Circulation: Cardiovascular Interventions. 2008;1:233
doi: 10.1161/CIRCINTERVENTIONS.108.813592
Images and Case Reports in Interventional Cardiology |
Apical Aortic Valve Implantation in a Patient With a Mechanical Valve Prosthesis in Mitral Position
Josep Rodés-Cabau, MD, FESC
;
Eric Dumont, MD
;
Santiago Miró, MD
;
Daniel Doyle, MD
;
Robert De Larochellière, MD
;
Marie-Annick Clavel, DVM, MSc
;
Jacques Villeneuve, MD
;
Sebastien Bergeron, MD
;
Mario Senechal, MD
and
Philippe Pibarot, PhD
From the Quebec Heart Institute/Laval Hospital, Quebec, Canada.
Correspondence to Josep Rodés-Cabau, MD, FESC, Quebec Heart Institute/Laval Hospital, 2725 Chemin Ste-Foy, G1V 4G5 Quebec, Canada. E-mail josep.rodes{at}crhl.ulaval.ca
A 67-year-old man diagnosed with severe aortic stenosis was admitted to our institution with pulmonary edema. The patient had a history of severe pulmonary fibrosis (total lung capacity, 57% of predicted value; diffusing capacity for carbon monoxide, 33% of predicted value) and had undergone coronary bypass grafting and mitral valve replacement with a St Jude mechanical valve (St Jude Medical, St Paul, Minn) 18 years ago. Doppler echocardiography showed a mean aortic gradient of 36 mm Hg, an aortic valve area of 0.50 cm2, and a left ventricular ejection fraction of 45%. Although the mean predicted operative mortality by the Society of Thoracic Surgeons score was 7.5%, the patient was considered at too high risk for surgical aortic valve replacement because of his pulmonary condition, and he was then evaluated for percutaneous aortic valve implantation (PAVI). Transesophageal echocardiography (TEE) showed an aortic annulus of 23 mm as well as proximity between the mitral prosthesis and the aortic annulus (Figure 1A). Contrast computed tomography showed the presence of moderate stenosis and severe calcification of both iliofemoral arteries precluding transfemoral PAVI, and the patient was then proposed for transapical PAVI.

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Figure 1. TEE images (long-axis view) showing the relationship between the mechanical valve prosthesis in mitral position and the aortic annulus before aortic valve implantation (A; white arrow indicates the lack of space between the mitral prosthesis and the aortic annulus) and after percutaneous valve implantation (B; white arrows indicate the aortic and ventricular ends of the percutaneously implanted aortic valve).
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The procedure was performed in the operating room under TEE
and fluoroscopy guidance by a team of cardiac surgeons and interventional
cardiologists using the techniques extensively described in
previous reports.
1–3 Concerns about the interference of
the mitral mechanical prosthesis with the expansion of the new
aortic valve and the potential increased risk of valve embolization
led us to perform balloon valvuloplasty by transfemoral approach
with a 23-mm balloon just before thoracothomy. After valvuloplasty
that showed the stability and complete expansion of the balloon,
a left anterior minithoracotomy was performed to expose the
apex, and 2 large pursestrings with pledgets were placed at
the left ventricular apex. After puncturing the apex, a stiff
guidewire was positioned in the descending aorta, and a 26F
sheath was inserted into the left ventricle over the wire. On
the basis of an aortic annulus measurement of 23 mm by TEE,
a 26-mm Edwards SAPIEN valve (Edwards Lifesciences Inc, Irvine,
Calif) was selected for implantation. Careful positioning of
the valve with TEE guidance was performed with about half of
the valve positioned above and half below the aortic annulus.
Valve implantation was performed under rapid pacing, and after
valve deployment, TEE showed the appropriate position of the
aortic valve, with no interference with the mitral prosthesis
(
Figure 1B). Three-dimensional computed tomography images of
the mitral and aortic prostheses are shown in
Figure 2 and Movies
I and II. Doppler echocardiography at hospital discharge 6 days
after the intervention showed a mean residual aortic gradient
and aortic valve area of 12 mm Hg and 1.46 cm
2, respectively,
and the absence of any detectable residual aortic regurgitation.
At 2-month follow-up, the patient was in New York Heart Association
functional class II, and transthoracic Doppler echocardiography
showed the correct position of the valve and the absence of
hemodynamic changes compared with the data obtained at hospital
discharge. Fluoroscopy images of the aortic and mitral prostheses
obtained at 2-month follow-up are shown in
Figure 3 and Movies
III and IV.

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Figure 2. Three-dimensional computed tomography images showing the mechanical valve prosthesis in mitral position (thick white arrows) and the percutaneous valve in aortic position (thin white arrows). A, Ventricular view. B, Aortic and auricular view.
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Figure 3. Fluoroscopic images showing the mechanical valve prosthesis in mitral position (white arrows) and the percutaneous valve in aortic position (black arrows). A, Right anterior oblique view showing the proximity between the mitral and aortic prostheses. B, Left anterior oblique view showing the adequate functioning of the mechanical valve in mitral position.
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This is the first report of PAVI in the presence of a mechanical
heart valve in mitral position. The presence of a mechanical
valve in mitral position might complicate PAVI because of (1)
the significant reduction or even absence of the mitroaortic
space to accommodate the balloon-expanded valve (
Figure 1A)
and (2) the presence of a mechanical structure instead of fibrous
tissue that can limit the expansion of the percutaneous valve.
Thus, these 2 mechanisms might favor valve underexpansion and
embolization.
4 In fact, the presence of previous mitral valve
surgery is considered an exclusion criterion in the currently
ongoing Placement of AoRTic TraNscathetER valves (PARTNER) trial
(clinicaltrial.org, NCT00530894), which compares PAVI and surgical
aortic valve replacement. The present report shows that PAVI
can be successfully performed in the presence of mechanical
heart prosthesis in mitral position. Importantly, the percutaneous
valve was fully expanded, with no deformation of the metallic
structure (
Figures 2 and 3
and Movies I through IV), only mild
residual gradient, and no aortic regurgitation. Moreover, no
distortion or malfunction of the mechanical valve in mitral
position occurred.
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Disclosures
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Drs Rodés-Cabau and Dumont are consultants for Edwards
Lifesciences Inc. Dr Pibarot has received honoraria from Edwards
Lifesciences Inc for speakers bureau appointments. All
other authors have no conflicts of interest to disclose.
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Footnotes
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The online-only Data Supplement is available at http://circinterventions.ahajournals.org/cgi/content/full/1/3/233/DC1.
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References
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1. Lichtenstein SV, Cheung A, Ye J, Thompson CR, Carere RG, Pasupati S, Webb JW. Transapical transcatheter aortic valve implantation in humans: initial clinical experience.
Circulation. 2006; 114: 591–596.
[Abstract/Free Full Text]2. Walther T, Simon P, Dewey T, Wimmer-Greinecker G, Falk V, Kasimir MT, Doss M, Borger MA, Schuler G, Glogar D, Fehske W, Wolner E, Mohr FW, Mack M. Transapical minimally invasive aortic valve implantation: multicentre experience. Circulation. 2007; 116: I240–I245.[Medline]
3. Rodés-Cabau J, Dumont E, DelaRochellière R, Doyle D, Lemieux J, Bergeron S, Clavel MA, Villeneuve J, Raby K, Bertrand OF, Pibarot P. Feasibility and initial results of percutaneous aortic valve implantation including selection of the transfemoral or transapical approach in patients with severe aortic stenosis. Am J Cardiol. 2008; 102: 1240–1246.[CrossRef][Medline]
4. Moss RR, Ivens E, Pasupati S, Humphries K, Thompson CR, Munt B, Sinhal A, Webb JG. Role of echocardiography in percutaneous aortic valve implantation. J Am Coll Cardiol Img. 2008; 1: 15–24.[Abstract/Free Full Text]
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