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Transcatheter Aortic Valve
      Implantation

 TAVI : Current Updates

         Magdy Mostafa, MD

   Professor of Cardio-Thoracic Surgery
          Ain-Shams University
• Europe in 2007 approved Edwards SAPIEN and CoreValve TAVI

•   It is described as a "runaway train“ phenomena in Europe.
•   TAVI procedures made up 1.2% of valve procedures in
2007, but are expected to exceed 30% in the first half of 2011 .
                     ( Cardiology News Digital Network, Dec,2011 )
•     TAVI statistics presented during CardioEgypt 2012 showed that
it exceeded 51% in Europe in the last year.


• USA in November 2011: Food and Drug Administration (FDA)
approved TAVI after PARTNER clinical trial study is concluded .
March 1, 2012

     AATS, STS , ACCF and SCAI representing cardiologists and cardiothoracic
 surgeons released initial recommendations for creating and maintaining
 transcatheter aortic valve replacement (TAVR) programs.


•    Cardiologists and cardiothoracic surgeons are the cornerstone for
establishing a successful program, noting that a program without both
specialties would be fundamentally deficient.


•     Heart team concept that is led by the surgeon and interventional
cardiologist. In all TAVR procedures, the interventional cardiologist and surgeon
must both be present during the entire procedure ensuring joint participation and
optimal patient-centered care.



( Tommaso et al., 2012 by the Society for Cardiovascular Angiography and
Interventions, The Journal of Thoracic and Cardiovascular Surgery, The Annals of
Thoracic Surgery, and The Journal of the American College of Cardiology )
The Team Approach for TAVI

CARDIOLOGISTS

    SURGEONS

           Anesthesiologists

                 Imaging specialists (Echo, CT, MRI)


                (EACTS/ESC/EAPCI , Eur Heart J, 2008; 29: 1463-1470,
                             Eur J Cardiothorac Surg 34 (2008) 1-8)
Where to perform TAVI?

  For optimal safety and results, a hybrid operating room with sophisticated fixed
imaging is essential. This includes having the facilities to:

1.   Perform angiographic imaging,
2.   Provide cardiac anesthesia with transesophageal echocardiography ( TEE )
3.   Access to all preoperative diagnostic imaging.
4.   Having the ability to convert to an open operation with cardiopulmonary bypass.
5.   General anesthesia
Inclusion Criteria for TAVI After assessment by the “Team”

1. Severe Symptomatic AS (valve area is < 1.0 cm² or < 0.6
cm²/m²) & Pressure gradient > 50 mm Hg with normal cardiac output
2. Life expectancy >1year
3. Contraindication for surgery ,or High Risk for Surgery :

    Clinical judgement + EuroScore (logistic) > 20%;
                        STS Score          >10%
4. AND/OR
    - Porcelain aorta
    - History of thoracic irradiation
    - Severe thoracic deformity
    - Patent coronary bypass



                                        (Alec Vahanian, 2008)
Access For TAVI

•   Femoral vein (Antigrade) : it is no longer used
•   Femoral artery ( Retrograde )
•   Left ventricular apex
•   Subclavian / axillary (left)
•   Ascending aorta ( NEW)




                           ( Michael Mack, 2010 )
TAVI Primary Operator

TF              Cardiologist/Surgeon

TA              Surgeon

Subclavian      Cardiologist (Access Surgeon)

Direct Aortic   Surgeon
TAVI Approaches
                                 TA
TF
                                 Shorter time
Less invasive                    Less radiation
Percutaneous                     Less contrast
Local anesthesia                 Easier delivery

        ---                              ---
Delivery more difficult          More invasive
More stroke?                     Less skilled operators
Not for all patients             Less experience
Subclavian                    Direct Aortic

• Minimally Diseased Vessel   • Most Direct Access
• Less Invasive Than TA       • Less Invasive Than TA
• Local Anesthesia Possible   • Surgeons More Comfortable
• Crosses Arch But Less       With Access?
Traumatic ?
• Direct Access To Valve
Balloon aortic valvuloplasty is typically performed with a Tyshak balloon. An
angiogram is performed to confirm proper positioning of the balloon, and during a
short period of rapid ventricular pacing, the balloon is inflated.
Transcatheter transfemoral retrograde approach. The valve is advanced over a stiff
guidewire into the aortic position in a retrograde manner. It is positioned such that
60% of the valve is on the ventricular side, and 40% of the valve is on the aortic
side of the annulus.
Transcatheter transfemoral approach – completion angiogram of the implanted
aortic valve is shown. Note that the contrast filled aortic root and ascending aorta are
clearly seen, along with the take-off of the right and left coronary arteries.
The cardiac apex is accessed and a transapical sheath is placed into the left ventricle. The
valve is advanced over a stiff wire in an antegrade manner. It is positioned such that 50%
of the valve lies on the ventricular side, and 50% of the valve lies on the aortic side.
A completion angiogram is performed after the transapical deployment of the valve.
The implanted aortic valve is shown. The completion angiogram should not only
confirm that the aortic root, ascending aorta, and the coronary ostia are intact, but
also that the mitral valve apparatus has not been disrupted by the transapical
approach.
Contra indications for TAVI
General contra indications
      1.Aortic annulus <18mm or >27mm
      2. Bicuspid valves
      3. Heavy calcification in front of LM
      4. LV Thrombus
Specific contraindications for transfemoral approach
Peripheral arteries
  1. Diameter < 8 - 9mm
  2. Severe tortuosity /calcification
  3. Aorto-Femoral by pass
Aorta
  1. Aneurysm of abdominal aorta with thrombosis
  2. Severe angulation
  3. Porcelain aorta
  4. Severe atheroma of the arch
Specific contraindications for transapical approach
  1.Previous surgery of the LV using a patch
  2. Calcified pericardium
  3. Severe respiratory disease
  4. Non-reachable apex                    (Alec Vahanian, 2008)
Diagnostic Workup for TAVI

.Measurement of Ilio-Femoral diameters by Angio & MS CT

.Measurements of Aortic Annulus diameter by TTE & MS CT

.Study Aortic Calcification distribution by TTE & MS CT

.Plane of Aortic Annulus by MS CT

.Distance Annulus/ Coronary Ostia by MS CT
Plane of the Aortic Annulus/ MSCT




              Welt F G et al. Circulation 2011;124:2944-2948
MSCT :Distance Annulus /Coronary Ostia




                 Welt F G et al. Circulation 2011;124:2944-2948
CT scan of thoracic aorta of patient with calcific aorta




    Welt F G et al. Circulation 2011;124:2944-2948



Copyright © American Heart Association
Devices
Current-: 1st Generation
• Edwards Sapien
• Medtronic Core valve

Future-: 2    nd   Generation
• Sadra
• Direct Flow
• St. Jude
• Symetis
• Medtronic Engager (Ventor)
• JenaValve

Michael Mack, Southern Thoracic Surgical Association, 2010
(A) Sapien balloon-expandable, stainless steel support structure, bovine pericardial valve;
(B) Core self-expanding, nitinol support structure, porcine pericardial valve.
Source

Clinical images provided by the American College of Cardiology Foundation ( 2008 )
Future Devices




Direct Flow Aortic Valve         Sadra               HLT Valve




 Medtronic/Ventor          Symetis ACURATE™ Device   JenaClip stent
Differences between the Medtronic CoreValve and Edwards Sapien valve systems

                                Medtronic CoreValve        Edwards Sapien valve

Minimum femoral artery          6.5 mm                     7 mm
diameter required

Composition                     Porcine pericardial with   Bovine pericardial with steel
                                nitinol stent              stent
Delivery system size required   18 French                  18 French (Sapien XT only)*
                                                           22 French (23 mm valve)
                                                           24 French (26 mm valve)



Native annulus size feasible for 19 mm to 27 mm            17 mm to 25 mm
implant
Mechanism of implantation       Self-expanding             Balloon expandable

Ventricular rhythm at time of   Beating heart              Rapid ventricular pacing
implant
Possible Complications post TAVI:
1. Stroke:
    A. EARLY:

Immediate ( 1st 24 hours ) post-procedural Thromboembolic risk may be due to:

• Periprocedural hypotension.
• Embolism of debris during valve implantation.
• Thrombi can form on devices/ wires during the procedure.

Newer devices that deflect or filter emboli are also currently being investigated.
.
                                             (Tay et al.,JACC, Dec, 2011)
B. Delayed

Persists up to the first 2 months after TAVI.

The bioprosthesis itself may be a source of thromboemboli before
endothelialization of the prosthesis is complete :

1. Aggregation of platelet and fibrin on valve leaflet within a few hours after
   implantation.
2. The native valve leaflets, may be fissured or denuded are left compressed
   adjacent to the stent frame, which again has thrombogenic consequences.

3. Incomplete Endothelialization of stent struts.

                                        (Tay et al.,JACC, Dec, 2011)
Pathological Images Showing
Incomplete Endothelialization

(A) Postmortem of a patient who
    died on day 25 from pulseless
    ventricular tachycardia.

(B) Postmortem of a patient who
died on day 28 after implantation
from stroke-related complications.

     Several stent struts are not
endothelialized (black arrow) in this
patient. Areas with tissue ingrowth
(white arrow) are also shown for
comparison.

    (Tay et al.,JACC, Dec, 2011)
2. Paravalvular leak:
• Post TAVI moderate to major paravalvular leak varies between (4%–35%)

• It results from inaccurate sizing of the native Aortic annulus.

• This is partly due to intrinsic anatomic properties of the aortic root—the
‘virtual ring’ is largely inhomogeneous, coursing through the muscular
septum, the membranous septum and the mitro-aortic curtain.




                                                ( Cerillo et al., 2012 )
3. New-onset AF after TAVI:
• NOAF occurred in about one-third of the patients with no prior
history of AF undergoing TAVI

• The 2 factors associated with the new-onset AF after TAVI :

1. Left atrial enlargement
2. Use of the transapical approach.

•    NOAF was associated with a higher rate of stroke/systemic
    embolism, but not a higher mortality, at 30 days and at 1-year
    follow-up.


      ( Amat - Santos et al., JACC, Dec. 2011 & Lung et al., JACC, 2012 )
4. Atrioventricular block:

  Complete atrioventricular block requiring pacemaker implantation at ≤30 days
was low (1.8% for the TF and 3.8% for TA approach), and it depends on the
depth and level of placement of the valve at the left ventricular outflow track.




                              (Lung et al., JACC, 2012 )
5. Other major adverse events:

•   Major ventricular tachyarrhythmia (0%–4%)
•   Myocardial infarction (0%–15%)
•   Cardiac tamponade (2%–10%),
•   Conversion to surgery (0%–8%),
•   Vascular complication (8%–17%),
•   Valve-in-valve procedure (2%–12%),
•   Aortic dissection/perforation (0%–4%).


               (Yan et al., J Thorac Cardiovasc Surg 2010 )
Post TAVI Anticoagulation management
• Dual antiplatelet therapy (DAPT) with clopidogrel and aspirin
for 3 to 6 months is a widely accepted strategy in (TAVI) patients
but this approach is not evidence based.

                    ( Lung et al., JACC Vol. 59, No. 2, 2012)

•  While the strategy of adding clopidogrel to aspirin for 3
months after TAVI was not found to be superior to aspirin alone.

                     ( Ussia et al, American J. of Cardiology, 2011)
Placement of AoRTic TraNscathetER Valve
                     (PARTNER) clinical trial Study

• This represents the first US 1: 1 randomized percutaneous aortic valve trial.

• A total of 1058 Patient included in 2 Parallel cohort studies individually
powered :

cohort A compared surgical aortic valve replacement versus transcatheter aortic
valve implantation (TAVI) among high-risk operative candidates ( 700 Patient )

cohort B examined outcomes in inoperable patients. ( 358 Patient )
One year follow-up of the multi-centre US PARTNER transcatheter heart
                              valve study


    I.   PARTNER cohort A :
     Included 700 elderly patients (median age 84.1) with severe aortic stenosis
   and a mean STS score of 11.8/logistic EuroSCORE 29.3 were randomized to either:

    TAVI or Conventional surgery at one of 25 centers.
   •     245 patients receiving the experimental device via transfemoral route
   •     105 via a transapical procedure
   •     350 conventional surgery

      Patients in the transapical group were slightly higher risk than patients in
   either the transfemoral-TAVI group or the aortic-valve-surgery group.
American College of Cardiology (ACC) 2011
                               US PARTNER cohort A
TAVI vs surgery outcomes:
     End point          TAVI           Surgery    p
    End point                   TAVI             Surgery   p
     Mortality
    Mortality
     30 d               3.4            6.5        0.07
    30 d                        3.4              6.5       0.07
     1y                 24.2           26.8       0.44
    1y                          24.2             26.8      0.44
     Major stroke

    Major stroke
    30 d                3.8            2.1        0.20

    30 y
     1d                 5.1     3.8    2.4       2.1
                                                  0.07     0.20

    1Major vascular
      y                  11.0   5.1    3.2       2.4
                                                  <0.001   0.07
     complications, 30 d
    Major vascular              11.0             3.2       <0.001
    complications, 309.3
     Major bleeding   d                19.5       <0.001

    Major bleeding
    New-onset AF        8.6     9.3    16.0      19.5
                                                  0.006    <0.001

    Moderate/severe
    New-onset AF                8.6              16.0      0.006
     PR

    Moderate/severe PR
    30 d          12.2                 0.9        <0.001

    30 y
     1d                 6.8     12.2   1.9       0.9
                                                  <0.001   <0.001

    1y                          6.8              1.9       <0.001
One year follow-up of the multi-centre US PARTNER
          transcatheter heart valve study


II . PARTNER cohort B :

It enrolled 358 patients with severe aortic disease unable to undergo
surgery at one of 21 centers and randomized them to either:

• Transcatheter valve implantation (Transfemoral, Sapien Valve)

or

• Best medical care, including balloon valvuloplasty.
TAVI vs standard therapy at one year: Primary end points

End point                TAVI     Standard (%)                         p
                         (%)

1-y all-cause death      30.7     50.7                                 <0.001

1-y all-cause death or   42.5     71.6                                 <0.001
repeat hospitalization




                                ( Leon MB et al. N Engl J Med 2010 )
TAVI vs standard therapy secondary end points

End point                                       TAVI (%)   Standard (%) p


30-d major stroke                               5.0        1.1              0.06


30-d vascular complications                     16.2       1.1              <0.001


1-y cardiac death                               19.6       41.9             <0.001


1-y major bleeding                              22.3       11.2             0.007


Survivors: Cardiac symptoms at 1 y              25.2       58.0             <0.001



                                     ( Leon MB et al. N Engl J Med 2010 )
One year follow-up of the multi-centre European PARTNER transcatheter
                           heart valve study
                                                Procedural outcome.




 Lefèvre T et al. Eur Heart J 2011;32:148-157
One year follow-up of the multi-centre European PARTNER transcatheter
                           heart valve study
                            (A) Overall survival for transapical patients.

                        (B) Overall survival for transfemoral patients




Lefèvre T et al. Eur Heart J 2011;32:148-157
Why TA results may not be as good as TF !

• Higher risk patients in TA
  * TF First programs bias against TA

• Procedure “less mature”
   * Surgeons with lesser “wire skills”
   * TA started later and there still is less experience with TA

• More invasive procedure, especially in high-risk patients



   Michael Mack, Southern Thoracic Surgical Association, 2010
Transaortic Transcatheter Aortic Valve
             Implantation
European Multi-Center Experience


  Out of 1236 patients underwent TAVI using the
Edwards SAPIEN valve, 158 patients (12.8%) the
transaortic approach was used

 Transaortic approach results :
• No postoperative strokes
• 30-day all-cause mortality rate of 7%
• Major bleeding rate of 1.3%.

           (Bapat et al.,, STS meeting,2011)
"Transcatheter aortic valve replacement with Edwards SAPIEN valve via
transaortic route: European Multi-Center Experience" STS 2011

•Initial protocol was to attempt:

    Transfemoral approach > Transapical > Transaortic.

But now:

    Transfemoral approach > Transaortic access.

• But why the Transaortic approach was not the first choice, given its excellent
outcomes, low risk of stroke.

    It is difficult to "sell" the transaortic approach to patients because it involves a 5-
cm incision in the chest, either via a mini-sternotomy or a mini-thoracotomy, as
opposed to a short incision at the groin.

                                     (Bapat et al.,, STS meeting,2011).
Conclusion

• Heart team concept should be adopted in every TAVI
procedure
• Transfemoral access need not be the default approach as
no data exist from randomized clinical trials showing that it is
better than the others .

• ‘Indications are slipping’ which means that operable
patients with moderate or low risk score are getting TAVI
when they should have surgery

• Trans Aortic approach is a good and more safe alternative
to both Transfemoral and Transapical approaches.
Thank You

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Tavi 3

  • 1. Transcatheter Aortic Valve Implantation TAVI : Current Updates Magdy Mostafa, MD Professor of Cardio-Thoracic Surgery Ain-Shams University
  • 2. • Europe in 2007 approved Edwards SAPIEN and CoreValve TAVI • It is described as a "runaway train“ phenomena in Europe. • TAVI procedures made up 1.2% of valve procedures in 2007, but are expected to exceed 30% in the first half of 2011 . ( Cardiology News Digital Network, Dec,2011 ) • TAVI statistics presented during CardioEgypt 2012 showed that it exceeded 51% in Europe in the last year. • USA in November 2011: Food and Drug Administration (FDA) approved TAVI after PARTNER clinical trial study is concluded .
  • 3. March 1, 2012 AATS, STS , ACCF and SCAI representing cardiologists and cardiothoracic surgeons released initial recommendations for creating and maintaining transcatheter aortic valve replacement (TAVR) programs. • Cardiologists and cardiothoracic surgeons are the cornerstone for establishing a successful program, noting that a program without both specialties would be fundamentally deficient. • Heart team concept that is led by the surgeon and interventional cardiologist. In all TAVR procedures, the interventional cardiologist and surgeon must both be present during the entire procedure ensuring joint participation and optimal patient-centered care. ( Tommaso et al., 2012 by the Society for Cardiovascular Angiography and Interventions, The Journal of Thoracic and Cardiovascular Surgery, The Annals of Thoracic Surgery, and The Journal of the American College of Cardiology )
  • 4. The Team Approach for TAVI CARDIOLOGISTS SURGEONS Anesthesiologists Imaging specialists (Echo, CT, MRI) (EACTS/ESC/EAPCI , Eur Heart J, 2008; 29: 1463-1470, Eur J Cardiothorac Surg 34 (2008) 1-8)
  • 5. Where to perform TAVI? For optimal safety and results, a hybrid operating room with sophisticated fixed imaging is essential. This includes having the facilities to: 1. Perform angiographic imaging, 2. Provide cardiac anesthesia with transesophageal echocardiography ( TEE ) 3. Access to all preoperative diagnostic imaging. 4. Having the ability to convert to an open operation with cardiopulmonary bypass. 5. General anesthesia
  • 6.
  • 7. Inclusion Criteria for TAVI After assessment by the “Team” 1. Severe Symptomatic AS (valve area is < 1.0 cm² or < 0.6 cm²/m²) & Pressure gradient > 50 mm Hg with normal cardiac output 2. Life expectancy >1year 3. Contraindication for surgery ,or High Risk for Surgery : Clinical judgement + EuroScore (logistic) > 20%; STS Score >10% 4. AND/OR - Porcelain aorta - History of thoracic irradiation - Severe thoracic deformity - Patent coronary bypass (Alec Vahanian, 2008)
  • 8. Access For TAVI • Femoral vein (Antigrade) : it is no longer used • Femoral artery ( Retrograde ) • Left ventricular apex • Subclavian / axillary (left) • Ascending aorta ( NEW) ( Michael Mack, 2010 )
  • 9. TAVI Primary Operator TF Cardiologist/Surgeon TA Surgeon Subclavian Cardiologist (Access Surgeon) Direct Aortic Surgeon
  • 10. TAVI Approaches TA TF Shorter time Less invasive Less radiation Percutaneous Less contrast Local anesthesia Easier delivery --- --- Delivery more difficult More invasive More stroke? Less skilled operators Not for all patients Less experience
  • 11. Subclavian Direct Aortic • Minimally Diseased Vessel • Most Direct Access • Less Invasive Than TA • Less Invasive Than TA • Local Anesthesia Possible • Surgeons More Comfortable • Crosses Arch But Less With Access? Traumatic ? • Direct Access To Valve
  • 12. Balloon aortic valvuloplasty is typically performed with a Tyshak balloon. An angiogram is performed to confirm proper positioning of the balloon, and during a short period of rapid ventricular pacing, the balloon is inflated.
  • 13. Transcatheter transfemoral retrograde approach. The valve is advanced over a stiff guidewire into the aortic position in a retrograde manner. It is positioned such that 60% of the valve is on the ventricular side, and 40% of the valve is on the aortic side of the annulus.
  • 14. Transcatheter transfemoral approach – completion angiogram of the implanted aortic valve is shown. Note that the contrast filled aortic root and ascending aorta are clearly seen, along with the take-off of the right and left coronary arteries.
  • 15. The cardiac apex is accessed and a transapical sheath is placed into the left ventricle. The valve is advanced over a stiff wire in an antegrade manner. It is positioned such that 50% of the valve lies on the ventricular side, and 50% of the valve lies on the aortic side.
  • 16. A completion angiogram is performed after the transapical deployment of the valve. The implanted aortic valve is shown. The completion angiogram should not only confirm that the aortic root, ascending aorta, and the coronary ostia are intact, but also that the mitral valve apparatus has not been disrupted by the transapical approach.
  • 17. Contra indications for TAVI General contra indications 1.Aortic annulus <18mm or >27mm 2. Bicuspid valves 3. Heavy calcification in front of LM 4. LV Thrombus Specific contraindications for transfemoral approach Peripheral arteries 1. Diameter < 8 - 9mm 2. Severe tortuosity /calcification 3. Aorto-Femoral by pass Aorta 1. Aneurysm of abdominal aorta with thrombosis 2. Severe angulation 3. Porcelain aorta 4. Severe atheroma of the arch Specific contraindications for transapical approach 1.Previous surgery of the LV using a patch 2. Calcified pericardium 3. Severe respiratory disease 4. Non-reachable apex (Alec Vahanian, 2008)
  • 18. Diagnostic Workup for TAVI .Measurement of Ilio-Femoral diameters by Angio & MS CT .Measurements of Aortic Annulus diameter by TTE & MS CT .Study Aortic Calcification distribution by TTE & MS CT .Plane of Aortic Annulus by MS CT .Distance Annulus/ Coronary Ostia by MS CT
  • 19. Plane of the Aortic Annulus/ MSCT Welt F G et al. Circulation 2011;124:2944-2948
  • 20. MSCT :Distance Annulus /Coronary Ostia Welt F G et al. Circulation 2011;124:2944-2948
  • 21. CT scan of thoracic aorta of patient with calcific aorta Welt F G et al. Circulation 2011;124:2944-2948 Copyright © American Heart Association
  • 22. Devices Current-: 1st Generation • Edwards Sapien • Medtronic Core valve Future-: 2 nd Generation • Sadra • Direct Flow • St. Jude • Symetis • Medtronic Engager (Ventor) • JenaValve Michael Mack, Southern Thoracic Surgical Association, 2010
  • 23. (A) Sapien balloon-expandable, stainless steel support structure, bovine pericardial valve; (B) Core self-expanding, nitinol support structure, porcine pericardial valve.
  • 24. Source Clinical images provided by the American College of Cardiology Foundation ( 2008 )
  • 25. Future Devices Direct Flow Aortic Valve Sadra HLT Valve Medtronic/Ventor Symetis ACURATE™ Device JenaClip stent
  • 26. Differences between the Medtronic CoreValve and Edwards Sapien valve systems Medtronic CoreValve Edwards Sapien valve Minimum femoral artery 6.5 mm 7 mm diameter required Composition Porcine pericardial with Bovine pericardial with steel nitinol stent stent Delivery system size required 18 French 18 French (Sapien XT only)* 22 French (23 mm valve) 24 French (26 mm valve) Native annulus size feasible for 19 mm to 27 mm 17 mm to 25 mm implant Mechanism of implantation Self-expanding Balloon expandable Ventricular rhythm at time of Beating heart Rapid ventricular pacing implant
  • 27. Possible Complications post TAVI: 1. Stroke: A. EARLY: Immediate ( 1st 24 hours ) post-procedural Thromboembolic risk may be due to: • Periprocedural hypotension. • Embolism of debris during valve implantation. • Thrombi can form on devices/ wires during the procedure. Newer devices that deflect or filter emboli are also currently being investigated. . (Tay et al.,JACC, Dec, 2011)
  • 28. B. Delayed Persists up to the first 2 months after TAVI. The bioprosthesis itself may be a source of thromboemboli before endothelialization of the prosthesis is complete : 1. Aggregation of platelet and fibrin on valve leaflet within a few hours after implantation. 2. The native valve leaflets, may be fissured or denuded are left compressed adjacent to the stent frame, which again has thrombogenic consequences. 3. Incomplete Endothelialization of stent struts. (Tay et al.,JACC, Dec, 2011)
  • 29. Pathological Images Showing Incomplete Endothelialization (A) Postmortem of a patient who died on day 25 from pulseless ventricular tachycardia. (B) Postmortem of a patient who died on day 28 after implantation from stroke-related complications. Several stent struts are not endothelialized (black arrow) in this patient. Areas with tissue ingrowth (white arrow) are also shown for comparison. (Tay et al.,JACC, Dec, 2011)
  • 30. 2. Paravalvular leak: • Post TAVI moderate to major paravalvular leak varies between (4%–35%) • It results from inaccurate sizing of the native Aortic annulus. • This is partly due to intrinsic anatomic properties of the aortic root—the ‘virtual ring’ is largely inhomogeneous, coursing through the muscular septum, the membranous septum and the mitro-aortic curtain. ( Cerillo et al., 2012 )
  • 31. 3. New-onset AF after TAVI: • NOAF occurred in about one-third of the patients with no prior history of AF undergoing TAVI • The 2 factors associated with the new-onset AF after TAVI : 1. Left atrial enlargement 2. Use of the transapical approach. • NOAF was associated with a higher rate of stroke/systemic embolism, but not a higher mortality, at 30 days and at 1-year follow-up. ( Amat - Santos et al., JACC, Dec. 2011 & Lung et al., JACC, 2012 )
  • 32. 4. Atrioventricular block: Complete atrioventricular block requiring pacemaker implantation at ≤30 days was low (1.8% for the TF and 3.8% for TA approach), and it depends on the depth and level of placement of the valve at the left ventricular outflow track. (Lung et al., JACC, 2012 )
  • 33. 5. Other major adverse events: • Major ventricular tachyarrhythmia (0%–4%) • Myocardial infarction (0%–15%) • Cardiac tamponade (2%–10%), • Conversion to surgery (0%–8%), • Vascular complication (8%–17%), • Valve-in-valve procedure (2%–12%), • Aortic dissection/perforation (0%–4%). (Yan et al., J Thorac Cardiovasc Surg 2010 )
  • 34. Post TAVI Anticoagulation management • Dual antiplatelet therapy (DAPT) with clopidogrel and aspirin for 3 to 6 months is a widely accepted strategy in (TAVI) patients but this approach is not evidence based. ( Lung et al., JACC Vol. 59, No. 2, 2012) • While the strategy of adding clopidogrel to aspirin for 3 months after TAVI was not found to be superior to aspirin alone. ( Ussia et al, American J. of Cardiology, 2011)
  • 35. Placement of AoRTic TraNscathetER Valve (PARTNER) clinical trial Study • This represents the first US 1: 1 randomized percutaneous aortic valve trial. • A total of 1058 Patient included in 2 Parallel cohort studies individually powered : cohort A compared surgical aortic valve replacement versus transcatheter aortic valve implantation (TAVI) among high-risk operative candidates ( 700 Patient ) cohort B examined outcomes in inoperable patients. ( 358 Patient )
  • 36. One year follow-up of the multi-centre US PARTNER transcatheter heart valve study I. PARTNER cohort A : Included 700 elderly patients (median age 84.1) with severe aortic stenosis and a mean STS score of 11.8/logistic EuroSCORE 29.3 were randomized to either: TAVI or Conventional surgery at one of 25 centers. • 245 patients receiving the experimental device via transfemoral route • 105 via a transapical procedure • 350 conventional surgery Patients in the transapical group were slightly higher risk than patients in either the transfemoral-TAVI group or the aortic-valve-surgery group.
  • 37. American College of Cardiology (ACC) 2011 US PARTNER cohort A TAVI vs surgery outcomes: End point TAVI Surgery p End point TAVI Surgery p Mortality Mortality 30 d 3.4 6.5 0.07 30 d 3.4 6.5 0.07 1y 24.2 26.8 0.44 1y 24.2 26.8 0.44 Major stroke Major stroke 30 d 3.8 2.1 0.20 30 y 1d 5.1 3.8 2.4 2.1 0.07 0.20 1Major vascular y 11.0 5.1 3.2 2.4 <0.001 0.07 complications, 30 d Major vascular 11.0 3.2 <0.001 complications, 309.3 Major bleeding d 19.5 <0.001 Major bleeding New-onset AF 8.6 9.3 16.0 19.5 0.006 <0.001 Moderate/severe New-onset AF 8.6 16.0 0.006 PR Moderate/severe PR 30 d 12.2 0.9 <0.001 30 y 1d 6.8 12.2 1.9 0.9 <0.001 <0.001 1y 6.8 1.9 <0.001
  • 38. One year follow-up of the multi-centre US PARTNER transcatheter heart valve study II . PARTNER cohort B : It enrolled 358 patients with severe aortic disease unable to undergo surgery at one of 21 centers and randomized them to either: • Transcatheter valve implantation (Transfemoral, Sapien Valve) or • Best medical care, including balloon valvuloplasty.
  • 39. TAVI vs standard therapy at one year: Primary end points End point TAVI Standard (%) p (%) 1-y all-cause death 30.7 50.7 <0.001 1-y all-cause death or 42.5 71.6 <0.001 repeat hospitalization ( Leon MB et al. N Engl J Med 2010 )
  • 40. TAVI vs standard therapy secondary end points End point TAVI (%) Standard (%) p 30-d major stroke 5.0 1.1 0.06 30-d vascular complications 16.2 1.1 <0.001 1-y cardiac death 19.6 41.9 <0.001 1-y major bleeding 22.3 11.2 0.007 Survivors: Cardiac symptoms at 1 y 25.2 58.0 <0.001 ( Leon MB et al. N Engl J Med 2010 )
  • 41. One year follow-up of the multi-centre European PARTNER transcatheter heart valve study Procedural outcome. Lefèvre T et al. Eur Heart J 2011;32:148-157
  • 42. One year follow-up of the multi-centre European PARTNER transcatheter heart valve study (A) Overall survival for transapical patients. (B) Overall survival for transfemoral patients Lefèvre T et al. Eur Heart J 2011;32:148-157
  • 43. Why TA results may not be as good as TF ! • Higher risk patients in TA * TF First programs bias against TA • Procedure “less mature” * Surgeons with lesser “wire skills” * TA started later and there still is less experience with TA • More invasive procedure, especially in high-risk patients Michael Mack, Southern Thoracic Surgical Association, 2010
  • 44. Transaortic Transcatheter Aortic Valve Implantation
  • 45. European Multi-Center Experience Out of 1236 patients underwent TAVI using the Edwards SAPIEN valve, 158 patients (12.8%) the transaortic approach was used Transaortic approach results : • No postoperative strokes • 30-day all-cause mortality rate of 7% • Major bleeding rate of 1.3%. (Bapat et al.,, STS meeting,2011)
  • 46. "Transcatheter aortic valve replacement with Edwards SAPIEN valve via transaortic route: European Multi-Center Experience" STS 2011 •Initial protocol was to attempt: Transfemoral approach > Transapical > Transaortic. But now: Transfemoral approach > Transaortic access. • But why the Transaortic approach was not the first choice, given its excellent outcomes, low risk of stroke. It is difficult to "sell" the transaortic approach to patients because it involves a 5- cm incision in the chest, either via a mini-sternotomy or a mini-thoracotomy, as opposed to a short incision at the groin. (Bapat et al.,, STS meeting,2011).
  • 47. Conclusion • Heart team concept should be adopted in every TAVI procedure • Transfemoral access need not be the default approach as no data exist from randomized clinical trials showing that it is better than the others . • ‘Indications are slipping’ which means that operable patients with moderate or low risk score are getting TAVI when they should have surgery • Trans Aortic approach is a good and more safe alternative to both Transfemoral and Transapical approaches.