57 results about "Extracorporeal" patented technology

A medical fluid management assembly includes a pneumatic manifold, at least one valve, and a fluid manifold. The pneumatic manifold includes at least one pneumatic passageway that is pneumatically connected to the at least one valve. The fluid manifold includes at least one chamber comprising upper and lower fluid chambers separated by a flexible membrane. The fluid manifold also includes fluid tube sections and fluid pathways that fluidly couple the one or more upper and lower fluid chambers to the at least one valve and at least one of a purified water line, a liquid concentrate line, a to-extracorporeal circuit fresh dialysis fluid line, a drain line, or a from-extracorporeal circuit used dialysis fluid line.

The utility model discloses an emergency treatment in-vitro cooling device, which belongs to the technical field of in-vitro cooling, and comprises a bottom plate, a groove is formed in the top of the bottom plate, bearings are fixedly connected to the opposite inner walls of the groove, rotating shafts are rotatably connected to the interiors of the two bearings, the opposite ends of the two rotating shafts are fixedly connected with the same screw rod, and the same screw rod is fixedly connected with the screw rod. The surface of the lead screw is in threaded connection with a threaded block, the top of the threaded block is fixedly connected with a connecting plate, the top of the connecting plate is fixedly connected with two sets of air cylinders, and the two sets of air cylinders are internally provided with blowing fans. And through operation of the blowing fan, the body of the patient can be cooled, and through operation of an electric push rod, the height of a frame plate can be adjusted.

A hemodiafiltration system with a disposable pumping unit is disclosed. An example system includes a medical fluid pump actuator, a medical fluid heater, a blood filter and a disposable unit. The example disposable unit includes a medical fluid cassette portion including a medical fluid cassette housing configured to be operatively connected to the medical fluid pump actuator to pump medical fluid through the medical fluid cassette portion when the medical fluid cassette portion is in fluid communication with a medical fluid source. The example medical fluid cassette portion is also configured to be placed in fluid communication with the blood filter and with an extracorporeal circuit communicating with the blood filter, the fluid communication enabling hemodiafiltration to be performed. The example disposable unit also includes a heater bag configured to be placed in operable communication with the medical fluid heater and in fluid communication with the medical fluid cassette portion.

A multi-layered bio purifier includes a plurality of layers. Each layer may include a membrane having a first side and a second side opposite the first side, a first channel formed on the first side, and a second channel formed on the second side. Further, each layer may include a first type of cells formed on the first side in the first channel and a second type of cells formed on the second side in the second channel. The multi-layered bio purifier includes a first manifold assembly to split incoming blood into the first channel and the second channel of the plurality of layers and a second manifold assembly to combine processed blood from the first channel and the second channel of the plurality of layers. The processed blood may include detoxified or purified blood.

A system for performing any of extracorporeal or intracorporeal wound closure, includes a suture cartridge 100 configured to be detachably coupled to a distal end of a handle of the system extracorporeal wound closure, or to a shaft assembly that is coupled to distal end of the handle for intracorporeal wound closure. On being coupled to any of the shaft assembly or the handle, a driving pulley 112A of the cartridge 100 gets operatively coupled to a driving mechanism in the handle to drive a belt 110 of the suture cartridge 100 to drive a suturing needle 106 for suturing tissues for the extracorporeal or intracorporeal wound closure. The cartridge 100 can be coupled with any of a robotic system, a hand held system and a minimal invasive surgical system.

The invention belongs to the technical field of pipeline fixing devices, and particularly relates to a cardiac surgery extracorporeal circulation pipeline fixing system which comprises a fixing base and a pipeline clamping module located at the top of the fixing base, and the pipeline clamping module comprises a fixing plate. The device is tightly adsorbed to the surface of an operating table through a fixed suction cup, a second supporting seat is automatically leveled through a hydraulic buffer, the second supporting seat is always in a horizontal stable state, and a first clamping block and a second clamping block are controlled to be buckled through a pipeline clamping module by extruding arc-shaped clamping plates on the two sides; a first clamping block and a second clamping block are fixed through rotation of a limiting block, a pipeline is preliminarily fixed, pressure adjusting plates on the two sides are controlled by a pressure adjusting knob to move in the opposite direction, and the clamping force can be finely adjusted according to the factors such as the material and thickness of the pipeline; the problem that the blood flow stability is influenced by the body position change of a patient or the traction of a surgical instrument and other factors of the pipeline fixing device in the surgical process is solved.

An EBDLR system includes a multi-layered bio purifier having a plurality of layers. Each layer includes a membrane, a first type of cells on a first side of the membrane in a first channel, and a second type of cells on a second side of the membrane in a second channel. The EBDLR includes a plasma separator to receive blood from a subject and separate a plasma component from the blood, a first reservoir to collect the plasma component, and a second pump to move the plasma component from the first reservoir to the multi-layered bio purifier. The multi-layered bio purifier distributes the plasma component into the first and second channels of each layer to purify the plasma component. The EBDLR includes a second reservoir to collect the purified plasma component and a third pump to infuse the purified plasma component from the second reservoir into the subject.

The portable self-adaptive extracorporeal shock wave orthopedic treatment device comprises a bandage, a treatment head and a fixing band, the bandage is composed of a bandage body and a base, and the section of the bandage body is in a U shape; the edge of the base is connected with the edge of the bandage body, and the base and the bandage body define a closed cavity. A plurality of mounting holes are formed in the substrate at intervals; the treatment head is mounted at the mounting hole in the base, and the action end of the treatment head extends towards one side far away from the cavity; the treatment heads at different positions can generate extracorporeal shock waves with different intensities and frequencies according to the bone mineral density loss condition to act on a human body part; the fixing bands are installed at the two ends of the bandage, and during use, the bandage surrounds the part, needing to be treated, of the body and is fixed through the fixing bands. The device self-adaptively recognizes the condition of a to-be-treated part of a patient, and accurately sends out shock waves to prevent and treat bone loss; the device is portable and small, can be used under microgravity, can be operated by a patient, and improves the treatment convenience.

The invention relates to a medical treatment machine with connection points for disposable tubing that can be connected to a patient's extracorporeal circuit. To improve hygiene, these connection points are optimally dried before the disposable tubing is connected.

The application provides a sinus intubation extracorporeal water absorption structure, and relates to the technical field of sinus intubation extracorporeal water absorption, which comprises a drainage tube, a sticking accessory, a negative pressure bag, a first one-way valve, a liquid storage bag and a second one-way valve. One end of the drainage tube is used for insertion into a sinus and for absorbing sinus exudate. The sticking accessory is connected with the drainage tube and is used for sticking to the skin of a patient, so as to detachably stick the drainage tube to the skin and block the sinus opening. The inlet end of the first one-way valve is connected with the end of the drainage tube away from the sinus, the outlet end of the first one-way valve is in communication with the inlet of the negative pressure bag, and the negative pressure bag is configured to automatically elastically recover and generate negative pressure on the drainage tube when it is released after being manually squeezed. The inlet end of the second one-way valve is in communication with the outlet of the negative pressure bag, and the outlet of the second one-way valve is detachably communicated with the liquid storage bag. The sinus intubation extracorporeal water absorption structure has the advantages of simple structure, low cost, self-management of the patient and no limitation on the activity of the patient.

The utility model relates to an anti-bruise drainage tube and a drainage tube assembly, and belongs to the technical field of drainage tubes. Comprising a drainage tube body, and the drainage tube body comprises an in-vivo tube section and an in-vitro tube section which are independent; a flow guide channel is arranged in the pressure-proof base; a first connecting end and a second connecting end which are communicated with the flow guide channel are arranged on the pressure-resistant base; the pressure-resistant base is provided with a bottom face used for being attached to the skin. Wherein one end of the in-body pipe section is fixedly connected with the first connecting end in a sealing manner; one end of the in-vitro pipe section is hermetically and rotatably connected with the second connecting end, so that the in-vitro pipe section can circumferentially rotate relative to the pressure-resistant base; and the bottom surface is provided with a bonding part fixed with the skin. The in-vitro pipe section can adjust the leading-out angle along with the actions of turning over, sitting up and the like of the patient, so that the lateral turning torque generated on the pressure-resistant base due to rigid traction of the pipeline is greatly reduced, and the bottom surface is always stably attached to the skin.

The invention belongs to the technical field of emergency nursing, and particularly relates to an emergency in-vitro cooling device which comprises a frame, a mounting plate is arranged at the bottom of the frame, and a water tank is mounted in the center of the top surface of the mounting plate; through cooperative use of a cooling plate and a heat exchange pipe, heat on a patient can be conducted to a heat conducting plate through the cooling plate and conducted to the heat exchange pipe through the heat conducting plate, then a first water pump is started, and the first water pump conveys water in a water tank into the heat exchange pipe through a first water outlet and conveys the water back into the water tank through a first water inlet; water liquid can circularly flow in the heat exchange pipe, when the water flow flows in the heat exchange pipe, heat on the heat exchange pipe and the heat conducting plate can be rapidly taken away, and the cooling plate can continuously conduct heat of the whole body of a patient, so that the whole body of the patient is effectively cooled, and the in-vitro cooling effect on the patient during emergency nursing is improved.

1. The name of the design product: brain-computer interface external machine. 2. The use of the design product: for electroencephalogram signal processing and information transmission. 3. The design points of the design product: in shape. 4. The picture or photo that best indicates the design points: perspective view 1.

Disclosed herein is an ultrasound barrier chamber for a fluid system, e.g., which facilitates the de-air of a fluid line using an ultrasound signal. In some examples, the fluid line may include, for example, an extracorporeal blood circuit for use in a dialysis process. In one example, a device for monitoring an extracorporeal circuit having a blood pump disposed therein to deliver blood may include one or more ultrasound transducers positioned in a predetermined vicinity of a vent of an instillation chamber of the extracorporeal circuit, one or more ultrasound transducers positioned in a predetermined vicinity of the vent of the instillation chamber of the extracorporeal circuit, and one or more ultrasound transducers positioned in a predetermined vicinity of the vent of the instillation chamber of the extracorporeal circuit. And a controller coupled to the one or more ultrasound transducers, the controller configured to enable the one or more ultrasound transducers to transmit an ultrasound signal that displaces particles in the contents of the instillation chamber away from the vent. Other embodiments are described.

The invention relates to the technical field of medical instruments, in particular to an oxygenator mounting support capable of being quickly fixed and an ECMO (extracorporeal membrane pulmonary oxygenation) rack car, which comprise a base, a central controller, a variable temperature water tank, an oxygenator, a centrifugal pump, a blood storage device and a power box, two connecting plates are fixedly connected to the inner sides of the four supporting rods, a central controller is placed on the upper surface of one connecting plate, a variable-temperature water tank is placed on the upper surface of the other connecting plate, a power box is placed on the upper surface of the base, and three movable assemblies are arranged on the outer surfaces of the three supporting rods correspondingly. Through the arrangement of the movable assembly and through the first connecting rod and the second connecting rod which can stretch and contract, the left-right position can be adjusted according to the actual situation, and operation is convenient and fast; and the locking assembly is used for limiting, so that the adjusting angles of the first connecting rod and the second connecting rod can be quickly and stably locked, and the displacement phenomenon of the first connecting rod and the second connecting rod is avoided.

The utility model relates to the technical field of medical instruments, in particular to an in-vitro fixing device for a cannula protector. The in-vitro fixing device for the cannula protector comprises a limiting plate, a binding piece and a clamping and fixing assembly, the limiting plate is used for being attached to the outside of the lips of a patient, the binding piece is connected between the two ends of the limiting plate and used for being bound to the head of the patient, a notch for a cannula to penetrate through is formed in the limiting plate, and the clamping and fixing assembly is connected with the limiting plate. The clamping and fixing assembly is arranged on the outer side of the notch of the limiting plate and used for clamping the insertion pipe penetrating through the notch. The cannula fixing device has the advantages that the structural design is simple and reasonable, the cannula can be effectively fixed after cannula insertion, and displacement of the cannula in the length direction of the cannula is avoided.

The invention discloses a conduit pump clamping device and an in-vitro simulation circulating system, the conduit pump clamping device comprises an inlet flange and an outlet flange, and fluid flows from the inlet flange to the outlet flange. A penetrating pipe is arranged in the outlet flange, one end of the penetrating pipe communicates with the first cavity, and the other end of the penetrating pipe penetrates through the side wall of the outlet flange and extends out of the outlet flange. The far end of the catheter pump can penetrate into the catheter pump clamping device through the penetrating pipe until the fluid inlet in the catheter pump is located in the first cavity, and the fluid outlet in the catheter pump is located in the penetrating pipe. At the moment, the fluid entering the outlet flange can flow out in two ways: the fluid is pumped out through the conduit pump or flows out from a fluid outlet on the outlet flange. In this way, the pumping flow of the conduit pump in the auxiliary process can be obtained by measuring the fluid flow of the penetrating pipe; and the fluid can be converged after flowing out, and the total flow of the artery can be obtained by measuring the converged flow, so that a tester can evaluate the real performance of the catheter pump.

The invention relates to the technical field of medical instruments, in particular to a special cardiac surgery head frame with a multi-body-position fixing structure, which comprises a mounting frame, a rotating rod is rotatably connected to the inner wall of the mounting frame, two round tubes are rotatably connected to the outer wall of the rotating rod, and a first fixing block and a second fixing block are fixedly connected to the outer walls of the round tubes respectively. Electromagnets are fixedly connected to the positions, corresponding to the first fixing block and the second fixing block, of the inner wall of the mounting frame, and through magnetic attraction control and arc-shaped limiting block design, switching of three modes of synchronous rotation of the head and the body, independent rotation of the head and independent rotation of the body is achieved; when the head is placed, a conical linkage structure is triggered by means of gravity, a supplementary air bag is extruded to supply air to a fixed air bag, placing, namely clamping and air bag attaching to the head are achieved, the risk of pressure sores is reduced, a fourth spring can drive the air bag to automatically return air and reset, manual operation is not needed, and operation is convenient. And the operation interference during the operation is reduced.

The invention discloses a simulation cycle test system for extracorporeal membrane oxygenation ECMO, and relates to the technical field of medical instrument extracorporeal test. The system comprises a training data acquisition module for acquiring blood flow characteristic parameters of users with different body characteristic parameters and generating a training sample data set. The prediction model training module establishes a neural network model and trains the blood flow feature extraction model. The physiological feature analysis module predicts blood flow feature parameters by simulating body feature parameters of a user and sets blood exchange flow velocity and pressure according to predicted values. The exchange parameter adjusting module is used for dynamically adjusting the set flow velocity and pressure and acquiring blood quality parameters under the operation condition. The blood quality adjusting module is used for correcting the gas flow of the membrane oxygenator according to the obtained blood quality parameters, the ECMO simulation cycle test is completed, refined gas flow management is achieved, and the oxygenation efficiency is improved.

A cannula (100) for an extracorporeal life support system may include a tubular element (110) and an actuation structure (140). The actuation structure (140) may be configured to be sensitive to an external stimulus such that an internal diameter of the tubular element (110) changes when the external stimulus changes. A system may include the cannula (100) and a control device (30) in electrical communication with the actuation structure (140). The control device may be configured by a user to set a desired value for an internal diameter of the tubular element (110). Figure for the abstract: Fig. 1

An advanced system and methods for treatment of cancer and other diseases including complications from late-stage viral infections by inducing hyperthermia in a patient relying on withdrawing blood from the patient and returning the withdrawn blood to the patient to establish a continuous extracorporeal flow circuit. Blood is heated by passing through the extracorporeal circuit at a controlled rate until a target body core temperature in is achieved. An innovative concept inherent in the instant invention is the incorporation of an ECMO machine to provide oxygenation. Usually, the blood will be subjected to a continuously re-circulating dialysis to balance electrolytes. Additionally, the blood will be subjected to a continuously recirculating regeneration through a carbon sorbent column where toxins and contaminants are removed. The blood temperature is maintained at the target blood temperature for a treatment period, and the blood is cooled after the treatment period has been completed.

The invention relates to the field of cooling devices, in particular to an emergency treatment in-vitro cooling device which comprises a bed plate, a limiting plate assembly, a trunk area cushion, a head area cushion, a cooling pipe, a cooling water tank, a water tank inlet and outlet pipe set, a head cooling assembly and a trunk cooling assembly. A limiting plate assembly used for limiting the fever patient from moving disorderly after lying down is installed on the rear side of the upper end of the bed plate. A fever patient is limited to move disorderly after lying down through the limiting assembly, the back, the head and the neck of the lying patient can be subjected to water cooling, heat of the body surface is effectively taken away, the body temperature is rapidly reduced, meanwhile, the chest area, the hand area and the leg area of the patient are all coated with alcohol through the alcohol smearing roller moving front and back, and therefore the patient feels comfortable. The cooling device is long in duration time, capable of reducing side effects or anaphylactic reactions possibly caused by drugs, high in automation degree and quite suitable for emergency treatment.

Extracorporeal blood flow circuit devices can be used during medical procedures such as on-pump open-heart surgery. For example, extracorporeal heat exchange and oxygenation devices can be used to facilitate surgical procedures such as coronary artery bypass grafting. In some embodiments, such an oxygenation device can include an integrated air removal structure. In particular embodiments, the air removal structure can comprise one or more porous hollow fibers.

The invention discloses an intervention pump in-vitro simulation cycle testing device which comprises a supporting system, a blood pump system, a bionic cardiovascular simulation system, a sensing and measuring system and a control system. The support system is used for bearing and fixing each component and integrating an electric signal input interface and a serial communication interface; the blood pump system comprises a servo motor and a base, and the servo motor rotates to drive the base and the bionic left ventricle model to rotate; the bionic cardiovascular simulation system comprises a bionic left ventricle model, a valve device and a simulated cardiovascular loop, and the sensing and measuring system is used for monitoring hemodynamic parameters of the loop in real time; and the control system is used for receiving the hemodynamic parameters and controlling the servo motor to output motion meeting physiological characteristics. The device is simplified in structure, high in integration level, modular in design, capable of supporting quick disassembly and assembly, improved in maintenance efficiency, capable of reducing operation difficulty and personal errors and capable of reducing blood injury risks at the same time. The system is high in control stability and high in physiological simulation precision.

Cardiopulmonary by-pass (CBP) during cardiac surgery leads to deleterious systemic inflammatory response. In a prospective cohort of 46 patients older than 18 years and eligible for non-urgent cardiac surgery with CPB, measurement of sTREM-1 in the plasma was performed immediately after the onset of anesthesia (H0) and 2 and 24 hours after CBP. After CBP, sTREM-1 significantly increased at H2 and at H24 (p<0.001). Based on both baseline sTREM-1 levels and variations. 3 patterns of patients were identified. Profile 1 group with high baseline sTREM-1 levels as well as high increase, developed more severe organ failure after CBP with higher norepinephrine dose at H24, higher SOFA score and more frequently AKI at both H24 and H48. Finally, acute atrial fibrillation at H24 was more frequent in profile 1 when compared to profile 2 / 3, Profile 1 group had longer ICU and hospital length of stay (LOS). In conclusion, early sTREM-1 variations after cardiac surgery identified a group of patients at high risk for post-operative AKI and prolonged length of stay. Thus sTREM-1 represents a relevant biomarker and biotarget in cardiac surgery with CBP.

The utility model discloses a trocar and an implantation system, and belongs to the technical field of medical instruments. The trocar comprises a trocar body and a channel penetrating in the length direction of the trocar body, the trocar body comprises a first trocar part and a second trocar part which are arranged in the length direction of the trocar body, the first trocar part is used for being located outside a body, the second trocar part can be implanted in the body, and the first trocar part is pre-formed with an open groove or can form an open groove; the slot extends from one end, away from the second tube part, of the first tube part to the other end, the side face of the tube body is communicated with the outside through the slot, and the channel and the slot are both used for allowing electrode wires to penetrate through. The trocar and the implantation system provided by the utility model can be compatible with a single electrode lead and a plurality of branched electrode leads, so that the use requirements are met.

The present invention is directed generally to a method and apparatus for human brain neuroprotection during surgery. The invention includes use of a heart-lung machine to generate periodic rectangular pulsation of blood flow. The invention uses a non-invasive CA monitor to continuously record transient functions such as dynamic autoregulation functions of a human brain cerebrovascular autoregulation system and process the data to generate an alarm to indicate CA impairment and take steps to minimize the CA impairment event.

To provide medical systems that use artificial intelligence to facilitate autonomous or semi-autonomous medical procedures.SOLUTION: There is provided a system for applying open heart surgery technique 200 to a patient 10, and the system includes a heart / lung machine 100, one or more monitoring devices 218, a database 206, and a computing system 200. In the technique, the computing system analyzes parameters from the one or more monitoring devices, and first medical data and second medical data, and determines, through comparison of analysis with third medical data, the prediction that operation data from the heat / lung machine or the parameters from the one or more monitoring devices tend to deviates from target ranges.SELECTED DRAWING: Figure 2A

The utility model discloses an inferior vena cava drainage tube for cardiac surgery extracorporeal circulation operation, which belongs to the technical field of medical instruments and comprises a drainage tube body, a plurality of external connection blocks are fixedly connected to the rear end of the outer wall of the drainage tube body at equal intervals, and guide grooves are formed in the inner walls of the external connection blocks. The left end and the right end of the inner wall of the guide groove are slidably connected with limiting blocks, the left end and the right end of the outer wall of each limiting block are fixedly connected with magnetic plates, and a flow guide mechanism is arranged in the middle of the inner wall of the drainage tube body and comprises a one-way valve installed in the middle of the inner wall of the drainage tube body. The inner wall of each external connection block is designed to be one sixth of that of a pipe body, the limiting blocks are rotated after the drainage pipe is clamped into a connector of the extracorporeal circulation machine, the limiting blocks in the two different external connection blocks can be attracted through the magnetic plates on the outer walls of the limiting blocks, and therefore a closed loop is formed, and the connection stability of the external connection blocks is guaranteed.

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.