CN214966284U - Thrombus removing device - Google Patents

Abstract

The utility model provides a thrombus clearing device, including sacculus pipe, driving tube and sheath pipe, the driving tube is located to sacculus pipe slip cap, the driving tube is located to the sheath pipe box outside, the distal end and the near-end of sacculus pipe are connected with the sacculus respectively and fill the unit, the driving tube rotates with the suction plug head and is connected, a fixed garrulous plug sword of distal end of driving tube, garrulous plug sword holding is in the suction plug head, the drive unit is connected to the near-end of driving tube, suction unit is connected to the near-end of sheath pipe, clearance between the outer wall of driving tube and the inner wall of sheath pipe constitutes the suction plug passageway, suction plug passageway and suction plug head intercommunication. The balloon catheter is provided with a filling channel, the perfusion unit injects or extracts first liquid into the balloon through the filling channel to control the expansion or contraction of the balloon, the perfusion unit also provides second liquid for an area between the balloon and the thrombus suction head, the suction unit sucks thrombus into the thrombus suction head through the thrombus suction channel, the driving unit drives the thrombus cutting knife to cut up the thrombus, and thrombus fragments are sucked out through the thrombus suction channel by the suction unit.

Description

Thrombus removing device

Technical Field

The utility model relates to the technical field of medical equipment, especially, relate to a thrombus clearing device.

Background

With the development of technology, in recent years, a mechanical thrombus removal (PMT) device has appeared, which is an apparatus for removing acute and subacute thrombus formation in blood vessels, and adopts the dissolving, crushing and suction modes to remove thrombus in blood vessels and restore blood circulation and valve function. PMT is the intracavitary thrombus clearing device of microtrauma, can clear away the thrombus fast, resumes blood flow, saves valve function.

US20140088610A1 discloses a mechanical thrombectomy device structure comprising a catheter having a plurality of side holes at the tip, a separate tube for carrying the perfusion fluid and a plurality of small holes at the tip of the tube. During operation, high-pressure normal saline is poured into the independent pipeline, so that the normal saline is sprayed out from a small hole in the top end of the pipeline, the normal saline sprayed at high speed is matched with a side hole in the top end of the catheter to generate a Bernoulli effect to suck thrombus into the catheter through the side hole, meanwhile, the normal saline sprayed at high speed breaks up the sucked massive thrombus and sucks the thrombus out of the body through negative pressure, and thrombolytic drugs can be poured into blood vessels through the catheter after operation to reduce residual thrombus. The patent solves the problem of sucking and discharging thrombus out of the body, but due to the design characteristic that water flow breaks up thrombus, the suction effect on old thrombus is poor, and high-pressure physiological saline hardly breaks up thrombus to a proper size for suction holes, so that the suction efficiency is not high; meanwhile, the thrombus breaking process is carried out outside the catheter, and the normal saline sprayed at high speed destroys red blood cells in blood, and the destroyed red blood cells are not completely sucked out of the body, so that complications such as hematuria, renal failure and the like are easy to occur.

WO2019001245A1 discloses a mechanical thrombus removal device structure which mainly comprises a thrombus breaking system, a thrombus suction system and a medicine perfusion system, wherein thrombolytic medicines are firstly injected to a pathological change position through the medicine perfusion system during working, and the thrombus breaking system and the thrombus suction system are opened after the medicines fully react with the pathological change. The negative pressure provided by the peristaltic pump in the thrombus suction system sucks thrombus near the thrombus suction head of the catheter into the catheter, and the thrombus is cut by a thrombus cutting knife of the thrombus cutting system and is pumped out of the body by the thrombus suction system. The medicine perfusion system of the system needs to use an injector to discontinuously perfuse medicine to lesion, so that the thrombolysis effect is limited, and in the process, the medicine perfused to blood vessels easily causes thrombus to flow to the lung along with blood; although the thrombus breaking process is carried out in the catheter, the hematuria problem is solved, a large amount of blood loss of a patient is caused by long-time suction, and the patient with bad physical condition is in danger.

Aiming at the defects of the existing mechanical thrombus removal device, the technical personnel in the field always seek a solution to improve the thrombus removal efficiency and prevent thrombus drift.

SUMMERY OF THE UTILITY MODEL

An object of the utility model is to provide a thrombus clearing device can improve and get and tie efficiency and prevent the thrombus drift to improve the effect of cleaing away of thrombus.

In order to achieve the above object, the present invention provides a thrombus clearing device, which comprises a balloon catheter, a transmission tube and a sheath tube, wherein the balloon catheter is slidably sleeved in the transmission tube, and the sheath tube is sleeved outside the transmission tube;

the far end and the near end of the balloon catheter are respectively connected with a balloon and a perfusion unit, the far end of the sheath catheter is connected with a suction plug head, the transmission tube is rotatably connected with the suction plug head, a broken-plug knife is fixed at the far end of the transmission tube and is contained in the suction plug head, and the near end of the transmission tube is connected with a driving unit and the near end of the sheath catheter is connected with a suction unit;

an inflation channel is arranged in the balloon catheter, the perfusion unit injects or extracts a first liquid into or out of the balloon through the inflation channel to control the inflation or the deflation of the balloon, a first perfusion channel is arranged in the balloon catheter, the first perfusion channel is provided with at least one first perfusion opening positioned between the balloon and the thrombus absorption head, and the perfusion unit provides a second liquid to a region between the balloon and the thrombus absorption head through the first perfusion channel and the first perfusion opening;

the thrombus sucking device comprises a driving pipe, a sheath pipe, a sucking bolt head, a sucking bolt channel, a sucking unit, a driving unit and a sucking bolt unit, wherein a gap between the outer wall of the driving pipe and the inner wall of the sheath pipe forms the sucking bolt channel, the sucking bolt channel is communicated with the sucking bolt head, the sucking unit is used for sucking thrombus into the sucking bolt head, the driving unit is used for driving a thrombus cutter to cut up the thrombus to form thrombus fragments, and the sucking unit is used for sucking out the thrombus fragments through the sucking bolt channel.

Optionally, the balloon catheter is a multi-channel tube, a guide wire channel is arranged at the center of the balloon catheter, and the filling channel and the first perfusion channel are axially arranged in the tube wall of the balloon catheter.

Optionally, the filling channel and the first perfusion channel are symmetrically arranged along the center of the guide wire channel.

Optionally, the sheath pipe overcoat is equipped with the outer tube, set up at least one second along the axial in the outer tube and pour into the passageway, the second fills the passageway and has at least one and be located the second of the distal end of outer tube fills the mouth, it passes through to pour into the unit the second fill the passageway and the second fills the mouth to the sacculus with regional the third liquid that provides between the head of the suction plug.

Optionally, the distal end of the outer tube is flared.

Optionally, the filling unit includes a first filling unit and a second filling unit, the first filling unit is used for outputting or sucking out the first liquid, and the second filling unit is used for outputting the second liquid.

Optionally, first filling unit includes first adaptor, first transfer line and syringe, be equipped with in the syringe first liquid, the distal end of first transfer line is passed through first adaptor with filling the passageway intercommunication, the proximal end of first transfer line with the syringe intercommunication.

Optionally, the second fills the unit and includes second adaptor, second transfer line and fills the liquid storage bag, it is equipped with in filling the liquid storage bag the second liquid, the distal end of second transfer line passes through second adaptor and first filling passageway intercommunication, the proximal end of second transfer line with fill the liquid storage bag intercommunication, be provided with first peristaltic pump on the second transfer line.

Optionally, the distal end of the plunger tip and/or the side wall of the plunger tip is provided with a plurality of plunger holes through which thrombus enters the plunger tip.

Optionally, the suction unit includes that third connecting piece, third transfer line and thrombus collect the bag, the bag is collected to the thrombus is used for collecting the thrombus piece, the third transfer line passes through the third connecting piece with inhale the thrombus passageway intercommunication, the near-end of third transfer line with bag intercommunication is collected to the thrombus, be provided with the second peristaltic pump on the third transfer line.

Optionally, the first liquid is a developing solution, and the second liquid is a thrombolytic drug solution and/or normal saline.

In addition, the utility model also provides a thrombus clearing device, which comprises a balloon catheter, a transmission tube, a sheath tube and an outer tube, wherein the balloon catheter is slidably sleeved in the transmission tube, the sheath tube is sleeved outside the transmission tube, and the outer tube is sleeved outside the sheath tube;

the far end and the near end of the balloon catheter are respectively connected with a balloon and a perfusion unit, the far end of the sheath tube is connected with a suction plug head, the transmission tube is rotatably connected with the suction plug head, a broken plug knife is fixed at the far end of the transmission tube and is contained in the suction plug head, and the near end of the transmission tube and the near end of the sheath tube are respectively connected with a driving unit and a suction unit;

an filling channel is arranged in the balloon catheter, the filling unit injects or extracts first liquid into or out of the balloon through the filling channel to control the balloon to expand or contract, a plurality of second filling channels are axially arranged in the outer tube wall, a second filling port is arranged at the far end of the outer tube, and the filling unit provides the second liquid to the area between the balloon and the embolectomy head through the second filling channels and the second filling port;

the thrombus sucking device is characterized in that a thrombus sucking channel is formed by a gap between the outer wall of the transmission tube and the inner wall of the sheath tube, the thrombus sucking channel is communicated with the thrombus sucking head, thrombus is sucked into the thrombus sucking head by the sucking unit, the thrombus is cut into thrombus fragments by the driving unit driving the thrombus cutter, and the thrombus fragments are sucked out by the sucking unit through the thrombus sucking channel.

The utility model provides an among the thrombus clearing device, fill into the unit and inject into or take first liquid out in order to control in to the sacculus through filling the passageway the sacculus inflation or shrink can make the laminating of the blood vessel inner wall of the distal end portion of sacculus and thrombus to can be when cleaing away the thrombus, the blood vessel of thrombus distal end portion is plugged up to the sacculus, prevents that thrombus fragment from escaping from the blood vessel of thrombus distal end portion. The infusion unit also provides a second liquid for the area between the thrombus suction head and the balloon, the second liquid can be a thrombolytic liquid medicine and/or normal saline and the like, the thrombolytic liquid medicine and/or normal saline can apply an extra impact force to the thrombus when the thrombus is washed away, so that the thrombus is promoted to fall off from the inner wall of the blood vessel, and the thrombolytic liquid medicine can promote the thrombus to dissolve, so that the operation time is shortened, the thrombus taking efficiency is improved, and meanwhile, in the process of sucking thrombus fragments, the infusion unit can clamp the thrombolytic liquid medicine and/or normal saline infused to the area near the thrombus suction head, the thrombus fragments are sucked by the suction unit, the blood in the blood vessel can be prevented from being excessively sucked by the thrombus suction unit, and then the blood loss of a patient is reduced.

Drawings

Fig. 1 is a schematic structural view of a thrombus removal device according to a first embodiment of the present invention;

FIG. 2 is a view of the thrombus removal device according to a first embodiment of the present invention from the A direction;

FIG. 3 is a cross-sectional view of a pipette tip according to a first embodiment of the present invention;

fig. 4 is a schematic structural view of a balloon catheter according to a first embodiment of the present invention;

fig. 5 is a cross-sectional view of a balloon catheter in accordance with a first embodiment of the present invention;

fig. 6 is a front view of a balloon catheter in accordance with a first embodiment of the present invention;

fig. 7 is a top view of a balloon catheter according to a first embodiment of the present invention;

FIG. 8 is a schematic structural view of a thrombus removal device according to a second embodiment of the present invention;

FIG. 9 is a view of the thrombus removal device according to the second embodiment of the present invention from the A direction;

fig. 10 is a schematic structural view of an outer tube according to a second embodiment of the present invention;

FIG. 11 is a view of the thrombus removal device according to the third embodiment of the present invention from the A direction;

fig. 12 is a cross-sectional view of a balloon catheter in a third embodiment of the present invention;

wherein the reference numbers are as follows:

1000-a thrombus removal device; 1100-balloon; 1110-a development ring; 1200-a balloon catheter; 1210-filling the mouth; 1220-a first infusion port; 1230-filling channels; 1240-a first perfusion channel; 1250-a guidewire channel; 1300-suction plug head; 1310-pipette holes; 1400-transmission tube; 1410-crushing the bolt; 1420-a drive unit; 1500-sheath; 1600-outer tube; 1610-a second perfusion channel; 1620-a second perfusion port; 1700-a suction unit; 1710-a third connector; 1720-a third infusion tube; 1730-a second peristaltic pump; 1740-thrombus collection bag; 1750-a thrombus-aspiration channel; 1800-a perfusion unit; 1810-a first perfusion unit; 1811-first connector; 1812-a first infusion tube; 1813-syringe; 1820-a second perfusion unit; 1821-a second connector; 1822-a second infusion tube; 1823-a first peristaltic pump; 1824-filling a liquid storage bag;

2000-guide wire; 2100-a guidewire locking unit.

Detailed Description

The following description of the embodiments of the present invention will be described in more detail with reference to the drawings. The advantages and features of the present invention will become more apparent from the following description. It should be noted that the drawings are in simplified form and are not to precise scale, and are provided for convenience and clarity in order to facilitate the description of the embodiments of the present invention.

The definitions of "proximal" and "distal" herein are: "proximal" generally refers to the end of the medical device that is near the operator during normal operation, while "distal" generally refers to the end of the medical device that first enters the patient during normal operation.

Thrombi are small pieces formed on the surface of the inner wall of a blood vessel where tissue has been stripped or repaired. Thrombi consist of insoluble fibrin, deposited platelets, accumulated white blood cells and entrapped red blood cells. Thrombus can cause blood flow to slow down, the blood flow generates vortex and the like, and then human body discomfort is caused, so that the life of limbs is endangered and even life safety is threatened.

The thrombus eliminating device is one thrombus eliminating instrument for eliminating thrombus and has dissolving, crushing and sucking modes to eliminate thrombus inside blood vessel and to improve blood circulation.

Fig. 1 is a schematic structural view of a thrombus removal device in this embodiment, fig. 2 is a view of the thrombus removal device in this embodiment taken along direction a, and fig. 3 is a sectional view of a pipette head in this embodiment. As shown in fig. 1, fig. 2 and fig. 3, the thrombus removal device 1000 includes a balloon catheter 1200, a transmission tube 1400 and a sheath tube 1500, wherein the balloon catheter 1200 is slidably sleeved in the transmission tube 1400, and the sheath tube 1500 is sleeved outside the transmission tube 1400.

The distal end and the proximal end of the balloon catheter 1200 are respectively connected with a balloon 1100 and an infusion unit 1800, the distal end of the sheath 1500 is connected with a suction plug head 1300, the transmission tube 1400 is rotatably connected with the suction plug head 1300, and a cork cutter 1410 is fixed at the distal end of the transmission tube 1400 and is accommodated in the suction plug head 1300. The distal end of the transmission tube 1400 is connected to the plunger tip 1300, and the distal end of the sheath tube 1500 is also connected to the plunger tip 1300, so that the transmission tube 1400 and the sheath tube 1500 do not slide relative to each other in the axial direction. The proximal end of the transmission tube 1400 is connected with a driving unit 1420, the proximal end of the sheath tube 1500 is connected with a suction unit 1700, a gap between the outer wall of the transmission tube 1400 and the inner wall of the sheath tube 1500 forms a suction plug channel 1750, and the suction plug channel 1750 is communicated with the suction plug head 1300. The suction unit 1700 sucks thrombus into the thrombus head 1300, the driving unit 1420 drives the thrombus cutter 1410 to cut up thrombus, and thrombus fragments are sucked out by the suction unit 1700 via the thrombus channel 1750.

With continued reference to fig. 1, 2 and 3, the side wall of the pipette head 1300 is provided with a plurality of pipette holes 1310 through which thrombus is drawn into the pipette head 1300. The peg breaking blade 1410 is a tubular hollow structure with at least one blade, and the blade is partially facing the peg suction hole 1310. Thus, the cutting blades 1410 in cooperation with the cutting holes 1310 can cut thrombus. Since the thrombus channel 1750 communicates with the stopper head 1300, the suction unit 1700 sucks thrombus fragments and also provides negative pressure inside the stopper head 1300, so that thrombus can be sucked by the stopper head 1300 through the stopper hole 1310. The driving unit 1420 drives the thrombus cutting knife 1410 located in the thrombus head 1300 to cut up thrombus.

Optionally, the driving unit 1420 may be a rotary motor, the material of the suction plug head 1300 is metal or a composite material of medical polymer and metal, and the material of the transmission tube 1400 is metal or a composite material of medical polymer and metal.

An filling channel 1230 is provided in the balloon catheter 1200, and the perfusion unit 1800 injects or pumps a first liquid into or out of the balloon 1100 through the filling channel 1230 to control the contraction or expansion of the balloon 1100. And the priming unit 1800 also provides a second liquid to the vicinity of the pipette head 1300. Specifically, the area near the pipette tip 1300 is the area between the balloon 1100 and the pipette tip 1300.

In one embodiment of the present invention, the first liquid is a developing solution. The developing solution enters the balloon 1100, so that the balloon 1100 can be easily developed under a medical imaging device, and an operator can conveniently observe the balloon.

In yet another embodiment of the present invention, the first liquid and the second liquid are both normal saline. The saline is infused to the lesion area during the operation, and the blood loss of the patient can be reduced during the process that the suction unit 1700 sucks out the thrombus fragment.

In yet another embodiment of the present invention, the second liquid is a thrombolytic drug solution, and the thrombolytic drug solution has a thrombolytic drug (e.g., urokinase) dissolved therein, so that the thrombolytic drug solution can dissolve the thrombus. The sacculus 1100 with the region between the suction plug head 1300 is pathological change region (the thrombus is located pathological change region), and through pouring the thrombolysis liquid medicine into pathological change region, the volume of thrombus can be reduced to the thrombolysis liquid medicine thrombolysis, and then can reduce when the operation, can improve and get a thrombus efficiency.

Fig. 4 is a schematic structural view of the balloon catheter in this embodiment, fig. 5 is a sectional view of the balloon catheter in this embodiment, fig. 6 is a front view of the balloon catheter in this embodiment, and fig. 7 is a plan view of the balloon catheter in this embodiment. As shown in fig. 4-7, to implement the infusion unit 1800, a second liquid can be provided to the area between the balloon 1100 and the pipette head 1300. The balloon catheter 1200 is a multi-channel tube, a first perfusion channel 1240 is further arranged in the balloon catheter 1200, the first perfusion channel 1240 is axially arranged in the tube wall of the balloon catheter 1200, the first perfusion channel 1240 has at least one first perfusion port 1220 positioned between the balloon 1100 and the pipette head 1300, and the perfusion unit 1800 provides the second liquid for the area near the pipette head 1300 through the first perfusion channel 1240. The number of the first infusion ports 1220 includes, but is not limited to, one, two, three, or four. The number of the first filling ports 1220 can be set according to the requirement of the second liquid by the skilled person, it should be understood that the aperture of the first filling ports 1220 can also affect the filling amount of the second liquid, and it is obvious that the skilled person can adjust the filling amount of the second liquid by changing the aperture of the first filling ports 1220 and the number of the first filling ports 1220.

Referring to fig. 1, optionally, the perfusion unit 1800 includes a first perfusion unit 1810 and a second perfusion unit 1820, the first perfusion unit 1810 is used for outputting or sucking out the first liquid, and the second perfusion unit 1820 is used for outputting the second liquid. That is, the second perfusion unit 1820 communicates with the first perfusion opening 1220 through the first perfusion channel 1240.

Further, the second perfusion unit 1820 includes a second connector 1821, a second perfusion tube 1822, and a perfusion reservoir 1824, a distal end of the second perfusion tube 1822 is communicated with the first perfusion channel 1240 through the second connector 1821, a proximal end of the second perfusion tube 1822 is communicated with the perfusion reservoir 1824, and the second perfusion tube 1822 is provided with a first peristaltic pump 1823. In this way, the second liquid (thrombolytic drug solution and/or physiological saline) in the perfusion reservoir 1824 can be delivered to the first perfusion port 1220 by the first peristaltic pump 1823 and then discharged. It should be appreciated that a one-way valve is provided in the second connector 1821 to prevent blood from flowing back into the priming reservoir 1824. It should be appreciated that the first peristaltic pump 1823 may be replaced with a syringe 1813, and the operator manipulates the syringe 1813 to inject the second fluid into the lesion in the form of a manual injection.

With continued reference to fig. 2, 5 and 7, a filling opening 1210 is disposed at the distal end of the balloon catheter 1200 corresponding to the balloon 1100, the filling opening 1210 communicates with the filling passage 1230, and the filling passage 1230 is axially disposed in the wall of the balloon catheter 1200. That is, the first perfusion unit 1810 communicates with the filling opening 1210 via the filling channel 1230, and then injects or withdraws the first liquid into or from the balloon 1100 to control the inflated state or the deflated state of the balloon 1100.

With continued reference to fig. 1, further, the first perfusion unit 1810 includes a first connector 1811, a first perfusion tube 1812 and a syringe 1813, the syringe 1813 contains the first fluid, the distal end of the first perfusion tube 1812 communicates with the filling channel 1230 through the first connector 1811, and the proximal end of the first perfusion tube 1812 communicates with the syringe 1813. A check valve is arranged in the first connecting piece 1811. It should be appreciated that the first infusion unit 1810 may not require the first infusion tube 1812, and the first infusion tube 1812 is provided to allow more space for the syringe 1813 to move, and the placement of the syringe 1813 may be selected to facilitate the operation.

It should be noted that in the operation of removing thrombus, the operator injects the first liquid into the balloon 1100 to expand the balloon 1100 at the distal end of the thrombus, and in the expanded state, the volume of the balloon 1100 is increased to make the surface of the balloon 1100 closely fit with the inner wall of the blood vessel, so that the balloon 1100 separates the distal end of the diseased region, and during the operation, thrombus fragments can be prevented from entering the blood circulation system from the distal end of the diseased region, and complications such as hematuria and renal failure of the patient can be further prevented. Meanwhile, the thrombus fragment can be prevented from flowing to the lung along with the blood to cause pulmonary embolism.

Further, two ends of the balloon 1100 are fixed on the balloon catheter 1200 through the developing rings 1110, that is, two ends of the balloon 1100 are wound on the balloon catheter 1200 through the developing rings 1110, and the developing rings 1110 are also easy to develop under the medical imaging device. This can facilitate the surgeon in obtaining the exact location of the balloon 1100 in the vessel.

Preferably, the balloon 1100 is made of medical silica gel, latex or elastomer polymer material. The balloon catheter 1200 is made of a medical polymer material or a medical polymer and metal composite material. Further, the balloon catheter 1200 is a flexible tube, so that it can follow the trend of the blood vessel to bend.

It should be appreciated that, since the balloon catheter 1200 is slidably sleeved in the transmission tube 1400, the balloon catheter 1200 can move in the axial direction of the transmission tube 1400, and thus, the distance between the balloon 1100 disposed at the distal end of the balloon catheter 1200 and the pipette head 1300 can be adjusted by moving the balloon catheter 1200. Since the distance between the balloon 1100 and the plunger head 1300 is adjustable, in the operation of removing thrombus, the operator can adjust the distance between the balloon 1100 and the plunger head 1300 according to the size of the thrombus to adapt to the size of the thrombus.

In another embodiment of the present invention, the operator can push the balloon catheter 1200 back and forth to drive the balloon 1100 to move back and forth in the blood vessel, so as to draw the thrombus to the area near the thrombus suction head 1300, so that the thrombus suction head 1300 can suck the thrombus and crush it.

Further, thrombus with a longer existence period can be attached to the inner wall of a blood vessel, and in the later stage of a thrombus removing operation, an operator can drive the balloon 1100 to move back and forth in the blood vessel by adjusting the distance between the balloon 1100 and the thrombus absorbing head 1300, and the balloon 1100 scratches and rubs the inner wall of the blood vessel in the moving process, so that the thrombus attached to the wall can be peeled off by the balloon 1100 in the withdrawing process of the balloon 1100 and is discharged out of the body after passing through the thrombus absorbing head 1300 and the thrombus absorbing channel 1750, and the thrombus removing effect is improved.

Optionally, a guide wire channel 1250 is disposed in the center of the balloon catheter 1200, the filling channel 1230 and the first perfusion channel 1240 are both axially disposed in the tube wall of the balloon catheter 1200, and the filling channel 1230 and the first perfusion channel 1240 are symmetrically disposed along the center of the guide wire channel 1250. It should be understood that the filling channel 1230 and the first perfusion channel 1240 may be disposed in the wall of the balloon catheter 1200 in various ways, and may not be symmetrical, and may not have the same cross-sectional size, and is not limited herein.

The guide wire channel 1250 is used for passing through the guide wire 2000, and in an embodiment of the present invention, a guide wire locking unit 2100 is usually disposed at the proximal end of the balloon catheter 1200, and the closing or opening of the guide wire channel 1250 is adjusted by controlling the locking or unlocking of the guide wire locking unit 2100. When the guidewire locking unit 2100 is locked, the proximal end of the balloon catheter 1200 is locked so that the guidewire 2000 cannot be accessed or moved. When the guide wire locking unit 2100 is released, the guide wire channel 1250 opens and may allow the guide wire 2000 to be accessed or moved.

The guide wire 2000 is used to guide the thrombus removal device 1000 to a designated position, and during the operation, the blood vessel is punctured, and then one end (i.e., the distal end) of the guide wire 2000 is inserted into the diseased blood vessel and penetrates through the thrombus, and at the same time, the other end (the proximal end) of the guide wire 2000 is inserted into the guide wire channel 1250 (i.e., the guide wire channel 1250 in the middle of the balloon catheter 1200) of the thrombus removal device 1000. The distal end of the thrombus removal device 1000 is fed into a blood vessel along the guide wire 2000, and the thrombus removal device 1000 is delivered to a position where thrombus exists. Further, the balloon 1100 and a portion of the balloon catheter 1200 disposed at the front end of the thrombectomy device 1000 are passed through the thrombi along the guide wire 2000, such that the balloon 1100 and the thrombus-aspiration head 1300 are located at the distal end and the proximal end of the thrombi, respectively.

Referring to fig. 1, the suction unit 1700 includes a third connector 1710, a third infusion tube 1720 and a thrombus collection bag 1740, the third infusion tube 1720 is communicated with the thrombus collection channel 1750 through the third connector 1710, the proximal end of the third infusion tube 1720 is communicated with the thrombus collection bag 1740, and the third infusion tube 1720 is provided with a second peristaltic pump 1730.

The third connecting piece 1710 is also commonly called an intermediate connector, the appearance of the third connecting piece 1710 is Y-shaped, the third connecting piece 1710 is a double-pass design, the transmission tube 1400 can pass through without restriction in the third connecting piece, the far end of the third connecting piece is connected with the sheath tube 1500, the Y-shaped end of the third connecting piece is connected with the far end of the third infusion tube 1720, the near end of the third infusion tube 1720 is communicated with the thrombus collection bag 1740. Thrombus debris and blood mix fluid can be aspirated from the thrombus channel 1750 into the thrombus collection bag 1740 by the second peristaltic pump 1730. Preferably, the third connecting member 1710 is made of a medical polymer material.

For better understanding of the thrombus removal device 1000 of the present invention, the following detailed description of the process of using the thrombus removal device 1000 with reference to fig. 1 to 7 is as follows:

before the operation starts, the first peristaltic pump 1823 is connected to the second connector 1821, the first peristaltic pump 1823 in the second perfusion unit 1820 is started, the thrombolytic drug liquid in the perfusion liquid storage bag 1824 is collected from the first perfusion port 1220, and then the first peristaltic pump 1823 is stopped. The thrombus removal device 1000 is placed in the mixed solution of the normal saline and the heparin by the thrombus removal head 1300, and the second peristaltic pump 1730 in the suction unit 1700 is started until the mixed solution of the normal saline and the heparin is visible in the thrombus collection bag 1740, and the second peristaltic pump 1730 is stopped. The pipette tip is then removed from the mixed solution of saline and heparin (heparin has an anticoagulant effect and prevents blood from clotting within the pipette tip 1300, the pipette channel 1750, the third adapter 1710, and the third tubing 1720, which in turn causes aspiration failure). Syringe 1813 in first infusion unit 1810 is connected to first connector 1811 via first infusion tube 1812 so that syringe 1813 is connected to filling channel 1230 and filling port 1210, and suction is initiated until balloon 1100 no longer becomes smaller and one-way valve 1811 is locked. The purpose of the above operation is to evacuate the air from the thrombectomy device 1000.

In the operation process, a blood vessel is punctured, the distal end of the thrombus removal device 1000 is sent into the blood vessel along the guide wire 2000, the developing rings 1110 at the two ends of the balloon 1100 are scanned by means of a medical imaging device, the thrombus removal device 1000 is sent to the position before thrombus, the first peristaltic pump 1823 is started to perfuse a certain amount of thrombolytic liquid medicine into the blood vessel, then the first peristaltic pump 1823 is closed, then the guide wire 2000 is used for penetrating into the guide wire channel 1250 of the balloon catheter 1200, the distal end of the guide wire 2000 is used for penetrating through the thrombus, then the proximal end of the balloon catheter 1200 is pushed, and the balloon catheter 2 is moved towards the distal end along the guide wire 2000 until the balloon 1100 penetrates through the thrombus. Thus, the balloon 1100 and the pipette tip 1300 are located distal and proximal to the thrombus, respectively.

The injector 1813 is pushed to inject the developing solution into the balloon 1100 through the first infusion tube 1812, and whether the outer wall of the balloon 1100 is attached to the inner wall of the blood vessel is checked on the medical imaging device. When the outer wall of the balloon 1100 is attached to the inner wall of the blood vessel, the driving unit 1420 is activated, and the driving unit 1420 drives the driving tube 1400 to rotate the embolectomy knife 1410. The second peristaltic pump 1730 is then activated, followed by the first peristaltic pump 1823. The first peristaltic pump 1823 delivers the saline solution in the perfusion reservoir 1824 to the region between the balloon 1100 and the thrombus head 1300, i.e., the lesion (thrombus) site, through the second infusion tube 1822, the second connector 1821, the first perfusion channel 1240 and the first perfusion port 1220. The second peristaltic pump 1730 rotates to make the suction unit 1700 provide negative pressure to the thrombus suction head 1300 and the thrombus suction channel 1750, a part of thrombus is sucked into the thrombus suction head 1300, the rotating thrombus crushing knife 1410 is matched with the thrombus suction hole 1310 fixed on the thrombus suction head 1300 to crush the thrombus sucked into the thrombus suction head 1300, the crushed thrombus fragments are sucked into the thrombus collection bag 1740 through the thrombus suction channel 1750, the third adapter and the third 1720, and meanwhile, the physiological saline and a part of thrombolytic medicine liquid which are injected through the first injection port 1220 are also sucked into the thrombus collection bag 1740.

In the operation process, the thrombus clearing device 1000 can be moved back and forth along the guide wire 2000 according to the specific position of thrombus in the blood vessel, so that the thrombus removing efficiency is improved. The balloon catheter 1200 can also be withdrawn to drive the balloon 1100 to move in the blood vessel so as to draw the thrombus to the front of the thrombus suction head 1300, so that the thrombus suction head 1300 can suck and crush the thrombus, thereby improving the thrombus extraction efficiency, and the balloon catheter 1200 can also be withdrawn to drive the balloon 1100 to move towards the thrombus suction head 1300 so as to scrape and rub the thrombus to cause the thrombus to fall off.

In the operation process, the thrombolytic liquid medicine in the perfusion liquid storage bag 1824 can be replaced by normal saline or the mixed liquid of the thrombolytic liquid medicine and the normal saline, so that excessive blood loss caused by excessive blood suction of the suction unit 1700 can be avoided. It should be appreciated that the perfusion amount of the second perfusion unit 1820 and the suction amount of the suction unit 1700 can be adjusted by matching the rotational speed of the first peristaltic pump 1823 and the second peristaltic pump 1730.

After the thrombus is sucked, the driving unit 1420 is firstly closed, then the first peristaltic pump 1823 and the second peristaltic pump 1730 are sequentially closed, and then the developing solution in the balloon 1100 is extracted through the syringe 1813, so that the balloon 1100 is contracted. Finally, the thrombectomy device 1000 and the guide wire 2000 are withdrawn from the body together.

Example two

The same portions as those in the first embodiment will not be described again, and only different points will be described below.

Fig. 8 is a schematic structural view of the thrombus removal device in this embodiment, fig. 9 is a view of the thrombus removal device in this embodiment taken along direction a, and fig. 10 is a schematic structural view of the outer tube in this embodiment. As shown in fig. 8 to 10, the difference between the present embodiment and the first embodiment is that the thrombus removal device 1000 further includes an outer tube 1600, the outer tube 1600 is sleeved outside the sheath tube 1500, and a gap exists between the outer tube 1600 and the sheath tube 1500, so that the outer tube 1600 can freely move back and forth outside the sheath tube 1500. The outer tube 1600 has a plurality of second perfusion channels 1610 axially arranged along the outer tube 1600 in the tube wall, and the second perfusion unit 1820 provides the third liquid to the vicinity of the pipette tip 1300 through the second perfusion channels 1610. The distal end of the outer tube 1600 is provided with a second perfusion port 1620, and the third liquid is perfused into the region between the pipette tip 1300 and the balloon 1100 through the second perfusion channel 1610 via the second perfusion port 1620. In detail, the area near the pipette tip 1300 is the area between the balloon 1100 and the pipette tip 1300, and in one embodiment, the third liquid and the second liquid are the same, and the third liquid and the second liquid are thrombolytic drug solution and/or normal saline. In yet another embodiment, the third liquid is different from the second liquid, the third liquid is normal saline, and the second liquid is a thrombolytic drug.

In one embodiment of this embodiment, the thrombus removal device includes two second infusion units 1820 in communication with the first infusion channel 1240 and the second infusion channel 1610, respectively. The first perfusion channel 1240 is filled with thrombolytic drug solution only, and the second perfusion channel 1610 is filled with physiological saline only. Thus, the infusion amount of the thrombolytic liquid medicine and the physiological saline can be more accurately adjusted. In another embodiment of this embodiment, both the first perfusion channel 1240 and the second perfusion channel 1610 can be filled with thrombolytic drug and saline, so that a sufficient perfusion amount can be obtained when a large perfusion amount of saline is required.

It should be appreciated that the cross-sectional area of the second perfusion channels 1610 disposed on the outer tube 1600 is generally larger than the cross-sectional area of the first perfusion channels 1240, and the number of the second perfusion channels 1610 is greater than the number of the first perfusion channels 1240. Based on this, the second perfusion channel 1610 can provide a larger perfusion volume.

In the application process of the thrombus removal device 1000 of the present embodiment, before the operation, the thrombolytic drug solution can be infused only through the first infusion channel 1240, so that the infusion amount of the thrombolytic drug solution can be controlled, and the infusion of too much thrombolytic drug solution can be avoided.

In the operation process, the second perfusion channels 1610 are perfused with physiological saline, and the second perfusion channels 1610 with a larger number and a larger cross-sectional area can supplement sufficient physiological saline, so that the blood loss of the human body is further reduced.

Further, the distal end of the outer tube 1600 is trumpet-shaped. The outer tube 1600 with the horn-shaped opening can reduce the gap between the outer tube 1600 and the inner wall of the blood vessel, and after the second perfusion unit 1820 is opened, the physiological saline is sprayed out from the horn-shaped opening at the far end of the outer tube 1600, so that the free thrombus which is not cut into pieces at the position of the suction plug head 1300 can be prevented from flowing into the blood circulation system through the gap between the outer tube 1600 and the inner wall of the blood vessel.

Further, the cross-sectional shape of the second perfusion channel 1610 of the outer tube 1600 may be different, and the perfusion amount of the second liquid may be more finely adjusted through the second perfusion channels 1610 with different cross-sectional sizes when necessary. It is understood that the cross-sectional shape of the second irrigation channel 1610 includes, but is not limited to, a fan, a circle, or a rectangle.

Preferably, the material of the outer tube 1600 is medical polymer material or medical polymer and metal composite material.

EXAMPLE III

The same portions as those in the first and second embodiments will not be described again, and only different points will be described below.

Fig. 11 is a view of the thrombus removal device in this example from the direction a, and fig. 12 is a sectional view of a balloon catheter in this example. As shown in fig. 11 and 12, the difference between the present embodiment and the second embodiment is that the thrombus removal device 1000 further includes an outer tube 1600, the outer tube 1600 is sleeved outside the sheath 1500, a plurality of second perfusion channels 1610 are axially disposed along the outer tube 1600 in the wall of the outer tube 1600, the balloon catheter 1200 is not provided with the first perfusion channel 1240, and the second liquid is provided to the vicinity of the thrombus suction head 1300 only through the second perfusion unit 1820 and the second perfusion channels 1610.

It should be appreciated that such an arrangement may allow the structure of the balloon catheter 1200 to be simpler, which may further reduce the manufacturing cost of the thrombus removal device 1000.

To sum up, the embodiment of the utility model provides a thrombus clearing device, including sacculus pipe, driving tube and sheath pipe, sacculus pipe slip cap is located in the driving tube, the sheath pipe box is located outside the driving tube, the distal end and the near-end of sacculus pipe are connected with the sacculus respectively and fill the unit, the distal end of driving tube reaches the distal end of sheath pipe all is connected with a bolt head, the near-end of driving tube reaches drive unit and suction unit are connected respectively to the near-end of sheath pipe, the outer wall of driving tube with clearance between the inner wall of sheath pipe constitutes inhales the bolt passageway, inhale the bolt passageway with inhale bolt head intercommunication. Be provided with among the sacculus pipe and fill the passageway, the unit that pours into through fill the passageway to inject into in the sacculus or take out first liquid in order to control the sacculus inflation or shrink, just the unit that pours into still for the area near the suction plug head provides the second liquid, the suction unit passes through the suction plug passageway with thrombus suction into the suction plug head, drive unit drive the broken embolus sword in the suction plug head cuts up the thrombus, thrombus fragment via the suction plug passageway by the suction unit suction. The utility model provides an among the thrombus clearing device, fill into the unit and inject into or take first liquid out in order to control in to the sacculus through filling the passageway the sacculus inflation or shrink can make the laminating of the blood vessel inner wall of the distal end portion of sacculus and thrombus to can be when cleaing away the thrombus, the blood vessel of thrombus distal end portion is plugged up to the sacculus, prevents that thrombus fragment from escaping from the blood vessel of thrombus distal end portion. The infusion unit also provides a second liquid for the area near the suction plug head, the second liquid can be a thrombolysis liquid medicine and/or normal saline and the like, the thrombolysis liquid medicine and/or normal saline can apply an extra impact force to the thrombus when the thrombus is washed away, so that the thrombus is promoted to fall off from the inner wall of the blood vessel, the thrombolysis liquid medicine can promote the thrombus to dissolve, the operation time is shortened, the thrombus taking efficiency is improved, and meanwhile, in the process of sucking thrombus fragments, the infusion unit can clamp the thrombus fragments with the thrombolytic liquid medicine and/or normal saline infused to the area near the suction plug head and suck the thrombus fragments by the suction unit, so that the blood in the blood vessel can be prevented from being excessively sucked by the suction unit, and the blood loss of a patient is reduced.

The above description is only for the preferred embodiment of the present invention, and does not limit the present invention. Any technical personnel who belongs to the technical field, in the scope that does not deviate from the technical scheme of the utility model, to the technical scheme and the technical content that the utility model discloses expose do the change such as the equivalent replacement of any form or modification, all belong to the content that does not break away from the technical scheme of the utility model, still belong to within the scope of protection of the utility model.

Claims (12)

1. A thrombus removal device, comprising: the balloon catheter is sleeved in the transmission pipe in a sliding manner, and the sheath pipe is sleeved outside the transmission pipe;

the far end and the near end of the balloon catheter are respectively connected with a balloon and a perfusion unit, the far end of the sheath catheter is connected with a suction plug head, the transmission tube is rotatably connected with the suction plug head, a broken-plug knife is fixed at the far end of the transmission tube and is contained in the suction plug head, and the near end of the transmission tube is connected with a driving unit and the near end of the sheath catheter is connected with a suction unit;

an inflation channel is arranged in the balloon catheter, the perfusion unit injects or extracts a first liquid into or out of the balloon through the inflation channel to control the inflation or the deflation of the balloon, a first perfusion channel is arranged in the balloon catheter, the first perfusion channel is provided with at least one first perfusion opening positioned between the balloon and the thrombus absorption head, and the perfusion unit provides a second liquid to a region between the balloon and the thrombus absorption head through the first perfusion channel and the first perfusion opening;

the thrombus sucking device comprises a driving pipe, a sheath pipe, a sucking bolt head, a sucking bolt channel, a sucking unit, a driving unit and a sucking bolt unit, wherein a gap between the outer wall of the driving pipe and the inner wall of the sheath pipe forms the sucking bolt channel, the sucking bolt channel is communicated with the sucking bolt head, the sucking unit is used for sucking thrombus into the sucking bolt head, the driving unit is used for driving a thrombus cutter to cut up the thrombus to form thrombus fragments, and the sucking unit is used for sucking out the thrombus fragments through the sucking bolt channel.

2. The thrombus removal device according to claim 1, wherein the balloon catheter is a multi-channel tube, and a guide wire channel is provided at the center of the balloon catheter.

3. The thrombus removal device of claim 2, wherein the filling channel and the first perfusion channel are symmetrically disposed along a central axis of the guidewire channel.

4. The thrombectomy device of claim 2, wherein the sheath is externally sleeved with an outer tube, at least one second perfusion channel is axially disposed in the outer tube, the second perfusion channel has at least one second perfusion port located at a distal end of the outer tube, and the perfusion unit provides a third liquid to a region between the balloon and the thrombus head through the second perfusion channel and the second perfusion port.

5. The thrombectomy device of claim 4, wherein the distal end of the outer tube is flared.

6. The thrombectomy device of claim 1, wherein the infusion unit comprises a first infusion unit for outputting or aspirating the first liquid and a second infusion unit for outputting the second liquid.

7. A thrombectomy device according to claim 6, wherein said first infusion unit comprises a first adapter, a first infusion tube and a syringe, said syringe containing said first fluid, a distal end of said first infusion tube communicating with said filling channel through said first adapter, and a proximal end of said first infusion tube communicating with said syringe.

8. A thrombus removal device according to claim 6, wherein the second infusion unit comprises a second adapter, a second infusion tube and an infusion reservoir bag, the infusion reservoir bag contains the second liquid, the distal end of the second infusion tube is communicated with the first infusion channel through the second adapter, the proximal end of the second infusion tube is communicated with the infusion reservoir bag, and the second infusion tube is provided with a first peristaltic pump.

9. The thrombectomy device of claim 1, wherein the distal end of the plunger head and/or the side wall of the plunger head is provided with a plurality of plunger holes.

10. A thrombus removal device according to claim 1, wherein the aspiration unit comprises a third connector, a third infusion tube and a thrombus collection bag, the third infusion tube is communicated with the thrombus aspiration channel through the third connector, a proximal end of the third infusion tube is communicated with the thrombus collection bag, and a second peristaltic pump is provided on the third infusion tube.

11. The thrombus removal device according to claim 1, wherein the first liquid is a developing solution and the second liquid is a thrombolytic drug solution and/or a physiological saline.

12. A thrombus removal device, comprising: the balloon catheter is sleeved in the transmission pipe in a sliding manner, the sheath pipe is sleeved outside the transmission pipe, and the outer pipe is sleeved outside the sheath pipe;

the far end and the near end of the balloon catheter are respectively connected with a balloon and a perfusion unit, the far end of the sheath tube is connected with a suction plug head, the transmission tube is rotatably connected with the suction plug head, a broken plug knife is fixed at the far end of the transmission tube and is contained in the suction plug head, and the near end of the transmission tube and the near end of the sheath tube are respectively connected with a driving unit and a suction unit;

an filling channel is arranged in the balloon catheter, the filling unit injects or extracts first liquid into or out of the balloon through the filling channel to control the balloon to expand or contract, a plurality of second filling channels are axially arranged in the outer tube wall, a second filling port is arranged at the far end of the outer tube, and the filling unit provides second liquid to the area between the balloon and the embolectomy head through the second filling channels and the second filling port;

the thrombus sucking device is characterized in that a thrombus sucking channel is formed by a gap between the outer wall of the transmission tube and the inner wall of the sheath tube, the thrombus sucking channel is communicated with the thrombus sucking head, thrombus is sucked into the thrombus sucking head by the sucking unit, the thrombus is cut into thrombus fragments by the driving unit driving the thrombus cutter, and the thrombus fragments are sucked out by the sucking unit through the thrombus sucking channel.

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