Due to increasing of life expectancy, patients with von Willebrand disease are exposed to age-related pathologies such as cancer or cardiovascular diseases. Management of thrombotic events is challenging given the inherent bleeding risk in von Willebrand disease. Few data are currently available in the literature. The aim of the study is to describe the frequency and nature of arterial and venous thromboembolic events and atrial fibrillation in patients with von Willebrand disease in the West of France. The investigators will perform a retrospective multicenter study conducted in the von Willebrand population of the French West. Von Willebrand adult patients followed in one of the French West medical centers participating in the study, who presented deep vein thrombosis, pulmonary embolism, ischemic stroke, transient ischemic attack, acute coronary syndrome, acute limb ischemia, atrial fibrillation, arteriopathy of the lower limbs, angina will be eligible.
Von Willebrand disease is the most common hereditary bleeding disorder. Due to the development of therapies, life expectancy and life quality are increasing in affected patients. However, certain treatments and/or certain comorbidities associated with venous and arterial thrombotic risks may be present in these patients. In the general population, venous thromboembolic disease, arterial thrombosis and atrial fibrillation are frequent. Their management requires the use of antiaggregants and anticoagulant molecules, themselves associated with a bleeding risk. Few data are currently available in the literature concerning the occurrence of venous and arterial thromboembolic events in patients with von Willebrand disease and their management, in the face of a hemorrhagic risk inherent to their pathology and its increase by anti-aggregant treatments and anticoagulants. The aim of the study is to describe the frequency and nature of arterial and venous thromboembolic events and atrial fibrillation in patients with von Willebrand disease in the West of France. The investigators will perform a retrospective multicenter study on data conducted in the French West. The study population is composed of patients with von Willebrand disease followed in a reference center in the French West, have consented to be included in the BERHLINGO database (Base d'Etude et de Recherche pour Les INvestigateurs en Hémostase du Grand-Ouest), and who presented deep vein thrombosis, pulmonary embolism, ischemic stroke, transient ischemic attack, acute coronary syndrome, acute limb ischemia, atrial fibrillation, arteriopathy of the lower limbs, angina. Data about von Willebrand disease, risk factors, event, treatment such as antiaggregants and anticoagulants and complications such as hemorrhage or recurrence, will be collected.
Study Type
OBSERVATIONAL
Enrollment
100
CHU d'Angers
Angers, France
NOT_YET_RECRUITINGCHU de Brest
Brest, France
RECRUITINGCHU de Caen
Caen, France
NOT_YET_RECRUITINGCH le MANS
Le Mans, France
NOT_YET_RECRUITINGCHU de Nantes
Nantes, France
NOT_YET_RECRUITINGCHU de Rennes
Rennes, France
NOT_YET_RECRUITINGTo describe the frequency of arterial and venous thromboembolic events and cardiac arrhythmia due to atrial fibrillation in patients with Willebrand disease in the Greater West.
Occurrence of a thromboembolic event validated by an adjudication committee
Time frame: 12 months
To describe the nature of arterial and venous thromboembolic events and cardiac arrhythmia due to atrial fibrillation in patients with Willebrand disease in the Greater West.
Occurrence of a thromboembolic event validated by an adjudication committee
Time frame: 12 months
Identify potential risk factors
identify whether certain risk factors are more prevalent in the population than others
Time frame: 12 months
Number of revascularisation procedures, anticoagulants and antiaggregants prescribed for these conditions
Prescription of anticoagulant and/or antiaggregant treatment
Time frame: 12 months
Evaluate the nature of treatments prescribed for these pathologies: revascularisation procedures, anticoagulants and antiaggregants
Revascularisation procedure (endovascular or surgical)
Time frame: 12 months
Evaluate the tolerance of these treatments
Occurrence of clinical haemorrhage
Time frame: 12 months
Evaluate the effectiveness of these treatments
Occurrence of a cardio-embolic event
Time frame: 12 months
Evaluate the effectiveness of these treatments
Occurrence of a thromboembolic recurrence
Time frame: 12 months
Evaluate the effectiveness of these treatments
Death from haemorrhage and/or thromboembolic causes.
Time frame: 12 months
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