36 results about "Fluid replacement" patented technology

The invention relates to the technical field of medical resource allocation, in particular to a medical resource allocation system for war wound rescue, which comprises the following steps of: acquiring monitoring curve segments of different time periods corresponding to physiological indexes of each dimension of all target patients in a war wound rescue process; analyzing the data abnormal degree of each time period to screen out each abnormal monitoring curve segment corresponding to each dimension physiological index of each target patient; determining an abnormal change degree of each abnormal monitoring curve segment corresponding to each dimension physiological index, and further determining a kidney injury risk index of each target patient during each monitoring, so as to determine a fluid infusion effective index of each target patient during the current monitoring; and in combination with the fluid infusion effective index and the renal injury risk index of each target patient, determining a priority index of each target patient during medical resource allocation during current monitoring. According to the invention, the medical resource allocation priority conditions of different target patients in the war wound rescue process can be accurately obtained.

The invention discloses a spinal post-operation erect hypotension volume management method and system and a terminal. The method comprises the steps that individual physiological features, preoperative evaluation data, intraoperative monitoring data and post-operation monitoring data of a target patient are obtained; constructing an artificial intelligence model, and training, verifying and testing the artificial intelligence model to obtain a target evaluation model; inputting the preoperative evaluation data, the intraoperative monitoring data and the postoperative monitoring data into a target evaluation model for evaluation to obtain a risk probability; according to the individual physiological features, the preoperative evaluation data, the intraoperative monitoring data and the risk probability, making a personalized fluid infusion management scheme for the target patient; according to the fluid infusion management scheme, fluid infusion is conducted on the target patient, the patient condition is monitored in real time, and early warning information is sent out to take first-aid measures. Multi-source data are fused, the occurrence risk of the erect hypotension of the patient is evaluated and managed in real time, fluid infusion management is enhanced, and fluid infusion efficiency is improved.

The invention provides a method, a system and a device for determining an active fluid infusion deceleration compensation torque, and relates to the technical field of vehicle control. When a vehicle is in non-braking sliding and has an active fluid infusion deceleration compensation demand, a target sliding torque is determined based on a vehicle running state; calculating an initial active liquid supplementing deceleration compensation torque by combining a target allowable energy recovery torque determined by the motor allowable recovery power; and the initial compensation torque is dynamically corrected by further combining the road adhesion rate and the tire slip rate, so that the target active fluid infusion deceleration compensation torque at the current moment is determined. The deceleration consistent with the normal recovery working condition is still kept when the vehicle is in the non-braking sliding working condition and the recovery capacity is limited, the problems that the deceleration is unstable and the driving experience is poor under the pure sliding working condition at present are solved, and the smooth, comfortable and safe sliding energy recovery control effect is achieved.

The application provides a method for determining the longitudinal wave velocity after fluid replacement in an anisotropic medium and related equipment. The method comprises the following steps: determining an average bulk modulus based on a matrix bulk modulus; determining a first bulk modulus when the medium contains fluid based on first property data; determining a second bulk modulus when the medium does not contain fluid based on the first property data, the matrix bulk modulus, the average bulk modulus and the first bulk modulus; determining a second vertical stiffness coefficient when the medium does not contain fluid based on the first property data, the average bulk modulus, the first bulk modulus and the second bulk modulus; obtaining second property data of each predetermined replacement fluid; and determining the longitudinal wave velocity after the fluid in the medium is replaced by the predetermined replacement fluid based on the first property data, the average bulk modulus, the second bulk modulus, the second vertical stiffness coefficient and the second property data. The technical problem that the longitudinal wave velocity determined after fluid replacement in an anisotropic medium is not accurate in the prior art is solved.

The application relates to a corneal drug delivery scleral lens, which comprises a lens body, the lens body comprises a treatment area, a reverse area and a landing area from the center to the outside, the treatment area is located in the center, the reverse area is arranged around the treatment area and is used for connecting the treatment area and the landing area, the landing area is arranged around the reverse area and is used for supporting a scleral surface, so that a liquid accumulation layer is formed between a corneal front surface and the lens body; a flow guide pipe is arranged in the lens body in the radial direction, forming a liquid injection end and a drug delivery hole. The scleral lens of the application can supplement liquid medicine through the flow guide pipe without taking off the lens, dynamic fluid replacement is realized, and the cornea is prevented from being damaged by repeated taking off and wearing. When the lens is designed, the height of the reverse area is taken as a core variable parameterization design, the thickness of the liquid accumulation area and the drug concentration are accurately controlled. The overflow hole is normally sealed, and the risk of infection is reduced. The liquid medicine is diffused from the edge to the center, the whole surface of the cornea is uniformly soaked, and the bioavailability is improved.

The purpose of the present invention is to suppress the replacement frequency of a cleaning solution in an automatic analysis device using a plurality of cleaning solutions, and a method for controlling the same. An automatic analysis device according to the present invention comprises: a dispensing probe that sucks and discharges at least one of a reagent and a sample; the liquid conveying mechanism is used for conveying first cleaning liquid and second cleaning liquid which are used for cleaning the dispensing probe respectively; different types of cleaning liquid areas in which the first cleaning liquid and the second cleaning liquid can exist; and a storage unit (referring to Figure 5) that stores the type of cleaning fluid present in the different type of cleaning fluid region.

This invention discloses a suspended automatic intravenous infusion hanger, comprising a telescopic rod, a hook, a fixed shaft, a bag-hanging assembly, and a bag-changing assembly. The hook is installed at the top of the telescopic rod, the fixed shaft is installed at the bottom of the telescopic rod, the bag-hanging assembly is located outside the fixed shaft, and the bag-hanging assembly is used to suspend and hold the infusion bag. The bag-changing assembly is located at the bottom of the fixed shaft, and the bag-changing assembly is linked with the bag-hanging assembly. The bag-changing assembly is used to drive the infusion plug puncture device to puncture and connect with the infusion bag on the bag-hanging assembly. This invention utilizes the coordinated use of the telescopic rod, hook, bag-hanging assembly, fixed shaft, and bag-changing assembly. Under the action of the telescopic rod, the height of the bag-hanging assembly and the bag-changing assembly can be adjusted, thereby facilitating the installation or removal of infusion bags by medical personnel. Furthermore, with the coordinated use of the bag-hanging assembly and the bag-changing assembly, the function of automatic bag changing infusion can be achieved after the infusion fluid inside the bag has been completely infused.

The application discloses a fluid supplement method and a fluid supplement device. The method comprises the following steps: receiving a fluid replacement instruction, wherein the fluid replacement instruction indicates that the target cooling circuit is to be filled with fluid; in response to the fluid replacement instruction, performing a leakage detection operation on the target cooling circuit to obtain a detection result; in the case that the detection result indicates that the target cooling circuit does not have a leakage fault, performing a fluid filling operation on the target cooling circuit; in the process of performing the fluid filling operation, the progress of the fluid filling operation is determined according to a flow curve, and the flow curve is used to quantitatively represent the change trend of the injection amount of the fluid over time; and in the case that the progress of the fluid filling operation reaches a preset progress, performing a gas discharge operation on the target cooling circuit. The application solves the technical problems that the related art relies on manual operation to fill the cooling fluid for the vehicle, which is time-consuming and cannot detect the leakage of the cooling system.

A vial cap is configured to releasably contain a portion of a material, for example a powdered medication, for dispensing into a container. Via operation of a depressable plunger, the material is released into the container for rehydrating and mixing with a liquid, and thereafter may be extracted, such as via a needle. In this manner, a rehydrated medication may be provided in a predetermined amount and at a desired time.

In the present invention, a control unit (90) of an extracorporeal circulation device (1) capable of ensuring an ideal blood flow rate for a patient when performing VA-ECMO comprises: a calculation unit (91) that calculates an ideal flow rate and pump head pressure from patient-specific information; and a transmission unit (92) that transmits, to a fluid replacement device (70) for performing fluid replacement, water amount data obtained through measurement by a measurement device (80) for measuring the water amount of the patient. The control unit (90) gives a fluid replacement instruction to the fluid replacement device (70) via the transmission unit (92) on the basis of the pressure of the inside of a blood circuit (20) measured by pressure measurement units (45, 46), the flow rate of the inside of the blood circuit (20) measured by a flow rate measurement unit (47), and the water amount data obtained through measurement by the measurement device (80).

This present disclosure relates to fluid therapy based on adjusted urine output rate and / or sodium output rate, and associated systems, devices, and methods. Exemplary methods can include receiving a sodium excretion input for the patient; receiving a urine output rate; determining an adjusted urine output rate based on the sodium excretion input and the urine output rate; and providing fluid therapy based on the adjusted urine output rate. By determining the amount and / or rate of the infused diuretic and / or hydration fluid based on a patient's actual sodium excretion levels, embodiments of the present technology can optimize and / or customize all or a subset of a diuretic therapy to an individual patient's physiology.

The invention relates to the technical field of medical instruments, in particular to a tissue preservation device for pathology analysis of the digestive system department. A cabinet body is arranged on a moving trolley, a cylindrical groove is formed in the middle of a disc-shaped base with the bottom end connected to a top plate of the cabinet body in a sleeving mode, and a plurality of cylindrical cavities are formed in the outer edge of the disc-shaped base; a central hole and a through hole are formed in the disc-shaped shell sleeved at the top end of the disc-shaped seat; the sample cabin is sleeved in the cylindrical cavity; the liquid supplementing tank and the sterile gas tank are arranged in the cabinet body; a gas path input end and a liquid path input end of the gas-liquid distribution part are respectively connected to output ends of the sterile gas tank and the liquid supplementing tank, the liquid nitrogen assembly comprises a tank seat fixed on the bottom surface of the cylindrical groove, a liquid nitrogen tank and a one-way valve arranged at the bottom of the liquid nitrogen tank, and the tank seat is communicated with an inner cavity of the sample cabin; a sealing plate is arranged in a through hole in the outer edge of the disc-shaped shell rotationally sleeved in the disc-shaped shell; the driving part is used for driving the turntable to rotate; a gas-liquid input piece is arranged at the bottom of the sample container, and stationary liquid adopts a new formula. Pathological analysis tissue samples collected by the digestive system department can be safely and effectively stored.

A circulating device comprises a first tee joint (1), a first three-way valve (2), a second tee joint (3), a second three-way valve (4), a buffer bottle (5), a liquid supplementing pump (6), a third three-way valve (7) and a controller (8), the first tee joint (1) is connected with the first three-way valve (2), the third three-way valve (7) and a solvent bottle (13), and the first three-way valve (2) is connected with the first tee joint (1), a liquid phase pump (9) and the second tee joint (3). The second three-way valve (3) is connected with the first three-way valve (2), the surge flask (5) and the second three-way valve (4), the second three-way valve (4) is connected with the detector (12), the second three-way valve (3) and the collecting end (17), the surge flask (5) is connected with the second three-way valve (3) and the liquid supplementing pump (6), a solvent overflow port (16) is formed in the upper portion of the surge flask (5), and the liquid supplementing pump (6) is located between the surge flask (5) and the third three-way valve (7). The third three-way valve (7) is connected with the first three-way valve (1), the liquid supplementing pump (6) and the waste liquid port (15). The circulating device has the advantages that diffusion is avoided, pressure fluctuation is absorbed, normal internal circulation of the liquid phase pump is ensured, internal collection can be achieved in a circulating mode, and cleaning is easy.

The utility model relates to an automatic liquid adding device with a simple structure, which comprises a first container, a second container and a first cover body, the first cover body is respectively connected and fixed with the first container and the second container, a gap between the first container and the second container is filled with the first cover body, and the joint of the first container and the second container is sealed; a first liquid outlet is formed in the bottom of the first container, a second liquid outlet is formed in the bottom of the second container, and a ventilation pipeline is arranged in the first container and extends downwards from an inner cavity of the first container to an inner cavity of the second container. The liquid supplementing device only comprises two containers and a sealing upper cover, the containers are sealed, a ventilation pipeline communicated with the first container and the second container is arranged in the first container, the air pressure difference in the two containers can be caused by the change of the liquid level height of the containers, and the automatic liquid supplementing process can be achieved according to the air pressure balance principle; and the device is simple in structure and free of redundant parts, so that the device is easy to disassemble and clean.

To provide management of fluid levels in a patient and associated devices, systems and methods.SOLUTION: Devices, systems, and methods for delivering fluid therapy to a patient are disclosed herein. An exemplary method can comprise the steps of: obtaining a urine output rate from a patient; causing a diuretic to be provided to the patient at a dosage rate, where the dosage rate is increased over a period of time such that the urine output rate increases to be above a predetermined threshold within the period of time; and causing a hydration fluid to be provided to the patient at a hydration rate. The hydration rate can be set based on the urine output rate to drive net fluid loss from the patient.SELECTED DRAWING: Figure 1

The invention discloses a medical fluid replacement multi-cavity catheter, and relates to the technical field of replacement catheters, and the medical fluid replacement multi-cavity catheter has the advantages that the liquid medicine foaming time is shortened, the liquid medicine foaming efficiency is improved, and one person can operate with one hand. A connecting pipe is integrally formed at the near end of the catheter body, a partition plate assembly dividing the connecting pipe into a plurality of chambers with different purposes is integrally formed in the connecting pipe, the partition plate assembly extends into an inner cavity of the catheter body and divides the inner cavity of the catheter body into a plurality of chambers, and a plurality of extension pipes are fixed to the connecting pipe. Each extension pipe is communicated with one cavity of the inner cavity of the connecting pipe, a preparation cylinder is fixed to the end, away from the connecting pipe, of one extension pipe, a liquid medicine injection pipe communicated with the preparation cylinder is arranged on the preparation cylinder, and a foaming assembly for primarily foaming liquid medicine is arranged at the joint of the liquid medicine injection pipe and the preparation cylinder.

The present application relates to a kind of liquid supplement monitoring system and method, system includes urine control module and doctor end with hospital management cloud communication connection, urine control module includes urine volume detection component, urinary tube opening and closing component and bladder pressure detection component;Urine control module is based on the bladder pressure detection component collected bladder pressure intelligent switch urinary tube opening and closing component;The urine volume detection component of urine control module detects the urine volume in urine bag in real time;Hospital management cloud can generate first threshold and second threshold in combination with the real-time urine volume of patient, and send the judgment benchmark related with first threshold and second threshold to urine control module;When the bladder pressure detected by bladder pressure detection component is in the range with first threshold and second threshold as critical point, urine control module controls the program of patient urination with patient through personal control terminal manually opening and closing the urinary tube opening and closing component of urine control module as the first priority.

A system suitable for remotely monitoring and maintaining improved hydration of a user, in particular a user suffering from a mineral metabolism disorder. The system comprises a server, a user device in communication with the server, a processing unit operating on the user device, wherein the processing unit is configured to acquire the user's urine parameters, and a care provider device in communication with the server. The system further comprises a prescription unit configured to generate a prescription comprising a recommendation relating to hydration fluid intake by the user, the prescription being based on the user's urine parameters.

The utility model relates to the technical field of medical instruments, and discloses a dynamic L-carnitine supplementing device which comprises a shell, a containing groove is formed in the front end of the lower surface of the shell, a plurality of first limiting clamping plates are fixedly connected to the front end of the inner top face of the containing groove, and liquid storage tanks are arranged on the lower surfaces of the first limiting clamping plates. And one side of the outer wall of the liquid storage tank is fixedly connected with a liquid supplementing opening, and the outer wall of the front end of the liquid storage tank is fixedly connected with a connecting block. According to the utility model, the liquid medicine pump is arranged in the liquid storage tank of the supplementing device, so that the liquid medicine pump can be replaced when the liquid storage tank is replaced, the operation steps are simplified, the replacement efficiency is improved, the possibility that the same liquid medicine pump is in contact with different liquid medicines is reduced, the risk of cross contamination is reduced, and the safety of medical equipment is improved; and the liquid medicine pump and the liquid storage tank are combined together to form a whole, so that maintenance and replacement are facilitated, and the possibility that the device breaks down is reduced.

The present invention relates to the field of fluid transport technology, and in particular to a fluid system, which includes a fluid container for storing fluid; a control valve group, including a primary valve group and multiple secondary valve groups, each of which is connected to the primary valve group and the fluid container; a flow pool, wherein the flow pool is connected to the outlet of the primary valve group via a common pipeline; a first power module, wherein the first power module is connected to the outlet of the flow pool, and the outlet of the first power module is connected to a waste liquid container and / or the fluid container; and a second power module, wherein the second power module is connected to the bypass port of the primary valve group via a bypass pipeline, and the outlet of the second power module is connected to the waste liquid container and / or the fluid container. The present invention can reduce waste caused by fluid replacement while improving flexibility.

The application provides a kind of pancreatitis patient fluid intake and output quantity comprehensive monitoring method, comprising the following steps: obtaining the fluid intake and output quantity data and blood gas analysis data of pancreatitis patient and other data;Set liquid demand quantity prediction model, according to the preprocessed multidimensional monitoring data set and liquid demand quantity prediction model, liquid demand quantity prediction is carried out;Set the time series risk early warning model based on LSTM, according to the preprocessed multidimensional monitoring data set and liquid demand quantity prediction model, risk prediction is carried out;According to the prediction result of risk prediction, generate liquid management early warning information and fluid replacement scheme adjustment suggestion;According to the prediction result of liquid demand quantity prediction, the risk probability of future occurrence of liquid overload, hypovolemia or abdominal cavity high pressure syndrome of patient is predicted.The application can realize the intelligent prediction of individualized liquid demand quantity and the early dynamic early warning of complication risk, generate liquid management suggestion, to assist clinical precise and predictive liquid treatment.

The invention relates to the technical field of fungus diagnosis, in particular to a fungus culture device for skin infection diagnosis. A mother culture dish and a son culture dish are embedded in the culture box; and a medicine bottle and a liquid storage tube are fixedly mounted in the incubator. A fixed sleeve is fixedly mounted in the mounting frame, and a dropping pipette is fixedly mounted in the fixed sleeve; a plurality of groups of guide pipes are slidably mounted in the culture box, and collecting bags are fixedly mounted on the guide pipes; a collecting structure, a transferring structure and a liquid supplementing structure are arranged on the incubator; the transfer structure can drive the guide pipe to move in the vertical direction and the radial direction of the fixing table. When the catheter moves, the collection structure extrudes the collection bag to collect a fungus sample; the liquid supplementing structure can increase the flow speed of liquid medicine in the medicine bottle to the mother culture dish so as to supplement sample loss; the transfer structure, the collection structure and the liquid injection structure are matched with one another, so that fungus samples can be automatically transferred to the sub-culture dishes containing different inhibition drugs under the condition that the internal environment of the culture box is not changed.

The application provides an oxygen treatment system and a control method thereof, wherein the oxygen treatment system comprises an oxygen treatment device for treating oxygen through an electrochemical reaction and a liquid supplementing device for supplementing liquid to the oxygen treatment device, and the control method comprises: detecting a liquid level drop rate of the liquid supplementing device; judging whether the liquid level drop rate of the liquid supplementing device is greater than a preset drop rate threshold; if yes, locating a leakage point of the oxygen treatment system; and performing an alarm measure corresponding to the leakage point. By using the method, the oxygen treatment system has the liquid leakage self-monitoring capability and the leakage point locating capability, so that the user can take targeted remedial measures. According to the scheme of the application, the oxygen regulation function of the oxygen treatment device can be reduced or avoided from being disabled due to liquid leakage, and the surrounding environment is protected from being eroded by electrolyte.

The utility model relates to the field of otorhinolaryngological nursing, and discloses a nasal irrigator for otorhinolaryngological nursing, which comprises a mounting column, one end of the mounting column is provided with an annular groove, the inside of the annular groove is in threaded connection with a replacement cylinder, the inside of the mounting column is provided with a mounting groove, the inside of the mounting groove is provided with a water pump, and the water pump is connected with the replacement cylinder. A positioning groove is formed in one end of the replacement cylinder, the positioning groove and the annular groove are rotationally inserted, a water pumping hole is formed in the bottom end of the interior of the positioning groove, a sealing piece is detachably arranged in the water pumping hole, a fixing cylinder is fixed to one end of the interior of the replacement cylinder, and a communicating hole is formed in one end of the fixing cylinder; an extraction pipe is fixed to one end of the fixing cylinder, and the central axis of the communication hole and the central axis of the extraction pipe are located on the same straight line. According to the utility model, one patient can correspond to one bottle or a plurality of bottles filled with cleaning liquid by medical staff, so that the replacement cylinder is prevented from being repeatedly used, and the risk of cross infection is reduced.

This application discloses a blood purification device and storage medium. The blood purification device includes a memory and a processor. When the processor executes a computer program, it performs the following: In the pre-charge test phase, it controls a heating plate to heat the replacement fluid in the fluid replenishment branch. When the detected first temperature of the replacement fluid is within a preset safe temperature range, it switches to the blood treatment phase. Then, it controls the heating plate to start heating at the initial heating temperature, receives the user-set heating target temperature, and obtains the first flow rate of the fluid replenishment branch based on the detected rotation speed of the first peristaltic pump. It determines a temperature lookup table based on the first flow rate, finds the corresponding first heating temperature of the heating plate in the temperature lookup table based on the heating target temperature, and adjusts the heating power of the heating plate using PI control feedback based on the detected actual heating temperature and the first heating temperature. In this way, this application can improve the stability and accuracy of intelligent control of the temperature of the replacement fluid in the fluid replenishment branch.

The utility model relates to a dipping tank applied to an automatic dipping coating device, which comprises a liquid medicine tank with an opening at the upper end, at least one vertically arranged vertical partition plate is arranged in the liquid medicine tank, the liquid medicine tank is divided into a dipping cavity and a backflow cavity by the vertical partition plate, and the top end of the vertical partition plate is lower than the edge of the upper opening of the liquid medicine tank. Liquid medicine in the dipping cavity flows into the backflow cavity in an overflowing mode, a liquid supplementing opening communicated with the dipping cavity and a backflow opening communicated with the backflow cavity are formed in the bottom of the liquid medicine pool, the liquid supplementing opening is communicated with the liquid medicine storage tank through a guide pipe and a liquid supply pump, and the backflow opening is communicated with the liquid medicine storage tank through a guide pipe. According to the utility model, the stability of the liquid level height of liquid medicine is ensured in a liquid medicine overflowing manner, so that the dipping depth of workpieces is kept constant in the dipping and coating process, and the consistency of the dipping and coating effects of all the workpieces is ensured.

Aspects of the invention include methods of managing pain in a subject by applying a transdermal delivery device containing a dexmedetomidine composition formulated to deliver a pain relieving effective amount of dexmedetomidine to a subject. In practicing methods according to certain embodiments, a transdermal delivery device having a dexmedetomidine composition is applied to a subject and is maintained in contact with the subject in a manner sufficient to deliver an amount of dexmedetomidine effective to manage pain in the subject. In some embodiments, methods include hydrating the subject, such as by administering a hydration fluid composition to the subject. Methods according to certain embodiments may also include co-administering an opioid to the subject. Also provided is a transdermal delivery device configured to deliver dexmedetomidine sufficient for practicing the subject methods, as well as kits containing the transdermal delivery device.

The invention belongs to the technical field of clinical medicine, and discloses an intelligent liquid drug delivery system, the specific technical scheme is that the intelligent liquid drug delivery system is composed of a front-end user interface, a rear-end data processing module and a database, the front-end user interface is responsible for interacting with a user, and the user inputs the body weight, dehydration degree, physiological indexes and blood examination results of a patient through the front-end user interface; the system receives input data and displays a calculation result, the rear-end data processing module is responsible for processing the data and calculating a recommended fluid infusion scheme according to a fluid infusion amount calculation formula and specific physiological indexes of a patient, and the system displays the fluid infusion scheme obtained through calculation to a user in the form of charts and characters. A user manually adjusts a recommended fluid infusion scheme according to actual conditions, a medical institution performs drug administration according to the recommended or adjusted fluid infusion scheme, and a database is used for storing patient information, the fluid infusion scheme and system configuration and storing liquid therapy calculation historical records of the user. The system can significantly improve the administration efficiency of medical institutions and the safety of patients.

Fluid replacement structures used in immersion cooling tanks can include various enhancements to make them functional beyond simply taking up space. For example, the density of fluid replacement structures can be variable to assist with buoyancy control. As another example, fluid replacement structures can be designed to enable vaporized working fluid to be directed to a desired location. As another example, fluid replacement structures can include emergency cooling features, such as different substances that cause an endothermic reaction to occur when they are mixed together. The substances can be separated by a membrane that melts when the temperature reaches a certain point. As another example, a fluid replacement structure can provide structural support for an immersion cooling tank when negative pressure operations are performed. Fluid replacement structures can also include alignment features, lifting features, locking features, mating guides, fiducial markers, or the like.