U01 IP001158
6 · The paper itself

Abstract

backgroundRhinovirus (RV) associated acute respiratory illness (ARI) data come mostly from infants and young children. We present data from 5 to 17-year-olds to characterize RV species A, B and C.

methodsDuring December 1, 2016-Nov 30, 2017, seven U.S. New Vaccine Surveillance Network (NVSN) sites performed active pediatric ARI surveillance of inpatients (IP) and emergency department (ED) patients using molecular platforms to detect multiple respiratory pathogens. RV or RV/enterovirus (EV) positive specimens without co-detections were sequenced. Demographic and clinical data collected via parent interview and chart review were analyzed descriptively by RV species, month, and hospital setting, using chi-squared tests for comparisons.

resultsRV or RV/EV was detected in 581/2298 (25.3 %) ARI patients; 529 were single detections, 516 of these had sufficient sample for sequencing, and 420 (81.4 %) yielded sequence results: RV-A (183, 35.5 %), RV-B (16, 3.1 %), RV-C (210, 40.7 %), non-typeable RV (2, 0.4 %), and EV (9, 1.7 %). Among 52 RV-A, 8 RV-B and 44 RV-C unique types identified, A49 (32, 61.5 %), B6 (5, 62.5 %) and C15 (22, 50 %) were predominant. History of asthma was reported in 65.4 % RV-A, 50 % RV-B and 78.5 % RV-C patients (p = 0.005). Hospitalization occurred in 63.4 % RV-A, 37.5 % RV-B and 71.4 % RV-C patients (p = 0.012). RV-C detections peaked during winter and RV-A peaked during summer-fall.

conclusionsRV exhibited genetic diversity in 5-17-year-old ARI patients, and circulation differed by RV species. Among children seeking care in ED or hospital settings, with confirmed RV or RV/EV single detections, hospitalization was more common with RV-A and -C than RV-B.

Indexed as

Genetic VariationPicornaviridae InfectionsRespiratory Tract InfectionsRhinovirusAcute DiseaseAdolescentChildChild, PreschoolFemaleGenotypeHumansMaleUnited StatesGenotypic diversityMulti-siteRhinovirusSchool-aged children

Identifiers

PMID40479933
PMCPMC12798460

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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.