Evidence map›Paper›PMID 32367406›Full record

ArticleClinical rheumatology2020

Clinical manifestations of Kawasaki disease in different age groups: retrospective data from Southwest China.

Lianjie Shi, Jianhong Li, Di Qie, Xintian Hua, Jinyong Pan, Xiaoqing Shi, Liang Zhao, Li Li, Jiangtao Li, Hanmin Liu and 1 more

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2020. 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
1.0field-weighted citation impact, top 24% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
  4. Article
  5. Article
  6. [Diagnosis and treatment of incomplete Kawasaki disease in children].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Review
  7. 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

11 authors at 3 institutions in 1 country.

Lianjie ShiDepartment of Rheumatology and Immunology, Peking University International Hospital, Beijing, 102206, China.
Jianhong LiDepartment of Nuclear Medicine, Peking University International Hospital, Beijing, 102206, China.
Di QieDepartment of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, NO. 20, section 3, Renmin South Road, Chengdu, 610041, Sichuan, China.
Xintian HuaDepartment of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, NO. 20, section 3, Renmin South Road, Chengdu, 610041, Sichuan, China.
Jinyong PanDepartment of Pediatrics, The First Affiliated Hospital of Medical College, Shihezi University, Shihezi, 832008, China.
Xiaoqing ShiDepartment of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, NO. 20, section 3, Renmin South Road, Chengdu, 610041, Sichuan, China.
Liang ZhaoDepartment of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, NO. 20, section 3, Renmin South Road, Chengdu, 610041, Sichuan, China.
Li LiDepartment of Rheumatology and Immunology, Binzhou People's Hospital, Binzhou, 256600, China.
Jiangtao LiDepartment of Rheumatology, The First People's Hospital of Yibin, Yibin, 644000, China.
Hanmin LiuDepartment of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, NO. 20, section 3, Renmin South Road, Chengdu, 610041, Sichuan, China. hanmin@vip.163.com.
Lina QiaoDepartment of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, NO. 20, section 3, Renmin South Road, Chengdu, 610041, Sichuan, China. iaqiao@163.com.
Sichuan University · CNPeking University · CNFirst Affiliated Hospital of Shihezi University Medical College · CN

Funding

Peking University International Hospital Research Funds YN2017QX01Young Scientists Fund 81501396
6 · The paper itself

Abstract

objectivesThe aim of the present study is to identify the clinical manifestations and laboratory findings of children with Kawasaki disease (KD) in different age groups and to recognize and treat KD in a timely manner.

methodsA total of 213 children with KD were divided into the following age groups: (1) infants, (2) toddlers, and (3) preschool age. Retrospective analysis of clinical data was performed among the groups. Categorical data were statistically compared by Chi-square analysis, and measurement data were compared using one-way ANOVA analysis.

resultsOur study showed that (1) cough (40.5%), diarrhea (16.9%), and vomiting (8.5%) were also very common in KD patients. (2) Patients in the infant group more commonly developed cough and diarrhea, but were less frequently documented with lymphadenopathy and skin rash. (3) Elevation of platelets was more common in the infant group. When urine tests were compared among the three groups, the toddler group had a higher proportion of sterile pyuria, and infants younger than 1 year old had a lower proportion of proteinuria and positive urine ketones.

conclusionCough, diarrhea, vomiting, and sterile pyuria were very common in infant KD patients less than 1 year old. They should be noted in patients with suspected KD for earlier diagnosis and timely treatments. Key Points • Patients with Kawasaki disease (KD) in different age groups showed different clinical manifestations and laboratory findings. • Cough, diarrhea, vomiting, and sterile pyuria were very common in infant KD patients less than 1 year old. • Paying more attentions to respiratory, gastrointestinal, and urinary manifestations or abnormalities might be helpful for earlier diagnosis of KD, especially incomplete KD, though they were not list in the diagnostic criteria.

Indexed as

Mucocutaneous Lymph Node SyndromePyuriaChild, PreschoolChinaEarly DiagnosisHumansInfantRetrospective StudiesAge groupKawasaki diseaseLaboratory parametersManifestation

Identifiers

PMID32367406
OpenAlexW3022040834

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.