Evidence map›Paper›PMID 33045237›Full record

ArticleThe Journal of pediatrics2021

Year-Round, Routine Testing of Multiple Body Site Specimens for Human Parechovirus in Young Febrile Infants.

Cristina Tomatis Souverbielle, Huanyu Wang, John Feister, Jason Campbell, Alexandra Medoro, Asuncion Mejias, Octavio Ramilo, Domenico Pietropaolo, Douglas Salamon, Amy Leber and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 19 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

11 authors at 1 institution in 1 country.

Cristina Tomatis SouverbielleDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Huanyu WangDepartment of Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH.
John FeisterDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Jason CampbellDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Alexandra MedoroDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Asuncion MejiasDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Octavio RamiloDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Domenico PietropaoloDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Douglas SalamonDepartment of Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH.
Amy LeberDepartment of Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH.
Guliz ErdemDivision of Infectious Diseases, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Nationwide Children's Hospital · US

Funding

Project 3: Dr. LiP01AI112524 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI LI, JIANRONG · 2015 to 2019
$6.8M
NIAID NIH HHS P01 AI112524
6 · The paper itself

Abstract

objectivesTo test our hypothesis that routine year-round testing of specimens from multiple body sites and genotyping of detected virus would describe seasonal changes, increase diagnostic yield, and provide a better definition of clinical manifestations of human parechovirus (PeV-A) infections in young febrile infants. STUDY

designPeV-A reverse-transcriptase polymerase chain reaction (RT-PCR) analysis was incorporated in routine evaluation of infants aged ≤60 days hospitalized at Nationwide Children's Hospital for fever and/or suspected sepsis-like syndrome beginning in July 2013. We reviewed electronic medical records of infants who tested positive for PeV-A between July 2013 and September 2016. Genotyping was performed with specific type 3 RT-PCR and sequencing.

resultsOf 1475 infants evaluated, 130 (9%) tested positive for PeV-A in 1 or more sites: 100 (77%) in blood, 84 (65%) in a nonsterile site, and 53 (41%) in cerebrospinal fluid (CSF). Five infants (4%) were CSF-only positive, 31 (24%) were blood-only positive, and 20 (15%) were nonsterile site-only positive. PeV-A3 was the most common type (85%) and the only type detected in CSF. Although the majority (79%) of infections were diagnosed between July and December, PeV-A was detected year-round. The median age at detection was 29 days. Fever (96%), fussiness (75%), and lymphopenia (56%) were common. Among infants with PeV-A-positive CSF, 77% had no CSF pleocytosis. The median duration of hospitalization was 41 hours. Four infants had bacterial coinfections diagnosed within 24 hours of admission; 40 infants had viral coinfections.

conclusionsAlthough most frequent in summer and fall, PeV-A infections were encountered in every calendar month within the 3-year period of study. More than one-half of patients had PeV-A detected at more than 1 body site. Coinfections were common. PeV-A3 was the most common type identified and the only type detected in the CSF.

Indexed as

Cerebrospinal FluidDiagnostic Tests, RoutineFemaleFeverGenotyping TechniquesHumansInfantInfant, NewbornMaleParechovirusPicornaviridae InfectionsReal-Time Polymerase Chain ReactionRetrospective StudiesSeasonsbacterial coinfectionneonatal infectionrapid diagnosisviral typing

Identifiers

PMID33045237
PMCPMC7546655
OpenAlexW3092635228

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.