Table 1.
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