US3587115A - Prosthetic sutureless heart valves and implant tools therefor - Google Patents

Abstract

AN INNER RING CARRYING A CHECK VALVE IS ROTATABLY MOUNTED WITHIN AN OUTER RING, AND A SERIES OF SPACED WIRES ARE CONFINED BETWEEN THE RINFS WITH THEIR FREE ENDS POSITIONED IN OPENINGS IN THE OUTER RING. ROTATING THE INNER RING WITH RESPECT TO THE OUTER RING FORCES THE WIRE ENDS OUTWARDLY TO

PIERCE A FABRIC RING AND THE SURROUNDING HEART TISSUE AND THEN CURL BACK TOWARDS THE VALVE.

Description

United States Patent 3,371,352 3/1968 Siposs et a1. 3/1

3,409,013 11/1968 Berry 128/303 3,445,916 5/1969 Schu1te..... 29/458 3,464,065 9/1969 Cromic 3/1 OTHER REFERENCES Sutureless Prosthetic Heart Valves by G. J. Magovern et 21., The Journal of Thoracic & Cardiovascular Surgery, V01. 46, No.6, Dec. 1963, pp. 726-- 736. 3-1 HV.

Primary Examiner-Dalton L. Truluck Assistant ExaminerRonald L. Frinks Attorney--Knobbe and Martens Fowler [72] Inventor Dong]!!! S liiley 122229 8 99 Santa Ana, Calif. [21] Appl. No. 687,249 [22] Filed Dec. 1,1967 [45] Patented June 28, 1971 Continuation-impart 01 application Ser. No. 1. 8 My 1 12% mhenq ps [54] PROS'IHETIC SUTURELESS HEART VALVES ANDIMPLANT TOOLS THEREFOR 49 Claims, 30 Drawing Figs.

[52] [1.8.01 3", 128/334, 128/303 [51] Int. Cl. A6li 1/22 [50] Field oiSearch 3/1,l (HV); 128/334 [56] References Cited UNITED STATES PATENTS 3,143,742 8/1964 Cromie 3/1 PATENTEnJummn 3,5 11 15 sum 3 [1F 9 I INVENTOR. DONALD P SH/LE/ B Y Fan/4 5e, k/vase a GAME/G524.

4 T TOP/VE/S'.

PATENTEU JUH28 12m SHEET 5 OF 9 INVENTOR. 00NALD P .S'HILEy POM/L 51?, (NOBBIE 64/1454 54 4 4 7' TOIPNE/S,

PATENIEn Junzslsn 3.587.115

SHEET 7 UF 9 INVENTOR DONALD Sl-l/LE/ POM/LEE, K/V0555 a MA]? TENS ,QTTO/Q/VEYS.

lPRQSTlHlETlIC SUTURELESS HEART VALVES AND llMPlLANT TOQLS THEREFOR Cross-Reference to Related Application This invention is a continuation-in-part of U.S. Pat. application Ser. No. 547,580, filed May 4, 1966.

BACKGROUND OF THE INVENTION This invention relates to improvements in prosthetic devices, and, more particularly, to improvements in so-called sutureless prosthetic heart valves, which are really valves with self-contained sutures. The latter will be used to exemplify the operation of the invention.

with surgical techniques currently available, the complete replacement of a malfunctioning aortic, mitral or tricuspid heart valve is often attempted. While the mortality rate for such replacements, both short and long term, has improved considerably during the past few years, it still remains relative ly high. And, this is true even though the basic causes for most failures are fairly well understood.

The overall construction of the prosthetic, replacement valve is quite important. Projections or interruptions of the profile of the valve promote the formation of blood clots. Culde-sacs of low blood velocity at the margins of a replacement valve and the heart tissue encourage thrombus formation. Moreover, insufficient washing of the metallic parts of the prosthetic replacement contributes to high coronary failure rates.

There is also the recognized incidence of failure due to the trauma occasioned by the replacement operation itself. For most prior art prosthetic heart valves, fastening the valve in place requires an extended period of time. A number of hours of extra-corporeal prefusion and coronary pulmonary bypass is necessary, in part because the valve must be secured by sutures connecting the valve's sewing ring to the tissue surrounding the valvular orifice. While the sutures, the suture knots and various parts of the prosthetic valve itself all contribute to forming nidi which lead to thrombus formation, the extended periods of time alone often prove too much for the patients lowered resistance, and death results.

lt is one of the principal objects of this invention, therefore, to provide a prosthesis which can be fastened to the tissues surrounding a passageway in the body, e.g. the valvular opening in the heart, quickly and rapidly. In the case of heart valves, this will minimize coronary prefusion and reduce the danger of thrombus formation.

While the idea of a sutureless heart valve per se is not new, for example US. Pat. No. 3,143,742 which issued on Aug. 1], 1964 to H. W. Cromie, discloses one such valve, the sutureless heart valves of the prior art all have certain disadvantages. in some, it is necessary for a portion of the prosthetic valve to rest in overlying relation on both sides of the tissue defining the valvular opening in the heart. This increases the probability of the tissue surrounding the valve opening being torn upon insertion of the: valve. In others, the excessive exposed metal surfaces create difficulties since they uncertainly define the boundary between the valve structure itself and the heart tissue. in other prosthetic valves, the sewing ring is not attached to the periphery of the prosthetic valve properly. The sewing ring not only provides retention means for sutures when they are used to anchor the valve body to the tissue, but also provide a good matrix for the tissue to establish a fluid tight margin between the prosthetic valve body and the valvular opening.

Summary of the invention These and other shortcomings of prior art devices, of both the sutureless and suture-type prosthetic heart valves, are obviated by the present invention without changing the external appearance of the valve. A plurality of wire sutures are retained interior of the ring body of the novel prosthetic valve for movement to radially extended positions in which they firmly engage the tissue defining the valvular opening in the heart. The wire sutures which are normally contained between an outer and inner ring of the prosthetic device move into the tissue and back toward the rings without exposing any of their metal surface to the action of blood flow through the valve. Thus, the tendency of these metal surfaces in prior art devices to contribute to the unsteady margins between the prosthetic device and the endothelium lining or covering of the heart are reduced. The result is that thrombus formations and clot potentials are reduced.

Broadly speaking, the present prosthetic device has a plurality of wirelike sutures coupled to means for providing a retracted position wherein a substantial portion of each suture has a retracted configuration, and an operative position wherein these portions have a tissue piercing configuration different from that of the retracted position.

The heart valve of this invention, irrespective of whether it is a replacement for an aortic, mitral or tricuspid valve, comprises an outer ring having a plurality of peripherally spacedapart guide slots formed through it, an inner ring concentrically mounted interior of the outer ring for rotation with respect to it, a movable check valve assembly of either the ball-type or disc-type including a valve seat and longitudinally movable check member associated with the inner ring, the wire sutures have portions substantially fixed with respect to the inner ring at peripherally spaced-apart points and a set of their ends extend into the guide slots in the outer ring when the inner ring is in a rotationally retracted position with respect to the outer ring. Means are provided for maintaining the inner ring interior of the outer ring and for rotating the rings with respect to each other so that the wire sutures can move radially outward beyond the outer surface of the outer .ring into tissue-piercing piercing positions.

In one specific embodiment of the prosthetic heart valve of the present invention, the outer ring has a recessed shoulder to journal an outward projecting shoulder of the inner ring. When the inner ring is in its retracted position with respect to the outer ring, the wire sutures reside in an annulus between the inner and outer rings. Upon rotation of the inner ring with respect to the outer ring, the wire sutures are guided by the radial slots in the outer ring beyond the outer ring into generally circular shapes with the points of the suture wires coming to rest immediately adjacent the periphery of the outer ring. A cloth-sewing ring mounted around the outer edge of the outer ring overlying the radial slots is pierced and held by the extended wire sutures. The inner ring is held interior of the outer ring by the retaining force of the wire pins, and the inner ring is prevented from moving beyond the retracted and tissue-piercing positions by selecting the depth of the annulus, the thickness of the wire pins, their number and angular separation.

in a second embodiment of the prosthetic heart valve disclosed herein, there is provided an outer ring having a plurality of spaced-apart generally radial notches formed in its lower surface, an upper inner ring concentrically mounted interior of the outer ring, and a lower inner ring integrally attached to the lower part of the upper inner ring so that its flat upper surface contacts the shoulders defining the notches in the outer ring. The outer ring is trapped by the two inner rings which combine to form a U-shaped groove to hold the outer ring in rotatable relation thereto. Deformable wire sutures are positioned intermediate the innerand outer rings in an annulus with one set of their ends retained by the lower inner ring at spaced-apart radial points and the other set lying interior of the slots formed by the notches of the outer ring and the upper surface of the lower inner ring.

in yet a third embodiment of the present invention, the inner ring is L-shaped and has a series of angularly displaced shoulders defining a series of longitudinal notches which cooperate with an annular groove adjacent thereto to retain the pins. The wire pins are bent at their inner set of ends to ride in the longitudinal slots and the annular groove rather than in radial holes formed in the inner ring. The third embodiment also includes a series of serrations formed along the lower edge of the outer ring which engage the outer flared leg on the L-shaped inner ring to hold a fabric-sewing ring about the periphery of the outer ring in a position overlying the radial slots through which the wire pins are extended into tissuepiercing positions.

In a fourth embodiment of the present invention, two series of spaced slots or openings are formed in one ring for receiving opposite ends of U-shaped sutures. The legs of the sutures are confined within a pair of annular grooves in the outer surface of the other ring while the bight of each suture is retained within a slot formed in a rib extending between the two grooves. Utilizing two rows of tissue-piercing sutures improves the connection between the valve and the adjacent heart tissue. To further enhance the connection, the sutures of one series are advantageously circumferentially offset with respect to those of the other series.

In addition to the various embodiments of the prosthetic sutureless heart valves constructed in accordance with the present invention which are disclosed herein, there is disclosed a series of tools for implanting the valves. These tools generally comprise an elongate outer tubular body having a lower locking cup adapted to rotatably hold the outer ring ofa prosthetic valve assembly, an inner shaft slideably and rotatably supported interior of the tubular body, an intermediate tubular member rotatably disposed between the body and the inner shaft with its lower end having a locking cup adapted to rotationally lock the inner ring of the valve assembly to the intermediate member at the same time the outer ring is rotationally locked to the tubular body. The inner shaft member has retaining means associated with its lower end operable to retain the inner ring adjacent the lower end of the intermediate tubular member. Means are also provided at the upper end of the tool to operate the retaining means and to rotate the intermediate member with respect to the body.

These tools permit the various prosthetic valves disclosed herein to be positioned adjacent a valvular opening in the heart and permit the inner ring to be rotated with respect to the outer ring to set" the wire pins into the tissue adjacent the outer edge of the outer ring.

In addition to the prosthetic heart valves and implant tools therefor, there is also disclosed herein a means of assembling a sutureless heart valve of the type described comprising the steps of mounting the inner ring in the outer ring with the peripherally spaced-apart apertures of the outer ring aligned with the peripherally spaced-apart wire retention points of the inner ring, positioning individual suture wires in the apertures and attaching each to a retention point, and rotating the inner ring to a retracted position with respect to the outer ring to draw the suture wires interior of the outer-inner ring configuration.

DETAILED DESCRIPTION AND DRAWINGS These and other objects, advantages and features of the present invention will be more fully understood when the following detailed description is read with reference to the drawings, in which:

FIG. 1 is a perspective view of a first embodiment of an aorta disc type prosthetic valve constructed in accordance with the present invention and an exemplary implant tool used to install the prosthetic valve in the aorta valve opening of the heart;

FIG. 2 is a side cross section view of the aortic prosthetic valve and implant tool of FIG. 1 with the valve retained by the implant tool adjacent the aortic-ventricle opening in the heart;

FIG. 3 is a plan section view of the implant tool means for setting the prosthetic valve to its tissue-piercing position taken along line 3-3 of FIG. 1;

FIG. 4 is an exploded perspective of the lower end of the implant tool illustrated in FIGS. 1 and 2 which retains the prosthetic valve and sets it during installation in the heart;

FIG. 5 is an enlarged horizontal sectional view of the prosthetic valve of FIG. I with the valve in its retracted positron;

FIG. 6 is also an enlarged horizontal sectional view of the prosthetic valve of FIG. I but with the valve in its tissue-piercing position;

FIG. 7 is an enlarged partial diametral section view of one side of the aortic prosthetic valve constructed in accordance with the invention to illustrate the interrelationship of the inner and outer rings and wire sutures thereof;

FIG. 8 is an enlarged perspective of the bottom of the aortic prosthetic valve of FIG. 1 in its retracted position with certain parts cut away to more clearly show the construction thereof;

FIG. 9 is an enlarged perspective of the bottom of the valve of FIG. 1 in a position intermediate its retracted and tissuepiercing positions with certain parts cut away to more clearly show the construction thereof;

FIG. 10 is an enlarged plan view of the disc valve of FIG. 1;

FIG. 11 is a partial enlarged plan view of a modification of the disc valve of FIG. 1;

FIG. 12 is an exploded perspective of the lower end of an implant tool for holding and setting a ball-type aortic prosthetic valve constructed in accordance with a second embodiment of the present invention to minimize the radial thickness of the valve rings;

FIG. 13 is an enlarged partial diametral section view of an aortic prosthetic valve taken along line 13-13 of FIG. 12 to illustrate the relationship between the outer ring, the inner rings and the wire sutures;

FIG. 14 is a section view of the aortic valve of FIGS. 12-13 taken along line 14-14 of FIG. 13;

FIG. 15 is an enlarged exploded perspective of the outer ring, inner rings and wire sutures of the mitral valve of FIGS. 12-44;

FIG. 16 is a top perspective of a dual cage aortic prosthetic valve constructed in accordance with a third embodiment of the present invention with certain parts cut away to more clearly show the construction thereof;

FIG. 17 is an enlarged partial section view taken along line 17-17 of FIG. 16 to show the disc and valve seat;

FIG. 18 is a section view taken along line 18-18 of FIG. 17 to illustrate the cloth retention means of the third embodiment;

FIG. 19 is an enlarged section taken along a line such as 17-17 of FIG. 16 to illustrate a modification of the third embodiment of the invention as illustrated in FIG. 17;

FIG. 20 is a side view of an implant tool positioning a mitral disc valve in the heart;

FIG. 21 is a side cross section view of the mitral prosthetic valve and implant tool of FIG. 20 with the valve retained by the implant tool adjacent the left auricle-ventricle opening in the heart;

FIG. 22 is an enlarged exploded perspective of the lower end of the implant tool of FIG. 20 and the mitral prosthetic valve which it is designed to set;

FIG. 23 is a perspective view of a prosthetic valve constructed in accordance with a fourth embodiment of the present invention;

FIG. 24 is a perspective exploded view of the valve of FIG. 23;

FIG. 25 is an enlarged, cross-sectional, elevational view of one side of the valve of FIG. 23;

FIG. 26 is an enlarged cross-sectional view of a circumferential portion of the valve on line 16-26 of FIG. 25, showing the sutures in a retracted position;

FIG. 27 is a view similar to that of FIG. 26 but with the sutures in their tissue-piercing positions;

FIG. 28 is a linear development of a portion of the side of the valve with a portion of the outer ring cut away to illustrate the position of the sutures in the fully retracted position;

FIG. 29 is a developmental view similar to that of FIG. 28 but with the sutures in their extended positions; and,

FIG. 30 is a fragmentary linear developmental view of a side of the valve illustrating the manner in which the inner and outer rings are assembled.

In the descriptions to follow, the orientation of the valve and implant tools will be described with the upper part of the valve being the part defining a valve seat and having the movable check member, whether of a ball or disc-type, cooperating therewith. This procedure will be followed irrespective of whether the valve is designed to be used to replace a mitral, tricuspid or aortic valve. Similarly, the implant tools will be described with reference to their vertical orientation in FIGS. 2 and 21. The upper'part of the tools being those parts towards the upper part of the drawings. The lower part of the tools are adapted to cooperate with the prosthetic valves during the im plant operation.

Valve Embodiment of FIGS. l

A first specific embodiment of the sutureless prosthetic heart valve of the present invention is disclosed in FIGS. 1- --1t) in conjunction with an exemplary implant tool for setting it in the valvular opening presented after a mitral or tricuspid valve has been removed from the heart. This exemplaryprosthetic heart valve 10 comprises broadly anouter ring 11,

aninner ring 12 mounted for rotation interior of the outer ring, a plurality of wire sutures or pins 13 cooperating with or coupled to the outer andinner rings 11 and 12, avalve seat 14 formed on the upper side of theinner ring 12 and amovable check member 15 cooperating. therewith. There are also provided for cooperation with the basic components of theprosthetic valve 10, asewing ring 16 which is mounted peripherally around theouter ring 11 and a retainingcage 17 adapted to retain themovable check member 15 in operative juxtaposition to thevalve seat 14.

Whereas FIG. 1 illustrates the first embodiment in assembled condition adjacent the end of an implant tool 71 for setting the valve, the various parts of the valve itself can be more easily seen if reference is made to FIGS. 59. FIG. 5 illustrates theinner ring 11 in its retracted position with respect to the outer ring 12 (wire pins 13 retracted), whereas FIG. 6 illustrates the two rings in the expanded position (wire pins 13 in extended tissue-piercing positions). FIG. 7 is a partial cross section which illustrates the manner in which theouter ring 11 and theinner ring 12 cooperate with the wire sutures or pins 13. FIGS. 8 and 9 also clarify the cooperation of the parts.

Theouter ring 11 is circular in cross section and has an inwardly extending shoulder 31 which acts to journal theinner ring 12 for rotation with respect thereto. It also prevents theinner ring 12 from moving through (i.e., below) the openouter ring 11 as will be explained in more detail hereinafter. There are a series of fourupstanding lugs 33 formed at peripherally spaced-apart points along the upper, outer surface of theouter ring 11 to cooperate with an implant tool such as 71.

Towards the center portion of the outer ring 11 (with respect to the longitudinal axis of thevalve 10 along which the valve disc or check member moves), there are provided a plurality ofradial slots 35 at circumferentially spaced-apart points on thering 11. Theseslots 35 act to receive the wire sutures 13 which are expanded into tissue-piercing positions. Towards the lower part of theouter ring 11 and on its outer surface there is provided agroove 37 which is adapted to receive the retaining means for thesewing ring 16.

Theinner ring 12, which is journaled for rotation in theouter ring 11, includes an outwardly projectingshoulder 39 on its upper end which is adapted to ride on the shoulder 31 of theouter ring 11. Theinner ring 12 has a plurality of apertures 41 formed at peripherally spaced-apart points about its outer surface to receive one set ofends 43 of the wire sutures 13 with which it isdesigned to cooperate. There is also, as noted above, avalve seat 14 formed on the upper surface of theinner ring 12 to cooperate with themovable valve disc 15.

Theinner ring 12 is journaled for rotation by theouter ring 11 by the upper projectingshoulder 39 and a lower outwardly projecting shoulder 45 formed integral with theinner ring 12. These contact the surfaces formed by the inwardly extending shoulder 31 of theouter ring 11 and thesurface 47 at the lower part of theouter ring 11.

The wire sutures 13 are equalin number to the number ofradial slots 35 formed in theouter ring 11 and the number of apertures 41 formed in theinner ring 12. One set ofends 43 of the wire pins 13 are secured in the apertures 41 formed in peripherally spaced-apart points on theinner ring 12 and the other set ofends 49 are disposed freely in therespective slots 35 formed peripherally about and through the outer ring 1 1.

Thebody portions 50 of the suture pins 13 are disposed in an elongated chamber in the fonn of anannulus 52 formed between the adjacent sides of the inner andouter rings 11 and 12. Theannulus 52 is of sufficient depth along the longitudinal axis 55-55 of the valve and implant tool to accommodate thebodies 50 of those wire suture pins 13 which are held between pairs ofslots 35 and retaining points 41.

In order to assemble thevalve 10 of this first embodiment, theinner ring 12 is concentrically mounted in theouter ring 11 as illustrated particularly in FIG. 7, and the series ofslots 35 are aligned with the apertures 41 in theinner ring 12. Since the angular separation a between theadjacent slots 35 coincides with the separations between the apertures 41 and theinner ring 12, all of the pairs align. At this point, a series of wires that are to form the wire pins 13 are inserted from the outside through theslots 35 into the retention points formed by the apertures 41 of theinner ring 12. Thereafter, theinner ring 12 is rotated counterclockwise with respect to the outer ring 11 (when viewed from the top of the prosthetic valve as illustrated in FIGS. 5 and 6) causing the wires to conform to the elongated shape of theannulus 52. Theinner ring 12 is rotated counterclockwise (approximately 30 until it reaches its fully retracted position. At this point theinner ring 12 is rotated a small distance clockwise with respect to theouter ring 11 and the wires are cut off and the outer set ofends 49 are pointed as illustrated in FIGS. 5 and 6.

As illustrated in FIG. 6, the tissue piercing positions are the fully expanded positions for the wire suture pins 13 and are defined by the point at which thepins 13 have been curled back on themselves and ends 49 are adjacent the outer surface of theouter ring 11.

The retracted position is determined by rotation of the inner ring with respect to the outer ring through the angle a, which in the exemplary embodiment is approximately 30 (see FIGS. 5 and 6). The retracted position itself is normally determined by the longitudinal depth of theannulus 52 as it is related to the peripheral spacing of theslots 35 and apertures 41 and the diameter of the wire pins 13. As can be seen particularly in FIG. 7, the longitudinal height or depth of theannulus 52 is selected so that a pair of the wire pins 13 can be longitudinally stacked in theannulus 52 without binding. As soon as theinner ring 12 is rotated with respect to theouter ring 11 to the point where athird wire pin 13 needs to move into theannulus 52 along with the two then occupying it, it binds or jams theinner ring 12 with respect to theouter ring 11. This point roughly defines the fully retracted position.

The defining of the retracted position can be understood by examining FIGS. 8 and 9. FIG. 8 illustrates the exemplary prosthetic heart valve in its fully retracted position where two adjacent wire pins 13 lie one over the other in theannulus 52. As theinner ring 12 is rotated to the tissue-piercing position with respect to theouter ring 11, the wire pins 13 move outwardly from theouter ring 11. FIG. 9 illustrates an intermediate point of this movement. In the tissue-piercing position, twoadjacent pins 13 barely overlap in theannulus 52. Upon relative rotation in the opposite direction, a position is reached in which athird wire pin 13 must move into the longitudinal annulus space already shared by the two.

The height of the annulus and the diameters of the wires are such that the movement of the third pin tends to jam the inner andouter rings 11 and 12 together, thereby resisting further clockwise rotation of theinner ring 12. A note of caution must be interjected as to the embodiment illustrated in FIGS. 1- -10, however, since excessive clockwise rotation of the inner ring will cause the third wire pin to cam theinner ring 12 upward and out of theouter ring 11 unless some position stop at the retracted position is provided or the inner ring is axially locked to the outer ring. This is done in some embodiments, e.g. the modification of FIG. 11, but in this first embodiment no such restraint is imposed.

ln this first embodiment, the camming out" is avoided by using an implant tool to load the wires. As will be explained hereinafter, the implant tools have positive stops for the retracted and expanded or tissue-piercing positions which will not permit the valves to be overretracted or overexpanded. Of course, the resistance the third pin creates acts to warn an as sembler that the retracted position has been reached.

As noted above, FIG. illustrates the prosthetic heart valve of the type disclosed in FIGS. l-10 in its retracted position with theouter tips 49 of thesutures 13 interior of theslots 35. FIG. 6 illustrates the same plan view of the prosthetic valve when theinner ring 12 has been rotated to the tissue-piercing position. At this point, the wire sutures 13 have been caused to curl back on themselves to complete a circle and terminate theends 49 of the wire pins 13 adjacent the outer surface of theouter ring 11. This curling can be guided by the shape ofslots 35 if the wire is deformable or precurled wires can be used which are straightened out in the annulus before the valve is set.

There can be a plurality of indentations orsmall depressions 57 formed on the outer surface of theouter ring 11 intermediate theslots 35 to receive thetips 49 of the suture pins 13 and anchor them firmly after the valve has been set."

The wovenfabric sewing ring 16 which is mounted about the periphery of theouter ring 11 is affixed in thegroove 37 by a circular retaining ring 59 formed of Teflon or some similar material which is expandable to permit it to snap into place. By containing the ring 59 completely within thesewing ring 16, it is possible to assure that only thesewing ring fabric 16 contacts thetissue 18 of the heart defining the valvular open mg.

A modification of the prosthetic heart valve illustrated in FIGS. 1-10 is shown in FIG. 11. Basically, the organization of the various parts are identical except that there is provided a positive lock to maintain theinner ring 12 interior of theouter ring 11 after the wire pins 13 have been inserted and theinner ring 12 has been rotated to its retracted position. There is provided a series of fourupstanding lugs 61, which are similar to theupstanding lugs 33 used in connection with the embodiment of FlGS. 110, that cooperate with an implant tool. In the modification illustrated in FIG. 11, however, theupstanding lugs 61 have inwardly projectinglips 63 thereon so that they overlie the upper surface of theinner ring 12. In normal operation, theinner ring 12 is prevented from moving upward and out of theouter ring 11 by the inwardly extendinglips 63 on thelugs 61, and is prevented from moving downwardly and out of concentric relation toouter ring 11 by virtue of the outwardly extendingshoulder 39 which contacts the annular shoulder 31 on theouter ring 11.

In order to initially place theinner ring 12 interior of theouter ring 11, there are a number oflongitudinal slots 65 formed along the outer surface of theinner ring 12 at angular separations identical to those defining the positions of theupstanding lugs 61. By rotating theinner ring 12 with respect to theouter ring 11 to register thelug 61 with theslots 65, it is possible to place theinner ring 12 in theouter ring 11 with the inwardly extendinglip 63 in registration with theslots 65. Once theinner ring 12 is concentrically mounted in theouter ring 11, however, theinner ring 12 is rotated with respect thereto to displace the inwardly extendinglips 63 from theslots 65 so that theinner ring 12 cannot be removed during normal operation. The location of theslots 65 is selected so that they do not register withlips 63 when theinner ring 12 is in its retracted position, its tissue-piercing position or anywhere between these positions. Hence, there is no way for the inner ring to ride out of the outer ring.

Before describing the other embodiments of the prosthetic heart valve disclosed and claimed herein, it is appropriate to consider the implant tool used to set the valve illustrated in FIGS. 1 11 in the valvular opening of the heart. Such a tool is illustrated in FIGS. 1-4. Before describing the implant tool itself, it is worthwhile noting the particular operations that have to be performed to set" the prosthetic valve in an opening of the heart.

Taking as an example the setting of a valve in the aortic opening of the heart, it can be appreciated that the natural valve will have been removed leaving a roughly circular opening of muscular tissue defining the aperture between the aorta and the left ventricle (as illustrated, for example, in FIG. 20).

To implant the valve therein, it is necessary to hold the valve in the opening defining the aorta and left ventricle while rotating theinner ring 12 with respect to theouter ring 11 to cause thewire 13 to move outwardly into tissue-piercing positions. Basically, therefore, it is necessary to support the prosthetic valves outer ring in a nonrotatable position in the opening while providing means for rotating the inner ring with respect to the outer ring. This is precisely what the implant tool illustrates in FIGS. 1-4 does.

The implant tool 71 includes generally a hollowcircular body 73 having an enlargedopen cup 75 at its lower end adapted to overlie the upper surface of theouter ring 11 and to hold theouter ring 11 in a nonrotatable position with respect to thebody 73. To do this, the lowercircular member 75 has formed in its lower edge a series ofnotches 77 which are angularly spaced from each other to coincide with the angular separation between thelugs 33 formed on theouter ring 11 of the disc-type valve of FIGS. 1--10. The notches orslots 77 engage theupstanding lugs 33 to rotatably lock thebody member 73 and theouter ring 11 together.

A solidinner shaft 79 is supported interior of thebody 73 for rotation and axial movement. The lower end of theshaft 79 has a flat generally rectangular-shapedretainer plate 81 attached to it (see FIG. 4). Theshaft 79 is biased upwardly by acoil spring 83 which coacts between anexterior cap 85 attached to the upper end of theshaft 79 and theupper surface 86 of thebody 73.

There is also provided in the implant tool 71 a hollowintermediate shaft 89 which is journaled for rotation by the lowercircular member 75 of thebody 73 and an interior upper part of thebody 91. Apinion gear 93 is staked to the upper end of the intermediaterotatable member 89 and acts to journal that end of themember 89 in thebody 73. Attached to the lowermost end of theintermediate member 89 is aninverted cuplike member 95 having a pair of symmetricallyopposite slots 96 formed in parallel planes and adapted to correspond to the separation between thewire cages 17 of thevalve 10. As previously noted, thelower end 95 ofintermediate member 89 is joumaled by the interior surface of thelower cup 75.

Theinner shaft 79 normally rotates freely with theintermediate shaft 89 and in conjunction therewith acts to lock theinner ring 12 against the interior of the downwardly dependingcup 95 which is attached to the lowermost end of theintermediate member 89.

The width of theretainer plate 81 onshaft 79 is selected so that it can move freely between the pair ofcages 17 of the disc valve illustrated in FIGS. 1-10. When thecap 85 is pushed downwardly, theshaft 79 moves theretention plate 81 down so that it may be moved through the twoU-shaped cage members 17. Thereafter, it is rotated (as illustrated generally in FIG. 4 by the dotted line perspective) to a position where the outer edges thereof engage the under sides of thecages 17 to firmly hold the cages against the cup on theintermediate member 89. This, in turn, holds thecup 75 against the upper surface of theouter ring 11. By this means, the implant tool 71 provides a positive support for thedisc valve 10 and rotationally locks theouter ring 11 to fixed position of thebody 73.

Theintermediate member 89 is rotated by way of thepinion gear 93 through aworm gear 97 which is rotatably mounted in the upper part of thebody 91 at right angles to thepinion 93. Ahandle 99 is provided exterior of thebody 73 to permit the ummm nan:

worm gear 97 to be rotated thereby rotating theintermediate member 119.

In operation, the implant tool 71 is used as follows: thelower part 75 of thebody 73 depends over the upper part of thevalve 111 as illustrated in FIG. 1 so that theslots 77 engage theupstanding lugs 33. At the same time, theinner shaft 79 is rotated by way ofknob 85 until theretainer plate 81 at its lower end can be moved between thewire cages 17. At that point, theinner shaft 79 is moved downwardly against thespring 33 and rotated approximately 90 so that the outer ends of theretainer member 81 engages the underside of thecages 17 to hold theinner ring 12 firmly inside of the dependingcup 95 attached to theintermediate member 89. Since there are provided a pair ofparallel slots 96 in the outer edge of the dependingcup 95, these fit over thewire cages 17 and permit theinner ring 12 to be rotated by the rotation of the intermediate member.Shaft 79 rotates withintermediate member 89.

Once the prosthetic valve has been properly attached to the lower end of the implant tool 71, the valve is positioned in the aortic opening with the surgeon holding theimplant tool body 73 in one hand. Once properly positioned, thehandle 99 may be rotated to cause theintermediate shaft 89 to rotate. This moves the wire pins 13 outwardly towards their tissue-piercing positions. To avoid any excessive retraction or extension of the wire pins 13, thepinion 93 has aslot 101 out in one edge thereof corresponding to the angle a through which theinner ring 12 rotates with respect to theouter ring 11 between the fully retracted and the fully extended or tissue-piercing positions. An inwardly extendingpin 103 is attached to theupper part 91 of the body and projects into theslot 101 to act as a stop between the retracted and fully extended positions of the valve. These positions are shown on the upper end of tool 71 as the retracted (R) and open positions which cooperate with index line 104. By this positive means, it is impossible to overset" thepins 13 when a valve is being implanted in an opening of the heart; Moreover, if valves such as 111 are assembled by using implant tool 71 or a similar type of device, it is impossible to draw the pins too far into the retracted position thereby causing the inner and outer rings to separate along the longitudinal axis 55-55 of the valve. In this case, the outwardlydisposed lips 63 on the FIG. 11 modification of the first embodiment are not needed.

Valve Embodiment of FIGS. 13

A second embodiment of a prosthetic valve constructed in accordance with the present invention is disclosed in FIGS. 13-15. The concept of this embodiment is similar to that disclosed in F IGS. 110, but the modifications are designed to minimize the radial thickness of the inner and outer rings so that a maximum prosthetic valve orifice area is obtained.

Thevalve 110 includes anouter ring 111, an upperinner ring 112 and a lower inner ring 1113. In order to reduce the width of the valve structure, the plurality of wire pins 115 are secured in the lowerinner ring 113 which is generally below theouter ring 111. By positioning the retention points 117 for the inner set ofends 118 of the wire pins 1 15 outwardly of the part of the inner ring which includes the valve seat, it is possible to minimize the overall thickness of the valve structure.

Theouter ring 111 is constructed somewhat similarly to ring 11 of the embodiment of FIGS. 1-10 in that it includes an inwardly extendingshoulder 119 and a series ofupstanding lugs 121 adapted to cooperate with an implant tool such as 71. However, rather than having a series of slots such as 35 formed peripherally about and through the outer ring, thelower surface 123 of theouter ring 111 has a series of spacedapart radially orientednotches 125 formed therein through which the wire pins 115 are adapted to move between their retracted and tissue-piercing positions. Thelowermost surface 123 contacts theupper surface 127 of the lowerinner ring 113 to form the series ofslots 129 which are comparable toslots 35 of the first embodiment.

In assembling the embodiment illustrated in FIGS. 1315, the lowerinner ring 113 has the plurality of wire pins retained in the series of spaced-apart apertures 117 with the outer or free ends 130 of thewires 115 lying along theupper surface 127 thereof. At this point, theouter ring 111 is placed over the lower inner ring 113 (as illustrated particularly in FIG. 15) to form the series ofradial slots 129 in spaced peripheral relation between theouter ring surface 123 and the lowerinner ring surface 127.

Thereafter, the upperinner ring 112 is disposed concentric to theouter ring 111 and the lower inner ring 113 (as is most clearly illustrated in FIG. 13). Once the outer ring and two inner rings are mounted with the series of wire pins 115 disposed in theretention apertures 117 and in theslots 129, the lowerinner ring 113 and the upperinner ring 112 are welded or otherwise bonded together, e.g. by forming a bead at 131. Thus, theinner rings 112 and 113 form a generally U- shaped inner ring member concentrically mounting theouter ring 111 in the bite of the U for rotation with respect thereto. Again, as in the preceeding embodiment of FIGS. 110, there is provided an elongated, interior chamber in the form of anannulus 133 to receive and stack the wire pins 115. The longitudinal depth of this annulus and the diameter of the wires are selected to again provide a stop for the retracted position of theinner ring assembly 112--1 13 as it rotated with respect to theouter ring 111.

It can be appreciated in connection with this embodiment, that it is not possible to assemble the wires and inner and outer ring elements in the same manner as was possible and desirable with the embodiment disclosed in FIGS. 110. Instead, the wire pins 115 are desirably preformed and disposed in theinner ring 113 and in the slots formed by theouter ring 111 and theinner ring 113 in advance of assembling thedevice 110. It will be noted that this particular arrangement permits the necessary radial spaced taken up by thelower retention points 117 for the wire pins 115 to under lie theslots 129 formed between theupper ring 111 and the lowerinner ring 113 so that a double radial width need not be provided.

It will also be noticed in the exemplary embodiment of FIGS. 13-15 that the prosthetic valve employs a ball rather than a flat disc check valve member. While the advantages and disadvantages of ball-type prosthetic devices as opposed to disc types are well known, for the purposes of the present invention it is immaterial which is used, although the embodiment of FIGS. 1315 utilizes a ball-type to show the interchangeability of the two types of check members.

In this particular embodiment, thevalve seat 135 is formed on the inner upper part of the upperinner ring 112 and theball 137 seats against it. A retainingcage 139 is provided for theball 137 which includes threepost members 141 connected to the upperinner ring 112 at spaced-apart points and terminating at acommon point 142 overlying thecheck valve 137.

While no sewing ring is shown on the second embodiment of FIGS. 1315, one can and would be used to facilitate attachment of the valve in a valvular opening. The ring could be attached to cover the outer edge of the outer ring and lower inner ring in a manner similar to that illustrated in FIGS. 1 1.

The implant tool used to set the prosthetic valve illustrated in FIGS. 13-15 is substantially similar to implant tool 71 used to set the prosthetic valves illustrated in FIGS. 111. The only difference in the implant tools resides in the lower parts of theinner shaft 79,intermediate member 89 and theouter body 73. For this reason, only the changed parts of the implant tool will be given different numbers and the other numbers will be continued for this and the implant tool 71 for the valves of the first embodiment. It should also be noted that the use and operation of the implant tool is identical for both prosthetic valves. It is only the hardware that has to be changed to accommodate thetriangular cage 139 and the balltype valve structure (see FIG. 12).

Thelower cuplike member 75 on thebody 73 is similar to 75 but differs in that there are three spaced-apart slots or notches 77' formed in its lower edge to engage threeupstanding lugs 121 which are formed intermediate theposts 141 around the periphery of the valve'souter ring 111.

Theintermediate member 89 has a dependingopen cup 95 attached to is lower end which includes three peripherally spaced-apart deep slots 96' formed in its lower edge. These telescope over thelegs 141 of the triangular shapedcage 139 to allow thecup 95 to rest against the upper part of the upperinner ring 112.

in order to hold thecage 139 against the cup 95', theinner shaft 79 has attached to its lower end, an open cup type member 81' which cooperates with the upper part ofcage 139. The cuplike member 31 includes three L-shaped slots including spaced-apartvertical slots 143 andhorizontal extensions 145. The slots are adapted to permit thecuplilce member 81 to fit over the top of thecage 131 and thereafter to be rotated to lock the threelegs 141 in thehorizontal slots 145 formed in the cup member 81'.

In operation, the implant tool is telescoped over the top of the ball-type prosthetic valve as illustrated in FIGS. 1315 and theinner shaft 79 rotated to cause thecup member 81 to lock thecage 139 interior of the cup 95'. With this locked in place, theouter cup member 75 rests against the notchedouter ring 111. Hence, it is possible to rotate theintermediate member 89 to set thepins 115 which cooperate with the outer and inner ring assemblies.

Again, as in the case of the implant tool illustrated in FIGS. 1-4, the tool is designed to set an aortic prosthetic valve since the implant tool engages the cage side of the valve rather than the lower part thereof. As will be seen in discussing a modification of the prosthetic valve below, certain modifications in the positions of the lugs and the engagement means must be made in order to set a prosthetic valve in the mitral or tricuspid opening of the heart.

Valve Embodiment of FIGS, 16-18 Turning to FIGS. 1618, there is illustrated yet a third embodiment of a prosthetic valve constructed generally in accordance with the present invention. The principal distinguishing characteristics of this third embodiment of the prosthetic valve is found in retaining the innermost ends of the wire sutures in an annular ledge on the inner ring directly overlying the chamber in which the wires nest between the outer and inner ring assembly, holding the sewing ring between the outer and inner rings by a series of serrated teeth and employing upper and lower open cages to retain the discshaped check member.

More specifically, this third specific embodiment includes anouter ring 151 journaled on an L-shapedinner ring 153. Theouter ring 151 is also generally L-shaped and fits in an inverted position over the L-shapedinner ring 153 with the lowermost surface of the outer ring having a series ofserrations 155 formed therein. These cooperate with the flatinner surface 159 of theinner ring 153 to hold a circular cloth-sewing ring 161 therebetween.

At the upper inwardly disposed shoulder of theouter ring 151 there extends a plurality of L-shapedcage legs 163 which are connected at one set of theirends 164 at spaced-apart peripheral points about theouter ring 151 and having their other ends moving inwardly to retain the disc-type valve 165 during operation of the prosthetic valve.

A plurality of radially orientedslots 167 are also formed about the periphery of theouter ring 151 at spaced-apart relation and, in the exemplary embodiment, are 12 in numberjust as they are in the case of the first and second embodiments previously described.

Theinner ring 153 includes five inwardly disposedcage members 169 which prevent thedisc valve 165 from moving downwardly through the valve orifice during operation of the valve. Thevalve seat 173 is formed on the interior upper part of theinner ring 153 and acts in cooperation with the outer lower edge of thedisc valve 165 to form a seal.

The outer surface of the upright leg of the inner L-ring 153 has an outwardly projectingshoulder 175 formed annularly thereabouts to retain the wire sutures 177 in place and also to form an elongated chamber in the form of an annulus 179 between theouter ring 151 and theinner ring 153 in which thewire bodies 178 lie. Specifically, the wire suture pins 177 are formed generally in an S-shape with one set of theirends 181 lying on the upper surface of theshoulder 175 and with theirintermediate part 183 lying in thelongitudinal grooves 185 formed in spaced-apart relation peripherally about the outer surface of the projectingshoulder 175. The other ends 187 of the wire pins 177 are guided interior of theslots 167 formed in theouter ring 151. The longitudinal width of the nesting annulus 179 is again selected so that thepins 177 act to jam as theinner ring 153 is rotated with respect to theouter ring 151 towards a fully retracted position. However, inasmuch as the addition ofpins 177 interior of the annulus 179 merely causes theouter ring 151 to ride upward away from theinner ring 153, care must be taken in setting the valve to its retracted position.

It must be noted that as theouter ring 151 rides upward away from theinner ring 153, it will cause theserrated teeth 155 on theouter ring 151 to move away from the surface of theinner ring 153 thereby tending to release thesewing ring 161 normally held in place by these serrations. Of course, as soon as the inner ring and outer ring are rotated with respect to each other to force the outer ends of thepins 177 into their tissue-piercing positions, the pins hold the two rings together. They also hold thesewing ring 161 in place inasmuch as it is pierced in a plurality of points by thepins 177, both when the pins move through it initially and also when they curl back towards the outer surface of theouter ring 151 when fully expanded to their tissue-piercing positions. In this sense, the construction is quite similar to that of the other embodiments heretofore disclosed.

Again, as in connection with the other embodiments, a series of small depressions or holes in theouter body 151 may be formed intermediate theslots 167 to retain the outer ends 187 of the wire pins 177 after they are curled back adjacent the outer surface of theouter ring 151. These retention points, of course, can be used in connection with any of the embodiments heretofore disclosed.

A modification of the embodiment illustrated in F108. 16- -18 is shown in FIG. 19. In this case, the upper andlower cage members 163 and 169 are formed as an integral,

generally U-shaped member which is attached at peripherally spaced-apart points to the inner ring 153'. This construction will work just as well as that of providing separate upper and lower cages as in the embodiment of FIGS. 16-18, but the unitary construction transfers both cages to the inner ring. However, it would necessitate carefully smoothing and proportioning of the interior dimensions of the retaining cage 163'169 and the inner ring 153' so that they do not provide any discontinuities or cul-dc-sacs where low blood velocity is present, a situation which would encourage thrombus formation. Moreover, in this case the disc-type valve should have a flexibleouter end 193 so that as it moves down against thelower leg 169 of the cage, it distorts against theinnermost edge 195 of the inner ring 153' to form a seal.

As heretofore explained, the implant tool 71 described in connection with the first embodiments of the prosthetic valves is designed to "set a prosthetic valve wherein the cage part of the valve is engaged by the lower end of the tool. While this is perfectly satisfactory for replacing aortic valves, it is not possible to use this type of implant tool for replacing mitral or tricuspid valves. ln order to replace them, it is necessary for the implant tool to engage the lower part of the prosthetic valve, i.e. that part opposite from the cage structure. Such animplant tool 211 is illustrated in connection with a diagram of the heart in FIG. 20, and the details of theimplant tool 211 are shown in F165. 21 and 22. While a number of the parts of theimplant tool 211 are substantially identical to those of implant tool 71, it will be less confusing to assign different numbers to the various components in the explanation which follows.

Valve Embodiment of FIGS. 20-22 The prosthetic valve illustrated in FIGS. 20-22 is identical to that illustrated in FIGS. 1-10 except that it is designed for insertion as a mitral or tricuspid replacement. The upstanding projectinglugs 33 are not placed on the upper surface of the inner ring; instead, a series of lugs are formed on the lower surfaces of the inner andouter rings 11 and 12 to permit cooperation with theimplant tool 211 which must grasp the lower or bottom side of the valve.

The valve has aninner ring 12 cooperating with anouter ring 11 and a plurality of wire suture pins 13 cooperating with both. The disc-type check member 15 cooperates with thevalve seat 14 formed on theinner ring 12 and acloth sewing ring 16 is disposed around the outer periphery ofring 11. A pair of retainingcages 17 are provided to hold thevalve disc 15 adjacent tovalve seat 14.

Instead of theupstanding lugs 33, however, there are provided a series of three angularly spaced-apart dependinglugs 221 on the lowermost surface of theinner ring 12 and a group of similar depending spaced-apart lugs 222 on the lower surface of theouter ring 11. The use of these downwardly de pendinglugs 221 and 222 will be explained in connection with theimplant tool 211 of FIG. 22.

Tool 211, similar to tool 71, includes anouter body 231, an intermediate hollowtubular member 233 and aninner shaft 235. Theintermediate member 233 has apinion 237 attached to its upper end and is rotatably mounted interior of thebody member 231. Theinner shaft 235 is slideably mounted interior of theintermediate member 233 and is adapted to rotate with theintermediate member 233.

While the function of theinner shaft 235, theintermediate member 233 and thebody 231 are identical to those for implant tool 71, the hardware with which they accomplish their operations are different. Theouter body 231 has a lower flange orshallow cup 241 attached to it with a dependingannular shoulder 243 formed about its outer periphery. A series of threenotches 245 are cut in spaced-apart points around the periphery of the dependingshoulder 243 to engage the dependinglugs 222 formed on the lower surface of the outer ring 1 1.

Theintermediate member 233 has a flatcircular plate 247 attached to its lowermost end which also includes a reduced radii, dependingannular shoulder 249. The dependingshoulder 249 defines acircular opening 251 adapted to act as a retention chamber for acoil spring 253 which cooperates with theinner shaft 235 as hereinafter explained to retain theinner ring 12 adjacent the end of theintermediate shaft 233 and theflange plate 247.

Theflange plate 247 includes a series of three notches 261 formed in its outermost edge at spaced-apart positions to coincide with the dependinglugs 221 formed on theinner ring 12. When the plate is in place adjacent the valve, notches 261 receive the downwardly dependinglugs 221 to lock theinner ring 12 rotationally with respect to theflange 247.

Since there is no way for theinnermost shaft 235 to engage thecage 17 of the prosthetic valve illustrated in FIGS. 2022, it is necessary to provide other means for locking the inner ring assembly to theintermediate shaft 233 and theflange plate 247. This is provided by generally rectangular-shaped retaining member orplate 271 which is attached at the lowermost end of theshaft 235. The outer lower edge of this generallyrectangular plate 271 has a groove or excisedportion 273 which is adapted to ride on the inside upper surface of theinner ring 12.

Normally, thecoil spring 253 acts between theflange plate 247 and the adjacent surface of the rectangular-shapedmember 271 to urge theshaft 235 and therectangular member 271 downwardly. Anut 281 is threaded on theupper end 277 of theinner shaft 235 to act to stop against the downward movement of theshaft 235 beyond a preselected position. The upper end of theshaft 235 is split at 291 and apin 293 rides therein.Pin 293 is staked to theintermediate shaft 233 so thatshaft 235 cannot rotate with respect tomember 233. This is desirable due to the different manner in which a valve is attached to and disengaged from thetool 211.

In order to useimplant tool 211, the threadednut 281 on theinner shaft 235 is loosened so that theinner shaft 235 is movable in a vertical or longitudinal direction under the force of thecompressed spring 253. Thenut 281 is loosened so that the shaft and therectangular retention member 271 on its end can move substantially away from thedisc 247 and the lower end of theimplant tool 21 1. Once this is accomplished, theimplant tool 211 is tilted so that one end 271a of themember 271 can be moved through the valvular opening of the prosthetic valve before it is tilted the other way to move the other end 271b through the opening so that both parts are on the top part of theinner ring 12. The ultimate position is illustrated in FIG. 21 most clearly.

Once therectangular member 271 has been moved through the bottom opening of the prosthetic valve and placed against the upper surface of theinner ring 12, thecoil spring 253 is compressed and the valve is pulled up against theintermediate flange 247 by rotating the threadedn'ut 281 in a clockwise direction. At the same time that the inner ring assembly is firmly held against theplate 247 by theretention member 271, thegrooves 245 and 261 in the lower portion of thebody 231 and theflange plate 247, respectively, act to engage the dependinglugs 222 and 221 on the outer andinner rings 11 and 12.

Once'the prosthetic valve is held by thetool 211, theintermediate shaft 233 can be rotated with respect to the outer body member in order to rotate theinner ring 12 with respect to theouter ring 11 and set the wire pins 13, as was done in connection with the valve illustrated in FIGS. 1--10.

In order to rotate theintermediate shaft 233, there is provided aworm gear 283 which is rotatably supported in the upper part of thebody 231 to rotate thepinion 237. Anexternal handle 285 is provided outside ofbody 231 for rotating theworm gear 283.

Valve Embodiment of FIGS. 23-30 Refer now to FIGS. 23-30 for a description of a prosthetic valve made in accordance with another embodiment of the invention. As seen in FIGS. 23-25, thevalve 300 includes an inner ring ormember 302 surrounded by an outer ring ormember 304, in turn surrounded by asewing ring 306. Theinner ring 302 is formed with an inwardly extendingshoulder 303 on its upper end, as viewed in the drawings, which forms a valve seat cooperating with avalve disc 308 that is limited in its opening movement by a cage defined by the twowires 310 supported by and extending upwardly from theinner ring 302.

As can be seen from FIG. 25, theouter ring 304 fits snugly and slideably around the central portion of theinner ring 302 with the inner upper end of the outer ring engaging ashoulder 311 formed by an outwardly extendingflange 312 on the upper end of theinner ring 302. Within the outer surface of theinner ring 302 there are formed a pair of annular spaces orgrooves 314 and 316 separated by anannular rib 318. Each of these grooves has a considerably greater axial dimension than radial dimension, as can be seen in FIG. 25. Thegrooves 314 and 316 are connected by a plurality of circumferentially spaced, axially extendingslots 320 in therib 318, which are most easily seen in FIGS. 28 and 29.

The upper end of thegroove 314 is defined by acam surface 322a, angled at approximately 45 with respect to the axis of the valve, and by anannular shoulder 322. The lower end of thegroove 316 is defined by asimilar cam surface 324a and by anannular rib 324. Therib 324 is further formed with a plurality of axially extendingslots 326 which are equally circumferentially spaced. The number ofslots 326 is equal to the number ofslots 320 and theslots 326 are circumferentially offset a slight amount with respect to theslots 320, as best seen in FIGS. 28 and 29. Also, theslots 320 and 326 have approximately the same circumferential dimension.

Theouter ring 304 is formed with an upper series of circumferentially spacedopenings 328 and a lower series ofopenings 330 separated by acentral portion 329 and a surroundingannular channel 331. Theopenings 328 and 330 extend from the inner surface of theouter ring 304 to its outer surface in planes substantially perpendicular to the axis of the valve. Rather than being radially oriented, theopenings 328 and 330 are, in a preferred arrangement, angled approximately 35 with respect to a radial line, as is indicated by the angle shown in FIG. 26. As best seen from FIG. 25, the upper series ofopenings 328 are aligned with the upper end of theannular groove 314 in theinner ring 302. The axial dimension of theannular groove 314 is approximately two or three times that of the diameter of theopenings 328. Theopenings 330, which are of similar size with respect to theannular groove 316, are aligned with the lower end of the groove.

The number ofopenings 328 is equal to the number ofopenings 330 and also equal to the number ofslots 320 and 326 formed in theribs 318 and 324. With an outer ring of about an eighth of an inch inner diameter, a preferred arrangement is aboutl6 openings 328, spaced about 225. As seen in FIG. 28, theopenings 328 are circumferentially offset with respect to theopenings 330. The amount of offset in the example illustrated is about 4, and is equal to the offset between theslots 320 and 326. A measure of the offset is also indicated by the angle d in FIG. 28 formed by a line 321 between the centers of the outer ends of an adjacent pair of the openings 328a and 330a and aline 331 parallel to the valve axis and extending through the center of the outer end of the opening 330a. In the example given, the distance between the center planes of theopenings 328 and 330 is about 0.1 10 inches, and the angle dis approximately A similar angular relationship exists between theslots 320 and 326.

Note from FIG. that therib 318 on theinner ring 302 engages the surface between the series ofopenings 328 and 330 in theouter ring 304. Also, the lower end 304a of theouter ring 304 engages therib 324 on theinner ring 302.

Within theannular grooves 314 and 316, there is nested a plurality ofwirelike elements 332 which form self-contained sutures for retaining the valve in surrounding tissue. Eachelement 332 is formed with a generally U-shape as may be seen in FIGS. 28 and 29 with thebight 332a of the U being positioned within a respective one of theslots 320 in therib 318, and with thelegs 332b and 332c forming the sutures. Theupper leg 332b of eachelement 332 extends circumferentially within thegroove 314 while the lower leg 332c extends within thegroove 316. The outer end of the upper leg orsuture 332b extends partially into anopening 328 as may be seen in FIG. 25; similarly, the outer end of the lower leg or suture 332c extends into anopening 330. With the arrangement illustrated in FIGS. 28 and 29, the upper leg orsuture 332b is slightly longer than the lower leg or suture 332c in view of the circumferential offset of a pair ofopenings 328 and 330 in the outer member.

As can also be seen from FIGS. 28 and 29, as well as from FIG. 25, thesutures 332b are confined within the elongated chamber formed by theannular groove 314 in an axial direction by theshoulder 322 and itscam surface 322a, and by the upper surface of therib 318. Thesutures 3320 are similarly confined axially in the elongated chamber formed by thegroove 316 by therib 324 and itsadjacent cam surface 324a and by the lower surface of therib 318. Also, thebight 332a of theU-shaped elements 332 is confined circumferentially by the portions of therib 318 defining theslots 320. Thebight 332a of each suture is prevented from radially outward movement by the central portion of theouter ring 304 and prevented from radially inward movement by theinner ring 302. Thus, thebight 332a of each element is substantially fixed with respect to the inner ring. The outer ends of thesutures 332 are, however, free to move through theopenings 328 and 330 upon slideable rotation of theinner ring 302 with respect to theouter ring 304. The axially downward movement of theouter ring 304 is limited by the presence of the ends of the wire sutures 332 within theopenings 328 and 330. The upward movement is of course limited by the interference between theshoulder 311 on theinner ring 302 and the upper surface of theouter ring 304.

Referring to FIGS. 25, thesewing ring 306 is in the form ofa flattened tube surrounding theouter ring 304. Thesewing ring 306 is retained in this position by awasherlike retainer 340 positioned within the lower end of the sewing ring and an annularelastic retainer 344 in the upper end of thering 306. Theretainer 340, which has an inner diameter approximately equal to the inner diameter of theouter ring 304, is positioned adjacent the lower end of the outer ring while the fabric forming the sewing ring extends between the retainingring 340 and the inner and outer valve rings 302 and 304. Note that anannular notch 342 is formed in the lower end of the inner ring and that the fabric forming the sewing ring partially extends into this notched area. As can be seen from FIG. 25, theretainer 344 has a circular cross section and an inner diameter less than the outer diameter of theouter ring 304, with the result that thesewing ring 306 is effectively positioned by the tworetainers 340 and 344.

Refer now to FIG. 30 for an explanation of the fabrication of theelements 332 and their assembly with the inner andouter rings 302 and 304. The ends of sections of suture wires are inserted from the inside of thering 304 through theopenings 328 and 330, respectively, to their fullest extent thereby forming a U-shape with thebight 332a extending from anopening 328 to anopening 330. Note that thebight 332a is angled about 20 with respect to a line parallel to the valve axis because of the circumferential offset of theopenings 328 and 330, shown in FIG. 28. With asuture wire 332 positioned in this fashion in each pair ofopenings 328 and 330, the upper end of theouter ring 304 is started onto the lower end of theinner ring 302 and thebight 325a of each suture is aligned with aslot 326 in thelower rib 324. By moving the outer ring axially onto theinner ring 302 and simultaneously slightly rotating the outer ring with respect to the inner ring, therings 302 and 304 may be moved to the position indicated in FIG. 30 wherein thebight 332a of theelement 332 has entered theslot 320 in therib 318. Note that the diameter of theelement 332 is considerably less than the width of theslots 320 and 326. With continued rotary and axial movement, the outer ring may be completely positioned onto the inner ring so that its upper end engages theshoulder 311 on the inner ring as seen in FIG. 25.

Thering 302 is then rotated with respect to thering 304 so that the suture wires are drawn into theannular grooves 314 and 316. This movement causes the main portions of the wires to conform to the shape of the groove or chamber and deforms thebights 332a to the shorter length, shown in FIG. 28. The movement is limited by the axial dimensions of the grooves and the diameter of the suture wire in that the sutures will interfere with each other and the axial ends of thegrooves 314 and 316 to prevent further movement. The totally retracted position is indicated in FIG. 28 wherein it can be seen that each suture extends a circumferential distance an amount slightly greater than twice the distance betweenadjacent slots 320 in therib 318, and three diameters of suture wire are positioned above and below eachslot 320.

The suture wires may be precut to the desired length or alternatively they may be cut after being installed. With the latter method, theelements 328 are fully retracted as shown in FIG. 28. Then, the inner ring is rotated slightly in a counterclockwise direction with respect to the outer ring an amount equal to about half the length of theopenings 328 and 330. The ends of the sutures are then severed at the outer periphery of theouter ring 304 and the ends suitably sharpened to form thesutures 332b and 332c. The amount severed should be such that when the sutures are once more fully retracted, their outer ends will still remain in theopenings 328 and 330 so that they will be properly guided when extended. Also, the ends of the wires are utilized to prevent theinner ring 302 from being withdrawn upwardly from within theouter ring 304.

After the sutures have been properly installed and the inner ring positioned with respect to the outer ring, thesewing ring 306 may be added by expanding the elasticupper retainer 344 to permit thesewing ring 306 to be slipped over theouter ring 304 into the position shown in FIG. 25.

Thevalve 302 is installed in a heart in a manner similar to that described with respect to the other embodiments of the invention. Theouter ring 304 is held in a fixed position by a suitable tool (not shown) having prongs cooperating with the sockets 346 (FIG. 24) formed in the upper end of theouter ring 304. The elasticity of the retainingelement 344 permits insertion of the tool prongs. When the valve is positioned in the proper location, theinner ring 302 is then slideably rotated within theouter ring 304 in a counterclockwise direction as indicated by the arrow in FIG. 29. This action causes the ends of thesutures 332 to be cammed outwardly by thecam surfaces 322a and 324a through theopenings 328 and 330. The angle of theopenings 328 and 330 causes thesutures 332 to extend outwardly through the material of thesewing ring 306, through the surroundingheart tissue 348, and then back inwardly toward the valve and back through the sewing ring so that at the fully extended position, the sutures look as shown in FIGS. 27 and 29. Note from FIG. 27, that the upper legs of the sutures form an upper series and the lower legs form a lower series and that due to the circumferential offset of theopenings 328 and 330, the two series of sutures are similarly circumferentially offset. Such an arrangement improves the attachment of the sutures to the surrounding heart tissue in that a minimum of strain is imposed on the tissue 248 at a given location. With the sutures fully extended, the valve is firmly implanted in the heart and, consequently, the tool may be withdrawn and the valve is ready to operate.

While the present invention has been disclosed by way of a number of exemplary embodiments, it should be apparent to those skilled in the art that various modifications are possible without departing from the spirit and scope of the invention. Therefore, the invention should only be limited by the limitations set forth in the appended claims.

I claim:

1. A prosthetic heart valve comprising, in combination:

an outer ring having a plurality of spaced-apart guide slots formed therethrough;

an inner ring concentrically mounted interior of said outer ring for rotation with respect thereto;

a movable check valve assembly including a valve seat formed on said inner ring and a movable check member to cooperate therewith;

a plurality of wire sutures having the innermost set of their ends retained by said inner ring at peripherally spacedapart points, said wire sutures having a first arcuate configuration and the outermost set of their ends freely extending interior of but not radially beyond respective ones of said guide slots when said inner ring is in a rotationally retracted position with respect to said outer ring;

means retaining said inner ring interior of said outer ring;

and,

means operable to rotate said inner ring with respect to said outer ring so that said wire sutures move radially outward I beyond the outer surface of said outer ring into a tissuepiercing position wherein they assume a second arcuate configuration which is more sharply curved than said first arcuate configuration.

2. A prosthetic heart valve in accordance with claim 1 wherein said wire sutures nest in an annulus formed in the outermost surface of said inner ring between said inner and outer rings and generally in a common plane therewith before being extended to the tissue-piercing position and said wire sutures act as the retaining means for said inner ring.

3. A prosthetic heart valve in accordance with claim 2, wherein the depth of the nesting area annulus in a direction perpendicular to said common plane is such that no more than two wire sutures can be nested therein without binding the inner and outer rings.

4. A prosthetic heart valve in accordance with claim 1, wherein the means for retaining said inner ring interior of said outer ring include a plurality of radially oriented lugs attached to peripherally spaced-apart parts of one side of said outer ring and which extend radially inward to overlie said inner ring, and including a plurality of radial notches formed in the outer edge of said inner ring at points corresponding to the peripherally spaced-apart locations of said lugs to permit said inner ring to pass said retaining lugs as it is positioned with said outer ring for rotation to a tissue-piercing position.

5. A prosthetic heart valve in accordance with claim 1, and including means to cause the outermost ends of said wire s utures to curl back toward the outer surface of said outer ring as said inner ring is rotated to said tissue-piercing position.

6. A prosthetic heart valve in accordance with claim 5, and including a fabric-sewing ring affixed to said outer ring to overlie the outer edge of the guide slots therethrough. I

7. A prosthetic heart valve in accordance with claim 5, wherein the wire sutures are caused to curl back toward the outer ring by the configuration of the generally radially disposed guide slots in the outer ring, the outermost ends of said wire sutures contacting said outer ring when the inner ring is in said tissue-piercing position to lock the valve in situ.

8. A prosthetic heart valve in accordance with claim 5, and including a plurality of recesses formed in the outer surface of said outer ring intermediate said guide slots to receive the outer tips of said curled wire sutures when said inner ring is rotated to the tissue-piercing position.

9. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve comprising, in combination:

an outer ring having an inner recessed shoulder and a plurality of circumferentially spaced-apart radial guide slots formed therethrough;

an inner ring having an outwardly projecting annular shoulder adapted to ride in the recessed shoulder of said outer ring when the inner ring is rotatably supported in the outer ring;

a valve seat formed on said inner ring and a movable check member cooperating therewith;

a plurality of flexible wire pins having pointed outer tips nesting between said inner and outer rings in a generally transverse plane;

the innermost set of their ends retained by said inner ring at spaced-apart peripheral points and the outermost set of their ends freely extending interior of respective ones of said guide slots;

said inner ring held interior of said outer ring by the retaining force of said wire pins;

means operable to rotate said inner ring with respect to said outer ring so that said wire pins move from retracted positions where their tips do not project beyond the outer surface of said outer ring to tissue-piercing positions; and,

stop means to prevent said inner ring from moving beyond said retracted and said tissue-piercing positions.

10. A prosthetic heart valve in accordance with claim 9, wherein the stops are obtained by selecting the longitudinal distance between the points of attachment of the wire pins to said inner ring and the lower surface of the annular shoulder on said inner ring so that no more than a preselected number of wire pins can be nested without binding on the inner and outer rings.

11. A prosthetic heart valve in accordance withclaim 10, wherein the angular separation between the stops directly subtends the arc length between the peripherally spaced adjacent slots in said outer ring and the peripherally spaced adjacent retention points in said inner ring.

12. A prosthetic heart valve comprising, in combination:

an upper ring having a plurality of spaced-apart, generally radial notches formed in its lower surface;

an inner ring concentrically mounted interior of said upper ring for rotation with respect thereto;

a lower ring integrally attached to the lower part of said inner ring so that its flat upper surface contacts the shoulders defining the notches in said outer ring;

a movable check valve assembly including a valve seat formed on said inner ring and a movable check member to cooperate therewith;

a plurality of wire pins having one set of their ends retained by said lower ring at spaced-apart radial points and the other set of their ends pointed and lying interior of the slots formed by said notches and the upper surface of the lower ring;

said pointed wires extending into, but not radially beyond, the outside of said outer ring when said inner and lower rings are in a retracted position with respect to said outer ring;

means associated with said inner and lower rings to retain said inner ring interior of said outer ring; and,

means operable to rotate said inner and lower rings with respect to said outer ring so that said wire pins move radially outward beyond the outer surface of said outer ring into a tissue-piercing position.

13. A prosthetic heart valve in accordance with claim l2, wherein said wire pins nest between said inner and outer rings and generally in a common plane therewith before being extended to said tissue-piercing position.

14. A prosthetic heart valve in accordance withclaim 13, wherein the inner ring is restricted in its rotation to movement between the retracted and tissue-piercing positions by proportioning the depth of the nesting area for the wire pins in a direction perpendicular to said common plane whereby no more than two wire pins can be nested without binding against the adjacent surfaces of said inner and outer rings.

15. A prosthetic heart valve in accordance withclaim 12, and including means to cause the outermost ends of said wire pins to curl back toward the outer surface of said outer ring as said inner ring is rotated to the tissue-piercing position.

16. A prosthetic heart valve in accordance withclaim 15, and including a fabric-sewing ring affixed to said lower ring overlying the outer edges of the radial notches in the outer ring.

17. A prosthetic heart valve in accordance withclaim 15, wherein the wire pins are caused to curl back toward the outer ring by the configuration of the radial notches in the outer ring, the outermost ends of said wire pins contacting said outer ring to lock the valve in situ when the inner ring is in the tissue-piercing position.

18. A prosthetic heart valve in accordance withclaim 17, and including a plurality of recesses formed in the outer surface of said outer ring intermediate said radial slots to receive the pointed ends of said curled wire pins when said inner ring is rotated to the tissue-piercing position.

19. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve comprising, in combination:

an outer ring having a plurality of circumferentially spacedapart radial guide slots formed through it and an inwardly extending shoulder;

an inner ring having an outwardly projecting annular shoulder at its lower edge to cooperate with said outer ring when it is rotatably supported therein;

a valve seat formed on said inner ring and a movable check member cooperating therewith;

a plurality of flexible wire pins having pointed outer tips and being held to assume a first shape between said inner and outer rings in a generally transverse plane;

the innermost set of their ends retained by said inner ring and said outer ring shoulder at spaced-apart peripheral points and the outermost set of their ends freely extending interior of respective ones ofsaid guide slots;

said inner ring held interior of said outer ring by the retaining force of said wire pins;

means operable to rotate said inner ring with respect to said outer ring so that said wire pins move from retracted positions where their tips do not project beyond the outer surface of said outer ring to tissue-piercing positions in which they assume a second and different shape; and,

stop means to prevent said inner ring from moving beyond said retracted and said tissue-piercing positions.

20. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve in accordance with claim 19, and including forming the radial slots to cause the outermost ends of said wire sutures to curl back toward the outer surface of said outer ring as said inner ring is rotated to said tissue-piercing position.

21. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve in accordance with claim 20, and including a fabric sewing ring cooperating with said outer ring to overlie the outer edge of the radial guide slots therethrough.

22. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve in accordance withclaim 21, wherein the lowermost edge of said outer ring is serrated to engage the sewing ring and hold it against the outwardly projecting shoulder on said inner ring.

23. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve in accordance with claim 22, wherein the inner ring has an intermediate outwardly extending shoulder which is notched at peripherally spaced-apart points to receive the innermost set of ends of said wire pins and the inside of said outer ring and the inwardly extending shoulder thereon hold said innermost ends in situ on said inner ring.

24. A prosthetic heart valve having a one-way check member adapted to move along the longitudinal axis of the valve in accordance with claim 20, and including a plurality of recesses formed in the outer surface of said outer ring intermediate said guide slots to receive the outer tips of said curled wire sutures when said inner ring is rotated to the tissue-piercing position.

25. A sutureless prosthetic device comprising, in combination:

an upper member having a plurality of spaced-apart notches formed in its lower surface;

an inner member mounted interior of said upper member for rotation with respect thereto;

a lower member fixedly attached to the lower part of said inner member so that its upper surface contacts the shoulders defining the notches in said outer member;

a plurality of wirelike elements having one set of their ends retained by said lower member at spaced-apart points and the other set of their ends lying at least partially interior of the slots formed by said notches and the upper surface of the lower member; and,

means operable to rotate said inner-lower members with respect to said outer member so that the wirelike elements move radially outward beyond the outer surface of said outer member into tissue-piercing positions.

26. A prosthetic device, comprising:

a first member having a plurality of openings formed therethrough;

a second member rotatably mounted with respect to said first member between a retracted position and an operative position;

a plurality of flexible wirelike suture elements, each having a portion substantially fixed with respect to the second member and each being held in a first, retracted configuration in which an end extends into respective ones of said openings when said second member is in its retracted position and a second, tissue-piercing configuration which is different from said retracted configuration, and in which said suture element ends are moved beyond the surface of said first member and through said openings when said second member is rotated to its operative position.

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