阅读说明：本技术 一种血栓处理平台 (Thrombus treatment platform ) 是由 王晓天 张磊 冯海全 李晓强 王永刚 关丽鹃 李靖 于 2020-06-12 设计创作，主要内容包括：本发明涉及血栓处理平台,包括具有抽吸通道的抽吸导管、与抽吸导管的近端相连通的抽吸泵、搅拌装置以及滤网组件,滤网组件包括滤杆、滤网；搅拌装置包括第一导管、滑动套设在第一导管外的第二导管、设置在第一导管的远端且具有打开状态和收拢状态的搅拌器、设置在第一导管和第二导管之间且能够使第一导管和第二导管相对滑动从而使搅拌器在打开状态和收拢状态之间转换的操作装置；血栓处理平台还包括与第一导管或第二导管相连接且能够带动搅拌器转动的驱动装置。本发明可以在保证相对安全的情况下去除血栓,特别适合去除下腔静脉中大量血栓,保护静脉瓣膜与静脉血管壁,失血量可控,操作步骤简单,缩短手术时间,减轻患者住院费用。(The invention relates to a thrombus treatment platform, which comprises an aspiration catheter with an aspiration channel, an aspiration pump communicated with the proximal end of the aspiration catheter, a stirring device and a filter screen assembly, wherein the filter screen assembly comprises a filter rod and a filter screen; the stirring device comprises a first guide pipe, a second guide pipe, a stirrer and an operating device, wherein the second guide pipe is sleeved outside the first guide pipe in a sliding manner, the stirrer is arranged at the far end of the first guide pipe and is provided with an opening state and a folding state, and the operating device is arranged between the first guide pipe and the second guide pipe and can enable the first guide pipe and the second guide pipe to slide relatively so as to enable the stirrer to be switched between the opening state and the folding state; the thrombus treatment platform also comprises a driving device which is connected with the first catheter or the second catheter and can drive the stirrer to rotate. The invention can remove thrombus under the condition of ensuring relative safety, is particularly suitable for removing a large amount of thrombus in inferior vena cava, protects venous valves and venous blood vessel walls, has controllable blood loss, simple operation steps, shortens operation time and lightens hospitalization cost of patients.)

1. A thrombus treatment platform comprising an aspiration catheter (10) having an aspiration channel characterized by: the thrombus treatment platform also comprises a suction pump (19) communicated with the proximal end of the suction catheter (10), a stirring device and a filter screen assembly,

the filter screen assembly comprises a filter rod (31) and a filter screen (32) which is fixedly arranged at the far end of the filter rod (31) and has an opened state and a folded state;

the stirring device comprises a first guide pipe (51), a second guide pipe (52) sleeved outside the first guide pipe (51) in a sliding manner, a stirrer (53) which is arranged at the far end of the first guide pipe (51) and has an opened state and a folded state, and an operating device which is arranged between the first guide pipe (51) and the second guide pipe (52) and can enable the first guide pipe (51) and the second guide pipe (52) to slide relatively so as to enable the stirrer (53) to be switched between the opened state and the folded state;

the thrombus treatment platform also comprises a driving device which is connected with the first catheter (51) or the second catheter (52) and can drive the stirrer (53) to rotate.

2. A thrombus treatment platform comprising an aspiration catheter (10) having an aspiration channel characterized by: the thrombus treatment platform also comprises a suction pump (19) communicated with the proximal end of the suction catheter (10), a stirring device and a filter screen assembly,

the filter screen assembly comprises a filter rod (31) passing through the suction channel, and a filter screen (32) fixedly arranged at the distal end of the filter rod (31) and having an opened state and a closed state; said sieve (32) being located at the distal end of said suction duct (10);

the stirring device comprises a first guide pipe (51) penetrating through the suction passage, a second guide pipe (52) penetrating through the suction passage and slidably sleeved outside the first guide pipe (51), a stirrer (53) arranged at the distal end of the first guide pipe (51) and having an opened state and a folded state, and an operating device arranged between the first guide pipe (51) and the second guide pipe (52) and capable of enabling the first guide pipe (51) and the second guide pipe (52) to relatively slide so as to enable the stirrer (53) to be switched between the opened state and the folded state; when said agitator (53) is in an open position, said agitator (53) being located between said sieve (32) and the distal end of said suction duct (10), said agitator (53) moving back and forth in the blood vessel when said first duct (51) is drawn;

the thrombus treatment platform also comprises a driving device which is connected with the first catheter (51) or the second catheter (52) and can drive the stirrer (53) to rotate.

3. A thrombus treatment platform according to claim 1 or 2, wherein: when the stirrer (53) is in a furled state, the outer diameter of the stirrer (53) is less than or equal to 6F.

4. A thrombus treatment platform according to claim 1 or 2, wherein: the agitator (53) enables the degree of deployment to be controlled by the second conduit (52).

5. A thrombus treatment platform according to claim 4, wherein: the stirrer (53) is formed by weaving a plurality of silk threads (56), and two ends of each silk thread (56) are respectively fixed at the near end and the far end of the first catheter (51).

6. A thrombus treatment platform according to claim 4, wherein: the distal end of the first conduit (51) extends out of the second conduit (52); the stirrer (53) comprises a plurality of wires (56); the distal end of each wire (56) is fixedly connected with the first catheter (51), and the proximal end of each wire is fixedly connected with the second catheter (52).

7. A thrombus treatment platform according to claim 5 or 6, wherein: at least some of said filaments (56) intersecting; -at least part of said wire (56) is rotated by a certain angle around said first duct (51); the silk thread (56) is made of one or more of nickel-titanium alloy, stainless steel wire and high polymer.

8. A thrombus treatment platform according to claim 5 or 6, wherein: the stirring device also comprises a plurality of first ultrasonic generators (81) fixedly arranged on the silk thread (56), a first power line (82) connected with the first ultrasonic generators (81), and a first ultrasonic joint (84) arranged on the operating device and capable of supplying power to the first power line (82).

9. A thrombus treatment platform according to claim 8, wherein: the wire (56) has an internal lumen, the first catheter (51) or the second catheter (52) also has an internal lumen, and the first power cord (82) is located within the internal lumen of the wire (56) and the internal lumen of the first catheter (51) or the second catheter (52).

10. A thrombus treatment platform according to claim 9, wherein: the diameter of the first ultrasonic generator (81) is 0.2-0.4 mm, the outer diameter of the silk thread (56) is 0.2-0.3 mm, and the inner diameter of the silk thread (56) is 0.1-0.2 mm.

11. A thrombus treatment platform according to claim 1 or 2, wherein: the operating device comprises a handle (54) sleeved on the first guide pipe (51) and/or the second guide pipe (52), a locking assembly arranged between the first guide pipe (51) and the second guide pipe (52) and capable of locking the first guide pipe and the second guide pipe relatively, and an operating assembly which is connected with the handle (54) in a sliding manner and can be matched and locked with the first guide pipe (51) or the second guide pipe (52); when the locking assembly is in an unlocked state and the operating assembly is in a locked state, and the operating assembly slides relative to the handle (54), the first guide pipe (51) and the second guide pipe (52) slide relative to each other to enable the stirrer (53) to be switched between an opened state and a folded state; when the locking assembly is in a locking state, the relative positions of the first guide pipe (51) and the second guide pipe (52) are locked, and the driving device can drive the first guide pipe (51) and the second guide pipe (52) to rotate.

12. A thrombus treatment platform according to claim 11, wherein: the locking assembly comprises a first locking member (60) fixedly connected with one of the first conduit (51) and the second conduit (52), a second locking member (61) rotatably connected with the other of the first conduit (51) and the second conduit (52), and a third locking member (62) arranged between the first locking member (60) and the second locking member (61) and capable of being matched and locked with the other of the first conduit (51) and the second conduit (52), wherein when the locking assembly is in a locking state, the third locking member (62) is matched and locked with the other of the first conduit (51) and the second conduit (52), the first locking member (60) and the second locking member (61).

13. A thrombus treatment platform according to claim 12, wherein: the third locking piece (62) is made of a material capable of generating elastic deformation, and when the locking assembly is in a locking state, the third locking piece (62) generates elastic deformation and is respectively tightly matched with the other one of the first guide pipe (51) and the second guide pipe (52), the first locking piece (60) and the second locking piece (61).

14. A thrombus treatment platform according to claim 12 or 13, wherein: second locking piece (61) on be formed with the recess, the cell wall of recess on be formed with the internal thread, the surface of first locking piece (60) on be formed with can with internal thread complex external screw thread, first locking piece (60) insert and establish the recess of second locking piece (61) in and through the internal thread with external screw thread with second locking piece (61) rotate and be connected, third locking piece (62) be located first locking piece (60) with the appearance intracavity that second locking piece (61) formed.

15. A thrombus treatment platform according to claim 11, wherein: the operating component comprises an operating part (55) which is connected with the handle (54) in a sliding way, an engaging part (64) which is formed on the operating part (55) and can be matched and locked with the first conduit (51) or the second conduit (52), and an elastic part (67) which makes the engaging part (64) have the tendency of moving towards the state of being matched and locked with the first conduit (51) or the second conduit (52); when the operating assembly is in a locking state, the matching part (64) is matched and locked with the first conduit (51) or the second conduit (52); when the operating assembly is in the unlocked state, the fitting portion (64) is separated from the first conduit (51) or the second conduit (52).

16. A thrombus treatment platform according to claim 14, wherein: the operating assembly further comprises a sliding rail (65) fixedly arranged on the inner wall of the handle (54), a sliding block (66) connected with one end of the elastic piece (67) and capable of sliding in a matched mode with the sliding rail (65), and the other end of the elastic piece (67) is connected with the matching portion (64).

17. A thrombus treatment platform according to claim 15, wherein: the stirring device also comprises a plurality of first ultrasonic generators (81) fixedly arranged on the silk thread (56), a first power line (82) connected with the first ultrasonic generators (81), and a first ultrasonic joint (84) which is arranged on the operating device and can supply power to the first power line (82); said wire (56) having an internal lumen, said second catheter (52) also having an internal lumen, said first power cord (82) being located within the internal lumen of said wire (56) and the internal lumen of said second catheter (52); the stirring device also comprises a conductive ring (91) fixedly arranged at the proximal end of the first power line (82); the first catheter (51) comprises a flexible pipe section, a metal pipe and an insulating layer, wherein the far end of the metal pipe is fixedly connected with the near end of the flexible pipe section, and the insulating layer is sleeved on the part of the metal pipe; the material of the matching part (64) is an inductive material, the first ultrasonic joint (84) is connected with the matching part (64), the conductive ring (91) is contacted with the metal pipe of the first conduit (51) in the effective stroke of the relative movement of the first conduit (51) and the second conduit (52), and the matching part (64) can be contacted with the metal pipe of the first conduit (51); the first ultrasonic connector (84) is capable of supplying power to the first ultrasonic generator (81) when the fitting portion (64) is in contact with the metal tube of the first conduit (51).

18. A thrombus treatment platform according to claim 1 or 2, wherein: the driving device comprises a motor (20) connected with the first conduit (51) or the second conduit (52) and a power supply capable of supplying power to the motor (20).

19. A thrombus treatment platform according to claim 1 or 2, wherein: the first guide pipe (51) is sleeved on the filtering rod (31), and the outer diameter of the filtering rod (31) is 0.1-1 mm.

20. A thrombus treatment platform according to claim 1 or 2, wherein: an injection hole (58) for injecting thrombolytic drugs is formed at the proximal end of the first catheter (51), and a plurality of thrombolytic holes (59) for the thrombolytic drugs to enter a blood vessel are formed at the distal end of the first catheter (51) and/or the stirrer (53).

21. A thrombus treatment platform according to claim 1 or 2, wherein: the suction catheter (10) comprises a catheter part with the suction channel, an operating part (4) movably connected to the near end of the catheter part, a fixing part (15) fixedly arranged on the catheter part, and a connecting part (14) which is respectively connected with the operating part (4) and the fixing part (15) and can bend the far end of the catheter part by operating the operating part (4).

22. A thrombus treatment platform according to claim 21, wherein: the operation part (4) is rotatably connected with the catheter part, the connecting piece (14) is provided with a proximal end and a distal end, the proximal end of the connecting piece (14) is wound on the operation part (4), and the distal end of the connecting piece (14) is arranged at the distal end of the catheter part; or, the connecting piece (14) is provided with two far-end parts and a near-end part, the two far-end parts are respectively arranged at two opposite sides of the catheter part, and the near end is wound on the operating part (4).

23. A thrombus treatment platform according to claim 21, wherein: the operating part comprises a first operating part (41) movably connected with the proximal end of the catheter part and a second operating part (42) movably connected with the proximal end of the catheter part, and the connecting piece comprises a first connecting piece (21) and a second connecting piece (22); the first connecting piece (21) and the second connecting piece (22) are respectively provided with two far-end parts and a near-end part, the two far-end parts of the first connecting piece (21) are respectively arranged at two opposite sides of the catheter part, and the near end of the first connecting piece (21) is wound on the first operating part (41); the two distal ends of the second connecting piece (22) are respectively arranged on the two opposite sides of the catheter part, and the proximal end of the second connecting piece (22) is wound on the second operating part (42); the two distal ends of the first connecting piece (21) and the two distal ends of the second connecting piece (22) are uniformly distributed along the circumferential direction of the catheter part; when the first operation part (41) and the second operation part (42) are operated, the front end of the conduit part can directionally rotate in a three-dimensional space.

24. A thrombus treatment platform according to claim 21, wherein: the aspiration catheter (10) further comprising a dilation catheter coupled to the distal end of the catheter portion and having an open position and a collapsed position, the dilation catheter being positioned within the catheter portion when the dilation catheter is in the collapsed position; when the dilation catheter is in an open state, the diameter of the distal end of the dilation catheter is larger than the diameter of the catheter portion.

25. A thrombus treatment platform according to claim 24, wherein: the dilating catheter comprises a soft film (71) and a dilating ring (72), wherein the proximal end of the soft film (71) is fixedly connected with the distal end of the catheter part, and the dilating ring is fixedly connected with the distal end of the soft film (71).

26. A thrombus treatment platform according to claim 25, wherein: the expansion ring (72) is made of memory material or air bag.

27. A thrombus treatment platform according to claim 1 or 2, wherein: the thrombus treatment platform also comprises a second ultrasonic generator (5) arranged at the far end of the suction catheter (10), a second power line (16) and a signal transmission line (17) which are connected with the second ultrasonic generator (5) and arranged in the tube wall of the suction catheter (10), and a second ultrasonic joint (6) which is arranged at the near end of the suction catheter (10) and connected with the second power line (16) and the signal transmission line (17).

28. A thrombus treatment platform according to claim 1 or 2, wherein: the thrombus treatment platform also comprises a sheath tube (18) which can pass through the suction channel and the far end of which extends to the near end of the filter screen (32), and the near end of the sheath tube (18) is connected with a suction pump (19).

29. A thrombus treatment platform according to claim 28, wherein: the sheath (18) comprises a first channel (181) capable of allowing a guide wire to pass through and a second channel (182) capable of allowing thrombus to pass through or capable of receiving the filter screen (32).

30. A thrombus treatment platform according to claim 1 or 2, wherein: the filter screen (32) is in a basket or pocket shape with an opening facing to the near end, or the filter screen (32) is in a shuttle shape.

Technical Field

The invention belongs to the field of medical instruments, and particularly relates to a thrombus treatment platform.

Background

The existing treatment methods mainly comprise vascular incision embolectomy, catheter contact thrombolysis and percutaneous mechanical puncture embolectomy, wherein the incision embolectomy needs to be performed through dissection separation and blood vessel incision, such as femoral artery, femoral vein or brachial artery incision, and with the development of intracavity intervention technology and the innovation of materials, the open operation mode is gradually replaced by minimally invasive interventional intracavity treatment, namely catheter contact thrombolysis and percutaneous mechanical puncture embolectomy. Catheter contact thrombolysis is not beneficial to many patients because of the high risk of thrombolysis drug bleeding and the extreme severity of the surgical indications, and a large proportion of patients have catheter contact thrombolysis contraindications.

Based on the existing medical cognition, the deep venous thrombosis is often large in capacity, and the acute-phase thrombosis is soft and fragile in texture; arterial thrombosis often has small volume, and thrombus in an acute stage is soft in texture; old thrombi tend to adhere to the vessel wall. For old thrombus, the old thrombus is mainly scraped mechanically by the vessel wall or falls off by thrombolytic drugs at present.

For example, a thrombectomy catheter system, such as an X-sizer thrombectomy catheter system, in which a spiral cutter at the front end of the catheter is used to cut thrombus and blood clots are sucked out of the body, chinese patent CN204092102U discloses a novel peripheral vascular disease thrombus suction connector, which includes: the rotary tail seat comprises a pipe body, a rotary rod, a spiral rotary piece, an arc joint and a connecting tail seat, wherein the pipe body is in a hollow tubular shape, the upper end of the pipe body is movably connected with the arc joint through threads, a rectangular groove is formed in the middle upper portion of the pipe body, the rotary rod is inserted into the pipe body, and the spiral rotary piece is sleeved on the periphery of the rotary rod. However, the thrombus removal device has a complicated structure, high production cost, and cumbersome use, and when the thrombus on the vascular wall is detached by the rotation of the spiral cutter or the spiral rotary blade in the blood vessel, the vascular endothelium is easily damaged, and the thrombus removal sequelae are easily caused.

For another example, the Angiojet thrombus remover can spray a certain amount of thrombolytic agent into the thrombus at high pressure to break up the thrombus, increase the contact area with the thrombus, and perform thrombus suction (called chemical-physical coupling thrombus volume reduction), and is suitable for acute stage thrombus of iliac, femoral and popliteal veins. However, the patient often loses too much blood due to the overlong negative pressure time, and meanwhile, the red blood cell injury may be caused by the high-pressure rapid stirring, so that the hemolysis is caused, and the thrombus extraction sequelae are easy to occur.

Disclosure of Invention

The invention aims to provide a thrombus treatment platform capable of reducing thrombus taking sequelae.

In order to solve the technical problems, the invention adopts the following technical scheme:

from the viewpoint of product structure, the thrombus treatment platform comprises an aspiration catheter with an aspiration channel, and further comprises an aspiration pump, an agitating device and a filter screen assembly which are communicated with the proximal end of the aspiration catheter,

the filter screen assembly comprises a filter rod and a filter screen which is fixedly arranged at the far end of the filter rod and has an opening state and a folding state;

the stirring device comprises a first guide pipe, a second guide pipe sleeved outside the first guide pipe in a sliding manner, a stirrer arranged at the far end of the first guide pipe and having an opening state and a folding state, and an operating device arranged between the first guide pipe and the second guide pipe and capable of enabling the first guide pipe and the second guide pipe to slide relatively so as to enable the stirrer to be switched between the opening state and the folding state;

the thrombus treatment platform also comprises a driving device which is connected with the first catheter or the second catheter and can drive the stirrer to rotate.

From the use state of the product, the thrombus treatment platform comprises an aspiration catheter with an aspiration channel, and the thrombus treatment platform also comprises an aspiration pump, an agitating device and a filter screen assembly which are communicated with the proximal end of the aspiration catheter,

the filter screen assembly comprises a filter rod penetrating through the suction channel, and a filter screen fixedly arranged at the distal end of the filter rod and having an opened state and a closed state; said screen being located at the distal end of said suction duct;

the stirring device comprises a first conduit passing through the suction channel, a second conduit passing through the suction channel and sleeved outside the first conduit in a sliding manner, a stirrer arranged at the distal end of the first conduit and having an opened state and a folded state, and an operating device arranged between the first conduit and the second conduit and capable of enabling the first conduit and the second conduit to slide relatively so as to enable the stirrer to be switched between the opened state and the folded state; said agitator being positioned between said screen and said distal end of said suction catheter when said agitator is in an open position, said agitator moving back and forth in the blood vessel as said first catheter is drawn;

the thrombus treatment platform also comprises a driving device which is connected with the first catheter or the second catheter and can drive the stirrer to rotate.

Preferably, when the stirrer is in a furled state, the outer diameter of the stirrer is less than or equal to 6F, further preferably, the outer diameter of the stirrer is less than or equal to 5.5F, and more preferably, less than or equal to 5F.

Preferably, the agitator is a wire-formed mesh basket.

Preferably, the stirrer can be controlled by the second catheter to be unfolded, so that medical personnel can conveniently control the distance between the stirrer and the vessel wall and the fitting degree according to actual needs, and the stirrer is more convenient to use; in addition, the stirrer is woven by silk threads, and the outer diameter can be very small in a furled state, so that the size of the second catheter can be reduced, a larger space is reserved for the suction channel, and the thrombus extraction efficiency is improved.

It is further preferred that the agitator is formed by braiding a plurality of said wires and that the two ends of each of said wires are located at the proximal and distal ends of said first conduit, respectively, i.e. the length of each wire is substantially along the axial direction of the first conduit, rather than along a direction perpendicular to the axial direction of the first conduit.

More preferably, at least some of said filaments intersect.

More preferably, at least part of the wire is rotated around the first conduit by an angle, wherein the angle may be dependent on the length of the wire and the desired maximum outer diameter of the agitator when in the open position.

According to one embodiment, the distal and proximal ends of the plurality of wires are fixedly disposed on the first conduit, and the agitator is disposed within the second conduit when the agitator is in a collapsed state; when said agitator is in an open position, at least a portion of said agitator is disengaged from said second conduit; this embodiment may control the diameter of the agitator after it has been collapsed by controlling the inner diameter of the second conduit.

According to another embodiment, the distal end of the first catheter extends beyond the second catheter; the stirrer comprises a plurality of wires; the distal end of each silk thread is fixedly connected with the first catheter, and the proximal end of each silk thread is fixedly connected with the distal end of the second catheter; the agitator is opened when the first conduit is moved proximally relative to the second conduit, and the outer diameter of the agitator is larger as the degree of expansion of the agitator is larger as the first conduit is moved a longer distance; when the first catheter is moved distally relative to the second catheter until the wire is straightened, the agitator is in a collapsed state in which the outer diameter of the agitator is at a minimum and substantially conforms to the first catheter.

Preferably, the silk thread is made of one or more of nickel-titanium alloy, stainless steel wire, high molecular polymer and the like.

Preferably, the stirring device further comprises a plurality of first ultrasonic generators fixedly arranged on the filament, a first power line connected with the first ultrasonic generators, and a first ultrasonic joint arranged on the operating device and capable of supplying power to the first power line.

Further preferably, the wire has an internal lumen, the first catheter or the second catheter also has an internal lumen, and the first power cord is located in the internal lumen of the wire and the internal lumen of the first catheter or the second catheter.

More preferably, the diameter of the first ultrasonic generator is 0.2-0.4 mm, and the outer diameter of the silk thread is 0.2-0.3 mm.

Still preferably, the silk thread internal diameter be 0.1 ~ 0.2 mm.

With the solution in which both ends of the wire are fixed to the first catheter, the structure of the operating device can be very simple, comprising only one handle.

Specifically, the operating device comprises a handle sleeved on the first catheter and/or the second catheter, a locking component arranged between the first catheter and the second catheter and capable of locking the first catheter and the second catheter relatively, and an operating component which is connected with the handle in a sliding manner and capable of being matched and locked with the first catheter or the second catheter; when the locking assembly is in an unlocked state and the operating assembly is in a locked state, and the operating assembly slides relative to the handle, the first guide pipe and the second guide pipe slide relative to each other so that the stirrer can be switched between an opened state and a folded state; when the locking assembly is in a locking state, the relative positions of the first guide pipe and the second guide pipe are locked, and the driving device can drive the first guide pipe and the second guide pipe to rotate.

Further, the locking assembly includes a first locking member fixedly connected to one of the first conduit and the second conduit, a second locking member rotatably connected to the other of the first conduit and the second conduit, and a third locking member disposed between the first locking member and the second locking member and capable of being locked in cooperation with the other of the first conduit and the second conduit, wherein when the locking assembly is in a locked state, the third locking member is locked in cooperation with the other of the first conduit and the second conduit, the first locking member, and the second locking member.

Furthermore, the third locking element is made of a material capable of generating elastic deformation, and when the locking assembly is in a locking state, the third locking element generates elastic deformation and is respectively tightly matched with the other one of the first guide pipe and the second guide pipe, the first locking element and the second locking element.

Furthermore, a groove is formed in the second locking piece, an internal thread is formed on the groove wall of the groove, an external thread capable of being matched with the internal thread is formed on the outer surface of the first locking piece, the first locking piece is inserted into the groove of the second locking piece and is rotatably connected with the second locking piece through the internal thread and the external thread, and the third locking piece is located in a cavity formed by the first locking piece and the second locking piece.

Specifically, the operating assembly comprises an operating part which is connected with the handle in a sliding way, an engaging part which is formed on the operating part and can be matched and locked with the first conduit or the second conduit, and an elastic part which enables the engaging part to have the tendency of moving towards the state of being matched and locked with the first conduit or the second conduit; when the operating component is in a locking state, the matching part is matched and locked with the first guide pipe or the second guide pipe; when the operating assembly is in the unlocked state, the mating portion is separated from the first conduit or the second conduit.

Furthermore, the operating assembly further comprises a slide rail fixedly arranged on the inner wall of the handle and a slide block connected with one end of the elastic piece and capable of sliding in a matched mode with the slide rail, and the other end of the elastic piece is connected with the matched part, so that when the operating piece slides relative to the handle, the elastic piece can smoothly slide along with the operating piece.

According to a specific and preferred embodiment, the stirring device further comprises a plurality of first ultrasound generators fixedly arranged on the wire, a first power line connected to the first ultrasound generators, and a first ultrasound connector arranged on the operating device and capable of supplying power to the first power line; the wire is provided with an inner cavity, the second catheter is also provided with an inner cavity, and the first power line is positioned in the inner cavity of the wire and the inner cavity of the second catheter; the stirring device also comprises a conducting ring fixedly arranged at the near end of the first power line; the first catheter comprises a flexible pipe section, a metal pipe and an insulating layer, wherein the far end of the metal pipe is fixedly connected with the near end of the flexible pipe section, and the insulating layer is sleeved on the metal pipe; the material of the matching part is an inductive material, the first ultrasonic joint is connected with the matching part, the conductive ring is contacted with the metal pipe of the first guide pipe in the effective stroke of the relative movement of the first guide pipe and the second guide pipe, and the matching part can be contacted with the metal pipe of the first guide pipe; the first ultrasonic connector is capable of powering the first ultrasonic generator when the mating portion is in contact with the metal tube of the first conduit.

Specifically, the driving device includes a motor connected to the first conduit or the second conduit, and a power source capable of supplying power to the motor, wherein the power source may be a dry battery or a power cord capable of being connected to an external power source.

Preferably, the first catheter is sleeved on the filter rod, and the outer diameter of the filter rod is 0.1-1 mm, so that the filter rod can be used as a guide wire, and other components required for removing thrombus can be guided to enter the position required by the blood vessel.

Preferably, the proximal end of the first catheter is provided with an injection hole for injecting thrombolytic drugs, and the distal end of the first catheter and/or the stirrer are/is provided with a plurality of thrombolytic holes for the thrombolytic drugs to enter the blood vessel.

Preferably, the filter screen is in a basket or a pocket shape with an opening facing to the proximal end, or the filter screen is in a shuttle shape.

Preferably, the suction catheter comprises a catheter part with the suction channel, an operating part movably connected with the near end of the catheter part, a fixing part fixedly arranged on the catheter part, and a connecting part which is respectively connected with the operating part and the fixing part and can bend the far end of the catheter part by operating the operating part.

In the present invention, the axis of the connector is parallel to and does not coincide with the axis of the conduit part.

According to the invention, the operation part is operated by medical staff, so that the operation part moves to drive the connecting piece to move, the connecting piece further pulls the fixing piece, and the catheter part is bent, so that the far end of the catheter part and the near end of the catheter part are deviated in angle, and the angle of the head part of the suction catheter is convenient to adjust according to clinical needs, such as convenient insertion into a bifurcated vessel and the like.

In the invention, the fixing piece and the conduit part can be fixedly connected in a hot melting or welding mode, and the connecting piece and the fixing piece can be fixedly connected in a knotting, hot melting or welding mode and the like.

In the invention, the operation part and the catheter part can be connected in a sliding way or in a rotating way, but when in sliding connection, the operation part needs to move a certain distance in the axial direction of the suction catheter, so that the operation of medical personnel is not convenient, and the volume of the suction catheter is increased.

According to one embodiment, the connecting element has a proximal end and a distal end, wherein the distal end is fixed to the fixing element and the proximal end is arranged around the operating element, wherein the connecting element has only one connection point with the fixing element, so that the catheter section can be bent only in one direction when the operating element is rotated.

According to another embodiment, the connector has two distal portions at a distal end and a proximal portion, the two distal portions being disposed on opposite sides of the catheter portion, and the proximal portion being disposed around the operation portion; when the operation part rotates towards one direction, the connecting piece on one side is extended, the connecting piece on the other side is correspondingly shortened, the extension length and the shortening length are consistent, and at the moment, the front end of the guide pipe part is bent towards one side; when the operation part rotates towards the other direction, the original extended connecting piece is shortened, the original shortened connecting piece is extended, and the front end of the conduit part is bent towards the other side.

According to another embodiment, the operating part comprises a first operating part movably connected with the proximal end of the catheter part and a second operating part movably connected with the proximal end of the catheter part, and the connecting part comprises a first connecting part wound on the first operating part and a second connecting part wound on the second operating part; the first connecting piece and the second connecting piece are respectively provided with two distal end parts positioned at the distal ends and a part positioned at the proximal end, the two distal end parts of the first connecting piece are respectively arranged at two opposite sides of the catheter part, and the proximal end of the first connecting piece is wound on the first operating part; two distal end parts of the second connecting piece are respectively arranged on two opposite sides of the catheter part, and the proximal end of the second connecting piece is wound on the second operating part; the two far ends of the first connecting piece and the two far ends of the second connecting piece are uniformly distributed along the circumferential direction of the catheter part; when the first operating part and the second operating part are operated, the front end of the conduit part can directionally rotate in a three-dimensional space, namely the head end of the conduit part realizes 360-degree rotation.

Preferably, the aspiration catheter further comprises a dilation catheter coupled to the distal end of the catheter portion and having an open position and a collapsed position, the dilation catheter being positioned within the catheter portion when the dilation catheter is in the collapsed position; when the dilation catheter is in an open state, the diameter of the distal end of the dilation catheter is larger than the diameter of the catheter portion.

Further preferably, the dilating catheter comprises a flexible membrane material fixedly connected with the proximal end of the catheter part and a dilating ring fixedly connected with the distal end of the flexible membrane material.

More preferably, the expansion ring is made of memory material or a balloon; when the memory material is adopted, the memory material can be self-expanding memory material, and also can be memory material which needs to be expanded through an expander; when a balloon is used, the medical interventional catheter also includes a channel for inflating and deflating the balloon.

In the present invention, when the operation part is operated in one direction, the front end of the conduit part can be bent in an oriented manner by 0 to 180 degrees, preferably by 0 to 90 degrees, and more preferably by 0 to 30 degrees.

Preferably, the connecting member is a metal wire, such as 304 stainless steel wire, nitinol wire, or the like.

Preferably, the fixing part is a developing ring, and the developing ring is used as the fixing part, so that an operator can conveniently know the position of the suction catheter while the fixed connection between the connecting part and the catheter part is realized.

Preferably, the catheter part comprises a first tube part located at the near end, a second tube part located at the far end and a third tube part located between the first tube part and the second tube part, the hardness of the third tube part is smaller than that of the first tube part and that of the second tube part, and the far end of the connecting piece is located on the third tube part, so that when the operation part operates, the connecting piece can well drive the second tube part to bend.

Further preferably, the conduit portion includes a first wall layer located on the inner side, a second wall layer located on the outer side, and a support member provided between the first wall layer and the second wall layer, the support member including a plurality of repetitions arranged in series along an axial direction of the conduit portion, wherein a distance between two adjacent repetitions of the first pipe portion and two adjacent repetitions of the second pipe portion is smaller than a distance between two adjacent repetitions of the third pipe portion, so that a hardness of the third pipe portion is smaller than that of the first pipe portion and the second pipe portion.

Preferably, the suction catheter further comprises a second ultrasonic generator arranged at the distal end of the suction catheter, a second power line and a signal transmission line which are connected with the second ultrasonic generator and arranged in the wall of the suction catheter, and a second ultrasonic joint arranged at the proximal end of the suction catheter and connected with the second power line and the signal transmission line.

Preferably, the thrombus treatment platform further comprises a sheath tube capable of passing through the suction channel and extending from the distal end to the proximal end of the filter screen, and the proximal end of the sheath tube is connected with a suction pump, wherein the suction pump and the suction pump connected with the suction catheter can be the same or two different pumps.

Further preferably, the sheath comprises a first channel capable of allowing a guide wire to pass through and a second channel capable of allowing thrombus to pass through or capable of receiving the filter screen.

When the filter screen assembly is used, thrombus can be prevented from flowing into other parts along the blood flow by arranging the filter screen assembly at the downstream of the blood flow; the stirrer moves back and forth in the blood vessel by introducing thrombolytic drugs and dragging the stirring device back and forth, the stirrer scrapes the blood vessel wall back and forth and stirs thrombus in the blood vessel, or the stirrer is driven to rotate by the driving device to break the thrombus, or ultrasonic turbulence is carried out, so that the thrombus falls off from the blood vessel wall, the thrombus is broken, and the thrombus is captured; and the thrombus is sucked by matching with a suction catheter, so that a large amount of deep vein thrombus and old thrombus can be quickly taken out, the vascular wall and vein valves are not damaged, and the thrombus taking sequelae are reduced.

The proximal end is defined herein as the side that is proximal to the medical practitioner when the thrombus treatment platform is in use; the distal end is defined on the side away from the medical personnel when the thrombus treatment platform is in use.

On the premise that the suction catheter has the thrombus removal function, the suction catheter can provide a passage for other thrombus removal equipment, so that doctors can conveniently select operation schemes aiming at different thrombi, and the thrombus treatment platform is wide in adaptation diseases.

Of course, for some thrombotic conditions that can be treated by aspiration through an aspiration catheter only, the medical practitioner may use the aspiration catheter of the present invention without the use of an agitator device and screen assembly or the like.

In the present invention, the suction catheter, the filter screen assembly, the stirring device, the sheath tube, the driving device, and the suction pump are packaged separately, and each of the separately packaged components may be sold as a whole or sold separately, so as to facilitate selective use by medical personnel.

According to one embodiment, the thrombus treatment platform further comprises a guidewire. This product can be equipped with the seal wire and sell together, also can use the seal wire of other producers.

Due to the implementation of the technical scheme, compared with the prior art, the invention has the following advantages:

the invention can remove thrombus under the condition of ensuring relative safety, is particularly suitable for removing a large amount of thrombus in inferior vena cava, protects venous valves and venous blood vessel walls, has controllable blood loss, simple operation steps, shortens operation time and lightens hospitalization cost of patients.

Drawings

FIG. 1 is a schematic view showing the construction of an aspiration catheter of examples 1 and 2;

FIG. 2 is a schematic partial sectional view of an aspiration catheter of embodiment 1;

FIG. 3 is an enlarged fragmentary view of FIG. 2;

FIG. 4 is a schematic view of the suction catheter of example 1 at 0 and 30 bends;

FIG. 5 is a schematic partial sectional view of an aspiration catheter of embodiment 2;

FIG. 6 is an enlarged fragmentary view of FIG. 5;

FIG. 7 is a schematic transverse cross-sectional view of FIG. 5;

FIG. 8 is a schematic view of the suction catheter of example 2 at a + -30 deg. bend;

FIG. 9 is a schematic view showing the construction of a suction catheter of embodiment 3;

FIG. 10 is a schematic partial sectional view of an aspiration catheter of example 3;

FIG. 11 is an enlarged fragmentary view of FIG. 10;

FIG. 12 is a schematic transverse cross-sectional view of FIG. 10;

FIG. 13 is a schematic view of the suction catheter of example 3 in a plane at a + -30 deg. bend;

FIG. 14 is a schematic illustration of a screen assembly of the basket screen;

FIG. 15 is a schematic illustration of a screen assembly of the shuttle screen;

FIG. 16 is a schematic view of a screen assembly of a tuck-net type screen;

FIG. 17 is a schematic structural view of the stirring apparatus of embodiment 5in a collapsed state;

FIG. 18 is a schematic structural view of the stirring apparatus of example 5in an open state;

FIG. 19 is an enlarged view at A of FIG. 18;

FIG. 20 is a schematic structural view of the stirring apparatus of the embodiment 6 in a collapsed state;

FIG. 21 is a schematic structural view of the stirring apparatus of embodiment 6 in an open state;

FIG. 22 is a sectional view taken along line A-A of FIG. 21;

FIG. 23 is an enlarged view at B of FIG. 21;

FIG. 24 is a cross-sectional view taken along line C-C of FIG. 23;

FIG. 25 is a partial cross-sectional view of the stirring assembly with the operating assembly in the locked position and the stirrer in the collapsed position (the stirring device does not include ultrasonic functionality);

FIG. 26 is a partial cross-sectional view of the stirring assembly with the operating assembly in the locked position and the stirrer in the open position (the stirring device does not include ultrasonic functionality);

FIG. 27 is a schematic structural view of the operating assembly in an unlocked state and the locking assembly in a locked state (the stirring device does not include ultrasonic functionality);

FIG. 28 is a schematic view showing the construction of the suction catheter of example 4 (the dilating catheter in a collapsed state);

FIG. 29 is a cross-sectional view showing the expanded catheter of example 4 in a collapsed state;

FIG. 30 is a schematic view showing the construction of the suction of example 4 (the dilating catheter in an open state);

FIG. 31 is a cross-sectional view showing an opened state of the dilating catheter of example 4;

FIG. 32 is a schematic view of the dilator;

FIG. 33 is a schematic view of a sheath;

FIG. 34 is a sectional view taken along line A-A of FIG. 33;

FIG. 35 is a view showing a state where a sheath tube transports the screen assembly;

FIG. 36 is a cross-sectional view taken along line A-A of FIG. 35;

FIG. 37 is a view of the suction catheter (without the sonotrode) in engagement with the screen assembly;

FIG. 38 is a view of the suction catheter (including the ultrasonic generator) in engagement with the screen assembly;

FIG. 39 is a view of the suction catheter (with the sonotrode) and the agitator (without the sonotrode) in combination with a sieve assembly;

FIG. 40 is a view of the suction catheter (without the sonotrode) and an agitator (without the sonotrode) in combination with a sieve assembly;

FIG. 41 is a view showing a state in which a suction duct (without an ultrasonic generator), an agitating device (with an ultrasonic generator) and a screen assembly are engaged (a driving device is omitted and not shown);

FIG. 42 is a view showing the state in which the suction catheter (including the dilatation catheter), the agitation device (including the sonotrode) and the screen assembly are engaged (the driving means are omitted and not shown);

FIG. 43 is a view showing a state in which a suction duct (including an ultrasonic generator), a stirring device (including an ultrasonic generator) and a screen assembly are engaged (a driving device is omitted and not shown);

FIG. 44 is a view of the suction catheter (without the sonotrode) with the sheath engaged with the screen assembly;

FIG. 45 is a view of the suction catheter (including the dilation catheter), sheath and screen assembly in combination;

FIG. 46 is a view of the suction catheter (including the ultrasonic generator), sheath and screen assembly in combination;

FIG. 47 is a partial cross-sectional view of the agitation assembly with the operating assembly in the locked position (the agitation device includes ultrasonic functionality);

FIG. 48 is a partial cross-sectional view of the agitation assembly with the operating assembly in the locked position (the agitation device including ultrasonic functionality);

fig. 49 is an enlarged view at a of fig. 47 and 48.

Detailed Description

The present invention will be described in further detail with reference to specific examples. It is to be understood that these embodiments are provided to illustrate the basic principles, essential features and advantages of the present invention, and the present invention is not limited by the following embodiments.

The thrombus treatment platform of the present invention comprises an aspiration catheter 10 having an aspiration channel, an aspiration pump 19, an agitation device, a screen assembly, and the like.

Fig. 1 to 13 are schematic structural views of the suction duct 10 of embodiments 1 to 3, and fig. 28 to 31 are schematic structural views of the suction duct 10 of embodiment 4. The suction duct 10 includes a duct portion having a suction passage extending in an axial direction of the duct portion and penetrating the duct portion, and an outer diameter of the duct portion is 12 to 14F.

The catheter section comprises a first wall layer 11 on the inner side, a second wall layer 12 on the outer side, a support 13 arranged between the first wall layer 11 and the second wall layer 12, the support 13 comprising a plurality of repetitions arranged consecutively in the axial direction of the catheter section, wherein the spacing between the repetitions of the support 13 varies from the proximal end to the distal end, such that the catheter parts are a first tube part 1 at the proximal end, a second tube part 2 at the distal end, a third tube part 3 between the first tube part 1 and the second tube part 2, and the distance between two adjacent repetitions at the position of the first tubular portion 1 and the distance between two adjacent repetitions at the position of the second tubular portion 2 is smaller than the distance between two adjacent repetitions at the position of the third tubular portion 3, thereby make the hardness of third pipe portion 3 be less than the hardness of first pipe portion 1 and second pipe portion 2, and then can be better realize the bending of second pipe portion 2 relative first pipe portion 1.

The supporting member 13 formed by a plurality of repeating bodies can be spiral like a spring, and can also be in an accordion like structure, when the supporting member 13 is in a spiral shape, the pitch of the repeating bodies is the pitch, and when the supporting member 13 is in an accordion structure, the pitch of the repeating bodies is the distance between two adjacent wave crests. In this embodiment, the supporting member 13 preferably has a spiral shape.

As for the bending angle of the second tube 2 relative to the first tube 1, it can be realized by adjusting the distance between the repeating bodies and the material of the conduit tube, in this embodiment, the material of the supporting member 13 is selected from metals, such as 304 stainless steel, nitinol wire, etc.; the first wall layer 11 and the second wall layer 12 are made of Polytetrafluoroethylene (PTFE), block polyether amide (Pcbax), Polyimide (PI), Polyamide (PA), Polyethylene (PE), a metal film, and the like, preferably, the first wall layer 11 is made of Polytetrafluoroethylene (PTFE) with better lubricity, the second wall layer 12 is made of block polyether amide (Pcbax), a metal film, and the like, and the second wall layers 12 of the first pipe portion 1, the second pipe portion 2, and the third pipe portion 3 can be spliced by different materials.

The suction catheter 10 further comprises a fixing member 15 fixedly arranged at the distal end of the third tube part 3 of the catheter part, the fixing member 15 of this embodiment being a developer ring. For the embodiments of 1 to 3, the developing ring is fixed between the first wall layer 11 and the second wall layer 12 by heat fusion or welding or the like.

The suction catheter 10 further includes a coupling member 14 having a distal end fixedly connected to the fixing member 15, and an operation portion 4 rotatably connected to a proximal end of the catheter portion. The connecting piece 14 is located between the first wall layer 11 and the second wall layer 12 and extends along the axial direction of the pipe portion, so that the axial lead of the connecting piece 14 is parallel to and does not coincide with the axial lead of the pipe portion, and the connecting piece 14 can drive the second pipe portion 2 to bend.

The aspiration catheter 10 further comprises a second ultrasound generator 5 arranged at the distal end of the catheter section (i.e. at a distal position of the second catheter section 2), a second power line 16 and a second signal transmission line 17 connected to the second ultrasound generator 5 and arranged within the wall of the catheter section (i.e. between the first wall layer 11 and the second wall layer 12), a second ultrasound connector 6 arranged at the proximal end of the catheter section and connected to the second power line 16 and the second signal transmission line 17, the second ultrasound connector 6 being connectable to other equipment.

As shown in fig. 1 to 4, embodiment 1 is shown, in which the connecting member 14 is only a steel wire, the distal end of the connecting member 14 is fixedly connected to the developing ring, and the proximal end is wound around the operating portion 4, and at this time, the connecting member 14 is only a connection point with the developing ring, so that when the operating portion 4 is rotated, the conduit portion can be bent only in one direction, and the bendable angle range is 0 to 90 °, and the angle range shown in fig. 4 is 0 ° and 30 °.

As shown in fig. 1, 5 to 8, an embodiment 2 is shown, in which the connecting member 14 is also a steel wire, but both end portions of the connecting member 14 (i.e. the distal end of the connecting member 14) are fixedly connected to opposite sides of the fixing member 15, respectively, and the middle position of the connecting member 14 is wound around the operating portion 4, so that the connecting member 14 is divided into two parts by the operating portion 4, which is expressed in terms of upper and lower parts, for example, when the operating portion 4 is rotated clockwise, the upper connecting member 14 is extended, the lower connecting member 14 is correspondingly shortened, and the second tube portion 2 of the catheter portion is rotated downward by a certain angle; when the operating part 4 is rotated counterclockwise, the upper connecting member 14 is shortened, the lower connecting member 14 is correspondingly extended, and the second pipe part 2 of the conduit pipe part is rotated upward by a certain angle. The description here is made with the second pipe portion 2 being on the same line as the first pipe portion 1 and the third pipe portion 3, that is, with the second pipe portion 2 having a bending angle of 0 ° as a starting position. The duct section of example 2 can thus be bent in both directions, both of which can be bent in the range of 0 to 90 °, and the angle ranges shown in fig. 8 are 0 ° and ± 30 °.

As shown in fig. 9 to 13, the embodiment 3 is shown in which the operation portion includes a first operation portion 41 movably connected to the proximal end of the catheter portion, and a second operation portion 42 movably connected to the proximal end of the catheter portion, the connection members include a first connection member 21 wound around the first operation portion 41, and a second connection member 22 wound around the second operation portion 42, two distal ends of the first connection member 21 are respectively disposed on two opposite sides of the fixing member 15, two distal ends of the second connection member 22 are respectively disposed on two opposite sides of the fixing member 15, and the two distal ends of the first connection member 21 and the two distal ends of the second connection member 22 are uniformly distributed along the circumferential direction of the fixing member 15, so that the tip end of the catheter portion can be rotated by 360 ° by simultaneously operating the first operation portion 41 and the second operation portion 42. That is, the embodiment 3 corresponds to the embodiment 2 in which a set of the operation portion and the connection member is added.

The operation portion 4 of embodiments 1 to 3 may be provided at the proximal end portion of the catheter portion, or may be provided at the proximal end side portion of the catheter portion, preferably at the proximal end side portion of the catheter portion, so that it is possible to facilitate the placement of the hemostatic valve 7 at the proximal end portion of the catheter portion. With embodiment 3, the first operating portion 41 and the second operating portion 42 are located on both sides of the duct portion, so that the layout at the handle 54 of the suction duct 10 is more reasonable.

Fig. 28 to 31 are schematic structural views of an aspiration catheter 10 of example 4, which is configured by adding a dilatation catheter to examples 1 to 3, and has the following specific structure:

the suction catheter 10 further includes an expansion catheter connected to the distal end of the catheter portion and having an open state and a collapsed state, the expansion catheter being positioned within the catheter portion when the expansion catheter is in the collapsed state; the distal end of the dilation catheter has a diameter greater than the diameter of the catheter portion when the dilation catheter is in the open state. The dilating catheter comprises a soft film material 71 and a dilating ring 72, wherein the proximal end of the dilating catheter is fixedly connected with the distal end of the catheter part, and the dilating ring is fixedly connected with the distal end of the soft film material 71. The stent ring 72 can be made of memory material or material such as a balloon which can keep the distal end of the dilatation catheter expanded; when the memory material is adopted, the memory material can be self-expanding memory material, or memory material which needs to be expanded through an expander, the memory material can be nickel titanium material, and the like, and at the moment, the material of the soft membrane material 71 is PTFE or ePTFE; when a balloon is used, the aspiration catheter 10 further includes a channel for inflating and deflating the balloon, and the flexible membrane 71 may be a biocompatible latex-based elastic polymer material. When the aspiration catheter 10 having the dilatation catheter at the distal end is used, the outer diameter of the catheter section can be 12F; the expanded outer diameter of the dilating catheter can reach 14F, so that the suction catheter 10 can be more conveniently inserted into and withdrawn from a human body and can adapt to more blood vessels.

The structure of the catheter section of the aspiration catheter 10 can be referred to the structure of the catheter section of example 1, in which the first wall layer 11 and the second wall layer 12 are slidable relative to each other, and the proximal end of the flexible film 71 of the dilatation catheter is fixedly connected to the distal end of the first wall layer 11 and the distal end of the second wall layer 12, respectively, so that the dilatation catheter can be pushed out of the catheter section by moving the first wall layer 11 distally when the dilatation catheter needs to be opened, and can be retracted into the catheter section by moving the first wall layer 11 proximally when the dilatation catheter needs to be retracted. Wherein, the first wall layer 11 and the second wall layer 12 need to have better flexibility and anti-rolling ability, the material of the first wall layer 11 and the second wall layer 12 is preferably soft material film such as ePTFE, PTFE, etc., and the structure of the supporting member 13 is the same as that of the embodiments 1 to 3.

Since the first wall layer 11 and the second wall layer 12 of this embodiment can slide relative to each other, the fixing member 15 is preferably fixed to the second wall layer 12.

In this embodiment, the suction catheter 10 further comprises a handle 73 fixedly connected to the first wall layer 11, the handle 73 being rotatably connected to the second wall layer 12, so that the handle 73 can be rotated to rotate and move the first wall layer 11 in the axial direction relative to the second wall layer 12, thereby pushing and retracting the dilating catheter. The hemostatic valve 7, the first operation portion 41, and the second operation portion 41 are mounted on the handle 73, and the three-way valve 8 is mounted on the handle 73 and communicates with the internal cavity of the first wall layer 11.

The bending direction and the bending angle of the front end of the conduit pipe part can be accurately controlled by rotating the operation part 4, for example, the diameter of the operation part 4 can be calculated and adjusted, so that the front end of the conduit pipe part can be bent by a certain angle, such as 1 degree, 2 degrees, 3 degrees and the like, every time the operation part 4 is rotated for one circle, and naturally, in order to avoid overlarge working intensity of medical staff, the bending angle of the conduit pipe part caused by every rotation of the operation part 4 can be set to be 5 degrees and the like.

The aspiration catheter 10 of the present invention further includes a three-way valve 8 communicating with the proximal end of the catheter portion, and a medical worker can introduce physiological saline, thrombolytic drug, etc. into the catheter portion through the three-way valve 8, and can also perform aspiration of thrombus by connecting an aspiration pump 19 to the three-way valve 8.

According to the invention, the operator operates the operation part 4, so that the operation part 4 moves to drive the connecting part 14 to move, the connecting part 14 further pulls the catheter wall, the catheter part is bent, and the angle deviation is generated between the far end of the catheter part and the near end of the catheter part, so that the angle of the head part of the suction catheter 10 can be conveniently adjusted according to clinical needs, for example, the suction catheter 10 can be used for entering blood vessels, and the bifurcation blood vessels and the like can be more conveniently inserted through the adjustment of the angle of the head end.

Fig. 14-16 show three different configurations of screen assemblies, each of which can be used with the four embodiments of suction ducts 10 described above.

The screen assembly includes a filter rod 31, a screen 32 fixedly mounted to a distal end of the filter rod 31 and having an open position and a collapsed position. The screen 32 shown in fig. 14 is in the form of a basket open towards the proximal end, the screen 32 shown in fig. 15 is in the form of a shuttle, and the screen 32 shown in fig. 16 is in the form of a pocket open towards the proximal end.

The outer diameter of filter rod 31 is 0.1-1 mm, preferably 0.035in, so that filter rod 31 can be used as a guide wire to facilitate other components to enter a desired position along filter rod 31.

Fig. 33 and 34 are schematic structural views of the sheath 18, wherein the sheath 18 includes a first passage 181 for passing a guide wire and a second passage 182 capable of allowing thrombus to pass or receiving the filter screen 32.

The manner in which the screen assembly is advanced into the vessel and extended distal of the thrombus can be accomplished by conventional methods known in the art, such as by loading the screen assembly into the sheath 18 and then advancing the sheath 18 over the guidewire to the desired location. The filter screen 32 can be loaded in the sheath tube 18 in the furled state, and in the opened state, the outer diameter of the filter screen 32 (i.e. the maximum distance of the cross section after the expansion of the filter screen 32) is larger than or equal to the inner diameter of the blood vessel, so that the filter screen 32 can filter thrombus passing through the filter screen 32 well, and the thrombus is prevented from flowing to other parts.

Fig. 17 to 24 are schematic structural views of the stirring apparatuses of examples 5 and 6.

The stirring device comprises a first guide pipe 51, a second guide pipe 52 sleeved outside the first guide pipe 51 in a sliding manner, a stirrer 53 arranged at the far end of the first guide pipe 51 and having an opened state and a folded state, and an operating device arranged between the first guide pipe 51 and the second guide pipe 52 and capable of enabling the first guide pipe 51 and the second guide pipe 52 to slide relatively so as to enable the stirrer 53 to be switched between the opened state and the folded state. The thrombus treatment platform further comprises a driving device which is connected with the first conduit 51 or the second conduit 52 and can drive the stirrer 53 to rotate.

The driving device comprises a motor 20 connected with the first conduit 51 or the second conduit 52, and a power supply capable of supplying power to the motor 20, wherein the power supply can be a dry battery or a power line capable of being connected with an external power supply.

Wherein the agitator 53 is a mesh basket woven by a plurality of wires 56, and both ends of each wire 56 are respectively located at the proximal end and the distal end of the first conduit 51, i.e. the axial direction of each wire 56 extends along the axial direction of the first conduit 51, but at least a part of the wires 56 rotate around the first conduit 51 at a certain angle and at least a part of the wires 56 intersect, wherein the specific angle can be set according to the required density and size of the woven mesh basket. The wire 56 is made of nitinol, stainless steel wire, high molecular polymer, or the like. When the stirrer 53 is in the collapsed state, the outer diameter of the stirrer 53 is 6F or less, more preferably 5.5F or less, and still more preferably 5F or less.

The deployment degree of the stirrer 53 can be controlled by the second catheter 52, so that medical personnel can conveniently control the distance between the stirrer 53 and the vessel wall and the fitting degree according to actual needs, and the use is more convenient; in addition, the stirrer 53 of the present invention is woven by using the wires 56, and the outer diameter is very small in the collapsed state, so that the size of the second catheter 52 can be reduced, a larger space is reserved for the aspiration path, and the efficiency of thrombus aspiration is improved.

Fig. 17 to 19 show an embodiment of the stirring device of example 5, in which the distal end of the first guide tube 51 extends out of the second guide tube 52; the distal end of each wire 56 is fixedly connected with the first catheter tube 51, and the proximal end is fixedly connected with the second catheter tube 52; when the first guide duct 51 is moved toward the proximal end with respect to the second guide duct 52, the agitator 53 is opened, and the larger the degree of expansion of the agitator 53 as the first guide duct 51 is moved the longer, the larger the outer diameter of the agitator 53, as shown in fig. 18; when the first catheter tube 51 is moved distally relative to the second catheter tube 52 until the wire 56 is straightened, the agitator 53 is in a collapsed state, in which the outer diameter of the agitator 53 is at a minimum, substantially conforming to the first catheter tube 51, as shown in fig. 17. In embodiment 5 described above, the structure of the operating device is as shown in fig. 25 to 27: the operating device comprises a handle 54 sleeved on the first guide pipe 51 and the second guide pipe 52, a locking component arranged between the first guide pipe 51 and the second guide pipe 52 and capable of locking the first guide pipe 51 and the second guide pipe 52 relatively, and an operating component which is connected with the handle 54 in a sliding mode and capable of being matched and locked with the first guide pipe 51. The first guide tube 51 passes through the handle 54 and extends from the front end of the handle 54.

The locking assembly includes a first locking member 60, a second locking member 61, a third locking member 62, and the like.

The first locking member 60 is fixedly connected to the distal end of the second conduit 52, wherein the first locking member 60 and the second conduit 52 are fixedly connected by heat melting, welding or the like, or integrally formed by extrusion molding or injection molding. The first locking member 60 has an external thread formed on an outer surface thereof.

The distal end of the handle 54 is provided with an accommodating groove capable of accommodating the second locking member 61, the second locking member 61 is capable of rotating in the accommodating groove, a plurality of ribs are formed on the outer surface of the second locking member 61, and the ribs can increase the friction force on the outer surface of the second locking member 61, so that the second locking member 61 can be rotated to lock and unlock the locking assembly. The second locking member 61 is sleeved on the first guide pipe 51 and can rotate around the first guide pipe 51, a groove is formed on the second locking member 61, and an internal thread is formed on a groove wall of the groove.

The first locking member 60 is inserted into the groove of the second locking member 61, and the first locking member 60 and the second locking member 61 are rotatably connected through internal threads and external threads so that the distance from the proximal end of the first locking member 60 to the bottom of the groove can be adjusted, and a cavity is formed between the proximal end of the first locking member 60 and the bottom of the groove, and the third locking member 62 is located in the cavity.

The third locking member 62 is made of a material capable of being elastically deformed, such as silicone rubber.

When the locking assembly is in the unlocked state, the third locking member 62 is in a natural state in which the third locking member 62 is still in contact with the first locking member 60, the second locking member 61 and the first guide pipe 51, but the fit is not so tight that the first guide pipe 51 and the second guide pipe 52 can slide relative to each other when an external force greater than the frictional force between the third locking member 62 and the first guide pipe 51 is applied to the first guide pipe 51.

When the locking assembly needs to be locked, the second locking piece 61 is rotated to enable the second locking piece 61 to move towards the far end, so that the cavity between the first locking piece 60 and the second locking piece 61 is reduced, at the moment, the third locking piece 62 is extruded to generate elastic deformation so as to enable the third locking piece 62 to be matched with the first locking piece 60, the second locking piece 61 and the first guide pipe 51 more tightly, at the moment, the friction force between the third locking piece 62 and the first guide pipe 51 is greatly increased, the relative position of the first guide pipe 51 and the second guide pipe 52 is locked, and when the first guide pipe 51 is driven to rotate around the axis line of the first guide pipe 51 by the motor 20, the second guide pipe 52 can rotate along with the first guide pipe 51, so that the stirrer 53 rotates around the axis line of the first guide pipe to play a role in breaking thrombus.

In order to allow the locking assembly to function as a hemostatic valve with good sealing effect while having the function of locking the first and second catheters 51, 52 relative to each other, the locking assembly further comprises a spacer 63 disposed between the third locking member 62 and the first locking member 60.

The operating assembly includes a sliding slot 57 formed on the handle 54 and extending in the proximal and distal directions, an operating member 55 inserted in the sliding slot 57 and slidably connected to the handle 54, an engaging portion 64 formed on the operating member 55 and capable of engaging and locking with the first guide tube 51, a sliding rail 65 fixedly disposed on the inner wall of the handle 54, a sliding block 66 capable of engaging and sliding with the sliding rail 65, and an elastic member 67 having two end portions disposed on the bottom of the engaging portion 64 and the upper surface of the sliding block 66, respectively. The elastic members 67 are springs, and the number of the elastic members 67 is two along the axial direction of the handle 54.

When the operating component is in a locking state, the upper surface of the matching part 64 and the lower surface of the first conduit 51 are tightly matched under the elastic force of the elastic piece 67 to be locked relatively, and when the locking component is in an unlocking state, the operating piece 55 is slid towards the near end, so that the first conduit 51 is driven to slide towards the near end, and the stirrer 53 is opened; and conversely the agitator 53 may be collapsed.

When the motor 20 is required to drive the stirrer 53 to rotate, the second locking member 61 is rotated to lock the locking assembly, the operating member 55 is pressed downward to overcome the elastic force of the elastic member 67, so that the matching portion 64 is separated from the first guide pipe 51 to unlock the operating assembly, and at this time, the motor 20 is started to drive the first guide pipe 51 to rotate, so that the stirrer 53 can rotate.

Fig. 20 to 24 show the stirring device of the embodiment 6 having the function of emitting ultrasonic waves to break thrombus, wherein the stirring device further comprises a plurality of first ultrasonic generators 81 fixedly provided on the wire 56, a first power line 82 connected to the first ultrasonic generators 81, and a first ultrasonic connector 84 provided on the operation device and capable of supplying power to the first power line 82. In this embodiment, the wire 56 has an internal lumen, the first catheter tube 51 or the second catheter tube 52 also has an internal lumen, and the first power cord 82 passes through the internal lumen of the wire 56 and the internal lumen of the first catheter tube 51 or the second catheter tube 52 to connect the first ultrasonic generator 81 and the first ultrasonic connector 84. For the solution that both ends of the filament 56 are fixed on the first conduit 51, the first power line 82 passes through the wall of the first conduit 51; for the arrangement in which the distal end of the wire 56 is secured to the first catheter tube 51 and the proximal end is secured to the second catheter tube 52, the first power wire 82 is threaded through the wall of the second catheter tube 52.

In this embodiment, the diameter of the first ultrasonic generator 81 is 0.2 to 0.4mm, preferably 0.3mm, the outer diameter of the filament 56 is 0.2 to 0.3mm, preferably 0.25mm, and the inner diameter of the filament 56 is 0.1 to 0.2mm, preferably 0.15 mm.

The first ultrasonic generator 81 is fixed to the wire 56 by welding.

The operating device of this example was constructed substantially the same as the operating device used in the mixer of example 5, except that: the connection of the first power cord 82 to the first ultrasonic connector 84.

In this scenario, the first power cord 82 is located within the internal lumen of the wire 56 and the internal lumen (i.e., wall) of the second conduit 52; the stirring device further comprises a conductive ring 91 fixedly arranged at the proximal end of the first power line 82; the conductive ring 91 is fixedly connected to the second conduit 52, slidably sleeved on the first conduit 51 and contacting the first conduit 51; the first catheter 51 comprises a flexible pipe section, a metal pipe with a far end fixedly connected with a near end of the flexible pipe section, and an insulating layer sleeved on the metal pipe, wherein the metal pipe is made of stainless steel and the like; the matching part 64 is made of an electro-sensitive material, the first ultrasonic connector 84 is connected with the matching part 64, the conductive ring 91 is contacted with the metal tube of the first guide tube 51 in the effective stroke of the relative movement of the first guide tube 51 and the second guide tube 52, and the matching part 64 can be contacted with the metal tube of the first guide tube 51; the first ultrasonic connector 84 is capable of supplying power to the first ultrasonic generator 81 when the fitting portion 64 is in contact with the metal tube of the first guide tube 51.

In another embodiment (not shown), the distal and proximal ends of the plurality of wires are fixedly disposed on the first catheter, and the opening and closing of the agitator and the degree of deployment of the agitator are determined by how much the agitator is closed within the second catheter. When the stirrer is in a furled state, the stirrer is completely positioned in the second guide pipe; when the agitator is in the open state, at least a portion of the agitator disengages the second conduit; when the agitator is completely detached from the second conduit, the agitator is opened to a maximum state. This embodiment may control the diameter of the agitator after it has been collapsed by controlling the inner diameter of the second conduit.

In this embodiment, the structure of the operation device may be the same as that of the above-described embodiment, but since the wires of the stirrer are all disposed on the first guide tube, the second guide tube may not rotate together when the driving device drives the first guide tube to rotate, and therefore, the locking assembly may be omitted from the operation device in this embodiment, and the structure of the operation assembly may be maintained, which is not described herein again.

The stirrer 53 of both embodiments can also be used in combination with the suction catheter 10 shown in examples 1 to 3.

In the present invention, the stirring assembly also has a function of introducing thrombolytic drugs, and the specific structure can be as shown in fig. 17 to 19, the first conduit 51 has a thrombolytic channel extending along the axial direction inside, the proximal end of the first conduit 51 is provided with an injection hole 58 communicated with the thrombolytic channel and used for injecting thrombolytic drugs, the distal end of the first conduit 51 and/or the stirrer 53 is provided with a plurality of thrombolytic holes 59 for the thrombolytic drugs to enter the blood vessel, wherein fig. 19 shows a structure in which the thrombolytic holes 59 are located on the first conduit 51, the plurality of thrombolytic holes 59 are uniformly distributed along the axial direction of the first conduit 51, and the plurality of thrombolytic holes 59 are located between the proximal end and the distal end of the stirrer 53.

The steps of the operation by adopting the thrombus treatment platform are as follows:

1. firstly, feeding a 0.035in guide wire into a specified position;

2. after the 6F sheath 18 loaded with the filter screen assembly is pushed to the position where the thrombus passes through by the 0.035in guide wire, the 6F sheath 18 is withdrawn to open the filter screen 32, as shown in fig. 35, the 6F sheath 18 is withdrawn;

3. inserting the dilator 9 (the structure is shown in fig. 32) into the suction catheter 10, then pushing along the filter rod 31 to the designated position of the human body, and withdrawing the dilator as shown in fig. 37 or fig. 38;

4. the stirring device is inserted into the suction catheter 10 along the filter rod 31 and pushed to the thrombus site, and the stirrer 53 is positioned between the distal end of the suction catheter 10 and the filter screen 32, so that the thrombolysis or the back-and-forth dragging or rotation of the stirrer 53 can be performed according to actual requirements. For example, firstly, thrombolytic drugs are injected into a thrombolytic channel of the first catheter 51 from the injection hole 58 and then enter a thrombus position from the thrombolytic hole 59 to dissolve thrombus, after the thrombolytic is finished, the operation piece 55 is operated to slide towards the proximal end to drive the first catheter 51 to slide towards the proximal end, so that the stirrer 53 is opened, the handle 54 is repeatedly dragged back and forth to break and collect the undissolved thrombus, then the operation piece 55 is pressed to unlock the operation component and lock the locking component, and the motor 20 is started to drive the first catheter 51, the second catheter 52 and the stirrer 53 to rotate together; or the first ultrasonic generator 81 is switched on to generate ultrasonic waves to vibrate the thrombus; meanwhile, the suction pump 19 is arranged on the three-way valve 8 at the proximal end of the suction catheter 10, negative pressure is applied to the suction catheter 10 for suction, and the recovery bag 23 is connected to the suction pump 19 and is used for collecting thrombus, so that the drift of large thrombus in the dragging process can be prevented, as shown in fig. 39 to 43;

5. after the operation is finished, after the stirring device is removed from the body, the 0.035in guide wire is pushed to the front end of the filter screen assembly through the suction catheter 10 again, the 6F sheath 18 is inserted into the suction catheter 10 along the 0.035in guide wire and pushed to the front end of the filter screen assembly, the suction pump 19 is connected to the three-way valve 8 of the 6F sheath 18, negative pressure is applied to the 6F sheath 18 to suck the broken small thrombus intercepted in the filter screen 32, the recovery bag 23 is connected to the suction pump 19 for collecting the thrombus, and the suction negative pressure is preferably not more than 0.02Mpa so as to reduce the influence on the deformability of the erythrocyte and reduce the occurrence of hemolysis as much as possible, as shown in fig. 45 or 46;

6. after the suction is finished, the 6F sheath tube 18 and the 0.035in guide wire are withdrawn out of the body together, then the suction pump 19 is connected to the suction catheter 10 for suction operation again to remove residual thrombus, then the suction catheter 10 is pushed to the far end along the filter rod 31 until the filter screen 32 is completely withdrawn into the suction catheter 10, the hemostatic valve 7 is locked, and the whole system is withdrawn to finish the operation.

The invention can not block the blood flow in the blood vessel in the operation process, and can avoid the drift of the thrombus to the downstream of the blood flow in the dragging, thrombolysis and suction processes. The invention can effectively remove large-area acute and subacute thrombus in the inferior vena cava by combining the venous thrombus removal agent and the venous thrombus removal agent in the vein. Can dissolve the thrombus earlier when reply old thrombus of inferior vena cava, then drag through agitator 53 to cooperation suction and filter screen protection use this apparatus can remove a large amount of thrombus in the inferior vena cava under the circumstances of guaranteeing relative safety, protection venous valve and venous blood vessel wall, and the blood loss is controllable, and operating procedure is simple, shortens operating time, alleviates patient's cost of being in hospital.

As described above, the present invention has been explained fully in accordance with the gist of the present invention, but the present invention is not limited to the above-described examples and implementation methods. A practitioner of the related art can make various changes and implementations within a range allowed by the technical idea of the present invention.