tavr: the latest information & team strategy...cleveland clinic aortic stenosis –“typical”...
TRANSCRIPT
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Cleveland Clinic
TAVR: The Latest Information & Team Strategy
Samir Kapadia, MD
Professor of Medicine
Section head, Interventional Cardiology
Director, Cardiac Catheterization Laboratory
Cleveland Clinic
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Cleveland Clinic
TAVR – Where Did We Start?
Questions in 2003-4
1. Is there an unmet need for patients with AS?
- May be for inoperable patients
2. How can one improve on outstanding results of SAVR?
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Cleveland Clinic
Aortic Stenosis – “typical” patient2003
• 75 year old patient
• No prior cardiac history
• Presents with shortness of breath with exertion
• No CP
• No lightheadedness
• O/E BP 120/80, HR 90
• No JVD
• S1 normal A2 not heard, late peaking systolic murmur
• No edema
• Lungs clear
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Cleveland Clinic
Sternotomy
Courtesy Dr. Mick
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Cleveland Clinic
Aorta Cross-clamped
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Cleveland Clinic
Surgical Aortic Valve Replacement
Courtesy of Dr. Gosta Pettersson
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Cleveland Clinic
Surgical AVR
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Cleveland Clinic
• 88 yr old, male Ht:171.5cm Wt: 70.1kg BMI: 23• NYHC III
• HTN, CAD, A fib
• Mild CAD
• Former Smoker- Quit 1973
• Hb:12.3 Ht: 37.1
• FEVI: 1.5 L
• Cr 1.8
• EF 45%
• AVA 0.7, peak gradient 64, mean gradient 40 mm
• STS score 8
Clinical Presentation - 2006
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Retrograde Approach
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Final Result
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Cleveland Clinic
Outcome of Patients TF-TAVR at Cleveland Clinic
2006-12 (Initial 262 TF TAVR patients)
2006 2007 2008 2009 2010 2011 2012
Major Stroke 0 1 0 0 2 2 0
Total Procedure 11 11 14 19 39 69 92
Nu
mb
er
of
Pati
en
ts Major Stroke
Total Procedure
2006 2007 2008 2009 2010 2011 2012
Major Bleeding 1 0 0 1 1 6 4
Total Procedure 11 11 14 19 39 69 92
Num
be
r o
f P
atie
nts
Major Bleeding
2006 2007 2008 2009 2010 2011 2012
Vascular Complications 1 2 1 0 6 7 7
Total Procedure 11 11 14 19 39 69 92
Nu
mb
er
of
Pa
tie
nts
Vascular…Total Procedure
2006 2007 2008 2009 2010 2011 2012
30-Day Mortality 0 0 0 0 0 1 0
Total Procedure 11 11 14 19 39 69 92
Num
be
r o
f P
atie
nts
30-DayMortality
30 day mortality
Major bleeding Vascular Complications
Stroke
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History: 88M
6’2’’, 162lb (73 kg)
Relevant PMH:
-Prostate CA
-PAD
-AF
-s/p PPM
-Asbestosis nmlPFT
-Iliac aneurysm
Allergies: NKDA
Labs BUN/Cr: 16/1.1
Hgb/Hct: 11/31
Plt: 112
INR: 1.1
Echo (6/11/15)EF: 63%
AVA, Gradients:
0.77 cm2, 52/29 mmHg
DI: 0.22, SVI 32 ml/m2
Trivial AI, 2+ MR/TR
RV: dilated, nml fxn
RVSP 56
Annular Area
CTA
Annulus 594 mm2 (AG)
LHC/PCI
LMT:, Mild
LAD:, long 40% narrowing
LCX: 60% proximal narrowing
RCA: 40% proximal narrowing
Access: TF (commercial)
Valve size: #29 S3
Coronary dist: RCA 23, LMT 23
Angles: RAO 0/Cau 25
LAO 25/Cran 15
Procedural issues
- Right CIA aneurysm w/ thrombus
- Tortuous left CIA and abd ao
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Cleveland Clinic
Planning : Heart Team
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Cleveland Clinic
• Co-leadership
• Continuous and open
communication
• Early conflict resolution
• Consensus building
• Shared resources
• Shared credits
• Great facility
Cardiologist – Surgeon Collaboration
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Cleveland Clinic
Hybrid Room
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Cleveland Clinic
Minimalist ApproachConscious sedation, No SG, TTE
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Cleveland Clinic
One Perclose and Same Side Sheath
Valve
Access
Pigtail
Access
Pacer
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Cleveland Clinic
Sentinel
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Cleveland Clinic
Valve Deployment
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Cleveland Clinic
Final Picture
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Cleveland Clinic
Procedural Log
8:47 to 9:15 = 28 minutes
Access, temp wire, Sentinel, Valve deployment
Closure of groin
Fluorotime 11 miutes
Radiation 159 mGy
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BalloonExpandable
SelfExpandable
OtherDesigns
SAPIEN (Edwards)*no longer available
SAPIEN XT (Edwards) S3 (Edwards)
HLT (Heart Leaflet Technologies)
Colibri Heart Valve
CoreValve (Medtronic) Portico (St. Jude Medical)Evolut R (Medtronic) Centera (Edwards) Venus (Medtech)
Lotus (Boston Scientific) Direct Flow Valve (DFM) Acurate (Symetis Inc) Engager (Medtronic) JenaValve
Inovare valve (Braile Biomedica )
Commercially available and investigational devices for TAVI
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STS/ACC TVT Registry Participating Sites
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TVT RegistryTAVR and TAVR ViV Procedures
4,666
8,946
16,301
24,819
38,276
51,303 51,643
225 499 1318 2358 3153 3244
0
10,000
20,000
30,000
40,000
50,000
60,000
2012 2013 2017 2018 Q1-Q32014 2015 2016
TVT Registry Datamart Data as of 1/22/2019
TAVR ViV
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Cleveland Clinic
Which Patients?
Extreme
Risk
Intermediate
Risk
Low RiskHigh RiskF
utile
RCT
PARTNER1B PARTNER1B
CoreValve
S3i
SURTAVI
NOTION
P3 & CoreValve
Standard
Vs
TAVR
SAVR
Vs
TAVR
SAVR
Vs
TAVR
SAVR
Vs
TAVR
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RCT - TAVR versus SAVR
Mack, JACC 2018, 72, 18, 2018, 2106-8
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P1ATAVR
N=348
P1ASAVR
N=351
CoreValveHigh Risk
TAVRN=390
CoreValveHigh Risk
SAVRN=357
PIIAXT
N=994
PIIASAVR
N=1021
S3i S3
N=1077
NotionTAVR
N=145
Notion SAVR
N=135
All Stroke 5.5 2.4 4.9 6.2 5.5 6.1 2.7 2.8 3.0
Disabling Stroke
3.8 2.1 3.9 3.1 3.2 4.3 1.0 1.4 3.0
TIA 0.9 0.3 0.8 0.3 0.9 0.4 NA 1.4 0
MajorVascular
11.0 3.2 5.9 1.7 7.9 5.0 5.6 5.6 1.5
Bleeding 9.3 19.5 13.6 35.0 10.4 43.4 5.4 11.3 20.9
AKI 2.9 3.0 6.0 15.1 1.3 3.1 0.5 0.7 6.7
New Afib 8.6 16.0 11.7 30.5 9.1 26.4 5.0 16.9 57.8
Complications For TAVR versus SAVR
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Stroke After TAVR and SAVR
CONCLUSION
Despite similar early-peaking (<1 day
post-procedure) neurological risk
profiles, SAVR is associated
with a higher risk of early major
stroke than TF-TAVR.
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What to Expect from Low Risk Trials
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CharacteristicSurgery P1A
(n = 351)
Surgery P2A
(n = 944)
Anesthesia Time (min) 330 333
Procedure Time (min) 230 237
Aortic Cross-clamp Time (min) 74 75
Total CPB Time (min) 105 104
Median ICU Stay (days) 5.0 4.0
Median Total Length of Stay (days) 12 9.0
Surgery Data ComparisonHigh to Intermediate Risk
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Events (%)30 Days
Surgery P1A
(n = 351)
Surgery P2A
(n = 1021)
Death (all-cause)
and Stroke (disabling)8.2 8.0
Death
All-cause 6.5 4.1
Cardiovascular 3.0 3.2
Neurological Events
All Stroke 2.4 6.1
Disabling Stroke 2.1 4.3
TIA 0.3 0.4
Surgical Data Comparison
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Cleveland Clinic
Events (%)
30 Days
P1A
Sapien
N=348
PIIA
XT
N=994
S3i
S3
N=1077
Death (all-cause)
and Stroke (disabling)6.9 6.1 2.0
Death
All-cause 3.4 3.9 1.1
Cardiovascular 3.2 3.3 0.9
Neurological Events
All Stroke 5.5 5.5 2.7
Disabling Stroke 3.8 3.2 1.0
TIA 0.9 0.9 NA
TAVR Data Comparison
*Event rates are KM estimates, p-values are point in time
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Complication P1A
(n = 348)
P2A
(n = 994)
S3i
(n = 1076)
Procedural deaths (0-3 days) 3 (0.9%)* 12 (1.2%) 2 (0.2%)
≥ 2 transcatheter valves 7 (2.0%) 26 (2.6%) 2 (0.2%)
Valve embolization 7 (2.0%) 10 (1.0%) 0 (0%)
Coronary Occlusion 0.0 0.4 0.4
Annular Rupture NA 0.3 0.2
Fluoro time 31 20 19
Procedure Time 133 103 90**
ICU stay 3 2 2
LOS 8 6 4
TAVR Comparison
** Preliminary * During procedure
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Events (%)30 Days
P1A
(n = 348)
P2A
(n = 1011)s3i
(n = 1077)
Rehospitalization 4.4 6.5 4.6
MI 0 1.2 0.3
Major Vascular
Complications7.9 7.9 5.6
Life-Threatening / Disabling
Bleeding9.3 10.4 5.4
AKI (Stage III) 2.9 1.3 0.5
New Atrial Fibrillation 8.6 9.1 5.0
New Permanent Pacemaker 3.8 8.5 10.2
TAVR Outcomes Overtime
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LRT – Prospective Study of Low Risk Patients
Waksman et al, J Am Coll Cardiol 2018;72:2095–105
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The PARTNER 3 Trial
High
Risk
Interm
Risk
Extreme
Risk
Low
Risk
PARTNER 1B
PARTNER 1APARTNER 2A
PARTNER 3• RCT 1:1
• vs. Standard Rx
• N = 358 pts
• RCT 1:1
• vs. SAVR
• N = 699 pts
• RCT 1:1
• vs. SAVR
• N = 2032 pts
• RCT 1:1
• vs. Surgery
• N = 1000 pts
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Low Risk/TF ASSESSMENT by Heart Team
(STS < 4%)
1:1 Randomization
1000 Patients
TAVR(SAPIEN 3 THV)
Surgery
(Surgical Bioprosthetic Valve)
Symptomatic Severe Aortic Stenosis
Follow-up: 30 day, 6 mos, and annually through 10 years
PRIMARY ENDPOINT:
Composite of all-cause mortality, stroke, or CV re-hospitalization
at 1 year post-procedure
PARTNER 3 Study Design
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Severe Calcific Aortic Stenosis
• AVA ≤ 1.0 cm2 or AVA index ≤ 0.6 cm2/m2
• Jet velocity ≥ 4.0 m/s or mean gradient ≥ 40 mmHg, AND
▪ NYHA Functional Class ≥ 2, OR
▪ Abnormal exercise test with severe SOB, abnormal BP
response, or arrhythmia, OR
▪ Asymptomatic with LVEF < 50%
Low Surgical Risk
• Determined by multi-disciplinary heart team
• STS < 4%
• Adjudicated by case review board
Key Inclusion Criteria
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Anatomic• Aortic annulus diameter < 16 mm or > 28 mm (3D imaging)
• Bicuspid valve (CT imaging)
• Severe AR (> 3+) or MR (> 3+) Severe LV dysfunction (LVEF < 30%)
• Severe calcification of aortic valvar complex (esp. LVOT)
• Vascular anatomy not suitable for safe femoral access
• Complex CAD: ULM, Syntax score > 32, or not amenable for PCI
• Low coronary takeoff (high risk for obstruction)
Clinical• Acute MI within 1 month
• Stroke or TIA within 90 days
• Renal insufficiency (eGFR < 30 ml/min) and/or renal replacement Rx
• Hemodynamic or respiratory instability
• Frailty (objective assessment; > 2/4+ metrics)
Key Exclusion Criteria
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SAPIEN Valve Evolution
Valve
Technology
SAPIEN SAPIEN XT SAPIEN 3
Sheath
Compatibility
Available
Valve Sizes23 mm 26 mm 20 mm 23 mm 26 mm 29 mm
22-24F 16-20F 14-16F
23 mm 26 mm 29 mm
PARTNER 1 PARTNER 3PARTNER 2
2011 2014 2015
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Primary Endpoint
• Non-hierarchical composite of all-cause mortality,
all strokes, or CV re-hospitalization at 1 year
▪ Primary analysis was non-inferiority, followed by superiority
▪ Analysis cohort was the ‘as-treated’ (AT) population, defined
as all randomized patients in whom the procedure was
initiated.
▪ Multiple sensitivity analyses performed
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Patient DispositionAs Treated Population
N=950
TAVR with complete 30-day
follow up for primary endpoint
N = 496/496
(100%)
TAVR Initiated (AT) N = 496
1 Conversion to surgery
1 Withdrawal
2 Missed visits
Surgery Initiated (AT) N = 454
1 Aborted procedure
Surgery with complete 30 day
follow-up for primary endpoint
N = 450/454
(99.1%)
Surgery with complete 1 year
follow-up for primary endpoint
N = 442*/454
(97.4%)
*4 patients who withdrew from the surgery arm
are considered to have complete 1-yr follow-up
b/c they had already experienced an endpoint
event prior to withdrawing from the study.
TAVR with complete 1 year
follow-up for primary endpoint
N = 493/496
(99.4%)
11 Withdrawals
1 Lost to follow-up
Valve Implanted (VI)
N = 495
Valve Implanted (VI)
N = 453
98.4% Follow-up for Primary Endpoint
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Baseline Patient Characteristics
Demographics &
Vascular Disease
TAVR
(N=496)
Surgery
(N=454)
Other
Co-Morbidities
TAVR
(N=496)
Surgery
(N=454)
Age (years) 73.3 ± 5.8 73.6 ± 6.1 Diabetes 31.3% 30.2%
Male 67.5% 71.1% COPD (any) 5.1% 6.2%
BMI – kg/m2 30.7 ± 5.5 30.3 ± 5.1 Pulmonary Hypertension 4.6% 5.3%
STS Score 1.9 ± 0.7 1.9 ± 0.6 Creatinine > 2mg/dL 0.2% 0.2%
NYHA Class III or IV* 31.3% 23.8% Frailty (overall; > 2/4+) 0 0
Coronary Disease 27.7% 28.0% Atrial Fibrillation (h/o) 15.7% 18.8%
Prior CABG 3.0% 1.8% Permanent Pacemaker 2.4% 2.9%
Prior CVA 3.4% 5.1% Left Bundle Branch Block 3.0% 3.3%
Peripheral Vascular Disease 6.9% 7.3% Right Bundle Branch Block 10.3% 13.7%
% or mean ± SD
*p = 0.01
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Baseline Echo and CT Characteristics
Characteristic TAVR
(N=496)
Surgery
(N=454)
Aortic Valve Area (cm2) 0.8 ± 0.2 0.8 ± 0.2
Mean Gradient (mmHg) 49.4 ± 12.8 48.3 ± 11.8
LVEF (%) 65.7 ± 9.0 66.2 ± 8.6
LV Mass Index (g/m2) 104.5 ± 25.7 101.5 ± 25.4
≥ Moderate MR 1.3% 3.2%
≥ Moderate AR 3.9% 2.5%
≥ Moderate TR 1.7% 2.3%
CT – Annulus Perimeter (mm) 78.1 ± 6.9 78.6 ± 7.2
CT – Annulus Area (mm2) 473.5 ± 83.3 479.6 ± 87.6
% or mean ± SD
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VariableTAVR
(N=496)
Surgery
(N=454)P-value
Conscious Sedation 65.1% NA NA
Procedure Time (min) 58.6 ± 36.5 208.3 ± 62.2 <0.001
Fluoroscopy Time (min) 13.9 ± 7.1 NA NA
Aortic Cross-Clamp Time (min) NA 74.3 ± 27.8 NA
Total CPB Time (min) NA 97.7 ± 33.8 NA
Median ICU Stay (days) 2.0 3.0 <0.001
Median Total LOS (days) 3.0 7.0 <0.001
Discharge to Home/Self-care 96.0% 73.1% <0.001
Concomitant Procedures 7.9% 26.4% <0.001
Procedural & Hospital Findings
% or mean ± SD
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Procedural ComplicationsIn-Hospital
*Valve-in-valve
ComplicationTAVR
(N=496)
Surgery
(N=454)P-value
In-hospital Death 0.4% (2) 0.9% (4) 0.43
> 2 Transcatheter Valves Implanted* 0.2% (1) NA NA
Valve Embolization 0 NA NA
Aortic Dissection 0 NA NA
Annular Rupture 0.2% (1) NA NA
Ventricular Perforation 0.2% (1) 0.4% (2) 0.61
Coronary Obstruction 0.2% (1) 0.4% (2) 0.61
Access Site Infections 0.4% (2) 1.3% (6) 0.16
% or mean ± SD
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Primary Endpoint
0 3 6 9 12
496 475 467 462 456454 408 390 381 377
Number at risk:
TAVRSurgery
Months after Procedure
451374
TAVRSurgery
Psuperiority= 0.001
HR [95% CI] =
0.54 [0.37, 0.79]
Death
, S
troke, or
Rehosp
(%)
Pnon-inferiority< 0.001
Upper 95% CI of
risk diff = -2.5%
8.5%9.3%
15.1%
4.2%
0
10
20
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All-Cause Mortality
All-
Cause M
ort
alit
y (
%)
494 494 493 492454 445 438 433 431
488427
Months from ProcedureNumber at risk:
1.0%1.1% 2.5%
0
10
0.4%
20HR [95% CI] =
0.41 [0.14, 1.17]
496TAVRSurgery
P = 0.09
0 3 6 9 12
TAVRSurgery
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All Stroke
All
Str
oke (
%)
491 491 489 487454 435 427 423 421
484417
Months from ProcedureNumber at risk:
HR [95% CI] =
0.38 [0.15, 1.00]
496TAVRSurgery
1.2%
2.4% 3.1%
P = 0.04
0
10
20
0.6%0 3 6 9 12
TAVRSurgery
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Death or Disabling StrokeD
eath
or
Dis
ablin
g S
troke (
%)
494 494 493 491454 444 436 432 430
488426
Months from ProcedureNumber at risk:
HR [95% CI] =
0.34 [0.12, 0.97]
496TAVRSurgery
1.0%
2.9%1.3%
P = 0.03
0
10
20
0.4%0 3 6 9 12
TAVRSurgery
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RehospitalizationR
ehospitaliz
ation
(%)
477 469 465 459454 416 399 389 385
453382
Months from ProcedureNumber at risk:
HR [95% CI] =
0.65 [0.42, 1.00]
496TAVRSurgery
7.3%
11.0%
6.5%
P < 0.05
0
10
20
0 3 6 9 12
TAVRSurgery
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Other Secondary Endpoints
Outcomes
30 Days 1 Year
TAVR
(N=496)
Surgery
(N=454) P-valueTAVR
(N=496)
Surgery
(N=454) P-value
Bleeding - Life-threat/Major 3.6% (18) 24.5% (111) <0.001 7.7% (38) 25.9% (117) <0.001
Major Vascular Complics 2.2% (11) 1.5% (7) 0.45 2.8% (14) 1.5% (7) 0.19
AKI - stage 2 or 3* 0.4% (2) 1.8% (8) 0.05 0.4% (2) 1.8% (8) 0.05
New PPM (incl baseline) 6.5% (32) 4.0% (18) 0.09 7.3% (36) 5.4% (24) 0.21
New LBBB 22.0% (106) 8.0% (35) <0.001 23.7% (114) 8.0% (35) <0.001
Coronary Obstruction 0.2% (1) 0.7% (3) 0.28 0.2% (1) 0.7% (3) 0.28
AV Re-intervention 0% (0) 0% (0) NA 0.6% (3) 0.5% (2) 0.76
Endocarditis 0% (0) 0.2% (1) 0.29 0.2% (1) 0.5% (2) 0.49
Asymp Valve Thrombosis 0.2% (1) 0% (0) 0.34 1.0% (5) 0.2% (1) 0.13
Event rates are KM estimates (%) and p-values are based on Log-Rank test
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0
10
20
30
40
50
Surgery
TAVR
441 426 390
483 490 469
Mean G
radie
nt
(mm
Hg)
11.2
49.448.3
13.7
11.6
TAVRSurgery
12.8
No. of EchosBaseline 30D 1 Year
Echocardiography Findings Mean Gradient
P < 0.001 P < 0.001
P-values are based on the ANCOVA for TAVR vs Surgery adjusted by baseline.
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0.0
0.5
1.0
1.5
2.0
Surgery
TAVR
423 395 371
458 470 446
Valv
e A
rea (
cm
2)
0.8
1.8
1.7
1.8
1.7
TAVRSurgery
0.8
No. of EchosBaseline 30D 1 Year
Echocardiography Findings Aortic Valve Area
P = 0.05P = 0.04
P-values are based on the ANCOVA for TAVR vs Surgery adjusted by baseline.
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70.4
97.1
70.0
97.4
28.7
2.9
29.4
2.1
0%
20%
40%
60%
80%
100%
TAVR(N=487)
Surgery(N=421)
TAVR(N=466)
Surgery(N=381)
Perc
enta
ge o
f P
atients
1 Year30 Days
≥ Moderate
Mild
None/Trace
Paravalvular Regurgitation
P-values are based on the Wilcoxon rank-sum test.
0.8 0.6 0.5
≥ mod PVR: P = 0.13 ≥ mod PVR: P = 1.00
0
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The PARTNER 3 TrialConclusions (1)
In a population of severe symptomatic aortic stenosis patients who were at
low surgical risk, TAVR (using the SAPIEN 3 valve) compared to surgery:
• Significantly reduced the primary endpoint of death, stroke, or
rehospitalization by 46% at 1-year
▪ Components of the primary endpoint favored TAVR, both at
30 days and 1 year
▪ Multiple sensitivity analyses confirmed robustness of the
primary endpoint findings
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The PARTNER 3 TrialClinical Implications
• Based upon these findings, TAVR, through 1-year, should be considered
the preferred therapy in low surgical risk aortic stenosis patients!
• PARTNER randomized trials over the past 12 years, clearly indicate
that the relative value of TAVR compared with surgery
is independent of surgical risk profiles.
• The choice of TAVR vs. surgery in aortic stenosis patients should be
a shared-decision making process, respecting patient preferences,
understanding knowledge gaps (esp. in younger patients), and
considering clinical and anatomic factors.
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Study Design
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Mean ± SD or % TAVR (N=725) SAVR (N=678)
Age, years 74.1 ± 5.8 73.6 ± 5.9
Female sex 36.0 33.8
Body surface area, m2 2.0 ± 0.2 2.0 ± 0.2
STS PROM, % 1.9 ± 0.7 1.9 ± 0.7
NYHA Class III or IV 25.1 28.5
Hypertension 84.8 82.6
Chronic lung disease (COPD) 15.0 18.0
Cerebrovascular disease 10.2 11.8
Peripheral arterial disease 7.5 8.3
There are no significant differences between groups.
Baseline Characteristics
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-0.1 -0.05 0 0.05 0.1 0.15
PP>0.999
TAVR 5.3% SAVR 6.7%
Posterior probability of
noninferiority > 0.999
TAVR –SAVR difference = -1.4% (95% BCI; -4.9, 2.1)
Primary Endpoint Met
TAVR is noninferior to
SAVR
Primary EndpointAll-Cause Mortality or Disabling Stroke at 2 Years
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0%
2%
4%
6%
8%
10%
0 1 2 3 4 5 6 7 8 9 10 11 12
TAVR
SAVR
De
ath
or
Dis
ab
ling
Str
oke
(%
)
Months
30 Days
2.5
0.7
1 Year
4.6
2.7
No. at riskTAVR
725 718 648 435
SAVR
678 656 576 366
K-M All-Cause Mortality or Disabling Stroke at 1 Year
Log-rank P = 0.065
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0%
2%
4%
6%
8%
10%
0 1 2 3 4 5 6 7 8 9 10 11 12
TAVR
SAVR
65
No. at risk
K-M Rates of All-Cause Mortality at 1 Year
All-
Ca
use
Mo
rta
lity (
%)
Months Post Procedure
TAVR 725 720 651 435
SAVR 678 665 583 373
30 Days
1.20.4
1 Year
3.02.3
Log-rank P = 0.412
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0%
2%
4%
6%
0 1 2 3 4 5 6 7 8 9 10 11 12
K-M Disabling Stroke at 1 Year
Log-rank P = 0.024
No. at riskTAVR
725 720 648 435
SAVR
678 656 576 366
Months
Dis
ab
ling
Str
oke
(%
)
1 Year
2.30.7
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TAVR may be a preferred strategy to surgery in patients with severe aortic stenosis at low risk of
surgical mortality.
Conclusion
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0%
2%
4%
6%
8%
10%
0 1 2 3 4 5 6 7 8 9 10 11 12
TAVR
SAVR
Months
K-M Heart Failure Hospitalization at 1 Year
No. at riskTAVR
725 712 636 420
SAVR
678 649 561 358
He
art
Fa
ilure
Ho
sp
ita
liza
tio
n
(%)
6.4
3.1
Log-rank P = 0.006
1 Year
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Cleveland Clinic TAVR Outcomes - 2018
• 2018 = ~495 patients
• 60% High risk, 40% Int risk
• 89% Conscious Sedation
Mortality - 0.2%
Stroke - 0.2%
AR(>=2+) - 0.8%
New PPM - 5%
Question in 2018 - HOW CAN YOU PROVIDE A BETTER TREATMENT OPTION
Isolated SAVR mortality was 0%! – Mostly low risk patients
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Unanswered Question(s)
Durability
1. What is the gold standard?
2. What are the predictors? (HALT etc)
3. What is the penalty for this?
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Surgical Valve Durability
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Durability
Douglas et al, JAMA Cardiol, 2017
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Structural Valve Deterioration
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Prevalence of reduced leaflet motionTranscatheter vs. surgical bioprosthetic aortic valves: p=0.001
Reduced leaflet motion was present in 106
(11.9%) patients
Transcatheter valves
13.4% (101 out of 752)
Surgical valves
3.6% (5 out of 138)
Chakravarty et al, Lancet 2017; 389: 2383–92
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Reduced Leaflet Motionand Increased Gradients
Baseline Pre-discharge Time of CT
10
20
30
40
50
Mean g
radie
nt
(mm
Hg)
Chakravarty et al, Lancet 2017; 389: 2383–92
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Predictors of Valve Hemodynamic Degeneration after TAVR
1521 patients undergoing TAVR
Valve hemodynamic degeneration = 10mmHg rise in transvalvular gradients
BMI
Valve ≤ 23mm
Valve in valve
No anticoagulation
at discharge
Del Trigo M. et al. JACC 2016
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THV expansion and Leaflet Thrombus
Fuchs et al, Eurointervention, 2017 Jul 25. pii: EIJ-D-17-00373
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Neo-sinus and Anatomical Sinus
Neo-sinus
Anatomical
Sinus
TranscatheterValve Leaflets
Covering
Kapadia et al, Circulation 2017, in press
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-8
-6
-4
-2
0
2
4
6
8
-200 200 400 600 800 1000 1200 1400 1600 1800
Follow-up (Days)
Group: p=0.15
change: p=0.014
Group x change: p = 0.008
Valve depth > 6.5mm
Valve depth ≤ 6.5mm
0
ΔM
ea
n g
rad
ien
t (m
mH
g)
0-30 30-300 300-600 600-1000 1000-1400 > 1400 days
Depth > 6.5 28 24 17 14 7 11
Depth ≤ 6.5 83 65 40 34 17 20
Depth of Implant
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What is the correct thinking?
Surgery for low surgical risk patients
OR
TAVR for low TAVR risk patients
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Devices Likely to Approved This Year
PORTICO LOTUS
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ACURATE neo Aortic Valve
Supra-annular Valve
• Porcine pericardium leaflets• BioFix™ anti-calcification
process• Low gradients
Stabilization Arches
• Axial self-aligning
Pericardial Skirt
• Inner and outer anti-leak skirts
Lower Crown
• Minimal protrusion into LVOT• Low risk of conduction system
interference
Upper Crown
• Minimal supra-annular anchoring
• Captures native leaflets and provides coronary clearance
Self-expanding Nitinol Frame
• Treats annulus from 21mm to 27mm
Information not intended for use in France. CE mark received 2014. Information for the ACURATE Valve System is for use in countries
with applicable product registrations. Indications, contraindications, warnings and instructions for use can be found in the product
labeling supplied with each device.
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ACURATE neo2 Aortic Valve
ACURATE neo2 maintains key features of the ACURATE neo valve• Self-expanding nitinol frame with porcine pericardium leaflets
• Supra-annular positioning; two-step top-down deployment
• Treats annuli from 21mm to 27mm
Stabilization Arches• Axial; self-aligning
Upper Crown• Captures native leaflets and provides
coronary clearance
Lower Crown• Minimal protrusion into LVOT
ACURATE neo2 incorporates
“Advanced Sealing” technology • Inner and outer pericardial skirts (outer skirt
covers to waist of stent)
• Designed to improve conformability to
irregular, calcified anatomy and enhance
reduction of PVL
The ACURATE neo2 Valve System is an investigational device only. Not approved for sale or use.
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23mm, 26mm, and
29mm valve sizes
Centera: Self-Expanding TAVR Valve Design
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Centera Self-Expanding TAVR SystemExCEED U.S. Clinical Trial
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Important Areas
• Early TAVR - Asymptomatic
• Bicuspid AS
• Valve in Valve
• Unload LV – Moderate AS and LV dysfunction
• Isolated AR
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Stress-Test Abnormal
Treadmill Stress-Test
Stress-Test Normal
Early-TAVR Randomized Trial
CTA and Angiography TF- TAVR eligibility
Randomization 1:1Stratified by STS (<3 vs >3)
TF- TAVRClinical
Surveillance
Early TAVR Registry
Primary Endpoint (superiority): 2-year composite of all-cause mortality, all strokes,
and repeat hospitalizations (CV)
EARLY TAVR