63 results about "Great vessels" patented technology

A valve prosthesis is sized and configured to rest within a blood path subject to antegrade and retrograde blood flow. A trestle element on the prosthesis extends across the blood path. A leaflet assembly is suspended from the trestle element and extends into the blood path in alignment with blood flow. At least one mobile leaflet member on the leaflet assembly is sized and configured to assume orientations that change according to blood flow direction. The mobile leaflet member has a first orientation that permits antegrade blood flow and a second orientation that resists retrograde blood flow. The valve prosthesis, when implanted in a heart chamber or great vessel, serves to supplement and/or repair and/or replace native one-way heart valve function.

Artificial disc replacement (ADR) systems with intradiscal components feature non anterior-posterior (A-P) or oblique-oriented keels such that the great vessels do not require as much retraction during insertion. The system may further include guides for aligning the ADR prior to insertion, and for cutting an oblique slot into a vertebral endplate to receive the keel. A screw adapted to penetrate a vertebral body may be used in conjunction with the keel. The screw and keel may converge, diverge or intersect. The screw may further include a mechanism providing a locking relationship with the keel. The system may further including a guide to direct drill bits and screws through holes in the keel. ADRs according to the invention may additionally, independently include a non-symmetrical endplate shaped so as to decrease the risk of injuring the great vessels. By virtue of the invention, a second ADR may be installed at a second level having a keel oriented differently from that of the ADR having an orientation other than anterior-to-posterior.

A system and method for the intra corporal, telemetric measuring of blood pressure, particularly within the heart or a great vessel, includes a substantially rigid sensor chip mounted in a holder and an antenna. The holder is anchored within an appropriate location in the cardiovascular system, such as in the cardiac septum, via a catheter or other minimally-invasive procedure to position at least one capacitive pressure sensor on the chip in the blood flow to be sensed. Measured values are transmitted telemetrically from the chip to an extra corporal monitoring device.

The invention relates to clinical cardiology and cardiovascular surgery. The method for forming a blood flow in research stands and in surgically reconstructed segments of the blood circulation system comprises diagnosing the individual condition of a patient's blood circulation system; measuring the blood flow velocity field in the heart chambers and great vessels; comparing the parameters measured against the physiological norm; determining parameters forming a swirled blood flow; and modeling an individual swirled blood current in the blood circulation system being diagnosed, the streamlined surfaces and guide elements of flow channels of the blood circulation system reconstructed being given shapes conforming to the flow lines of the restored normally swirled blood flow in accordance with formulas:

wherein: V_r, V_z, and V_φ are the radial, longitudinal, and tangential velocities of the swirled current; v is the kinematic viscosity of the medium; φ₀ is the initial swirling angle in relation to the flow axis normal; φ, z and r are current values of the angular, longitudinal, and radial coordinates along the flow line; and Q(t), Z₀(t), k(t), Γ₀(t), and C₀(t) are parameters of the swirled blood flow variable over time because of the non-stationary current and corresponding to the individual normal indicators for a physiologically swirled blood flow. The normal indicators are established by routine examination of a representative sample of patients having no changes in the cardiovascular system. A vessel prosthesis comprises a tube having an internal surface in contact with the blood flow provided with a pattern to swirl the blood flow in accordance with formulas (1.1 to 1.3) conforming to a specific localization of the segment being reconstructed. A cannula for para-corporeal perfusion devices comprises a flow channel having an internal surface that is provided with a longitudinal pattern to swirl the blood flow, the shape of the pattern being determined from formulas (1.1 to 1.3), relative to the specific localization of the point where the cannula is inserted into the vessel channel. A heart valve prosthesis comprises one or more shutoff elements arranged symmetrically in the center of a body of round and/or oval cross-section, the streamlined surfaces of the valve being provided with a pattern in accordance with formulas (1.1 to 1.3). A blood pump comprises a flow swirling unit, a flow channel, and valves at the inlet and outlet of the channel, the surface washed over by blood being provided with a relief variable over time in accordance with formulas (1.1 to 1.3). A swirling device comprises an end piece having a streamlined surface provided with guides in the form of ribs, grooves, or blades of a shape defined by formulas (1.1 to 1.3), the swirling angle of the guides relative to the flow axis being varied optionally an operator or by a special-purpose device for modeling different current conditions.

The invention provides devices and methods for performing less-invasive surgical procedures within an organ or vessel. In an exemplary embodiment, the invention provides a method of closed-chest surgical intervention within an internal cavity of a patient's heart or great vessel. According to the method, the patient's heart is arrested and cardiopulmonary bypass is established. A scope extending through a percutaneous intercostal penetration in the patient's chest is used to view an internal portion of the patient's chest. An internal penetration is formed in a wall of the heart or great vessel using cutting means introduced through a percutaneous penetration in an intercostal space in the patient's chest. An interventional tool is then introduced, usually through a cannula positioned in a percutaneous intercostal penetration. The interventional tool is inserted through the internal penetration in the heart or great vessel to perform a surgical procedure within the internal cavity under visualization by means of the scope. In a preferred embodiment, a cutting tool is introduced into the patient's left atrium from a right portion of the patient's chest to remove the patient's mitral valve. A replacement valve is then introduced through an intercostal space in the right portion of the chest and through the internal penetration in the heart, and the replacement valve is attached in the mitral valve position.

Improved methods and apparatus render ADR insertion safer and more precise. Certain surgical instruments according to the invention include a level enabling a user to align the instrument for proper placement of a surgical implant. A different surgical instrument includes two or more scopes mounted relative to the instrument permitting a user to simultaneously view more than one side of the instrument. A device for use with a surgical instrument having a long shaft includes a holder that surrounds at least a portion of the shaft allowing a user to control the instrument with both hands. A further surgical instrument comprises a set of retractors and one or more guards placed over the retractors for protecting the great vessels, nerves or other delicate structures during a surgical procedure. Surgical apparatus according to the invention comprises a platform mountable to an operating room table over a patient undergoing a surgical procedure, enabling a user to place their hands or attach an instrument while operating. Different surgical instruments include an indicator showing angular displacement or a wedge-shaped portion used for disc distraction. Also disclosed are blades designed for use with a power tool featuring a cutting edge configured such that rapid oscillation of the cutting tool reduces the pressure a user must apply the tool.

Natural and/or synthetic materials to form a strong barrier between the skeletal system and the great vessels. In the preferred embodiments, a natural or synthetic material is used to prevent scar tissue from forming around the vessels and/or to act as barrier placed between the vessels and the skeletal system, including the spine. Devices according to the invention may also be used over the dura and nerves following laminectomy procedures, between the sternum and the pericardium or heart following cardiac procedures, in intra-abdominal procedures such as intestinal or vascular surgery, over the brain in intra-cranial surgery, over the ovaries or other organs or tissues in the female genitourinary system, over the prostate or other organ or tissues in the male genitourinary system, or in other surgeries on humans or animals.

The invention relates to a liver tumor radiofrequency ablation technology, and aims at providing a method for precisely simulating radiofrequency ablation technology by utilizing ellipsoid to cover tumor. The method for precisely simulating radiofrequency ablation technology by utilizing ellipsoid to cover tumor comprises the following steps: preprocessing tumor images; clustering the tumor images into a plurality of ellipsoidal subclasses under reasonable constraint conditions; calculating the minimal coverage ellipsoids of each obtained class; giving an initial radiofrequency scheme by utilizing the number of the minimal ellipsoids automatically determined; determining an adjustable conical area, and manually adjusting the initial radiofrequency direction so as to completely keep away from great vessels and ribs, thus completing the establishment of the final radiofrequency scheme. According to the method, the purpose of designing the radiofrequency treatment scheme before operation can be realized, three-dimensional navigation can be conducted during operation, the adopted optimized algorithm can help a doctor more precisely and efficiently do operation, the harm of the operation to normal tissues can be reduced as far as possible, and the peripheral organs can be avoided, so that the radiofrequency ablation operation is safer and more effective.

The invention relates to medical healthcare equipment, in particular to a wearable multi-field radiation whole-body hyperthermia device. Heat is introduced into a radiating target (i.e., a great vessel) by means of probe beams, and the energy of ultrasound, infrared, laser, microwave, radio frequency and electromagnetic probes at each frequency range is introduced into a vascular circulation system through the radiation probe network composed of probe beams distributed on an attachment in the form of optimum biological heat absorption, and then heat is transferred throughout the body through a hemoperfusion method, so that the vivo tissue is rapidly heated through conduction of biological heat in the tissue. The device has the characteristics of high thermal utilization ratio, high blood flow rate and high specific heat, and thermal convection is rapidly conducted between the radiant heat and the tissue to realize whole-body hyperthermia, therefore, the device not only can realize the purposes of uniformity of the machine body and rapid temperature rise, but also avoid the phenomenon of local overheating, simultaneously, has the accessibility of a wearable device and is a high-efficiency hyperthermia equipment without ache.

Adhesions and scar formation following a surgical procedure are controlled by providing a human recombinant phage antibody, and introducing the antibody onto or into an area of the body following the procedure to inhibit adhesions, or scar formation. According to one embodiment, the antibody is used to prevent the formation of scar tissue following spinal surgery. This may be carried out by placing the antibody over the dura lining the spinal nerves and spinal cord. Alternatively, the antibody may be used to inhibit adhesions following abdominal surgery, or placed around the great vessels following an anterior approach to the spine or other regions. Importantly, the antibody may be used to inhibit adhesion formation adjacent to areas where growth factors are used to stimulate healing. The invention may further include the step of protecting the growth factors and/or the area of the body where stimulated healing is desired from the antibodies to the growth factors. As a further option, other medications or therapeutic substances may be added to the antibody(ies) to enhance healing or effectiveness.

The invention discloses a starch stypticum and a preparation method thereof, belonging to the field of medical preparations. The preparation method comprises the following steps: refining waxy maize starch to 4,000 to 10,000 meshes; centrifugally filtering after crosslinking, acidolysis and enzymolysis are completed; cleaning with distilled water; blasting and drying at constant temperature until the weight is constant; crushing, and screening through a 200-mesh screen; radiating by Co60 to disinfect to prepare the starch stypticum. The water absorption rate of the starch stypticum prepared by adopting the method is 2 to 3 times that of the conventional styptic materials, the starch stypticum can quickly stop bleeding in actual application, has quick styptic function in great vessel hemorrhage, even massive bleeding wound surface, and can be widely applied to surgeries of cardiothoracic and vascular surgery department, hepatobiliary surgery department, orthopedics department, general surgery department, obstetrics and gynecology department, urology surgery department and ear-nose-throat department and the like.

The invention relates to a positioning method for magnetic resonance. The method comprises the following steps: a, displaying a schematic diagram with a human body model and a scanning coil on visible human-machine interactive equipment which is arranged in a magnetic resonance equipment scanning room; b, starting a positioning beam after a patient lies on a bed in a magnetic resonance cavity, and positioning the positioning beam according to the position of the scanning coil; c, selecting the part to be scanned of the patient on the human-machine interactive equipment; d, moving the bed until the selected scanning part displayed on the human-machine interactive equipment is positioned under the positioning beam. The positioning method can be used for effectively positioning coils for performing combined scanning on the belly or great vessels and the like, so that coordinate information of unfixed important coil units can be acquired, and an operator can carry out positioning operation without repeatedly entering the scanning room. Therefore, the scanning efficiency is greatly improved, and the cost on scanning time of coil positioning in a pre-scanning mode can be eliminated.

A debranching Great vessel stent graft and methods for its use, where the stent graft comprises, a main body stent graft with a first bifurcation defining a first leg and a second leg, the main body stent graft has distal and proximal ends, the main body stent graft has a diameter at the proximal end in the range from about 18 mm to about 28 mm, the first leg and the second leg each have a diameter in the range from about 12 mm to about 18 mm, the distance from the proximal end of the main body to the distal end of the first leg is in the range from about 30 mm to about 50 mm, and the distance from the proximal end of the main body to the distal end of the second leg is in a range from about 50 mm to about 70 mm.

The invention relates to a process and a device for sterile blood sampling of live pigs. The process comprises: fixing a live pig in a sterilized hermetic blood sampling system; puncturing the heart the live pig and the great vessel connected with the heart through a puncture needle to perform sterile blood sampling; and connecting the puncture needle with a blood collection container through a duct to collect blood, wherein the blood sampling speed is 0.5 to 5 L/1 to 10 minutes, and the blood sampling amount is 0.5 to 5 L/100 kg/pig. Compared with the prior art, the process has the advantages of simplicity, easy implementation, effective prevention of microbial contamination to pig blood, low cost and the like.

An electromagnetic controllability occlusion system for celiac great vessels comprises an internal magnetic vessel occlusion device, an external electromagnet element and central control equipment, wherein the internal magnetic vessel occlusion device corresponds to an external electromagnet element which is connected with the central control equipment; the internal magnetic vessel occlusion device is placed on the surface of an infrahepatic vena cava and used for pressing and occluding vessels; the external electromagnet element is integrated into an operating bed mattress and used for locating the internal magnetic vessel occlusion device and gradually increasing the current of the external electromagnet element; and occlusion of postcava or aorta abdominalis is realized through attraction between the external electromagnet element and the internal magnetic vessel occlusion device. The electromagnetic controllability occlusion system can be operated simply, conveniently, quickly and safely, avoids defects of longer operation time, vessel injury and the like, which are caused by vessel separation in an open appendectomy or laparoscopic surgery , and simultaneously solves the problem of instable systemic hemodynamics probably caused by a traditional vessel occlusion method.

The invention relates to a covered stent used in a chest great vessel cavity. Compared with the prior art, the defects that a covered stent is incapable of overcoming straightening force and is poor in practicability are overcome. The covered stent comprises artificial blood vessels (1) and support frames (2), wherein each artificial blood vessel (1) comprises a plurality of straight pipes and a plurality of pleated pipes; the straight pipes are connected at intervals through the pleated pipes; the support frames (2) are wrapped on each straight pipe respectively; the straight pipes are arranged at the two ends of each artificial blood vessel (1) respectively. The covered stent has certain longitudinal stretching deformation capacity, can fit the physiological bending of an aorta, and eliminates the straightening force after a traditional stent is bent, so that the blood vessel wall of the aorta is uniformly stressed.