US20200146688A1 - Guidewire - Google Patents

Abstract

Embodiments include a transition section for coupling a distal section and a proximal section of the guidewire. The transition section includes a main body having a first outer diameter; proximal and distal pin extensions having second and third outer diameters, wherein the proximal pin extension is configured to be fixed to the proximal section of the guidewire, and the distal pin extension is configured to be inserted into and fixed to the distal section of the guidewire. The distal pin extension includes a bore for receiving an inner core of the distal section of the guidewire. The first outer diameter may be greater than the second and third outer diameters. Also disclosed are methods of manufacturing a guidewire with such a transition section.

Description

CROSS REFERENCE TO RELATED APPLICATIONS
• The present application is a Continuation of U.S. patent application Ser. No. 15/719,792 filed Sep. 29, 2017 (Allowed); which claims the benefit of U.S. Provisional Application No. 62/402,852 filed Sep. 30, 2016; the full disclosures which are incorporated herein by reference in their entirety for all purposes.
BACKGROUND OF THE INVENTION
• The invention relates to guidewires suitable for use in the deployment of implants for lung volume reduction.
• In chronic obstructive pulmonary disease, damage to tissue in certain parts of the lungs means that normal muscular inflation and deflation of the lungs becomes less efficient. One method to improve this situation is lung volume reduction, in which the diseased tissue is compressed or collapsed so that the remaining tissue can behave more normally. In one form of lung volume reduction, one or more elongate spring implants are deployed into the airways in the diseased lung tissue and are allowed to contract, gathering up the diseased tissue as they do so. Implants and systems for such treatments are disclosed in WO 2007/106495 and WO 2010/030993. In both cases, implants are deployed into the airways from catheter systems. The airways of the lungs are highly branched and tortuous, and lung tissue can be easily damaged. Therefore guidewires are used to determine the path to the airway to be treated, the catheter for delivery of the implant being advanced over the guidewire, which is then removed so that the implant can be deployed through the properly positioned catheter.
• The guidewire must be capable of being pushed out of the catheter and into airway, and rotated so that it advances in the desired direction, while at the same time being small enough that the delivery catheter can fit over it to be advanced into the lung for proper delivery of the implant. In order to reduce the likelihood of kinking due to the combination of compression and torsion, a composite structure has been proposed for the guidewire, comprising an inner core extending through an outer coil sheath. In order to allow the guidewire to be advanced through the catheter, the proximal part of the core is relatively thicker than the distal part, which is thinner to provide the necessary flexibility to be directed through the airways without damaging the lung tissue. One result of this is that applying torque at the proximal end of the guidewire to steer the distal end in the required direction can result in significant wind-up between the core and coil, making accurate control of the distal end difficult.
• The invention attempt to address the problem of how to provide more accurate control of the distal end while retaining the necessary flexibility in the system.
SUMMARY
• The various aspects of the present invention relate to improved guidewires for use in deployment of lung volume reducing implants, such as coils. One aspect provides a guidewire, comprising: an outer sheath having a proximal end and a distal end, and comprising a proximal section, a transition section, and a distal section, wherein the proximal section extends from the proximal end of the outer sheath to the transition section, and the distal section extends from the transition section to the distal end of the outer sheath, and wherein the distal section defines a bore extending from the transition section to the distal end of the outer sheath; and an inner core having a proximal end and a distal end, wherein the inner core extends through the bore of the distal section of the outer sheath, wherein the inner core is fixed to the outer sheath at the transition section, and wherein the distal end of the inner core is fixed to the distal end of the outer sheath at the distal end of the sheath.
• By fixing the inner core to the outer sheath at the transition section, it is not necessary for the core to extend the whole length of the sheath and so allows different physical properties to be provided for the proximal and distal sections of the sheath.
• In one configuration, the proximal section of the outer sheath defines a bore extending from the proximal end of the sheath to the transition section. In this case, the bore of the proximal section of the outer sheath can be substantially unobstructed between the proximal end of the sheath and the transition section.
• The proximal section of the outer sheath and the distal section of the outer sheath can comprise coils. In this case, the coil comprising the proximal section of the outer sheath can have different mechanical properties to the coil comprising the distal section of the outer sheath. For example, the proximal section can be configured to apply torque to the transition section and distal section, and the distal section can be configured for flexibility.
• The transition section can comprise an adapter to which the coils comprising the proximal and distal sections of the outer sheath are fixed. In one example, the transition section comprises a cylindrical body having a proximal pin extension for insertion into and fixture to an open end of the coil comprising the proximal section of the outer sheath, and a distal pin extension for insertion into and fixture to an open end of the coil comprising the distal section of the outer sheath, the distal pin extension also comprising a bore for receiving and fixing the inner core. This configuration allows a substantially constant outer diameter across the transition section and so helps avoid snagging.
• The proximal end of the inner core can be fixed to the outer sheath at the transition section. The distal end of the outer sheath and the distal end of the inner core can be fixed to a ball structure. Thus the end of the structure can have a atraumatic shape and so avoid damage to lung tissue as it is advanced.
• The inner core can comprise a wire having a flattened portion intermediate the proximal and distal ends. The proximal and distal ends of the wire can have substantially the same diameter. This allows modification from a simple wire structure to provide a core that preferentially bends in one plane, assisting in directing the guidewire though lung airways.
• The outer sheath is dimensioned to pass through a catheter for introduction into an airway of the lung of a patient.
• The guidewire can further comprise an end fitting connected to the proximal end of the proximal section and configured to allow a user to apply torque to the proximal section. The end fitting can comprise a hub that is permanently or removably connected to the proximal end of the proximal section.
• Another aspect provides a system comprising a first catheter, a guidewire as defined above, and a second catheter, wherein the first catheter is configured for introduction into the major airways of the lung of a patient, the guidewire is configured to be advanced from a lumen of the first catheter and further into a predetermined airway in the lung of the patient, and the second catheter is configured to be advanced through the lumen of the first catheter and over the guidewire into the predetermined airway of the lung of the patient. The system can further comprise an implant configured for delivery through a lumen in the second catheter and deployment into the predetermined airway of the lung of the patient.
• Another aspect provides method of deploying a lung volume reduction implant into a predetermined airway of a lung of a patient, comprising advancing the first catheter and the guidewire into a major airway of the lung; advancing the second catheter and guidewire through the lumen of the first catheter; advancing the guidewire from the lumen of the second catheter and directing the distal end of the guidewire further into the predetermined airway by rotating the proximal end of the outer sheath so as to point the distal end of the outer sheath in the direction of the predetermined airway; withdrawing the guidewire from the second catheter; and advancing a lung volume reduction implant through the lumen of the second catheter and deploying the implant into the predetermined airway.
• Another aspect provides a system comprising: a first catheter configured for introduction into the major airways of the lung of a patient; a second catheter configured to be advanceable through the lumen of the first catheter and further into a predetermined airway in the lung of the patient; and a guidewire according to any preceding aspects and configured to be advanced through a lumen of the second catheter and further into the predetermined airway, wherein the second catheter is configured to be further advancable over the guidewire and further into the predetermined airway of the lung of the patient. The system can further comprise an implant configured for delivery through a lumen in the second catheter and deployment into the predetermined airway of the lung of the patient.
• Another aspect provides a method of deploying a lung volume reduction implant into a predetermined airway of a lung of a patient, comprising: advancing the first catheter into a major airway of the lung; advancing the second catheter and guidewire through the lumen of the first catheter so as to extend into a predetermined airway of the lung; further advancing the guidewire from the lumen of the second catheter and directing the distal end of the guidewire further into the predetermined airway by rotating the proximal end of the outer sheath so as to point the distal end of the outer sheath in the direction of the predetermined airway; further advancing the second catheter over the guidewire further into the predetermined airway; withdrawing the guidewire from the second catheter; and advancing a lung volume reduction implant through the lumen of the second catheter and deploying the implant into the predetermined airway.
• Other aspects of the invention will be apparent from the following description.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIGS. 1 and 2 illustrate the human respiratory system:
• FIG. 3 shows an example of a guidewire;
• FIG. 4 shows further detail of the distal end of the outer sheath;
• FIG. 5 shows further detail of the transition section;
• FIG. 6 shows further detail of the distal end of the core;
• FIG. 7 shows the distal sheath section, the core, and the transition section;
• FIG. 8 shows further detail of the core;
• FIG. 9 shows a system for placing a lung volume reduction implant;
• FIGS. 10 and 11 show details of an implant;
• FIG. 12 illustrates delivery of the implant;
• FIG. 13 shows a fluoroscopic image of an implant in the position illustrated inFIG. 12;
• FIG. 14 shows a fluoroscopic image of an implant in a lung as the delivery catheter is removed;
• FIG. 15 illustrates the system after delivery of the implant.
DETAILED DESCRIPTION OF THE INVENTION
• FIGS. 1 and 2 illustrate the human respiratory system, including thetrachea12, which directs air from the nose8 ormouth9 into theprimary bronchus16. Air enters thelung20 from theprimary bronchus16. As is shown inFIG. 2, theprimary bronchus16 branches into thesecondary bronchus22,tertiary bronchus24,bronchioles26,terminal bronchioles28, and finally into thealveoli30.
• FIGS. 3-8 illustrate various aspects of the guidewire.FIG. 3 shows a schematic view of an outer sheath of a guidewire, comprising aproximal section40, atransition section42, and adistal section44. Theproximal section40 is formed of a spun coil which has a tight pitch and is substantially gapless. An example of such a coil is an HHS® (Helical Hollow Strand) Tube obtainable from Fort Wayne Metals of Fort Wayne, Ind., USA. A suitable tube can be formed from a single layer of 304V Spring Temper stainless steel filament(s) of approximately 0.029 cm thickness to give a coil tube of approximately 0.17 cm OD. Theproximal section40 can have a bore that is substantially unobstructed so as to give substantially consistent torque transmission and bending capability along its length. Thedistal section44 is formed from a wound coil, such as 304V Spring Temper stainless steel wire of approximately 0.025 cm thickness. Ashort section46 near the distal end of thedistal section44 is wound at a looser pitch so as to provide a highly flexible region as is shown inFIG. 4. The proximal anddistal sections40,44 are connected to each other by means of thetransition section42.FIG. 5 shows thetransition section42 in more detail. Thetransition section42 comprises a substantially cylindricalmain body48 having proximal anddistal extensions50,52 extending coaxially from opposite ends. Theextensions50,52 are of reduced OD compared to the OD of themain body48 and are sized to fit inside the respective bores of the proximal anddistal sections40,44. The OD of themain body48 is substantially the same as that of the proximal anddistal sections40,44. The transition section can also be made from stainless steel and connected to the proximal and distal sections by welding. A deviation can be provided in thetransition section42 so that the outer coil tube is naturally in a slightly bent configuration.
• Ahub54 is affixed at the proximal end of theproximal section40 by which a user can apply torque to the guidewire. The hub can be permanently affixed, such as by gluing, or can be removable. Aball56 can be welded to the distal end of thedistal section44 to provide an atraumatic surface. Theproximal section40 can also include amarker section58 to assist a user in determining the extend of insertion of the guidewire into a delivery system.
• A core is provided inside the coil forming thedistal section44, as shown inFIGS. 6 and 7. The core is formed of awire60 that is connected at one end in abore61 in thedistal extension52 of thetransition section42, and at the other end is a bore in theball56. Thewire60 is substantially cylindrical at its ends, but has been flattened to a thickness of about half of the original wire diameter at aposition62 close to the proximal end so that it will preferably bend in a direction perpendicular to the plane of the flattened section and assist in steering the end in use. As is shown inFIG. 8, a series ofmarkers64 are positioned along the core between thetransition section42 and the flattenedsection62. The markers can be made of a material visible in a fluoroscopic imaging system, such as Pt/Ir.
• In the configuration shown in these figures,distal section44 is approximately half as long as the proximal section. The overall length can be of the order of 120 cm, although other lengths and ratios can be used according to requirements.
• FIGS. 9-15 illustrate systems and methods using the guidewire described above.
• The system ofFIG. 9 comprises a bronchoscope including abronchoscope catheter100 having acamera102 at its distal end connected to a video processing system104. Adelivery catheter106 extends through the lumen of thebronchoscope catheter100. Thedistal end108 of thedelivery catheter106 is provided withmarkers110 visible to afluoroscopic imaging system112. Aguidewire114 of the type described above extends through the lumen of thedelivery catheter106 and can be advanced out of thedistal end108. The end of theguidewire114 also has markers116 (corresponding tomarkers64 described above). Adilator118 can be provided to endure a smooth transition between the outer surface of theguidewire114 and the outer surface of thedelivery catheters106.
• The system ofFIG. 9 is intended for use with an implant of the type shown inFIGS. 10 and 11, although other shapes may also be used. In its normal state, the implant comprises anelongate member120 that adopts acomplex shape122 comprising a series of curved sections, each curve centered on a separate axis. Theimplant120 can be made from Nitinol wire and can have atraumatic terminals at the ends and one or more length markers (not shown). For delivery, theimplant120 is distorted into a relativelystraight configuration124 and constrained in adelivery cartridge126.
• In use, thebronchoscope catheter100 ofFIG. 9 is advanced into the upper airways of a patient either to the extent of its available length, or until its physical size prevents further insertion without damage to the lung tissue. Thedelivery catheter106, together with theguidewire114, is advanced through the lumen of the bronchoscope catheter and into the airway. Theguidewire114 is then further advanced along thedelivery catheter106 from the proximal end so as to extend from thedistal end108 and project further into the airway. Themark58 can be positioned so as to indicate when the distal end of theguidewire114 is at the distal end of thecatheter108. As theguidewire114 is advanced further, it can be steered by applying a torque to thehub54, the deviation allowing the distal end to be pointed in a required direction and theflexible section46 and flattenedcore section62 allowing the end to be eased into the required airway on contact with the wall of the airway. Progress can be monitored either via the viewing field of the bronchoscope, or by use of the remotefluoroscopic imaging system112 once the end has passed out of this field of view. Thedeployment catheter106 can be advanced with theguidewire114 until itsdistal end118 is at or near the distal end of theguidewire114 in the airway of interest.
• Theproximal section40 is not configured to extend beyond thedistal end118 of thedelivery catheter106. Consequently, theproximal section40 can be configured for axial compression and torque transmission, together with the necessary degree of flexibility to be fed into thebronchoscope catheter100. In the example described above, this is achieved using the tight pitch spun coil structure for theproximal section40. By avoiding the need for the core60 to extend to thehub54, theproximal section40 can be more flexible than the previously proposed structure and so provides for easier insertion into thecatheter106. Themarker58 can be positioned so as to indicate that the distal end of theguidewire114 is at or near thedistal end118 of thedelivery catheter106, indicating to the user that further progress must be monitored using one or other of theimaging systems104,112.
• By providing an asymmetry in the guidewire construction, such as a deviation at thetransition section42, the distal end can be directed off axis. This, together with theflexible region46 and the flattenedportion62 of the core60 means that when the distal end reaches anairway junction128, torque can be applied at thehub54 to cause the distal end to move radially in the airway, the flattenedsection62 providing for preferential bending in the plane perpendicular to the plane of the flattenedsection62. The provision of theatraumatic ball58 andflexible end46 mean that the airway tissue can provide a reaction surface to allow control of the position without damage to the tissue.
• Once thedelivery catheter106 is in position, it can be secured and theguidewire114 withdrawn from thedelivery catheter106. Thecartridge126 carrying theimplant120 can then be connected in its place, and theimplant120 advanced along thedelivery catheter106 by a pusher device having adetachable connector130 as shown inFIG. 12.FIG. 13 shows remote imaging system view of theimplant120 at the end of thedelivery catheter106. Theimplant120 is held in place by thepusher device130 and thedelivery catheter106 is withdrawn, allowing theimplant120 to return to its as-manufactured shape (FIG. 14), reducing the volume of lung tissue in that region as it does so. Once theimplant120 is completely outside thedelivery catheter106, theconnector130 is detached (FIG. 15) and the bronchoscope anddelivery catheters100,106 can be withdrawn from the lung.
• Other variations are within the spirit of the present invention. Thus, while the invention is susceptible to various modifications and alternative constructions, certain illustrated embodiments thereof are shown in the drawings and have been described above in detail. It should be understood, however, that there is no intention to limit the invention to the specific form or forms disclosed, but on the contrary, the intention is to cover all modifications, alternative constructions, and equivalents falling within the spirit and scope of the invention, as defined in the appended claims.
• In the previous description, various embodiments of the present invention are described. For purposes of explanation, specific configurations and details are set forth in order to provide a thorough understanding of the embodiments. However, it will also be apparent to one skilled in the art that the present invention may be practiced without the specific details. Furthermore, well-known features may be omitted or simplified in order not to obscure the embodiment being described.
• The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The terms “comprising,” “having,” “including,” and “containing” are to be construed as open-ended terms (i.e., meaning “including, but not limited to,”) unless otherwise noted. The term “connected” is to be construed as partly or wholly contained within, attached to, or joined together, even if there is something intervening. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate embodiments of the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.
• Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors expect skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.
• All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.

Claims (21)

What is claimed is:

1. A transition section for coupling a distal section and a proximal section of a guidewire, the transition section comprising:

a main body having a first outer diameter;

a proximal pin extension having a second outer diameter, wherein the proximal pin extension extends proximally from the main body, and wherein the proximal pin extension is configured to be fixed to the proximal section of the guidewire; and

a distal pin extension having a third outer diameter, wherein the distal pin extension extends distally from the main body, and wherein the distal pin extension is configured to be inserted into and fixed to the distal section of the guidewire, the distal pin extension comprising a bore for receiving an inner core of the distal section of the guidewire;

wherein the first outer diameter is greater than the second and third outer diameters.

2. The transition section ofclaim 1, wherein the proximal section of the guidewire comprises a coil, and wherein the proximal pin extension is configured to be fixed to an open end of the coil.

3. The transition section ofclaim 1, wherein the distal section of the guidewire comprises a coil, and wherein the distal pin extension is configured to be fixed to an open end of the coil.

4. The transition section ofclaim 1, wherein the proximal section of the guidewire comprises a first coil and the distal section of the guidewire comprises a second coil.

5. The transition section ofclaim 1, wherein the second outer diameter and the third outer diameter are substantially same.

6. The transition section ofclaim 1, wherein the first outer diameter is substantially same as an outer diameter of the distal section of the guidewire and an outer diameter of the proximal section of the guidewire.

7. The transition section ofclaim 1, wherein the proximal pin extension and the distal pin extension extend coaxially from opposite ends of the main body.

8. The transition section ofclaim 7, wherein the proximal pin extension and the distal pin extension are cylindrical.

9. The transition section ofclaim 8, wherein the main body is cylindrical.

10. The transition section ofclaim 1, wherein the transition section is welded to the proximal section of the guidewire and the distal section of the guidewire.

11. The transition section ofclaim 10, wherein the transition section comprises a steel material.

12. The transition section ofclaim 1, wherein the transition section is dimensioned to pass through a catheter for introduction into an airway of a lung of a patient.

13. The transition section ofclaim 1, wherein the main body is cylindrical.

14. A method of manufacturing a guidewire with a distal section and a proximal section coupled together, the method comprising:

disposing a proximal pin extension of a transition section according toclaim 1 within a bore of the proximal section of the guidewire, wherein the proximal pin extension extends from a main body of the transition section according toclaim 1;

disposing ng a distal pin extension of the transition section according toclaim 1 within a bore of the distal section of the guidewire, wherein the distal pin extension extends from the main body of the transition section according toclaim 1;

fixing the transition section according toclaim 1 to the proximal section of the guidewire and the distal section of the guidewire; and

fixing an inner core of the distal section of the guidewire within a bore of the distal pin extension, wherein the inner core comprises a wire that extends through the distal section of the guidewire.

15. The method ofclaim 14, further comprising fixing a ball structure at a distal end of the guidewire.

16. The method ofclaim 15, wherein fixing the ball structure at the distal end of the guidewire comprises disposing the inner core of the distal section of the guidewire within a bore of the ball structure.

17. The method ofclaim 15, wherein fixing the ball structure at the distal end of the guidewire comprises welding the ball structure to the distal end of the distal section of the guidewire.

18. The method ofclaim 14, further comprising flattening a segment at a distal portion of the inner core, wherein the flattened segment is configured to assist in steering a distal tip of the guidewire.

19. The method ofclaim 18, further comprising disposing one or more markers between the transition section according toclaim 1 and the flattened segment of the inner core, wherein the markers allow for remote monitoring by an imaging system.

20. The method ofclaim 14, further comprising welding the transition section according toclaim 1 to a portion of the proximal section of the guidewire and a portion of the distal section of the guidewire.

21. The method ofclaim 14, further comprising forming the distal section of the guidewire from a wound coil, wherein a distal region of the distal section is wound at a looser pitch than a proximal region of the distal section, so as to provide flexibility at the distal region.

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