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The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
European Journal of Clinical Microbiology & Infectious Diseases ( IF 3.7 ) Pub Date : 2020-10-02 , DOI: 10.1007/s10096-020-04033-0
Jingjiao Zhou 1, 2 , Yudie Wang 1, 2 , Juan Zhao 3 , Lixing Gu 1, 2 , Cheng Yang 1, 2 , Jun Wang 1, 2 , Heng Zhang 3 , Yu Tian 1, 2 , Hu Tuo 3 , Dan Li 3 , Min Wei 4 , Bing He 3, 5
Affiliation  

Our aim was to investigate whether SARS-CoV-2 infection raised high risks of late pregnancy complications, and posed health problems in fetuses and neonates. We analyzed the data of COVID-19 pregnant women with COVID-19 during late pregnancy and their neonates. Eleven out of 16 (69%) pregnant women with COVID-19 had ++ or +++ of ketone body in urine. The blood uric acid of pregnant patients was 334 μmol/L (IQR, 269–452). D-dimer and FDP in pregnant patients were 3.32 mg/L (IQR, 2.18–4.21) and 9.6 mg/L (IQR, 5.9–12.4). Results of blood samples collected at birth showed that 16 neonates had leukocytes (15.7 × 109/L (IQR, 13.7–17.2)), neutrophils (11.1 × 109/L (IQR, 9.2–13.2)), CK (401 U/L (IQR, 382–647)), and LDH (445 U/L (IQR, 417–559)). Twenty-four hours after birth, a neonate from COVID-19 woman had fever and positive of SARS-CoV-2 gene. Another woman had strongly positive for SARS-CoV-2 gene (+++) for 4 weeks, and delivered one neonate who had SARS-CoV-2 IgM (46 AU/mL) and IgG (140 AU/mL) on day 1 after birth. In the third trimester, COVID-19 infection in pregnant patients raised high risks of ketonuria, hypercoagulable state, and hyperfibrinolysis, which may lead to severe complications. COVID-19 increased the inflammatory responses of placenta, and fetuses and neonates had potential organ dysregulation and coagulation disorders. There was a potential intrauterine transmission while pregnant women had high titer of SARS-CoV-2, but it is necessary to detect SARS-CoV-2 in the blood cord, placenta, and amniotic fluid to further confirm intrauterine infection of fetuses.



中文翻译:


COVID-19孕妇及其新生儿的代谢和免疫学特征



我们的目的是调查 SARS-CoV-2 感染是否会增加妊娠晚期并发症的高风险,并给胎儿和新生儿带来健康问题。我们分析了妊娠晚期感染 COVID-19 的 COVID-19 孕妇及其新生儿的数据。 16 名感染 COVID-19 的孕妇中有 11 名 (69%) 尿液中酮体含量为 ++ 或 +++。妊娠患者血尿酸为334μmol/L(IQR,269~452)。妊娠患者的 D-二聚体和 FDP 分别为 3.32 mg/L(IQR,2.18-4.21)和 9.6 mg/L(IQR,5.9-12.4)。出生时采集血样结果显示,16名新生儿的白细胞(15.7×10 9 /L(IQR,13.7-17.2))、中性粒细胞(11.1×10 9 /L(IQR,9.2-13.2))、CK(401 U) /L(IQR,382–647))和 LDH(445 U/L(IQR,417–559))。一名 COVID-19 妇女新生儿出生后 24 小时出现发烧症状,且 SARS-CoV-2 基因呈阳性。另一名妇女的 SARS-CoV-2 基因 (+++) 呈强阳性,持续 4 周,并在第一天生下一名新生儿,该新生儿具有 SARS-CoV-2 IgM (46 AU/mL) 和 IgG (140 AU/mL)出生后。在妊娠晚期,孕妇感染COVID-19会增加酮尿、高凝状态和纤溶亢进的高风险,从而可能导致严重的并发症。 COVID-19增加了胎盘的炎症反应,胎儿和新生儿存在潜在的器官失调和凝血障碍。孕妇SARS-CoV-2滴度较高时,存在潜在的宫内传播风险,但需要检测血脐带、胎盘、羊水中的SARS-CoV-2,以进一步确诊胎儿宫内感染。

更新日期:2020-10-02
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