AU2007216618A1 - Minimally invasive mitral valve repair method and apparatus - Google Patents

Description

Regul tion 3.2 Revi$ed 2/98

AUSTRALIA

Patents Act, 1990

ORIGINAL

COMPLETE SPECIFICATION TO BE COMPLETED BY THE APPLICANT NAME OF APPLICANT: ACTUAL INVENTORS: ADDRESS FOR SERVICE: INVENTION TITLE: DETAILS OF ASSOCIATED APPLICATION NO(S): Edwards Lifesciences Corpora ion William J Allen Alan Bachman Scott Reed Ray Adams Robert R Steckel Peter Maxwell and Associates Level 6 Pitt Street SYDNEY NSW 2000 MINIMALLY INVASIVE MITRAL VALVE REPAIR METHOD AND

APPARATUS

Divisional of Australia Patent Application No. 2004 229 028 file 11 November 2004 which is a divisional of Australia Patent Application No. 775,796 filed on October 2000 j on 0eo The following statement is a full description of this invention including the bi method of performing it known to us:m:\docs\20001359\126707.doc The present invention relates to the repair of heart valves, ai particularly, to methods and apparatuses for the repair of heart vali In vertebrate animals, the heart is a hollow muscular organ I pumping chambers: the left and right atria and the left and right ver provided with its own one-way overflow valve. The natural heart v; identified as the aortic, mitral (or bicuspid), tricuspid and pulmonar The valves separate the chambers of the heart, and are each mou annulus therebetween. The annuluses comprise dense fibrous rin either directly or indirectly to the atrial and ventricular muscle fiber' leaflets are flexible collagenous structures that are attached to anc inward from the annuluses to meet at coapting edges. The aortic valves have three leaflets, while the mitral and pulmonary valves t Various problems can develop with heart valves, for a numl reasons. Stenosis in heart valves is a condition in which the valve open properly. Insufficiency is a condition which a valve does not properly. Repair or replacement of the aortic or mitral valves are r because they reside in the left side of the heart where pressures C are the greatest. In a valve replacement operation, the damaged excised and the annulus sculpted to receive a replacement prosth id, more res.

laving four itricles, each lives are valves.

ited in an ]s attached .The extend ind tricuspid ave two.

er of clinical s do not close nost common nd stresses eaflets are etic valve.

In many patients who suffer from valve dysfunction, surgical rep ir "valvuloplasty") is a desirable alternative to valve replacement. Remode ing of the valve annulus "annuloplasty") is central to many reconstructive val loplasty procedures. Remodeling of the valve annulus is typically accomplished by implantation of a prosthetic ring "annuloplasty ring") to stabilize the annulus c and to correct or prevent valvular insufficiency that may result from a dysfunction of the valve annulus. Annuloplasty rings are typically constructed of a resilient

O

C ~core covered with a fabric sewing ring. Annuloplasty procedures are performed not only to repair damaged or diseased annuli, but also in conjunction with other 10 procedures, such as leaflet repair.

SMitral valve regurgitation is caused by dysfunction of the mitral alve structure, or direct injury to the mitral valve leaflets. A less than perfect understanding of the disease process leading to mitral valve regurgitation complicates selection of the appropriate repair technique. Though impla ntation of an annuloplasty ring, typically around the posterior aspect of the mitral valve, has proven successful in a number of cases, shaping the surrounding annulus does not always lead to optimum coaptation of the leaflets.

More recently, a technique known as a "bow-tie" repair has been advocated. The bow-tie technique involves suturing the anterior and posterior leaflets together in the middle, causing blood to flow through the two si e openings thus formed. This process was originally developed by Dr. Otavio Alfieri, and involved placing the patient on extracorporeal bypass in order to access and suture the mitral valve leaflets.

A method for performing the bow-tie technique without the need for bypass has been proposed by Dr. Mehmet Oz, of Columbia University. The method and a device for performing the method are disclosed in PCT publication WO 99/00059, dated January 7, 1999. In one embodiment, the device consists of a forceps-like grasper device that can be passed through a sealed aperture in the apex of the left ventricle. The two mitral valve leaflets meet and curve into the left ventricular cavity at their mating edges, and are thus easy to grasp from inside the entricle.

The mating leaflet edges are grasped from the ventricular side and held ogether, and various devices such as staples are utilized to fasten them together. The teeth of the grasper device are linearly slidable with respect to one another so as to align the mitral valve leaflets prior to fastening. As the procedure is done beating heart, and the pressures and motions within the left ventricle severe, the procedure is thus rendered fairly skill-intensive.

There is presently a need for an improved means for performi bowtie technique of mitral valve repair.

SUMMARY OF THE INVENTION The present invention provides a number of methods for fastE "approximating" tissue pieces together. The term "tissue pieces" is t understood to means discrete pieces that may be straight, curved, tL so long as the pieces are initially disconnected. For example, many embodiments of the invention disclosed herein are especially useful two leaflets of a heart valve. The coapting edges of the leaflets thus the "tissue pieces." In other contexts, the invention can be used to a two vessels, either end-to-end, in a T-junction, or otherwise. In thes, the two vessels define the "tissue pieces". One specific application invention to perform an anastomosis is in a coronary artery bypass c (CABG) procedure. Another example of an application of the preser is in wound closure, wherein the facing edges of the wound are joinE the present invention in its broadest sense should not be construed 1 limited to any particular tissue pieces, although particular examples i shown and disclosed.

The present invention includes a number of methods for both the tissue pieces to be joined, and fastening them together. Some embodiments disclose only the stabilizing function, others only the f" function, and still others show combination stabilizing and fastening should be understood that certain of the stabilizing devices can be u certain of the fastening devices, even though they are not explicitly n a are ng the ning or be bular, etc., of the for joining constitute nastomose 3 cases, f using the raft it invention d. In sum, o be nay be stabilizing Lstening jevices. It sed with ;hown in joint operation. In other words, based on the explanation of the par device, one of skill in the art should have little trouble combining the certain of two such devices. Therefore, it should be understood that the stabilizing and fastening devices are interchangeable, and the in' covers all permutations thereof.

According to one aspect of the invention there is provided a ry joining heart valve tissue, the method comprising: temporarily stabilizing a first valve leaflet to a probe; temporarily stabilizing a second valve leaflet to the probe; engaging a tissue securing device to the first valve leaflet; engaging the tissue securing device to the second valve leafli releasing the first valve leaflet from the probe; releasing the second valve leaflet from the probe; and securing the first valve leaflet to the second valve leaflet, whe first valve leaflet is released from the probe prior to securing the first leaflet to the second valve leaflet.

Furthermore, many of the fastening devices disclosed herein icular features of many of iention iethod for ;t; rein the valve ,,an be deployed separately from many of the stabilizing devices, and the two can therefore be deployed in parallel. Alternatively, and desirably, however, the C fastening and stabilizing functions are performed with one device.

SThe stabilizing and fastening devices of the present invention can be utilized in either standard open surgical procedures, endoscopic procedures, or percutaneous procedures. In one embodiment the devices can be delivered through an open chest either transapically or transatrially. In another embodiment, the 00 stabilizing and fastening devices can be introduced through an incision performed I N- over the roof of the left.atrium. In yet another embodiment the devices can be delivered into the left ventricle through the right chest via a thorascope. The devices can also be delivered percutaneously, via a catheter or catheters, into the patient's arterial system through the femoral or brachial arteries). Other objects, features, and advantages of the present invention will become apparent from a consideration of the following detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a perspective view of an exemplary tissue stabilizer of the present invention that uses a vacuum; Figure la is an elevational view of a first step in a valve repair procedure using the tissue stabilizer of Figure 1; Figure lb is an elevational view of a second step in a valve repair procedure using the tissue stabilizer of Figure 1; Figure 2 is a perspective view of a further tissue stabilizer of the present invention that also uses a vacuum; Figure 2a is an elevational view of a step in a valve repair procedure using the tissue stabilizer of Figure 2; Figures 3a-3c are perspective views of several embodiments of vacuumbased tissue stabilizers having tissue separating walls; Figure 3d and 3e are sectional views of two different vacuum p rt configurations for the tissue stabilizers shown in Figures 3a-3c, the stabilizers shown in operation; Figure 4a is an elevational view of a first step in a valve repair procedure using a mechanical tissue stabilizer with linearly displaceable tissue clamps; Figure 4b is an elevational view of a second step in a valve repair procedure using the tissue stabilizer of Figure 4a; Figure 4c is a detailed perspective view of a clamp of the tissue stabilizer of Figure 4a extended to grasp a valve leaflet from both sides; Figure 5a is a perspective view of a suture-based tissue fastener of t e present invention having toggles; Figure 5b is a sectional view of the suture-based tissue fastener ofFi gure loaded into a delivery needle; Figure 6a-6c are elevational views of several steps in a valve repair procedure using a tissue stabilizer of the present invention and the suture-b sed tissue fastener shown in Figure Figure 7a is a perspective view of an exemplary tissue stabilizing ad fastening device of the present invention that uses a vacuum and needles to deliver suture-based fasteners having toggles through the tissue; Figure 7b is an elevational view of a step in a valve repair procedure using the tissue stabilizing and fastening device of Figure 7a; Figure 8 is an elevational view of an alternative tissue stabilizing and fastening device similar to that shown in Figure 7a; Figure 9a is a perspective view of a further tissue stabilizing and fastening device of the present invention that uses a vacuum and needles to deliver suturebased fasteners having toggles through the tissue; Figure 9b is a plan view of the distal tip of the device of Figure 9a; Figures 10a-10c are several photographs of tissue being connected wth suture-based fasteners having toggles; Figures 11 a-1 Ic are elevational views of a tissue stabilizing and fastening device of the present invention having members deployable on a blind side of the tissue being connected; Figures 12a-12e are elevational views of a tissue stabilizing and fastening device of the present invention having needles deployable on a blind side f the tissue being connected and a suture-based fastener, Figure 13a is a perspective view of a further tissue stabilizing and astening device of the present invention that uses a vacuum and deployable needles to deliver suture-based fasteners through the tissue; Figure 13b is a plan view of the distal tip of the device of Figure 13a; 0 Figures 14a-14b are elevational view of a still further tissue stabilizing and NC fastening device of the present invention that uses vacuum and deploya le needles J to deliver suture-based fasteners through the tissue; Figures 15a-15h are elevational and plan views of several steps in a valve Srepair procedure using the tissue stabilizing and fastening device of Fig re 14; Figures 16a-16c are sectional views of several steps in a tissue joining 00 procedure using an exemplary tissue stabilizing and fastening device ha ing IN needles.for delivering a suture-based fastener; Figure 16d is.a detailed perspective view of a portion of the device seen in Figure 16b; Figures 16e and 16f are isolated views of suture ties used with t e suturebased fastener of Figure 16a; Figures 17a-17c are elevational views of several steps in a valve repair procedure using an exemplary tissue stabilizing and fastening device fol delivering a suture-based axial needle fastener, Figure 18a is an elevational view of a first step in a valve repair procedure using an exemplary tissue fastening device of the present invention for delivering a spiral suture-based leaflet fastener, Figure 18b is a detailed perspective view of a second step in a v Ive repair procedure using the spiral suture-based leaflet fastener of Figure 18a; Figure 18c is an elevational view of a completed valve repair procedure utilizing the spiral suture-based leaflet fastener of Figure 18a; Figure 18d is a detailed view of a pledget anchoring device used with the spiral suture-based leaflet fastener of Figure 18a; Figures 19a-19d are elevational views of several steps in a valve repair procedure using an exemplary tissue stabilizing and fastening device of the present invention having vacuum stabilization and mechanical clamping; Figure 20 is an elevational view of a mechanical tissue stabilizer with pivoting tissue clamps; Figures 21a and 21b are elevational views of two steps in a valve repair procedure using the mechanical tissue stabilizer of Figure 21; Figures 22a and 22b are elevational views of two steps in a valve repair U procedure using a mechanical tissue stabilizer of the present invention having Spreformed hooks; Figure 22c is a detailed perspective view of a hook of the tissue stabilizer Cof Figure 22a extended to grasp a valve leaflet from the side opposite the tissue stabilizer; OC Figures 23a and 23b are elevational views of two steps in a valve repair I procedure using a mechanical tissue stabilizer of the present invention havi g Sspring-biased hooks; 6 Figure 23c is a detailed perspective view of two hooks of the tissue stabilizer of Figure 23a extended to grasp the valve leaflets from the side opposite the tissue stabilizer; Figures 24a-24d are elevational views of several steps in a valve repair procedure using a mechanical tissue stabilizer of the present invention to deliver a non-suture-based fastener, Figure 25a is a perspective view of an exemplary tissue staple usefu with the methods and devices of the present invention and shown in an open configuration; Figure 25b is a perspective view of the tissue staple of Figure 25a shown in a closed configuration; Figures 26a-26c are elevational views of several steps in a valve repair procedure using an exemplary tissue fastening device of the present invention for delivering the tissue staple of Figure Figure 27a is a perspective view of a further tissue stabilizing and f stening device of the present invention that uses a vacuum and delivers a staple to fasten tissue pieces; Figure 27b is a sectional view of a step in a valve repair procedure using the tissue stabilizing and fastening device of Figure 27a; Figure 27c is a perspective view of a completed valve repair procedure utilizing the tissue stabilizing and fastening device of Figure 27a; Figure 28a is an elevational view of a further tissue fastening device of the present invention for delivering an alternative "toggle-like" tissue clip, the lip shown open; Figure 28b is an elevational view of the tissue fastening device of Figure cJ 28a, the clip shown closed; Figure 29a is a detailed perspective view of a first step in a talve repair procedure using the tissue fastening device of Figure 28a; o00 Figures 29b and 29c are elevational views of two steps in a valve repair IND 5 procedure using the tissue fastening device of Figure 28a; c Figure 30a is a perspective view of an alternative "toggle-like" tissue 0 fastening clip, the clip shown open; Figure 30b is a perspective view of the tissue fastening clip of Figure shown closed; Figures 31a-31d are elevational views of several steps in a valve repair procedure using an exemplary tissue fastening device of the pres nt invention for delivering the tissue fastening clip of Figure Figures 32a 32d are elevational views of various tissue fastening clips having barbed ends; Figures 33a and 33b are sectional views of two steps in a valve repair procedure using an exemplary tissue fastening device of the present invention for delivering a barbed tissue fastening clip of Figure 32a; Figure 33c is an elevational view of a third step in a valve repair procedure using the tissue fastening device of Figure 33a; Figure 34a 34f are elevational and perspective views of a tissue fastener of the present invention having spring -loaded jaws; Figure 35a is a sectional view of a tissue fastening device or delivering the tissue fastener of Figure 34a; Figures 35b and 35c are sectional views of the tissue fast ener of Figure 34a in both closed and opened positions around the tissue being onnected; Figures 36a 36c are elevational views of a further tissue fastener of the present invention having spring-loaded jaws; Figure 37a is a sectional view of a tissue fastening device fcr delivering the tissue fastener of Figure 36a; Figure 37b is a sectional view of the tissue fastener of Figure 36a in a closed position around the tissue being connected; Figure 38 is a perspective view of an exemplary integrated issue stabilizer and fastening device of the present invention; to Figure 39 is a perspective view of the device of Figure 38 wherein the needle carrier is extended; Figure 40 is a perspective view of the device of Figure 38 showing te initial release of the needles; Figure 41 is a perspective view of the device ofFigure38 showing the needles captured within the vacuum ports; I Figure 42 is an exploded view of various components of the device of CN Figure 38; O Figure 43 is a perspective view of the device of Figure 38 whereinthe CN 10 needle carrier has been removed to clearly show the.vacuum ports; Figure 44 is a perspective view of an exemplary embodiment of a handpiece that is utilized with the device of Figure 38; Figures 45a and 45b illustrate perspective views of alternate suture configurations used to practice the invention; and Figure 46 is a perspective view of another exemplary embodiment o a handpiece that is utilized with the device of Figure 38.

DESCRIPTION OF THE PREFERRED EMBODIMENTS Exemplary Stabilizing Devices Figure 1 shows a tissue stabilizer 20 of the present invention that uses a vacuum to hold two tissue pieces. In this case, the tissue pieces are heart v lve leaflets 22 and a valve repair procedure using the stabilizer 20 is depicted in Figures la and lb. The tissue stabilizer 20 comprises a cylindrical probe 24 with at least one internal lumen (not shown) and having a flat distal end 26, a pa r of vacuum ports 28 being disposed in the distal end 26. The ports 28 may be n communication with a common vacuum source, may be separately communicable with the source with internal valves (not shown), or may be in communicati on with different vacuum sources. The size of the ports 28 and magnitude of suction applied may vary depending on the application, but the ports 28 are desirably spaced apart a minimum distance to create two distinct suctions. In this manner, one leaflet or the other may be stabilized with one of the ports 28 without unduly influencing the other. In one example, the ports 28 have a minimum diameter of about 1/8 inch, and are spaced apart with a wall of at least 0.020 inches Q therebetween.

t )The probe 24 desirably has a size suitable for minimally invasive s rgery.

In one embodiment probe 24 is part of a catheter based percutaneous deliv ry system. In that case probe 24 is a catheter tube having a lumen or lumens connecting vacuum ports 28 to the vacuum source or sources. The catheter would oo be long enough and have sufficient steerability and maneuverability to rea h the Sheart valve from a peripheral insertion site, such as the femoral or brachial artery.

I One particular advantage of the present invention is the ability to perform valve repair surgery on a beating heart. The procedure shown in Figures la and lb is a O 10 o mitral valve repair with an approach of the probe 24.from the left atrium The -1 .atrium 30 has lower pressures than the ventricle 31, and thus there is less bood leakage and less turbulence imparted to the probe 24. First, the anatomica structures, including the location of the leaflets 22, can be visualized using echo technology, or other means. One leaflet 22 may be stabilized with one of he ports 28, and that leaflet 22 then manipulated toward the other leaflet 22, which is then also stabilized. Again, any of the fasteners disclosed herein may then be used to secure the leaflets 22 together.

Figure 2 is illustrates another tissue stabilizer 32 similar to that shown in Figure 1 and that also uses a vacuum. The tissue stabilizer 32 includes a probe body 34 having at least one internal lumen (not shown) and an angled or Utpered nose 36 on a distal end. A vacuum port 38 is provided on each face of the tapered nose 36. Figure 2a shows a valve repair procedure using the tissue stabilizer 32 of Figure 2, wherein a distal tip 40 of the nose 36 is exposed to the ventricular 31 side of the leaflets 22. Because of this exposure, various leaflet fastening devices can be delivered through the probe 34 to the ventricular side of the leaflets 22, as will be seen below.

Figures 3a-3c show three vacuum-based tissue stabilizers having tissue separating walls. In Figure 3a, a tissue stabilizer 40 includes a flat distal face 42 having a pair of distally-directed tissue separating walls 44 extending therefrom, and defining a gap 46 therebetween. The stabilizer 40 contains one or mo e lumens in communication with vacuum ports 48 that open on both sides of the walls 44. There are four such ports 48 shown, one on each side of each w 1144. In addition, a fastener channel 50 opens at the distal face 42 between the walls 44, o and facing the gap 46 therebetween. The fastener channel 50 can be used to Sdeliver tissue fasteners, as described below.

In Figure 3b, a tissue stabilizer 52 includes a flat distal face 54 having a single distally-directed tissue separating wall 56 extending therefrom. The stabilizer 52 contains one or more lumens in communication with circular vacuum 00 ports 58 that open on both sides of the wall 56. There are two such ports 58 IND shown, one on each side of each wall 56.

C In Figure 3c, a tissue stabilizer 60 includes a flat distal face 62 having a O single distally-directed tissue separating wall 64 extending therefrom. The C' 10 stabilizer 60 contains one or more lumens in communication with semi-circular vacuum ports 66 that open on both sides of the wall 64. There are two such ports 66 shown, one on each side of each wall 64.

Figure 3d and 3e show two different vacuum port configurations for the tissue stabilizers 40, 52, or 60 shown in Figures 3a-3c. As mentioned abo e, the stabilizers 40, 52, or 60 may have one or more lumens in communication with one or more ports. In Figure 3d, two lumens 68a and 68b provide separate suction control to the associated ports. Thus, one tissue piece 70a is seen stabilized by the right-hand vacuum port, while the left-hand port is not operated. Alternatively, a single lumen 72 in communication with two vacuum ports is seen in Figure 3e, and both tissue pieces 70a, 70b are stabilized simultaneously. In both these vies, the tissue separating wall 74 is shown between the tissue pieces to be joined.

SFastening devices can thus be delivered via the wall 74, or through a gap formed for that purpose, such as the gap 46 and fastener channel 50 seen in Figure 3a.

Figures 4a-4c show a mechanical tissue stabilizer 80 with a four-part, linearly displaceable tissue clamp 82. On each side, a lower clamp 84 is separated from an upper clamp 86 and inserted between two tissue pieces (in this case valve leaflets 22). As the lower and upper clamps 84, 86 are brought together, a, seen in Figure 4b, they physically clamp and stabilize the leaflet 22. Small teeth 8 on the clamps 84, 86 may be provided for traction. The clamps 84 and 86 on each side are individually actuated to enable grasping of one leaflet 22 at a time.

Exemplary Suture-Based Tissue Fasteners Figure 5a illustrates a suture-based tissue fastener 90 of the present 14 invention including toggles 92 secured to the end of suture threads 94. Figure 5b is Sa sectional view through a needle 96 used to deliver the tissue fastener Specifically, the toggle 92 and suture thread 94 is seen loaded into the lumen of the c r needle 96, and a pusher 98 is provided to urge the tissue fastener 90 from the distal end thereof.

00 Figure 6a-6c depict several steps in a valve repair procedure using he IN tissue fasteners 90 shown in Figure 5a. A probe, such as the probe 20 seer in C-i Figure I having vacuum ports for tissue stabilization, provides lumens for two of the needles 96 of Figure 5b. The lumens with the vacuun parts 96 may re eive the Cg 10 needles 96 or additional lumens may be provided.. The sharp ends of the needles 96 pierce the leaflets, and the pushers 98 are displaced (separately or in conjunction) to deploy the tissue fasteners 90. After the needles 96 are ret acted, the toggles 92 anchor the tissue fasteners 90 on the ventricular 31 side of tie leaflets 22. The suture threads 94 are then tied off on the atrial 30 side to secure the leaflets 22 together, as seen in Figure 6c.

Figure 7a is a perspective view of an exemplary tissue stabilizing and fastening device 100 that uses the principles of vacuum stabilization and a suturebased toggle fastener, as seen in Figures Sa and 5b. The device 100 includes a probe 102 defining several lumens (not shown) therein that open on a dists face.

Two lumens 104 open at a proximal end and receive two of the needles 96 for delivering the fasteners. Two other lumens communicate through two side arms 106 with sources of vacuum. Figure 7b shows the device 100 in use in a valve repair procedure, with the two needles 96 having pierced the leaflets 22 and delivered the fasteners 90. The leaflets 22 are held to the probe 102 using the vacuum ports.

Figure 8 illustrates an alternative tissue stabilizing and fastening device 108 similar to the device 100 of Figure 7a, but having a pointed nose with two concave faces 110 in which the vacuum ports are located. The device 108 functions as described above, with a fastener deliver needle shown in phantom having ierced the left leaflet 22.

Figures 9a and 9b show a still further tissue stabilizing and fastening device 112 that uses a vacuum and needles to deliver suture-based fasteners having toggles through the tissue. The device 112 is quite similar in function to tle device o 102 of Figure 7a, but has a modified distal end, as best seen in the plan view f ;Z Figure 9b. Specifically, a central tissue separating wall 114 is provided with a pair of vacuum ports 116a on one side, and another pair 116b on the other. Again, the port 116 may be separately or commonly supplied with vacuum. Fastener delivery 5 lumens 118a and 118b are located on each side of the wall. The aforementioned 00 needles 96 or other such device may be delivered through the lumens 118 to pierce IN and fasten the tissue pieces.

Cl Figures 10a-10c are several photographs of tissue being connected w th O suture-based fasteners having toggles. Figure 10a illustrates the toggle 92 being C1 10 deployed. Figure O1b illustrates the needles 96 being retracted, and Figure 1Oc illustrates the sutures 94 being tied.

Figures 1 la-1 Ic show a tissue stabilizing and/or fastening device 120 having members deployable on a blind side of the tissue being connected, n this context, "blind side" means the side of the tissue pieces opposite the side to which the device has direct access. The deployable members may be clamps to stabilize the tissue pieces, or fastening devices that contact the tissue pieces on the blind side.

The device 120 includes a probe 122 with lumens, and a distal tip 123 that is narrower than the probe 122 and defines concave transition faces 124. A vacuum port 126 may be provided in each transition face 124 for tissue stabilization, or a clamping mechanism may be stowed in a space 128 in the distal tip 123. Figure 1 c shows the clamp 129 (or fastener) in a deployed state.

Figures 12a-12e illustrate a tissue stabilizing and fastening device 1 0 having needles 132 deployable on a blind side of the tissue being connected. The device 130 may be configured like the device 120 of Figure 1 la, with the space 128 receiving needles 132. A common suture thread 134 connects the needles 132 and is used to secure the tissue pieces 70 together. Thus, as seen in the seq ence of Figures 12a-12e, the needles 132 are first advanced to the blind side of the issue pieces 70 and deployed outboard of the distal tip. The entire device 130 is retracted, as in Figure 12c, to cause the needles 132 to pierce the tissue pieces The two needles 132 are then disengaged from the device 130, and each other, as in Figure 12d, and the entire device 130 once again retracted to pull the needles 132 out from the pieces 70, leaving the connected suture joining the two pi ces (Figure 12e). The suture 132 can then be tied off, or otherwise secured on he Supper side of the tissue pieces Figure 13a is a more detailed view of a tissue stabilizing and fastening c device 140 similar to that shown in Figures 12a-12e. The device 140 features two semi-circular vacuum ports 142 that stabilize the tissue pieces being joined The 00 Sdistal tip includes a centered and distally-directed frame 144 defining a spae 146

ID

I therein. The needles 148 are connected to the frame 144 and reside within the C- space 146. Although not shown, a deployment mechanism is also provided that O causes the needles to pivot outward about their distal ends, and also disengages the C, 10 needles 148 from the frame 144.

Figures 14a-14b illustrate a tissue stabilizing and fastening device 150 having needles 152 deployable on a blind side of the tissue being connecte The device 150 includes a probe 154 having two vacuum ports 156a, 156b for stabilizing the tissue pieces 70 being joined. A distal tip includes an extension member 158 having a centered and distally-directed frame 160 defining a pace 162 therein. The extension member 158 may be configured relatively narr w in one direction such that it can enter the ventricle 31 between the leaflets 22 with minimum risk to the chordae (not shown). The frame 160 may be extendea and retracted within the probe 154. The needles 152 are connected to the frame 160 and reside within the space 162. A deployment mechanism (not shown) is provided that causes the needles 152 to pivot outward about their distal end, and also disengages the needles 152 from the frame 160. A common suture th ead 166, which is stored within the probe 154, connects the needles 152 and is used to secure the tissue pieces 70 together. In the embodiment shown in Figure 14, the device 150 includes two needles 152 and a single suture 166. Other em diments may include four needles with separate sutures. Additional needles may b provided if needed.

Figures 15a-1 5h illustrate several steps in a tissue joining procedure using the tissue stabilizing and fastening device 150. Referring to Figure 15a, the probe 154 is passed through the atrium 30 via an access cannula or catheter 164. During this stage, the frame 160 is in its retracted position. The probe 154 is secured to the atrium 30 with a purse string 166 or any other manner known to one s illed in the art. Figures 15b-15d illustrate stabilization of the leaflets 22 being joi ed.

o Suction is provided to the first vacuum port 156a, and the probe 154 is manipulated to capture the first leaflet 22. With the first leaflet 22 captured, suction is pr vided to the second vacuum port 156b, and the second leaflet 22 is captured. Refe ring to Figure 15e, the frame 160 is advanced into the ventrical 31 by extending e 00 5 frame 160, and the needles 152 pivot outward about their distal end. The frame S160 is returned to its retracted position, and the needles 152 pierce the leafle s 22 and are directed into needle receivers 168, as shown in Figure 15f. As shown in

N

C Figure 15g, suction to the vacuum ports 156a, 156b is terminated, and the leaflets -0 22 are released. The needle receivers 168 pullthe ieedles 152 though the l1aflets (N 10 22, and the suture 166 "pays-out" behind the needles 152. The suture 166 tr tils out as the probe 154, withhe needles 152 stored wthn the probe 154, is withd awn from the access cannula or catheter 144 (see Figure 15g). The two needles 152 are then disengaged from the probe 154, and the suture 166 can then be tied off or otherwise secured on the upper side of the leaflets 22.

Figures 16a-16c are sectional views of several steps in a tissue joini g procedure using a tissue stabilizing device 170 having a fastening device 172 with two needles 174 for delivering a suture-based fastener. The stabilizing device 170 includes a distal tip with oppositely-facing concave surfaces 176 for contacting and stabilizing the tissue pieces 70 (with, vacuum ports). Although not shown, the fastening device 172 is stowed in a channel within the stabilizing device 170 and may be linearly deployed through apertures formed in the concave surfaces 176.

The device 170 further includes a sliding plate 178 with two throug holes 180 in the distal end, as seen in Figure 16d. The fastening device 172 has a spring bias that causes the needles 174 to curve inward when permitted. Therefore, as seen in Figure 16b, the fastening device 172 has been freed from the chan els past the concave surfaces 176 and the needles 174 have curved inward to be received in the plate holes throughholes 180. The needles 174 first pass twice through each respective tissue piece 70. The plate 178 is then retracted upward into the device 1170, thus pulling the needles 174 through the tissue pieces 70. The fastening device 172 is desirably made of a highly pliable material, such as a supere astic like Nitinol, so that it can be pulled through sharp angles. Suture threads 182 are connected to each needle 174 and are also pulled through the tissue pieces Figure 16c shows the result, with the suture thread 182 passed through bo h tissue pieces 70. Figures 16e and 16f illustrate two suture ties to complete the procedure.

Figures 17a-17c illustrate several steps in a valve repair procedure using a tissue stabilizing and fastening device 190 for delivering a suture-based axia needle fastener 192. The device 190 includes a clamping mechanism 194, iuch like the clamping device 82 seen in Figures 4a-4c. The two sides are independently controllable, so as to grasp and pierce one leaflet 22 and then the other. The fastener 192 includes a pair of needles 196 initially mounted in fie lower portion of the clamping mechanism 194 and facing upward. The two needles 196 are connected with a sutuie thread 198. Whenthe clamping mechanism 194 actuates, the needles 198 pierce the respective leaflet 22. Tie upper portion of each side then pulls the needle 196 completely through the leaflet 22, and the lower portion is retracted from the blind side of the leaflets 22. 'he resulting suture loop is tied off, as seen in Figure 17c.

Figures 18a-18d illustrate a valve repair procedure using a tissue fastening device 200 and a spiral suture-based leaflet fastener 202. The leaflets 22 arn stabilized, using one of the means disclosed herein (such as suction from two angled faces 204), and the fastener 202 is deployed. The fastener 202 comprises a helical needle 206, a trailing suture thread 208, and a pair of pledget anchoring devices 210. Figure 18d is a detailed view of the pledget 210 used with the spiral suture-based leaflet fastener 202.

Figures 19a-19d illustrate a tissue stabilizing and fastening device 220 that uses the principles of vacuum stabilization/mechanical clamping and a sutu ebased toggle fastener. The device 220 includes a probe 222 having two vacuum ports for initial tissue stabilization. In addition to the vacuum ports 224, the device 220 includes a mechanical tissue stabilizer 226 with a four-part, rotatable and linearly extendable capture hooks 228. The distal tip includes a centered a d distally-directed frame 230 defining a space 232 therein. The capture hooks 228 are folded flat within the space 232 and are rotatably and slidingly coupled to the probe 222 so that the capture hooks 228 may be rotated about 90 degrees and retracted to a capture position, wherein the leaflets 22 are "pinched" between distal ends of the capture hooks 228 and shoulders 234 of the probe 222. The two vacuum ports 224 also provide lumens for two of the needles 96 of Figure 5b. The sharp ends of the needles 96 pierce the leaflets 22, and the pushers 98 are displaced (separately or in conjunction) to deploy the tissue fastener 90. After the ne dles 96 are retracted, the toggles 92 anchor the tissue fasteners 90 on the ventricular 31 side of the leaflets. The suture threads 94 are then tied off on the atrial 30 side to Ssecure the leaflets 22 together, as seen in Figure 6c.

Figures 19a-l 9d illustrate several steps in a valve repair procedure using OC the tissue stabilizing and fastening device 220. The stabilizing and/or fastening ID elements of the device 220 is formed relatively narrow in one dimension to enable it to be slipped between the two leaflets 22, wherein the capture hooks 228 are stored in a folded and extended position. The two leaflets 22 are initially s abilized by the vacuum ports 224. To.further stabilize the leaflets 22,.the capture hooks 228 are rotated 90 degrees and retracted, wherein the leaflets 22 are physic ally clamped against the shoulders 234 of the probe 222 and the distal ends of e capture hooks 228. It is noted that both vacuum stabilization and mechani al clamping do not have to be implemented to stabilize the leaflets 22. In ce ain applications, implementing only one of the mechanisms may be desireable, With the leaflets 22 properly stabilized, the needles 96 are driven forward to pierce the leaflets 22. The capture hooks 228 reduce the likelihood of losing grasp o the leaflets 22 during the piercing process. As shown in Fig. 5b, the pushers 98 are displaced (separately or in conjunction) to deploy the tissue fastener 90. After the needles 96 are retracted, the toggles 92 anchor the tissue fasteners 90 on th ventricular 31 side of the leaflets 22. The suture threads 94 are then tied offon the atrial 30 side to secure the leaflets 22 together, as shown in Figure 6c.

Exemplary Mechanical Stabilizers and Fasteners Figure 20 shows a mechanical tissue stabilizer 240 that can be used to grasp tissue pieces 70 to be joined. The stabilizer 240 includes a probe 242 having a pair of pivoting arms 244 on a distal end. The arms 244 each have teeth 246 for added purchase on the tissue. Figures 21 a and 21b illustrate a valve repair procedure initiated in accordance with the present invention using the tissue stabilizer 240.

Figures 22a and 22b illustrate steps in a valve repair procedure usi g a mechanical tissue stabilizer 250 having preformed hooks 252. The hooks !52 are curled into approximately a three-quarter circle and deployed on the blind fide of the leaflets 22 to grasp and stabilize them. The linear displacement ofeac hook

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N 252 is separately controllable.

SFigures 23a-23c illustrate steps in a valve repair procedure using a mechanical tissue stabilizer 260 having spring-biased hooks 262. The hoos 262 C curl into approximately a three-quarter circle when deployed, and are adva ced on the blind side of the leaflets 22 to grasp and stabilize them. Again, the linear OC displacement of each hook 252 is separately controllable.

N Figures 24a-24d illustrate a valve repair procedure using a mechani al tissue stabilizer 270 similar to both the stabilizers shown in Figures 22 and 23.

After hooks 272 have stabilized the leaflets 22, a retainer 274 is slid down ink, rods 276 of each hook 272 (Figure 24c). Figure 24d shows the retainer 274 having reached the curvature of the hooks 272, at which point the link rods 276 an severed using conventional means. For example, the link rods 276 may be made of a polymer material, and a cutter deployed adjacent the device 270 to sever them.

Again, the link rods 276 are separately displaceable as seen in Figure 24b.

Exemplary Staple and Clip-Type Fasteners Figure 25a shows an exemplary tissue staple 280 for joining two tissue pieces in an open configuration. The staple 280 includes a bridge portion 282 and four gripping arms 244, two on each side. The gripping arms 284 are initii ly curled in a semi-circle upward from the plane of the bridge portion 282 and terminate in sharp points approximately in the plane of the bridge portion 82.

Figure 25b shows the staple 280 when closed, with the gripping arms 284 urled underneath the plane of the bridge portion 282 toward each other.

Figures 26a-26c illustrate several steps in a valve repair procedure ising an exemplary tissue fastening device 290 for delivering the tissue staple 280. The device 290 includes a probe 292 with an internal lumen 294 within which a pusher 296 is slidable. A stop member 298 is also provided underneath the bridge portion 282 of the staple 280 to prevent displacement of the bridge portion 282 toward the leaflets 22. After stabilizing the leaflets 22, the pusher 296 displaces downward which causes the staple 280 to undergo a plastic deformation from the configuration of Figure 25a to that of Figure 25b. The sharp points of the ipping arms 284 pass through the leaflets 22 and anchor the staple 280 therein. F nally, the stop member 298 is disengaged from under the bridge portion 282, and the to device 290 is retracted.

;Z Figure 27a illustrate the use of a tissue stabilizing and fastening device 300 for deploying the staple 280 of Figure 25. The device 300 is quite similar to the device 290 of Figure 26, with an exemplary stabilizing means shown in the nnm of vacuum chamber(s) 302 on each side of the staple deployment mechanism.

00 Figures 28a and 28b illustrate a further tissue fastening device 310 o the

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IN present invention for delivering an alternative "toggle-like" tissue clip 312. In Ci Figure 28a the clip 312 is shown open, while in Figure 28b the clip 312 is s own closed. The clip 312 is plastically deformed from open to close using a cla ping (C 10 mechanism 314 that flattens a ring-shaped head portion 316 of the clip 312. Two pincher arms 318 thus pivot toward each other and grasp and hold tissue therebetween.

Figures 29a-29c depict steps in a valve repair procedure using the tissue fastening device 310 of Figure 28. One method for inserting the device 31 as well as many other devices of the present invention, between the two leaflet 22 is detailed in Figure 29a. Specifically, the stabilizing and/or fastening elements of the devices of the present invention can be formed relatively narrow in one dimension to enable them to be slipped between two tissue pieces so that the pieces can then be fastened together from the blind side. Thus, for example, the ti sue fastening device 310 is seen in Figure 29a rotated to orient the narrow dimension in line with the gap between the leaflets 22.

Figures 30a-30b and 31a-31d illustrate an alternative tissue fasteni g device 320 for delivering another "toggle-like" tissue fastening clip 322. I contrast to the clip 312 of Figure 28, the clip 322 pierces the tissue pieces 70 from the front side, and is then deformed to clamp the tissue pieces 70 together.

Figures 32a-32d illustrate various embodiments of barbed clips 330, 332, 334, 336 used to fasten tissue pieces together using the principles of the present invention. The barbed clips include a bridge portion 338, 340, 342, 344 and terminate in sharp points.

Figures 33a-33c illustrate several steps in a valve repair procedure using an exemplary barbed clip deployment device 350 for delivering the barbed clip 330. The device 350 includes a probe 352 with an internal lumen 354 wit in which an internal driver 356 is slidable. A stop member 358 is provided at the distal end of the probe 352 to spread the two barbs away from each other as it is Spushed forward. The tips of the barbed clip 330 are displaced towards the Ilaflets 22 by downwardly sliding the driver 356. After the clip 330 pierces the lea lets 22

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c from the front side, the clip 330 is disengaged from the device 350 as shown in Figure 33c. When the clip 330 is disengaged from the device 350, it return to its 00 retracted position and compresses the leaflets 22 together. Again, any ofthe \stabilizers of the present invention can be used in conjunction with the depl ayment C, device 350.

Figures 34a-34f illustrate a spring-loaded clip 360 used to fasten tissue pieces 70 together. The clip 360 comprises a spring portion 362 and two aims 364, and the anns 364 include a plurality of barbs 366. The distal ends of the ar s 364 are tapered to enable the clip 350 to pierce the leaflets 22, and the arms 364 are configured to overlap each other after closure (see Figure 34c). Figures 35 illustrate a valve repair procedure using a clip deployment device 370 for delivering the spring-loaded clip 360. The device 370 includes a probe 37 with an internal lumen 374, and a pusher 376 is slidably coupled to the internal umen 374. A sleeve 378 is disposed between the pusher 376 and the internal wa 1 of the lumen 374. The spring portion 362 of the clip 360 is housed within the sleeve 378 in its open position, wherein the spring portion 362 is compressed by the s eeve 378. As seen in the sequence of Figures 35a-35c, downward movement o the pusher 376 causes the clip 360 to move downward and pierce the leaflets 22 from the front side. The clip 360 is pushed downward at a velocity adequate to insure penetration without dislodging the leaflets 22 from the vacuum source. As the clip 360 is disengaged from the device 370, the clip 360 automatically springs to its closed position and compresses the leaflets together.

Figures 36a-36c illustrate another embodiment of a spring-loaded clip 380 used to fasten tissue pieces together. The clip 380 comprises a spring portion 382 and two arms 384 having distal ends which are tapered and extend inwardly to pierce and lockingly secure the leaflets 22. A gap 386 exits between mid ortions of the arms 384 when the clip 380 is in its closed position.

Figures 37a and 37b illustrate a clip deployment device 390 havi g a probe 392 with an internal lumen 394 and a pusher 396 slidably coupled to the internal lumen 394. The spring portion 382 is retained in a compressed state b3) within a housing member 398 such that the clip 380 is held in an open position.

Downward movement of the pusher 396 causes the clip 380 to move downward and pierce the leaflets 22 from the front side. As the spring portion 384 exits the housing member 398, the clip 380 automatically springs into its closed position 00 5 and lockingly secures and compresses the leaflets 22.

\I0 Exemplary Integrated Stabilizing and Fastening Device Figures 38-46 illustrate another exemplary embodiment of an integrated Stissue stabilizing and fastening device 400 which captures tissue pieces, such as valve leaflets, with vacuum and fastens the tissue pieces with sutures. The device 400 is similar to the devices illustrated in Figures 11-15 in that it comprises a slender distal portion which accesses the heart valve trans-atrially. The device 400 is placed through a specialized cannula and it has a proximal handpiece porion which provides user controls. In an exemplary embodiment the distal portion is approximately 10 mm in diameter and it terminates in vacuum ports and a eedle array as depicted in Figures 38 through 41. The handpiece portion contain individual vacuum port controls and needle deployment controls as general y depicted in Figure 44. The device 400 is connected to a vacuum source via a flexible hose. The illustrated device 400 is utilized to grasp the tissue pieces and place the sutures correctly. Remote tying and cutting of the sutures can be accomplished with a separate device. The following description of the use f the device 400 will be made with respect to the stabilizing and fastening of the leaflets of a mitral valve. However, those of skill in the art will appreciate that the device can also be used to stabilize and fasten other physiological tissues. A more detailed description of the device 400 follows.

Figures 38-41 illustrate device 400 in various modes of operation. Device 400 comprises vacuum ports 402 and 404 at the distal tip of device 400 which are connected to the vacuum source 418 (shown in Figure 44). Needle carrier 406 is centrally disposed at the distal end of device 400 and is configured to be extended from and retracted back into device 400. Needles 408 are mounted on mo nting blocks 410 within carrier 406 and mounting blocks 410 are pivotably attacl ed to carrier 406 via pivot pin 412. Needle catchers 414 are retained in ports 402 and 404 to grip and retain needles 408 when needle carrier is retraced back intc device C( 400 upon completion of the procedure.

to Figure 44 illustrates an exemplary handpiece 416 which connects v cuum source 418 to device 400 and delivers vacuum to vacuum ports 402, 404 at the CrC distal tip of the device. Pinch valves 420 mounted on the handpiece 416 of the device normally constrict the vacuum lines. By individually manipulating each 00 valve, the operator can differentially control access to the vacuum source. By IN partially deflecting one valve, the operator permits momentary access by one of the vacuum ports to the vacuum source. By fully deflecting one of the valves, the operator permits continuous access to the vacuum source. The provision o separate, individually controlled valves permits the delivery of differential vacuum to one or. the other of ports 402 and 404. This may be very helpful in cert in cases of valve prolapse where it is necessary to capture one leaflet and move it 1aterally with respect to the second leaflet to facilitate final capture.

The vacuum system has, of necessity, two different operating modes.

Initially, it is necessary to capture the leaflets. This requires relatively high flow rates to attract a leaflet to a vacuum port. In an exemplary embodiment the flow rate is approximately 10 cc per second. Since this flow rate is capable of exsanguinating and destabilizing the beating heart, the invention provides for quick and efficient leaflet capture. Efficient capture requires that the vacu m port be close to the leaflet when the vacuum is turned on. Proper placement of device 400 with respect to the leaflets is facilitated by placement ofechogenic members at or near vacuum ports 402 and 404 to enhance visualization by echo.

Echogenicity is enhanced by the proper choice of materials. The d vice, being entirely of plastic except for small metal parts in the immediate vicinity of the ports, takes advantage of the relatively high visibility of metal while avoiding the shadowing properties of large masses of metal. The metal parts in question are needle catchers 414, needles 408 and pivot pin 412. Since these parts are ocated near the vacuum ports 402 and 404 in the long axis of the device, they ser e to locate ports 402 and 404 axially relative to the valve leaflets prior to vacuum application. Since they are discontinuous and symmetrical about ports 402 and 404 in the short axes, they facilitate the correct radial orientation of the pots relative to the valve leaflets. Echogenicity is further enhanced by a polymer coating which can be wholly or selectively applied to the ports 402 and 404. This o) coating creates a microscopic boundary layer which effectively separates the ports ;Z from the blood under echo visualization.

In an exemplary embodiment, the vacuum surfaces of the ports 402 a d 404 are angled between zero and ninety degrees relative to a plane normal to the ong 0 5 axis of the device. This is intended to conform somewhat to the shape of the valve r leaflets. In another exemplary embodiment the ports are angled between 15 to IN degrees relative to a plane normal to the long axis of the device. In yet anot er Sembodiment the ports are angled at about 25 degrees relative to that plane.

Once the leaflets have been captured, the second operating mode of the Cl 10 vacuum system is to hold the leaflets in position for sutuiire application without additional exsanguination. This implies high holding force and no flow. These properties are primarily a function of pressure differential, port area and por shape. In one embodiment, adequate holding force is obtained at a maximum differential pressure with port areas in the approximate range of 0.03-0.04 s uare inch per port. In the embodiment illustrated in Figure 43, a geometrically optimized cylindrical device is shown having two separate shaped port 404 and 404. The illustrated device 400 has about 10 mm in diameter. Since a acuum port with the highest ratio of area to perimeter a circle) will have the h ghest average peel away strength, some modification of the shaped port is us ful for functional optimization. This is accomplished in the device by filling in the corners of the where the arc meets the straight portion at acute angles. This can be seen clearly on port 402 in Figure 38. The comers which have been eliminated represent the part of the shape least resistant to peel away ofthe leaflet which is being held by vacuum.

Vacuum ports 402 and 404 further have barriers 422 which serve tvo distinct purposes. Barriers 422 support the valve leaflet to prevent it from being sucked deep into the ports 402 and 404, thereby minimizing tissue trauma. This has the further useful effect of controlling the position of the leaflet relative to the suture needles so that the latter penetrate the leaflet in a predictable way, placing sutures the correct distance from the edge of the leaflet for reliable repair. In the illustrated embodiment of Figure 43, the barriers are recessed below the perimeter of the slot. In an exemplary embodiment the barriers are recessed about 0.02 inches. This slightly distorts the valve tissue and creates resistance to disp acement 24 of tissue as it is moved laterally by the device to approximate the leaflets. If the o i barriers were not recessed, the only resistance to lateral drag would be the coefficient of friction between the port surface and the leaflet which is likey to be ¢q low in the bloody environment.

A pre-evacuated sterile bottle 418 serves as a passive vacuum sourc e for 00 capturing and holding the leaflets. In an exemplary embodiment, the systei is INO designed to minimize total exsanguination to about 200 cc per procedure. A standard 2 liter bottle can provide that amount of flow with negligible incr ase in absolute pressure. This offers a significant advantage over utility vacuum sources in hospital operating rooms and dedicated active pumps. Utility sources are not well controlled and active pumps present cost, convenience and sterility issues.

Once captured, leaflets will be fastened by remotely applied sutures. The mechanism by which this is accomplished is shown in Figures 39 through 42 as will be discussed below. Figures 45a and 45b illustrates two exemplary suture configurations which the system can provide, depending on the way in which the sutures and needles are loaded into the device.

In one embodiment, two lengths of suture (not shown) are used with a straight needle 408 attached to each suture end. Sutures are inserted into a coaxial hole in the end of the needle opposite the point and the body of the needle is crimped to retain the suture using conventional suture technology. A groo ve near the tip of the needle provides a means for grasping and pulling the needle hrough after it has pierced the valve leaflet. Sutures can be monofilament or brai ed or other types suitable for cardiovascular use. In an exemplary embodiment, a size 4- 0 monofilament suture capable of gamma sterilization Novafil) is used since the internal configuration of the device favors radiation sterilization and it is desirable to be able to sterilize the entire system at one time. The needles ill receive a lubricious coating silicone) to reduce penetration force and raction.

In one embodiment, the needles and sutures are an integral part of a single use completely disposable device. In a second embodiment, the needles, utures and associated hardware may be packaged as a cartridge which plugs into a reusable device. This device can be limited to multiple use in a single procedure, or reusable for multiple procedures.

Needle carrier 406 further comprises needle driver assembly 424. Driver assembly 424 includes blocks 410; axle 412, needle driver 426, and cams 42 ;Z Needles 408 are slidably mounted in blocks 410 which pivot about axle 412.

Blocks 410 may be slotted in the area of the hole which receives the needle so that the needles can be held in place by controlled friction. Sutures (not shown) 00 5 protruding from the ends of the needles can be routed along the sides of the eedle Scarrier 406 in grooves provided for that purpose. The needles are initially re essed into the body of the device 400 by virtue of the recessed position of carrier 4 6, as C-I shown in Figure 38. The position of the needles in this state is shown in Fig ure 39.

The needle mounting blocks 410 are pivoted so that needles 408 lie in a sing le row C1 10 within the confines of the needle carrier 406. One end of driver element 426 which drives the needle carrier 406 in and out of the distal device tip is positioned just above the needle points so that the needles 408 are retained in their holders against any drag which might tend to dislodge them. The other end of the iver element 426 is connected to a control at the proximal end of the device by which the operator manipulates the needles 408.

After the valve leaflets are captured as described above, needle carrir 406 is advanced from the position shown in Figure 38 to that of Figure 39. The needle mechanism at this stage is compactly configured to avoid entangling chordae tendineae or papillary muscles during capture of the leaflets and initial need deployment. Cams 428 are then advanced, pivoting the needle mounting bl cks 410 and causing the needles 408 to deploy as shown in Figure 40. Protruding stops on blocks 410 limit the angular deployment of the needles to the proper po ition for penetrating the valve leaflets. These stops come to rest against the needle carrier 406. The individual parts can be seen clearly in Figure 42.

With the needles deployed, the needle carrier 406 is retracted prox* ally, causing the needle points to penetrate valve leaflets (not shown) and enter the vacuum ports 402 and 404. As the needles continue to move proximally, the points enter the needle catchers 414 which are essentially one way gripping devices. The needles advance until their grooves engage the jaws of the needle catchers 414. Needle catchers 414 are retained in the ports 402 and 404 by a vacuum adapter 430, shown in Figure 42.

The needle carrier 406 advances distally pulling the needle mounti g blocks 410 away from the needles which are retained by the needle catchers 414.

The vacuum is disconnected and the device is withdrawn from the heart along with the needles 408 which are firmly held by the catchers 414. As the needles move outward, the sutures, which are loosely deployed in the body of the device 400, are pulled through the leaflets 432 and 434 to one of the positions shown in Figures 45a and 45b. Once the device is free of the access cannula, sutures 436 and 438, or 440 and 442, are cut from the needles and tied remotely using a knot rundovn tool with an integral cutter to remove excess suture material.

The proximal control handpieces 416 shown in Figures 44 and 46 are illustrative of alternate approaches to controlling the system. One objective is to permit single handed control of the vacuum ports and suture needles without destabilizing the device. It is useful to locate and hold the device precisely in relation to the beating heart in order to accomplish the surgical procedure vith minimal blood loss. In operation, the surgeon will use one hand to stabilize the distal end of the device via the cannula where it enters the atrium and the other hand to operate the vacuum and suturing controls. Control functions are described below.

In the device shown in Figure 44, handpiece 416 has a pistol-like configuration which includes a shaft portion 446 and a handle portion 448. A pair of vacuum controls 420 are positioned akin to pistol hammers at the back f shaft portion 446 and at the top of handle portion 448. In this embodiment vacuum controls 420 are thumb operated. Vacuum controls 420 are separately cap ble of being partially activated or fully activated by a toggle mechanism (not sho When partially activated, the associated vacuum line is momentarily opened, allowing blood to flow into the vacuum source 418. If one of the controls 420 is released it will return to its normally closed position and flow to the associ ated line will stop immediately. Once a leaflet has been captured the control 420 can be moved to its extreme position where it will remain due to an internal toggle action.

In this case vacuum is applied to retain the leaflet which, in turn, blocks tl e port, preventing blood flow.

In another embodiment shown in Figure 46, the pair of vacuum co trols 420 -are located in the body 416 below the shaft portion 446 and in front o the handle portion 448. In this embodiment the vacuum controls 420 function like a pistol trigger, just above the needle control trigger 444, so that they can be t3j operated individually by the index finger. In the arrangement shown, it will be ;Z necessary to actuate the control nearest the index finger first The first action momentarily opens the vacuum line as described above. When the leaflet is captured the control is depressed further, causing it to latch into place by an internal toggle action. The second control 420 is now accessible to the inde

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finger for capture of the second leaflet in similar manner.

IN In the embodiments shown in Figures 44 and 46 the trigger 444 is p votably C1 mounted in body 416 to control needle deployment after the leaflets are captured.

The trigger is connected to needle driver 426 by a linkage iriteinai't6 the boiy 416 C1 10 which establishes the correct direction aid 'stroke. The device is supplied v ith the trigger fully depressed to hold the needle array in the position shown in Figure 38 relative to the vacuum ports 402 and 404. An internal latch in 416 retains t e trigger. Once the leaflets have been captured the trigger is released, allowing the needles to advance to the position shown in Figure 39. Near the end of the trigger stroke, needle driver 426 bears on cams 428 which, in turn, bear on blocks 410 causing the needles to deploy outward as in Figure Squeezing the trigger 444 moves the needles proximally through the valve leaflets and into the vacuum ports 402 and 404 where they will be trapped as previously described. The trigger stroke will be internally limited so that it will not achieve the latched condition in which the cycle began. Releasing the trigg er moves the needle carrier 406 forward, separating the needles from blocks 410. The entire device can now be removed, drawing sutures through the leaflets as previously described. The distal tip of the device 400 is rotatable relative t) the body 416 for precise angular positioning of the ports 402 while maintaining a comfortable handle position for the user.

The present invention may be embodied in other specific forms wiout departing from its spirit, and the described embodiments are to be consider d in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the claims and their equivalents rather than by the foregoing description.

Claims (7)

1. A method for joining heart valve tissue, the method comprisin, temporarily stabilizing a first valve leaflet to a probe; temporarily stabilizing a second valve leaflet to the probe; engaging a tissue securing device to the first valve leaflet; engaging the tissue securing device to the second valve leaflk releasing the first valve leaflet from the probe; releasing the second valve leaflet from the probe; and securing the first valve leaflet to the second valve leaflet, whe first valve leaflet is released from the probe prior to securing the first leaflet to the second valve leaflet.

2. The method of claim 1, wherein the second valve leaflet is rel the probe prior to securing the first valve leaflet to the second valve 1

3. The method of claim 1, wherein the tissue securing device co suture, and engaging the tissue securing device to the first valve lea comprises passing the suture through the first valve leaflet.

4. The method of claim 2, wherein securing the first valve leaflet second valve leaflet comprises tying the suture.

The method of claim 2, wherein engaging the tissue securing the second valve leaflet comprises passing the suture through the s( leaflet.

6. The method of claim 5, wherein the first valve leaflet is tempo stabilized prior to passing the suture through the first valve leaflet, ar second valve leaflet is temporarily stabilized prior to passing the sutt the second valve leaflet. "ein the valve )ased from eaflet. nprises a let to the device to cond valve rarily Id the ire through 30/08/07 b1t

7. A method for joining heart valve tissue substantially as hereir before described with reference to the accompanying drawings. Dated this 30 day of August 2007 00 -IN INO Edward Lifesciences Corporation Patent Attorneys for the Applicant SPETER MAXWELL ASSOCIATES 30/08/07