Maternal Fetal Medicine Division, Department of Obstetrics and Gynecology, Mayo Clinic College of Medicine, Rochester, MN.
Division of Research, Department of Obstetrics and Gynecology, Mayo Clinic College of Medicine, Rochester, MN.
Mayo Clin Proc. 2020 Aug;95(8):1750-1765. doi: 10.1016/j.mayocp.2020.05.011. Epub 2020 May 30.
The global pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the cause of coronavirus disease 2019 (COVID-19), has been associated with worse outcomes in several patient populations, including the elderly and those with chronic comorbidities. Data from previous pandemics and seasonal influenza suggest that pregnant women may be at increased risk for infection-associated morbidity and mortality. Physiologic changes in normal pregnancy and metabolic and vascular changes in high-risk pregnancies may affect the pathogenesis or exacerbate the clinical presentation of COVID-19. Specifically, SARS-CoV-2 enters the cell via the angiotensin-converting enzyme 2 (ACE2) receptor, which is upregulated in normal pregnancy. Upregulation of ACE2 mediates conversion of angiotensin II (vasoconstrictor) to angiotensin-(1-7) (vasodilator) and contributes to relatively low blood pressures, despite upregulation of other components of the renin-angiotensin-aldosterone system. As a result of higher ACE2 expression, pregnant women may be at elevated risk for complications from SARS-CoV-2 infection. Upon binding to ACE2, SARS-CoV-2 causes its downregulation, thus lowering angiotensin-(1-7) levels, which can mimic/worsen the vasoconstriction, inflammation, and pro-coagulopathic effects that occur in preeclampsia. Indeed, early reports suggest that, among other adverse outcomes, preeclampsia may be more common in pregnant women with COVID-19. Medical therapy, during pregnancy and breastfeeding, relies on medications with proven safety, but safety data are often missing for medications in the early stages of clinical trials. We summarize guidelines for medical/obstetric care and outline future directions for optimization of treatment and preventive strategies for pregnant patients with COVID-19 with the understanding that relevant data are limited and rapidly changing.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引发的 2019 年冠状病毒病(COVID-19)全球大流行与包括老年人和患有慢性合并症的患者在内的多个患者群体的不良结局相关。先前的大流行和季节性流感数据表明,孕妇感染相关发病率和死亡率可能增加。正常妊娠的生理变化和高危妊娠的代谢和血管变化可能影响 COVID-19 的发病机制或使临床症状恶化。具体而言,SARS-CoV-2 通过血管紧张素转换酶 2(ACE2)受体进入细胞,而 ACE2 在正常妊娠中上调。ACE2 的上调介导血管紧张素 II(血管收缩剂)转化为血管紧张素-(1-7)(血管扩张剂),并导致相对较低的血压,尽管肾素-血管紧张素-醛固酮系统的其他成分上调。由于 ACE2 表达增加,孕妇可能面临 SARS-CoV-2 感染并发症的风险增加。SARS-CoV-2 与 ACE2 结合后会导致其下调,从而降低血管紧张素-(1-7)水平,这可能模拟/加重子痫前期发生的血管收缩、炎症和促凝血病。事实上,早期报告表明,在其他不良结局中,COVID-19 孕妇子痫前期可能更常见。妊娠期和哺乳期的医疗治疗依赖于已证实安全性的药物,但在临床试验的早期阶段,许多药物的安全性数据通常缺失。我们总结了医疗/产科护理指南,并概述了优化 COVID-19 孕妇治疗和预防策略的未来方向,需要理解的是,相关数据有限且正在迅速变化。