Clinical Presentation and Outcome of Multisystem Inflammatory Syndrome in Children in Dhaka Shishu (Children) Hospital

S. Afroz, T. Ferdaus, A. Jabbar, Umme Tanjila, A. Hasnat, Sabrina Akter, Tarannum Khondoker, Tanjina Haque Silvi, J. Ferdous, R. Rima, M. Mamun, Jonaki Khatun
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引用次数: 1

Abstract

Background: The increasing trend in multisystem inflammatory syndrome in children (MIS-C) during Covid-19 pandemic is alarming. Understanding the clinical course and outcome will give the clinical and public health implications of this syndrome. Objectives: This study was conducted to find out the clinical presentation, course of the disease and outcome of the children and adolescents of MIS-C. Methods: This observational study was conducted in the department of Pediatric Nephrology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh, from August 2020 to October 2020. Total 12 children of MIS-C diagnosed according to WHO diagnostic criteria of MIS-C were included after taking written informed consent from the parents. Mean, median and standard deviation were calculated for the continuous variables. Results: The age ranged from 17 days to 13 years, 56% were male, 17% were positive for SARS-CoV-2 by RT-PCR and 4(33%) had history of the COVID-19 exposure. Organsystem involvement included bilateral pneumonia in 92%, myocarditis in 78%, swollen hands and feet in 67%, mucocutaneous involvement in 50%, diarrhea in 50%, musculoskeletal involvement in 50%, acute kidney injury (AKI) in 33% patients and acute pancreatitis in 25% patients. The median duration of hospitalization was 11 days and ICU stay was 5 days. Mean duration of fever was 8.66 days. Kawasaki’s diseaselike features were documented in 50% patients and 4 of them had elevated level of procalcitonin and troponin I. Markedly elevated C reactive protein (CRP), Ferritin and D dimer in all patients were present. All patients with cardiac involvement had left ventricular dysfunction and ejection fraction was as low as 38.5%. Coronary-artery dilatation was documented in 33%. About 67% received intensive care with oxygen support by low flow nasal cannula or face mask, 33% received vasoactive support and systemic glucocorticoid, 50% received intravenous immunoglobulin (IVIG) plus methyl prednisolone. Antiplatelet and anticoagulant therapy was given in 75% and 33% patients respectively. Out of 12 patients 2 died, the contributing cause of death included complications like hypotension, shock, myocarditis, coagulopathy and AKI. Conclusion: MIS-C led to serious and life-threatening complications especially when there are cardiac involvement, hypotension and acute kidney injury. DS (Child) H J 2020; 36(2): 87-94
达卡Shishu(儿童)医院儿童多系统炎症综合征的临床表现和预后
背景:在Covid-19大流行期间,儿童多系统炎症综合征(MIS-C)的增加趋势令人担忧。了解临床过程和结果将给出该综合征的临床和公共卫生意义。目的:探讨儿童及青少年MIS-C的临床表现、病程及转归。方法:本观察性研究于2020年8月至2020年10月在孟加拉国达卡Shishu(儿童)医院儿科肾脏病科进行。经父母书面知情同意,纳入12例符合WHO诊断标准的MIS-C患儿。计算连续变量的均值、中位数和标准差。结果:年龄17天~ 13岁,男性56%,RT-PCR阳性17%,有COVID-19暴露史4例(33%)。器官系统受累包括92%的双侧肺炎、78%的心肌炎、67%的手脚肿胀、50%的粘膜皮肤受累、50%的腹泻、50%的肌肉骨骼受累、33%的急性肾损伤(AKI)和25%的急性胰腺炎。中位住院时间为11天,ICU住院时间为5天。平均发热时间8.66 d。50%的患者有川崎病样特征,其中4例患者降钙素原和肌钙蛋白i水平升高。所有患者均出现C反应蛋白(CRP)、铁蛋白和D二聚体明显升高。所有心脏受累的患者均有左心室功能障碍,射血分数低至38.5%。33%的患者出现冠状动脉扩张。约67%接受重症监护,低流量鼻插管或面罩供氧,33%接受血管活性支持和全身糖皮质激素治疗,50%接受静脉注射免疫球蛋白(IVIG)加甲基强的松龙治疗。抗血小板和抗凝治疗分别占75%和33%。在12例患者中,2例死亡,导致死亡的原因包括低血压、休克、心肌炎、凝血功能障碍和AKI等并发症。结论:misc可导致严重的危及生命的并发症,特别是在心脏受累、低血压和急性肾损伤时。DS(儿童)[J] 2020;36 (2): 87 - 94
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