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Multiple and mixed valvular heart disease (MMVD) is a common condition in clinical practice. It corresponds to a combination of stenotic or leaky lesions on two or more heart valves (multiple valve disease), or a combination of stenotic and leaky lesions on the same valve (mixed valve disease). However, the management of their clinical, biological and cardiovascular imaging is not well established. Current European Society of Cardiology (ESC) recommendations primarily address the various valve diseases in isolation. This results in an absence of reliable recommendations for managing MMVD, with different approaches being adopted by care centres.
In order to address this knowledge gap regarding MMVD, it is crucial to assess its prevalence, the cardiovascular imaging methods employed and the management strategies, as well as to identify prognostic factors for the various combinations of valve disease.
The multicentre MMVD study will be a valuable resource as it will improve our understanding of the prognosis for patients with MMVD. It will highlight imaging and biological markers associated with the prognosis of different combinations of MMVD.
National, Prospective, Multicentric Registry. Patients with a diagnosis of MMVD identified by echocardiography will be included and followed up at 1, 2, 3, 4 and 5 years.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with a diagnosis of MMVD | Patients with a diagnosis of MMVD based on cardiovascular imaging and defined as follows: At least two cases of moderate to severe valvular heart disease, as assessed by a cardiologist and defined by transthoracic echocardiography (TTE) on one or more valves. This is in line with the recommendations of the European Society of Cardiology (ESC), the American Society of Echocardiography (ASE) and expert opinion. |
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| Measure | Description | Time Frame |
|---|---|---|
| To assess the association between cardiovascular imaging parameters (echocardiography and cardiac MRI) and cardiovascular event-free survival in a population of MMVD. | Survival without cardiovascular event | 1 year after inclusion |
| Measure | Description | Time Frame |
|---|---|---|
| To assess the association between cardiovascular imaging parameters and survival | at 1, 2, 3, 4 and 5 years after inclusion | |
| Proportion of patients who did not experience a cardiovascular event | at 1, 2, 3, 4 and 5 years after inclusion |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with a diagnosis of MMVD based on cardiovascular imaging and defined as follows:
At least two cases of moderate to severe valvular heart disease, as assessed by a cardiologist and defined by transthoracic echocardiography (TTE) on one or more valves. This is in line with the recommendations of the European Society of Cardiology (ESC), the American Society of Echocardiography (ASE) and expert opinion.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Théo PEZEL | Contact | 01 44 90 70 28 | +33 | multivalve@sfcardio.fr |
| Augustin COISNE | Contact | 01 44 90 70 28 | +33 | multivalve@sfcardio.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chu Lille- Hopital Cardiologique | Recruiting | Lille | France |
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| ID | Term |
|---|---|
| D006349 | Heart Valve Diseases |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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optional blood sample <56ml
| Proportion of patients who are alive | at 1, 2, 3, 4 and 5 years after inclusion |
| Proportion of patients who did not experience a cardiovascular event depending on the type of treatment (medical, surgical or percutaneous) | at 1, 2, 3, 4 and 5 years after inclusion |
| Proportion of patients who are alive depending on the type of treatment (medical, surgical or percutaneous) | at 1, 2, 3, 4 and 5 years after inclusion |
| To assess the progression of the stage of severity of valvulopathy | Echocardiography | at 1, 2, 3, 4 and 5 years after inclusion |
| % of patients with MMVD combinations | during 5 years after inclusion |
| Measurement of cardiovascular biomarkers | BNP or NT-pro-BNP and troponin | at baseline and 1, 2, 3, 4 and 5 years after inclusion |
| Assessing the association between cardiovascular biomarkers in patients with MMVD and survival | BNP or NT-pro-BNP and troponin, vital status | during 5 years after inclusion |
| Assessing the association between cardiovascular biomarkers in patients with MMVD and cardiovascular event-free survival | BNP or NT-pro-BNP and troponin, Survival without cardiovascular event | during 5 years after inclusion |
| Exploring the value of cardiovascular biomarkers analysed in a centralised laboratory (optional) | Biobank (optional) | at baseline |
| Chu Lariboisiere (Aphp) | Recruiting | Paris | France |
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