BACKGROUND OF THE INVENTION The present invention relates generally to apparatus and methods for removing occluding materials from body lumens. More particularly, the present invention relates to the construction and use of atherectomy catheters for excising atheroma and other materials from blood vessels.
Cardiovascular disease frequently arises from the accumulation of atheromatous material on the inner walls of vascular lumens, particularly arterial lumens of the coronary and other vasculature, resulting in a condition known as atherosclerosis. Atherosclerosis occurs naturally as a result of aging, but may also be aggravated by factors such as diet, hypertension, heredity, vascular injury, and the like. Atheromatous and other vascular deposits restrict blood flow and can cause ischemia which, in acute cases, can result in myocardial infarction. Atheromatous deposits can have widely varying properties, with some deposits being relatively soft and others being fibrous and/or calcified. In the latter case, the deposits are frequently referred to as plaque.
Atherosclerosis can be treated in a variety of ways, including drugs, bypass surgery, and a variety of catheter-based approaches which rely on intravascular widening or removal of the atheromatous or other material occluding a blood vessel. Of particular interest to the present invention, a variety of methods for cutting or dislodging material and removing such material from the blood vessel have been proposed, generally being referred to as atherectomy procedures. Atherectomy catheters intended to excise material from the blood vessel lumen generally employ a rotatable and/or axially translatable cutting blade which can be advanced into or past the occlusive material in order to cut and separate such material from the blood vessel lumen. In particular, side-cutting atherectomy catheters generally employ a housing having an aperture on one side, a blade which is rotated or translated by the aperture, and a balloon or other deflecting structure to urge the aperture against the material to be removed.
Although atherectomy catheters have proven to be very successful in treating many types of atherosclerosis, some catheter designs suffer from certain limitations. For example, many side-cutting atherectomy catheters have difficulty in capturing occluding material in the cutting aperture. To facilitate material capture, the cutting aperture is frequently elongated. Although improving material capture, such lengthening makes it more difficult to introduce the distal end of the catheter through torturous regions of the vasculature. Additionally, it is often difficult for conventional atherectomy cutters to apply the requisite pressure to cut off the targeted material. When higher pressures are applied, damage to the artery (barotrauma) can occur. High pressures can also compress plaque, subsequently reducing the cutter's ability to capture the occlusive material. This decreases the effectiveness of these cutters and limits the cutter and catheter designs.
For these reasons, it is desired to provide atherectomy catheters which can access small, tortuous regions of the vasculature and which can remove atheromatous and other occluding materials from within blood vessels in a controlled fashion with minimum risk of injuring the blood vessel wall. In particular, it is desired to provide atherectomy catheters which can facilitate capturing of occlusive material. It would also be particularly desirable to decrease the amount of force required to cut off occlusive material from the body. At least some of these objectives will be met by the catheter and method of the present invention described hereinafter and in the claims.
SUMMARY OF THE INVENTION The present invention provides catheters, kits, and methods for removing material from a body lumen. The catheters and methods of the present invention are for use in a variety of body lumens, including but not limited to intravascular lumens such as the coronary artery and other blood vessels. In general, the catheter of the present invention has a cutting element that cuts material engaged by a material capture device on the catheter body. Preferably, the material capture device tensions the material during cutting, which reduces the amount of cutting force required. The material capture device typically follows a path that draws material into the catheter body. Preferably, but not necessarily, the material capture device is arranged on the catheter body to advance along a path outwardly from the catheter body into the material and then inwardly towards the catheter body to tension the material. In some embodiments, the material capture device may extend in an outwardly direction but not beyond the outer diameter of the catheter body. The cutting element on the catheter body moves between a first position and a second position to cut the material while in tension, where motion of the cutting element urges the material capture device to draw cut material into the catheter body.
Desirably, the blade or blades of the catheter will be actuable with the application of reasonable mechanical forces which are capable of being transmitted along even rather lengthy catheters. Further desirably, the catheters will be suitable for directional removal of occluding material and may include mechanisms for engaging cutting blades against selected portions of a vascular wall. Optionally, the engaging mechanisms should permit blood perfusion during performance of an atherectomy procedure.
In one embodiment, the catheter of the present invention uses a material capture device in the form of a material capture needle. The needle will be deployed in a radially outward direction from the catheter body. Preferably, but not necessarily, the needle will capture material while the catheter remains stationary. Some embodiments may use a plurality of material capture needles. The material capture needle may follow a path outwardly from the catheter body in various manners. In one embodiment, the needle has a portion that advances through an elongate slot on the catheter body to move the needle along a path outwardly from the catheter body. Another embodiment uses a curved needle rotatably mounted about a pivot pin. As the needle is rotated, it will protrude outwardly from the catheter body. A preferred embodiment uses a needle having a bias element which urges the needle outwardly when the catheter is in position. Typically, a material cutting element will engage the material that has been captured and sheer off the material into the catheter.
In a further embodiment, a material capture device of the present invention uses a penetrating member mounted to extend through an aperture on the catheter body to penetrate material in advance of the cutting blade and to draw material into the catheter body as the cutting blade is advanced past the aperture. The penetrating member is rotatably mounted to the slidable cutting blade on the catheter body. A cam surface on the catheter body engages a surface of the penetrating member to guide the member along a path to engage the material and draw the material into the catheter body. In a still further embodiment, an abutment or raised portion on the catheter body is mounted to engage one end of the penetrating member. This contact caused the penetrating member to rotate about its pivot point on the cutting blade and thus engage material and draw material into the catheter body.
In another aspect of the present invention, a method is provided for excising occlusive material from within a body lumen. The method involves engaging the occlusive material with a material capture device on a catheter body. The material is drawn in a radially inward direction by the device to tension the material to be cut. A blade is advanced through the tensioned material to sever the material from the body lumen. As mentioned previously, tensioning the material reduces the amount of cutting force required. The tensioning of the occlusive material may also comprise moving the material capture device towards a catheter body while the material capture device is in contact with the occlusive material. Typically, the engaging and tensioning steps may also be performed with a single motion by the user to facilitate cutting.
In a still further aspect, kits according to the present invention will comprise a catheter having a material capture device. The kits will further include instructions for use setting forth a method as described above. Optionally, the kits will further include packaging suitable for containing the catheter and the instructions for use. Exemplary containers include pouches, trays, boxes, tubes, and the like. The instructions for use may be provided on a separate sheet of paper or other medium. Optionally, the instructions may be printed in whole or in part on the packaging. Usually, at least the catheter will be provided in a sterilized condition. Other kit components, such as a guidewire, may also be included.
A further understanding of the nature and advantages of the invention will become apparent by reference to the remaining portions of the specification and drawings.
BRIEF DESCRIPTION OF THE DRAWINGSFIG. 1 is a perspective view of an atherectomy catheter constructed in accordance with the principles of the present invention.
FIGS. 2-4 show various embodiments of a material capture device and a material cutting element according to the present invention.
FIGS. 5A-5C illustrate a material cutting sequence using one embodiment of a material capture device and material cutting element according to the present invention.
FIGS. 6A-6B show cross-sectional views of a further embodiment of a material capture device and material cutting element.
FIGS. 7-8 show still further embodiments of a material capture device and material cutting element.
FIGS. 9-11 show cross-sectional views of a preferred embodiment of the material capture device;
FIGS. 12, 13,14,14A-C, and15 show alternative embodiments of the device show inFIGS. 9-11.
FIGS. 16-18 depict various embodiments of a cam surface according to the present invention.
FIGS. 19-22 are cross-sectional views of a telescoping cutter having a material capture device according to the present invention.
FIGS. 23-24 show a still further embodiment of the material capture device.
FIG. 25 shows a kit according to the present invention.
FIGS. 26 and 27 illustrate a catheter having material capture devices and material cutting elements oriented at various angles on the catheter body.
FIG. 28 shows a preferred embodiment of the present invention for use with a material imaging device according to the present invention.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS The present invention provides devices, methods, and kits for use in removing material from a body lumen. The present invention may be used in a variety of body lumens, including but not limited to coronary and other arteries. Advantageously, the present invention reduces the amount of force required to cut material and facilitates material capture into apertures of the catheter.
Apparatus according to the present invention will comprise catheters having catheter bodies adapted for intraluminal introduction to the target body lumen. The dimensions and other physical characteristics of the catheter bodies will vary significantly depending on the body lumen which is to be accessed. In the exemplary case of atherectomy catheters intended for intravascular introduction, the catheter bodies will typically be very flexible and suitable for introduction over a guidewire to a target site within the vasculature. In particular, catheters can be intended for “over-the-wire” introduction when a guidewire lumen extends fully through the catheter body or for “rapid exchange” introduction where the guidewire lumen extends only through a distal portion of the catheter body.
Catheter bodies intended for intravascular introduction will typically have a length in the range from 50 cm to 200 cm and an outer diameter in the range from 1 French (0.33 mm; Fr.) to 12 Fr., usually from 3 Fr. to 9 Fr. In the case of coronary catheters, the length is typically in the range from 125 to 200 cm, the diameter is preferably below 8 Fr., more preferably below 7 Fr., and most preferably in the range from 2 Fr. to 7 Fr. Catheter bodies will typically be composed of an organic polymer which is fabricated by conventional extrusion techniques. Suitable polymers include polyvinylchloride, polyurethanes, polyesters, polytetrafluoroethylenes (PTFE), silicone rubbers, natural rubbers, and the like. Optionally, the catheter body may be reinforced with braid, helical wires, axial filaments, or the like, in order to increase rotational strength, column strength, toughness, pushability, and the like. Suitable catheter bodies may be formed by extrusion, with one or more lumens being provided when desired. The catheter diameter can be modified by heat expansion and shrinkage using conventional techniques. The resulting catheters will thus be suitable for introduction to the vascular system, often the coronary arteries, by conventional techniques.
The cutting blades used in the present invention will usually be formed from a metal, but could also be formed from hard plastics, ceramics, or composites of two or more materials, which can be honed or otherwise formed into the desired cutting edge. In the exemplary embodiments, the cutting blades are formed as coaxial tubular blades with the cutting edges defined in aligned apertures therein. It will be appreciated that the present invention is not limited to such preferred cutting blade assemblies, in a variety of other designs, such as the use of wiper blades, scissor blades or the like. Optionally, the cutting edge of either or both the blades may be hardened, e.g., by application of a coating. A preferred coating material is titanium nitride, available from Brycoat, Inc., which may be applied according to manufacturer's instructions.
Referring now toFIG. 1, acatheter10 constructed in accordance with the principles of the present invention comprises acatheter body12 having aproximal end14 and adistal end16. Acutting mechanism18 comprises anouter cutter20, aninner cutter22 is attached to the distal end of thecatheter body12, and aneedle23 as a material capture device. Anatraumatic tip24 is attached to the distal end of theouter cutter20, and aguidewire lumen25 extends through the entire catheter body, cuttingmechanism18, and terminates inport25 at the distal tip oftip section24. Aproximal hub30 is attached to the proximal end ofcatheter body12 and comprises a perfusion/aspiration connector32, aguidewire connector34, and aslider36. Theslider36 is attached to the proximal end of anactuator rod37 which extends from thehub30 through the lumen ofcatheter body12 into thecutting mechanism18 where it is attached at a proximal end of theinner cutter22. In this way, manual actuation ofslider36 in the direction ofarrow38 movesinner cutter22 in the direction ofarrow40.
Referring toFIGS. 2A and 2B, this embodiment of thecatheter10 uses thematerial capture needle23 to capture the material and tension it towards thecutters20 and22. Thematerial capture needle23 follows a path where the material capture needle extends outwardly from the catheter body and moves inwardly towards the catheter body to tension the material. In this embodiment, when thematerial capture needle23 is deployed, it angles out from theaperture42 and a portion of the material capture needle typically runs parallel to the window with the sharpened tip located near the proximal end of the aperture. The inner cutter or cuttingelement22 is reciprocated to open and close theaperture42 formed in the wall of thecatheter body12. Movement of theinner cutter22 also controls the deployment of the material capture needle. When theinner cutter22 opens theaperture42, thematerial capture needle23 is biased outwardly from thecatheter body12. Thematerial capture needle23 is preferably spring-loaded, where in its resting condition, the material capture needle extends outwardly from thecatheter body12. Thematerial capture needle23 is otherwise constrained within thecatheter body12 when theinner cutter22 closesaperture42. Thematerial capture needle23 may be made of a variety of materials such as stainless steel or a superelastic material.
With thematerial capture needle23 deployed as shown inFIG. 2B, the material capture needle may penetrate into the material when thecatheter body12 is pulled in the proximal direction. Theinner cutter22 is then closed, as indicated byarrow40, to push thematerial capture needle23 towards thecatheter body12 as indicated byarrow44. Preferably, closing ofcutter22 will tension the material and draw it into thecatheter body12 when thecutters20 and22 will shear off the material. It is also preferred that theinner cutter22, upon finishing the closing motion, will wipe the piece of cut-off material off thematerial capture needle23 and into the catheter for storage. Thematerial capture needle23 andcutting mechanism18 may then be readied to make a subsequent cut. Thematerial capture needle23 typically has a diameter between about 0.1 to 0.5 mm, preferably 0.2 to 0.3 mm, with a length between about 1 to 5 mm, preferably 3 to 4 mm.
Referring toFIGS. 3-4, a variety of catheter embodiments may incorporate a needle as a material capture device. Like the catheter ofFIG. 2, these catheters rely on the motion of a cutter to control positioning of the material capture needle during cutting. TheFIGS. 3A-3B show the distal portion of acatheter50 having anouter cutter52 which reciprocates to control the deployment of thematerial capture needle54. Additionally, in this embodiment, thematerial capture needle54 is deployed to have a forward pointing sharpened tip. With thematerial capture needle54 deployed, thecatheter50 would be pushed forward as indicated byarrow56 to penetrate target material T. Thecatheter50 may also incorporate aski mechanism58 to urge the cutting side of the catheter radially against the target material T. Such a ski mechanism is described in detail in commonly assigned, copending U.S. patent application Ser. No. 08/982,231 (Attorney Docket No. 18489-000200) filed Dec. 17, 1997, the full disclosure of which is incorporated herein by reference. All of the catheter structures herein may optionally employ such mechanisms.
FIGS. 4A and 4B show acatheter70 having atelescoping cutter72 for use with amaterial capture needle74. Thetelescoping cutter72 is used to decrease the rigid length of thecatheter70 and may be used to create a larger window oraperture76 for removing greater amounts of material. As thetelescoping cutter72 is drawn proximally, thematerial capture needle74 will be pushed into theaperture76 as indicated byarrow78, along with material attached to the material capture needle. As seen inFIG. 4B, thematerial capture device74 may also include one ormore barbs79 which keep the material from sliding off once it is excised.
Thecatheter70 is quite useful and an improvement over conventional atherectomy catheters even without incorporation of thematerial capture needle74. The decrease in the rigid length of the distal portion ofcatheter70 is a significant advantage, particularly when the catheter is introduced to the highly tortuous regions of the coronary vasculature. Once at a desired location, however, the rigid cutter portion of the catheter can be extended in length by 50% or more, with a theoretical limit of 100% for a two-portion telescoping region. In the illustrated embodiment, the cuttingaperture76 is defined only on one of the cutter blades. In other embodiments, it will possible to define the aperture on both of the cutting blades and/or in a variety of configurations. While the cutting blades will preferably employ the cutting edges at each end, the advantages of the telescoping cutter can be enjoyed even without the cutting edges.
Referring now toFIGS. 5A-5C, another embodiment of anatherectomy catheter100 uses amaterial capture needle102 which rotates about apivot pin104. As indicated byarrow106 inFIG. 5A, thematerial capture needle102 will rotate upward as thedrawbar108 is pulled proximally. As seen in the cross-section ofFIG. 5B, thedrawbar108 is coupled toslider110 which has cuttingblade112. Acam106 about thepivot pin104 will pull against thematerial capture needle102 asdrawbar108 is moved. Thedrawbar108 will be retracted until theblade112, as shown inFIG. 5C, has sheared off any material captured by thematerial capture needle102.
FIGS. 6A and 6B show a catheter embodiment similar to that ofFIGS. 5A-5C. Thematerial capture needle120 ofFIG. 6A rotates about apivot122 to engage material M to be excised from the luminal wall. The needle actuator for this embodiment differs from that ofcatheter100. Thematerial capture needle120 of the present embodiment sits betweentabs124 and126 which are attached to thedrawbar130. Thedrawbar130 rotates theneedle120 while pulling onslider132 havingblade134. Of course, it should be understood that the motion of the pivotingmaterial capture needle120 may be dependent or independent of the motion of the cutting element orblade134. Thematerial capture needle120 may also be constructed of existing devices such as a suture needle used in procedures such as coronary anastomoses.
FIG. 7 shows, amaterial capture needle150 mounted on a base152 which slides within elongate slots orgrooves154 and156. Theslots154 and156 guide theneedle150 along a path that carries the needle outward and then inwardly towards thecatheter body158 after the needle has engaged the catheter body. Theinner cutter160 has a cut-out162 which holds the base152 as the cutter is moved with thematerial capture needle150. The base may move vertically within the cut-out162 to follow theslots154 and156.
In a still further embodiment of the cutting mechanism,FIG. 8 shows acutter170 which is controlled by adrawbar172 which is separate from the material capture needles180 anddrawbar182. The material capture needles180 continue to pivot as indicated byarrows184. Pulling of thecutter drawbar172 will reciprocate thecutter170 without interacting with the positioning of thematerial capture needle180. Such separate control may be desirable in particular situations where the timing of the engagement of thematerial capture needle180 and thecutter170 must be more accurately controlled.
Referring now toFIG. 9, a preferred embodiment of the present invention having a material capture device will now be described in further detail.FIG. 9 shows aninner cutter200 mounted coaxially within anouter cutter202 and in a fully distal position to open thewindow204. The material capture device in this embodiment comprises a penetratingmember206 and acam surface208. The penetratingmember206 is pivotably mounted on the inner cutter about apivot pin210. The penetratingmember206 has acurved surface212 that is designed to slide over thecam surface208. Thecurved surface212 is typically a lower or underside surface of the penetratingmember206. As theinner cutter200 is advanced during the cutting motion, thecam surface208 will guide the penetratingmember206 in a radially outward direction along a path that brings the member into engagement with targeted material. By varying the shape of thecurved surface212 and the height of thecam surface208, the penetratingmember206 may have a variety of material-engaging positions, e.g., where the sharpenedtip214 extends radially beyond the outer diameter of theouter cutter202, where the sharpenedtip214 is radially aligned with the outer diameter of the outer cutter or theinner cutter200, or where thetip214 is within the inner cutter. It should be understood that thecurved surface212 may be also contain longitudinal grooves and be contoured as desired to best follow and maintain contact with thecam surface208 during the cutting motion. As shown inFIG. 9, the penetratingmember206 includes alower protrusion216 which helps move tissue proximally away from the cutters after the tissue has been excised.
Referring now toFIG. 10, adrive wire220 mounted within adrive tube222 is used to move theinner cutter200 from a first, open position to a second, closed position. Of course, other push/pull elements or separate push elements and pull elements may be used to control the movement of theinner cutter200. Thedrive wire220 may be made of material such as stainless steel or nickel titanium. Thedrive tube222 may also be made of a variety of materials such as a polymer like polyimide, polyurethane, or polyethylene or a flexible metal such as nickel titanium. Thedrive tube222 may also be made from a composite of metal and polymer, or a metal that has material selectively removed to increase its flexibility. Further details of the drive tube can be found in commonly assigned, copending U.S. patent application Ser. No. 08/982,231 (Attorney Docket No. 18489-000200US), filed on Dec. 17, 1997, the full disclosure of which is incorporated herein by reference.
As seen inFIGS. 10 and 11, thecam surface208 is fixedly secured to theouter cutter202 and remains stationary relative to the penetratingmember206 during the cutting motion. Theinner cutter200 typically includes a slot or cut-out portion to accommodate thecam surface208. Movement of theinner cutter200 brings the sharpenedend214 into contact with target material which is pushed towards the first blade224 (FIG. 10). Referring now toFIG. 11 as thewindow204 is closed, asecond blade226 on theinner cutter200 will complete the cutting motion by shearing off the material against thefirst blade224. Thecam surface208 will push against thelower surface212 of the penetratingmember206 and force the sharpenedtip214 of the penetrating member to retract into the inner cutter as shown inFIG. 11.
Referring now toFIGS. 12-14, other embodiments of the penetrating member, cam surface, and inner cutter will now be described.FIG. 12 shows an embodiment of the penetratingmember230 where the member has a more aggressively designed sharpenedtip232. The additional length of thetip232 allows the penetratingmember230 to engage materials further away from theouter cutter202. Thelower surface234 of the penetratingmember230 includes a recessedportion236 that allows the penetrating member to be retracted into theouter cutter202 when theinner cutter200 is in its distal most position.
FIG. 13 shows a material capture device where the sharpenedtip240 of the penetratingmember242 is even with the outer diameter of theouter cutter202 when the penetrating member is in its tissue-engaging position. Thecam surface244 has a decreased height and the location of the pivot pin246 has also been lowered to change the position of the sharpenedtip240. The extension distance may vary depending on the desired function of the cutter. For example, the extension distance of the penetrating member (where the outer edge of the inner cutter is 0.000) may range between about −0.05 to 0.10 inches (as shown in phantom), preferably between about 0.00 to 0.04 inches, and most preferably between about 0.01 to 0.02 inches for a 0.100 maximum diameter cutter. The length of the sharpenedtip240 may also be used to change the maximum extension distance of the material capture device.
FIG. 14 shows an embodiment of the penetratingmember250 used with a reduced lengthinner cutter252. Using a shorterinner cutter252 can reduce the rigid length of the catheter and improve tracking of the catheter through tortuous vasculature. Unlike the inner cutters shown inFIGS. 9-11, theinner cutter252 inFIG. 14 has the side-openingaperture254 located at the proximal end of the cutter. In other embodiments, this side-opening aperture is located away from the ends of the cutter. Moving theaperture254 to the end of thecutter252 allows the reduction in rigid length. In this embodiment, thedrive wire220 is repositioned to be on the lower surface of theinner cutter252.
The embodiments ofFIGS. 12-14 may further be provided with positioner wires as shown inFIGS. 14A-14C. Thecutter mechanism500 comprises a penetratingmember502, aninner cutter504, an outertubular cutter506, and a pair of positioner wires510 (only one of which is visible in the figures). Theinner cutter504 is shown in its closed (fully proximally advanced) configuration inFIG. 14A. The penetratingmember502 is fully radially retracted within the cutter assembly, and the positioning wires are also fully retracted.
Thepositioning wires510 form from a resilient material, typically stainless steel ribbon or a shape memory alloy ribbon, such as nitinol. The proximal ends of each wire are attached in slots formed near the proximal end of the outertubular cutter506 and extend inwardly through openings (not shown) so that their distal ends extend radially inwardly into the interior of the outer tubular cutter, as shown in the left-hand side ofFIG. 14A. With theinner cutter504 closed, as shown inFIG. 14A, thecutter mechanism500 can be advanced through the vasculature with a minimum profile, i.e., neither the tissue-penetratingmember502 nor thepositioner wires510 extend out from the cutter mechanism.
Once positioned at the treatment location, theinner cutting blade504 may be distally retracted, both opening acutter window514 and causing thecam surface518 on the penetratingmember502 to engage acam element520, causing the penetrating tip of the penetratingelement502 to emerge through thecutter window514 as generally described with the embodiments ofFIGS. 12-14.Cutter mechanism500 differs from the earlier embodiments in that a lower portion of theinner cutter504 engages the curved distal ends522 of thepositioner wires510, as best seen inFIG. 14B. In particular, as theinner cutter504 moves in a distal direction, (i.e., toward the left inFIGS. 14A-14C), it depresses the curved ends522, causing the main body of thepositioner wires510 to emerge from theouter cutter506, as indicated at530 inFIG. 14B. As theinner cutter504 moves further in the distal direction, thepositioner wires510 are deployed fully outwardly, as best shown inFIG. 14C. Thecutter window514 is fully opened and the penetratingmember502 again retracted within thecutter mechanism500. With thepositioner wires510 fully deployed, the penetratingmember502 of the cutter mechanism is disposed to penetrate into target tissue as theinner cutter member504 is closed in the proximal direction. Preferably, thepositioner wires510 will apply a very low amount of force against the artery wall since the penetratingmember502 will be able to quickly engage and capture the tissue to be cut by themechanism500. Additionally, if the lesion being treated has a small diameter, the positioner wires will simply fold over as the inner cutter is moved distally to open thecutter window514. During the cutting operation, thepositioner wires510 will quickly spring back into the outertubular cutter506 since the tissue-penetrating member will act to maintain contact with the material to be cut during the remainder of the cutting operation.
FIGS. 15-18 show a still further embodiment of the material capture device using a penetrating member and a cam surface. InFIG. 15, the penetrating member comprise acurved needle260 which is fixedly secured to theinner cutter200 and biased against acam surface262. Thecurved needle260 may be integrally formed with theinner cutter200 or otherwise attached such as by welding or other methods known in the art. As theinner cutter200 is advanced, thecam surface262 will guide theneedle260 along a path outwardly to engage target material and then it back towards the catheter body. As discussed previously, theneedle260 need not move beyond theouter cutter202, instead remaining even with the outer diameter of the outer cutter as the needle engages material. Theinner cutter200 may also include amaterial imaging device264 such as an ultrasound transducer or optical fibers which will image tissue when thewindow204 is closed by the cutter. The optical fibers may be used for optical coherence tomography or optical coherence reflectometry. A suitable ultrasound transducer or transducer array may be found in commonly assigned, copending U.S. patent application Ser. No. 09/______ (Attorney Docket No. 18489-001000US), filed ______, the full disclosure of which is incorporated herein by reference.
FIGS. 16-18 shows various embodiments of thecam surface262.FIG. 16 shows a perspective view of thecam surface262 used in the device ofFIG. 15.FIGS. 17 and 18 show acam surface270 which hasseparate tracks272 and274 which can guide the needle266 along different needle paths when the needle is advanced and when the needle is retracted. Thecam surface270 has funneledportions276 and278 for guiding the needle into therespective tracks272 and274, depending on whether the needle is being advanced or retracted.
Referring now toFIGS. 19-22, a telescoping cutting device using a material capture device will be described in further detail. As shown inFIG. 19, thetelescoping portion300 in this embodiment of the cutting device extends outwardly from anaperture302 on thecatheter body304. Thecatheter body304 may include acutting blade305 for shearing material drawn into the cutting device. It should be understood, of course, that the blade may be located in a variety of positions such as on thetelescoping portion300 of the device or located on both the telescoping portion and the catheter body. As shown inFIG. 19, thedistal end306 of thetelescoping portion300 is preferably adapted to mount a soft, atraumatic distal tip (shown in phantom) to facilitate passage of the device through body lumens. The tip may, in some embodiments, be integrally formed with thetelescoping portion300.
As seen inFIG. 19, thetelescoping portion300 is in a distal position where oneedge307 of the telescoping portion is spaced apart from the catheter body and defines a cuttingwindow308. In some embodiments, theedge307 may comprise a cutting blade while in other embodiments the edge may be unsharpened, but pushing material into the cutting window, The cuttingwindow308 is preferably a directional cutting window which may open towards one side of the catheter where material may intrude to be cut off. A penetratingmember310 is preferably rotatably mounted about apivot pin312 on thetelescoping portion300 to engage the material. It should be understood that some embodiments of thetelescoping portion300 may not include the penetratingmember310. The penetratingmember310 is shown inFIG. 19 to be in a first, tissue-engaging position. A tether orleash element314 is rotatably coupled to the penetratingmember310 and can be pulled proximally as indicated byarrow316 to rotate the member into the tissue-engaging position. Thetether314 may be made of a variety of materials such as stainless steel or a polymer like polyimide or a fibrous material like Kevlar®.
FIG. 20 shows thetelescoping portion300 being retracted by adrive wire318 as indicated byarrow320. As one end of the penetratingmember310 contacts abutment ordeflection block322, the penetratingmember310 will begin to rotate as indicated byarrow324. Further retraction of thetelescoping portion300 will cause the sharpenedtip326 of the penetratingmember310 to be pushed within the boundaries of the catheter body. As seen inFIG. 21, the penetratingmember310 andtelescoping portion300 may be substantially retracted into thecatheter body304. Thetether314 has abent portion330 that allows the penetrating member to rotated to the position shown inFIG. 22. Retraction of the penetratingmember310 into the catheter body as shown inFIG. 22 also functions to push tissue proximally into the catheter body where it can be stored.
Referring now toFIGS. 23 and 24, a still further embodiment of the tissue capture device will be described.FIG. 23 shows a penetratingmember340 that is rotatably mounted to theouter cutter342, instead of the inner,slidable cutter344 as shown in previous embodiments. Theinner cutter344 can be reciprocated to cut off materials captured in thewindow346. Theinner cutter344 includes a pushingelement348 that contacts the penetratingmember340 to rotate the penetrating member into the target material and then return to the inside of theouter cutter342. The pushingelement348 traverses over the top of the surface of the penetrating member and wipes off any tissue, directing it into the catheter. The penetratingmember340 may be reset to its starting position by a variety of methods such as through the use of a leash element as described above or by using a bias element to create a return force.
Referring now toFIG. 25, the present invention will further comprisekits including catheters400, instructions foruse402, and packages404.Catheters400 will generally be described above, and the instruction for use (IFU)402 will set forth any of the methods described above.Package404 may be any conventional medical device packaging, including pouches, trays, boxes, tubes, or the like. The instructions foruse402 will usually be printed on a separate piece of paper, but may also be printed in whole or in part on a portion of thepackaging404.
While all the above is a complete description of the preferred embodiments of the inventions, various alternatives, modifications, and equivalents may be used. For example, the cutters and material capture devices may be oriented in a variety of angles on the catheter body. As seen inFIGS. 26 and 27, thecatheters430 and440 havecutters432 and442 which are oriented perpendicularly or at other inclined angles to alongitudinal axis450 of the catheter. A plurality of material capture devices may be used with a single or a plurality of cutting blades. Additionally, as discussed above forFIG. 15, another embodiment of the device includes anultrasound transducer460 as shown inFIG. 28. In place of an ultrasonic transducer, the device may use one or more optical fibers for optical coherence tomography or optical coherence reflectometry. Although the foregoing invention has been described in detail for purposes of clarity of understanding, it will be obvious that certain modifications may be practiced within the scope of the appended claims.