MODULAR MEDICAL GUIDE WIRE ASSEMBLY
20180193608 · 2018-07-12
Assignee
Inventors
Cpc classification
A61M2025/0175
HUMAN NECESSITIES
A61M2025/09116
HUMAN NECESSITIES
A61M2025/09075
HUMAN NECESSITIES
A61M2205/0216
HUMAN NECESSITIES
International classification
Abstract
A guide wire assembly for medical use includes at least a portion which is formed of a plurality of inter-cooperating elements forming a flexible section of the guide wire assembly, and specifically a section that can have varying flexibility. A control device passes through a lumen extending for the whole length of the guide wire and is typically fixed at a distal end of the assembly. The control device is used to change the flexibility of the guidewire assembly and in some embodiments to lock it in position. The elements have tapering internal lumens for accommodating the control device, particularly when the guide wire is bent.
Claims
1. A medical guide wire of elongate form comprising, a longitudinal dimension, a distal end and a proximal end; at least a portion of the guide wire being formed of a plurality of inter-cooperating elements disposed longitudinally in series, the inter-cooperating elements having cooperating facing surfaces able to slide relative to one another so as to cause the guide wire to be bendable in at least one lateral dimension; each inter-cooperating element having a bore extending from a first end to a second end thereof, the bore having a taper from the first end to the second end; and a control device extending through the bores of the inter-cooperating elements; the control device having at least one operating state enabling the inter-cooperating elements to slide relative to one another.
2. A medical guide wire according to claim 1, wherein the control device has a first operating state in which the inter-cooperating elements can slide relative to one another and in which the guide wire is relatively flexible, and a second operating state limiting sliding of the inter-cooperating elements and in which the guide wire is relatively less flexible.
3. A medical guide wire according to claim 2, wherein the control device has an operating state preventing sliding of the inter-cooperating elements and in which the guide wire is stiff.
4. A medical guide wire according to claim 1, wherein the cooperating facing surfaces are textured, toothed or friction surfaces.
5. A medical guide wire according to claim 1, wherein at least one of the cooperating facing surfaces is curved.
6. A medical guide wire according to claim 1, wherein both of the cooperating facing surfaces are curved.
7. A medical guide wire according to claim 1, wherein at least one of the facing cooperating surfaces is rounded.
8. A medical guide wire according to claim 7, wherein the cooperating surface or surfaces are part-circular.
9. A medical guide wire according to claim 1, wherein cooperating surfaces are respectively convex and concave.
10. A medical guide wire according to claim 1, wherein each inter-cooperating element includes at the first end a convex surface and at the second end a concave surface.
11. A medical guide wire according to claim 1, wherein the inter-cooperating elements include a rounded outer surface at the first end and an inner surface at the second end, the second end being sized to envelop the first end of an adjacent inter-cooperating element.
12. A medical guide wire according to claim 11, wherein the first end is radially compressible.
13. A medical guide wire according to claim 12, wherein the first end includes at least one longitudinally extending slot allowing the first end to compress radially.
14. A medical guide wire according to claim 12, wherein the second end is shaped so as to cause a first end of an element coupled thereto to compress when fitted into or removed from the second end.
15. A medical guide wire according to claim 12, wherein the bore extending in the inter-cooperating elements has a smaller diameter at the first end relative to the second end.
16. A medical guide wire according to claim 15, wherein the control device has a diameter smaller than the bore when the first end is radially compressed on insertion into or withdrawal form a second end of a coupled inter-cooperating element.
17. A medical guide wire according to claim 1, wherein the bore of each or at least one inter-cooperating element has a uniform taper from the first end to the second end.
18. A medical guide wire according to claim 1, wherein the bore of each or at least inter-cooperating element has a non-uniform taper from the first end to the second end.
19. A medical guide wire according to claim 1, wherein the inter-cooperating elements have tapering bores in the same orientation along the length of the guide wire.
20. A medical guide wire according to claim 1, including inter-cooperating elements of different lengths.
21. A medical guide wire according to claim 20, wherein longer inter-cooperating elements are located proximally relative to shorter inter-cooperating elements along at least part of the length of the guide wire.
22. A medical guide wire according to claim 1, wherein the control device is a wire or cable connected at the distal end of the guide wire.
23. A medical guide wire according to claim 1, wherein the control device is connected to a driving mechanism at the proximal end of the guide wire.
24. A medical guide wire according to claim 1, wherein the control device is made of a metal, metal alloy, carbon fibre, a stretchable material or an elastomeric material.
25. A medical guide wire according to claim 1, including a covering or sleeve disposed over the inter-cooperating elements.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0029] Embodiments of the present invention are described below, by way of example only, with reference to the accompanying drawings, in which:
[0030]
[0031]
[0032]
[0033]
[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0040] Various embodiments of medical guide wire assembly are described below and shown in the accompanying drawings. It is be understood that the drawings are schematic only and are not intended to show the various components of the assembly to scale. In many cases, the assembly has been depicted in enlarged form for the sake of clarity of disclosure. The skilled person will appreciate that the assembly may be configured to a variety of different sizes, and shapes, in order to correspond to the vessel or other organ in which the device is to be deployed. In practical embodiments, the guide wire assembly can be produced to have a very small diameter, including of less than a millimetre. Where dimensions are given in drawings these are solely for exemplary purposes. The elements may be formed to have different dimensions and different proportions.
[0041] Referring first to
[0042] The guide wire, which is in practice an assembly of components, includes a plurality of pivotable or rotatable elements of which two are shown in
[0043] The surfaces 14, 22 in at least some embodiments are able to engage with one another in non-sliding manner so as to lock the elements 12 and 20 together non-rotatably. For this purpose, the surfaces 14 and 22 may be roughened, may have corresponding keying elements such as inter-engaging teeth or other relief patterns, may simply make friction contact with one another, and so on.
[0044] Each element 12, 20 has an internal channel or lumen therein, not visible in
[0045] The left-most sketch of
[0046] The surfaces 14, 22 may, in some embodiments, have different shapes in order to limit their angular rotation relative to one another. For instance, the surfaces 14, 22 could be at least part-cylindrical so as to rotate around a single axis of rotation, or could be shaped to rotate along two or more axes of rotation, or the like. It is preferred, though, that the surfaces 14, 22 are part-spherical.
[0047] In sketch B of
[0048] Referring now to
[0049] The guide wire 50 includes an outer tubular element 52 having a distal end 54 and a proximal end 56. At the distal end 54 there may be provided a soft tip 60 made, for example, of a plastics or elastomeric material. In some embodiments the tip 60 may be a weld joint or other relatively rigid tip and in all cases is preferably rounded so as to be atraumatic. The proximal end 56 is attached to a handle assembly 70, of which an example of only the principal components is shown. Disposed within a lumen (not shown in
[0050] In the embodiment shown in
[0051] There may be provided a spring or other biasing mechanism between the handle portions 72 and 74 to bias them apart from one another and therefore the assembly into a less flexible or locked condition. There may also, or in the alternative, be provided other control mechanisms such as locking pins, drive elements or the like for adjusting the tension of the control device and for fixing this during operation of the guide wire.
[0052] It is to be appreciated that
[0053] The main portion 80 of the guide wire 50 may be in the form of a catheter or cannula of unitary elongate form with a lumen extending therethrough, and with a distal end 100 formed of a series of inter-cooperating elements 100 of the types disclosed herein. The control device 58 extends through the lumen of the proximal portion 80 and through the internal, aligned, lumens of the elements 100 to the tip 54 of the guide wire 50. In this manner, the control device 58 can control the configuration of the guide wire, in the manner described in further detail below.
[0054] The proximal portion 80 of the guide wire 50 is preferably flexible and may be made in any conventional form and with known materials. Equally, in some embodiments, the portion 80 of the guide wire may be made from a rigid cannula.
[0055] In this example of
[0056] In use, the guide wire 50 can be fed endoluminally through a patient's vasculature, with the control device 58 in its relaxed condition, that is with the segments 100 able to rotate relative to one another, such that the guide wire 50 is very flexible. In this condition, the guide wire 50 can pass through tortuous vasculature and also through delicate vessels including, for example, the neural vessels.
[0057] It will be appreciated that the elements or segments 100 will rotate relative to one another to allow the segmented portion 90 of the guide wire 50 to adopt with little resistance complex curved shapes, in dependence upon the direction of curvature and bending of the vessels through which it passes. The guide wire 50 can be stiffened or locked in the configuration in which it is variably curved, by pulling on, that is tightening, the control device 58. This can reduce the flexibility of the distal portion 90 and preferably lock the segments 100 relative to one another. Locking can be done for a variety of reasons. For instance, the guide wire elements 100 can be locked relative to one another to assist in feeding the guide wire 50 through a patient's vasculature, for example for directing the distal end 54 of the guide wire 50 through a bifurcation or into a branch vessel. After positioning, the guide wire sections 100 can be loosened again. The guide wire 50 can also be locked into its configuration once it has been positioned within a patient's vessels at the site at which treatment is to be carried out, so as to support an introducer assembly passed through the patient's vasculature over the guide wire 50.
[0058] Referring now to
[0059] The first end 102 has a rounded convex outer surface, which in the preferred embodiment is preferably part-spherical. At its extremity, the first end 102 has a generally flat surface 314 with, in the embodiment shown, an internally flared and rounded opening to lumen 120. The flared opening avoids any sharp edges which may damage or prematurely wear the control device 58.
[0060] The second end 304 is larger than the first end 102 and specifically has a rounded concave internal wall 106 having a shape which is preferably consistent with or substantially identical to the outer shape of the first end 102. The internal wall 106 defines a chamber having a diameter which is the same as or only slightly larger than the outer diameter of the first end 102, such that, as described below, the first end 102 of one element 100 can fit into the chamber of the second end 104 of another element 100.
[0061] The second end 104 has an outer wall, which in this example is rounded in similar manner to the internal wall 106, that is preferably part-spherical. The outer shape of the second end 104 does not affect the functioning of the element 100 but that shown reduces the amount of material needed for the element, thereby reducing volume and weight, and provides a smooth rounded outer surface to the assembly.
[0062] The second end 104 terminates in a flat end 116 and, as depicted in the drawings, the inner wall 106 of the second end 104 curves smoothly at the opening 316 towards the outer surface of the second end 104.
[0063] The neck 110, in this embodiment, has an outer surface which tapers from the second end 104 to the first end 102 and terminates in a rounded collar 118 leading to the first end 102.
[0064] The bore formed by the internal wall 112 widens from the opening 114 of the first end 102 to the junction of the internal wall 306 of the second end 104 and in practice has a frusto-conical shape.
[0065] The outer surface of the neck 110 widens in a similar manner to the internal bore 110, although this is not a necessary characteristic. In fact, in other embodiments, the outer surface of the neck 110 need not taper and may, for example, be cylindrical.
[0066] The combination of the internal wall 112 and the internal surface 106 of the second end 104, together with the open ends, provides an open lumen which extends through the entire length of the element 100.
[0067] Referring now specifically to
[0068] The maximum diameter of the outer surface of the first end 102 is preferably larger than the minimum diameter of the opening 116 of the second end 104, by preferably no more than the width 124 of the slots. The first end 102 is resiliently deformable, that is compressible, such that it can be pushed into the opening 116 of the second end 104 of a mating element 100. The skilled person will understand that the walls of the first end 102 can also change shape, by radial compression, as a result of the provision of the slots 122. In other embodiments the element 100 may be made of a naturally resilient material and in some circumstances resilient enough that slots are not necessary.
[0069] In other embodiments, the second end 104 may additionally or alternatively be provided with longitudinally extending slots similar to the slots 122, although the arrangement shown in
[0070]
[0071] Two or more elements 100 can be fitted together in series, in the manner shown in
[0072] Any number of elements 100 can be coupled together in dependence upon the desired characteristics for the guide wire 50. In this regard too, while
[0073] The lumen 120 accommodates a control device 58, typically a wire, of the type described elsewhere herein. The control device 58 will extend through the inter-cooperating elements 100 to the distal extremity 54 of the guide wire and typically be attached to a distal most element 100 or to a tip 60 of the assembly. As explained above, the proximal end of the control device 58 is attached to a handle assembly 70.
[0074] In the preferred embodiments, the control device 58 has a diameter which is the same as or only slightly smaller than the diameter of the bore 120 at its narrow end, that is at the opening 114 of the first end 102. Any diameter difference is preferably less than the amount by which the first end 102 must compress to slide into or out of the second end 104. In this manner, when the control device 58 is fitted into the lumen, the elements 100 cannot separate form one another because there is no space for the first ends 102 to compress to be able to be pulled out of the opening 116 of the second ends 104. This provides a mechanism for securely attaching the elements 100 together and preventing their separation, for example when the guide wire 50 is being pulled out of a patient.
[0075] The elements 100 shown in
[0076] The surfaces are the inter-cooperating elements 100, in particular the outer surface of the first end 102 and the inner surface 106 of the second end 104, may be smooth, textured, toothed or friction surfaces, for the purposes herein described. The outer diameter of the first end 102 is preferably less than the inner diameter of the chamber 106 of the second section 104 such that when the first end 102 of section 100 is fitted into the second end 104 of an adjacent inter-cooperating element 100, the two elements 100 are able to pivotal, or rotate, relative to one another easily. In this case, the control device 58 is held in a relatively loose configuration.
[0077] When the control device 58 is tightened, by suitable operation of the handle assembly 70, in the example shown by pulling the end element 74 in a proximal direction that is away from the handle element 72, the elements 100 will be pressed together. In this manner, the outer surface of the first end 102 would be pressed against the inner surface 106 of the second end 104 in which it is located. Where the surfaces are smooth, the pressure imparted on the surfaces will reduce their ability to slide relative to one another and will therefore stiffen the guide wire section 90. Where the surfaces are roughened, textured or otherwise friction surfaces, as they are pressed together the guide wire will lock, preventing any further pivoting or rotation of the elements 100 relative to one another and as a result will lock the guide wire section 90. As a result, the section 90 of the guide wire 50 will retain the shape it has when it is locked, providing a solid and stable support for any further devices fed over the guide wire.
[0078] When the control device 58 is loosened, particularly by bringing the proximal handle portion 74 closer to the distal handle portion 72, the guide wire section 90 will loosen as the elements 100 no longer press against one another and the relevant surfaces are able to slide relative to one another again. The guidewire section 90 will therefore retain its maximum flexibility.
[0079] It is not necessary for the elements 100 to lock tight to one another when the control device 58 is fully deployed, although it is preferred if this occurs, in which case the control device 58 could be considered to be a locking device.
[0080] Referring now to
[0081] Preferably, the internal wall at the second end 220 has a curvature which is the same as or approximates the curvature of the outer surface of the first end 204, such that the first end 204 of one element 200 can fit into the concave recess formed by the internal wall at the second end 206 of an adjacent element 200. When so positioned, the elements 200 provide an internal lumen for receiving a control device 58 for the type disclosed herein.
[0082] With reference to
[0083] The bore formed by the internal wall 206 of the different versions of element 200 shown in
[0084] With the examples of elements 200 shown in
[0085] As with the embodiments described above, the surfaces of the first and second ends 204, 206 of the elements 200 may be smooth or non-smooth, such as roughened, textured or otherwise high friction surfaces. In this manner, a guide wire made up of sections 200 may exhibit the operational characteristics described above in connection with the embodiment of
[0086] The internal taper of the bore or lumen shown in the various embodiments of inter-cooperating elements 100, 200 disclosed herein provides room for the control device 58, particularly when the guide wire elements 100, 200 are pivoted so as to cause the guide wire to bend or curve. In the absence of a tapering internal lumen, either the assembly must be provided with a relatively large lumen, which restricts the dimensions to the guidewire and weakening the assembly, or will impart a straightening effect on the inter-cooperating elements 100, 200. The tapering internal lumen, therefore, aids in maintaining the guide wire in a bent configuration even as the control device 58 is tightened to retain a curved shape of the guide wire.
[0087] In
[0088] The bore of each or at least one inter-cooperating element 100, 200 may have a uniform taper from the first end to the second end. In practice, this can be accomplished by the internal wall of the element that forms the bore being substantially straight in longitudinal cross-section, as can be seen for example with the embodiments of
[0089] As explained above, in the preferred embodiments the assembly is provided with a covering sheath or cladding over at least that part of the guide wire assembly formed of the inter-cooperating elements 100, 200. This can ensure that the guide wire maintains a smooth outer surface even when it is curved, and also ensures that the elements 100, 200 remain coupled to one another, for instance on breakage of the internal control wire. The sheath or cladding may also provide lubricity to the guide wire, for instance when made of or covered by a lubricious material.
[0090] Referring first to the embodiment of
[0091] The assembly shown in
[0092] The cladding 220 preferably extends all the way to the tip 60, leaving the tip 60 exposed. In practice, as will be appreciated, the strip 232 will be less than 1 mm in thickness, preferably of no more than 0.05 to 0.50 mm, so as not to contribute unduly to the diameter of the assembly. The strip 232 may be made of any suitable material of which many are available in the art. Examples include a polymer material such as a polyamide (for instance Nylon), polyethylene terephthalate (PET), a polyether block amide (such as PEBAX); or a metal material such as nitinol, platinum, stainless steel or a combination of polymer and metal. The cladding 220 could advantageously be made of a lubricious material or be provided with a lubricious coating, such as a Hydrofil coating.
[0093] The strip 232 may be laid edge to edge along the length of the guidewire or may be laid with the edges overlapping.
[0094] The strip 232 may be simply wound tightly over the inter co-operating elements 200, although some embodiments may be attached to itself or to the core of the guide wire, for example by a suitable adhesive.
[0095] As explained, the cladding 220 provides a smooth outer surface to the guidewire and also ensures continued integrity of the assembly during its use and in the unlikely event that the control wire 58 were to break.
[0096]
[0097] It is not necessary for the braided sleeve 240 to be attached to the inter-cooperating elements 200, allowing the elements 200 to slide within the sleeve 240 and providing optimum flexibility of the assembly.
[0098] The braiding may be formed of any suitable metal or metal alloy, stainless steel, platinum and Nitinol being preferred.
[0099] The assembly can be provided with radiopaque properties. This may be in the form of an additive or filler to the cladding and/or to the material used in the formation of the inter co-operating elements 100, 200.
[0100] The guidewire assembly may be provided with a proximal portion not formed of inter co-operating elements of the types disclosed herein. In this case, the proximal portion is preferably made of a flexible tubular element of the type typically used for catheters. It may also be made as a hypotube, for instance of stainless steel, Nitinol or other suitable material. The hypotube may be transversely slotted, in known manner, to increase its flexibility.
[0101] With the arrangement disclosed it is possible to provide a guide wire with a soft locking section and having selectively varying flexure characteristics.
[0102] The control device may be a metal or metal alloy wire or a wire made from, for example, an ultrahigh molecular weight polyamide such as Dynema.
[0103] The elements 100, 200 may be made of metal or a metal alloy but in other embodiments may be made of a polymer material, such as a polyamide (for example Nylon), or any other suitable and preferably biocompatible material.
[0104] In practice, the assemblies taught herein can provide a very soft guide wire able to be made more rigid or locked into a shape during a medical procedure. The guide wire can retain that shape and in effect become stiff when locked. This can provide more optimal support for a microcatheter introduced over the guide wire. The guide wire can be manipulated, unlocked or otherwise made soft again and this can be controlled entirely by the clinician and repeated over and again during the procedure. In other words, the guide wire can be softened and stiffened or locked repeatedly as required.
[0105] The guide wire may have an outer diameter in the region of 0.35 mm to around 0.9 mm for neurovascular procedures but could equally have greater diameters, for instance of a millimetre or more, for other vessels. The portion of the guide wire formed of inter-cooperating elements may have a length of a few centimetres up to around 5 to 10 centimetres in some instances. The skilled person will appreciate that in many cases it is a design choice how long to make the lockable part of the guide wire.
[0106] All optional and preferred features and modifications of the described embodiments and dependent claims are usable in all aspects of the invention taught herein. Furthermore, the individual features of the dependent claims, as well as all optional and preferred features and modifications of the described embodiments are combinable and interchangeable with one another.
[0107] The disclosure in the abstract accompanying this application is incorporated herein by reference.