cardiology grand rounds - minneapolis heart institute...

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PLEASE SAVE A COPY OF THIS FLIER AS YOUR CERTIFICATE OF ATTENDANCE CARDIOLOGY GRAND ROUNDS Presentation: Use of CT to support appropriate selection of patients and devices / guide to nonsurgical mitral valve replacement Speaker: Jonathon A. Leipsic, MD, FRCPS, FSCCT Chairman, Department of Radiology, Providence Health Care, Vancouver, BC Vice Chairman – Research, University of British Columbia, Department of Radiology Associate Professor of Radiology and Cardiology, University of British Columbia Canada Research Chair, Advanced Cardiopulmonary Imaging Date: Monday, October 26, 2015, 7:00 8:00 AM Location: ANW Education Building, Watson Room OBJECTIVES At the completion of this activity, the participants should be able to: 1. Review the role of MDCT for structural heart disease and transcatheter valvular assessment. 2. Review the current data for the use of MDCT for mitral valvular assessment and annular sizing for TMVI. 3. Discuss the unanswered questions that remain in transcatheter mitral valve implantation and how MDCT may provide some answers. ACCREDITATION Physicians: This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of Allina Health and Minneapolis Heart Institute Foundation. Allina Health is accredited by the ACCME to provide continuing medical education for physicians. Allina Health designates this live activity for a maximum of 1.0 AMA PRA Category 1 Credit TM . Physicians should only claim credit commensurate with the extent of their participation in the activity. Nurses: This activity has been designed to meet the Minnesota Board of Nursing continuing education requirements for 1.2 hours of credit. However, the nurse is responsible for determining whether this activity meets the requirements for acceptable continuing education. Others: Individuals representing other professional disciplines may submit course materials to their respective professional associations for 1.0 hours of continuing education credit. DISCLOSURE STATEMENTS Speaker(s): Dr. Leipsic has declared following relationships. Consultant: Neovasc Inc. and Tendyne Holdings Inc. Planning Committee: Dr. Michael Miedema, and Eva Zewdie have declared that they do not have any conflicts of interest associated with the planning of this activity. Dr. Robert Schwartz declared the following relationships stockholder: Cardiomind, Interface Biologics, Aritech, DSI/Transoma, InstyMeds, Intervalve, Medtronic, Osprey Medical, Stout Medical, Tricardia LLC, CoAptus Inc, Augustine Biomedical; scientific advisory board: Abbott Laboratories, Boston Scientific, MEDRAD Inc, Thomas, McNerney & Partners, Cardiomind, Interface Biologics; options: BackBeat Medical, BioHeart, CHF Solutions; speakers bureau: Vital Images; consultant: Edwards LifeSciences.

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Page 1: CARDIOLOGY GRAND ROUNDS - Minneapolis Heart Institute ...mplsheart.org/wp-content/uploads/2015/11/Leipsic_CT-Guide-to-Mitral-Valve... · CARDIOLOGY GRAND ROUNDS ... Isolated prolapse

PLEASE SAVE A COPY OF THIS FLIER AS YOUR CERTIFICATE OF ATTENDANCE 

  

C A R D I O L O G Y   G R A N D   R O U N D S  Presentation:  Use of CT to support appropriate selection of patients and devices 

/ guide to non‐surgical mitral valve replacement 

Speaker:  Jonathon A. Leipsic, MD, FRCPS, FSCCTChairman, Department of Radiology, Providence Health Care, Vancouver, BC  Vice Chairman – Research, University of British Columbia, Department of Radiology Associate Professor of Radiology and Cardiology, University of British Columbia Canada Research Chair, Advanced Cardiopulmonary Imaging 

Date:  Monday, October 26, 2015, 7:00 – 8:00 AM

Location:  ANW Education Building, Watson Room 

OBJECTIVES At the completion of this activity, the participants should be able to: 1.  Review the role of MDCT for structural heart disease and transcatheter valvular assessment. 2.  Review the current data for the use of MDCT for mitral valvular assessment and annular sizing for TMVI. 3.  Discuss the unanswered questions that remain in transcatheter mitral valve implantation and how MDCT may 

provide some answers.  

ACCREDITATION Physicians: This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of Allina Health and Minneapolis Heart Institute Foundation.  Allina Health is accredited by the ACCME to provide continuing medical education for physicians.   

Allina Health designates this live activity for a maximum of 1.0 AMA PRA Category 1 CreditTM.  Physicians should only claim credit commensurate with the extent of their participation in the activity.  

Nurses: This activity has been designed to meet the Minnesota Board of Nursing continuing education requirements for 1.2 hours of credit.  However, the nurse is responsible for determining whether this activity meets the requirements for acceptable continuing education.  

Others: Individuals representing other professional disciplines may submit course materials to their respective professional associations for 1.0 hours of continuing education credit.  

DISCLOSURE STATEMENTS  Speaker(s): Dr. Leipsic has declared following relationships. Consultant: Neovasc Inc. and Tendyne Holdings Inc.  

Planning Committee: Dr. Michael Miedema, and Eva Zewdie have declared that they do not have any conflicts of interest associated with the planning of this activity. Dr. Robert Schwartz declared the following relationships ‐ stockholder: Cardiomind, Interface Biologics, Aritech, DSI/Transoma, InstyMeds, Intervalve, Medtronic, Osprey Medical, Stout Medical, Tricardia LLC, CoAptus Inc, Augustine Biomedical; scientific advisory board: Abbott Laboratories, Boston Scientific, MEDRAD Inc, Thomas, McNerney & Partners, Cardiomind, Interface Biologics; options: BackBeat Medical, BioHeart, CHF Solutions; speakers bureau: Vital Images; consultant: Edwards LifeSciences.   

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MDCT to Guide Mitral Valve Interventions

Jonathon Leipsic MD FRCPC FSCCTVice Chairman of Radiology

Associate Professor Radiology and Cardiology UBC

President Society of Cardiovascular CTCanada Research Chair Advanced Cardiac 

Imaging

Disclosures

Speaker’s bureau: GE Healthcare and Edwards LifeSciences

Grant Support‐ CIHR, NIH, GE Healthcare, Heartflow

Consultant‐Heartflow, 

Edwards LifeSciences, Neovasc, Circle CVI

Corelab‐ NIH, Edwards Lifesciences, Neovasc, Tendyne

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Learning Lessons from TAVI 

The Virtual Basal Ring

Source: Leipsic et al JACC Img April 2011

Sinotubular junctionAortic leafletsAortic Annulus

Aortic Annular Diameter

RC = Right coronary cusp; NC = Non-coronary cusp; LC = Left coronary cusp

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Live Case Summary‐TCT

• 89 year old female

• Severe degenerative mitral regurgitation

• NYHA III

• Coronary artery bypass grafting ‐ 2008

• Chronic kidney disease ‐ eGFR 40mL/min

• Chronic bronchitis/COPD 

• 6 minute walk test – 340m

• STS – 16.1%

Neovasc Tiara Transcatheter Mitral Valve• Anatomically shaped (D‐shaped)

• Nitinol based, self‐expanding frame

• Bovine pericardium leaflets

• Ventricular anchors to fix the valve onto fibrous trigone and posterior annulus

• Captures the anterior and posterior leaflets

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Annular Segmentation

Angle Prediction and coronary sinus localization 

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Device Cloning and Neo LVOT

How did we get to this point together?

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1‐MDCT aids in the diagnosis of valvular disease

Temporal Resolution

• Echo > 30 fps (<33 msec)

• 64‐slice CT 165 msec

• Dual‐source CT 83 msec (2nd Gen. 75msec)

CT Limitations Assessing Valves

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CT Limitations Assessing Valves

• Irregular rhythms (variability, gating)

• Difficult images and artifacts

–Obesity

–Calcium and leads

–Motion artifacts

Strength of CT is Anatomical DetailUnicuspid Valve Quadricuspid

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Normal Mitral Valve Anatomy on MDCT

Mitral Valvular Disease

• Patient with rheumatic mitral valve and mild mitral stenosis (valve area 1.6 cm2)

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Mitral valve stenosis‐ Limited Data

Planimetry by CT vs. Echocardiography 

Messika-Zeitoun et al. JACC 2006

Moderate Mitral Stenosis

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Mitral Regurgitation

MR can be isolated in location (involved

scallops) or timing (part of systole)

Minimum Intensity Projection

Any MR? Moderate MR by TEE

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• Most common valvular heart disease

Classification

• due to a primary abnormality of the valve apparatus 

– Mitral valve prolapse (aka "degenerative" or myxomatousmitral valve disease)

– Rheumatic heart disease

– Infective endocarditis

• secondary to another cardiac disease (functional)

– Ischemic cardiomyopathy

– Dilated cardiomyopathies 

Mitral regurgitationFacts

• abnormal systolic displacement of one or both leaflets into the left atrium (systolic billowing) due to a disruption or elongation of leaflets, chordae, or papillary muscles

• Echocardiography: Billowing of any portion of the mitral leaflets ≥2 mm above the annular plane in a long axis view (parasternal or apical three‐chamber) 

Mitral Valve Prolapse (MVP)

Definition

Classification

•abnormal movement of the valve: • Billowing: when the tips of leaflets remain in the left ventricle• Flail: when the tip(s) of one (or both) leaflets prolapses into the left atrium 

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Mitral Valve Prolapse (MVP)

Ethiology of MVP and mechanism of MR

Disease Mechanism of regurgitation

Primary MVP

Fibroelastic deficiencyIsolated prolapse of the mitral leaflet (commonly P2 scallop)Frequent chordal ruptureMild annular enlargement

Forme fruste Barlow disease Intermediate

Barlow diseaseDiffusely thickened, redundant mitral leafletsChordal elongation/ruptureSevere annular enlargement

Secondary MVP

Associated with connective tissue disease*

Diffusely thickened, redundant mitral leafletsChordal elongation/ruptureSevere annular enlargement

Associated with congenital heart disease

¶Thickened, redundant mitral leafletsChordal elongation/rupture possible

Acute myocardial ischemia Papillary muscle dysfunction with secondary prolapse/papillary muscle rupture

Acute rheumatic fever Chordal and leaflet destruction by acute inflammatory process

Endocarditis Chordal and leaflet destruction by infectious process; vegetations

Other (trauma, severe mitralannular calcification, hypertrophic

cardiomyopathy)Ruptured chordae, no myxomatous changes of mitral valve leaflets

Image: Adams et al. EHJ 2010 Table: Uptodate.com

Mitral valve apparatusLeaflet anatomy

MPR minIP

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Mitral valve apparatusPapillary muscles

Mitral Valve Prolapse

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Mitral Valve Prolapse

Mitral Valve Prolapse (MVP)

Importance of the employed view

MVP should never be diagnosed on 4 chamber reconstruction

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Mitral Valve Prolapse (MVP)

Importance of the employed view

https://depts.washington.edu/cvrtc/iafnew.gifLevine et al. Circulation 1989

Mitral Valve Prolapse (MVP)

Pseudoprolapse

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Diagnostic Accuracy of MDCT for MVP

Source: Feuchtner et al Radiology 2010

4 ways CT can help with TMVI in 2015

• Anatomic assessment of valvular apparatus

• Help with annular sizing and device selection 

• Understanding mechanisms and risk of LVOT obstruction

• Prediction of appropriate fluoroscopy angles for coaxial deployment 

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2‐MDCT allows for a granular and clear definition of the mitral 

annulus

MDCT to Guide TranscatheterMitral Valve Replacement

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Advantages to MDCT methods 

Greater reproducibility (less operator dependent)

Less sensitive to minor changes in obliquity

“3‐D”“3‐D”

“2D”Source: Gurvitch et al JACC Interventions Nov 2011

Mitral Annulus is non‐planar

Source: Levine et al Circulation 1989

Saddle shape with a valley and 2 peaks extending to the aortic root

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The mitral annulus is segmented posteriorly along the insertion of the posteriormitral valve leaflet and anteriorly along the insertion of the intervalvular fibrosa.

Mitral Annular Segmentation with MDCT

Source: Blanke et al. JACC Imaging 2015

Segmentation of the Saddle and D Shaped Annulus

Source: Blanke and Naoum et al JACC Imaging 2015

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Saddle Shaped Annulus

Mitral annulus

• Posterior peak: Insertion of the posterior mitralleaflet at atrioventricularjunction

• Anterior/aortic peak:insertion of intervalvularfibrosa at the left atrium, in part continuous with the aortic annulus  

• Nadirs: are located at the level of fibrous trigones. 

Lee et al. Circulation 2013

Flachskampf et al. Circulation 2000

The mitral annulus is segmented posteriorly along the insertion of the posteriormitral valve leaflet and anteriorly along the insertion of the intervalvular fibrosa.

Mitral Annular Segmentation with MDCT

Source: Blanke et al. JACC Imaging 2015

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Mitral annulusCT segmentation ‐ Saddle‐shaped annulus

Saddled Annulus

Projected area

Traditional Method for Mitral Annular Assessment 

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Mitral Annulus in the context of TMVI

Projected area

Source: Blanke et al JCCT 2014 and iJACC Imaging 2015

Re‐thinking the Mitral Annulus

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“unsaddled” annulus

TT

“unsaddled” annulus

TT

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Conformational similarities with an implanted device in vivo

Source: Cheung et al. JACC 2014

Aortic Annulus is Dynamic 

Source: Blanke et al JACC Int ; Leipsic et al Circ Imaging Jun 2013

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Dynamic Changes of the Aortic Annulus

CT for Valvular Heart Disease

CT……..

Atrial kick

LV largest

EarlyS

EndS

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Mitral Annulus is also Dynamic

Source: Unpublished data

3‐Different devices with different designs have different anatomical requirements

Tiara Fortis Tendyne

Source: Cheung et al JACC 2014; Bapat Euroint 2014; Moat et al JACC 2015 

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Different devices with different designs

Source: In press Blanke et al JACC Imaging

Confirmation of Mitral Valve Prolapse

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Anatomical assessment of device anchoring by MDCT

Device anchoring

Sufficient posterior shelfin the setting of dilatedLV, persisting in diastoleand systole

Sufficient posterior shelf in the setting of a focal basal scar and dilated LV, persisting in diastole and systole

Landing zone differs among mitral pathologies and patients 

LV

LA

MAd

MA disjuction

LV

LA

LV

LA

LV

LA

LA

LV

myocardialshelf

LA

LV

myocardialshelf

A

D

B

E

C

F

Landing Zone Characterization

MA disjuction

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Landing Zone CharacterizationMitral annular calcium

3‐Co‐planar angle prediction with MDCT

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Fluoroscopy angulation predictionLine of perpendicularity

Identificationof annulus

plane 

Adjusting toLAO 0˚ 

Adjusting toCAU 0˚

Adjusting toLAO 30˚

1                2                3 

1                   2                     3  Blanke, Leipsic  Radiology 2013

MDCT  vs 3‐D Angio CT for Angle Prediction

Source: Binder et al. TCT 2011 , Circ Interventions April 2012

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Not all preferred projections are feasible

Prediction of fluoroscopy angulation

• Corresponding LAO/RAO and CRA/CAU

Variable projections for different devices

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Coronary sinus segmentation to aid with deployment

Simulation of the coronary sinus wire (yellow line) and mitral annular plane in “compromise views” in 

two different patients.

Only some angles are feasible in the hybrid OR

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Clinical Implications for TMVI

Source: in press JCCT

4‐ Prediction of LVOT Obstruction

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Predisposing factors for LVOT obstruction 

Small LVOT‐diameter

Septal bulge

Larger Aorto‐mitral angle

Device protrusion into LV 

Device flaring 

Remaining systolic function

Mechanisms of LVOT Obstruction‐ Concept of the Neo‐LVOT

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Concept of the Neo‐LVOT

Mechanisms of LVOT Obstruction

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Implications for Sizing and LVOT Clearance

Source: Blanke et al JACC Imaging

Modeling the risk of LVOT Obstruction‐

Need dynamic data to more deeply understand individual risk

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Determination of LVOT Clearance 

Important lessons from post implant CT to understand device positioning and capture

Learning from post‐implant geometry

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Modeling the risk of LVOT Obstruction‐

Need dynamic data to more deeply understand individual risk

Mechanism of LVOT Obstruction in native Transcatheter Mitral Valve Implantation

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5‐ Aids in access localization to guide co‐planar device deployment

Source: Blanke et al JACC Imaging 2015

Historical approach for TA procedures may not be adequate in TMVI

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Echo views: Purple line rotational axis through apex, blue line ideal access trajectory

3CH‐View Dependent x‐plane90degrees

Plane through ideal access point

Blue line indicates view above

14mm Antero‐lateral

Varied offset of Optimal access point and traditional apex

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Whole thorax allows localization of the appropriate rib space for puncture

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Expanding to the Tricuspid Space

Clinical Experience to date

• 13 patients (Canada and Switzerland)

• Prohibitive risk for cardiac surgery per heart team (compassionate use)

• Left sided disease with secondary RV dilation

• Severe functional TR

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Edwards FORMA Repair System

FORMA System consists of:1. Spacer

– Positioned into the regurgitant orifice

– Creates a platform for native leaflet coaptation

2. Rail

– Tracks Spacer into position

– Distally and proximally anchored

Echo Confirmation of Severe TR

• Dilated annulus (>>40 mm)

• Dilated right atrium

• Leaflet mal‐coaptation

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Echo Confirmation of Severe TR

Echo Confirmation of Severe TR

Vena contracta

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Pre‐procedural Evaluation I

• Short axis view

• Large centralgap

Pre‐procedural Evaluation I

• Annular area = 20 cm2

• 15 mm Spacer area = 1.76 cm2

• Very low risk of Stenosis

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RAO42 CAU2 

Co‐planar angle prediction with MDCT

Localization of the cardiac apex

APEX projects anteriorto Trans‐section point with myocardium

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Orthogonal view LA048 CAU2

APEX

4 chamber view 

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Surgical Cut‐Down

Subclavian Vein

24 F Sheath in Left Subclavian Vein

Anchoring of the Delivery Rail

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Anchoring of the Delivery Rail

Spacer Positioning in the Tricuspid Valve 

Initial position Final position

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Intra‐procedural reduction of TR severity

Before spacer After spacer

Proximal locking and Closure

Proximal part of the delivery rail is coiled and secured in a subcutaneous pocket

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Final location of FORMA spacerin the Tricuspid Valve

Systole Diastole

Valve leaflet

Anchor

SpacerRail

A

B

Using CT to understand device positioning

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Conclusions

• Rapid evolution of transcatheter solutions for functional mitral regurgitation

• Role of MDCT is evolving particularly with regards to Transcatheter Mitral Valve Replacement

• Outcomes data is needed to better optimize the integration of MDCT to guide minimally invasive mitral valve interventions

• Continued learning to integrate MDCT into right sided valvular disease