CN214805306U

CN214805306U - A balloon and ablation device for cardiac surgery

Info

Publication number: CN214805306U
Application number: CN202120445204.1U
Authority: CN
Inventors: 杨士伟; 贾德安; 胡宾; 周玉杰
Original assignee: Beijing Anzhen Hospital
Current assignee: Beijing Anzhen Hospital
Priority date: 2021-03-02
Filing date: 2021-03-02
Publication date: 2021-11-23
Anticipated expiration: 2031-03-02

Abstract

The utility model relates to a balloon and an ablation device for cardiac surgery. The ablation device includes a catheter device and a balloon. The balloon comprises a capsule, which is covered to form a closed balloon body; an elastically deformable expansion structure arranged in the balloon body; wherein the balloon body is in a long strip when it is retracted into the tube sleeve. In the retracted state, the balloon is in a dumbbell-shaped expanded state when the sleeve is extended, and the balloon body forms a thin waist when in the expanded state. The dumbbell-shaped balloon of the utility model forms a thin waist after being expanded in the extended state, so that it can be easily stuck and fixed in the atrial septal wall hole between the left and right atria, and the operation is convenient for the operation; the balloon and ablation of the utility model The device supports liquid nitrogen filling, and the support strip structure is reinforced on the balloon membrane, so that the liquid nitrogen can not be leaked when the balloon is extended to form a thin waist and retracted into the hose.

Description

Balloon for cardiac surgery and ablation device

Technical Field

The utility model belongs to the technical field of medical instrument, especially, relate to a sacculus and ablation device for cardiac operation.

Background

With the advancement of medical technology, the related art of cardiac surgery has rapidly developed. For patients with heart failure, the pressure of the left atrium and blood cannot be released to the right atrium by themselves, at present, instruments are used for expansion, however, tissues can be contractured after the instruments are withdrawn, so that the expanded part is retracted, and the expansion effect is poor. In the operation using the ablation mode, the cooling liquid can perform frostbite on the tissue to form aseptic tissue necrosis, and the necrotic part can form permanent wounds. The method is used in cardiac operation to form permanent wound on the interatrial septum between the left atrium and the right atrium, and the pressure (blood) in the left atrium is released from the wound to the right atrium, so as to achieve the purpose of treatment. However, no relevant apparatus can achieve the above function at present, and during calcification of the atrial septal wall of the heart of a patient, the apparatus can slide up and down or left and right in a wound of the atrial septal wall, and is difficult to fix.

SUMMERY OF THE UTILITY MODEL

The utility model provides a sacculus and ablation device for cardiac operation aims at solving one of the technical problem that exists among the prior art at least.

The technical scheme of the utility model an aspect is a sacculus for cardiac surgery, it includes: a capsule membrane, which is coated to form a closed capsule body; an elastically deformable expandable structure disposed within the balloon; the balloon body is in a long strip-shaped retraction state when being retracted into the pipe sleeve and is in a dumbbell-shaped expansion state when being extended out of the pipe sleeve, and a slender waist part is formed when the balloon body is in the expansion state.

Further, the capsule membrane can be a single layer or a double layer.

Further, the balloon includes: and the supporting strips are uniformly distributed and fixed on the membrane wall of the capsular sac, wherein the length directions of the supporting strips are consistent with the length direction of the sac body.

Further, each of the support bars includes an elongated portion and a short and thick portion, wherein the short and thick portions are disposed at a central position of the balloon body where the thin waist portion is to be formed in the expanded state, and the elongated portions are disposed at both sides of the short and thick portions.

Furthermore, the supporting strip and the capsule membrane are integrally formed by injection molding, and the supporting strip is formed on the inner wall of the capsule body.

Further, the capsule membrane material is selected from polyimide, polytrifluorochloroethylene or ultra-high molecular weight polyethylene.

Furthermore, the expansion structure comprises a plurality of metal wires which are woven along the length direction of the bag body and can be expanded elastically, and the plurality of metal wires form an encircling shape at the extending end of the bag body.

Further, the expansion structure comprises a restraining ring which is arranged at the middle position of the thin waist part of the balloon body to be formed in the expansion state and is used for binding the plurality of metal wires.

The technical scheme on the other hand of the utility model is an ablation device for cardiac surgery, including catheter device and foretell balloon for cardiac surgery.

Further, the catheter device comprises: a flexible tube sleeve; the tail end of the outer sheath tube is hermetically connected with a balloon membrane at one end of the balloon; the end part of the inner sheath tube, which extends out of the outer sheath tube, is hermetically connected with the balloon membrane at the other end of the balloon; the guide wire is arranged in the inner sheath tube, and the tail end of the guide wire is provided with a sharp part; the guide wire can move in the length direction of the inner sheath, and the sharp part of the guide wire can extend out of the end part of the inner sheath.

Further, the ablation device further comprises: a steering end for the guide wire, the steering end being located at an end of the sheath remote from the balloon; and the liquid injection port is communicated with a channel between the outer sheath tube and the inner sheath tube.

The utility model has the advantages that:

the dumbbell-shaped saccule of the utility model forms a slender waist after being expanded in an extending state, thereby being easy to be clamped and fixed at the wound of the atrial septal wall between the left atrium and the right atrium, and providing convenient operation for the operation; the balloon and the ablation device of the utility model support liquid nitrogen filling, so that the tissue at the thin waist of the balloon is frostbitten to form a permanent wound; the expansion structure is matched with the balloon to form a dumbbell shape when the balloon is expanded, so that a thin waist part appears; the supporting strip structure is reinforced on the balloon membrane, so that liquid nitrogen can be prevented from leaking when the balloon extends out to form a thin waist part and retracts to a hose, and the inside of the balloon is protected from being abraded by the expansion structure; the pipe sleeve adopts a sleeve structure of an inner sheath pipe and an outer sheath pipe and a sealing connection mode of the inner sheath pipe and the outer sheath pipe and the balloon, and can be matched with each other to realize the conveying of liquid nitrogen and realize the movement of the balloon driven by the guide wire.

Drawings

Fig. 1 is a general schematic view of a balloon and ablation device in accordance with an embodiment of the present invention.

Fig. 2 is a schematic view of a balloon in a semi-retracted state according to an embodiment of the present invention.

Fig. 3 is a schematic view of a balloon in a fully expanded state according to an embodiment of the present invention.

Fig. 4 is a schematic view of a support strip with a balloon in a fully expanded state according to an embodiment of the present invention.

Fig. 5 and 6 are cross-sectional views of the balloon of fig. 4 in positions a and B, respectively.

Fig. 7 is a cross-sectional view of a balloon in a semi-retracted state in accordance with an embodiment of the present invention.

Fig. 8 is a cross-sectional view of a balloon in a fully expanded state according to an embodiment of the present invention.

Fig. 9-12 are exemplary illustrations of a balloon and ablation device in use in surgery, according to an embodiment of the present invention.

Detailed Description

The conception, specific structure and technical effects of the present invention will be described clearly and completely with reference to the accompanying drawings and embodiments, so as to fully understand the objects, aspects and effects of the present invention. It should be noted that the embodiments and features of the embodiments in the present application may be combined with each other without conflict.

It should be noted that, unless otherwise specified, when a feature is referred to as being "fixed" or "connected" to another feature, it may be directly fixed or connected to the other feature or indirectly fixed or connected to the other feature. Furthermore, the description of the upper, lower, left, right, top, bottom, etc. used in the present invention is only relative to the mutual position relationship of the components of the present invention in the drawings.

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

It will be understood that, although the terms first, second, third, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element of the same type from another. For example, a first element could be termed a second element, and, similarly, a second element could be termed a first element, without departing from the scope of the present disclosure.

Referring to fig. 1-3, in some embodiments, an ablation device for cardiac surgery according to the present invention includes a catheter device 200 and a balloon 100. The balloon 100 includes a membrane 110, and the membrane 110 is wrapped to form a closed balloon body. Referring to fig. 2 and 3, the bladder is in an elongate retracted state when received in sleeve 201. In an expanded state of a dumbbell-type shape when extended out of the cuff 201, and the balloon forms a waisted portion 140 in the expanded state.

Referring to fig. 4, in one embodiment, balloon 100 includes: a plurality of support bars 120 uniformly distributed on the membrane wall of the capsular sac 110, wherein the length direction of the plurality of support bars 120 coincides with the length direction of the balloon body. Each stay 120 may include an elongated portion 121 and a short and thick portion 122, wherein the short and thick portion 122 is disposed at a middle position of the balloon where the thin waist portion 140 is to be formed in the expanded state, and the elongated portion 121 is disposed at both sides of the short and thick portion 122. Because the thick and short portions 122 are closely arranged on the peripheral wall of the balloon body, the expanded diameter (as shown in fig. 5) of the thin waist portion 140 of the balloon 100 is smaller than the expanded diameter (as shown in fig. 6) of the rest of the balloon membranes 110 where the thin and long portions 121 are arranged, and the thin waist portion 140 in the expanded state is protected, so that the expansion structure 130 is prevented from wearing the balloon body, and the cooling liquid (such as liquid nitrogen) in the balloon 100 is prevented from leaking. Preferably, the size of the balloon 100 at the middle waistline may be in the range of 6-16 mm.

The support band 120 and the membrane 110 may be integrally injection molded, and the support band 120 is formed on the inner wall of the capsule body. This allows the outer wall of the balloon 110 to be smoothly retracted into or extended out of the sheath 201, and allows the outer wall of the balloon 110 to be more easily and smoothly withdrawn from the opening in the atrial septum 310 of the heart 300 during surgery.

In a preferred embodiment, an ablation device and balloon 110 according to the present invention are injected with liquid nitrogen, and the material of balloon 110 includes: polyimide, Polychlorotrifluoroethylene (PCTFE), or ultra high molecular weight polyethylene (UPE). At normal pressure, the liquid nitrogen temperature was-196 ℃. The polyimide can be used for a long time at the temperature of below 200 ℃ below zero. PCTFE has an outstanding low temperature resistance, does not crack or creep in liquid nitrogen, and can be used under a certain condition at a temperature close to absolute zero (-273 ℃). The minimum working temperature of UPE can reach 200 ℃ below zero, and the UPE is low-temperature resistant and has ductility under liquid nitrogen. The above materials are harmless to human body. In addition, a double-layer capsule 110 structure can be adopted, and the leakage-proof safety is improved.

Referring to fig. 7 and 8, balloon 100 includes an expandable structure 130 disposed within the balloon that is capable of elastic deformation and adjustment. The expandable structure 130 includes a plurality of elastically expandable wires 131 woven in the length direction of the balloon, and the plurality of wires 131 form a loop 133 at the extended end of the balloon. The stent 130 further comprises a constraining loop 132, the constraining loop 132 binding the plurality of wires 131 at a central location of the balloon that is to form a thin waist 140 in the expanded state. The hoops 133 and the constraining rings 132 allow the balloon 100 to be pre-expanded into a dumbbell shape by the expandable structure 130 as it extends from the cuff 201, and can continue to maintain a stable shape. By controlling the size of the constraining loops 132 of the expandable structure 130, the size of the waisted portion 140 of the balloon 100 can be adjusted so that the diameter of the waist 140 in the middle can be in the range of 10-40 mm.

In the preferred embodiment, the expansion and contraction of the expandable structure 130 is controlled by a single continuous wire having one end connected to the plurality of wires 131 and the other end passing out of the inner sheath 220 along with the guidewire 230. When an operator pulls the full-length metal wire outwards, the full-length metal wire drives the plurality of metal wires 131 to move towards the pipe sleeve 201, so that the pipe sleeve 201 can be retracted, and meanwhile, the volume or the expansion degree is reduced, so that the balloon 100 is contracted; when an operator pushes the full-length metal wire inwards, the full-length metal wire pushes the plurality of metal wires 131 to move towards the outside of the tube sleeve 201, and then the metal wires can extend out of the tube sleeve 201, and meanwhile, the volume or the expansion degree is increased, and the expansion structure 130 is increased, so that the balloon 100 is expanded into a dumbbell shape.

Referring now back to fig. 1, 4-6, in one embodiment, a catheter device 200 includes: a flexible tube sleeve 201; an outer sheath 210 arranged inside the sheath 201, wherein the end of the outer sheath 210 is hermetically connected with the balloon membrane 110 at one end of the balloon 100; an inner sheath tube 220 disposed inside the outer sheath tube 210, wherein the end of the inner sheath tube 220 extending out of the outer sheath tube 210 is hermetically connected with the capsular 110 at the other end of the balloon 100, i.e. the end of the inner sheath tube 220 is located inside the capsular 110; a guide wire 230 disposed inside the inner sheath 220, the guide wire 230 having a sharp portion 231 at a distal end thereof, the sharp portion 231 being capable of extending out of or retracting into the capsular sac 110; a steering end 240 for said guide wire 230, the steering end 240 being located at an end of the sheath 201 remote from the balloon 100; a liquid injection port 250, the liquid injection port 250 being communicated with the passage between the outer sheath tube 210 and the inner sheath tube 220; the guide wire 230 is movable in the longitudinal direction of the inner sheath 220, and the sharp portion 231 of the guide wire 230 can protrude from the end of the inner sheath 220.

With reference to fig. 5 and 6, specifically, the balloon 100 is disposed near the free end of the head of the outer sheath 210, the inner sheath 220 is disposed inside the outer sheath 210, the inner sheath 220 also penetrates through the balloon 100 and then penetrates out from the top end of the balloon 100, and the inner sheath 220 is not communicated with the inside of the outer sheath 210; the inner sheath 220 is internally penetrated by a guide wire 230, liquid nitrogen is injected into the outer sheath 210 through the liquid injection port 250, the liquid nitrogen flows through a passage between the outer sheath 210 and the inner sheath 220, and the liquid nitrogen flows into the balloon 100, so that the balloon 100 is expanded to a required size, and meanwhile, the liquid nitrogen does not enter the inner sheath 220.

The use of the balloon 100 and ablation device according to the present invention in surgery is described below by way of an example of use in fig. 9-12 to help understand the structure described in the above embodiments and the prominent substantial technical effect that results.

Referring to fig. 9, the free end of the catheter device 200 is extended into the left atrium of the heart 300.

Referring to fig. 10, at the manipulating end 240, the guide wire 230 is manipulated to move in the inner sheath 220 in the direction of the free end, so that the sharp portion 231 protrudes out of the balloon 100 and pierces the atrial septum 310 between the left atrium and the right atrium, thereby forming a wound.

Referring to fig. 11, the guide wire 230 pulls/leads the sheath 210 and the balloon 100 to penetrate into the wound, when the thin waist of the balloon 100 moves to the atrial septum wall 310, the movement is stopped, liquid nitrogen is filled into the balloon 100 through the liquid filling port 250, and simultaneously the balloon 100 is inflated under the action of the expansion structure 130 and the liquid nitrogen is filled, and the two ends and the thin waist 140 of the balloon 100 are inflated to the required size.

Referring to fig. 12, the thin waist 140 of the dumbbell-shaped balloon 100 is stuck between the left atrium and the right atrium, and after filling liquid nitrogen, the surrounding tissue is frozen and necrotized (aseptic tissue necrosis), forming permanent holes and calcified tissue 311. After a few minutes, the liquid nitrogen is pumped out, the balloon 100 is deflated, and the sheath 210 is removed as a whole. At the moment, a permanent wound is formed between the left atrium and the right atrium, and the pressure (blood) of the left atrium is released from the wound to the right atrium, so that the blood pressure of the two atria is balanced, and the treatment purpose is achieved.

The foregoing is merely a preferred embodiment of the present invention, and the present invention is not limited to the above embodiment, as long as the technical effects of the present invention are achieved by the same means, and any modifications, equivalent substitutions, improvements and the like made within the spirit and principle of the present disclosure should be included within the scope of the present disclosure. All belong to the protection scope of the utility model. The technical solution and/or the embodiments of the invention may be subject to various modifications and variations within the scope of the invention.

Claims

1. a balloon for cardiac surgery, characterized in that, comprising:

a capsule (110), the capsule (110) is coated to form a closed capsule;

an elastically deformable expansion structure (130) disposed in the balloon body;

Wherein, the balloon body is in an elongated retracted state when the tube sleeve (201) is received, and is in a dumbbell-shaped expansion state when the tube sleeve (201) is extended, and the balloon body is formed in the expanded state. Thin waist (140).

2. The balloon for cardiac surgery according to claim 1, wherein the balloon (100) comprises:

A plurality of evenly distributed support bars (120) fixed on the membrane wall of the capsule membrane (110), wherein the length directions of the plurality of support bars (120) are the same as the length directions of the capsule body Consistent.

3. The balloon for cardiac surgery according to claim 2, wherein

Each of the support bars (120) includes an elongated portion (121) and a short thick portion (122), wherein the short thick portion (122) is arranged at the thin waist portion (122) of the balloon body to be formed in the expanded state. 140), the elongated part (121) is arranged on both sides of the thick and short part (122).

4. The balloon for cardiac surgery according to claim 3, wherein

The support bar (120) and the bladder membrane (110) are integrally formed by injection molding, and the support bar (120) is formed on the inner wall of the bladder body.

5. The balloon for cardiac surgery according to claim 1, wherein

The material of the capsule film (110) is selected from polyimide, polychlorotrifluoroethylene or ultra-high molecular weight polyethylene.

6. The balloon for cardiac surgery according to claim 1, wherein

The expansion structure (130) includes a plurality of elastically expandable metal wires (131) woven along the length direction of the balloon body, and the plurality of metal wires (131) are stretched on the balloon body. The outgoing end forms an embracing shape (133).

7. The balloon for cardiac surgery according to claim 6, wherein the expansion structure (130) comprises a constraining ring (132), and the constraining ring (132) is provided on the side of the balloon body The middle position of the thin waist portion (140) to be formed in the expanded state is used for binding the plurality of metal wires (131).

8. An ablation device for cardiac surgery, characterized by comprising a catheter device (200) and the cardiac surgery balloon (100) according to any one of claims 1 to 7.

9. The ablation device for cardiac surgery according to claim 8, wherein the catheter device (200) comprises:

A flexible sleeve (201);

an outer sheath tube (210) disposed inside the tube sleeve (201), the end of the outer sheath tube (210) being sealedly connected with the capsule (110) at one end of the balloon (100);

The inner sheath tube (220) is arranged inside the outer sheath tube (210), the end of the outer sheath tube (210) extended from the inner sheath tube (220) and the other end of the balloon (100). The capsule (110) is sealingly connected;

a guide wire (230) arranged inside the inner sheath tube (220), the end of the guide wire (230) is provided with a sharp part (231);

Wherein, the guide wire (230) can move in the length direction of the inner sheath tube (220), and the sharp part (231) of the guide wire (230) can move from the end of the inner sheath tube (220) Department extends.

10. The ablation device for cardiac surgery according to claim 9, further comprising:

a manipulation end (240) for the guide wire (230), the manipulation end (240) being located at one end of the sleeve (201) away from the balloon (100);

A liquid injection port (250), the liquid injection port (250) communicates with the channel between the outer sheath tube (210) and the inner sheath tube (220).