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Percutaneous mitral valve repair using the MitraClip® device (e-valve)

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Presentation on theme: "Percutaneous mitral valve repair using the MitraClip® device (e-valve)"— Presentation transcript:

1 Percutaneous mitral valve repair using the MitraClip® device (e-valve)
Post-script Percutaneous mitral valve repair using the MitraClip® device (e-valve) Angela Hoye, Rajesh Nair, Farqad Alamgir Castle Hill Hospital, Hull

2 No conflict of interest in relation to this presentation

3 Introduction: MR Mitral regurgitation occurs due to:
valvular degeneration (50%) rheumatic disease (20%) ischaemia (17%) Where possible, surgical mortality is lower following MV repair rather than replacement However, after MV repair surgery, published data show a rate of recurrence of grade 3 or 4 MR of 17-20% at 5 yrs

4 Anatomy

5 The Alfieri technique The surgical “edge-to-edge” technique was first described in early 1990`s (Alfieri) Over 1,500 pts reported in the literature Safe, effective, durable No occurrence of mitral stenosis Facilitates proper leaflet coaptation Degenerative - anchor flail / prolapsing leaflets Functional - Coapt tethered leaflets to reduce time and force required to close valve Creates tissue bridge Tissue bridge limits annulus dilatation

6 The Alfieri technique Euro Heart Survey demonstrated that despite presence of severe MR and symptoms, HALF of all patients are not considered for surgery CE Mark approval in March 2008

7 MitraClip® procedure overview
Independent leaflet capture Arm on ventricular side; Gripper on atrial side Reduces potential for embolization Repositionable and removable Preserves surgical options in the future Polyester cover designed to promote tissue healing

8 Anatomic Suitability Leaflet mal-coaptation resulting in MR
>2mm >11mm <10mm <15mm Sufficient leaflet tissue for mechanical coaptation Non-rheumatic/endocarditic valve morphology Anatomic considerations Flail gap <10mm Flail width <15mm Mitral Area > 4.0cm Coaptation length > 2mm

9 Feasibility (completed)
Studies Enrollment Population n EVEREST I Feasibility (completed) Registry patients 55 EVEREST II Randomized n=279 Roll-in Randomized Clip Randomized Surgery 60 187 92 High Risk Registry 78 47 sites

10 Data: EVEREST Age 18 years or older
Moderate to severe (3+) or severe (4+) MR Symptomatic Asymptomatic with LVEF < 60% or LVESD > 40mm* MR originates from A2-P2 mal-coaptation Candidate for mitral valve surgery Key exclusions: EF < 25% or LVESD > 55 mm Renal insufficiency Endocarditis, rheumatic heart disease *ACC/AHA Guidelines, Circ. 114;450,2006

11 One or more Clips implanted in 90% of cases
Results EVEREST I + roll-in phase of EVEREST II One or more Clips implanted in 90% of cases

12 Clinical results 99% 97% 96% 96% 96% 92% 89% 85% 86% 84% 82% 75% 67%
Survival 96% 96% 96% 92% 89% Freedom from surgery 85% 86% 84% 82% 75% 67% 66% 65% 63% Freedom from death, surgery & MR > 2+

13 Reverse LV remodelling
LV Dysfunction Population (EF < 55% or LVIDs > 4.5cm)

14 Our experience All potential patients were discussed at MDT
Pre-procedural TTE and TOE to determine suitability Teamwork is vital Interventional cardiologist Cardiac anaesthetist ECHO specialist Lab staff – specialist training given to nursing staff All procedures performed with support from physicians from the company

15 Our experience Successfully treated 3 patients, all with degenerative MR 2 pts with a single clip, 1 with 2 clips No procedural MACE At 1 month, all patients report a marked improvement in symptoms / exercise capacity

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18 Amplatz Guide

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23 Conclusions Preliminary results of percutaneous mitral valve repair with the MitraClip® demonstrate that it is safe and feasible Steep learning curve and it is essential to understand MV anatomy and TOE images Definite place for this technology in a subset of patients with MR and suitable anatomy All potential candidates should be evaluated by a multidisciplinary team Patient selection is paramount


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