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1 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017 1 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017 Case of combined NIVL and PTS stenting Courtesy of Mr. Stephen Black United kingdom

Case Study: Combined NIVL and PTS Stenting · 12 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PIof 24 -494318 AA SEP2017 Stent Placement • An Over-The-Wire

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Page 1: Case Study: Combined NIVL and PTS Stenting · 12 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PIof 24 -494318 AA SEP2017 Stent Placement • An Over-The-Wire

1 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017 1 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017

Case of combined NIVL and PTS

stenting

Courtesy of Mr. Stephen Black

United kingdom

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2 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017

Patient History

25 y/o female

2011: Conservatively treated ilio-femoral DVT

2013-2015:

• Increasing c/o pain and swelling despite using adequate BK compression

stockings.

• On gabapentin to control pain

• Known family history of AT III deficiency and verified in patient.

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3 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017

Initial venogram

• A soft hydrophilic guidewire

(0.035”) is inserted under ultra-

sound guidance in the femoral

vein mid-thigh

• The cannula is replaced by a #9

sheath.

• An initial venogram is performed

through the sheath.

• A power injector and subtraction

technique was utilized

• 20ml at 8ml/s contrast dye,

pressure 900 psi

AP Venogram

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4 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017

Intravascular Ultrasound – (IVUS)

Initial IVUS - (left side) Images from IVC to

femoral vein acquired during pullback

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5 of 24 © 2017 Boston Scientific Corporation or its affiliates. All rights reserved. PI-494318-AA SEP2017

Central non-thrombotic iliac vein lesion (NIVL) >50%

Green -CIV stenosis at

vessel-crossing, focal,

normal wall – NIVL

Blue – reference

“normal” vein just central

to the inflow of the int.

iliac vein

Area % stenosis = (114.0-42.2/114) x 100 = 63%

Min diam % = (9.5-3.6/9.5) x 100 = 62%

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Postthrombotic occlusion EIV and CFV

Occluded EIV

Area % stenosis = 100%

Min diam % = 100%

Size of patent distal CFV

Min diam = 7.6mm

Max diam = 13.6 mm

Area 85.7 mm2

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Sizing of the Stent

Assess the diameter of the “normal” vein:

Take the average of the 2 diameters of the “normal”

For example 14.1 +9.5 = 23.5/2 = appr. 12;

Select a stent diameter at least 2 mm larger than the surrounding “normal” vessel.

“Normal” CIV

Max diam 14.1mm

Min diam 9.5 mm

Area 114 mm2

“Normal” CFV

Max diam 13.6mm

Min diam 7.6 mm

Area 86.7 mm2

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Identifying Central “Landing Zone”

Stenting from centrum to periphery

Starting >5mm central to lesion

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Identifying Peripheral “Landing Zone”

Pre-dilation IVUS

Stent lower

limit

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Deciding the Length of the Stent System

Appr. 24 cm

on the IVUS

catheter

With venogram May need several injections

Contralateral CFV injection

Oblique views

With IVUS Use the cm marking on the IVUS catheter to

indicate extent of stenting

Use IVUS head for exact positioning

The stent system should be at least 1 cm

longer than the lesion (5 mm centrally and

5 mm peripherally).

Plan the number and length of the

individual stents.

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Pre-dilation

• Directly to final size balloon

• In stages with increasingly larger

balloons

• Keep highest inflation pressure until

pressure stable

12-16 mm high-pressure balloon

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Stent Placement

• An Over-The-Wire system

• 0.035 in. (0.89 mm) guidewires

• 9 French introducer sheath

• Loosen the valve of the RHV.

• Magnify the central “landing zone”.

• Start deploying stent above intended level to “Martini-glass”

formation by securing the shaft hub and retract the RHV.

• Pull back the device to appropriate level and fully deploy.

Rotating Hemostatic Valve (RHV)

Shaft Hub

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Stent Deployment

“Martini-glass”

able to pull down

“Wine-glass”

committed

The VICI Venous Stent System

cannot be re-captured!

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Stent Deployment

“Martini-glass”

able to pull down

“Wine-glass”

committed

The VICI Venous Stent System

cannot be re-captured!

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Stent Placement and Example of Post-stent Dilation –

Upper Stent

This particular patient required three stents to adequately cover the lesion. Other

patients may require more or fewer stents to adequately cover their lesion(s).

Deployment and dilation

Notice the expected foreshortening of 10-20% of the

stent length at delivery as compared to the stent length

when restrained in the delivery sheath

IVUS Catheter Stent

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Middle and Lower Stent Placement and Dilation

If using >1 stent, the stents should overlap by at least 1 cm. (notice expected foreshortening from sheath to full deployment)

Deployment of the middle stent Deployment and dilation of lower stent

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Final IVUS –

Following stent placement and balloon dilation

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IVUS – Lower end of stent

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Final Venography

Final Venography Before Stenting After Stenting

16mm Vici Venous Stent 120mm, 120mm and 90mm

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Post-op DUS

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Post-op DUS - grayscale

Longitudinal Transverse

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Post-op DUS - colorflow

Mid-stent Central stent to IVC

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One year follow-up

• No swelling, no pain.

• Does not use compression stocking or

pain medication

• No secondary intervention.

• Maintained on Rivoxarban.

• Annual DUS follow-up planned

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VICI VENOUS STENT® is manufactured by Veniti®, Inc. and distributed by Boston Scientific Corporation.

All cited trademarks are the property of their respective owners. CAUTION: The law restricts these devices to sale by or on the order of

a physician. Indications, contraindications, warnings and instructions for use can be found in the product labelling supplied with each

device. Information for the use only in countries with applicable health authority product registrations. Indications, operating

specifications and availability may vary by country. Check with local product representation and country-specific Information For Use for

your country. This material is not approved for use or distribution in France. Illustrations for information purposes – not indicative of

actual size or clinical outcome.

© 2017 Boston Scientific Corporation or its affiliates. All rights reserved.