Evidence map›Paper›PMID 31136073›Full record

ArticlePediatrics international : official journal of the Japan Pediatric Society2019

Enterovirus D68 respiratory infection in a children's hospital in Japan in 2015.

Yu Funakoshi, Kenta Ito, Saeko Morino, Kazue Kinoshita, Yoshihiko Morikawa, Tatsuo Kono, Yen Hai Doan, Hiroyuki Shimizu, Nozomu Hanaoka, Masami Konagaya and 8 more

Abstract read
In one paragraph

Article in Pediatrics international : official journal of the Japan Pediatric Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
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

18 authors.

Yu FunakoshiDepartment of General Pediatrics, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0676-0719
Kenta ItoDivision of Infectious Diseases, Department of Pediatrics, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.
Saeko MorinoInfectious Disease Surveillance Center, National Institute of Infectious Diseases, Shinjuku, Tokyo, Japan.
Kazue KinoshitaDivision of Infectious Diseases, Department of Pediatrics, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.
Yoshihiko MorikawaClinical Research Support Center, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1437-0374
Tatsuo KonoDepartment of Radiology, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.
Yen Hai DoanDepartment of Virology II, National Institute of Infectious Diseases, Musashi-Murayama, Tokyo, Japan.
Hiroyuki ShimizuDepartment of Virology II, National Institute of Infectious Diseases, Musashi-Murayama, Tokyo, Japan.
Nozomu HanaokaInfectious Disease Surveillance Center, National Institute of Infectious Diseases, Shinjuku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1039-6278
Masami KonagayaInfectious Disease Surveillance Center, National Institute of Infectious Diseases, Shinjuku, Tokyo, Japan.
Tsuguto FujimotoInfectious Disease Surveillance Center, National Institute of Infectious Diseases, Shinjuku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4861-4349
Ai SuzukiDepartment of Microbiology, Tokyo Metropolitan Institute of Public Health, Shinjuku, Tokyo, Japan.
Takashi ChibaDepartment of Microbiology, Tokyo Metropolitan Institute of Public Health, Shinjuku, Tokyo, Japan.
Tetsuya AkibaDepartment of Microbiology, Tokyo Metropolitan Institute of Public Health, Shinjuku, Tokyo, Japan.
Yasuhiro TomaruDivision of Medical Science, Department of Virology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Bunkyo, Tokyo, Japan.
Ken WatanabeDivision of Medical Science, Department of Virology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Bunkyo, Tokyo, Japan.
Norio ShimizuDivision of Medical Science, Department of Virology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Bunkyo, Tokyo, Japan.
Yuho HorikoshiDivision of Infectious Diseases, Department of Pediatrics, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.

Funding

Japan Agency for Medical Research and Development 17fk0108204j0702Japan Agency for Medical Research and Development 18fk0108004j0003Tokyo project research grant H27-30
6 · The paper itself

Abstract

backgroundOutbreaks of enterovirus D68 (EV-D68) respiratory infections in children were reported globally in 2014. In Japan, there was an EV-D68 outbreak in the autumn of 2015 (September-October). The aim of this study was to compare EV-D68-specific polymerase chain reaction (PCR)-positive and EV-D68-specific PCR-negative patients.

methodsPediatric patients admitted for any respiratory symptoms between September and October 2015 were enrolled. Nasopharyngeal swabs were tested for multiplex respiratory virus PCR and EV-D68-specific reverse transcription-PCR. EV-D68-specific PCR-positive and -negative patients were compared regarding demographic data and clinical information.

resultsA nasopharyngeal swab was obtained from 76 of 165 patients admitted with respiratory symptoms during the study period. EV-D68 was detected in 40 samples (52.6%). Median age in the EV-D68-specific PCR-positive and -negative groups was 3.0 years (IQR, 5.5 years) and 3.0 years (IQR, 4.0 years), respectively. The rates of coinfection in the two groups were 32.5% and 47.2%, respectively. There was no significant difference in the history of asthma or recurrent wheezing, length of hospitalization, or pediatric intensive care unit admission rate between the groups. The median days between symptom onset and admission was significantly lower for the EV-D68-positive group (3.0 days vs 5.0 days, P = 0.001). EV-D68 was identified as clade B on phylogenetic analysis. No cases of acute flaccid myelitis were encountered.

conclusionsMore than half of the samples from the children admitted with respiratory symptoms were positive for EV-D68-specific PCR during the outbreak. Asthma history was not associated with the risk of developing severe respiratory infection.

Indexed as

Disease OutbreaksCase-Control StudiesChildChild, PreschoolDNA, ViralEnterovirus D, HumanEnterovirus InfectionsFemaleHospitals, PediatricHumansJapanLogistic ModelsMalePhylogenyProspective StudiesRespiratory Tract InfectionsDNA, Viralasthmachildrendisease outbreakenterovirus 68

Identifiers

PMID31136073
PMCPMC7167638

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.