Multisystem inflammatory syndrome in children
Disease of children; pediatric comorbidity from COVID-19 / From Wikipedia, the free encyclopedia
Dear Wikiwand AI, let's keep it short by simply answering these key questions:
Can you list the top facts and stats about Multisystem inflammatory syndrome in children?
Summarize this article for a 10 year old
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.[7] MIS-C has also been monitored as a potential, rare[8] pediatric adverse event following COVID-19 vaccination.[9] Research suggests that COVID-19 vaccination lowers the risk of MIS-C, and in cases where symptoms develop after vaccine, is likely extremely rare or related to factors like recent exposure to COVID-19.[10] It can rapidly lead to medical emergencies such as insufficient blood flow around the body (a condition known as shock).[7] Failure of one or more organs can occur.[11] A warning sign is unexplained persistent fever with severe symptoms following exposure to COVID-19.[12] Prompt referral to paediatric specialists is essential, and families need to seek urgent medical assistance.[7] Most affected children will need intensive care.[7]
This article needs to be updated. The reason given is: The content was largely intended to provide timely information (in 2020–2021) about an ongoing event. (January 2023) |
Paediatric multisystem inflammatory syndrome (PMIS/PIMS/PIMS-TS) | |
---|---|
Other names |
|
TEM image of SARS-CoV-2, the coronavirus responsible for COVID-19: PMIS / MIS-C is thought to be caused by an unusual biological response to infection in certain children | |
Specialty | Paediatrics |
Symptoms | Fever, abdominal pain, diarrhoea/vomiting, low blood pressure, insufficient blood supply (shock), pink eye, "strawberry tongue", rashes, large lymph nodes, swollen hands/feet, neurological disturbances, among others |
Complications | Cardiac dysfunction; coronary artery abnormalities, including aneurysms; acute kidney injury; coagulopathy |
Usual onset | typically 2–6 weeks[6] after COVID-19 exposure |
Causes | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) |
Diagnostic method | Clinical evaluation by specialists |
Differential diagnosis | Alternative infectious/non-infectious causes, Kawasaki disease |
Treatment | Intravenous immunoglobulin (IVIG); corticosteroids; oxygen, supportive care |
Prognosis | Response to treatment, generally good; long-term prognosis, unclear[7] |
Frequency | Rare |
Deaths | <2% of reported cases |
All affected children have persistent fever.[7] Other clinical features vary.[12] The first symptoms often include acute abdominal pain with diarrhoea or vomiting.[7] Muscle pain and general tiredness are frequent,[7] and low blood pressure is also common.[13] Symptoms can also include pink eye, rashes, enlarged lymph nodes, swollen hands and feet, and "strawberry tongue".[6] Various mental disturbances are possible.[6] A cytokine storm may take place,[14] in which the child's innate immune system stages an excessive and uncontrolled inflammatory response.[15] Heart failure is common.[13] Clinical complications can include damage to the heart muscle, respiratory distress, acute kidney injury, and increased blood coagulation.[16] Coronary artery abnormalities can develop (ranging from dilatation to aneurysms).[6]
This life-threatening disease has proved fatal in under 2% of reported cases.[7] Early recognition and prompt specialist attention are essential.[17] Anti-inflammatory treatments have been used, with good responses being recorded for intravenous immunoglobulin (IVIG), with or without corticosteroids.[18] Oxygen is often needed.[7] Supportive care is key for treating clinical complications.[16] Most children who receive expert hospital care survive.[7]
Knowledge of this newly described syndrome is evolving rapidly.[19] 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.[13] It can also show features of other serious inflammatory conditions of childhood, including toxic shock and macrophage activation syndromes.[13] Nevertheless, it appears to be a separate syndrome.[20] Older children tend to be affected.[21]
This emerging condition has been defined slightly differently (using different names), by the World Health Organization (WHO),[22] the Royal College of Paediatrics and Child Health (RCPCH),[11] and the Centers for Disease Control and Prevention (CDC).[1] Although the condition is thought to follow SARS-CoV-2 viral infection, antigen or antibody tests are not always positive.[3] Exclusion of alternative causes, including bacterial and other infections, is essential for differential diagnosis.[3] Some general clinical guidance has been provided by the RCPCH,[11] the National Institutes of Health,[21] the American College of Rheumatology,[23] and the American Academy of Pediatrics.[24]
Clusters of new cases have been reported two to six weeks after local peaks in viral transmission.[6] The disease is thought to be driven by a delayed biological mechanism in certain predisposed children.[18] The European Centre for Disease Prevention and Control (ECDC) has rated risk to children in Europe as being 'low' overall, based on a 'very low' likelihood of a child developing this 'high impact' disease.[3] 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.[17] Initial reports regarded children in various parts of Europe and the United States, and it was unclear to what extent the condition had gone unrecognized elsewhere.[22] Reports have since emerged of cases in various other countries around the world.[25][26] In adults, a similar condition has occasionally been reported, which has been called multisystem inflammatory syndrome in adults (MIS-A).[27]