3190results about "Pressure infusion" patented technology

In some embodiments, a system can include a fluid delivery assembly and a motor drive assembly. The fluid delivery assembly is configured to be releasably mechanically and, optionally, electrically coupled to the motor drive assembly. When the fluid delivery assembly is releasably coupled to the motor drive assembly, the motor drive assembly can control delivery of fluid from the fluid delivery assembly (e.g., to a patient). For example, the motor drive assembly can be releasably coupled to the fluid delivery assembly to control delivery of fluid from the fluid delivery assembly to provide continuous (e.g., non-pulsatile) fluid flow from the fluid delivery assembly.

A modular disease management system may provide medication management for a patient. The system may include a base configured to at least partially couple to a tissue site of a patient. The system may further include a medication bladder coupled to the base and configured to maintain medication. The system may further include a medication pump coupled to the medication bladder, comprising a conduit and muscle wire-actuated plungers, wherein the medication pump is configured to cause the medication to flow from the medication bladder through the conduit. The system may further include a cannula insertion device coupled to the medication pump via the conduit, wherein the cannula insertion device comprises a cannula, a spring, and a triggering component, wherein the cannula insertion device is configured to insert the cannula into the tissue site of the patient by actuation of the spring released by the triggering component.

A system for delivering a fluid to a target site of a patient's vasculature having a catheter having a proximal end, a distal end, and a lumen defined by an interior surface of the catheter extending longitudinally through the catheter between the proximal end and the distal end, a guiding element having a distal end, a proximal end, and an exterior surface, the guiding element positioned in the lumen creating an area, between the exterior surface of the guiding element and the interior surface of the catheter, having an effective cross-sectional area sized fluid communication while the guiding element is in the lumen. Also, a method of performing a neurovascular procedure includes providing a multi-catheter assembly including an access catheter, a guide catheter, and a procedure catheter, coupling the assembly to a robotic drive system, and injecting contrast media into the assembly without removing a guiding element.

This disclosure generally relates to medical devices that include a sensor transmitter assembly that includes a sensor assembly including a sensor module where a first sensor including a first sensor head having at least one first sensor contact pad is combined with a second sensor including a second sensor head having at least one second sensor contact pad. The sensor transmitter assembly also includes a transmitter assembly positioned on a top of the sensor assembly to form a single unit, the transmitter assembly having at least one transmitter contact disposed on a base of the transmitter assembly, where the first sensor contact pad(s) and the second sensor form a connection path with the transmitter contact(s).

A fluidics system includes a cassette having a saline subsystem, a contrast subsystem, and a vacuum subsystem. The fluidics system further includes a splitter and a first tubing set coupled to the cassette and splitter, the first tubing set having a single saline channel, a single contrast channel, and a single vacuum channel. The fluidics system further includes two or more hub assemblies, at least one of the two or more hub assemblies configured to have a third saline flow-path, a third contrast flow-path, and a third vacuum flow-path to provide saline, contrast and vacuum to the lumen of a catheter coupled to the at least one of the two or more hub assemblies. The fluidics system further includes a second tubing set having a plurality of tube groups, each tube group coupled to the splitter and to one of the two or more hub assemblies.

The invention discloses a spiral medicine storage mechanism and a patch type injection pump, and the medicine storage mechanism comprises a medicine storage part which is provided with a spiral liquid medicine cavity; the driving part is provided with a driving rod and a piston, the piston is arranged in the liquid medicine cavity, and the piston is driven by the driving rod to move along the spiral wall surface of the liquid medicine cavity. The liquid medicine cavity is arranged to be spiral, the space arrangement limitation of a horizontal circumferential plane is broken through, the liquid medicine cavity is expanded in the vertical direction, the space in the vertical direction is reasonably and effectively utilized, the path for expanding the liquid storage amount is increased, and even if the patch pump is arranged to be small and compact, the requirement for the large liquid storage amount can be met; the size of a smaller and more optimized patch pump is achieved, the wearing comfort of a patient is improved, and meanwhile the requirements for various liquid storage amounts are met.

The invention discloses an infusion monitoring system, which relates to the technical field of infusion monitoring, and comprises a controller with a display screen, an infusion pump arranged at the top of a main body case and used for regulating and controlling the infusion speed, an infusion tube fixing frame arranged on one side of the main body case, and an alarm device arranged on the surface of the main body case, a physiological parameter acquisition module, a medicine characteristic analysis module, a dynamic dripping speed regulation and control module, a liquid abnormity detection module, an AR interaction control module and an alarm cooperative processing module are arranged in the controller; a physiological parameter acquisition module, a medicine characteristic identification module, a dynamic dripping speed regulation module, a liquid abnormity detection module, an AR interaction control module and an alarm cooperative processing module are integrated. The intelligent and closed-loop infusion monitoring system is constructed, self-adaptive dripping speed adjustment based on the physiological state of the patient and the medicine characteristics is achieved, and the safety of infusion treatment is improved.

In an infusion pump system that includes a pump that may have a user interface for pump programming, one or more smartphones or other remote control devices that interface with the infusion pump, and / or an automated insulin delivery algorithm, there is a potential conflict between commands such as boluses being programmed on multiple devices and / or calculated by the AID algorithm at the same time. In order to avoid low glucose levels that could result from delivering multiple boluses from these various sources when only one bolus is needed, systems and methods disclosed herein provide a bolus permissions and prioritization scheme that prioritizes boluses programmed with the infusion pump and one or more remote control devices and calculated by a closed loop delivery algorithm.

The invention relates to the technical field of injection pump calibration, in particular to an injection pump automatic calibration method and system based on flow velocity stability, and the method comprises the following steps: S1, collecting flow velocity data in the operation process of an injection pump, and recognizing a boundary section of stable-to-unstable conversion based on a dynamic window; constructing a boundary drift indication map reflecting response delay, amplitude fluctuation and a rate inflection point; s2, identifying a consistency offset error mode from the atlas in combination with a multi-cycle drift behavior, marking a start window, a transfer window and a peak window, and generating a historical drift memory sequence; and S3, constructing a cross-cycle inheritance type calibration parameter template based on the memory sequence, and adaptively adjusting key parameters in input control logic to realize pre-calibration response before the injection pump is unstable. According to the method, by constructing the boundary drift map, the inheritance type calibration template and the dynamic parameter fusion mechanism, accurate pre-adjustment calibration and self-adaptive compensation optimization of the injection pump before the injection pump is in the unstable state are achieved.

An intracorporeal robot (1) for deployment in a body tract, comprising: - a permanent magnet constituting an effector magnet (2) configured to be guided by an extracorporeal actuating magnet (105), and - a medical device (3) coupled to the effector magnet, the medical device comprising a shape memory structure (4) configured for tetherless actuation by an extracorporeal shape memory actuator (105).

The embodiments described herein may relate to methods and systems for adjusting insulin delivery. Some methods and systems may be configured to adjust insulin delivery to personalize automated insulin delivery for a person with diabetes. Some methods and systems may be configured to adjust insulin delivery to a person with diabetes according to one or more conditions of an insulin delivery device. Some methods and systems may be configured to enable a lock-out mode where adjustment to insulin delivery to personalize automated insulin delivery is restricted.

The invention belongs to the technical field of anesthesia depth regulation and control, and particularly relates to an anesthesia depth self-adaptive regulation and control method and system based on a dynamic time sequence model, and the system comprises a portable computer which is used for operating a program, receiving electroencephalogram time sequence data output by a signal collection device, receiving a pressing event of a handle, and obtaining efficacy information of an effect part; a channel gating result is generated based on the information and used for conducting category division on a drug administration adjustment request, gating is conducted through a shared code LSTM and a two-channel LSTM head and an effect room concentration vector and a hysteresis band, the problem of rhythm dislocation caused by exponential smoothing lag and induction-waking asymmetry is solved, mistaken up-regulation or mistaken down-regulation and overshoot are reduced, and the accuracy of drug administration adjustment is improved. And the adjustment convergence time is shortened, so that the anesthesia depth is more stably maintained in a target interval.

The invention discloses a postoperative block analgesia curative effect evaluation system based on multi-modal data analysis, particularly relates to the technical field of medical information processing, and is used for solving the problem of poor analgesia evaluation standardization. An evaluation path of analgesia deviation quantification, state time sequence judgment and strategy generation is realized by constructing a structured comparison mechanism of an analgesia observation frame and an individualized analgesia baseline trajectory, pain, medication and activity deviations are dynamically calculated by fusing an anesthesia record, an analgesia pump log and clinical monitoring data, and an analgesia result is obtained. Typical states such as insufficient retardation effect are identified in combination with a time sequence inference model, a curative effect level and an early warning mark are automatically output, additional retardation, parameter adjustment and medicine remedy suggestions are generated according to a credibility level, and a state, disposal and result chain is constructed by continuously learning historical case data, so that the treatment efficiency is improved. The adaptive optimization of the baseline trajectory, the state threshold and the adjustment strategy is realized, and the individual matching performance, the response timeliness and the risk control capability of the analgesia strategy are improved.

The present invention relates to an infusion pump assembly. A wearable infusion pump assembly includes a reusable housing assembly including a mechanical control assembly including a pump assembly, at least one shape memory actuator configured to actuate the pump assembly, and at least one valve assembly. The wearable infusion pump assembly also includes a disposable housing assembly including a reservoir for receiving an infusible fluid. A releasable engagement assembly is configured to releasably engage the reusable housing assembly with the disposable housing assembly. A switch assembly is configured to enable a pairing function of the infusion pump assembly.

The invention discloses an intelligent control method for an analgesia pump based on deep learning. The intelligent control method comprises the following steps: S1, acquiring multi-modal original signals of a postoperative patient and synchronously normalizing the multi-modal original signals; s2, removing artifacts and noise in the synchronous data, and performing interpolation compensation on missing data; s3, carrying out modal reliability weight distribution on the sensing sequence based on a Hemma optimization algorithm; s4, inputting the node set into a PainNet relation statistical network to generate a dynamic graph topological structure; s5, predicting the pain score of the patient in the future, and generating a low-dose high-frequency micro-pulse administration instruction; s6, according to the circadian rhythm of the patient, dynamically adjusting the edge weight and the administration interval of the PainNet network; and S7, when the pain score fluctuation exceeds the limit, triggering an emergency mode, quickly converging to the most conservative parameter combination, and outputting a safety locking instruction. According to the invention, the control accuracy and safety of postoperative analgesia are improved.

The invention discloses an insulin pump safety reminding system based on remote communication, and the system comprises an insulin pump terminal which is used for collecting equipment operation parameters, and receiving and executing a verified operation instruction; the patient monitoring terminal is bridged with a data transfer interface, a local data encryption cache interface, a graded early warning display interface and a remote man-machine interaction interface of the insulin pump terminal and the hospital comprehensive management platform; the graded authorization user terminal receives early warning information related to the insulin pump terminal, checks the state of a patient and initiates a remote operation request; the hospital comprehensive management platform is in communication connection with each terminal, manages each terminal, performs data aggregation and intelligent analysis, generates early warning information based on a multi-dimensional rule, and performs authority management and auditing and multi-source data fusion application; and the safety communication and control module is used for guaranteeing data transmission safety, operation instruction compliance and system emergency fault-tolerant operation. According to the invention, cross-time-space safety protection and active early warning can be realized, the treatment safety and management efficiency are improved, and the method is suitable for medical and pension institutions at all levels.

The invention provides an intelligent insulin closed-loop infusion system for type 1 diabetes mellitus, and relates to the technical field of diabetes mellitus treatment equipment. The system comprises a blood glucose monitoring module, a control module, an insulin infusion module, a user interaction module, a wireless communication module and a power module, and closed-loop precise infusion of insulin is achieved through cooperation of the multiple modules. Wherein a closed-loop algorithm based on a dynamic basic rate formula is arranged in the control module, and the insulin infusion amount can be dynamically adjusted in combination with an LSTM blood glucose prediction model and a metabolic parameter least square method updating unit; the insulin infusion module adopts a micro peristaltic pump controlled by PWM (Pulse Width Modulation) and a current monitoring type blockage detection unit, so that the infusion precision and safety are guaranteed. According to the system, the blood glucose standard reaching time proportion can be increased to 78%, the hypoglycemia occurrence frequency is reduced to 0.8 times per week, the system is remarkably superior to a traditional insulin pump and a simple closed-loop system, meanwhile, the system has the advantages of being long in sensor service life and low in power consumption, and the treatment convenience and safety of type 1 diabetes patients are improved.

The invention relates to the related technical field of medical instruments, in particular to a contrast injection device for enhancing nuclear magnetic resonance, which comprises a base, a mounting shell arranged at the upper part of the base, a first barrel arranged at the left upper part in the mounting shell, a second barrel arranged at the right upper part in the mounting shell, and a mixing barrel arranged in the middle of the upper part of the mounting shell, a first piston rod is arranged in the first barrel, a second piston rod is arranged in the second barrel, communicating pipes are respectively communicated between the first barrel and the mixing barrel and between the second barrel and the mixing barrel, a one-way water inlet pipe is arranged at the top of the barrel, and the one-way water inlet pipe is communicated with an external liquid storage tank. By rotating the adjusting screw rod, the adjusting screw rod drives the first wedge-shaped block to move to the position of the needed dosage, then the rodless air cylinder controls the extrusion plate to move upwards, and after the extrusion plate moves upwards and makes contact with the plate body, the piston rods move upwards to inject the contrast agent and normal saline of the corresponding dosage into the mixing barrel to be mixed.

The invention relates to the technical field of medical auxiliary equipment, in particular to an automatic blood transfusion device for the blood transfusion department, which comprises a base, a blood bag and a blood transfusion tube, the blood bag is communicated with the blood transfusion tube, a mounting frame is mounted on the base, and a placing module for placing the blood bag and an adjusting module for adjusting the flow of the blood transfusion tube are mounted on the mounting frame. A monitoring module used for monitoring the blood remaining amount and the flow velocity in the blood bag in real time is installed on the placing module, the monitoring module is further used for monitoring pressure data generated by extrusion of the adjusting module in real time, the monitoring module is in signal connection with a controller, and the controller is in signal connection with the placing module and the adjusting module. The controller is used for adjusting the adjusting module according to the real-time allowance data and the flow velocity data monitored by the monitoring module. The system is used for accurately monitoring and intelligently adjusting the blood remaining amount and the flow velocity in the blood transfusion process and automatically judging and processing abnormal conditions such as blood transfusion tube blockage, and the safety and effectiveness of blood transfusion are improved.

Medical devices and related systems and methods are provided. A method of controlling medication delivery based on sensor input involves obtaining a measurement parameter representing an electrical response of a first instance of a sensing element to a physiological condition of a person. The measurement parameter is converted into a calibrated measurement parameter using calibration data specific to the first instance of the sensing element. The method further involves determining a measurement value using the calibrated measurement parameter as input to a performance model. The performance model is derived from historical calibrated measurement parameters and corresponding reference values. The historical calibrated measurement parameters are from other instances of the sensing element. A command is then determined based on the measurement value and sent to a medical device. The command causes the medical device to deliver a dose of medication influencing the physiological condition of the person.

In some embodiments, a system for operating a fluid injection system may include at least one processor to receive patient data related to a patient undergoing a fluid injection procedure, in one embodiment, at least one parameter of an injection protocol for a fluid injection procedure is automatically generated based on patient data and independently of an input associated with a dose of a medical fluid for the fluid injection procedure received through a user interface associated with a fluid injection system performing the fluid injection procedure, when the at least one parameter is automatically generated, the at least one processor is configured to determine a dose of the medical fluid for the fluid injection procedure and provide the at least one parameter of the injection protocol to the fluid injection system. Methods and computer program products are also disclosed.

Methods of insulin delivery may include selecting a basal insulin delivery rate responsive to a projected blood glucose level that approximates a target blood glucose level. Methods of insulin delivery may further include generating insulin delivery instructions for an insulin delivery device, the insulin delivery instructions corresponding to the basal insulin delivery rate and for a variable time duration relative to an intended time duration.

Provided is a vented needle hub assembly for infusion of a liquid into subcutaneous tissue. More specifically, the vented needle hub assembly is provided by a needle hub having an inlet side and an outlet side and a fluid passageway therebetween; an infusion needle in fluid contact with the fluid passageway and extending from the outlet side; a flexible tubing joined to the inlet side in fluid contact with the fluid passageway; at least one vent disposed in a sidewall of the needle hub, the vent in fluid contact with the fluid passageway; and a porous plug disposed within each at least one vent adjacent to the fluid passageway, the porous plug structured and arranged to distinguish gas from liquid, gas permitted to pass from the fluid passageway through the porous plug and out the at least one vent. An associated method of use is provided as well.

A technical solution for monitoring operation of a medical delivery device such as a wearable patch pump for occlusion is provided that employs sensing pump motor current during at least one of a dispense stroke and an aspirate in a pump cycle. The solution can be implemented alone or in combination with other occlusion sensing methods that use one or more of pump measurement data such as pump stroke duration (e.g., duration of aspirate stroke or dispense stroke in a rotational metering-type pump or a reciprocating-type pump), end-stop or limit switch activation, and duration difference between aspirate and dispense strokes to detect occlusion. Accuracy of occlusion detection based on measured data in a fluid delivery device is improved by using dead band normalization of loaded measured data to unloaded measured data.

The invention discloses a patient transfer intelligent monitoring platform based on the Internet of Things and the intelligent wearing technology, and relates to the technical field of transfer intelligent monitoring, and the platform comprises an intelligent wearing equipment module which is used for carrying out the time sequence collection of physical sign data in a transfer process, and obtaining a physical sign monitoring data sequence; the medical equipment interconnection module is used for carrying out simultaneous multi-terminal data acquisition; the data transmission network module is used for determining an infusion pump infusion speed analysis result, a physical sign abnormal mode analysis result, a monitoring terminal abnormal mode analysis result and an oxygen consumption reserve analysis result; and the alarm and display module is used for graded alarm and shared display of the electronic handover bill. The technical problems that in the prior art, continuous dynamic monitoring cannot be achieved in the transferring process of the invasive mechanical ventilation patient, the early warning capability is lacked, and handover communication is not smooth are solved, and the technical effects that physical sign data and medical equipment parameters in the transferring process of the patient are collected in real time, and transferring monitoring continuity and handover efficiency are improved are achieved.

The disclosed device, system and method manages medication delivery failures. An effective therapeutic range of a patient physiological property is determined based on a pharmacokinetic profile of a medication. During an administration of the medication to the patient, an expected trend in the measured physiological property is determined based on sensor data, the pharmacokinetic profile of the medication, a dose of the medication provided to the patient, and the at least one physical property of the patient, and an infusion device is caused to adjust the dose of the medication to cause the physiological property to follow the expected trend. Responsive to determining that a current trend in the physiological property has deviated from the expected trend, and will fall outside the effective therapeutic range within a predetermined time period, a delivery failure is determined and an alarm is provided.

The invention discloses a high-pressure injection system and method. The high-pressure injection system comprises an equipment body, an injection propelling device, a needle cylinder pipeline suite, a medicine bottle replacing device, a bubble induction sensor, a gravity sensor, a pressure sensor and a control system, wherein the injection propelling device, the needle cylinder pipeline suite, the medicine bottle replacing device, the bubble induction sensor, the gravity sensor and the pressure sensor are installed on the equipment body; wherein the medicine bottle replacing device is used for containing and automatically replacing medicine bottles; the needle cylinder pipeline suite is communicated with the needle cylinder pipeline suite through a puncture outfit, and can selectively suck liquid medicine and continuously inject multiple patients; the injection propulsion device drives a needle cylinder piston to realize precise injection; the bubble induction sensor, the gravity sensor and the pressure sensor are respectively used for monitoring pipeline bubbles, medicine bottle weight and needle cylinder pressure in real time; the control system coordinates all the components, and full-automatic execution of medicine bottle replacement, medicine liquid extraction, pipeline exhaust and injection control operation is achieved. Full automation of the injection preparation process is achieved, the radiography examination efficiency is remarkably improved, the labor intensity of medical workers is reduced, and the safety and accuracy of the injection process are ensured.

The invention discloses an infusion pump with a bubble detection function, and belongs to the field of infusion devices.The infusion pump comprises a shell, connecting mechanisms are arranged on the two sides of the shell, the shell is installed on an external infusion rod through the connecting mechanisms, the interior of the shell is hollow, an arc-shaped seat is fixedly installed on one side of the shell, and the infusion pump further comprises a penetrating opening and a notch; the upper end and the lower end of the arc-shaped base are each provided with an ultrasonic bubble sensor embedded into the arc-shaped base, a microcomputer system controller is installed on the shell and used for controlling the ultrasonic bubble sensors to work, and a peristaltic pump mechanism is arranged in the notch. The ultrasonic bubble sensors are embedded into the upper end and the lower end of the arc-shaped base, a surrounding type detection area for the infusion hose is formed, planar scanning is conducted on a medium in the hose, and misjudgment caused by the uneven surface of the hose or liquid medicine residues is reduced. The contact surface of the sensor and the hose is expanded from a point to an arc-shaped area, so that the influence of local wrinkles or particles on signals is reduced.

Disclosed herein, in part, are liquid pharmaceutical formulations comprising furosemide or a pharmaceutically acceptable salt thereof, one or more pharmaceutically acceptable excipients, and a pharmaceutically acceptable buffer. Methods of treating congestion, edema, fluid overload, or hypertension in a patient in need thereof are also provided.

Infusion devices and related medical devices, patient data management systems, and methods are provided for monitoring a physiological condition of a patient. An exemplary method of monitoring a physiological condition of a patient involves obtaining current measurement data for the physiological condition of the patient provided by a sensing arrangement, obtaining a user input indicative of one or more future events associated with the patient, and in response to the user input, determining a prediction of the physiological condition of the patient in the future based at least in part on the current measurement data and the one or more future events using one or more prediction models associated with the patient, and displaying a graphical representation of the prediction on a display device.