CN217246176U - Novel sacculus catheter subassembly - Google Patents

Novel sacculus catheter subassembly Download PDF

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Publication number
CN217246176U
CN217246176U CN202220850062.1U CN202220850062U CN217246176U CN 217246176 U CN217246176 U CN 217246176U CN 202220850062 U CN202220850062 U CN 202220850062U CN 217246176 U CN217246176 U CN 217246176U
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balloon
sub
main
channel
filling
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白会新
牛兴慧
褚晓莉
刘升华
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Beijing Yingxing Medical Technology Co ltd
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Beijing Yingxing Medical Technology Co ltd
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Abstract

The utility model discloses a novel saccule conduit assembly, which comprises a first conduit seat (1), a second conduit seat (2) and an outer conduit (4); a Y-shaped balloon (5) fixedly connected with the outer tube (4) is arranged at the far end of the outer tube (4), one end of a main balloon part of the Y-shaped balloon (5) is fixedly connected with the outer tube (4) and is communicated with the inside of the outer tube, the middle section of the main balloon part is forked and is internally provided with a separation membrane, and the separation membrane divides the far end inner side of the main balloon part into a first sub balloon (53) and a second sub balloon (54) which are independent of each other; the main balloon part, the first sub-balloon (53) and the second sub-balloon (54) are hermetically separated from each other. Adopt the utility model discloses, when the blood vessel that contains calcified plaque to blood vessel bifurcation position carries out the pre-expansion, can make Y type sacculus and branching vascular shape phase-match, realize vascular pre-expansion simultaneously fast to effectively shorten the operation time.

Description

Novel sacculus catheter subassembly
Technical Field
The utility model relates to the technical field of medical equipment, especially, relate to a novel sacculus pipe subassembly.
Background
Stroke, also known as stroke or cerebrovascular Accident (CVA), is an acute cerebrovascular disease, and belongs to a group of diseases in which Cerebral tissues are damaged due to sudden rupture of Cerebral vessels or blood failure to flow into the brain caused by vessel occlusion, including ischemic and hemorrhagic stroke.
The investigation shows that the number of people dying due to cerebral apoplexy exceeds the number of tumor and cardiovascular diseases every year in China, and the death is the first cause. Treatment in the acute phase is of paramount importance for the prognosis of stroke patients. The traditional treatment methods mainly comprise drug treatment and surgical treatment. However, the intracranial blood vessels have a complex structure, so that the treatment means has great limitations, and the treatment effect is poor.
With the rapid development of interventional therapy, the interventional therapy technology of intracranial vascular diseases is more and more advanced, and for example, the method of intracranial vascular stent formation and the like is utilized to bring great benefits to patients.
However, the blood vessel with a bifurcation part is often encountered in the operation process, when the calcified plaque is positioned at the bifurcation part of the blood vessel, when the blood vessel at the bifurcation part is pre-dilated by using the balloon dilatation catheter, the calcified plaque at the bifurcation part can not be pre-dilated simultaneously by using the conventional balloon dilatation catheter. Therefore, a high technical requirement is put on a new balloon dilatation catheter, which not only needs to have good delivery performance and retraction performance, but also needs to be capable of pre-dilating calcified plaques of blood vessels at bifurcation sites, but no suitable special balloon catheter product is available in the industry at present.
SUMMERY OF THE UTILITY MODEL
In view of this, the main objective of the present invention is to provide a novel balloon catheter assembly for pre-dilating a blood vessel when treating or removing a lesion tissue at a bifurcated blood vessel site, so as to enable a subsequent interventional operation to be performed more smoothly.
In order to achieve the above purpose, the technical scheme of the utility model is as follows:
a novel saccule catheter assembly comprises a first tube seat, a second tube seat and an outer tube; the far end of the outer tube is provided with a Y-shaped balloon fixedly connected with the outer tube, one end of a main balloon part of the Y-shaped balloon is fixedly connected with the outer tube and is communicated with the inside of the outer tube, the middle section of the main balloon part is forked and is internally provided with a separation membrane, and the separation membrane divides the far end inner side of the main balloon part into a first sub-balloon and a second sub-balloon which are independent respectively; the main balloon part, the first sub-balloon and the second sub-balloon are hermetically separated from each other.
A novel saccule catheter assembly comprises a first tube seat, a second tube seat and an outer tube; a first channel and a second channel are arranged inside the outer tube; the far end of the outer tube is provided with a Y-shaped balloon fixedly connected with the outer tube, one end of a main balloon part of the Y-shaped balloon is fixedly connected with the outer tube and is communicated with the inside of the outer tube, the middle section of the main balloon part is forked and is internally provided with a separation membrane to divide the outer side of the main balloon part into a first main balloon and a second main balloon which are respectively sealed; the separation film separates and seals the insides of the opposite sides of the first main balloon and the second main balloon at the bifurcation part to form a first sub balloon and a second sub balloon; the first channel provides an inflation medium channel and a guide wire channel for the first main balloon or/and the first sub balloon through the first inner tube; the second channel provides an inflation medium channel and a guide wire channel for the second main balloon or/and the second sub balloon through the second inner tube.
Wherein: and one end of the outer pipe, which is close to the first pipe seat and the second pipe seat, is surrounded by a protective sleeve, and the protective sleeve is fixedly connected with the contact part of the outer pipe.
The outer diameter of the protective sleeve close to one end of the first pipe seat and one end of the second pipe seat gradually changes slightly to be larger than the outer diameter of the fixed connection position of the outer pipe.
The first inner tube comprises a first filling channel and a first guide wire channel, and the first filling channel and the first guide wire channel are arranged at intervals along the axial direction of the first inner tube and are not communicated with each other; the second inner tube comprises a second filling channel and a second guide wire channel, and the second filling channel and the second guide wire channel are arranged in a spaced mode in the axial direction of the second inner tube and are not communicated with each other.
The first wire guide channel of the first inner tube is communicated with the inside of the first wire guide seat of the first tube seat at the near end, and the first wire guide channel of the first inner tube penetrates through the first main balloon or/and the first sub balloon at the far end and penetrates through the first sub balloon leg to be communicated with the outside;
the second wire guide channel of the second inner tube is communicated with the inside of the second wire guide seat of the second tube seat at the near end, and the second wire guide channel of the second inner tube penetrates through the second main balloon or/and the second sub balloon at the far end and is communicated with the outside after penetrating through the second sub balloon leg.
The first filling channel of the first inner tube is communicated with the interior of the first filling seat of the first tube seat at the proximal end, and the first filling channel is communicated with the interior of the first main balloon or/and the first sub balloon through a first filling opening and/or a second filling opening which are/is arranged in the Y-shaped balloon at the distal end;
the second filling channel of the second inner tube is communicated with the inside of the second filling seat of the second tube seat at the near end, and the second filling channel is communicated with the inside of the second main balloon or/and the second sub balloon through a third filling opening and/or a fourth filling opening which are/is arranged in the Y-shaped balloon at the far end.
The developing device is characterized in that a first developing mark is arranged at the fixed connection position of a main balloon leg and the outer tube in the Y-shaped balloon, a third developing mark is arranged at the tail end of a first sub-balloon in the Y-shaped balloon, namely near a third sub-balloon leg, and a second developing mark is arranged at the tail end of a second sub-balloon in the Y-shaped balloon, namely near the second sub-balloon leg.
In the filling state, the diameter of the main balloon part of the Y-shaped balloon is larger than the diameters of the first sub-balloon and the second sub-balloon.
In the filling state, the included angle alpha between the first sub-balloon and the second sub-balloon ranges from 10 degrees to 60 degrees.
In the filling state, the diameter range of the main balloon part is 4-10 mm, and the diameter ranges of the first sub-balloon and the second sub-balloon are 2-5 mm.
The main balloon leg of the Y-shaped balloon is welded and fixed with the outer tube; and two first sub-balloon legs and two second sub-balloon legs of the first sub-balloon and the second sub-balloon are respectively welded and fixed with the far end of the first inner tube and the far end of the second inner tube.
The Y-shaped balloon is a non-compliant balloon.
A method of manufacturing a novel balloon catheter assembly comprising:
respectively processing a tube seat group, an outer tube and a Y-shaped balloon of the balloon catheter assembly, arranging a separation membrane to separate the far-end inner side of a main balloon part into a first sub-balloon and a second sub-balloon which are independent of each other, and hermetically separating the main balloon part from the first sub-balloon and the second sub-balloon;
and welding and fixing one end of the outer tube and the Y-shaped saccule, and respectively welding and fixing two first sub-saccule legs and two second sub-saccule legs of the first sub-saccule and the second sub-saccule with the far end of the first inner tube and the far end of the second inner tube in the Y-shaped saccule.
A method of manufacturing a novel balloon catheter assembly comprising:
respectively processing a tube seat group, an outer tube and a Y-shaped balloon of the balloon catheter assembly, arranging a separation film at a main balloon part of the Y-shaped balloon, respectively arranging a first main balloon and a second main balloon which are hermetically separated from each other at the outer side of the main balloon part, arranging a separation film to separate the inner side of the far end of the main balloon part into a first sub balloon and a second sub balloon which are independent from each other, and hermetically separating the first main balloon, the second main balloon, the first sub balloon and the second sub balloon from each other;
and welding and fixing one end of the outer tube and the Y-shaped saccule, and respectively welding and fixing two first sub-saccule legs and two second sub-saccule legs of the first sub-saccule and the second sub-saccule with the far end of the first inner tube and the far end of the second inner tube in the Y-shaped saccule.
The utility model discloses a novel sacculus pipe subassembly has following beneficial effect:
in intracranial vascular stent plasty, use the utility model discloses a novel sacculus catheter subassembly when the blood vessel that contains calcified plaque to blood vessel bifurcation position carries out pre-expansion, can make Y type sacculus and branching blood vessel shape phase-match, can realize vascular pre-expansion simultaneously fast to effectively shorten operation time.
Drawings
Fig. 1 is a schematic structural view of a novel balloon catheter assembly according to an embodiment of the present invention;
fig. 2 is a partial cross-sectional view of a novel balloon catheter assembly according to an embodiment of the present invention;
fig. 3 is a cross-sectional view of a Y-shaped balloon of the novel balloon catheter assembly of the present invention;
fig. 4 is a schematic sectional view along the direction a-a of the novel balloon catheter assembly according to the present invention;
fig. 5 is a schematic view of an outer tube structure of the novel balloon catheter assembly according to the embodiment of the present invention;
fig. 6 is a schematic view of a first inner tube structure of the novel balloon catheter assembly according to an embodiment of the present invention;
fig. 7 is a schematic structural view of a Y-shaped balloon of the novel balloon catheter assembly according to an embodiment of the present invention;
fig. 8 is a schematic structural view of the novel balloon catheter assembly according to the embodiment of the present invention in a state where the balloon is not inflated;
FIG. 9 is a schematic view of a vascular structure of a bifurcation site with calcified plaque according to an embodiment of the present invention;
FIG. 10 is a schematic view of the guide wire feeding process in interventional operation using the novel balloon catheter assembly of the present invention;
fig. 11 is a schematic view of a balloon catheter delivery process during an interventional procedure using the novel balloon catheter assembly of the present invention;
FIG. 12 is a schematic view showing the balloon catheter being transported in place during an interventional procedure using the novel balloon catheter assembly of the present invention;
fig. 13 is a schematic view of the balloon filling after the novel balloon catheter assembly of the present invention is applied to an interventional operation.
[ main component/part symbol description ]
1: first stem 11: first guide wire holder 111: first guide wire 12: first filling seat
2: second stem 21: second guide wire holder 211: second guide wire 22: second filling seat
3: and (4) protective sleeve: outer tube 41: first passage 42: the second channel
5: y-shaped balloon 51: main balloon leg 52: first main balloon 52': the second main ball bag
53: first sub-balloon 54: second sub-balloon 55: first partial balloon leg 55': second sub-saccule leg
6: first inner pipe 61: first filling passage 62: first guidewire channel 611: first filling opening
612: second filling opening
7: second inner tube 71: second filling passage 72: second guidewire channel 711: third filling opening
712: fourth filling opening
81: first development mark 82: second development mark 83: and a third development mark.
Detailed Description
The present invention will be described in further detail with reference to the accompanying drawings and embodiments of the present invention.
For a more complete description and illustration of the embodiments of the present invention, reference is made to one or more of the accompanying drawings, and additional details or examples used to describe the figures are not intended to limit the scope of any of the inventive concepts of the present application, the presently described embodiments, or the preferred versions thereof. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terminology used in the description of the invention herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention.
It should be noted that the drawings are simplified form to assist in illustrating the objects of the embodiments of the present invention. The term "proximal" as used herein generally refers to a direction proximal to an operator of a balloon catheter assembly; "distal" refers to a direction away from the operator of the balloon catheter assembly.
Fig. 1 is a schematic structural view of the novel balloon catheter assembly according to an embodiment of the present invention. Fig. 2 is a partial cross-sectional view of a novel balloon catheter assembly according to an embodiment of the present invention. Fig. 3 is a cross-sectional view of the Y-shaped balloon of the novel balloon catheter assembly of the embodiment of the present invention. Fig. 4 is a schematic view of a cross-sectional structure along direction a-a of the novel balloon catheter assembly according to an embodiment of the present invention. Fig. 5 is a schematic view of an outer tube structure of the novel balloon catheter assembly according to an embodiment of the present invention. Fig. 6 is a schematic view of a first inner tube structure of the novel balloon catheter assembly according to an embodiment of the present invention.
As shown in fig. 1, the novel balloon catheter assembly comprises: the device comprises a first tube holder 1, a second tube holder 2, a protective sleeve 3, an outer tube 4, a Y-shaped balloon 5, a first inner tube 6 and a second inner tube 7. The first tube holder 1 and the second tube holder 2 are arranged at one end of the saccule catheter component and are called a tube holder group.
Wherein, two channels, namely a first channel 41 and a second channel 42, are arranged in the outer tube 4, and the cross section of the channels is circular or oval, preferably circular. The first channel 41 and the second channel 42 are symmetrically disposed on two sides of the axial section inside the outer tube 4 (see fig. 5).
In the first passage 41 and the second passage 42, a first inner tube 6 and a second inner tube 7 are respectively arranged (refer to fig. 4). The first inner tube 6 and the second inner tube 7 are symmetrically distributed in the first channel 41 and the second channel 42 of the outer tube 4, respectively (refer to fig. 4). The first inner pipe 6 and the second inner pipe 7 have the same structure, and the cross sections of the first inner pipe and the second inner pipe are circular. A first filling channel 61 and a first guide wire channel 62 are respectively arranged in the first inner tube 6 (refer to fig. 4 and 6); a second filling channel 71 and a second guide wire channel 72 are arranged in the second inner tube 7 (refer to fig. 4). The cross section of the first guide wire channel 62 and the second guide wire channel 72 is circular, so that guide wires can smoothly pass through the guide wire channels; the cross-sectional shapes of the first filling channel 61 and the second filling channel 71 are crescent or oval (please refer to fig. 4 and fig. 6), which not only can provide a pipeline for the filling medium to pass through the filling channels, but also ensures that the pipe wall provides a certain supporting function for the circulation of the filling medium.
In the present embodiment, the first pipe socket 1 is fixedly connected with the first inner pipe 6 in the outer pipe 4; the second pipe holder 2 is fixedly connected with a second inner pipe 7 in the outer pipe 4. The first inner tube 6 and the second inner tube 7 are respectively arranged in the outer tube 4 (see fig. 4), and the protective sleeve 3 is enclosed at one end of the outer tube 4 close to the first tube socket 1 and the second tube socket 2, i.e. the tube socket set. The protective sleeve 3 is fixedly connected with the outer pipe 4 at the contact position, and preferably, the outer diameter of the protective sleeve 3 near one end of the pipe seat group is gradually slightly larger than the outer diameter of the fixed connection position with the outer pipe 4.
The outer layer of the outer tube 4 is made of resin materials such as nylon, polyurethane or PEBAX (block polyether amide). The inner layer of the outer tube 4 is made of the same material as the outer layer of the outer tube. The middle layer of the outer pipe 4 is made of stainless steel wires or nickel-titanium wires by winding.
As shown in fig. 2, in the novel balloon catheter assembly, a first guide wire holder 11 is arranged at one end of a first tube holder 1, and a first filling holder 12 is further arranged beside an opening of the first guide wire holder 11. One end of the second pipe seat 2 is provided with a second wire guide seat 21, and a second filling seat 22 is arranged beside the opening of the second wire guide seat 21.
The first guide wire holder 11 of the first tube holder 1 communicates with the inside of a first guide wire passage 62 (see fig. 6) in the first inner tube 6. The first filling socket 12 beside the first tube socket 1 communicates with the interior of the first filling passage 61 (see fig. 4 and 6) in the first inner tube 6. The first filling channel 61 and the first guide wire channel 62 are arranged at a distance from each other in the axial direction of the first inner tube 6, and are not communicated with each other, and their cross-sections are shown in fig. 6.
The second guide wire holder 21 of the second stem 2 communicates with the inside of the second guide wire passage 72 (see fig. 4) in the second inner tube 7. The second filling socket 22 next to the second socket 2 communicates with the interior of the second filling passage 71 (see fig. 4) in the second inner tube 7. The second filling channel 71 (see fig. 4) and the second guide wire channel 72 (see fig. 4) are spaced apart from each other in the axial direction of the second inner tube 7 and do not communicate with each other.
The first filling passage 61 communicates with the first filling orifice 611 or/and the second filling orifice 612 (see fig. 3) in the first tube 6. The first filling port 611 or/and the second filling port 612 are open to the interior of the Y-balloon 5.
The second filling passage 71 communicates with the third filling orifice 711 or/and the fourth filling orifice 712 (see fig. 3) in the second internal tube 7. The third filling port 711 and/or the fourth filling port 712 open into and communicate with the interior of the Y-balloon 5.
The first channel 41 and the second channel 42 of the outer tube 4 of the novel balloon catheter assembly are respectively connected with the proximal ends of the first inner tube 6 and the second inner tube 7 in the Y-shaped balloon 5 in a welding mode at the distal ends and are communicated with the inside of the Y-shaped balloon; and a plurality of developing marks are further arranged on the outer tube 4 and the first inner tube 6 and the second inner tube 7 in the Y-shaped saccule 5. The method specifically comprises the following steps: the first development mark 81 of the outer tube 4 is fixed to the distal end of the outer tube 4; the third development mark 83 of the first inner tube 6 is fixed to the distal end of the first inner tube 6. The second visualization mark 82 of the second inner tube 7 is fixed to the distal end of the second inner tube 7.
The first visualization mark 81, the second visualization mark 82 and the third visualization mark 83 are all provided inside the Y-balloon 5 (see fig. 3). In this embodiment, the first development mark 81, the second development mark 82, and the third development mark 83 are made of a platinum-iridium alloy or a platinum-tungsten alloy.
Fig. 7 is a schematic structural view of a Y-shaped balloon (in an inflated state) of the novel balloon catheter assembly according to the present invention.
As shown in fig. 7, in one embodiment, the Y-shaped balloon 5 is provided with three balloon legs, a main balloon portion and two sub-balloons, namely a main balloon leg 51 and a first sub-balloon leg 55, a second sub-balloon leg 55', and a main balloon portion (which may be divided into a first main balloon 52 and a second main balloon 52'), a first sub-balloon 53 and a second sub-balloon 54. The main balloon portion, the first sub-balloon 53 and the second sub-balloon 54 together form a Y-shaped structure. The diameter of the main balloon portion is larger than the diameters of the first sub-balloon 53 and the second sub-balloon 54.
In this embodiment, the included angle α between the first sub-balloon 53 and the second sub-balloon 54 ranges from 10 degrees to 60 degrees, and preferably is 30 degrees. The diameter range of the main balloon part is 4-10 mm, and preferably 6 mm. The diameters of the first sub-balloon 53 and the second sub-balloon 54 are about 2-5 mm, preferably 3 mm.
In this embodiment, the main balloon leg 51 of the Y-shaped balloon 5 and the outer tube 4 are welded and fixed at the distal end. The two sub-balloon legs 55, 55' of the first sub-balloon 53 and the second sub-balloon 54 are respectively welded and fixed with the far end of the first inner tube 6 and the far end of the second inner tube 7.
In this embodiment, the Y-shaped balloon 5 is a non-compliant balloon, and the material thereof may be nylon.
The first guide wire seat 11 and the first guide wire channel 62 are used as a working channel for the first guide wire 111 to enter the outer tube 4 of the balloon catheter assembly and to pass through the first main balloon 52 (upper half part) and the first sub-balloon 53 of the Y-shaped balloon 5.
Similarly, the second guide wire seat 21 and the second guide wire channel 72 serve as a working channel for the second guide wire 211 to enter the outer tube 4 of the balloon catheter assembly and to pass through the second main balloon 52' (lower half) and the second sub balloon 54 of the Y-shaped balloon 5.
The first filling seat 12, the first filling channel 61, the first filling orifice 611 or/and the second filling orifice 612 serve as a delivery channel for filling medium to flow out of and into the interior of the Y-balloon 5. The second filling receptacle 22, the second filling passageway 71, the third filling port 711 and/or the fourth filling port 712 are similar and will not be described in detail herein.
The working principle of the novel balloon catheter assembly according to the embodiment of the present invention will be described in detail with reference to fig. 8 to 13.
Fig. 8 is a schematic structural view of the novel balloon catheter assembly according to the embodiment of the present invention in the state where the balloon is not inflated.
As shown in fig. 8, in the novel balloon catheter assembly, when the balloon is in an unfilled state, the Y-shaped balloon 5 is in an unfilled state; the first sub-balloon 53 and the second sub-balloon 54 of the Y-shaped balloon 5 with the first inner tube 6 and the second inner tube 7 are in a fit state, so that the interventional operation is convenient to carry out.
Fig. 9 is a schematic view of a vascular structure of a bifurcation site with calcified plaque according to an embodiment of the present invention.
As shown in fig. 9, the blood vessel at the bifurcation part with calcified plaque is, for example, the middle cerebral artery M2 segment, and the calcified plaque is formed at the bifurcation part due to the lesion.
Fig. 10 is a schematic view of the guide wire delivery process during interventional operation using the novel balloon catheter assembly of the present invention.
As shown in fig. 10, during the guide wire delivery process in the interventional operation of the novel balloon catheter, the first guide wire 111 and the second guide wire 211 are respectively passed through the first guide wire channel 62 and the second guide wire channel 72 to be delivered to the distal end of the bifurcated vessel in an interventional operation mode, so as to ensure that the first guide wire 111 and the second guide wire 211 are positioned at the distal end of the calcified plaque.
Fig. 11 is a schematic view of the balloon catheter conveying process when the novel balloon catheter assembly of the present invention is used for interventional operation.
As shown in fig. 11, in the interventional operation delivery process using the novel balloon catheter assembly, the first inner tube 6 of the novel balloon catheter is introduced into the blood vessel along the first guide wire 111 and the second inner tube 7 along the second guide wire 211 in an interventional operation mode, and during the delivery process, the Y-shaped balloon 5 is in a negative pressure state, and the first guide wire 111 and the second guide wire 211 are fixed to prevent the Y-shaped balloon 5 from being unable to be delivered in place.
Fig. 12 is a schematic diagram of balloon catheter delivery in place when the novel balloon catheter assembly of the present invention is used for interventional surgery.
As shown in fig. 12, after the novel balloon catheter assembly is delivered to the site in the interventional operation, when the novel balloon catheter is delivered to the proximal end of the bifurcated vessel, the novel balloon catheter is slowly pushed again, so that the first sub-balloon 53 and the second sub-balloon 54 of the novel balloon catheter enter the two sides of the bifurcated vessel respectively; until the second visualization marker 82 and the third visualization marker 83 are delivered to the distal end of the calcified plaque and the new balloon catheter is again confirmed in place by Digital Subtraction Angiography (DSA).
Fig. 13 is a schematic diagram of the balloon after being full when the novel balloon catheter assembly of the present invention is used for interventional operation. Please refer to fig. 3 and fig. 7.
As shown in fig. 13, in the balloon of the novel balloon catheter assembly, the first filling seat 12 connected with the first tube holder 1 by the punching device is used to fill the Y-shaped balloon 5 with the liquid filling medium through the first filling channel 61, the liquid filling medium flows out from the first filling port 611 and the second filling port 612 and is respectively filled into the main balloon portion (i.e. the first main balloon 52 and the second main balloon 52' are internally communicated into a whole or separated into two chambers separated and sealed by the arrangement of the separation film) and the first sub-balloon 53 (which is internally communicated with the second sub-balloon 54 or is separated from each other by the arrangement of the separation film) of the Y-shaped balloon 5, so that the Y-shaped balloon 5 is filled, the balloon profile is forced to expand, the calcified plaque at the blood vessel is expanded by the Y-shaped balloon 5, and the calcified plaque is squeezed to enlarge the uterine cavity of the blood vessel, the vascular stent is easy to implant.
In another embodiment, when the first sub-balloon 53 and the second sub-balloon 54 are not communicated internally, a liquid filling medium can be filled into the Y-shaped balloon 5 through the second filling channel 71, and the liquid filling medium flows out from the third filling port 711 and the fourth filling port 712 and is respectively filled into the second main balloon 52' and the second sub-balloon 54 of the main balloon portion of the Y-shaped balloon 5, so that the Y-shaped balloon 5 is filled, the balloon profile is forced to expand, the calcified plaque at the bifurcated blood vessel is expanded by the Y-shaped balloon 5, and the calcified plaque is squeezed, so that the uterine cavity of the bifurcated blood vessel is enlarged, and the blood vessel stent is easy to implant. The process of filling the liquid filling medium into the first main balloon 52 and the first sub-balloon 53 of the Y-shaped balloon 5 through the first filling channel 61 is similar, and will not be described herein.
Preferably, in a further embodiment, a separation membrane is disposed inside the main balloon portion, dividing the main balloon portion into an upper half portion and a lower half portion, namely the first main balloon 52 and the second main balloon 52'. The spaces of the first main balloon 52 and the first sub-balloon 53 can be respectively and independently arranged, the first main balloon 52 and the first sub-balloon 53 are respectively communicated with the inside of the first main balloon 52 and the first sub-balloon 53 through the first filling opening 611 and the second filling opening 612, the Y-shaped balloon 5 is expanded after the liquid filling medium is injected into the upper half main balloon 52 and the first sub-balloon 53, the upper half part of the bifurcated vessel with the calcified plaque is passively expanded, and therefore the cavity of the bifurcated vessel is enlarged through extrusion, and the vascular stent is easy to implant.
Similarly, after the second filling seat 22 of the second tube holder 2 is connected by the stamping device, the liquid filling medium can be respectively injected into the second main balloon 52' and the second sub-balloon 54 of the Y-shaped balloon 5 through the second filling channel 71.
Preferably, a separation membrane is arranged in the main balloon part to divide the main balloon part into an upper half part and a lower half part. The spaces of the second main balloon 52 'and the second sub-balloon 54 can be arranged independently from each other, and the liquid filling medium is respectively injected into the second main balloon 52' through the third filling port 711 and the second sub-balloon 54 through the fourth filling port 712 to realize internal communication. The liquid filling medium flows out of the third filling port 711 and the fourth filling port 712 and respectively enters the second main balloon 52 'and the second sub-balloon 54 of the Y-shaped balloon 5, so that the Y-shaped balloon 5 is filled, and the second main balloon 52' and the second sub-balloon 54 of the lower half portion expand after the liquid filling medium is injected, so that the lower half portion of the bifurcated vessel with the calcified plaque is passively expanded, and the cavity of the bifurcated vessel is enlarged by extrusion, so that the vessel stent can be easily implanted.
In the above embodiment, the first visualization mark 81, the second visualization mark 82 and the third visualization mark 83 are used for accurately guiding the novel balloon catheter to be delivered to the lesion site for interventional operation under the visual environment of the medical imaging device.
The utility model discloses a manufacturing method of novel sacculus pipe subassembly mainly includes following step:
respectively processing a tube seat group and an outer tube 4 of the balloon catheter assembly and a Y-shaped balloon 5, arranging a separation film to separate the far end inner side of a main balloon part into a first sub-balloon 53 and a second sub-balloon 54 which are independent of each other, and hermetically separating the main balloon part from the first sub-balloon 53 and the second sub-balloon 54;
one end of the outer tube 4 is welded and fixed with the Y-shaped balloon 5, and two first sub-balloon legs 55 and two second sub-balloon legs 55' of the first sub-balloon 53 and the second sub-balloon 54 are respectively welded and fixed with the distal end of the first inner tube 6 and the distal end of the second inner tube 7 in the Y-shaped balloon 5.
The utility model discloses a manufacturing method of another kind of novel sacculus pipe subassembly, include:
processing a tube seat group and an outer tube 4 of the balloon catheter assembly and a Y-shaped balloon 5 respectively, arranging a separation film at the main balloon part of the Y-shaped balloon 5, arranging a first main balloon 52 and a second main balloon 52 'which are hermetically separated from each other at the outer side of the main balloon part respectively, arranging a separation film to separate the far-end inner side of the main balloon part into a first sub balloon 53 and a second sub balloon 54 which are independent from each other, and hermetically separating the first main balloon 52, the second main balloon 52', the first sub balloon 53 and the second sub balloon 54 from each other;
one end of the outer tube 4 is welded and fixed with the Y-shaped balloon 5, and two first sub-balloon legs 55 and two second sub-balloon legs 55' of the first sub-balloon 53 and the second sub-balloon 54 are respectively welded and fixed with the distal end of the first inner tube 6 and the distal end of the second inner tube 7 in the Y-shaped balloon 5.
The above description is only a preferred embodiment of the present invention, and is not intended to limit the scope of the present invention.

Claims (13)

1. A novel saccule catheter assembly comprises a first tube holder (1), a second tube holder (2) and an outer tube (4); the method is characterized in that: a Y-shaped balloon (5) fixedly connected with the outer tube (4) is arranged at the far end of the outer tube (4), one end of a main balloon part of the Y-shaped balloon (5) is fixedly connected with the outer tube (4) and is communicated with the inside of the outer tube, the middle section of the main balloon part is forked and is internally provided with a separation membrane, and the separation membrane divides the far end inner side of the main balloon part into a first sub balloon (53) and a second sub balloon (54) which are independent of each other; the main balloon part, the first sub-balloon (53) and the second sub-balloon (54) are hermetically separated from each other.
2. A novel sacculus catheter assembly comprises a first tube seat (1), a second tube seat (2) and an outer tube (4); a first channel (41) and a second channel (42) are arranged in the outer tube (4); the method is characterized in that: a Y-shaped balloon (5) fixedly connected with the outer tube (4) is arranged at the far end of the outer tube (4), one end of a main balloon part of the Y-shaped balloon (5) is fixedly connected with the outer tube (4) and is communicated with the inside of the outer tube, the middle section of the main balloon part is forked and is internally provided with a separation membrane to divide the outer side of the main balloon part into a first main balloon (52) and a second main balloon (52') which are respectively closed; the separation film separates and seals the insides of the opposite sides of the first main balloon (52) and the second main balloon (52') at the bifurcation part to form a first sub balloon (53) and a second sub balloon (54); the first channel (41) provides a filling medium channel and a guide wire channel for the first main balloon (52) or/and the first sub balloon (53) through the first inner tube (6); the second channel (42) provides a filling medium channel and a guide wire channel for the second main balloon (52') or/and the second sub balloon (54) through the second inner tube (7).
3. The novel balloon catheter assembly of claim 1, wherein: one end of the outer pipe (4) close to the first pipe seat (1) and the second pipe seat (2) is surrounded by a protective sleeve (3), and the protective sleeve (3) is fixedly connected with the contact part of the outer pipe (4).
4. The novel balloon catheter assembly of claim 3, wherein: the outer diameter of one end of the protective sleeve (3) close to the first pipe seat (1) and the second pipe seat (2) is gradually changed slightly to be larger than the outer diameter of the fixed connection position of the outer pipe (4).
5. The novel balloon catheter assembly of claim 2, wherein: the first inner tube (6) comprises a first filling channel (61) and a first guide wire channel (62), and the first filling channel (61) and the first guide wire channel (62) are arranged at intervals along the axial direction of the first inner tube (6) and are not communicated with each other; the second inner tube (7) comprises a second filling channel (71) and a second guide wire channel (72), and the second filling channel (71) and the second guide wire channel (72) are arranged at intervals along the axial direction of the second inner tube (7) and are not communicated with each other.
6. The novel balloon catheter assembly of claim 2 or 5, wherein: the first guide wire channel (62) of the first inner tube (6) is communicated with the interior of the first guide wire seat (11) of the first tube seat (1) at the proximal end, and the first guide wire channel (62) of the first inner tube (6) penetrates through the first main balloon (52) or/and the first sub balloon (53) at the distal end and penetrates through the first sub balloon leg (55) to be communicated with the exterior;
the second guide wire channel (72) of the second inner tube (7) is communicated with the inside of the second guide wire seat (21) of the second tube seat (2) at the near end, and the second guide wire channel (72) of the second inner tube (7) penetrates through the second main balloon (52') or/and the second sub balloon (54) at the far end and penetrates through the second sub balloon leg (55') to be communicated with the outside.
7. The novel balloon catheter assembly of claim 2 or 5, wherein: the first filling channel (61) of the first inner tube (6) is communicated with the interior of the first filling seat (12) of the first tube seat (1) at the proximal end, and the first filling channel (61) is communicated with the interior of the first main balloon (52) or/and the first sub-balloon (53) at the distal end through a first filling opening (611) and/or a second filling opening (612) arranged in the Y-shaped balloon;
the second filling channel (71) of the second inner tube (7) is communicated with the inside of the second filling seat (22) of the second tube seat (2) at the proximal end, and the second filling channel (71) is communicated with the inside of the second main balloon (52') or/and the second sub balloon (54) at the distal end through a third filling opening (711) and/or a fourth filling opening (712) arranged in the Y-shaped balloon.
8. The novel balloon catheter assembly of claim 2, wherein: a first developing mark (81) is arranged at the fixed connection position of a main saccule leg (51) and the outer tube (4) in the Y-shaped saccule (5), a third developing mark (83) is arranged near a third saccule leg (55) which is the tail end of a first sub-saccule (53) in the Y-shaped saccule (5), and a second developing mark (82) is arranged near a second sub-saccule leg (55') which is the tail end of a second sub-saccule (54) in the Y-shaped saccule (5).
9. The novel balloon catheter assembly of claim 2, wherein: in the inflated state, the diameter of the main balloon part of the Y-shaped balloon is larger than the diameters of the first sub-balloon (53) and the second sub-balloon (54).
10. The novel balloon catheter assembly of claim 2 or 9, wherein: in the filling state, an included angle alpha between the first sub-balloon (53) and the second sub-balloon (54) ranges from 10 degrees to 60 degrees.
11. The novel balloon catheter assembly according to claim 2 or 9, wherein: in the filling state, the diameter range of the main balloon part is 4-10 mm, and the diameter ranges of the first sub-balloon (53) and the second sub-balloon (54) are 2-5 mm.
12. The novel balloon catheter assembly of claim 2, wherein: a main balloon leg (51) of the Y-shaped balloon (5) is welded and fixed with the outer tube (4); two first sub-balloon legs (55) and two second sub-balloon legs (55') of the first sub-balloon (53) and the second sub-balloon (54) are respectively welded and fixed with the far end of the first inner tube (6) and the far end of the second inner tube (7).
13. The novel balloon catheter assembly of claim 2, wherein: the Y-shaped balloon (5) is a non-compliant balloon.
CN202220850062.1U 2022-04-12 2022-04-12 Novel sacculus catheter subassembly Active CN217246176U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202220850062.1U CN217246176U (en) 2022-04-12 2022-04-12 Novel sacculus catheter subassembly

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202220850062.1U CN217246176U (en) 2022-04-12 2022-04-12 Novel sacculus catheter subassembly

Publications (1)

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CN217246176U true CN217246176U (en) 2022-08-23

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