Evidence map›Paper›PMID 36018446›Full record

ArticleClinical rheumatology2022

Multisystem inflammatory syndrome in children: clinical presentation, management, and short- and long-term outcomes.

Müge Sezer, Elif Çelikel, Zahide Ekici Tekin, Fatma Aydın, Tuba Kurt, Nilüfer Tekgöz, Cüneyt Karagöl, Serkan Coşkun, Melike Mehveş Kaplan, Nimet Öner and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Post-MIS-C cardiovascular outcomes: a systematic review.European journal of pediatrics · 2026
    Pooled it
  2. Pooled it
  3. Article
  4. MIS-C: Diagnosis, Management, and Outcomes.Open forum infectious diseases · 2026
    Review
  5. Article
  6. Article
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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

14 authors at 2 institutions in 2 countries.

Müge SezerDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey. muge2202@hotmail.com.ORCID http://orcid.org/0000-0002-9254-9935
Elif ÇelikelDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-0129-4410
Zahide Ekici TekinDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-5446-667X
Fatma AydınDepartment of Pediatric Rheumatology, Faculty of Medicine, Ankara University, Ankara, Turkey.ORCID http://orcid.org/0000-0003-0306-7473
Tuba KurtDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-3711-8347
Nilüfer TekgözDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-2235-4489
Cüneyt KaragölDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-2987-1980
Serkan CoşkunDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-2568-9329
Melike Mehveş KaplanDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-8012-2774
Nimet ÖnerDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-0403-151X
Merve Cansu PolatDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-3279-8435
Ayşe Esin Kibar GülDepartment of Pediatric Cardiology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-7833-7701
Aslınur Özkaya ParlakayDepartment of Pediatric Infectious Disease, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-5691-2461
Banu AcarDepartment of Pediatric Rheumatology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-1808-3655
Memorial Ankara Hospital · TRAnkara University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn this study, it was aimed to evaluate the demographic, clinical and laboratory characteristics of MIS-C patients in our hospital, to share our treatment approach, and to assess the outcomes of short- and long-term follow-up.

methodsMIS-C patients who were admitted and treated in our hospital between July 2020 and July 2021 were evaluated. Demographic, clinical, laboratory, and follow-up data were collected from patient records retrospectively.

resultsA total of 123 patients with MIS-C (median age, 9.6 years) were included the study. Nineteen (15.4%) were mild, 56 (45.6%) were moderate, and 48 (39%) were severe MIS-C. High CRP, ferritin, pro-BNP, troponin, IL-6, and D-dimer values were found in proportion to the severity of the disease (p < 0.001, p < 0.001, p < 0.001, p < 0.001, p = 0.005, p < 0.001), respectively. Two (1.6%) patients died. The mean follow-up period was 7.8 months. Valve failure, left ventricular dysfunction/hypertrophy, coronary involvement, and pericardial effusion were the most common cardiac pathologies in the short- and long-term follow-up of the patients. In the long-term follow-up, the most common reasons for admission to the hospital were recurrent abdominal pain (14.2%), cardiac findings (14.2%), pulmonary symptoms (8%), fever (7.1%), neuropsychiatric findings (6.2%) and hypertension (3.5%). Neuropsychiatric abnormalities were observed significantly more common in severe MIS-C patients at follow-up (p = 0.016). In the follow-up, 6.2% of the patients required recurrent hospitalization.

conclusionMIS-C is a serious and life-threatening disease, according to short-term outcomes. In addition to the cardiac findings of patients with MIS-C, long-term outcomes such as neuropsychiatric findings, persistent gastrointestinal symptoms, fever and pulmonary symptoms should be monitored. Key Points • In MIS-C patients, attention should be paid not only to cardiac findings, but also to symptoms related to other systems. • Patients should be followed up in terms of neuropsychiatric findings, persistent gastrointestinal symptoms, fever and pulmonary symptoms that may occur during follow-up.

Indexed as

Connective Tissue DiseasesCOVID-19ChildFeverHumansRetrospective StudiesSARS-CoV-2Systemic Inflammatory Response SyndromeCOVID-19HyperinflammationMIS-CPediatric

Identifiers

PMID36018446
PMCPMC9411826
OpenAlexW4293199564

What OpenQuestion holds

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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.