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Differentiating multisystem inflammatory syndrome in children: a single-centre retrospective cohort study.
Roberts, Jordan E; Campbell, Jeffrey I; Gauvreau, Kimberlee; Lamb, Gabriella S; Newburger, Jane; Son, Mary Beth; Dionne, Audrey.
  • Roberts JE; Pediatrics, Division of Immunology, Boston Children's Hospital, Boston, Massachusetts, USA Jordan.roberts2@childrens.harvard.edu.
  • Campbell JI; Harvard Medical School, Boston, Massachusetts, USA.
  • Gauvreau K; Harvard Medical School, Boston, Massachusetts, USA.
  • Lamb GS; Pediatrics, Division of Infectious Disease, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Newburger J; Harvard Medical School, Boston, Massachusetts, USA.
  • Son MB; Cardiology, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Dionne A; Harvard Medical School, Boston, Massachusetts, USA.
Arch Dis Child ; 107(3): e3, 2022 03.
Article in English | MEDLINE | ID: covidwho-1388470
ABSTRACT

OBJECTIVE:

Features of multisystem inflammatory syndrome in children (MIS-C) overlap with other febrile illnesses, hindering prompt and accurate diagnosis. The objectives of this study were to identify clinical and laboratory findings that distinguished MIS-C from febrile illnesses in which MIS-C was considered but ultimately excluded, and to examine the diseases that most often mimicked MIS-C in a tertiary medical centre. STUDY

DESIGN:

We identified all children hospitalised with fever who were evaluated for MIS-C at our centre and compared clinical signs and symptoms, SARS-CoV-2 status and laboratory studies between those with and without MIS-C. Multivariable logistic LASSO (least absolute shrinkage and selection operator) regression was used to identify the most discriminative presenting features of MIS-C.

RESULTS:

We identified 50 confirmed MIS-C cases (MIS-C+) and 68 children evaluated for, but ultimately not diagnosed with, MIS-C (MIS-C-). In univariable analysis, conjunctivitis, abdominal pain, fatigue, hypoxaemia, tachypnoea and hypotension at presentation were significantly more common among MIS-C+ patients. MIS-C+ and MIS-C- patients had similar elevations in C-reactive protein (CRP), but were differentiated by thrombocytopenia, lymphopenia, and elevated ferritin, neutrophil/lymphocyte ratio, BNP and troponin. In multivariable analysis, predictors of MIS-C included age, neutrophil/lymphocyte ratio, platelets, conjunctivitis, oral mucosa changes, abdominal pain and hypotension.

CONCLUSIONS:

Among hospitalised children undergoing evaluation for MIS-C, children with MIS-C were older, more likely to present with conjunctivitis, oral mucosa changes, abdominal pain and hypotension, and had higher neutrophil/lymphocyte ratios and lower platelet counts. These data may be helpful for discrimination of MIS-C from other febrile illnesses, including bacterial lymphadenitis and acute viral infection, with overlapping features.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: English Journal: Arch Dis Child Year: 2022 Document Type: Article Affiliation country: ARCHDISCHILD-2021-322290

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: English Journal: Arch Dis Child Year: 2022 Document Type: Article Affiliation country: ARCHDISCHILD-2021-322290