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High Plasma tPAPAI-1C Levels May Be Related to a Poor Prognosis in Patients with Severe or Critical COVID-19: A
Kunihiro Shirai1, Michiko Ishikawa1, Tomoyuki Kobayashi1
1Department of Emergency, Disaster and Critical Care Medicine, Hyogo Medical University, Nishinomiya 663-8501, Japan.
Insights
Severe COVID-19 patients often experience blood clots and death. This study found that higher levels of tissue plasminogen activator/plasminogen activator inhibitor-1 complex (tPAPAI-1C) predict poor outcomes in critical novel coronavirus disease 2019 (COVID-19) patients.
Area of Science:
- Hematology
- Critical Care Medicine
- Pathophysiology
Background:
- Severe novel coronavirus disease 2019 (COVID-19) is associated with high rates of thrombotic complications and mortality.
- The underlying pathophysiology involves coagulopathy, fibrinolytic system impairment, and vascular endothelial damage.
Purpose of the Study:
- To investigate coagulation and fibrinolytic markers as predictors of outcomes in severe COVID-19 patients.
- To identify specific hematological parameters associated with mortality in intensive care unit (ICU) admitted COVID-19 patients.
Main Methods:
- Retrospective observational study of 164 COVID-19 patients.
- Comparison of hematological parameters (platelets, PIC, tPAPAI-1C, D-dimer, FDP) on days 1, 3, 5, and 7 between survivors and nonsurvivors.
- Multivariate logistic regression analysis to identify independent predictors of mortality.
Main Results:
- Nonsurvivors had higher APACHE II, SOFA scores, and age compared to survivors.
- Nonsurvivors exhibited significantly lower platelet counts and higher levels of PIC, tPAPAI-1C, D-dimer, and FDP throughout the study period.
- Maximum tPAPAI-1C levels were identified as an independent predictor of mortality (AUC = 0.713).
Conclusions:
- COVID-19 patients with poor outcomes show exacerbated coagulopathy, fibrinolysis inhibition, and endothelial damage.
- Plasma tPAPAI-1C levels can serve as a valuable prognostic marker for severe or critical COVID-19.
- Monitoring tPAPAI-1C may aid in predicting patient outcomes and guiding treatment strategies.
Abstract:
Severe novel coronavirus disease 2019 (COVID-19) patients have a high incidence of thrombotic complications and mortality. The pathophysiology of coagulopathy involves fibrinolytic system impairment and vascular endothelial damage. This study examined coagulation and fibrinolytic markers as outcome predictors. In an observational study of 164 COVID-19 patients admitted to our emergency intensive care unit, hematological parameters on days 1, 3, 5, and 7 were retrospectively compared between survivors and nonsurvivors. Nonsurvivors had a higher APACHE II score, SOFA score, and age than survivors. Nonsurvivors also had a significantly lower platelet count and significantly higher plasmin/α2plasmin inhibitor complex (PIC), tissue plasminogen activator/plasminogen activator inhibitor-1 complex (tPAPAI-1C), D-dimer, and fibrin/fibrinogen degradation product (FDP) levels than survivors throughout the measurement period. The 7-day maximum or minimum values of the tPAPAI-1C, FDP, and D-dimer levels were significantly higher in nonsurvivors. A multivariate logistic regression analysis showed that the maximum tPAPAI-1C (OR = 1.034; 95% CI,1.014-1.061; p = 0.0041) was an independent factor affecting mortality, with an area under the curve (AUC) of 0.713 (optimum cut-off of 51 ng/mL; sensitivity, 69.2%; and specificity, 68.4%). COVID-19 patients with poor outcomes exhibit exacerbated coagulopathy with fibrinolysis inhibition and endothelial damage. Consequently, plasma tPAPAI-1C might be a useful predictor of the prognosis in patients with severe or critical COVID-19.
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