Suction device applied to coronary artery bypass grafting

By designing the attraction device for coronary artery bypass surgery, it can automatically attract the anastomotic blood and adsorb blood in the pericardial cavity, solving the problems of high difficulty in surgery and waste of resources in the prior art, and improving surgical efficiency and field of vision clarity.

CN116159195BActive Publication Date: 2025-07-11BEIJING ANZHEN HOSPITAL AFFILIATED TO CAPITAL MEDICAL UNIV
View PDF 1 Cites 0 Cited by

Patent Information

Application Number
CN202211534340.3
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2022-11-30
Publication Date
2025-07-11
Estimated Expiration
2042-11-30

AI Technical Summary

Technical Problem

In the prior art, cardiac fixators cannot handle the anastomotic bleeding problem, resulting in increased difficulty in surgery, waste of human resources and increased workload of medical staff, and conventional flushing methods increase the pericardial fluid, affecting surgical operations.

Method used

A suction device for coronary artery bypass surgery is designed, including a fixed base, a suction tube, a first universal shaped tube and a pressing suction head. It automatically attracts the anastomosis blood through the negative pressure suction device, and adsorbs the blood in the pericardial cavity through the second universal shaped tube and a suction suction head, reducing the difficulty of anastomosis and visual field occlusion.

Benefits of technology

实现了自动吸引吻合口血液,降低了手术难度,节约人力资源,清晰暴露手术视野,提高了手术效率。

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure CN116159195B_ABST
    Figure CN116159195B_ABST
Patent Text Reader

Abstract

The present invention discloses an aspiration device applied to coronary artery bypass grafting surgery, comprising: a fixed base, which is positioned and arranged on a bypass heart fixator or a sternal retractor; an aspirator pipeline, which is communicated with a negative pressure aspiration device and fixedly arranged on the fixed base; a first universal shaping tube, which is communicated with the aspirator pipeline and can be adjusted and positioned in any orientation; a push-button aspirator head, which has a cavity inside and is communicated with the aspirator pipeline through the first universal shaping tube, and a plurality of first liquid suction holes communicated with the inside of the push-button aspirator head are formed in the side part; the push-button aspirator head is adapted to be pressed on the anastomotic stoma of the coronary artery bypass graft vessel to adsorb blood, so as to expose the anastomotic stoma area of the coronary artery bypass graft vessel. The present invention can automatically aspirate the blood at the anastomotic stoma of the coronary artery bypass graft vessel during the operation, expose the anastomotic stoma area, and simultaneously assist the fixator to fix the anastomotic area, reduce the operation anastomosis difficulty, and save human resources.
Need to check novelty before this filing date? Find Prior Art

Description

Technical Field

[0001] The present invention relates to the technical field of cardiac surgical instruments, and particularly relates to a suction device applied to coronary artery bypass grafting surgery. Background Art

[0002] Off-pump coronary artery bypass grafting (OPCABG) is an important method for treating severe coronary heart disease. The heart stabilizer can reduce the movement amplitude of the myocardium around the coronary artery-bridge vessel anastomosis site, reduce the difficulty of vascular anastomosis, and is an essential surgical consumable in OPCABG surgery. In the conventional beating-heart coronary artery bypass grafting surgery, the heart stabilizer is fixed on the sternal retractor. The surgeon incises the sternum along the midline of the patient's chest, exposes the thoracic cavity, exposes the heart, and performs cardiac surgery.

[0003] However, the heart stabilizer itself cannot handle the bleeding problem at the anastomosis site during the operation. It is necessary for an assistant to hold a blowing tube or syringe to flush the bleeding at the anastomosis site. Moreover, due to the obstruction of the surgeon, the anastomosis area may not be fully exposed, which affects the surgical operation, increases the surgical difficulty, prolongs the operation time, and causes a waste of human resources. In addition, if the method of flushing the anastomosis site is adopted, the liquid in the pericardial cavity will increase, and an additional adsorption device is needed to adsorb the liquid in the pericardial cavity, which increases the workload of medical staff. Summary of the Invention

[0004] Therefore, the technical problem to be solved by the present invention is to overcome the defects that the method of flushing the anastomosis site to expose the anastomosis area in the prior art will increase the surgical difficulty, cause a waste of human resources, and increase the workload of medical staff, so as to provide a suction device applied to coronary artery bypass grafting surgery.

[0005] To achieve the above object, the technical solution adopted by the present invention is as follows:

[0006] A suction device applied to coronary artery bypass grafting surgery, comprising:

[0007] A fixed base, which is positioned on the bypass heart stabilizer or the sternal retractor;

[0008] A suction tube, which is connected to a negative pressure suction device and fixedly arranged on the fixed base;

[0009] A first universal shaping tube, which is connected to the suction tube and can be adjusted and positioned in any direction;

[0010] A push-type suction head, which is hollow inside and is connected to the suction tube through the first universal shaping tube, and is provided with a plurality of first liquid suction holes on the side part that are connected to the inside of the push-type suction head; the push-type suction head is adapted to be pressed on the coronary artery bridge vessel anastomosis site and adsorb blood to expose the coronary artery bridge vessel anastomosis area.

[0011] Further optimize the technical solution, and the pressing suction head is set to be U-shaped or annular.

[0012] Further optimize the technical solution, and the first liquid suction hole is opened on the inner ring side wall and / or the outer ring side wall of the pressing suction head.

[0013] Further optimize the technical solution, and a second universal shaping tube capable of adjusting and positioning in any direction is branched and communicated on the suction tube. The end of the second universal shaping tube is communicated with a liquid suction type suction head capable of adsorbing the blood in the pericardial cavity.

[0014] Further optimize the technical solution, and the suction tube includes:

[0015] A connecting main pipe, one end of which is communicated with a negative pressure suction device, and the other end is bifurcated into a first fixed pipe and a second fixed pipe respectively fixed to the fixed base;

[0016] A first telescopic pipe, which can be telescoped and folded inside the fixed base and extend out of the fixed base movably; one end of the first telescopic pipe is communicated with the first fixed pipe, and the other end of the first telescopic pipe is communicated with the first universal shaping pipe;

[0017] A second telescopic pipe, which can be telescoped and folded inside the fixed base and extend out of the fixed base movably; one end of the second telescopic pipe is communicated with the second fixed pipe, and the other end of the second telescopic pipe is communicated with the second universal shaping pipe.

[0018] Further optimize the technical solution, and switches are respectively arranged on the first fixed pipe and the second fixed pipe.

[0019] Further optimize the technical solution, and the liquid suction type suction head is set to be cylindrical or frustum-shaped. The inside of the liquid suction type suction head is set to be cavity-shaped, and a number of second liquid suction holes communicated with the inside of the liquid suction type suction head are arranged on the liquid suction type suction head.

[0020] Further optimize the technical solution, and a protrusion or a groove is arranged at the end of the liquid suction type suction head. The second liquid suction hole is opened on the outer side wall of the protrusion or the inner side wall of the groove.

[0021] Further optimize the technical solution, and a fixed buckle for fixing to a bypass heart fixator or a sternal retractor is arranged at the bottom end of the fixed base.

[0022] The technical solution of the present invention has the following advantages:

[0023] 1. The suction device applied to coronary artery bypass surgery provided by the present invention is installed on a bypass heart fixator or a sternal retractor, which can automatically suck the blood at the anastomosis of the coronary artery bypass graft during the operation, expose the anastomosis area, and at the same time assist the fixator to fix the anastomosis area, reducing the difficulty of surgical anastomosis and saving human resources. The present invention adjusts the position of the pressing suction head through the first universal shaping tube, so that the pressing suction head is pressed at the anastomosis of the coronary artery bypass graft, and the first universal shaping tube has a certain supporting strength. Therefore, when the pressing suction head is pressed at the anastomosis of the coronary artery bypass graft, the movement amplitude of the myocardium around the anastomosis of the coronary artery bypass graft can be reduced, and the difficulty of blood vessel anastomosis can be reduced. During the operation, the negative pressure suction device operates, and the first liquid suction hole can suck the blood at the anastomosis of the coronary artery bypass graft. The sucked blood can directly enter the negative pressure suction device through the first universal shaping tube and the suction pipeline to completely expose the anastomosis area of the coronary artery bypass graft and ensure the normal operation of the operation.

[0024] 2. The suction device applied to coronary artery bypass surgery provided by the present invention is also branch-connected with a second universal shaping tube on the suction pipeline, and the end of the second universal shaping tube is connected with a liquid-sucking suction head. The present invention can suck the excess blood in the pericardial cavity through the liquid-sucking suction head, increase the amount of blood suction on the basis of using the pressing suction head, and then expose the surgical field of view, facilitating the doctor's next operation. When the suction of the excess blood in the pericardial cavity is completed, the liquid-sucking suction head can be removed by adjusting the second universal shaping tube.

[0025] 3. The suction device applied to coronary artery bypass surgery provided by the present invention realizes the telescoping of the first universal shaping tube and the pressing suction head through the first telescopic pipeline, and realizes the second telescopic pipeline and the liquid-sucking suction head through the second telescopic pipeline, so as to better meet the actual use requirements.

[0026] 4. The suction device applied to coronary artery bypass surgery provided by the present invention is respectively provided with switches on the first fixed pipeline and the second fixed pipeline. By setting switches on the two pipelines respectively to control the overall working state of the device, it is very convenient. BRIEF DESCRIPTION OF THE DRAWINGS

[0027] In order to more clearly illustrate the specific embodiments of the present invention or the technical solutions in the prior art, the following will briefly introduce the drawings required for use in the description of the specific embodiments or the prior art. Obviously, the following drawings are some embodiments of the present invention. For those of ordinary skill in the art, other drawings can be obtained based on these drawings without creative efforts.

[0028] Figure 1It is a schematic diagram of the structure of the suction device of the present invention applied to coronary artery bypass surgery;

[0029] Figure 2 This is a schematic structural diagram of a fixed base of a suction device used in coronary artery bypass surgery according to the present invention when it is cut open;

[0030] Figure 3 It is a schematic structural diagram of a push-type suction device head of a suction device used in coronary artery bypass surgery of the present invention when the head is in a ring shape;

[0031] Figure 4 The present invention is applied to the suction device of coronary artery bypass surgery Figure 3 Top view of the .

[0032] Figure numerals: 1. Suction device pipeline, 11. First fixed pipeline, 12. First telescopic pipeline, 13. Second fixed pipeline, 14. Second telescopic pipeline, 15. Connecting main pipe, 2. Fixed base, 21. Fixed buckle, 3. Press-type suction device head, 31. First suction hole, 4. Suction type suction device head, 41. Second suction hole, 5. First universal shaping tube, 6. Second universal shaping tube, 7. First switch, 8. Second switch. DETAILED DESCRIPTION

[0033] The technical solution of the present invention will be described clearly and completely below in conjunction with the accompanying drawings. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. 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.

[0034] In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", etc., indicating the orientation or positional relationship, are based on the orientation or positional relationship shown in the drawings, and are only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and therefore cannot be understood as limiting the present invention. In addition, the terms "first", "second", and "third" are used for descriptive purposes only, and cannot be understood as indicating or implying relative importance.

[0035] In the description of the present invention, it should be noted that unless otherwise clearly defined and limited, the terms "installation", "connection", and "coupling" should be understood in a broad sense. For example, it can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be directly connected or indirectly connected through an intermediate medium, and it can be the communication inside two components. For those of ordinary skill in the art, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

[0036] In addition, the technical features involved in different embodiments of the present invention described below can be combined with each other as long as they do not conflict with each other.

[0037] As Figures 1 to 4 shown in the specific embodiment of the suction device applied to coronary artery bypass grafting surgery, it includes a fixed base 2, a suction tube 1, a first universal shaping tube 5, and a push-type suction head 3.

[0038] Among them, the fixed base 2 is positioned on a bypass heart fixator or a sternal retractor, and the bypass heart fixator and the sternal retractor are existing conventional devices. The distal end of the suction tube 1 is connected and fixed to the fixed base 2 in communication with a negative pressure suction device. The first universal shaping tube 5 is a rotatable gooseneck tube or a coiled tube, and the angle of the push-type suction head 3 can be adjusted arbitrarily. The first universal shaping tube 5 is in communication with the suction tube 1 and can be adjusted and positioned in any orientation. The inside of the push-type suction head 3 is in a cavity shape and is in communication with the suction tube 1 through the first universal shaping tube 5, and a plurality of first liquid suction holes 31 communicating with the inside of the push-type suction head are provided on the side.

[0039] For the above suction device applied to coronary artery bypass grafting surgery, the position of the push-type suction head 3 is adjusted through the first universal shaping tube 5, so that the push-type suction head 3 is pressed on the anastomosis of the coronary artery bypass graft vessel. And the first universal shaping tube 5 has a certain support strength. Furthermore, when the push-type suction head 3 is pressed on the anastomosis of the coronary artery bypass graft vessel, the movement amplitude of the myocardium around the anastomosis of the coronary artery bypass graft vessel can be reduced, and the difficulty of blood vessel anastomosis can be reduced. During the operation, the negative pressure suction device operates. The first liquid suction holes 31 in this embodiment can adsorb the blood at the anastomosis of the coronary artery bypass graft vessel, and the adsorbed blood can directly enter the negative pressure suction device through the first universal shaping tube and the suction tube 1 to completely expose the area of the anastomosis of the coronary artery bypass graft vessel and ensure the normal operation of the surgery.

[0040] Among them, the anastomosis is the junction point connecting two tissues in a surgical operation. The negative pressure suction device is an existing conventional device, and no detailed description is given here.

[0041] As an alternative embodiment, the negative pressure suction device may also be a surgical suction device, ensuring that the present invention can be applied to most surgical scenarios.

[0042] As a further improved embodiment, the pressing suction head 3 is set to be U-shaped or annular, and can be set according to actual usage requirements. As Figure 1 and Figure 2 shown, the pressing suction head 3 is set to be U-shaped; as Figure 3 and Figure 4 shown, the pressing suction head 3 is set to be annular. The inner cavity of the pressing suction head 3 is set to be hollow.

[0043] As a further improved embodiment, the first liquid suction hole 31 is opened on the inner ring side wall and / or the outer ring side wall of the pressing suction head 3. That is, the first liquid suction hole 31 in this embodiment can be opened at a lower position on the inner ring side wall of the U-shaped pressing suction head, or can be opened on the outer ring side wall of the U-shaped pressing suction head, or can be opened on both the inner ring side wall and the outer ring side wall of the U-shaped pressing suction head. Or the first liquid suction hole 31 can be opened on the inner ring side wall of the annular pressing suction head, or can be opened on the outer ring side wall of the annular pressing suction head, or can be opened on both the inner ring side wall and the outer ring side wall of the annular pressing suction head.

[0044] As a further improved embodiment, a second universal shaping tube 6 capable of adjusting and positioning in any direction is also branched and communicated on the suction tube 1. The second universal shaping tube 6 is a gooseneck tube or a snake tube, and can fix the liquid suction type suction head 4 at any position. The end of the second universal shaping tube 6 is communicated with a liquid suction type suction head 4 capable of adsorbing the blood in the pericardial cavity. When there is too much bleeding at the coronary artery bypass anastomosis, the speed of adsorbing blood only by setting the pressing suction head 3 is relatively slow, and the excess blood will continuously flow into the pericardial cavity. Therefore, in this embodiment, the second universal shaping tube 6 and the liquid suction type suction head 4 are provided. The liquid suction type suction head 4 can be adjusted in any direction, and the excess blood in the pericardial cavity can be adsorbed through the liquid suction type suction head 4, increasing the amount of blood adsorption on the basis of using the pressing suction head, thereby exposing the surgical field of view and facilitating the doctor's next operation. When the adsorption of the excess blood in the pericardial cavity is completed, the liquid suction type suction head 4 can be removed by adjusting the second universal shaping tube 6.

[0045] As a further improved embodiment, the suction device pipeline 1 includes a connecting main pipe 15, a first fixed pipeline 11, a second fixed pipeline 13, a first telescopic pipeline 12 and a second telescopic pipeline 14. One end of the connecting main pipe 15 is connected to the negative pressure suction device, and the other end is bifurcated into the first fixed pipeline 11 and the second fixed pipeline 13 respectively fixed to the fixed base 2. The fixed base 2 in this embodiment has a accommodating cavity. The first telescopic pipeline 12 can be telescopically folded inside the fixed base 2 and can be movably extended from the fixed base 2. One end of the first telescopic pipeline 12 is connected to the first fixed pipeline 11, and the other end of the first telescopic pipeline 12 is connected to the first universal shaping tube 5. The second telescopic pipeline 14 can be telescopically folded inside the fixed base 2 and can be movably extended from the fixed base 2; one end of the second telescopic pipeline 14 is connected to the second fixed pipeline 13, and the other end of the second telescopic pipeline 14 is connected to the second universal shaping tube 6. This embodiment realizes the extension and retraction of the first universal shaping tube 5 and the pressing type suction head 3 through the first telescopic pipeline 12, and realizes the second telescopic pipeline 14 and the liquid suction type suction head 4 through the second telescopic pipeline 14, thereby being able to better meet the needs of actual use.

[0046] As a further improved implementation, switches are respectively provided on the first fixed pipeline 11 and the second fixed pipeline 13, that is, the first fixed pipeline 11 is provided with a first switch 7, and the second fixed pipeline 13 is provided with a second switch 8. The overall working state of the device is controlled by respectively providing switches on the two pipelines. When the first switch 7 is turned on and the negative pressure suction device is in operation, the blood at the anastomosis of the coronary artery bridge vessel can be adsorbed by the press-type suction head 3. When the second switch 8 is turned on and the negative pressure suction device is in operation, the blood in the pericardial cavity can be adsorbed by the suction-type suction head 4. When the first switch 7 and the second switch 8 are turned on at the same time, and the negative pressure suction device is in operation, the synchronous operation function of the press-type suction head 3 and the suction-type suction head 4 is realized.

[0047] The first switch 7 and the second switch 8 can be water-stop buckles or infusion switches.

[0048] As a further improved embodiment, the suction head 4 is configured to be cylindrical or truncated cone-shaped, the interior of the suction head 4 is configured to be cavity-shaped, and the distal end of the suction head 4 is provided with a plurality of second suction holes 41 connected to the interior of the suction head.

[0049] The end of the suction type aspirator head 4 is provided with a protrusion or a groove, and the second suction hole 41 is provided on the outer side wall of the protrusion or on the inner side wall of the groove. The second suction hole 41 is provided at the side, which is more convenient for adsorbing blood. In this embodiment, four second suction holes 41 are provided.

[0050] As an alternative embodiment, the end of the suction type aspirator head 4 is configured as a multi-slot type, and the second suction hole 41 is disposed on the side wall of the slot.

[0051] As a further improved implementation, the bottom end of the fixing base 2 is provided with a fixing buckle 21 fixed to the bypass heart fixator or the sternal retractor. In this embodiment, the positioning of the device can be achieved through the fixing buckle 21. When the bottom end of the fixing base 2 is set on the bypass heart fixator, it is specifically fixedly connected to the movable arm of the bypass heart fixator.

[0052] The specific use process of the present invention is:

[0053] The device is fixed on a bypass heart fixator or a sternal retractor, and the position of the pressing suction device head 3 is adjusted through the first universal shaping tube 5 so that the pressing suction device head 3 is pressed to the anastomosis of the coronary artery graft vessel.

[0054] During the operation, the first switch 7 is turned on and the negative pressure suction device is started, so that the push-type suction head 3 is in a continuous negative pressure adsorption state, thereby continuously adsorbing the blood at the coronary artery graft anastomosis to ensure the normal progress of the operation.

[0055] When the pressure-type suction head 3 absorbs blood but the coronary artery graft anastomosis is still blocked by blood, the second switch 8 can be turned on and the suction-type suction head 4 can be used to absorb the blood in the pericardial cavity to expose the surgical field of view.

[0056] Furthermore, during the operation, the first switch 7 and the second switch 8 can be directly turned on at the same time, so that the pressure-type suction head 3 and the suction-type suction head 4 can absorb the blood at the same time.

[0057] Obviously, the above embodiments are merely examples for clear explanation, and are not intended to limit the implementation methods. For those skilled in the art, other different forms of changes or modifications can be made based on the above description. It is not necessary and impossible to list all the implementation methods here. The obvious changes or modifications derived from them are still within the protection scope of the invention.

Claims

1. An aspiration device applied to coronary artery bypass surgery, characterized in that, Comprising: A fixed base (2), positioned and set on a coronary artery bypass heart fixator or a sternal retractor; A suction tube (1), connected to a negative pressure suction device and fixedly set on the fixed base (2); A first universal shaping tube (5), connected to the suction tube (1) and capable of adjusting and positioning in any orientation, the first universal shaping tube (5) being a rotatable gooseneck tube or a snake tube; A push - type suction head (3), with a cavity inside and connected to the suction tube (1) through the first universal shaping tube (5), and having a number of first liquid suction holes (31) opened on the side and communicating with the inside of the push - type suction head; the push - type suction head (3) is adapted to be pressed on the anastomotic site of the coronary artery bypass graft vessel to adsorb blood, so as to expose the anastomotic area of the coronary artery bypass graft vessel.

2. The suction device applied to coronary artery bypass surgery according to claim 1, characterized in that, The push - type suction head (3) is set in a U - shape or a ring shape.

3. The aspiration device applied to coronary artery bypass surgery according to claim 2, wherein The first liquid suction holes (31) are opened on the inner ring side wall and / or the outer ring side wall of the push - type suction head (3).

4. The aspiration device applied to coronary artery bypass surgery according to any one of claims 1 to 3, characterized in that, On the suction tube (1), there is also a second universal shaping tube (6) branched and connected, which can be adjusted and positioned in any orientation. The end of the second universal shaping tube (6) is connected to a liquid - suction type suction head (4) capable of adsorbing blood in the pericardial cavity.

5. The suction device applied to coronary artery bypass surgery according to claim 4, characterized in that, The suction tube (1) includes: A connecting main pipe (15), one end connected to the negative pressure suction device, and the other end bifurcated into a first fixed pipe (11) and a second fixed pipe (13) respectively fixed to the fixed base (2); A first telescopic pipe (12), capable of telescoping and folding inside the fixed base (2) and extending out of the fixed base (2) movably; one end of the first telescopic pipe (12) is connected to the first fixed pipe (11), and the other end of the first telescopic pipe (12) is connected to the first universal shaping tube (5); A second telescopic pipe (14), capable of telescoping and folding inside the fixed base (2) and extending out of the fixed base (2) movably; one end of the second telescopic pipe (14) is connected to the second fixed pipe (13), and the other end of the second telescopic pipe (14) is connected to the second universal shaping tube (6).

6. The aspiration device applied to coronary artery bypass surgery according to claim 5, wherein Switches are respectively arranged on the first fixed pipe (11) and the second fixed pipe (13).

7. The suction device applied to coronary artery bypass surgery according to claim 4, wherein, The liquid - suction type suction head (4) is set in a cylindrical shape or a frustum - shaped shape, with a cavity inside, and a number of second liquid suction holes (41) are arranged on the liquid - suction type suction head (4) and communicate with the inside of the liquid - suction type suction head.

8. The aspiration device applied to coronary artery bypass surgery according to claim 7, wherein, The end of the liquid - suction type suction head (4) is provided with a protrusion or a groove, and the second liquid suction holes (41) are opened on the outer side wall of the protrusion or the inner side wall of the groove.

9. The aspiration device applied to coronary artery bypass surgery according to claim 1, characterized in that, The bottom end of the fixed base (2) is provided with a fixed buckle (21) fixed to a coronary artery bypass heart fixator or a sternal retractor.

Citation Information

Patent Citations

  • Suction device applied to coronary artery bypass surgery

    CN219440161U