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Published on: February 10, 2023
Venous Thromboembolism Management throughout the COVID-19 Era: Addressing Acute and Long-Term Challenges
Maddalena Alessandra Wu1,2, Alba Taino1, Pietro Facchinetti3
1Division of Internal Medicine, ASST Fatebenefratelli Sacco, Luigi Sacco Hospital, University of Milan, 20156 Milan, Italy.
Insights
COVID-19 patients with venous thromboembolism (VTE) showed fewer comorbidities and a lower mortality rate compared to non-COVID-19 patients. Management involved shorter anticoagulation courses for COVID-19-associated VTE, with no fatalities observed in this group.
Area of Science:
- Cardiology
- Infectious Diseases
- Hematology
Background:
- COVID-19 is linked to an increased risk of venous thromboembolism (VTE) via immunothrombosis mechanisms.
- Limited data compare VTE management and outcomes in acute and long-term follow-up between COVID-19 and non-COVID-19 patients.
Purpose of the Study:
- To investigate and compare the acute and long-term management and complications of VTE in patients with and without COVID-19.
Main Methods:
- Prospective, observational, single-center cohort study.
- Follow-up of VTE patients from acute care to 24 months post-diagnosis.
- Comparison of clinical characteristics, treatment, and outcomes between COVID-19-associated VTE and non-COVID-19 VTE cohorts.
Main Results:
- 157 patients (30 COVID-19, 127 non-COVID-19) were enrolled with a mean follow-up of 10.8 months.
- COVID-19 patients had fewer comorbidities, a higher proportion of pulmonary embolism at baseline, and a lower probability of remaining on anticoagulation therapy after three months.
- No fatalities occurred in COVID-19 patients, contrasting with a 9.4% mortality rate in the non-COVID-19 group (p=0.027). Major hemorrhagic events and VTE recurrence rates were similar between groups.
Conclusions:
- COVID-19-associated VTE patients demonstrate distinct clinical characteristics and outcomes, including significantly lower mortality.
- Personalized, risk-based approaches are crucial for VTE management, potentially involving shorter anticoagulation courses for COVID-19 patients.
- Further research into tailored anticoagulation strategies for different VTE risk subsets is warranted.
Abstract:
Background: COVID-19 increases the risk of venous thromboembolism (VTE) through a complex interplay of mechanisms collectively referred to as immunothrombosis. Limited data exist on VTE challenges in the acute setting throughout a dynamic long-term follow-up of COVID-19 patients compared to non-COVID-19 patients. The aim of the study was to investigate acute and long-term management and complications in VTE patients with and without COVID-19. Methods: A prospective, observational, single-center cohort study on VTE patients followed from the acute care stage until 24 months post-diagnosis. Results: 157 patients, 30 with COVID-19-associated VTE and 127 unrelated to COVID-19, were enrolled. The mean follow-up was 10.8 (±8.9) months. COVID-19 patients had fewer comorbidities (1.3 ± 1.29 vs. 2.26 ± 1.68, p < 0.001), a higher proportion of pulmonary embolism at baseline (96.7% vs. 76.4%, p = 0.01), and had a lower probability of remaining on anticoagulant therapy after three months (p < 0.003). The most used initial therapy was low-molecular-weight heparin in 130/157 cases, followed by long-term treatment with direct oral anticoagulants in 123/157. Two (6.7%) COVID-19 vs. three (2.4%) non-COVID-19 patients (p = 0.243) had major hemorrhagic events, all of them within the first three months. Four (3.1%) non-COVID-19 patients had VTE recurrence after six months. Three (2.4%) non-COVID-19 patients developed chronic thromboembolic pulmonary hypertension. There were no fatalities among patients with COVID-19, compared to a mortality of 12/127 (9.4%) in the non-COVID-19 subgroup (p = 0.027). Discussion: Our study offers a comprehensive overview of the evolving nature of VTE management, emphasizing the importance of personalized risk-based approaches, including a limited course of anticoagulation for most COVID-19-associated VTE cases and reduced-dose extended therapy for high-risk subsets.
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