Division of Rheumatology, Department of Pediatrics, University of Alabama at Birmingham, 1600 7th Ave. S., CPPN #G10, Birmingham, AL, 35233-1711, USA.
Division of Hospital Medicine, Department of Pediatrics, University of Alabama at Birmingham, 1600 7th Ave S, McWane Building, Suite 108, Birmingham, AL, 35233, USA.
Pediatr Rheumatol Online J. 2021 Feb 24;19(1):21. doi: 10.1186/s12969-021-00508-2.
Active pediatric COVID-19 pneumonia and MIS-C are two disease processes requiring rapid diagnosis and different treatment protocols.
To distinguish active pediatric COVID-19 pneumonia and MIS-C using presenting signs and symptoms, patient characteristics, and laboratory values.
Patients diagnosed and hospitalized with active COVID-19 pneumonia or MIS-C at Children's of Alabama Hospital in Birmingham, AL from April 1 through September 1, 2020 were identified retrospectively. Active COVID-19 and MIS-C cases were defined using diagnostic codes and verified for accuracy using current US Centers for Disease Control case definitions. All clinical notes were reviewed for documentation of COVID-19 pneumonia or MIS-C, and clinical notes and electronic medical records were reviewed for patient demographics, presenting signs and symptoms, prior exposure to or testing for the SARS-CoV-2 virus, laboratory data, imaging, treatment modalities and response to treatment.
111 patients were identified, with 74 classified as mild COVID-19, 8 patients as moderate COVID-19, 8 patients as severe COVID-19, 10 as mild MIS-C and 11 as severe MIS-C. All groups had a male predominance, with Black and Hispanic patients overrepresented as compared to the demographics of Alabama. Most MIS-C patients were healthy at baseline, with most COVID-19 patients having at least one underlying illness. Fever, rash, conjunctivitis, and gastrointestinal symptoms were predominant in the MIS-C population whereas COVID-19 patients presented with predominantly respiratory symptoms. The two groups were similar in duration of symptomatic prodrome and exposure history to the SARS-CoV-2 virus, but MIS-C patients had a longer duration between presentation and exposure history. COVID-19 patients were more likely to have a positive SAR-CoV-2 PCR and to require respiratory support on admission. MIS-C patients had lower sodium levels, higher levels of C-reactive protein, erythrocyte sedimentation rate, d-dimer and procalcitonin. COVID-19 patients had higher lactate dehydrogenase levels on admission. MIS-C patients had coronary artery changes on echocardiography more often than COVID-19 patients.
This study is one of the first to directly compare COVID-19 and MIS-C in the pediatric population. The significant differences found between symptoms at presentation, demographics, and laboratory findings will aide health-care providers in distinguishing the two disease entities.
活动性小儿 COVID-19 肺炎和 MIS-C 是两种需要快速诊断和不同治疗方案的疾病过程。
通过表现出的症状和体征、患者特征和实验室值来区分活动性小儿 COVID-19 肺炎和 MIS-C。
本回顾性研究在阿拉巴马州伯明翰市阿拉巴马儿童医院(Children's of Alabama Hospital)从 2020 年 4 月 1 日至 9 月 1 日期间,确定了被诊断和住院治疗的活动性 COVID-19 肺炎或 MIS-C 患儿。使用诊断代码定义活动性 COVID-19 和 MIS-C 病例,并使用当前美国疾病控制与预防中心的病例定义对其准确性进行验证。对所有临床记录进行审查,以确定 COVID-19 肺炎或 MIS-C 的记录,对临床记录和电子病历进行审查,以确定患者人口统计学特征、表现出的症状和体征、是否有接触或检测 SARS-CoV-2 病毒史、实验室数据、影像学检查、治疗方式以及对治疗的反应。
共确定了 111 名患儿,其中 74 名患儿被归类为轻度 COVID-19,8 名患儿为中度 COVID-19,8 名患儿为重度 COVID-19,10 名患儿为轻度 MIS-C,11 名患儿为重度 MIS-C。所有组均以男性为主,与阿拉巴马州的人口统计学特征相比,黑人及西班牙裔患儿占比更高。大多数 MIS-C 患儿的基线情况良好,而大多数 COVID-19 患儿至少有一种基础疾病。发烧、皮疹、结膜炎和胃肠道症状在 MIS-C 人群中更为常见,而 COVID-19 患者则主要表现为呼吸道症状。两组患者的症状前驱期和接触 SARS-CoV-2 病毒的病史持续时间相似,但 MIS-C 患者从就诊到接触病毒的时间间隔较长。COVID-19 患者更有可能进行 SARS-CoV-2 PCR 阳性检测,并在入院时需要呼吸支持。MIS-C 患者的钠水平较低,C 反应蛋白、红细胞沉降率、D-二聚体和降钙素水平较高。COVID-19 患者入院时乳酸脱氢酶水平较高。MIS-C 患者的超声心动图上更常出现冠状动脉变化,而 COVID-19 患者则较少。
本研究是首次直接比较小儿 COVID-19 和 MIS-C 的研究之一。在就诊时的症状、人口统计学特征和实验室发现方面存在的显著差异,将有助于医疗保健提供者区分这两种疾病实体。