U.S. patent application number 14/660791 was filed with the patent office on 2015-07-09 for prosthetic leaflet assembly for repairing a defective cardiac valve and methods of using the same.
The applicant listed for this patent is Jacques Seguin. Invention is credited to Jacques Seguin.
Application Number | 20150190229 14/660791 |
Document ID | / |
Family ID | 46319781 |
Filed Date | 2015-07-09 |
United States Patent
Application |
20150190229 |
Kind Code |
A1 |
Seguin; Jacques |
July 9, 2015 |
PROSTHETIC LEAFLET ASSEMBLY FOR REPAIRING A DEFECTIVE CARDIAC VALVE
AND METHODS OF USING THE SAME
Abstract
Methods and apparatus are provided for repairing or replacing a
defective cardiac valve including a prosthetic leaflet assembly
having an expandable frame with one or more anchors configured to
engage a predetermined region of the defective cardiac valve in an
expanded deployed state, and at least one prosthetic leaflet
coupled to the expandable frame. The prosthetic leaflet assembly is
configured such that the prosthetic leaflet is suspended within a
flow path of the defective cardiac valve and coapts with, and
improves functioning of, one or more native leaflets of the
defective cardiac valve.
Inventors: |
Seguin; Jacques; (Gstaad,
CH) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Seguin; Jacques |
Gstaad |
|
CH |
|
|
Family ID: |
46319781 |
Appl. No.: |
14/660791 |
Filed: |
March 17, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13527463 |
Jun 19, 2012 |
9011523 |
|
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14660791 |
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61498991 |
Jun 20, 2011 |
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Current U.S.
Class: |
623/2.11 |
Current CPC
Class: |
A61F 2/2436 20130101;
A61F 2/246 20130101; A61F 2/2454 20130101; A61F 2/2418 20130101;
A61F 2/2427 20130101 |
International
Class: |
A61F 2/24 20060101
A61F002/24 |
Claims
1-19. (canceled)
20. A catheter for delivering a prosthetic leaflet assembly at a
defective cardiac valve, the catheter comprising: a tube having a
distal end, a proximal end, and an internal lumen extending between
the distal and proximal ends; a stylet disposed within the internal
lumen, the stylet having an end cap disposed at a distal end of the
stylet; and a suture disposed within the internal lumen, the suture
engaging the prosthetic leaflet assembly when the prosthetic
leaflet assembly is disposed within the internal lumen in a
contracted delivery state, wherein the end cap contacts the distal
end of the tube in the contracted delivery state.
21. The catheter of claim 20, further comprising a suture tube
disposed within the internal lumen, the suture tube having a distal
end, a proximal end, and an internal lumen extending between the
proximal and distal ends of the suture tube, wherein the suture is
disposed within the internal lumen of the suture tube.
22. The catheter of claim 20, further comprising a locking member
disposed at the proximal end of the tube, the locking member
configured to lock the suture in place.
23. The catheter of claim 20, wherein the catheter is configured to
deliver the prosthetic leaflet assembly transvascularly using a
minimally invasive approach.
24. The catheter of claim 20, wherein the catheter is configured to
deliver the prosthetic leaflet assembly transapically.
25. The catheter of claim 20, wherein the catheter is adapted to
deliver the prosthetic leaflet assembly to one of a mitral valve, a
tricuspid valve, an aortic valve, or a pulmonary valve.
Description
I. CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims priority to U.S. Provisional
Application No. 61/498,991, filed Jun. 20, 2011, the entire
contents of which are incorporated herein by reference.
II. FIELD OF THE INVENTION
[0002] This application generally relates to apparatus and methods
for performing transcatheter or minimally invasive repair of a
defective cardiac valve, such as the mitral, tricuspid, and aortic
valves.
III. BACKGROUND OF THE INVENTION
[0003] The human heart has four major valves which moderate and
direct blood flow in the cardiovascular system. These valves serve
critical functions in assuring a unidirectional flow of an adequate
blood supply through the cardiovascular system. The mitral valve
and aortic valve control the flow of oxygen-rich blood from the
lungs to the body. The mitral valve lies between the left atrium
and left ventricle, while the aortic valve is situated between the
left ventricle and the aorta. Together, the mitral and aortic
valves ensure that oxygen-rich blood received from the lungs is
ejected into systemic circulation. The tricuspid and pulmonary
valves control the flow of oxygen-depleted blood from the body to
the lungs. The tricuspid valve lies between the right atrium and
right ventricle, while the pulmonary valve is situated between the
right ventricle and the pulmonary artery. Together the tricuspid
and pulmonary valves ensure unidirectional flow of oxygen-depleted
blood received from the right atrium towards the lungs.
[0004] Heart valves are passive structures composed of leaflets
that open and close in response to differential pressures on either
side of the valve. The mitral valve acts as the inflow valve to the
left side of the heart. Blood flows from the lungs, where it
absorbs oxygen, and into the left atrium. When the mitral valve
opens, blood flows from the left atrium to the left ventricle. The
mitral valve then closes to prevent blood from leaking back into
the lungs when the ventricle contracts to pump blood out to the
body. Whereas the aortic, pulmonary, and tricuspid valves have
three leaflets, the mitral valve has only two leaflets.
[0005] These heart valves may be rendered less effective by
congenital, inflammatory, or infectious conditions, or disease, all
of which may lead to dysfunction of the valves over time. Such
degradation may result in serious cardiovascular compromise or even
death. Because the left ventricle drives systemic circulation, it
generates higher pressures than the right ventricle, and
accordingly the aortic and mitral valves are more susceptible to
dysfunction, such as stenosis or regurgitation. A stenotic mitral
valve may impede blood flow into the heart, causing blood to back
up and pressure to build in the lungs. Consequently, the presence
of a stenotic valve may make it difficult for the heart to increase
the amount of blood pumped during exercise, producing shortness of
breath under physical activity. Regurgitation occurs when the
mitral valve leaflets do not coapt correctly, thus causing blood to
leak backwards into the left atrium and lungs each time the heart
pumps. Improper coaptation of the mitral valve leaflets thus
requires the heart to pump more blood with each contraction to
eject the necessary amount of blood for systemic circulation; a
process called volume overload. Although the heart may compensate
for this overload for months to years, provided the progression of
the leakage comes gradually, the heart will eventually begin to
fail, producing shortness of breath and fatigue. Mitral valve
dysfunction is rarely caused by congenital conditions, but is
largely the result of degenerative disease due to advancing age,
disease, or infection.
[0006] Previously known medical treatments to address diseased
valves generally involve either repairing the diseased native valve
or replacement of the native valve with a mechanical or biological
valve prosthesis. All previously-known valve prostheses have some
disadvantages, such as need for long-term maintenance with blood
thinners, the risk of clot formation, limited durability, etc.
Accordingly, valve repair, when possible, usually is preferable to
valve replacement. However, most dysfunctional valves are too
diseased to be repaired using previously know methods and
apparatus. Accordingly, a need exists for a prosthesis capable of
assisting heart valve function that enables treatment of a larger
patient population, while reducing the need to fully supplant the
native heart valve.
[0007] For many years, the standard treatment for such valve
dysfunction called for surgical repair or replacement of the valve
during open-heart surgery, a procedure conducted under general
anesthesia. An incision is made through the patient's sternum
(sternotomy), and the heart is accessed and stopped while blood
flow is rerouted through a heart-lung bypass machine. When
replacing the valve, the native valve is excised and replaced with
either a mechanical or biological prosthesis. However, these
surgeries are prone to many complications and long hospital stays
for recuperation.
[0008] More recently, transvascular techniques have been developed
for introducing and implanting a replacement valve, using a
flexible catheter in a manner less invasive than open-heart
surgery. In such techniques, a replacement valve is mounted in a
crimped state at the end of a flexible catheter, and then advanced
through the blood vessel of a patient until the prosthetic valve
reaches the implantation site. The valve then is expanded to its
functional size at the site of the defective native valve, usually
by inflating a balloon within where the valve has been mounted. By
expanding the prosthetic valve, the native valve leaflets are
generally pushed aside and rendered ineffective. Examples of such
devices and techniques, wherein the native valve is replaced in its
entirety by a substitute tissue valve, are described, for example,
in U.S. Pat. Nos. 6,582,462 and 6,168,614 to Andersen et al.
[0009] Mitral valve repair has become increasingly popular due to
its high rates of success and the clinical improvements noted after
repair. Several technologies have been developed to make mitral
repair less invasive. These technologies range from iterations of
the Alfieri stitch procedure; to coronary sinus-based modifications
of mitral anatomy, to subvalvular placations or ventricular
remodeling devices, which also may be employed to correct mitral
valve regurgitation. Unfortunately, for a significant percentage of
patients, mitral valve replacement is still necessary due to
stenosis or anatomical limitations, and few less-invasive options
are available for replacement procedures.
[0010] Prostheses have been produced and used for over forty years
to treat cardiac disorders. They have been made from a variety of
materials, both biological and artificial. Mechanical or artificial
valves generally are made from non-biological materials, such as
plastics or metals. Such materials, while durable, are prone to
blood clotting and thrombus formation, which in turn increases the
risk of embolization and stroke or ischemia. Anticoagulants may be
taken to prevent blood clotting that may result in thromboembolic
complications and catastrophic heart failure, however, such
anti-clotting medication may complicate a patient's health due to
the increased risk of hemorrhage.
[0011] In contrast, "bio-prosthetic" valves are constructed with
leaflets made of natural tissue, such as bovine, equine or porcine
pericardial tissue, which functions very similarly to the leaflets
of the natural human heart valve by imitating the natural action of
the heart valve leaflets, coapting between adjacent tissue
junctions known as commissures. The main advantage of valves made
from tissue is they are not as prone to blood clots and do not
absolutely require lifelong systemic anticoagulation. A major
disadvantage of tissue valves is they lack the long-term durability
of mechanical valves. This is so because naturally occurring
processes within the human body may stiffen or calcify the tissue
leaflets over time, particularly at high-stress areas of the valve
such as at the commissure junctions between tissue valve leaflets
and at the peripheral leaflet attachment points, or "cusps," at the
outer edge of each leaflet. Furthermore, valves are subject to
stresses from constant mechanical operation within the body. In
particular, the leaflets are in tension when in a closed position
and are in compression when in an open position. Such tension
causes prosthetic valves to wear out over time, requiring
replacement.
[0012] In recent years, bio-prosthetic valves have been constructed
by integrating valve leaflets made from natural tissue into the
stent-like supporting frame, which provides a dimensionally stable
support structure for the valve leaflets. In more advanced
prosthetic heart valve designs, besides providing dimensionally
stable support structure for the valve leaflets, the stent-like
supporting frame also imparts a certain degree of controlled
flexibility, thereby reducing stress on the leaflet tissue during
valve opening and closure and extending the lifetime of the
leaflets. In most designs, the stent-like supporting frame is
covered with a biocompatible cloth (usually a polyester material
such as Dacron.TM. or polytetrafluoroethylene (PTFE)) that provides
sewing attachment points for the leaflet commissures and leaflets
themselves. Alternatively, a cloth-covered suture ring may be
attached to the stent-like supporting frame, providing a site for
sewing the valve structure in position within the patient's heart
during a surgical valve replacement procedure.
[0013] While iterative improvements have been made on surgical
bioprosthetic valves over the last several decades, existing
bioprosthetic valves still have drawbacks. One drawback is the
mismatch in size and mass between opposing surfaces of the
stent-like supporting frame. The mismatch is often due to the
variability in the shapes and mechanical characteristics of the
stent-like supporting frame. For prosthetic valves with
balloon-expandable stent-like supporting frames, the recoil of the
supporting frames post-balloon-inflation may lead to perivalvular
leaks around the circumference of the prosthetic valve and
potential slippage and migration of the valve post-implantation.
Another risk associated with prosthetic valves having
balloon-expandable supporting frames is potential damage to the
leaflets of the prosthesis during implantation, when the leaflets
may be compressed between the balloon and the supporting frame. For
prosthetic valves with self-expanding stent-like supporting frames,
mismatch may arise due to the deformation/movement of the
supporting frame, e.g., slight deformation of the frame into a less
than circular shape during normal cardiac movement. Such mismatch
may lead to instability among components of a prosthetic valve,
resulting in perivalvular leaks and uneven stress distribution in
the valve leaflets, resulting in accelerated wear of the valve.
[0014] Another drawback in the construction of existing
bio-prosthetic valves with self-expanding supporting frames is the
potential for damage to the leaflet tissue arising from the spacing
between the struts of the frame. For example, when the stent-like
supporting frame is deployed, the distance between struts during
expansion of the frame may stretch both the surrounding tissue and
the leaflet tissue further apart than designed, potentially
resulting in damage to surrounding tissue and leaflet tissue. With
use of an oblong or circular radially self-expanding frame applied
on the majority of the mitral valve, there is risk of
left-ventricular outflow tract (LVOT) obstruction.
[0015] A mitral valve regurgitation often arises due to mitral
annulus dilatation, which may be treated using a surgical technique
to narrow and restore the natural shape the annulus. Usually the
mitral valve and annulus are shaped like a "D", but when dilated
the shape becomes more like an "O". Prosthetic annuloplasty rings
are therefore an important additional component in some mitral
valve repair techniques. A primary role of the annuloplasty ring is
to reduce the size of the annulus and decrease the tension on the
sutures while providing flexibility and mobility at the same time.
An annuloplasty ring thus is omitted during mitral valve repair
only exception in cases of infective endocarditis, in order to
avoid excess foreign material. When an annuloplasty ring is used,
three months of anticoagulation is often prescribed.
[0016] One recent technique for correcting mitral valve leakage, as
described for example in U.S. Pat. No. 6,269,819 to Oz et al.,
employs a percutaneously placed catheter to introduce a clipping
apparatus into a leaking mitral valve. Once positioned, the clip
arms are unfolded and advanced into the left ventricle below the
valve leaflets, after which it is retracted and closed over the
leaflets, holding them together to reduce mitral regurgitation. If
further improvements to regurgitation are to be made, the clip is
released and further advanced for repositioning. Once decrease of
leakage has been assessed, the clip is deployed to entrap together
the free edges of the mitral leaflets, and the catheter withdrawn.
The clip may be made of metal with a polyester fabric covering to
promote healing. Because the clip transforms the mitral orifice
into two orifices, the clip may significantly obstruct the flow of
blood through the valve.
[0017] In view of the above-noted drawbacks of previously-known
systems, it would be desirable to provide a device, and methods of
using the same, that assists the functioning of the native cardiac
valve, rather than removing or entirely supplanting the native
valve. The native structures (mitral leaflets, chordae, papillary
muscles, etc.) play an important role in left-ventricular function
and therefore any valve replacement system that does not respect
these elements may adversely impact the left-ventricular
function.
[0018] It would also be desirable to provide a device having
prosthetic leaflets, and methods of using the same that reduces
tension on the prosthetic leaflets, thereby increasing the life of
the prosthesis.
[0019] It further would be desirable to provide a device having a
support frame, and methods of using the same, wherein the
prosthesis is configured to firmly anchor to the native valve when
deployed, without deformation or movement of the supporting frame
at the annulus, thus reducing the risk of perivalvular leakage.
[0020] It still further would be desirable to provide a device, and
methods of using the same, that may be deployed with reduced risk
of obstructing blood flow relative to previously known mitral valve
repair techniques.
IV. SUMMARY OF THE INVENTION
[0021] The present invention provides leaflet assembly prostheses,
and methods of using the same, that overcomes the drawbacks of
previously-known systems. In particular, the present invention
provides a prosthetic leaflet assembly that may be suspended within
the flow path of a defective cardiac valve to improve functioning
of the native valve, while retaining much of the native valve
structure and function. Exemplary embodiments of the inventive
prosthetic leaflet assembly include an expandable frame and one or
more prosthetic leaflets coupled to the frame. The expandable frame
may be configured to transition from a contracted delivery state to
an expanded deployed state and may have one or more anchors
configured to engage a predetermined region, e.g., commissural
area, of the defective cardiac valve in the expanded deployed
state. Advantageously, the prosthetic leaflet assembly is
configured such that one or more prosthetic leaflets are suspended
within a flow path of the defective cardiac valve and coapt
therewith, thereby improving functioning of the native valve.
[0022] The expandable frame may further include at least one
stabilization member and at least one biasing member. The
stabilization member may be disposed upstream of the defective
native cardiac valve and configured to prevent the one or more
native leaflets from prolapsing when the leaflets are subjected to
backpressure, and also to prevent migration of the prosthetic
leaflet assembly. The biasing member may be configured to urge the
one or more anchors into engagement with the predetermined
region(s). Additionally, the expandable frame and the prosthetic
leaflets may be configured to self-expand between a delivery state
enabling transcatheter delivery and an expanded, deployed
state.
[0023] In accordance with one aspect of the invention, the
prosthetic leaflet assembly may be implanted using a transvascular
approach. Illustratively, implantation of a mitral valve embodiment
of the present invention, for example, may be accomplished by
passing a catheter through the femoral vein into the right atrium,
followed by a transeptal puncture to gain access to the mitral
valve from above. Alternatively, implantation may be accomplished
by passing the catheter through the femoral artery into the aorta
and through the aortic valve to gain access to the mitral valve
from below. As yet another alternative, a minimally-invasive
approach may be employed in which a catheter is inserted through a
keyhole opening in the chest and then transapically from below the
mitral valve. As yet a further alternative, an open heart surgery
approach may be used to gain access to the mitral valve. Notably,
the prosthetic leaflet assembly may be used with any cardiac valve
including tricuspid valve, aortic valve, and pulmonary valve.
[0024] In some embodiments the prosthetic leaflet assembly may
comprise a metal alloy, e.g., nickel-titanium, or polymer frame
covered by animal tissue or synthetic fabric that mimics the
leaflet valve configuration of the valve being repaired. The
expandable frame of the prosthetic leaflet assembly may comprise
the metal alloy or polymer frame and the leaflet assembly may
comprise the animal tissue or synthetic fabric.
[0025] In accordance with one aspect of the present invention, a
prosthetic leaflet assembly system is configured so as to enable
subsequent implantation of a previously-known replacement valve,
such that the replacement valve may be secured to the prosthetic
leaflet assembly. The replacement valve may be implanted seconds,
days, months, or years after the prosthetic leaflet assembly is
deployed, e.g., if the repaired valve undergoes further
deterioration due to disease progression or aging.
[0026] In accordance with another aspect of the present invention,
an exemplary catheter is provided for delivering a prosthetic
leaflet assembly transvascularly or transapically into a defective
cardiac valve. The catheter may include a tube having an internal
lumen, a stylet disposed within the internal lumen, and a suture
disposed within the internal lumen. The suture may engage the
prosthetic leaflet assembly when the prosthetic leaflet assembly is
disposed within the internal lumen in a contracted delivery state.
The stylet may have an end cap disposed at its distal end that may
contact the distal end of the tube in the contracted delivery
state. The catheter may further include a suture tube disposed
within the internal lumen through which the suture may be disposed.
The catheter may have a locking member disposed at the proximal end
of the tube configured to lock the suture in place.
[0027] Methods of using the prosthetic leaflet assembly and system
of the present invention also are provided.
V. BRIEF DESCRIPTION OF THE DRAWING
[0028] FIGS. 1A, 1B, and 1C depict an exemplary embodiment of a
prosthetic leaflet assembly constructed in accordance with the
principles of the present invention, suitable for use in mitral
valve repair, wherein FIG. 1A is a perspective view, FIG. 1B is a
bottom view, and FIG. 1C is an elevation front view.
[0029] FIGS. 2A through 2E are illustrative views of an exemplary
expandable frame of the prosthetic leaflet assembly constructed in
accordance with the principles of the present invention, wherein
FIG. 2A is an elevation view, FIG. 2B is a perspective view, FIG.
2C is a top view, FIG. 2D is a side view, and FIG. 2E is a bottom
view.
[0030] FIG. 3 depicts illustrative embodiments of a catheter for
transvascular delivery of the prosthetic leaflet assembly of the
present invention.
[0031] FIGS. 4A through 4D are illustrative views showing loading
of the prosthetic leaflet assembly into the delivery catheter in
accordance with aspects of the present invention.
[0032] FIG. 5 is a sectional view of the left ventricular portion
of a human heart showing a mitral valve being repaired using the
prosthetic leaflet assembly system of the present invention,
wherein the delivery catheter has been disposed proximate the
aortic valve.
[0033] FIGS. 6A through 6E are illustrative views showing
deployment of the prosthetic leaflet assembly using the delivery
catheter in a mitral valve undergoing repair in accordance with one
aspect of the present invention.
[0034] FIGS. 7A and 7B are illustrative views showing deployment of
a replacement valve prosthesis at the site of a deployed prosthetic
leaflet assembly of the present invention.
VI. DETAILED DESCRIPTION OF THE INVENTION
[0035] Referring to FIGS. 1A, 1B and 1C, an illustrative embodiment
of a prosthetic leaflet assembly in accordance with the principles
of the present invention is described. Illustratively, the
prosthetic leaflet assembly is designed for repairing a defective
mitral valve, although it could be readily adapted for other
cardiac valves such as the tricuspid valve, aortic valve, or
pulmonary valve. In FIG. 1A, prosthetic leaflet assembly 10 is
shown "upside down", such that the leaflets (at the top of the
figure) are configured to be positioned to extend into a patient's
left ventricle, while the support members (at the bottom of the
figure) preferably are configured to be disposed in the left
atrium, above the native leaflets. Prosthetic leaflet assembly 10,
includes animal tissue or synthetic leaflet assembly 20 mounted on
expandable frame 30. As further described below, prosthetic leaflet
assembly 10 preferably is configured to transition between an
expanded, deployed state and a contracted delivery state, such that
the device may be disposed within a delivery catheter for
transvascular or minimally-invasive surgical delivery.
[0036] Leaflet assembly 20 illustratively includes first and second
prosthetic leaflets 21 and 22 that may be coupled to expandable
frame 30 between first and second anchors 31 and 32 using sutures
or biocompatible adhesive. First prosthetic leaflet 21 has base 23
and free margin 25 and second prosthetic leaflet 22 has base 24 and
free margin 26. Base 23 substantially contacts base 24 when leaflet
assembly 20 is closed as illustrated in FIG. 1B. Prosthetic
leaflets 21 and 22 may be configured such that the length of bases
23 and 24 of each leaflet is inferior to the length of free margins
25 and 26, thereby inducing prosthetic leaflets 21 and 22 to bend
inward under forward blood flow, thereby improving the
transprosthetic gradient, and outward during retrograde blood flow,
improving coaptation of each prosthetic leaflet with the opposing
corresponding native cardiac leaflet as described further
below.
[0037] Leaflet assembly 20, including leaflets 21 and 22,
preferably comprise treated animal tissue, such as porcine, bovine,
or equine pericardial tissue fixed using glutaraldehyde as is per
se known in the art of prosthetic valve design. Alternatively,
leaflet assembly 20, including leaflets 21 and 22 may comprise any
of a number of synthetic fabrics, such as a polyethylene
terephthalate fabric, e.g., DACRON.RTM. (a registered trademark of
Invista North America S.A.R.L. Corporation). As a further
alternative, portions of leaflet assembly 20 may comprise synthetic
material, while other portions, such as leaflets 21 and 22, may
comprise animal tissue.
[0038] Although leaflet assembly 20 illustratively includes two
prosthetic leaflets, fewer or more leaflets may be included without
departing from the scope of the present invention. For example, in
an embodiment wherein the prosthetic leaflet assembly is configured
for repairing a defective aortic valve, the leaflet assembly may
include three prosthetic leaflets. As another example, in an
embodiment wherein one native leaflet is substantially
dysfunctional, the prosthetic leaflet assembly may be designed in a
semicircular configuration having a leaflet assembly including one
prosthetic leaflet.
[0039] As best shown in FIGS. 2A through 2E, in an embodiment
suitable for repairing a mitral valve, expandable frame 30 may
include first and second anchors 31 and 32, first and second
stabilization members 33 and 34, first and second body support
members 35 and 36, first and second biasing members 37 and 38, and
first and second attachment members 39 and 40. Expandable frame 30
may be configured for implantation in a circular-shaped or
oval-shaped cardiac valve and may comprise a superelastic material,
such as a nickel-titanium alloy. The superelastic material may be
treated to expand from a contracted delivery state to an expanded
deployed state as is well-known in the art for such materials.
Alternatively, expandable frame 30 may comprise non-superelastic
metal alloy, such as stainless steel or cobalt-chrome alloy, that
may be compressed onto a balloon catheter and then plastically
expanded during deployment. Expandable frame 30 may be covered with
treated animal tissue or any of a number of synthetic fabrics using
sutures or biocompatible adhesive.
[0040] Anchors 31 and 32 may be configured to engage predetermined
region(s) or surface(s) within a patient's heart, such as the
commissural areas of the defective cardiac valve, to anchor
prosthetic leaflet assembly 10 at a desired location within the
native valve structure. Beneficially, anchors 31 and 32 firmly
anchor prosthetic leaflet assembly 10 to the native cardiac valve
and move relatively with the motion of the native valve. Because
leaflet coaptation is insured by leaflet assembly 20, the risk of
perivalvular leakage is reduced.
[0041] First anchor 31 is coupled to first body support member 35
and second anchor 32 is coupled to second body support member 36.
Body support members 35 and 36 may be coupled to stabilization
members 33 and 34 and biasing members 37 and 38. Stabilization
members 33 and 34 preferably are configured to be disposed upstream
of the defective cardiac valve, so as prevent the native leaflets
from ballooning or prolapsing during backflow and to prevent
prosthetic leaflet assembly 10 migration.
[0042] Biasing members 37 and 38 preferably are configured to urge
anchors 31 and 32 into engagement with the predetermined region,
such as the commissural areas, when prosthetic leaflet assembly 10
is deployed. Biasing members 37 and 38 further may be configured to
urge anchors 31 and 32 in a specified direction to further ovalize
or modify the annulus of the defective cardiac valve, thereby
moving the native leaflet closer to the center of the valve and
enhancing coaptation with prosthetic leaflets 21 and 22 as
described below.
[0043] First biasing member 37 may include attachment member 39 and
second biasing member may include attachment member 40. Attachment
members 39 and 40, illustratively eyelets, are configured to attach
leaflet assembly 20 to expandable frame 30 with center attachment
member 41, shown in FIG. 1C. Center attachment member 41 may
comprise animal tissue or synthetic fabric, and may be coupled to
attachment members 39 and 40 and leaflet assembly 20 using sutures
or biocompatible adhesive. Alternatively, leaflet assembly 20 and
center attachment member 41 may comprise a single piece of
material.
[0044] Preferably, prosthetic leaflet assembly 10 is configured
such that prosthetic leaflets 21 and 22 coapt with, and improve
function of, one or more native leaflets of the defective cardiac
valve, for example, during backpressure. In one embodiment,
prosthetic leaflets 21 and 22 are configured to cover between 5 to
35 percent of the central opening of the native cardiac valve.
Advantageously, prosthetic leaflet assembly 10 works together with
the native cardiac valve, rather than pushing the leaflets of the
native cardiac valve aside and rending the native valve structures
ineffective. Additionally, stabilization members 33 and 34 and
biasing members 37 and 38 are positioned away from the path of the
native cardiac leaflets, thus reducing the risk of obstructing
blood flow through the cardiac valve.
[0045] Referring now to FIG. 3, an exemplary embodiment of a
delivery catheter for the prosthetic leaflet assembly of the
present invention is described. Delivery catheter 50 includes a
suitable length of tubing 51 having distal end 52, proximal end 53,
an internal lumen extending therebetween, handle portion 54, stylet
55 disposed in the internal lumen, and first and second suture
tubes 56 and 57 disposed in the internal lumen. Stylet 55
preferably has a length greater than that of tubing 51 and includes
proximal end 58, distal end 59, and end cap 60 disposed at distal
end 59. Stylet 55 and end cap 60 optionally may include a guide
wire lumen extending throughout to accommodate passage of a guide
wire. First suture tube 56 includes a length of tubing that may be
greater than the length of tubing 51 and has proximal end 61,
distal end 62, an internal lumen extending therebetween, and
locking member 63 disposed near proximal end 61. First suture 64 is
disposed in the internal lumen of first suture tube 56 and
preferably has a length at least twice the length of first suture
tube 56. Second suture tube 57 includes a length of tubing that may
be greater than the length of tubing 51 and has proximal end 65,
distal end 66, an internal lumen extending therebetween, and
locking member 67 disposed near proximal end 65. Second suture 68
is disposed in the internal lumen of second suture tube 57 and
preferably has a length at least twice the length of second suture
tube 57. In one embodiment, first and second sutures 64 and 68 are
each a single wire having a locking mechanism disposed at the
respective distal end to engage into a matching locking mechanism
on prosthetic leaflet assembly 10, e.g., on body support members 35
and 36. In another embodiment, first and second sutures 64 and 68
may be used as a lanyard to re-secure prosthetic leaflet assembly
10 to delivery catheter 50.
[0046] Delivery catheter 50 preferably comprises materials
conventionally used in catheter designs, and has lengths and
profiles suitable for the selected access path, i.e., either
transvascular or transapical. Tubing 51 is sized to permit
prosthetic leaflet assembly 10 to be compressed within, and
retained within, delivery catheter 50 for delivery. In one
embodiment, expandable frame 30 is self-expanding and causes
prosthetic leaflet assembly 10 to expand when deployed. In an
alternative embodiment, such as for plastically deformable
embodiments of expandable frame 30, stylet 55 may include an
expandable balloon or mandrel configured, as is conventional in the
art of balloon-catheters, to be inflated to cause prosthetic
leaflet assembly 10 to expand when deployed.
[0047] Referring to FIGS. 4A through 4D, an exemplary method of
loading the prosthetic leaflet assembly into the delivery catheter
is now described. As depicted in FIG. 4A, the distal end of first
suture 64 is looped around a portion of prosthetic leaflet assembly
10, illustratively the first anchor, and fed into distal end 62 of
first suture tube 56 until the distal end of first suture 64 passes
through the opening at proximal end 61 of first suture tube 56.
With both ends of first suture 64 exposed at proximal end 61,
locking member 63 is activated to lock first suture 64 in place.
The distal end of second suture 68 then is looped around a portion
of prosthetic leaflet assembly 10, illustratively the second
anchor, and fed into distal end 66 of second suture tube 57 until
the distal end of first suture 68 passes through the opening at
proximal end 65 of second suture tube 57. With both ends of second
suture 68 exposed at proximal end 65, locking member 67 is
activated to lock second suture 68 in place.
[0048] Next, proximal ends 61 and 65 of first and second suture
tubes 56 and 57 are pulled proximally to urge prosthetic leaflet
assembly 10 proximally until prosthetic leaflet assembly 10
contacts first and second suture tubes 56 and 57, as shown in FIG.
4B. Proximal ends 58, 61, and 65 of stylet 55 and first and second
suture tubes 56 and 57 then are pulled proximally to compress
prosthetic leaflet assembly 10 within the internal lumen of tubing
51 while urging prosthetic leaflet assembly 10 proximally, as
depicted in FIG. 4C. To assist in compressing prosthetic leaflet
assembly 10, assembly 10 may be cooled and inserted into a loading
tube, such as are known in the art. Proximal ends 58, 61, and 65
are pulled proximally until end cap 60 contacts distal end 52 of
tubing 51, as shown in FIG. 4D.
[0049] Referring to FIG. 5, a method of deploying the prosthetic
leaflet assembly of present invention is now described in the
context of repairing a defective mitral valve. In FIG. 5, the left
ventricular quadrant of a human heart H is shown having a mitral
valve MV with commissural areas CA and located within a mitral
valve annulus MVA. The leaflets L of the mitral valve MV are
tethered to the endocardium of the left ventricle LV via the
chordae tendineae CT and papillary muscles PM. The outflow tract of
the aortic valve AV is disposed immediately adjacent to the mitral
valve MV. This anatomical feature of the mitral valve makes
anchoring a prosthetic device directly to the mitral valve annulus
problematic, since it creates a risk that prosthetic device will
obstruct the outflow tract for the aortic valve. Alternatively,
having a prosthetic device expanded into direct engagement with the
mitral valve annulus may disrupt or remodel the aortic valve
annulus, causing mismatch of the leaflets of that valve and
possibly aortic valve regurgitation.
[0050] In FIG. 5, delivery catheter 50 is shown approaching the
aortic valve AV through the aorta to gain access to the mitral
valve MV from below.
[0051] Referring now to FIGS. 6A through 6E, as shown in FIG. 6A,
delivery catheter 50 is moved distally until end cap 60 and the
distal portion of tubing 51 pass through the leaflets L of the
mitral valve MV. Once delivery catheter 50 is disposed partially
through the mitral valve MV in a suitable position, as may be
determined, e.g., using fluoroscopy, tubing 51 is retracted
proximally as shown in FIG. 6B. Delivery catheter 50 may be rotated
and moved proximally and distally, e.g., by moving and/or rotating
handle 54 of delivery catheter 50, to properly align anchors 31 and
32 of prosthetic leaflet assembly 10 with the predetermined region,
e.g., commissural areas CA, of the mitral valve MV, e.g., using
fluoroscopic guidance. As tubing 51 of delivery catheter 50 is
withdrawn, prosthetic leaflet assembly 10 may expand as depicted in
FIG. 6C so that the prosthetic leaflets are deployed within the
flow path circumscribed by the native leaflets. First and second
suture tubes 56 and 57 may be curved outwardly to assist in
expanding prosthetic leaflet assembly 10.
[0052] As shown in FIG. 6D, anchors 31 and 32 engage commissural
areas CA of the mitral valve MV when the expandable frame of
prosthetic leaflet assembly 10 causes the assembly 10 to transition
to the expanded deployed state. Anchors 31 and 32 engage
predetermined regions of the native valve structure, e.g.,
commissural areas CA, such that portions of each anchor are located
above and/or below the mitral valve annulus MVA.
[0053] Once prosthetic leaflet assembly 10 is in the expanded
deployed state, locking mechanism 63 of first suture tube 56 and
locking mechanism 67 of second suture tube 57 may each be released
and one end of each suture 64 and 68 may be pulled proximally until
each suture is no longer looped around prosthetic leaflet assembly
10, freeing assembly 10. Alternatively, sutures 64 and 68 may be
cut using a suitable transvascular tool. Delivery catheter 50 then
is fully withdrawn leaving prosthetic leaflet assembly 10 deployed
in the mitral valve, as depicted in FIG. 6E. Advantageously, the
leaflets L of the mitral valve MV coapt against the expanded
deployed prosthetic leaflet assembly 10; illustratively, against
the two prosthetic leaflets of prosthetic leaflet assembly 10 such
that the two prosthetic leaflets are suspended within the flow path
defined by the leaflets L and the prosthetic leaflets coapt with,
and improve functioning of, the leaflets L.
[0054] In an alternative embodiment, prosthetic leaflet assembly 10
may be implanted with delivery catheter 50 using a
minimally-invasive approach wherein delivery catheter 50 is
inserted through a keyhole opening in the chest and delivery
catheter 50 is inserted transapically from below the mitral valve.
As yet another alternative, an open heart surgery approach may be
used to gain access to the mitral valve to implant prosthetic
leaflet assembly 10. In an embodiment where prosthetic leaflet
assembly is implanted using an alternative transvascular approach,
implantation of a mitral valve embodiment, for example, may be
accomplished by passing delivery catheter 50 through the femoral
vein into the right atrium, followed by a transeptal puncture to
gain access to the mitral valve from above. In this embodiment,
prosthetic leaflet assembly 10 may be loaded in delivery catheter
50 such that stabilization members 33 and 34 and biasing members 37
and 38 of prosthetic leaflet assembly 10 are loaded into delivery
catheter 50 first rather than last as depicted in the embodiment of
FIGS. 4A through 4D.
[0055] As will be appreciated by one of ordinary skill, leaflet
assembly 20 may comprise alternative leaflet configurations
designed to coapt against the native leaflets, such as balls,
flaps, duck-bill elements, etc., such as art known in the art,
without departing from the spirit of the present invention, so long
as such configurations can be contracted to a reduced delivery
state for transcatheter or minimally invasive implantation. In
addition, expandable frame 30 may comprise, for example, a suitably
trained shape memory alloy, that expands to a deployed shape for
use in a non-circular cardiac valve, such as an ovoid or D-shaped
configuration. In this latter case, leaflet assembly 20 should be
configured so that, when expandable frame 30 is fully deployed, the
leaflet assembly expands to a predetermined shape with the required
level of coaptation.
[0056] Referring to FIGS. 7A and 7B, a method for deploying a
replacement valve prosthesis, such as are known in the art, through
the deployed prosthetic leaflet assembly of the present invention
is now described. In FIG. 7A, catheter 70 having the replacement
valve disposed therein is shown approaching the mitral valve MV
wherein catheter 70 is directed, e.g., under fluoroscopic guidance,
between stabilization members 33 and 34 of prosthetic leaflet
assembly 10. Catheter 70 then is withdrawn and replacement valve
prosthesis 80 expands and compresses prosthetic leaflet assembly 10
toward the mitral valve MV, as depicted in FIG. 7B. As replacement
valve 80 expands, it preferably engages and anchors to prosthetic
leaflet assembly 10. For example, expanding replacement valve 80
may cause the stabilization members and/or biasing members to exert
force on valve 80, thereby securing valve 80 within prosthetic
leaflet assembly 10. Additionally, replacement valve 80 may be
secured to prosthetic leaflet assembly 10 using, for example,
sutures or biocompatible adhesive. In turn, because prosthetic
leaflet assembly 10 is firmly anchored to the mitral valve MV,
replacement valve 80 is anchored at the mitral valve MV.
[0057] Replacement valve 80 illustratively is constructed as
described in U.S. Pat. No. 4,490,859 to Black et al., which is
incorporated herein by reference, and/or the above-mentioned
patents to Andersen et al., and comprises treated animal tissue,
such as porcine, bovine or equine pericardial tissue, or any of a
number of synthetic fabrics, such as a polyethylene terephthalate
fabric, e.g., DACRON.RTM. (a registered trademark of Invista North
America S.A.R.L. Corporation), mounted on a collapsible metal alloy
or polymer frame. The collapsible frame 81 may include two or more
upstanding posts disposed on the sides of the frame to form
commissural points for the tissue or synthetic fabric leaflets 82.
As described in the foregoing patent, the tissue or fabric
components of the valve body may be cut from flat pieces of
material, and then sewn or bonded together, and to the upstanding
posts and the frame, to form a valve that mimics the functionality
of an intact non-diseased mitral valve. Alternatively, replacement
prosthesis 80 may be of any other construction suitable to be
collapsed to a reduced diameter so as to permit the prosthetic
valve to be delivered via catheter in a contracted delivery
state.
[0058] Replacement valve 80 may be implanted immediately after
prosthetic leaflet assembly 10 is deployed or may be implanted
minutes, days, months, or years after prosthetic leaflet assembly
10 is deployed. In one embodiment, replacement valve 80 is
implanted because a defective cardiac valve having prosthetic
leaflet assembly 10 deployed thereon further degenerates, for
example, due to disease progression or aging, such that valve
replacement is required. Replacement valve 80 may be implanted
using a transcatheter approach, a minimally invasive approach, or
an open heart surgery approach.
[0059] In accordance with an alternative embodiment of the present
invention, expandable frame 30 may be loaded and deployed without
leaflet assembly 20 in a manner similar to descriptions above with
respect to FIGS. 4-6. In this embodiment, anchors 31 and 32 apply
outward force to the annulus, preferably at the commissures of the
defective valve, to forcefully ovalize or modify the shape of the
annulus to enhance leaflet coaptation and thereby reduce cardiac
valve regurgitation.
[0060] While various illustrative embodiments of the invention are
described above, it will be apparent to one skilled in the art that
various changes and modifications may be made therein without
departing from the invention. The appended claims are intended to
cover all such changes and modifications that fall within the true
scope of the invention.
* * * * *