Implant-free suturing device for cardiac interventional operation
By using the adjustment and release components of the implant-free suture device for cardiac interventional surgery, the problems of non-adjustable suture device spacing and low suture efficiency have been solved, achieving a highly efficient and safe suture effect and avoiding inflammation caused by implants.
Patent Information
- Application Number
- CN202511498959.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-10-20
- Publication Date
- 2026-01-23
- Estimated Expiration
- 2045-10-20
AI Technical Summary
In current cardiac interventional surgery, implant suture devices have problems such as inflammatory reactions, thrombosis, displacement, and low suture success rate, while suture without implant devices has low suture efficiency.
An implant-free suture device for cardiac interventional surgery has been designed, comprising an adjustment component and a release component. The adjustment component adjusts the spacing between puncture needles via a threaded rod, and the release component uses an electric push rod to drive the clamps to tighten and a pressure sensor to control the clamping force, automatically releasing the suture to complete the suturing.
It enables flexible adjustment of the suture needle spacing, improves the suturing success rate, avoids inflammation caused by implants, and shortens the operation time.
Smart Images

Figure CN121370263A_ABST
Abstract
Description
TECHNICAL FIELD
[0001] The present application relates to the technical field of medical devices, in particular to a heart intervention surgery implant-free suturing device. BACKGROUND
[0002] With the continuous development of cardiovascular disease diagnosis and treatment technology, heart intervention surgery has gradually replaced traditional open chest surgery and become the mainstream means for treating coronary heart disease, arrhythmia, heart structure defects and other diseases due to its small trauma, fast recovery and definite effect. In common heart intervention surgeries such as percutaneous coronary intervention and transcatheter aortic valve replacement, effective closure of postoperative vascular puncture wounds or intra-cardiac operation wounds is a key link to ensure surgical safety and reduce the risk of complications. The mainstream treatment method in clinical practice is to use implant closure devices such as vascular suture devices and occluders, which achieve closure by implanting metal anchors, suture anchors, polymer occlusive pads and other implants at the wound site.
[0003] However, implant-dependent closure devices have many inherent defects in clinical application. Metal implants may cause local tissue inflammatory reactions, thrombosis, and even serious complications such as vascular stenosis and perforation due to implant migration. Polymer implants have problems such as incomplete degradation and poor compatibility with body tissues. Although existing implant-free suturing devices avoid the risks of implants, most suturing devices complete valve puncture suturing through barbed needles, which have a low success rate of hooking artificial sutures, reducing the success rate of surgery and prolonging the operation time. SUMMARY
[0004] In view of the problems in the prior art, the purpose of the present application is to provide a heart intervention surgery implant-free suturing device.
[0005] To solve the above problems, the technical scheme adopted by the present application is as follows.
[0006] A heart intervention surgery implant-free suturing device, comprising a handle, a fixed plate, a puncture needle and a cylinder, the fixed plate is provided with an adjusting assembly for adjusting the distance between the puncture needles, one end of the puncture needle close to the fixed plate is provided with a release assembly for automatically releasing the puncture needle:
[0007] The adjusting assembly comprises a sliding groove formed in the fixed plate, a plurality of sliding seats are slidably connected in the sliding groove, one end of the sliding seat away from the puncture needle is rotatably connected with a rotating plate, a adjusting plate is rotatably connected in the sliding groove, and the adjusting plate is rotatably connected with the rotating plate, a threaded rod is rotatably connected in the sliding groove, and the threaded rod is threadedly connected with the sliding seat away from the adjusting plate;
[0008] The releasing assembly comprises a top base fixedly connected to the sliding base, a light rod fixedly connected to one end of the top base close to the puncture needle, a circular table II fixedly connected to the other end of the light rod away from the top base, a sleeve fixedly connected to one end of the puncture needle close to the sliding base, two expansion grooves symmetrically formed in the sleeve, an expansion rod slidably connected to the expansion grooves, a clamping block fixedly connected to one end of the expansion rod close to the circular table II, and the clamping block is matched with the circular table II.
[0009] Optionally, a sliding groove is formed in the holding rod, a pull plate and a push plate are slidably connected to the sliding groove, two connecting plates are symmetrically installed on one end of the pull plate close to the push plate, and a mounting plate is fixedly connected to one end of the connecting plate close to the push plate.
[0010] Optionally, an electric rod is fixedly connected to the mounting plate, and an output end of the electric rod is fixedly connected to the fixed plate.
[0011] Optionally, a clamping groove is formed in the cylinder, a sliding rod is slidably connected to the clamping groove, and a limiting block is fixedly connected to one end of the sliding rod in the cylinder.
[0012] Optionally, a clamping groove is formed in the puncture needle, the limiting block is matched with the clamping groove, and a circular table I is slidably connected to the outer wall of the light rod.
[0013] Optionally, two rotating bases are installed on one side of the push plate away from the pull plate, the rotating bases are fixedly connected to the push plate, and pincers are rotatably connected to the rotating bases.
[0014] Optionally, an electric push rod is fixedly connected to the push plate, a guide plate is fixedly connected to an output end of the electric push rod, hinged plates are installed at both ends of the guide plate, the hinged plates are rotatably connected to the guide plate, and the hinged plates are rotatably connected to the pincers at one end away from the guide plate.
[0015] Optionally, a sleeve is slidably connected to the holding rod, the sleeve is fixedly connected to the pull plate, an adjusting groove is formed in the holding rod, an adjusting knob is slidably connected to the adjusting groove, and the adjusting knob is fixedly connected to the arc-shaped end of the sleeve.
[0016] Optionally, an adjusting rod is slidably connected to the sleeve, the adjusting rod is fixedly connected to the push plate, and the pull plate is slidably connected to the adjusting rod.
[0017] Optionally, a support plate is fixedly connected to one end of the holding rod away from the sliding groove, an insertion rod is slidably connected to the support plate, a plurality of insertion holes are uniformly formed in the adjusting rod, and the insertion rod is matched with the insertion holes.
[0018] Compared with the prior art, the technical scheme provided by the application has at least the following beneficial effects:
[0019] The adjusting assembly solves the problem that the distance between the stitching needles of the prior device cannot be adjusted, the threaded rods in the two fixed plates are driven to rotate by the adjusting assembly, the slide blocks in the sliding grooves are adjusted equidistantly, and then the positions of the puncture needle and the cylinder are adjusted synchronously; the position of the puncture needle is adjusted by pushing the adjusting knob, the position of the clamp is adjusted by pulling the adjusting rod, the surrounding tissue of the wound is prevented from being scratched during the movement of the holding rod, and the use range of the stitching device is effectively widened through the adjustment of the distance between the stitching needles.
[0020] The releasing assembly solves the problems that the implant of the prior device is prone to inflammation and the success rate of the needle hooking suture is low, the puncture needle is inserted into the cylinder through the suture site under the pushing of the electric rod, the cylinder is clamped with the puncture needle, the clamping of the puncture needle and the clamping block in the sleeve is released, and finally the automatic suture of the wound is completed by the puncture needle pulling the suture. This design avoids inflammation caused by the implant and significantly improves the stitching efficiency. BRIEF DESCRIPTION OF DRAWINGS
[0021] The accompanying drawings, which are incorporated herein and constitute part of the specification, illustrate embodiments of the application and, together with the description, further serve to explain the principles of the application and to enable a person skilled in the relevant art to implement and use the application.
[0022] Figure 1 It is a whole structure schematic diagram of the heart intervention surgery implant-free stitching device of the present application;
[0023] Figure 2 It is a holding rod cross-sectional structure schematic diagram of the heart intervention surgery implant-free stitching device of the present application;
[0024] Figure 3 It is a support plate structure schematic diagram of the heart intervention surgery implant-free stitching device of the present application;
[0025] Figure 4 It is a push plate structure schematic diagram of the heart intervention surgery implant-free stitching device of the present application;
[0026] Figure 5 It is a guide plate structure schematic diagram of the heart intervention surgery implant-free stitching device of the present application;
[0027] Figure 6 It is a cylinder cross-sectional structure schematic diagram of the heart intervention surgery implant-free stitching device of the present application;
[0028] Figure 7It is a schematic view of the sectional structure of the fixing plate of the non-implant suture device for the heart intervention surgery of the present application;
[0029] Figure 8 It is a schematic view of the sectional structure of the sleeve of the non-implant suture device for the heart intervention surgery of the present application;
[0030] Figure 9 It is a schematic view of the structure of the top base of the non-implant suture device for the heart intervention surgery of the present application.
[0031] [Reference signs]
[0032] In the figure: 1, holding rod; 2, adjusting rod; 3, adjusting groove; 4, supporting plate; 5, adjusting knob; 6, inserting rod; 7, sliding groove; 8, sleeve; 9, pulling plate; 10, pushing plate; 11, connecting plate; 12, mounting plate; 13, rotating base; 14, clamping; 15, electric push rod; 16, hinged plate; 17, guide plate; 18, fixing plate; 19, sliding groove; 20, sliding base; 21, cylinder; 22, clamping groove; 23, sliding rod; 24, limiting block; 25, clamping block; 26, threaded rod; 27, adjusting plate; 28, rotating plate; 29, electric rod; 30, sleeve; 31, clamping groove; 32, puncture needle; 33, top base; 34, light rod; 35, round table one; 36, round table two; 37, telescopic groove; 38, telescopic rod; 39, inserting hole.
[0033] As shown in the figure, in order to clearly realize the structure of the embodiment of the present application, specific structures and devices are marked in the figure, but this is only for the need of illustration, and is not intended to limit the present application in the specific structure, device and environment, and the devices and environment can be adjusted or modified by the ordinary skilled in the art according to the specific need. DETAILED DESCRIPTION
[0034] The present application will be described in detail below in conjunction with the drawings and specific embodiments. It should be noted that in order to make the embodiments more detailed, the following embodiments are the best, preferred embodiments, and other alternative ways can also be used by the skilled in the art to implement some known technologies; and the part of the drawings is only for more specific description of the embodiments, and is not intended to specifically limit the present application.
[0035] It should be noted that in the specification, "one embodiment", "embodiment", "exemplary embodiment", "some embodiments" and the like indicate that the described embodiments can include specific features, structures or characteristics, but not necessarily every embodiment includes the specific features, structures or characteristics. In addition, when a specific feature, structure or characteristic is described in conjunction with an embodiment, it should be within the knowledge of the skilled in the related art to realize this feature, structure or characteristic in conjunction with other embodiments (whether or not explicitly described).
[0036] In general, terminology can be understood at least in part from the usage in context. For example, the term "one or more" as used herein, depending at least in part upon context, can be used to describe any feature, structure, or characteristic in a singular sense or can be used to describe combinations of features, structures or characteristics in a plural sense. Additionally, the term "based on" can be understood as not necessarily intended to convey an exclusive set of factors, but rather can instead allow for existence of additional factors not necessarily expressly described, again, at least in part depending on context.
[0037] It is to be understood that the terms "on", "over", and "above", as used herein, should be interpreted in the broadest context possible so that "on" not only means "directly on" something but also includes the meaning of being "on" something with intervening features or layers therebetween, and "over" or "above" not only means "over" or "above" something but also can include the meaning of being "over" or "above" something with no intervening features or layers therebetween.
[0038] In addition, spatially relative terms, such as "beneath", "below", "lower", "above", "upper", and the like, can be used herein for ease of description to describe one element's or feature's relationship to another element(s) or feature(s) as illustrated in the figures. The spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientations depicted in the figures. The devices can be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly.
[0039] As shown in Figures 1 to 9 An embodiment of the present application provides a heart intervention surgery implant-free suturing device, which comprises a holding rod 1, two fixed plates 18, a puncture needle 32 and a cylinder 21. The fixed plates 18 are internally provided with an adjusting assembly for adjusting the distance between the puncture needles 32. The puncture needles 32 are provided with a releasing assembly at one end close to the fixed plates 18 for automatically releasing the puncture needles 32.
[0040] As shown in Figure 6 and Figure 7As shown, the adjusting assembly comprises a sliding groove 19 formed in a fixed plate 18, a plurality of sliding seats 20 slidably connected in the sliding groove 19, a rotating plate 28 rotatably connected to one end of the sliding seat 20 away from the puncture needle 32, an adjusting plate 27 rotatably connected in the sliding groove 19 and rotatably connected with the rotating plate 28, the rotating plate 28 rotatably connected between two adjacent sliding seats 20, and a threaded rod 26 rotatably installed on the fixed plate 18 and penetrating through the sliding groove 19. The threaded rod 26 comprises a light rod, and an external thread is formed on the light rod. The sliding seat 20 at the external thread is threadedly connected with the threaded rod 26, and the remaining sliding seats 20 are slidably installed on the light rod.
[0041] As shown in the drawings, Figure 2 As shown, a sliding groove 7 is formed in the handle 1, a pull plate 9 and a push plate 10 are slidably connected in the sliding groove 7, two connecting plates 11 are symmetrically installed on one end of the pull plate 9 close to the push plate 10, an installation plate 12 is fixedly connected to one end of the connecting plate 11 close to the push plate 10, two installation plates 12 are respectively installed on the two connecting plates 11, and two fixed plates 18 are respectively installed on the two installation plates 12. Specifically, as shown in the drawings, Figure 6 One of the two fixed plates 18 is fixedly installed on the installation plate 12, and a cylinder 21 is installed on the sliding seat 20 in the fixed plate 18; as shown in the drawings, Figure 7 The other fixed plate 18 is installed on the installation plate 12 by an electric push rod 29, and a top seat 33 and a puncture needle 32 are installed on the sliding seat 20 in the fixed plate. When the electric push rod 29 is started, the electric push rod 29 drives the fixed plate 18 to move towards the other fixed plate 18 until the puncture needle 32 is inserted into the cylinder 21.
[0042] As shown in the drawings, Figure 6 A clamping groove 22 is formed in the cylinder 21, a sliding rod 23 is slidably connected in the clamping groove 22, and a limiting block 24 is fixedly connected to one end of the sliding rod 23 in the cylinder 21. As shown in the drawings, Figure 2 A sleeve 8 is slidably connected in the handle 1 and fixedly connected with the pull plate 9, an adjusting groove 3 is formed in the handle 1, an adjusting knob 5 is slidably connected in the adjusting groove 3 and fixedly connected with the arc-shaped end of the sleeve 8, an adjusting rod 2 is slidably connected in the sleeve 8, the adjusting rod 2 is fixedly connected with the push plate 10, the pull plate 9 is slidably connected with the adjusting rod 2, a supporting plate 4 is fixedly connected to one end of the handle 1 away from the sliding groove 7, a plug rod 6 is slidably connected to the supporting plate 4, a spring is sleeved on the plug rod 6, one end of the spring is connected with the supporting plate and the other end is connected with the middle part of the plug rod 6, and a plurality of plug holes 39 are uniformly formed in the adjusting rod 2 and matched with the plug rod 6.
[0043] In order to improve the use range of the suture device, the adjusting assembly is arranged, the threaded rod 26 in the two fixed plates 18 is driven to rotate through the assembly, the sliding seat 20 in the sliding groove 19 is adjusted equidistantly, and then the positions of the puncture needle 32 and the cylinder 21 are synchronously adjusted; the position of the puncture needle 32 is adjusted by pushing the adjusting knob 5, the position of the clamp 14 is adjusted by pulling the adjusting rod 2, the surrounding tissue of the wound is prevented from being scratched in the moving process of the holding rod 1, and the use range of the suture device is effectively widened through the adjustment of the distance between the suture needles.
[0044] Specifically, first, the adjusting knob 5 is pushed, the sleeve 8 drives the pull plate 9 to move, the puncture needle 32 and the cylinder 21 on the mounting plate 12 are retracted into the sliding groove 7, the adjusting rod 2 is pulled, the push plate 10 and the clamp 14 are also retracted into the sliding groove 7, the surrounding tissue of the wound is prevented from being scratched in the moving process of the holding rod 1, the motor matched with the threaded rod 26 is controlled to rotate according to the size of the wound, the sliding seat 20 in the sliding groove 19 is driven to slide, it is worth noting that only one sliding seat 20 is threadedly connected with the threaded rod 26, and the rest of the sliding seats 20 are in sliding contact with the threaded rod 26, one sliding seat 20 moves, so that the rest of the sliding seats 20 are pulled along the sliding groove 19 formed in the fixed plate 18 under the pulling of the rotating plate 28, and the adjusting principles of the two fixed plates 18 are the same, the sliding seats 20 are equidistantly adjusted through rotation of the threaded rod 26, when the position of the suture needle is adjusted, the doctor holds the holding rod 1, slowly pushes the prepared suture device along the sheath tube reserved after the cardiac intervention operation is completed, and the accuracy of the positions of the puncture needle 32 and the clamp 14 is ensured through the matched DSA multi-angle projection.
[0045] Secondly, when the suture device reaches the specified position, the insertion rod 6 is pulled out along the insertion hole 39 on the adjusting rod 2, the adjusting rod 2 is slowly pushed, the push plate 10 extends along the sliding groove 7, the clamp 14 on the push plate 10 moves to the wound, the insertion rod 6 is inserted into the insertion hole 39 under the pushing of the spring arranged on the insertion rod 6, the position of the adjusting rod 2 is limited, the adjusting knob 5 is pushed along the adjusting groove 3, the sleeve 8 and the pull plate 9 extend along the sliding groove 7, and are moved to the position matched with the clamp 14, so that the wound is prepared for suturing.
[0046] As Figures 7 to 9As shown, the release assembly comprises a top seat 33 located on the fixed plate 18 on which the electric push rod 29 is mounted, specifically the top seat 33 fixedly connected to the sliding seat 20, a light rod 34 fixedly connected to one end of the top seat 33 close to the puncture needle 32, and a circular table two 36 fixedly connected to the other end of the light rod 34 away from the top seat 33. The puncture needle 32 is fixedly connected to a sleeve 30 close to the sliding seat 20, two expansion slots 37 are symmetrically formed in the sleeve 30, an expansion rod 38 is slidably connected in the expansion slot 37, a clamping block 25 is fixedly connected to one end of the expansion rod 38 close to the circular table two 36, the clamping block 25 is matched with the circular table two 36, a spring is sleeved on the expansion rod 38, one end of the spring is connected to the inner wall of the expansion slot 37, and the other end of the spring is connected to the clamping block. The mounting plate 12 is fixedly connected with the electric rod 29, the output end of the electric rod 29 is fixedly connected with the fixed plate 18, the puncture needle 32 is provided with a clamping groove 31, the limiting block 24 is matched with the clamping groove 31, and the outer wall of the light rod 34 is slidably connected with a circular table one 35.
[0047] As shown in the figure, Figure 5 The push plate 10 is provided with two rotating seats 13 away from the pull plate 9, and the rotating seats 13 are fixedly connected with the push plate 10, the rotating seats 13 are rotatably connected with the clamps 14, the push plate 10 is fixedly connected with the electric push rod 15, the output end of the electric push rod 15 is fixedly connected with the guide plate 17, the both ends of the guide plate 17 are provided with the hinged plates 16, the hinged plates 16 are rotatably connected with the guide plate 17, and the one end of the hinged plate 16 away from the guide plate 17 is rotatably connected with the clamp 14.
[0048] In order to improve the stitching efficiency, the release assembly is arranged, the clamp 14 is driven by the electric push rod 15 to clamp the part to be stitched, and the contact end of the clamp 14 with the stitching part is provided with a pressure sensor, the sensor is linked with the electric push rod 15, so that damage to the stitching part caused by excessive clamping force can be avoided; under the pushing of the electric rod 29, the puncture needle 32 penetrates through the stitching part and is inserted into the cylinder 21, the cylinder 21 forms clamping with the puncture needle 32, the puncture needle 32 is pressed to extrude the clamping block 25 in the sleeve 30, so that the clamping block 25 is automatically disengaged from the circular table two 36, and finally the puncture needle 32 pulls the suture to complete the automatic suture of the wound. This design not only avoids inflammation caused by the implant, but also significantly improves the stitching efficiency.
[0049] Specifically, first, the electric push rod 15 pulls the guide plate 17, so that the guide plate 17 pulls the clamp 14 to clamp the wound, and the clamp 14 is provided with a pressure sensor at the contact end of the wound, and the sensor is linked with the electric push rod 15. The electric push rod 15 automatically adjusts its extension according to the monitoring data of the pressure sensor to avoid damage to the suture site due to excessive clamping force. After the wound is clamped, the position of the micro-adjusting sleeve 8 is adjusted to adjust the position of the puncture needle 32. The puncture needle 32 and the cylinder 21 are moved close to each other by the electric rod 29 pushing the fixed plate 18 to move. It is worth noting that the mounting plate 12 is moved away from the clamp 14 under the pushing of the pull plate 9 and the connecting plate 11. The movement of the puncture needle 32 and the cylinder 21 will not contact the clamp 14. After the previous synchronous adjustment; the positions of the puncture needle 32 and the cylinder 21 are correspondingly arranged. When the puncture needle 32 passes through the wound clamped by the clamp 14, the puncture needle 32 is inserted into the cylinder 21, and the limiting block 24 in the cylinder 21 is clamped with the clamping groove 31 opened on the puncture needle 32. At the same time, the needle tip of the puncture needle 32 is inserted into the conical sleeve arranged in the cylinder 21 to fix the position of the puncture needle 32.
[0050] Secondly, with the further extension of the electric rod 29, the clamping block 25 in the sleeve 30 pushes the circular table one 35 to slide along the light rod 34, so that the circular table one 35 is tightly attached to the top seat 33. When the clamping block 25 passes the end of the circular table one 35 away from the top seat 33, the clamping block 25 slides along the conical end of the circular table one 35, and at this time the mounting plate 12 does not contact the suture site of the wound. At this time, the electric rod 29 is controlled to retract, and the clamping block 25 is pushed by the spring force of the spring arranged on the telescopic rod 38, so that the clamping block 25 clamps the circular table one 35 to move along the light rod 34, so that the circular table one 35 is attached to the circular table two 36. Under the pulling of the electric rod 29, the clamping block 25 and the telescopic rod 38 are retracted along the telescopic groove 37. When the clamping block 25 passes the contact end of the circular table one 35 and the circular table two 36, the clamping block 25 and the telescopic rod 38 rebound. At this time, the puncture needle 32 is pulled through the suture site under the pulling of the cylinder 21. The sleeve 30 is provided with a suture line, and the two ends of the suture line are fixedly connected with the sleeve 30 and the circular table two 36. At this time, the two ends of the wound will have a suture line, and the suture line can be knotted to complete the suture of the wound. The above components have been fully disinfected and sterilized before use. The suture line is a bioabsorbable suture line. After the suture is completed, the clamp 14 and the puncture needle 32 are retracted into the sliding groove 7 according to the above method, and the suture device is removed from the wound.
[0051] The working principle of the present application is as follows: first, push the adjusting knob 5, make the sleeve 8 drive the pull plate 9 to move, make the puncture needle 32 and the cylinder 21 on the mounting plate 12 retract into the sliding groove 7, pull the adjusting rod 2, make the push plate 10 and the clamp 14 also retract into the sliding groove 7, drive the sliding seat 20 in the sliding groove 19 to slide, when the position adjustment of the suture needle is completed, the prepared suture device is slowly pushed along the sheath tube reserved after the heart intervention operation is completed, and through the matched DSA multi-angle projection, the accuracy of the positions of the puncture needle 32 and the clamp 14 is ensured, when the suture device reaches the specified position, the insertion rod 6 is pulled out along the insertion hole 39 on the adjusting rod 2, the adjusting rod 2 is slowly pushed, the push plate 10 is extended along the sliding groove 7, when the clamp 14 on the push plate 10 moves to the wound, the insertion rod 6 is inserted into the insertion hole 39 under the pushing of the spring arranged on the insertion rod 6, the position of the adjusting rod 2 is limited, the adjusting knob 5 is pushed along the adjusting groove 3, the sleeve 8 and the pull plate 9 are extended along the sliding groove 7, and are moved to the position matched with the clamp 14, the clamp 14 is driven by the electric push rod 15 to clamp the suture part, and the contact end of the clamp 14 and the suture part is provided with a pressure sensor, the sensor is linked with the electric push rod 15, so that the damage to the suture part caused by the too large clamping force can be avoided; under the pushing of the electric rod 29, the puncture needle 32 penetrates the suture part and is inserted into the cylinder 21, the cylinder 21 forms a clamping connection with the puncture needle 32, the puncture needle 32 is pressed to extrude the clamping block 25 in the sleeve 30, so that the clamping block 25 is automatically disconnected with the circular table two 36, at this time, the puncture needle 32 penetrates the suture part under the pulling of the cylinder 21, at this time, the suture thread is arranged at both ends of the wound, and the suture thread is knotted, so that the suture of the wound is completed.
[0052] The present application encompasses any substitutions, modifications, equivalent methods and solutions made on the essence and scope of the present application. In order for the public to have a thorough understanding of the present application, specific details are described in the following preferred embodiments of the present application, and the present application can also be completely understood without the description of these details for those skilled in the art. In addition, in order to avoid unnecessary confusion to the essence of the present application, well-known methods, processes, flows, elements and circuits are not described in detail.
[0053] The above is only the preferred embodiment of the present application, and it should be pointed out that for ordinary skilled in the art, without departing from the principle of the present application, a number of improvements and refinements can also be made, and these improvements and refinements should also be regarded as the protection scope of the present application.
Claims
1. A non-implantable suture device for cardiac interventional surgery, comprising a handle, a fixation plate, a puncture needle, and a cylinder, characterized in that, An adjustment component for adjusting the distance between puncture needles is installed inside the fixing plate, and an automatic release component for releasing the puncture needle is installed at the end of the puncture needle closest to the fixing plate. The adjustment assembly includes a slide groove formed in a fixed plate, a plurality of slide seats are slidably connected in the slide groove, a rotating plate is rotatably connected to the end of the slide seat away from the puncture needle, an adjustment plate is rotatably connected in the slide groove and the adjustment plate is rotatably connected to the rotating plate, and a threaded rod is rotatably connected in the slide groove and the threaded rod is threadedly connected to the slide seat away from the adjustment plate. The release assembly includes a top seat fixedly connected to a slide. A light rod is fixedly connected to one end of the top seat near the puncture needle. A second truncated cone is fixedly connected to one end of the light rod away from the top seat. A sleeve is fixedly connected to one end of the puncture needle near the slide. Two telescopic grooves are symmetrically opened inside the sleeve. A telescopic rod is slidably connected inside the telescopic grooves. A locking block is fixedly connected to one end of the telescopic rod near the second truncated cone, and the locking block is adapted to the second truncated cone.
2. The implant-free suture device for cardiac interventional surgery according to claim 1, characterized in that: The grip bar has a sliding groove, and a pull plate and a push plate are slidably connected in the sliding groove. Two connecting plates are symmetrically installed on the pull plate near the push plate, and an installation plate is fixedly connected to the connecting plate near the push plate.
3. The implant-free suture device for cardiac interventional surgery according to claim 2, characterized in that: An electric rod is fixedly connected to the mounting plate, and the output end of the electric rod is fixedly connected to the mounting plate.
4. The implant-free suture device for cardiac interventional surgery according to claim 1, characterized in that: The cylinder has a snap-fit groove, and a slide rod is slidably connected in the snap-fit groove. A limit block is fixedly connected to one end of the slide rod located inside the cylinder.
5. The implant-free suture device for cardiac interventional surgery according to claim 4, characterized in that: The puncture needle has a slot, and the limiting block is adapted to the slot. A frustum is slidably connected to the outer wall of the optical rod.
6. The implant-free suture device for cardiac interventional surgery according to claim 2, characterized in that: Two rotating seats are installed on the side of the push plate away from the pull plate, and the rotating seats are fixedly connected to the push plate. A clamp is rotatably connected inside the rotating seat.
7. The implant-free suture device for cardiac interventional surgery according to claim 6, characterized in that: An electric actuator is fixedly connected to the push plate, and a guide plate is fixedly connected to the output end of the electric actuator. Hinges are installed at both ends of the guide plate, and the hinges are rotatably connected to the guide plate. The end of the hinge away from the guide plate is rotatably connected to the clamp.
8. The implant-free suture device for cardiac interventional surgery according to claim 1, characterized in that: A sleeve is slidably connected inside the grip, and the sleeve is fixedly connected to the pull plate. An adjustment groove is provided on the grip, and an adjustment knob is slidably connected inside the adjustment groove, and the adjustment knob is fixedly connected to the arc-shaped end of the sleeve.
9. The implant-free suture device for cardiac interventional surgery according to claim 8, characterized in that: An adjusting rod is slidably connected inside the sleeve. The adjusting rod is fixedly connected to the push plate, and the pull plate is slidably connected to the adjusting rod.
10. The implant-free suture device for cardiac interventional surgery according to claim 9, characterized in that: The end of the grip rod away from the sliding groove is fixedly connected to a support plate, and a plug rod is slidably connected to the support plate. The adjusting rod has multiple plug holes evenly distributed on it, and the plug rod is adapted to the plug holes.
Citation Information
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