Coagulation Studies Are Not Predictive of Hematological Complications of COVID-19 Infection.

Sarah Hadique, Varun Badami, Rahul Sangani, Michael Forte, Talia Alexander, Aarti Goswami, Adriana Garrison, Sijin Wen
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Abstract

Objectives  Thrombotic and bleeding complications are common in COVID-19 disease. In a prospective study, we performed a comprehensive panel of tests to predict the risk of bleeding and thrombosis in patients admitted with hypoxic respiratory failure due to severe COVID-19 infection. Methods  We performed a single center (step down and intensive care unit [ICU] at a quaternary care academic hospital) prospective study. Sequentially enrolled adult (≥18 years) patients were admitted with acute hypoxic respiratory failure due to COVID-19 between June 2020 and November 2020. Several laboratory markers of coagulopathy were tested after informed and written consent. Results  Thirty-three patients were enrolled. In addition to platelet counts, prothrombin time, and activated partial thromboplastin time, a series of protocol laboratories were collected within 24 hours of admission. These included Protein C, Protein S, Antithrombin III, ADAMTS13, fibrinogen, ferritin, haptoglobin, and peripheral Giemsa smear. Patients were then monitored for the development of hematological (thrombotic and bleeding) events and followed for 30 days after discharge. Twenty-four patients (73%) required ICU admissions. At least one laboratory abnormality was detected in 100% of study patients. Nine patients (27%) suffered from significant hematological events, and four patients had a clinically significant bleeding event requiring transfusion. No significant association was observed between abnormalities of coagulation parameters and the incidence of hematologic events. However, a higher SOFA score (10.89 ± 3.48 vs. 6.92 ± 4.10, p  = 0.016) and CKD (5/9 [22.2%] vs. 2/24 [12.5%] p  = 0.009) at baseline were associated with the development of hematologic events. 33.3% of patients died at 30 days. Mortality was similar in those with and without hematological events. Reduced ADAMTS13 level was significantly associated with mortality. Conclusion  Routine extensive testing of coagulation parameters did not predict the risk of bleeding and thrombosis in COVID-19 patients. Thrombotic and bleeding events in COVID-19 patients are not associated with a higher risk of mortality. Interestingly, renal dysfunction and a high SOFA score were found to be associated with increased risk of hematological events.

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凝血研究不能预测COVID-19感染的血液学并发症。
目的血栓和出血并发症在COVID-19疾病中很常见。在一项前瞻性研究中,我们进行了一组全面的测试,以预测因严重COVID-19感染而入院的缺氧呼吸衰竭患者出血和血栓形成的风险。方法我们进行了一项单中心前瞻性研究(一家四级护理学术医院的重症监护病房[ICU])。顺序入组的成人(≥18岁)患者于2020年6月至2020年11月因COVID-19引起的急性缺氧呼吸衰竭入院。在知情和书面同意后,测试了几种凝血功能障碍的实验室标志物。结果33例患者入组。除了血小板计数、凝血酶原时间和活化的部分凝血活酶时间外,入院24小时内收集了一系列方案实验室。包括蛋白C、蛋白S、抗凝血酶III、ADAMTS13、纤维蛋白原、铁蛋白、触珠蛋白和外周吉姆萨涂片。然后监测患者血液学(血栓形成和出血)事件的发展,并在出院后随访30天。24例患者(73%)需要进入ICU。在100%的研究患者中至少检测到一种实验室异常。9名患者(27%)出现了严重的血液学事件,4名患者出现了临床上显著的出血事件,需要输血。未观察到凝血参数异常与血液学事件发生率之间的显著关联。然而,基线时较高的SOFA评分(10.89±3.48比6.92±4.10,p = 0.016)和CKD(5/9[22.2%]比2/24 [12.5%]p = 0.009)与血液学事件的发生有关。33.3%的患者在30天内死亡。有和没有血液学事件的死亡率相似。ADAMTS13水平降低与死亡率显著相关。结论常规广泛检测凝血参数不能预测COVID-19患者出血和血栓形成的风险。COVID-19患者的血栓和出血事件与较高的死亡风险无关。有趣的是,肾功能不全和高SOFA评分被发现与血液学事件风险增加有关。
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