Double-wing-structure forceps holder for restraining mitral valve regurgitation and conveying equipment of double-wing-structure forceps holder

Through the design of a double-wing structure clamp, the blade composed of a support rod and an elastic rod is fixed below the mitral valve, following the movement of the mitral valve, and adjusting the clamping force by air pressure, the mitral valve clamp in the prior art is solved. The problem of poor damage and reflux inhibition improves the safety and effectiveness of the surgery.

CN119235509AActive Publication Date: 2025-01-03SUZHOU JINYI MEDICAL TECH CO LTD +1
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Patent Information

Application Number
CN202411442360.7
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2024-10-16
Publication Date
2025-01-03
Estimated Expiration
2044-10-16

AI Technical Summary

Technical Problem

The existing mitral valve clamps are prone to unnecessary damage to the mitral valve when used, resulting in the gradual weakening of the inhibitory effect of the clamp on mitral valve regurgitation, requiring multiple adjustments to the position, which increases the risk of surgery and secondary surgery. probability.

Method used

Using a double-wing structure clamp, the "blade" composed of a support rod and an elastic rod is fixed under the mitral valve, and the mitral valve is opened and closed accordingly, which enhances the clamping force, and defines the clamping force through air pressure to reduce the barbs and The number of mitral valve contacts improves the suitability and stability of the clamp.

Benefits of technology

It reduces mitral valve damage, improves the fixation effect between the clamp and the mitral valve, enhances the reflux inhibition ability, reduces the need for reoperation, and improves the practicality and safety of the clamp.

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Abstract

The invention discloses a double-wing structure forceps holder for inhibiting mitral valve regurgitation and conveying equipment thereof, and relates to the technical field of surgical operating instruments. Comprising a fixing seat, the fixing seat is fixedly connected with supporting rods which are distributed in a mirror image mode through elastic pieces, the supporting rods are fixedly connected with elastic rods which are distributed at equal intervals in a mirror image mode, the fixing seat is fixedly connected with fixing pieces which are distributed in a mirror image mode, and the fixing pieces are fixedly connected with a mounting plate through the elastic pieces. The opposite sides of the mounting plates distributed in a mirror image mode are fixedly connected with barbs at equal intervals. By changing the positions of the barbs, the number of times that the barbs make contact with the mitral valve in the operation process is reduced, then damage to the mitral valve is reduced, the good fixing effect is achieved between the forceps holder and the mitral valve, and then the forceps holder can more stably restrain reflux of the mitral valve of a patient; meanwhile, the blades composed of the supporting rods and the adjacent elastic rods are opened and closed along with the movement of the mitral valve, the effect similar to that of a one-way valve is achieved, and the effect of restraining mitral valve regurgitation is further enhanced.
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Description

Technical Field

[0001] The present invention relates to the technical field of surgical instruments, and in particular to a double-wing structure clamp for inhibiting mitral valve regurgitation and a conveying device thereof. Background Art

[0002] The mitral valve clamp is a small device used to treat mitral regurgitation (mitral valve regurgitation is a condition in which the mitral valve in the heart cannot be completely closed, causing some blood to flow back from the left ventricle to the left atrium). It is delivered to the mitral valve of the heart through the femoral vein through the mitral valve clamp delivery device, and the clamp is controlled by a traction wire to clamp the middle part of the mitral valve to relieve mitral valve regurgitation. After the clamp is fixed on the mitral valve, the mitral valve clamp delivery device needs to be separated from the clamp and withdrawn from the patient. The clamp is usually composed of an elastic upper clamp arm and a lower clamp arm. When in use, the lower clamp arm is opened and the lower clamp arm is located on one side of the mitral valve, and the upper clamp arm is located on the other side of the mitral valve. Then the upper clamp arm is released, so that the upper clamp arm opens under its own elastic action and finally cooperates with the adjacent lower clamp arm to fix the adjacent mitral valve. In order to improve the firmness of the clamp and the mitral valve, barbs are provided on the upper clamp arm, but After the clamp is fixed on the mitral valve, it is necessary to observe the regurgitation of the mitral valve through ultrasound. If the clamp cannot be clamped at the most appropriate position on the mitral valve in one time, the position of the clamp needs to be adjusted multiple times until the regurgitation reaches the ideal effect before the mitral valve clamp delivery device is separated from the clamp. However, after each fixation of the clamp, the barbs on the upper clamp arm will cause damage to the mitral valve, and if the final clamping position coincides with the previous clamping position, that is, the clamp is finally fixed on the damaged part of the mitral valve, in this case, with the relaxation and contraction movement of the mitral valve, the clamp is frequently subjected to the pulling force of the mitral valve, which can easily cause the damaged part of the mitral valve to tear, causing the clamp to slide relative to the mitral valve, causing the effect of the clamp in suppressing the patient's mitral valve regurgitation to gradually weaken, resulting in the patient needing to undergo surgery again to adjust the position of the clamp or increase the number of clamps, and the second surgery undoubtedly greatly increases the surgical risk of the patient. Summary of the invention

[0003] The present invention provides a double-wing structure clamp for inhibiting mitral valve regurgitation and a delivery device thereof, so as to overcome the disadvantage that the existing mitral valve clamp may cause unnecessary damage to the mitral valve when used, resulting in the gradual weakening of the inhibitory effect of the clamp on mitral valve regurgitation.

[0004] The technical implementation scheme of the present invention is: a double-wing structure clamp for inhibiting mitral valve regurgitation, including a fixed seat, the fixed seat is fixed with a mirror-distributed support rod through an elastic sheet, the support rod is fixed with equidistant and mirror-distributed elastic rods, a film is fixed between the elastic rod and the adjacent support rod, the fixed seat is hinged with a mirror-distributed lower clamp arm, the lower clamp arm is hinged with a hinge rod near the fixed seat, the mirror-distributed hinge rod is hinged with a connecting head on one side away from the lower clamp arm, the lower clamp arm is provided with evenly distributed grasping teeth on one side away from the connecting head, a connecting piece is rotatably connected in the fixed seat, the fixed seat is fixed with a mirror-distributed fixing plate, the fixing plate is fixed with an upper clamp arm on one side away from the connecting head through an elastic sheet, the upper clamp arm is made of elastic material, the fixing plate is fixed with a mounting plate on one side away from the connecting head through an elastic sheet, and the opposite sides of the mirror-distributed mounting plates are fixed with equidistant barbs.

[0005] Furthermore, a connecting plate is fixedly connected to one side of the mounting plate away from the adjacent fixing plate, the connecting plate is made of elastic material, and the facing sides of the connecting plates in mirror-image distribution are commonly fixedly connected to a middle plate.

[0006] Furthermore, a symmetrically distributed reinforcing plate is fixedly connected to one side of the lower clamp arm away from the connecting head, and evenly distributed gripping teeth are provided on one side of the reinforcing plate away from the connecting head. The upper clamp arm is composed of a U-shaped member and steps fixed thereto and equidistant therefrom. In a free state, the U-shaped member on the upper clamp arm tends to move toward the gap between the adjacent reinforcing plate and the adjacent lower clamp arm.

[0007] Furthermore, the position where the upper clamp arm is fixed to the adjacent fixing plate is located above the fixing seat to accommodate mitral valves of different specifications. The step of the upper clamp arm is close to the adjacent U-shaped piece and is provided with an inclined surface on one side away from the adjacent fixing plate.

[0008] Furthermore, a locking rod is fixedly connected to one side of the connector close to the fixing seat, and the locking rod is threadedly connected to the connector.

[0009] The present invention also aims to provide a delivery device for a double-wing structure clamp, comprising an operating handle and the above-mentioned double-wing structure clamp for inhibiting mitral valve regurgitation, the operating handle being fixedly connected to an outer sleeve, an inner sleeve fixedly connected to the operating handle inside the outer sleeve, a connecting rod slidably connected inside the inner sleeve, the operating handle being limitedly slidably connected to a mirror-distributed arc-shaped push block, a traction wire being connected to the inner thread of the arc-shaped push block, a mirror-distributed guide hole being arranged near the outer sleeve of the operating handle, a mounting sleeve being fixedly connected to the side of the operating handle away from the outer sleeve, a sealing cylinder fixedly connected to the connecting rod inside the mounting sleeve, and the sealing cylinder being rotatably connected to the outer sleeve. An operating ring is connected, the operating handle and the mounting sleeve are both slidably connected to the operating ring, a sealing plate is sealingly, slidingly and rotatably connected to the side of the sealing tube away from the outer sleeve, the mounting sleeve is sealingly and slidably connected to the sealing plate through a connecting rod, the sealing plate cooperates with the sealing tube to form a power chamber, gas is stored in the power chamber, a position close to the operating ring in the sealing tube is sealed and limitedly slidably connected to an annularly distributed limiting column, the operating ring is provided with annularly distributed hemispherical grooves that are respectively limited and matched with adjacent limiting columns, a limiting block is fixedly connected to the side of the operating handle close to the guide hole distributed in a mirror image, and the limiting block is limited and matched with the adjacent traction wire.

[0010] Furthermore, the mounting sleeve is rotatably connected to an adjusting shaft, and the adjusting shaft is threadedly connected to the sealing plate.

[0011] Furthermore, two groups of partitions in mirror-image distribution are fixedly connected in the outer sleeve, each group of the partitions includes the partitions in mirror-image distribution, and each group of the partitions corresponds to adjacent guide holes.

[0012] Furthermore, the operating ring is fixedly connected to a friction ring which is slidably connected to the mounting sleeve, a limit ring is slidably connected to a position close to the friction ring in the mounting sleeve, an extrusion piece is slidably connected to a position close to the limit ring in the mounting sleeve, the mounting sleeve is provided with limit grooves which are distributed in a mirror image, the limit grooves are limitedly matched with the extrusion piece, a spring is connected between the extrusion piece and the limit ring, and the limit ring is frictionally matched with the friction ring.

[0013] Furthermore, the arc-shaped push block on one side is connected to a synchronous ring for limiting rotation, and the arc-shaped push block on the other side is provided with a synchronous groove, and the synchronous groove is limitedly matched with the synchronous ring.

[0014] In summary, the present application includes at least one of the following beneficial technical effects: the present invention reduces the number of times the barbs come into contact with the mitral valve during surgery by changing the position of the barbs, thereby reducing damage to the mitral valve, ensuring a good combination of the barbs and the mitral valve, and ensuring a good fixing effect between the clamp and the mitral valve, thereby enabling the clamp to more stably suppress the regurgitation of the patient's mitral valve. At the same time, the "leafs" composed of the support rod and the adjacent elastic rods are fixed under the mitral valve by the clamp, so that the "leafs" composed of the support rod and the adjacent elastic rods open and close with the movement of the mitral valve, playing a role similar to a one-way valve, further enhancing the effect of suppressing mitral valve regurgitation, and reducing the probability of the patient requiring reoperation due to increased mitral valve regurgitation.

[0015] By increasing the distance between the upper clamp arm and the corresponding lower clamp arm when the clamp is opened, the applicability of the clamp is improved. At the same time, the connection plate and the middle plate cooperate to increase the contact area between the clamp and the mitral valve, thereby enhancing the firmness between the clamp and the mitral valve.

[0016] By adopting a threaded connection between the connecting piece and the locking rod, the probability of the clamp opening and falling off due to heart beating after the clamp is fixed is reduced, thereby improving the practicality of the clamp.

[0017] The clamping force of the clamp on the mitral valve is limited by air pressure to prevent the possibility of the clamp falling off due to insufficient clamping force or a "gap" in the mitral valve due to excessive clamping force. There is no need to rely entirely on the doctor's experience, which improves the practicality of the clamp delivery device. BRIEF DESCRIPTION OF THE DRAWINGS

[0018] Figure 1 It is a schematic diagram of the three-dimensional structure of the present invention; Figure 2 This is a three-dimensional structural state diagram of the mitral valve clamp of the present invention when it is closed; Figure 3 This is a three-dimensional structural state diagram of the mitral valve clamp of the present invention when it is opened; Figure 4 It is a three-dimensional structural schematic diagram of the fixing seat, the connecting head and the connecting piece of the present invention; Figure 5 It is a schematic diagram of the three-dimensional structure of the upper clamp arm, the mounting plate and the barbs of the present invention; Figure 6 The present invention is attached Figure 4 The enlarged view of point A in the middle; Figure 7 An exploded view of the mitral valve clamp of the present invention; Figure 8 It is a three-dimensional structural schematic diagram of the operating handle, arc-shaped push block and mounting sleeve of the present invention; Fig. 9 It is a three-dimensional structural schematic diagram of the arc-shaped push block, the sealing cylinder and the operating ring of the present invention; Fig.10 It is a schematic diagram of the three-dimensional structure of the operating ring, the sealing plate and the limiting column of the present invention; Fig.11 The present invention is attached Figure 8 The enlarged view of point B in the middle; Fig.12 The present invention is attached Figure 7 Enlarged view of point C in the middle; Fig.13 It is a three-dimensional structural cross-sectional view of the outer sleeve, the inner sleeve and the connecting rod of the present invention; Fig.14 It is a schematic diagram of the three-dimensional structure of the friction ring, the limit ring and the extrusion part of the present invention.

[0019] In the figure: 1-fixed seat, 101-support rod, 102-elastic rod, 2-lower clamping arm, 3-hinge rod, 4-connecting head, 5-connecting piece, 6-fixed plate, 7-upper clamping arm, 8-mounting plate, 9-barb, 10-connecting plate, 11-middle plate, 12-reinforcement plate, 13-locking rod, 14-operating handle, 15-outer sleeve, 151-partition, 16-inner sleeve, 17-connecting rod, 18-arc push block, 181-traction wire, 182-guide hole, 19-mounting sleeve, 20-sealing cylinder, 21-operating ring, 22-sealing plate, 221-power chamber, 23-limiting column, 24-limiting block, 25-adjusting shaft, 26-friction ring, 27-limiting ring, 28-extrusion piece, 281-limiting groove, 29-synchronizing ring, 291-synchronizing groove. DETAILED DESCRIPTION

[0020] In order to make the purpose, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below in conjunction with the drawings in the embodiments of the present invention. Obviously, the described embodiments are part of the embodiments of the present invention, not all of the embodiments. Generally, the components of the embodiments of the present invention described and shown in the drawings here can be arranged and designed in various different configurations.

[0021] It should be noted that during surgery, the end of the medical device close to the operator is the proximal end of the medical device, and the end of the medical device entering the patient's blood vessel is the distal end of the medical device, and the description of the proximal end and the distal end is only to help understanding.

[0022] Therefore, the following detailed description of the embodiments of the present invention provided in the accompanying drawings is not intended to limit the scope of the invention claimed for protection, but merely represents selected embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0023] When using a mitral valve clamp, the position of the clamp needs to be adjusted multiple times. However, each time the clamp is fixed, the barbs on the upper clamp arm will damage the mitral valve, resulting in poor fixation of the clamp to the mitral valve.

[0024] Example 1: A double-wing structure clamp for inhibiting mitral valve regurgitation, please refer to Figure 1-Figure 5 , including a fixing seat 1, the lower part of the fixing seat 1 is fixed with two support rods 101 (the support rods 101 are made of hard metal) distributed in front and back mirror images through an elastic sheet, the support rod 101 is fixed with a plurality of elastic rods 102 (the elastic sheet and the elastic rods 102 are nickel-titanium memory alloy) distributed in left and right mirror images at equal distances, and a film is fixed between the elastic rod 102 and the adjacent support rod 101. When in the outside world, the doctor folds the support rod 101 and the elastic rod 102 together (the folded state can be referred to the attached Figure 2 , attached Figure 2 The film is not shown in the figure). After entering the patient's heart, the elastic sheet and the elastic rod 102 restore their deformation and unfold the film to form a leaf-like shape (the specific shape can be found in the attached figure). Figure 3 ), after unfolding, the "leaf" as a whole is in a state of being higher in the middle and lower on the left and right sides. The lower part of the fixed seat 1 is hinged with two lower clamping arms 2 distributed in left and right mirror images, and the lower part of the lower clamping arm 2 is hinged with a hinge rod 3. The lower sides of the two hinge rods 3 distributed in mirror images are jointly hinged with a connecting head 4, and the upper side of the lower clamping arm 2 is provided with evenly distributed grasping teeth, and the grasping teeth are used to improve the firmness of the lower clamping arm 2 to fix the mitral valve. A connecting piece 5 is rotatably connected in the fixed seat 1, and the upper parts of the left and right sides of the fixed seat 1 are fixed with fixing plates 6, and the upper parts of the opposite sides of the two fixing plates 6 are fixed with upper clamping arms 7 through elastic sheets. The upper clamping arms 7 are made of elastic material, and the upper side of the fixing plate 6 is fixed with a mounting plate 8 through an elastic sheet, and the opposite sides of the two mounting plates 8 distributed in mirror images are fixed with equidistant barbs 9, and the barbs 9 are used to increase the fixing force of the clamp and the mitral valve.

[0025] Please refer to Figure 2-Figure 5 The facing sides of the upper parts of the two mirror-distributed mounting plates 8 are fixedly connected with connecting plates 10, which are made of elastic material. The facing sides of the two mirror-distributed connecting plates 10 are fixedly connected with a middle plate 11. A hole is provided in the middle of the middle plate 11 for the clamping conveying device to pass through. In the free state, the distance between the two mounting plates 8 from top to bottom gradually increases due to the action of the connecting plates 10 and the middle plate 11.

[0026] Please refer to Figure 2-Figure 7Two reinforcing plates 12 symmetrically distributed frontally and rearwardly are fixedly connected to the middle part of the upper side of the lower clamp arm 2, and evenly distributed gripping teeth are arranged on the upper side of the reinforcing plates 12. The upper clamp arm 7 is composed of a U-shaped piece and steps fixed thereto and equidistant therefrom, and the U-shaped piece is fixed to the adjacent elastic sheet. The steps on the uppermost side of the upper clamp arm 7 are provided with symmetrically distributed perforations for connection with the clamping and conveying device. In the free state, the U-shaped piece on the upper clamp arm 7 tends to move to the gap between the adjacent reinforcing plate 12 and the adjacent lower clamp arm 2. The position where the upper clamp arm 7 is fixed to the adjacent fixing sheet 6 is located above the fixing seat 1, so as to achieve the purpose of clamping mitral valves of different thicknesses. An inclined surface is arranged on the side of the step of the upper clamp arm 7 close to the adjacent U-shaped piece and away from the adjacent fixing sheet 6.

[0027] Please refer to Figure 5 A locking rod 13 is fixedly connected to the middle part of the upper side of the connecting head 4, and the locking rod 13 is threadedly connected to the connecting piece 5, which is used to lock the relative position of the connecting head 4 and the fixing seat 1, that is, to lock the distance between the two lower clamping arms 2, thereby reducing the probability of the clamp falling off due to vibration.

[0028] When performing mitral valve clamping, the doctor connects the fixing seat 1, the upper clamp arm 7 and the connecting piece 5 to the corresponding positions on the existing mitral valve clamp delivery device, and then the doctor controls the two upper clamp arms 7 to swing and finally to be in a closed state through the mitral valve clamp delivery device (the closed state of the clamp can be referred to in the attached figure). Figure 2 ), during the swinging of the upper clamp arm 7, the upper clamp arm 7 is attached to the adjacent mounting plate 8 and pushes the mounting plate 8 to swing to a folded state. During the swinging of the mounting plate 8, the mounting plate 8 pushes the middle plate 11 downward through the adjacent connecting plate 10, and the connecting plate 10 bends and deforms at the same time. Then the doctor controls the rotation of the connecting piece 5 through the mitral valve clamp delivery device, and the connecting piece 5 moves upward through the threaded transmission locking rod 13 and the connecting head 4. The connecting head 4 pushes the adjacent lower clamp arm 2 to swing through the two hinged rods 3 and is finally in a folded state.

[0029] After the lower clamp arm 2 is in the retracted state, the doctor uses the guiding device and the adjustable curved sheath tube to establish an interventional channel from outside the patient to inside the patient. When the end of the adjustable curved sheath tube is located at the mitral valve position of the patient's heart, the doctor withdraws the guiding device, and then the doctor retracts the two support rods 101 to make the support rod 101 in a vertical state. At the same time, the elastic sheet adjacent to the support rod 101 is bent. Then the doctor retracts several elastic rods 102 to reduce the angle between the elastic rod 102 and the adjacent support rod 101. After completing the retraction of the support rod 101 and the elastic rod 102, the doctor uses the mitral valve clamp delivery device to deliver the clamp through the adjustable curved sheath tube into the patient's body.

[0030] After the clamp is delivered to the patient's heart, the mitral clamp delivery device drives the clamp to extend out of the adjustable curved sheath tube. At this time, the support rod 101 opens under the action of its adjacent elastic sheet, and the elastic rod 102 recovers its deformation, so that several elastic rods 102 and adjacent support rods 101 open the thin film between them. Then, under the guidance of three-dimensional ultrasound, the doctor drives the "leaf" composed of the support rod 101 and the elastic rod 102 to move downward by the clamp until the two lower clamp arms 2 pass through the middle of the two leaflets of the mitral valve (the lower clamp arms 2 are located below the mitral valve at this time), and operates the mitral valve. The clamp delivery device causes the connecting piece 5 to rotate in the opposite direction and moves the locking rod 13 and the connecting head 4 downward through the threaded transmission. The connecting head 4 pulls the adjacent lower clamp arms 2 to swing to the open state through the two hinged rods 3. Then the clamp is pulled upward as a whole through the mitral clamp delivery device until the two lower clamp arms 2 respectively drag the two leaflets of the mitral valve, and at the same time, the two upper clamp arms 7 enter between the two leaflets. At this time, the doctor controls the mitral clamp delivery device to open the upper clamp arms 7 under the action of the adjacent elastic sheets (at the same time, the two mounting plates 8 are reset under the action of the adjacent connecting plates 10. This state can be referred to in the attached figure). Figure 3 ), so that the two leaflets of the mitral valve are respectively clamped between the adjacent upper clamp arms 7 and the adjacent lower clamp arms 2 (at this time, the mitral valve is in contact with the grasping teeth on the adjacent lower clamp arms 2 and the adjacent reinforcing plates 12, which is used to increase the firmness of the clamp to fix the mitral valve), and then the mitral valve clamp delivery device continues to pull the clamp upward as a whole, and at the same time, the mitral valve clamp delivery device controls the rotation of the connecting piece 5, and the connecting piece 5 moves upward through the threaded transmission locking rod 13 and the connecting head 4, and the connecting head 4 pushes the two lower clamp arms 2 to swing through the two hinged rods 3 until they are about to reach the folded state and stop (at this time, the barbs 9 are not in contact with the adjacent leaflets).

[0031] The main cause of mitral regurgitation is due to abnormal mitral valve structure. One of the causes of abnormal mitral valve structure is thickening of the mitral valve. In the existing clamps, since the swing axis of the upper clamp arm 7 coincides with the swing axis of the adjacent lower clamp arm 2, during the opening of the upper clamp arm 7, the lower part of the upper clamp arm 7 first contacts the end of the adjacent leaflet, and then the upper clamp arm 7 stops moving. At this time, only the lower part of the upper clamp arm 7 contacts the adjacent leaflet. In this case, the clamp does not firmly clamp the mitral valve. By separating the swing axis of the upper clamp arm 7 from the swing axis of the adjacent lower clamp arm 2 and leaving a distance between the swing axes of the two to accommodate leaflets of different thicknesses, the specific operation is as follows: during the opening of the upper clamp arm 7 (since the distance between the lower part of the upper clamp arm 7 and the adjacent lower clamp arm 2 is greater than the thickness of the leaflet end, the lower part of the upper clamp arm 7 is not in contact with the leaflet end). The upper part of the upper clamp arm 7 first contacts the adjacent leaflet, and then under the action of the adjacent elastic sheet of the upper clamp arm 7, the upper part of the upper clamp arm 7 bends and fits against the surface of the adjacent leaflet (at this time, the lower part of the upper clamp arm 7 has not yet contacted the end of the adjacent leaflet), increasing the contact area between the upper clamp arm 7 and the adjacent leaflet, and then in the process of retracting the lower clamp arm 2, the lower clamp arm 2 drives the adjacent upper clamp arm 7 to swing through the adjacent leaflet. Since the swing axis of the lower clamp arm 2 is inconsistent with the swing axis of the adjacent upper clamp arm 7, during the swinging of the lower clamp arm 2, the upper clamp arm 7 moves upward relative to the adjacent lower clamp arm 2. At this time, the leaflet follows the movement of the adjacent lower clamp arm 2 under the action of the grasping teeth on the adjacent lower clamp arm 2 and the adjacent reinforcing plate 12, so that the upper clamp arm 7 slides along the adjacent leaflet (in this process, the inclined surface on the step of the upper clamp arm 7 guides the upper clamp arm 7 to slide along the adjacent leaflet).

[0032] When the lower clamp arm 2 is swung to a closed state, the doctor observes the patient's mitral regurgitation through ultrasound. If the patient's mitral regurgitation is not significantly relieved, the doctor repeats the above operation in reverse, opens the lower clamp arm 2, and closes the upper clamp arm 7 through the mitral clamp delivery device, then adjusts the position of the clamp, and clamps the leaflet again until the patient's mitral regurgitation is significantly relieved. The doctor continues to control the rotation of the connecting piece 5 through the mitral clamp delivery device, repeats the above steps of rotating the connecting piece 5, and swings the lower clamp arm 2 to a closed state.

[0033] When the lower clamp arm 2 swings to the folded state, the lower clamp arm 2 squeezes the adjacent upper clamp arm 7 through the adjacent leaflet to swing, so that the adjacent elastic sheet of the upper clamp arm 7 is deformed. As the lower clamp arm 2 swings, the distance between the lower clamp arm 2 and the swing axis of the adjacent upper clamp arm 7 gradually decreases until the end of the leaflet contacts the lower part of the adjacent upper clamp arm 7, the upper part of the upper clamp arm 7 contacts the upper part of the adjacent mounting plate 8, and pushes the adjacent mounting plate 8 to swing, so that the adjacent elastic sheet of the mounting plate 8 is deformed, and the connecting plate 10 adjacent to the mounting plate 8 is deformed. The reaction force of the connecting plate 10 on the mounting plate 8 pushes the upper part of the adjacent upper clamp arm 7 to bend and deform, thereby increasing the contact area between the upper clamp arm 7 and the leaflet. While the upper part of the upper clamp arm 7 contacts the upper part of the adjacent mounting plate 8, the barb 9 at the lower part passes through the adjacent upper clamp arm 7 and contacts the leaflet. The barb 9 further improves the firmness of the fixation of the leaflet.

[0034] After the lower clamp arm 2 swings to the folded state, the fixation of the mitral valve is completed. Then the doctor releases the clamping connection between the mitral valve clamping delivery device and the fixing seat 1, and withdraws the mitral valve delivery device from the patient's body. At this point, the mitral valve clamping operation is completed, and the large hole of the patient's mitral valve when it is open is divided into two small holes (at this time, the "leaf" composed of the support rod 101 and the adjacent elastic rod 102 is located directly below the adjacent small hole). At the same time, when the mitral valve is diastolic, blood impacts the "leaf" composed of the support rod 101 and the adjacent elastic rod 102 from top to bottom, causing the support rod 101 to be The elastic sheets adjacent to 101 are deformed, and at the same time, the elastic rod 102 is bent relative to the adjacent support rod 101, so that the projected area of ​​the "leaf" in the horizontal direction is reduced, and the flow of the patient's blood is not hindered. When the mitral valve contracts, the support rod 101 and the elastic rod 102 resume their deformation, and as the blood impacts the "leaf" in the opposite direction, the distance between the leaf and the mitral valve hole is reduced, thereby hindering the backflow of blood. In this way, the "leaf" composed of the support rod 101 and the adjacent elastic rod 102 opens and closes with the movement of the mitral valve, further suppressing mitral valve regurgitation.

[0035] When performing mitral valve clamping, the force with which the clamp holds the mitral valve is entirely determined by the doctor's feeling. If the clamp holds the mitral valve with little force, the clamp will not hold the mitral valve firmly enough, and the clamp may easily fall off in the patient's future life. If the clamp holds the mitral valve with great force, it may easily create a "gap" in the mitral valve, causing damage to the patient's mitral valve.

[0036] Example 2: Based on Example 1, a conveying device for a double-wing structure clamp is provided. Figure 1 and Figure 8-Figure 11, including an operating handle 14, an outer sleeve 15 is fixedly connected to the left side of the operating handle 14, an inner sleeve 16 is fixedly connected to the outer sleeve 15, the inner sleeve 16 is fixedly connected to the operating handle 14, the left end of the inner sleeve 16 protrudes out of the outer sleeve 15, a connecting rod 17 is slidably connected to the inner sleeve 16, the left end of the connecting rod 17 is roughly rectangular, and is used to drive the connecting member 5 to rotate, and two arc-shaped push blocks 18 distributed in front and behind are slidably connected to the left and right limit positions in the middle of the operating handle 14, and the arc-shaped push blocks 18 are internally threadedly connected with a traction wire 181 (the traction wire 181 is composed of a silk thread and a threaded rod, and the traction wire 181 can be seen in the attached Figure 8 ), the left part of the operating handle 14 is provided with two guide holes 182 distributed in front and back mirror images, the guide holes 182 are used to guide the movement of adjacent traction wires 181, the rear side of the operating handle 14 is fixedly connected with a mounting sleeve 19, a sealing cylinder 20 is fixedly connected in the mounting sleeve 19, the left side of the sealing cylinder 20 is fixedly connected to the connecting rod 17, the left part of the sealing cylinder 20 is rotatably connected with an operating ring 21, the right side of the operating handle 14 and the left side of the mounting sleeve 19 are both slidably connected with the operating ring 21, the right part of the sealing cylinder 20 is sealed, slidably and rotatably connected with a sealing plate 22, the right side of the mounting sleeve 19 is sealed and slidably connected to the sealing plate 22 left and right through two connecting rods, and the left side of the sealing plate 22 cooperates with the sealing cylinder 20 to form a power chamber 221, gas is stored in the power chamber 221, the left part of the sealing tube 20 is sealed and limitedly slidably connected with four limiting columns 23 distributed in an annular shape, the side of the limiting column 23 away from the central axis of the sealing tube 20 is hemispherical, the operating ring 21 is provided with a hemispherical groove distributed in an annular shape, the hemispherical groove of the operating ring 21 is limitedly matched with the adjacent limiting column 23, the left part of the operating handle 14 is fixedly connected with two limiting blocks 24 distributed in front and back mirror images, the limiting block 24 is provided with a semicircular groove and a horizontal groove in the semicircular groove, the height of the horizontal groove in the vertical direction is less than the diameter of the wire in the traction wire 181, the limiting block 24 is limitedly matched with the adjacent traction wire 181, and is used to fix the wire of the traction wire 181.

[0037] Please refer to Fig.10 and Fig.14 The right side of the mounting sleeve 19 is rotatably connected with an adjusting shaft 25 , and the adjusting shaft 25 is threadedly connected to the sealing plate 22 for adjusting the volume of the power chamber 221 .

[0038] Please refer to Fig.12 and Fig.13 Two groups of partitions 151 are fixedly connected in the outer sleeve 15 in a front-to-back mirror-distributed manner. Each group of partitions 151 includes two partitions 151 in an upper-lower mirror-distributed manner. Each group of partitions 151 corresponds to an adjacent guide hole 182 for guiding the wire of the traction wire 181 to pass through the outer sleeve 15 .

[0039] Please refer to Fig.14A friction ring 26 is fixedly connected to the right side of the operating ring 21, and the friction ring 26 is slidably connected to the mounting sleeve 19. The left part of the mounting sleeve 19 is slidably connected to a limit ring 27, and the left part of the mounting sleeve 19 is slidably connected to an extrusion piece 28. The mounting sleeve 19 is provided with two limit grooves 281 distributed in upper and lower mirror images. The limit groove 281 consists of a connecting groove in the middle and six card grooves symmetrically distributed on the front and rear sides, and the horizontal cross-section shape of the limit groove 281 is roughly in the shape of a "non" character. The card groove of the limit groove 281 is limitedly matched with the extrusion piece 28, and a spring is connected between the left side of the extrusion piece 28 and the limit ring 27, and the limit ring 27 is frictionally matched with the friction ring 26.

[0040] Please refer to Fig. 9 The front arc-shaped push block 18 is connected to the synchronous ring 29 for limited rotation, and the rear arc-shaped push block 18 is provided with a synchronous groove 291, which cooperates with the synchronous ring 29 to control whether the two arc-shaped push blocks 18 move synchronously.

[0041] When performing mitral valve clamping, the doctor clamps the inner sleeve 16 with the fixing seat 1, and makes the connecting rod 17 and the connecting piece 5 limitedly slidably connected, then respectively passes the wire ends of the two traction wires 181 through the adjacent arc-shaped push blocks 18 and makes the threaded rods of the traction wires 181 threadably connected with the adjacent arc-shaped push blocks 18, the wires of the traction wires 181 pass through the adjacent guide holes 182 and move along the gap between the two adjacent partitions 151, and finally pass through the outer sleeve 15, at this time, the doctor passes the wires of the traction wires 181 through the perforations on the upper clamping arm 7 on the same side, and re-inserts the wires of the traction wires 181 along the original path. The wire passes through the guide hole 182 on the same side, and then the doctor stretches the silk thread of the traction wire 181 to swing the upper clamp arm 7 to the retracted state. The doctor clamps the silk thread of the traction wire 181 in the horizontal groove of the adjacent limit block 24. At this time, the assembly of the device is completed. Then the doctor rotates the adjustment shaft 25 according to the condition of the patient's mitral valve (the mitral valve of some patients will undergo hardening). The adjustment shaft 25 moves the sealing plate 22 left and right through the threaded transmission to adjust the pressure of the gas in the power chamber 221 (the pressure is proportional to the clamping force of the clamp on the mitral valve) to an appropriate pressure. At this point, the preparation work is completed.

[0042] After the preparation work is completed, the mitral valve clamping operation begins, the clamp is delivered to the patient's heart, and then the doctor rotates the operating ring 21, and the operating ring 21 drives the sealing cylinder 20 to rotate through the four limit columns 23, and the sealing cylinder 20 drives the connecting rod 17 to rotate, and the connecting rod 17 drives the connecting head 4 to move through the threaded cooperation between the connecting piece 5 and the locking rod 13, and the connecting head 4 drives the opening or closing of the two lower clamping arms 2 on the clamp through the two hinged rods 3. When the two lower clamping arms 2 on the clamp are closed, if the clamping force of the clamp reaches the initial set force, the reaction force of the clamp on the connecting rod 17 causes the sealing cylinder 20 to stop rotating, and the doctor When the doctor continues to rotate the operating ring 21, the hemispherical groove of the operating ring 21 squeezes the adjacent limiting post 23 toward the central axis of the operating ring 21, and causes the hemispherical groove of the operating ring 21 to lose contact with the adjacent limiting post 23, thereby releasing the limiting effect of the limiting post 23 on the operating ring 21. As the operating ring 21 continues to rotate, the limiting post 23 gradually corresponds to the next adjacent hemispherical groove above and below the operating ring 21, and enters the hemispherical groove under the push of the gas in the power chamber 221, thereby re-limiting the operating ring 21. At this time, the doctor notices the above situation and stops rotating the operating ring 21, thereby ensuring that the clamping force of the clamp on the mitral valve is at an appropriate level.

[0043] When performing mitral valve clamping, the arc-shaped push block 18 is pushed to the left to relax the wires of the adjacent traction wires 181. At this time, the upper clamping arm 7 on the ipsilateral mitral valve swings and opens under the action of the adjacent elastic sheet. When it is necessary to control the two upper clamping arms 7 at the same time, the doctor rotates the synchronization ring 29 on the front arc-shaped push block 18 to make the synchronization ring 29 enter the synchronization groove 291 of the rear arc-shaped push block 18. At this time, when the doctor pushes any one of the arc-shaped push blocks 18, the two arc-shaped push blocks 18 move together.

[0044] When the doctor rotates the operating ring 21, the operating ring 21 drives the friction ring 26 to rotate, and the friction ring 26 and the limiting ring 27 are in friction cooperation to prevent the operating ring 21 from rotating when the doctor is not in contact with the operating ring 21, thereby affecting the doctor's operation. Therefore, before the mitral valve clamping operation begins, the doctor rotates the extrusion piece 28 counterclockwise (the rotation angle of this embodiment is from right to left) to make the extrusion piece 28 lose contact with the adjacent slot on the limiting groove 281. Then the doctor moves the extrusion piece 28 left and right to change the elastic force of the adjacent spring on the left side of the extrusion piece 28. When the elastic force of the adjacent spring of the extrusion piece 28 pushes the limiting ring 27 to squeeze the friction ring 26, and the friction force between the limiting ring 27 and the friction ring 26 is sufficient to keep the operating ring 21 stationary when the doctor is not operating, the extrusion piece 28 is stopped from moving and rotated clockwise to make the extrusion piece 28 enter the adjacent slot on the limiting groove 281. At this time, the adjustment of the extrusion piece 28 is completed.

[0045] After the clamp is fixed in place, the doctor first removes the wire of the traction wire 181 from the horizontal groove of the adjacent limit block 24, then releases the threaded connection between the threaded rod of the traction wire 181 and the arc-shaped push block 18 on the same side, and pulls out the traction wire 181. The doctor then releases the clamping connection between the inner sleeve 16 and the fixing seat 1, and withdraws the delivery device from the patient's body.

[0046] As described above, the above embodiments are only used to illustrate the technical solutions of the present invention, rather than to limit the same. Although the present invention has been described in detail with reference to the aforementioned embodiments, those skilled in the art should understand that the technical solutions described in the aforementioned embodiments may still be modified, or some of the technical features thereof may be replaced by equivalents. However, these modifications or replacements do not deviate the essence of the corresponding technical solutions from the spirit and scope of the technical solutions of the embodiments of the present invention.

Claims

1. A double-wing structure clamp for inhibiting mitral valve regurgitation, comprising a fixing seat (1), wherein the fixing seat (1) is fixedly connected to a mirror-distributed support rod (101) through an elastic sheet, wherein the support rod (101) is fixedly connected to an equidistant and mirror-distributed elastic rod (102), wherein a film is fixedly connected between the elastic rod (102) and the adjacent support rod (101), wherein the fixing seat (1) is hingedly connected to a mirror-distributed lower clamp arm (2), wherein the lower clamp arm (2) is hingedly connected to a hinge rod (3) at a position close to the fixing seat (1), wherein the mirror-distributed hinge rod (3) is hingedly connected to a connecting head (4) at a side away from the lower clamp arm (2), wherein the side of the lower clamp arm (2) away from the connecting head (4) is provided with evenly distributed gripping teeth, wherein: The device further comprises a connecting member (5), wherein the connecting member (5) is rotatably connected to the fixing seat (1), the fixing seat (1) is fixedly connected with a fixing plate (6) in a mirror-image distribution, the fixing plate (6) is fixedly connected with an upper clamping arm (7) via an elastic plate on a side away from the connecting head (4), the upper clamping arm (7) is made of an elastic material, the fixing plate (6) is fixedly connected with a mounting plate (8) via an elastic plate on a side away from the connecting head (4), and the opposite sides of the mirror-image mounting plates (8) are fixedly connected with equidistant barbs (9).

2. The double-wing structure clamp for inhibiting mitral regurgitation according to claim 1, characterized in that: A connecting plate (10) is fixedly connected to one side of the mounting plate (8) away from the adjacent fixing plate (6); the connecting plate (10) is made of elastic material; and the opposite sides of the mirror-distributed connecting plates (10) are commonly fixedly connected to a middle plate (11).

3. The double-wing structure clamp for inhibiting mitral regurgitation according to claim 2, characterized in that: A symmetrically distributed reinforcing plate (12) is fixedly connected to one side of the lower clamping arm (2) away from the connecting head (4), and evenly distributed gripping teeth are arranged on one side of the reinforcing plate (12) away from the connecting head (4). The upper clamping arm (7) is composed of a U-shaped member and steps fixedly connected thereto and equidistant therefrom. In a free state, the U-shaped member on the upper clamping arm (7) tends to move toward the gap between the adjacent reinforcing plate (12) and the adjacent lower clamping arm (2).

4. The double-wing structure clamp for inhibiting mitral regurgitation according to claim 3, characterized in that: The position where the upper clamp arm (7) is fixedly connected to the adjacent fixing plate (6) is located above the fixing seat (1) to accommodate mitral valves of different specifications. The step of the upper clamp arm (7) is provided with an inclined surface on one side close to the adjacent U-shaped member and away from the adjacent fixing plate (6).

5. The double-wing structure clamp for inhibiting mitral regurgitation according to claim 4, characterized in that: A locking rod (13) is fixedly connected to one side of the connector (4) close to the fixing seat (1), and the locking rod (13) is threadedly connected to the connector (5).

6. A conveying device for a double-wing structure clamp, characterized in that: The invention comprises an operating handle (14) and a double-wing structure clamp for inhibiting mitral valve regurgitation as claimed in claim 5, wherein the operating handle (14) is fixedly connected to an outer sleeve (15), an inner sleeve (16) fixedly connected to the operating handle (14) is fixedly connected inside the outer sleeve (15), a connecting rod (17) is slidably connected inside the inner sleeve (16), the operating handle (14) is limitedly slidably connected to an arc-shaped push block (18) distributed in a mirror image, the arc-shaped push block (18) is internally threadedly connected to a traction wire (181), a mirror-shaped guide hole (182) is provided at a position of the operating handle (14) close to the outer sleeve (15), a mounting sleeve (19) is fixedly connected to a side of the operating handle (14) away from the outer sleeve (15), a sealing cylinder (20) fixedly connected to the connecting rod (17) is fixedly connected inside the mounting sleeve (19), an operating ring (21) is rotatably connected to the sealing cylinder (20), and the operating The operating handle (14) and the mounting sleeve (19) are both slidably connected to the operating ring (21); a sealing plate (22) is sealingly slidably and rotatably connected to the side of the sealing sleeve (20) away from the outer sleeve (15); the mounting sleeve (19) is sealingly slidably connected to the sealing plate (22) via a connecting rod; the sealing plate (22) cooperates with the sealing sleeve (20) to form a power chamber (221); gas is stored in the power chamber (221); a position close to the operating ring (21) in the sealing sleeve (20) is sealed and slidably connected to an annularly distributed limiting column (23); the operating ring (21) is provided with an annularly distributed hemispherical groove that is respectively limited and matched with adjacent limiting columns (23); a limiting block (24) is fixedly connected to the side of the operating handle (14) close to the mirror-distributed guide hole (182); the limiting block (24) is limited and matched with the adjacent traction wire (181).

7. A conveying device for a double-wing structure clamp according to claim 6, characterized in that: The mounting sleeve (19) is rotatably connected to an adjusting shaft (25), and the adjusting shaft (25) is threadedly connected to the sealing plate (22).

8. The conveying device of the double-wing structure clamp according to claim 7 is characterized in that: Two groups of partition plates (151) distributed in a mirror image are fixedly connected inside the outer sleeve (15), each group of the partition plates (151) includes partition plates (151) distributed in a mirror image, and each group of the partition plates (151) corresponds to adjacent guide holes (182).

9. The conveying device of the double-wing structure clamp according to claim 8, characterized in that: The operating ring (21) is fixedly connected to a friction ring (26) which is slidably connected to the mounting sleeve (19); a limit ring (27) is slidably connected to a position in the mounting sleeve (19) close to the friction ring (26); an extrusion piece (28) is slidably connected to a position in the mounting sleeve (19) close to the limit ring (27); the mounting sleeve (19) is provided with a limit groove (281) distributed in a mirror image; the limit groove (281) is limitedly matched with the extrusion piece (28); a spring is connected between the extrusion piece (28) and the limit ring (27); and the limit ring (27) is frictionally matched with the friction ring (26).

10. The conveying device of the double-wing structure clamp according to claim 9, characterized in that: The arc-shaped push block (18) on one side is connected to a synchronization ring (29) for limited rotation, and the arc-shaped push block (18) on the other side is provided with a synchronization groove (291), and the synchronization groove (291) is limitedly matched with the synchronization ring (29).

Citation Information

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