CN218685681U - Dilation device and guidance system - Google Patents

Abstract

The utility model relates to an expansion device and guide system. The expansion device comprises an expansion pipe, a connecting pipe and a switching piece, wherein the expansion pipe comprises a supporting pipe and an expansion pipe arranged outside the supporting pipe in a sleeved mode, a filling cavity is formed in the expansion pipe, the expansion pipe has a contraction state and an expansion state which is expanded along the radial direction after the filling cavity is filled with a medium, the connecting pipe is connected with the expansion pipe, the connecting pipe is provided with a filling channel, the filling channel is communicated with the filling cavity, and the switching piece is provided with a filling opening communicated with the filling channel. The expansion device can expand the tortuous vessels with plaques and ulcers or the cramped spastic vessels, reduce the resistance of the vessel wall and ensure that surgical instruments such as a guide catheter or an angiography catheter and the like smoothly pass through the tortuous or spastic positions of the vessels.

Description

Dilation device and guidance system

Technical Field

The utility model relates to the technical field of medical equipment, especially, relate to an expansion device and guide system.

Background

Percutaneous Coronary Intervention (PCI) is mainly used for the treatment of obstructive coronary artery disease, which is rapidly developing due to the advantages of being minimally invasive, time-saving, safe and efficient. In addition, PCI has high operation success rate and good curative effect on diseases such as left trunk lesion, chronic Total Occlusion (CTO) lesion, severe calcification lesion and the like. Currently, the radial approach to PCI has become the preferred approach. In the operation, an interventional device such as a guide wire, a balloon, or a stent needs to be delivered to a lesion site, but due to the tortuous path of a blood vessel and the action of a blood flow force, it is difficult for the interventional device such as a flexible guide wire, a balloon, or a stent to reach the lesion site through the blood vessel. It is therefore necessary to now pass a guiding catheter through the blood vessel, through which the interventional instrument is guided to the lesion.

However, when the radial artery is in tortuosity or spasm, the guide catheter cannot smoothly pass through the artery, and if violent operation is performed, vascular injury, local pain or local hematoma are easily caused, and even serious complications such as periosteum syndrome and the like are caused. However, if the contralateral radial or femoral access is changed, the pain, the probability of serious complications and the high operation cost of the patient are increased, and the operation time and the exposure time of the patient and the operator to the radiation are increased.

SUMMERY OF THE UTILITY MODEL

In view of this, it is necessary to provide an expansion device and a guidance system for solving the problem of how to make it difficult to guide a catheter through a blood vessel due to the occurrence of blood vessel tortuosity or spasm in an artery.

In one aspect, the present application provides a stent comprising:

the expansion pipe comprises a supporting pipe and an expansion pipe sleeved outside the supporting pipe, an inflation cavity is formed in the expansion pipe, and the expansion pipe has a contraction state and an expansion state of expanding along the radial direction after the inflation cavity is filled with a medium;

the connecting pipe is connected with the expansion pipe and provided with an filling channel which is communicated with the filling cavity;

the adaptor, the adaptor be equipped with fill sufficient mouth that the passageway is linked together.

The technical solution of the present application is further described below:

in one embodiment, the outer diameter of the expansion tube decreases in a direction away from the connection tube.

In one embodiment, the expansion device is provided with a guide wire channel, which extends through the expansion tube, the connection tube and the adapter.

In one embodiment, the peripheral side of the expansion tube is provided with a drainage hole which is communicated with the guide wire channel.

In one embodiment, the outer peripheral side of the dilating tube, the outer peripheral side of the connecting tube and the inner wall of the guide wire channel are provided with a lubricating coating.

In one embodiment, the outer periphery of the connecting pipe is provided with threads; and/or the presence of a gas in the gas,

an annular bulge is arranged on the outer peripheral side of the connecting pipe, and the outer diameter of the annular bulge is gradually increased along the direction from the expansion pipe to the adaptor; and/or the presence of a gas in the gas,

a reticulate pattern structure is arranged on the outer peripheral side of the connecting pipe; and/or the presence of a gas in the gas,

the periphery side of the connecting pipe is provided with a medicine hole, and the medicine hole is used for bearing medicines.

In one embodiment, the connecting pipe comprises an inner pipe and an outer pipe sleeved outside the inner pipe, the filling channel is formed between the inner pipe and the outer pipe, one end of the inner pipe is connected with the supporting pipe, the other end of the inner pipe is connected with the adapter, one end of the outer pipe is connected with the expansion pipe, and the other end of the outer pipe is connected with the adapter.

In one embodiment, the connecting pipe comprises an inner pipe and an outer pipe sleeved outside the inner pipe, the filling passage is formed between the inner pipe and the outer pipe, the inner pipe is connected with the supporting pipe, the outer pipe is connected with the expansion pipe, a connecting hole is formed in one end, away from the expansion pipe, of the filling passage, the expansion device further comprises a pushing pipe, one end of the pushing pipe penetrates through the connecting hole and penetrates into the filling passage, and the other end of the pushing pipe is communicated to the filling port.

In one embodiment, the material of the expansion pipe is a biocompatible polymer material; the support tube is made of biocompatible metal material.

In another aspect, the present application further provides a guiding system, which includes a guiding catheter and the above-mentioned expansion device, the expansion device is disposed through the guiding catheter, the expansion tube is disposed through one end of the guiding catheter, and the adaptor is disposed through the other end of the guiding catheter.

In another aspect, the present application further provides a guidance system, including:

the expansion pipe comprises a supporting pipe and an expansion pipe sleeved outside the supporting pipe, an inflation cavity is formed in the expansion pipe, and the expansion pipe has a contraction state and an expansion state of expanding along the radial direction after the inflation cavity is filled with a medium;

the connecting pipe is connected with the expansion pipe and provided with an filling channel, the filling channel is communicated with the filling cavity, the connecting pipe comprises a soft section, a bending section and a supporting section which are sequentially connected, the soft section is connected with the expansion pipe, and at least one bending structure which is bent relative to the supporting section or the soft section is formed in the bending section; and (c) a second step of,

the adapter is connected with the support section and provided with a filling opening communicated with the filling channel;

wherein, instrument channels for surgical instruments to pass through are formed in the expansion tube, the connecting tube and the adaptor.

The expansion device and the guiding system are characterized in that the expansion pipe is configured to comprise a supporting pipe and an expansion pipe sleeved outside the supporting pipe, the supporting pipe can effectively increase the supporting strength of the expansion pipe, so that the expansion pipe can smoothly penetrate into the tortuous or spasm position of the blood vessel, and the expansion pipe is configured to have a contraction state and an expansion state, so that after the expansion pipe penetrates into the tortuous or spasm position of the blood vessel, a medium such as liquid or gas is injected into a filling cavity of the expansion pipe through a filling channel of the connecting pipe through a filling opening of the adapter, the expansion pipe is radially expanded, a tortuous blood vessel with plaques and ulcers or a tight spasm blood vessel is expanded, the resistance of the blood vessel wall is reduced, and the guiding pipe or a contrast catheter and other surgical instruments can smoothly penetrate through the tortuous or spasm position of the blood vessel. When encountering the problem of blood vessel tortuosity or spasm in the interventional operation, the guiding catheter and other surgical instruments can be ensured to smoothly penetrate to the pathological change position without changing the access path, the operation is simple, the operation time is saved, and the time of exposing the patient and the operator to rays is reduced.

Drawings

The accompanying drawings, which are incorporated in and constitute a part of this application, are included to provide a further understanding of the invention, and are incorporated in and constitute a part of this specification.

In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings used in the description of the embodiments will be briefly described below, and it is obvious that the drawings in the description are only some embodiments of the present invention, and it is obvious for those skilled in the art that other drawings can be obtained without creative efforts.

FIG. 1 is a schematic view showing the construction of the stent of the first embodiment;

FIG. 2 is a sectional view showing the construction of an expansion tube and a connection tube of the expansion means shown in FIG. 1;

FIG. 3 is a schematic structural view of the dilation tube of the dilation device shown in FIG. 1;

FIG. 4 is a schematic view of a thread of a connecting pipe according to an embodiment;

FIG. 5 is a schematic structural diagram of an annular protrusion of a connecting tube according to an embodiment;

FIG. 6 is a schematic diagram of a cross-hatched structure of a connecting tube according to an embodiment;

FIG. 7 is a schematic diagram of the structure of the drug hole of the connecting tube according to one embodiment;

FIG. 8 is a schematic structural view of the stent of the second embodiment;

FIG. 9 is a sectional view showing the structure of an expansion tube, a connection tube and a push tube of the expansion device shown in FIG. 8;

FIG. 10 is a side view of a connection tube of the stent shown in FIG. 8;

FIG. 11 is a schematic view of an embodiment of a guiding catheter.

Description of reference numerals:

10. an expansion device; 11. an expansion tube; 111. supporting a tube; 112. an expansion tube; 113. filling the cavity; 114. A drainage hole; 12. a connecting pipe; 121. an inner tube; 122. an outer tube; 123. filling the channel; 124. a thread; 125. an annular projection; 126. a cross-hatched structure; 127. a drug aperture; 13. an adaptor; 131. filling the mouth; 14. a guidewire channel; 20. an expansion device; 21. expanding the tube; 213. filling the cavity; 22. a connecting pipe; 221. An inner tube; 222. an outer tube; 223. filling the channel; 2231. connecting holes; 23. an adapter; 231. filling the mouth; 24. pushing the pipe; 30. a guide catheter; 31. an expansion tube; 32. a connecting pipe; 321. a soft segment; 322. Bending the section; 323. a support section; 33. an adapter; 331. the mouth is filled.

Detailed Description

In order to make the above objects, features and advantages of the present invention more comprehensible, embodiments of the present invention are described in detail below with reference to the accompanying drawings. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. The present invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein, as those skilled in the art will be able to make similar modifications without departing from the spirit and scope of the present invention.

In particular, one aspect of the present application provides an expansion device for expanding a blood vessel to assist in guiding a surgical instrument, such as a catheter, through the blood vessel. Specifically, the expansion device of an embodiment includes expansion pipe, connecting pipe and adaptor, and wherein the expansion pipe includes that stay tube and cover establish the expansion pipe outside the stay tube, is formed with full chamber in the expansion pipe, and the expansion pipe has the expansion state of contraction state and following the expansion state of radial expansion after filling the full medium of full chamber, and the connecting pipe is connected with the expansion pipe, and the connecting pipe is equipped with full passageway, fills passageway and full chamber intercommunication, and the adaptor is equipped with the full mouth that is linked together with full passageway.

Specifically, the above-mentioned dilatation device can be used with a guide catheter or a contrast catheter when in use, when the guide catheter or the contrast catheter cannot be passed into the blood vessel due to the problem of blood vessel tortuosity or spasm, the dilatation device can be passed into the guide catheter or the contrast catheter and passed through the guide catheter or the contrast catheter to the tortuosity or spasm of the blood vessel, the adapter can be used for connecting with an injector, then the injector injects a medium such as liquid or gas into the filling cavity of the dilatation catheter through the filling opening of the adapter, the medium can radially expand the dilatation catheter after filling the filling cavity, thereby supporting the tortuosity or spasm of the blood vessel, expanding the inner diameter of the blood vessel to ensure that the surgical instruments such as the guide catheter or the contrast catheter can smoothly pass through the tortuosity or the spasm of the blood vessel and pass into the lesion, and then the dilatation device is withdrawn from the guide catheter or the contrast catheter, so that the surgical instruments can be conveyed to the lesion through the guide catheter or the contrast catheter.

The expansion device comprises an expansion pipe and an expansion pipe, wherein the expansion pipe is sleeved outside the support pipe, the support pipe can effectively increase the support strength of the expansion pipe, so that the expansion pipe can smoothly penetrate into a tortuous or spasm position of a blood vessel, and the expansion pipe is configured to have a contraction state and an expansion state, so that after the expansion pipe penetrates into the tortuous or spasm position of the blood vessel, a medium such as liquid or gas is injected into a filling cavity of the expansion pipe through a filling channel of a connecting pipe through a filling opening of an adapter, the expansion pipe is radially expanded, a tortuous blood vessel with plaques and ulcers or a tight spasm blood vessel is expanded, the resistance of the blood vessel wall is reduced, and surgical instruments such as a guide catheter or a contrast catheter can be guaranteed to smoothly pass through the tortuous or spasm position of the blood vessel. When encountering the problem of blood vessel tortuosity or spasm in the interventional operation, the guiding catheter and other surgical instruments can be ensured to smoothly penetrate to the pathological change position without changing the access path, the operation is simple, the operation time is saved, and the time of exposing the patient and the operator to rays is reduced.

Various embodiments of the stent of the present application will be further described with reference to the drawings.

Specifically, referring to fig. 1 and 2, fig. 1 and 2 illustrate a structural schematic view of the expansion device 10 of the first embodiment, specifically, the expansion device 10 of the first embodiment includes an expansion tube 11, a connection tube 12 and an adaptor 13, wherein the expansion tube 11 includes a support tube 111 and an expansion tube 112 sleeved outside the support tube 111, an inflation cavity 113 is formed in the expansion tube 112, the expansion tube 112 has a contracted state and an expanded state radially expanded after the inflation cavity 113 is filled with a medium, one end of the connection tube 12 is connected to the expansion tube 11, the connection tube 12 is provided with an inflation channel 123, the inflation channel 123 is communicated with the inflation cavity 113, the other end of the connection tube 12 is connected to the adaptor 13, and the adaptor 13 is provided with an inflation port 131 communicated with the inflation channel.

Further, in the present embodiment, the material of the expansion tube 112 is a biocompatible polymer material, for example, a composite material formed by mixing one or more of polyethylene, polypropylene, polytetrafluoroethylene, polyurethane, polyamide, polyether block polyamide, polyester, and silicone rubber can be selected. The expansion tube 112 may be formed by injection molding, extrusion, pressing, calendering, or thermoforming, among other processes. Preferably, in the present embodiment, the expansion tube 112 is a double-layer tube, and includes an inner layer covering the outer peripheral surface of the support tube 111 and an outer layer sleeved outside the inner layer, and the filling cavity 113 is formed between the inner layer and the outer layer. In another embodiment, the expansion tube 112 may also be a single-layer tubing, with the inflation lumen 113 formed between the expansion tube 112 and the support tube 111.

Further, in the present embodiment, the material of the support tube 111 is a biocompatible metal material, for example, a composite material formed by mixing one or more of titanium, magnesium, nickel, cobalt, stainless steel, and the like is selected. Preferably, the structure of the support tube 111 is a woven mesh tube structure, so as to effectively increase the support rigidity of the expansion tube 11, thereby ensuring that the expansion tube 11 can penetrate and ensuring that the support tube 111 can support the flexible expansion tube 112.

Referring to fig. 3, the outer diameter of the dilating tube 11 gradually decreases towards a direction away from the connecting tube 12, i.e. the dilating tube 11 is tapered as a whole, so as to improve the dilating performance of the dilating tube 11, ensure that the dilating tube 11 can smoothly penetrate into a narrower tortuous or spastic position in the blood vessel without damaging the blood vessel, and effectively dilate the blood vessel in combination with the capability of the dilating tube 11 to be inflated.

Further, the expansion device 10 is provided with a guide wire channel 14, and the guide wire channel 14 penetrates through the expansion tube 11, the connection tube 12 and the adaptor 13. Specifically, in use, a guidewire may be threaded into the guidewire channel 14 of the expansion device 10 such that the guidewire can be delivered to a designated area along the expansion device 10. Including but not limited to a guide wire, a contrast wire, a rotational milled wire, etc.

Furthermore, the outer peripheral side of the expanding tube 11 is provided with a drainage hole 114, and the drainage hole 114 is communicated with the guide wire channel 14. Therefore, after the expansion device 10 is delivered to the lesion part, the blood flow of the branch blood vessel can circulate through the drainage hole 114 and the guide wire channel 14, and the blood circulation of the branch blood vessel is ensured. Further, the drainage aperture 114 is spaced from the filling lumen 113 to prevent blood from entering the filling lumen 113 and to prevent the medium in the filling lumen 113 from leaking into the blood vessel.

Further, the outer peripheral side of the stent 11 and the outer peripheral side of the connection tube 12 are provided with a lubricant coating, so that the friction force between the blood vessel wall and the stent 10 is reduced, the smoothness of the stent 10 when it penetrates into the blood vessel is improved, and the blood vessel is prevented from being damaged. Further, the inner wall of the guide wire channel 14 is also provided with a lubricating coating, thereby improving the smoothness when the guide wire is inserted. Preferably, the lubricant coating is selected from a hydrophilic coating such as polyvinylpyrrolidone, or a hydrophobic coating such as silicone oil, polytetrafluoroethylene, or the like.

Further, referring to fig. 2, in the present embodiment, the connection tube 12 includes an inner tube 121 and an outer tube 122 sleeved outside the inner tube 121, an inflation channel 123 is formed between the inner tube 121 and the outer tube 122, one end of the inner tube 121 is connected to the support tube 111, the other end of the inner tube 121 is connected to the adaptor 13, one end of the outer tube 122 is connected to the expansion tube 112, and the other end of the outer tube 122 is connected to the adaptor 13. That is, in the present embodiment, the connection tube 12 has a double-layer structure, and the expansion tube 11 and the adaptor 13 are connected by the connection tube 12 having a double-layer structure, so that the support and the torque control performance of the expansion device 10 are improved.

Specifically, the material of the outer tube 122 is a biocompatible polymer material, such as a composite material formed by mixing one or more of polyethylene, polypropylene, polytetrafluoroethylene, polyurethane, polyamide, polyether block polyamide, polyester, and silicone rubber. Further, the hardness of the material of the outer tube 122 is greater than that of the expansion tube 112, so that the outer tube 122 of the connection tube 12 is prevented from being expanded and deformed when the expansion tube 112 is filled with the medium.

The material of the inner tube 121 is a biocompatible metal material, for example, a composite material formed by mixing one or more of titanium, magnesium, nickel, cobalt, stainless steel, and the like. Preferably, the inner tube 121 and the support tube 111 are integrally formed, that is, the inner tube 121 is also a braided mesh tube structure, so as to effectively improve the support and torsion control of the connection tube 12.

Further, the outer circumference side of the outer tube 122 of the connection tube 12 may be provided with some texture structure, thereby improving the functionality of the connection tube 12. Specifically, referring to fig. 4, in an embodiment, the outer periphery of the connecting tube 12 is provided with a thread 124, so that when the expansion device 10 passes through tortuous and spastic blood vessels, the rotating adaptor 13 drives the connecting tube 12 to rotate, and since the outer periphery of the connecting tube 12 is provided with the thread 124, the blood vessel wall and the thread 124 act to apply an axial force to the expansion device 10, thereby helping the expansion device 10 pass through tortuous and spastic blood vessels, and further improving the pushing performance, the passing performance and the twisting performance of the expansion device 10.

Referring to fig. 5, the outer periphery of the connection tube 12 may further be provided with an annular protrusion 125, and the outer diameter of the annular protrusion 125 gradually increases along the direction from the expansion tube 11 to the adaptor 13, i.e. the annular protrusion 125 has a tapered structure, and the outer diameter of the end of the annular protrusion 125 close to the expansion tube 11 is smaller, so as to be easier to penetrate into the tortuous and spasm part of the blood vessel. The annular protrusion 125 has a larger outer diameter at the end close to the dilating tube 11, so that the connecting tube 12 has a certain expandability, and when the connecting tube 12 passes through tortuous and spastic vessels, the vessel can be further dilated, thereby improving the expandability of the dilating device 10. Preferably, the outer circumferential side of the connection pipe 12 is provided with a plurality of annular protrusions 125, and the plurality of annular protrusions 125 are arranged along the axial direction of the connection pipe 12.

Referring to fig. 6, the outer periphery of the connecting tube 12 may also be provided with a texture 126, and preferably, the texture 126 may be a metal texture, which may improve the rigidity of the connecting tube 12, thereby improving the supporting performance and the twisting performance of the supporting tube 111.

Referring to fig. 7, the outer circumference of the connecting tube 12 may also be provided with a drug hole 127, and the drug hole 127 is used for carrying drugs, wherein the drugs include but are not limited to drugs for treating vasospasm, so that the vasospasm can be treated while dilating the blood vessel. Preferably, the plurality of medicine holes 127 are provided, and the plurality of medicine holes 127 are spaced apart on the outer circumferential side of the connection pipe 12.

Referring to fig. 8 to 10, fig. 8 to 10 illustrate a structural schematic view of the expansion device 20 of the second embodiment, and specifically, unlike the first embodiment, the expansion device 20 of the second embodiment further includes a push pipe 24, and the push pipe 24 is used for connecting the connecting pipe 22 and the adaptor 23. Specifically, in the second embodiment, the connecting tube 22 includes an inner tube 221 and an outer tube 222 sleeved outside the inner tube 221, a filling passage 223 is formed between the inner tube 221 and the outer tube 222, the inner tube 221 is connected to the support tube, the outer tube 222 is connected to the expansion tube, one end of the filling passage 223, which is far away from the expansion tube 21, is provided with a connecting hole 2231 communicated with the filling passage 223, the other part of one end of the filling passage 223, which is far away from the expansion tube 21, except for the connecting hole 2231 is a closed structure, one end of the pushing tube 24 penetrates through the connecting hole 2231 and penetrates into the filling passage 223, and the other end of the pushing tube 24 is communicated to the filling port 231.

Specifically, the push tube 24 is a hollow tubular structure with two open ends, and the diameter of the push tube 24 is smaller than the radial dimension of the filling passage 223, so as to ensure that one end of the push tube 24 penetrates into the filling passage 223 to communicate the filling passage 223 with the filling port 231 through the push tube 24, and ensure that when a liquid or gas medium is injected into the filling port 231, the medium can enter the filling cavity 213 and make the dilating tube 21 enter the dilating state to dilate the blood vessel. And because the diameter of the push tube 24 is small, the push tube occupies a small space in the blood vessel, so that other surgical instruments can not be influenced to pass through the blood vessel, and the push tube is beneficial to assisting in delivering other interventional instruments.

Further, the material of the pushing pipe 24 is a biocompatible metal material, for example, a composite material formed by mixing one or more of titanium, magnesium, nickel, cobalt, stainless steel, and the like is selected, so that the support property and the torsion control property of the pushing pipe 24 are improved. Further, the cross section of the pushing rod may be circular, oval, rectangular, etc., without limitation.

It is understood that other technical features of the expanding tube 21, the connecting tube 22 and the adaptor 23 of the second embodiment may be the same as those of the first embodiment without any contradiction in the combination of the technical features, and are not described herein.

The present application further provides a guiding system, and in particular, the guiding system of an embodiment includes a guiding catheter and the expansion device of any of the above embodiments, the expansion device is disposed through the guiding catheter, the expansion tube is disposed through one end of the guiding catheter, and the adaptor is disposed through the other end of the guiding catheter.

Specifically, when the guiding catheter is used, the guiding catheter can be firstly passed through a blood vessel, when the guiding catheter encounters the problem of blood vessel tortuosity or spasm and cannot be continuously passed through the blood vessel, the expansion device can be passed through the guiding catheter, the expansion tube passes through the distal end of the guiding catheter, the adaptor is left at the proximal end of the guiding catheter and is used for being connected with the injector, then gas or liquid medium is injected into a filling port of the adaptor through the injector, the medium can enter a filling cavity of the expansion tube through a filling channel, so that the expansion tube is radially expanded and supports the tortuosity or spasm part of the blood vessel, the inner diameter of the blood vessel is expanded, at the moment, the guiding catheter can smoothly pass through the tortuosity or spasm position of the blood vessel and is passed to the lesion position, and then the expansion device is withdrawn from the guiding catheter to convey a surgical instrument to the lesion position through the guiding catheter or the contrast catheter.

The aforementioned dilation devices generally need to be used in conjunction with a guiding catheter to achieve the function of dilating the vessel and delivering the device. In another embodiment of the present invention, a guiding system 30 having functions of expanding a blood vessel and guiding an instrument is provided, and specifically, referring to fig. 11, the guiding system 30 of an embodiment includes an expanding tube 31, a connecting tube 32 and an adaptor 33, wherein the expanding tube 31 includes a supporting tube and an expanding tube sleeved outside the supporting tube, an inflation cavity is formed in the expanding tube, the expanding tube has a contraction state and an expansion state expanded along a radial direction after the inflation cavity is filled with a medium, one end of the connecting tube 32 is connected to the expanding tube 31, the connecting tube 32 is provided with an inflation channel, the inflation channel is communicated with the inflation cavity, the other end of the connecting tube 32 is connected to the adaptor 33, and the adaptor 33 is provided with an inflation port 331 communicated with the inflation channel.

Further, in this embodiment, the connection tube 32 includes a flexible section 321, a bending section 322 and a supporting section 323 connected in sequence, the flexible section 321 is connected to the dilation tube 31, the bending section 322 is formed with at least one bending structure bending relative to the supporting section 323 or the flexible section 321, and a bending angle of the bending structure can be adjusted according to a physiological structure (such as a coronary artery opening position, an inclination angle, etc.) of the patient and an operation path (such as a left coronary artery or a right coronary artery), so that the connection tube 32 can smoothly hang the coronary artery opening after entering the aorta.

Further, the guiding system 30 is provided with an instrument channel, which penetrates through the dilating tube 31, the connecting tube 32 and the adaptor 33, so that a surgical instrument such as a guide wire, a balloon, a stent, etc. can be delivered to the lesion site through the instrument channel.

It is understood that, in the case that there is no contradiction in the combination of the technical features, other technical features of the expanding tube 31, the connecting tube 32 and the adaptor 33 of the guiding system 30 of the present embodiment may be the same as the technical features of the expanding tube 31, the connecting tube 32 and the adaptor 33 of the expanding device of the first embodiment, and are not described herein again.

The guiding system 30 is disposed at one end of the connecting tube 32, the expanding tube 31 is configured to include a support tube and an expanding tube sleeved outside the support tube, the support tube can effectively increase the support strength of the expanding tube 31, so that the expanding tube 31 can smoothly penetrate into the tortuous or spasm position of the blood vessel, and the expanding tube is configured to have a contracted state and an expanded state, so that after the expanding tube 31 penetrates into the tortuous or spasm position of the blood vessel, a medium such as liquid or gas is injected into the filling cavity of the expanding tube 31 through the filling channel of the connecting tube 32 through the filling opening 331 of the adaptor 33, so that the expanding tube radially expands, thereby expanding the tortuous blood vessel with plaque and ulcer or the tight spasm blood vessel, reducing the resistance of the blood vessel wall, ensuring that the guiding system 30 smoothly passes through the tortuous or spasm position of the blood vessel and enters the lesion site, and simultaneously, by disposing an instrument channel in the guiding system 30, the guiding system 30 can assist the guiding wire, balloon, stent, and other instruments to smoothly pass through the tortuous or spasm position of the blood vessel and reach the lesion site.

The technical features of the embodiments described above may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the embodiments described above are not described, but should be considered as being within the scope of the present specification as long as there is no contradiction between the combinations of the technical features.

The above-mentioned embodiments only represent some embodiments of the present invention, and the description thereof is specific and detailed, but not to be construed as limiting the scope of the present invention. It should be noted that, for those skilled in the art, without departing from the spirit of the present invention, several variations and modifications can be made, which are within the scope of the present invention. Therefore, the protection scope of the present invention should be subject to the appended claims.

In the description of the present invention, it is to be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", "axial", "radial", "circumferential", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and for simplicity of description, and do not indicate or imply that the device or element referred to must have a particular orientation, be constructed and operated in a particular orientation, and thus, should not be construed as limiting the present invention.

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 at least one of the feature. In the description of the present invention, "a plurality" means at least two, e.g., two, three, etc., unless specifically limited otherwise.

In the present invention, unless otherwise expressly stated or limited, the terms "mounted," "connected," and "fixed" are to be construed broadly and may, for example, be fixedly connected, detachably connected, or integrally formed; can be mechanically or electrically connected; they may be directly connected or indirectly connected through intervening media, or they may be connected internally or in any other suitable relationship, unless expressly stated otherwise. The specific meaning of the above terms in the present invention can be understood according to specific situations by those skilled in the art.

In the present application, unless expressly stated or limited otherwise, the first feature may be directly on or directly under the second feature or indirectly via intermediate members. Also, a first feature "on," "above," and "over" a second feature may be directly on or obliquely above the second feature, or simply mean that the first feature is at a higher level than the second feature. A first feature being "under," "below," and "beneath" a second feature may be directly under or obliquely under the first feature, or may simply mean that the first feature is at a lesser elevation than the second feature.

It will be understood that when an element is referred to as being "secured to" or "disposed on" another element, it can be directly on the other element or intervening elements may also be present. When an element is referred to as being "connected" to another element, it can be directly connected to the other element or intervening elements may also be present. The terms "vertical," "horizontal," "upper," "lower," "left," "right," and the like as used herein are for illustrative purposes only and do not denote a unique embodiment.

Claims (11)

1. An expansion device, comprising:

the expansion pipe comprises a supporting pipe and an expansion pipe sleeved outside the supporting pipe, an inflation cavity is formed in the expansion pipe, and the expansion pipe has a contraction state and an expansion state of expanding along the radial direction after the inflation cavity is filled with a medium;

the connecting pipe is connected with the expansion pipe and provided with an filling channel which is communicated with the filling cavity; and the number of the first and second groups,

the adaptor, the adaptor be equipped with fill sufficient mouth that the passageway is linked together.

2. The stent of claim 1, wherein the outer diameter of the stent tube gradually decreases away from the connecting tube.

3. The expansion device of claim 1, wherein a guide wire channel is provided through the expansion tube, the connecting tube and the adaptor.

4. The expanding device of claim 3, wherein the outer circumference of the expanding tube is provided with a drainage hole, and the drainage hole is communicated with the guide wire channel.

5. The stent of claim 3, wherein the outer circumferential side of the stent, the outer circumferential side of the connecting tube, and the inner wall of the guide wire channel are provided with a lubricating coating.

6. The stent according to claim 1, wherein an outer peripheral side of the connection tube is provided with a thread; and/or the presence of a gas in the gas,

an annular bulge is arranged on the outer peripheral side of the connecting pipe, and the outer diameter of the annular bulge is gradually increased along the direction from the expansion pipe to the adaptor; and/or the presence of a gas in the gas,

a reticulate pattern structure is arranged on the outer peripheral side of the connecting pipe; and/or the presence of a gas in the gas,

the periphery side of the connecting pipe is provided with a medicine hole, and the medicine hole is used for bearing medicines.

7. The dilation device according to any one of claims 1 to 6 wherein the connection tube comprises an inner tube and an outer tube sleeved outside the inner tube, the inner tube and the outer tube forming the filling passage therebetween, one end of the inner tube being connected to the support tube and the other end of the inner tube being connected to the adaptor, one end of the outer tube being connected to the inflation tube and the other end of the outer tube being connected to the adaptor.

8. The stent according to any one of claims 1 to 6, wherein the connecting tube comprises an inner tube and an outer tube sleeved outside the inner tube, the inner tube and the outer tube form the filling passage therebetween, the inner tube is connected to the support tube, the outer tube is connected to the expansion tube, a connecting hole is provided at one end of the filling passage away from the expanding tube, the stent further comprises a pushing tube, one end of the pushing tube is inserted into the connecting hole and penetrates into the filling passage, and the other end of the pushing tube is communicated to the filling port.

9. The stent of any of claims 1-6, wherein the material of the inflation tube is a biocompatible polymeric material; the support tube is made of biocompatible metal material.

10. A guide system comprising a guide catheter and an expansion device according to any one of claims 1 to 8, the expansion device being disposed through the guide catheter and the expansion tube extending through one end of the guide catheter and the adaptor extending through the other end of the guide catheter.

11. A guidance system, comprising:

the expansion pipe comprises a supporting pipe and an expansion pipe sleeved outside the supporting pipe, an inflation cavity is formed in the expansion pipe, and the expansion pipe has a contraction state and an expansion state of expanding along the radial direction after the inflation cavity is filled with a medium;

the connecting pipe is connected with the expansion pipe and provided with an filling channel, the filling channel is communicated with the filling cavity, the connecting pipe comprises a soft section, a bending section and a supporting section which are sequentially connected, the soft section is connected with the expansion pipe, and at least one bending structure which is bent relative to the supporting section or the soft section is formed in the bending section; and the number of the first and second groups,

the adaptor is connected with the support section and provided with a filling opening communicated with the filling channel;

wherein, instrument channels for surgical instruments to pass through are formed in the expansion tube, the connecting tube and the adaptor.

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