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. 2021 May 20;17(4):335–340. doi: 10.1007/s12519-021-00435-y

Table 1.

Differences of multiple inflammatory syndrome in children associated with COVID-19 and Kawasaki disease

Items MIS-C KD
Age Median age: 6–10 years 76% cases < 5 years
Sex More common in male Male: female about 1.5:1
Ethnic distribution High proportion of African ethnicity or ancestry, as well as Hispanic subjects Asian children have the highest incidence in the world
Clinical features
Fever 100% 100%
Rash 50–75% Above 90%
Mucous membrane involvement 60–94% Above 90%
Conjunctivitis 48–69% Above 90%
Hands and feet erythema/edema 26–68% About 75%
Cervical lymphadenopathy 30–70% 50–70%
Classic and incomplete KD presentation 25–65.5% 100%
Shock (KDSS) 33–87% 2–7%
MAS 3–50% 1.1–1.9%
Other clinical features
Gastrointestinal symptoms 60–100% Rare
Respiratory distress 12–46% Rare
Cardiac manifestation 18–87% Rare
CAA 14–36% 4%
Laboratory features
Lymphopenia 37–81% Rare
Platelets Decreased Increased
Level of inflammatory markers Noticeably increased Increased
Troponin T More common Rare
BNP Marked increased Mild increased
Ferritin Highly elevated Normal
D-dimer Significantly increase Normal
SARS-Cov2 positive (serology or PCR) 80–100% None
Treatment
Intropes/vasopressors 25–100% Rare
Mechanical ventilation 13–57% Rare
Aspirin 3–28% Very rare
ECMO In some cases (0%-75%) 100%
IVIG 54–100% 100%
Steroid 20–83% In some cases
Biologic drugs 7–80% Occasionally reported
Outcomes
Mortality About 2.1–18% About 0.17%

MIS-C multiple inflammatory syndrome in children, MAS macrophagic activation syndrome, CAA coronary artery aneurysm, IVIG intravenous immunoglobulin, KD Kawasaki disease, PCR polymerase chain reaction, ECMO extracorporeal membrane oxygenation, KDSS Kawasaki disease shock syndrome, BNP brain natriuretic peptide