34 results about "Clinical laboratory test" patented technology

The determination of analyte concentration in physiological samples is of ever increasing importance to today's society. Such assays find use in a variety of applications, including clinical laboratory testing, home testing, etc., where the results of such testing play a prominent role in the diagnosis and management of a variety of disease conditions. An apparatus is described herein which may be used for the manufacture of medical devices which include an integrated lancet and sensor.

The determination of analyte concentration in physiological samples is of ever increasing importance to today's society. Such assays find use in a variety of applications, including clinical laboratory testing, home testing, etc., where the results of such testing play a prominent role in the diagnosis and management of a variety of disease conditions. In the present application, a method is described which may be used for the manufacture of medical devices which include an integrated lancet and sensor.

The invention provides for a novel dynamically configurable point-of-care device for clinical diagnostics and research for analysis of activity associated with pluripotent stem cells, tumor cells, drug metabolites, immunological response, glucose monitoring, cardiovascular diseases, liver cell therapy, cell-cell signaling, epidemic outbreaks, hospital based infectious diseases, pathogens, germ cells, pharmacological compounds, oxidation reduction, microscopy, tomography, flow cytometry, clinical lab testing, and for providing immunoassays, ELISA, electrophoresis, PCR, chromatography, and other laboratory functions. The device comprises a biochemical processing module further comprising a processor and at least one controller, receiving microfluidic elements, sensors, software scripts, an electrically operated interface, flow ports, a user interface, memory, and a communications link, configurable based on analysis of patient data. The invention further provides for multiple-criteria decision analysis for hospital administrators, a wearable device, mobile medical device, molecular electronics configuration, touchscreen recognition, data analytics application, and a drone delivery based point-of-care system.

Computerized systems and methods are provided for coordinating clinical laboratory testing from initial order entry to results notification. A laboratory testing manager provides a centralized conduit for interfacing entities placing orders for laboratory testing and laboratories performing testing. Entities, such as healthcare providers, patients, and the like, may access the laboratory testing manager to enter orders for laboratory testing. The laboratory testing manager may determine an eligible laboratory to perform the laboratory testing based on information provided in each order, such as the type of testing requested and insurance coverage information. After a laboratory performs testing specified in an order, the laboratory may enter the testing results, which are routed to recipients indicated for the results.

The present invention relates to a clinical laboratory test apparatus capable of simply and quickly attaching and detaching a microchip. The clinical laboratory testing apparatus comprises a microchip having a measuring cell that holds a sample liquid; a rotation body; a rotation drive mechanism that rotates the rotation body; a lock mechanism that locks the microchip on the rotation body; a measurement room that holds the microchip and the rotation body and that has an attachment and detachment opening; a protection cover that closes the attachment and detachment opening; a light source that irradiates the measuring cell; and a light receiving unit that receives the light, wherein a centrifugal separation processing of a specimen in the sample liquid is performed in the microchip by the rotation drive mechanism rotating the rotation body, and wherein the protection cover has a pressing-down member that presses down a wall face of the microchip when the protection cover is closing the attachment and detachment opening.

Reference intervals are established and / or validated based on existing clinical data and exclusion criteria, such as diagnosis coding. A Reference Interval Test Engine is designed to statistically analyze large volumes of existing clinical lab test results to establish and evaluate reference intervals for specific population subgroups and / or to provide other applications.

The invention discloses an intelligent control system for text quality of a medical clinical laboratory. According to quality control data parameters set by the clinical laboratory, the intelligent control system can automatically receive quality control data sent by an automatic analytical instrument of the laboratory, send the quality control data to a professional third-party clinical laboratory test quality comparison system in real time to perform comparison and return comparison results to a laboratory information management system in real time. The invention further discloses an intelligent control method for the test quality of the medical clinical laboratory. By the intelligent control method, real-time data interaction between the laboratory information management system and the third-party clinical laboratory test quality comparison system can be realized without manual intervention, and accordingly, accuracy and reliability of clinical text results are guaranteed.

The present invention relates to a disease prognosis prediction modeling method for preparing a model for predicting the prognosis of a specified disease from clinical laboratory test values for the disease by means of a computer, the method comprising the steps of: inputting a plurality of actually measured clinical laboratory test values for the disease and actual measured values of the prognoses into the computer; processing these values by a data mining method to determine one or a plurality of clinical laboratory test items which have an influence on the prognosis of the disease; determining a priority of the items with respect to the prognosis in a case where there are a plurality of the items; and establishing a judgment routine in which correlation of the plurality of clinical laboratory test items and the clinical laboratory test value ranges of the test items with the predicted value of the prognosis is stipulated on the basis of the priority, wherein the judgment routine is used as the model.

This invention relates to the use of thermodynamically incompatible surfaces in agglutination assays for the express purpose of using the sample as a key component of the detection instrument. Specifically, the invention relates to formation of a lense and a virtual container for rapid mixing via thermal energy by a sample liquid disposed on a superhydrophobic surfaces, and a subsequent specific analyte or overall protein concentration assay using particles agglutination for use in the industrial, environmental, and clinical laboratory test fields.

A clinical laboratory test information system comprises: a memory configured to store time information regarding a plurality of stages included in a clinical-laboratory-test-relating operation; an operating device; a display unit; and a controller configured to: cause the display unit to display, based on the time information stored in the memory, first information indicating a temporal transition of a required time for each of the plurality of stages, such that each stage is selectable; and if one of the plurality of stages is selected by the operating device indicated in the first information, cause the display unit to display second information indicating a temporal transition of the required time for the selected stage.

This invention relates to the use of thermodynamically incompatible surfaces in agglutination assays for the express purpose of using the sample as a key component of the detection instrument. Specifically, the invention relates to formation of a lense and a virtual container for rapid mixing via thermal energy by a sample liquid disposed on a superhydrophobic surfaces, and a subsequent specific analyte or overall protein concentration assay using particles agglutination for use in the industrial, environmental, and clinical laboratory test fields.

The invention discloses a hospital clinical laboratory test tube oscillation device with a hydraulic reset function. The hospital clinical laboratory test tube oscillation device comprises a base, a bracket, an oscillation mechanism, an adjusting mechanism, a test tube and a reset mechanism, wherein the two supports are installed on the front side and the rear side of the top end of the base correspondingly. The oscillating mechanism is assembled at the top end of the base; the adjusting mechanism is assembled on the inner side of the bracket; the test tube is arranged in an inner cavity of the adjusting mechanism; and the reset mechanism is assembled at the top of the test tube. The device can simultaneously oscillate a plurality of test tubes with different or same calibers at one time, is higher in practicability, replaces a manual oscillation mode, realizes all-directional reciprocating oscillation of liquid in inner cavities of the test tubes from all angles, is more uniform and efficient in oscillation effect, and is higher in practicability. Besides, the device can balance the pressure intensity of the inner cavity of the test tube after oscillation, so that the normal resetting of liquid in the inner cavity of the test tube is effectively ensured, and the use requirements are satisfied well.

A clinical laboratory test information system comprising: a memory configured to store time information regarding a plurality of stages included in a clinical-laboratory-test-relating operation; an operating device; a display unit; and a controller configured to: cause the display unit to display, based on the time information stored in the memory, first information indicating a temporal transition of a required time for each of the plurality of stages, such that each stage is selectable; and if one of the plurality of stages is selected by the operating device indicated in the first information, cause the display unit to display second information indicating a temporal transition of the required time for the selected stage. Also, a non-transitory storage medium.

The invention belongs to the field of test tube clamps, and particularly provides a high-stability clinical laboratory test tube clamp which comprises a handle, a holding column, a first fixing columnand a second fixing column; one end of the handle is connected with the holding column, the other end of the handle is hinged to the first fixing column, and a bending power mechanism is arranged between the holding column and the first fixing column; the bottom end of the first fixing column is fixedly connected with a second fixing column through a connecting column, the other end of the firstfixing column and the other end of the second fixing column are each hinged to two symmetrically-arranged clamping jaws, the clamping jaws are each hinged to an action rod, the first fixing column andthe second fixing column are each sleeved with a movable ring in a sliding mode, and the movable rings are hinged to two action rods located on the same horizontal plane. According to the invention,two parts of a test tube can be clamped and fixed, the stability is good, the test tube is not prone to falling off in the operation process, the two clamping parts can be driven to move at the same time through pulling of one pull rod to achieve rapid clamping, and operation is convenient and rapid.

The invention discloses a multifunctional experimental platform for clinical examination, which comprises a platform body, a disinfection cabinet is fixed at the left end of the top of the platform body, and the disinfection cabinet is in the shape of a "cuboid", and a control touch screen is provided at the right end of the disinfection cabinet, and the control touch screen The screen is embedded in the platform body, a workbench is arranged in the middle of the top of the platform body, and the workbench is embedded in the platform body, and a reagent rack is arranged at the rear end of the workbench. This kind of multifunctional experimental platform for clinical examination is equipped with a zigzag rod and a pulley. The bottom of the zigzag rod is provided with a pulley, and the pulley is movably connected with the zigzag rod. It is bent at ten degrees, and the bottom of the bending rod is equipped with a pulley, so that the platform body can slide and move, which is convenient for handling and solves the problem of troublesome handling of the platform body in the past, wasting manpower and time, and is suitable for multifunctional experimental platforms for clinical testing. Production and use have good development prospects.

The utility model discloses a clinical laboratory test paper daubing device which comprises a bottom plate and a supporting frame, a placing groove is formed in one side of the bottom plate, a first water storage tank is fixedly arranged on the other side of the bottom plate, the supporting frame is movably arranged at the upper end of the bottom plate, and a daubing structure is arranged on the supporting frame. The smearing structure comprises a mounting frame, a smearing wheel and a middle box, the mounting frame is movably arranged between the supporting frames, and a sample is conveniently smeared on the test paper through the smearing structure; a plurality of spray heads are fixedly arranged on the mounting frame, a first connecting pipe is arranged between the middle box and the spray heads, the spray heads are communicated with the middle box through the first connecting pipe, a plurality of first adding ports are formed in the upper end of the middle box, and a plurality of second adding ports are formed in the lower end of the middle box. And a second water storage tank is fixedly arranged at the side end of the supporting frame, so that the sample is conveniently sprayed on the smearing wheel by the spraying head.

A clinical laboratory test apparatus of a health care information system includes a reading section that reads an optically readable code array, an extraction section that extracts, from a plurality of the code arrays read by the reading section, a rule that is common between the plurality of code arrays, a storage section that stores the rule extracted by the extraction section, and a determination section that determines authenticity of each of the code arrays read by the reading section based on the rule stored in the storage section. In testing a sample, in a case where it is determined by the determination section that the code array read by the reading section is true, the test is executed, and in a case where it is determined that the code array is false, the execution of the test is suspended.

The invention discloses an intelligent control system for text quality of a medical clinical laboratory. According to quality control data parameters set by the clinical laboratory, the intelligent control system can automatically receive quality control data sent by an automatic analytical instrument of the laboratory, send the quality control data to a professional third-party clinical laboratory test quality comparison system in real time to perform comparison and return comparison results to a laboratory information management system in real time. The invention further discloses an intelligent control method for the test quality of the medical clinical laboratory. By the intelligent control method, real-time data interaction between the laboratory information management system and the third-party clinical laboratory test quality comparison system can be realized without manual intervention, and accordingly, accuracy and reliability of clinical text results are guaranteed.

The present invention is a blood coagulation reaction inhibitor comprising phosphatidylserine, phosphatidylcholine, and phosphatidylethanolamine. The present invention is also a thrombin generation inhibitor comprising phosphatidylserine, phosphatidylcholine, and phosphatidylethanolamine. The blood coagulation reaction inhibitor and the thrombin generation inhibitor of the present invention are useful as an antithrombotic agent, a clinical laboratory test reagent for the blood coagulation-fibrinolysis system, and the like.

A clinical laboratory test apparatus of a health care information system includes a reading section that reads an optically readable code array, an extraction section that extracts, from a plurality of the code arrays read by the reading section, a rule that is common between the plurality of code arrays, a storage section that stores the rule extracted by the extraction section, and a determination section that determines authenticity of each of the code arrays read by the reading section based on the rule stored in the storage section. In testing a sample, in a case where it is determined by the determination section that the code array read by the reading section is true, the test is executed, and in a case where it is determined that the code array is false, the execution of the test is suspended.

The utility model relates to the technical field of test tube cleaning, in particular to a hospital clinical laboratory test tube cleaning device which comprises a shell. The device further comprises first electric telescopic rods, sleeves, motors, second electric telescopic rods, bunching rings, nylon ropes, connecting blocks, semicircular plates, fixing plates and fixing rods, the first electric telescopic rods are arranged on the upper surface of the interior of the shell in a bilateral symmetry mode, the output ends of the first electric telescopic rods are connected with the sleeves, and the motors are arranged on the upper surfaces of the interiors of the sleeves. The first electric telescopic rod is arranged to drive the sleeve to move downwards to the specified depth of the test tube, then the motor is started to drive the second electric telescopic rod to pull the bunching ring to tighten the nylon rope, and the semicircular closed assembly is lifted through the connecting block to be tightly attached to the top of the sleeve to form a closed structure and completely make contact with the inner wall of the test tube. At the moment, the first telescopic rod reversely drives the sleeve to move upwards, the closed semicircular assembly mechanically scrapes along the inner wall of the test tube, and residual attachments and liquid traces are efficiently removed.

To precisely evaluate adverse events.SOLUTION: The information processing system includes a clinical laboratory test value extraction unit that extracts a clinical laboratory test value for a drug, a specification unit that specifies a worst value of the clinical laboratory test value or an average value of the clinical laboratory test value for each clinical laboratory test item during a prescription period of the drug, a grade determination unit that determines one of a plurality of grades based on the worst value of the clinical laboratory test value or the average value of the clinical laboratory test value, and an evaluation unit that evaluates whether or not there is an adverse event according to the one of the plurality of grades.SELECTED DRAWING: Figure 2

The present invention recognizes that current clinical laboratory testing methods for multiparametric single cell analysis are limited to analysis of intact live cells, and are insufficient for identification of signaling activation profile defining certain cell types, including but not limited to neoplastic and immunologically activated cell subsets. One aspect of the present invention generally relates to marker selection in panels to include proteins routinely assessed in standard FCM, while preferably also incorporating markers for surface receptor proteins within activated signaling cascades. A further aspect of the present invention generally relates to panel design for the following indications in neoplastic and non-neoplastic clinical applications as examples of the technology: (a) identification of CML progenitor cell subsets in the setting of disease recurrence after treatment discontinuation or relapse due to treatment resistance, and (b) characterization of activated basophils to predict the severity of an allergic response. Another aspect of the present invention generally relates to methods to measure levels of surface and IC biomarkers in separate or combined assays for robust characterization of each or select cell compartment, and data analysis based on results from each or all method(s) used for optimal detection of the markers. A further aspect of the present invention generally relates to the identification and profiling of cell subpopulations based on analysis of surface markers including those associated with lineage and maturation of cell types and receptor proteins, and the corresponding IC phosphoproteins including those in activated signaling cascades to predict certain disease states or response to treatment.

The invention discloses a clinical laboratory test tube storage device with an anti-collision function. The clinical laboratory test tube storage device comprises a test tube rack, a top cover is arranged at the top end of the test tube rack, a loading groove is formed in the top end of the test tube rack, a ventilation mechanism is arranged in an inner cavity of the top cover, and a clamping mechanism is arranged in an inner cavity of the test tube rack. Through the ventilation mechanism, sealed test tubes can be selectively ventilated or sealed, and corresponding operation treatment can be carried out according to different test tube containing components.

The invention discloses a clinical laboratory test result interference factor acquisition method and device and a computer readable storage medium, which can automatically extract a medication condition possible interference factor and / or a physiological condition possible interference factor and / or a pathological condition possible interference factor corresponding to a specific clinical laboratory test result. Comprising the steps that first information and second information are obtained, the first information comprises a clinical laboratory inspection result of an inspector, and the second information comprises at least one of medication condition information, physiological condition information and pathological condition information of the inspector; and according to a preset corresponding relationship between the test result and the interference factor, automatically extracting a drug use condition possible interference factor and / or a physiological condition possible interference factor and / or a pathological condition possible interference factor corresponding to the test result of the specific clinical laboratory from the first information and the second information.

The invention provides an intelligent clinical laboratory test tube cleaning and drying all-in-one machine which comprises a cleaning outer frame, supporting legs, a liquid storage hopper, a guide-out valve, a sterilizing lamp, a rotary storage frame structure, a lifting positioning frame structure, a positioning driving frame structure, a rotary cleaning frame structure, a fan, a cleaning liquid conveying pipe, a dropping pipette, a guide-in valve, a control frame, a controller, a control panel and an electric heating wire. The supporting legs are installed at the four corners of the lower portion of the cleaning outer frame through bolts. The liquid storage hopper is embedded into the middle lower part of the cleaning outer frame; the sterilizing lamps are embedded in the left side and the right side of the lower portion of the cleaning outer frame. An angle rotating motor is installed on the lower portion of the left side of the cleaning outer frame through screws, and test tubes in a transverse frame can be flexibly turned over in the using process. And the threaded groove is in threaded fit with the lifting screw rod, so that the heights of the positioning driving frame structure and the rotary cleaning frame structure can be flexibly adjusted according to requirements during use.

A computerized method for normalizing the results of clinical laboratory tests to a reference scale includes providing a measured value of a clinically significant parameter, providing a set of patient data, and providing a set of method data, including an indication of a method used by a testing instrument used to measure the measured value. One or more correlation factors are retrieved including a method correlation factor from a computer readable database based on the method data. The method correlation factor corresponds to the method used by the testing instrument used to measure the measured value. A normalized value of the clinically significant parameter is calculated based upon the one or more correlation factors. The normalized value may correspond to a value on the reference scale regardless of the method used by the testing instrument.