Service de Médecine Intensive Réanimation, Nouvel Hôpital Civil, Hôpitaux universitaires de Strasbourg, 1, Place de l'Hôpital, 67091, Strasbourg Cedex, France.
ImmunoRhumatologie Moléculaire, INSERM UMR_S1109, LabEx TRANSPLANTEX, Centre de Recherche d'Immunologie et d'Hématologie, Faculté de Médecine, Fédération Hospitalo-Universitaire (FHU) OMICARE, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg (UNISTRA), Strasbourg, France.
Intensive Care Med. 2020 Jun;46(6):1089-1098. doi: 10.1007/s00134-020-06062-x. Epub 2020 May 4.
Little evidence of increased thrombotic risk is available in COVID-19 patients. Our purpose was to assess thrombotic risk in severe forms of SARS-CoV-2 infection.
All patients referred to 4 intensive care units (ICUs) from two centers of a French tertiary hospital for acute respiratory distress syndrome (ARDS) due to COVID-19 between March 3rd and 31st 2020 were included. Medical history, symptoms, biological data and imaging were prospectively collected. Propensity score matching was performed to analyze the occurrence of thromboembolic events between non-COVID-19 ARDS and COVID-19 ARDS patients.
150 COVID-19 patients were included (122 men, median age 63 [53; 71] years, SAPSII 49 [37; 64] points). Sixty-four clinically relevant thrombotic complications were diagnosed in 150 patients, mainly pulmonary embolisms (16.7%). 28/29 patients (96.6%) receiving continuous renal replacement therapy experienced circuit clotting. Three thrombotic occlusions (in 2 patients) of centrifugal pump occurred in 12 patients (8%) supported by ECMO. Most patients (> 95%) had elevated D-dimer and fibrinogen. No patient developed disseminated intravascular coagulation. Von Willebrand (vWF) activity, vWF antigen and FVIII were considerably increased, and 50/57 tested patients (87.7%) had positive lupus anticoagulant. Comparison with non-COVID-19 ARDS patients (n = 145) confirmed that COVID-19 ARDS patients (n = 77) developed significantly more thrombotic complications, mainly pulmonary embolisms (11.7 vs. 2.1%, p < 0.008). Coagulation parameters significantly differed between the two groups.
Despite anticoagulation, a high number of patients with ARDS secondary to COVID-19 developed life-threatening thrombotic complications. Higher anticoagulation targets than in usual critically ill patients should therefore probably be suggested.
在 COVID-19 患者中,几乎没有增加血栓形成风险的证据。我们的目的是评估严重 SARS-CoV-2 感染患者的血栓形成风险。
本研究纳入了 2020 年 3 月 3 日至 31 日期间,因 COVID-19 导致急性呼吸窘迫综合征(ARDS)而被转诊至法国两家三级医院 4 个重症监护病房(ICU)的所有患者。前瞻性收集了患者的病史、症状、生物学数据和影像学结果。采用倾向评分匹配分析非 COVID-19 ARDS 和 COVID-19 ARDS 患者的血栓栓塞事件发生情况。
共纳入 150 例 COVID-19 患者(男 122 例,中位年龄 63[53;71]岁,SAPSII 49[37;64]分)。150 例患者中诊断出 64 例有临床意义的血栓并发症,主要为肺栓塞(16.7%)。29 例(96.6%)接受连续肾脏替代治疗的患者发生了体外循环凝血。12 例(8%)接受 ECMO 支持的患者中有 3 例发生了离心泵血栓阻塞(2 例患者各 1 例)。大多数患者(>95%)的 D-二聚体和纤维蛋白原水平升高。无患者发生弥漫性血管内凝血。血管性血友病因子(vWF)活性、vWF 抗原和 FVIII 显著升高,57 例检测患者中有 50 例(87.7%)存在狼疮抗凝物阳性。与非 COVID-19 ARDS 患者(n=145)比较证实,COVID-19 ARDS 患者(n=77)发生血栓并发症的比例显著更高,主要为肺栓塞(11.7%比 2.1%,p<0.008)。两组间凝血参数存在显著差异。
尽管进行了抗凝治疗,仍有大量 COVID-19 相关性 ARDS 患者发生危及生命的血栓并发症。因此,此类患者的抗凝目标可能需要高于一般危重症患者。