JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
VOL. 67, NO. 7, 2016
ª 2016 BY THE AMERICAN COLLEGE OF CARDIOLOGY FOUNDATION
ISSN 0735-1097/$36.00
PUBLISHED BY ELSEVIER
Letters Transfemoral Tricuspid Valve Repair Using a Percutaneous Mitral Valve Repair System
repair therapy might potentially also be applied for TR. A 77-year-old woman presented with increasing dyspnea and signs of right heart failure in New York Heart Association functional class III. Within the past 6 months, she had several hospital admissions despite intensive diuretic therapy. Her medical history included severe chronic obstructive pulmonary fibrillation.
There is increasing evidence that severe tricuspid
disease
regurgitation (TR) is associated with a poor prognosis.
revealed severe TR. The right ventricle was enlarged
Recently, less invasive transcatheter tricuspid repair
(43
technologies are emerging as alternative therapeutic
(tricuspid annular plane systolic excursion 27 mm).
options for high surgical risk patients. One percuta-
Systolic pulmonary artery pressure was 50 mm Hg,
neous mitral valve repair system (MitraClip, Abbott
and the left ventricular ejection fraction was normal
Vascular, Santa Clara, California) has demonstrated
with moderate MR.
and
mm)
atrial
with
preserved
Echocardiography
ventricular
function
safety and long-term clinical benefit. Very similar to
Based on the heart team’s discussion, the surgical
functional mitral regurgitation (MR), TR is mainly due
risk for this patient was unacceptably high. The patient
to ventricular enlargement, annulus dilation, and loss
gave her written informed consent for the procedure
of leaflet coaptation. Thus, percutaneous mitral valve
on the basis of a compassionate use of the device.
F I G U R E 1 Percutaneous Mitral Valve Repair Therapy for Tricuspid Regurgitation
(A) Three-dimensional transesophageal echocardiography and 2-dimensional color Doppler at baseline. (B) Three-dimensional transesophageal echocardiography and 2-dimensional Doppler after percutaneous mitral valve repair system (arrow) implantation.
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JACC VOL. 67, NO. 7, 2016
Letters
FEBRUARY 23, 2016:889–94
The procedure was performed with the patient
When considering the percutaneous mitral valve
under general anesthesia with access from the right
repair system for tricuspid valve repair, several
femoral vein. The 24-F steerable guide catheter was
requirements must be met: 1) a large right atrium
positioned over a stiff guidewire into the right atrium.
for guide catheter steering; 2) sufficient coaptation
The guide catheter was then slightly pulled back, and
to get enough tissue for the (first) clip; 3) good
the tip was flexed. Thereafter, the clip was advanced
echocardiographic visibility, which is crucial and
forward until the bullet nose protruded from the tip of
might be a problem in the presence of valve pros-
the guide catheter. The clip was positioned perpen-
thesis or severe calcification of the mitral annulus;
dicular to the tricuspid valve by anterior movement
4) avoiding deep diving into or extensive move-
and bending of the guide catheter. Using deep trans-
ments of the clip in the right ventricle to prevent
gastric mid- and deep esophageal 2- and 3-dimensional
chordae rupture.
transesophageal echocardiography views, the appro-
This is the first description of a new interventional
priate clip arm orientation was adjusted, the clip was
approach for transfemoral tricuspid repair using the
advanced into the right ventricle slightly under the
percutaneous mitral valve repair system. Larger
leaflets, which were then captured. After implantation of a single clip, TR was reduced from severe to mild (Figure 1). At discharge, the
studies are required to confirm the feasibility, safety, and efficacy of the percutaneous mitral valve repair therapy in patients with severe TR.
patient’s symptoms significantly improved, transthoracic echocardiography demonstrated a stable clip position and sustained reduction of TR. We report the first transfemoral implantation of the MitraClip in a tricuspid valve with severe functional TR that resulted in a significant TR reduction. Therapeutic options for those patients are limited. Therefore, less invasive and safer therapeutic solutions are needed for this ever-growing patient population. A few transcatheter-based treatment options for TR are currently under evaluation. Laule et al. (1) reported on 3 patients with single or dual implantation with the SAPIEN XT prosthesis (Edwards Lifesciences, Irvine, California) for severe TR. This approach does not address TR itself, but may reduce the regurgitation of blood into the vena cava. With
*Joachim Schofer, MD, PhD Claudia Tiburtius, MD Christoph Hammerstingl, MD Per-Olof Dickhaut, MD Julian Witt, MD Lorenz Hansen, MD Friedrich-Christian Riess, MD, PhD Klaudija Bijuklic, MD *Albertinen Heart Center Süntelstrasse 11a 22457 Hamburg, Germany E-mail:
[email protected] http://dx.doi.org/10.1016/j.jacc.2015.11.047 Please note: Dr. Hammerstingl has received honoraria from Abbott, Mitralign, and Valtech for serving as a proctor. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
improvement in 2- and 3-dimensional TEE, advanced imaging of the tricuspid valve became possible.
REFERENCES
Targeting malcoaptation, the results of 7 high-risk
1. Laule M, Stangl V, Sanad W, et al. Percutaneous transfemoral management of severe secondary tricuspid regurgitation with Edwards Sapien XT bio-
patients with severe TR who received the Forma Repair System (Edwards Lifesciences) were recently published (2). We reported on the first-in-humans transcatheter tricuspid valve repair by using a pledgeted suture (Mitralign System, Mitralign Inc., Tewksbury, Massachusetts) (3).
prosthesis: first-in-man experience. J Am Coll Cardiol 2013;61:1929–31. 2. Campelo-Parada F, Perlman G, Philippon F, et al. First-in-man experience of a novel transcatheter repair system for treating severe tricuspid regurgitation. J Am Coll Cardiol 2015;66:2475–83. 3. Schofer J, Bijuklic K, Tiburtius C, et al. First-in-human transcatheter tricuspid valve repair in a patient with severely regurgitant tricuspid valve. J Am Coll Cardiol 2015;65:1190–5.
Our patient had no shelf to use for pledget placement, but the right atrium was large enough to steer
Bridging Anticoagulation
the guide catheter and a coaptation was sufficient to grasp the leaflets in the area of significant TR. Therefore, she was deemed a suitable candidate for
The recent comprehensive and thoughtful review by
the percutaneous mitral valve repair procedure.
Drs. Rechenmacher and Fang (1) emphasizes that the
Theoretically, this procedure can be performed from
benefit of bridging anticoagulation therapy (i.e.,
the internal jugular or femoral vein. We chose the
decreasing thromboembolic events by limiting the
femoral vein as the access site because it gives more
duration of anticoagulation interruption) must be
stability to the guide catheter and facilitates steering
carefully balanced against its risk of untoward peri-
maneuvers.
procedural bleeding.