CN113729852A

CN113729852A - Bolt taking system

Info

Publication number: CN113729852A
Application number: CN202110820049.1A
Authority: CN
Inventors: 陈学明; 李建民; 周祥; 王永胜
Original assignee: Hangzhou Wei Qiang Medical Technology Co ltd
Current assignee: Hangzhou Wei Qiang Medical Technology Co ltd
Priority date: 2021-04-09
Filing date: 2021-07-20
Publication date: 2021-12-03
Anticipated expiration: 2041-07-20
Also published as: CN113729853B; CN113729853A; CN113729854B; CN113729854A; WO2022214020A1; CN113729852B; CN115192139A

Abstract

The invention relates to a bolt taking system, comprising: the thrombus taking device comprises a thrombus taking support and a traction catheter, wherein the traction catheter is connected with the thrombus taking support, the thrombus taking support is used for scraping thrombus on the inner wall of a blood vessel, and the scraped thrombus enters the thrombus taking support; the plug crushing bracket and the conveying pipe can be slidably connected in the traction guide pipe; the conveying pipe is connected with the broken bolt support to drive the broken bolt support to be discharged from the far end of the traction catheter and enter the bolt taking support, and the conveying pipe drives the broken bolt support to rotate circumferentially in the bolt taking support to carry out broken bolt; after the thrombus is broken, the conveying pipe can also drive the thrombus support to enter the traction guide pipe from the far end of the traction guide pipe and drive the thrombus support to be discharged from the near end of the traction guide pipe.

Description

Bolt taking system

Technical Field

The invention relates to the technical field of medical instruments, in particular to a embolectomy system.

Background

Venous Thromboembolism (VTE) includes lower limb Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE).

Deep Vein Thrombosis (DVT) of the lower limb is a highly vascular surgical disorder, and is often caused by an obstruction of blood reflux due to abnormal clotting of blood in the veins of the lower limb. Pulmonary Embolism (PE) has become the third leading cause of death from cardiovascular disease. Risk factors for pulmonary embolism include both environmental factors and personal factors, including age, past VTE history, tumor history, cardiopulmonary failure, congenital or acquired coagulation disorders, hormonal therapy, and the like. Acute PE can lead to systemic hypotension and even total heart failure, leading to death of the patient.

Therefore, the thrombus can be quickly and effectively removed as soon as possible, the vein occlusion can be relieved, the PE can be effectively prevented, the valve function can be protected, and the recurrence rate of the thrombus can be reduced.

The existing mechanical thrombus taking or suction catheter thrombus taking system has poor thrombus removing effect.

Disclosure of Invention

The present application provides a thrombectomy system.

A embolectomy system, comprising:

the thrombus taking device comprises a thrombus taking support and a traction catheter, wherein the traction catheter is connected with the thrombus taking support, the thrombus taking support is used for scraping thrombus on the inner wall of a blood vessel, and the scraped thrombus enters the thrombus taking support;

the plug crushing bracket and the conveying pipe can be slidably connected in the traction guide pipe;

the conveying pipe is connected with the broken bolt support to drive the broken bolt support to be discharged from the far end of the traction catheter and enter the bolt taking support, and the conveying pipe drives the broken bolt support to rotate circumferentially in the bolt taking support to carry out broken bolt; after the thrombus is broken, the conveying pipe can also drive the thrombus support to enter the traction guide pipe from the far end of the traction guide pipe and drive the thrombus support to be discharged from the near end of the traction guide pipe.

In one embodiment, the thrombus removal device further comprises an aspiration catheter, wherein after the thrombus support is withdrawn from the proximal end of the traction catheter, the aspiration catheter extends into the traction catheter and is used for externally connecting an aspiration power, and the externally connecting aspiration power sucks thrombus in the thrombus support through the aspiration catheter and/or the traction catheter.

In one embodiment, after the thrombus stent is withdrawn from the proximal end of the traction catheter, the traction catheter is used for externally connecting suction power, and the externally connecting suction power sucks thrombus in the thrombus stent through the traction catheter.

In one embodiment, the embolectomy system further comprises a suction device, wherein the suction device comprises a joint conduit and a branch conduit, the joint conduit is communicated with the traction conduit, and the branch conduit is communicated with the joint conduit or the branch conduit; the branch conduit is used for connecting external suction power, and the joint conduit is connected with a switch for controlling the opening and closing of the joint conduit;

the delivery tube is capable of driving the embolic stent out of the proximal end of the traction catheter and into the adaptor catheter and out of the proximal end of the adaptor catheter.

In one embodiment, the switch comprises a screw cap and a seal ring with elasticity, wherein the seal ring is provided with a central hole at least when not pressed by the rotation; the rotary cover is rotatably connected to the joint guide pipe; the sealing ring is clamped between the screw cap and the proximal port of the joint catheter, and the central hole is communicated with the inner cavity of the joint catheter; and rotating the rotary cover, and elastically extruding or releasing the sealing ring by the rotary cover so as to open or close the central hole.

In one embodiment, when the delivery pipe passes through the central hole, the screw cap is rotated, and the screw cap elastically presses or releases the sealing ring to control the size of the central hole, so that the delivery pipe is clamped and fixed or loosened.

In one embodiment, a branch switch for opening and closing the branch conduit is connected to the branch conduit.

In one embodiment, the stent is radially expanded after being withdrawn from the pull catheter.

In one embodiment, the bolt taking system further comprises a loading pipe, wherein the loading pipe can move and is sleeved on the bolt breaking bracket, so that the bolt breaking bracket is contained in the loading pipe in a compression mode in the radial direction, and the bolt breaking bracket can be loaded into the traction catheter.

In one embodiment, the loading tube is movably sleeved on the conveying tube, the loading tube is moved to the proximal end of the conveying tube, the distal end of the conveying tube and the broken bolt support extend into the traction guide tube together, and the loading tube stays outside the traction guide tube.

In one embodiment, the embolectomy system further comprises an outer sheath, the embolectomy stent and the traction catheter are both connected within the outer sheath and are transitioned between a slidable state and a fixed state within the outer sheath, at least the embolectomy stent being slidable out of the outer sheath.

In one embodiment, the outer sheath tube is connected with a sheath tube joint, the sheath tube joint is rotatably connected with an adjusting knob, and a silica gel ring with an inner hole is clamped between the adjusting knob and the sheath tube joint;

the traction catheter penetrates through the sheath pipe joint, the adjusting knob and the silica gel ring, the adjusting knob is rotated, and the silica gel ring is extruded to change the size of the inner hole so as to clamp or loosen the traction catheter.

In one embodiment, a compression ring is clamped between the adjusting knob and the sheath pipe joint, and the compression ring and the adjusting knob clamp the silica gel ring together.

In one embodiment, the sheath joint is communicated with a branch hose.

In one embodiment, the proximal end of the delivery tube is fixedly sleeved with a stainless steel tube.

In one embodiment, the thrombectomy stent is slidably coupled to the traction catheter such that the thrombectomy stent is axially movable relative to the traction catheter.

In one embodiment, a sliding groove is formed in the peripheral wall of the traction catheter, the thrombus taking support is movably sleeved in the sliding groove, and the thrombus taking support is connected with a pull wire.

In one embodiment, the thrombectomy stent is fixedly connected with the traction catheter.

According to the technical scheme, the embodiment of the invention at least has the following advantages and positive effects:

the traction catheter is used for driving the thrombus taking support to move in the blood vessel, thrombus on the inner wall of the blood vessel is scraped off by the thrombus taking support, and the scraped thrombus enters the thrombus taking support; the crushed thrombus support enters the thrombus taking support through the traction catheter by utilizing the conveying pipe; driving the thrombus crushing support to rotate in the thrombus taking support along the circumferential direction by utilizing the conveying pipe, and crushing thrombus in the thrombus taking support; after the thrombus is broken, the thrombus breaking support is pulled out through a traction catheter through a delivery pipe; the broken thrombus blocks in the thrombus taking support can be sucked away through the traction catheter. The large thrombus is crushed into small pieces by the thrombus crushing bracket, so that the thrombus blocks are easier to be sucked out through the traction catheter. Because after the bits of broken glass were tied, the bits of broken glass tied support can be demolishd, can prevent that the bits of broken glass tied support from hindering the process of absorbing the thrombus piece, improves work efficiency, and prevents that the bits of broken glass tied support from blockking the thrombus piece and through pulling the pipe, and then can be with getting the cleaner that the thrombus piece in the support was clear away, reduce to omit, improve the effect of cleaing away the thrombus.

Drawings

Fig. 1 is a schematic overall structure diagram of a thrombus removal system according to a first embodiment of the present invention.

Fig. 2 is a partial perspective view of the embolectomy system of fig. 1.

FIG. 3 is a schematic view of the construction of the tampon support of FIG. 1.

Fig. 4 is a top view of fig. 3.

Fig. 5 is an enlarged schematic view of the region a in fig. 4.

Fig. 6 is a schematic view of the structure of the separation bracket of fig. 3.

Fig. 7 is a side view of fig. 6.

Fig. 8 is a schematic structural view of the support bracket of fig. 3.

Fig. 9 is a side view of fig. 8.

Fig. 10 is a schematic view of the structure of the screen film of fig. 3.

Fig. 11 is a side view of fig. 10.

FIG. 12 is a schematic view of the embodiment of the thrombectomy device of FIG. 1.

FIG. 13 is a schematic structural view of the first embodiment of the embolic support of FIG. 12.

Fig. 14 is a side view of fig. 13.

Fig. 15 is a top view of fig. 13.

FIG. 16 is a schematic structural view of a second embodiment of the embolic support of FIG. 12.

Fig. 17 is a side view of fig. 16.

Fig. 18 is a top view of fig. 16.

Fig. 19 is a schematic structural view of the first bracket of fig. 16.

Fig. 20 is a structural view of the second bracket of fig. 16.

FIG. 21 is a schematic structural view of a third embodiment of the embolic support of FIG. 12.

Fig. 22 is a side view of fig. 21.

FIG. 23 is a schematic structural view of a fourth embodiment of the embolic support of FIG. 12.

Fig. 24 is a schematic structural view of the sheath tube in fig. 1.

Fig. 25 is a schematic view of the structure of the sheath adapter of fig. 24.

Fig. 26 is a schematic view of the structure of the pull catheter, the connector catheter and the branch catheter in fig. 1.

Figure 27 is a cross-sectional view of the connector conduit of figure 26.

FIG. 28 is a schematic view of a diseased portion of the inferior vena cava of a human.

FIG. 29 is a schematic view of the access system of FIG. 1 penetrating into a lesion.

FIG. 30 is a schematic view of the initial release of the thrombectomy stent.

FIG. 31 is a schematic illustration of the release and adjustment of the thrombectomy stent.

FIG. 32 is a schematic view of the thrombectomy stent after release.

FIG. 33 is a schematic illustration of an embolectomy stent separating and collecting intravascular thrombi.

FIG. 34 is an operational view of the thrombectomy device in thrombus clearing within the thrombectomy stent.

FIG. 35 is a schematic illustration of the morcellating device being withdrawn after the morcellating is completed.

FIG. 36 is a schematic view of aspiration of a thrombus.

FIG. 37 is a schematic view of the thrombectomy stent again detaching and collecting the thrombus.

FIG. 38 is a schematic view of the embolic device reentering the adaptor catheter and the pull catheter.

FIG. 39 is a schematic view of thrombus aspiration of the second embodiment of the present invention.

Fig. 40 is a schematic structural view of a thrombus removal device in a third embodiment of the present invention.

Fig. 41 is a schematic view of the structure of fig. 40 in another state.

FIG. 42 is a schematic structural diagram of a fourth embodiment of the present invention.

Fig. 43 is a schematic structural view of a fifth embodiment of the present invention.

Fig. 44 is a schematic structural view of a sixth embodiment of the present invention.

The reference numerals are explained below:

01. a venous blood vessel; 02. thrombus tissue; 03. a guide wire; 04. a puncture hole; 1. an outer sheath tube; 11. a sheath pipe joint; 12. adjusting a knob; 13. a compression ring; 14. a silica gel ring; 15. a branch hose; 16. compressing the balloon; 111. a branch joint; 2. a traction catheter; 21. a fixed cover; 22. a chute; 3. a thrombus taking support; 31. separating the bracket; 32. a support bracket; 33. a screen film; 34. a guide head; 35. a silk thread; 310. a first diamond-shaped grid cell; 311. a support body; 312. a connecting rod; 313. a connecting ring; 320. a second diamond-shaped grid cell; 321. a support bar; 322. a fixing ring; 331. mesh openings; 332. a small hole; 3131. a pull wire; 4. a delivery pipe; 41. a drive handle; 42. a loading tube; 401. a drive terminal; 402. a stainless steel tube; 411. a drive interface; 412. driving the wrench; 413. a rechargeable battery; 414. a drive motor; 415. a control button; 5. a broken bolt support; 51. a fixed tube; 52. a first bracket; 53. a second bracket; 54. a third circular ring; 511. a first stationary tube; 512. a second stationary tube; 521. a first cutting bar; 522. a first circular ring; 531. a second cutting bar; 532. a second circular ring; 5111. a clamping groove; 5112. a first opening; 5121. the clamping bulge; 5122. a second opening; 6. a connector conduit; 61. a branch conduit; 62. screwing a cover; 63. a seal ring; 64. a suction syringe; 65. a suction catheter; 601. a pipe dividing joint; 611. a branch switch.

Detailed Description

Exemplary embodiments that embody features and advantages of the invention are described in detail below in the specification. It is to be understood that the invention is capable of other embodiments and that various changes in form and details may be made therein without departing from the scope of the invention and the description and drawings are to be regarded as illustrative in nature and not as restrictive.

In the description of the present application, it is to be understood that the terms "center," "longitudinal," "lateral," "length," "width," "thickness," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," "outer," "clockwise," "counterclockwise," and the like are used in the orientations and positional relationships indicated in the drawings for convenience in describing the present application and for simplicity in description, and are not intended to indicate or imply that the referenced devices or elements must have a particular orientation, be constructed in a particular orientation, and be operated in a particular manner, and are not to be construed as limiting the present application.

Furthermore, the terms "first", "second" and "first" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly indicating the number of technical features indicated. Thus, features defined as "first", "second", may explicitly or implicitly include one or more of the described features. In the description of the present application, "a plurality" means two or more unless specifically limited otherwise.

In the description of the present application, it is to be noted that, unless otherwise explicitly specified or limited, the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either a fixed connection, a removable connection, or an integral connection; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meaning of the above terms in the present application can be understood in a specific case by those of ordinary skill in the art.

In the description of the present application, "radial" and "axial" are to be understood in a broad sense. "radial" is not limited to absolute circular objects nor is "axial" limited to absolute cylindrical objects.

In the description of this application, "proximal" refers to the end of the thrombectomy support or the thrombectomy support that is proximal to the operating end (drive handle 41) and "distal" refers to the end of the thrombectomy support or the thrombectomy support that is distal to the operating end (drive handle 41).

Referring to fig. 1, an embodiment of the invention provides an embolectomy system, which can be used for rapid and more complete removal of an occluded thrombus in a blood vessel. The thrombus taking system of the embodiment of the invention mainly comprises an outer sheath tube 1, a thrombus taking device, a thrombus crushing device and a suction device.

Referring to FIG. 1 in conjunction with FIGS. 28 to 31, the outer sheath 1 serves as a loading container for receiving the thrombectomy device and the thrombectomy device, and for pulling or guiding the thrombectomy device and the thrombectomy device into the diseased site within the vessel.

Referring to fig. 1 and 2, the embolectomy device includes a traction catheter 2 and an expandable embolectomy stent 3.

The traction catheter 2 is movably inserted into the outer sheath 1 and can move relative to the outer sheath 1 along the axial direction.

The thrombus taking support 3 is arranged at the far end of the traction catheter 2, and the thrombus taking support 3 can be driven by the traction catheter 2 to move axially in the sheath tube 1, so that the thrombus taking support 3 extends out of the sheath tube 1 or contracts into the sheath tube 1.

The thrombectomy stent 3 is a stent structure which can be contracted and expanded in the radial direction so that the thrombectomy stent 3 can be compressed into the sheath tube 1. Meanwhile, when the thrombus taking support 3 extends out of the outer sheath tube 1, the thrombus taking support 3 can be naturally expanded and is attached to the inner wall of the blood vessel.

The proximal end of the thrombectomy stent 3 is provided with an opening and is matched with the peripheral wall of the thrombectomy stent 3 to perform thrombectomy, so that the thrombi in the blood vessel can enter the inner space of the thrombectomy stent 3 through the opening. It will be appreciated that the opening may be provided in plural. Meanwhile, the distal end of the thrombus taking support 3 is closed so as to gather and capture thrombus, so that the thrombus is collected in the thrombus taking support 3. It should be noted that "distal end closed" in this application means that the distal end of the thrombectomy stent 3 is sufficient to capture thrombi, for example, the distal end may be provided with pores for blood or a guide wire to pass through, and the size of the pores at the distal end is smaller than that of the openings at the proximal end as a whole.

Referring to fig. 3 to 5, the embolectomy support 3 includes a self-expandable separation support 31, a self-expandable support 32, a filter membrane 33 and a guide head 34. When the thrombus removing bracket is in operation, an operator can move the thrombus removing bracket 3 back and forth along the axial direction of a blood vessel, and thrombus on the inner wall of the blood vessel is scraped off by the separation bracket 31.

Referring to fig. 6 and 7 in conjunction with fig. 3 to 5, a detachment bracket 31 is formed at the proximal end of the thrombectomy bracket 3. The split stent 31 is a stent structure that is radially capable of contracting and expanding.

The proximal end of the detachment scaffold 31 is connected to the traction catheter 2. The connection may be a fixed connection in the axial direction or a sliding connection in the axial direction, and the fixed connection is described first in this embodiment, and the sliding connection is described in the following embodiments. The proximal end of the separation stent 31 is formed with an opening which serves as a proximal end opening of the thrombectomy stent 3 for collecting thrombi in the vessel. The distal end of the separation bracket 31 is connected to the proximal end of the support bracket 32 so that the separation bracket 31 is engaged with the support bracket 32 and the interior of the separation bracket 31 communicates with the interior of the support bracket 32. It should be noted that "the separation bracket 31 is connected to the support bracket 32" means that the separation bracket 31 and the support bracket 32 may be separately processed and then connected together, or the separation bracket 31 and the support bracket 32 may be directly and integrally formed into a whole.

Referring to fig. 6 and 7, the separation bracket 31 of the present embodiment includes a supporting body 311 having a distal end connected to the supporting bracket 32, a plurality of connecting rods 312 connected to a proximal end of the supporting body 311, and a connecting ring 313 connected to a proximal end of the plurality of connecting rods 312, wherein the connecting ring 313 may be a connecting member having another structure without a through hole.

Referring to fig. 6 in combination with fig. 2, the connection ring 313 is sleeved on the traction catheter 2 to connect the thrombectomy support 3 with the traction catheter 2.

Still referring to fig. 6 and 7, the supporting body 311 is a bare stent structure, and is a tubular stent structure in a circumferential closed loop in a deployed state; or the support body 311 is annular in the circumferential direction and has a mesh-like support structure. The support body 311 can provide good radial support force for the separation stent 31, so that the separation stent 31 can be better attached to the inside of a blood vessel, and then complete cutting, separation and collection are carried out between thrombus in the blood vessel and the inner wall of the blood vessel, and the thrombus can completely enter the thrombus taking stent 3.

In this embodiment, the support body 311 includes a plurality of circumferentially and axially contiguous V-shaped rods. A plurality of circumferentially connected V-shaped rods may form a wave ring. The wave ring has circumferentially staggered peaks and troughs, the peaks facing the proximal end and the troughs facing the distal end. Depending on the number of circumferentially adjacent V-shaped bars, a different number of valleys may be formed at the distal end of the support body 311 as connection points to facilitate attachment to the support stent 32.

The plurality of axially connected V-shaped rods may form a plurality of first diamond-shaped lattice cells 310, which first diamond-shaped lattice cells 310 are also capable of directly cutting thrombus to allow thrombus to enter the separation stent 31 when the support body 311 is expanded. The proximal and distal ends of the first diamond-shaped lattice element 310 may also form peaks and valleys, respectively. The number of V-shaped bars at the proximal end of the support body 311 may be adjusted stepwise to form a different number of peaks to facilitate interfacing with a different number of connecting bars 312 at the proximal end. In this embodiment, the number of wave troughs at the distal end of the supporting body 311 is greater than the number of wave crests at the proximal end of the supporting body 311. It should be noted that the grid cells in the present application are not limited to the diamond-shaped grid cells 310, and may be grid cells with other shapes, such as oval, triangle, etc., and the sides of the grid cells may be straight sides or curved sides.

It can be understood that the first diamond-shaped mesh unit 310 can be deformed in a telescopic manner along the axial direction of the supporting body 311, so that the supporting body 311 has strong radial supporting force and vessel adherence ability, and the separation stent 31 can be compressed and expanded in the radial direction.

The strainer membrane 33 is connected to at least the support stent 32, and the strainer membrane 33 is provided with a porous structure so that the strainer membrane 33 is used for filtering thrombus and passing blood.

As shown in fig. 3, the elastic support strength of the separation holder 31 is greater than the elastic support strength of the support holder 32, and the compliance of the support holder 32 is greater than the compliance of the separation holder 31. The support body 311 and/or the connection rod 312 in the separation stent 31 are used to scrape away thrombus located on the inner wall of the blood vessel. The separation support 31 provides better elastic support strength through self higher elastic performance, and the contact force between the separation support 31 and the inner wall of the blood vessel is larger, so that thrombus on the inner wall of the blood vessel is easier to scrape off. The filter membrane 33 is connected to the support frame 32, and the support frame 32 provides support for the filter membrane 33, so that the filter membrane 33 maintains a relatively stable shape, and since the support frame 32 is not used as a core part for scraping thrombus, the elastic support strength of the support frame 32 can be smaller than that of the separation frame 31. Because filter screen film 33 connects in support holder 32 at least, support holder 32's compliance is greater than the compliance of separation holder 31, support holder 32's compliance is good to can be better be suitable for filter screen film 33's deformation, can prevent support holder 32 because self elasticity supports intensity great and support easy to prop filter screen film 33 broken, perhaps prop great with the area of the pore structure on filter screen film 33, and lead to filter screen film 33 not good to the interception effect of thrombus.

The connecting rod 312 is disposed at the proximal end of the supporting body 311, and the distal end of the connecting rod 312 is connected to the wave peak at the proximal end of the supporting body 311. The plurality of connecting rods 312 are arranged at intervals in the circumferential direction, the proximal ends of the plurality of connecting rods 312 are connected to the connecting ring 313 in a converging manner, and a proximal opening of the separation bracket 31 is formed between the adjacent connecting rods 312 and the supporting body 311.

As shown in fig. 7, the portion having the first diamond-shaped grid cells 310 on the left side in fig. 7 is a support 311, and the elastic support strength of the support 311 is greater than that of the support bracket 32. Wherein the size may be different between the plurality of first diamond-shaped grid cells 310; the connecting rod 321 is a strip structure, and two ends of the connecting rod 321 are respectively connected with the supporting body 311 and the connecting ring 313. For example, in the embodiment shown in fig. 6, there are two connecting rods 312, the distal ends of the two connecting rods 312 are respectively connected to different first diamond-shaped lattice units 310, and the proximal ends of the two connecting rods 312 are gathered and connected to the connecting ring 313, where the gathering means that a plurality of objects are close to each other, may be connected to each other, or may not be connected to each other.

The connection ring 313 is used for connecting the traction catheter 2. In this embodiment, the connection ring 313 is fixedly secured to the distal end of the traction catheter 2. It is understood that the connection ring 313 may be disposed on the axial center of the support 311, or may be disposed eccentrically.

It should be noted that the entire separation stent 31 can be made of a nickel-titanium alloy tube by a laser cutting process and a heat setting process.

Referring to fig. 8 and 9, the support bracket 32 of the present embodiment is disposed at the distal end of the separation bracket 31. The support stent 32 is a stent structure that is radially collapsible and expandable. The proximal end of the support stent 32 is axially contiguous with the support body 311 of the detachment stent 31. The distal end of the support stent 32 forms a gradually converging closed end to facilitate capturing and collecting thrombus separated from the blood vessel by the separation stent 31.

Referring to fig. 8 and 9 in combination with fig. 5, in the present embodiment, a plurality of second diamond-shaped grid cells 320 are formed at the proximal end of the supporting frame 32, and the plurality of second diamond-shaped grid cells 320 may also be formed by connecting a plurality of V-shaped rods along the circumferential direction and the axial direction. The proximal ends of the second diamond-shaped lattice units 320 form peaks, which may be used as connection points to correspond to the valleys at the distal end of the supporting body 311 one by one, and are wound and connected by the wires 35, as shown in fig. 5.

The second diamond-shaped grid cells 320 can be deformed in a telescopic manner along the axial direction of the support stent 32, so that the support stent 32 has strong radial supporting force and vessel adherence ability, and the support stent 32 can be compressed and expanded in the radial direction. It is understood that the second diamond-shaped lattice cells 320 may be arranged in one or more layers in the axial direction of the support stent 32. The greater the number of layers of the second diamond-shaped lattice cells 320, the greater the radial bending ability of the support stent 32. It should be noted that the support stent 32 does not serve as a main structure for scraping thrombus on the thrombus wall, and therefore the support stent 32 is smaller in elastic support strength than the separation stent 31. In order to adapt the support stent 32 to the deformation of the filter membrane 33, prevent the filter membrane 33 from being broken or the pore structure on the filter membrane 33 from being enlarged, the compliance of the support stent 32 is greater than that of the separation stent 31, for example, the compliance of the second diamond-shaped mesh unit 320 is greater than that of the separation stent 31, further, the compliance of the second diamond-shaped mesh unit 320 is greater than that of the first diamond-shaped mesh unit 310, and the elastic support strength of the second diamond-shaped mesh unit 320 is less than that of the first diamond-shaped mesh unit 310.

Still referring to fig. 8 and 9, a plurality of support rods 321 circumferentially distributed and a fixing ring 322 connected to the distal ends of the support rods 321 are formed at the distal end of the support bracket 32. The support rods 321 may extend along the axial direction of the support bracket 32, and in a direction from the proximal end to the distal end, the radial dimension of the support rods 321 is gradually reduced, so that the distal ends of the plurality of support rods 321 are gradually gathered and connected to the fixing ring 322. When the distal ends of the support rods 321 are close together, the radial dimension of the structure surrounded or defined by the support rods 321 is gradually reduced in the direction from the proximal end to the distal end; alternatively, the radial dimension of the structure surrounded or defined by the plurality of support rods 321 may be constant and then gradually reduced; alternatively, the radial dimension of the structure surrounded or defined by the plurality of support rods 321 may first increase and then gradually decrease.

Referring to fig. 3 to 5, it should be noted that, similar to the separation stent 31, the support stent 32 may also be made of a nickel titanium alloy tube by a laser cutting process and a heat setting process. However, the wall thickness of support stent 32 is less than the wall thickness of separation stent 31, i.e., the wall thickness of the tubing used for support stent 32 is less than the wall thickness of the tubing used for separation stent 31, so that separation stent 31 and support stent 32 are adapted to the resilient support strength and compliance relationships of the embodiments described above; the wall thickness refers to the thickness of the tubular stent structure in the direction from the outer surface to the inner surface. Therefore, the support stent 32 maintains certain flexibility while providing certain radial support force, and performs proper bending deformation by using the characteristic that the second rhombic grid cells 320 are not symmetrical and fixed, so as to better fit the tortuous characteristic of the blood vessel of the patient. Namely, the radial supporting force of the separation bracket 31 is larger than that of the support bracket 32, and the separation bracket 31 has better vessel adherence capability. Meanwhile, the flexibility of the support stent 32 is greater than that of the separation stent 31, and the support stent 32 can adapt to the tortuous characteristics of the blood vessel.

Referring to fig. 10 to 11 and fig. 3 to 5, the filter membrane 33 is sewn to the peripheral wall of the support frame 32. The pore structure of the filter screen film 33 may be a microporous structure, and the size of the microporous structure may be selected according to actual needs. That is, the screen film 33 can be made of a film material having a micro-porous structure, and the screen film 33 is densely provided with the meshes 331. It will be appreciated that the microporous structure is adapted to allow blood to pass through and to intercept thrombi.

As shown in fig. 3, the screen film 33 may be sewn to the inner circumferential wall of the support bracket 32. Since the support frame 32 is compressed in the sheath tube 1 during transportation and the mesh membrane 33 is sewn to the inner peripheral wall of the support frame 32, the mesh membrane 33 can be prevented from being scraped or crushed when the support frame 32 slides in the sheath tube 1.

The screen film 33 may be sewn to the support rod 321 of the support bracket 32 using a wire harness. The proximal open edge of the screen membrane 33 may be sewn to the proximal attachment point of the support bracket 32. In the support frame 32, the axial deformation amount of the support rod 321 is smaller than that of the first diamond-shaped grid unit 310, so that the structure of the proximal connection point of the filter membrane 33 and the support frame 32 can be protected relatively stably without breakage. The center of the far end of the filter screen film 33 is provided with a small hole 332, and the position of the small hole 332 corresponds to the fixing ring 322.

Referring to fig. 3-5 in conjunction with fig. 8 and 9, a guide head 34 is provided at the distal end of the support bracket 32. The guide head 34 may be attached to a securing ring 322 at the distal end of the support stent 32. The distal end of the guide head 34 is pointed to guide and enhance the pushability of the embolectomy device. The centers of the guide head 34 and the fixing ring 322 can be penetrated by guide wires, and the guide wires play a guiding role.

Referring to FIG. 12 in conjunction with FIG. 1, the morcellating device includes a delivery tube 4, an expandable morcellating stent 5, a drive handle 41 and a loading tube 42.

The delivery pipe 4 is movably arranged in the traction catheter 2 in a penetrating way. The delivery tube 4 is axially movable with respect to the towing conduit 2 and is circumferentially rotatable with respect to the towing conduit 2.

The broken bolt support 5 is arranged at the far end of the conveying pipe 4, the broken bolt support 5 can be driven by the conveying pipe 4 to move axially in the traction guide pipe 2, so that the broken bolt support 5 extends out of the far end of the traction guide pipe 2, the broken bolt support 5 is released in the bolt taking support 3, or the broken bolt support 5 is contracted into the traction guide pipe 2, and the broken bolt support 5 can be driven to completely withdraw from the traction guide pipe 2. When conveyer pipe 4 carries out the rotation in a circumferential direction simultaneously, can also drive garrulous bolt support 5 and tie support 3 inside and carry out synchronous rotation in a circumferential direction getting to cut, smash the thrombus of tying support 3 inside getting. Specifically, after the thrombectomy stent 3 cuts the thrombus in the blood vessel, the thrombus enters the inner space enclosed by the thrombectomy stent 3 through the opening of the separation stent 31 in the thrombectomy stent 3. After that, the conveying pipe 4 can be pushed from the proximal end of the conveying pipe 4 to the distal direction, so that the conveying pipe 4 pushes the thrombus support 5 to be discharged from the traction catheter 2, and the thrombus support 5 can expand along the circumferential direction under the self elastic force due to the separation from the limitation of the traction catheter 2, so that the thrombus support 5 can crush the thrombus in the thrombus taking support 3.

Fig. 13 to 15 are schematic structural views of a first embodiment of the support 5 for the thrombus.

Referring to fig. 13 to 15 in combination with fig. 1, in the present embodiment, the plug breaking bracket 5 includes a fixing tube 51, a first bracket 52 and a second bracket 53. The fixing tube 51 may not have a tubular structure, but may be a fixing member such as a solid rod structure or a frame structure.

The fixed pipe 51 is fixedly sleeved on the conveying pipe 4, so that the broken bolt support 5 is fixedly connected with the conveying pipe 4. The fixing tube 51 and the delivery tube 4 can be connected and fixed by bonding, for example, medical glue or hot melt adhesive is selected for fixing.

Be equipped with the trompil on fixed pipe 51's the perisporium, the inner chamber of fixed pipe 51 of trompil intercommunication, medical glue or hot melt adhesive accessible this trompil part infiltration fixed pipe 51's inner chamber to make fixed pipe 51 bond on conveyer pipe 4, in order to improve the bonding area between garrulous bolt support 5 and the conveyer pipe 4, make the connection between garrulous bolt support 5 and the conveyer pipe 4 more firm, and make garrulous bolt support 5 have better antitorque circular property.

Referring to fig. 13 to 15, the first bracket 52 includes two first rods 521 symmetrically distributed in the circumferential direction, and the bolt breaking bracket includes a first ring 522 disposed at the distal end of the first rods 521. The proximal end of the first cutter bar 521 is attached to the fixed tube 51 and the distal end of the first cutter bar 521 is attached to the first ring 522.

The first cut rod 521 has a variable radial dimension in a proximal-to-distal direction, and the first circular ring 522 is coaxially disposed with the fixed tube 51 and movably sleeved on the delivery tube 4, so that the first circular ring 522 can move axially relative to the fixed tube 51, and the first cut rod 521 can freely compress and expand, thereby forming the first stent 52 into a stent structure capable of contracting and expanding in a radial direction.

When the first bracket 52 rotates along with the fixed tube 51 in the circumferential direction, the first cutting rod 521 can form a first rotary cutting curved surface, and can cut thrombus. The first cutting bar 521 may have a semicircular shape, a semi-elliptical shape, a V-shape, a W-shape, or the like to form various shapes of the rotary cutting curved surface. It is understood that the first cutting bars 521 may be provided in three, four or more numbers and arranged at circumferential intervals.

Still referring to fig. 13 to 15, the second bracket 53 includes two second cutting rods 531 symmetrically distributed in the circumferential direction, and the plug bracket includes a second ring 532 disposed at the distal end of the second cutting rods 531. The proximal end of the second cutting bar 531 is attached to the fixed tube 51, and the distal end of the second cutting bar 531 is attached to the second ring 532. The second cutting rods 531 and the first cutting rods 521 are arranged in a staggered and spaced mode in the circumferential direction, meanwhile, the second circular rings 532 and the first circular rings 522 are coaxially arranged, and a space is formed between each second circular ring 532 and each first circular ring 522.

The second cutting rod 531 has a varying radial dimension in a proximal-to-distal direction, and the second ring 532 is movably fitted over the delivery tube 4 such that the second ring 532 is able to move axially relative to the fixed tube 51 and the second cutting rod 531 is able to freely compress and expand, thereby forming the second stent 53 into a stent structure that is able to contract and expand in a radial direction. That is, the fixing members such as the fixing tube 51 are connected to one ends of the first cutting rod 521 and the second cutting rod 531, the fixing members such as the fixing tube 51 are fixedly connected to the delivery pipe 4, the first circular ring 522 is connected to one end of the first cutting rod 521, which is far away from the fixing tube 51, the second circular ring 532 is connected to one end of the second cutting rod 531, which is far away from the fixing tube 51, and both the first circular ring 522 and the second circular ring 532 are slidably connected to the delivery pipe 4. That is, the first and

second brackets

52 and 53 are slidably coupled to the feed pipe 4 at ends thereof remote from the fixing member such as the fixing pipe 51.

Meanwhile, when the second stent 53 is circumferentially rotated with the fixed tube 51, the second cutting bar 531 can form a second rotary cutting curved surface, and the thrombus can be cut. The second cutting bar 531 may also be formed in a semicircular shape, a semi-elliptical shape, a V-shape or a W-shape, etc. to form rotary cutting curved surfaces of different shapes. It is understood that the second cutting bar 531 may be provided in plurality and arranged at circumferential intervals. And the plurality of first cutting bars 521 and the plurality of second cutting bars 531 may be arranged in a crossed or staggered interval to alternately cut the thrombus. For example, one of the first cut levers 521, one of the second cut levers 531, the other first cut lever 521, and the other second cut lever 531 are arranged in this order in a counterclockwise or clockwise direction in the circumferential direction.

The whole of the plug crushing support 5 can be manufactured by a nickel-titanium tube through a laser cutting process and a heat setting process.

Referring to fig. 13 to 15, in the present embodiment, the connection point between the second cutting rod 531 and the fixed tube 51 is located at the distal end of the connection point between the first cutting rod 521 and the fixed tube 51, the second circular ring 532 is located at the proximal end of the first circular ring 522, and the radial dimension of the first cutting rod 521 is larger than that of the second cutting rod 531. Therefore, the second rotary cutting curved surface and the first rotary cutting curved surface are arranged at an inner interval and an outer interval, namely the second rotary cutting curved surface is wrapped inside the first rotary cutting curved surface, and the second rotary cutting curved surface and the first rotary cutting curved surface form rotary spherical surfaces with different inner and outer layers of sizes. The structure can lead the thrombus tissue entering the inside of the thrombus bracket 5 to be cut by the first rotary cutting curved surface and the second rotary cutting curved surface in a crossing way, so as to smash the thrombus tissue to be smaller.

In one embodiment, a fixed member such as a fixed tube 51 is rotatable about a rotational axis to rotate the first support to form a first rotationally cut surface and to rotate the second support to form a second rotationally cut surface. The surface of revolution should be understood broadly herein to allow it to have a certain thickness. The maximum radial distance of the first support from the axis of rotation is greater than the maximum radial distance of the second support from the axis of rotation. Wherein, the plane perpendicular to the rotation axis intersects with the rotation axis and the first support or the second support, the radial distance refers to the distance between the intersection point of the plane and the first support and the intersection point of the rotation axis, and the same is true for the radial distance of the second support.

In some embodiments, if the first bracket includes a plurality of first cutting bars 521, the plurality of first cutting bars 521 are rotated about the rotation axis to form a plurality of first rotary cutting curved surfaces, which may or may not coincide, depending on the respective configurations of the first cutting bars 521. For example, when a plurality of first cutting bars 521 are arranged around the rotation axis array, that is, the first cutting bars 521 are identical in shape, the first rotating cutting curved surfaces coincide; for example, if the first cutting rods 521 have different shapes, the first rotational cutting curves formed by the rotation of the first cutting rods 521 around the rotation axis are not completely overlapped or overlapped.

In some embodiments, the first and second curved rotary cutting surfaces are at least partially spaced apart. The first bracket rotates around the first rotating axis to form the first rotating cutting curved surface, and the second bracket rotates around the second rotating axis to form the second rotating cutting curved surface. When the first rotation axis is coaxial with the second rotation axis, the first rotary cutting curved surface and the second rotary cutting curved surface are coaxial. And a connecting line between the plane perpendicular to the first rotating axis and the first rotating axis is called as one radial direction of the first rotating cutting curved surface. Similarly, at any point on the intersection line of the plane perpendicular to the second rotation axis and the second rotating cutting surface, the line connecting the second rotation axis and the plane perpendicular to the second rotation axis is called as one radial direction of the second rotating surface. The first rotary cutting curved surface and the second rotary cutting curved surface have at least one part with interval in the same vertical plane, and the vertical plane can be a plane perpendicular to the first rotation axis or a plane perpendicular to the second rotation axis.

It will be appreciated that the first and second curved rotary cutting surfaces are spaced apart when the second curved rotary cutting surface is spaced inwardly and outwardly from the first curved rotary cutting surface.

It will be appreciated that when the second rotary cutting surface is positioned with one portion inside the first rotary cutting surface and another portion outside the first rotary cutting surface, the portion of the second rotary cutting surface intersecting the first rotary cutting surface is not spaced.

It should be noted that both the first bracket 52 and the second bracket 53 can be freely contracted and expanded during the entire rotation of the bracket 5. And because the first ring 522 at the far end of the first support 52 and the second ring 532 at the far end of the second support 53 are separated from each other and do not interfere with each other, in the rotary cutting thrombus process, when the first rotary cutting curved surface formed by the first support 52 positioned at the outer side is deformed due to thrombus compression, the deformation of the first rotary cutting curved surface does not influence the second rotary cutting curved surface formed by the second support 53 positioned at the inner side, so that the cutting space of the inner rotary cutting curved surface can be ensured, the thrombus can be completely cut, and the thrombus breaking effect can be further improved.

FIGS. 16 to 20 are schematic structural views of a second embodiment of a bracket 5 for a plug according to the present invention.

Referring to fig. 16 to 20 in combination with fig. 12, the tumbler bracket 5 of the present embodiment has the same main structure as the tumbler bracket 5 of the first embodiment, except that the front end of the tumbler bracket 5 has a different structure.

In the morcellating bracket 5 of the present embodiment, the fixed tube 51 is divided into a first fixed tube 511 and a second fixed tube 512. The second fixing tube 512 is spliced at the far end of the first fixing tube 511 along the axial direction, and the first fixing tube 511 and the second fixing tube 512 are both fixed on the delivery pipe 4 in a sleeved manner. The proximal end of the first cutter bar 521 is connected to the first stationary tube 511. The proximal end of the second cutting bar 531 is attached to the second stationary tube 512.

It should be noted that the bracket 5 of the present embodiment can be divided into two first brackets 52 and two second brackets 53 separated from each other. The first bracket 52 and the second bracket 53 can be respectively made of a nickel-titanium tube by a laser cutting process and a heat setting process, and are finally spliced into a whole. The scheme can simplify the structures of the first support 52 and the second support 53 respectively and reduce the difficulty of the laser cutting process.

In this embodiment, the distal end of the first fixing tube 511 is concavely provided with a retention groove 5111, and the proximal end of the second fixing tube 512 is convexly provided with a retention projection 5121 matched with the retention groove 5111. The catching projection 5121 is engaged and connected to the catching groove 5111, so that the second fixing tube 512 is coaxially connected to the distal end of the first fixing tube 511. It is understood that the retention groove 5111 can also be provided at the proximal end of the second stationary tube 512, while the retention projection 5121 is provided at the distal end of the first stationary tube 511.

One or more first openings 5112 are formed in the peripheral wall of the first fixing tube 511, and the first openings 5112 are communicated with the lumen of the first fixing tube 511. One or more second openings 5122 are formed in the peripheral wall of the second fixing tube 512, and the second openings 5122 are communicated with the tube cavity of the second fixing tube 512. Glue can enter the lumen of the first fixing tube 511 through the first opening 5112 to improve the connection firmness between the first fixing tube 511 and the delivery tube 4, and can also enter the lumen of the second fixing tube 512 through the second opening 5122 to improve the connection firmness between the second fixing tube 512 and the delivery tube 4.

FIGS. 21 to 22 are schematic structural views of a bracket 5 for a bolt breaker according to a third embodiment of the present invention.

Referring to fig. 21 to 22 in combination with fig. 12, the main structure of the bracket 5 of this embodiment is the same as that of the bracket 5 of the second embodiment, except that the structure of the distal end of the bracket 5 is different.

In the bolt breaking bracket 5 of the embodiment, the first ring 522 at the distal end of the first bracket 52 and the second ring 532 at the distal end of the second bracket 53 are connected into a whole, i.e. the third ring 54 is formed. The distal ends of the first cutting rod 521 and the second cutting rod 531 are both connected to the third ring 54, and the third ring 54 is movably sleeved on the conveying pipe 4. Of course, the third ring 54 may not be formed by fixedly connecting the first ring 522 and the second bracket 53, but may be directly manufactured as a separate component.

It should be noted that in the bolt breaking bracket 5 of the present embodiment, the distal end of the first bracket 52 is connected to the distal end of the second bracket 53, so that the first rotational cutting curve formed by the first bracket 52 and the second rotational cutting curve formed by the second bracket 53 have a certain influence on each other.

FIG. 23 is a schematic structural view of a fourth embodiment of a bracket 5 for a thrombi of the present invention.

Referring to FIG. 23 in conjunction with FIG. 12, the bracket 5 of this embodiment has the same main structure as the bracket 5 of the first embodiment, except that the proximal end of the first bracket 52 and the second bracket 53 have different structures.

In the morcellating bracket 5 of the present embodiment, the connection point of the first cutter bar 521 to the fixed tube 51 is located on the distal end side of the connection point of the second cutter bar 531 to the fixed tube 51. The distal end of the first stent is located on the distal side of the distal end of the second stent, where "the distal end of the first stent" refers to the junction of the first cutting bar 521 and the third ring 54, and "the distal end of the second stent" refers to the junction of the second cutting bar 531 and the third ring 54.

Therefore, the first rotary cutting curved surface formed by the first cutter bar 521 and the second rotary cutting curved surface formed by the second cutter bar 531 are staggered at the proximal portion. That is, the first rotary cut surface and the second rotary cut surface intersect. This kind of structural scheme can make first rotary cutting curved surface and second rotary cutting curved surface form the space sphere of crisscross each other, can improve the bits of broken glass bolt effect of bits of broken glass bolt support 5 better.

Still referring to FIG. 12, the driving handle 41 is used to drive the delivery tube 4 and the bracket 5 to rotate circumferentially. In this embodiment, a drive handle 41 is removably disposed at the proximal end of delivery tube 4. The proximal end of the delivery tube 4 is provided with a drive terminal 401. The driving handle 41 is provided with a driving interface 411, and the driving interface 411 can be butted with the driving terminal 401 of the delivery pipe 4. A gear assembly is arranged in the driving handle 41, a driving wrench 412 is hinged on the driving handle 41, and the driving wrench 412 is in transmission connection with the driving interface 411 through the gear assembly. Drive spanner 412 is held through pressing, can drive the gear assembly and rotate to drive interface 411 fast revolution through the variable speed of gear assembly, and then rotate through the drive terminal 401 with the butt joint of drive interface 411, and then drive the bits of broken glass support 5 of conveyer pipe 4 and the conveyer pipe 4 distal end with drive terminal 401 body coupling and carry out fast circumference rotation, cut the thrombus tissue of parcel in getting to tie support 3 and smash.

The thrombus material-crushing stent 5 is rotated in the circumferential direction within the thrombus removal stent 3, and cuts and crushes the thrombus tissue enclosed in the thrombus removal stent 3. The supporting bracket 32 is arranged to support the filter membrane 33, so that the filter membrane 33 can keep a relatively stable shape, the supporting bracket 32 and the filter membrane 33 are prevented from being compressed inwards along the radial direction due to the extrusion of the inner wall of the blood vessel, and the thrombus stent 5 is contacted with the supporting bracket 32 or the filter membrane 33, so that the thrombus stent 5 is prevented from rotating in the circumferential direction in the thrombus removal stent 3. That is, the support stent 32 needs to have a certain radial support property in addition to a certain flexibility, and a certain radially outward supporting force is provided by the support stent 32, so that a certain interval is formed between the support stent 32 and the plug support 5, or a certain interval is formed between the screen film 33 and the plug support 5.

It will be appreciated that a spring mechanism may be provided in the drive handle 41 in communication with the drive wrench 412 to allow the drive wrench 412 to spring back and maintain the drive wrench 412 in a repeatable gripping relationship.

Still referring to fig. 12, the loading tube 42 is movably sleeved on the conveying tube 4, and the loading tube 42 is used for loading the broken bolt support 5. The loading tube 42 can move to the distal end of the conveying tube 4 and is sleeved on the plug support 5, so that the plug support 5 is accommodated in the loading tube 42, and the first support 52 and the second support 53 can be accommodated in the loading tube 42.

When it is desired to use the thrombi stent 5, the loading tube 42 can be moved to the proximal end of the delivery tube 4, the distal end of the delivery tube 4 and the thrombi stent 5 can be used together by extending into the traction catheter 2, and the loading tube 42 can stay outside the traction catheter 2.

When the broken bolt support 5 is used, the far end of the conveying pipe 4 and the broken bolt support 5 can be completely withdrawn from the traction guide pipe 2, and the loading pipe 42 is sleeved on the broken bolt support 5 again, so that the broken bolt support 5 is prevented from contacting with the external environment as far as possible.

Still referring to fig. 12, the proximal end of the delivery tube 4 is also sleeved with a stainless steel tube 402. The proximal end of the delivery tube 4 is connected to the proximal end of a stainless steel tube 402. In this embodiment, the proximal end of the stainless steel tube 402 is connected to the drive terminal 401. It will be appreciated that by releasing or fixing the stainless steel tube 402, the axial movement of the delivery tube 4 can be defined and controlled.

Referring to fig. 24 and 25 in combination with fig. 1, in the present embodiment, a sheath joint 11 is disposed at a proximal end of the outer sheath 1, and an adjusting knob 12 is disposed at a proximal end of the sheath joint 11. An adjusting knob 12 is rotatably connected to the proximal end of the sheath joint 11, and a compression ring 13 and a silicone ring 14 are interposed between the adjusting knob 12 and the sheath joint 11. The silicone ring 14 is clamped between the adjusting knob 12 and the compression ring 13.

The traction catheter 2 sequentially penetrates through the adjusting knob 12, the silica gel ring 14, the compression ring 13 and the sheath pipe joint 11, and then extends into the outer sheath pipe 1. The silicone ring 14 has an inner bore. The silica gel ring 14 can be extruded by rotating the adjusting knob 12, so that the inner diameter (namely the size of an inner hole) of the center of the silica gel ring 14 is changed, the traction catheter 2 can be clamped or loosened, and whether the traction catheter 2 and the outer sheath tube 1 can move relatively or not is controlled.

In the present embodiment, a branch joint 111 is further formed on the circumferential side of the sheath joint 11, and the branch joint 111 communicates with the inside of the clamp ring 13, and further communicates with the sheath joint 11 and the inside of the outer sheath 1. The branch fitting 111 may circumscribe the branch hose 15. The other end of the branch hose 15 may be connected to a standard luer fitting.

Referring to fig. 26 and 27 in conjunction with fig. 1, the suction device comprises a connector duct 6 and a branch duct 61 connected to the connector duct 6.

The distal end of the adapter catheter 6 is axially connected to the proximal end of the pull catheter 2. In this embodiment, the proximal end of the traction catheter 2 is provided with a fixed cap 21, and the distal end of the adapter catheter 6 can be screwed with the fixed cap 21 to communicate the adapter catheter 6 and the traction catheter 2. The delivery tube 4 is movably disposed through the adapter catheter 6 and the pull catheter 2, and the delivery tube 4 can be completely withdrawn from the adapter catheter 6 from the proximal end of the adapter catheter 6.

The near end of the joint conduit 6 is provided with a switch which is used for controlling the opening and closing of the near end opening of the joint conduit 6. The switch closes the proximal port of the adaptor catheter 6 after the delivery tube 4 and the crash bolt support 5 have completely withdrawn the pull catheter 2 and the adaptor catheter 6 from the proximal end of the adaptor catheter 6.

In this embodiment, the switch includes a screw cap 62 and a packing 63. A screw cap 62 is screwed to the proximal end of the connector catheter 6. The seal ring 63 is provided in the proximal port of the connector catheter 6 and is interposed between the screw cap 62 and the proximal port of the connector catheter 6. The delivery pipe 4 is axially movably inserted into the screw cap 62 and the seal ring 63, and can completely withdraw from the seal ring 63.

The seal ring 63 has elasticity and deformability. After the delivery pipe 4 completely exits the joint conduit 6 and the sealing ring 63, the screw cap 62 is rotated forward or backward, and the sealing ring 63 is synchronously pressed or released, so as to change the size of the central hole of the sealing ring 63. And when the center hole of the seal ring 63 disappears due to extrusion deformation, the proximal port of the joint conduit 6 can be closed. When the central hole of the sealing ring 63 is present, the proximal port of the adapter catheter 6 can be opened. Meanwhile, when the conveying pipe 4 penetrates through the joint guide pipe 6 and the sealing ring 63, the size of the central hole of the sealing ring 63 is changed by rotating the screw cap 62 and extruding, so that the sealing ring 63 can clamp and fix or loosen the conveying pipe 4, and whether the conveying pipe 4 and the joint guide pipe 6 and the traction guide pipe 2 can move relatively along the axial direction or not is further controlled. It will be appreciated that the central aperture is provided in the seal ring 63 only and need not be provided in the centre of the seal ring 63.

One end of the branch conduit 61 is connected to the peripheral wall of the joint conduit 6 and communicated with the inner cavity of the joint conduit 6, and the other end of the branch conduit 61 is externally connected with suction power. The external suction power can be the suction syringe 64, when the proximal port of the adapter catheter 6 is closed, the thrombus at the proximal port of the traction catheter 2 can be collected inside the suction syringe 64 by the suction syringe 64 through the traction catheter 2, the adapter catheter 6 and the branch catheter 61. In this case, the pull catheter 2 is used as a suction catheter, i.e. the pull catheter 2 can also be considered as an integral part of the suction device.

In this embodiment, a branch pipe connector 601 communicating with the inside of the connector duct 6 is provided on the side wall of the connector duct 6, and the branch duct 61 is detachably connected to the branch pipe connector 601 to be connected to the connector duct 6.

Referring to fig. 28 to fig. 38, the operation principle of the embolectomy system of the present embodiment will be described in detail.

Referring to FIG. 28, FIG. 28 is a schematic view of the inferior vena cava 01 of a human being. Within the inferior vena cava vessel 01 there is thrombus tissue 02. A guide wire 03 is introduced through a femoral vein or popliteal vein puncture 04 to establish a pathway for vein embolectomy.

Referring to fig. 29, a guidewire 03 is advanced out of the guide head 34 at the distal end of the embolectomy device. The thrombus taking device enters the vein 01 from the puncture hole 04 along the guide wire 03 and is gradually conveyed forwards.

Referring to fig. 30, the thrombectomy device is advanced along the guidewire 03 until the distal end of the sheath 1 passes through the thrombus tissue 02.

Referring to fig. 31, the sheath connector 11 is fixed, and the traction catheter 2 and the connector catheter 6 are pushed continuously, so that the thrombectomy stent 3 extends out of the distal end of the outer sheath 1, and the thrombectomy stent 3 can be released gradually in the blood vessel. And when the proximal end of the embolectomy stent 3 completely extends out of the distal end port of the sheath catheter 1, the traction catheter 2 and the joint catheter 6 are stopped being pushed.

During release of the thrombectomy stent 3, the screw cap 62 may be loosened to allow axial movement of the delivery tube 4 relative to the traction catheter 2. And through to distal end propelling movement conveyer pipe 4, make the distal end of conveyer pipe 4 support and lean on getting to tie the guide head 34 of 3 distal ends of support, in order to drive and get to tie support 3 and stretch out sheath pipe 1, and when getting the near-end of tying support 3 and stretch out the distal end port of sheath pipe 1 completely, through fixed traction pipe 2 and joint pipe 6, and withdraw conveyer pipe 4, make and get to tie support 3 and release completely in the blood vessel, get to tie support 3 and arrange by wall in the blood vessel.

It should be noted that during the forward pushing of the delivery tube 4, the thrombus support 5 can extend out of the traction catheter 2 and into the thrombus removal support 3. During the retraction of the delivery tube 4, the stent 5 may be forced to compress into the pull catheter 2.

It will be appreciated that the pull catheter 2 and adapter catheter 6 may also be secured and the thrombectomy stent 3 released by withdrawal of the sheath 1.

Referring to fig. 32, fig. 32 is a schematic view of the thrombus removal stent 3 fully released at the distal end of the thrombus tissue 02.

Referring to fig. 33, the embolectomy system is withdrawn integrally, that is, the sheath tube 1, the traction catheter 2 and the delivery tube 4 are withdrawn integrally, so as to drive the embolectomy stent 3 to withdraw. The thrombus tissue 02 is peeled off from the inner wall of the vein vessel 01 by utilizing the opening at the near end of the thrombus removal support 3 and the support structure, enters the thrombus removal support 3, and is wrapped and collected by the filter screen film 33.

Referring to FIG. 34 in conjunction with FIG. 33, the tube 4 is pushed forward to re-enter the thrombus support 5 into the thrombus support 3. Drive interface 411 with actuating handle 41 docks with the drive terminal 401 of conveyer pipe 4, through repeatedly pressing and holding drive spanner 412, drive interface 411 fast turn, and then drive garrulous bolt support 5 fast revolution, will wrap up the cutting of the inside thrombus tissue 02 of filter screen film 33 and smash.

Referring to FIG. 35, after completion of the thrombolysis, the whole of the thrombolysis devices such as the thrombolysis stent 5 and the delivery tube 4 are withdrawn proximally and completely from the proximal end of the adapter catheter 6. After the broken bolt support 5 is withdrawn from the connector guide tube 6, the loading tube 42 is sleeved on the broken bolt support 5, so that the broken bolt support 5 is compressed into the loading tube 42.

Referring to fig. 36, the proximal end of the adapter catheter 6 is rotated to rotate the cap 62, compressing the inner seal 63 and closing the proximal port of the adapter catheter 6. The suction syringe 64 is communicated with the branch catheter 61. By pulling the suction cylinder 64, the broken thrombus can be sucked into the interior of the suction cylinder 64 through the traction catheter 2 and the branch catheter 61 and taken out.

A branch switch 611 is provided between the suction cylinder 64 and the branch catheter 61, and the branch switch 611 is used to control whether or not the branch catheter 61 and the suction cylinder 64 communicate with each other. It is understood that branch switch 611 may also be used to control whether branch conduit 61 is in communication with the outside.

Referring to FIG. 37, the thrombus removal stent 3 is continuously withdrawn, and the thrombus is continuously separated and collected in the filter membrane 33.

Referring to fig. 38, the proximal end of the adapter catheter 6 is rotated in reverse to screw cap 62, releasing the inner seal 63 and opening the proximal port of the adapter catheter 6. The crushed thrombus stent 5 and the delivery pipe 4 are pushed into the connector catheter 6 again through the loading pipe 42 and are pushed into the traction catheter 2 continuously, the operations in the figures 34 to 36 are repeated until the thrombus tissue 02 is taken out of the vein vessel 01 completely, finally, the thrombus taking stent 3 is retracted into the outer sheath pipe 1 through the fixed sheath pipe connector 11 and the connector catheter 6 is withdrawn, and the thrombus taking is finished.

FIG. 39 is a schematic view of thrombus aspiration in accordance with the second embodiment of the present invention.

Referring to FIG. 39, in a second embodiment of the present invention, a second alternative for aspirating thrombi is provided.

In this embodiment, when the whole of the thrombectomy device is withdrawn from the proximal end of the adapter catheter 6 after the thrombectomy is completed, a suction catheter 65 may be extended into the traction catheter 2 through the adapter catheter 6 and out of the traction catheter 2, so that the distal end of the suction catheter 65 extends into the thrombectomy stent 3. The proximal end of the aspiration catheter 65 is connected to an aspiration device for performing a thrombus aspiration operation through the distal end of the aspiration catheter 65. In this process, the traction catheter 2 is used as a passage for the suction catheter 65. Of course, when in operation, the distal end of the suction catheter 65 does not extend into the thrombus extraction support 3, and the thrombus can be sucked, particularly, the thrombus can be sucked by the suction catheter 65 and the traction catheter 2 together. For example, when the distal end of the aspiration catheter 65 is positioned within the traction catheter 2, the thrombus inside the thrombectomy stent 3 first enters the traction catheter 2 and then enters the aspiration catheter 65 through the distal end of the aspiration catheter 65.

It should be noted that during the aspiration operation, the distal end of the pull catheter 2 is attached to the proximal end of the thrombectomy stent 3, without accessing the interior of the thrombectomy stent 3.

Fig. 40 and 41 are schematic structural views of a thrombus removal device according to a third embodiment of the present invention.

Referring to fig. 40 to 41, in a third embodiment of the present invention, a second connection scheme of the thrombectomy stent 3 in the thrombectomy device and the traction catheter 2 is provided, wherein the proximal end of the thrombectomy stent 3 is movably connected to the distal end of the traction catheter 2.

In this embodiment, the peripheral wall of the distal end of the traction catheter 2 is concavely provided with a sliding groove 22, and the proximal end of the separation bracket 31 in the thrombectomy bracket 3 is movably sleeved on the sliding groove 22, i.e. the connection ring 313 is slidably sleeved on the sliding groove 22. The connection ring 313 is axially slidable within the confines of the slide slot 22. The connection ring 313 is provided with a pulling wire 3131, and the distal end of the pulling wire 3131 is connected to the connection ring 313, i.e., the pulling wire 3131 is connected to the separation bracket 31. The pull wire 3131 may be used to pull the detachment bracket 31 and the entire embolectomy bracket 3 to slide along the slide groove 22 toward the proximal end of the traction catheter 2, thereby controlling the position of the distal port of the traction catheter 2 inside the embolectomy bracket 3. The scheme structure can effectively suck residual thrombus tissue 02 at the proximal part of the thrombus bracket 3 in the process of sucking thrombus.

FIG. 42 is a schematic structural diagram of a thrombus removal system according to a fourth embodiment of the present invention.

Referring to FIG. 42, in a fourth embodiment of the present invention, an improved version of an outer sheath 1 is provided.

In this embodiment, a compression balloon 16 is sleeved outside the distal end of the sheath tube 1. Compression balloon 16 may be in communication with an external high pressure device. When the thrombus stripping of the thrombus taking support 3 is finished, the high-pressure equipment can inject physiological saline into the compression balloon 16, so that the compression balloon 16 is expanded and is tightly attached to the inner wall of the blood vessel. The compressed balloon 16 can effectively prevent the thrombus tissue 02 from flowing reversely, and the thrombus tissue 02 is completely extruded into the thrombus taking support 3, so that thrombus crushing and thrombus suction are completed, and a better thrombus removing effect is achieved.

FIG. 43 is a schematic structural diagram of a embolectomy system according to a fifth embodiment of the present invention.

Referring to FIG. 43, in a fifth embodiment of the present invention, an integrated design of a deadbolt breaking device is provided. The present embodiment differs from the first embodiment in the structure of the drive handle 41.

In this embodiment, the drive handle 41 is integrally formed on the delivery tube 4. The proximal end of the delivery tube 4 extends through the drive handle 41. When the driving wrench 412 is pressed, the gear assembly in the driving handle 41 can directly drive the conveying pipe 4 to rotate circumferentially.

FIG. 44 is a schematic structural diagram of a thrombus removal system according to a sixth embodiment of the present invention.

Referring to FIG. 44, in a sixth embodiment of the present invention, an electrically driven deadbolt reduction scheme is provided. The present embodiment differs from the first embodiment in the structure of the drive handle 41.

In this embodiment, the driving handle 41 does not have the driving wrench 412, while the rechargeable battery 413 and the driving motor 414 are provided inside the driving handle 41. The rechargeable battery 413 powers the drive motor 414, causing the drive motor 414 to rotate. The driving motor 414 can drive the gear assembly to rotate, and further drive the driving interface 411 to rotate at a high speed. The driving handle 41 is further provided with a control button 415, and the control button 415 is used for controlling the driving motor 414 to work.

Based on the technical scheme, the embodiment of the invention at least has the following advantages and positive effects:

in the thrombus removal system of the embodiment of the invention, the outer sheath tube 1 is used for accommodating the thrombus removal bracket 3 and the traction catheter 2; the traction catheter 2 can be used for accommodating the thrombus support 5 and the delivery pipe 4; the traction catheter 2 and the thrombus taking bracket 3 are matched with the sheath tube 1, so that thrombus in the blood vessel is accommodated in the thrombus taking bracket 3; then, the thrombus bracket 5 is matched with the conveying pipe 4, so that the thrombus bracket 5 extends into the thrombus taking bracket 3 to rotate, and the thrombus in the thrombus taking bracket 3 is cut into fine particles, thereby being beneficial to crushing intractable, large and hard thrombus; finally, the delivery pipe 4 is utilized to drive the thrombus-breaking support 5 to retreat from the traction catheter 2, the traction catheter 2 can be used as a suction catheter at the same time, and the small thrombus in the thrombus taking support 3 is sucked through the inner cavity of the traction catheter 2, so that pulmonary embolism caused by the omission of the small thrombus is effectively prevented, and the thrombus taking effect is improved.

While the present invention has been described with reference to several exemplary embodiments, it is understood that the terminology used is intended to be in the nature of words of description and illustration, rather than of limitation. As the present invention may be embodied in several forms without departing from the spirit or essential characteristics thereof, it should also be understood that the above-described embodiments are not limited by any of the details of the foregoing description, but rather should be construed broadly within its spirit and scope as defined in the appended claims, and therefore all changes and modifications that fall within the meets and bounds of the claims, or equivalences of such meets and bounds are therefore intended to be embraced by the appended claims.

Claims

1. A thrombectomy system, comprising:

2. The embolectomy system of claim 1, further comprising an aspiration catheter extending into the traction catheter after the fragmented embolus stent is withdrawn from the proximal end of the traction catheter, the aspiration catheter being configured to receive external aspiration power that aspirates thrombus within the embolus stent through the aspiration catheter and/or the traction catheter.

3. The embolectomy system of claim 1, wherein after the crushed thrombus support is withdrawn from the proximal end of the traction catheter, the traction catheter is configured to be externally connected with an aspiration power, and the externally connected aspiration power aspirates thrombus within the embolectomy support through the traction catheter.

4. The embolectomy system of claim 1, further comprising a suction device comprising a connector conduit in communication with the traction conduit and a branch conduit in communication with either the connector conduit or the branch conduit; the branch conduit is used for connecting external suction power, and the joint conduit is connected with a switch for controlling the opening and closing of the joint conduit;

5. The embolectomy system of claim 4, wherein the switch comprises a screw cap and a resilient sealing ring, the sealing ring having a central aperture at least when not compressed by the rotation; the rotary cover is rotatably connected to the joint guide pipe; the sealing ring is clamped between the screw cap and the proximal port of the joint catheter, and the central hole is communicated with the inner cavity of the joint catheter; and rotating the rotary cover, and elastically extruding or releasing the sealing ring by the rotary cover so as to open or close the central hole.

6. The embolectomy system of claim 5, wherein the screw cap is rotated when the delivery tube passes through the central hole, and the screw cap elastically presses or releases the sealing ring to control the size of the central hole, so as to clamp or release the delivery tube.

7. The embolectomy system of claim 4, wherein a branch switch for opening and closing the branch conduit is connected to the branch conduit.

8. The embolectomy system of claim 1, wherein the crushed thrombus support expands radially after being withdrawn from the traction catheter.

9. The embolectomy system of claim 1, further comprising a loading tube capable of being moved and sleeved over the fragmented embolus holder such that the fragmented embolus holder is radially compressed and contained within the loading tube such that the fragmented embolus holder can be loaded into the traction catheter.

10. The embolectomy system of claim 9, wherein the loading tube is movably sleeved on the delivery tube, and is moved to the proximal end of the delivery tube, so that the distal end of the delivery tube and the fragmented embolus stent together extend into the pull catheter, and the loading tube stays outside the pull catheter.

11. The embolectomy system of claim 1, further comprising an outer sheath, wherein the embolectomy stent and traction catheter are both connected within the outer sheath and transition between a slidable state and a fixed state within the outer sheath, at least the embolectomy stent being slidable out of the outer sheath.

12. The embolectomy system of claim 11, wherein the outer sheath is connected with a sheath connector, the sheath connector is rotatably connected with an adjusting knob, and a silicone ring with an inner hole is clamped between the adjusting knob and the sheath connector;

13. The embolectomy system of claim 12, wherein a clamp ring is clamped between the adjusting knob and the sheath joint, and the clamp ring and the adjusting knob clamp the silicone ring together.

14. The embolectomy system of claim 12, wherein the sheath hub is in communication with a branch hose.

15. The embolectomy system of claim 1, wherein the proximal end of the delivery tube is fixedly sheathed with a stainless steel tube.

16. The embolectomy system of claim 1, wherein the embolectomy support is slidably coupled to the traction catheter such that the embolectomy support is axially movable relative to the traction catheter.

17. The thrombus removal system according to claim 16, wherein a sliding groove is formed in a peripheral wall of the traction catheter, the thrombus removal support is movably sleeved in the sliding groove, and a pull wire is connected to the thrombus removal support.

18. The embolectomy system of claim 1, wherein the embolectomy support is fixedly attached to the traction catheter.