mitral valve replacement
Conditions
Interventions
Group 1: The aim of this study is to examine the findings of patients who have had a mitral valve replacement with and without retethering since 2017. In addition, the findings of all patients who wil
Sponsors
Universitätsklinikum Magdeburg A.ö.R. Klinik für Herz- und Thoraxchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: • Patients who have had mitral valve replacement surgery since 2017
Exclusion criteria
Exclusion criteria: • Lack of patient consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Leftventricular ejectionfraction after 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints will be: 1. Patient mortality (up to 3 years) 2. Frequency of an LVR 3. Echocardiographic data on ventricle and valve function before surgery and in the short and long term as well as integrity of the patch (intrahospital , 30 days, 6 months, 1 year, max. 3 years if applicable) 4. Frequency of secondary bleeding and reoperation during hospital stay 5. Rate of pacemaker requirement during hospital stay 6. Length of hospital stay 8. Course parameters of the hospital stay: laboratory values, transfusions | — |
Countries
Germany
Contacts
Public ContactMax Wacker
Universitätsklinikum Magdeburg A.ö.R. Klinik für Herz- und Thoraxchirurgie
Outcome results
None listed