TRANSCATHETER VALVE

Abstract

A synthetic heart valve is made from a valve graft of synthetic material and more particularly expanded polytetrafluoroethylene (ePTFE). The valve graft has an upper portion defined by a first thickness and a lower portion defined by a second thickness which is greater than the first thickness. The valve graft is formed into a cylindrical sleeve having a diameter and a folded region. A flexible stent overlays the cylindrical sleeve, wherein a series of leaflets are formed in the lower portion of the sleeve, the leaflets defining a semicircular perimeter. The leaflets are sutured to the cylindrical sleeve and the cylindrical sleeve is sutured to the flexible stent, the stent having a plurality of bent cylindrical wire segments that are welded together and in which the sleeve is sutured to the wire, including the welded areas of the stent. The formed valve can be implanted using a balloon catheter.

Claims

1. A synthetic heart valve comprising: a valve graft made from a synthetic material and more particularly ePTFE, the valve graft having an upper portion having a first thickness and a lower portion having a second thickness which is greater than the first thickness, the sheet being formed into a cylindrical sleeve having a diameter; and a flexible stent overlaying the cylindrical sleeve, wherein a series of leaflets are formed in the lower portion of the sleeve, the leaflets defining a semicircular perimeter which is sutured to the cylindrical sleeve, the stent comprising a plurality of wire segments that are welded together, the cylindrical sleeve being sutured to the stent including weld areas of the stent.

2. The valve according to claim 1, wherein the valve graft is formed from one of a sheet or a cylinder.

3. The valve according to claim 1, in which the wire segments of the stent are made from a wire comprising platinum and iridium.

4. The valve according to claim 1, wherein the valve is a tricuspid valve.

5. The valve according to claim 1, wherein the sutures are made from expanded polytetrafluoroethylene.

6. A method for manufacturing a synthetic heart valve, the method comprising: providing a valve graft made from a synthetic biocompatible material, the valve graft including an upper portion having a first thickness and a lower region having a second thickness which is greater than the first thickness; cutting a plurality of leaflets from the lower portion of the valve graft; forming the graft into a cylindrical sleeve; suturing the leaflets to the cylindrical sleeve; and suturing the cylindrical sleeve to a flexible stent.

7. The method according to claim 6, wherein the synthetic material is expanded polytetrafluoroethylene.

8. The method according to claim 7, in which the sutures are made from expanded polytetrafluoroethylene.

9. The method according to claim 7, in which the valve is a tricuspid valve.

10. The method according to claim 7, in which the flexible stent is defined by a plurality of wire segments formed in a pattern, the segments being welded together to form a cylindrical form and in which the stent overlays the cylindrical sleeve.

11. The method according to claim 10, in which the wire segments comprise platinum and iridium.

12. The method according to claim 10, further comprising the step of securing the stent on a balloon catheter for implanting the valve.

13. The method according to claim 12, including the step of inflating the balloon catheter to radially expand the valve during implantation.

14. The method according to claim 13, wherein the valve graft is one of a sheet or a cylinder made from the synthetic material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIGS. 1(a)-1(b) represent sequential views of the manufacture of a synthetic valve in accordance with an embodiment;

[0015] FIG. 1(c) depicts a partial assembly view taken in section depicting the securement of a valve leaflet by suturing to a flexible stent;

[0016] FIG. 2 is a longitudinal representation of the valve leaflets of a synthetic valve made in accordance with an embodiment;

[0017] FIG. 3 is a detailed representation of a leaflet for a synthetic heart valve in accordance with an embodiment, the valve being made to an exemplary (specific) size;

[0018] FIG. 4 is a bottom perspective view of an assembled synthetic valve in accordance with an embodiment;

[0019] FIG. 5 is a top view of the assembled synthetic valve of FIG. 4;

[0020] FIG. 6 illustrates an assembled synthetic valve as further assembled to a balloon catheter for purposes of implantation;

[0021] FIGS. 7A and 7B are representative views of a synthetic valve that is made in accordance with another embodiment; and

[0022] FIGS. 7C and 7D are representative view of the synthetic valve of FIGS. 7A and 7B as sutured to a flexible stent.

DETAILED DESCRIPTION

[0023] The following description relates to the manufacture of a heart valve (such as a pulmonary valve), fabricated from a graft formed from a specific synthetic biocompatible material, namely expanded polytetrafluoroethylene (ePTFE) in accordance with various embodiments. According to one embodiment, the graft is formed from a multi-layered sheet and according to another embodiment the graft is made from a cylinder made from the synthetic biocompatible material. As described herein, the heart valve is a tri-leaflet valve having a plurality (three) of semicircular leaflets, in which the formed graft or sleeve of the valve and the leaflets are sutured to a flexible stent for implementation to a patient site using a balloon catheter. It will be readily understood that there can be other variations and modifications of the herein described valve design herein intended to be within the ambits of the invention.

[0024] First, and with reference to FIGS. 1(a) and 1(b), the formation of a valve graft 200 in accordance with a first embodiment is herein described. The valve graft 200 is formed from a sheet 202 of expanded polytetrafluoroethylene (ePTFE), commonly referred to under the tradename of Gore-Tex. The sheet 202 is cut initially longitudinally and is defined by a pericardial membrane having a thickness, according to this embodiment of 0.1 mm. The sheet 200 of the ePTFE material is further formed into a cylindrical sleeve having an upper portion 204 that is defined by a wall comprising of two layers (and therefore a thickness of 0.2 mm) and a lower portion 208 having a wall comprising of three layers (and therefore a thickness of 0.3 mm). The sheet 200 is formed into the cylindrical sleeve 216, as shown in FIG. 1(a). A folded region 220 is created at the respective edges of the sheet 200 to create a periphery having an interior diameter. The folded region 220 according to this embodiment is created proximate the respective edges of the sheet as formed by a vertically disposed fold line 224 extending over the height of the formed sleeve 216. When created the folded region 220, as herein represented, has a thickness in the upper portion 204 of 0.6 mm and a thickness in the lower portion 208 of 0.9 mm based on the overlap of sheet material in the folded region 220. According to this version, the folded region 220 is maintained by a continuous suture extending along the length of the fold line 224.

[0025] With reference to FIG. 1(b), the upper portion 204 and the lower portion 208 of the formed cylindrical sleeve 216 are divided (as shown by phantom line 228) and in which a series of connected leaflets 234 are formed in the lower (thickened) portion 208, as shown most closely in FIG. 1(b), indicating a total of three (3) identical valve leaflets 234. The leaflets 234 are each formed as semi-circular segments having a semi-circular perimeter that is sutured to the sleeve 216. The cylindrical sleeve 216 is secured by sutures 238 to the wire segments of a flexible stent 400, which is only partially shown in the vertical cross-sectioned view of FIG. 1(c). According to this embodiment, the sutures 238 which are also preferably made from ePTFE are CV-7 sutures having a diameter of 0.119 mm. Each formed valve leaflet 234 has a thickness of 0.1 mm and represents one layer of the formed graft 200.

[0026] FIG. 2 illustrates the three (3) leaflets 234 according to this tri-leaflet valve design, which includes the semicircular area of each leaflet 234 itself, the valve including a junction area or region 244 extending from the intersect point of adjacent leaflets and having a defined height dimension, shown by line 248, the junction region 244 extending along the entire circumference of the formed graft 200, which is shown in sheet form 202 in FIG. 2. In this example, the junction region above the dotted line is about 3-5 mm in height.

[0027] With reference to FIGS. 2 and 3, the parameters of an exemplary synthetic valve leaflet and graft are herein described. More specifically, the herein described valve has a diameter (D) of 26 mm. The circumference of the valve is measured by a r (or 7C D). Therefore and according to this specific embodiment, the circumference c is equal to 81.68 mm. The width of each leaflet 234 of the valve is equal to one third the circumference c, since the valve is a tri-leaflet valve as shown in FIG. 2. Therefore, the width (W) of each valve leaflet 234 at the phantom line 248 defining the junction region 244 according to this embodiment is 27.23 mm. The height (h) of each valve leaflet 234 due to its semi-circular configuration is determined (3/2)the leaflet width (W). Therefore and for this specific valve, the height h is 23.58 mm, which includes the height of the junction region 244 as shown in FIG. 3. Based on the sample herein described, the valve leaflet radius (r) is determined by the height of the leaflet shown as 2400.75. According to this embodiment, the value of r is equal to 17.68 mm. The height of the junction region 244 is defined as the leaflet height (h)leaflet radius (r), which according to this embodiment is equal to 5.89 mm. Finally, the total length (L) of the valve according to this embodiment is determined by the height of the leaflets (h)+6 mm, the latter dimension being a margin of 3 mm added to the top and bottom of the valve graft 200. This latter dimension can be suitably varied. According to this specific version, the total length of the 26 mm diameter valve is 29.58 mm.

[0028] Alternatively and with reference to FIGS. 7A-7D, a valve graft in accordance with another embodiment can be made from a cylinder of ePTFE pericardial membrane having a wall thickness of 0.1 mm. The dimensions of the valve leaflets 334 are identical according to this version, with the exception of the elimination of the folded area previously required by the layered sheet, which therefore further eliminates 6 layers or 0.6 mm from the wall of the formed valve and accordingly reduces the profile of the valve. As discussed herein and when mounted on the balloon of a delivery catheter, the nominal wall thickness of the sheet made from ePTFE is 1.2 mm as compared to a reduced maximal wall thickness of 0.6 mm in the case of a sleeve formed from a cylinder of ePTFE creating a 50 percent reduction in overall material thickness.

[0029] The following table summarizes the above-described valve parameters for a range of diameters (D) made in accordance with this embodiment, the diameter range extending between 14 mm and 34 mm.

TABLE-US-00001 TABLE I Valve Diameter Circumference Width Height Leaflet radius Junction Total Length 3.14 14.00 43.98 14.66 12.70 9.52 3.17 18.70 3.14 15.00 47.12 15.71 13.60 10.20 3.40 19.60 3.14 16.00 50.27 16.76 14.51 10.88 3.63 20.51 3.14 17.00 53.41 17.80 15.42 11.56 3.85 21.42 3.14 18.00 56.55 18.85 16.32 12.24 4.08 22.32 3.14 19.00 59.69 19.90 17.23 12.92 4.31 23.23 3.14 20.00 62.83 20.94 18.14 13.60 4.53 24.14 3.14 21.00 65.97 21.99 19.04 14.28 4.76 25.04 3.14 22.00 69.11 23.04 19.95 14.96 4.99 25.95 3.14 23.00 72.26 24.09 20.86 15.64 5.21 26.86 3.14 24.00 75.40 25.13 21.77 16.32 5.44 27.77 3.14 25.00 78.54 26.18 22.67 17.00 5.67 28.67 3.14 26.00 81.68 27.23 23.58 17.68 5.89 29.58 3.14 27.00 84.82 28.27 24.49 18.36 6.12 30.49 3.14 28.00 87.96 29.32 25.39 19.04 6.35 31.39 3.14 29.00 91.11 30.37 26.30 19.73 6.58 32.30 3.14 30.00 94.25 31.42 27.21 20.41 6.80 33.21 3.14 31.00 97.39 32.46 28.11 21.09 7.03 34.11 3.14 32.00 100.53 33.51 29.02 21.77 7.26 35.02 3.14 33.00 103.67 34.56 29.93 22.45 7.48 35.93 3.14 34.00 106.81 35.60 30.83 23.13 7.71 36.83

[0030] With reference to FIGS. 4 and 5, a flexible stent 400 is placed in overlaying relation onto the formed ePTFE sleeve. For purposes of this discussion, the valve graft 200 is shown, although the cylindrical graft 300 would be similarly attached. The flexible stent 400 utilized according to this embodiment is defined by a cylindrical body that is made from a plurality of fine wire segments 406. The fine wire segments 406 are joined together to form a tubular or cylindrical member. Each wire segment 406 is fabricated from a soft, highly malleable metal alloy that has been fully annealed in order to remove as much spring memory as possible. Preferably and for purposes of this embodiment, the wire material is fabricated from an alloy consisting of about 90 percent platinum and 10 percent iridium and having a tensile strength of between about 150,000 psi and 175,000 psi. Although a platinum-iridium wire is preferred, other alloys having similar properties, such as, for example, a gold nickel alloy may also be employed. More specifically, each of the wire segments 406 have a diameter of 0.33 mm according to this exemplary embodiment. Prior to winding the wire segments 406 into a cylindrical shape, each section is formed so that it contains a series of alternating sinusoidal bends. The bends can be formed, according to one version, by winding each strand of wire between rows of vertical pins projecting from the surface of a flat planar substrate (not shown) as described in WO 95/11720 and WO 98/14137, the entire contents of each document being incorporated herein by reference. The strand can be wound about the pins to create a desired sinusoidal shape with the appropriate number of bends with a free length of wire at each end of the formed segment forming a serpentine pattern.

[0031] Each wire segment 406 is wound into a cylinder and the cylinders are placed in axial alignment so that the apex of each bend section is located in close proximity with the apex of a bend section of an adjacent wound segment. The adjacent bend sections are then welded together at weld joints 408 in order to cojoin the segments and form the cylindrical body. The fee ends of the adjacent cylindrical wire segments 406 are bent into parallel overlapping alignment and are also conjoined using similar welds.

[0032] Each weld joint 408 is formed, preferably, so that the weld joint 408 lies inside the boundaries of the cylindrical stent 400 as described by the inside diameter and the outside diameter of the formed cylinder. Accordingly, the weld joint 408 does not protrude beyond the boundaries of the wire cylinder into regions where rough edges of the welds 408 might come into contact with tissue. The platinum-iridium wires of the stent 400 are laser welded at each weld joint and brazed with 24 carat gold.

[0033] As noted, the flexible stent 400 is disposed in overlaying fashion onto the formed valve graft 200, which includes the valve leaflets 234 that are already sutured to the sleeve 216 using CV-7 Gore-Tex sutures having a diameter of 0.05 mm. The cylindrical sleeve 216 is sutured to the stent 400, which may include the weld joints 408, as shown pictorially in FIGS. 1(c), 4 and 5.

[0034] As shown in FIG. 6, a valve made in accordance with the present invention can be attached onto a balloon catheter 500, which is part of an implantation delivery system. An exemplary catheter is described in greater detail in U.S. Pat. No. 5,860,966, which is incorporated herein by reference in its entirety and a catheter such as the Balloon-in-Balloon (BIB) catheter commercially manufactured and sold by NuMed, Inc. of Hopkinton, N.Y. The annealed nature of the wire material of the formed flexible stent 400 permits the sutured valve graft to be radially expanded by the balloon in which the stent 400 is configured to maintain the expanded configuration after expansion and removal of the catheter to complete implantation at the patient site.

[0035] As shown in FIG. 6 and by way of specific example, a 20 mm valve is mounted to a 20 mm BIB balloon, fitting a FR 20 opening in a catheter scale 510.

PARTS LIST FOR FIGS. 1-7D

[0036] 200 valve graft [0037] 202 sheet, synthetic material [0038] 204 upper portion [0039] 206 lower portion [0040] 216 cylindrical sleeve [0041] 220 folded region [0042] 224 fold line [0043] 228 phantom line [0044] 234 valve leaflets [0045] 238 sutures [0046] 240 height, leaflet [0047] 244 junction region or zone [0048] 248 line [0049] 300 valve graft [0050] 302 cylinder [0051] 334 valve leaflets [0052] 400 flexible stent [0053] 406 wire segments [0054] 408 welds or weld joints [0055] 500 balloon catheter [0056] 510 catheter scale

[0057] It will be readily apparent that other variations and modifications are possible within the inventive ambits described herein and in accordance with the following claims. For example, other flexible intraluminar stents can be used in conjunction with the valve graft tube or cylinder or other suitable stent delivery systems.