Not provided
Not provided
Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| ID RCB : 2018-A02844-51 | Other Identifier | ANSM |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Venous thromboembolic disease is a common pathology in the general population (1.5/1000), the prognosis of which depends in particular on the risk of recurrence. This risk depends essentially on whether the thrombotic episode was provoked or not. Thus, patients who present a thromboembolic event without any contributing factor have a high risk of recurrence, which encourages clinicians to continue anticoagulant treatment for a long time. However, anticoagulant treatment is the leading cause of hospitalization for iatrogenic causes and the leading cause of iatrogenic mortality. The benefit-risk balance of treatment must be evaluated regularly, which requires a good knowledge of the risk factors for thrombotic recurrence and the risk factors for hemorrhage.
Several tools have been established and validated to help clinicians assess patients' bleeding risk, notably using the HAS BLED, haemorrage, and more recently the VTE BLED score. This latest score, published very recently, is the only one to have been validated in patients treated with direct oral anticoagulants. At the same time, we have recurrence risk scores such as HERDOO2, which allow us to identify patients at low risk of recurrence.
In order to improve the management of patients with venous thromboembolic disease, multidisciplinary thrombosis RCPs have been established since 2015, bringing together hemostasis specialists, internists, oncologists, and private vascular physicians to assist clinicians in managing complex cases. • Dedicated post-emergency consultations twice a week to streamline outpatient care for less serious patients This study aims to evaluate the effectiveness of these tools: score and RCP in the management of patients with venous thromboembolic disease.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patient having experienced at least one venous thromboembolic episode |
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Rate of recurrence in patients treated with venous thromboembolic disease (VTE) | Evaluation of the number of hospitalizations or consultations for a venous thrombotic recurrence | 12 years |
| Rate of bleeding complications in patients treated with venous thromboembolic disease (VTE) | Evaluation of the number of hospitalizations or consultations for a hemorrhagic complication. | 12 years |
| Measure | Description | Time Frame |
|---|---|---|
| Long-term complication rates | Assessment of the occurrence of long-term complications | At enrollment visit, 6 months, 1 years and each year during 12 years |
| Long-term complication rates | Assessment of mortality |
Not provided
Inclusion Criteria:
Any patient over 18 years of age who has experienced at least one venous thromboembolic episode:
Hospitalization in the Internal Medicine Department
Consultation by an Internal Medicine physician
File presented at the thrombosis multidisciplinary meeting
Exclusion Criteria:
Thrombosis not meeting the inclusion criteria (cerebral venous thrombosis, mesenteric)
Not provided
Not provided
Not provided
Patient having experienced at least one venous thromboembolic episode
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| David DM MALLET, Director | Contact | 02 32 88 82 65 | +33 | David.Mallet@chu-rouen.fr |
| Vincent VF FERRANTI, ARC | Contact | 02 32 88 82 65 | +33 | Vincent.Ferranti@chu-rouen.fr |
| Name | Affiliation | Role |
|---|---|---|
| Sébastien SM MIRANDA, Doctor | University Hospital, Rouen | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital of Rouen | Recruiting | Rouen | 76031 | France |
The data provided will be the property of the sponsor and will be used solely for its own research activities.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| At enrollment visit, 6 months, 1 years and each year during 12 years |