Distinguishing active pediatric COVID-19 pneumonia from MIS-C

Pediatr Rheumatol Online J. 2021 Feb 24;19(1):21. doi: 10.1186/s12969-021-00508-2.

Abstract

Importance: Active pediatric COVID-19 pneumonia and MIS-C are two disease processes requiring rapid diagnosis and different treatment protocols.

Objective: To distinguish active pediatric COVID-19 pneumonia and MIS-C using presenting signs and symptoms, patient characteristics, and laboratory values.

Design: Patients diagnosed and hospitalized with active COVID-19 pneumonia or MIS-C at Children's of Alabama Hospital in Birmingham, AL from April 1 through September 1, 2020 were identified retrospectively. Active COVID-19 and MIS-C cases were defined using diagnostic codes and verified for accuracy using current US Centers for Disease Control case definitions. All clinical notes were reviewed for documentation of COVID-19 pneumonia or MIS-C, and clinical notes and electronic medical records were reviewed for patient demographics, presenting signs and symptoms, prior exposure to or testing for the SARS-CoV-2 virus, laboratory data, imaging, treatment modalities and response to treatment.

Findings: 111 patients were identified, with 74 classified as mild COVID-19, 8 patients as moderate COVID-19, 8 patients as severe COVID-19, 10 as mild MIS-C and 11 as severe MIS-C. All groups had a male predominance, with Black and Hispanic patients overrepresented as compared to the demographics of Alabama. Most MIS-C patients were healthy at baseline, with most COVID-19 patients having at least one underlying illness. Fever, rash, conjunctivitis, and gastrointestinal symptoms were predominant in the MIS-C population whereas COVID-19 patients presented with predominantly respiratory symptoms. The two groups were similar in duration of symptomatic prodrome and exposure history to the SARS-CoV-2 virus, but MIS-C patients had a longer duration between presentation and exposure history. COVID-19 patients were more likely to have a positive SAR-CoV-2 PCR and to require respiratory support on admission. MIS-C patients had lower sodium levels, higher levels of C-reactive protein, erythrocyte sedimentation rate, d-dimer and procalcitonin. COVID-19 patients had higher lactate dehydrogenase levels on admission. MIS-C patients had coronary artery changes on echocardiography more often than COVID-19 patients.

Conclusions and relevance: This study is one of the first to directly compare COVID-19 and MIS-C in the pediatric population. The significant differences found between symptoms at presentation, demographics, and laboratory findings will aide health-care providers in distinguishing the two disease entities.

MeSH terms

  • Abdominal Pain / physiopathology
  • Adolescent
  • Asthma / epidemiology
  • Black or African American
  • C-Reactive Protein / metabolism
  • COVID-19 / epidemiology
  • COVID-19 / metabolism
  • COVID-19 / physiopathology*
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Comorbidity
  • Conjunctivitis / physiopathology
  • Coronary Artery Disease
  • Diabetes Mellitus / epidemiology
  • Diarrhea / physiopathology
  • Dilatation, Pathologic
  • Echocardiography
  • Exanthema / physiopathology
  • Female
  • Fever / physiopathology
  • Heart Defects, Congenital / epidemiology
  • Hispanic or Latino
  • Humans
  • Hyponatremia / metabolism
  • Male
  • Nausea / physiopathology
  • Neoplasms / epidemiology
  • Neurodevelopmental Disorders / epidemiology
  • Obesity / epidemiology
  • SARS-CoV-2
  • Severity of Illness Index
  • Sex Distribution
  • Stroke Volume
  • Systemic Inflammatory Response Syndrome / epidemiology
  • Systemic Inflammatory Response Syndrome / metabolism
  • Systemic Inflammatory Response Syndrome / physiopathology*
  • Time Factors
  • Vomiting / physiopathology

Substances

  • C-Reactive Protein

Supplementary concepts

  • pediatric multisystem inflammatory disease, COVID-19 related