CN215018480U - Guiding device - Google Patents

Guiding device Download PDF

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Publication number
CN215018480U
CN215018480U CN202121382635.4U CN202121382635U CN215018480U CN 215018480 U CN215018480 U CN 215018480U CN 202121382635 U CN202121382635 U CN 202121382635U CN 215018480 U CN215018480 U CN 215018480U
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Prior art keywords
outer tube
hole
tube
fluid
inner tube
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CN202121382635.4U
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Chinese (zh)
Inventor
孙权权
叶萍
张一�
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Shanghai Achieva Medical Suzhou Co ltd
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Shanghai Achieva Medical Suzhou Co ltd
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Priority to CN202121382635.4U priority Critical patent/CN215018480U/en
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Abstract

The utility model provides a guiding device, including the inner tube, outer tube and expandable member, the inner tube outside is located to the outer pipe box, form fluid passage between outer tube and the inner tube, expandable member locates the outside of outer tube, at least one through-hole has been seted up to the outer tube, expandable member injects the fluid when inflation state, form the fluid chamber between outer tube and the expandable member, through-hole intercommunication fluid passage and fluid chamber, the outer tube still has two at least concave parts, every concave part is sunken towards the inner tube and is fixed in the inner tube, on the circumferencial direction of outer tube, every through-hole is located between two adjacent concave parts. The at least two concave parts of the outer pipe are respectively sunk towards the inner pipe and fixed on the inner pipe, the concave parts and the inner pipe can provide supporting force for the part between the two adjacent concave parts of the outer pipe, so that the part between the two adjacent concave parts of the outer pipe is arched, and when fluid in the fluid cavity is pumped out, the situation that the part of the outer pipe around the through hole is tightly attached to the wall of the inner pipe to block the through hole is avoided.

Description

Guiding device
Technical Field
The utility model relates to a blood vessel intervention medical instrument especially relates to a guiding device.
Background
Cerebral thrombosis is mainly caused by cerebral thrombosis, and is the most common lethal and disabling disease of the central nervous system. Cerebral thrombosis has the characteristics of high morbidity, high disability rate, high mortality rate and high recurrence rate.
The recanalization of blood vessels is the key for treating cerebral thrombosis, one treatment method of the cerebral thrombosis at present is mechanical thrombus extraction, an interventional medical instrument is adopted to complete the treatment, a thrombus extraction device is pushed to the position of a target thrombus through an inner cavity of a balloon guide catheter, then fluid is injected between an inner tube and an outer tube of the balloon guide catheter, the fluid flows into a balloon tube coated on the periphery of the outer tube through a through hole on the outer tube, so that the balloon tube is expanded and attached to the inner wall of the blood vessel, the blood flow is temporarily blocked, then the thrombus extraction device is cut into the target thrombus to hang the whole thrombus, then the thrombus extraction device is withdrawn to extract the thrombus, the fluid in the balloon tube is sucked to enable the balloon tube to be contracted to be attached to the outer surface of the outer tube, and the blood flow returns to normal flow.
However, when fluid is sucked, the flow rate of the fluid at the through hole is the largest, and the negative pressure borne by the part of the outer tube around the through hole is far larger than that borne by other parts of the outer tube, so that the part of the outer tube around the through hole is easily sunk to the inner tube, the distance between the outer tube and the inner tube is reduced, the time required by the contraction of the balloon tube is increased, and even the part of the outer tube around the through hole is tightly attached to the wall of the inner tube to block the through hole, so that the fluid is remained in the balloon tube to prevent the balloon tube from continuously contracting, the time for blocking the blood flow is increased, and the operation risk is increased.
Disclosure of Invention
In order to solve the technical problem, the utility model provides a guiding device to when solving the suction fluid, the outer tube is sunken to the inner tube easily around the through-hole or hug closely even and block up the through-hole in the inner tube wall, and leads to the unable smooth exhaust problem of fluid in the sacculus.
In order to realize one of the above objects of the present invention, an embodiment of the present invention provides a guiding device, including an inner tube, an outer tube and an expandable member, the outer tube is sleeved on the outer side of the inner tube, and the outer tube and the inner tube form a fluid channel therebetween, the expandable member is disposed on the outer side of the outer tube, at least one through hole has been disposed on the outer tube, the expandable member injects fluid in an expanded state, the outer tube and the expandable member form a fluid chamber therebetween, the through hole communicates the fluid channel with the fluid chamber, the outer tube further has at least two concave portions, each of which faces towards the inner tube is recessed and fixed on the inner tube, in a circumferential direction of the outer tube, each of the through holes is disposed adjacent to each other between the concave portions, and the through hole is disposed in the balloon tube.
As a further improvement of an embodiment of the present invention, in the circumferential direction of the outer tube, a distance between each of the through holes and two of the concave portions adjacent thereto is equal.
As a further improvement of an embodiment of the present invention, two of the concave portions adjacent to the through hole are located on the same circumference of the outer tube and arranged at an interval of 180 °.
As a further improvement of an embodiment of the present invention, the inflatable member is a balloon.
As a further improvement of an embodiment of the present invention, in an axial direction of the outer tube, both ends of the expandable member are respectively fixed to the outer tube, and the concave portion is located outside the expandable member.
As a further improvement of an embodiment of the present invention, the recess is located on a side of the expandable member near the proximal end of the outer tube.
As a further improvement of an embodiment of the present invention, the outer tube includes a first section and a second section which are sequentially arranged from a proximal end to a distal end thereof, the expandable member is disposed in an outer side of the second section, the through hole is disposed in the second section, and an outer diameter of the second section is not greater than a maximum diameter of the first section.
As a further improvement of an embodiment of the present invention, the concave portion extends in an axial direction of the outer tube.
As a further improvement of an embodiment of the present invention, the concave portion is fixed to the inner pipe by welding, bonding, or fusion.
As a further improvement of an embodiment of the present invention, the hardness of the outer tube is gradually decreased from the proximal end to the distal end, and/or the hardness of the inner tube is gradually decreased from the proximal end to the distal end.
Compared with the prior art, the utility model discloses following beneficial effect has: the guiding device of the utility model, through at least two concave parts of the outer tube respectively towards the inner tube sunken and fixed in the inner tube, the concave parts and the inner tube can provide supporting force for the part between two adjacent concave parts of the outer tube, thereby the part between two adjacent concave parts of the outer tube is arched, the radial distance from the highest point of the arch to the inner tube is increased, when the bolt taking is completed, the fluid in the fluid cavity is drawn out from the through hole between the two adjacent concave parts, under the supporting force action of the concave parts and the inner tube, even if the fluid flow speed at the through hole is the largest, the negative pressure born by the part of the outer tube around the through hole is far larger than that born by other parts of the outer tube, the part of the outer tube around the through hole can not be sunken too much towards the inner tube, the part of the outer tube around the through hole still has a certain space between the inner tube and the part of the outer tube, so that the fluid smoothly flows out of the fluid cavity, under the condition that the diameter of the outer pipe is not increased, the situation that the part of the outer pipe around the through hole is tightly attached to the wall of the inner pipe to block the through hole is avoided, the expandable part can be restored to the contracted state from the expanded state as soon as possible, the expandable part is separated from the inner wall of the blood vessel, the blocked blood flow is restored to flow, the guide device is convenient to take out, and the operation risk is reduced.
Drawings
The accompanying drawings, which are included to provide a further understanding of the application and are incorporated in and constitute a part of this application, illustrate embodiment(s) of the application and together with the description serve to explain the application and not to limit the application. In the drawings:
fig. 1 is a schematic cross-sectional view of a guiding device according to an embodiment of the present invention, in which a balloon is shown in a contracted state;
fig. 2 is a schematic cross-sectional view of a guiding device according to an embodiment of the present invention, showing a balloon in an inflated state;
fig. 3 is a schematic cross-sectional view of a guiding device according to an embodiment of the present invention, illustrating a cross-section of the balloon at the maximum diameter in the inflated state.
Detailed Description
In order to make the objects, technical solutions and advantages of the present application more apparent, the technical solutions of the present application will be described in detail and completely with reference to the following specific embodiments of the present application and the accompanying drawings. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
In the various figures of the present invention, certain dimensions of structures or portions are exaggerated relative to other structures or portions for ease of illustration, and thus, are used only to illustrate the basic structure of the subject matter of the present invention.
It is to be understood that, unless otherwise expressly specified or limited, in the description of the invention, the terms "inner", "outer", and the like refer to an orientation or positional relationship based on that shown in the drawings, which is for convenience in describing the invention and simplifying the description, and do not indicate or imply that the device or element referred to must have a particular orientation, be constructed in a particular orientation, and be operated, and therefore should not be considered as limiting the invention. Furthermore, the terms "first" and "second" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance.
Referring to fig. 1, the present invention provides a guiding device 100, which comprises an inner tube 1, an outer tube 2, a connecting tube 3 and an expandable member, wherein the outer tube 2 is sleeved on the outer side of the inner tube 1 and coaxially arranged with the inner tube 1, a fluid passage 6 is formed between the outer tube 2 and the inner tube 1, and a sealing portion 5 extending from the distal end of the outer tube 2 to the inner tube 1 along the radial direction of the outer tube 2 is further provided at the distal end of the guiding device 100, so as to prevent the fluid from flowing out of the guiding device 100 and entering the blood vessel. One end of the connecting pipe 3 is connected to the outer pipe 2, and the pipe cavity of the connecting pipe 3 is communicated with the fluid channel 6, but the pipe cavity of the connecting pipe 3 is isolated from the pipe cavity of the inner pipe 1, so that the fluid can be conveniently injected into the fluid channel 6 from the connecting pipe 3, and the fluid can not enter the pipe cavity of the inner pipe 1.
Referring to fig. 1 to 2, the expandable member is disposed outside the outer tube 2, the outer tube 2 is provided with at least one through hole 21, the expandable member has an expanded state and a contracted state tightly attached to an outer surface of the outer tube 2, when the expandable member injects a fluid into the expanded state, a fluid cavity 41 is formed between the outer tube 2 and the expandable member, the through hole 21 communicates the fluid channel 6 and the fluid cavity 41, at this time, the fluid flows into the fluid cavity 41 from the fluid channel 6 and fills the fluid cavity 41, and the expandable member expands along an axial direction thereof to be attached to an inner wall of a blood vessel, thereby playing a role of temporarily blocking blood flow and avoiding an influence of blood flow on a thrombus removal process. The fluid here is a mixed solution of contrast agent and saline to facilitate viewing of the inflated state of the inflatable member.
Specifically, in this embodiment, the expandable member is a balloon 4, the balloon 4 is disposed at the periphery of the outer tube 2, the outer tube 2 is provided with a through hole 21 communicating the fluid channel 6 with the balloon 4, the balloon 4 has an expanded state and a contracted state attached to the outer surface of the outer tube 2, when the balloon 4 injects a fluid in the expanded state, a fluid cavity 41 is formed between the outer tube 2 and the balloon 4, the fluid flows into the fluid cavity 41 from the fluid channel 6 and fills the fluid cavity 41, and the balloon 4 expands along the axial direction thereof to the inner wall attached to the blood vessel, thereby playing a role of temporarily blocking the blood flow and avoiding the influence of the blood flow on the embolectomy process. The fluid here is a mixed solution of contrast agent and saline to facilitate observation of the inflated state of the balloon 4.
Referring to fig. 3, the outer tube 2 further has at least two recesses 22, each recess 22 being recessed toward the inner tube 1 and fixed to the inner tube 1, the recesses 22 being disposed adjacent to the through holes 21, and each through hole 21 being disposed between two adjacent recesses 22 in the circumferential direction of the outer tube 2, the through holes 21 being located inside the balloon 4. Thus, the concave portion 22 and the inner tube 1 will provide a supporting force for the portion between two adjacent concave portions 22 of the outer tube 2, so that the portion between two adjacent concave portions 22 of the outer tube 2 is arched, and the radial distance from the highest point of the arch to the inner tube 1 is increased, so that the radial distance from the through hole 21 to the inner tube 1 is increased, when the fluid in the fluid chamber 41 is pumped out of the fluid chamber 41 after the embolectomy is completed, even if the fluid flow rate at the through hole 21 is the maximum, the negative pressure borne by the portion of the outer tube 2 around the through hole 21 is much larger than the negative pressure borne by the other portion of the outer tube 2, under the supporting force of the concave portion 22 and the inner tube 1, the portion of the outer tube 2 around the through hole 21 will not be depressed too much towards the inner tube 1, and a certain space is still existed between the portion of the outer tube 2 around the through hole 21 and the inner tube 1 for the fluid to smoothly flow out of the fluid chamber 41, under the condition that the diameter of the outer tube 2 is not increased, the situation that the through hole 21 is blocked due to the fact that the part of the outer tube 2 around the through hole 21 is tightly attached to the wall of the inner tube 1 is avoided, the balloon 4 can be made to return to the shrinking state from the expansion state as soon as possible, the balloon 4 is separated from the inner wall of the blood vessel, the blocked blood flow is recovered, meanwhile, the guiding device 100 is convenient to take out, and the operation risk is reduced.
Preferably, the expandable member is provided at the distal end of the outer tube 2, at least one through hole 21 is also provided at the distal end of the outer tube 2, and at least two recesses 22 are also provided at the distal end of the outer tube 2.
Specifically, in the present embodiment, the balloon 4 is disposed outside the distal end of the outer tube 2, and the through hole 21 and the at least two recesses 22 are also disposed at the distal end of the outer tube 2, so that it can block the blood flow near the location of the target thrombus and prevent the debris embolus generated during the embolectomy from flowing to the distal end of the blood vessel along with the blood flow.
In the present invention, the terms "distal end" and "proximal end" should be understood as meaning the end closer to the operator and the end farther away from the operator during operation, as viewed from the direction of the operator, the direction indicated by the arrow in the figure being the direction from the proximal end to the distal end.
Preferably, the through holes 21 are formed between every two adjacent recesses 22, so that the fluid in the fluid chamber 41 can be shunted through the plurality of through holes 21, the negative pressure at each through hole 21 is reduced, the speed can be increased, the time for the fluid chamber 41 to move from the expanded state to the contracted state is shortened, the blood can be restored to flow as soon as possible, and the operation risk is reduced.
Referring to fig. 3, in the present embodiment, the outer tube 2 has two recesses 22, and the recesses 22 and the through holes 21 are alternately arranged in the circumferential direction of the outer tube 2, that is, the through holes 21 are arranged between two adjacent recesses 22, and the recesses 22 are also arranged between two adjacent through holes 21. Of course, the number of the outer tube 2 and the recesses 22 provided is not limited thereto, and in other embodiments, the recesses 22 and the through holes 21 may be each provided in plural and alternately provided in the circumferential direction of the outer tube 2.
Further, at least two recesses 22 are arranged at intervals in the circumferential direction of the outer tube 2. Thus, each concave portion 22 provides a supporting force for the other part of the outer tube 2 along the tangential direction of the position, under the action of the supporting force, the part between two adjacent concave portions 22 of the outer tube 2 is arched outwards along the circumferential direction, the negative pressure which can be born by the part between two adjacent concave portions 22 is increased, when the fluid in the fluid cavity 41 is pumped out of the fluid cavity 41, the supporting force can provide a radial inward pressure which is generated on the outer tube 2 by the fluid flowing from the fluid cavity 41 to the outer tube 2, the collapse amplitude of the outer tube 2 to the inner tube 1 is reduced, the outer tube 2 is not collapsed until the outer tube 2 is attached to the inner tube 1 to block the through hole 21, in addition, the part between two adjacent concave portions 22 of the outer tube 2 is arched outwards along the circumferential direction, the distance between the part 2 between two adjacent concave portions 22 and the inner tube 1 is also increased, that is, the space for the outer tube 2 to move to the inner tube 1 is increased, the possibility that the outer tube 2 collapses to close against the inner tube 1 and blocks the through-hole 21 is reduced.
Preferably, the distance between each through hole 21 and its adjacent two recesses 22 is equal in the circumferential direction of the outer tube 2. As can be seen from the above analysis, each concave portion 22 provides a supporting force to the other portion of the outer tube 2 along the tangential direction of the position thereof, and under the supporting force, the portion between two adjacent concave portions 22 of the outer tube 2 is arched outward along the circumferential direction, so that the distance from the middle point of the two adjacent concave portions 22 of the outer tube 2 to the inner tube 1 is the largest, and the component of the supporting force provided by the two adjacent concave portions 22 to the inner tube is the largest, so that the negative pressure can be borne by the outer tube is the largest, the collapse amplitude is the smallest when the fluid flows from the fluid chamber 41 to the outer tube 2 through the through hole 21, and the space for collapsing the outer tube 2 is the largest, so that the influence on the fluid flowing from the fluid chamber 41 to the fluid channel 6 through the through hole 21 is the smallest, and the occurrence of the situation that the outer tube 2 collapses to the inner tube 1 to block the through hole 21 is avoided.
Referring to fig. 3, taking the present example as an example, two recesses 22 are arranged at 180 ° intervals on the same circumference of the outer tube 2, and the through-hole 21 and two recesses 22 adjacent thereto are respectively arranged at 90 ° intervals in the circumferential direction of the outer tube 2, so that the distance from the through-hole 21 to the inner tube 1 is maximized, and the component of the supporting force applied to the outer tube 2 around the through-hole 21 by the adjacent two recesses 22 is also maximized.
In the axial direction of the outer tube 2, both ends of the expandable member are fixed to the outer tube 2, respectively, and the recess 22 is located outside the expandable member, and the portion between both ends of the expandable member is expanded when injecting the fluid, so that it is possible to prevent the outer diameter of the distal end of the guide device 100 from being excessively large because the recess 22 and the expandable member are located on the same circumference of the outer tube 2. Preferably, the recess 22 is located on the side of the expandable member near the proximal end of the outer tube 2.
In other embodiments, at least part of the through hole 21 and two adjacent recesses 22 may be located on the same circumference of the outer tube 2, so that the space between the outer tube 2 and the inner tube 1 around the through hole 21 is maximized, and the supporting force provided by the inner tube 1 and the two adjacent recesses 22 is maximized, so that the negative pressure can be maximized, the collapse amplitude is minimized when the fluid flows from the fluid chamber 41 to the outer tube 2 through the through hole 21, and the outer tube 2 is prevented from collapsing to be close to the inner tube 1 to block the through hole 21. Preferably, the recess 22 is at least partially provided at the intersection of the cross section of the axial center of the expandable member and the outer tube 2, so that the supporting force of the inner tube 1 and the recess 22 on the rest of the outer tube 2 is mainly concentrated on the cross section of the axial center of the expandable member, the outer tube 2 is arched outwards along the cross section and has the largest amplitude at the cross section, and the arched amplitude has a gradually decreasing trend from the cross section to the two ends of the expandable member along the axial direction of the outer tube 2, and the trend is consistent with the trend of the expansion amplitude of the expandable member, thereby facilitating the fluid to flow from the fluid chamber 41 to the fluid channel 6 through the through hole 21.
Preferably, the through hole 21 is provided at the intersection of the cross section of the axial center of the expandable member and the outer tube 2, such that the through hole 21 also arches outwardly with the outer tube 2 along the cross section, which increases the distance between the through hole 21 and the inner tube 1, which facilitates the smooth flow of fluid from the fluid chamber 41 through the through hole 21 to the fluid channel 6, and avoids the risk of the through hole 21 being blocked.
Further, the concave portion 22 extends along the axial direction of the outer tube 2, so that the arched area of the outer tube 2, especially the area extending along the axial direction of the outer tube 2, can be further increased, and the area of the through hole 21 can be enlarged, or a plurality of through holes 21 can be arranged along the axial direction, so as to increase the speed of the fluid flowing from the fluid chamber 41 to the fluid channel 6, shorten the time, and further to remove the blockage of the blood flow and withdraw the guiding device 100 as soon as possible, complete the surgical procedure as soon as possible, and reduce the surgical risk.
Referring to fig. 1 to 2, further, at least two through holes 21 are arranged between two adjacent recesses 22 at intervals along the axial direction of the outer tube 2, so as to disperse the fluid pressure in the fluid chamber 41, and avoid that the fluid pressure in the fluid chamber 41 is totally concentrated on the outer tube 2 near one through hole 21 when the fluid flows out from the one through hole 21, so that the pressure of the part of the outer tube 2 is too high to be tightly attached to the inner tube 1.
The inner tube 1 and the outer tube 2 can adopt a single-layer structure prepared from nylon elastomer, nylon, polyurethane, polyimide or polytetrafluoroethylene, so that the inner tube 1 and the outer tube 2 have certain flexibility and strength so as to be convenient to intervene in a blood vessel; the inner tube 1 and the outer tube 2 can also be formed by compounding a multilayer structure, specifically, the inner tube comprises an outer layer, an inner layer and a reinforcing layer arranged between the outer layer and the inner layer, the flexibility of the inner tube 1 and the outer tube 2 is kept, meanwhile, the strength of the inner tube 1 and the strength of the outer tube 2 are improved, preferably, the outer layer adopts nylon elastomer, nylon or polyurethane, the inner layer adopts nylon elastomer, nylon, polyurethane or polytetrafluoroethylene, and the reinforcing layer is a woven mesh or a spring mesh prepared by stainless steel, nickel titanium or high polymer materials; of course, the inner tube 1 and the outer tube 2 may include only an outer layer and a reinforcing layer, and the strength of the inner tube 1 and the outer tube 2 may be increased.
Further, the concave portion 22 is fixed to the inner tube 1 by welding, bonding or welding, so that the outer tube 2 can be supported by the inner tube 1 to reduce the collapse range of the outer tube 2 and even prevent the collapse of the outer tube 2, the welding or welding mode is selected based on the materials of the outer tube 2 and the inner tube 1 and the limitation of the sizes of the outer tube 2 and the inner tube 1 by the diameter of the blood vessel, the concave portion 22 of the outer tube 2 is favorably fixed to the inner tube 1, the outer tube 2 and the inner tube 1 cannot be damaged, the inner diameter of the inner tube 1 cannot be reduced, and the thrombus taking device can be ensured to smoothly pass through the guiding device 100 to reach the target thrombus.
Referring to fig. 1 to 2, further, the outer tube 2 includes a first section 23 and a second section 24 arranged in sequence from the proximal end to the distal end thereof, the expandable member is arranged outside the second section 24, the through hole 21 is arranged in the second section 24, the recess 22 is arranged at one end of the first section 23 close to the expandable member to ensure that the blood flow near the target thrombus is blocked, and the outer diameter of the second section 24 is not larger than the maximum diameter of the first section 23, so as to avoid the size increase of the distal end of the guiding device 100 caused by the arrangement of the expandable member, and to ensure that the inner diameter of the inner tube 1 is as large as possible in the case of being limited by the inner diameter of the blood vessel, thereby facilitating the insertion of the thrombus taking device.
Further, the stiffness of the outer tube 2 tapers from the proximal end to the distal end and/or the stiffness of the inner tube 1 tapers from the proximal end to the distal end, thereby increasing the flexibility of the distal end of the guiding device 100 to avoid damage to the vessel during insertion of the guiding device 100 into the vessel and during expansion of the expandable member.
In addition, visualization rings may be mounted at both the distal end of the inner tube 1 and the proximal end of the expandable member to facilitate determination of the target thrombus location and the state of the expandable member.
In summary, in the guiding device 100 of the present invention, at least two concave portions 22 of the outer tube 2 are respectively recessed toward the inner tube 1 and fixed to the inner tube 1, the concave portions 22 and the inner tube 1 provide a supporting force for the portion between two adjacent concave portions 22 of the outer tube 2, so that the portion between two adjacent concave portions 22 of the outer tube 2 is arched, and the radial distance from the highest point of the arch to the inner tube 1 is increased, when the embolectomy is completed, the fluid in the fluid chamber 41 is pumped out from the through hole 21 disposed between two adjacent concave portions 22, under the supporting force of the concave portions 22 and the inner tube 1, even though the fluid flow speed at the through hole 21 is the largest, the negative pressure borne by the portion of the outer tube 2 around the through hole 21 is much larger than that borne by other portions of the outer tube 2, the portion of the outer tube 2 around the through hole 21 will not be too much recessed toward the inner tube 1, and a certain space is still left between the portion of the outer tube 2 around the through hole 21 and the inner tube 1 for the fluid to smoothly flow out of the fluid chamber 41, under the condition that the diameter of the outer tube 2 is not increased, the situation that the part of the outer tube 2 around the through hole 21 is tightly attached to the wall of the inner tube 1 to block the through hole 21 is avoided, the expandable part can be quickly restored to the contracted state from the expanded state, the expandable part is separated from the inner wall of the blood vessel, the blocked blood flow is recovered, the guide device 100 is convenient to take out, and the operation risk is reduced.
It should be understood that although the present description refers to embodiments, not every embodiment contains only a single technical solution, and such description is for clarity only, and those skilled in the art should make the description as a whole, and the technical solutions in the embodiments can also be combined appropriately to form other embodiments understood by those skilled in the art.
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, many modifications and improvements can be made without departing from the inventive concept, and all of them belong to the protection scope of the present invention.

Claims (10)

1. A guiding device comprises an inner tube, an outer tube and an expandable part, wherein the outer tube is sleeved outside the inner tube, a fluid channel is formed between the outer tube and the inner tube, the expandable part is arranged outside the outer tube, at least one through hole is formed in the outer tube, a fluid cavity is formed between the outer tube and the expandable part when the expandable part injects fluid in an expansion state, and the through hole is communicated with the fluid channel and the fluid cavity.
2. The guide device of claim 1, wherein the distance between each through hole and two adjacent recesses is equal in the circumferential direction of the outer tube.
3. The guide device of claim 2, wherein two of said recesses adjacent to said through hole are located on the same circumference of said outer tube and are spaced 180 ° apart.
4. The guide device of claim 1, wherein the expandable member is a balloon.
5. The guide device according to claim 1, wherein both ends of the expandable member are fixed to the outer tube, respectively, in an axial direction of the outer tube, and the recess is located outside the expandable member.
6. The guide device of claim 5, wherein the recess is located on a side of the expandable member proximate the proximal end of the outer tube.
7. The guide device of claim 1, wherein the outer tube comprises a first section and a second section sequentially arranged from the proximal end to the distal end thereof, the expandable member is arranged outside the second section, the through hole is arranged in the second section, and the outer diameter of the second section is not larger than the maximum diameter of the first section.
8. The guide device of claim 1, wherein the recess extends in an axial direction of the outer tube.
9. The guide device of claim 1, wherein the recess is secured to the inner tube by welding, gluing, or fusing.
10. The guide device of claim 1, wherein the outer tube tapers in stiffness from the proximal end to the distal end and/or the inner tube tapers in stiffness from the proximal end to the distal end.
CN202121382635.4U 2021-06-22 2021-06-22 Guiding device Active CN215018480U (en)

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Application Number Priority Date Filing Date Title
CN202121382635.4U CN215018480U (en) 2021-06-22 2021-06-22 Guiding device

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Application Number Priority Date Filing Date Title
CN202121382635.4U CN215018480U (en) 2021-06-22 2021-06-22 Guiding device

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CN215018480U true CN215018480U (en) 2021-12-07

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Application Number Title Priority Date Filing Date
CN202121382635.4U Active CN215018480U (en) 2021-06-22 2021-06-22 Guiding device

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115501456A (en) * 2021-06-22 2022-12-23 上海加奇生物科技苏州有限公司 Guiding device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115501456A (en) * 2021-06-22 2022-12-23 上海加奇生物科技苏州有限公司 Guiding device
CN115501456B (en) * 2021-06-22 2024-04-26 上海加奇生物科技苏州有限公司 Guiding device

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