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TAVI: New indications<br />

Prof. Flavio L. <strong>Ribichini</strong><br />

Director Division and School of Cardiology<br />

University of Verona, Italy


No conflict of interest<br />

Proctor for Edwards and Medtronic<br />

Prof. Flavio L. <strong>Ribichini</strong><br />

Director Division and School of Cardiology<br />

University of Verona, Italy


New indications now: the intermediate risk


New indications now: the intermediate risk


TAVI: new indications in the near future<br />

Low-risk AS patients<br />

Asymptomatic AS patients


TAVI: new indications (off label)<br />

Pure, non-calcific aortic regurgitation<br />

Bridge o Heart Mate or heart transplant<br />

AS and aortic dissection<br />

AS and associated mitral valve disease<br />

Bicuspid aortic valve<br />

Mitral and tricuspid VIV<br />

Aortic VIV and severe high-risk CAD


Emergency TAVI for severe aortic regurgitation –<br />

procedural and technical considerations<br />

We report 14 consecutive inoperable patients with non-calcific, pure Aortic Regurgitation and<br />

advanced heart failure treated with emergency percutaneous trans-femoral implantation with<br />

self-expandable CoreValves at our institution, between July 2011 and February 2018.<br />

✓ Computed tomography scan (CTS) of the aortic root was performed in 11 patients to obtain<br />

accurate measures of the aortic annulus and root.<br />

✓ Extremely unstable hemodynamics in 3 patients prevented CTS, and the valve sizing was<br />

decided by intra-procedural trans-esophageal echocardiography (TEE).<br />

✓ The immediate and long-term clinical outcome was prospectively assessed according to the<br />

VARC-2 criteria for device success and safety.


Pure AR in extensive aortic dissection<br />

Two cases of massive residual AR after aortic valve reconstruction performed during the replacement of the ascending aorta due to<br />

acute type 1 aortic dissection, with a residual type III dissection from the aortic arch to the iliac arteries.


Diagnostic catheterization


Aortic Dissection<br />

as seen with the<br />

intra-procedural IVUS


Pure AR in extensive<br />

aortic dissection


Pure AR and aortic Root Aneurysm<br />

Patient’s and procedural characteristic<br />

Pt #2 was implanted electively two 31mm CoreValves in a large aortic root aneurysm, as a planned strategy. The first 31mm CoreValve was<br />

used for anchoring a second 31mm device with optimal final result and complete resolution of the AR.<br />

CT scan of pt #2<br />

• c-d) dilated ascending aorta (55mm);<br />

• e) diameters perimeter and area of the aortic annulus;<br />

• f) sagital view of its aortic valve without calcifications;<br />

• g) sagital view of a thoracic CT scan after the implantation of two<br />

CoreValves in the aortic annulus;<br />

• h) frontal view with the two valves in place.


CT scan at level of the aneurysm of the<br />

Valsalva simus (56mm)


“Valve in valve” implantation of two self-expandable trans-catheter aortic<br />

valves to exclude aortic root aneurysm and treat massive aortic regurgitation.<br />

75 years old male<br />

Massive aortic<br />

insufficiency,<br />

LVEF 50%<br />

Large aneurysm of<br />

the aortic root.<br />

Two previous<br />

cardiac surgeries:<br />

CABG and plastic of<br />

the aortic valve.<br />

Aortic dissection<br />

with implantation of<br />

a Dacron tube in<br />

ascending aorta.


First CoreValve 31mm in the ascending aorta<br />

Valve implantation in the conventional<br />

possition


After 5 years the patient is in NHYA class I


CT scan of the aortic root showing the<br />

valve in valve in correct possition.


Pure AR secondary to Heart Mate or as bridge to<br />

transplant<br />

Heart-Mate II<br />

CT scan showing non-calcified aortic valves<br />

All of them presented multiorgan failure at<br />

the time of TAVI.<br />

One patient had an extremely dilated and<br />

calcified homograft<br />

Now performing TAVI BEFORE Heart Mate<br />

to avoid emergency treatment


Patient survvived, underwent heart transplantation and is alive after 6 years


Intra-op TEE showing AR pre and post<br />

Heart Mate<br />

After the activation of the LVAD<br />

the CO decreased from 3.0l/min<br />

to 2.0 l/min due to the worsening<br />

of the AR


2014: Traumatic aortic aneurysm treated with<br />

Thoracic Endovascular Aortic Repair (TEVAR)<br />

Before…<br />

After TEVAR…


10/2017: Endoleak type 1a at the level<br />

of aortic arch with growth of aneurysm


10/2017: Complete resolution of the endoleak with 2nd endovascular prothesis<br />

(after debranching of the supraortic trunks)<br />

Anastomosis with<br />

supraortic trunks<br />

2nd endovascular prothesis<br />

Calcifications on the aortic valve


11/2017: worsening of aortic stenosis<br />

For episodes of chest pain and dyspnea<br />

(NYHA III) echocardiography was<br />

performed with evidence<br />

of severe aortic stenosis (Peak<br />

Gradient 62mmHg, Mean Gradient 42<br />

mmHg)<br />

The aortic stenosis was confirmed at the heart catheterization<br />

with a peak to peak gradient of 45 mmHg.


PRE-TAVI Evaluation<br />

At the CT scan evidence of an horizontal aorta<br />

with a LVOT diameters of 27,9 mm and 22,1 mm,<br />

perimeter of 79,7 mm, area of 479,5 mm 2 and no<br />

signs of residual dissections.<br />

A CoreValve Evolute R 29 mm was chosen.


1/2018: TAVI Procedure<br />

Evidence of a false lumen due to<br />

an undiagnosed Type 1 aortic<br />

dissection during aortography<br />

prior to TAVI: The 5F pigtail<br />

catheter easily entered a large<br />

false lumen at the level of the<br />

aortic root/ascending aorta<br />

while negotiating the noncoronary<br />

Valsalva synus.


1/2018: TAVI Procedure<br />

5Fr Amplatz AL-1 was used to opacify the true lumen and direct<br />

the straight soft 0.35’’ angiographic wire through the aortic valve<br />

into that horizontal aortic root.<br />

After crossing the aortic valve, thus confirming the correct<br />

placement of the wire, a 2 nd supportive 0.35’’ wire was placed into<br />

the LV, to act as a rail for the CoreValve through the endoprostheses<br />

and the horizontal aortic root.


Before deployment of the CoreValve the buddy wire was removed<br />

from the LV to avoid unwanted trapping and possible<br />

dislodgement of the valve during retrieval<br />

1/2018: TAVI Procedure<br />

Final angiogram showing satisfactory position of the<br />

CoreValve, no relevant aortic regurgitation and no acute aortic<br />

damages or clear images of dissection left.


Post-TAVI CT-SCAN<br />

Evidence of dissection<br />

of ascendent aorta<br />

partially covered at the<br />

entry site by the Evolute<br />

R.<br />

10 months f-up, OK.


Associated mitral valve disease


Male 83. Mitral para-valvular leak<br />

1 2<br />

Four chamber echo view showing the mitral bioprosthesis<br />

Trans-esophagic image showing severe mitral peri-prosthetic leak<br />

EDV pre intervention showing severe LV chamber diatation


…and severe aortic valve regurgitation<br />

Short and<br />

long axis<br />

images and<br />

color Doppler<br />

(long axis and<br />

M mode)<br />

showing<br />

severe aortic<br />

regurgitation.<br />

The aortic<br />

valve has mild<br />

calcifications<br />

without<br />

gradient


Mitral valve intervention<br />

Release of the vascular plug AGA III 10x5mm<br />

Percutanaous occlusion of the mitral peri-valvular leak


Aortic valve intervention<br />

Percutaneous Trans-catheter Aortic Valve Implantation<br />

CoreValve in place with a trivial<br />

residual aortic insufficiency


TTE at discharge<br />

Trans-aortic Doppler before discharge<br />

Residual mean aortic gradient: 9 mmHg.<br />

4 years<br />

F-up in<br />

NYHA<br />

class I


Male, 77 yo, severe AVS and severe MR cord rupture<br />

Percutaneous Trans-catheter Aortic Valve Implantation


Male, 77 yo, severe AVS and severe MR cord rupture<br />

Percutaneous Trans-catheter Mitral Valve Repair


Male, 77 yo, severe AVS and<br />

severe MR cord rupture


VIV of a tricuspid bioprosthesis<br />

- Male born in 1954, aged 62 at the time of referral.<br />

- Rheumatic fever in childhood<br />

- Chronic AF since the age of 25 and since then in OAC<br />

- 1981: Aortic and mitral valve replacement (mechanic valves)<br />

- 2001: Severe tricuspid regurgitation: Perimount Magna<br />

31mm bioprosthesis.<br />

- COPD with recent worsening, in domiciliary oxygen therapy<br />

- Several recurrent TIA of embolic origin<br />

- Severe right heart failure with anasarca


Thoracic angio CT scan<br />

Right atrium volume= 1300-1400 ml


Balloon inflation and valve release<br />

N


Operative result<br />

Intra-operative mean<br />

gradient 3.2 mmHg<br />

Prosthesis in-place


Pre-discharge echographic control: 4 chambers<br />

Mean gradient: 4.1 mmHg<br />

5 years f-up: uneventful with normal function of the valve


Evolut R 34 in Bicuspid<br />

Aortic Valve<br />

76 y o female<br />

Normal coronary arteries<br />

Higly fragile<br />

Severe reumatoid artritis on steroids<br />

CKD (eGFR 30)<br />

Several major bleedings<br />

TF TAVI performed February 10 2017


Calcium<br />

distribution<br />

Implanting view


The valve


• Elective follow-up at 12 months<br />

• Clinically uneventful<br />

• CT scan 12/02/2018<br />

• TTE 31/01/2018


Valve at LVOT and lack of contact to the annulus<br />

Valve at the leaflets @10mm (raphe)


VIV on high risk stentless bioporsthesis and low<br />

coronary ostia<br />

89 years old female<br />

Previous AVR in 2000 with Stentless Sorin 23mm<br />

Well being until beginning of 2015<br />

Rapid progression to NYHA class III-IV<br />

TT echocardio: (oct 2015) mean aortic gradient 58mmHg<br />

Normal coronary arteries<br />

Preserved LV function (EF 66%)<br />

Moderate renal dys-function (eGFR 45)


CT scan and type of valve<br />

CT scan showing the distance beween the aortic valve<br />

annulus and the origin of the coronary arteries (4.7<br />

and 5.4mm)<br />

SORIN Pericarbon Freedom 23mm<br />

stentless aortic bio-prosthesi (a),<br />

and the surgical technique of valve<br />

sewing very close to coronary ostia (b)<br />

a<br />

b


Two BMW guide wires in the coronaries<br />

Left femoral access for the<br />

valve sheath.<br />

The rigth femoral artery<br />

was used for the left<br />

coronary artery guiding<br />

catheter.<br />

The right coronary guiding<br />

catheter was advanced<br />

through the right radial artery


Rapid pacing and<br />

valve inflation


Implantation of the stent in the RCA first and then in the left main


Final aortic<br />

angiogram


Complete normalization of the<br />

rhythm, ECG QRS width, and<br />

blood pressure after implantation of the<br />

two stents.<br />

Aortic angio shows the XT Sapien 3<br />

valve in place, and patent RCA and left<br />

coronary artery.<br />

Intra-operatory TT echo shows no<br />

residual aortic leak in diastole (a)<br />

Residual trans-valvular<br />

PG (18mmHg) (b).<br />

a<br />

b<br />

The patient<br />

had<br />

uneventful<br />

Hospital stay<br />

and was<br />

discharged on<br />

day 6 on DAPT<br />

advised for 6


Considerations<br />

Currently available TAVI technology allows<br />

treatment of a wide spectrum of complex heart<br />

valvular disease, in particular in patients that have<br />

undergone previous cardiac surgery and present<br />

high risk of re-operation.<br />

The success of the procedure is based on a<br />

thougthful planning of the strategy before hand.

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