The main objective is to determine the early and late survival and reoperation outcome of VSARR in patients suffering from aortic root aneurysm with or without aortic regurgitation. Furthermore, we will evaluate the quality of using a SF-36 form.…
ID
Source
Brief title
Condition
- Cardiac valve disorders
- Cardiac therapeutic procedures
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Reoperation
Secondary outcome
Survival outcome and Quality of life and Valve related complications.
Background summary
Provide insight in VSARR performed in Erasmus MC
Study objective
The main objective is to determine the early and late survival and reoperation
outcome of VSARR in patients suffering from aortic root aneurysm with or
without aortic regurgitation. Furthermore, we will evaluate the quality of
using a SF-36 form. The second objective is evaluate the valve related
complications after VSARR.
Study design
Single-centre hospital-based retrospective/prospective cohort study .
Study burden and risks
We expect that the burden associated with participation will be mainly
emotional due to the SF-36 questionnaire. Patients have to visit our outpatient
clinic which may have organizational burdens (taking a few ours off from work
etc.) and to travel to the Erasmus MC..There is no further risk associated with
participation because our study population consist of patients who are compos
mentis and to collect our data, we use the hospital information systems.
Patients may benefit from the knowledge of a potential change in the
hemodynamics or change in valve function seen on the echocardiogram, which may
lead to an altered, improved treatment.
's Gravendijkwal 230
ROTTERDAM 3015 CE
NL
's Gravendijkwal 230
ROTTERDAM 3015 CE
NL
Listed location countries
Age
Inclusion criteria
•All patients aged 18 years or older who received a valve sparing root reimplantation (Tirone David) at the Erasmus MC since 2000
•Signed informed consent by the patient and the investigator.
Exclusion criteria
•Patients who are unable or uncapable to give informed consent
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL50604.078.14 |
Other | NTR nr volgt |