Multisystem inflammatory syndrome in children (MIS-C), or paediatric inflammatory multisystem syndrome (PIMS / PIMS-TS), or systemic inflammatory syndrome in COVID-19 (SISCoV), is a rare systemic illness involving persistent fever and extreme inflammation following exposure to SARS-CoV-2, the virus responsible for COVID-19. Studies have suggested that MIS-C occurred in 31.6 out of 100,000 people under 21 who were infected with COVID-19. It can rapidly lead to medical emergencies such as insufficient blood flow around the body (a condition known as shock). Failure of one or more organs can occur. A warning sign is unexplained persistent fever with severe symptoms following exposure to COVID-19. Prompt referral to paediatric specialists is essential, and families need to seek urgent medical assistance. All affected children have persistent fever. Other clinical features vary. The first symptoms often include acute abdominal pain with diarrhea or vomiting. Muscle pain and general fatigue are frequent, and low blood pressure is also common. Symptoms can also include pink eye, rashes, enlarged lymph nodes, swollen hands and feet, and "strawberry tongue". Various mental disturbances are possible. A cytokine storm may take place, in which the child's innate immune system stages an excessive and uncontrolled inflammatory response. Heart failure is common. Clinical complications can include damage to the heart muscle, respiratory distress, acute kidney injury, and increased blood coagulation. Coronary artery abnormalities can develop (ranging from dilatation to aneurysms). As of 2020, the disease proved fatal in under 2% of reported cases. Early recognition and prompt specialist attention are essential. Anti-inflammatory treatments have been used, with good responses being recorded for intravenous immunoglobulin (IVIG), with or without corticosteroids. Oxygen is often needed, and supportive care is key for treating clinical complications. Mortality is low for children who receive expert hospital care. Knowledge of the syndrome evolved rapidly through the course of the COVID-19 pandemic (2020–2023). Its clinical features may appear somewhat similar to Kawasaki disease, a rare disease of unknown origin that typically affects young children, in which blood vessels become inflamed throughout the body.> It can also show features of other serious inflammatory conditions of childhood, including toxic shock and macrophage activation syndromes. This emerging condition has been defined slightly differently (using different names), by the World Health Organization (WHO), the Royal College of Paediatrics and Child Health (RCPCH) in the UK, and the Centers for Disease Control and Prevention (CDC) in the US. Although the condition is thought to follow SARS-CoV-2 viral infection, antigen or antibody tests are not always positive. Exclusion of alternative causes, including bacterial and other infections, is essential for differential diagnosis. Some general clinical guidance has been provided by the RCPCH, the National Institutes of Health, the American College of Rheumatology, and the American Academy of Pediatrics. Clusters of new cases have been reported two to six weeks after local peaks in viral transmission. The disease is thought to be driven by a delayed biological mechanism in certain predisposed children. In May 2020, the European Centre for Disease Prevention and Control (ECDC) rated risk to children in Europe as being "low" overall, based on a "very low" likelihood of a child developing this "high impact" disease. Regarding ethnicity, the condition seems to affect more children of African, Afro-Caribbean, and Hispanic descent, whereas Kawasaki disease affects more of East Asian ancestry. In adults, the condition is called multisystem inflammatory syndrome in adults (MIS-A) in the US. As of August 2026, in the Anglosphere, only the United States and Australia continue to publish an ongoing tally of cases. At this date, the CDC reports a total number of cases of MIS as 9,808, with 80 deaths recorded in the United States (population c. 350 million. In Australia (population c. 28 million), there have been 217 confirmed cases in total, the number peaking in 2022. Vaccination against COVID-19 is cconsidered the best defence against developing PIMS.
Name The disorder has been called by various names, including:
Multisystem inflammatory syndrome in children (MIS-C) Multisystem inflammatory syndrome (MIS) in children and adolescents temporally related to COVID-19 Paediatric inflammatory multisystem syndrome (PIMS) Paediatric inflammatory multisystem syndrome, temporally associated with SARS-CoV-2 infection (PIMS-TS) Paediatric multisystem inflammatory syndrome (PMIS) Kawa-COVID-19 Systemic inflammatory syndrome in COVID-19 (SISCoV)
Background
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