The primary objective of this study is to determine the efficacy, safety and feasibility of next day discharge home in patients undergoing self-expandable transfemoral TAVR utilizing the Vancouver 3M Clinical Pathway.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
315
Vancouver Clinical Pathway
The composite of all-cause mortality or stroke
Time frame: 30 days post-procedure
The proportion of patients undergoing elective transfemoral TAVR using the Vancouver Clinical Pathway, who are discharged the next day
Time frame: Discharge 1 day after procedure
All-cause mortality
Time frame: 30 days post-procedure
Stroke
Time frame: 30 days post-procedure
Major vascular complications
Time frame: 30 days post-procedure
Major/Life-threatening bleed
Time frame: 30 days post-procedure
Any hospital readmission
Time frame: 30 days post-procedure
>mild paravalvular regurgiation
Time frame: Immediately after a procedure is performed or at time immediately prior to discharge, up to 48 hours after procedure
New permanent pacemaker
Time frame: 30 days post-procedure
Patient is converted from local to general anaesthetic/receives intubation during procedure
Time frame: This happens during the procedure
Myocardial infarction
Time frame: This happens during the procedure
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Repeat procedure for valve-related dysfunction
Time frame: 30 days post-procedure
Stage 3 acute kidney injury (need for dialysis)
Time frame: 30 days post-procedure
Patient-centred outcomes including health related quality of life as measured by KCCQ at baseline, 30 days and 1 year
Time frame: Baseline, and 30 days and 1 year post-procedure