Time series analysis and modelling of MIS-C cases: can we predict MIS-C cases by new cases in the 0–18 age group?

Background : Multisystem Inflammatory Syndrome in Children (MIS-C) is a rare but severe complication following SARS-CoV-2 infection. Early recognition and forecasting may support preparedness and clinical resource allocation. Objective : We aimed to model the temporal relationship between COVID-19 incidence and MIS-C cases using time series analysis. Materials and methods : We retrospectively analyzed data from 51 children with MIS-C (age 0–18 years) hospitalized in a single center between November 2020 and April 2021. A regression model with ARIMA(1,0,0) errors was applied to predict MIS-C cases based on weekly COVID-19 incidence in individuals aged 0–18 years. Results : The majority of children were male (n = 37, 72.5%) and older than 5 years (n = 40, 78%), with a mean age of 8.82 ± 4.16 years. Abdominal symptoms were predominant (n = 38, 74%), and nearly half experienced respiratory (n = 23, 45%) or cardiac (n = 26, 51%) involvement. The ARIMA model identified a lag of 5–6 weeks between COVID-19 cases and MIS-C incidence (R² = 0.41). A selection-aware Monte Carlo simulation confirmed the robustness of the model’s significant regressors when extrapolated beyond the original data period. Conclusion : The moderate predictive power of the ARIMA model supports the potential of syndromic surveillance to forecast MIS-C clusters, aiding early intervention. Larger datasets could further enhance prediction accuracy.

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Publication Details

Journal
Pharmacia
Published
2026-01-22
DOI
https://doi.org/10.3897/pharmacia.73.e167298
Primary Topic
Kawasaki Disease and Coronary Complications
Type
article
Field-Weighted Citation Impact
0.00

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article

Time series analysis and modelling of MIS-C cases: can we predict MIS-C cases by new cases in the 0–18 age group?

Tsvetelina Velikova, Iren Tzotcheva, L Tomov, Dimitrina Georgieva Miteva et al.
Pharmacia
Kawasaki Disease and Coronary Complications
article

Time series analysis and modelling of MIS-C cases: can we predict MIS-C cases by new cases in the 0–18 age group?

Tsvetelina Velikova, Iren Tzotcheva, L Tomov, Dimitrina Georgieva Miteva, Ali Hassan, Snejina Lazova
article en

Abstract

Background : Multisystem Inflammatory Syndrome in Children (MIS-C) is a rare but severe complication following SARS-CoV-2 infection. Early recognition and forecasting may support preparedness and clinical resource allocation. Objective : We aimed to model the temporal relationship between COVID-19 incidence and MIS-C cases using time series analysis. Materials and methods : We retrospectively analyzed data from 51 children with MIS-C (age 0–18 years) hospitalized in a single center between November 2020 and April 2021. A regression model with ARIMA(1,0,0) errors was applied to predict MIS-C cases based on weekly COVID-19 incidence in individuals aged 0–18 years. Results : The majority of children were male (n = 37, 72.5%) and older than 5 years (n = 40, 78%), with a mean age of 8.82 ± 4.16 years. Abdominal symptoms were predominant (n = 38, 74%), and nearly half experienced respiratory (n = 23, 45%) or cardiac (n = 26, 51%) involvement. The ARIMA model identified a lag of 5–6 weeks between COVID-19 cases and MIS-C incidence (R² = 0.41). A selection-aware Monte Carlo simulation confirmed the robustness of the model’s significant regressors when extrapolated beyond the original data period. Conclusion : The moderate predictive power of the ARIMA model supports the potential of syndromic surveillance to forecast MIS-C clusters, aiding early intervention. Larger datasets could further enhance prediction accuracy.

PharmaciaVol. 73
New Bulgarian University (BG), Government College University, Faisalabad (PK), Medical University of Sofia (BG), National Institute of Emergency Medicine "Pirogov" (BG), Sofia University "St. Kliment Ohridski" (BG)
European Commission
Openalex Percentile: Top 81%
Kawasaki Disease and Coronary Complications
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