Major bleeding complications in critically ill patients with COVID-19 pneumonia

被引:40
作者
Godier, Anne [1 ,2 ,4 ]
Clausse, Darless [1 ]
Meslin, Simon [1 ]
Bazine, Myriame [1 ]
Lang, Elodie [1 ]
Huche, Florian [1 ]
Cholley, Bernard [1 ,2 ]
Hamada, Sophie Rym [1 ,3 ]
机构
[1] Univ Paris, Dept Anaesthesiol & Crit Care, European Georges Pompidou Hosp, AP HP, Paris, France
[2] Univ Paris, INSERM, UMRS 1140, Paris, France
[3] Univ Paris Saclay, Univ Paris Sud, CESP, INSERM, Paris, France
[4] Hop Pompidou, Serv Anesthesie Reanimat, 20 Rue Leblanc, F-75015 Paris, France
关键词
Anticoagulant; Bleeding; COVID-19; Fibrinogen; Inflammation; Thrombosis;
D O I
10.1007/s11239-021-02403-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As patients with COVID-19 pneumonia admitted to intensive care unit (ICU) have high rates of thrombosis, high doses of thromboprophylaxis have been proposed. The associated bleeding risk remains unknown. We investigated major bleeding complications in ICU COVID-19 patients and we examined their relationship with inflammation and thromboprophylaxis. Retrospective monocentric study of consecutive adult patients admitted in ICU for COVID-19 pneumonia requiring mechanical ventilation. Data collected included demographics, anticoagulation status, coagulation tests and outcomes including major bleeding and thrombotic events. Among 56 ICU COVID-19 patients, 10 (18%) patients had major bleeding and 16 (29%) thrombotic events. Major bleeding occurred later than thrombosis after ICU admission [17(14-23) days versus 9(3-11) days respectively (p = 0.005)]. Fibrinogen concentration always decreased several days [4(3-5) days] before bleeding; D-dimers followed the same trend. All bleeding patients were treated with anticoagulants and anticoagulation was overdosed for 6 (60%) patients on the day of bleeding or the day before. In the whole cohort, overdose was measured in 22 and 78% of patients receiving therapeutic anticoagulation during fibrinogen increase and decrease respectively (p < 0.05). Coagulation disorders had biphasic evolution during COVID-19: first thrombotic events during initial hyperinflammation, then bleeding events once inflammation reduced, as confirmed by fibrinogen and d-dimers decrease. Most bleeding events complicated heparin overdose, promoted by inflammation decrease, suggesting to carefully monitor heparin during COVID-19. Thromboprophylaxis may be adapted to this biphasic evolution, with initial high doses reduced to standard doses once the high thrombotic risk period ends and fibrinogen decreases, to prevent bleeding events.
引用
收藏
页码:18 / 21
页数:4
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