Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome

Background: Multisystem inflammatory syndrome in children (MIS-C) is a novel disease associated with COVID-19. The COVID-19 epidemic peaked in May 2022 in Taiwan, and we encountered our first case of MIS-C in late May 2022. We aimed to present patients’ clinical manifestations and identify risk fact...

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Main Authors: Chi-Hsien Wu, Tu-Hsuan Chang, Boon-Fatt Tan, Jong-Lin Wu, Song-Ming Huang, Ting-Yu Yen, En-Ting Wu, Ching-Chia Wang, Min-Tai Lin, Chun-Yi Lu, Luan-Yin Chang, Li-Min Huang
Format: Article
Language:English
Published: Elsevier 2024-04-01
Series:Journal of the Formosan Medical Association
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0929664623004035
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author Chi-Hsien Wu
Tu-Hsuan Chang
Boon-Fatt Tan
Jong-Lin Wu
Song-Ming Huang
Ting-Yu Yen
En-Ting Wu
Ching-Chia Wang
Min-Tai Lin
Chun-Yi Lu
Luan-Yin Chang
Li-Min Huang
author_facet Chi-Hsien Wu
Tu-Hsuan Chang
Boon-Fatt Tan
Jong-Lin Wu
Song-Ming Huang
Ting-Yu Yen
En-Ting Wu
Ching-Chia Wang
Min-Tai Lin
Chun-Yi Lu
Luan-Yin Chang
Li-Min Huang
author_sort Chi-Hsien Wu
collection DOAJ
description Background: Multisystem inflammatory syndrome in children (MIS-C) is a novel disease associated with COVID-19. The COVID-19 epidemic peaked in May 2022 in Taiwan, and we encountered our first case of MIS-C in late May 2022. We aimed to present patients’ clinical manifestations and identify risk factors for shock. Methods: We included patients diagnosed with MIS-C at two medical centers from May 2022 to August 2022. We separated those patients into two groups according to whether they experienced shock. We collected demographic, clinical manifestation, and laboratory data of the patients and performed statistical analysis between the two groups. Results: We enrolled 28 patients, including 13 (46 %) with shock and 15 (54 %) without shock. The median age was 6.4 years (IQR: 1.9–7.5). In single variable analysis, patients with shock tended to be older, had more neurological symptoms, more conjunctivitis and strawberry tongue, lower lymphocyte count, lower platelet counts, and higher C-reactive protein, higher procalcitonin, higher ferritin, and higher D-dimer levels than those without shock. The area under the ROC curve that used procalcitonin to be the risk factor of shock with MIS-C was 0.815 (95 % CI 0.644 to 0.987). The cutoff value obtained by ROC analysis of procalcitonin was 1.68 ng/mL. With this cutoff, the test characteristics of procalcitonin were as follows: sensitivity 77 %, specificity 93 %, positive predictive value 91 %, negative predictive value 82 %. Multivariable analysis revealed that procalcitonin was the only independent risk factor of shock with MIS-C on admission (OR, 26.00, 95 % CI, 1.01–668.89). Conclusions: MIS-C patients with high initial procalcitonin levels have higher risks of experiencing shock and may need ICU admission.
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spelling doaj.art-9fd7db5be1e849469eac78dca11b23d92024-04-10T04:28:32ZengElsevierJournal of the Formosan Medical Association0929-66462024-04-011234496500Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndromeChi-Hsien Wu0Tu-Hsuan Chang1Boon-Fatt Tan2Jong-Lin Wu3Song-Ming Huang4Ting-Yu Yen5En-Ting Wu6Ching-Chia Wang7Min-Tai Lin8Chun-Yi Lu9Luan-Yin Chang10Li-Min Huang11Department of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, Chi-Mei Medical Center, Tainan, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, Hsin-Chu Branch, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanDepartment of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan; Corresponding author. Department of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, No. 8, Chung Shan S. Rd., Taipei 10041, Taiwan.Department of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan; Corresponding author. Department of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, No. 8, Chung Shan S. Rd., Taipei 10041, Taiwan.Department of Pediatrics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, TaiwanBackground: Multisystem inflammatory syndrome in children (MIS-C) is a novel disease associated with COVID-19. The COVID-19 epidemic peaked in May 2022 in Taiwan, and we encountered our first case of MIS-C in late May 2022. We aimed to present patients’ clinical manifestations and identify risk factors for shock. Methods: We included patients diagnosed with MIS-C at two medical centers from May 2022 to August 2022. We separated those patients into two groups according to whether they experienced shock. We collected demographic, clinical manifestation, and laboratory data of the patients and performed statistical analysis between the two groups. Results: We enrolled 28 patients, including 13 (46 %) with shock and 15 (54 %) without shock. The median age was 6.4 years (IQR: 1.9–7.5). In single variable analysis, patients with shock tended to be older, had more neurological symptoms, more conjunctivitis and strawberry tongue, lower lymphocyte count, lower platelet counts, and higher C-reactive protein, higher procalcitonin, higher ferritin, and higher D-dimer levels than those without shock. The area under the ROC curve that used procalcitonin to be the risk factor of shock with MIS-C was 0.815 (95 % CI 0.644 to 0.987). The cutoff value obtained by ROC analysis of procalcitonin was 1.68 ng/mL. With this cutoff, the test characteristics of procalcitonin were as follows: sensitivity 77 %, specificity 93 %, positive predictive value 91 %, negative predictive value 82 %. Multivariable analysis revealed that procalcitonin was the only independent risk factor of shock with MIS-C on admission (OR, 26.00, 95 % CI, 1.01–668.89). Conclusions: MIS-C patients with high initial procalcitonin levels have higher risks of experiencing shock and may need ICU admission.http://www.sciencedirect.com/science/article/pii/S0929664623004035COVID-19MIS-CShockProcalcitoninRisk factor
spellingShingle Chi-Hsien Wu
Tu-Hsuan Chang
Boon-Fatt Tan
Jong-Lin Wu
Song-Ming Huang
Ting-Yu Yen
En-Ting Wu
Ching-Chia Wang
Min-Tai Lin
Chun-Yi Lu
Luan-Yin Chang
Li-Min Huang
Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
Journal of the Formosan Medical Association
COVID-19
MIS-C
Shock
Procalcitonin
Risk factor
title Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
title_full Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
title_fullStr Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
title_full_unstemmed Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
title_short Clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
title_sort clinical manifestations and risk factors of shock in children with multisystem inflammatory syndrome
topic COVID-19
MIS-C
Shock
Procalcitonin
Risk factor
url http://www.sciencedirect.com/science/article/pii/S0929664623004035
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