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Published on: November 26, 2013
Thromboprophylaxis and clinical outcomes in moderate COVID-19 patients: A comparative study
Asmaa S Mohamed1, Hosam M Ahmad2, Alyaa S A Abdul-Raheem3
1Clinical Pharmacy Department, Faculty of Pharmacy, Port Said University, Port Said, Egypt.
Insights
Enoxaparin and rivaroxaban showed similar efficacy and safety for preventing blood clots in moderate COVID-19 patients. Neither anticoagulant demonstrated a clear advantage in clinical outcomes or complications.
Area of Science:
- Internal Medicine
- Pharmacology
- Infectious Diseases
Background:
- Coronavirus disease 2019 (COVID-19) is associated with a high risk of thrombotic complications.
- Antithrombotic therapy is crucial for preventing these events in COVID-19 patients.
Purpose of the Study:
- To compare the efficacy and safety of enoxaparin versus rivaroxaban for thromboprophylaxis in moderate COVID-19.
- To evaluate clinical outcomes, including mortality and complication rates, between the two anticoagulant groups.
Main Methods:
- A study involving 124 patients with moderate COVID-19 (pneumonia without hypoxia).
- Patients were randomized to receive either enoxaparin (0.5 mg/kg SC every 12h) or rivaroxaban (10 mg orally once daily) until hospital discharge.
- Outcomes assessed included ICU transfer, length of stay, mortality, and thrombotic/bleeding complications.
Main Results:
- No significant differences were found in intermediate care unit (IMCU) duration, ICU duration, or total hospital stay between enoxaparin and rivaroxaban groups.
- The rates of ICU admission, in-hospital mortality, thrombotic complications, and mild bleeding were comparable between the two treatment arms.
- Specific p-values indicated no statistically significant variations in any of the primary or secondary outcomes.
Conclusions:
- Enoxaparin and rivaroxaban can be utilized as effective thromboprophylaxis agents in patients with moderate COVID-19.
- Current evidence suggests no definitive advantage of one agent over the other in this patient population.
Background:
Many thrombotic complications are linked to coronavirus disease 2019 (COVID-19). Antithrombotic treatments are important for prophylaxis against these thrombotic events.
Objectives:
This study was designed to compare enoxaparin and rivaroxaban as prophylactic anticoagulants in moderate cases of COVID-19 in terms of efficacy, safety, and clinical outcomes.
Methods:
The study involved 124 patients with moderate COVID-19 (pneumonia without hypoxia) divided into two groups. The first group (G1) comprised 66 patients who received enoxaparin subcutaneously at a dose of 0.5 mg/kg every 12 h until discharge from the hospital. The second group (G2) comprised 58 patients who received oral rivaroxaban at a dose of 10 mg once daily until discharge from the hospital. The outcomes evaluated in this study were as follows: intermediate care unit (IMCU) duration, the number of patients transferred from the IMCU to the intensive care unit (ICU), ICU duration, the total length of hospital stay, in-hospital mortality, and thrombotic and bleeding complications.
Results:
No significant differences in IMCU duration (p = 0.39), ICU duration (p = 0.96), and total length of hospital stay (p = 0.73) were observed between the two groups. The percentage of patients requiring ICU admission after hospitalization was 21.2% in G1 and 22.4% in G2 (p = 0.87). The mortality rate was 12.1% in G1 and 10.3% in G2 (p = 0.76). The proportion of patients who had thrombotic complications was 9.1% in G1 and 12.1% in G2 (p = 0.59). The incidence of mild bleeding was 3% in G1 and 1.7% in G2 (p = 0.64).
Conclusion:
Either enoxaparin or rivaroxaban may be used as thromboprophylaxis agents in managing patients with moderate COVID-19. Either medication has no clear advantage over the other.
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