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Published on: February 28, 2012
Oral anticoagulants (NOAC and VKA) in chronic thromboembolic pulmonary hypertension
Marc Humbert1, Gérald Simonneau1, David Pittrow2
1Université Paris-Saclay, Inserm U999, Service de Pneumologie et Soins Intensifs Respiratoires, Hôpital Bicêtre, Assistance Publique Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
Insights
This study compared anticoagulants in chronic thromboembolic pulmonary hypertension (CTEPH) patients. While hemorrhagic events were similar, embolic/thrombotic events were higher with non-vitamin K antagonist oral anticoagulants (NOACs) versus vitamin K antagonists (VKAs).
Area of Science:
- Cardiology
- Pulmonology
- Pharmacology
Background:
- Pulmonary hypertension poses significant risks.
- Chronic thromboembolic pulmonary hypertension (CTEPH) requires effective anticoagulation.
- Riociguat is a treatment option for pulmonary hypertension.
Purpose of the Study:
- To compare adverse events (AEs) and serious AEs (SAEs) in CTEPH patients on different anticoagulants.
- To evaluate hemorrhagic and embolic/thrombotic event rates based on anticoagulant type.
- To assess long-term anticoagulation effects in CTEPH.
Main Methods:
- Prospective, uncontrolled, non-interventional cohort study (EXPERT).
- Follow-up of 1-4 years in patients with CTEPH.
- Comparison of patients receiving vitamin K antagonists (VKAs) versus non-vitamin K antagonist oral anticoagulants (NOACs).
Main Results:
- Overall AEs and SAEs were reported in 64.1% and 37.6% of VKA patients, versus 68.2% and 37.4% of NOAC patients.
- Exposure-adjusted hemorrhagic event rates were similar between VKA and NOAC groups.
- Exposure-adjusted embolic/thrombotic event rates were higher in the NOAC group, though event numbers were small.
Conclusions:
- Anticoagulation strategies in CTEPH patients show comparable hemorrhagic event rates between VKA and NOACs.
- Higher embolic/thrombotic event rates observed in the NOAC group warrant further investigation.
- Additional research is needed to fully understand long-term anticoagulation effects in CTEPH.
Abstract:
EXPERT was an international, multicenter, prospective, uncontrolled, non-interventional cohort study in patients with pulmonary hypertension treated with riociguat. Patients were followed for 1-4 years, and the primary outcomes were adverse events (AEs) and serious AEs (SAEs), including embolic/thrombotic and hemorrhagic events. Here we report data on patients with chronic thromboembolic pulmonary hypertension (CTEPH) receiving a vitamin K antagonist (VKA; n = 683) or a non-vitamin K antagonist oral anticoagulant (NOAC; n = 198) at baseline. AEs and SAEs were reported in 438 patients (64.1%) and 257 patients (37.6%), respectively, in the VKA group, and in 135 patients (68.2%) and 74 patients (37.4%) in the NOAC group. Exposure-adjusted hemorrhagic event rates were similar in the two groups, while exposure-adjusted embolic and/or thrombotic event rates were higher in the NOAC group, although the numbers of events were small. Further studies are required to determine the long-term effects of anticoagulation strategies in CTEPH.
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