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Published on: February 26, 2013
Antithrombotic Therapy for Patients With Left Ventricular Mural Thrombus
Benoit Lattuca1, Nesrine Bouziri1, Mathieu Kerneis1
1Sorbonne Université, ACTION Study Group, INSERM UMR_S 1166, Institut de Cardiologie, Pitié-Salpêtrière Hospital (AP-HP), Paris, France.
Insights
Left ventricular thrombus (LVT) is linked to high risks. Anticoagulant therapy can lead to LVT regression, reducing mortality but potentially increasing bleeding risk. Further research is needed for optimal management.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Thrombosis Management
Background:
- Contemporary data on left ventricular thrombus (LVT) prognosis and management are limited.
- Understanding LVT evolution and treatment outcomes is crucial for patient care.
Purpose of the Study:
- To quantify the effect of anticoagulation therapy on LVT evolution using sequential imaging.
- To determine the impact of LVT regression on thromboembolism, bleeding, and mortality.
Main Methods:
- Retrospective analysis of 90,065 echocardiogram reports from January 2011 to January 2018.
- Inclusion of 159 patients with confirmed LVT, assessing treatment with anticoagulants and antiplatelets.
- Evaluation of major adverse cardiovascular events (MACE), major bleeding, and all-cause mortality during follow-up.
Main Results:
- LVT regression occurred in 62.3% of patients within a median of 103 days; nonischemic cardiomyopathy and smaller baseline thrombus size were correlates.
- The overall incidence of MACE was 37.1%, mortality 18.9%, stroke 13.3%, and major bleeding 13.2%.
- Total LVT regression was associated with reduced mortality (HR: 0.48) but persistent LVT increased major bleeding risk (HR: 0.34).
Conclusions:
- Left ventricular thrombus (LVT) presence is associated with high risks of MACE and mortality.
- Anticoagulant therapy can achieve LVT regression, which is linked to decreased mortality.
- Optimizing anticoagulation duration and considering factors like LVEF are important for managing LVT patients.
Background:
Contemporary data are lacking regarding the prognosis and management of left ventricular thrombus (LVT).
Objectives:
The purpose of this study was to quantify the effect of anticoagulation therapy on LVT evolution using sequential imaging and to determine the impact of LVT regression on the incidence of thromboembolism, bleeding, and mortality.
Methods:
From January 2011 to January 2018, a comprehensive computerized search of LVT was conducted using 90,065 consecutive echocardiogram reports. Only patients with a confirmed LVT were included after imaging review by 2 independent experts. Major adverse cardiovascular events (MACE), which included death, stroke, myocardial infarction, or acute peripheral artery emboli, were determined as well as major bleeding events (BARC ≥3) and all-cause mortality rates.
Results:
There were 159 patients with a confirmed LVT. Patients were treated with vitamin K antagonists (48.4%), parenteral heparins (27.7%), and direct oral anticoagulants (22.6%). Antiplatelet therapy was used in 67.9% of the population. A reduction of the LVT area from baseline was observed in 121 patients (76.1%), and total LVT regression occurred in 99 patients (62.3%) within a median time of 103 days (interquartile range: 32 to 392 days). The independent correlates of LVT regression were a nonischemic cardiomyopathy (hazard ratio [HR]: 2.74; 95% confidence interval [CI]: 1.43 to 5.26; p = 0.002) and a smaller baseline thrombus area (HR: 0.66; 95% CI: 0.45 to 0.96; p = 0.031). The frequency of MACE was 37.1%; mortality 18.9%; stroke 13.3%; and major bleeding 13.2% during a median follow-up of 632 days (interquartile range: 187 to 1,126 days). MACE occurred in 35.4% and 40.0% of patients with total LVT regression and those with persistent LVT (p = 0.203). A reduced risk of mortality was observed among patients with total LVT regression (HR: 0.48; 95% CI: 0.23 to 0.98; p = 0.039), whereas an increased major bleeding risk was observed among patients with persistent LVT (9.1% vs. 12%; HR 0.34; 95% CI: 0.14 to 0.82; p = 0.011). A left ventricular ejection fraction ≥35% (HR: 0.46; 95% CI: 0.23 to 0.93; p = 0.029) and anticoagulation therapy >3 months (HR: 0.42; 95% CI: 0.20 to 0.88; p = 0.021) were independently associated with less MACE.
Conclusions:
The presence of LVT was associated with a very high risk of MACE and mortality. Total LVT regression, obtained with different anticoagulant regimens, was associated with reduced mortality.
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