U.S. patent application number 11/737474 was filed with the patent office on 2007-08-16 for prosthesis for annuloplasty comprising a perforated element.
This patent application is currently assigned to Sorin Biomedica Cardio. Invention is credited to Pietro Arru, Giovanni Bergamasco, Carla Stacchino.
Application Number | 20070191940 11/737474 |
Document ID | / |
Family ID | 27798967 |
Filed Date | 2007-08-16 |
United States Patent
Application |
20070191940 |
Kind Code |
A1 |
Arru; Pietro ; et
al. |
August 16, 2007 |
PROSTHESIS FOR ANNULOPLASTY COMPRISING A PERFORATED ELEMENT
Abstract
A prosthesis for annuloplasty comprising a laminar or tubular
element having a plurality of apertures along at least one portion.
Preferably, the shape, dimensions, and arrangements of the
apertures in this prosthesis are chosen in such a way as to give
the prosthesis a differentiated flexibility in dependence on the
location and direction of application of an external stress.
Inventors: |
Arru; Pietro; (Fraz. Vernone
(Torino), IT) ; Bergamasco; Giovanni; (Torino,
IT) ; Stacchino; Carla; (Torino, IT) |
Correspondence
Address: |
FAEGRE & BENSON LLP;PATENT DOCKETING
2200 WELLS FARGO CENTER
90 SOUTH SEVENTH STREET
MINNEAPOLIS
MN
55402-3901
US
|
Assignee: |
Sorin Biomedica Cardio
Saluggia
IT
|
Family ID: |
27798967 |
Appl. No.: |
11/737474 |
Filed: |
April 19, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10393448 |
Mar 20, 2003 |
7220277 |
|
|
11737474 |
Apr 19, 2007 |
|
|
|
Current U.S.
Class: |
623/2.37 ;
623/2.36 |
Current CPC
Class: |
A61F 2250/0018 20130101;
A61F 2/2448 20130101 |
Class at
Publication: |
623/002.37 |
International
Class: |
A61F 2/24 20060101
A61F002/24 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 27, 2002 |
EP |
02425190.2 |
Claims
1. An annuloplasty prosthesis for repair of a cardiac valve annulus
by affecting the dimensions or shape of the valve annulus, so as to
improve performance of the cardiac valve, the prosthesis
comprising: a ring element having a longitudinal axis, a curved
portion, and a generally straight portion, the ring element
configured to have a shape generally corresponding to a desired
shape of a normal cardiac valve annulus; and a sheath covering at
least a portion of the ring element; wherein the ring element
defines a plurality of apertures each having a characteristic
selected to effect the flexibility of the annuloplasty
prosthesis.
2. The annuloplasty prosthesis of claim 1 wherein the
characteristic includes one or more of a size, a shape, and a
location along the longitudinal axis.
3. The annuloplasty prosthesis of claim 1 wherein the apertures are
configured such that the curved portion is more flexible than at
least the straight portion.
4. The annuloplasty prosthesis of claim 1 wherein the ring element
is an open ring having a first end and a second end.
5. The annuloplasty prosthesis of claim 1 wherein the ring element
has a tubular cross-section.
6. The annuloplasty prosthesis of claim 1 wherein the ring element
has a laminar cross-section.
7. An annuloplasty prosthesis comprising a ring element having a
size and a shape generally corresponding to a cardiac valve
annulus, the ring element including a plurality of apertures for
controlling the flexibility of the annuloplasty prosthesis.
8. The annuloplasty prosthesis of claim 7 wherein the apertures are
disposed along at least a portion of the ring element and are
configured such that the prosthesis has a desired non-uniform
flexibility along its length.
9. The annuloplasty prosthesis of claim 7 wherein the apertures are
configured such that the prosthesis has a differentiated
flexibility depending on the location and direction of application
of an external stress.
10. The annuloplasty prosthesis of claim 7 wherein the prosthesis
is generally planar, and wherein the apertures are configured such
that the prosthesis has a first flexibility in response to a first
external stress acting in the general plane of the prosthesis and a
second flexibility in response to a second external stress acting
generally transverse to the general plane of the prosthesis.
11. The annuloplasty prosthesis of claim 7 wherein: the ring
element has a first portion and a second portion; and at least one
of a size, a shape, or a position of each aperture is selected such
that the first portion is more flexible than at least a part of the
second portion.
12. The annuloplasty prosthesis of claim 7 wherein the ring element
has a curved portion and a straight portion, and wherein the
apertures are configured such that the curved portion is more
flexible than the straight portion.
13. The annuloplasty prosthesis of claim 12 wherein the curved
portion includes first and second end regions and a center region
therebetween, and wherein the apertures are configured such that
the center region is more flexible than the first and second end
regions.
14. The annuloplasty prosthesis of claim 7 wherein the ring element
is an open ring having first and second ends.
15. A method of forming an annuloplasy prosthesis, the method
comprising: forming a plurality of apertures in a laminar or
tubular element, including configuring the apertures such that the
laminar or tubular element has a desired non-uniform flexibility
along its length; and forming the laminar or tubular element into a
ring element having a shape generally corresponding to a shape of a
natural cardiac valve annulus.
16. The method of claim 15 wherein forming the plurality of
apertures includes selecting at least one of a size, a shape, and a
location of each aperture such that the laminar or tubular element
has a desired non-uniform flexibility along its length.
17. The method of claim 15 wherein forming the plurality of
apertures includes configuring the apertures such that the
prosthesis has a differentiated flexibility depending on the
location and direction of application of an external stress.
18. The method of claim 15 wherein: forming the laminar or tubular
element into a ring element includes forming a generally planar
ring element; and forming the plurality of apertures includes
configuring the apertures such that the annuloplasty prosthesis has
a first flexibility in response to a first external stress acting
in the general plane of the ring element and a second flexibility
in response to a second external stress acting generally transverse
to the general plane of the ring element.
19. The method of claim 15 wherein: forming the laminar or tubular
element includes forming the laminar or tubular element into a ring
element having a curved portion and a generally straight portion;
and forming the plurality of apertures includes configuring the
apertures such that the curved portion is more flexible than at
least a part of the straight portion.
20. The method of claim 15 wherein forming the laminar or tubular
element includes forming the laminar or tubular element into an
open ring element having a center portion and first and second
ends.
Description
CROSS REFERENCE TO RELATED APPLICATION
[0001] The present application is a continuation of U.S. patent
application Ser. No. 10/393,448, entitled "PROSTHESIS FOR
ANNULOPLASTY COMPRISING A PERFORATED ELEMENT" filed Mar. 20, 2003
by Pietro Arru et al., which claims the benefit of European Patent
Application No. 02425190.2 filed Mar. 27, 2002. Each of the
foregoing U.S. and European patent applications is incorporated
herein by reference in its entirety. Any disclaimer of claim scope
that may have occurred during the prosecution of the
above-referenced application(s) is hereby expressly rescinded.
TECHNICAL FIELD
[0002] The present invention relates in general to a device for
cardiac valve repair operations and, in particular, to a prosthesis
for annuloplasty.
BACKGROUND
[0003] The human heart has four cardiac valves: the mitral valve,
the tricuspid valve, the pulmonary valve and the aortic valve. The
mitral valve is situated in the left atrio-ventricular ostium and
regulates the unidirectionally of the flow of blood from the atrium
to the ventricle. It opens in the diastole and closes in the
systole, preventing blood from flowing back from the ventricle to
the atrium. The annulus of a normally functioning mitral valve is
characterized by shape, dimensions and flexibility such as to allow
a correct closure of the valve lips during the systolic phase. For
example, the mitral annulus has a characteristic "kidney" shape (of
"D" shape), and is more flexible in the portion corresponding to
the posteria lip of the valve. Illnesses or genetic defects can
cause deformations or dilatations of the annulus of the mitral
valve, resulting in an incomplete closure thereof with consequent
regurgitation of blood. The same phenomena can occur in the
tricuspid valve, situated between the right atrium and right
ventricle.
[0004] A frequently used method for eliminating some pathological
alterations of the mitral and tricuspid valves is that of
reinstating the correct shape and dimensions of the valve annulus
by means of surgical procedures known as annuloplasty. Annuloplasty
comprises surgically implanting a supporting prosthesis on the
dilated or deformed annulus for the purpose of reinstating its
dimensions and/or physiological shape in such a way as to allow the
cardiac valve to function correctly.
[0005] Support prostheses utilized in valve repair operations are
called annuloplasty prostheses. In the majority of cases such
prostheses are constituted by a closed or open ring structure
comprising an inner core and an outer cladding of biocompatible
material which allows surgical suture.
[0006] Annuloplasty prostheses of various types have been described
in the prior art. Initially, the prostheses proposed were
predominantly of the rigid type for the purpose of drastically
reducing the dilatation of the valve annulus. Such prostheses are
generally constituted by a metal core (for example, a titanium
alloy), an optional sheath of cladding around the core, and an
outer cladding of textile for suturing. Rigid annuloplasty
prostheses are described, for example, in U.S. Pat. No. 4,055,861
by Carpentier et al., issued Nov. 1, 1977, and U.S. Pat. No.
3,656,185 by Carpentier et al., issued Apr. 18, 1972.
[0007] Rigid prostheses, although satisfactory as far as
reinstatement of the shape and dimensions of the valve annulus are
concerned, do not allow the annulus of the valve to flex along the
base of the posterior cuspid in such a way as to assist the cardiac
muscle movements. Consequently, significant stress is imposed on
the suture points subjected to torsion and traction, which prevents
natural behavior of the valve.
[0008] Subsequently, semi-rigid or completely flexible prosthesis
models were proposed. Completely flexible annuloplasty prostheses
are described, for example, in U.S. Pat. No. 5,041,130 by
Carpentier et al., issued Aug. 20, 1991, U.S. Pat. No. 5,716,397 by
Myers et al. issued Feb. 10, 1998, U.S. Pat. No. 6,102,945 by
Campbell et al., issued Aug. 15, 2000, and U.S. Pat. No. 5,064,431
by Gilbertson et al., issued Nov. 12, 1991. The completely flexible
prostheses follow the movements of the annulus during the cardiac
cycle in an optimal manner. However, they have the disadvantage of
not allowing the shape to be reconstructed in an optimal
manner.
[0009] Semi-rigid prostheses seek to unite the advantages of the
rigid type with those of the completely flexible type while
avoiding the disadvantages of each. Semi-rigid annuloplasty
prostheses are described, for example, in U.S. Pat. No. 5,061,277
by Carpentier et al., issued Oct. 29, 1991, U.S. Pat. No. 5,104,407
by Lam et al., issued Apr. 14, 1992, U.S. Pat. No. 5,674,279 by
Wright et al., issued Oct. 7, 1997, U.S. Pat. No. 5,824,066 by
Gross et al., issued Oct. 20, 1998, U.S. Pat. No. 5,607,471 by
Seguin et al., issued Mar. 4, 1997, and U.S. Pat. No. 6,143,024 by
Campbell et al., issued Nov. 7, 2000.
[0010] In particular, U.S. Pat. No. 5,104,407 describes a ring
prosthesis comprising an annular support element which is
substantially more rigid in one part than in the remainder. This
more rigid part projects transversely with respect to the general
plane in which the remaining part of the support element lies. On
the other hand, U.S. Pat. No. 5,607,471 describes a ring prosthesis
having variable transverse sections, and therefore differentiated
rigidity along its circumferential extent.
[0011] All these known prostheses have, however, limitations in
relation to the possibility of exhibiting a variable rigidity in
dependence on the point and/or mode of application of the stresses.
For example, U.S. Pat. No. 5,104,407 provides a structure with
variable rigidity in the plane of the ring, but with a limited
possibility of flexure outside this plane. On the other hand, U.S.
Pat. No. 5,607,471 describes technical arrangements able to
guarantee an improved flexibility out of the plane of the annulus.
However, the possibility of effectively obtaining characteristics
of variable rigidity of the prosthesis, for example, in its
localised portions as well, appears significantly limited by the
necessity to vary the area of the entire resistant section of the
internal element. Moreover, the technical arrangements described in
U.S. Pat. No. 5,607,471 do not allow an optimal behavior of the
prosthesis in response to stresses in a tangential direction to be
obtained (that is to say stresses directed along its longitudinal
axis, which is usually closed in a ring), the rigidity in response
to traction and compression at the same point of the internal
element being substantially undifferentiated.
SUMMARY
[0012] The present invention provides a prosthesis for
annuloplasty, the rigidity of which can be made variable in a
described manner in dependence on the point, direction and mode
(traction, compression, flexion, torsion) of application of the
stresses. According to the invention, this is achieved thanks to a
prosthesis for annuloplasty comprising a laminar or tubular element
having a plurality of apertures in at least one portion. This
element can then be defined hereinafter in the present description
as "perforated." In the perforated element, the apertures can be
formed substantially according to any arrangement and with any
shape and dimensions, so as to obtain the desired rigidity
variation. For example, a prosthesis provided with such a
perforated element can have markedly different rigidity whilst
having a constant transverse section, so as to satisfy possible
requirements of uniformity of dimensions.
[0013] The perforated element can be formed in its laminar form
both with a flat development and with various three-dimensional
shapes. Preferably, however, the perforated element is made in a
tubular shape because this shape allows a more flexible and
efficient arrangement of the apertures for the purpose of
influencing the properties of rigidity of prosthesis. As a matter
of fact, the transverse section of the perforated tubular element
can be of any shape. A circular transverse section is preferred for
reasons of practicality and simplicity of production.
[0014] The prostheses of the invention have the additional
advantage of an easier suturability since the apertures formed in
the perforated element can constitute, if necessary, preferential
transit ways for the passage of a suture needle.
[0015] There are no particular limitations in relation to the
material usable for the production of the perforated element. The
perforated element can be produced in metal, polymeric, or
composite material. For their part, the apertures can be formed in
the perforated element with any conventional technology. For
example, if the perforated element is made of metal, the apertures
can be formed by piercing a pre-formed tube by a laser,
electroerosion, or cutting. If the perforated element were formed
of polymeric material, it could be directly formed into its
definitive shape by moulding technologies. Overall, therefore, the
production of the prosthesis of the invention is simple and
economical.
[0016] Further advantages and characteristics of the invention will
become apparent from the following detailed description provided
purely by way of non-limitative example, with reference to the
attached drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] FIG. 1 is a plan view, partially in section, of a prosthesis
of the invention of closed ring type (or "closed loop type").
[0018] FIG. 2 is a prospective view, on an enlarged scale, of a
tubular element forming part of the prosthesis of FIG. 1.
[0019] FIGS. 3 to 6 are perspective views of respective alternative
embodiments of the tubular element of FIG. 2.
[0020] FIG. 7 is a plan view, partially in section, of a further
alternative open ring type (or "open loop type") embodiment of the
prosthesis of the invention.
DETAILED DESCRIPTION
[0021] The reference 10 indicates in FIG. 1 a prosthesis for
annuloplasty. The shape of this prosthesis generally reproduces the
geometry of the annulus of a mitral valve. This prosthesis has a
closed ring shaped in the form of a D with an approximately
rectilinear intertrigonal section 12 and a curved section 14. The
prosthesis 10 is externally clad, in a manner known per se by a
sheath 16 of biocompatible material. Preferably the sheath is made
from materials chosen from the group consisting of polymers,
synthetic textiles, biological tissues and their combinations. The
sheath 16 covers a tubular ring element 18 having a transverse
section of constant circular shape over its entire extent. The
element 18 has in its wall (FIG. 2) a plurality of circular
apertures 20 spaced along two lines parallel to the longitudinal
axis 22 of the element 18 and diametrically opposite one another
across the axis 22 in such a way that the apertures 20 have a
spatial orientation substantially parallel to the general plane of
the prosthesis 10. Preferably, there are no such apertures in the
intertrigonal section 12, which must be more rigid, whilst they
gradually become more closely spaced towards the central part of
the curved section 14, which must be more flexible. The internal
cavity of the element 18 may possibly be filled, partially or
totally, with elastomeric material 23, in particular silicone,
polyurethane and their mixtures, as for example described in U.S.
Pat. No. 10/164,358, filed Jun. 5, 2002, the contents of which are
hereby incorporated herein by reference.
[0022] The surface of the tubular element 18 and/or of the sheath
16 can be clad partially or totally with a thin layer of
hemocompatible carbon, for example turbostratic carbon. The
procedure for the production of such a cladding is, for example,
described in U.S. Pat. Nos. 5,084,151, 5,387,247, 5,370,684,
5,133,845 and 5,423,886, the contents of each of which are hereby
incorporated herein by reference. This cladding contributes to an
improved hemocompatibility of the prosthesis 10 and to a controlled
tissue growth of the receiving organism.
[0023] FIG. 3 illustrates an alternative embodiment of the tubular
element 18, which has, in addition to the apertures illustrated in
the preceding FIG., further apertures 20 disposed along two lines
parallel to the longitudinal axis 22 of the element 18 and
diametrically opposite across the axis 18 so as to have a
substantially transverse spatial orientation with respect to the
general plane of the prosthesis 10. The presence of apertures 20 in
the arrangement just described influences the rigidity
characteristics of the prosthesis 10 under the action of stresses
which act both in the general plane and transversely with respect
to it. In particular, the prosthesis can be rendered, for example,
less rigid against stresses which act in its general plane along an
antero-posterior direction (that is to say in a direction
distinguished by the reference numeral 24 in FIG. 1), with respect
to stresses which act in the general plane along a direction
orthogonal to the antero-posterior direction. As far as the
rigidity characteristics against stresses which act transversely
with respect to the general plane of the prostheses 10 are
concerned, they are for example chosen in such a way as to
facilitate the assumption of a saddle shape in certain phases of
the cardiac cycle.
[0024] The desired characteristics of variation in flexibility can
also be obtained with a suitable variation of the dimensions of the
apertures 20 of the element 18, as illustrated for example in FIG.
4.
[0025] FIG. 5 illustrates a further embodiment of the tubular
element 18, in which the apertures 20 are formed in the shape of
rings interrupted along a generatrix by a bridge 26 connecting
adjacent portions 28, also of annular shape, of the tubular element
18. Such apertures 20 can be characterized by their extent (a) in
the axial direction, the extent (b) in the axial direction of the
tubular portions 28 interposed between two adjacent apertures 20,
and the extent (c) of the bridges 26 in the circumferential
direction. The values of (a), (b), and (c) can be selected
independently at will and maintained constant or made to vary along
the axial extent of the element 18 so as to determine the rigidity
of the prosthesis 10 in a desired manner in dependence on the point
and direction of application of the stresses.
[0026] FIG. 6 illustrates a further embodiment of the tubular
element 18, in which the apertures 20 have a sinuous shape limited
in one or more portions by edges 30 in contact, or almost in
contact, in the absence of external stresses. A prosthesis provided
with a perforated tubular element 18 of this type opposes
enlargement of the apertures 20 with a predetermined force in
response to a traction stress, allowing the prosthesis to extend in
the axial direction, whilst further closure of the apertures 20 in
response to a compression stress is in fact prevented by the
contacting edges 30, so that the behavior of the prosthesis is
similar in this case to that of a rigid body. Such a prosthesis
thus has differentiated rigidity in response to stresses acting in
the axial direction, being rather rigid in response to compression
stresses but on the other hand deformable in response to traction
stresses acting in the opposite sense along the same direction.
Such behavior is particularly convenient for encouraging, on the
one hand, the natural dilatation of the annulus in the diastolic
phase and, on the other hand, to guarantee the absence of
compression and corrugation phenomena (pleating) following surgical
suture during a valve repair operation.
[0027] It goes without saying that the arrangements of the
apertures 20 previously illustrated and/or described can be
combined in any way in different portions of the same perforated
element 18 so as to regulate the rigidity of the prosthesis 10 in a
desired manner in dependence on the point and direction of
application of the stresses. Equally it is also possible, in
embodiments of the perforated element 18 not illustrated, to
arrange the apertures in an irregular manner rather than in a
regularly repeating pattern.
[0028] FIG. 7 illustrates a further embodiment of the prosthesis of
the invention having an open ring shape and having a perforated
element 18 of laminar or tubular structure. In this case, too, by
varying the shape, dimensions and/or spacing of the apertures 20 it
is possible to obtain the desired variations in rigidity.
[0029] Naturally, the principle of the invention remaining the
same, the details of construction and the embodiments can be widely
varied with respect to what has been described purely by way of
example, without by this departing from its ambit.
* * * * *