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Elevated Troponin, D-Dimers and D-Dimers/Fibrinogen Ratio Increase Mortality Risk in Remdesivir-Treated COVID-19
Georgia Ragia1,2, Gavriela Voulgaridou1,2, Vasileios Tsirozis3
1Laboratory of Pharmacology, Medical School, Democritus University of Thrace, Dragana Campus, 68100 Alexandroupolis, Greece.
Insights
Biomarkers like troponin and D-dimers predict mortality in COVID-19 patients treated with remdesivir. Remdesivir treatment impacts coagulation markers, potentially mitigating hypercoagulability and improving outcomes.
Area of Science:
- Biochemistry
- Critical Care Medicine
- Pharmacology
Background:
- Effective COVID-19 treatment requires monitoring biomarkers linked to severe illness and death.
- Identifying prognostic markers is crucial for patient management.
Purpose of the Study:
- To evaluate troponin, D-dimers, fibrinogen, and D-dimers/fibrinogen ratio (DFR) as mortality predictors in remdesivir-treated COVID-19 patients.
- To assess remdesivir's impact on these biomarkers during treatment.
Main Methods:
- Retrospective analysis of 549 hospitalized COVID-19 patients treated with remdesivir.
- Evaluation of demographic, biochemical, and clinical data.
- Statistical analysis of mortality risk and biomarker level changes.
Main Results:
- Elevated baseline troponin and D-dimers increased mortality risk.
- Post-remdesivir treatment, elevated troponin, D-dimers, and DFR remained associated with higher death risk.
- Remdesivir decreased fibrinogen in both survivors and non-survivors.
- Remdesivir decreased troponin and D-dimers in survivors but increased DFR and D-dimers in non-survivors.
Conclusions:
- Troponin, D-dimers, and DFR are critical predictors of mortality in remdesivir-treated COVID-19 patients.
- Remdesivir treatment influences coagulation biomarkers, potentially counteracting COVID-19-induced hypercoagulability.
- These biomarkers can help identify high-risk patients for targeted interventions.
Abstract:
Background/Objectives: Identification, monitoring, and modulation of biochemical markers that increase risk of severe illness and death from COVID-19 are crucial for effective disease treatment. This study aims to investigate the prognostic value of baseline troponin, D-dimers, fibrinogen, and D-dimers/fibrinogen ratio (DFR) as biomarkers for mortality in remdesivir-treated patients, and additionally, to investigate the impact of remdesivir treatment on troponin, D-dimers, fibrinogen, and DFR levels during disease course. Methods: We retrospectively analyzed the demographic, biochemical, and clinical characteristics of 549 (47.5% male, mean age 69.6 ± 14.7) hospitalized COVID-19 patients, all treated with remdesivir. Results: A total of 106 patients (19.3%) died during hospitalization. Elevated baseline troponin levels and D-dimers increased risk of death (HR 2.374, 95% CI 1.343-4.197; p = 0.003, adjusted for comorbidities and HR 1.862, 95% CI 1.127-3.076, p = 0.015, unadjusted, respectively). After remdesivir treatment, death risk was increased by elevated troponin (HR 2.010, 95% CI 1.219-3.316, p = 0.006), D-dimers (HR 2.207, 95% CI 1.254-3.882, p = 0.006) and DFR (HR, 3.816, 95% CI 1.567-9.291, p = 0.003) levels, in models adjusted for age, sex, and comorbidities. Remdesivir treatment decreased fibrinogen levels both in survivors (p < 0.001) and non-survivors (p < 0.001). In survivors, remdesivir treatment significantly decreased troponin levels (p < 0.001) and D-dimers (p < 0.001), whereas in non-survivors, it increased DFR (p < 0.001) and D-dimers (p < 0.001). Conclusions: In addition to its antiviral action, remdesivir treatment was associated with changes in coagulation biomarkers, potentially preventing patients from the COVID-19-provoked hypercoagulable state. Troponin, D-dimers, and DFR hold a critical role in predicting mortality risk among COVID-19 patients treated with remdesivir and can aid in identifying individuals at increased risk of death.
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