Medical analysis equipment initialization method, device, equipment and medium

Abstract

The present invention relates to the technical field of medical analysis equipment, and in particular to a method, device, equipment and medium for initializing medical analysis equipment. When the medical analysis equipment is turned on, the power-on and power-off status of a reagent compartment of the medical analysis equipment when it was last shut down is determined. If the reagent compartment was powered on when it was last shut down, the first interval duration from the last shutdown to the current startup of the medical analysis equipment is obtained. Finally, according to the first interval duration, a condensate pumping function module is controlled to pump water from the reagent compartment to complete the initialization of the medical analysis equipment. This allows the present invention to determine whether there is enriched condensate in the condensate compartment when performing a startup initialization operation on the medical analysis equipment, and to pump out the condensate when performing the startup initialization operation, thereby ensuring the normal operation of the medical analysis equipment after startup.

Description

Technical Field

[0001] The present invention relates to the technical field of medical analysis equipment, and in particular to a method, device, equipment and medium for initializing medical analysis equipment. Background Art

[0002] When the medical equipment is in use, the reagent chamber is in a low temperature state, and the reagent chamber in a low temperature state will produce condensed water. In the prior art, the usual practice is that after the medical equipment completes the medical analysis work, the condensed water is drained when the medical analysis equipment is turned off. Then when it is turned on for use next time, the medical analysis equipment needs to be initialized first. The process of performing conventional initialization operations on medical analysis equipment is that the terminal user logs in, and the power-on initialization process cannot be skipped. Then the power-on initialization executes instructions such as whole machine reset, hardware self-test, fault elimination, and liquid circuit maintenance. After the terminal user logs in to the account, it is necessary to wait for the standby initialization to be completed before entering the software interface and performing sample testing. For emergency samples, the test results cannot be reported in time. This initialization method can solve the problem that before the user goes to work, the instrument can automatically start up within the set time, and complete the power-on initialization and related maintenance actions, so that the instrument enters the ready state. After the user goes to work, he directly performs sample analysis on the instrument, saving time.

[0003] However, although the initialization operation performed at startup can make the medical analysis equipment meet the use requirements, it cannot accurately determine whether condensed water is still accumulated in the condensation chamber, affecting the normal operation of the medical analysis equipment. Summary of the invention

[0004] The main purpose of the present invention is to provide a method, device, equipment and medium for initializing medical analysis equipment, aiming to solve the technical problem in the related art that it is impossible to accurately judge whether condensed water is still enriched in the condensation chamber, which affects the normal operation of the medical analysis equipment.

[0005] To achieve the above object, in a first aspect, the present invention provides a method for initializing a medical analysis device, comprising the following steps:

[0006] When the medical analysis device is turned on, determining the power-on / off state of the reagent compartment of the medical analysis device when it was last shut down;

[0007] If the reagent compartment was powered on when the device was last shut down, obtaining a first interval between the last shutdown and the current startup of the medical analysis device;

[0008] According to the first interval duration, the condensed water pumping function module is controlled to pump water from the reagent chamber to complete the initialization of the medical analysis device.

[0009] Optionally, the step of controlling the condensed water pumping function module to pump water from the reagent chamber according to the first interval duration to complete the initialization of the medical analysis device includes:

[0010] determining a number of first interval hours included in the first interval duration;

[0011] Determining a first pumping duration according to the first interval hours;

[0012] According to the first pumping time, the condensed water pumping function module is controlled to pump water from the reagent bin.

[0013] Optionally, before the step of determining the power-on / off state of the reagent compartment of the medical analysis device when the medical analysis device was last shut down when the medical analysis device is turned on, the step further includes:

[0014] When receiving the shutdown instruction, obtaining the startup operation time of the medical analysis device;

[0015] According to the startup operation time, the condensate water pumping function module is controlled to perform a condensate water pumping operation on the reagent compartment.

[0016] Optionally, the step of controlling the condensate pumping operation of the reagent bin according to the startup operation time includes:

[0017] Determining the number of second interval hours included in the startup operation time;

[0018] Determining the second pumping duration according to the second interval hours;

[0019] According to the second pumping time, the condensed water pumping function module is controlled to pump water from the reagent bin.

[0020] Optionally, the method further comprises:

[0021] Performing abnormal state detection on various basic functional modules of the medical analysis device;

[0022] When at least one of the basic function modules is in an abnormal state, the initialization task is terminated.

[0023] Optionally, after the step of performing abnormal state detection on the various basic function modules of the medical analysis device, the method further includes:

[0024] Performing a closing state detection on a plurality of closeable covers of the medical analysis device;

[0025] When at least one closable cover is in an open state, the initialization task is terminated.

[0026] Optionally, after the step of controlling the condensed water pumping function module to pump water from the reagent chamber according to the first interval duration to complete the initialization of the medical analysis device, the method further includes:

[0027] When it is monitored that the sample liquid collected in the collection component drips into the calibration module, the temperature sensor is controlled to collect the sample liquid temperature of the calibration module;

[0028] If the sample liquid temperature is lower than the preset temperature, the collection component is heated so that the temperature of the sample liquid stored in the collection component reaches the preset temperature.

[0029] Based on the same technical concept, in a second aspect, the present invention proposes a medical analysis device, which includes a processor and a memory, wherein a medical analysis device initialization program is stored in the memory, and when the medical analysis device initialization program is executed by the processor, the medical analysis device initialization method described in the first aspect is implemented.

[0030] Optionally, it also includes:

[0031] A sample supply module, the sample supply module comprising a reagent carrier and a sample carrier, the reagent carrier and the sample carrier are spaced apart and distributed in a horizontal direction;

[0032] There is a height difference between the bottom of the sample carrier and the bottom of the reagent carrier in the height direction.

[0033] Based on the same technical concept, in a third aspect, the present invention proposes a computer storage medium, on which a computer program is stored. When the computer program is executed by one or more processors, the medical analysis equipment initialization method described in the first aspect is implemented.

[0034] The technical solution of the present invention has the following beneficial effects:

[0035] The technical solution of the present invention first determines the power-on and power-off status of the reagent compartment of the medical analysis equipment when the medical analysis equipment was last shut down when the medical analysis equipment was turned on. If the reagent compartment was in the power-on state when the medical analysis equipment was last shut down, the first interval duration from the last shutdown to the current startup of the medical analysis equipment is obtained. Finally, according to the first interval duration, the condensate pumping function module is controlled to pump water from the reagent compartment to complete the initialization of the medical analysis equipment. This allows the present invention to determine whether there is enriched condensate in the reagent compartment of the medical analysis equipment when the startup initialization operation is performed on the medical analysis equipment, and use the condensate pumping function module to pump water from the reagent compartment when it is determined that the condensate compartment was in the startup state when the medical analysis equipment was last shut down. This allows the present invention to determine whether there is enriched condensate in the condensate compartment when the startup initialization operation is performed on the medical analysis equipment, and at the same time, the condensate is pumped out when the startup initialization operation is performed, thereby ensuring the normal operation of the medical analysis equipment after startup. BRIEF DESCRIPTION OF THE DRAWINGS

[0036] In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on the structures shown in these drawings without paying creative work.

[0037] Figure 1 A flowchart of a method for initializing a medical analysis device according to an example of the present invention;

[0038] Figure 2 for Figure 1 A detailed flowchart of step S300 in the example;

[0039] Figure 3 for Figure 1 Flowcharts of some embodiments exemplified in;

[0040] Figure 4 for Figure 3 A detailed flowchart of step S20 in the example;

[0041] Figure 5 Flow charts of some specific embodiments of the present invention;

[0042] Figure 6 Schematic diagram of the hardware structure of the medical analysis device according to the present invention.

[0043] The purpose, features and advantages of the present invention will be further described with reference to the accompanying drawings in conjunction with the embodiments. DETAILED DESCRIPTION

[0044] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0045] It should be noted that all directional indications (such as up, down, left, right, front, back, etc.) in the embodiments of the present invention are only used to explain the relative position relationship, movement status, etc. between various mechanisms under a certain specific posture (as shown in the accompanying drawings). If the specific posture changes, the directional indication will also change accordingly.

[0046] In the present invention, unless otherwise clearly specified and limited, the terms "connection", "fixation", etc. should be understood in a broad sense. For example, "fixation" can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium, it can be the internal connection of two elements or the interaction relationship between two elements, unless otherwise clearly defined. For ordinary technicians in this field, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

[0047] In addition, if there are descriptions involving "first", "second", etc. in the embodiments of the present invention, the descriptions of "first", "second", etc. are only used for descriptive purposes and cannot be understood as indicating or implying their relative importance or implicitly indicating the number of technical features indicated. Therefore, the features defined as "first" and "second" may explicitly or implicitly include at least one of the features. In addition, the meaning of "and / or" appearing in the full text includes three parallel schemes. Taking "A and / or B" as an example, it includes scheme A, or scheme B, or a scheme that satisfies both A and B. In addition, the technical solutions between the various embodiments can be combined with each other, but it must be based on the ability of ordinary technicians in the field to implement. When the combination of technical solutions is contradictory or cannot be implemented, it should be deemed that such a combination of technical solutions does not exist and is not within the scope of protection required by the present invention.

[0048] The inventive concept of the present invention is further described below in conjunction with some specific implementation methods.

[0049] See also Figures 1 to 6 The present invention proposes a specific embodiment of a method, device, equipment and medium for initializing medical analysis equipment.

[0050] See also Figures 1 to 5 The medical analysis device initialization method of the present invention includes the following steps:

[0051] In this embodiment, the specific process is:

[0052] First, step S10 is executed to obtain the startup operation time of the medical analysis device when a shutdown instruction is received.

[0053] In an exemplary embodiment, for example, if a medical analysis device receives a shutdown command at 6 p.m., the startup time of the medical analysis device on that weekday and before receiving the shutdown command is first determined, and the working hours of the medical analysis device on that weekday are determined based on the duration between the startup time and the time corresponding to the shutdown command. For example, if the startup time is 8 a.m., the running time of the medical analysis device on that weekday is 10 hours.

[0054] S20. According to the startup operation time, control the condensate water pumping function module to perform the condensate water pumping operation on the reagent bin.

[0055] In this embodiment, the specific process is: first, executing step S21, determining the number of second interval hours included in the startup operation time;

[0056] S22, determining the second pumping duration according to the number of the second interval hours;

[0057] S23. According to the second pumping time, control the condensed water pumping function module to pump water from the reagent bin.

[0058] After determining the startup time and before performing the condensate pumping operation, it is also necessary to select the corresponding condensate pumping strategy. Specifically, the pumping strategy is to complete 8 seconds of pumping every 1 hour from the startup time. After determining the corresponding pumping strategy, the second pumping time is determined based on the startup time and the pumping strategy. The second pumping time is determined by multiplying the startup time and the pumping strategy, that is, the second pumping time is 80 seconds. Specifically, the pumping time for controlling the condensate pumping function module to perform the condensate pumping operation on the reagent bin is the second pumping time, that is, 80 seconds.

[0059] S100, when the medical analysis device is turned on, determining the power-on / off state of the reagent compartment of the medical analysis device when it was last shut down;

[0060] In this embodiment, during specific use, since the reagent compartment in the medical analysis equipment in the prior art can be powered independently, when executing this step, it is possible to determine whether the reagent compartment was powered independently at the last shutdown, and the power on and off status of the reagent compartment in the medical analysis equipment can be obtained.

[0061] S200, if the reagent compartment was powered on when the device was last shut down, obtaining a first interval time from when the medical analysis device was last shut down to when it is turned on this time;

[0062] In this embodiment, specifically, the process of determining the first interval duration is that, when executing this startup, the technician can determine the shutdown time of the last shutdown by consulting the work log, etc. After determining the shutdown time, the first interval duration from the last shutdown to the current startup can be obtained according to the time interval between the shutdown time and the startup time of the current startup. For example, the shutdown time of the last shutdown is 6 o'clock in the evening of the previous day, and the startup time of the current startup is 8 o'clock in the morning of the same day, then the first interval duration is 14 hours.

[0063] S300. According to the first interval duration, control the condensed water pumping function module to pump water from the reagent chamber to complete the initialization of the medical analysis equipment.

[0064] In this embodiment, the specific process of step S300 is: firstly, step S310 is executed to determine the number of first interval hours included in the first interval duration;

[0065] S320, determining a first pumping duration according to the number of first interval hours;

[0066] S330. According to the first pumping time, control the condensed water pumping function module to pump water from the reagent bin.

[0067] More specifically, after determining the first interval duration and before executing the condensate pumping operation during the startup initialization process, it is also necessary to select the corresponding condensate pumping strategy. Specifically, the pumping strategy is to complete 8 seconds of pumping for every 1 hour from the shutdown time. After determining the corresponding pumping strategy, the first pumping duration is determined based on the first interval duration and the pumping strategy. The first pumping duration is determined by multiplying the first interval duration by the pumping strategy, that is, the first pumping duration is 112 seconds. Specifically, the pumping duration for controlling the condensate pumping function module to perform the condensate pumping operation on the reagent bin is the first pumping duration, that is, 112 seconds.

[0068] The technical solution of the present invention first determines the power-on and power-off status of the reagent compartment of the medical analysis equipment when the medical analysis equipment was last shut down when the medical analysis equipment was turned on. If the reagent compartment was in the power-on state when the medical analysis equipment was last shut down, the first interval duration from the last shutdown to the current startup of the medical analysis equipment is obtained. Finally, according to the first interval duration, the condensate pumping function module is controlled to pump water from the reagent compartment to complete the initialization of the medical analysis equipment. This allows the present invention to determine whether there is enriched condensate in the reagent compartment of the medical analysis equipment when the startup initialization operation is performed on the medical analysis equipment, and use the condensate pumping function module to pump water from the reagent compartment when it is determined that the condensate compartment was in the startup state when the medical analysis equipment was last shut down. This allows the present invention to determine whether there is enriched condensate in the condensate compartment when the startup initialization operation is performed on the medical analysis equipment, and at the same time, the condensate is pumped out when the startup initialization operation is performed, thereby ensuring the normal operation of the medical analysis equipment after startup.

[0069] Of course, in some specific embodiments, the medical analysis device initialization method of the present invention further includes:

[0070] S400, performing abnormal state detection on various basic functional modules of the medical analysis equipment;

[0071] In this embodiment, when executing step S400, the main contents that need to be detected include self-test of the software system, detection of hardware such as the RFID module, the whole machine protection cover sensor, the reagent compartment cover sensor, the room temperature reagent micro switch, the syringe, etc., detection of equipment or devices that perform mechanical movements in the medical analysis equipment (such as sample needles, reagent needles, grippers, cup pusher resets, etc.), detection of the optical system and temperature control system in the medical analysis equipment, and detection of whether there are any equipment left over from the previous analysis operation in the medical analysis equipment.

[0072] S500: When at least one basic function module is in an abnormal state, the initialization task is terminated.

[0073] In this embodiment, if a hardware anomaly is detected, the initialization will be terminated, the system will enter the boot state, and an alarm will be sounded. After the anomaly is eliminated, the system will be restored and the system will enter the waiting state for testing to perform sample analysis.

[0074] Furthermore, the optical system and temperature control system should reach a stable state within 20 minutes of startup. The optical system should be turned on during the startup initialization process. When the sample is analyzed 15 minutes later, the AD value of the optical system should be tested to see if it meets the sample analysis requirements. The temperature control system should start timing from the time the temperature control system is turned on during the startup initialization process. The incubation / detection module should enter a stable state when it reaches 37±0.5℃ for 3 consecutive minutes. If the temperature does not reach 37±0.5℃ for 3 consecutive minutes after 20 minutes of startup, the system will alarm.

[0075] Furthermore, when there are devices left over from the last analysis operation in the medical analysis device, it is necessary to execute a clean-up instruction for the entire device. For example, when there are reaction cups left over from the last analysis operation in the medical analysis device, a clean-up instruction for the entire device is executed for the medical analysis device. In this embodiment, the exemplary clean-up instruction for the entire device can directly adopt the existing technology, which will not be described in detail in this embodiment.

[0076] In some specific embodiments, after the step of performing abnormal state detection on various basic functional modules of the medical analysis device, the method further includes:

[0077] S600: Detect the closing status of multiple closeable covers of the medical analysis equipment.

[0078] In this embodiment, the example coverable cover body includes a whole machine protection cover and a reagent compartment cover. When executing step S600, if it is detected that the whole machine protection cover and the reagent compartment cover are in the open state, the relevant detection items are skipped, and the next step of detection is performed until the initialization is completed and the machine enters the power-on state, and an alarm prompts.

[0079] S700: When at least one closable cover is in an open state, the initialization task is terminated.

[0080] It should be further emphasized that after the medical analysis equipment completes the boot operation in the process of executing steps S400 to S700, it is not allowed to perform sample analysis, and the corresponding defects must be completely eliminated and the system restarted before entering the standby state.

[0081] In some specific embodiments, when using a medical analysis device to analyze a sample, if the temperature of the sample cannot meet a preset temperature, the accuracy of the analysis result will be affected. Therefore, after the step of controlling the condensed water pumping function module to pump water from the reagent tank according to the first interval duration to complete the initialization of the medical analysis device, the method further includes:

[0082] S800, when it is monitored that the sample liquid collected in the collection component drips into the calibration module, control the temperature sensor to collect the sample liquid temperature of the calibration module;

[0083] In this embodiment, the calibration module includes a calibration pool, a heat preservation structure for heat preservation of the calibration pool, and a temperature detector for detecting the real-time temperature in the calibration pool. The heat preservation structure can maintain the temperature at a preset temperature. Specifically, the heat preservation structure can maintain the temperature of the calibration pool at 37°C or a temperature close to human body temperature. Of course, in specific use, in order to make the temperature in the calibration pool more constant, some liquids (such as saline, etc.) can also be placed in the calibration pool, and then the heat preservation structure can be used to keep these liquids warm.

[0084] It can be further explained that when the temperature of the sample liquid collected by the collection component is detected, the sample liquid collected by the collection component can be dropped into the liquid agent. Since the liquid agent is in a constant temperature state, when the sample liquid is dropped into the liquid agent, if the temperature of the sample liquid and the liquid agent is different, the temperature result detected by the temperature sensor will inevitably change. That is, the temperature of the sample liquid can be detected in this way.

[0085] It should be particularly and clearly stated that, for example, the collection component is a sampling needle, and at least part of the sampling needle is provided with a heating device for preheating or heating the sampling needle so that the liquid in the sampling needle reaches a preset temperature.

[0086] S900: If the sample liquid temperature is lower than the preset temperature, the collection component is heated to make the temperature of the liquid stored in the collection component reach the preset temperature.

[0087] In this embodiment, the calibration process is as follows: the liquid in the collection component that has been heated within a set time range (consistent with the normal working time) is dropped into the liquid in the calibration pool, and the temperature sensor detects the temperature change of the liquid to determine the drift amount of the heating of the collection component; and the detection result is fed back to the controller to control the heater set on the collection component to heat the collection component and the sample liquid stored in the collection component.

[0088] In this embodiment, during specific implementation, a calibration module is used to detect the sample liquid temperature, and then the collection component is heated according to the detection result, so that the present invention can ensure that the sample liquid temperature is maintained at a preset temperature when in use, thereby improving the accuracy of the analysis result.

[0089] Based on the same technical concept, in a second aspect, the present invention proposes a medical analysis device, which includes a processor and a memory. The memory stores a medical analysis device initialization program. When the medical analysis device initialization program is executed by the processor, the medical analysis device initialization method of the first aspect is implemented.

[0090] Medical analysis equipment refers to terminal equipment or network equipment that can achieve network connection. Medical analysis equipment can be terminal equipment such as mobile phones, computers, tablets, embedded industrial computers, or network equipment such as servers and cloud platforms.

[0091] like Figure 6 , which is a schematic diagram of the hardware structure of a medical analysis device. The medical analysis device may include: a processor 1001 , such as a CPU (Central Processing Unit), a communication bus 1002 , a user interface 1003 , a network interface 1004 , and a memory 1005 .

[0092] Those skilled in the art will understand that Figure 6 The hardware structure shown in the figure does not constitute a limitation on the medical analysis device of the present invention, and may include more or less components than shown in the figure, or a combination of certain components, or a different arrangement of components.

[0093] Specifically, the communication bus 1002 is used to realize the connection and communication between these components;

[0094] The user interface 1003 is used to connect to the client and perform data communication with the client. The user interface 1003 may include an output unit, such as a display screen, and an input unit, such as a keyboard;

[0095] The network interface 1004 is used to connect to the backend server and perform data communication with the backend server. The network interface 1004 may include an input / output interface, such as a standard wired interface, a wireless interface, such as a Wi-Fi interface;

[0096] The memory 1005 is used to store various types of data, which may include, for example, instructions for any application or method in the medical analysis device, and data related to the application. The memory 1005 may be a high-speed RAM memory or a stable memory, such as a disk memory. Optionally, the memory 1005 may also be a storage device independent of the processor 1001, as described in detail below. Figure 6 , the memory 1005 may include an operating system, a network communication module, a user interface module, and a medical analysis device initialization program;

[0097] The processor 1001 is used to call the medical analysis device initialization program stored in the memory 1005 and perform the following operations:

[0098] In some specific embodiments, it also includes:

[0099] A sample supply module, the sample supply module includes a reagent carrier and a sample carrier, the reagent carrier and the sample carrier are spaced apart in a horizontal direction;

[0100] There is a height difference between the bottom of the sample carrier and the bottom of the reagent carrier in the height direction.

[0101] In this embodiment, during specific implementation, the sample supply module is used to provide samples and / or reagents to the analyzer;

[0102] The sample supply module includes a sample carrier for carrying samples, a reagent carrier for carrying reagents, a collection component for collecting samples and / or reagents, and a sample supply conveying component for conveying the sample carrier and / or reagent carrier;

[0103] The reagent carriers include refrigerated reagent carriers and room temperature reagent carriers; the refrigerated reagent carriers and room temperature reagent carriers are distributed separately, that is, they are not connected in the three dimensions of XYZ, and the projections in at least two dimensions do not overlap;

[0104] The sample carrier and the reagent carrier are distributed in a step-like manner, that is, there is a height difference △H between the bottom of the sample carrier and the bottom of the reagent carrier in the height direction; further, there is also a certain height difference △h in the height direction between the collection positions of the collection components on the reagent carrier and the sample carrier; △H and △h can be equal or different.

[0105] In this embodiment, the sample carrier and the reagent carrier are arranged in a step-wise manner, so that the present invention can make the structure of the entire sample supply module more compact when in use.

[0106] Of course, in an exemplary embodiment, the medical analysis device of the present invention also includes the following functional modules:

[0107] A detection module is used to detect a sample or a sample and a reagent; the detection module includes an incubation component for incubating the sample / sample and a reagent, a mixing component for mixing the sample / sample and the reagent, a measuring component for measuring the sample / sample and the reagent, a dilution component for diluting the sample, and a gripper component for transferring a reaction cup between the incubation component, the mixing component, the dilution component and the measuring component; wherein the gripper component can be a set of grippers or a combination of multiple sets of grippers; the measuring module can be an optical measuring module or / and a magnetic bead measuring module, the optical measuring module uses an optical method to measure the optical properties of the sample / sample and the reagent during the reaction; the magnetic bead measuring module measures the movement characteristics of the magnetic beads in the sample / sample and the reagent during the reaction.

[0108] The cup supply module is used to provide reaction cups to the analyzer; the cup supply module includes a cup bin for receiving and storing reaction cups, a cup arrangement component for arranging the reaction cups into cups with specific placement features, and a temporary storage component for receiving reaction cups transferred from the cup arrangement component and temporarily storing and transferring them to the gripper component; wherein the temporary storage component includes at least two temporary storage positions.

[0109] The HIL module is used to perform HIL analysis on the sample; the HIL module includes a colorimetric cell for analyzing the sample / sample and reagent to determine the type of the sample / sample and reagent so as to select a suitable measurement module for detection and analysis; it also includes a transfer module for transferring the sample / sample and reagent to the corresponding measurement module according to the sample type; the transfer module can be partially or fully shared with the transfer component.

[0110] The cleaning module is used to clean the collection component and the waste cup; the cleaning module includes a cleaning tank and a cup throwing component; the cleaning tank includes a first cleaning tank and a second cleaning tank, and the cup throwing component is used to throw the waste cups that have been tested into the waste cup box through the pipeline.

[0111] The emergency module is used to provide emergency testing; the emergency module includes an emergency position, which is arranged adjacent to a conventional sampling position, wherein the sampling needle travels a first stroke to the conventional sampling position to collect conventional samples, and travels a second stroke to the emergency position to collect emergency samples.

[0112] The controller includes multiple modules and is used to control the operation and collaboration of each module. The controller can be an independent controller or integrated into a host computer, or integrated with the analyzer display screen and control the display format of the display screen.

[0113] Based on the same technical concept, in a third aspect, the present invention proposes a computer storage medium having a computer program stored thereon. When the computer program is executed by one or more processors, the medical analysis device initialization method of the first aspect is implemented.

[0114] Based on the same inventive concept, this embodiment provides a computer-readable storage medium, such as a flash memory, a hard disk, a multimedia card, a card-type memory (for example, an SD or DX memory, etc.), a random access memory (RAM), a static random access memory (SRAM), a read-only memory (ROM), a programmable read-only memory (PROM), an erasable programmable read-only memory (EPROM), an electrically erasable programmable read-only memory (EEPROM), a magnetic memory, a disk, an optical disk, a server, etc., on which a computer program is stored. The computer program can be executed by one or more processors. When the computer program is executed by the processor, all or part of the steps of each embodiment of the medical analysis device initialization method of the present invention can be implemented.

[0115] The above descriptions are only optional embodiments of the present invention, and are not intended to limit the patent scope of the present invention. All equivalent structural changes made using the contents of the present invention's specification and drawings, or directly / indirectly applied in other related technical fields, are included in the patent protection scope of the present invention.

Claims

1. A method for initializing a medical analysis device, characterized in that: The steps include: When the medical analysis device is turned on, determining the power-on / off state of the reagent compartment of the medical analysis device when it was last shut down; If the reagent compartment was powered on when the device was last shut down, obtaining a first interval between the last shutdown and the current startup of the medical analysis device; According to the first interval duration, controlling the condensed water pumping function module to pump water from the reagent compartment to complete the initialization of the medical analysis device; The step of controlling the condensed water pumping function module to pump water from the reagent compartment according to the first interval duration to complete the initialization of the medical analysis device includes: determining a number of first interval hours included in the first interval duration; Determining a first pumping duration according to the first interval hours; According to the first pumping time, the condensed water pumping function module is controlled to pump water from the reagent bin.

2. The method for initializing a medical analysis device according to claim 1, characterized in that: Before the step of determining the power-on / off state of the reagent compartment of the medical analysis device when the medical analysis device was last shut down when the medical analysis device is turned on, the method further includes: When receiving the shutdown instruction, obtaining the startup operation time of the medical analysis device; According to the startup operation time, the condensate water pumping function module is controlled to perform a condensate water pumping operation on the reagent compartment.

3. The method for initializing a medical analysis device according to claim 2, characterized in that: The step of controlling the condensate pumping function module to perform a condensate pumping operation on the reagent bin according to the startup operation time includes: Determining the number of second interval hours included in the startup operation time; Determining the second pumping duration according to the second interval hours; According to the second pumping time, the condensed water pumping function module is controlled to pump water from the reagent bin.

4. The method for initializing a medical analysis device according to claim 1, wherein: The method further comprises: Performing abnormal state detection on various basic functional modules of the medical analysis device; When at least one of the basic function modules is in an abnormal state, the initialization task is terminated.

5. The method for initializing a medical analysis device according to claim 4, characterized in that: After the step of performing abnormal state detection on the various basic function modules of the medical analysis device, the method further includes: Performing a closing state detection on a plurality of closeable covers of the medical analysis device; When at least one closable cover is in an open state, the initialization task is terminated.

6. The method for initializing a medical analysis device according to claim 1, wherein: After the step of controlling the condensed water pumping function module to pump water from the reagent chamber according to the first interval duration to complete the initialization of the medical analysis device, the method further includes: When it is monitored that the sample liquid collected in the collection component drips into the calibration module, the temperature sensor is controlled to collect the sample liquid temperature of the calibration module; If the sample liquid temperature is lower than the preset temperature, the collection component is heated so that the temperature of the sample liquid stored in the collection component reaches the preset temperature.

7. A medical analysis device, characterized in that: The medical analysis device comprises a processor and a memory, wherein a medical analysis device initialization program is stored in the memory, and when the medical analysis device initialization program is executed by the processor, the medical analysis device initialization method according to any one of claims 1 to 6 is implemented.

8. The medical analysis device according to claim 7, characterized in that Also includes: A sample supply module, the sample supply module comprising a reagent carrier and a sample carrier, the reagent carrier and the sample carrier are spaced apart and distributed in a horizontal direction; There is a height difference between the bottom of the sample carrier and the bottom of the reagent carrier in the height direction.

9. A computer storage medium, characterized in that: The storage medium stores a computer program, and when the computer program is executed by one or more processors, the medical analysis device initialization method according to any one of claims 1 to 6 is implemented.

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