mitral valve repair for mitral regurgitation
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Written informed consent is obtained from the patient or his/her parental authority Patients scheduled mitral valve repair for mitral regurgitation Patients with more than 20 years old
Exclusion criteria
Exclusion criteria: emergency operation Patients under 20 years old Patients with mitral regurgitation due to infection (infective endocarditis) Patients contraindicated for transesophageal echocardiography (postoperative esophageal cancer, esophageal diverticulum, esophageal varix) Patients deemed as inappropriate for participating in the study Pationts who we can not take consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between the size of annuloplasty ring size and predicted size by using 3D-TEE | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate whether the discrepancy between the annuloplasty ring size and predicted size by using 3D-TEE affect the postoperative residual mitral regurgitation. Correlation between the size of annuloplasty ring size and predicted size by using 3D-TEE due to the difference of the lesion site (anterior leaflet or posterior leaflet) Complication of transesophageal echocardiography Postoperative complication Postoperative recovery (respiration time, stay in intensive care unit, hospital stay) | — |
Countries
Japan
Contacts
National Cerebral and Cardiovascular Center Department of Anesthesiology