
18
Table 7:
Cohort B (Inoperable) Clinical Outcomes at 30 days for NR1, NR4 and NR6
(AT Population)*
Outcome
a
SAPIEN XT Valve
(N = 265)
Death from any cause
21/265 (7.9%)
Major Stroke
5/265 (1.9%)
Repeat hospitalization
b
8/265 (3.0%)
Death from any cause or major stroke or repeat hospitalization
31/265 (11.7%)
Myocardial Infarction
4/265 (1.5%)
Major Vascular Complications
15/265 (5.7%)
Renal Failure
c
7/265 (2.6%)
Disabling Bleeding Event
d
30/265 (11.3%)
Cardiac Reintervention
e
8/265 (3.0%)
Endocarditis
0/265 (0.0%)
New Atrial Fibrillation
f
9/167 (5.4%)
New pacemaker
12/265 (4.5%)
* AT = As Treated, NA = not applicable, TAVR = transcatheter aortic valve replacement. Data presented as n/N
(%) of patients.
a. CEC adjudicated.
b. Repeat hospitalizations were included if they were due to aortic stenosis or complications of the valve
procedure (e.g., TAVR).
c.
Renal failure is defined as stage III acute kidney injury: Increase in serum creatinine to ≥ 300% (3 x increase
compared with base
line) or serum creatinine of ≥ 4 mg/d (≥ 354 μmol/L) with an acute increase of at least 0.5
mg/dl (44 μmol/L).
d. Disabling bleeding: Fatal bleeding OR bleeding in a critical area or organ, such as intracranial, intraspinal,
intraocular, or pericardial necessitating pericardiocentesis, or intramuscular with compartment syndrome OR
bleeding causing hypovolemic shock or severe hypotension requiring vasopressors or surgery OR overt source
of bleeding with drop in hemoglobin of ≥ 5 g/dL or whole blood of packed red blood cells (RBC) transfusion ≥ 4
units.
e. Cardiac reintervention includes any intervention that repairs, alters or replaces a previously operated valve
OR balloon aortic valvuloplasty OR Surgical aortic valve replacement OR valve in valve
f. Based on 167 patients at 30 days.
Table 8:
Conduction Disturbance Requiring Pacemaker to 30 Days for NR1, NR4 and NR6 (CEC Adjudicated) (AT
Population)
SAPIEN XT Valve
(TA/TAo)
(N = 265)
Event
Events
Patients with
Event
New Permanent Pacemaker- All Patients
1
0-30 Days
12
12/265 (4.5%)
New Permanent Pacemaker – Patients without pre-procedural pacemaker
2
0-30 Days
12
12/222 (5.4%)
1
Subjects with pacemaker or ICD at baseline are included (all patients included in denominator).
2
Subjects with pacemaker or ICD at baseline are excluded (patients with baseline pacemaker/ICD subtracted
from denominator).
Note: The patients who received a new pacemaker in both rows are the same patients. The only difference is the
denominators.