1. Field of the Invention
The present invention relates to medical devices. More particularly, the invention relates to wire guides and a method for making wire guides.
2. Background of the Invention
Often elongated, flexible wire guides are used to gain access to specific inner areas of the body. The wire guide may enter the body through a small opening and travel to parts of the body through body channels. For example, wire guides may be passed through the body via peripheral blood vessels, gastrointestinal tract, or the urinary tract. Wire guides are commercial available and are currently used in cardiology, gastroenterology, urology, and radiology. Once in place at a desired location in the body, wire guides are commonly used as guides for the introduction of additional medical instruments, e.g., catheters.
One design challenge for wire guides is that they have sufficient column strength to be pushed through a patient's vascular system or other body lumen without kinking. The wire guide must also be flexible enough to avoid damaging the blood vessel or other body channel through which it is being advanced. Improved strength and enhanced flexibility, however, are two properties which for the most part are diametrically opposed to one another. That is, an increase in one of these properties usually involves a decrease in the other. Accordingly, further improvements and enhancements in the strength and flexibility of wire guides may be desirable.
In at least one embodiment of the present invention, a method for making a wire guide is provided. The method comprises forming a distal end portion of a proximal core wire. The distal end portion has a first variable diameter that is less than a maximum diameter of the proximal core wire. The first variable diameter is configured to flare distally along at least a partial length of the distal end portion. A proximal end portion of a distal core wire is formed. The proximal end portion has a second variable diameter that is less than the maximum diameter of the distal core wire. The second variable diameter is configured to flare proximally along at least a partial length of the proximal end portion. Polymer material is overmolded onto the distal and proximal end portions to form a joining member that couples the distal and proximal end portions together.
In at least one other embodiment of the present invention, a wire guide is provided. The wire guide comprises a proximal core wire having a distal end portion. The distal end portion has a first variable diameter that is less than a maximum diameter of the proximal core wire. The first variable diameter is configured to flare distally along at least a partial length of the distal end portion. A distal core wire has a proximal end portion that has a second variable diameter that is less than a maximum diameter of the distal core wire. The second variable diameter is configured to flare proximally along at least a partial length of the proximal end portion. A joining member is formed of polymeric material overmolded onto the distal and proximal end portions. The joining member couples the distal and proximal end portions together.
In at least one other embodiment of the present invention, a catheter kit is provided. The catheter kit comprises the wire guide as described in the foregoing paragraph and a guide catheter for insertion into a patient. The wire guide provides the guide catheter a path during insertion into the patient.
Further objects, features, and advantageous of the present invention will become apparent from consideration of the following description and appended claims when taken in conjunction with the accompanying drawings.
Detailed embodiments of the present invention are disclosed herein. It is understood, however, that the disclosed embodiments are merely exemplary of the invention and may be embodied in various and alternative forms. The figures are not necessarily to scale; some figures may be configured to show the details of a particular component. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting but merely as a representative basis for the claims and teaching one skilled in the art to practice the present invention.
Examples of the present invention seek to overcome some of the concerns associated with providing a wire guide for guiding various medical devices through a body channel or cavity of a patient while providing sufficient column strength and flexibility to the wire guide so that the wire guide can be pushed through the patients' body without kinking and causing damage to the surrounding body tissue.
Employing the principles of the present invention is, for example, a wire guide, a method for making the wire guide and a catheter kit. The wire guide comprises two separate core wires. The core wires are joined together by a joining member that has been overmolded about one end of each of the core wires. The overmolded ends of the core wires are configured to mechanically anchor to the joining member. By having two discrete core wires joined together, the mechanical properties of each of the core wire can be respectively selected to provide corresponding sections of the wire guide with unique mechanical properties. In one example, the wire guide has a proximal section with relatively high column strength for pushing the wire guide through a patients' body lumen without kinking. In another example, the wire guide has a distal section with relatively high flexibility to avoid damage to a body channel or cavity when the wire guide is advanced therethrough.
Referring to
The core wires 10 and 12 may be made by any suitable wire forming process known to those skilled in the art, such as for example, pultrusion or extrusion of a metal alloy through a mold or die that has a circular opening. The core wires 10 and 12 each have an elongated cylindrical form with a corresponding diameter 22 and 24. Various diameters 22 and 24 for the core wires 10 and 12 are within the scope and spirit of the present invention with many medical procedures preferably having wire guides with a core wire diameter not exceeding about 0.020 inches. In one embodiment, the core wires 10 and 12 have the same or substantially the same (“substantially the same” is hereinafter understood to mean within manufacturing tolerances) diameters 22 and 24. In an alternative embodiment, one of the core wires 10 or 12 has a smaller diameter than the other core wire 10 or 12. For example, the distal core wire 12 may have a smaller diameter 24 than the diameter 22 of the proximal core wire 10 to form a wire guide having a relatively more flexible distal section.
The core wires 10 and 12 may each be comprised of different materials. For example, the proximal core wire 10 may comprise a material that is relatively stiffer and more kink resistant than the material of the distal core wire 12. In one embodiment, the proximal core wire 10 is made from stainless steel and the distal core wire 12 is made from Nitinol.
Referring to
The machining or grinding process is preferably capable of machining away material from the core wires 10 and 12 to produce intricate shapes with varying dimensions and geometries. Accordingly, the grinding wheel 30 may be accurately controlled for movement over numerous axes. In one example, this is accomplished by using an automated computer numerically controlled (CNC) multi-axis grinding machine. Preferably, the CNC grinding machine is capable of controlled movement over at least two axes, e.g., the X and Y axis. One such machine is a CAM.2 Profile Grinder manufactured by Glebar Company Inc. The CAM.2 Profile Grinder has direct interface with CAD/CAM and includes a fully integrated multi-axis servo controller. This arrangement may allow for machining of very intricate shapes which have been designed using a CAD based program. In one example, the grinding machine is capable of machining the shape within the core wires 10 and 12 to within several microns of a targeted dimension.
In one embodiment, the distal end 16 of the proximal core wire 10 is machined while the proximal core wire 10 is rotated about its longitudinal axis 34 to form substantially circular cross-sections along the distal end portion 26 with corresponding diameters 32. The diameters 32 are configured to vary (i.e. variable diameter 32) along the distal end portion 26 to define the shape of the distal end portion 26. Because material is removed from the proximal core wire 10 to form the distal end portion 26, the variable diameter 32 is less than the diameter 22 of the proximal core wire 10.
In one embodiment, the variable diameter 32 is configured to flare distally along a distal most length 36 of the distal end portion 16. For example, the variable diameter 32 may vary substantially linearly along the distal length 36 to form a partial cone shape or frustoconical section 38. Alternatively, the variable diameter 32 may vary in a non-linear fashion along the distal length. In another embodiment, the variable diameter 32 is configured to taper distally along a partial length 40 of the distal end portion 16 which is proximal to the distal most length 36. Other suitable configurations and/or arrangements for the distal end portion 16 may also be used without departing from the scope or spirit of the present invention.
The proximal end portion 28 of the distal core wire 12 is formed at 102. Similar to forming of the distal end portion 26, the proximal end portion 28 is formed by removing material from the proximal end 18 of the distal core wire 12 by machining or grinding with the grinding wheel 30 or mill. In one embodiment, the proximal end 18 of the distal core wire 12 is machined while the distal core wire 12 is rotated about its longitudinal axis 42 to form substantially circular cross-sections along the proximal end portion 28 with corresponding diameters 44. The diameters 44 are configured to vary (i.e. variable diameter 44) along the proximal end portion 28 to define the shape of the proximal end portion 28. The variable diameter 44 is less than the diameter 24 of the distal core wire 12.
In one embodiment, the variable diameter 44 is configured to flare proximally along a proximal most length 46 of the proximal end portion 28. For example, the variable diameter 44 may vary substantially linearly along the proximal length 46 to form a partial cone shape or frustoconical section 48. Alternatively, the variable diameter 44 may vary non-linearly. In another embodiment, the variable diameter is configured to taper proximally along a partial length 50 of the proximal end portion 28 which is distal to the proximal most length 46. Other suitable configuration and/or arrangement for the proximal end portion 28 may also be used without departing from the spirit of the present invention.
Referring to
In one embodiment, the mold 52 interfaces with an injection molding machine 56 which is configured to deliver molten polymeric material into the cavity 54 of the mold 52 via a runner/gate arrangement 58 formed in the mold 52. The polymeric material may be a thermoplastic or thermoset plastic material. Non-limiting examples of the polymeric material include polyamide, polyester, polyurethane, ABS, polycarbonate, epoxy or blends/mixtures thereof. Other suitable processes and/or systems may also be used for delivering the polymer material into the cavity 54 of the mold 52.
The distal and proximal end portions 16 and 28 are overmolded with the molten polymeric material. That is, the polymeric material is injected into the cavity 54 of the mold 52 around, over, under and/or through the distal and proximal end portions 16 and 28. The mold 52 further facilitates cooling and/or curing of the polymer material to form a solid structure defining a joining member 60. The joining member 60 couples the distal and proximal end portions 16 and 28 together and preferably has a substantially cylindrical form aligned with the proximal and distal core wires 10 and 12 which corresponds to their diameters 22 and 24.
Referring to
In one embodiment, the guide wire 62 has a recessed portion 68 formed in the distal core wire 12 distal from the proximal end portion 28. The recessed potion 68, for example, may be formed be removing material from the distal core wire 12 as part of the machining process described in the foregoing paragraphs. The recessed portion 68 has a reduced axial cross-sectional dimension 70 relative to the diameter 24 of the distal core wire 12. This reduced dimension 70 may provide the distal end 20 of the core wire 12 with greater flexibility.
A collar 72 may be positioned adjacent to the distal tip 74 of the wire guide 62 about the recessed portion 68. The distal tip 74, which may be formed for example by soldering or welding the distal end 20, preferably has an outside diameter corresponding to the diameter of the collar 72 so as to retain the collar 72 about the recessed portion 68. The collar 72 may be a coil spring 76 as depicted in
In one example, the collars 72 attaches to the core wire 12 to form the wire guide 62 by bonding with adhesive. Alternatively, the collar 72 may be attached via soldering or welding. Other suitable means know to those skilled in the art for attaching a collar to a core wire may also be used.
The collar 72 may also include a radio pacifier that is detectible by X-ray and/or fluoroscopic visualization. The radio pacifier may be incorporated directly into the material of the collar 72 or coated thereon. Alternatively, the radio pacifier may be included as part of the adhesive, welding material or solder that is used to attach the collar 72 to the core wire 12.
Referring to
Referring to
The kit 150 further includes the wire guide 62 as discussed in the foregoing paragraphs. The wire guide 62 provides a guide catheter 162 (discussed in more detail below) a path during insertion of the guide catheter 162 within the body channel or cavity. The size of the wire guide 62 is based on the inside diameter of the guide catheter 162.
The guide catheter 162 or sheath is typically made from polytetrafluoroethylene (PTFE) and is for percutaneously introducing the microcatheter 152 into the body of the patient. Of course, any other suitable material may be used without falling beyond the scope or spirit of the present invention. The guide catheter 162 may have a size of between about 4-French to 8-French and allows the microcatheter 152 to be inserted therethrough to a desired location in the body channel or cavity. The guide catheter 162 receives the microcatheter 152 and provides stability of the microcatheter 152 at a desired location within the body. For example, the guide catheter 152 may stay stationary within a common visceral artery, e.g., a common hepatic artery, and adds stability to the microcatheter 152 as the microcatheter 152 is advanced through the guide catheter 162 to a desired point in a connecting artery, e.g., the left or right hepatic artery.
When the distal end 156 of the microcatheter 152 is at the desired point in the body, the medical device may be loaded at the proximal end 154 of the microcatheter 152 and is advanced through the microcatheter 152 for deployment through the distal end 156. In one embodiment, a push wire 164 is used to mechanically advance or push the medical device through the microcatheter 152. The size of the push wire 164 depends on the diameter of the microcatheter 152.
It is to be understood that the catheter kit 150 described above is merely one example of a kit that may be used with the wire guide 62. Of course, other kits, assemblies, and systems may be used with the wire guide 62 without falling beyond the scope or spirit of the present invention.
As a person skilled in the art will readily appreciate, the above description is meant as an illustration of the implementation of the principles of this invention. This description is not intended to limit the scope of application of this invention in that the invention is susceptible to modification, variation, and change, without departing from the spirit of this invention, as defined in the following claims.
This application is related to and claims all available benefit of U.S. provisional patent application 61/141,268 filed Dec. 30, 2009, the entire contents of which are herein incorporated by reference.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2009/069674 | 12/29/2009 | WO | 00 | 6/28/2011 |
Number | Date | Country | |
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61141268 | Dec 2008 | US |