Department of Pediatric Immunology-Hematology and Rheumatology, Hôpital Necker Enfants Malades, Paris, France.
Division of Pediatric Cardiology, Zucker School of Medicine, Cohen Children's Medical Center of NY, Northwell Health, New York, USA.
J Cardiovasc Magn Reson. 2021 Dec 30;23(1):140. doi: 10.1186/s12968-021-00841-1.
Recent evidence shows an association between coronavirus disease 2019 (COVID-19) infection and a severe inflammatory syndrome in children. Cardiovascular magnetic resonance (CMR) data about myocardial injury in children are limited to small cohorts. The aim of this multicenter, international registry is to describe clinical and cardiac characteristics of multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19 using CMR so as to better understand the real extent of myocardial damage in this vulnerable cohort.
Hundred-eleven patients meeting the World Health Organization criteria for MIS-C associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), having clinical cardiac involvement and having received CMR imaging scan were included from 17 centers. Median age at disease onset was 10.0 years (IQR 7.0-13.8). The majority of children had COVID-19 serology positive (98%) with 27% of children still having both, positive serology and polymerase chain reaction (PCR). CMR was performed at a median of 28 days (19-47) after onset of symptoms. Twenty out of 111 (18%) patients had CMR criteria for acute myocarditis (as defined by the Lake Louise Criteria) with 18/20 showing subepicardial late gadolinium enhancement (LGE). CMR myocarditis was significantly associated with New York Heart Association class IV (p = 0.005, OR 6.56 (95%-CI 1.87-23.00)) and the need for mechanical support (p = 0.039, OR 4.98 (95%-CI 1.18-21.02)). At discharge, 11/111 (10%) patients still had left ventricular systolic dysfunction.
No CMR evidence of myocardial damage was found in most of our MIS-C cohort. Nevertheless, acute myocarditis is a possible manifestation of MIS-C associated with SARS-CoV-2 with CMR evidence of myocardial necrosis in 18% of our cohort. CMR may be an important diagnostic tool to identify a subset of patients at risk for cardiac sequelae and more prone to myocardial damage.
The study has been registered on ClinicalTrials.gov, Identifier NCT04455347, registered on 01/07/2020, retrospectively registered.
最近的证据表明,2019 年冠状病毒病(COVID-19)感染与儿童严重炎症综合征之间存在关联。关于儿童心肌损伤的心血管磁共振(CMR)数据仅限于小队列。本多中心、国际注册研究的目的是使用 CMR 描述与 COVID-19 相关的儿童多系统炎症综合征(MIS-C)的临床和心脏特征,以更好地了解这一脆弱人群中心肌损伤的真实程度。
从 17 个中心纳入了 111 名符合世界卫生组织(WHO)定义的与严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)相关的 MIS-C 且有临床心脏受累并接受 CMR 成像扫描的患者。发病时的中位年龄为 10.0 岁(IQR 7.0-13.8)。大多数儿童的 COVID-19 血清学呈阳性(98%),27%的儿童血清学和聚合酶链反应(PCR)仍为阳性。CMR 中位时间为症状发作后 28 天(19-47)。111 名患者中有 20 名(18%)符合 CMR 急性心肌炎标准(根据路易斯湖标准定义),其中 18 名患者显示心外膜下延迟钆增强(LGE)。CMR 心肌炎与纽约心脏协会(NYHA)心功能分级 IV 级显著相关(p=0.005,OR 6.56(95%-CI 1.87-23.00))和需要机械支持(p=0.039,OR 4.98(95%-CI 1.18-21.02))。出院时,111 名患者中有 11 名(10%)仍存在左心室收缩功能障碍。
在我们的大多数 MIS-C 队列中,没有发现 CMR 心肌损伤的证据。然而,急性心肌炎是与 SARS-CoV-2 相关的 MIS-C 的一种可能表现,我们队列中有 18%的患者有心肌坏死的 CMR 证据。CMR 可能是一种重要的诊断工具,可识别出具有心脏后遗症风险和更易发生心肌损伤的亚组患者。
该研究已在 ClinicalTrials.gov 上注册,标识符为 NCT04455347,于 2020 年 1 月 7 日注册,为回顾性注册。