CN217566214U

CN217566214U - Conveying structure and have its catch and tie conveyor

Info

Publication number: CN217566214U
Application number: CN202221156478.XU
Authority: CN
Inventors: 刘辰洋
Original assignee: Shanghai Li Kai Technology Co ltd
Current assignee: Shanghai Li Kai Technology Co ltd
Priority date: 2022-05-06
Filing date: 2022-05-06
Publication date: 2022-10-14
Anticipated expiration: 2032-05-06

Abstract

The application relates to a conveying structure, comprising: supporting part, pars contractilis and carry the seal wire, and the pars contractilis is the development nature material, wears to establish to fix and carries the seal wire and be close to distal end position department, and the supporting part is the development nature material, wears to establish to fix on carrying the seal wire, lies in one side setting of pars contractilis at least, and supporting part and pars contractilis paste and pay or have between supporting part and the pars contractilis and predetermine the clearance. On the premise of ensuring the stability of mechanical transmission, the supporting part further applies axial force through the telescopic part to control the limiting and positioning of the supporting part, so that the element failure in the releasing and recovering processes is avoided. Meanwhile, the telescopic part has higher compliance and is used for improving the overall compliance of the instrument, reducing the overall rigidity of the instrument, improving the passing capacity of the instrument, reducing the resistance in the pushing process, improving the operation hand feeling of an operator and reducing the clinical risk. On the other hand, the application also provides a bolt catching conveying device.

Description

Conveying structure and have its catch and tie conveyor

Technical Field

The application relates to the technical field of medical instruments, in particular to a conveying structure and a thrombus capturing conveying device with the same.

Background

Minimally invasive interventional surgery is a common treatment for internal carotid stenosis. At present, different methods such as balloon expansion, balloon-expandable stent implantation, self-expandable stent implantation and the like are used as main treatment technologies for carotid artery stenosis. Among them, the stent implantation for treating the stenosis of the internal carotid artery is a common treatment technique.

However, during treatment of stenotic lesions, the plaque manipulation by the device can cause tiny plaque to detach and be flushed by the blood flow towards the distal vessels of the brain, causing blockage of the distal vessels. Therefore, in the treatment process, an embolus capturing device is required to capture escaping emboli so as to avoid blocking the far-end blood vessel. Based on this, for the thrombus capturing device, the action parts are all positioned at the far end of the focus to play a role in blocking. Therefore, the thrombus-capturing device has higher requirements on the in-place capability and the capability of passing through the narrow focus. And on the premise that the requirement of proper conveying system cooperation and the requirement of mechanical property transmission, the flexibility is better, and the thrombus capturing device can smoothly pass through the focus and reach an ideal position.

In summary, the thrombus capture device can be advanced or withdrawn in the blood vessel through the delivery of the delivery guide wire, but when the thrombus capture device passes through the blood vessel with a serious stenotic lesion, the smoothness of the pushing and withdrawing of the thrombus capture device in the prior art needs to be improved.

SUMMERY OF THE UTILITY MODEL

In view of the above, the present application provides a delivery structure, which is suitable for intravascular delivery or retraction, and includes a support portion, an expansion portion, and a delivery guide wire; the telescopic part is made of developing materials and is fixedly arranged at the position, close to the far end, of the conveying guide wire in a penetrating way; the supporting part is made of developing materials, is fixedly arranged on the conveying guide wire in a penetrating mode and is at least arranged on one side of the telescopic part, and the supporting part is attached to the telescopic part or a preset gap is formed between the supporting part and the telescopic part.

In a possible implementation, when the support portions are provided on both sides of the telescopic portion, the support portions comprise a conveying element and a recovery element; the conveying element is arranged at the far end of the telescopic part, the recovery element is arranged at the near end of the telescopic part, and the structure of the conveying element is the same as that of the recovery element.

In a possible realization, the conveying element and the recovery element are arranged symmetrically on both sides of the telescopic part.

In a possible implementation manner, the telescopic part is of a hollow cylindrical structure, the supporting part is of a hollow cylindrical shape, and the diameters of the telescopic part and the supporting part are the same.

In a possible implementation manner, the area of the end surface of the supporting portion, which is close to one end of the telescopic portion, to the end surface of the supporting portion, which is far from one end of the telescopic portion, is gradually increased.

In one possible implementation, the support is in the form of a hypotube structure; the supporting part is provided with a plurality of hollow holes at intervals, the hollow holes are long-strip-shaped, and the hollow holes are formed along the radial direction of the supporting part or at the position with the radial direction of the supporting part and with a preset inclination angle.

In a possible implementation manner, the telescopic part is a variable pitch spring, and the pitch length of the middle section of the telescopic part is greater than the pitch lengths of the two sides of the telescopic part.

In a possible implementation manner, the telescopic part is a reducing spring, and the radius length of the middle section of the telescopic part is greater than the radius lengths of the two sides of the telescopic part.

In a possible implementation, the preset gap is less than or equal to 1mm.

In one possible implementation, the delivery guidewire is a cylindrical wire and comprises a proximal end section, a conical section and a distal end section which are connected in sequence from the proximal end direction to the distal end direction; the diameter of the proximal section is larger than that of the distal section, and the end of the distal section is provided with a flexible section; the diameter of the tapered section gradually decreases from the proximal end to the distal end; the telescopic part and the supporting part are arranged on the far end section in a penetrating mode.

In one possible implementation, the length of the support portion in the axial direction of the delivery guidewire has a predetermined ratio to the length of the telescoping portion in the axial direction of the delivery guidewire, the predetermined ratio being within [ 1: 1.5, 1: 5 ].

In one possible implementation, the preset ratio is 1: 3.

On the other hand, the application also provides a thrombus capturing and conveying device, which comprises the conveying structure, the thrombus capturing component and the sheath tube in any one of the possible implementation modes; the catching bolt component is hollow, two ends of the catching bolt component are fixed on the conveying structure through fixing points, the arrangement positions of the telescopic part and the supporting part are located between the two fixing points, and the telescopic part and the supporting part do not interfere with the catching bolt component; the sheath pipe is sleeved on the outer sides of the conveying structure and the whole catching bolt component.

In one possible implementation, the thrombus capture member, the telescoping portion, and the support portion are coaxially disposed along the delivery guidewire.

The beneficial effect of this application: through attaching mutually or having supporting part and the pars contractilis of predetermineeing the clearance and setting up on carrying the seal wire, the art person is when operating this transport structure and carry out mechanical pushing, in the mode that supporting part and pars contractilis combined, the tip that the setting of supporting part made the transport seal wire can be more smooth and easy carry out propelling movement or retrieve along its axial when mechanical pushing, the setting of pars contractilis can guarantee that this transport structure wholly has certain pliability, be convenient for remove in narrow blood vessel, thereby reach distal end focus position. Moreover, the supporting part further exerts axial force through the pars contractilis and is used for controlling the spacing location of supporting part under the prerequisite of guaranteeing mechanics transmission stability, avoids producing the component inefficacy in release, recovery process. Meanwhile, the telescopic part has higher compliance and is used for improving the overall compliance of the instrument, reducing the overall rigidity of the instrument, improving the passing capacity of the instrument, reducing the resistance in the pushing process, improving the operation hand feeling of an operator and reducing the clinical risk.

Other features and aspects of the present application will become apparent from the following detailed description of exemplary embodiments, which proceeds with reference to the accompanying drawings.

Drawings

The accompanying drawings, which are incorporated in and constitute a part of the specification, illustrate exemplary embodiments, features, and aspects of the application and, together with the description, serve to explain the principles of the application.

FIG. 1 shows a side view of a conveying structure according to an embodiment of the present application;

FIG. 2 shows a cross-sectional view of a thrombus-capturing delivery device according to an embodiment of the present application;

FIG. 3 is a partial enlarged view of a support portion of a cylindrical structure according to an embodiment of the present application;

FIG. 4 shows a partial enlarged view of a support portion of a cone-shaped structure according to an embodiment of the present application;

FIG. 5 shows an enlarged partial view of a support portion of a hypotube structure according to an embodiment of the present application;

FIG. 6 shows an enlarged partial view of a support portion of another embodiment of the hypotube structure of the present application;

FIG. 7 shows a close-up view of a larger pitch telescoping section of an embodiment of the present application;

FIG. 8 shows a partial enlarged view of a variable pitch telescoping section of an embodiment of the present application;

fig. 9 is a partially enlarged view of the variable diameter telescopic part according to the embodiment of the present application.

Detailed Description

Various exemplary embodiments, features and aspects of the present application will be described in detail below with reference to the accompanying drawings. In the drawings, like reference numbers indicate functionally identical or similar elements. While the various aspects of the embodiments are presented in drawings, the drawings are not necessarily drawn to scale unless specifically indicated.

It will be understood, however, that the terms "central," "longitudinal," "lateral," "length," "width," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," "outer," "clockwise," "counterclockwise," "axial," "radial," "circumferential," and the like are used in an orientation or positional relationship indicated in the drawings for convenience in describing the present application or for simplicity of description, and do not indicate or imply that the device or element so referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore should not be considered limiting of the present application.

Furthermore, the terms "first", "second" and "first" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly indicating the number of technical features indicated. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of the present application, "a plurality" means two or more unless specifically limited otherwise.

The word "exemplary" is used exclusively herein to mean "serving as an example, embodiment, or illustration. Any embodiment described herein as "exemplary" is not necessarily to be construed as preferred or advantageous over other embodiments.

Furthermore, in the following detailed description, numerous specific details are set forth in order to provide a better understanding of the present application. It will be understood by those skilled in the art that the present application may be practiced without some of these specific details. In some instances, methods, means, elements and circuits that are well known to those skilled in the art have not been described in detail so as not to obscure the present application.

FIG. 1 shows a side view of a conveying structure according to an embodiment of the present application; FIG. 2 shows a cross-sectional view of a thrombus delivery device according to an embodiment of the present application; FIG. 3 is a partially enlarged view of the support portion of the cylindrical structure according to the embodiment of the present application;

FIG. 4 shows a partial enlarged view of a support portion of a cone-shaped structure according to an embodiment of the present application; FIG. 5 illustrates an enlarged partial view of a support portion of a hypotube structure according to an embodiment of the present application; FIG. 6 shows an enlarged partial view of a support portion of another embodiment of the hypotube structure of the present application; FIG. 7 shows a close-up view of a larger pitch telescoping section of an embodiment of the present application; FIG. 8 shows a partial enlarged view of a variable pitch telescoping section of an embodiment of the present application; fig. 9 is a partially enlarged view of the variable diameter telescopic part according to the embodiment of the present application.

As shown in fig. 1 to 9, the conveying structure includes: the supporting portion 100, the expansion portion 102 and the conveying guide wire 420, the expansion portion 102 is made of developing material and is fixed at the position, close to the far end, of the conveying guide wire 420 in a penetrating mode, the supporting portion 100 is made of developing material and is fixed on the conveying guide wire 420 in a penetrating mode, the supporting portion 100 is at least located on one side of the expansion portion 102, and the supporting portion 100 is attached to the expansion portion 102 or a preset gap is formed between the supporting portion 100 and the expansion portion 102.

In this embodiment, the supporting portion 100 and the telescopic portion 102 are attached to each other or have a predetermined gap, so that when an operator operates the conveying structure to perform mechanical pushing, in a manner that the supporting portion 100 is combined with the telescopic portion 102, the end of the conveying guide wire 420 can be pushed or recovered along the axial direction thereof more smoothly during the mechanical pushing due to the arrangement of the supporting portion 100, and the telescopic portion 102 can ensure that the whole conveying structure has certain flexibility, so that the conveying structure can move in a narrow blood vessel conveniently, thereby reaching a far-end focus position. Moreover, on the premise of ensuring the mechanical transmission stability, the supporting portion 100 further applies an axial force through the telescopic portion 102 to control the limiting and positioning of the supporting portion 100, thereby avoiding the element failure in the releasing and recovering processes. Meanwhile, the telescopic part 102 has high compliance, so that the overall compliance of the instrument is improved, the overall stiffness of the instrument is reduced, the passing capacity of the instrument is improved, the resistance in the pushing process is reduced, the operation hand feeling of an operator is improved, and the clinical risk is reduced.

More specifically, the predetermined gap between the support portion 100 and the telescoping portion 102 is less than 1mm, and the axial length of the support portion 100 and the telescoping portion 102 having the predetermined gap is longer on the delivery guidewire to facilitate the fitting of the longer tether capturing member 202, and the distance between the support portion 100 and the telescoping portion 102 is longer to fit and act on the longer tether capturing member 202 while ensuring sufficient stability of the axial mechanical transmission of the delivery guidewire 420.

In one embodiment, the length of the strut 100 in the axial direction of the delivery guidewire 420 is within a predetermined ratio of [ 1: 1.5, 1: 5] to the length of the telescoping portion 102 in the axial direction of the delivery guidewire 420.

In this embodiment, it should be noted that the supporting portion 100 may serve as two ends of the telescopic portion 102 in this embodiment, and the too short telescopic portion 102 cannot provide better flexibility for the whole delivery structure of the present application, so that the preset ratio is limited to [ 1: 1.5, 1: 5], and the telescopic portion 102 has higher flexibility to improve the flexibility of the whole delivery structure of the present application on the premise of ensuring the reasonable design of the delivery structure of the present application, and the transcranial blood vessel has better trafficability, and the un-captured member 202 can provide enough supporting strength during pushing or withdrawing.

In one embodiment, the ratio of the length of the support portion 100 to the telescoping portion 102 in the axial direction of the delivery guidewire 420 is preferably 1: 3.

The delivery structure with the ratio of the axial length of the supporting part 100 to the axial length of the telescopic part 102 in the axial direction of the delivery guide wire 420 being 1: 3 can meet most of use scenes of delivering or withdrawing the catching bolt part 202, the delivery structure in the ratio can be used as a conventional device, and the ratio can better take part batch production and most of non-extreme use scenes or examples into consideration.

In one embodiment, when the supporting portion 100 is disposed on both sides of the telescopic portion 102, the supporting portion 100 comprises a delivery element 101 and a recovery element 103, the delivery element 101 is disposed on the distal end of the telescopic portion 102, the recovery element 103 is disposed on the proximal end of the telescopic portion 102, and the structure of the delivery element 101 is the same as that of the recovery element 103.

In this embodiment, preferably, the supporting portion 100 is disposed on two sides of the telescopic portion 102 and attached to each other, the supporting portion 100 includes a conveying element 101 located at a distal end of the telescopic portion 102 and a recovery element 103 located at a proximal end, the conveying element 101 located at the distal end provides a better propelling force for the capture element 202 during pushing, the recovery element 103 located at the proximal end provides a better withdrawing force for the capture element 202 during withdrawing the whole body, the telescopic portion 102 attached between the two is generally a spring, and the spring disposed between the conveying element 101 and the recovery element 103 is convenient for fixing the conveying element 101 and the recovery element 103 relatively on the premise of ensuring stability of axial mechanical transmission, so as to avoid slippage and failure of the elements during clinical use.

More specifically, compared with the supporting portion 100 having a predetermined gap with the telescopic portion 102, the two portions are attached to each other to ensure that the pushing force or the retracting force transmitted along the delivery guide wire 420 during pushing or retracting can be transmitted more effectively, so as to reduce the loss of the distal end force during the operation, thereby saving the physical strength of the operator and reducing the error rate during the operation.

In one embodiment, the conveying element 101 and the recovery element 103 are symmetrically arranged on both sides of the telescopic part 102.

In this embodiment, the delivery member 101, optionally made of a developable material such as platinum, platinum iridium, platinum tungsten, tantalum, etc., may be bonded or welded to the delivery wire 420;

the recovery element 103, which is made of platinum, platinum-iridium, platinum-tungsten, tantalum, or other developable materials, is bonded or welded to the delivery guidewire 420.

Preferably, the conveying element 101 and the recovery element 103 are identical in structure and symmetrically arranged with respect to the telescopic portion 102, and the conveying element 101 and the recovery element 103 with the same structure are beneficial to production and preparation on the premise of ensuring better stability. The conveying element 101, the telescopic part 102 and the recovery element 103 made of developing materials are helpful for operators to know the in-place condition of the components at the far-end lesion site from the external environment, are beneficial to detailed operation during surgery and improve the surgery efficiency.

In one embodiment, the extension portion 102 has a hollow cylindrical structure, the support portion 100 has a hollow cylindrical structure, and the extension portion 102 and the support portion 100 have the same diameter.

In this embodiment, the expansion part 102 of the hollow cylindrical structure is mechanically stable.

In one embodiment, the area of the end surface of the support portion 100 near the end of the expansion portion 102 increases gradually to the end surface far from the end of the expansion portion 102.

In this embodiment, the tapered direction is the direction from the proximal telescopic portion 102 to the distal telescopic portion 102, the end surface of the support portion 100 is gradually enlarged, and the tapered design of the support portion 100 can reasonably and effectively improve the engagement capability of the end surface, thereby preventing the force-bearing portion of the instrument from being unloaded during the pushing process to the distal end and the withdrawing process of the captive bolt.

The catch member 202 is provided coaxially with the extendable portion 102 and the support portion 100 in the circumferential direction, and outside thereof, the catch member 202 is independent from the extendable portion 102 and the support portion 100. The hollow trap member 202 can ensure that the trap member 202 does not interfere with each other, and only the end surface of the support portion 100 far away from one end of the telescopic portion 102 can contact the trap member 202 when being pushed or retracted, so that the pushing force or the retracting force can be transmitted to the trap member 202.

In one embodiment, the supporting portion 100 is a hypotube structure, wherein the supporting portion 100 is formed with a plurality of spaced hollow holes, the hollow holes are long, and the hollow holes are formed along the radial direction of the supporting portion 100 or at a predetermined inclined angle with respect to the radial direction of the supporting portion 100.

In this embodiment, the conveying element 101 and the recovering element 103 may be of a hypotube structure, and the cross-sectional shape thereof includes a rectangle, a trapezoid, or a rectangle with a thread cutting pattern. The flexibility of the supporting parts 100 at the two ends in the tortuous blood vessels is improved, the pushing resistance is reduced, and the supporting parts have certain rigidity and are not easy to deform.

It should also be noted that the telescoping feature of the telescoping section 102 does not play a role in the delivery or retraction process, and the main role of the telescoping section 102 in this application is to provide better compliance, which is used to facilitate delivery or retraction of the delivery structure. Therefore, the flexible portion 102 is fixed on the delivering guide wire 420 by single-point fixing, multi-point fixing and filling fixing, which will not affect the flexible characteristic.

More specifically, when the expansion portion 102 is bonded or welded, two ends of the expansion portion may be fixed on the delivery guide wire 420 for fixing, or the inner cavity may be completely filled, for example, by filling glue or solder balls, so the fixing manner of the expansion portion 102 is not limited in this document.

In one embodiment, the telescoping portion 102 is a variable pitch spring, with the pitch length in the midsection of the telescoping portion 102 being greater than the pitch length on either side of the telescoping portion 102.

In this embodiment, the expansion part 102 is a variable pitch spring with a pitch length in the middle section greater than the pitch lengths on both sides of the expansion part 102, i.e. the expansion part 102 has both ends loosely wound and the middle tightly wound, and forms a transition from large stiffness to small stiffness and then large stiffness with the two-end elements. The overall flexibility of the parts is improved on the premise of ensuring the fixing effect of the telescopic part 102.

In one embodiment, the expansion portion 102 is a reducing spring, and the radius length of the middle section of the expansion portion 102 is greater than the radius lengths of the two sides of the expansion portion 102.

In this embodiment, the telescoping portion 102 is designed to have a variable outer diameter, and the outer diameter of the middle portion of the telescoping portion 102 is increased to ensure a larger inner cavity for enhancing the connection between the telescoping portion 102 and the delivery guide wire 420, thereby avoiding the failure of the device due to the unloading of the telescoping portion 102, and the outer diameters of both ends are consistent with the outer diameter of the delivery and recovery element 103 for protecting the end of the telescoping portion 102 from being damaged. Compared with the overall increase of the outer diameter of the telescopic part 102, the telescopic part 102 with the variable-diameter design can avoid the influence on the progress of the operation caused by too much resistance when pushing or retracting due to too much rigidity.

In the above embodiment, the telescopic portion 102 may be made of developing wire materials such as platinum, platinum-iridium, platinum-tungsten, tantalum, etc., or common metal wire materials such as stainless steel, nickel titanium, cobalt-chromium, etc., or polymer wire materials such as silica gel, polyurethane, etc., and the transportation guide wire 420 are connected together by bonding, welding, etc.

In one embodiment, the delivery guidewire 420 is a cylindrical wire, and comprises a proximal section, a tapered section and a distal section which are connected in sequence from the proximal direction to the distal direction, wherein the diameter of the proximal section is larger than that of the distal section, the distal section is provided with a flexible section 305 at the end, the diameter of the tapered section is gradually reduced from the proximal end to the distal end, and the telescopic portion 102 and the supporting portion 100 are all arranged on the distal section in a penetrating manner.

Further, the end of the distal segment of the delivery guide wire 420 is provided with the flexible segment 305, and the flexible segment 305 can effectively prevent the delivery structure from harming the human body, thereby playing a role in buffering.

In this embodiment, the delivery guidewire 420 may be made of stainless steel or nickel titanium, and the soft segment at the distal end may be made of platinum, platinum iridium, platinum tungsten, tantalum, or other developable materials, and is bonded to the delivery guidewire 420 by bonding, welding, or the like.

On the other hand, the application also provides a thrombus-capturing conveying device, which comprises the conveying structure, the thrombus-capturing component 202 and the sheath 270 described in any one of the above embodiments, wherein the inside of the thrombus-capturing component 202 is hollow, two ends of the thrombus-capturing component 202 are fixed on the conveying structure through fixing points, the arrangement positions of the expansion part 102 and the supporting part 100 are located between the two fixing points, the expansion part 102 and the supporting part 100 do not interfere with the thrombus-capturing component 202, the sheath 270 is sleeved on the outer side of the conveying structure and the whole thrombus-capturing component 202, and the thrombus-capturing component 202 and the expansion part 102 are coaxially arranged along the conveying guide wire 420.

Based on the conveying structure of any one of the preceding, this application still provides a catch bolt conveyor. The thrombus-capturing delivery device of the embodiment of the application comprises the delivery structure. By penetrating the conveying structure into the sleeve and installing the trapping component 202 outside the supporting part 100 and the telescopic part 102, when the operator carries out mechanical pushing or mechanical withdrawing through the conveying guide wire 420, the stability of axial mechanical transmission of the conveying guide wire 420 and relative fixation to the supporting part 100 can be effectively ensured, so that the trapping and conveying device is easier for the operator to operate, the operation at the near end is smoother, and the operation efficiency is further improved.

In this embodiment, the center points of the fixed points at both ends of the trap member 202 coincide with the center points of the conveying member 101, the recovery member 102, and the recovery member 103, that is, the conveying member 101, the recovery member 102, and the recovery member 103 are disposed at the right middle position of the trap member 202.

It should be noted that the specific structure of the catch member 202 is not modified in the present application, and the catch delivery device of the present application can be adapted to the catch member 202 only by ensuring that the end surface of the support portion 100 away from the telescoping portion 102 can contact the catch member 202 during pushing and transmitting the force to the catch member 202, so the structure of the catch member 202 is not limited in detail herein.

In conclusion, in carotid artery stenosis stenting, the specific working flow of the thrombus capturing and conveying device of the application is as follows:

1. the capture member 202 is compressed within the sheath 270, advanced over a 0.014 micro-wire to the vessel distal to the stenotic lesion, and the delivery wire 420 is then advanced proximally, bringing the delivery element 101 into contact with the capture device and pushing it out of the sheath 270;

2. after the embolectomy component 202 is completely released in the internal carotid blood vessel and smoothly opened, the guide wire 420 is conveyed by the embolectomy component 202 to guide and implant the carotid stent, the carotid stent is released at the narrow focus, in the releasing process of the stent, unstable plaque at the narrow focus is separated with the carotid stent, and rushes to the far end of the blood vessel along the blood flow, and at the moment, the embolectomy device which is smoothly opened at the far end of the focus can capture emboli in the blood flow, so as to avoid the encephalic blood vessel blockage caused by the embolectomy device entering the intracranial blood vessel;

3. after the capture of the embolus is completed, the delivery guide wire 420 is retracted, the recovery element 103 is contacted with the embolus capturing component 202, and is slightly retracted with force, so that the embolus capturing component 202 is smoothly recovered into the sheath 270, and the captured escape embolus and the embolus capturing component 202 are recovered into the sheath 270 together;

4. then the whole thrombus-capturing delivery device is withdrawn until the outside of the body is removed, and carotid artery stenting operation and intraoperative thrombus-capturing operation are smoothly completed.

Having described embodiments of the present application, the foregoing description is intended to be exemplary, not exhaustive, and not limited to the disclosed embodiments. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the described embodiments. The terminology used herein is chosen in order to best explain the principles of the embodiments, the practical application, or improvements made to the technology in the marketplace, or to enable others of ordinary skill in the art to understand the embodiments disclosed herein.

Claims

1. A conveying structure is suitable for conveying or withdrawing in blood vessels and is characterized by comprising a supporting part, a telescopic part and a conveying guide wire;

the telescopic part is made of developing materials and is fixedly arranged at the position, close to the far end, of the conveying guide wire in a penetrating way;

the supporting part is a developing material, is fixed on the conveying guide wire in a penetrating mode, is at least located on one side of the telescopic part, and is attached to the telescopic part or a preset gap is formed between the supporting part and the telescopic part.

2. The conveying structure according to claim 1, wherein when the supporting portion is provided on both sides of the stretching portion, the supporting portion includes a conveying member and a recovery member;

the conveying element is arranged at the far end of the telescopic part, the recovery element is arranged at the near end of the telescopic part, and the structure of the conveying element is the same as that of the recovery element.

3. The conveying structure according to claim 2, wherein the conveying element and the recovery element are symmetrically arranged on both sides of the telescopic part.

4. The conveying structure according to claim 1, wherein the telescopic part is a hollow cylindrical structure, the support part is a hollow cylindrical structure, and the telescopic part and the support part have the same diameter.

5. The conveying structure according to claim 1, wherein the area of the end surface of the support portion near the end of the telescopic portion gradually increases to the end surface far from the end of the telescopic portion.

6. The conveying structure according to claim 1, wherein the support is of a hypotube structure;

the supporting part is provided with a plurality of hollow holes at intervals, the hollow holes are long-strip-shaped, and the hollow holes are formed along the radial direction of the supporting part or at the position with the radial direction of the supporting part and with a preset inclination angle.

7. The transport structure of claim 1, wherein the telescoping section is a variable pitch spring, the pitch length of the midsection of the telescoping section being greater than the pitch length of the sides of the telescoping section.

8. The conveying structure as claimed in claim 1, wherein the expansion part is a reducing spring, and the radius length of the middle section of the expansion part is greater than the radius lengths of both sides of the expansion part.

9. The conveying structure according to claim 1, wherein the preset gap is less than or equal to 1mm.

10. The delivery structure according to claim 1, wherein said delivery guidewire is a cylindrical wire comprising a proximal section, a tapered section and a distal section connected in sequence from a proximal direction to a distal direction;

the diameter of the proximal section is larger than that of the distal section, and the end of the distal section is provided with a flexible section;

the diameter of the tapered section gradually decreases from the proximal end to the distal end;

the telescopic part and the supporting part are arranged on the far end section in a penetrating mode.

11. The delivery structure according to any one of claims 1 to 10, wherein the length of the support portion in the axial direction of the delivery guidewire has a preset ratio to the length of the telescoping portion in the axial direction of the delivery guidewire, the preset ratio being within [ 1: 1.5, 1: 5 ].

12. The conveying structure according to claim 11, wherein the preset ratio is 1: 3.

13. A thrombus-capturing delivery device comprising the delivery structure of any one of claims 1-12, a thrombus-capturing member, and a sheath;

the bolt catching component is hollow, two ends of the bolt catching component are fixed on the conveying structure through fixing points, the arrangement positions of the telescopic part and the supporting part are located between the two fixing points, and the telescopic part and the supporting part do not interfere with the bolt catching component;

the sheath pipe is sleeved on the outer sides of the conveying structure and the whole catching bolt component.

14. The embolus capturing delivery device of claim 13, wherein the embolus capturing member, the telescoping portion, and the support portion are coaxially disposed along the delivery guidewire.