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TAVI – IMAGING 
+ICE 
+IVUS 
+HYBRID
Use of Imaging for TAVI 
§ Assessment pre TAVI 
§ TTE, MSCT, 3DE, coronary angiography 
§ Assessment during TAVI 
§ TOE/TTE, Fluroscopy 
§ Assessment post TAVI 
§ TTE, MSCT
Assessment pre TAVI 
• TTE 
– Diagnosis: severe AS, morphology 
– Aortic regurgitation 
– LVOT/subaortic stenosis 
– Mitral & tricuspid valves 
– LV & RV function 
– Pericardial effusion 
– LV hypertrophy 
– LV/LA thrombus 
• MSCT/3DE 
– Annulus size 
– Prosthesis type and size 
– Coronary height 
– Sinus of valsalva diameter 
– Femoral access 
• Coronary angiography 
– Proximal CAD 
– PCI 
• CMR – LGE – interstitial fibrosis 
• Dobutamine stress ECHO 
SCREENING
Is 
it 
severe 
AS? 
• “Flow dependent” parameters 
• Post-VPC accentuation of gradient 
• Atrial fibrillation 
• Aortic regurgitation 
• “Classical” LG LF severe AS reduced 
LVEF (DSE) 
• “Paradoxical” LG LF severe AS normal 
LVEF 
• NF, LG, N LVEF severe AS
(SV 
= 
TVI 
LVOT 
x 
CSA 
LVOT) 
or 
SVI
Dobutamine 
stress 
ECHO 
in 
paFent 
with 
LGSAS 
Baseline 
CW 
tracing: 
Peak 
velocity 
3.2 
m/s 
Mean 
grad 
25 
mmHg 
AVA 
0.45 
cm2 
CW 
10ug/kg/min 
dobutamine 
Peak 
velocity 
4.1 
m/s 
Mean 
grad 
39 
mmHg 
AVA 
0.5 
cm2
DSE in a patient with Pseudo-severe AS 
Baseline 
5 
ug/kg/min 
Peak 
velocity 
stable, 
AVA 
increased, 
contracFle 
reserve 
+, 
absence 
of 
severe 
AS 
10 
ug/kg/min 
20 
ug/kg/miin
NFHG 
N 
EF 
LFLG 
N 
EF 
NFLG 
N 
EF 
LFLG 
Low 
EF 
Algorithm 
for 
classificaFon 
of 
paFents 
with 
LGSAS 
MSCT 
– 
extent 
of 
AV 
calcium
Imaging for aortic annulus sizing 
prosthesis type/sizing 
TTE/TOE 
MSCT 
3D-­‐ECHO
Circ 
Cardiovasc 
Interv: 
2008 
Piazza 
et 
al
Understanding Annulus Anatomy 
VIRTUAL 
ANNULUS 
Most basal point of aortic leaflet attachment 
Measured during systole, ensure alignment, 
Circ 
Cardiovasc 
Interv: 
2008 
Piazza 
et 
al 
trailing edge to leading edge – PLAX TTE/TOE
MSCT 
ECHO 
3D 
2D 
AorFc 
annulus 
is 
oval 
In 
shape 
in 
majority 
of 
PaFents 
RaFo 
of 
longD/shortD 
1.28
Basal SAX view of Aortic Valve 
RC 
LC 
NC 
Circ 
Cardiovasc 
Interv: 
2008 
Piazza 
et 
al
AORTIC 
ANNULUS 
SIZING 
-­‐ 
2D 
vs 
3D
Histology of Aortic Valvar Complex 
Circ 
Cardiovasc 
Interv: 
2008 
Piazza 
et 
al
ECHO vs Surgical Assessment 
Annulus Diameter
2-D TOE 
Underestimate 35% 
Correct 55% 
Overestimate 10% 
3-D TOE 
Mylofe 
et 
al, 
JACC 
CV 
Intervent 
2014
INCORRECT 
SIZING 
• WRONG 
VALVE 
USED 
IN 
50 
% 
OR 
CASES
Aortic annulus – diameter variation 
during cardiac cycle 
Aortic annulus: 4-5% larger in systole vs diastole
Which 
MSCT 
Measurement 
to 
use…… 
• Short 
diameter 
• Long 
diameter 
• Mean 
diameter: 
SAPIEN 
• Area-­‐derived 
diameter 
• Perimeter-­‐derived 
diameter 
• Area: 
SAPIEN 
• Perimeter: 
CoreValve
Oversizing 
– 
does 
it 
mafer? 
• 10-­‐20% 
oversizing 
recommended 
• Area/perimeter/mean 
diameter 
• TransiFon 
zone 
– Annulus 
falls 
between 
two 
valve 
sizes 
• Presences 
of 
LVOT 
calcium 
– Important: 
• balloon-­‐expandable 
valves: 
root 
rupture 
• Self-­‐expanding 
valves: 
para-­‐valvular 
leak 
• Any 
post-­‐TAVI 
BAV: 
root 
rupture/valvular 
AR
CONSEQUENCES 
OF 
INACCURATE 
AORTIC 
ANNULUS 
SIZING 
• ANNULUS 
RUPTURE 
– BALLOON 
EXPANDABLE 
– SELF-­‐EXPANDING 
• PARAVALVULAR 
AORTIC 
REGURGITATION 
– LINKED 
TO 
PROGNOSIS 
• VALVULAR 
AORTIC 
REGURGITATION 
• PROSTHESIS 
EMBOLISATION 
• PPM 
REQUIREMENT 
POST 
TAVI 
• POST-­‐TAVI 
BAV 
– ASSOCIATED 
WITH 
INCREASED 
RISK 
OF 
CVA
Aortic Annulus Sizing
3D 
ANALYSIS 
OF 
3-­‐DIMENSIONAL 
STRUCTURE
AORTIC 
ANNULUS 
– 
INACCURATE 
SIZING
Imaging for aortic annulus sizing 
prosthesis type/sizing 
TTE/TOE 
MSCT 
3D-­‐ECHO
GA required for 3D TOE
Contrast requirement
When should 3DE be a surrogate, 
alternative or preferred for TAVI sizing 
• When MSCT cannot be obtained but 3D available 
– No local expertise with MSCT 
• When MSCT is contraindicated/risky 
– Severe renal impairment 
• When there is doubt regarding the quality of the 
MSCT 
– Motion artifact/difficult to repeat
MSCT for assessment of peripheral access
3-­‐MENSIO 
VALVES 
(MSCT 
BASED 
FEM 
ART 
ACCESS 
ANALYSIS)
MSCT 
GOLD 
STANDARD 
FOR 
AORTIC 
ANNULUS 
SIZING 
2D 
TEE 
AND 
TTE 
UNDERESTIMATES 
AORTIC 
ANNULUS 
DIMENSIONS 
AORTIC 
ANNULUS 
DIMENSIONS 
IMPORTANT 
FOR 
ACCURATE 
PROSTHESIS 
SIZING
OR 
SLIDE 
FROM 
JAMES’ 
TAVI 
Talk 
on 
peripheral 
access
Assessment 
during 
TAVI 
PROCEDURE
TAVI 
-­‐ 
PROCEDURAL 
STEPS 
• Baseline ECHO 
• Peripheral access 
• Identify ideal projection 
• Cross valve 
• BAV 
• TAVI valve positioning 
• TAVI valve deployment 
• Post deployment final assessment 
– Haemodynamic 
– Aortography 
– TOE/TTE 
• Real-time monitoring for complications during procedure
Baseline TOE/TTE at start of 
procedure 
• Confirm gradients 
• Baseline aortic regurgitation 
• Baseline mitral valve assessment 
• LVOT 
• Baseline LV/RV wall motion 
• Baseline pericardial effusion 
• Online monitoring of valve procedure/complications 
• Repeat all at end of procedure + check for complications
M85, 
CKD, 
COPD, 
PAF, 
T2D 
Class 
IV 
NYHA, 
no 
significant 
CAD
SUPPORTIVE 
HYBRID 
REAL-­‐TIME 
GUIDANCE 
Overlay 
of 
3D 
MSCT 
images 
from 
pre-­‐procedure 
Screening 
on 
top 
of 
live 
X-­‐Ray 
fluoroscopy
PSAX 
TTE 
Day 
1 
Post 
TAVI 
CDF
Procedural Findings 
Assessment 
of 
Post-­‐Procedural 
AR: 
Requires 
agreement 
of 
three 
assessment 
tools 
Echocardiography 
Hemodynamics 
Aortography 
PVAR 
vs 
VAR 
Severity 
ComplicaFons 
AR 
Valve 
posiFon 
Gradient/AVI 
Coronary 
perfusion 
TCT 2013 Procedural Outcomes Extreme Risk Study | Iliofemoral Pivotal 67
Cath 
Lab 
Assessment 
Immediate 
Post 
Deployment 
• Haemodynamic 
– AV 
index: 
Ao 
diastolic 
pressure-­‐LVEDP 
(<25 
= 
significant 
AR) 
– Peak 
to 
Peak 
gradient 
+ 
mean 
gradient 
(PT 
Ao-­‐LVPT) 
• Aortography 
– PVAR/VAR 
– 
use 
enough 
contrast/RAO 
projecFon 
– Coronary 
artery 
perfusion 
– Competence 
of 
aorFc 
root 
• ECHO: 
TOE/TTE 
– AorFc 
paravalvular 
and 
valvular 
leak 
– Systolic 
valve 
funcFon: 
PG, 
MG, 
AVA 
– LV/RV 
systolic 
funcFon 
– Pericardial 
effusion 
– 
compare 
with 
baseline 
– Mitral 
valve 
funcFon 
– 
mitral 
regurgitaFon, 
AML 
hinge 
point 
– Tricuspid 
valve/pulmonary 
pressure
ComplicaFons 
& 
Management 
AorFc 
RegurgitaFon 
• Typically paravalvular mild 
or mild-moderate severity 
• Most of AR disappears or 
reduces at 1 yr follow-up 
[13% absent, 80% mild AR] 
Cardiol 
Clin 
29 
(2011) 
211–222 
J. 
Am. 
Coll. 
Cardiol. 
2012;59;1200-­‐1254
Aortography 
Mild 
PVAR
Annular and leaflet calcification may limit 
prosthesis expansion – cause of PVAR
Paravalvular/valvular 
aorFc 
regurgitaFon 
post 
TAVI 
• AeFology 
(paravalvular) 
– MalposiFon 
• Supra-­‐annular 
• Infra-­‐annular 
– Underexpansion 
• Focal/widspread 
calcificaFon 
– Prosthesis 
mismatch 
• Undersizing 
– Horizontal 
aorta: 
• AeFology 
(valvular) 
significant 
VAR 
uncommon 
– Incorrect 
prosthesis 
size 
• Oversizing 
– Valve 
damage 
during 
procedure 
– Underexpanded 
valve 
– 
calcium 
– Overexpansion 
of 
valve 
– 
post 
TAVI 
BAV
Assessment 
of 
para-­‐valvular 
aorFc 
regurgitaFon 
post 
TAVI 
** 
Not 
well-­‐validated 
and 
may 
overesFmate 
the 
severity 
compared 
with 
the 
quanFtaFve 
doppler 
PVAR 
assessment 
cont’d…….. 
TOE: 
Deep 
transgastric 
permits 
best 
axial 
alignment 
for 
the 
quanFtaFve 
doppler 
measurement 
of 
regurgitant 
pressure 
half-­‐Ame. 
PLAX 
and 
PSAX 
ME: 
indenFficaFon 
of 
site, 
number 
and 
extent 
of 
PVAR 
jets. 
Vena 
contracta 
diameter 
and 
area 
can 
be 
assessed 
using 
2D 
and 
3D 
colour 
doppler 
but 
may 
not 
be 
a 
reliable 
measure 
of 
PVAR 
post 
TAVI 
(mulFple, 
small, 
irregular 
shape, 
eccentric 
jets)
Para-­‐valvular 
AR 
post 
TAVI 
ME 
PSAX 
ME 
PLAX
Native aortic valve regurgitation post 
balloon aortic valvuloplasty
Deep 
Transgastric 
view 
– 
PHT
US Pivotal Extreme Risk Study 
Surgical 
AVR 
paravalvular 
leak: 
2-­‐4%
US Pivotal Extreme Risk Study
Malposition – infra-annular 
SAPIEN 
Balloon-­‐expandable
Malposition – infra-annular 
Different Mechanism: CoreValve self-expanding
Coronary Occlusion
Pericardial Tamponade
Annular Rupture, Aortic Dissection…
TAVI IMAGING at follow-up 
• Imaging modalities 
– TTE –valve function 
– MSCT – valve 
deformity 
– CMR – LV/RV 
assessment 
FOLLOW-­‐UP
Suggested time for routine ECHO 
follow up post TAVI 
§ 24-48 hrs, pre-discharge 
§ 30 days 
§ 6 month 
§ 12 months 
§ Then yearly thereafter
Routine ECHO assessment of 
TAVI valve 
• Valve position 
• Valve morphology 
• Valve function 
– Systolic 
– Diastolic 
• LV size and systolic function +RV 
• Mitral + tricuspid 
• Pulmonary pressure 
• Pericardial effusion
How is TAVI different from SAVR 
• TAVI (vs SAVR) 
– No sewing ring 
– Much longer prosthesis (up to 55 mm) 
• Flow acceleration 
• LVOT diameter 
• Valve type 
• PVAR 
– Native valve in situ 
• Calcium, leaflets, prosthesis type, size, expansion 
– LBBB more common
Definition of new valve dysfunction at 
follow-up 
• Suspected structural TAVI failure: compare to patient’s 
baseline ECHO eg TTE post-procedure (Day 1) 
• Significant changes: 
– An increase in the mean gradient >10 mmHg 
– A decrease in the AVA >0.3-0.4 cm2 
– A reduction in the DVI >0.10-0.13 
• Exclude measurement error – 
– Baseline (Day 1) LVOT diameter 
– Depends on valve depth in LVOT and valve type 
– LVOT diameter and LVOT velocity for AVA should be measured in same 
location outside the stent frame 
– LVOT non-circular 
– Flow acceleration inside stent frame prox to valve cusps with elevated 
velocity 
• Note changes in LV function and allow for effect on gradient
Definition of new valve dysfunction at 
follow-up 
• Suspected structural TAVI failure: compare 
to patient’s baseline ECHO eg TTE post-procedure 
(Day 1) 
• Significant changes: 
– An increase in the mean gradient >10 mmHg 
– A decrease in the AVA >0.3-0.4 cm2 
– A reduction in the DVI >0.10-0.13
Long-­‐term 
Valve 
Performance
Post-implantation follow up of 
TAVI patients 
• Similar to follow up of surgically implanted 
prostheses but two important differences 
– Calculation of EOA as an index of valve opening: 
• Founded in ratio of post- to pre-valvular velocities 
• Flow acceleration within transcatheter valve proximal to 
the valve cusps 
• Pre-valvular velocity should be recorded proximal to the 
stent (PW doppler with sample situated where LVOT 
diameter measured) and the post-valvular velocity 
recorded with CW doppler reflects that distal to the 
stented valve 
• If the LVOT velocity used in the calculations is 
erroneously recorded inside the stent but proximal to the 
cusps the result will be an increased velocity with an 
overestimation of the valve area and DVI
Prosthetic Aortic Stenosis 
• Limitation of flow independent parameters 
– The absolute EOA does not account for the cardiac output 
requirements in relation to the patients body size 
– The indexed EOA may overestimate the haemodynamic burden in 
obesity; hence lower criteria may be more appropriate in patients 
with a BMI>30kg/m2 
– DVI severity criteria are dependent on LVOT size ie a lower 
threshold may be more appropriate if LVOT>25mm 
– The LVOT should be measured just beneath the ventricular margin 
of the valve stent/skirt 
– Unlike the surgically implanted valve, the transcatheter prosthetic 
valve EOA is defined not only by the size of the valve but also by 
the patient’s aortic valve/annular anatomy and procedural variables. 
Thus, well-established normal trans- catheter valve gradients and 
EOAs based on preimplant aortic annular dimensions do not 
currently exist.
• In 
condiFons 
of 
normal 
or 
near 
normal 
SV
DSE
Assessment 
of 
para-­‐valvular 
and 
valvular 
prostheFc 
AR 
post 
TAVI 
** 
Not well-validated, assumes continuity of flow and may overestimate the severity 
compared with the quantitative doppler 
PLAX 
and 
PSAX 
TTE: 
Number/distribution and extent of PVAR jets. A3C and A5C for 
further assessment of jets: PHT.
MSCT 
post 
TAVI 
Coronal 
Oblique 
View 
3D 
volume 
rendered 
view 
Medtronic 
CoreValve 
2 
weeks 
post 
TAVI 
-­‐Adequate 
deployment 
-­‐No 
instent 
restenosis 
-­‐Patent 
coronary 
art 
-­‐Good 
valve 
posiFon 
-­‐Integrity 
of 
stent 
struts 
-­‐thrombus/vegetaFon 
visible 
on 
leaflets 
-­‐Assymmetric 
expansion
Medtronic 
CoreValve/Evolut
Edwards 
Sapien 
XT/3
TTE 
PRE 
TAVI 
PLAX: 
CDF 
VAR/MR 
& 
A5C: 
CDF 
VAR
PORTICO 
TAVI 
post-­‐implantaFon: 
LVOT 
measurement
A5C 
TTE 
Day 
1 
Post 
TAVI 
VTI 
LVOT
A5C 
TTE 
Day 
1 
Post 
TAVI 
CW 
AorFc 
Valve
PORTICO 
TAVI 
D1 
LVOT 
measurement
A5C 
TTE 
Day 
2 
Post 
TAVI 
PW 
LVOT 
outside 
valve 
and 
inside 
valve
A5C 
TTE 
Day 
2 
Post 
TAVI 
CW 
AorFc 
Valve
SECOND 
GENERATION 
TAVI 
DEVICES
PORTICO 
Day 
1 
– 
Post 
TAVI 
Baseline 
TTE 
Day 
1 
post 
TAVI
TTE 
PRE 
TAVI 
PLAX: 
CDF 
VAR/MR 
& 
A5C: 
CDF 
VAR
PORTICO 
Day 
1 
– 
Post 
TAVI 
Baseline 
TTE 
Day 
1 
post 
TAVI
A4C 
TTE 
Day 
2 
Post 
TAVI 
Simpsons 
Biplane 
for 
LVEF
PLAX 
TTE 
Day 
1 
Post 
TAVI
PSAX 
TTE 
Day 
1 
Post 
TAVI 
CDF
PSAX 
2D 
TTE 
Day 
1 
Post 
TAVI
A5C 
TTE 
Day 
1 
Post 
TAVI
A5C 
TTE 
Day 
1 
Post 
TAVI 
PVAR 
PHT
PSAX 
TTE 
Day 
1 
Post 
TAVI 
Mitral 
Valve 
CDF
PSAX 
TTE 
Day 
1 
Post 
TAVI 
CDF 
RVOT/PV/TV/AV
Pre 
TAVI
A5C 
TTE 
Day 
2 
Post 
TAVI 
CDF 
PVAR 
and 
PHT 
PVAR
The 
color 
Doppler 
jet 
of 
a 
paravalvular 
leak 
is 
ouen 
best 
appreciated 
from 
the 
deep 
transgastric 
TEE 
view 
(Figure 
19). 
This 
view 
usually 
permits 
the 
best 
axial 
alignment 
for 
the 
quanFtaFve 
Doppler 
measure 
of 
regurgitant 
pressure 
half-­‐Fme. 
The 
midesophageal 
views 
provide 
the 
cross-­‐ 
secFonal 
and 
long-­‐ 
axis 
views 
to 
facilitate 
idenFficaFon 
of 
the 
site 
and 
extent 
of 
paravalvular 
leak. 
The 
vena 
contracta 
diameter 
and 
area 
can 
be 
assessed 
using 
2D 
and 
3D 
color 
Doppler 
applicaFon, 
respecFvely 
(Figure 
20).
Valve 
funcFon 
• Valve 
Academic 
Research 
ConsorFum-­‐2 
maintains 
the 
original 
recommendaFons 
to 
use 
echocardiography 
as 
the 
primary 
imaging 
modality 
for 
the 
assessment 
of 
prostheFc 
valve 
funcFon.39 
This 
should 
include 
the 
valve 
posiFon, 
morphology, 
funcFon, 
and 
evaluaFon 
of 
the 
leu 
ventricle 
(LV) 
and 
right 
ventricle 
(RV) 
size 
and 
funcFon. 
The 
sug-­‐ 
gested 
Fme 
points 
for 
rouFne 
follow-­‐up 
transthoracic 
echo-­‐ 
cardiography 
(TTE) 
following 
valve 
implantaFon 
are:immediately 
(before 
discharge) 
following 
the 
implantaFon 
for 
transarterial 
approaches 
or 
within 
30 
days 
for 
transapi-­‐ 
cal 
or 
transaorFc 
approaches, 
6 
months 
following 
implantaFon, 
1 
year 
following 
implantaFon, 
and 
yearly 
thereauer. 
At 
these 
endpoints, 
prostheFc 
aorFc 
valve 
steno-­‐ 
sis 
and 
regurgitaFon 
should 
be 
reported.
Diagnosis 
of 
aorFc 
stenosis 
• Establishing 
diagnosis 
of 
severe 
AS 
– AVA 
<0.8-­‐1.0 
or 
AVAI 
<0.6cm/m2 
– MG 
>40 
mmHg 
– Peak 
velocity 
>4.0 
m/s 
• Pixalls 
in 
ECHO 
diagnosis 
– Gradient 
post-­‐ectopic 
– Hyperdynamic 
states 
eg 
anaemia 
– AorFc 
regurgitaFon 
– Doppler 
beam 
not 
parallel 
to 
valve 
being 
assessed 
– Low 
LVEF 
“classical” 
LF 
LG 
severe 
AS 
(DSE 
of 
use): 
severe 
vs 
pseudosevere 
AS 
and 
contracFle 
reserve 
– Normal 
LVEF 
“paradoxical” 
LF 
LG 
severe 
AS: 
hypertrophied 
low 
volume 
LV, 
low 
SV
• TTE 
(pre-­‐TAVI 
planning) 
– Annular 
dimension 
for 
accurate 
valve 
sizing 
• LimitaFons 
of 
TTE 
and 
TOE 
• TAVI 
CT 
method 
of 
choice 
• Undersizing 
may 
cause 
PVL, 
valve 
migraFon 
• Oversizing 
may 
cause 
root 
rupture 
and 
incomplete 
expansion 
of 
valve 
leaflets 
with 
valvular 
AR, 
reducFon 
in 
valve 
durability 
• Annular 
diameter 
measure 
in 
systole 
(annulus 
is 
bigger 
in 
systole), 
in 
PSLAX, 
at 
point 
of 
inserFon 
of 
aorFc 
cusps 
(virtual 
annulus), 
from 
Fssue 
blood 
interface 
to 
Fssue 
blood 
interface: 
trailing 
edge 
to 
leading 
edge 
• TTE 
underesFmates 
the 
annulus 
in 
most 
cases 
(not 
measuring 
true 
diameter, 
annulus 
no 
circular 
but 
oval 
in 
most 
cases) 
• TOE 
2D 
sFll 
underesFmates 
annulus 
in 
30% 
of 
cases, 
but 
overesFmates 
annulus 
in 
10-­‐20% 
of 
cases 
making 
valve 
sizing 
difficult 
• TOE 
3D 
is 
more 
accurate 
and 
correlates 
well 
with 
TAVI 
CT 
measurements 
but 
resoluFon 
much 
lower 
and 
equipment 
and 
experience 
required 
to 
be 
useful
• TTE 
(pre-­‐TAVI 
planning) 
– Bicuspid 
vs 
tricuspid 
valve 
– LV 
and 
RV 
dimensions 
and 
funcFon 
– AorFc 
regurgitaFon 
– Structure 
and 
funcFon 
of 
other 
valves 
– LVOT 
obstrucFon 
– Basal 
septal 
hypertrophy 
– LV 
thrombus 
– Pre-­‐exisFng 
echolucent 
pericardial 
space 
eg 
fluid 
or 
fat 
and 
calcificaFon 
(trans-­‐apical)
• TOE 
(pre-­‐TAVI 
planning) 
– Not 
rouFnely 
done 
pre-­‐procedure 
since 
rouFne 
TAVI 
CT 
performed 
– used 
in 
our 
insFtuFon 
intra-­‐procedurally 
(annulus 
measurements 
confirmed) 
– If 
doubt 
re: 
aorFc 
root, 
annular 
size, 
bicuspid 
vs 
tricuspid, 
LVOT 
calc 
– TOE 
assumes 
annular 
circularity 
– 
almost 
never 
the 
case 
– Annulus 
to 
RCA 
osFum 
can 
be 
measured 
but 
not 
the 
annulus 
to 
LCA 
osFum 
(requires 
3D-­‐TOE 
or 
MSCT) 
– AorFc 
arch 
atheroma 
– 
important 
to 
know 
but 
MSCT 
also 
good 
and 
devices 
smaller 
more 
stearable 
with 
less 
risk 
of 
embolisaFon
• Role 
of 
2D-­‐ECHO 
limited 
during 
TAVI 
– Immediate 
detecFon 
of 
complicaFons 
at 
any 
stage 
– Eg 
causes 
for 
hypotension: 
• Tamponade, 
severe 
PVL, 
root 
rupture, 
new 
LV 
dysfuncFon 
(coronary 
obstrucFon) 
– Assessment 
of 
valve 
funcFon 
auer 
deployment 
• Mechanism 
of 
AR 
• PVL 
• Valvular 
regurgitaFon 
• Systolic 
valve 
funcFon: 
eg 
remaining 
gradient/area, 
need 
for 
further 
postdilataFon 
– Deep 
TG 
view: 
CW, 
PW, 
CF 
• Prosthesis 
impingement 
of 
the 
AML 
if 
prosthesis 
extends 
past 
the 
AML 
hinge 
point 
• Complemented 
by 
haemodynamic 
assessment 
and 
aortography
• Role 
of 
3D-­‐TEE 
during 
TAVI 
– Annulus 
dimension 
confirmaFon 
if 
doubt 
– 
important 
for 
accurate 
prosthesis 
sizing 
– Assessment 
of 
severity 
of 
PVL 
post 
TAVI 
deployment 
• Planimetry 
of 
regurgitant 
orifice 
(eg 
DTG, 
Mid-­‐oesophageal) 
• Planimetry 
of 
vena 
contracta 
– Other 
imaging 
modaliFes: 
• Intracardiac 
ECHO 
(ICE) 
• Trans-­‐nasal 
TOE
Follow 
up 
assessment 
• The 
follow-­‐up 
assessment 
should 
also 
begin 
with 
valve 
imaging 
and 
documentaFon 
of 
changes 
in 
morphology. 
When 
determining 
whether 
a 
paFent 
has 
developed 
haemodynamically 
significant 
structural 
valve 
failure, 
the 
paFent’s 
own 
baseline 
echocardiographic 
parameters 
should 
be 
used 
as 
a 
reference. 
• An 
increase 
in 
the 
mean 
gradient 
>10 
mm 
Hg, 
a 
decrease 
in 
the 
EOA>0.3-­‐0.4 
cm2, 
or 
a 
reducFon 
in 
the 
DVI>0.1-­‐0.13 
probably 
indicates 
a 
change 
in 
valve 
funcFon 
and 
should 
trigger 
a 
comprehensive 
haemody-­‐ 
namic 
evaluaFon 
• Whenever 
valve 
dysfuncFon 
is 
suspected, 
the 
careful 
evaluaFon 
of 
valve 
morphology 
should 
confirm 
a 
structurally 
abnormal 
valve. 
In 
addiFon, 
measurement 
error 
must 
be 
excluded; 
the 
use 
of 
a 
consistent 
LVOT 
diameter 
for 
more 
accurate 
follow-­‐up 
study 
comparisons 
is 
recommended. 
• Finally, 
changes 
in 
ventricular 
morphology 
would 
be 
expected 
in 
the 
se}ng 
of 
long-­‐standing 
significant 
valvular 
dysfuncFon 
and 
this 
parameter 
may 
support 
the 
clinical 
assessment 
of 
severity.
TAVI 
-­‐ 
PROCEDURAL 
GUIDANCE
TAVI 
– 
IMAGING 
MODALITIES 
• ECHO 
• MSCT 
• FLUORO 
• CMR 
• HYBRID 
– 
MSCT+FLUORO 
• OTHERS 
– 
IVUS, 
ICE
ICE 
for 
TAVI
IVUS 
FOR 
TAVI 
VOLCANO 
CorporaFon 
-­‐ 
9F 
-­‐ 
60 
mm 
field 
of 
depth 
IVUS 
MSCT
3MENSIO
PHILIPS 
– 
MSCT 
(NAVIGATOR)
TAVI
Key TAVI Exclusion Criteria by 
ECHO 
• Bicuspid or unicuspid valve 
• Severe valvular regurgitation (any) 
• Pre-existing prosthetic heart valve 
• Moderate/severe MS 
• Hypertrophic obstructive cardiomyopathy 
• Severe basal septal hypertrophy with 
LVOT gradient 
• Aortic annulus<20 or >29 mm 
• Asc aorta diameter >43 mm (>40 for small 
annulus)
PLAX 
of 
typical 
severe 
AS 
with 
gradients 
and 
AVA 
on 
side
PLAX 
Mr 
Neville 
Pseudosevere 
AS 
or 
Mr 
Ferris 
(gradient 
and 
AVA)
DSE 
Features 
to 
look 
for 
to 
disFnguish 
between 
true 
severe 
and 
pseudo 
severe 
AS
Paradoxical 
LF 
LG 
N 
LVEF
Circ 
Cardiovasc 
Interv: 
2008 
Piazza 
et 
al
• The 
immediate 
post-­‐TAVI 
evaluaFon 
documents 
iniFal 
valve 
appearance 
(posiFon 
and 
circularity 
of 
the 
stent, 
and 
leaflet 
morphology 
and 
moFon) 
and 
a 
comprehensive 
haemodynamic 
evaluaFon. 
Valve 
Academic 
Research 
ConsorFum-­‐2 
advocates 
using 
the 
integraFve 
approach 
• Using 
1 
flow 
dependent 
(eg, 
mean 
gradient) 
and 
1 
flow 
independent 
criterion 
(eg, 
EOA) 
for 
the 
iniFal 
haemodynamic 
evaluaFon 
• If 
there 
is 
discordance 
between 
these 
measurements, 
then 
the 
DVI 
should 
be 
calculated. 
An 
abnormal 
DVI 
indicates 
possible 
prostheFc 
valve 
dysfuncFon 
• A 
normal 
DVI 
indicates 
intrinsically 
normal 
prostheFc 
valve 
funcFon, 
and 
the 
indexed 
EOA 
can 
then 
be 
used 
to 
determine 
the 
reason 
for 
the 
iniFal 
measurement 
discordance. 
When 
the 
indexed 
EOA 
is 
low 
in 
the 
se}ng 
of 
a 
normal 
DVI, 
the 
paFent 
probably 
has 
a 
prosthesis–paFent 
mismatch 
(PPM), 
an 
indicator 
of 
the 
intrinsic 
relaFonship 
of 
the 
implanted 
valve 
to 
the 
cardiac 
output 
requirements 
of 
the 
paFent 
• Prosthesis–paFent 
mismatch 
occurs 
in 
the 
se}ng 
of 
a 
morphologically 
normal 
valve 
and 
is 
considered 
to 
be 
haemodynamically 
insignificant 
if 
the 
indexed 
EOA 
is 
>0.85 
cm2/m2, 
moderate 
if 
between 
• 0.65 
and 
0.85 
cm2/m2, 
and 
severe 
if<0.65 
cm2/m2. 
However, 
for 
obese 
paFents 
(body 
mass 
index 
>30 
kg/ 
m2) 
lower 
criteria 
may 
be 
more 
appropriate
• There 
is 
growing 
evidence 
suggesFng 
a 
significant 
associaFon 
of 
post-­‐ 
procedural 
paravalvular 
aorFc 
regurgitaFon 
(AR) 
with 
short-­‐ 
and 
long-­‐ 
term 
mortality. 
• As 
the 
number 
of 
implanted 
transcatheter 
heart 
valves 
increases, 
valve 
durability 
and 
dysfuncFon 
become 
more 
crucial 
issues. 
• EvaluaFng 
the 
presence 
and 
severity 
of 
regurgitaFon 
should 
include 
an 
assessment 
of 
both 
central 
and 
para-­‐valvular 
components, 
with 
a 
combined 
measurement 
of 
‘‘total’’ 
aorFc 
regurgitaFon 
(AR) 
reflecFng 
the 
total 
volume 
load 
imposed 
on 
the 
LV 
• The 
quanFtaFve 
and 
semi-­‐quanFtaFve 
haemodynamic 
assessment 
of 
AR 
severity 
should 
be 
performed 
with 
Doppler 
echocardiography 
according 
to 
the 
guidelines 
• Color 
Doppler 
evaluaFon 
should 
be 
performed 
just 
below 
the 
valve 
stent 
for 
para-­‐valvular 
jets, 
and 
at 
the 
co-­‐aptaFon 
point 
of 
the 
leaflets 
for 
central 
regurgitaFon
• Although 
all 
imaging 
windows 
should 
be 
used, 
the 
parasternal 
short-­‐axis 
view 
is 
criFcal 
in 
assessing 
the 
number 
and 
severity 
of 
paravalvular 
jets 
• Whenever 
possible, 
the 
quanFficaFon 
of 
the 
prostheFc 
regurgitant 
volume, 
effecFve 
regurgitant 
orifice 
area, 
and 
regurgitant 
fracFon 
(Table 
10) 
should 
be 
performed 
• The 
regurgitant 
volume 
may 
be 
calculated 
as 
the 
difference 
between 
the 
stroke 
volume 
across 
any 
non-­‐regurgitant 
orifice 
(RVOT 
or 
mitral 
valve) 
and 
the 
stroke 
volume 
across 
the 
LVOT 
• It 
is 
important 
to 
realize 
that 
at 
this 
Fme 
the 
body 
of 
evidence 
supporFng 
the 
numerical 
criteria 
used 
in 
Table 
10 
as 
well 
as 
Figure 
4 
may 
be 
limited. 
These 
criteria 
should 
be 
used 
as 
guidelines 
for 
clinical 
decision-­‐making 
and 
require 
further 
validaFon 
as 
our 
experience 
conFnues 
to 
expand
– Accurate 
quanFficaFon 
of 
AR 
post 
TAVI 
• May 
consist 
of 
valvular 
and 
para-­‐valvular 
AR 
(usually 
just 
PVR) 
• Valvular 
AR: 
CF 
doppler, 
– length 
of 
jet 
unreliable 
indicator 
of 
severity, 
– proximal 
jet 
width 
or 
cross-­‐secFonal 
area 
preferred, 
– following 
criteria: 
<25% 
mild, 
26-­‐64% 
moderate, 
>65% 
severe, 
limited 
to 
valvular 
AR 
as 
PVR 
ouen 
mulFple 
jets, 
irregular 
shaped 
jets 
and 
eccentric 
jets 
• Valvular 
AR: 
Vena 
Contracta 
– VC 
esFmate 
of 
EROA 
– AcousFc 
shadowing 
from 
stent/sewing 
ring 
may 
interfere 
with 
measurements 
– VC 
measured 
at 
the 
level 
of 
the 
cusps 
of 
the 
bioprostheFc 
valve 
• QuanFtaFve 
measurements 
– Total 
SV-­‐non-­‐regurgitant 
valve 
SV=RV 
– EROA: 
SV/VTI 
– Based 
on 
several 
measurements 
with 
potenFal 
for 
errors 
significant
• Para-­‐valvular 
AR: 
• ASE/EAE 
guidelines 
• Vena 
Contracta 
– Measured 
at 
the 
prox 
end 
of 
the 
stent 
skirt 
– No 
validaFon 
for 
adding 
the 
vena 
contracta 
of 
mulFple 
jets 
• ProporFon 
of 
the 
circumference 
of 
the 
sewing 
ring/proximal 
stent 
skirt 
occupied 
by 
the 
jet 
gives 
a 
semi-­‐quanFtaFve 
guide 
to 
severity: 
– <10% 
mild 
– 10-­‐20% 
moderate 
– >20% 
severe 
– Assumes 
conFnuity 
of 
the 
jet 
which 
may 
not 
be 
the 
case 
for 
transcatheter 
valves 
and 
thus 
may 
overesFmate 
the 
severity 
of 
PVAR 
in 
the 
se}ng 
of 
mulFple 
small 
jets 
– This 
approach 
does 
not 
consider 
the 
that 
the 
radial 
extent 
of 
PV 
jets 
may 
vary 
(eg 
surgical 
PVL) 
and 
in 
the 
case 
of 
transcatheter 
valves 
may 
be 
very 
small 
ie 
not 
a 
big 
problem 
– AfempFng 
to 
add 
the 
degrees 
of 
involvement 
when 
the 
jets 
are 
small 
is 
challenging 
• QuanFtaFve 
methods 
for 
assessment 
of 
severity 
of 
PVAR 
post 
TAVI 
– RV: 
– comparison 
of 
SV 
across 
AV 
(forward+regurg 
vol) 
LVOT 
and 
a 
non-­‐regurgitant 
valve 
eg 
mitral 
or 
tricuspid 
(RV 
ouxlow), 
can 
be 
used 
for 
prostheFc 
valves 
and 
for 
TAVI 
– Total 
stroke 
volume 
also 
measured 
by: 
subtracFng 
LVESV 
(forward) 
from 
LVEDV(forward+regurgitant), 
not 
accurate 
with 
2D, 
3D 
may 
be 
the 
method 
of 
choice, 
growing 
evidence 
for 
3D 
evaluaFon 
of 
RV 
by 
this 
method 
for 
naFve 
AR 
– EROA: 
– Shore 
pressure 
half 
Fme 
of 
CW 
doppler 
signal 
of 
AR: 
problem: 
mulFple 
jets, 
eccentric, 
irregular 
shape, 
– Density 
of 
spectral 
display: 
best 
if 
one 
single 
jet 
– Diastolic 
flow 
reversal 
in 
the 
desc 
aorta: 
PW 
doppler 
from 
the 
suprasternal 
notch/abdominal 
aorta 
from 
subcostal 
view 
• CombinaFon 
of 
above, 
iniFal 
haemodynamic 
assessment 
and 
aortography 
is 
ouen 
required 
as 
well 
as 
clinical 
parameters 
during 
follow 
up 
• CMR 
auer 
7 
weeks 
in 
experienced 
centres 
with 
the 
right 
magnet 
is 
the 
most 
accurate 
and 
limited 
evidence 
suggests 
that 
the 
echo 
assessment 
underesFmates 
the 
degree 
of 
severity 
of 
PVR 
post 
TAVI
Echocardiography in TAVI patients 2014

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Echocardiography in TAVI patients 2014

  • 1. TAVI – IMAGING +ICE +IVUS +HYBRID
  • 2. Use of Imaging for TAVI § Assessment pre TAVI § TTE, MSCT, 3DE, coronary angiography § Assessment during TAVI § TOE/TTE, Fluroscopy § Assessment post TAVI § TTE, MSCT
  • 3. Assessment pre TAVI • TTE – Diagnosis: severe AS, morphology – Aortic regurgitation – LVOT/subaortic stenosis – Mitral & tricuspid valves – LV & RV function – Pericardial effusion – LV hypertrophy – LV/LA thrombus • MSCT/3DE – Annulus size – Prosthesis type and size – Coronary height – Sinus of valsalva diameter – Femoral access • Coronary angiography – Proximal CAD – PCI • CMR – LGE – interstitial fibrosis • Dobutamine stress ECHO SCREENING
  • 4.
  • 5. Is it severe AS? • “Flow dependent” parameters • Post-VPC accentuation of gradient • Atrial fibrillation • Aortic regurgitation • “Classical” LG LF severe AS reduced LVEF (DSE) • “Paradoxical” LG LF severe AS normal LVEF • NF, LG, N LVEF severe AS
  • 6.
  • 7. (SV = TVI LVOT x CSA LVOT) or SVI
  • 8.
  • 9. Dobutamine stress ECHO in paFent with LGSAS Baseline CW tracing: Peak velocity 3.2 m/s Mean grad 25 mmHg AVA 0.45 cm2 CW 10ug/kg/min dobutamine Peak velocity 4.1 m/s Mean grad 39 mmHg AVA 0.5 cm2
  • 10. DSE in a patient with Pseudo-severe AS Baseline 5 ug/kg/min Peak velocity stable, AVA increased, contracFle reserve +, absence of severe AS 10 ug/kg/min 20 ug/kg/miin
  • 11. NFHG N EF LFLG N EF NFLG N EF LFLG Low EF Algorithm for classificaFon of paFents with LGSAS MSCT – extent of AV calcium
  • 12. Imaging for aortic annulus sizing prosthesis type/sizing TTE/TOE MSCT 3D-­‐ECHO
  • 13. Circ Cardiovasc Interv: 2008 Piazza et al
  • 14. Understanding Annulus Anatomy VIRTUAL ANNULUS Most basal point of aortic leaflet attachment Measured during systole, ensure alignment, Circ Cardiovasc Interv: 2008 Piazza et al trailing edge to leading edge – PLAX TTE/TOE
  • 15. MSCT ECHO 3D 2D AorFc annulus is oval In shape in majority of PaFents RaFo of longD/shortD 1.28
  • 16.
  • 17. Basal SAX view of Aortic Valve RC LC NC Circ Cardiovasc Interv: 2008 Piazza et al
  • 18. AORTIC ANNULUS SIZING -­‐ 2D vs 3D
  • 19. Histology of Aortic Valvar Complex Circ Cardiovasc Interv: 2008 Piazza et al
  • 20.
  • 21. ECHO vs Surgical Assessment Annulus Diameter
  • 22. 2-D TOE Underestimate 35% Correct 55% Overestimate 10% 3-D TOE Mylofe et al, JACC CV Intervent 2014
  • 23. INCORRECT SIZING • WRONG VALVE USED IN 50 % OR CASES
  • 24. Aortic annulus – diameter variation during cardiac cycle Aortic annulus: 4-5% larger in systole vs diastole
  • 25. Which MSCT Measurement to use…… • Short diameter • Long diameter • Mean diameter: SAPIEN • Area-­‐derived diameter • Perimeter-­‐derived diameter • Area: SAPIEN • Perimeter: CoreValve
  • 26. Oversizing – does it mafer? • 10-­‐20% oversizing recommended • Area/perimeter/mean diameter • TransiFon zone – Annulus falls between two valve sizes • Presences of LVOT calcium – Important: • balloon-­‐expandable valves: root rupture • Self-­‐expanding valves: para-­‐valvular leak • Any post-­‐TAVI BAV: root rupture/valvular AR
  • 27.
  • 28. CONSEQUENCES OF INACCURATE AORTIC ANNULUS SIZING • ANNULUS RUPTURE – BALLOON EXPANDABLE – SELF-­‐EXPANDING • PARAVALVULAR AORTIC REGURGITATION – LINKED TO PROGNOSIS • VALVULAR AORTIC REGURGITATION • PROSTHESIS EMBOLISATION • PPM REQUIREMENT POST TAVI • POST-­‐TAVI BAV – ASSOCIATED WITH INCREASED RISK OF CVA
  • 29.
  • 31. 3D ANALYSIS OF 3-­‐DIMENSIONAL STRUCTURE
  • 32.
  • 33.
  • 34. AORTIC ANNULUS – INACCURATE SIZING
  • 35. Imaging for aortic annulus sizing prosthesis type/sizing TTE/TOE MSCT 3D-­‐ECHO
  • 36.
  • 37.
  • 38.
  • 39.
  • 40.
  • 41. GA required for 3D TOE
  • 43.
  • 44. When should 3DE be a surrogate, alternative or preferred for TAVI sizing • When MSCT cannot be obtained but 3D available – No local expertise with MSCT • When MSCT is contraindicated/risky – Severe renal impairment • When there is doubt regarding the quality of the MSCT – Motion artifact/difficult to repeat
  • 45. MSCT for assessment of peripheral access
  • 46. 3-­‐MENSIO VALVES (MSCT BASED FEM ART ACCESS ANALYSIS)
  • 47. MSCT GOLD STANDARD FOR AORTIC ANNULUS SIZING 2D TEE AND TTE UNDERESTIMATES AORTIC ANNULUS DIMENSIONS AORTIC ANNULUS DIMENSIONS IMPORTANT FOR ACCURATE PROSTHESIS SIZING
  • 48. OR SLIDE FROM JAMES’ TAVI Talk on peripheral access
  • 50. TAVI -­‐ PROCEDURAL STEPS • Baseline ECHO • Peripheral access • Identify ideal projection • Cross valve • BAV • TAVI valve positioning • TAVI valve deployment • Post deployment final assessment – Haemodynamic – Aortography – TOE/TTE • Real-time monitoring for complications during procedure
  • 51. Baseline TOE/TTE at start of procedure • Confirm gradients • Baseline aortic regurgitation • Baseline mitral valve assessment • LVOT • Baseline LV/RV wall motion • Baseline pericardial effusion • Online monitoring of valve procedure/complications • Repeat all at end of procedure + check for complications
  • 52.
  • 53. M85, CKD, COPD, PAF, T2D Class IV NYHA, no significant CAD
  • 54.
  • 55.
  • 56.
  • 57.
  • 58.
  • 59.
  • 60.
  • 61. SUPPORTIVE HYBRID REAL-­‐TIME GUIDANCE Overlay of 3D MSCT images from pre-­‐procedure Screening on top of live X-­‐Ray fluoroscopy
  • 62.
  • 63.
  • 64. PSAX TTE Day 1 Post TAVI CDF
  • 65.
  • 66.
  • 67. Procedural Findings Assessment of Post-­‐Procedural AR: Requires agreement of three assessment tools Echocardiography Hemodynamics Aortography PVAR vs VAR Severity ComplicaFons AR Valve posiFon Gradient/AVI Coronary perfusion TCT 2013 Procedural Outcomes Extreme Risk Study | Iliofemoral Pivotal 67
  • 68. Cath Lab Assessment Immediate Post Deployment • Haemodynamic – AV index: Ao diastolic pressure-­‐LVEDP (<25 = significant AR) – Peak to Peak gradient + mean gradient (PT Ao-­‐LVPT) • Aortography – PVAR/VAR – use enough contrast/RAO projecFon – Coronary artery perfusion – Competence of aorFc root • ECHO: TOE/TTE – AorFc paravalvular and valvular leak – Systolic valve funcFon: PG, MG, AVA – LV/RV systolic funcFon – Pericardial effusion – compare with baseline – Mitral valve funcFon – mitral regurgitaFon, AML hinge point – Tricuspid valve/pulmonary pressure
  • 69. ComplicaFons & Management AorFc RegurgitaFon • Typically paravalvular mild or mild-moderate severity • Most of AR disappears or reduces at 1 yr follow-up [13% absent, 80% mild AR] Cardiol Clin 29 (2011) 211–222 J. Am. Coll. Cardiol. 2012;59;1200-­‐1254
  • 71.
  • 72. Annular and leaflet calcification may limit prosthesis expansion – cause of PVAR
  • 73. Paravalvular/valvular aorFc regurgitaFon post TAVI • AeFology (paravalvular) – MalposiFon • Supra-­‐annular • Infra-­‐annular – Underexpansion • Focal/widspread calcificaFon – Prosthesis mismatch • Undersizing – Horizontal aorta: • AeFology (valvular) significant VAR uncommon – Incorrect prosthesis size • Oversizing – Valve damage during procedure – Underexpanded valve – calcium – Overexpansion of valve – post TAVI BAV
  • 74.
  • 75.
  • 76.
  • 77.
  • 78. Assessment of para-­‐valvular aorFc regurgitaFon post TAVI ** Not well-­‐validated and may overesFmate the severity compared with the quanFtaFve doppler PVAR assessment cont’d…….. TOE: Deep transgastric permits best axial alignment for the quanFtaFve doppler measurement of regurgitant pressure half-­‐Ame. PLAX and PSAX ME: indenFficaFon of site, number and extent of PVAR jets. Vena contracta diameter and area can be assessed using 2D and 3D colour doppler but may not be a reliable measure of PVAR post TAVI (mulFple, small, irregular shape, eccentric jets)
  • 79. Para-­‐valvular AR post TAVI ME PSAX ME PLAX
  • 80.
  • 81.
  • 82. Native aortic valve regurgitation post balloon aortic valvuloplasty
  • 84. US Pivotal Extreme Risk Study Surgical AVR paravalvular leak: 2-­‐4%
  • 85. US Pivotal Extreme Risk Study
  • 86. Malposition – infra-annular SAPIEN Balloon-­‐expandable
  • 87. Malposition – infra-annular Different Mechanism: CoreValve self-expanding
  • 90. Annular Rupture, Aortic Dissection…
  • 91. TAVI IMAGING at follow-up • Imaging modalities – TTE –valve function – MSCT – valve deformity – CMR – LV/RV assessment FOLLOW-­‐UP
  • 92. Suggested time for routine ECHO follow up post TAVI § 24-48 hrs, pre-discharge § 30 days § 6 month § 12 months § Then yearly thereafter
  • 93. Routine ECHO assessment of TAVI valve • Valve position • Valve morphology • Valve function – Systolic – Diastolic • LV size and systolic function +RV • Mitral + tricuspid • Pulmonary pressure • Pericardial effusion
  • 94. How is TAVI different from SAVR • TAVI (vs SAVR) – No sewing ring – Much longer prosthesis (up to 55 mm) • Flow acceleration • LVOT diameter • Valve type • PVAR – Native valve in situ • Calcium, leaflets, prosthesis type, size, expansion – LBBB more common
  • 95. Definition of new valve dysfunction at follow-up • Suspected structural TAVI failure: compare to patient’s baseline ECHO eg TTE post-procedure (Day 1) • Significant changes: – An increase in the mean gradient >10 mmHg – A decrease in the AVA >0.3-0.4 cm2 – A reduction in the DVI >0.10-0.13 • Exclude measurement error – – Baseline (Day 1) LVOT diameter – Depends on valve depth in LVOT and valve type – LVOT diameter and LVOT velocity for AVA should be measured in same location outside the stent frame – LVOT non-circular – Flow acceleration inside stent frame prox to valve cusps with elevated velocity • Note changes in LV function and allow for effect on gradient
  • 96. Definition of new valve dysfunction at follow-up • Suspected structural TAVI failure: compare to patient’s baseline ECHO eg TTE post-procedure (Day 1) • Significant changes: – An increase in the mean gradient >10 mmHg – A decrease in the AVA >0.3-0.4 cm2 – A reduction in the DVI >0.10-0.13
  • 98. Post-implantation follow up of TAVI patients • Similar to follow up of surgically implanted prostheses but two important differences – Calculation of EOA as an index of valve opening: • Founded in ratio of post- to pre-valvular velocities • Flow acceleration within transcatheter valve proximal to the valve cusps • Pre-valvular velocity should be recorded proximal to the stent (PW doppler with sample situated where LVOT diameter measured) and the post-valvular velocity recorded with CW doppler reflects that distal to the stented valve • If the LVOT velocity used in the calculations is erroneously recorded inside the stent but proximal to the cusps the result will be an increased velocity with an overestimation of the valve area and DVI
  • 99. Prosthetic Aortic Stenosis • Limitation of flow independent parameters – The absolute EOA does not account for the cardiac output requirements in relation to the patients body size – The indexed EOA may overestimate the haemodynamic burden in obesity; hence lower criteria may be more appropriate in patients with a BMI>30kg/m2 – DVI severity criteria are dependent on LVOT size ie a lower threshold may be more appropriate if LVOT>25mm – The LVOT should be measured just beneath the ventricular margin of the valve stent/skirt – Unlike the surgically implanted valve, the transcatheter prosthetic valve EOA is defined not only by the size of the valve but also by the patient’s aortic valve/annular anatomy and procedural variables. Thus, well-established normal trans- catheter valve gradients and EOAs based on preimplant aortic annular dimensions do not currently exist.
  • 100.
  • 101. • In condiFons of normal or near normal SV
  • 102. DSE
  • 103.
  • 104.
  • 105. Assessment of para-­‐valvular and valvular prostheFc AR post TAVI ** Not well-validated, assumes continuity of flow and may overestimate the severity compared with the quantitative doppler PLAX and PSAX TTE: Number/distribution and extent of PVAR jets. A3C and A5C for further assessment of jets: PHT.
  • 106. MSCT post TAVI Coronal Oblique View 3D volume rendered view Medtronic CoreValve 2 weeks post TAVI -­‐Adequate deployment -­‐No instent restenosis -­‐Patent coronary art -­‐Good valve posiFon -­‐Integrity of stent struts -­‐thrombus/vegetaFon visible on leaflets -­‐Assymmetric expansion
  • 109. TTE PRE TAVI PLAX: CDF VAR/MR & A5C: CDF VAR
  • 110.
  • 112. A5C TTE Day 1 Post TAVI VTI LVOT
  • 113. A5C TTE Day 1 Post TAVI CW AorFc Valve
  • 114. PORTICO TAVI D1 LVOT measurement
  • 115. A5C TTE Day 2 Post TAVI PW LVOT outside valve and inside valve
  • 116. A5C TTE Day 2 Post TAVI CW AorFc Valve
  • 118. PORTICO Day 1 – Post TAVI Baseline TTE Day 1 post TAVI
  • 119. TTE PRE TAVI PLAX: CDF VAR/MR & A5C: CDF VAR
  • 120. PORTICO Day 1 – Post TAVI Baseline TTE Day 1 post TAVI
  • 121. A4C TTE Day 2 Post TAVI Simpsons Biplane for LVEF
  • 122. PLAX TTE Day 1 Post TAVI
  • 123. PSAX TTE Day 1 Post TAVI CDF
  • 124. PSAX 2D TTE Day 1 Post TAVI
  • 125. A5C TTE Day 1 Post TAVI
  • 126. A5C TTE Day 1 Post TAVI PVAR PHT
  • 127. PSAX TTE Day 1 Post TAVI Mitral Valve CDF
  • 128. PSAX TTE Day 1 Post TAVI CDF RVOT/PV/TV/AV
  • 130.
  • 131.
  • 132. A5C TTE Day 2 Post TAVI CDF PVAR and PHT PVAR
  • 133.
  • 134.
  • 135.
  • 136.
  • 137.
  • 138.
  • 139.
  • 140.
  • 141.
  • 142.
  • 143.
  • 144.
  • 145.
  • 146.
  • 147.
  • 148.
  • 149.
  • 150.
  • 151. The color Doppler jet of a paravalvular leak is ouen best appreciated from the deep transgastric TEE view (Figure 19). This view usually permits the best axial alignment for the quanFtaFve Doppler measure of regurgitant pressure half-­‐Fme. The midesophageal views provide the cross-­‐ secFonal and long-­‐ axis views to facilitate idenFficaFon of the site and extent of paravalvular leak. The vena contracta diameter and area can be assessed using 2D and 3D color Doppler applicaFon, respecFvely (Figure 20).
  • 152. Valve funcFon • Valve Academic Research ConsorFum-­‐2 maintains the original recommendaFons to use echocardiography as the primary imaging modality for the assessment of prostheFc valve funcFon.39 This should include the valve posiFon, morphology, funcFon, and evaluaFon of the leu ventricle (LV) and right ventricle (RV) size and funcFon. The sug-­‐ gested Fme points for rouFne follow-­‐up transthoracic echo-­‐ cardiography (TTE) following valve implantaFon are:immediately (before discharge) following the implantaFon for transarterial approaches or within 30 days for transapi-­‐ cal or transaorFc approaches, 6 months following implantaFon, 1 year following implantaFon, and yearly thereauer. At these endpoints, prostheFc aorFc valve steno-­‐ sis and regurgitaFon should be reported.
  • 153. Diagnosis of aorFc stenosis • Establishing diagnosis of severe AS – AVA <0.8-­‐1.0 or AVAI <0.6cm/m2 – MG >40 mmHg – Peak velocity >4.0 m/s • Pixalls in ECHO diagnosis – Gradient post-­‐ectopic – Hyperdynamic states eg anaemia – AorFc regurgitaFon – Doppler beam not parallel to valve being assessed – Low LVEF “classical” LF LG severe AS (DSE of use): severe vs pseudosevere AS and contracFle reserve – Normal LVEF “paradoxical” LF LG severe AS: hypertrophied low volume LV, low SV
  • 154. • TTE (pre-­‐TAVI planning) – Annular dimension for accurate valve sizing • LimitaFons of TTE and TOE • TAVI CT method of choice • Undersizing may cause PVL, valve migraFon • Oversizing may cause root rupture and incomplete expansion of valve leaflets with valvular AR, reducFon in valve durability • Annular diameter measure in systole (annulus is bigger in systole), in PSLAX, at point of inserFon of aorFc cusps (virtual annulus), from Fssue blood interface to Fssue blood interface: trailing edge to leading edge • TTE underesFmates the annulus in most cases (not measuring true diameter, annulus no circular but oval in most cases) • TOE 2D sFll underesFmates annulus in 30% of cases, but overesFmates annulus in 10-­‐20% of cases making valve sizing difficult • TOE 3D is more accurate and correlates well with TAVI CT measurements but resoluFon much lower and equipment and experience required to be useful
  • 155. • TTE (pre-­‐TAVI planning) – Bicuspid vs tricuspid valve – LV and RV dimensions and funcFon – AorFc regurgitaFon – Structure and funcFon of other valves – LVOT obstrucFon – Basal septal hypertrophy – LV thrombus – Pre-­‐exisFng echolucent pericardial space eg fluid or fat and calcificaFon (trans-­‐apical)
  • 156. • TOE (pre-­‐TAVI planning) – Not rouFnely done pre-­‐procedure since rouFne TAVI CT performed – used in our insFtuFon intra-­‐procedurally (annulus measurements confirmed) – If doubt re: aorFc root, annular size, bicuspid vs tricuspid, LVOT calc – TOE assumes annular circularity – almost never the case – Annulus to RCA osFum can be measured but not the annulus to LCA osFum (requires 3D-­‐TOE or MSCT) – AorFc arch atheroma – important to know but MSCT also good and devices smaller more stearable with less risk of embolisaFon
  • 157. • Role of 2D-­‐ECHO limited during TAVI – Immediate detecFon of complicaFons at any stage – Eg causes for hypotension: • Tamponade, severe PVL, root rupture, new LV dysfuncFon (coronary obstrucFon) – Assessment of valve funcFon auer deployment • Mechanism of AR • PVL • Valvular regurgitaFon • Systolic valve funcFon: eg remaining gradient/area, need for further postdilataFon – Deep TG view: CW, PW, CF • Prosthesis impingement of the AML if prosthesis extends past the AML hinge point • Complemented by haemodynamic assessment and aortography
  • 158. • Role of 3D-­‐TEE during TAVI – Annulus dimension confirmaFon if doubt – important for accurate prosthesis sizing – Assessment of severity of PVL post TAVI deployment • Planimetry of regurgitant orifice (eg DTG, Mid-­‐oesophageal) • Planimetry of vena contracta – Other imaging modaliFes: • Intracardiac ECHO (ICE) • Trans-­‐nasal TOE
  • 159.
  • 160. Follow up assessment • The follow-­‐up assessment should also begin with valve imaging and documentaFon of changes in morphology. When determining whether a paFent has developed haemodynamically significant structural valve failure, the paFent’s own baseline echocardiographic parameters should be used as a reference. • An increase in the mean gradient >10 mm Hg, a decrease in the EOA>0.3-­‐0.4 cm2, or a reducFon in the DVI>0.1-­‐0.13 probably indicates a change in valve funcFon and should trigger a comprehensive haemody-­‐ namic evaluaFon • Whenever valve dysfuncFon is suspected, the careful evaluaFon of valve morphology should confirm a structurally abnormal valve. In addiFon, measurement error must be excluded; the use of a consistent LVOT diameter for more accurate follow-­‐up study comparisons is recommended. • Finally, changes in ventricular morphology would be expected in the se}ng of long-­‐standing significant valvular dysfuncFon and this parameter may support the clinical assessment of severity.
  • 161.
  • 163.
  • 164. TAVI – IMAGING MODALITIES • ECHO • MSCT • FLUORO • CMR • HYBRID – MSCT+FLUORO • OTHERS – IVUS, ICE
  • 166. IVUS FOR TAVI VOLCANO CorporaFon -­‐ 9F -­‐ 60 mm field of depth IVUS MSCT
  • 168. PHILIPS – MSCT (NAVIGATOR)
  • 169. TAVI
  • 170.
  • 171.
  • 172.
  • 173. Key TAVI Exclusion Criteria by ECHO • Bicuspid or unicuspid valve • Severe valvular regurgitation (any) • Pre-existing prosthetic heart valve • Moderate/severe MS • Hypertrophic obstructive cardiomyopathy • Severe basal septal hypertrophy with LVOT gradient • Aortic annulus<20 or >29 mm • Asc aorta diameter >43 mm (>40 for small annulus)
  • 174.
  • 175.
  • 176.
  • 177.
  • 178. PLAX of typical severe AS with gradients and AVA on side
  • 179. PLAX Mr Neville Pseudosevere AS or Mr Ferris (gradient and AVA)
  • 180. DSE Features to look for to disFnguish between true severe and pseudo severe AS
  • 181. Paradoxical LF LG N LVEF
  • 182.
  • 183. Circ Cardiovasc Interv: 2008 Piazza et al
  • 184.
  • 185. • The immediate post-­‐TAVI evaluaFon documents iniFal valve appearance (posiFon and circularity of the stent, and leaflet morphology and moFon) and a comprehensive haemodynamic evaluaFon. Valve Academic Research ConsorFum-­‐2 advocates using the integraFve approach • Using 1 flow dependent (eg, mean gradient) and 1 flow independent criterion (eg, EOA) for the iniFal haemodynamic evaluaFon • If there is discordance between these measurements, then the DVI should be calculated. An abnormal DVI indicates possible prostheFc valve dysfuncFon • A normal DVI indicates intrinsically normal prostheFc valve funcFon, and the indexed EOA can then be used to determine the reason for the iniFal measurement discordance. When the indexed EOA is low in the se}ng of a normal DVI, the paFent probably has a prosthesis–paFent mismatch (PPM), an indicator of the intrinsic relaFonship of the implanted valve to the cardiac output requirements of the paFent • Prosthesis–paFent mismatch occurs in the se}ng of a morphologically normal valve and is considered to be haemodynamically insignificant if the indexed EOA is >0.85 cm2/m2, moderate if between • 0.65 and 0.85 cm2/m2, and severe if<0.65 cm2/m2. However, for obese paFents (body mass index >30 kg/ m2) lower criteria may be more appropriate
  • 186. • There is growing evidence suggesFng a significant associaFon of post-­‐ procedural paravalvular aorFc regurgitaFon (AR) with short-­‐ and long-­‐ term mortality. • As the number of implanted transcatheter heart valves increases, valve durability and dysfuncFon become more crucial issues. • EvaluaFng the presence and severity of regurgitaFon should include an assessment of both central and para-­‐valvular components, with a combined measurement of ‘‘total’’ aorFc regurgitaFon (AR) reflecFng the total volume load imposed on the LV • The quanFtaFve and semi-­‐quanFtaFve haemodynamic assessment of AR severity should be performed with Doppler echocardiography according to the guidelines • Color Doppler evaluaFon should be performed just below the valve stent for para-­‐valvular jets, and at the co-­‐aptaFon point of the leaflets for central regurgitaFon
  • 187. • Although all imaging windows should be used, the parasternal short-­‐axis view is criFcal in assessing the number and severity of paravalvular jets • Whenever possible, the quanFficaFon of the prostheFc regurgitant volume, effecFve regurgitant orifice area, and regurgitant fracFon (Table 10) should be performed • The regurgitant volume may be calculated as the difference between the stroke volume across any non-­‐regurgitant orifice (RVOT or mitral valve) and the stroke volume across the LVOT • It is important to realize that at this Fme the body of evidence supporFng the numerical criteria used in Table 10 as well as Figure 4 may be limited. These criteria should be used as guidelines for clinical decision-­‐making and require further validaFon as our experience conFnues to expand
  • 188. – Accurate quanFficaFon of AR post TAVI • May consist of valvular and para-­‐valvular AR (usually just PVR) • Valvular AR: CF doppler, – length of jet unreliable indicator of severity, – proximal jet width or cross-­‐secFonal area preferred, – following criteria: <25% mild, 26-­‐64% moderate, >65% severe, limited to valvular AR as PVR ouen mulFple jets, irregular shaped jets and eccentric jets • Valvular AR: Vena Contracta – VC esFmate of EROA – AcousFc shadowing from stent/sewing ring may interfere with measurements – VC measured at the level of the cusps of the bioprostheFc valve • QuanFtaFve measurements – Total SV-­‐non-­‐regurgitant valve SV=RV – EROA: SV/VTI – Based on several measurements with potenFal for errors significant
  • 189. • Para-­‐valvular AR: • ASE/EAE guidelines • Vena Contracta – Measured at the prox end of the stent skirt – No validaFon for adding the vena contracta of mulFple jets • ProporFon of the circumference of the sewing ring/proximal stent skirt occupied by the jet gives a semi-­‐quanFtaFve guide to severity: – <10% mild – 10-­‐20% moderate – >20% severe – Assumes conFnuity of the jet which may not be the case for transcatheter valves and thus may overesFmate the severity of PVAR in the se}ng of mulFple small jets – This approach does not consider the that the radial extent of PV jets may vary (eg surgical PVL) and in the case of transcatheter valves may be very small ie not a big problem – AfempFng to add the degrees of involvement when the jets are small is challenging • QuanFtaFve methods for assessment of severity of PVAR post TAVI – RV: – comparison of SV across AV (forward+regurg vol) LVOT and a non-­‐regurgitant valve eg mitral or tricuspid (RV ouxlow), can be used for prostheFc valves and for TAVI – Total stroke volume also measured by: subtracFng LVESV (forward) from LVEDV(forward+regurgitant), not accurate with 2D, 3D may be the method of choice, growing evidence for 3D evaluaFon of RV by this method for naFve AR – EROA: – Shore pressure half Fme of CW doppler signal of AR: problem: mulFple jets, eccentric, irregular shape, – Density of spectral display: best if one single jet – Diastolic flow reversal in the desc aorta: PW doppler from the suprasternal notch/abdominal aorta from subcostal view • CombinaFon of above, iniFal haemodynamic assessment and aortography is ouen required as well as clinical parameters during follow up • CMR auer 7 weeks in experienced centres with the right magnet is the most accurate and limited evidence suggests that the echo assessment underesFmates the degree of severity of PVR post TAVI