Valve replacement thread and use method thereofTechnical Field
The invention relates to the technical field of medical instruments, in particular to a valve replacement wire and a using method thereof.
Background
Valves are membranous structures that can be opened and closed inside the organs of humans or some animals. Each individual has four valves in the heart, namely an aortic valve that joins the left ventricle and the aorta, a pulmonary valve that joins the right ventricle and the pulmonary arteries, a mitral valve that joins the left atrium and the left ventricle, and a tricuspid valve that joins the right atrium and the right ventricle, all of which act as one-way valves that allow blood to flow only in one direction and not in the other. Multiple causes can lead to valve damage, early stage valve pathological changes have no obvious symptoms, symptoms such as dyspnea (labored dyspnea, paroxysmal nocturnal dyspnea, acute pulmonary edema), cough, expectoration, hemoptysis, listlessness, cyanosis and the like can appear until left heart failure, symptoms such as jugular vein anger, liver swelling with tenderness, lower limb concave edema and the like can appear when right heart failure, and ascites and cardiogenic cirrhosis can occur at the late stage.
Valve replacement is currently the means to address most valve diseases, as it is performed by securing it to the annulus with sutures. In order to fix the valve on the valve ring without displacement, the knots of the valve changing line cannot be loosened, a surgeon usually takes a certain time to make a plurality of knots, and the increased operation time can correspondingly increase the operation risk; in addition, minimally invasive surgeries such as endoscopic surgeries are developing faster and faster in cardiac surgery, the visual field exposure of the endoscopic surgeries is poor, and the knotting difficulty and the operation time are further increased.
Disclosure of Invention
The invention aims to provide a valve replacement wire and a using method thereof, which solve the problem that the valve replacement wire cannot be reliably knotted in a narrow space of an endoscopic surgery; the valve replacement wire is not required to be knotted in the valve replacement process, the fixation is reliable, the whole operation is simple and convenient, the operation time is saved, and the quick rehabilitation of a patient is facilitated.
In order to achieve the purpose, the valve replacement wire provided by the invention comprises a replacement suture, a limiting component, a fixing component, a connecting component and a guiding component, wherein the limiting component and the replacement suture are connected into a whole, the fixing component and the limiting component are matched and installed to form a self-locking structure, one end of the connecting component is detachably connected with the end part of the replacement suture, the other end of the connecting component is detachably connected with the tail part of the guiding component, and the head part of the guiding component is in a sharp arc shape.
Preferably, the limiting component is in a barb shape, and the fixing component is provided with a mounting hole groove corresponding to the barb-shaped limiting component.
Preferably, the limiting assembly and the replacement suture are connected into a whole to form a taper, an annular groove is formed in the middle of the limiting assembly, the fixing assembly is annular, the inner side of the fixing assembly is made of elastic materials, and the diameter of the inner ring of the fixing assembly is smaller than that of the annular groove in the middle of the limiting assembly.
Preferably, the limiting assemblies are distributed on the replacement suture line at intervals.
Preferably, the upper part of the connecting component is provided with a connecting hole corresponding to the replacement suture, the lower part of the connecting component is provided with a thread groove, and the rear end of the guide component is in threaded connection with the thread groove at the lower part of the connecting component.
Preferably, a rubber pad is arranged at the joint of the guide assembly and the connecting assembly.
Preferably, the surface of the guide assembly is provided with an oxidation resistant coating.
Preferably, the surface of the replacement suture is provided with an anti-infective coating.
Preferably, the surface of the replacement suture is provided with scale marks.
Further, a method for using the valve replacement wire is as follows:
firstly connecting the guide component at the end part of the replacement suture through the connecting component, then installing a fixing component, matching the fixing component with the limit component on the replacement suture to form a self-locking structure, simultaneously penetrating the artificial valve prefabricated on the human valve ring tissue and the human valve ring tissue through the guide component, then installing a fixing component, clamping and fixing the human valve ring tissue and the artificial valve by the front fixing component and the rear fixing component, then repeating the steps to enable the replacement suture to pass through the part needing to be fixed and fixing the whole artificial valve by using the self-locking structure formed by the limit component and the fixing component, and finally recording the value of the scale mark on the replacement suture and cutting off the redundant replacement suture to complete the valve replacement process.
Compared with the prior art, the invention has the following technical effects:
1. the invention solves the problem that the valve replacement thread can not be reliably knotted in a narrow space of an endoscopic surgery;
2. in the valve replacement process, the valve replacement wire does not need to be knotted;
3. the invention can firmly fix the artificial valve on the valve ring tissue of the human body;
4. the invention makes the whole operation process of valve replacement simpler and more convenient, saves the operation time and is beneficial to the quick recovery of patients.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present application, the drawings that are required to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present application and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained from the drawings without inventive effort.
FIG. 1 is a schematic view of the overall structure of the embodiment;
FIG. 2 is a schematic view of an assembly of the connecting assembly and the guide assembly of the embodiment;
FIG. 3 is a schematic structural diagram of a positioning assembly according to the first embodiment;
icon: 1-replacement suture, 2-limiting component, 3-fixing component, 4-connecting component, 401-connecting component lower part, 402-connecting component upper part, 403-connecting hole, 5-guiding component and 6-rubber pad.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present application clearer, the technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the drawings in the embodiments of the present application, and it is obvious that the described embodiments are some embodiments of the present application, but not all embodiments. The components of the embodiments of the present application, generally described and illustrated in the figures herein, can be arranged and designed in a wide variety of different configurations.
Thus, the following detailed description of the embodiments of the present application, presented in the accompanying drawings, is not intended to limit the scope of the claimed application, but is merely representative of selected embodiments of the application. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
It should be noted that the embodiments and features of the embodiments in the present application may be combined with each other without conflict.
It should be noted that: like reference numbers and letters refer to like items in the following figures, and thus, once an item is defined in one figure, it need not be further defined and explained in subsequent figures.
In the description of the embodiments of the present application, it should be noted that the indication of orientation or positional relationship is based on the orientation or positional relationship shown in the drawings, or the orientation or positional relationship which is usually placed when the product of the application is used, or the orientation or positional relationship which is usually understood by those skilled in the art, or the orientation or positional relationship which is usually placed when the product of the application is used, and is only for the convenience of describing the application and simplifying the description, but does not indicate or imply that the indicated device or element must have a specific orientation, be constructed in a specific orientation, and be operated, and thus, should not be construed as limiting the application. Furthermore, the terms "first," "second," "third," and the like are used solely to distinguish one from another and are not to be construed as indicating or implying relative importance.
In the description of the embodiments of the present application, it should also be noted that, unless otherwise explicitly stated or limited, the terms "disposed," "mounted," and "connected" are to be construed broadly, and may for example be fixedly connected, detachably connected, or integrally connected; may be directly connected or indirectly connected through an intermediate. The specific meaning of the above terms in the present application can be understood in a specific case by those of ordinary skill in the art.
Examples
The utility model provides a valve replacement line, includesreplacement suture 1,spacing subassembly 2, fixedsubassembly 3, coupling assembling 4,guide assembly 5,spacing subassembly 2 is connected as an organic wholely withreplacement suture 1, fixedsubassembly 3 forms auto-lock structure withspacing subassembly 2 cooperation installation, and coupling assembling 4 can be dismantled with the tip ofreplacement suture 1 and be connected, and coupling assembling 4 another can be dismantled with the afterbody ofguide assembly 5 and be connected, makes things convenient for the postoperative to retrieve, the disinfection, and the head ofguide assembly 5 is sharp-pointed arc form, is convenient forguide replacement suture 1.
Thelimiting component 2 is in a barb shape, and thefixing component 3 is provided with a mounting hole groove corresponding to the barb-shapedlimiting component 2.
Thelimiting assemblies 2 are provided with a plurality of limitingassemblies 2 which are evenly distributed on thereplacement suture 1 at intervals.
The coupling memberupper part 402 of the coupling member 4 is provided with a coupling hole 403 corresponding to thereplacement suture 1, the coupling member lower part 401 of the coupling member 4 is provided with a screw groove, and the rear end of theguide member 5 is screw-coupled to the screw groove of the coupling member lower part 401.
Therubber pad 6 is arranged at the joint of theguide assembly 5 and the connecting assembly 4, and therubber pad 6 plays a role in fastening theguide assembly 5 and prevents theguide assembly 5 from loosening and falling off in the operation.
The surface of theguide member 5 is provided with an oxidation-resistant coating which prevents oxidation of the surface of theguide member 5.
The surface of thereplacement suture 1 is provided with an anti-infection coating, the main component of the anti-infection coating is TiCagrilor, the Chinese name of the TiCagrilor is Ticagrelor, the anti-infection coating is a platelet aggregation inhibitor, the TiCagrilor is uniformly sprayed on the outer surface of thereplacement suture 1 by adopting a high-density spraying technology, the risk of infecting endocarditis can be reduced, and meanwhile, the rapid coagulation of platelets can be prevented from influencing the threading process.
The surface of thereplacement suture 1 is provided with graduation marks for recording the length of thepenetrated replacement suture 1.
Firstly, theguide component 5 is connected to the end part of thereplacement suture 1 through the connecting component 4, then afixing component 3 is installed, thefixing component 3 is matched with thelimiting component 2 on thereplacement suture 1 to form a self-locking structure, the artificial valve prefabricated on the human valve ring tissue and the human valve ring tissue are penetrated through theguide component 5 at the same time, then thefixing component 3 is installed, the human valve ring tissue and the artificial valve are clamped and fixed by thefront fixing component 3 and therear fixing component 3, then the steps are repeated to enable thereplacement suture 1 to penetrate through the part needing to be fixed and fix the whole artificial valve by using the self-locking structure formed by thelimiting component 2 and thefixing component 3, and finally the value of the scale mark on thereplacement suture 1 is recorded and theredundant replacement suture 1 is cut off, so that the valve replacement process can be.
Example one
Spacing subassembly 2 is connected as an organic whole withreplacement suture 1 and is the taper, the middle part ofspacing subassembly 2 is equipped with the annular groove, andfixed subassembly 3 is cyclic annular, and the inboard offixed subassembly 3 is elastic material, and the inner ring diameter of fixedsubassembly 3 is less than the diameter ofspacing subassembly 2 middle part annular groove, embolias the annular groove ofspacing subassembly 2 withfixed subassembly 3 in, plays spacing, the fixed action to artificial valve.
The present invention is capable of other embodiments, and various changes and modifications may be made by one skilled in the art without departing from the spirit and scope of the invention.