儿童和青少年多系统炎症综合征(MIS-C)的流行病学、临床特征和结局——一项实时系统综述和荟萃分析

IF 3.6 Q1 PEDIATRICS
Current pediatrics reports Pub Date : 2022-01-01 Epub Date: 2022-05-06 DOI:10.1007/s40124-022-00264-1
Li Jiang, Kun Tang, Omar Irfan, Xuan Li, Enyao Zhang, Zulfiqar Bhutta
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引用次数: 0

摘要

综述的目的:COVID-19是一种发生在儿童和青少年身上的多系统炎症,在全球范围内得到越来越多的认可和广泛研究。本综述旨在调查和综合有关其临床特征、管理和儿科患者预后的最新证据:我们从 PubMed、EMBASE、Cochrane Library、WHO COVID-19 数据库、Google Scholar 和预印本数据库中检索了数据,时间跨度为 2019 年 12 月 1 日至 2021 年 7 月 31 日。最终的描述性分析和风险因素分析共纳入了 123 项符合条件的研究。我们全面回顾了已发表和预发表的各种设计研究中报告的儿童多系统炎症综合征(MIS-C)病例,以提供有关流行病学、临床、实验室和影像学发现、管理和短期结果的最新证据。最新证据表明,非洲黑人和非西班牙裔白人是最常见的两个种族群体,分别占MIS-C人群的24.89%(95% CI 23.30-26.48%)和25.18%(95% CI 23.51-26.85%)。MIS-C 的典型症状包括发热(90.85%,95% CI 89.86-91.84%)、未指定的胃肠道症状(51.98%,95% CI 50.13-53.83%)、皮疹(49.63%,95% CI 47.80-51.47%)、腹痛(48.97%,95% CI 47.09-50.85%)、结膜炎(46.93%,95% CI 45.17-48.69%)、呕吐(43.79%,95% CI 41.90-45.68%)、呼吸道症状(41.75%,95% CI 40.01-43.49%)和腹泻(40.10%,95% CI 38.23-41.97%)。与川崎病患者相比,MIS-C 患者发生结膜炎(OR 0.27,95% CI 0.11-0.67)、宫颈腺病(OR 0.21,95% CI 0.07-0.68)和皮疹(OR 0.44,95% CI 0.26-0.77)的几率较低。我们的研究显示,大多数 MIS-C 病例(95.21%)完全康复,只有 2.41% 的患者死于该综合征。我们发现,中低收入国家与高收入国家在临床结果方面存在明显差异。摘要:MIS-C 似乎与 COVID-19 有关,可导致器官和组织的严重炎症。尽管关于该综合征的特征、风险因素和临床预后的新证据不断涌现,但关于其因果关系、最佳预防和治疗干预措施以及 MIS-C 患者的长期预后,仍有许多未知因素:在线版本包含补充材料,可在 10.1007/s40124-022-00264-1 网站上查阅。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiology, Clinical Features, and Outcomes of Multisystem Inflammatory Syndrome in Children (MIS-C) and Adolescents-a Live Systematic Review and Meta-analysis.

Purpose of review: A multisystem inflammatory condition occurring in children and adolescents with COVID-19 has become increasingly recognized and widely studied globally. This review aims to investigate and synthesize evolving evidence on its clinical characteristics, management, and outcomes in pediatric patients.

Recent findings: We retrieved data from PubMed, EMBASE, Cochrane Library, WHO COVID-19 Database, Google Scholar, and preprint databases, covering a timeline from December 1, 2019, to July 31, 2021. A total of 123 eligible studies were included in the final descriptive and risk factor analyses. We comprehensively reviewed reported multisystem inflammatory syndrome in children (MIS-C) cases from published and preprint studies of various designs to provide an updated evidence on epidemiology, clinical, laboratory and imaging findings, management, and short-term outcomes. Latest evidence suggests that African black and non-Hispanic white are the two most common ethnic groups, constituting 24.89% (95% CI 23.30-26.48%) and 25.18% (95% CI 23.51-26.85%) of the MIS-C population, respectively. Typical symptoms of MIS-C include fever (90.85%, 95% CI 89.86-91.84%), not-specified gastrointestinal symptoms (51.98%, 95% CI 50.13-53.83%), rash (49.63%, 95% CI 47.80-51.47%), abdominal pain (48.97%, 95% CI 47.09-50.85%), conjunctivitis (46.93%, 95% CI 45.17-48.69%), vomiting (43.79%, 95% CI 41.90-45.68%), respiratory symptoms (41.75%, 95% CI 40.01-43.49%), and diarrhea (40.10%, 95% CI 38.23-41.97%). MIS-C patients are less likely to develop conjunctivitis (OR 0.27, 95% CI 0.11-0.67), cervical adenopathy (OR 0.21, 95% CI 0.07-0.68), and rash (OR 0.44, 95% CI 0.26-0.77), in comparison with Kawasaki disease patients. Our review revealed that the majority of MIS-C cases (95.21%) to be full recovered while only 2.41% died from this syndrome. We found significant disparity between low- and middle-income countries and high-income countries in terms of clinical outcomes.

Summary: MIS-C, which appears to be linked to COVID-19, may cause severe inflammation in organs and tissues. Although there is emerging new evidence about the characteristics of this syndrome, its risk factors, and clinical prognosis, much remains unknown about the causality, the optimal prevention and treatment interventions, and long-term outcomes of the MIS-C patients.

Supplementary information: The online version contains supplementary material available at 10.1007/s40124-022-00264-1.

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