CN214484746U - Delivery guide wire and treatment device - Google Patents

Abstract

The utility model relates to a carry seal wire and treatment device, treatment device is including carrying seal wire, medical implant and conveyer pipe, carry the seal wire include the dabber with set up in the epaxial drive member of dabber, be formed with the depressed part on the drive member, medical implant quilt the conveyer pipe compression sleeve is established carry on the seal wire, just medical implant at least part imbeds in the depressed part to increase medical implant and carry the area of contact between the seal wire, be favorable to medical implant reduces the transport degree of difficulty along with carrying seal wire synchronous motion.

Description

Delivery guide wire and treatment device

Technical Field

The utility model relates to the technical field of medical equipment, concretely relates to carry seal wire and treatment device.

Background

Intracranial aneurysms are usually abnormal bulges on the wall of an intracranial artery, and are the first causes of subarachnoid hemorrhage. In cerebrovascular diseases, the incidence of intracranial aneurysm is second to cerebral thrombosis and hypertensive cerebral hemorrhage, and the intracranial aneurysm has great harm.

In the prior art, there are three main methods for treating intracranial aneurysms: (1) the surgical clamping method adopts a metal clamp to clamp the neck of the aneurysm to block intracranial aneurysm and cerebral circulation blood flow, and prevents the rupture and bleeding of the aneurysm while recovering normal blood supply of the parent artery. (2) The intratumoral embolization method adopts embolization materials to fill the aneurysm, so that thrombus is formed in the body of the aneurysm, and the rupture hemorrhage caused by further expansion of the body of the aneurysm is avoided. (3) The intravascular stent method is to implant a stent into a blood vessel to interfere the blood flow entering an aneurysm from a parent artery, so that the blood in the aneurysm is blocked and deposited, thereby forming aneurysm thrombus and further promoting the closure of the aneurysm body to prevent the rupture of the aneurysm body. Since aneurysms are generally longer than the periphery of the cerebral arterial loop, there are many important blood vessels, nerves and brain tissue around the cerebral arterial loop. When the surgical clamping method is used for treating the aneurysm, the medical requirements of doctors are extremely high, and the death rate of patients who treat the aneurysm by the surgical clamping method is still as high as 50 percent. When the intratumoral embolization method is simply used for treating large or huge complicated aneurysms, the recurrence rate of patients is high. Currently, the most widely used treatment for intracranial aneurysms is endovascular stenting.

Fig. 1 shows a treatment device for intracranial aneurysm treatment by using an intravascular stent method in the prior art, the treatment device includes a delivery guide wire 10 and a delivery tube 20, the delivery tube 20 has an inner cavity that axially penetrates through, a stent 30 to be delivered is accommodated in the inner cavity and sleeved on the delivery guide wire 10, and the delivery guide wire 10, the stent 30 and the delivery tube 20 are in an interference state. In this way, when the operator pushes the delivery guide wire 10 to move in the delivery tube 30, a first friction force is generated between the delivery guide wire 10 and the stent 20, and under the action of the first friction force, the stent 30 can move synchronously with the delivery guide wire 10 and finally reach the preset position. During which a second friction force, opposite to the first friction force, is generated between the stent 30 and the inner wall of the delivery tube 20 to resist movement of the stent 30 with the delivery guidewire 10. When the intracranial aneurysm is treated by adopting the intravascular stent method, the stent plays a role in guiding blood flow, so the stent has higher metal coverage rate, and the intracranial blood vessel is thin and roundabout, and needs to be conveyed by a small and flexible conveying device. This means that the fit between the stent and the delivery device is tighter than with a larger delivery device, resulting in a second friction force generated during delivery that is too high to make stent pushing difficult.

In order to smoothly push the delivery guide wire 10 in the delivery tube 30, the existing delivery guide wire 10 has a smooth outer surface, and in order to increase the first friction between the delivery guide wire 10 and the stent 30, a part of the delivery guide wire 10 is provided with a driving member having a relatively high friction coefficient. However, the arrangement of the entraining member causes the outer diameter of the stent loaded on the delivery guidewire 10 to increase, causing a second frictional force between the stent and the inner wall of the delivery tube 30 to increase, and at the same time, the outer diameter of the entire treatment device may also increase, making the treatment device difficult to use for the treatment of distal end vascular lesions. Also, if too many entraining members are provided or the length is too long, this may result in reduced compliance of the distal end of the delivery guidewire 10.

SUMMERY OF THE UTILITY MODEL

An object of the utility model is to provide a carry seal wire and treatment device can reduce the transport degree of difficulty of support.

In order to achieve the above object, the present invention provides a delivering guide wire for delivering medical implant, comprising a core shaft and a driving member disposed on the core shaft, wherein a recess is formed on the driving member.

Optionally, the carrying member includes a body and a groove formed on an outer surface of the body, and the groove forms the recess.

Optionally, the structure of the recess matches at least part of the structure of the medical implant in the compressed state.

Optionally, the recess is a mirror image of the inner surface of the medical implant in the compressed state.

Optionally, the groove has a width of 0.0008 inch to 0.004 inch, and/or a depth of 0.0002 inch to 0.004 inch.

Optionally, the groove comprises one or more sub-grooves, and a plurality of the sub-grooves are arranged on the outer surface of the body in a staggered arrangement, a continuous arrangement or an interval arrangement.

Optionally, the groove is helically wound along the axis of the body to form one or more helical grooves in the outer surface of the body.

Optionally, the carrying member is spirally wound by a winding wire along the axis of the mandrel to form one or more spiral structures, and the winding wire of two adjacent circles are arranged at intervals to form the recess.

Optionally, the winding wire is a polymer wire or a metal wire coated with a polymer coating.

Optionally, the wire is developable, and/or the wire is a platinum tungsten alloy wire or a platinum iridium alloy wire.

Optionally, the driving member includes an inner layer and an outer layer, wherein the inner layer is made of a metal material and fixedly sleeved on the mandrel; the outer layer piece is made of high polymer materials and is fixedly sleeved on the inner layer piece.

Optionally, the inner layer has a void structure, the outer layer partially or completely fills the void structure, and at least a portion of the outer layer is connected to the mandrel through the void structure.

Optionally, the outer surface of the inner layer member is provided with a recess, and the recess constitutes the void structure.

Optionally, the inner layer member includes a plurality of coils, the plurality of coils are sequentially arranged along the axial direction of the mandrel, and the void structure is formed between two adjacent coils.

Optionally, the inner layer member is a tube net structure woven by silk threads, and the mesh holes of the tube net structure form the gap structure.

Optionally, the filaments have a diameter of less than or equal to 0.001 inch and/or the number of braid intersections contained on the inner layer per inch of length is 15-50.

Optionally, the inner layer is at least one tubular structure, and the outer layer partially or completely covers the inner layer.

Optionally, the inner layer member is a helical structure formed by a wire helically wound around the axis of the mandrel, and the void structure is formed between two adjacent turns of the wire.

Optionally, the wire has a diameter of less than or equal to 0.001 inch and/or the wire forms a helix having a pitch of 0.001-0.007 inch.

Optionally, the inner layer member is made of a metal material having developability, wherein the metal material is selected from one or more of platinum, gold, tungsten, platinum-gold alloy, platinum-tungsten alloy, platinum-iridium alloy, and platinum-nickel alloy.

Optionally, the inner layer is welded or glued to the mandrel and/or the outer layer covers the inner layer and extends to connect to the mandrel.

Optionally, the material of the outer layer member includes any one or more of block polyether amide resin, thermoplastic polyurethane elastomer, silicone, nylon and acrylic polymer.

Optionally, the outer layer is formed on the inner layer by hot pressing and/or dip coating, or the inner layer and the outer layer are bonded.

Optionally, the mandrel is provided with at least two driving members, and the at least two driving members are arranged along the axial direction of the mandrel at intervals.

Optionally, the distance between two adjacent driving members is 0.5mm-150 mm.

Optionally, the distance between two adjacent driving members is 0.5mm-5 mm.

Optionally, one or more driving members are arranged on the mandrel, the outer diameter of each driving member is 0.01-0.03 inch, and the length of each driving member is 0.5-8 mm.

Optionally, each of the entraining members has a length of 0.5mm to 4 mm.

Optionally, the guide wire further comprises a first developing part and a second developing part, the first developing part is arranged at the end part of the far end of the mandrel, the second developing part is arranged on the mandrel, and the driving component is arranged between the first developing part and the second developing part.

In order to achieve the above object, the present invention also provides a therapeutic device, which comprises a delivery tube, a medical implant and the above delivery guide wire; the delivery pipe is provided with an inner cavity which is axially communicated and is used for accommodating the medical implant, and the wall of the inner cavity extrudes the medical implant so as to enable the medical implant to be in a compressed state; the medical implant in a compressed state is sleeved on the driving component, and at least part of the medical implant is embedded into the concave part.

Optionally, the lumen has a radial dimension in a range of 0.017 inches to 0.029 inches.

Optionally, the medical implant is a self-expanding stent.

Compared with the prior art, the utility model discloses a carry seal wire and treatment device has following advantage:

the treatment device comprises a delivery guide wire, a medical implant and a delivery pipe, wherein the delivery guide wire comprises a mandrel and a driving component arranged on the mandrel, and a concave part is formed on the driving component. Utilize the conveying seal wire carries medical implant, medical implant is held in the conveyer pipe, just the pipe wall of conveyer pipe is used for the compression medical implant, the compression state medical implant cover is established drive on the component, just medical implant at least part embedding depressed part, thereby the increase the support with the area of contact who drives the component improves medical implant with carry frictional force between the seal wire, and can make medical implant with the part of conveyer pipe contact tends towards levelly and smoothly and reduces medical implant with conveyer pipe and frictional force between with, reduces medical implant's the transport degree of difficulty. Meanwhile, the outer diameter of the medical implant compressed in the delivery pipe is reduced, and the outer diameter of the delivery pipe can be correspondingly reduced, so that the treatment device can reach a more remote target treatment position, the treatment range is expanded, the overall flexibility of the treatment device can be improved, a tortuous blood vessel can be smoothly passed, and the success rate of the operation is improved.

Meanwhile, in some embodiments, the driving member includes an inner layer piece and an outer layer piece, the inner layer piece is made of a metal material and is fixedly sleeved on the mandrel; the outer layer piece is made of high polymer materials and is fixedly sleeved on the inner layer piece. Because the inner layer piece is fixed (such as welded) on the mandrel, and the inner layer piece and the mandrel are both made of metal materials, the bonding strength is very high, and the inner layer piece and the mandrel cannot be displaced. The outer layer piece and the inner layer piece made of high polymer materials are fixedly connected through a specific structure, for example, a gap structure is arranged on the inner layer piece, and the gap structure is partially or completely filled in the outer layer piece, so that the inner layer piece and the outer layer piece are mutually embedded and matched; if the outer layer piece is used for coating the inner layer piece and further extends to be connected with the mandrel, the outer layer piece, the inner layer piece and the mandrel are in tight fit. The outer layer piece is arranged on the mandrel through the inner layer piece, and the inner layer piece and the outer layer piece have larger contact area, so that the connection strength is further improved. The connection mode in the prior art is changed by the above modes, so that the whole driving component can be firmly fixed on the mandrel, the phenomena of looseness, folds and displacement of the driving component in the process of conveying the bracket are avoided, and the reliability of the conveying guide wire in the process of conveying the medical implant is improved.

Drawings

FIG. 1 is a schematic view of a prior art treatment apparatus;

FIG. 2 is a schematic view of a pushwire according to an embodiment of the present invention, with the depression not shown;

FIG. 3 is a schematic view of a pushwire according to an embodiment of the present invention showing a depression;

fig. 4 is a schematic structural view of a bracket according to an embodiment of the present invention;

FIG. 5 is a schematic view of a modified version of the delivery guidewire of FIG. 3;

FIG. 6 is a schematic view of another alternative configuration of the delivery guidewire of FIG. 3;

FIG. 7 is an enlarged schematic view at A of the delivery guidewire of FIG. 6;

FIG. 8 is a schematic view of yet another alternative configuration of the delivery guidewire of FIG. 3;

FIG. 9 is an enlarged schematic view at B of the delivery guidewire shown in FIG. 8;

FIG. 10 is a schematic view of yet another alternative configuration of the delivery guidewire of FIG. 3;

fig. 11 is a schematic structural view of a pushwire according to another embodiment of the present invention;

fig. 12 is a schematic structural view of a pushwire according to yet another embodiment of the present invention;

fig. 13 is a schematic structural view of a pushwire according to yet another embodiment of the present invention.

In the figure:

10, 100-delivery guide wire;

110-a mandrel;

120-driving component, 121-body, 122-groove, 123-gap, 124-inner layer piece, 125-outer layer piece, 126-gap structure;

130-a first development;

140-a second development;

20-a delivery pipe;

30, 300-scaffold;

310-weaving silk;

311-weaving points.

Detailed Description

To make the objects, advantages and features of the present invention clearer, the present invention will be described in further detail with reference to the accompanying drawings. It should be noted that the drawings are in simplified form and are not to precise scale, and are provided for convenience and clarity in order to facilitate the description of the embodiments of the present invention.

As used in this specification, the singular forms "a", "an" and "the" include plural referents, and the plural forms "a plurality" includes more than two referents unless the content clearly dictates otherwise. As used in this specification, the term "or" is generally employed in its sense including "and/or" unless the content clearly dictates otherwise, and the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either fixedly connected, detachably connected, or integrally connected. Either mechanically or electrically. Either directly or indirectly through intervening media, either internally or in any other relationship. The specific meaning of the above terms in the present invention can be understood according to specific situations by those skilled in the art. The same or similar reference numbers in the drawings identify the same or similar elements.

As used herein, the terms "proximal" and "distal" refer to the relative orientation, relative position, and orientation of elements or actions with respect to one another from the perspective of an operator using the medical device, although "proximal" and "distal" are not intended to be limiting, but generally refers to the end of the medical device that is closer to the operator during normal operation, and generally refers to the end that is first introduced into the patient.

The present embodiments provide a delivery guidewire for delivering a medical implant to a predetermined location within a patient. The medical implant is, for example, a self-expanding stent (i.e., a self-expanding stent), which may be, in particular, a braided stent or a cut stent. In other embodiments, the medical implant may also be a medical embolic coil, a vascular occlusion device, or the like, without limitation. Hereinafter, for the convenience of description, the medical implant is described as a self-expandable stent, and for the sake of simplicity, the self-expandable stent is uniformly referred to as a "stent".

Referring to fig. 2 and 3, the guide wire 100 includes a core shaft 110 and a driving member 120 disposed on the core shaft 110, wherein a recess is formed on the driving member 120.

When the stent is delivered, the stent is compressed in the lumen of a delivery tube (at this time, the stent is in a compressed state), and tightly sleeved on the driving member 120, so that the stent generates a radial pressure on the driving member 120, and at least a portion of the stent is embedded in the recess. Thus, the contact area between the bracket and the driving member 120 can be greatly increased. When the operator pushes the delivery guidewire 100 to move axially in the delivery tube, the first friction force generated between the stent and the driving member 120 can also be greatly increased, thereby facilitating the stent to move synchronously with the delivery guidewire 100. For the braided stent, the braided wires used for braiding the stent are different in thickness; similarly, for the cutting stent, the wave bars on the cutting stent have different thicknesses, and at this time, the thicker braided wire or wave bars can be embedded into the concave parts more under the pressure of the delivery pipe so that the surface of the stent, which is in contact with the delivery pipe (namely the outer surface of the stent), tends to be flat, thereby reducing the second friction force generated between the stent and the inner wall of the delivery pipe and reducing the pushing resistance of the stent during delivery.

Similar to conventional delivery guidewires, the delivery guidewire 100 of the present embodiment further includes a first visualization member 130 and a second visualization member 140. The core shaft 110 has a first distal end and a first proximal end opposite to each other, the first developing member 130 may be a developing spring and disposed at an end of the first distal end, the second developing member 140 is disposed on the core shaft 110, and the driving member 120 is disposed between the first developing member 130 and the second developing member 140, so that the bracket is disposed between the first developing member 130 and the second developing member 140.

In some embodiments, the driving member 120 may be made of a polymer material such as silicone, thermoplastic polyurethane elastomer rubber (TPU), polyimide, thermoplastic elastomer (Pebax), Polytetrafluoroethylene (PTFE), or the like. In other embodiments, the driving member 120 may be made of a metal material such as stainless steel, nitinol, platinum-tungsten alloy, etc.

The mandrel 110 is provided with a plurality of driving members 120, such as one, two, three, four, five, six, etc., and the specific number of the driving members 120 is determined according to the length of the stent to be delivered (i.e., the size of the stent in the axial direction). Generally, if the length of each of the driving members 120 is fixed, the greater the length of the stent, the greater the pushing resistance generated during the delivery, and more driving members 120 are needed to increase the first friction between the delivery guidewire 100 and the stent, so as to ensure that the stent moves synchronously with the delivery guidewire 100. In this embodiment, the outer diameter of each of the driving members 120 may be between 0.01 inch and 0.03 inch, the length of each of the driving members 120 is between 0.5mm and 8mm, and preferably, the length of each of the driving members 120 is between 0.5mm and 4 mm. When the mandrel 110 is provided with more than two driving members 120, the more than two driving members 120 are arranged at intervals along the axial direction of the mandrel 110. Optionally, the distance between two adjacent driving members 120 is between 0.5mm and 150mm, and preferably the distance is between 0.5mm and 5 mm.

On the one hand, compared with the method of increasing the first friction force by simply increasing the friction coefficient of the driving members 120, the larger first friction force can be obtained more easily by designing the number of the driving members 120 arranged on the mandrel 110 and the size of each driving member 120. On the other hand, compared to a continuous longer driving member disposed on the mandrel 110, the at least two spaced and shorter driving members 120 disposed on the mandrel 110 can reduce the total length of the driving members 120 and increase the recoverable rate of the stent (i.e., the smaller the total length of the driving members 120, the higher the recoverable rate of the stent). On the other hand, the plurality of short driving members 120 at intervals are arranged, so that the flexibility of the conveying guide wire 100 can be improved, the conveying guide wire 100 can conveniently pass through tortuous blood vessels, and meanwhile, the plurality of short driving members 120 are adopted, so that the driving members 120 can be made of materials with relatively high hardness (relatively low friction coefficient), the tolerance is convenient to control, and the manufacturing difficulty is reduced. It will be appreciated that the recoverability of the scaffolds described herein is well known in the art and will be apparent to those skilled in the art: the recovery rate of the stent is (total length of the stent-the distance from the proximal end of the stent to the distal end of the driver member)/total length of the stent is 100%.

Next, the structure of the entraining member 120 will be described with reference to the accompanying drawings. It should be understood that the specific structure of the driving member 120 described in the following embodiments is only an optional implementation manner of the present invention, and it should not limit the present invention.

Referring to fig. 2-4, in an embodiment, the driving member 120 includes a body 121, the body 121 is a hollow tubular body, the body 121 is sleeved on the core shaft 110, a groove 122 is formed on an outer surface of the body 121, and the groove 122 forms the recess. It is understood that the "groove" of the present embodiment includes an elongated concave structure, and also includes a circular, square or irregular concave structure (i.e. a pit), and the groove 122 has different forms according to actual needs.

For example, with continued reference to FIG. 3, the grooves 122 are configured to match at least a portion of the configuration of the stent in a compressed state. Specifically, the shape and position of the groove 122 are matched with those of the stent, and the size of the groove 122 is also matched with that of the wave bar or the weaving wire of the stent, for example, the width of the groove 122 is greater than, equal to or slightly smaller than that of the weaving wire or the wave bar, the depth of the groove 122 (the distance between the bottom of the groove 122 and the outer surface of the body 121 at the top of the groove 122) is greater than, equal to or smaller than the radial size of the weaving wire or the wave bar, and the like. Depending on the size of the stent, the width of the grooves 122 is between 0.0008 inches and 0.004 inches, and the depth of the grooves 122 is between 0.0002 inches and 0.004 inches. It will be understood that the width of the grooves 122 corresponds to the width of the braided wires or struts of the stent, for example, when the braided wires of the stent extend in the circumferential direction of the stent, the width of the braided wires refers to the dimension of the braided wires in the axial direction of the stent, and the width of the grooves 122 refers to the dimension of the grooves 122 in the axial direction of the stent.

The groove 122 may be a continuous structure formed on the outer surface of the body 121, and may also include a plurality of sub-grooves, which may be staggered, arranged continuously or arranged at intervals on the outer surface of the body 121.

Taking the stent 300 shown in fig. 4 as an example, the stent 300 is woven by a plurality of weaving wires 310. Corresponding to the stent 300, the grooves 122 may include a plurality of sub-grooves, and the sub-grooves are staggered such that the grooves 122 and the inner surface of the stent in a compressed state are mirror images of each other (as shown in fig. 3), i.e., the size and arrangement of the grooves 122 are matched with the size and arrangement of the braided wires 310 of the stent in a compressed state. Each of the braided wires 310 may be at least partially embedded in the recess when the stent 300 is fitted over the delivery guidewire 100.

The recess 122 may be shaped in a variety of ways in this embodiment. The body 121 is made of a polymer material, and when the body 121 is formed but not cured, a wire is wound on the body 121 along an axis of the body 121 in a spiral or staggered manner, and the wire is in close contact with a surface of the body 121 to apply a radial acting force to the body 121. Under the extrusion of the wire, the contact part of the outer surface of the body 121 and the wire is deformed in a concave manner toward the axis of the body 121 to form the groove 122, and then the wire is removed. The silk threads can be metal threads, polymer threads or silk threads made of other materials. In this embodiment, the diameter of the filament is the same as the diameter of the woven filament of the stent 300 that needs to be sleeved on the delivery guidewire 100, and in other embodiments, the diameter of the filament may be slightly larger or smaller than the diameter of the woven filament of the stent 300. The groove 122 may also be formed after the body 121 has been cured, for example, by first heating the body 121 to soften the body 121, and then forming the groove 122 with a wire; alternatively, after the body 121 is cured, the groove 122 is carved on the outer surface of the body 121 by using a carving process.

When the material of the body 121 is metal, the groove 122 may also be formed on the outer surface of the body 121 by an engraving process (e.g., laser engraving).

For the stent formed by the cutting process, a groove 122 matched with the stent may be formed on the surface of the body 121 by an engraving process.

Referring to fig. 5 to 10, in some embodiments, the driving member 120 includes an inner layer 124 and an outer layer 125, the inner layer 124 is made of a metal material and is fixed on the core shaft 110, and the outer layer 125 is made of a polymer material and is fixed on the inner layer 124.

The inner layer 124 is made of a metal material and may be fixed to the core shaft 110 by bonding or welding or other means, and the bonding strength between the two is very high, so that the inner layer 124 does not shift on the core shaft 110, and the outer layer 125 is connected to the core shaft 110 through the inner layer 124, which indirectly increases the connection area between the outer layer 125 and the core shaft 110, thereby enhancing the adhesion of the outer layer 125 to the core shaft 110, and reducing the possibility of the outer layer 125 loosening, wrinkling or shifting during stent delivery. It is understood that there are two cases of the "sleeving" described herein, one of which is that the inner layer 124 is an independent component with respect to the mandrel 110, and the two are assembled into a whole after being processed separately; secondly, during the machining process, the inner layer 125 is integrally formed with the mandrel 110, but the inner layer 124 protrudes from the outer surface of the mandrel 110.

Further, a void structure 126 may be formed on the inner layer 124, and the outer layer 125 partially or completely fills the void structure 126 to increase a connection area between the outer layer 125 and the inner layer 124.

In the present embodiment, the inner layer 124 can have various structures, and the preferred structure of the inner layer 124 will be described with reference to the accompanying drawings. It should be understood that the inner layer 124 in the following embodiments is only an optional implementation of the present invention, and should not be construed as limiting the present invention.

As shown in fig. 5, in one embodiment, the inner layer 124 includes a plurality of coils that are hooped on the mandrel 110, and the plurality of coils are arranged along the axial direction of the mandrel 110. In this embodiment, since the coils may be made of metal wires with a circular or elliptical cross section, two adjacent coils may contact each other, so that a concave portion with a cross section similar to a V shape may be formed between two adjacent coils, and the concave portion constitutes the void structure 126. In other embodiments, the recess may also be in the shape of a U-shaped groove, a cube, a cuboid, or a hemispherical dimple, depending on the shape of the radial cross-section of the coil. The outer surface of the coil is shaped and cooled by a mold by hot pressing and/or dip coating, etc. to form the outer layer member 125. The hot pressing mode is as follows: firstly, sleeving a polymer tube on the inner layer member 124, sleeving a heat-shrinkable tube on the polymer tube, heating the heat-shrinkable tube, shaping by using a mold, so that the polymer tube is melted and permeates into the gap structure 126 of the inner layer member 124, and removing the heat-shrinkable tube after the polymer material is cooled and solidified. The material of the outer layer 125 includes a thermoplastic elastomer, such as any one or a combination of more of block polyether amide resin (Pebax) or thermoplastic polyurethane elastomer (TPU), silicone, nylon, acrylic polymer, and other polymer materials. The polymer material fills the void structure 126, thereby increasing the contact area between the outer layer 125 and the inner layer 124 and enhancing the connection therebetween. Even more, when uncured, the polymer material penetrates the surface of the mandrel 110 from between two adjacent coils, and may also extend from two ends of the inner layer 124 to the surface of the mandrel 110, so that the outer layer 125, the inner layer 124 and the mandrel 110 may be tightly bonded to each other, thereby further reducing the possibility of wrinkling, loosening and displacement of the outer layer 125. In other embodiments, the outer layer may be formed first, and the inner layer 124 and the outer layer 125 are connected by gluing or the like.

In some embodiments, a plurality of the coils may be distributed on the core shaft at intervals, and a gap between two adjacent coils forms the void structure, in which case, the outer layer, the inner layer and the core shaft are all bonded to each other.

Referring to fig. 6 and 7, in another embodiment of the present invention, the inner layer 124 is a spiral structure formed by a wire spirally wound along the axis of the mandrel 110. Similar to the previous embodiment, for the inner layer 124 of the spiral structure, the wires of two adjacent turns may be in contact with each other or separated from each other. In this embodiment, the mandrel 110 may be provided with only one driving member 120, or a plurality of driving members 120.

Alternatively, the inner layer 124 in this embodiment may be wound with polymer wires or metal wires. For the inner layer 124 of metal, the helical structure is flexible and pliable, so that the pushwire 100 as a whole has better flexibility.

Optionally, the diameter of the wire of the inner layer 124 in this embodiment is less than or equal to 0.001 inches. Wherein the wires of the inner layer 124 form a helix having a pitch of 0.001 to 0.007inch, and in some embodiments, 0.004 to 0.007 inch. The larger the pitch, the more glue or the like can enter between the inner layer 124 and the mandrel 110, the more the bond strength between the inner layer 124/outer layer 125 and the mandrel 110 can be improved, and the flexibility of the delivery guidewire can not be affected while the bond strength between the inner layer 124 and the mandrel 110 is not reduced.

Referring to fig. 8 and 9, in another embodiment of the present invention, the inner layer 124 is a tube net structure woven by silk threads, and the mesh holes of the tube net structure form the void structure 126.

In this embodiment, the mandrel 110 may be provided with only one driving member 120, or a plurality of driving members 120. For each entraining member 120, the wires used to weave the inner layer 124 should be as thin as possible, e.g., the diameter of the wires (or the cross-sectional width of the wires) is less than or equal to 0.001 inch. In addition, the number of braid intersections per inch of the inner layer 124 should not be excessive, and preferably, the number of braid intersections per 1 inch of the inner layer 124 may be between 15 and 50. As such, the entraining member 120 does not affect the flexibility of the delivery guidewire 100 while enhancing the securement of the connection to the mandrel 110.

Fig. 10 shows a schematic view of a further embodiment of the invention. Referring to fig. 10, one or more inner layers 124 are welded to the mandrel 110, and the inner layers 124 are metal pipes. In this embodiment, the metal tube has a tubular structure with a flat surface. The metal tube may be 0.3-2mm in length to avoid affecting the compliance of the pushwire 100. When there are at least two metal tubes, the outer layer 125 may be configured to cover all of the metal tubes as a whole, and extend to the mandrel 110, and also cover the exposed portion of the mandrel 110 between the metal tubes (the portion constitutes the gap structure 126), or the outer layer 125 may be disposed on a single metal tube (as shown in fig. 9), that is, a single outer layer 125 covers a single inner layer 124, different outer layers 125 cover different inner layers 124, respectively, and the outer layer 125 also covers the mandrel 110 between the metal tubes (the portion constitutes the gap structure 126). The wrapping of the outer layer 125 to the inner layer 124 may be accomplished by dip coating or hot pressing.

In other embodiments, the metal tube may further be provided with pits, grooves, or through holes by laser etching, etc. to form more void structures 126, so as to further increase the contact area between the outer layer 125 and the inner layer 124 and improve the connection strength.

The inner layer member 124 described in the above embodiments may be made of a metal having no developability or a metal having developability. The metal without developability includes, but is not limited to, stainless steel, and the metal with developability includes, but is not limited to, platinum-tungsten alloy or platinum-iridium alloy. Preferably, the inner layer 124 is made of a metal with developability (or referred to as a radiopaque metal) to make the carrying member 120 have developability, and specifically, the material of the inner layer may be selected from one or more of platinum, gold, tungsten, platinum alloy, platinum-tungsten alloy, platinum-iridium alloy and platinum-nickel alloy, for example, the inner layer is made of platinum-tungsten alloy alone, or platinum-iridium alloy alone, or both platinum-tungsten alloy and platinum-iridium alloy (for example, the inner layer is woven by platinum-tungsten alloy wires and platinum-iridium alloy wires together to form the tube network structure). The advantage of setting up like this is, in transportation process, the operator can in time, accurately judge whether the support can also retrieve. Specifically, in actual use, the stent is sleeved over the delivery guidewire and compressed in a delivery tube having opposite first proximal and distal ends, with a visualization ring (not shown) disposed on the first distal end. In the conveying process, when the driving member 120 starts to coincide with the developing ring, if the bracket is pushed to the far end, the bracket can not be recovered any more, so that if the driving member 120 has developing performance, an operator can accurately perform positioning judgment through the developing device, and the operation of the operator is greatly facilitated.

In the embodiment of fig. 5-10, on one hand, by disposing the driving member 120 as two parts, i.e., an inner layer 124 and an outer layer 125, and disposing the inner layer 124 as a metal structure and fixedly covering the core shaft 110, the outer layer 125 is made of a polymer material and fixedly covering the inner layer 124, the inner layer 124 indirectly enhances the bonding force between the outer layer 125 and the core shaft 110, so that the driving member 120 is not easily loosened, folded or displaced during stent delivery, and the safety and reliability of the delivery guidewire 100 during delivery of a medical implant are improved. On the other hand, at least part of the medical implant in a compressed state is embedded into the groove 122 through the groove 122 on the outer surface of the outer layer 125 of the driving member 120, so that the contact area between the stent and the driving member 120 is increased, the friction force between the medical implant and the delivery guide wire 100 is improved, the contact part between the medical implant and the delivery pipe tends to be flat, the friction force between the medical implant and the delivery pipe is reduced, and the delivery difficulty of the medical implant is reduced.

In some embodiments, referring to fig. 11, the groove 122 may be a continuous groove formed on the body 121, and the continuous groove is spirally wound along the axis of the body 121 to form a spiral groove on the outer surface of the body 121. In this embodiment, the grooves 122 are preferably formed by using a wire to form the grooves 122.

For another example, referring to fig. 12, the groove 122 may include at least two sub-grooves spaced apart from each other on the body 121. The sub-grooves may be in various shapes such as a circle, a square, a prism, etc. (i.e., the sub-grooves are recesses), and when the number of the sub-grooves is more than two, a plurality of sub-grooves are distributed on the outer surface of the body 121 as required. The groove 122 may be formed by engraving or the like in this embodiment.

Still taking the stent 300 shown in fig. 4 as an example, the knitting points 311 where the knitting filaments 310 intersect have a larger radial thickness than other portions of the stent 300, and the knitting points 311 may be partially embedded in the sub-grooves when the stent 300 is mounted on the pushwire 100. Alternatively, in other stents, a site of greater radial dimension may be present at a location on the stent, and the site of greater radial dimension may be partially or fully embedded in the sub-groove when the stent is placed over the delivery guidewire. Thus, when the stent 300 is sleeved on the delivery guidewire 100 and inserted into the lumen of the delivery tube, the contact area between the braided wire or wave rod of the stent 300 and the body 121 is increased, so that the first friction between the stent 300 and the driving member 120 is increased; meanwhile, the outer diameter of the stent 300 tends to be uniform as a whole, and the surface of the stent 300 in contact with the delivery pipe (i.e., the outer surface of the stent 300) is smoother, so that the second friction between the stent and the inner wall of the delivery pipe is reduced, and the pushing resistance of the stent during delivery is reduced.

In another embodiment of the present invention, as shown in fig. 13, the driving member 120 is formed by a winding wire wound around the mandrel 110. The winding wire is spirally wound around the axis of the mandrel 110 for a plurality of turns to form a spiral structure, and a gap 123 exists between two adjacent turns of the winding wire, wherein the gap 123 constitutes the recess.

In this embodiment, the number of turns and the pitch of the winding wire can be adjusted as required. For example, when the stent to which the delivery guidewire 100 is mated has a relatively large PPI (PPI refers to the number of braid points contained within a unit length of the braided stent, where the length is the axial dimension of the stent), the number of windings of the wire on the mandrel 110 may be increased and the pitch may be decreased to provide a greater contact area between the stent and the driver member 120.

Alternatively, the winding filament may be a polymer filament, which preferably has a large surface friction coefficient, and may be selected according to the requirement.

Optionally, the winding wire is composed of a metal wire and a polymer coating layer coated on the outer surface of the metal wire. Preferably, the metal wire is a metal wire having developability, such as a platinum-tungsten alloy wire or a platinum-iridium alloy wire, so that the carrying member 120 has developability. Since the driving member 120 has developability, when the stent is delivered, an operator can conveniently judge the specific position of the stent in the body, and can further judge whether the partially released stent can be recovered into the delivery tube. Specifically, the conveying pipe for conveying through the stent has a second distal end and a second proximal end which are opposite to each other, and the second distal end is provided with the third developing member, and when the operator observes through the developing device that the driving member 120 starts to coincide with the third developing member while conveying the stent, the operator can judge that the stent cannot be recovered any more.

It is understood that in the embodiment of fig. 11-12, the entraining member 120 can also have an inner layer 124 and an outer layer 125 as in any of fig. 5-9, and the specific structure and materials can be the same as in the above-described embodiment and will not be repeated here.

Further, the present embodiments also provide a treatment apparatus comprising a delivery tube, a medical implant, and a delivery guidewire as described above. The delivery tube has an axially through lumen for receiving the medical implant, and the wall of the lumen compresses the medical implant so that it is compressed. The compressed medical implant is tightly sleeved on the driving member 120, a first friction force is generated between the compressed medical implant and the driving member 120, and at least part of the medical implant is embedded in the recess to increase the first friction force. The medical implant described herein is, for example, a self-expanding stent, and may be, in particular, a woven stent or a cut stent.

It should be noted that, in order to improve the matching degree between the driving member 120 and the medical implant and simplify the assembling process of the therapeutic device, the delivery guidewire 100 according to this embodiment is preferably manufactured according to a specific medical implant. That is, in the process of producing the delivery guidewire 100, the medical implant to be delivered is first provided, then the form of the entrainment member 120 and the recess portion is determined according to the structure of the medical implant, and finally the production of the delivery guidewire 100 is performed.

In addition, the inner cavity of the delivery pipe has different radial sizes according to actual requirements, and preferably, the radial size of the inner cavity ranges from 0.017 inches to 0.029 inches. More preferably, the radial dimension of the lumen is less than or equal to 0.027 inches, or the radial dimension of the lumen is less than or equal to 0.021 inches. Because the transport seal wire has adopted the drive component that has the depressed part, can reduce the external diameter of medical implant under compression state, therefore the utility model discloses a less conveyer pipe of radial dimension of inner chamber can be adopted to the treatment device, and this treatment device can reduce the external diameter of conveyer pipe correspondingly, and thinner conveyer pipe can reach the blood vessel of more distal end or more tiny pathological change position, enlarges the treatment range, has also improved the holistic compliance of treatment device simultaneously, more is favorable to reaching pathological change position smoothly through comparatively tortuous blood vessel, improves the operation success rate.

Although the present invention is disclosed above, it is not limited thereto. Various modifications and alterations of this invention may be made by those skilled in the art without departing from the spirit and scope of this invention. Thus, if such modifications and variations of the present invention fall within the scope of the claims and their equivalents, the present invention is also intended to include such modifications and variations.

Claims (40)

1. The utility model provides a carry seal wire for carry medical implant, its characterized in that, including the dabber with set up in drive component on the dabber, be formed with the depressed part on the drive component, drive the component including the body with form in the recess of body surface outside, the recess constitutes the depressed part, it includes inlayer spare and inlayer spare to drive the component.

2. The pushwire of claim 1, wherein said groove is configured to match at least a portion of the configuration of said medical implant in a compressed state.

3. The pushwire of claim 2, wherein said groove mirrors an inner surface of said medical implant in a compressed state.

4. The pushwire of claim 2 wherein said groove has a width of 0.0008 inches to 0.004 inches and/or a depth of 0.0002 inches to 0.004 inches.

5. The pushwire of claim 1, wherein said groove comprises one or more sub-grooves, a plurality of said sub-grooves being staggered, consecutive, or spaced on an outer surface of said body.

6. The pushwire of claim 1, wherein said groove spirals along the axis of said body to form one or more helical grooves in the outer surface of said body.

7. The pushwire of claim 1, wherein said inner member is formed of a metallic material and is secured to said mandrel;

the outer layer piece is made of high polymer materials and is fixedly sleeved on the inner layer piece.

8. The pushwire of claim 7, wherein said inner member has a void structure, said outer member partially or completely filling said void structure, at least a portion of said outer member being coupled to said mandrel through said void structure.

9. The pushwire of claim 8, wherein said inner member is provided with a depression in an outer surface thereof, said depression defining said void structure.

10. The pushwire of claim 8, wherein said inner member comprises a plurality of coils arranged in series along an axial direction of said mandrel, said void structure being formed between adjacent ones of said coils.

11. The pushwire of claim 8, wherein said inner layer is a tubular mesh woven from filaments, the pores of said tubular mesh forming said void structure.

12. The pushwire of claim 11, wherein said wire has a diameter of less than or equal to 0.001 inch and/or wherein said inner layer comprises between 15 and 50 braid intersections per inch of length.

13. The pushwire of claim 1, wherein said inner member is at least one tubular structure, and said outer member partially or completely covers said inner member.

14. The pushwire of claim 8, wherein said inner member is a helical structure formed by a wire helically wound around the axis of said mandrel, said void structure being formed between adjacent turns of said wire.

15. The pushwire of claim 14, wherein said wire has a diameter of less than or equal to 0.001 inch and/or wherein said wire forms a helix having a pitch of 0.001-0.007 inch.

16. The pushwire of any of claims 1-15, wherein said inner member is made of a developable metallic material.

17. The pushwire of claim 16, wherein said metallic material is selected from the group consisting of platinum, gold, tungsten, platinum alloys, platinum tungsten alloys, platinum iridium alloys, and platinum nickel alloys.

18. The pushwire of any of claims 1 to 15, wherein said inner member is welded or glued to said mandrel and/or said outer member covers said inner member and extends to join said mandrel.

19. The pushwire of any of claims 1 to 15, wherein said outer layer comprises any of a block polyether amide resin, a thermoplastic polyurethane elastomer, silicone, nylon, and an acrylic polymer.

20. The pushwire of any of claims 1 to 15, wherein said outer layer is formed on said inner layer by hot pressing and/or dip coating, or said inner and outer layers are bonded.

21. The pushwire of claim 20, wherein said depression is formed on an outer surface of said outer member; and/or the structure of the recess matches at least part of the structure of the medical implant in a compressed state.

22. The pushwire of claim 21, wherein said depression comprises one or more sub-grooves, a plurality of said sub-grooves being staggered, continuous, or spaced on the outer surface of said outer member.

23. The pushwire of any of claims 1-15, wherein said mandrel has at least two of said plurality of.

24. The pushwire of claim 23, wherein the distance between adjacent pairs of said entraining members is in the range of 0.5mm to 150 mm.

25. The pushwire of claim 24, wherein the distance between adjacent pairs of said entraining members is 0.5mm-5 mm.

26. The pushwire of any of claims 1-15, wherein said mandrel has one or more of said plurality of driver members, said driver members having an outer diameter of 0.01 inch to 0.03 inch, and each of said driver members having a length of 0.5mm to 8 mm.

27. The pushwire of claim 26, wherein each said entraining member has a length of 0.5mm to 4 mm.

28. The pushwire of any of claims 1-15, further comprising a first visualization member disposed at a distal end of said mandrel and a second visualization member disposed on said mandrel, said entraining member being disposed between said first visualization member and said second visualization member.

29. The conveying guide wire is used for conveying a medical implant and is characterized by comprising a mandrel and a driving component arranged on the mandrel, wherein a concave part is formed on the driving component, the driving component is spirally wound by a winding wire along the axis of the mandrel to form one or more spiral structures, and the winding wire of two adjacent circles is arranged at intervals to form the concave part.

30. The pushwire of claim 29, wherein said winding wire is a polymer wire or a metal wire coated with a polymer coating.

31. The pushwire of claim 30, wherein said wire is developable and/or said wire is a platinum-tungsten alloy wire or a platinum-iridium alloy wire.

32. The pushwire of any of claims 29-31, wherein said mandrel has at least two of said plurality of.

33. The pushwire of claim 32, wherein the distance between adjacent pairs of said entraining members is in the range of 0.5mm to 150 mm.

34. The pushwire of claim 33, wherein the distance between adjacent pairs of said entraining members is between 0.5mm and 5 mm.

35. The pushwire of any of claims 29-31, wherein said mandrel has one or more of said plurality of driver members, said driver members having an outer diameter of 0.01 inch to 0.03 inch, and each of said driver members having a length of 0.5mm to 8 mm.

36. The pushwire of claim 35, wherein each said entraining member has a length of 0.5mm to 4 mm.

37. The pushwire of any one of claims 29-31, further comprising a first visualization member disposed at a distal end of said mandrel and a second visualization member disposed on said mandrel, said entraining member being disposed between said first visualization member and said second visualization member.

38. A treatment device comprising a delivery tube, a medical implant, and a delivery guidewire according to any one of claims 1-37; the delivery pipe is provided with an inner cavity which is axially communicated and is used for accommodating the medical implant, and the wall of the inner cavity extrudes the medical implant so as to enable the medical implant to be in a compressed state; the medical implant in a compressed state is sleeved on the driving component, and at least part of the medical implant is embedded into the concave part.

39. The treatment device of claim 38, wherein the lumen has a radial dimension in a range of 0.017 inches to 0.029 inches.

40. The treatment device of claim 38, wherein the medical implant is a self-expanding stent.

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