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In-hospital and long-term outcome of patients with mitral valve replacement with and without retethering technique

Conditions
mitral valve replacement
Registration Number
DRKS00032902
Lead Sponsor
niversitätsklinikum Magdeburg A.ö.R. Klinik für Herz- und Thoraxchirurgie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

•Patients who have had mitral valve replacement surgery since 2017

Exclusion Criteria

•Lack of patient consent

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary endpoint will be periprocedural mortality as defined by VARC-3 criteria. <br>
Secondary Outcome Measures
NameTimeMethod
Secondary endpoints will be: <br>1.Patient mortality (up to 3 years)<br>2.Frequency of an LVR<br>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)<br>4.Frequency of secondary bleeding and reoperation during hospital stay<br>5.Rate of pacemaker requirement during hospital stay<br>6.Length of hospital stay<br>8.Course parameters of the hospital stay: laboratory values, transfusions<br>
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