Table 5.
Institution | US Centers for Disease Control and Prevention196 | World Health Organization201 | Royal College of Pediatrics and Child Health194 |
---|---|---|---|
Age group | An individual aged <21 y presenting with the following: | Children and adolescents 0–19 y of age with the following: | A child presenting with the following: |
Fever | fever ≥38.0°C for ≥24 h, or report of subjective fever lasting ≥24 h | fever ≥3 d | persistent fever >38.5⁰C |
AND | AND | AND | |
Inflammation | Laboratory evidence of inflammation including, but not limited to, 1 or more of the following: elevated C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), fibrinogen, procalcitonin, D-dimer, ferritin, lactic acid dehydrogenase (LDH), or interleukin 6 (IL-6), elevated neutrophils, reduced lymphocytes and low albumin | Elevated markers of inflammation such as ESR, CRP, or procalcitonin | Inflammation (neutrophilia, elevated CRP, and lymphopenia) |
AND | AND | AND | |
Severity of illness | Evidence of clinically severe illness requiring hospitalization | ||
AND | |||
Organ system involvement | With multisystem (≥2) organ involvement (cardiac, renal, respiratory, hematologic, gastrointestinal, dermatologic, or neurologic) | 2 of the following: (1) Rash or bilateral nonpurulent conjunctivitis or muco-cutaneous inflammation signs (oral, hands or feet). (2) Hypotension or shock. (3) Features of myocardial dysfunction, pericarditis, valvulitis, or coronary abnormalities (including echocardiogram findings or elevated troponin/NT-proBNP. (4) Evidence of coagulopathy (by PT, PTT, elevated d-Dimers). (5) Acute gastrointestinal problems (diarrhea, vomiting, or abdominal pain). | Evidence of single or multi-organ dysfunction (shock, cardiac, respiratory, renal gastrointestinal or neurologic disorder) |
AND | AND | AND | |
with additional featuresa | |||
AND | |||
Alternative explanations | No alternative for plausible diagnoses | No other obvious microbial cause of inflammation, including the following: | Exclusion of any other microbial cause including the following: |
Bacterial sepsis | Bacterial sepsis | ||
Staphylococcal or streptococcal shock syndromes | Staphylococcal or streptococcal shock syndromes | ||
Infections associated with myocarditis (such as enterovirus) | |||
AND | AND | AND | |
Virologic testing | Positive for current or recent SARS-CoV-2 infection by RT-PCR, serology, or antigen test; or exposure to a suspected or confirmed COVID-19 case within the 4 wk before the onset of symptoms | Evidence of COVID-19 (RT-PCR, antigen test or serology positive), or likely contact with patients with COVID-19 | SARS-CoV-2 PCR testing may be positive or negative |
Additional comments | Some individuals may fulfill full or partial criteria for Kawasaki disease but should be reported if they meet the case definition for MIS-C | This may include children fulfilling full or partial criteria for Kawasaki disease | |
Consider MIS-C in any pediatric death with evidence of SARS-CoV-2 infection |
Abbreviations: COVID-19, coronavirus disease 2019; MIS-C, multisystem inflammatory syndrome in children; NT-proBNP, N-terminal pro brain natriuretic peptide; PT, prothrombin time; PTT, partial thromboplastin time; RT-PCR, reverse-transcriptase polymerase chain reaction; SARS-CoV-2, severe acute respiratory distress syndrome coronavirus 2.
Additional features: abnormal fibrinogen, high D-dimer, high ferritin, hypoalbuminemia, acute kidney injury, anemia, coagulopathy, high interleukin (IL)-10, high IL-6, proteinuria, raised creatine kinase, raised lactate dehydrogenase, raised triglycerides, raised troponin, thrombocytopenia, transaminitis.