Clinical Characteristics and Histopathology of Coronavirus Disease 2019-Related Deaths in African Children.

Fikile C Mabena, Vicky L Baillie, Martin J Hale, Bukiwe N Thwala, Nonhlanhla Mthembu, Toyah Els, Natali Serafin, Jeanine du Plessis, Peter Swart, Sithembiso C Velaphi, Karen L Petersen, Jeannette Wadula, Nelesh P Govender, Charl Verwey, David P Moore, Fatima Y Moosa, Firdose L Nakwa, Basetsana V Maroane, Grace Okudo, Theodore M Mabaso, Ziyaad Dangor, Marta C Nunes, Shabir A Madhi
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引用次数: 9

Abstract

Background: Globally, very few childhood deaths have been attributed to coronavirus disease 2019 (COVID-19). We evaluated clinical, microbiologic and postmortem histopathologic findings in childhood deaths in whom severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was identified antemortem or postmortem.

Methods: Surveillance of childhood deaths was ongoing during the initial COVID-19 outbreak in South Africa from April 14, 2020, to August 31, 2020. All children hospitalized during this time had a SARS-CoV-2 test done as part of standard of care. Postmortem sampling included minimally invasive tissue sampling (MITS) of lung, liver and heart tissue; blood and lung samples for bacterial culture and molecular detection of viruses (including SARS-CoV-2) and bacteria. The cause of death attribution was undertaken by a multidisciplinary team and reported using World Health Organization framework for cause of death attribution.

Results: SARS-CoV-2 was identified on antemortem and/or postmortem sampling in 11.7% (20/171) of deceased children, including 13.2% (12/91) in whom MITS was done. Eighteen (90%) of 20 deaths with SARS-CoV-2 infection were <12 months age. COVID-19 was attributed in the causal pathway to death in 91.7% (11/12) and 87.5% (7/8) cases with and without MITS, respectively. Lung histopathologic features in COVID-19-related deaths included diffuse alveolar damage (n = 6, 54.5%), type 2 pneumocyte proliferation (n = 6, 54.5%) and hyaline membrane formation (n = 5, 36.4%). Culture-confirmed invasive bacterial disease was evident in 54.5% (6/11) of COVID-19 attributed deaths investigated with MITS.

Conclusions: COVID-19 was in the causal pathway of 10.5% (18/171) of all childhood deaths under surveillance. The postmortem histopathologic features in fatal COVID-19 cases in children were consistent with reports on COVID-19 deaths in adults; although there was a high prevalence of invasive bacterial disease in the children.

2019年非洲儿童冠状病毒病相关死亡的临床特征和组织病理学
背景:在全球范围内,很少有儿童死亡归因于2019年冠状病毒病(COVID-19)。我们评估了在死前或死后发现严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的儿童死亡的临床、微生物学和死后组织病理学结果。方法:在2020年4月14日至2020年8月31日南非首次暴发COVID-19期间,对儿童死亡进行监测。在此期间住院的所有儿童都进行了SARS-CoV-2检测,作为标准护理的一部分。死后取样包括肺、肝和心脏组织的微创组织取样(MITS);血液和肺部样本用于细菌培养和病毒(包括SARS-CoV-2)和细菌的分子检测。死因归属由一个多学科小组进行,并使用世界卫生组织的死因归属框架进行报告。结果:11.7%(20/171)的死亡儿童在死前和/或死后取样中发现了SARS-CoV-2,其中13.2%(12/91)的死亡儿童进行了MITS。结论:在监测的所有儿童死亡病例中,10.5%(18/171)存在COVID-19的因果通路。儿童死亡COVID-19病例的死后组织病理学特征与成人COVID-19死亡报告一致;虽然在儿童中浸润性细菌疾病的患病率很高。
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