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Published on: February 28, 2012
Anticoagulation as a therapeutic strategy for hospitalised patients with COVID-19
S Cullivan1,2,3, M Sholzberg4,5, F Ní Áinle2,3,6,7,8
1Department of Respiratory Medicine, Mater Misericordiae University Hospital, Dublin, Ireland.
Insights
Therapeutic heparin anticoagulation showed no benefit for critically ill COVID-19 patients. However, it improved outcomes and survival for non-critically ill hospitalized patients with COVID-19.
Area of Science:
- Critical Care Medicine
- Pharmacology
- Infectious Diseases
Background:
- COVID-19 is linked to hypercoagulability and increased thrombosis risk, especially in critically ill patients.
- Early data suggested anticoagulants might improve outcomes beyond preventing clots in COVID-19.
- Randomized trials investigated therapeutic heparin's efficacy and safety in hospitalized COVID-19 patients.
Purpose of the Study:
- To evaluate the effect of therapeutic heparin anticoagulation on clinical outcomes in hospitalized COVID-19 patients.
- To determine if therapeutic heparin improves organ support-free days and reduces mortality.
- To assess differential effects in critically ill versus non-critically ill patients.
Main Methods:
- Summarized data from three major randomized controlled trials: REMAP-CAP, ACTIV-4a, ATTACC, and the RAPID trial.
- Compared therapeutic heparin with usual care or prophylactic heparin in hospitalized COVID-19 patients.
- Analyzed outcomes including organ support-free days, mechanical ventilation, ICU admission, and all-cause mortality.
Main Results:
- Therapeutic heparin did not benefit critically ill COVID-19 patients (OR 0.83; futility 99.9%).
- In non-critically ill patients, therapeutic heparin increased organ support-free days (OR 1.27).
- The RAPID trial showed therapeutic heparin did not significantly reduce composite outcomes but lowered all-cause mortality (OR 0.22) in non-critically ill patients.
Conclusions:
- Therapeutic heparin may reduce illness severity and improve survival in hospitalized, non-critically ill COVID-19 patients.
- No benefit was observed for therapeutic heparin in critically ill COVID-19 patients.
- Treatment decisions for therapeutic heparin in moderately ill COVID-19 patients should be individualized.
Abstract:
The COVID-19 pandemic has devastated the global community and continues to cause significant morbidity and mortality worldwide. The development of effective vaccines has represented a major step towards reducing transmission and illness severity but significant challenges remain, particularly in regions where vaccine access has been limited. COVID-19 is associated with hypercoagulability and increased risk of thrombosis, with greatest risk among the critically ill. Interestingly, early observational data suggested that anticoagulant therapy might improve clinical outcomes, aside from thrombotic events, in patients with COVID-19. In this review we summarise data generated from three published randomised clinical trials which have sought to determine the effect of therapeutic heparin anticoagulation on efficacy and safety outcomes in hospitalised patients with COVID-19: the multiplatform REMAP-CAP, ACTIV-4a and ATTACC randomised controlled trials and the RAPID trial. In the multiplatform REMAP-CAP, ACTIV-4a and ATTACC randomised controlled trials, therapeutic heparin was not associated with benefit in critically ill patients with COVID-19 compared with usual care (adjusted proportional odds ratio (OR) for increased organ-support free days up to day 21: 0.83; 95% credible interval, 0.67-1.03, posterior probability of futility 99.9%). Conversely, among hospitalised patients without critical illness, therapeutic heparin was associated with an increased probability of organ support-free days alive (adjusted OR, 1.27; 95% credible interval, 1.03-1.58). The RAPID trial also evaluated the effect of therapeutic heparin compared with prophylactic heparin in non-critically ill patients. In this study, therapeutic heparin did not significantly reduce the odds of the primary composite outcome (death, mechanical ventilation or intensive care unit admission) (OR 0.69; 95% confidence interval [CI], 0.43 to 1.10; p = 0.12) but was associated with a significant reduction in all-cause mortality [OR, 0.22 (95%-CI, 0.07 to 0.65)]. Collectively these studies suggest that therapeutic anticoagulation with heparin may reduce the severity of illness and potentially even confer a survival benefit in hospitalised, non-critically ill patients with COVID-19. No benefit for therapeutic anticoagulation with heparin was evident in critically ill patients with COVID-19. Therefore, while the results of additional studies in this evolving field are pending, it is important to approach decisions regarding therapeutic heparin in moderately ill hospitalised patients with COVID-19 in a measured and individualised manner.
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