aortic valve stenosis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients scheduled to undergo transcatheter aortic valve implantation (TAVI) at our institution Patients capable of providing written informed consent
Exclusion criteria
Exclusion criteria: Patients with pacemaker or implantable cardioverter-defibrillator (ICD), in whom bioelectrical impedance analysis (BIA) is contraindicated Emergency cases Patients on chronic dialysis Valve-in-valve cases (redo transcatheter valve implantation within a previously implanted bioprosthetic valve) Patients undergoing TAVI via non-transfemoral approaches Patients converted to open surgical aortic valve replacement
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is all-cause mortality within 1 year after TAVI. Mortality will be ascertained from hospital electronic medical records, outpatient clinic records, and, if necessary, telephone follow-up. The time point of evaluation is defined as one year after the date of the TAVI procedure. | — |
Countries
Japan
Contacts
Osaka Medical and Pharmaceutical University Department of Anesthesiology