CN211094508U - Shock wave device for treating calcification of heart valve - Google Patents

Abstract

The application discloses treatment calcified shock wave device of heart valve, the shock wave device includes: a shock wave generator generating voltage/current pulses; a shock wave transmitter comprising an electrode cable and an electrode probe, the electrode cable receiving a conducted voltage/current pulse, the electrode probe receiving the voltage/current pulse to generate a shock wave; the conducting electrode is positioned in the conducting system and conducts voltage/current pulses generated by the shock wave generator to the shock wave emitter; the saccule is wrapped outside the shock wave emitter and is provided with a through hole for electrolyte liquid to flow into; a visualization member located on the shock wave emitter and/or the balloon. Shock waves generated by the shock wave emitter are conducted to an area to be treated through electrolyte liquid in the balloon, calcified parts are softened under the action of shock wave energy, the opening and closing state of valve leaflets during working is improved, and the purposes of treating calcification, facilitating release of heart valves, accurately positioning, attaching blood vessels to the periphery and reducing peripheral leakage are achieved.

Description

Shock wave device for treating calcification of heart valve

Technical Field

The application belongs to the technical field of medical treatment, concretely relates to shock wave device of treatment heart valve calcification.

Background

Calcification of heart valves is the main pathological manifestation of heart valve stenosis and regurgitation, and generally occurs in the elderly; vascular calcification is a common pathological manifestation of atherosclerosis, hypertension, diabetic vasculopathy, vascular injury, chronic kidney disease, aging and the like.

Currently, therapeutic approaches to heart valve and vascular calcification include: drug therapy, surgical replacement or interventional replacement.

The inventor of the application finds that the existing drug treatment effect is very limited in the long-term development process, and the existing mode of replacement by surgical operation or interventional operation has the defects of great trauma to the patient and long time consumption.

SUMMERY OF THE UTILITY MODEL

The application provides a shock wave device of treatment heart valve calcification can adopt the shock wave to soften the calcification position, can effectively accomplish the treatment to the calcification position fast.

In order to solve the technical problem, the application adopts a technical scheme that: a shock wave device for treating calcification of a heart valve, comprising: the shock wave transmitter comprises an electrode cable and an electrode probe, wherein the electrode cable receives and conducts voltage/current pulses, and the electrode probe is electrically connected with the electrode cable and used for receiving the voltage/current pulses to generate shock waves; the balloon is wrapped outside the shock wave emitter and is provided with a through hole for electrolyte liquid to flow into, and the electrolyte liquid is used for conducting the shock wave; a visualization member located on the shock wave emitter and/or the balloon.

According to one embodiment of the application, the balloon is provided with one, the balloon is in an 8 shape, and the radial width of the balloon is gradually reduced from one end connected with the shock wave emitter to the other end not connected with the shock wave emitter to the middle part; at least two electrode probes are arranged in the saccule and are respectively positioned at two ends of the saccule so as to respectively act on the inner wall and the outer end of the calcified valve.

According to an embodiment of the application, the sacculus is provided with at least two and is arranged in a circumferential array, and at least one electrode probe is arranged in each sacculus.

According to an embodiment of the application, the electrode probe is curved outwardly towards the circumference of the balloon array.

According to an embodiment of the present application, the developing member includes the electrode probe including a material having a developing action; and/or the developing piece comprises developing rings which are positioned at two ends of the saccule.

According to an embodiment of the present application, the method includes: the shock wave generator is connected with an external power supply to generate the voltage/current pulse; the conduction system is connected with the through hole of the balloon and is used for conducting the electrolyte liquid, so that the electrolyte liquid is circulated in the conduction system and the balloon; and the conducting electrode is positioned in the conducting system, one end of the conducting electrode is connected with the shock wave generator, and the other end of the conducting electrode is connected with the shock wave emitter so as to receive and conduct the voltage/current pulse.

According to an embodiment of the present application, the method includes: the guide head end is connected to one end, far away from the conduction system, of each sacculus, and the guide head end is conical, smooth in tail end and free of sharp corners.

According to an embodiment of the present application, the guide head end is made of a flexible material.

According to an embodiment of the present application, the method includes: a reserve channel extending inside the conduction system, inside or between the balloons, and inside the guide head.

According to an embodiment of the present application, the method includes: a handle connected to an exterior of the conduction system.

According to an embodiment of the present application, the method includes: and the one-way valve is arranged on the conveying path of the electrolyte liquid so as to control the on-off of the electrolyte liquid.

According to an embodiment of the present application, the developing member includes a developer mixed in the electrolytic liquid.

The beneficial effect of this application is: the saccule can enter the way through the femoral artery until the saccule is contacted with a target area to be treated, shock waves generated by the shock wave emitter are conducted to the target area to be treated through electrolyte liquid in the saccule, calcified parts in the target area to be treated are softened under the action of shock wave energy, the opening and closing state of valve leaflets during working is improved, and therefore the purposes of treating calcification, facilitating release of heart valves, accurate positioning and peripheral fitting of blood vessels and reducing peripheral leakage are achieved. Compared with the traditional medicine treatment, the treatment effect is remarkable; compared with the traditional mode of replacement by surgical operation or interventional operation, the shock wave device has the advantages that the wound on a patient is small, the time consumption is short, for example, the problem that the valve possibly encountered in the operation process is seriously calcified and the heart valve cannot be accurately placed is solved, the shock wave device provided by the application can effectively avoid the risks that the artificial valve is difficult to position and fix, the artificial valve is not properly released and is difficult to remove and the like in the operation process, the operation time is shortened, and the operation and prognosis are greatly improved. In addition, still include the development piece among the shock wave device that this application provided, this development piece is located shock wave transmitter and/or sacculus, can help the doctor to pinpoint the shock wave device, ensures that shock wave transmitter and/or sacculus treat at the target area of treating.

Drawings

In order to more clearly illustrate the technical solutions in the embodiments of the present application, the drawings needed to be used in the description of the embodiments are briefly introduced below, it is obvious that the drawings in the following description are only some embodiments of the present application, and other drawings can be obtained by those skilled in the art without inventive efforts, wherein:

FIG. 1 is a schematic front view of an embodiment of a shockwave device for treating calcification of a heart valve according to the present application;

FIG. 2 is a schematic cross-sectional view of a conduction system of an embodiment of the shock wave device of the present application for treating calcification of a heart valve;

FIG. 3 is a schematic view of a further embodiment of a shockwave device of the present application for treating calcification of a heart valve;

fig. 4 is a schematic view of another embodiment of a shockwave device of the present application for treating calcification of a heart valve.

Detailed Description

The technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the drawings in the embodiments of the present application, and it is obvious that the described embodiments are only a part of the embodiments of the present application, and not all of the embodiments. 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.

Referring to fig. 1 to 2, fig. 1 is a schematic front view of an embodiment of a shockwave device for treating calcification of a heart valve according to the present application; fig. 2 is a schematic cross-sectional view of a conduction system of an embodiment of the shock wave device for treating calcification of a heart valve of the present application.

A shock wave device 100 for treating calcification of a heart valve, as shown in fig. 1, includes a shock wave emitter 20, a balloon 10, and a developer. The shock wave transmitter 20 comprises an electrode cable 21 and an electrode probe 22, wherein the electrode cable 21 receives and conducts the voltage/current pulse, and the electrode probe 22 is electrically connected with the electrode cable 21 and used for receiving the voltage/current pulse to generate the shock wave. The energy of the shock wave can soften the calcified and hardened positions of the heart valves and the blood vessels or loosen the adhesive parts, and the shock wave does not affect and damage healthy and elastic tissues and only has a treatment effect on the calcified and hardened positions.

The balloon 10 is wrapped outside the shock wave emitter 20 and is provided with a through hole for electrolyte liquid to flow into, and the electrolyte liquid is used for conducting shock waves; in this embodiment, the balloon 10 has telescoping, collapsible, and insulating properties; the electrolyte liquid may be physiological saline, glycerin, or the like. The balloon 10 may be designed as a disposable or reusable consumable, which when used is sterilized prior to use.

The development member is located on the shock wave emitter 20 and/or the balloon 10. In this embodiment, the developing member can be observed in its position in the human body of the patient by an external developing apparatus (e.g., an X-ray imaging apparatus, etc.).

The target area to be treated may be calcified sites on the vessel wall, or the target area to be treated may also be sites of valve stenosis and regurgitated stiff leaflets or valve annuli. The saccule 10 can enter the way through the femoral artery until the saccule is contacted with a target area to be treated, shock waves generated by the shock wave emitter 20 are conducted to the target area to be treated through electrolyte liquid in the saccule 10, calcified parts in the target area to be treated are softened under the action of shock wave energy, the opening and closing state of valve leaflets during working is improved, and therefore the purposes of treating calcification, facilitating release of heart valves, accurate positioning and peripheral attachment of blood vessels and reducing peripheral leakage are achieved. Compared with the traditional medicine treatment, the treatment effect is remarkable; compared with the traditional mode of replacement by surgical operation or interventional operation, the shock wave device 100 has the advantages that the trauma to a patient is smaller, the time consumption is short, for example, the valve calcification possibly encountered in the operation process is serious, and the problem that a heart valve cannot be accurately placed is solved. In addition, the shock wave device 100 provided by the present application further includes a visualization member, which is located on the shock wave emitter 20 and/or the balloon 10, and can help a doctor precisely position the shock wave device 100, so as to ensure that the shock wave emitter 20 and/or the balloon 10 is treated in a target area to be treated.

In one embodiment, with continued reference to fig. 1, at least two balloons 10 are provided and are arranged in a circumferential array, with at least one electrode probe 22 disposed within each balloon 10. Because the sacculus 10 is provided with a plurality of sacculus 10, a plurality of sacculus 10 have the clearance of blood supply liquid, can guarantee to operate under the condition of unblocked blood. In addition, the plurality of electrode probes 22 can circumferentially treat calcified parts, thereby enhancing the effect. In this embodiment, the balloon 10 is provided with three, in other embodiments, the balloon 10 may also be provided with two, four, or more; in this embodiment, one electrode probe 22 is disposed within each balloon 10, and in other embodiments, there may be two, three, or more electrode probes 22 within the balloon 10.

The electrode probe 22 transmits the shock wave to the periphery through the electrolyte liquid, and in order to improve the effect of the electrode probe 22 on the calcified part, further, referring to fig. 1, the electrode probe 22 is bent outward toward the circumference where the balloon 10 array is located, so as to better act on the calcified part and shorten the treatment time. In other embodiments, the electrode probe 22 can be bent at any angle according to actual needs, and is not limited herein.

Wherein the diameter of the balloon is 6-10mm, such as 6mm, 8mm or 10mm, and the length of the balloon is 20-60mm, such as 20mm, 35mm, 40mm, 55mm or 60 mm. Preferably, the balloon has a diameter by length of 8mm by 40mm, 6mm by 40mm or 10mm by 40mm, at which specification the balloon is best used.

In another embodiment, referring to fig. 3, fig. 3 is a schematic view of a state of use of another embodiment of the shock wave device for treating calcification of a heart valve of the present application, in which one balloon 10 is provided, and the balloon 10 has a shape of "8", and the radial width of the balloon gradually decreases from one end connected with the shock wave emitter 20 to the other end not connected with the shock wave emitter 20 to the middle. At least two electrode probes 22 are arranged in the balloon 10 and are respectively positioned at two ends of the balloon 10 so as to respectively act on the inner wall and the outer end of the calcified valve 200. The 8-shaped flexible balloon 10 is positioned at the calcified valve 200, so that the fixation with the calcified valve 200 can be enhanced, and the displacement and over-expansion of the balloon 10 can be avoided. The electrode probe 22 inside the balloon 10 can directly clamp the calcified valve 200, and the generated shock wave can be fully contacted with the clamped calcified valve 200, so that the shock wave can better act on the calcified valve 200, and the operation time can be shortened. In addition, one, two, or more electrode probes 22 may be provided within the balloon 10. By controlling the number, frequency or duration of the electrode probes 22, the stenotic, rigid, adherent calcified structure of the valve is softened, and the treatment process can be completed quickly and effectively.

In one embodiment, with continued reference to FIG. 1, the visualization element includes an electrode probe 22, and the electrode probe 22 includes a material having a visualization effect such that it may be visualized by an X-ray imaging device or the like to assist the physician in positioning the shockwave device 100. The developing part further comprises developing rings 11, the developing rings 11 are located at two ends of the balloon 10, the developing rings 11 can be made of metal materials and the like, the developing rings 11 can be developed under the action of X-ray imaging equipment and the like, a doctor is better helped to accurately position the shock wave device 100, and the shock wave emitter 20 and/or the balloon 10 are ensured to be used for treating a target area to be treated. In other embodiments, the developing ring 11 may be formed in other shapes, such as a developing block fixed to the balloon 10.

In yet another embodiment, referring to fig. 1, the developer includes a developer mixed in an electrolyte liquid. The developing agent may be one commonly used in the art of medical technology, which can be developed in an X-ray developing device or a blood vessel imaging device DSA. The blood vessel imaging apparatus can monitor the amount of the electrolyte liquid in the balloon 10 by the developer when the balloon 10 is filled with the electrolyte liquid containing the developer, and stop filling the balloon 10 with the electrolyte liquid when the balloon 10 expands under the filling of the electrolyte liquid and clings to the blood vessel wall of the target area. In this way, on the one hand, the balloon 10 can be made to be as close as possible to the vessel wall, and on the other hand, the excessive filling of the electrolyte liquid in the balloon 10, which in turn can cause damage to the vessel wall, can be avoided.

In one embodiment, referring to FIG. 1, a shockwave device 100 of the present application further comprises a shockwave generator 40, a conducting system 30, and a conducting electrode 60. The shock wave generator 40 is connected to an external power source to generate voltage/current pulses. The conductive electrode 60 is located inside the conductive system 30, and has one end electrically connected to the shock wave generator 40 and the other end electrically connected to the electrode cable 21 of the shock wave emitter 20, so as to conduct the voltage/current pulse generated by the shock wave generator 40 to the shock wave emitter 20. Besides providing an extending path for the conductive electrode 60, the conductive system 30 is connected to the through hole of the balloon 10, so that the conductive system 30 is communicated with the inside of the balloon 10 and forms a sealed cavity, and the conductive system 30 is provided with a first hole through which external electrolyte liquid can flow into the conductive system 30 and then into the balloon 10.

Of course, in another embodiment, referring to fig. 4, a pipe 33 may be disposed at the first hole, and the pipe 33 may be only located outside the conducting system 30 and connected to the first hole, or the pipe 33 may extend from the outside of the conducting system 30 into the conducting system 30 along the first hole. Similarly, the electrolyte liquid in the balloon 10 can also flow out through the conduction system 30 and the first hole. The conductive system 30 may be formed of a flexible material that is stretchable, foldable, and insulative. The surface of the conducting system 30 is curved, for example, the conducting system 30 may be shaped as a sphere, such as a sphere, an ellipsoid, a convex sphere with curvature, or the like.

Further, the shock wave device 100 further includes a check valve 32, and the check valve 32 is disposed on a delivery path of the electrolyte liquid and is used for controlling on/off of the electrolyte liquid. In particular, a one-way valve may be provided on the above-mentioned conduit 33, thereby facilitating control by the medical staff.

In one embodiment, referring to fig. 1, the shockwave device 100 of the present application further comprises a guide tip 70, wherein the guide tip 70 is connected to an end of the balloon 10 away from the conduction system 30, and the guide tip 70 is tapered to provide a guide function for facilitating partial entry of the balloon 10 into a vessel or valve; and the tail end of the guide head end 70 is smooth and has no sharp corner, so that the blood vessel or the valve is prevented from being scratched.

Further, referring to fig. 1, the leading end 70 is made of a flexible material so as to have a certain variability capability and to bend with the shape of the blood vessel.

Further, referring to fig. 1, the shockwave device 100 of the present application further includes a reserve channel 80, the reserve channel 80 extending within the conduction system 30, within or between the balloon 10, and within the guide tip 70. An external wire or other suitable instrument may be passed through the channel 80 and, once the external wire enters the channel 80, the direction of advancement of the shockwave device 100 may be guided.

In another embodiment, as shown in fig. 4, fig. 4 is a schematic view of another embodiment of the shockwave device 100 for treating calcification of a heart valve of the present application in a use state, and the shockwave device further comprises a handle 90, so as to be suitable for an interventional treatment mode; the handheld shock wave device 100 may be designed to be used when a patient is to be treated surgically. In particular, the handle 90 may be connected to the exterior of the conduction system 30, for example by screwing or snapping. The handle 90 is held by the operator during the operation, and the handle 90 may be formed in an arc shape or the like for the operator to hold. In order to reduce the possibility of the handle 90 slipping, a concave-convex structure may be provided on the outside of the handle 90 or the roughness of the outer surface of the handle 90 may be increased to increase the contact area and the friction between the handle 90 and the human hand. The handle 90 is also connected with a connection joint 31, and the connection joint 31 is electrically connected with the conductive electrode 60 and is used for connecting the shock wave generator, thereby connecting the shock wave generator and the shock wave emitter 20.

In one embodiment, the handle 90 or shock wave generator 40 is further provided with a control switch system for adjusting the output of different current/voltage pulse intensities, repetition frequencies, and durations according to the calcification degree of the target region (e.g., valve leaflet, blood vessel, etc.) of the patient to be treated, further, a light source may be provided at the handle 90, and the L ED light source may be used for illumination during the operation.

In a specific implementation scenario, when the shockwave device 100 of the present application is used, the guiding tip 70 drives the balloon 10 into the human body to perform a guiding function; the health care professional can view the position of the visualization ring 11 through a visualization device (e.g., an X-ray visualization device, etc.) to position the shock wave device 100 at the target area to be treated.

Electrolyte liquid enters the balloon 10 through the conduction system 30, the shock wave generator 40 generates voltage/current pulses, the conduction system 30 conducts the voltage/current pulses to the shock wave emitter 20, the shock wave emitter 20 emits shock waves, and the electrolyte liquid conducts the shock waves to a target area to be treated; the developing member further includes a developer mixed in the electrolyte liquid, and the blood vessel imaging apparatus monitors the amount of the electrolyte liquid in the balloon 10, and stops filling the balloon 10 with the electrolyte liquid when the balloon 10 expands under the filling of the electrolyte liquid and clings to the blood vessel wall of the target area. In this way, on the one hand, the balloon 10 can be made to be as close as possible to the vessel wall, and on the other hand, the excessive filling of the electrolyte liquid in the balloon 10, which in turn can cause damage to the vessel wall, can be avoided.

After treatment is complete, the electrolyte fluid exits the balloon 10 and the shock wave device 100 is removed from the body.

The methods provided above are applicable to interventional and surgical procedures.

Taking the intervention operation as an example, the working process is as follows: the shock wave device 100 for treating the calcification of heart valves and blood vessels is delivered to the target area to be treated by a delivery system through a hemostatic valve, along the path of a pathway product, into the human body and under the action of the developing ring 11; under the action of a blood vessel imaging device DSA, the balloon 10 expands and clings to the blood vessel wall under the filling of electrolyte liquid containing a developer; turning on the control switch system, adjusting parameters, and starting the shock wave emitter 20 to work to emit shock waves to treat the target area to be treated; after the treatment is finished, electrolyte liquid containing a developing agent in the balloon 10 flows out of the balloon 10 so as to relieve the pressure of the balloon 10; the shockwave device 100 is withdrawn through the access product, completing the treatment procedure.

For example, the operation is as follows: after the patient opens the chest by means of a surgical operation, an incision is made on the apex of the heart, and a medical staff holds the shock wave device 100 to enter the heart along a pre-established access path and reach a target area to be treated under the action of the developing ring 11; under the action of a blood vessel imaging device DSA, the balloon 10 expands and clings to the blood vessel wall under the filling of electrolyte liquid containing a developer; turning on the control switch system, adjusting parameters, and starting the shock wave emitter 20 to work to emit shock waves to treat the target area to be treated; after the treatment is finished, electrolyte liquid containing a developing agent in the balloon 10 flows out of the balloon 10 so as to relieve the pressure of the balloon 10; the shockwave device 100 is withdrawn through the access product, completing the treatment procedure.

The above description is only an example of the present application and is not intended to limit the scope of the present application, and all modifications of equivalent structures and equivalent processes, which are made by the contents of the specification and the drawings, or which are directly or indirectly applied to other related technical fields, are intended to be included within the scope of the present application.

Claims (13)

1. A shock wave device for treating calcification of a heart valve, comprising:

the shock wave transmitter comprises an electrode cable and an electrode probe, wherein the electrode cable receives and conducts voltage/current pulses, and the electrode probe is electrically connected with the electrode cable and used for receiving the voltage/current pulses to generate shock waves;

the balloon is wrapped outside the shock wave emitter and is provided with a through hole for electrolyte liquid to flow into, and the electrolyte liquid is used for conducting the shock wave;

a visualization member located on the shock wave emitter and/or the balloon.

2. The device of claim 1, wherein the balloon is provided with one, the radial width of which is gradually reduced from the end connected with the shock wave emitter and the end not connected with the shock wave emitter to the middle part; at least two electrode probes are arranged in the saccule and are respectively positioned at two ends of the saccule so as to respectively act on the inner wall and the outer end of the calcified valve.

3. The device of claim 1, wherein the balloons are provided in at least two and circumferential arrays, and wherein at least one of the electrode probes is disposed within each of the balloons.

4. The apparatus of claim 3, wherein the electrode probe is curved outward of a circumference in which the balloon array is located.

5. The device of claim 3, wherein the balloon has a diameter of 6-10mm and a length of 20-60 mm.

6. The apparatus according to any one of claims 1 to 5, wherein the developing member includes the electrode probe including a material having a developing action; and/or the presence of a gas in the gas,

the developing part comprises developing rings, and the developing rings are positioned at two ends of the saccule.

7. The apparatus of any one of claims 1-5, comprising:

the shock wave generator is connected with an external power supply to generate the voltage/current pulse;

the conduction system is connected with the through hole of the balloon and is used for conducting the electrolyte liquid, so that the electrolyte liquid is circulated in the conduction system and the balloon;

and the conducting electrode is positioned in the conducting system, one end of the conducting electrode is connected with the shock wave generator, and the other end of the conducting electrode is connected with the shock wave emitter so as to receive and conduct the voltage/current pulse.

8. The apparatus of claim 7, comprising:

the guide head end is connected to one end, far away from the conduction system, of each sacculus, and the guide head end is conical, smooth in tail end and free of sharp corners.

9. The device of claim 8, wherein the guide tip is a flexible material.

10. The apparatus of claim 8, comprising:

a reserve channel extending inside the conduction system, inside or between the balloons, and inside the guide head.

11. The apparatus of claim 7, comprising:

a handle connected to an exterior of the conduction system.

12. The apparatus of claim 1, comprising:

and the one-way valve is arranged on the conveying path of the electrolyte liquid so as to control the on-off of the electrolyte liquid.

13. The apparatus according to claim 1, wherein said developing member includes a developer, said developer being mixed in said electrolytic liquid.

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