CN219354296U - Close net support and conveying system - Google Patents

Abstract

The utility model relates to the technical field of medical equipment and provides a dense net support and a conveying system, wherein the dense net support comprises a tubular main body, the tubular main body is formed by interweaving two or more than two braided wires, the tubular main body comprises a proximal end and a distal end which are oppositely arranged along the axial direction of the tubular main body, and part of the braided wires are disconnected and form at least one pair of oppositely arranged free ends. According to the dense net support and the conveying system, the problem that the existing dense net support is shifted in the curved intracranial artery wall after being unfolded is well solved.

Description

Close net support and conveying system

Technical Field

The utility model relates to the technical field of medical equipment, in particular to a dense net support and a conveying system.

Background

This section provides merely background information related to the present disclosure and is not necessarily prior art.

Intracranial aneurysms are mostly abnormal bulging occurring on the wall of intracranial arteries, and are the first causative agent of subarachnoid hemorrhage. Subarachnoid hemorrhage is one of the main types of clinical hemorrhagic stroke. The method for treating the aneurysm mainly comprises two steps of surgical clamping and interventional treatment, and clinical tests show that the mortality rate of interventional treatment of patients with the aneurysm is lower than that of surgical treatment.

The dense net stent is an emerging intracranial aneurysm treatment method in recent years, and the principle of the dense net stent is that the correct path of a blood vessel at an aneurysm is rebuilt, the blood flow direction of the intracranial blood vessel is restored, the blood flow direction of the intracranial blood vessel can be remodeled, the aneurysm is gradually reduced until the aneurysm disappears, and compared with spring coil embolism treatment, the dense net stent has higher safety and better effect, and has obvious treatment advantages for the large-scale and huge type aneurysms.

After the dense net stent is released in the intracranial artery tube, the dense net stent is released and unfolded and has poor fitting property with the intracranial artery tube wall, so that the dense net stent is unfolded and then easily shifted in the bent intracranial artery tube wall.

Disclosure of Invention

The utility model aims to at least solve the problem that the existing dense net stent is shifted in the curved intracranial artery wall after being unfolded. The aim is achieved by the following technical scheme:

the first aspect of the utility model provides a dense net support, which comprises a tubular main body, wherein the tubular main body is formed by interweaving two or more than two braiding wires, the tubular main body comprises a proximal end and a distal end which are oppositely arranged along the axial direction of the tubular main body, and part of the braiding wires are disconnected and form at least one pair of oppositely arranged free ends.

According to the dense net stent provided by the utility model, as part of the braided wires are cut off, the flexibility of the tubular main body is enhanced, and for a blood vessel with a bending angle, the expanded tubular main body can be bent along with the blood vessel, and the bent section of the tubular main body can be tightly attached to the wall of the blood vessel.

In conclusion, the dense net stent provided by the utility model well solves the problem that the existing dense net stent is shifted in the curved intracranial artery wall after being unfolded.

In addition, the dense net support according to the utility model can also have the following additional technical characteristics:

in some embodiments of the utility model, an anchor is provided on the free end, and the radial dimension of the anchor is greater than or equal to the radial dimension of the braided wire.

In some embodiments of the utility model, the anchors are in a plurality of pairs, the tubular body including a plurality of pairs of the free ends, the anchors of the plurality of pairs of the free ends forming a circumferential ring structure along an axis perpendicular to the tubular body.

In some embodiments of the utility model, the number of circumferential ring structures is a plurality, and adjacent circumferential ring structures are spaced apart along the axial direction of the tubular body.

In some embodiments of the utility model, the number of the anchors on any two of the circumferential annular structures is the same, and the anchors on any two of the circumferential annular structures are arranged in a superposition manner along the axial direction of the tubular main body.

In some embodiments of the utility model, the number of anchors on any two of the circumferential ring structures is the same, and the anchors on adjacent circumferential ring structures are staggered along the axial direction of the tubular body.

In some embodiments of the utility model, the proximal and/or distal ends of the braided wires are provided with the anchors.

In some embodiments of the utility model, the anchor is formed by hot-melting the ends of the braided filaments into a ball or sphere-like structure;

alternatively, the anchoring element is formed into a sphere or sphere-like structure by wrapping the ends of the braided wires with glue.

In some embodiments of the utility model, the braided filaments include a first braided filament and a second braided filament, and the first braided filament has a diameter greater than the diameter of the second braided filament, and a portion of the second braided filament is broken and forms at least one pair of oppositely disposed free ends.

In a second aspect, the present utility model provides a delivery system, including a dense mesh stent according to any one of the preceding claims, and further including a delivery assembly, where the dense mesh stent is disposed on the delivery assembly, and the delivery assembly is configured to deliver the dense mesh stent to a lesion site.

The dense mesh stent according to the present utility model has the same advantages as the transport system according to the present utility model and will not be described in detail here.

Drawings

Various other advantages and benefits will become apparent to those of ordinary skill in the art upon reading the following detailed description of the preferred embodiments. The drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the utility model. Also, like reference numerals are used to designate like parts throughout the figures. In the drawings:

fig. 1 schematically shows a front view of a dense net support according to a first embodiment of the present utility model;

fig. 2 schematically shows a side view of a dense mesh support according to a first embodiment of the utility model;

fig. 3 schematically shows a front view of a dense net support according to a second embodiment of the present utility model;

fig. 4 schematically shows a side view of a dense mesh support according to a second embodiment of the present utility model;

fig. 5 schematically shows a front view of a dense net support according to a third embodiment of the present utility model;

fig. 6 schematically shows a front view of a dense net support according to a fourth embodiment of the present utility model;

FIG. 7 schematically illustrates a schematic structural view of an anchor according to some embodiments of the present utility model;

fig. 8 schematically shows a first structural view in a state where a dense net stand is mounted in accordance with a first embodiment of the present utility model

Fig. 9 schematically shows a second structural diagram in a state where a dense net stand is mounted in accordance with the first embodiment of the present utility model;

fig. 10 schematically illustrates a front view of a delivery system according to some embodiments of the utility model.

Reference numerals illustrate:

100 is a transport system;

10 is a tubular body, 20 is a delivery assembly, 201 is a loading catheter, 202 is a delivery guidewire, 203 is a microcatheter;

1 is a braided wire, 11 is a first braided wire, 12 is a second braided wire, and 2 is an anchor.

Detailed Description

Exemplary embodiments of the present disclosure will be described in more detail below with reference to the accompanying drawings. While exemplary embodiments of the present disclosure are shown in the drawings, it should be understood that the present disclosure may be embodied in various forms and should not be limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the disclosure to those skilled in the art.

It is to be understood that the terminology used herein is for the purpose of describing particular example embodiments only, and is not intended to be limiting. As used herein, the singular forms "a", "an" and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise. The terms "comprises," "comprising," "includes," "including," and "having" are inclusive and therefore specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. The method steps, processes, and operations described herein are not to be construed as necessarily requiring their performance in the particular order described or illustrated, unless an order of performance is explicitly stated. It should also be appreciated that additional or alternative steps may be used.

Although the terms first, second, third, etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms may be only used to distinguish one element, component, region, layer or section from another region, layer or section. Terms such as "first," "second," and other numerical terms when used herein do not imply a sequence or order unless clearly indicated by the context. Thus, a first element, component, region, layer or section discussed below could be termed a second element, component, region, layer or section without departing from the teachings of the example embodiments.

For ease of description, spatially relative terms, such as "inner," "outer," "lower," "below," "upper," "above," and the like, may be used herein to describe one element or feature's relationship to another element or feature as illustrated in the figures. Such spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over, elements described as "below" or "beneath" other elements or features would then be oriented "above" or "over" the other elements or features. Thus, the example term "below … …" may include both upper and lower orientations. The device may be otherwise oriented (rotated 90 degrees or in other directions) and the spatial relative relationship descriptors used herein interpreted accordingly.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this utility model belongs. The terminology used herein in the description of the utility model is for the purpose of describing particular embodiments only and is not intended to be limiting of the utility model. The term "and/or" as used herein includes any and all combinations of one or more of the associated listed items.

In the present application, a range expressed by "one value to another value" is a general expression which avoids the specification from listing all the values in the range. Thus, recitation of a particular numerical range includes any numerical value within that range, as well as the smaller numerical range bounded by any numerical value within that range, as if the any numerical value and the smaller numerical range were written in the specification in the clear.

In this application, the end that is closer to the operator when used is referred to as the "proximal end", the end that is farther from the operator is referred to as the "distal end", and the "proximal end" and "distal end" of any of the components of the dense mesh stent are defined according to this principle. "axial" generally refers to the length of the dense mesh stent as it is being delivered, and "radial" generally refers to the direction of the dense mesh stent perpendicular to its "axial" direction, and defines the "axial" and "radial" directions of any of the components of the dense mesh stent in accordance with this principle.

Referring to fig. 10, a delivery system 100 of the present application includes a dense stent and a delivery assembly 20, the delivery assembly 20 being configured to deliver the dense stent to a lesion (e.g., an aneurysm).

Specifically, the delivery assembly 20 includes a loading catheter 201, a delivery guidewire 202, and a microcatheter 203, and the delivery process of the delivery assembly 20 is: (1) Firstly, binding the dense net support on a conveying guide wire 202, and loading the dense net support in a loading catheter 201, wherein the dense net support is in a compressed state; (2) Delivering microcatheter 203 to the site of the lesion (e.g., at an aneurysm); (3) Connecting the loading tube 201 to the proximal end of the microcatheter 203, then distally advancing the delivery guidewire 202, pushing the dense mesh stent from the loading tube 201 into the microcatheter 203; (4) Continuing to push the conveying guide wire 202 distally, after reaching the target position, making the dense net support deviate from the micro-catheter 203, expanding and abutting against the vessel wall; (5) proximally withdrawing microcatheter 203 and delivering guidewire 202.

Specifically, the dense mesh stent comprises a tubular main body 10, wherein the tubular main body 10 is formed by interweaving two or more than two braided wires 1, the tubular main body 10 comprises a proximal end and a distal end which are oppositely arranged along the axial direction of the tubular main body, and part of the braided wires 1 are cut off and form at least one pair of oppositely arranged free ends.

Referring to fig. 9, since a portion of the braided wire 1 is cut to form a free end, flexibility of the tubular body 10 is enhanced, the deployed tubular body 10 can be bent following a blood vessel with a bending angle, a bent section of the tubular body 10 can be closely attached to the blood vessel wall, and since the bent section of the tubular body 10 is closely attached to the blood vessel wall, blood flow guidance is not affected.

Further, an anchor 2 is arranged on the free end, and the radial dimension of the anchor 2 is larger than or equal to the radial dimension of the braided wire 1. In the illustrated embodiment, an anchor 2 is provided on each free end. Of course, it is also possible to selectively provide the anchor 2 at a specific free end.

Referring to fig. 8, an anchor 2 is provided at the free end, and the radial dimension of the anchor 2 is greater than or equal to the radial dimension of the braided wire 1, so that when the dense net stent is placed in a blood vessel and expanded to be adhered to the wall of the blood vessel, the anchor 2 can be recessed in the wall of the blood vessel, thereby enhancing the adhesion of the dense net stent and further enabling the dense net stent to be tightly adhered to the wall of the blood vessel.

Specifically, the free ends are formed by cutting part of the braided wires, the number of the free ends is not limited, one braided wire 1 can be provided with a plurality of pairs of free ends, or one braided wire 1 can be provided with only one pair of free ends, the braided wire 1 is made of nickel-titanium or cobalt-chromium metal wires or developing core-spun wires, and thus the tubular body 10 formed by braiding the braided wires 1 has shape memory, and the dense net stent is expanded and unfolded by itself after being separated from the microcatheter 203. In the illustrated embodiment, the braided filaments are broken along their direction of extension without purposely altering their own direction of extension after the break.

The tubular main body 10 is woven by a weaving wire 1 on a weaving core rod, the appearance and the size of the weaving core rod are determined according to the shape of the specific tubular main body 10, the tubular main body is placed into a heating furnace for heat setting after the weaving is completed, a section of tubular main body is cut after the setting is completed, the cutting length can be determined according to the actual operation condition, the cutting length is not limited, and finally, the anchor 2 is completed by a laser spot welder, or the end part of the weaving wire is wrapped by glue to form the anchor 2.

The diameter range of the tubular main body 10 after knitting and forming is 2-7mm, the number of the knitting wires 1 for knitting the tubular main body 10 is 32-72, the diameter of the knitting wires 1 is selected to be 0.01-0.05mm, and the PPI (PPI is knitting weft density, i.e. mesh number in the axial length of the 1-inch tubular main body 10) of the tubular main body 10 is 230-300. Preferably, the number of the braided filaments 1 of the braided tubular body 10 is 36, 48 or 64, the diameter of the braided filaments 1 is selected in the range of 0.02-0.03mm, and the PPI of the tubular body 10 is in the range of 250-280.

Referring to fig. 7, the anchor 2 is preferably formed into a ball or ball-like structure by hot-melting the ends of the braided wire 1; alternatively, the anchoring piece 2 is formed into a sphere or sphere-like structure by wrapping the end of the braided wire 1 with glue; the surface of the ball or the ball-like structure is smooth, when the dense net support is unfolded and is clung to the vessel wall, the ball or the ball-like structure can be sunken in the vessel wall after contacting the vessel wall, so that the adhesion of the dense net support is improved, the dense net support is clung to the vessel wall tightly, and the problem of displacement in the intracranial artery wall after the existing dense net support is unfolded is solved; in addition, because the surface of the sphere or sphere-like structure is smooth, no sharp section exists, the sharp section cannot penetrate into the vessel wall, the vascular structure cannot be damaged, the use safety of the stent is improved, and secondary injury after operation cannot be caused. However, the structure and shape of the anchor are not limited thereto, and may be cylindrical or the like.

Further, referring to fig. 1, 3 and 6, the proximal distance between the anchor 2 and the proximal end of the braided wire 1 is greater than 1mm; and/or the distance of the anchor 2 near the distal end from the distal end of the braided wire 1 is greater than 1mm; the distance should be kept not too close to avoid that the anchor 2 is too close to the proximal or distal end, resulting in the braid wires 1 coming out of the tubular body 10; with continued reference to fig. 1, 3 and 6, the distance between adjacent anchors 2 should not be too short or too long along the axial direction of the tubular body 10, when the distance between adjacent anchors 2 is too short, the braided wire 1 is easily separated from the tubular body 10, and when the distance between adjacent anchors 2 is too long, the anchoring performance of the anchors 2 and the flexibility of the tubular body 10 are affected, so that the fitting tightness of the tubular body 10 and the vessel wall is affected; the spacing between adjacent anchors 2 is preferably 2mm-5mm. In this application, the spacing of adjacent anchors refers to the axial distance between adjacent pairs of free ends of the same braided wire.

The free ends are preferably provided in a plurality of pairs, and at least one pair of free ends may be provided on each of the braided wires 1, or only a part of the braided wires 1 may be provided with the free ends, and the plurality of pairs of free ends may be uniformly provided or unevenly provided on the braided wires 1, so long as the anchoring performance and the flexibility of the tubular body 10 can be ensured. The following embodiments are preferably a plurality of embodiments formed by the arrangement between the plurality of anchors 2.

Example 1

Referring to fig. 1, the tubular body 10 includes a plurality of pairs of free ends, the anchors 2 of the plurality of pairs of free ends form a circumferential ring structure along an axial direction perpendicular to the tubular body 10, the number of the circumferential ring structures may be 1, 2 or 3 or more, and when the number of the circumferential ring structures is 1, the plurality of pairs of anchors 2 form 1 circumferential ring structure, and the tubular body 10 including 1 circumferential ring structure has inferior anchoring performance and compliance performance compared to the plurality of circumferential ring structures.

With continued reference to fig. 1, preferably, the number of circumferential annular structures is plural, and adjacent circumferential annular structures are disposed at intervals along the axial direction of the tubular body 10, and the number of support points between the tubular body 10 and the vessel wall is increased by the plural circumferential annular structures constituted by the plural pairs of anchors 2, further increasing the anchoring performance of the tubular body 10 and further increasing the compliance performance of the tubular body 10.

With continued reference to fig. 1 and 2, when the number of the circumferential annular structures is plural, the number of the anchors 2 on any two circumferential annular structures is the same, and the anchors 2 on any two circumferential annular structures are arranged in a superposed manner along the axial direction of the tubular main body 10; also, the number of support points between the tubular body 10 and the vessel wall of this arrangement increases, further increasing the anchoring properties of the tubular body 10, and further increasing the compliance properties of the tubular body 10.

Example 2

In embodiment 2, the same reference numerals are given to the same structures as those in embodiment 1, and the same description is omitted, and embodiment 2 is modified on the basis of embodiment 1:

referring to fig. 3, the plurality of pairs of anchors 2 form a circumferential ring structure perpendicular to the axial direction of the tubular body 10, and the number of the circumferential ring structures may be 1, 2, or 3 or more, and when the number of the circumferential ring structures is 1, the tubular body 10 including 1 circumferential ring structure is inferior in anchoring performance and compliance performance as compared to the plurality of circumferential ring structures constituted by the plurality of pairs of anchors 2.

With continued reference to fig. 3, preferably, the number of circumferential annular structures is plural, and adjacent circumferential annular structures are disposed at intervals along the axial direction of the tubular body 10, so that the plural pairs of anchors 2 form plural circumferential annular structures, the number of support points between the tubular body 10 and the vessel wall increases, the anchoring performance of the tubular body 10 is further increased, and the compliance performance of the tubular body 10 is further increased.

With continued reference to fig. 3 and 4, when the number of circumferential annular structures is plural, the number of anchors 2 on any two circumferential annular structures is the same, and the anchors 2 on adjacent circumferential annular structures are staggered along the axial direction of the tubular body 10; the tubular body 10 of example 2 is more densely circumferentially distributed with anchors 2 at different angles, and the tubular body 10 is wider circumferentially anchored in the vessel, increasing the anchoring force and thus reducing the risk of stent displacement, although the number of anchors 2 is not increased, compared to the tubular body 10 of example 1.

Example 3

In embodiment 3, the same reference numerals are given to the same structures as those in embodiment 1, and the same description is omitted, and embodiment 3 is modified on the basis of embodiment 1:

the existing tubular main body 10 is cut off in a cutting mode, so that the braided wires 1 at two ends of the tubular main body 10 form a section, the two ends of the braided wires 1 are sharp, when the tubular main body 10 is implanted into a blood vessel, the tubular main body 10 is clung to the wall of the blood vessel after being released, and when the two sharp ends contact the wall of the blood vessel, the sharp section part is led to penetrate the wall of the blood vessel, the vascular structure is damaged, and the risk of damage to the inner layer of the blood vessel is caused.

Therefore, referring to fig. 5, the tubular main body 10 of the present embodiment is also provided with the anchor 2 at the proximal end and/or the distal end of the braided wire 1, the surface of the anchor 2 is smoother, has no sharp cross section, and does not cause the sharp cross section to penetrate into the vessel wall, thereby not causing damage to the vessel structure, increasing the use safety of the stent, and not causing post-operation secondary injury.

Example 4

In embodiment 4, the same reference numerals are given to the same structures as those in embodiment 1, and the same description is omitted, and embodiment 4 is modified on the basis of embodiment 1:

since the cutting of a portion of the braided wire 1 affects the radial supporting force of the tubular body 10, when the tubular body 10 is released in the blood vessel, the expansion ability of the tubular body 10 itself in the radial direction thereof is affected, thereby causing the deployment of the tubular body 10 in the blood vessel.

Referring to fig. 6, the braided wire 1 is configured as a first braided wire 11 and a second braided wire 12, and the diameter of the first braided wire 11 is larger than that of the second braided wire 12, and a part of the second braided wire 12 is broken and constitutes at least one pair of oppositely disposed free ends, and it is particularly noted that the free ends are not cut off on the first braided wire 11, in other words, no break point is provided on the first braided wire 11; therefore, since the diameter of the first braided wire 11 is large and no break point is provided, the radial supporting force of the tubular body 10 is enhanced, and when the tubular body 10 is released in the blood vessel, the tubular body 10 can be smoothly deployed in the blood vessel.

Preferably, the diameter of the first braided wire 11 is twice that of the second braided wire 12, and the first braided wires 11 are uniformly distributed so as to ensure that the tubular main body 10 is unfolded simultaneously, thereby avoiding the problem that one side of the tubular main body 10 cannot be unfolded or is unfolded slowly, and further influencing the fitting degree of the tubular main body 10 and the vascular wall; the number of first filaments 11 is preferably 4 to 8.

In a second aspect, the present utility model proposes a delivery system 100, including a dense mesh stent according to any one of the preceding claims, and further including a delivery assembly 20, where the dense mesh stent is disposed on the delivery assembly 20, and the delivery assembly 20 is configured to deliver the dense mesh stent to a lesion site.

The dense mesh stent according to the present utility model has the same advantages as the delivery system 100 according to the present utility model and will not be described in detail herein.

The present utility model is not limited to the above-mentioned embodiments, and any changes or substitutions that can be easily understood by those skilled in the art within the technical scope of the present utility model are intended to be included in the scope of the present utility model. Therefore, the protection scope of the utility model is subject to the protection scope of the claims.

Claims (10)

1. The utility model provides a close net support which characterized in that includes tubular main part, tubular main part is woven by two or more than two braided wire crisscross, tubular main part includes the proximal end and the distal end of setting relatively along its axial, and part braided wire breaks off and constitutes at least a pair of free end that sets up relatively.

2. The dense mesh stent of claim 1 wherein the free end is provided with an anchor and the radial dimension of the anchor is equal to or greater than the radial dimension of the braided wires.

3. The dense mesh stent of claim 2 wherein the tubular body includes a plurality of pairs of the free ends, the anchors of the plurality of pairs of free ends forming a circumferential ring structure in a direction perpendicular to an axial direction of the tubular body.

4. A dense mesh stent according to claim 3 wherein the number of circumferential ring structures is a plurality and adjacent circumferential ring structures are spaced apart along the axial direction of the tubular body.

5. The dense mesh stent of claim 4 wherein the number of anchors on any two of the circumferential annular structures is the same, and the anchors on any two of the circumferential annular structures are disposed in registry along the axial direction of the tubular body.

6. The dense mesh stent of claim 4 wherein the number of anchors on any two of the circumferential rings is the same, and wherein the anchors on adjacent circumferential rings are offset along the axial direction of the tubular body.

7. The dense mesh stent of claim 2 wherein the proximal and/or distal ends of the braided wires are provided with the anchor.

8. The dense mesh stent of claim 7 wherein the anchor is formed by hot-melting the ends of the braided filaments into a sphere or sphere-like structure;

alternatively, the anchoring element is formed into a sphere or sphere-like structure by wrapping the ends of the braided wires with glue.

9. The dense mesh stent of claim 1 wherein the braided wires comprise a first braided wire and a second braided wire, and wherein the first braided wire has a diameter greater than the diameter of the second braided wire, and wherein a portion of the second braided wire is broken and forms at least one pair of oppositely disposed free ends.

10. A delivery system comprising a dense mesh stent according to any one of claims 1 to 9, and a delivery assembly disposed in the delivery assembly for delivering the dense mesh stent to a lesion site.