Change in Severity and Clinical Manifestation of MIS-C Over SARS-CoV-2 Variant Outbreaks in Korea

被引:8
|
作者
Choe, Young June [1 ]
Choi, Eun Hwa [2 ,13 ]
Choi, Jong Woon [3 ]
Eun, Byung Wook [4 ]
Eun, Lucy Youngmin [5 ]
Kim, Yae-Jean [7 ]
Kim, Yeo Hyang [6 ]
Kim, Young A. [8 ]
Kim, Yun-Kyung [9 ]
Kwak, Ji Hee [10 ]
Lee, Hyukmin [11 ]
Park, June Dong [2 ]
Jung, Yeon Haw [11 ]
Gwack, Jin [12 ]
Lee, Sangwon [12 ]
机构
[1] Korea Univ, Anam Hosp, Dept Pediat, Seoul, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Pediat, Seoul, South Korea
[3] Bundang Jesaeng Gen Hosp, Dept Pediat, Seongnam, South Korea
[4] Nowon Eulji Univ Hosp, Dept Pediat, Seoul, South Korea
[5] Yonsei Univ, Coll Med, Dept Pediat, Seoul, South Korea
[6] Sungkyunkwan Univ, Sch Med, Dept Pediat, Seoul, South Korea
[7] Kyungpook Natl Univ, Sch Med, Dept Pediat, Daegu, South Korea
[8] Pusan Natl Univ, Sch Med, Dept Pediat, Yangsan, South Korea
[9] Korea Univ, Dept Pediat, Coll Med, Seoul, South Korea
[10] Kangbuk Samsung Hosp, Dept Pediat, Seoul, South Korea
[11] Yonsei Univ, Coll Med, Dept Lab Med, Seoul, South Korea
[12] Korea Dis Control & Prevent Agcy, Gen Publ Hlth Emergency Preparedness, Cheongju, South Korea
[13] Seoul Natl Univ, Coll Med, Dept Pediat, 101 Daehak Ro, Seoul 03080, South Korea
关键词
MIS-C; COVID-19; SARS-CoV-2; MULTISYSTEM INFLAMMATORY SYNDROME; OMICRON VARIANT; SOUTH-KOREA; COVID-19; DISEASE; CHILDREN; SURVEILLANCE; VACCINE;
D O I
10.3346/jkms.2023.38.e225
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There is difference in the incidence of multi-system inflammatory syndrome in children (MIS-C) in patients with different variants of severe acute respiratory syndrome coronavirus 2, however, little is known about the epidemiology in Asian countries. We investigated and compared the epidemiology of the MIS-C during omicron-dominant period with that of previous periods in South Korea. Methods: We obtained clinical, epidemiological and laboratory data on MIS-C cases from national MIS-C surveillance in South Korea. We defined pre-delta period as January 2020-May 2021; delta period as June 2021-December 2021; and omicron period as January 2022-April 2022. We describe the clinical characteristics and outcomes of MIS-C patients by period. Results: A total of 91 cases were assessed to be MIS-C cases. Number of MIS-C cases have increased from six cases during pre-delta period to 66 cases during omicron period, while the incidence rate (the number of MIS-C cases per 100,000 cases of reported coronavirus disease 2019) has decreased from 38.5 cases per 100,000 (95% confidence interval [CI], 14.1-83.9) during pre-delta period to 1.6 cases per 100,000 (95% CI, 1.2-2.0) during omicron periods. During pre-delta period, 66.7% and 100% had hypotension and gastrointestinal involvement, respectively; while during omicron period, 12.1% and 6.1% had such clinical manifestations. Fifty percent of pre-delta MIS-C patients were taken intensive care unit (ICU) cares, while 10.6% of patients during omicron periods were in ICUs. Conclusion: Omicron period were associated with less severe clinical manifestation compared to pre-delta and delta periods. Although incidence rate of MIS-C was lower for the omicron period than pre-delta and delta periods, number of patients reported with MIS-C may pose a substantial clinical burden.
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页数:9
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