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10.1097/ALN.0000000000003685

http://scihub22266oqcxt.onion/10.1097/ALN.0000000000003685
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33417674!7864605!33417674
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suck abstract from ncbi


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pmid33417674      Anesthesiology 2021 ; 134 (3): 457-467
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  • Greater Fibrinolysis Resistance but No Greater Platelet Aggregation in Critically Ill COVID-19 Patients #MMPMID33417674
  • Heinz C; Miesbach W; Herrmann E; Sonntagbauer M; Raimann FJ; Zacharowski K; Weber CF; Adam EH
  • Anesthesiology 2021[Mar]; 134 (3): 457-467 PMID33417674show ga
  • BACKGROUND: The hemostatic balance in patients with coronavirus disease 2019 (COVID-19) seems to be shifted toward a hypercoagulable state. The aim of the current study was to assess the associated coagulation alterations by point-of-care-diagnostics, focusing on details of clot formation and lysis in these severely affected patients. METHODS: The authors' prospective monocentric observational study included critically ill patients diagnosed with COVID-19. Demographics and biochemical data were recorded. To assess the comprehensive hemostatic profile of this patient population, aggregometric (Multiplate) and viscoelastometric (CloPro) measures were performed in the intensive care unit of a university hospital at a single occasion. Coagulation analysis and assessment of coagulation factors were performed. Data were compared to healthy controls. RESULTS: In total, 27 patients (21 male; mean age, 60 yr) were included. Impedance aggregometry displayed no greater platelet aggregability in COVID-19 in comparison with healthy controls (area under the curve [AUC] in adenosine diphosphate test, 68 +/- 37 U vs. 91 +/- 29 U [-27 (Hodges-Lehmann 95% CI, -48 to -1); P = 0.043]; AUC in arachidonic acid test, 102 +/- 54 U vs. 115 +/- 26 U [-21 (Hodges-Lehmann 95% CI, -51 to 21); P = 0.374]; AUC in thrombin receptor activating peptide 6 test, 114 +/- 61 U vs. 144 +/- 31 U [-31 (Hodges-Lehmann 95% CI, -69 to -7); P = 0.113]). Comparing the thromboelastometric results of COVID-19 patients to healthy controls, the authors observed significant differences in maximum clot firmness in fibrin contribution to maximum clot firmness assay (37 +/- 11 mm vs. 15 +/- 4 mm [21 (Hodges-Lehmann 95% CI, 17 to 26); P < 0.001]) and lysis time in extrinsic activation and activation of fibrinolysis by tissue plasminogen activator assay (530 +/- 327 s vs. 211 +/- 80 s [238 (Hodges-Lehmann 95% CI, 160 to 326); P < 0.001]). CONCLUSIONS: Thromboelastometry in COVID-19 patients revealed greater fibrinolysis resistance. The authors did not find a greater platelet aggregability based on impedance aggregometric tests. These findings may contribute to our understanding of the hypercoagulable state of critically ill patients with COVID-19.
  • |*COVID-19[MESH]
  • |*Fibrinolysis[MESH]
  • |Critical Illness[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Platelet Aggregation[MESH]
  • |Prospective Studies[MESH]
  • |SARS-CoV-2[MESH]
  • |Thrombelastography[MESH]


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