Multisystem Inflammatory Syndrome (MIS-C) Clinical Pathway — Emergency, ICU and Inpatient

ED Evaluation for Possible Multisystem Inflammatory Syndrome in Children (MIS-C)

On April 27th, an alert was issued by the Pediatric Intensive Care Society (PICS) in the UK, reporting a rise in the number of patients presenting with a multisystem inflammatory process, which appeared to share features with toxic shock syndrome, atypical Kawasaki disease, and Kawasaki shock syndrome.

Multiple reports from the US and Europe have since emerged; this syndrome was referred to variably as “Pediatric Multisystem Inflammatory Syndrome (PMIS)” or “Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 (PIMS-TS).”

On May 14th , the CDC published a Health Advisory proposing a case definition which they termed “Multisystem Inflammatory Syndrome in Children (MIS-C).

CDC Health Advisory – MIS  

MIS-C Information

Case Definition

Note that this definition is for surveillance, and subtle differences exist between criteria prompting evaluation for MIS-C and this definition.

  • An individual aged < 21 years presenting with fever1, laboratory evidence of inflammation2, and evidence of clinically severe illness requiring hospitalization, with multisystem (≥ 2) organ involvement (cardiac, renal, respiratory, hematologic, gastrointestinal, dermatologic or neurological); AND
  • No alternative plausible diagnoses; AND
  • Positive for current or recent SARS-CoV-2 infection by RT-PCR, serology, or antigen test; or COVID-19 exposure within the 4 weeks prior to the onset of symptoms
  1. Fever > 38.0°C for ≥ 24 hours, or report of subjective fever lasting ≥ 24 hours
  2. Including, but not limited to, one or more of the following: an elevated C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), fibrinogen, procalcitonin, d-dimer, ferritin, lactic acid dehydrogenase (LDH), or interleukin 6 (IL-6), elevated neutrophils, reduced lymphocytes and low albumin

Note

It is hypothesized that this inflammatory syndrome is an immune mediated vasculitis/vasculopathy following SARS-CoV-2 infection.

The guidance here is based on expert opinion derived from the small number of cases reported thus far.

As this guidance will evolve, consultation for further evaluation and treatment with ID, Rheumatology, Dysregulated Immune Response Team, Cardiology, Hematology, and Critical Care Medicine is important for individualized recommendations for suspected cases. The guidance here will be updated as new data, experience and consensus becomes available, so look for updates.

For patients whose presentation is consistent with Kawasaki Disease, please also refer to the Kawasaki Disease pathway as a resource for diagnosis, evaluation and treatment.