Key points

MIS-C Case Definition
As described in the Council for State and Territorial Epidemiologists' (CSTE) position statement, "Standardized Case Definition for Surveillance of Multisystem Inflammatory Syndrome in Children" the CSTE/CDC case definition for MIS-C is as follows:
Any illness in a person <21 years of age that meets:
- The clinical AND the laboratory criteria (Confirmed); OR
- The clinical criteria AND epidemiologic linkage criteria (Probable); OR
- The vital records criteria (Suspect)
An illness characterized by all of the following, in the absence of a more likely alternative diagnosis*
- Subjective or documented fever (temperature ≥38.0⁰ C)
- Clinical severity requiring hospitalization or resulting in death
- Evidence of systematic inflammation indicated by C-reactive protein ≥3.0 mg/dL (30 mg/L
- New onset manifestations in at least two of the following categories:
- Cardiac involvement indicated by:
- Left ventricular ejection fraction <55% OR
- Coronary artery dilatation, aneurysm, or ectasia, OR
- Troponin elevated above laboratory normal range, or indicated as elevated in a clinical note
- Mucocutaneous involvement indicated by:
- Rash, OR
- Inflammation of the oral mucosa (e.g., mucosal erythema or swelling, drying or fissuring of the lips, strawberry tongue), OR
- Conjunctivitis or conjunctival injection (redness of the eyes), OR
- Extremity findings (e.g., erythema [redness] or edema [swelling] of the hands or feet)
- Shock**
- Gastrointestinal involvement indicated by:
- Abdominal pain, OR
- Vomiting, OR
- Diarrhea
- Hematologic involvement indicated by:
- Platelet count <150,000 cells/μL, OR
- Absolute lymphocyte count (ALC) <1,000 cells/μL
*If documented by the clinical treatment team, a final diagnosis of Kawasaki Disease should be considered an alternative diagnosis. These cases should not be reported to national MIS-C surveillance.
**Clinician documentation of shock meets this criterion.
- Detection of SARS-CoV-2 RNA in a clinical specimen*** up to 60 days prior to or during hospitalization, or in a post-mortem specimen using a diagnostic molecular amplification test (e.g., polymerase chain reaction [PCR]), OR
- Detection of SARS-CoV-2 specific antigen in a clinical specimen*** up to 60 days prior to or during hospitalization, or in a post-mortem specimen, OR
- Detection of SARS-CoV-2 specific antibodies^ in serum, plasma, or whole blood associated with current illness resulting in or during hospitalization
***Positive molecular or antigen results from self-administered testing using over-the-counter test kits meet laboratory criteria.
^Includes a positive serology test regardless of COVID-19 vaccination status. Detection of anti-nucleocapsid antibody is indicative of SARS-CoV-2 infection, while anti-spike protein antibody may be induced either by COVID-19 vaccination or by SARS-CoV-2 infection
- Close contact‡ with a confirmed or probable case of COVID-19 disease in the 60 days prior to hospitalization.
‡Close contact is generally defined as being within 6 feet for at least 15 minutes (cumulative over a 24-hour period). However, it depends on the exposure level and setting; for example, in the setting of an aerosol generating procedure in healthcare settings without proper personal protective equipment (PPE), this may be defined as any duration.
- A person whose death certificate lists MIS-C or multisystem inflammatory syndrome as an underlying cause of death or a significant condition contributing to death.
MIS-A Case Definition
CDC defines Multisystem Inflammatory Syndrome in Adults (MIS-A) as an illness in a person ≥ 21 years of age with:
- Hospitalization for ≥ 24 hours* AND
- Subjective or documented fever (≥38.0 C) for ≥24 hours prior to hospitalization or within the first THREE days of hospitalization AND
- An illness meeting the following clinical and laboratory criteria:
*Or hospitalized for any length of time with an illness resulting in death
- No alternative diagnosis (e.g. bacterial sepsis, exacerbation of a chronic medical condition) AND
- At least THREE of the following clinical criteria occurring prior to hospitalization or within the first THREE days of hospitalization. At least ONE must be a primary clinical criterion.
- Severe cardiac illness** (Includes myocarditis, pericarditis, coronary artery dilatation/aneurysm, new-onset right or left ventricular dysfunction [LVEF<50%], 2nd/3rd degree AV block, or ventricular tachycardia.)
- Rash AND non-purulent conjunctivitis
**Cardiac arrest alone does not meet this criterion
- New-onset neurologic signs and symptoms (Includes encephalopathy in a patient without prior cognitive impairment, seizures, meningeal signs, or peripheral neuropathy including Guillain-Barré syndrome)
- Shock or hypotension not attributable to medical therapy (e.g., sedation, renal replacement therapy)
- Abdominal pain, vomiting, or diarrhea
- Thrombocytopenia (platelet count <150,000/μL)
- Evidence of SARS-CoV-2 infection AND
- Positive SARS-CoV-2 nucleic acid amplification (NAAT), serology, or antigen test
- Evidence of systemic inflammation
- Elevated levels of at least 2 of the following: C-reactive protein (CRP), ferritin, interleukin-6 (IL-6), erythrocyte sedimentation rate (ESR), procalcitonin
Reporting
CDC recommends all state, local, territorial, and tribal health departments use the updated CSTE/CDC MIS-C surveillance definition and case report form to conduct surveillance and report all confirmed, probable, or suspected MIS-C cases to CDC.
See the guidance document for instructions on completing the case report form.
Cases of MIS-A can be reported to CDC using the MIS-A surveillance case report form.
MIS-C Data Available
View health department-reported cases of Multisystem Inflammatory Syndrome in Children (MIS-C) in the United States.