Hemostatic imbalance underlying preterm delivery in COVID-19 convalescent patients

Q3 Medicine
M. G. Nikolaeva, A. V. Korchagina, A. Momot, E. V. Grigoreva
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引用次数: 0

Abstract

Aim: to study the role of the hemostatic system in pretem delivery in pregnant women who have had COVID-19 in the gestation period from 14 to 16 weeks.Materials and Methods. A prospective single-center observational study was conducted by enrolling 63 pregnant women with verified COVID-19 at 14–16 weeks of gestation. The main group consisted of 37 patients with preterm birth (PB), comparison group – 26 patients labour activity that occurred at least at gestational age of 37 weeks. Clinical and anamnestic data and dynamic changes in fibrinogen and D-dimer level, activity of tissue factor (TF), tissue factor pathway inhibitor (TFPI), plasminogen activator inhibitor-1 (PAI-1), tissue plasminogen activator (t-PA), urokinase plasminogen activator (u-PA) were analyzed; thrombin generation assay (TGA) was performed.Results. It was found that severity of COVID-19 infection did not determine the timing of delivery that depended on patient comorbid condition. All PB observations (37 out of 63, 58.7 %) were caused by decompensated placental function manifested by acute obstetrical complications: increasing intrauterine fetal hypoxia (64.9 %) along with intrauterine growth retardation (51.4 %), severe preeclampsia (13.5 %) and premature abruption of the normally located placenta (5.0 %). In both study groups, COVID-19 experienced at 14–16 weeks of pregnancy was associated with coagulation and fibrinolytic imbalances. At the same time, at least 6 weeks post-COVID-19 infection, patients with PB had higher level of the “Peak thrombin” vs. comparison group (3050 vs. 2527 pmol/L; p = 0.0433). Also, patients with term vs. preterm delivery had TF activity decreased significantly: by 47.1% and 28.1%, respectively (p = 0.0546). Patients in preterm delivery group were characterized by fibrinolytic imbalance. At the first time point, suppressed fibrinolysis (PAI-1 level – 18.4 vs. 12.5 ng/ml in the comparison group; p = 0.0209) was concomitant with elevated level of u-PA (1.5 vs. 0.55 ng/ml in comparison group, p = 0.0015), which suggests a potential prolonged immunoinflammatory response in patients with PB. Magnitude of fibrinogen concentration and D-dimer level during post-COVID-19 follow-up study was within the reference values specific to gestational age.Conclusion. A significant increase in coagulation potential was found and verified by elevated activity of tissue factor and potential to thrombin generation in COVID-19 convalescent patients. In the case of preterm delivery, there was an imbalance in fibrinolysis system revealed by decreased blood fibrinolytic activity elevating along with increasing gestational age.
COVID-19康复患者早产背后的止血失衡问题
目的:研究止血系统在孕 14-16 周 COVID-19 孕妇预产期中的作用。该研究是一项前瞻性的单中心观察研究,共招募了 63 名在妊娠 14-16 周时确诊为 COVID-19 的孕妇。主组包括 37 名早产(PB)患者,对比组--26 名至少在孕 37 周时有分娩活动的患者。分析了临床和病理数据、纤维蛋白原和 D-二聚体水平的动态变化、组织因子(TF)、组织因子通路抑制剂(TFPI)、纤溶酶原激活剂抑制剂-1(PAI-1)、组织纤溶酶原激活剂(t-PA)、尿激酶纤溶酶原激活剂(u-PA)的活性,并进行了凝血酶生成测定(TGA)。结果发现,COVID-19感染的严重程度并不能决定分娩时间,分娩时间取决于患者的合并症。所有 PB 观察结果(63 例中的 37 例,58.7%)均由胎盘功能失代偿引起,表现为急性产科并发症:胎儿宫内缺氧加重(64.9%)、宫内发育迟缓(51.4%)、重度子痫前期(13.5%)和正常位置胎盘早剥(5.0%)。在两个研究组中,怀孕 14-16 周时出现的 COVID-19 与凝血和纤溶失衡有关。同时,在感染 COVID-19 后至少 6 周,PB 患者的 "凝血酶峰值 "水平高于对比组(3050 vs. 2527 pmol/L;p = 0.0433)。此外,与早产患者相比,足月产患者的凝血酶活性显著降低:分别降低了 47.1%和 28.1%(p = 0.0546)。早产组患者的特点是纤维蛋白溶解失衡。在第一个时间点,纤溶受抑(PAI-1 水平为 18.4 ng/ml 对对比组的 12.5 ng/ml;p = 0.0209)的同时,u-PA 水平升高(1.5 ng/ml 对对比组的 0.55 ng/ml;p = 0.0015),这表明早产儿患者可能会出现持续的免疫炎症反应。在COVID-19后的随访研究中,纤维蛋白原浓度和D-二聚体水平的幅度均在孕龄的参考值范围内。COVID-19康复患者的凝血潜能明显增加,组织因子活性和凝血酶生成潜能的升高证实了这一点。在早产病例中,血液纤维蛋白溶解活性随着胎龄的增加而升高,显示出纤维蛋白溶解系统的失衡。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
68
审稿时长
12 weeks
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