U.S. patent application number 14/602894 was filed with the patent office on 2015-07-30 for stationary intra-annular halo designs for paravalvular leak (pvl) reduction-passive channel filling cuff designs.
The applicant listed for this patent is St. Jude Medical, Cardiology Division, Inc.. Invention is credited to Peter N. Braido, Mina S. Fahim, Andrea L. McCarthy, Kent J. Smith.
Application Number | 20150209141 14/602894 |
Document ID | / |
Family ID | 52394956 |
Filed Date | 2015-07-30 |
United States Patent
Application |
20150209141 |
Kind Code |
A1 |
Braido; Peter N. ; et
al. |
July 30, 2015 |
STATIONARY INTRA-ANNULAR HALO DESIGNS FOR PARAVALVULAR LEAK (PVL)
REDUCTION-PASSIVE CHANNEL FILLING CUFF DESIGNS
Abstract
A prosthetic heart valve may include a collapsible and
expandable stent extending in a flow direction between a proximal
end and a distal end, a cuff attached to an annulus section of the
stent, a plurality of prosthetic valve leaflets each having a belly
attached to the cuff between a first location and a second location
downstream of the first location in a flow direction, and a sealing
structure attached to the annulus section of the stent. The annulus
section of the stent may be adjacent the proximal end. The stent
may include a plurality of struts shaped to form a plurality of
cells connected to one another in a plurality of annular rows
around the stent. The sealing structure may have a deployed
condition with a diameter greater than a diameter of the proximal
end of the stent when the stent is in an expanded use
condition.
Inventors: |
Braido; Peter N.; (Wyoming,
MN) ; Smith; Kent J.; (Shoreview, MN) ;
McCarthy; Andrea L.; (Vadnais Heights, MN) ; Fahim;
Mina S.; (Shoreview, MN) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
St. Jude Medical, Cardiology Division, Inc. |
St. Paul |
MN |
US |
|
|
Family ID: |
52394956 |
Appl. No.: |
14/602894 |
Filed: |
January 22, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
61931208 |
Jan 24, 2014 |
|
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|
Current U.S.
Class: |
623/2.17 |
Current CPC
Class: |
A61F 2250/0069 20130101;
A61F 2230/0095 20130101; A61F 2210/0061 20130101; A61F 2/2418
20130101; A61F 2250/001 20130101 |
International
Class: |
A61F 2/24 20060101
A61F002/24 |
Claims
1. A prosthetic heart valve configured to be expanded between
native leaflets of a native aortic annulus of a patient, the
prosthetic heart valve comprising: a collapsible and expandable
stent extending in a flow direction between a proximal end and a
distal end, the stent including an annulus section adjacent the
proximal end and a plurality of struts shaped to form a plurality
of cells connected to one another in a plurality of annular rows
around the stent, the flow direction being defined from the
proximal end toward the distal end; a cuff attached to the annulus
section of the stent; a plurality of prosthetic valve leaflets each
having a belly attached to the cuff between a first location and a
second location downstream of the first location in the flow
direction; and a sealing structure attached to the annulus section
of the stent, the sealing structure having a deployed condition
with a diameter greater than a diameter of the proximal end of the
stent when the stent is in an expanded use condition.
2. The prosthetic heart valve of claim 1, wherein the sealing
structure is entirely located between the proximal end of the stent
and the first location.
3. The prosthetic heart valve of claim 1, wherein the sealing
structure is located partially between the proximal end of the
stent the first location, and partially between the first location
and the second location.
4. The prosthetic heart valve of claim 1, further comprising an
underwire supporting a portion of the cuff and extending in a
circumferential direction about a perimeter of the stent along
locations where the bellies of the leaflets are attached to the
cuff, wherein the sealing structure is attached to the stent and
the cuff along the underwire.
5. The prosthetic heart valve of claim 4, wherein the underwire is
located within an interior of the sealing structure.
6. The prosthetic heart valve of claim 1, wherein the sealing
structure extends continuously around a circumference of the
stent.
7. The prosthetic heart valve of claim 6, wherein the sealing
structure has a top surface facing the distal end of the stent, the
top surface including a plurality of openings in fluid
communication with an interior of the sealing structure.
8. The prosthetic heart valve of claim 1, wherein the sealing
structure has a saddle ring shape with at least two peaks and at
least two valleys, the valleys being closer to the proximal end of
the stent than the peaks.
9. The prosthetic heart valve of claim 1, wherein the sealing
structure has a zigzag ring shape with at least three peaks and at
least three valleys, the valleys being closer to the proximal end
of the stent than the peaks.
10. The prosthetic heart valve of claim 9, wherein the peaks
include at least one low peak that extends to a first height above
the valleys and at least one high peak that extends to a second
height above the valleys, the second height being greater than the
first height.
11. The prosthetic heart valve of claim 9, wherein the stent
includes commissure features each located at a juncture of adjacent
ones of the bellies of the leaflets, at least a portion of the
belly of each leaflet being attached to one of the commissure
features, and the peaks are substantially aligned with the
commissure features in the flow direction.
12. The prosthetic heart valve of claim 9, wherein the stent
includes commissure features each located at a juncture of adjacent
ones of the bellies of the leaflets, at least a portion of the
belly of each leaflet being attached to one of the commissure
features, and the valleys are substantially aligned with the
commissure features in the flow direction.
13. The prosthetic heart valve of claim 9, wherein at least one of
the valleys includes a portion that extends in a direction
orthogonal to the flow direction, the portion not being attached to
the cuff and stent and being configured to be under tension when
the stent is in the expanded use condition.
14. The prosthetic heart valve of claim 13, wherein the stent
includes commissure features each located at a juncture of adjacent
ones of the bellies of the leaflets, at least a portion of the
belly of each leaflet being attached to one of the commissure
features, and the portion is substantially aligned with the
commissure features in the flow direction.
15. The prosthetic heart valve of claim 1, wherein the sealing
structure comprises at least one discontinuous ring portion
extending circumferentially about at least a portion of a perimeter
of the stent, the at least one discontinuous ring portion having a
high end and a low end that are vertically displaced from one
another in the flow direction.
16. The prosthetic heart valve of claim 15, wherein the high end
and the low end are aligned in the flow direction with one another,
such that an imaginary line extending in the flow direction
intersects the high end and the low end.
17. The prosthetic heart valve of claim 1, wherein the sealing
structure comprises at least two discontinuous ring portions each
extending circumferentially about at least a portion of a perimeter
of the stent, the high end being an end of a first one of the
discontinuous ring portions, and the low end being an end of a
second one of the discontinuous ring portions.
18. The prosthetic heart valve of claim 1, wherein the sealing
structure comprises a continuous ring structure and at least one
discontinuous ring portion, the at least one discontinuous ring
portion being disposed between the distal end of the stent and the
continuous ring structure.
19. The prosthetic heart valve of claim 18, wherein the stent
includes commissure features each located at a juncture of adjacent
ones of the bellies of the leaflets, at least a portion of the
belly of each leaflet being attached to one of the commissure
features, and each discontinuous ring portion is substantially
aligned with a corresponding one of the commissure features in the
flow direction.
20. The prosthetic heart valve of claim 1, wherein the sealing
structure comprises two continuous ring structures, each of the
continuous ring structures extending completely around a
circumference of the stent.
Description
CROSS-REFERENCE TO RELATED APPLICATION
[0001] The present application claims the benefit of the filing
date of U.S. Provisional Patent Application No. 61/931,208 filed
Jan. 24, 2014, the disclosure of which is hereby incorporated
herein by reference.
BACKGROUND OF THE INVENTION
[0002] The present disclosure relates in general to heart valve
replacement and, in particular, to collapsible prosthetic heart
valves. More particularly, the present disclosure relates to
devices and methods for positioning and sealing collapsible
prosthetic heart valves within a native valve annulus.
[0003] Prosthetic heart valves that are collapsible to a relatively
small circumferential size can be delivered into a patient less
invasively than valves that are not collapsible. For example, a
collapsible valve may be delivered into a patient via a tube-like
delivery apparatus such as a catheter, a trocar, a laparoscopic
instrument, or the like. This collapsibility can avoid the need for
a more invasive procedure such as full open-chest, open-heart
surgery.
[0004] Collapsible prosthetic heart valves typically take the form
of a valve structure mounted on a stent. There are two common types
of stents on which the valve structures are ordinarily mounted: a
self-expanding stent or a balloon-expandable stent. To place such
valves into a delivery apparatus and ultimately into a patient, the
valve must first be collapsed or crimped to reduce its
circumferential size.
[0005] When a collapsed prosthetic valve has reached the desired
implant site in the patient (e.g., at or near the annulus of the
patient's heart valve that is to be replaced by the prosthetic
valve), the prosthetic valve can be deployed or released from the
delivery apparatus and re-expanded to full operating size. For
balloon-expandable valves, this generally involves releasing the
entire valve, and then expanding a balloon positioned within the
valve stent. For self-expanding valves, on the other hand, the
stent automatically expands as the sheath covering the valve is
withdrawn.
BRIEF SUMMARY OF THE INVENTION
[0006] Prosthetic heart valves and methods of expanding a
prosthetic heart valve between native leaflets of a native aortic
annulus of a patient are disclosed.
[0007] A prosthetic heart valve configured to be expanded between
native leaflets of a native aortic annulus of a patient may include
a collapsible and expandable stent extending in a flow direction
between a proximal end and a distal end, a cuff attached to an
annulus section of the stent, a plurality of prosthetic valve
leaflets each having a belly attached to the cuff between a first
location and a second location downstream of the first location in
a flow direction, and a sealing structure attached to the annulus
section of the stent.
[0008] The annulus section of the stent may be adjacent the
proximal end. The stent may include a plurality of struts shaped to
form a plurality of cells connected to one another in a plurality
of annular rows around the stent. The flow direction may be defined
from the proximal end toward the distal end. The sealing structure
may have a deployed condition with a diameter greater than a
diameter of the proximal end of the stent when the stent is in an
expanded use condition.
[0009] The sealing structure may be entirely located between the
proximal end of the stent and the first location. The sealing
structure may be located partially between the proximal end of the
stent the first location, and partially between the first location
and the second location. The prosthetic heart valve may also
include an underwire supporting a portion of the cuff and extending
in a circumferential direction about a perimeter of the stent along
locations where the bellies of the leaflets are attached to the
cuff. The sealing structure may be attached to the stent and the
cuff along the underwire. The underwire may be located within an
interior of the sealing structure.
[0010] The sealing structure may extend continuously around a
circumference of the stent. The sealing structure may have a top
surface facing the distal end of the stent, the top surface
including a plurality of openings in fluid communication with an
interior of the sealing structure. The sealing structure may have a
saddle ring shape with at least two peaks and at least two valleys,
the valleys being closer to the proximal end of the stent than the
peaks.
[0011] The sealing structure may have a zigzag ring shape with at
least three peaks and at least three valleys, the valleys being
closer to the proximal end of the stent than the peaks. The peaks
may include at least one low peak that extends to a first height
above the valleys and at least one high peak that extends to a
second height above the valleys, the second height being greater
than the first height. The stent may include commissure features
each located at a juncture of adjacent ones of the bellies of the
leaflets, at least a portion of the belly of each leaflet being
attached to one of the commissure features, and the peaks may be
substantially aligned with the commissure features in the flow
direction.
[0012] The stent may include commissure features each located at a
juncture of adjacent ones of the bellies of the leaflets, at least
a portion of the belly of each leaflet being attached to one of the
commissure features. The valleys may be substantially aligned with
the commissure features in the flow direction. At least one of the
valleys may include a portion that extends in a direction
orthogonal to the flow direction, the portion not being attached to
the cuff and stent and being configured to be under tension when
the stent is in the expanded use condition.
[0013] The stent may includes commissure features each located at a
juncture of adjacent ones of the bellies of the leaflets, at least
a portion of the belly of each leaflet being attached to one of the
commissure features. The portion may be substantially aligned with
the commissure features in the flow direction. The sealing
structure may include at least one discontinuous ring portion
extending circumferentially about at least a portion of a perimeter
of the stent. The at least one discontinuous ring portion may have
a high end and a low end that are vertically displaced from one
another in the flow direction. The high end and the low end may be
aligned in the flow direction with one another, such that an
imaginary line extending in the flow direction intersects the high
end and the low end.
[0014] The sealing structure may include at least two discontinuous
ring portions each extending circumferentially about at least a
portion of a perimeter of the stent. The high end may be an end of
a first one of the discontinuous ring portions, and the low end may
be an end of a second one of the discontinuous ring portions. The
sealing structure may include a continuous ring structure and at
least one discontinuous ring portion. The at least one
discontinuous ring portion may be disposed between the distal end
of the stent and the continuous ring structure.
[0015] The stent may include commissure features each located at a
juncture of adjacent ones of the bellies of the leaflets, at least
a portion of the belly of each leaflet being attached to one of the
commissure features. Each discontinuous ring portion may be
substantially aligned with a corresponding one of the commissure
features in the flow direction. The sealing structure may include
two continuous ring structures. Each of the continuous ring
structures may extend completely around a circumference of the
stent.
BRIEF DESCRIPTION OF THE DRAWINGS
[0016] Various embodiments of heart valves are disclosed herein
with reference to the drawings, wherein:
[0017] FIG. 1 is a side elevational view of a conventional
prosthetic heart valve;
[0018] FIG. 2A is a highly schematic cross-sectional view taken
along line A-A of FIG. 1 and showing the prosthetic heart valve
disposed within a native valve annulus;
[0019] FIG. 2B is a highly schematic cross-sectional view showing a
prosthetic mitral valve disposed within a native valve annulus;
[0020] FIGS. 3A and 3B are highly schematic side views of another
embodiment of a heart valve having a sealing ring intended to fill
irregularities between the heart valve and the native valve
annulus;
[0021] FIG. 3C is a schematic end view of the prosthetic heart
valve of FIGS. 3A and 3B after formation of the sealing ring as
seen from the annulus end toward the aortic end of the heart
valve;
[0022] FIGS. 3D is a highly schematic side view of a variation of
the embodiment shown in FIGS. 3A-3C;
[0023] FIG. 4A is a highly schematic side view of another
embodiment of a heart valve having an undulating sealing ring
intended to fill irregularities between the heart valve and the
native valve annulus;
[0024] FIG. 4B is a schematic end view of the prosthetic heart
valve of FIG. 4A after formation of the undulating sealing ring as
seen from the annulus end toward the aortic end of the heart
valve;
[0025] FIG. 4C is a side view of another embodiment of a heart
valve having an undulating sealing ring intended to fill
irregularities between the heart valve and the native valve
annulus;
[0026] FIG. 4D is a side view of another embodiment of a heart
valve having an undulating sealing ring intended to fill
irregularities between the heart valve and the native valve
annulus;
[0027] FIGS. 5A-5F are highly schematic perspective views of
alternative sealing ring embodiments that can be used with the
stent, cuff, and leaflets of FIG. 4C;
[0028] FIG. 6A is a highly schematic side view of another
embodiment of a heart valve having a halo sealing ring intended to
fill irregularities between the heart valve and the native valve
annulus;
[0029] FIG. 6B is a schematic end view of the prosthetic heart
valve of FIG. 6A after formation of the halo sealing ring as seen
from the annulus end toward the aortic end of the heart valve;
[0030] FIG. 6C is a schematic end view an alternative sealing ring
embodiment that can be used with the stent, cuff, and leaflets of
FIG. 6A;
[0031] FIG. 6D is an enlarged partial side view of a heart valve
having the sealing ring of FIG. 6C attached thereto;
[0032] FIG. 7 is a side view of another embodiment of a heart valve
having a higher cuff height;
[0033] FIG. 8A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0034] FIG. 8B is a side view of a heart valve having the stent,
sealing ring, and leaflets of FIG. 8A;
[0035] FIGS. 8C-8E are developed views of variations of the stent,
sealing ring, and leaflets of FIG. 8A;
[0036] FIG. 9A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0037] FIG. 9B is a side view of a heart valve having the stent,
sealing ring, and leaflets of FIG. 9A;
[0038] FIG. 9C is a developed view of a variation of the stent,
sealing ring, and leaflets of FIG. 9A;
[0039] FIG. 10A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0040] FIG. 10B is a side view of a heart valve having the stent,
sealing ring, and leaflets of FIG. 10A;
[0041] FIGS. 10C and 10D are developed views of variations of the
stent, sealing ring, and leaflets of FIG. 10A;
[0042] FIG. 11A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0043] FIG. 11B is a side view of a heart valve having the stent,
sealing ring, and leaflets of FIG. 11A;
[0044] FIG. 11C is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0045] FIG. 11D is a side view of a heart valve having the stent,
sealing ring, and leaflets of FIG. 11C;
[0046] FIGS. 11E-11H are developed views of variations of the
stent, sealing ring, and leaflets of FIG. 11A;
[0047] FIG. 12A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0048] FIG. 12B is a side view of a heart valve having the stent,
sealing ring, and leaflets of FIG. 12A;
[0049] FIGS. 12C-12K are developed views of variations of the
stent, sealing ring, and leaflets of FIG. 12A;
[0050] FIG. 13A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0051] FIGS. 13B-13E are developed views of variations of the
stent, sealing ring, and leaflets of FIG. 13A;
[0052] FIG. 14A is a developed view of the stent, sealing ring, and
leaflets of another embodiment of a heart valve having a sealing
ring intended to fill irregularities between the heart valve and
the native valve annulus;
[0053] FIG. 14B is a side view of a variation of the stent, sealing
ring, and leaflets of FIG. 14A; and
[0054] FIG. 14C is a developed view of another variation of the
stent, sealing ring, and leaflets of FIG. 14A.
[0055] Various embodiments of the present disclosure will now be
described with reference to the appended drawings. It is to be
appreciated that these drawings depict only some embodiments of the
disclosure and are therefore not to be considered limiting of its
scope.
DETAILED DESCRIPTION
[0056] With conventional self expanding valves, clinical success of
the valve is dependent on accurate deployment and anchoring.
Inaccurate deployment and anchoring of the valve increases risks,
such as those associated with valve migration, which may cause
severe complications and possibly death due to the obstruction of
the left ventricular outflow tract. Inaccurate deployment and
anchoring may also result in the leakage of blood between the
implanted heart valve and the native valve annulus, commonly
referred to as perivalvular leakage (also known as "paravalvular
leakage"). In aortic valves, this leakage enables blood to flow
from the aorta back into the left ventricle, reducing cardiac
efficiency and putting a greater strain on the heart muscle.
Additionally, calcification of the aortic valve may affect
performance and the interaction between the implanted valve and the
calcified tissue is believed to be relevant to leakage, as will be
outlined below.
[0057] Moreover, anatomical variations from one patient to another
may cause a fully deployed heart valve to function improperly,
requiring removal of the valve from the patient. Removing a fully
deployed heart valve increases the length of the procedure as well
as the risk of infection and/or damage to heart tissue. Thus,
methods and devices are desirable that would reduce the need to
remove a prosthetic heart valve from a patient. Methods and devices
are also desirable that would reduce the likelihood of perivalvular
leakage due to gaps between the implanted heart valve and patient
tissue.
[0058] As used herein, the term "proximal," when used in connection
with a prosthetic heart valve, refers to the end of the heart valve
closest to the heart when the heart valve is implanted in a
patient, whereas the term "distal," when used in connection with a
prosthetic heart valve, refers to the end of the heart valve
farthest from the heart when the heart valve is implanted in a
patient. When used in connection with devices for delivering a
prosthetic heart valve or other medical device into a patient, the
terms "trailing" and "leading" are to be taken as relative to the
user of the delivery devices. "Trailing" is to be understood as
relatively close to the user, and "leading" is to be understood as
relatively farther away from the user. Also as used herein, the
terms "generally," "substantially," "approximately," and "about"
are intended to mean that slight deviations from absolute are
included within the scope of the term so modified.
[0059] When used to indicate relative locations within the aortic
annulus, the aortic root, and the ascending aorta of a patient, the
terms "above" and "below" are to be taken as relative to the
juncture between the aortic annulus and the left ventricle. "Above"
is to be understood as relatively farther from the left ventricle,
and "below" is to be understood as relatively closer to the left
ventricle.
[0060] When used to indicate relative locations within the
prosthetic heart valve, the terms "longitudinal" and "vertical" are
to be taken as the direction of the axis extending between the
proximal end and the distal end of the stent of the heart valve,
along the direction of intended blood flow; the term "flow
direction" is to be taken as the direction from the proximal end to
the distal end of the stent of the heart valve, along the direction
of intended blood flow; and the terms "above," "below," "high," and
"low" are to be taken as relative to the proximal end of the stent.
"Above" and "high" are to be understood as relatively farther from
the proximal end of the stent in the flow direction toward the
distal end of the stent, and "below" and "low" are to be understood
as relatively closer to the proximal end of the stent in the flow
direction. When used to indicate relative locations within the
prosthetic heart valve, the term "circumferential" is to be taken
as the direction of rotation about an axis extending in the flow
direction of the stent.
[0061] The sealing portions of the present disclosure may be used
in connection with collapsible prosthetic heart valves. FIG. 1
shows one such collapsible stent-supported prosthetic heart valve
100 including a stent 102 and a valve assembly 104 as is known in
the art. The prosthetic heart valve 100 is designed to replace a
native tricuspid valve of a patient, such as a native aortic valve.
It should be noted that while the inventions herein are described
predominantly in connection with their use with a prosthetic aortic
valve and a stent having a shape as illustrated in FIG. 1, the
valve could be a bicuspid valve, such as the mitral valve, and the
stent could have different shapes, such as a flared or conical
annulus section, a less-bulbous aortic section, and the like, and a
differently shaped transition section.
[0062] The stent 102 may be formed from biocompatible materials
that are capable of self-expansion, such as, for example, shape
memory alloys, such as the nickel-titanium alloy known as "Nitinol"
or other suitable metals or polymers. The stent 102 extends from a
proximal or annulus end 130 to a distal or aortic end 132, and
includes an annulus section 140 adjacent the proximal end 130, a
transition section 141, and an aortic section 142 adjacent the
distal end 132. The annulus section 140 has a relatively small
cross-section in the expanded condition, while the aortic section
142 has a relatively large cross-section in the expanded condition.
The annulus section 140 may be in the form of a cylinder having a
substantially constant diameter along its length. The transition
section 141 may taper outwardly from the annulus section 140 to the
aortic section 142.
[0063] Each of the sections of the stent 102 includes a plurality
of struts 160 forming cells 162 connected to one another in one or
more annular rows around the stent. For example, as shown in FIG.
1, the annulus section 140 may have two annular rows of complete
cells 162 and the aortic section 142 and the transition section 141
may each have one or more annular rows of partial cells 162. The
cells 162 in the aortic section 142 may be larger than the cells
162 in the annulus section 140. The larger cells in the aortic
section 142 better enable the prosthetic valve 100 to be positioned
in the native valve annulus without the stent structure interfering
with blood flow to the coronary arteries.
[0064] The stent 102 may include one or more retaining elements 168
at the distal end 132 thereof, the retaining elements 168 being
sized and shaped to cooperate with female retaining structures (not
shown) provided on the deployment device. The engagement of the
retaining elements 168 with the female retaining structures on the
deployment device helps maintain the prosthetic heart valve 100 in
assembled relationship with the deployment device, minimizes
longitudinal movement of the prosthetic heart valve relative to the
deployment device during unsheathing or resheathing procedures, and
helps prevent rotation of the prosthetic heart valve relative to
the deployment device as the deployment device is advanced to the
target location and the heart valve deployed.
[0065] The prosthetic heart valve 100 includes a valve assembly 104
preferably positioned in the annulus section 140 of the stent 102
and secured to the stent. The valve assembly 104 includes a cuff
176 and a plurality of leaflets 178 which collectively function as
a one-way valve by coapting with one another. As a prosthetic
aortic valve, the prosthetic heart valve 100 has three leaflets
178. However, it will be appreciated that other prosthetic heart
valves with which the sealing portions of the present disclosure
may be used may have a greater or lesser number of leaflets
178.
[0066] Although the cuff 176 is shown in FIG. 1 as being disposed
on the luminal or inner surface of the annulus section 140, it is
contemplated that the cuff 176 may be disposed on the abluminal or
outer surface of the annulus section 140 or may cover all or part
of either or both of the luminal and abluminal surfaces. Both the
cuff 176 and the leaflets 178 may be wholly or partly formed of any
suitable biological material or polymer such as, for example,
polytetrafluoroethylene (PTFE), polyvinyl alcohol (PVA), ultra-high
molecular weight polyethylene (UHMWPE), silicone, urethane, and the
like.
[0067] The leaflets 178 may be attached along their belly portions
to the cells 162 of the stent 102, with the commissure between
adjacent leaflets 178 attached to commissure features 166. As can
be seen in FIG. 1, each commissure feature 166 may lie at the
intersection of four cells 162, two of the cells being adjacent one
another in the same annular row, and the other two cells being in
different annular rows and lying in end-to-end relationship.
Preferably, the commissure features 166 are positioned entirely
within the annulus section 140 or at the juncture of the annulus
section 140 and the transition section 141. The commissure features
166 may include one or more eyelets which facilitate the suturing
of the leaflet commissure to the stent 102.
[0068] The prosthetic heart valve 100 may be used to replace a
native aortic valve, a surgical heart valve, or a heart valve that
has undergone a surgical procedure. The prosthetic heart valve 100
may be delivered to the desired site (e.g., near the native aortic
annulus) using any suitable delivery device. During delivery, the
prosthetic heart valve 100 is disposed inside the delivery device
in the collapsed condition. The delivery device may be introduced
into a patient using a transfemoral, transapical, transseptal,
transradial, transsubclavian, transaortic or any other percutaneous
approach. Once the delivery device has reached the target site, the
user may deploy the prosthetic heart valve 100. Upon deployment,
the prosthetic heart valve 100 expands so that the annulus section
140 is in secure engagement within the native aortic annulus. When
the prosthetic heart valve 100 is properly positioned inside the
heart, it works as a one-way valve, allowing blood to flow from the
left ventricle of the heart to the aorta, and preventing blood from
flowing in the opposite direction.
[0069] Problems may be encountered when implanting the prosthetic
heart valve 100. For example, in certain procedures, collapsible
valves may be implanted in a native valve annulus without first
resecting the native valve leaflets. The collapsible valves may
have critical clinical issues because of the nature of the stenotic
leaflets that are left in place. Additionally, patients with uneven
calcification, bi-cuspid aortic valve disease, and/or valve
insufficiency cannot be treated well, if at all, with the current
collapsible valve designs.
[0070] The reliance on unevenly-calcified leaflets for proper valve
placement and seating could lead to several problems, such as
perivalvular leakage ("PV leak"), which can have severe adverse
clinical outcomes. To reduce these adverse events, the optimal
valve would anchor adequately and seal without the need for
excessive radial force that could harm nearby anatomy and
physiology.
[0071] PV leak may also be caused by the implantation of a valve
having an expanded diameter that is too small relative to the
native aortic annulus diameter, a prosthetic valve that is deployed
in a tilted orientation relative to the native aortic annulus (such
that the longitudinal axis of the valve and the native aortic
annulus are misaligned), lack of full radial expansion of the valve
due to the stent catching on calcific nodules in the native aortic
annulus, and placing the valve at a non-optimal longitudinal
position relative to the native aortic annulus (either too high or
too low along a longitudinal axis of the native aortic
annulus).
[0072] FIG. 2A is a highly schematic cross-sectional illustration
of the prosthetic heart valve 100 disposed within a native valve
annulus 250A. As seen in the figure, the valve assembly 104 has a
substantially circular cross-section which is disposed within the
non-circular native valve annulus 250A. At certain locations around
the perimeter of the heart valve 100, gaps 200A form between the
heart valve 100 and the native valve annulus 250A. Blood flowing
through these gaps and past the valve assembly 104 of the
prosthetic heart valve 100 can cause regurgitation and other
inefficiencies which reduce cardiac performance. Such improper
fitment may be due to suboptimal native valve annulus geometry due,
for example, to calcification of the native valve annulus 250A or
to unresected native leaflets.
[0073] FIG. 2B is a similar cross-sectional illustration of a
prosthetic mitral valve 100B disposed within a native valve annulus
250B. As seen in the figure, the valve assembly 104B has a
substantially D-shaped cross-section that is disposed within the
irregularly-shaped annulus 250B. At certain locations around the
perimeter of the heart valve 100B, gaps 200B form between the heart
valve 100B and the native valve annulus 250B. Regurgitation and
other inefficiencies may thus result after deployment of a
prosthetic mitral valve. Though the following examples show aortic
valves, it will be understood that the present devices and methods
may be equally applicable to mitral heart valves.
[0074] FIGS. 3A-3C illustrate a prosthetic heart valve 300 in
accordance with another embodiment. As can be seen in FIG. 3A, the
prosthetic heart valve 300 extends between a proximal end 302 and a
distal end 304, and may generally include a stent 306 formed of a
plurality of struts 307, and a valve assembly 308 having a
plurality of leaflets 310 and a cuff 312. The cuff 312 may include
a surplus portion 322 that extends proximally of the proximal end
302 of the stent 306. In some examples, the surplus portion 322 in
its straight condition may extend between about 10 mm and about 20
mm proximally of the proximal end 302 of the stent 306. The surplus
portion 322 may be formed of the same material as the rest of the
cuff 312 and may be formed integrally therewith from a single piece
of material. Alternatively, the surplus portion 322 may be formed
of the same material or a different material than the cuff 312 that
is sutured, glued or otherwise affixed to the proximal end of the
cuff.
[0075] FIG. 3B illustrates the prosthetic heart valve 300 after the
surplus portion 322 has been rolled to form a sealing ring 350A.
After assembly of the cuff 312 to the stent 306, the surplus
portion 322 may be rolled outwardly in the direction of the distal
end 304 to form the sealing ring 350A such that a proximal surface
323 of the sealing ring is substantially aligned in the flow
direction of the stent with the proximalmost junctions 309A (FIG.
3A) of the stent. In this example, the surplus portion 322 is
rolled into a generally toroidal-shaped sealing ring 350A near the
proximal end 302 of the prosthetic heart valve 300 (e.g., at a
position that will lie at least partially below the native valve
annulus when the prosthetic heart valve is deployed into a
patient). The sealing ring 350A may be formed of one complete
revolution of the surplus portion 322, or of a series of
revolutions (e.g., two, three or more revolutions of the surplus
portion 322).
[0076] Although the sealing ring 350A is shown in FIG. 3A as having
a circular cross-section, that need not be the case. The sealing
ring 350A may be flattened in the flow direction, or it may have a
cross-section that is square, rectangular, triangular, or other
shapes. It is to be understood that all of the "sealing rings"
described herein are not to be understood to be limited to having a
circular cross-section. Any of the sealing rings described herein
may be flattened in the flow direction, or they may have a
cross-section that is square, rectangular, triangular, or other
shapes.
[0077] The sealing ring 350A may maintain its shape through a
variety of methods, such as by being tied to select struts 307 of
the stent 306. In one example, as seen in the enlarged schematic
view of FIG. 3B, end struts 360a and 360b of the stent 306 meet to
form a horseshoe-shaped end 370 having a partial slot 372
therebetween. A number of locking stitches LS1 may be tied around
the horseshoe-shaped ends 370, and specifically through each slot
372 and around the sealing ring 350A to keep the sealing ring from
unfurling. The locking stitches LS1 may be formed of a suture,
string, or any other suitable biocompatible thread.
[0078] It will be understood that, though three locking stitches
are shown around the circumference of the prosthetic heart valve to
couple the sealing ring 350A to the stent 306, any number of
locking stitches may be used. Although the locking stitches LS1 are
shown in FIGS. 3A and 3B as extending completely around the sealing
ring 350A, that need not be the case. In other examples, the
sealing ring 350A may be attached to the stent 306 by sutures
stitched through a portion of an inner diameter of the sealing
ring.
[0079] Other techniques for maintaining the shape of the sealing
ring 350A may also be used including adhesive, glue, shape memory
fabric, or the like. The sealing ring 350A may have a radius larger
than that of the valve assembly 308, the larger radius of the
sealing ring being capable of filling and/or blocking blood flow
through gaps between the prosthetic heart valve 300 and the native
valve annulus (not shown).
[0080] FIG. 3C illustrates the prosthetic heart valve 300 in native
valve annulus 380 after formation of the sealing ring 350A as seen
from the proximal end 302 (e.g., as seen from the annulus end
toward the aortic end of the heart valve). The sealing ring 350A
has been secured to the stent 306 via a series of locking stitches
LS1. The outer diameter of the stent 306 at the proximal end is
indicated with a dashed line. The sealing ring 350A extends
radially outward from the outer diameter of the stent 306 at the
proximal end of the prosthetic heart valve 300 by a radial distance
r1. In at least some examples, the radial distance r1 may be
between about 1.0 mm and about 2.5 mm. The radial distance r1 may
preferably be between at least 2.0 mm.
[0081] As can be seen in FIGS. 3B and 3C, the sealing ring 350A is
configured to radially expand to a diameter greater than the
diameter of the proximal end 302 of the stent 306 when the stent is
radially expanded, extending radially outward from the outer
diameter of the stent by the radial distance r1, for example. To
ensure that the sealing ring 350A radially expands to a diameter
greater than the diameter of the proximal end 302 of the stent 306
when the prosthetic heart valve 300 is deployed into a patient, the
sealing ring 350A, and all of the other sealing rings described
herein, may have sufficient elasticity that it has a spring bias
that tends to provide a force in a radially outward direction when
the sealing ring is radially compressed.
[0082] However, the outward spring bias of the sealing ring 350A,
and of all of the other sealing rings described herein, is
preferably small enough that the sealing ring may expand a greater
radial distance at locations along the circumference of the sealing
ring at which there is minimal radial force applied to the sealing
ring from the native anatomy (i.e., at locations at which voids or
gaps between the stent 306 and the native anatomy are present),
while the sealing ring may expand a lesser radial distance at
locations along the circumference of the sealing ring at which
there is greater radial force applied to the sealing ring from the
native anatomy (i.e., locations at which there are no such voids or
gaps).
[0083] FIG. 3D illustrates a heart valve 300D, which is a variant
of the heart valve 300 of FIGS. 3A-3C. The heart valve 300D has a
sealing ring 350D disposed at a higher location along the stent 306
than the sealing ring 350A of FIG. 3B, which may permit the
prosthetic heart valve 300D to achieve improved sealing against the
native annulus and the native leaflets in some patients.
[0084] Compared to the sealing ring 350A of FIGS. 3A-3C, all of the
other sealing rings described herein, including the sealing ring
350D, have structures that may provide different surface areas and
thicknesses of material at different longitudinal and
circumferential locations relative to the stent to provide
different advantages in sealing voids or gaps between the stent and
the native anatomy when the heart valves are deployed into a
patient. Such differences in surface areas and thicknesses of
material at certain longitudinal and circumferential locations may
make some sealing ring configurations preferable for certain native
anatomies and other sealing ring configurations preferable for
other native anatomies, depending on the anticipated locations of
voids or gaps between a deployed prosthetic heart valve and the
native anatomy. Such anticipated locations of voids or gaps between
a deployed prosthetic heart valve and the native anatomy may be
determined by a variety of methods, including imaging of the native
anatomy before deployment of a prosthetic heart valve, for
example.
[0085] The heart valve 300D extends between a proximal end 302 and
a distal end 304, and may generally include a stent 306 formed of
struts 307, and a valve assembly 308 having a plurality of leaflets
310 and a cuff 312. A surplus portion 322D of the cuff 312 has been
rolled to extend around the proximal end 302 of the stent 306 to
form a sealing ring 350D in a manner similar to that described
above, except that the sealing ring 350D has been rolled so that
the proximal surface 323D of the sealing ring lies above the
proximal end 302 of the stent 306 and closer to the leaflets 310
than the sealing ring 350A (e.g., at a position that will lie
within the native valve annulus when the prosthetic heart valve is
deployed into a patient). After rolling the surplus portion 322D
and forming the sealing ring 350D at the appropriate position,
locking stitches LS2 may be coupled to the sealing ring 350D and
upper junctions 309B of the proximalmost struts 307 of the stent
306 to secure the sealing ring in place.
[0086] FIGS. 4A-4B illustrate a prosthetic heart valve 400 in
accordance with another embodiment. The heart valve 400 extends
between a proximal end 402 and a distal end 404, and may generally
include a stent 406 formed of struts 407, and a valve assembly 408
having a plurality of leaflets 410 and a cuff 412. The cuff 412 may
include a surplus portion 422 that extends proximally of the
proximal end 402 of the stent 406 before rolling as described above
with reference to FIG. 3B. In some examples, the surplus portion
422 in its straight condition may extend between about 5 mm and
about 20 mm proximally of the proximal end 402 of the stent 406.
The surplus portion 422 may be formed of the same material as the
rest of the cuff 412 and may be integrally formed therewith from a
single piece of material.
[0087] In this example, the surplus portion 422 is formed of a
thickened material that is configured to circumferentially fold in
an accordion-like fashion at certain locations to form an
undulating sealing ring 450 when the prosthetic heart valve 400 is
released from a delivery device. The undulating sealing ring 450
may include thin porcine pericardial tissue between about about
0.005 inches and about 0.007 inches in thickness, or UHMWPE or PET
fabric between about 0.003 inches and about 0.005 inches in
thickness, and alternates between a series of peaks 460 and valleys
470. Compared to the sealing rings 350A and 350D described above,
the undulating sealing ring 450 distributes tissue over a greater
distance in the flow direction of the stent 406, thereby allowing
for filling in and around voids over a greater longitudinal
distance when the prosthetic heart valve 400 is deployed into a
patient. Furthermore, because the undulating sealing ring 450 is
configured to circumferentially fold, the sealing ring 450 may be
more easily folded in an organized manner for loading into a
delivery device.
[0088] Terminal sutures TS1 may attach portions of the surplus
portion 422 to selected struts 407 to aid in the formation of the
undulating ring 450. In some examples, the sutures TS1 may be the
same sutures that are used to attach the cuff 412 to the struts 407
so that no extra steps or bulk is added. In its rolled condition,
the undulating ring 450 may be annularly disposed around the stent
406 so that the valleys 470 of the sealing ring are substantially
aligned in the flow direction with the proximal end 402 of the
stent. As shown in FIG. 4A, the undulating ring 450 may be attached
to the cuff 412 and/or the stent 406 without following the contour
of the struts 407. However, in a preferred embodiment, the
undulating ring 450 may be attached to the cuff 412 and/or the
stent 406 following the contour of the struts 407 (FIG. 4C).
[0089] FIG. 4B illustrates the prosthetic heart valve 400 in a
native valve annulus 480 after formation of the undulating sealing
ring 450, as seen from the proximal end 402 (e.g., as seen from the
annulus end toward the aortic end of the prosthetic heart valve).
The outer diameter of the stent 406 at the proximal end is
indicated with a dashed line. The undulating ring 450 extends
radially outward from the outer diameter of the stent 406 at the
proximal end of heart valve 400 by a radial distance r2. In at
least some examples, the radial distance r2 may be between about
1.0 mm and about 10.0 mm, or between about 1.0 mm and about 2.5
mm.
[0090] FIG. 4C illustrates a heart valve 400C, which is a variant
of the heart valve 400 of FIGS. 4A-4B. The heart valve 400C extends
between a proximal end 402 and a distal end 404, and may generally
include a stent 406 formed of struts 407, and a valve assembly 408
having a plurality of leaflets 410 and a cuff 412.
[0091] A sealing ring 450C may be annularly disposed around the
abluminal surface of the stent 406 at the proximal end 402 of the
prosthetic heart valve 400. The sealing ring 450C may alternate
between a series of peaks 460C and valleys 470C and may radially
expand to a diameter greater than the diameter of the proximal end
of the stent 406, as described above with reference to the sealing
ring 350A of FIGS. 3A-3C.
[0092] Similar to the sealing ring 450 shown in FIGS. 4A-4B, the
sealing ring 450C may be formed of a thickened material that is
configured to circumferentially fold in an accordion-like fashion
at certain locations to form an undulating sealing ring when the
prosthetic heart valve 400C is released from a delivery device.
[0093] As shown in FIG. 4C, the valleys 470C of the sealing ring
450C may be stitched to the proximalmost junctions 409A of the
stent 406, and the peaks 460C of the sealing ring may be stitched
to upper junctions 409B of the proximalmost struts 407 of the
stent. As shown in FIG. 4C, in a preferred embodiment, the
undulating ring 450C may be attached to the cuff 412 and/or the
stent 406 following the contour of the struts 407. Such an
attachment of the undulating ring 450C following the contour of the
struts 407 may permit a reduction in the number of sutures needed
to attach the sealing ring to the cuff 412 and/or the stent 406,
which may help to reduce the crimped diameter of the prosthetic
valve 400C.
[0094] The sealing ring 450C may be formed, for example, from a
long, thin rectangle of material about 10 mm in width that is
folded approximately in half longitudinally, and the opposed
longitudinal edges may be stitched to one another to create a
flattened tube about 5 mm in diameter. The lateral ends of the
flattened tube may be stitched to one another to create the sealing
ring 450C.
[0095] The longitudinal seam of the sealing ring 450C may be
stitched to an abluminal surface of the cuff 412 and select struts
407 of the stent 406 by sutures that secure the sealing ring in
place. In some examples, the sutures are the same sutures as are
used to attach the cuff 412 to the struts 407 so that no extra
steps or bulk is added. Alternatively, the sealing ring 450C may be
formed from a surplus portion of the cuff 412 that is rolled to
form a sealing ring in a manner similar to that described above.
Any of the sealing rings disclosed herein may be formed using any
one of the aforementioned formation methods.
[0096] In one example, the sealing ring 450C may be made of a thin
tubular fabric material. In other examples, the sealing ring 450C
may include thin porcine pericardial tissue between about about
0.005 inches and about 0.007 inches in thickness, or UHMWPE or PET
fabric between about 0.003 inches and about 0.005 inches in
thickness. Alternatively, a variety of other materials may be used,
including bovine tissue (e.g., glycerol impregnated or freeze
dried), tissue with support structures therein, wire mesh,
radiopaque wire, fabric, braided or woven fabric (e.g., PTFE, PTE,
or UHMWPE), fabric coated with PTFE or collagen, or a multi-layered
composite of one or more of the aforementioned materials (e.g., a
fabric and tissue composite). Any of the sealing rings disclosed
herein may be made of any one of the aforementioned materials or a
combination thereof.
[0097] The sealing ring 450C may be at least partially radiopaque,
i.e., the sealing ring may include one or more materials having
enhanced visibility to a user under fluoroscopy. For example, the
sealing ring 450C may be include fabric or wire mesh material
having radiopaque fibers or entirely comprised of radiopaque
fibers. The sealing ring 450C may include radiopaque marker beads,
a thin radiopaque wire, radiopaque paint, or impregnation by
soaking in a radiopaque material such as silver, iodine, barium,
platinum, or the like. Any of the sealing rings disclosed herein
may be made of any one of the aforementioned radiopaque materials
or a combination thereof.
[0098] FIG. 4D illustrates a prosthetic heart valve 400D, which is
a variant of the prosthetic heart valve 400C of FIG. 4C. The
prosthetic heart valve 400D may be identical to the prosthetic
heart valve 400C, except for the sealing ring 450D, in which the
valleys 470D are stitched to the proximalmost junctions 409A of the
stent 406, but the peaks 460D may be located about half-way between
the proximalmost junctions and upper junctions 409B.
[0099] The peaks 460D of the sealing ring 450D may be stitched to
the abluminal surface of the cuff 412, or alternatively, the
portions of the sealing ring containing the peaks may not be
stitched to the cuff or the struts 407. In embodiments in which the
portions of the sealing ring 450D containing the peaks are not
stitched to the cuff 412 or the struts 407, the unstitched portions
of the sealing ring may be able to move relative to the cuff and
struts during sheathing or resheathing of the prosthetic heart
valve 400D, thereby reducing the tissue bulk at any particular
longitudinal location along the stent 406, which may help reduce
the profile (i.e., diameter) of the prosthetic heart valve when it
is in a radially-compressed condition in the delivery device.
[0100] FIGS. 5A-5E illustrate variants of sealing rings that may be
used with prosthetic heart valves 400, 400C, or 400D in place of
the sealing rings shown in FIGS. 4A-4D. Each of the sealing rings
550A-550E shown in FIGS. 5A-5E may be formed in the same manner,
attached to the stent and cuff in the same manner, and made of the
same material or materials described above with reference to the
sealing rings 450, 450C, and 450D. Each of the sealing rings
550A-550E may be attached to a stent in any location along the
longitudinal axis of the stent. A prosthetic heart valve, such as
the prosthetic heart valve 400C, may include one of the sealing
rings 550A-550E, or alternatively, the prosthetic heart valve may
include two or more of the sealing rings, as will be described in
more detail below.
[0101] FIG. 5A shows a sealing ring 550A in the shape of a toroid
similar to the toroidal-shaped sealing ring 350A shown in FIGS. 3B
and 3C. FIG. 5B shows a sealing ring 550B in the shape of a bent or
saddle-shaped toroid that alternates between peaks 560B and valleys
570B around the circumference of the sealing ring, the peaks and
valleys being substantially evenly distributed about the
circumference. As shown in FIG. 5B, the sealing ring 550B has two
peaks 560B and two valleys 570B, but the sealing ring may have
other numbers of peaks and valleys, such as three, for example.
[0102] FIG. 5C shows a sealing ring 550C having a zigzag shape,
similar to the zigzag shape shown in FIG. 4C. The sealing ring 550C
alternates between peaks 560C and valleys 570C around the
circumference of the sealing ring, the peaks and valleys being
substantially evenly distributed about the circumference. As shown
in FIG. 5C, the sealing ring 550C has nine peaks 560C and nine
valleys 570C, but the sealing ring may have other numbers of peaks
and valleys, such as three or six, for example. As shown in FIG.
4C, a sealing ring having a zigzag shape may be stitched to the
stent and the cuff along the struts. However, in other embodiments,
the sealing ring 550C may be stitched to the stent and/or the cuff
at other locations.
[0103] FIG. 5D shows a sealing ring 550D having a zigzag shape with
alternating peak heights. The sealing ring 550D alternates between
peaks 560D and valleys 570D around the circumference of the sealing
ring, the peaks and valleys being substantially evenly distributed
about the circumference. As shown in FIG. 5D, the sealing ring 550D
has eight peaks 560D and eight valleys 570D, but the sealing ring
may have other numbers of peaks and valleys, such as four or six,
for example.
[0104] The peaks 560D include low peaks 561 that extend by a first
height H1 above the valleys 570D and high peaks 562 that extend by
a second height H2 above the valleys, the second height being
greater than the first height. As shown in FIG. 5D, the peaks 560D
may include four low peaks 561 and four high peaks 562, with one
low peak separating adjacent ones of the high peaks. In other
embodiments, there may be other numbers of high and low peaks. For
example, a sealing ring having varying peak heights may include six
low peaks and three high peaks, with two low peaks separating
adjacent ones of the high peaks. In another example, a sealing ring
having varying peak heights may include three low peaks and six
high peaks, with two high peaks separating adjacent ones of the low
peaks.
[0105] FIG. 5E shows a stacked arrangement of two sealing rings
550D each having a zigzag shape with alternating peak heights. As
shown in FIG. 5E, the two sealing rings 550D are identical in
structure and are aligned with one another such that the peaks 560D
and valleys 570D of the upper sealing ring are substantially
aligned longitudinally with the peaks and valleys of the lower
sealing ring, and such that the low peaks 561 and high peaks 562 of
the upper sealing ring are substantially aligned longitudinally
with the low peaks and high peaks of the lower sealing ring. In
other embodiments, the peaks 560D and valleys 570D of the two
sealing rings 550D, and the low peaks 561 and the high peaks 562 of
the two sealing rings need not be longitudinally aligned. In other
embodiments, the two sealing rings need not have an identical
structure.
[0106] FIG. 5F shows a sealing ring 550F having a toroidal shape,
similar to the toroidal-shaped sealing ring 550A shown in FIG. 5A.
The sealing ring 550F has openings 563 in a top surface 564
thereof. The openings 563 may be round holes or may be holes having
any other shape or slits having any shape. The sealing ring 550F
may be attached to a stent and cuff of a prosthetic heart valve in
a similar manner as that described above with reference to the
sealing ring 450C shown in FIG. 4C.
[0107] When the sealing ring 550F is attached to a stent and cuff
of a prosthetic heart valve, the openings 563 and the top surface
564 will preferably face toward the distal end of the stent. When
deployed in a patient, the openings 563 may allow the sealing ring
550F to fill with blood, which may augment the sealing ability of
the sealing ring against the native aortic annulus or other native
tissue structures. Instead of or in addition to the openings 563,
the sealing ring 550F may include expanding materials within the
interior of the sealing ring, such as polyacrylimide or other
hydroscopic materials, PVA, shape memory foam, bovine gelatin or
collagen, or the like.
[0108] In another variation shown in FIGS. 6A-6B, a prosthetic
heart valve 600 extends between a proximal end 602 and a distal end
604, and may generally include a stent 606 formed of struts 607,
and a valve assembly 608 having a plurality of leaflets 610 and a
cuff 612. The cuff 612 may include an extended surplus portion 622
that extends proximally of the proximal end 602 of the stent 606.
In some examples, the surplus portion 622 may extend in its
straight condition between about 5.0 mm and about 10.0 mm
proximally of the proximal end 602 of the stent 606. The surplus
portion 622 may be formed of the same material as the rest of the
cuff 612 and may be formed integrally therewith from a single piece
of material.
[0109] In this example, the surplus portion 622 deploys into a
substantially flat sealing ring 650, which extends radially outward
to a diameter greater than the diameter of the proximal end of the
stent 606. FIG. 6B illustrates the prosthetic heart valve 600 in a
native valve annulus 680 after formation of the sealing ring 650,
as seen from the proximal end 602 (e.g., as seen from the annulus
end toward the aortic end of the heart valve. The outer diameter of
the stent 606 at the proximal end is indicated with a dashed line.
The sealing ring 650 extends radially outward from the outer
diameter of the stent 606 at the proximal end of the prosthetic
heart valve 600 by a radial distance r3. In at least some examples,
the radial distance r3 is between about 2 mm and about 10 mm. In
this embodiment, the sealing ring 650 does not fill the gaps
between the prosthetic heart valve 600 and the native annulus 650,
but rather extends over the gaps to occlude blood flow through
them.
[0110] In a variation of the sealing ring 650, FIGS. 6C-6D show a
sealing ring 650C that may be made from a material separate from
the cuff 612, such as a thin flat skirt cut from a strip or circle
of porcine tissue without a seam. In one example, the circle of
tissue comprising the sealing ring 650C may have an inner diameter
D1 of about 29 mm, an outer diameter D2 of about 34 mm, and a width
W1 between the inner diameter and an outer diameter of about 5 mm.
As shown in FIG. 6D, an inner edge 651 of the sealing ring 650C may
be sutured to the stent 606 and the cuff 612 near the proximal end
602, using a running stitch, for example. An outer edge 652 of the
sealing ring 650C may be a free edge that is not sutured to the
stent 606 or the cuff 612, and the outer edge may undulate
naturally as shown in FIG. 6D. In this example, the outer edge 652
of the sealing ring 650C may extend up to 5 mm radially outward
from the stent 606.
[0111] FIG. 7 illustrates a prosthetic heart valve 700, which is a
variant of the prosthetic heart valve 100 of FIG. 1. The heart
valve 700 extends between a proximal end 702 and a distal end 704,
and may generally include a stent 706 formed of struts 707, and a
valve assembly 708 having a plurality of leaflets 710 and a cuff
712.
[0112] As shown in FIG. 7, in the prosthetic heart valve 700, the
cuff 712 may extend over a greater distance in a flow direction of
the stent 706 compared to the cuff 112 of FIG. 1. For example, when
the stent 706 is in an expanded use condition, a landing zone
(i.e., continuous cylindrical portion) of the cuff 712 may extend
over a length of about 16 mm to about 18 mm in the flow direction
from the proximal end 702 toward the distal end 704, compared to a
landing zone of about 8 mm to about 10 mm for the cuff 112 of the
prosthetic heart valve 100. Furthermore, the bellies of the
leaflets 710 may be attached to the stent 706 and the cuff 712 a
greater distance away from the proximal end 702 in the flow
direction than the bellies of the leaflets 110 of the prosthetic
heart valve 100. In one example, the belly of each of the leaflets
710 may be attached to the stent 706 and the cuff 712 a distance D3
of at least 10 mm from the proximal end 702 of the stent.
[0113] The prosthetic valve 700 having a cuff 712 having a
relatively large landing zone may be used with any of the sealing
rings disclosed herein. The large landing zone of the cuff 712 may
permit a plurality of sealing rings to be attached thereto, the
sealing rings separated from one another in the flow direction
(e.g., FIG. 14B).
[0114] FIGS. 8A-8E illustrate prosthetic heart valve configurations
that have sealing rings that are variants of the sealing ring 450C
shown in FIG. 4C, in which the sealing ring embodiments are
attached to the stent and cuff below (i.e., closer to the proximal
end of the stent) the locations at which the bellies of the
leaflets are attached to the stent and cuff. In each of these
embodiments, as well as the embodiments described below, the
sealing ring has a generally tubular configuration which, in its
expanded condition, projects radially outward from the annulus
section of the prosthetic heart valve.
[0115] FIGS. 8A-8B illustrate a heart valve 800 that extends
between a proximal end 802 and a distal end 804, and that may
generally include a stent 806 formed of struts 807, and a valve
assembly 808 having a plurality of leaflets 810 and a cuff 812. The
sealing ring 850 may have a shape that is similar to the bent or
saddle-shaped toroid of the sealing ring 550B shown in FIG. 5B.
[0116] The sealing ring 850 alternates between peaks 860 and
valleys 870 around the circumference of the sealing ring, the peaks
and valleys being substantially evenly distributed about the
circumference. The sealing ring 850 has three peaks 860 and three
valleys 870 positioned between adjacent ones of the peaks. The
peaks 860 are substantially aligned in the flow direction with the
commissure features 866, and the valleys 870 are substantially
aligned in the flow direction with the lowest portion 811 of the
attachment of the bellies of the leaflets 810 to the stent 806 and
the cuff 812.
[0117] The entirety of the sealing ring 850 is attached to the
stent 806 and cuff 812 below the positions at which the bellies of
the leaflets 810 are attached to the stent and cuff. Such a
configuration may more evenly distribute the material of the
leaflets and the sealing ring along the length of the prosthetic
heart valve 800, which may permit a smaller crimped diameter of the
prosthetic heart valve when loaded into a delivery device.
[0118] In one example, a single suture may be stitched around the
entire circumference of the stent 806 to attach the sealing ring
850 to the stent and the cuff 812. The sealing ring 850 may be
stitched to the struts 807 at each location at which the sealing
ring crosses a strut, and the sealing ring may be stitched to the
tissue of the cuff 812 at locations between the struts. As
described above with reference to FIGS. 4A and 4B, the sutures used
to attach the sealing ring 850 to the struts 807 (and any of the
other sealing rings described herein) may be the same sutures that
are used to attach the cuff 812 to the struts so that no extra
steps or bulk is added.
[0119] As can be seen in FIG. 8A, the valleys 870 of the sealing
ring 850 may be attached to the proximalmost junctions 809A of the
stent 806, and the peaks 860 of the sealing ring may be attached to
upper junctions 809B of the proximalmost struts 807 of the
stent.
[0120] FIG. 8C shows a sealing ring 850C that is a variant of the
sealing ring 850 of FIGS. 8A-8B. The sealing ring 850C may have a
shape that is similar to the bent or saddle-shaped toroid of the
sealing ring 850 with three peaks and three valleys, but the peaks
860C of the sealing ring 850C are attached to the stent 806 and/or
the cuff 812 above the upper junctions 809B of the proximalmost
struts of the stent. Thus, in this embodiment, the entire sealing
ring 850C does not lie below the positions at which the bellies of
the leaflets 810 are attached to the stent 806 and the cuff 812,
but rather there is some overlap between the sealing ring and the
leaflets. While this embodiment provides a greater sealing area
between the prosthetic heart valve and the surrounding tissue, the
crimped profile of the prosthetic valve is not as small as that
achievable with the sealing ring 850.
[0121] FIG. 8D shows the sealing ring 850 of FIGS. 8A-8B in another
location relative to the leaflets 810. In this variation, the
valleys 870 of the sealing ring 850 are substantially aligned in
the flow direction with the commissure features 866, and the peaks
860 are substantially aligned in the flow direction with the lowest
attached portions 811 of the bellies of the leaflets 810. As with
the embodiment of FIGS. 8A-8B, the entirety of the sealing ring 850
lies below the positions at which the bellies of the leaflets 810
are attached to the stent 806 and the cuff 812, enabling a smaller
crimp profile to be achieved.
[0122] FIG. 8E shows a sealing ring 850E that is another variant of
the sealing ring 850 of FIGS. 8A-8B. The sealing ring 850E has five
peaks 860E and five valleys 870E forming a zigzag shape somewhat
similar to that of the sealing ring 550C of FIG. 5C, but
alternating legs of the zigzag configuration have different
lengths. That is, legs 863 have a longer length than legs 864. This
enables the legs 864 to directly overlie and be attached to certain
struts 807 of the stent 806, while the legs 863 may not be attached
to the stent 806 or the cuff 812. Such method of attachment
provides for easier expanding and collapsing of the prosthetic
heart valve. One of the peaks 860E is substantially aligned in the
flow direction with a commissure feature 866, while others of the
peaks are close to being aligned in the flow direction with the
lowest attached portions 811 of the bellies of the leaflets 810.
Some of the valleys 870E are substantially aligned in the flow
direction with the lowest attached portions 811 of the bellies of
the leaflets 810, while others of the valleys are close to being
aligned in the flow direction with the commissure features 866.
[0123] FIGS. 9A-9C illustrate prosthetic heart valve configurations
that have embodiments of sealing rings that are variants of the
sealing ring 450C shown in FIG. 4C, in which the sealing ring
embodiments are attached to the stent and cuff both above and below
the locations at which the bellies of the leaflets are attached to
the stent and cuff. In these embodiments, the material of the
sealing ring may be more evenly distributed along the length of the
prosthetic heart valve than an embodiment where the sealing ring is
distributed along a very small portion of the length of the
prosthetic heart valve (e.g., the sealing ring 550A), which may
permit a smaller crimped diameter of the prosthetic heart valve
when loaded into a delivery device.
[0124] FIGS. 9A-9B illustrate a heart valve 900 that extends
between a proximal end 902 and a distal end 904, and that may
generally include a stent 906 formed of struts 907, and a valve
assembly 908 having a plurality of leaflets 910 and a cuff 912. The
sealing ring 950 may have a shape with alternating height zigzag
features similar to those of the sealing ring 550D shown in FIG.
5D, but the sealing ring 950 has six peaks 960 and six valleys 970,
including three low peaks 961 that extend to a first height H1
above the valleys and three high peaks 962 that extend to a second
height H2 above the valleys, the second height being greater than
the first height.
[0125] As can be seen in FIG. 9A, each low peak 961 is disposed
between adjacent ones of the high peaks 962, and each high peak is
disposed between adjacent ones of the low peaks. The low peaks 961
are substantially aligned in the flow direction with the commissure
features 966, while the high peaks 962 are substantially aligned in
the flow direction with the lowest attached portions 911 of the
bellies of the leaflets 910.
[0126] Such a configuration of a sealing ring having low peaks 961
and high peaks 962 at alternating heights may permit a smaller
crimped diameter of the prosthetic heart valve when loaded into a
delivery device. When the prosthetic heart valve is crimped into a
delivery device, the low peaks 961 will be disposed at a different
longitudinal location along the stent 906 than the high peaks 962,
thereby distributing the bulk of the peaks so that only half of the
peaks are at any single longitudinal location.
[0127] In one example, a single suture may be stitched around the
entire circumference of the stent 906 to attach the sealing ring
950 to the stent and the cuff 912. The sealing ring 950 may be
stitched to the struts 907 along the entire circumference of the
sealing ring. As can be seen in FIG. 9A, the valleys 970 of the
sealing ring 950 may be attached to the proximalmost junctions 909A
of the stent 906, and the low peaks 961 of the sealing ring may be
attached to upper junctions 909B of the proximalmost struts 907 of
the stent. The high peaks 962 may be attached to upper junctions
909C of certain cells in a first full row 913 of complete cells 915
adjacent the proximal end 902 of the stent 906.
[0128] FIG. 9C shows a sealing ring 950C that is a variant of the
sealing ring 950 of FIGS. 9A-9B. The sealing ring 950C has three
peaks 960C and three valleys 970C. The valleys 970C of the sealing
ring 950C are substantially aligned in the flow direction with the
commissure features 966, while the peaks 960C are substantially
aligned in the flow direction with the lowest attached portions 911
of the bellies of the leaflets 910.
[0129] FIGS. 10A-10D illustrate prosthetic heart valve
configurations that have embodiments of sealing rings that are
variants of the sealing ring 450C shown in FIG. 4C, in which the
sealing ring embodiments are attached to the stent and cuff both
above and below the locations at which the bellies of the leaflets
are attached to the stent and cuff, and in which portions of the
sealing ring extending substantially orthogonally to the
longitudinal axis may be attached to the cuff along their length or
held up under tension when the stent is expanded.
[0130] In embodiments in which portions of the sealing ring are not
attached to the valve stent, the material of the sealing ring may
readily move along the length of the prosthetic heart valve when
the valve is loaded into a delivery device, which may permit a
smaller crimped diameter of the prosthetic heart valve. For
example, in embodiments such as those shown in FIGS. 10A-10D, the
portions of the sealing rings that are unattached to the cuff may
be pushed to a different longitudinal location along the stent than
the bellies of the leaflets during crimping of the prosthetic heart
valve, thereby permitting a smaller crimped diameter of the
prosthetic heart valve.
[0131] FIGS. 10A-10B illustrate a heart valve 1000 that extends
between a proximal end 1002 and a distal end 1004, and that may
generally include a stent 1006 formed of struts 1007, and a valve
assembly 1008 having a plurality of leaflets 1010 and a cuff 1012.
The sealing ring 1050 may have a shape with zigzag features similar
to those of the sealing ring 550C shown in FIG. 5C, but the sealing
ring 1050 has three peaks 1060 and three valleys 1070, and the
three valleys may include linear portions that extend substantially
orthogonally to the longitudinal axis and that are either attached
to the cuff 1012 along the length thereof or unattached to the cuff
and stent 1006, but held up under tension when the stent is
expanded.
[0132] As can be seen in FIG. 10A, the peaks 1060 are substantially
aligned in the flow direction with the lowest attached portions
1011 of the bellies of the leaflets 1010, while the valleys 1070
are substantially aligned in the flow direction with the commissure
features 1066. The peaks 1060 may be attached to upper junctions
1009C of certain cells in a first full row 1013 of complete cells
1015 adjacent the proximal end 1002 of the stent 1006. The valleys
1070 may be attached to upper junctions 1009B of the proximalmost
struts 1007 of the stent 1006 and to the cuff 1012 between the
upper junctions, or they may not be attached to either the cuff or
the stent, but held up under tension when the stent is expanded. In
the attached position of the sealing ring 1050, the valleys 1070
may be substantially aligned in the circumferential direction with
the lowest attached portions 1011 of the bellies of the leaflets
1010.
[0133] FIG. 10C shows a sealing ring 1050C that is the same as the
sealing ring 1050 of FIGS. 10A-10B, except that the valleys 1070C
are located closer to the proximal end 1002 of the stent. In that
regard, the valleys 1070C of the sealing ring 1050C include linear
portions that extend substantially orthogonally to the longitudinal
axis and that may not be attached to the cuff 1012 or the stent.
These linear portions may be located about half-way between the
lower junctions 1009A and the upper junctions 1009B of the
proximalmost struts 1007 of the stent.
[0134] FIG. 10D shows a sealing ring 1050D that is another variant
of the sealing ring 1050 of FIGS. 10A-10B. The sealing ring 1050D
has three peaks 1060D and three valleys 1070D, however, the peaks
include linear portions that extend substantially orthogonally to
the longitudinal axis and the valleys have a substantially V-shape.
The peaks 1060D are substantially aligned in the flow direction
with the commissure features 1066, while the valleys 1070D are
substantially aligned in the flow direction with the lowest
attached portions 1011 of the bellies of the leaflets 1010. The
valleys 1070D may be attached to the proximalmost 1009A of the
stent. The peaks 1060D may be attached to the cuff 1012 between the
upper junctions 1009C of certain cells in the first full row 1013
of complete cells 1015 adjacent the proximal end 1002 of the stent
1006, or they may not be attached to either the cuff or the stent,
but held up under tension when the stent is expanded. Between the
peaks 1060D and the valleys 1070D, the sealing ring 1050D may be
attached directly to struts 1007 of the stent 1006.
[0135] FIGS. 11A-11H illustrate prosthetic heart valve
configurations that have embodiments of sealing rings that are
variants of the sealing ring 450C shown in FIG. 4C, in which the
sealing ring embodiments are attached to the stent and cuff at
least partially along the attachment contour of the bellies of the
valve leaflets to the stent/cuff, so that the sealing ring can
integrate or replace an existing underwire that may be used to
reinforce the cuff where the bellies of the leaflets attach to
same.
[0136] FIGS. 11A-11B illustrate a heart valve 1100 that extends
between a proximal end 1102 and a distal end 1104, and that may
generally include a stent 1106 formed of struts 1107, and a valve
assembly 1108 having a plurality of leaflets 1110 and a cuff 1112.
The sealing ring 1150 has a generally scalloped shape including
three sharp peaks 1160 and three smoothly-curved valleys 1170.
[0137] As can be seen in FIG. 11A, the sealing ring 1150 is
attached to the stent 1106 and the cuff 1112 at the same locations
that the leaflets 1110 are attached to the stent and cuff. As a
result, the peaks 1160 are substantially aligned in the flow
direction with the commissure features 1166, while the valleys 1170
are substantially aligned in the flow direction with the lowest
attached portions 1111 of the bellies of the leaflets 1110. The
peaks 1160 may be attached to the commissure features 1166 or to
upper junctions 1109D of certain cells in a second full row 1117 of
complete cells 1115 above the first full row 1113. The valleys 1170
may be attached to upper junctions 1109B of the proximalmost struts
1107 of the stent and to the cuff 1112 between the upper
junctions.
[0138] In this embodiment, a single underwire formed of the same
material as the struts 1107 may be used to provide reinforcement to
both the sealing ring 1150 and the cuff 1112. In one example, an
underwire may be stitched to a surface of the cuff 1112, and the
stitches that attach the sealing ring 1150 to the cuff 1112 may
extend around the underwire. In another example, an underwire may
be disposed inside of the sealing ring 1150, and the stitches that
attach the bellies of the leaflets 1110 to the cuff 1112 may extend
into the sealing ring and around the underwire. Thus, in this
arrangement, the leaflets, the underwire, and the sealing ring may
be attached to the prosthetic valve with a single set of sutures.
In a particular example in which the sealing ring 1150 is made of a
fabric material, the fabric material may provide sufficient
reinforcement to the cuff 1112 that an underwire may be omitted
from the prosthetic heart valve 1100.
[0139] FIGS. 11C-11D show a sealing ring 1150C that is the same as
the sealing ring 1150 of FIGS. 11A-11B, except that the peaks 1160C
are truncated so as to be located closer to the proximal end 1102
of the stent. As can be seen in FIGS. 11C-11D, the peaks 1160C may
include linear portions that extend substantially orthogonally to
the longitudinal axis and that may not be attached to the cuff 1112
or the stent 1106. These linear portions may be located about
half-way between the upper junctions 1109B of the proximalmost
struts of the stent and the upper junctions 1109D of certain cells
in the second full row 1117 of complete cells.
[0140] FIG. 11E shows a sealing ring 1150E that is another variant
of the sealing ring 1150 of FIGS. 11A-11B. The sealing ring 1150E
is the same as the sealing ring 1150 of FIGS. 11A-11B, except that
the valleys 1170E extend down to the proximalmost junctions 1109A
of the stent 1106, and the contour of the valleys does not follow
the contour of the bellies of the leaflets 1110.
[0141] FIG. 11F shows a sealing ring 1150F that is the same as the
sealing ring 1150 of FIGS. 11A-11B, with sharp peaks 1162F and
smoothly curved valleys 1172F. However, in this embodiment, the
valleys 1172F each include a lower peak 1161F that does not follow
the contour of the bellies of the leaflets 1110. The upper peaks
1162F follow the contour of the bellies of the leaflets 1110, but
the lower peaks 1161F extend above the lowest attached portions
1111 of the bellies of the leaflets, and are attached to the stent
1106 at the upper junctions 1109C of the first full row 1113 of
complete cells 1115.
[0142] FIG. 11G shows a sealing ring 1150G that is the same as the
sealing ring 1150F of FIG. 11F, except that the upper peaks 1162G
are truncated. That is, the second peaks 1162G include linear
portions that extend substantially orthogonally to the longitudinal
axis and that are either attached to the cuff 1112 along their
lengths or are not attached to the cuff or the stent 1106, but
rather are held up under tension when the stent is expanded. The
linear portions of the second peaks 1162G may be located about
half-way between the upper junctions 1109B of the proximalmost
struts of the stent and the upper junctions 1109D of certain cells
in the second full row 1117 of complete cells 1115.
[0143] FIG. 11H shows a sealing ring 1150H that is the same as the
sealing ring 1150E of FIG. 11E, except that sealing ring 1150H is
attached to the stent 1106 and the cuff 1112 along the contour of
certain struts 1107 of the stent, only partially following the
attachment contour of the bellies of the leaflets 1110 to the stent
1106 and the cuff 1112.
[0144] FIGS. 12A-12K illustrate that have embodiments of sealing
rings that are variants of the sealing ring 450C shown in FIG. 4C,
in which the sealing ring embodiments have at least one vertical
discontinuity, such that the sealing ring does not extend
continuously around the entire circumference of the stent.
[0145] FIGS. 12A-12B illustrate a heart valve 1200 that extends
between a proximal end 1202 and a distal end 1204, and that may
generally include a stent 1206 formed of struts 1207, and a valve
assembly 1208 having a plurality of leaflets 1210 and a cuff 1212.
As shown in FIG. 12A, the sealing ring 1250 may have three
discontinuous sections 1251, each such section extending around
about one-third of the circumference of the stent 1206. Each
section 1251 may extend from a location below the lowest point at
which the bellies of the leaflets 1210 are attached to the stent
1206 and cuff 1212 to a location above that lowest point.
[0146] As can be seen in FIG. 12A, each discontinuous section 1251
extends in both a circumferential direction and a flow direction of
the stent 1206, from a low end 1252 adjacent the proximal end 1202
of the stent to a high end 1253 spaced apart from the distal end
1204. The low end 1252 of each section 1251 may be attached to
proximalmost junctions 1209A of the stent 1206, and the high end
1253 may be attached to upper junctions 1209C of certain cells in
the first full row 1213 of complete cells 1215.
[0147] The high end 1253 of each section 1251 is aligned in the
flow direction with, but vertically displaced from, the low end
1252 of an adjacent discontinuous section, such that, for each
discontinuous section, an imaginary line L can be drawn in the flow
direction that intersects the high end of the section and the low
end of the adjacent section. As shown in FIG. 12A, the imaginary
line L that intersects the high end 1253 of one section 1251 and
the low end 1252 of the adjacent discontinuous section is located
circumferentially between a commissure feature 1266 and the lowest
attached portion 1211 of a corresponding one of the bellies of the
leaflets 1210.
[0148] FIG. 12C shows a sealing ring 1250C that is the same as the
sealing ring 1250 of FIGS. 12A-12B, except that the sealing ring
1250C includes four discontinuous sections 1251C, each such section
extending around part of the circumference of the stent 1206. As
shown in FIG. 12C, each section 1251C extends around 2/9 of the
circumference of the stent 1206, such that the four discontinuous
sections together extend around 8/9 of the circumference of the
stent, leaving 1/9 of the circumference of the stent without a
portion of the sealing ring 1250C. In other embodiments, each of
the four sections 1251C may extend around 1/4 of the circumference
of the stent 1206, so that the four sections together extend around
the entire circumference of the stent.
[0149] FIG. 12D shows another sealing ring 1250D that is the same
as the sealing ring 1250 of FIGS. 12A-12B, except that the sealing
ring 1250D includes nine discontinuous sections 1251D. Each section
1251D extends around about 1/9 of the circumference of the stent
1206, so that the nine sections together extend around the entire
circumference of the stent 1206. As can be seen in FIG. 12D, each
section 1251D of the sealing ring 1250D may be attached to the
stent 1206 and the cuff 1212 along the contour of certain struts
1207.
[0150] FIG. 12E shows a further sealing ring 1250E that is the same
as the sealing ring 1250 of FIGS. 12A-12B, except that the
discontinuous sections 1251E are circumferentially offset relative
to the locations of the discontinuous sections 1251 of FIGS.
12A-12B. As shown in FIG. 12E, the imaginary vertical line L1 that
intersects the high end 1253 of one section 1251E and the low end
1252 of the adjacent discontinuous section may extend through or
very close to the lowest attached portion 1211 of a corresponding
one of the bellies of the leaflets 1210.
[0151] FIG. 12F shows yet another sealing ring 1250F that is the
same as the sealing ring 1250 of FIGS. 12A-12B, except that the
sealing ring 1250F includes a single discontinuous section 1251F.
The single discontinuous section 1251F extends around the entire
circumference of the stent 1206. The high end 1253 of the section
1251F is aligned in the flow direction with, but vertically
displaced from, the low end 1252 of the section, such that an
imaginary line L2 can be drawn in the flow direction that
intersects the high end and the low end of the section.
[0152] FIG. 12G shows a sealing ring 1250G that is the same as the
sealing ring 1250F of FIG. 12F, but positioned lower on the stent
1206. That is, the sealing ring 1250G is attached to the stent 1206
and cuff 1212 so as to lie entirely below the positions at which
the bellies of the leaflets 1210 are attached to the stent and
cuff.
[0153] FIG. 12H shows a sealing ring 1250H that is a variant of the
sealing ring 1250 of FIGS. 12A-12B. The sealing ring 1250H similar
to the sealing ring 1250 of FIGS. 12A-12B, except that the sealing
ring 1250H includes five discontinuous sections 1251H that together
extend around the entire circumference of the stent 1206. Three of
the discontinuous sections 1251H each extend around about 2/9 of
the circumference of the stent 1206, and the remaining two
discontinuous sections each extend around about 1/6 of the
circumference of the stent.
[0154] As shown in FIG. 12H, the high end 1253 of each section
1251F is aligned in the flow direction with, but vertically
displaced from, the low end 1252 of an adjacent discontinuous
section, such that an imaginary line L3 can be drawn in the flow
direction that intersects the high end of one section and the low
end of an adjacent discontinuous section. The discontinuous
sections 1251H together extend around the entire circumference of
the stent without any significant overlap in the flow direction.
Each section 1251H of the sealing ring 1250H may be attached to the
stent 1206 and the cuff 1212 along the contour of certain struts
1207. Some of the sections 1251H have a falling portion 1254 and a
rising portion 1255 that meet at a vertex 1256 at the proximalmost
junctions 1209A of the stent 1206.
[0155] FIG. 121 shows a sealing ring 12501 that is the same as the
sealing ring 1250H of FIG. 12H, except that the sealing ring 12501
includes five discontinuous sections, four of which each extend
around about 2/9 of the circumference of the stent 1206, and the
remaining one of which extends around about 1/9 of the
circumference of the stent. Similar to the discontinuous sections
1251H, the sections 12511 together extend around the entire
circumference of the stent without any significant overlap in the
flow direction.
[0156] FIG. 12J shows a sealing ring 1250J that is a variant of the
sealing ring 1250 of FIGS. 12A-12B. The sealing ring 1250J is
similar to the sealing ring 1250 of FIGS. 12A-12B, except that the
sealing ring 1250J includes five discontinuous sections 1251J, each
section extending around part of the circumference of the stent
1206 and partially overlapping the adjacent section in the
circumferential direction.
[0157] As shown in FIG. 12J, each discontinuous section 1251J
extends around 5/18 of the circumference of the stent 1206 and
overlaps the adjacent discontinuous section by at least 1/18 of the
circumference of the stent, such that the five discontinuous
sections together extend around the entire circumference of the
stent 1206. The high end 1253 of each discontinuous section 1251J
overlaps the low end 1252 of an adjacent discontinuous section in
the circumferential direction by at least an amount T, such that an
imaginary line L4 in the flow direction can be drawn within the
circumferentially overlapping area that intersects both
discontinuous sections.
[0158] In the embodiment of FIG. 12J, the discontinuous sections
1251J of the sealing ring 1250J are attached to the stent 1206 and
cuff 1212 so as to lie entirely below the positions at which the
bellies of the leaflets 1210 are attached to the stent and cuff. In
other embodiments (e.g., FIG. 12K), that need not be the case.
[0159] FIG. 12K shows a sealing ring 1250K that is the same as the
sealing ring 1250J of FIG. 12J, except that each discontinuous
section 1251K has a first portion 1257 that extends from the low
end 1252 to a vertex 1254, and a second portion 1258 that extends
from the vertex to the high end 1253. The first portion 1257 does
not follow the contour of the struts 1207, while the second portion
1258 is attached to the stent 1206 and cuff 1212 along the contour
of certain ones of the struts, thereby forming each section 1251K
with a dogleg shape. As can be seen in FIG. 12K, each section 1251K
may extend from a location below the lowest point at which the
bellies of the leaflets 1210 are attached to the stent 1206 and
cuff 1212 to a location above that lowest point.
[0160] FIGS. 13A-13E illustrate prosthetic heart valve
configurations that have embodiments of sealing rings that are
variants of the sealing ring 850 shown in FIGS. 8A-8B, in which the
sealing ring embodiments have a plurality of separately formed
portions that may or may not be discontinuous with one another.
[0161] FIG. 13A shows a sealing ring 1350 that is a variant of the
sealing ring 850 of FIGS. 8A-8B (and a variant of the sealing ring
550C of FIG. 5C). The sealing ring 1350 is the same as the sealing
ring 850 of FIGS. 8A-8B, except that the sealing ring 1350 includes
a continuous portion 1351 and three discrete portions 1352 disposed
adjacent the continuous portion. The continuous portion 1351 and
the discrete portions 1352 may be formed separately and attached to
the stent 1306 adjacent one another, or they may be formed together
as a single continuous piece of fabric, for example.
[0162] As can be seen in FIG. 13A, the continuous portion 1351 has
the zigzag shape of the sealing ring 550C shown in FIG. 5C, and
extends completely around the circumference of the stent 1306. The
continuous portion 1351 is attached to the stent 1306 and the cuff
following the zigzag contour of the proximalmost struts 1307 of the
stent 1306.
[0163] Each of the three discrete portions 1352 of the sealing ring
1350 points down and is aligned below a corresponding commissure
feature 1366 in the flow direction. Each portion 1352 may be
attached to the stent 1306 and the cuff following the contour of
the struts 1307 between the continuous portion 1351 and the
locations where the bellies of the leaflets 810 are attached to the
stent and cuff. An exemplary portion 1352 is shown in the circle A
in FIG. 13A.
[0164] As shown in FIG. 13A, the continuous portion 1351 and the
discrete portions 1352 may be attached to the stent 1306 and cuff
entirely below the locations at which the bellies of the leaflets
1310 are attached to the stent and cuff. In other embodiments, that
need not be the case.
[0165] FIG. 13B shows a sealing ring 1350B that is the same as the
sealing ring 1350 of FIG. 13A, except that, rather than a
continuous portion that extends completely around the circumference
of the stent 1306, the sealing ring 1350B includes three lower
discrete portions 1351B that are spaced from one another in the
circumferential direction. The sealing ring 1350B also includes
three upper discrete portions 1352B that point down and are
disposed longitudinally above the row of discrete portions 1351B,
but above the spaces between adjacent ones of the portions
1351B.
[0166] The three upper discrete portions 1352B are disposed in the
same locations on the stent 1306 as the three discrete portions
1352 shown in FIG. 13A, and are generally aligned in the flow
direction below a corresponding commissure feature 1366. The three
lower discrete portions 1351B are disposed on portions of the stent
1306 circumferentially offset from the three upper discrete
portions, and are generally aligned in the flow direction with the
lowest portions 1311 at which the bellies of the leaflets 1310 are
attached to the stent 1306 and the cuff. Each of the upper discrete
portions 1352B extends around about 1/9 of the circumference of the
stent 1306, and each of the lower discrete portions 1351B extend
around about 2/9 of the circumference of the stent, such that
together, the upper and lower discrete portions extend around the
entire circumference of the stent.
[0167] FIG. 13C shows a sealing ring 1350C that is the same as the
sealing ring 1350B of FIG. 13B, except that, rather than forming
two peaks, the three lower discrete portions 1351C each form a
single peak that extends farther from the proximal end of the
stent. That is, each lower discrete portion 1351C points up and
extends from the proximalmost junctions 1309A of the stent 1306 to
the upper junctions 1309C of certain cells in the first full row
1313 of complete cells 1315, such that each lower discrete portion
extends both above and below the locations at which the bellies of
the leaflets 1310 are attached to the stent 1306 and cuff.
[0168] FIG. 13D shows another sealing ring 1350D that is similar to
the same as the sealing ring 1350 of FIG. 13A, except that the
continuous portion 1351D has the same alternating height zigzag
shape as the sealing ring 950 shown in FIG. 9A. The continuous
portion 1351D has low peaks 1361D substantially aligned in the flow
direction with the commissure features 1366 and with the upper
discrete portions 1352D, and high peaks 1362D substantially aligned
in the flow direction with the lowest attached portions 1311 of the
bellies of the leaflets 1310. Like the sealing ring 950 of FIG. 9A,
the continuous portion 1351D extends both above and below the
locations at which the bellies of the leaflets 1310 are attached to
the stent 1306 and cuff. The three upper discrete portions 1352D of
the sealing ring 1350D may be the same as the discrete portions
1352 of FIG. 13A.
[0169] FIG. 13E shows a further sealing ring 1350E that is similar
to the sealing ring 1350 of FIG. 13A, except that the sealing ring
1350E includes six discrete portions 1352E disposed above the
continuous portion 1351E. Three of the discrete portions 1352E are
the same as the discrete portions 1352 of FIG. 13A, which point
down and are each substantially aligned in the flow direction with
a corresponding commissure feature 1366. The other three discrete
portions 1352E point up and are disposed between the discrete
portions just described, and are substantially aligned in the flow
direction above the lowest attached portions 1311 of the bellies of
the leaflets 1310.
[0170] FIGS. 14A-14C illustrate prosthetic heart valve
configurations that have embodiments of sealing rings that are
variants of the sealing rings shown and described above, in which
the sealing ring embodiments include two sealing ring members each
extending around the circumference of the stent.
[0171] FIG. 14A shows a sealing ring 1450 that is a variant of the
sealing ring 950 of FIGS. 9A-9B. The sealing ring 1450 has a lower
continuous member 1451 and an upper continuous member 1452 adjacent
thereto. The upper continuous member 1452 has the same alternating
height zigzag shape as the sealing ring 950 shown in FIG. 9A, while
the lower continuous member 1451 has the same zigzag shape as the
sealing ring 550C shown in FIG. 5C. The lower member 1451 and the
upper member 1452 may be formed separately and attached to the
stent 1406 adjacent one another, or they may be formed together as
a single continuous piece of fabric, for example.
[0172] FIG. 14B shows a sealing ring 1450B that is a variant of the
sealing ring 450C of FIG. 4C. The sealing ring 1450B has a lower
continuous member 1451B and an upper continuous member 1452B
adjacent thereto. The upper member 1451B and the lower member 1452B
have the same zigzag shape as the sealing ring 550C shown in FIG.
5C and are spaced apart from one another in the flow direction of
the stent 1406. It is preferred that the lower member 1451B and the
upper member 1452B of the sealing ring 1450B be attached to a cuff
having a higher cuff height in the flow direction of the stent
1406, such as the cuff 712 of FIG. 7.
[0173] The lower member 1451B is attached to the stent 1406 and the
cuff following the zigzag contour of certain struts 1407 between
the proximalmost junctions 1409A of the stent, and the upper
junctions 1409B of the proximalmost struts of the stent. The upper
member 1452B may be attached to the stent 1406 and the cuff
following the zigzag contour of certain struts 1407 between the
upper junctions 1409C of the first full row 913 of complete cells
915 and the upper junctions 1409D of the second full row 1417 of
complete cells 1415 above the first full row.
[0174] FIG. 14C shows a sealing ring 1450 that is a variant of the
sealing ring 950 of FIGS. 9A-9B. The sealing ring 1450C has a
continuous member 1451C and discontinuous sections 1452C that
partially overlap one another.
[0175] The continuous member 1451C has the same alternating height
zigzag shape as the sealing ring 950 shown in FIG. 9A, but is
shifted longitudinally and circumferentially on the stent 1406 so
that the high peaks intersect with the commissure features 1466.
That is, the low peaks 1461 are substantially aligned in the flow
direction with the lowest attached portions 1411 of the bellies of
the leaflets 1410, while the high peaks 1462 are substantially
aligned in the flow direction with the commissure features 1466.
The low peaks 1461 are disposed at the upper junctions 1409C of the
first full row 1413 of complete cells 1415, and the high peaks 1462
are disposed at the commissure features 1466 which are at the upper
junctions 1409D of the second full row 1417 of complete cells 1415
above the first full row.
[0176] The discontinuous sections 1452C are the same as the
discontinuous sections 1251E of FIG. 12E, but the low end 1453 of
each discontinuous section may be attached approximately at the
height of the upper junctions 1409B of the proximalmost struts 1407
of the stent 1406, rather than being attached at the proximalmost
junctions 1409A of the stent.
[0177] Although the various sealing structures have been described
herein as "sealing rings," it is to be understood that the term
"sealing ring" as used herein may describe one or more
discontinuous sealing structures that do not completely extend
around the circumference of the stent of a prosthetic heart
valve.
[0178] Although the invention herein has been described with
reference to particular embodiments, it is to be understood that
these embodiments are merely illustrative of the principles and
applications of the present invention. It is therefore to be
understood that numerous modifications may be made to the
illustrative embodiments and that other arrangements may be devised
without departing from the spirit and scope of the present
invention as defined by the appended claims.
[0179] It will be appreciated that the various dependent claims and
the features set forth therein can be combined in different ways
than presented in the initial claims. It will also be appreciated
that the features described in connection with individual
embodiments may be shared with others of the described
embodiments.
* * * * *