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Published on: February 26, 2013
Incidence and impact of atrial arrhythmias on thrombotic events in MPNs
Kristell Mahé1, Aurélien Delluc2,3, Aurélie Chauveau4
1Service d'Hématologie Clinique, Institut de Cancéro-Hématologie, Hôpital Morvan, CHRU de Brest, Avenue Foch, 29609, Brest Cedex, France.
Insights
Atrial arrhythmias (AA) significantly increase thrombosis risk in patients with essential thrombocythemia (ET) or polycythemia vera (PV). Careful management of anticoagulants like low-dose aspirin (LDA), vitamin K antagonists (VKA), or direct oral anticoagulants (DOAC) is crucial.
Area of Science:
- Cardiology
- Hematology
- Thrombosis Research
Background:
- Atrial arrhythmias (AA) are associated with increased thrombotic events, necessitating anticoagulation with vitamin K antagonists (VKA) or direct oral anticoagulants (DOAC).
- Essential thrombocythemia (ET) and polycythemia vera (PV) are myeloproliferative neoplasms (MPN) that also carry a high risk of thrombosis, typically managed with cytoreductive therapy and low-dose aspirin (LDA).
Purpose of the Study:
- To investigate the incidence and complications of atrial arrhythmias (AA) in patients diagnosed with essential thrombocythemia (ET) or polycythemia vera (PV).
- To evaluate the impact of AA on thrombotic risk and survival in patients with ET or PV.
- To assess the effectiveness and safety of current antithrombotic strategies in this patient population.
Main Methods:
- A case-control study was conducted involving 713 patients with ET or PV.
- Identified 96 patients (13.5%) with co-existing atrial arrhythmias (AA).
- Compared demographic data, cardiovascular risk factors, thrombosis history, and survival outcomes between patients with and without AA.
Main Results:
- Patients with AA were older (median 72.1 vs. 61.3 years) and had more cardiovascular risk factors (80% vs. 61%).
- A significantly higher incidence of thrombosis was observed before (27.1% vs. 14.6%) and after (35% vs. 18.8%) MPN diagnosis in patients with AA.
- Thrombosis-free survival was shorter in patients with AA (11.0 vs. 21.6 years), with LDA use associated with increased thrombotic events and VKA showing limited benefit.
Conclusions:
- The co-occurrence of atrial arrhythmias (AA) and myeloproliferative neoplasms (MPN) like ET and PV is more frequent than anticipated.
- Atrial arrhythmias (AA) significantly elevate the thrombotic risk in patients with ET or PV.
- Optimal anticoagulation strategies, potentially involving DOACs or combined therapies, require careful consideration and collaboration between cardiologists and hematologists to mitigate thrombotic events in this high-risk group.
Abstract:
Atrial arrhythmias (AA) induce a high rate of thromboses and require vitamin K antagonists (VKA) or direct anticoagulants (DOAC) prescriptions. Essential thrombocythemia (ET) and polycythemia vera (PV) are also pro-thrombotic diseases. The prevention of thromboses is based on the association of cytoreductive drug and low-dose aspirin (LDA). We studied the incidence and complications of AA among patients with ET or PV. We identified 96/713 patients (13.5%) carrying AA. These patients were older (median 72.1 vs. 61.3 years old, p < 0.0001). In a case-control analysis, we observed that patients with AA had a higher frequency of cardiovascular risk factors (77/96, 80% vs. 61/96, 61%; p = 0.01). A higher incidence of thromboses before and after myeloproliferative neoplasm (MPN) diagnosis was seen in this group: 26/96, 27.1% vs. 14/96, 14.6% (p = 0.03) and 34/96, 35% vs. 18/96, 18.8% (p = 0.009). Most of the events were arterial (82 vs. 61%, p = 0.09). This translates into a shorter thrombosis-free survival (11.0 vs. 21.6 years, p = 0.01). Continuation of LDA in this situation exposed patients to more thrombotic events (p = 0.04) but VKA did not seem to be good anticoagulant drugs either. The association of AA and MPN is more frequent than expected. AA clearly increased the thrombotic risk of these patients. Anticoagulant drugs should be carefully managed between cardiologists and hematologists. Association of LDA and VKA or the role of DOAC in such population should be rapidly discussed to reduce the thrombotic rate.
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