Steerable Guidewire and Method of Use
20230149671 · 2023-05-18
Assignee
Inventors
Cpc classification
A61M2025/0004
HUMAN NECESSITIES
A61M25/0147
HUMAN NECESSITIES
A61M2025/09116
HUMAN NECESSITIES
A61M25/0138
HUMAN NECESSITIES
A61M25/0013
HUMAN NECESSITIES
A61M25/0102
HUMAN NECESSITIES
International classification
Abstract
A steerable endoluminal access device, such as a guidewire or guide catheter. The steerable endoluminal access device includes an inner tube within an outer tube, with the inner tube fixed to the outer tube near the distal end of the device. The steerable endoluminal access device includes a releasably detachable hub for tensioning or compressing the inner tube relative to the outer tube.
Claims
1. A steerable endoluminal access device comprising: an outer tube characterized by a proximal end, a distal end, and a flexible region at said distal end of the outer tube, said flexible region also characterized by a proximal and a distal end; and an inner tube characterized by a proximal end and a distal end, and a flexible region near said distal end of the inner tube; said inner tube being disposed within the outer tube, extending from the proximal end of the outer tube to the distal end of the outer tube, and terminating distally proximate the distal end of the outer tube, said inner tube longitudinally fixed to the outer tube at a point in the outer tube proximate the distal end of the flexible region of the outer tube; and a hub assembly comprising a first compression fitting disposed about the proximal end of the outer tube and a second compression fitting disposed about the proximal end of the inner tube, said first compression fitting operable to be longitudinally fixed to the outer tube and said second compression fitting operable to be longitudinally fixed to the inner tube.
2. The steerable guidewire of claim 1 wherein: the flexible region of the outer tube comprises a segment of the outer tube which is snake-cut with a plurality of radially oriented slots in the wall of the outer tube, said radially oriented slots being radially aligned along one side of the outer tube; and the flexible region of the inner tube comprises a segment of the inner tube with a longitudinally oriented slot, wherein said longitudinally oriented slot divides the flexible region of the inner tube into a first partial cylinder segment and a second partial cylinder segment.
3. The steerable guidewire of claim 1 wherein: a separation adjusting mechanism which controls the distance between the first compression fitting and the second hub fitting.
4. A method of accessing a lumen of a patient with an endoluminal access device, said method comprising the steps of: providing an endoluminal access device comprising: an outer tube characterized by a proximal end, a distal end, and a flexible region at said distal end of the outer tube, said flexible region also characterized by a proximal and a distal end; and an inner tube characterized by a proximal end and a distal end, and a flexible region near said distal end of the inner tube; said inner tube being disposed within the outer tube, extending from the proximal end of the outer tube to the distal end of the outer tube, and terminating distally proximate the distal end of the outer tube, said inner tube longitudinally fixed to the outer tube at a point in the outer tube proximate the distal end of the flexible region of the outer tube; inserting the endoluminal access device into a lumen of the patient and navigating the distal end of the endoluminal access device toward a target site within the patient; securing a first compression fitting about the proximal end of the outer tube such that the first compression fitting is longitudinally fixed to the outer tube; securing a second compression fitting about the proximal end of the inner tube such that the second compression fitting is longitudinally fixed to the inner tube; and manipulating the first compression fitting and second compression fitting to tension or compress the inner tube relative to the outer tube to cause deflection of the distal end of the endoluminal access device.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0021] A general architecture that implements the various features of the invention will now be described with reference to the drawings. The drawings and the associated descriptions are provided to illustrate embodiments of the invention and not to limit the scope of the invention. Throughout the drawings, reference numbers are re-used to indicate correspondence between referenced elements.
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
DETAILED DESCRIPTION OF THE INVENTIONS
[0028] In accordance with current terminology pertaining to medical devices, the proximal direction, or end, is defined herein as that direction, or end, on the device that is furthest from the patient and closest to the user, while the distal direction, or end, is that direction, or end, closest to the patient and furthest from the user. These directions and locations are applied along the longitudinal axis of the device, which is generally an axially elongate structure optionally having one or more lumens or channels extending through the proximal end to the distal end and running at least a portion of the length of the device. A catheter size given in the units of “French” or “Fr” is defined as three times (approximately pi) the diameter in millimeters. Thus, a device that is 2 mm in diameter can be said to have a diameter of 6 French.
[0029] In an embodiment, the invention is an endoluminally, transvascularly, or endovascularly placed steerable guidewire, with internal deflectability or the ability to articulate, at its distal end, in a direction away from its longitudinal axis. The steerable guidewire is generally fabricated from stainless steel, nitinol, or the like and comprises an outer tube, an inner tube, and a distal articulating region. The deflecting or articulating mechanism is integral to the steerable guidewire. The steerable guidewire is useful for animals, including mammals and human patients and is routed through body lumens or other body structures to reach its target destination.
[0030] In an embodiment, the steerable guidewire comprises an inner tube and an outer tube. The steerable guidewire can also comprise a stylet or obturator, which can be removable or non-removable. The steerable guidewire further comprises a hub at its proximal end which permits grasping of the steerable guidewire as well as features, or control mechanisms, for controlling the articulation at the distal end. Such features can comprise control knobs, handles, levers, or the like. The proximal end further can optionally be terminated with a female Luer or Luer lock port or hemostasis valve, which is suitable for attachment of pressure monitoring lines, dye injection lines, vacuum lines, a combination thereof, or the like. The steerable guidewire can comprise a center channel operably affixed to the Luer or Luer lock port, said channel being useful for dye injection, material or fluid administration or removal, pressure monitoring, or the like. In some embodiments, it is beneficial that a catheter be advanceable over the guidewire beginning at the proximal end of the guidewire. In these embodiments, the hub, which comprises controlling mechanisms for the distal deflection, is beneficially detachable from the guidewire and can be releasably or non-releasably affixed to the guidewire following advancement of a catheter past the proximal end of the guidewire.
[0031] The steerable guidewire or catheter can be fabricated so that it is substantially straight from its proximal end to its distal end. Manipulation of a control mechanism at the proximal end of the steerable guidewire causes a distal region of the steerable guidewire to bend or curve away from its longitudinal axis. The bending, steering, deflecting, or articulating region is located near the distal end of the steerable guidewire and can be a flexible region or structure placed under tension or compression through control rods or tubular structures routed from the control handle at the proximal end of the steerable guidewire to a point distal to the flexible region.
[0032] Other embodiments of the inventions comprise methods of use. One method of use involves inserting the central core wire or stylet so that it protrudes out the distal end of the steerable guidewire. A percutaneous or cutdown procedure is performed to gain access to structures such as, but not limited to, the vasculature, either a vein, an artery, a body lumen or duct, a hollow organ, musculature, fascia, cutaneous tissue, the abdominal cavity, the thoracic cavity, and the like. An introducer, which is usually a hollow, large diameter, hypodermic needle, and the steerable guidewire are placed within the vasculature and the steerable guidewire is routed proximate to the target treatment site. The introducer can be removed at this time or substantially at the time the guidewire is introduced into the body lumen. A guiding catheter, preferably with a removable central obturator or dilator having a core lumen sized to slidably fit over the steerable guidewire, with a tapered distal tip pre-inserted, is routed over the steerable guidewire to the target site. The steerable guidewire can be adjusted so that it assumes a substantially straight configuration. In other procedural embodiments, the steerable guidewire can be advanced through the central lumen of an already placed catheter, sheath, introducer, or guide catheter. The steerable guidewire or catheter comprises a generally atraumatic, non-sharp, distal tip. The distal tip can be rounded, oval, or the like, but can also be sharpened or include electrodes for RF ablation, cryoablation, or HIFU.
[0033] The distal end of the steerable guidewire, and optionally the body of the guidewire or catheter as well, is sufficiently radiopaque that it is observable clearly under fluoroscopy or X-ray imaging. The steerable guidewire, especially near its distal end, can be configured with asymmetric radiopaque markers that provide some indication regarding the side of the steerable guidewire that deflection can occur. The location of the steerable guidewire and the amount of deflection and curvature of the distal end are observed and controlled using the aforementioned fluoroscopy or X-ray imaging, or other imaging method such as MRI, PET scan, ultrasound imaging, and the like. The primary structure of the steerable guidewire or catheter shaft is stainless steel or nitinol, or the like. These materials should preferably comprise spring or superelastic temper. A Leak resistant coating can be applied to the exterior or the interior lumen of the inner tube or outer tube. One or more radiopaque markers can be affixed to the distal end of the steerable guidewire to further enhance visibility under fluoroscopy. Such radiopaque markers can comprise materials such as, but not limited to, thick ferrous metals, tantalum, gold, platinum, platinum iridium, and the like.
[0034] Deflection of the distal tip to varying degrees of curvature, under control from the proximal end of the guidewire can be performed. The curve can be oriented along the direction of a branching vessel or vessel curve so that the steerable guidewire can then be advanced into the vessel by way of its high column strength and torqueability. Alignment with any curvature of the catheter can be completed at this time. When correctly positioned under fluoroscopy, ultrasound, or other imaging system, dye can be injected into the central lumen of the steerable guidewire at its proximal end and be expelled out of the distal end of the steerable guidewire to provide for road-mapping, etc. This steering function can be very beneficial in device placement and is also especially useful in highly tortuous vessels or body lumens which may further include branching structures such as bifurcations, trifurcations, and the like.
[0035] In some embodiments, the inner tube, the outer tube, or both can have slots imparted into their walls to impart controlled degrees of flexibility. The slots can be configured as “snake cuts” to form a series of ribs with one or more spines. The spines can be oriented at a given circumferential position on the outer tube, the inner tube, or both. The spines can also have non-constant orientations. In some embodiments, only the outer tube is slotted. The slots can be generated within the distal portion of the outer tube where the curve is generated. This distance can range between about 0.5-cm and 15-cm of the end and preferably between 1-cm and 5-cm of the distal end. The slot widths can range between 0.001 inches and 0.100 inches with a preferable width of 0.003 to 0.010 inches. In exemplary embodiments, the slot widths are about 0.008 inches. In some embodiments, it is desirable to have the outer tube bend in one direction only but not in the opposite direction and not in either lateral direction. In this embodiment, cuts can be made on one side of the outer tubing within, for example, the distal 10-cm of the tube length. Approximately 5 to 30 cuts can be generated with a width of approximately 0.010 to 0.040 inches. The cut depth, across the tube diameter from one side, can range between 0.1 and 0.9 of the tube diameter. In an embodiment, the cut depth can be approximately 0.4 to 0.6 of the tube diameter with a cut width of 0.025 inches. A second cut can be generated on the opposite side of the tube wherein the second cut is approximately 0.005 inches or less. In an embodiment, the outer tube can be bent into an arc first and then have the slots generated such that when the tube is bent back toward the 0.005 inch wide cuts, the tube will have an approximately straight configuration even through each tube segment between the cuts is slightly arced or curved.
[0036]
[0037] Referring to
[0038] A thread pitch for the jackscrew traveler 114 and the control knob 116 can range from about 16 to about 64 threads per inch (TPI) with a preferred range of about 24 TPI to about 48 TPI and a more preferred range of about 28 to about 36 TPI.
[0039] In some embodiments, the hub assembly is removable from the steerable guidewire so that the proximal end of the steerable guidewire 100 retains the same (or smaller) diameter or profile as the intermediate and distal ends of the guidewire. In these embodiments, catheters, guide catheters, introducers, sheaths, or other axially elongate medical devices comprising an internal guidewire lumen can be slipped over the proximal end of the steerable guidewire and advanced into the patient over an already placed steerable guidewire. This embodiment, or approach, provides for catheter exchange, replacement, swapping, or the like. Once the catheter is advanced such that its proximal end is located distal to the proximal end of the steerable guidewire, the hub assembly can be releasably affixed to the proximal end of the steerable guidewire so that the distal end of the guidewire can be deflected under control at the proximal end. The hub assembly illustrated in
[0040]
[0041] The polymeric outer coating 106 is optional but beneficial and can comprise materials such as, but not limited to, fluoropolymers such as PTFE, PFA, FEP, polyester, polyamide, PEEK, and the like. The polymeric outer coating 106 can render the coiled embodiment of the intermediate segment 108 of the outer tube, as illustrated, to retain a relatively smooth exterior surface and provide for friction reduction which is useful when passing a long, slender guidewire through a long, catheter lumen. The distal segment 102 of the outer tube can be affixed to the intermediate segment 108 of the outer tube by means of a weld, fastener, adhesive bond, embedment with polymeric, metallic, or ceramic materials, or the like. The intermediate segment 108 of the outer tube, illustrated in this embodiment as a coil structure with substantially no spacing between the coils, is highly flexible and the flexibility can be controlled by the elastic modulus, thickness, and other material properties of the outer coating 106. The intermediate segment 108 of the outer tube, in other embodiments, can comprise structures such as, but not limited to, an unperforated or unfenestrated tube, a tube with partial lateral cuts, a spiral cut tube, a ribcage with a backbone, or the like.
[0042]
[0043] Referring to
[0044]
[0045] Referring to
[0046] As described in relation to the previous figures, the flexible region of the inner tube is disposed within the longitudinal extent of the flexible region of outer tube. In the illustrated embodiment, that slotted portion of the inner tube defines the flexible region of the inner tube, and the snake cut segment of the outer tube defines the flexible region of the outer tube.
[0047] The number of lateral cuts 216 or, optionally, the number of lateral cuts 216 with T-cuts 218 can number between about four and about 50 with a preferred number being between about six and about 25 and a more preferred number of about eight to about fifteen. In the illustrated embodiment, there are 12 partial lateral cuts 216, each modified with a “T” or “H”-shaped slot 218. In other embodiments, the partial lateral cuts 216 can be shaped differently. For example, the partial lateral cuts 216 can be at angles other than 90 degrees to the longitudinal axis, curved, V-shaped, Z-shaped, W-shaped or the like. In other embodiments, the ‘T’ slots 218 can have, for example, further cuts approximately lateral to the longitudinal axis, along any portion of the “T” cut 218. This construction provides the outer tube with a flexible region at its distal end. The flexible region is a region at the distal end of the outer tube that is significantly more flexible and susceptible to deflection than the remaining proximal region of the outer tube.
[0048] The distal segment 102 of the outer tube can have an outer diameter of about 0.010 to about 0.1 inches with a preferred outside diameter of about 0.015 to about 0.050 inches and a more preferred diameter of about 0.020 inches to about 0.035 inches. In the illustrated embodiment, the outside diameter is about 0.048 inches while the inner diameter is about 0.036 inches. The inside diameter of the distal segment 102 of the outer tube can range from about 0.0.005 inches to about 0.090 inches.
[0049] The lead in 228 to the longitudinal slot 226 is beneficially angled to prevent other guidewires, stylets, or other devices, which are inserted through the central lumen 224 from being caught or bumping against an edge. The angled lead in 228 serves a guide to assist with traverse of a stylet, obturator, or guidewire past the lead in 228 and into the distal region of the steerable guidewire. The lead in 228 can be angled from between about −80 degrees (the angle can be retrograde) from the longitudinal axis (fully lateral) to about +2 degrees and preferably from about +5 degrees to about +20 degrees with a most preferred angle of about +8 degrees and about +15 degrees. In the illustrated embodiment, the angle of the lead in slot 228 is about 10 degrees from the longitudinal axis. A second feature of the lead in 228 is that it be positioned or located proximally to the most proximal “T” slot 218 in the outer tube 102 when the two tubes 102, 104 are affixed to each other (see
[0050] The inner tube 104 can have an outside diameter that is slightly smaller than the inside diameter of the outer tube 102 so that the inner tube 104 can be constrained to move longitudinally or axially within the outer tube 102 in a smooth fashion with relatively little force exerted. In the illustrated embodiment, the outside diameter of the inner tube 104 is about 0.033 inches giving about a 0.0015 inch radial clearance between the two tubes 102 and 104. The inside diameter of the inner tube 104 can range from about 0.006 to about 0.015 inches less than the outside diameter of the inner tube 104. In the illustrated embodiment, the wall thickness of the intermediate tube is about 0.006 inches so the inside diameter of the intermediate tube is about 0.021 inches. The lumen 224 of the inner tube 104 can be sized to slidably accept a stylet or obturator 140 such as illustrated in
[0051] The inner tube 104 transmits force along its proximal non-slotted region 222 from the proximal end of the inner tube 104 to the lead in 228 where the force continues to be propagated along the connected side 232 to the distal end 230. The outer tube 102 transmits force along its proximal non-slotted region 212. Longitudinal forces applied to the distal, flexible region with the slots 216 cause deformation of the outer tube in an asymmetrical fashion with the side of the outer tube 102 comprising the partial lateral slots 216 forming an outer curve if the slots 216 are expanded and an inside curve if the slots 216 are compressed. Forces to cause bending are preferably exerted such that the partial lateral slots 216 are compressed up to the point where the gap closes, but no further, however forces can also be exerted to expand the slots 216, however limits on curvature are not in place because the lateral slots 216 can open in an unrestrained fashion except for the material properties of the outer tube 102.
[0052] The disconnected side 234 of the inner tube 104, separated from the connected side 232 by the longitudinal slot 226 and the lead in 228, serves to maintain an undistorted tube geometry and provide resistance to deformation while helping to maintain the inner lumen 224 in a round configuration and provide a shoehorn or funnel effect to guide an obturator, guidewire, or stylet 140 therethrough as they are advanced distally. The disconnected side 234, being separated from the force transmitting member 222 cannot provide any substantial longitudinal load bearing structure, although at its distal end, where it is integral or affixed to the distal end 230, some tension load carrying capability exists. The inner tube 104 can be considered a split tube and does not carry a load in compression or tension along substantially the entire length of the disconnected side 234. A main advantage of keeping the disconnected side 234 is to maintain the off-center positioning of the force transmitting member 222.
[0053] The partial lateral slot 216 in the inner, or intermediate, tube 104 and the T-Slot 218 in the outer tube 102, as well as the longitudinal slot 226 in the inner tube 104, and the lead in slot 228 can be fabricated by methods such as, but not limited to, electron discharge machining (EDM), wire EDM, photo chemical etching, etching, laser cutting, conventional milling, or the like. In other embodiments, different slot configurations can also be employed, such as curved slots, complex slots, zig-zag slots, or the like. In some embodiments, the partial lateral slot 216 can be configured with a tongue and groove or dovetail design to prevent or minimize lateral movement or torqueing of the outer tube 102 in the flexible region. In some embodiments, the tongue and groove or dovetail (not shown) can be generally centered between two “T” slots, for example. The parts can be ganged and fixtured such that, using wire EDM, for example, a plurality of tubes can be cut to reduce manufacturing costs. As many as 20 to 30 tubes, or more, can be fixtured, secured, and etched by the aforementioned methods.
[0054]
[0055] Referring to
[0056] In embodiments using compression fittings, a first compression fitting, such as a collet or Tuohy-Borst compression fitting can be affixed to the proximal end of the outer tube and a second compression fitting can be affixed to the proximal end of the inner tube, which beneficially protrudes out the proximal end of the outer tube when the system is unstressed. Thus, the user can move the inner tube axially relative to the outer tube. The axial forces needed to cause tip deflection on these small diameter devices need not be great so simple hand movement can be used to adjust the tip deflection. A Tuohy-Borst compression fitting may comprise a compressible sleeve, distal cap (at item 312) and proximal cap (at 310) both disposed about the compressible sleeve, with the proximal cap and distal cap disposed on either side of the compressible sleeve and configured with internal and external threads so that the threads one cap can engage the threads of the other and the caps may be rotated relative to each other to compress the compressible sleeve and force it to deform radially inwardly to securely engage the tube on which it is disposed. The compression fittings may be configured, as in
[0057] The method of using the steerable guidewire can comprise the user assembling the hub fittings to the tubes of the steerable guidewire and then clamping the hub fittings in place using the locking or compression mechanisms. The user can next grasp the hub body 314 of the first hub fitting 306 and the hub body 314 of the second hub fitting 308. By moving (manually or by means of an actuator) the first hub fitting 306 axially relative to the second hub fitting 308, the user can articulate the distal end of the steerable guidewire. Moving the first hub fitting 306 closer to the second hub fitting 308 causes the distal end of the steerable guidewire to deflect in one direction out of the long axis of the steerable guidewire. Moving the first hub fitting 306 away from the second hub fitting 308 causes the distal end of the steerable guidewire to move in a direction opposite that of when the first hub fitting is moved closer to the first hub fitting. Circumferential orientation of the steerable guidewire 300 distal end can be achieved by rotating or torqueing the guidewire about its longitudinal axis. The steerable guidewire 300 of this construction retains the ability to transmit rotation applied to the hub all the way to the distal end.
[0058] After the steerable guidewire is routed to its end location, both the first hub fitting 306 and the second hub fitting 308 can be removed from their respective tubes 304 and 302 by loosening the compression mechanisms 312 by way of rotating the knobs 310 and pulling the first 306 and second hub 308 fittings axially off of the proximal end of the steerable guidewire 300. At this point, lumens of other catheters (not shown) can be routed over the proximal end of the steerable guidewire 300 and on to the target location.
[0059] The proximal ends of the inner tube 302 and the outer tube 302 can be roughened, finished with circumferential grooves, or the like, to enhance the grip of the compression mechanisms 312 of the hub fittings 306 and 308, while still allowing for loosening and release of the hub fittings 306 and 308.
[0060]
[0061] The steerable guidewire system 400 further comprises a separation adjusting mechanism which controls the distance between the first hub fitting 406 and the second hub fitting 408. The separation adjusting mechanism comprises the distal fixation device 418, the proximal fixation device 410, a distal linkage 416, a proximal linkage 412, and a control mechanism 414.
[0062] Referring to
[0063] However, a tubular or cylindrical central control device can maintain its structure in compression, maintain circumferential location within the outer cylindrical, axially elongate tube, maintain precise control, maintain sufficient tensile strength to exert forces, and maintain a central lumen larger than any other type of steerable device. The resistance to buckling occurs even when the inner tube is slotted longitudinally because the inner tube is constrained within the outer tube using very tight tolerances that will not let the inner tube bend out of its straight orientation, even under compression.
[0064] Intermediate sections of the tubes 302 and 304 can comprise coils, snake cut structures with or without backbones, or the like. The use of coils can be facilitated by a tensioner wire disposed through a part or all of the coil area to prevent excessive opening of the coils and thus allow for tensile strength as well as compressive strength when the coils close. Such intermediate tube sections can facilitate routing through tortuous vasculature or body lumens.
[0065] A steerable guidewire, as disclosed herein, can be used to route very large, stiff catheters through vasculature of body lumens such that orientation changes can be made without the large diameter, stiff catheter causing the guidewire to straighten out or lose its track because the guidewire can impart its own forces to maintain its curvature. The curvature can be controlled to be small, such as tip deflection, to large and arc shaped, for example to traverse the aortic arch, or turn a 180 degree angle to approach the mitral valve superiorly using an inferior approach through a femoral vein.
[0066] The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. For example, guidewires can have very similar diameters as the diameters of microcatheters. Thus, the structures and methods disclosed herein can be identically applied to a microcatheter. The forces are very small and compression fittings could easily grasp the movable parts of a microcatheter and pull an inner tube relative to an outer tube. This, of course blurs the line between a microcatheter and a guidewire, the difference being primarily that a microcatheter attempts to maximize the central lumen and this is not so important in a guidewire, if at all. The scope of the invention is therefore indicated by the appended claims rather than the foregoing description. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.