36 results about "Aortic wall" patented technology

A device comprises an implantable blood pump receivable in a sheath for percutaneous delivery. The implantable blood pump comprises a collapsible impeller mounted in a collapsible impeller cage, and a drive device mounted in a housing. The housing is in connection between a first end of a catheter and the collapsible impeller cage. The drive device is adapted for rotating the collapsible impeller. A retractable support structure is adapted to extend from the catheter. The extended retractable support structure is adapted to engage with the wall of the aorta for allowing the implantable blood pump to be secured in the left ventricle. The collapsible impeller cage comprises an inlet and an outlet. The inlet is adapted to receive blood from the left ventricle. The outlet directs blood in the direction of the atrioventricular valve.

A valve stent and an artificial valve. The valve stent (100) comprises: a stent main body (110), a plurality of first support arms (120), and at least one second support arm (130). The plurality of first support arms are arranged in a circumferential direction of the stent main body. One end of each of the first support arms is connected to an outflow end (112) of the stent main body, and the other end (121) of each of the first support arms is arranged outside the stent main body and extends toward the direction of an inflow end (111) of the stent main body. One end of the second support arm is connected to the outflow end of the stent main body, and the other end (131) of the second support arm is arranged outside the stent main body. The stent main body is used for placement at an aortic valve. A native valve leaflet (11) is accommodated between the stent main body and the first support arms, and the other end of each of the first support arms is used for extending into a corresponding aortic sinus to provide anchoring. In each aortic sinus, at least one first support arm is arranged, and the second support arm is used for expanding an aortic wall. When a pure aortic regurgitation valve is replaced, the valve stent can provide stable and reliable anchoring by means of the first support arms and the second support arm, can be prevented from interfering and blocking the coronary artery ostia by means of the second support arm, and can expand the aortic wall during delivery.

The invention relates to the technical field of neutrophile granulocyte separation, in particular to a mouse neutrophile granulocyte separation method which comprises the following steps: (1) anesthetizing and disinfecting a mouse; (2) tissue sampling; (3) tissue digestion; (4) preparing a cell suspension; (5) purifying cells; (6) cell culture; according to the method disclosed by the invention, isoflurane is adopted in the anesthesia disinfection step, so that central nervous activity of mice can be rapidly inhibited, tissue damage caused by stress reaction is avoided, and chemical stimulation can be reduced while body surface microorganisms are cleared through combination of ethanol disinfection and sterile normal saline flushing, and aortic tissues with intact activity are provided for subsequent material taking. In the compound enzyme digestive juice, collagenase I can specifically degrade aortic wall collagenous fibers, trypsin dissociates adhesion connection between cells, neutral protease assists in decomposing elastic fibers, and DNA enzyme I is supplemented to inhibit cell aggregation, so that the contradiction between incomplete digestion and large cell damage of the traditional enzyme juice is effectively solved.

The utility model discloses an aortic arch support which comprises a body, the body is arranged to be in a pre-bending shape, a concave portion is arranged on the body, and a first branch pipe, a second branch pipe and a third branch pipe which are matched with an aortic arch are arranged on the concave portion. The first branch pipe, the second branch pipe and the third branch pipe all protrude out of the surface of the body; according to the aortic arch support, a gap can be formed between the concave part and the aortic wall, the aortic arch support is suitable for most branch variation situations, and the phenomenon that the inner diameter of the aortic trunk is reduced cannot occur; besides, the contact area of the branch blood vessel and the main blood vessel can be increased, and the contact area is changed into a surface from a point, so that the phenomenon of internal leakage is well avoided; and the aortic arch stent is integrally designed, so that the integrity of the whole stent does not need to be damaged in an operation, and the risk is low.

The invention discloses a proximal anastomosis auxiliary device in coronary artery bypass grafting, and relates to the technical field of medical instruments. Comprising a puncture needle, a puncture cannula and an annular compressor. The puncture needle is sleeved with the puncture cannula, and a bulged ball is arranged at the head end of the puncture cannula; the annular compressor is arranged outside the puncture cannula in a sleeving mode and can slide in the axial direction, a compression ring with a notch is arranged at the head end of the annular compressor, and the inner diameter of the compression ring is smaller than the outer diameter of the bulging ball. During puncture, the annular compressor is pressed down after puncture enters the aorta, and the compression ring and the bulging ball cooperate to clamp and close a puncture point to achieve blood-free operation; after the aorta wall in the compression ring is cut off, the bridge vessel is matched with the aorta, and the suture passes through the compression ring together; after suturing is completed, the annular compressor is rotated, the suture retreats from the notch, the suture is tightened and knotted after the whole device is withdrawn, and anastomosis is completed. The aorta forceps clip operation is avoided, the plaque falling risk is eliminated, anastomosis can be completed only through a single hole, operation is easy and convenient, hemostasis is reliable, and cost is low.

The invention provides a biomarker composition and an application thereof. The biomarker composition comprises the following proteins: MMP12, UMOD, HbA1c, FGF9, NINJ1 and PRSS8. According to the biomarker composition provided by the invention, through combination of matrix metalloproteinase 12, uromodulin, glycosylated hemoglobin, FGF9, NINJ1 and serine protease 8, the problem of lack of a specific marker for aortic wall structure damage in the prior art is solved.

An endoanchor for anchoring an endograft to an aortic wall. The endoanchor comprises a first end, a second end, and a body helically extending between the first end and the second end. The endoanchor has a deployed state in which the endoanchor is configured to apply a radial force around the circumference of the endograft to anchor the endograft to the aortic wall.

The utility model provides an aorta abdominalis graft infection stent extraction device, which comprises a main body, a stent recovery clamp and an operating handle, an accommodating cavity is arranged in the main body, the accommodating cavity is exposed at the front end of the main body, the surface of the main body is smooth, the operating handle is positioned at the rear end of the main body, and the stent recovery clamp is arranged in the accommodating cavity. The operation handle pushes and pulls the support recovery clamp. The main body comprises an outer layer, an inner layer and a barb recovery part, the inner layer is arranged in the outer layer, and the front end of the inner layer is located on the rear side of the front end of the outer layer; the barb recovery part is located between the inner layer and the outer layer, and the barb recovery part is connected with the front end of the inner layer, so that the safety of taking out the stent graft is guaranteed, and damage to the aorta wall is avoided.

The invention relates to the technical field of animal model construction, and discloses a mouse abdominal aortic aneurysm model construction method. The construction method comprises the step that in a 18-month-old mouse, a sterile cotton piece soaked with elastinase is used for wrapping the kidney subabdominal aorta to induce formation of the abdominal aortic aneurysm. The mouse model can better reflect the degenerative change of the aortic wall of an elderly patient, better fits the clinical manifestation in the development speed and severity of aortic aneurysm, can more stably simulate the development process of the abdominal aortic aneurysm of the elderly patient, can be used as an effective tool for studying senescence-related aneurysm diseases, and has a wide application prospect. The method is helpful for revealing acceleration and aggravation processes of the elderly individuals in pathological development, and provides a more targeted theoretical basis and experimental support for designing and evaluating a new treatment method.

The present invention discloses a minimally invasive coronary artery bypass grafting proximal anastomosis instrument kit and anastomosis control system. It includes a puncher, a suturer and an anvil segment holder; the puncher includes a puncher body and an anvil segment, the puncher body includes an inner shaft, a cutting tube and an outer tube arranged in sequence from the inside to the outside, and the end of the inner shaft is threadedly connected with the anvil segment; the suturer includes a main cylinder, an eccentric rotating shaft and a needle storage bin, the eccentric rotating shaft is slidably connected and rotatably connected to the main cylinder; the end of the eccentric rotating shaft is connected to the needle storage bin; a needle insertion position for inserting a straight threaded suture needle is provided in the needle storage bin, and the socket of the needle insertion position faces the main cylinder; a connection structure for threading the anvil segment is provided on the side of the needle storage bin away from the main cylinder. The straight threaded suture needle of the present invention is hidden in the needle storage bin, and enters the aortic cavity together with the suturer, and then the needle storage bin is separated from the main cylinder by rotating, and then the straight threaded suture needle passes through the aortic wall from the inside to the outside in the aortic cavity to complete a needle suture.

The present application relates to the application of delta-Viniferin in the preparation of drugs for preventing or treating metabolic cardiovascular diseases. Delta-Viniferin can inhibit the expression level of aging and inflammation related genes / proteins of vascular endothelial cells, reduce endothelial dysfunction, and clarify its anti-hypertensive effect. Delta-Viniferin can inhibit the expression level of vascular smooth muscle cell phenotype conversion related genes / proteins, improve the contraction function of vascular smooth muscle, and significantly alleviate the degradation of elastic fibers of the vascular wall and the rupture of the intima of the aortic wall in vivo, and clarify its effect on preventing and treating aortic dissection. Delta-Viniferin can inhibit the expression level of myocardial fibroblast fibrosis related genes / proteins, and clarify its anti-myocardial fibrosis effect. Delta-Viniferin can promote white adipose tissue browning by targeting the SIRT1-FOXO1 axis, increase energy consumption, and clarify its effect on resisting obesity. In summary, the compound delta-Viniferin has the effect of protecting various metabolic cardiovascular diseases, and can be used to prepare drugs for preventing and treating metabolic cardiovascular diseases.

The present invention relates to the technical field of medical devices for cardiovascular diseases. Disclosed is an aortic covered stent. The aortic covered stent comprises a supporting stent, a sealing layer, and an elastic connecting layer. The sealing layer is spaced apart from and sleeved on the outer periphery of the supporting stent. The sealing layer comprises a first covering film. The elastic connecting layer is connected between the supporting stent and the sealing layer, such that blood flow can circulate between the supporting stent and the sealing layer. With the pulsation of the aorta, the sealing layer and the elastic connecting layer undergo elastic deformation, so that the first covering film is always closely attached to the aortic blood vessel wall adjacent to the sealing layer. The aortic covered stent can be well adapted to the special morphology of ascending aortic dissection and the mechanical characteristics of blood flow, offering high stability and exhibiting good sealing performance on the ascending aortic wall.

The application provides a valve stent and artificial valve, which comprises a stent body, a plurality of first support arms arranged along the circumference of the stent body, one end of the first support arm being connected with the outflow end of the stent body, the other end being arranged outside the stent body and extending towards the inflow end of the stent body, and a second support arm, one end of the second support arm being connected with the outflow end of the stent body, the other end being arranged outside the stent body; the stent body can be placed at the aortic valve, the stent body and the first support arm accommodate the native valve leaflet, the other end of the first support arm extends into the corresponding aortic sinus to provide anchoring, at least one first support arm can be arranged in each aortic sinus, and the second support arm can support the aortic wall. The application can replace the aortic valve regurgitation, realize stable and reliable anchoring through the unique anchoring structure, and is not easy to block the coronary artery opening.

The invention discloses a personalized valved aorta model manufacturing method based on iconography data, and belongs to the technical field of experimental apparatus design methods. The core innovation of the method is that an interlayer wrapping integrated forming process is adopted to replace a traditional bonding method. The method comprises the following steps: firstly, manufacturing a flexible valve assembly comprising valve leaflets, part of sinus canal walls and part of left ventricular outflow tracts by utilizing a special valve dipping mold; then, an aorta spin-coating mold with a reserved valve mounting position is used, preliminary spin-coating is conducted firstly, part of the aorta wall is formed, then the prefabricated valve assembly is mounted at the reserved position of the aorta mold, and then spin-coating continues to be conducted. In the process, a base (part of the sinus canal wall) of the valve assembly is seamlessly wrapped and fused into a silica gel layer of the aorta wall. And finally, dissolving the internal mold to obtain a seamless model in which the valve and the aorta are completely fused into a whole.

The invention relates to an application of delta-Viniferin in preparation of a medicine for preventing or treating metabolic cardiovascular diseases. Delta-Viniferin reduces endothelial dysfunction by inhibiting vascular endothelial cell senescence and inflammation related gene / protein expression level, and defines the antihypertensive effect of delta-Viniferin; delta-Viniferin improves the contraction function of vascular smooth muscle by inhibiting the expression level of gene / protein related to phenotype transformation of vascular smooth muscle cells, meanwhile, the in-vivo level remarkably relieves degradation of elastic fibers of vascular walls and rupture of intima of aortic walls, and the effect of the delta-Viniferin on preventing and treating aortic dissection is defined; delta-Viniferin defines the anti-myocardial fibrosis effect of delta-Viniferin by inhibiting the myocardial fibroblast fibrosis related gene / protein expression level; the delta-Viniferin promotes the browning of white fat by targeting an SIRT1-FOXO1 axis and increases the energy consumption, so that the effect of the delta-Viniferin on resisting obesity is defined. In conclusion, it is proved that the compound delta-Viniferin has the effect of protecting various metabolic cardiovascular diseases and can be used for preparing the medicine for preventing and treating the metabolic cardiovascular diseases.

This invention relates to the field of finite element stress calculation technology, specifically to an aortic stress calculation system based on finite element analysis. In this invention, multiple sets of aortic displacement vectors and element stress vectors are spliced ​​into a response matrix according to the sequence of nodal degrees of freedom and element numbering. The Gram-Schmidt orthogonalization method is introduced to process the retained vectors, compressing the directional coincident components and linearly correlated components, resulting in stronger stability of the reduced-order basis space and smoother conversion of high-dimensional discrete equations to low-dimensional expressions. The Newton-Raphson algorithm is introduced in the path state update stage, where load step difference, nodal displacement increment, and integral point stress tensor are continuously recorded. The path turning state and load propagation form are adjusted synchronously. Facing high internal pressure, large deformation, and nonlinear response scenarios, peak tracking continuity is stronger, the frequency of solving repeated integral models is reduced, the high-risk area of ​​the aortic wall is more concentrated, and the numerical support for scheme comparison, parameter scanning, and risk pre-assessment is more sufficient.

The invention provides an aortic dissection acute and chronic stage classification method and device based on deep learning, a medium and a program product, and relates to the field of intelligent medical treatment. The method comprises the following steps: acquiring two adjacent aorta cross-section interface ultrasonic images of a subject at the same position of at least two different time points; extracting aorta wall features and inner diaphragm features in the ultrasonic image; constructing a coordinate system comprising an x axis and a y axis by taking an intersection point of the aorta wall and the inner diaphragm features as an original point, and indexing areas where the inner diaphragm features in the two ultrasonic images are located by taking the x axis and the y axis as references to obtain two groups of coordinate point sets; the difference value of the inner diaphragm feature points at the same position on the x axis and / or the y axis is calculated; and outputting an auxiliary prediction result that the subject is acute or chronic according to the difference value. According to the method, by introducing the deep learning technology, automatic classification of the acute stage and the chronic stage of the aortic dissection is achieved, rapid and objective diagnosis and evaluation are expected to be achieved, and clinical decision making is assisted.

The present application relates to cardiovascular disease medical equipment technical field, disclose a kind of aortic covered stent, the aortic covered stent includes support stent, closure layer and elastic connecting layer, closure layer is spaced apart and is set to the outer periphery of support stent, closure layer includes first covering, elastic connecting layer is connected between support stent and closure layer, blood flow can flow between support stent and closure layer;With aortic pulsation, closure layer and elastic connecting layer produce elastic deformation, so that first covering is always close to aortic and the blood vessel wall adjacent to closure layer.The aortic covered stent can be better applied to the special form of ascending aortic dissection and the mechanical characteristics of blood flow, higher stability, better closure for ascending aortic wall.

The application discloses a blood pressure calculation method and equipment based on cross-scale fluid-solid coupling and considering nonlinear biomechanical characteristics of an aorta, and the method comprises the following steps: establishing a three-dimensional ideal aorta geometric model; establishing a zero-dimensional heart lumped parameter model to simulate the process that the heart pumps blood to the aorta inlet through periodic contraction and diastole; establishing a zero-dimensional three-element Windkessel model of small arteries to simulate blood flow microcirculation of peripheral small arteries; establishing a blood vessel wall biomechanical model containing residual stress of the aorta wall and active contraction of smooth muscle cells to obtain a pressure-radius relationship of the aorta wall as a fluid wall boundary condition to simulate the change process of the aorta radius in blood circulation; and coupling the three-dimensional ideal geometric model of the aorta, the zero-dimensional heart lumped parameter model and the zero-dimensional three-element Windkessel model to construct a cross-scale fluid-solid coupling system of hemodynamics, and the blood pressure in the aorta is calculated through iterative solution.

The invention discloses an application of valerian triester in preparation of products for preventing and treating aortic dissection, which can reduce the occurrence rate of aortic events, relieve the reduction of survival rate caused by aortic dissection, inhibit aortic dilatation caused by aortic dissection, reduce the number of elastic fiber fractures caused by aortic dissection and improve the survival rate of aortic dissection. The hematoma and the false cavity between aortic walls caused by the aortic dissection are improved, and the structural damage of the aortic walls caused by the aortic dissection is improved. According to the technical scheme provided by the invention, a brand new compound option is provided for the drug treatment of the aortic dissection.

The present invention relates to a local blood flow shield for the aortic wall, belonging to the technical field of medical surgical instruments. The shield consists of two rods that are cross-hinged to each other and are divided into a pair of rod arms and a pair of rod handles that can be opened and closed relative to each other with the hinge point as the boundary. A chuck is provided at the end of one rod arm; a hood is provided at the end of the other rod arm, and a slidable sleeve is sleeved on the rod arm below the hood; the hood is composed of a telescopic skeleton and a diaphragm covering the skeleton; when the sleeve slides up or down along the other rod arm, it respectively sleeves the skeleton to make the hood form a contracted state or an expanded state; during the operation, when the pair of rod arms are closed and the hood is in the expanded state, the hood and the chuck respectively adhere to the inner surface and the outer surface of the local aortic wall and are opposed to each other. The shield can create a local bloodless surgical field through the enclosed three-dimensional space formed by the hood and the inner surface of the local aortic wall, and at the same time eliminate the sequelae caused by conventional clamping of the aortic wall.

The utility model discloses an aortic cannula, and relates to the technical field of aortic cannulas. Comprising a cannula body, a first positioning airbag, a second positioning airbag and a connecting hose. The first positioning air bag and the second positioning air bag are arranged on the outer side of the cannula body and can be tightly pressed on the inner side and the outer side of an aorta adventitia respectively during use, and the problems that high-pressure blood flow enters an aorta cavity, and aorta dissection or false aneurysm is formed are solved; meanwhile, when the intubation tube body needs to be separated from extracorporeal circulation for tube drawing operation, air in the second positioning air bag is completely discharged, then the intubation tube body is pulled out, the first positioning air bag can play a role in blocking sprayed blood flow, and the operator can be effectively protected; the problems that in a traditional aortic cannula, the aortic wall structure is prone to being damaged in the cannula inserting process, and false aneurysm or aortic dissection is formed are solved; the blood pressure in the aorta blood vessel is high, the purse string is easy to avulsion, the aorta wall is damaged, and the intubation tube is easy to fall off.

The invention belongs to the technical field of biological medicine, and particularly discloses application of a bioactive composition in prevention, treatment and improvement of aortic dissection. The invention provides application of a bioactive composition in preparation of a medicine for preventing, treating and improving aortic dissection. The bioactive composition comprises docosahexaenoic acid and resveratrol. The invention discloses application of a bioactive composition in prevention, treatment and improvement of aortic dissection, and the aortic dissection is treated by repairing damaged aortic wall, retarding aortic dilatation, protecting elastic structure of aortic smooth muscle layer and recovering elastic phenotype of smooth muscle cells.

The three-legged aortic valve forceps comprise three supporting arms and an outer ring, the supporting arms are elastic and can be folded inwards, measuring rings are connected to the outer sides of the supporting arms in a sleeving mode, grabbing parts are arranged at the lower ends of the supporting arms, the upper ends of the supporting arms are fixedly connected, the lower sides of the supporting arms are separated and unfolded outwards, and the outer ring is arranged on the outer ring. The valve leaflet clamping device has the advantages that the valve leaflet can be rapidly and safely clamped and fixed, and the inner diameter of a prosthesis for replacing the aorta wall can be measured in an auxiliary mode.

Systems and methods for treatment of an aortic tear or dissection (such as in the thoracic aortic region) are provided. Some methods disclosed herein include inserting an endoprosthesis near an inlet flap of an aortic tear or dissection, inserting an infusion catheter near the inlet flap of the aortic tear or dissection, positioning said infusion catheter between an outer surface of the endoprosthesis and an aortic wall, expanding the endoprosthesis so that the infusion catheter is in contact with aortic tissue near the inlet flap, infusing a stabilization treatment compound through the infusion catheter, wherein the stabilization treatment compound comprises a contrast media agent, a stabilizing agent, and one or more excipients, and removing the infusion catheter.

A balloon occlusive aortic cannula having a hollow cannula and an inflation lumen having a distal end and an expandable element surrounding the hollow cannul and having an exterior surface. The expandable element is disposed on the distal end of the inflation lumen. The expandable element having a micro surface texture formed on the exterior surface. The micro surface texture having a plurality of surface features configured to engage an aortic wall and form a fluidic seal therebetween during a cardiopulmonary bypass procedure.

Cannulas for apical cannulation and methods of making and using the same are provided. The cannula includes a first elongated body defining a primary lumen, a second elongated body defining a first secondary lumen, a third elongated body defining a second secondary lumen, and a fourth elongated body defining a third secondary lumen. The primary lumen is configured to allow blood to flow therethrough. The first secondary lumen is configured to inflate an inflatable body, which is configured to engage an aortal wall proximate the aortic valve of the patient's heart to define a treatment space. The second secondary lumen is configured to selectively remove blood from the treatment space or introduce a cardioplegic solution into the treatment space. The third secondary lumen is configured to administer active decompression of the left ventricle of the patient's heart via suction.

The embodiment of the utility model provides a blood vessel broken end connecting device which comprises a first artificial blood vessel section provided with a near end of the first artificial blood vessel section and a far end of the first artificial blood vessel section, and the part, close to the near end of the first artificial blood vessel section, of the first artificial blood vessel section forms the near end of the first artificial blood vessel section; the inner supporting ring is arranged on the peripheral side of the near end part of the first artificial blood vessel section; the peripheral side of the first artificial blood vessel section is sleeved with the second artificial blood vessel section, the far end of the second artificial blood vessel section is connected with the far end of the first artificial blood vessel section, and the near end of the second artificial blood vessel section and the near end of the first artificial blood vessel section are free ends. Blood leakage between the first artificial blood vessel section and the ascending aorta wall is avoided, the suturing time and suturing difficulty in the aorta root reconstruction process can be well shortened, and the requirement for suturing operation is lowered.

The present invention relates to the field of medical device technology, and discloses a functional aortic arch in situ fenestration special covered stent, the proximal end of the aortic covered stent is provided with 2-3 Z-shaped wave stent rings (proximal Z-shaped wave stent ring group), the distal end is provided with 3-4 Z-shaped wave stent rings (distal Z-shaped wave stent ring group), the middle section of the aortic covered stent is provided with a saddle-shaped metal stent ring, the aortic stent is fully covered with a coating, the coating is provided with a mesh-like reinforcing wire, the outer peripheral side of the coating of the first Z-shaped wave stent ring of the proximal Z-shaped wave stent ring group is wrapped with a sponge-like structure, and the inside of the mesh reinforcing wire is provided with mutually cooperating latitudes and warps. The present invention mainly provides a special covered stent for in situ fenestration for in situ fenestration technology, which improves the success rate of fenestration, reduces the probability of stenosis caused by compression of the branch stent by the angle of the metal ring, reduces the damage of the proximal end of the stent to the aortic wall, and reduces the risk of recurrent dissection at the proximal end.

An auxiliary device for proximal aortic anastomosis in coronary artery bypass grafting (CABG) includes a puncture needle, a puncture cannula, a cutting cannula, and a ring compressor. The puncture cannula is fitted over the puncture needle, with a bulging ball at its tip and an annular groove at its tail end. The ring compressor is fitted over the puncture cannula and can slide axially; its tip has a notched compression ring with an inner diameter smaller than the outer diameter of the bulging ball. During puncture, after the aorta is penetrated, the ring compressor is pressed down, and the compression ring and bulging ball work together to clamp the puncture site, achieving a bloodless procedure. The cutting cannula is then pressed down, and the aortic wall within the compression ring is removed. The graft vessel is then anastomosed to the aorta, with the suture passing through the compression ring. After suturing, the ring compressor is rotated, and the suture exits through the notch. The entire device is then withdrawn, and the suture is tightened and knotted to complete the anastomosis. This invention avoids aortic clamping, eliminates the risk of plaque dislodgement, requires only a single port for anastomosis, and is simple to operate with reliable hemostasis.