A method, apparatus, device and medium for managing a sampling needle

Abstract

The application relates to the field of sampling needle detection, in particular to a sampling needle management method and device, equipment and medium. The method comprises the following steps: when a data acquisition instruction is detected, sampling data information of a sampling needle is acquired; whether the sampling needle has an abnormal condition is judged according to the sampling data information; if the sampling needle has an abnormal condition, current time information is acquired; and based on the current time information and the abnormal condition of the sampling needle, maintenance information is generated; and the maintenance information is controlled to be displayed. The application has the effect of improving the maintenance efficiency of the sampling needle.

Description

Technical Field

[0001] This application relates to the field of sampling needle detection, and in particular to a method, apparatus, equipment and medium for managing sampling needles. Background Technology

[0002] Clinical testing instruments often involve using a sampling needle to extract the sample from a sample tube, and then placing the sample from the sampling needle into a detection reaction loop. The samples used in clinical testing instruments include various liquids such as blood, urine, cerebrospinal fluid, and saliva, with blood samples being the most widely used.

[0003] During blood sample collection, sampling needles may encounter abnormalities. For example, the blood may have been left to stand for too long or hemolysis may occur during separation, leading to blood clots. When using a sampling needle to draw blood, the needle is prone to blockage. Detecting clotted blood not only wastes the sampling needle but also delays patient test results. Currently, pressure sensors are used to detect the pressure signal of the sampling needle in the fluid path to determine whether blockage has occurred during blood sample collection.

[0004] Regarding the aforementioned technologies, the inventors believe that when the sampling needle is being tested for blockage, if the sampling needle becomes blocked or other abnormal, the cause of the abnormality cannot be determined in a timely manner, thereby reducing the maintenance efficiency of the sampling needle. Summary of the Invention

[0005] To improve the maintenance efficiency of sampling needles, this application provides a method, apparatus, equipment, and medium for managing sampling needles.

[0006] Firstly, this application provides a method for managing sampling needles, employing the following technical solution: A method for managing a sampling needle, comprising: When a data acquisition command is detected, the sampling data information of the sampling needle is acquired; Determine whether the sampling needle is abnormal based on the sampling data information; If the sampling needle is abnormal, the current time information is obtained, and maintenance information is generated based on the current time information and the abnormality of the sampling needle. The control displays the maintenance information.

[0007] By adopting the above technical solution, when managing and maintaining the sampling needle, it is determined whether there is any abnormality in the sampling needle based on the sampling data information. When there is an abnormality, the current time information is obtained and combined with the abnormality to generate maintenance information for the current time period. Medical staff can determine the cause of the abnormality based on the displayed maintenance information and take further maintenance measures for the sampling needle according to the cause, thereby improving the maintenance efficiency of the sampling needle.

[0008] In another possible implementation, acquiring the sampling data information of the sampling needle includes: The system acquires device status information, blood detection information, and personnel identification information. The personnel identification information includes personnel location information and personnel behavior information. The device status information includes sensor status information and sampling needle status information. The blood detection information is the blood information collected by the sampling needle. The device status information, the blood test information, and the personnel identification information are processed to generate sampling data information.

[0009] By adopting the above technical solution, the main factors affecting the sampling needle's data collection include the status of the sampling needle and sensor equipment, the blood parameters of the extracted blood, and the behavior of the person using the sampling needle. The controller and data acquisition unit can obtain the status information of the sampling needle and sensor equipment; the sensors and MCU chip can obtain blood test information; and the monitor installed inside the sampling needle can obtain personnel identification information. The equipment status information, blood test information, and personnel identification information are packaged together to obtain the sampling needle data.

[0010] In another possible implementation, determining whether the sampling needle is abnormal based on the sampling data information includes: Based on the device status information, determine whether the sampler has a device malfunction; If the sampling needle has a device malfunction, then the sampling needle is determined to have a first malfunction; If the sampling needle does not have any equipment malfunction, then the presence of blood abnormalities in the blood is determined based on the blood test information. If the blood sample shows an abnormality, then the sampling needle is determined to have a second abnormality. If the blood sample does not show any abnormalities, then the presence of any abnormalities in the sampling needle is determined based on the personnel identification information. If there is an abnormality in the sampling needle, then it is determined that there is a third abnormality in the sampling needle; If there is no abnormality in the sampling needle, then it is determined that there is no abnormality in the sampling needle.

[0011] By adopting the above technical solution, the sampling data information, including equipment status information, blood test information, and personnel identification information, corresponds to the sampling needle device, the state of the blood collected by the sampling needle, and the behavior of the person using the sampling needle, respectively. First, based on the equipment status information, equipment abnormalities are judged. If an equipment abnormality exists, a first abnormality is identified. If no equipment abnormality exists, then based on the blood test information, it is judged whether there is a blood abnormality. If a blood abnormality exists, a second abnormality is identified. If no blood abnormality exists, then based on the personnel identification information, it is judged whether there is a personnel abnormality. If a personnel abnormality exists, a third abnormality is identified. If no personnel abnormality exists, it proves that there is no abnormality in the current sampling needle. By adopting a step-by-step judgment process, equipment abnormalities, blood abnormalities, and personnel abnormalities are judged sequentially. As long as any abnormality exists, it can be concluded that there is an abnormality in the sampling needle, thus achieving a comprehensive inspection of abnormalities within the sampling needle.

[0012] In another possible implementation, determining whether the sampler has a device malfunction based on the device status information includes: Based on the device status information, determine the device status of the sampling needle and the pressure sensor; Determine whether the device state does not conform to the preset state safety standard; If the device status does not meet the preset safety standard, then it is determined that the sampling needle has a device malfunction. If the device status does not meet the preset safety standard, then it is determined that the sampling needle does not have a device malfunction.

[0013] By adopting the above technical solution, the status of the sampling needle and pressure sensor devices corresponding to the device status information is collected, and the collected status of the sampling needle and pressure sensor devices is matched with the preset status safety standards to determine whether there is a device malfunction in the current sampling needle and / or pressure sensor. If so, it is determined that there is a device malfunction in the sampling needle. Medical staff maintain the sampling needle according to the corresponding malfunction information in the device malfunction, thereby avoiding the occurrence of abnormal blood collection due to malfunction of the sampling needle and / or pressure sensor.

[0014] In another possible implementation, determining whether the blood has any abnormalities based on the blood test information includes: Based on the blood test information, determine the blood parameters in the blood; Determine whether any of the blood parameters do not meet the preset blood parameter thresholds; If any of the blood parameters do not meet the preset blood parameter threshold, then it is determined that the sampling needle has a blood abnormality. If no blood parameter does not meet the preset blood parameter threshold, then it is determined that the sampling needle does not have the blood abnormality.

[0015] By adopting the above technical solution, after confirming that there is no equipment malfunction, the blood parameters in the blood test information are tested to determine whether the blood parameters match the preset blood parameter thresholds. If they do not match, it indicates that there is a blood abnormality, that is, there is a clot in the blood. Medical staff will then perform blood screening based on the blood abnormality to remove the clots in the blood and avoid clogging of the sampling needle.

[0016] In another possible implementation, determining whether the sampling needle has any abnormal personnel based on the personnel identification information includes: Based on the personnel identification information, determine the personnel location information and personnel behavior information; The location information of the sampling needle is determined based on the personnel location information; The behavior specifications for the location information are determined according to the preset sampling needle management specifications; Determine whether the person's behavior conforms to the behavioral norms; If the behavior does not conform to the stated code of conduct, it is determined that there is an abnormality in the personnel present when sampling. If the behavior conforms to the aforementioned behavioral guidelines, it is determined that there is no abnormality in the personnel present when sampling.

[0017] By adopting the above technical solution, after confirming that there are no equipment abnormalities or blood abnormalities, the personnel location information and personnel behavior information in the personnel identification information are monitored to determine whether the personnel behavior information meets the preset sampling needle management specifications of the personnel's location. If it does not meet the preset sampling needle management specifications, it indicates that the current personnel has an abnormality, that is, the personnel have abnormal operation. The abnormal operation is displayed on the designated terminal device in the form of maintenance information to inform the current personnel to correct the abnormal error in time and avoid subsequent sampling needle blockage abnormalities.

[0018] In another possible implementation, the method further includes: Determine whether personnel abnormalities related to the sampling needle will cause abnormalities in the blood and equipment. If the abnormality of the person would cause the abnormality of the blood, a blood restoration plan will be generated to restore the blood to normal. If the abnormality of the personnel would cause the abnormality of the equipment, the abnormality of the equipment would be handled to ensure that the sampling needle equipment is functioning normally. If the personnel abnormality can simultaneously cause the blood abnormality and the equipment abnormality, the equipment abnormality is dealt with first to restore the equipment in the sampling needle to normal operation. It is then determined whether the blood abnormality is related to the equipment abnormality. If not, the blood abnormality is restored according to the blood restoration plan.

[0019] By adopting the above technical solution, after handling and eliminating personnel-related abnormalities in the sampling needle, it is still possible that these abnormalities could lead to blood and equipment malfunctions. For example, a personnel abnormality might occur when personnel fail to clean the sampling needle promptly after use, causing residual blood to coagulate and clog the needle tip, thus causing equipment malfunction. Another personnel abnormality might occur when blood is not promptly placed in the designated storage location after collection, leading to blood clots and blood malfunctions. Therefore, it is necessary to determine whether personnel abnormalities will cause blood and equipment malfunctions. If personnel abnormalities will cause blood abnormalities, then these abnormalities should be addressed, such as promptly screening for blood clots and placing the blood in the designated storage location. If personnel abnormalities will cause equipment malfunctions, then the equipment malfunctions should be addressed to ensure the normal operation of the equipment during subsequent blood collection, thereby further reducing the occurrence of sampling needle clogging.

[0020] Secondly, this application provides a sampling needle management device, which adopts the following technical solution: A sampling needle management device, comprising: The acquisition module is used to acquire the sampling data information of the sampling needle when a data acquisition command is detected; The judgment module is used to determine whether there is any abnormality in the sampling needle based on the sampling data information; The information generation module acquires the current time information when the sampling needle is in an abnormal condition, and generates maintenance information based on the current time information and the abnormal condition of the sampling needle. The control display module is used to control the display of the maintenance information.

[0021] By adopting the above technical solution, when managing and maintaining the sampling needle, it is determined whether there is any abnormality in the sampling needle based on the sampling data information. When there is an abnormality, the current time information is obtained and combined with the abnormality to generate maintenance information for the current time period. Medical staff can determine the cause of the abnormality based on the displayed maintenance information and take further maintenance measures for the sampling needle according to the cause, thereby improving the maintenance efficiency of the sampling needle.

[0022] In one possible implementation, the acquisition module, when acquiring the sampling data information of the sampling needle, is specifically used for: The system acquires device status information, blood detection information, and personnel identification information. The personnel identification information includes personnel location information and personnel behavior information. The device status information includes sensor status information and sampling needle status information. The blood detection information is the blood information collected by the sampling needle. The device status information, the blood test information, and the personnel identification information are processed to generate sampling data information.

[0023] In another possible implementation, when the judgment module determines whether the sampling needle has an abnormality based on the sampling data information, it is specifically used for: Based on the device status information, determine whether the sampler has a device malfunction; If the sampling needle has a device malfunction, then the sampling needle is determined to have a first malfunction; If the sampling needle does not have any equipment malfunction, then the presence of blood abnormalities in the blood is determined based on the blood test information. If the blood sample shows an abnormality, then the sampling needle is determined to have a second abnormality. If the blood sample does not show any abnormalities, then the presence of any abnormalities in the sampling needle is determined based on the personnel identification information. If there is an abnormality in the sampling needle, then it is determined that there is a third abnormality in the sampling needle; If there is no abnormality in the sampling needle, then it is determined that there is no abnormality in the sampling needle.

[0024] In another possible implementation, when the determination module determines whether the sampler has a device malfunction based on the device status information, it is specifically used for: Based on the device status information, determine the device status of the sampling needle and the pressure sensor; Determine whether the device state does not conform to the preset state safety standard; If the device status does not meet the preset safety standard, then it is determined that the sampling needle has a device malfunction. If the device status does not meet the preset safety standard, then it is determined that the sampling needle does not have a device malfunction.

[0025] In another possible implementation, when the judgment module determines whether there is a blood abnormality in the blood based on the blood detection information, it is specifically used for: Based on the blood test information, determine the blood parameters in the blood; Determine whether any of the blood parameters do not meet the preset blood parameter thresholds; If any of the blood parameters do not meet the preset blood parameter threshold, then it is determined that the sampling needle has a blood abnormality. If no blood parameter does not meet the preset blood parameter threshold, then it is determined that the sampling needle does not have the blood abnormality.

[0026] In another possible implementation, when the judgment module determines whether there is an abnormality in the sampling needle based on the personnel identification information, it is specifically used for: Based on the personnel identification information, determine the personnel location information and personnel behavior information; The location information of the sampling needle is determined based on the personnel location information; The behavior specifications for the location information are determined according to the preset sampling needle management specifications; Determine whether the person's behavior conforms to the behavioral norms; If the behavior does not conform to the stated code of conduct, it is determined that there is an abnormality in the personnel present when sampling. If the behavior conforms to the aforementioned behavioral guidelines, it is determined that there is no abnormality in the personnel present when sampling.

[0027] In another possible implementation, the device further includes: a linkage judgment module, a first processing module, a second processing module, and a third processing module, wherein, The linkage judgment module is used to determine whether a personnel abnormality in the sampling needle will cause a blood abnormality or a device abnormality. The first processing module is used to generate a blood restoration plan when the abnormality of the person causes the abnormality of the blood, so as to restore the blood to normal. The second processing module is used to process the equipment malfunction when the personnel malfunction causes the equipment malfunction, so as to ensure that the sampling needle equipment is normal. The third processing module is used to first process the equipment malfunction to ensure that the equipment in the sampling needle is functioning normally when the personnel malfunction causes both the blood malfunction and the equipment malfunction. Then, it determines whether the blood malfunction is related to the equipment malfunction. If not, it performs abnormal blood recovery according to the blood recovery plan.

[0028] Thirdly, this application provides an electronic device that adopts the following technical solution: An electronic device comprising: At least one processor; Memory; At least one application, wherein the at least one application is stored in memory and configured to be executed by at least one processor, the at least one application being configured to: execute the above-described management method for sampling needles.

[0029] Fourthly, this application provides a computer-readable storage medium, which adopts the following technical solution: A computer-readable storage medium includes: a computer program that can be loaded by a processor and execute the above-described sampling needle management method.

[0030] In summary, this application includes the following beneficial technical effects: 1. When managing and maintaining the sampling needle, the sampling data information of the sampling needle is used to determine whether there is any abnormality in the sampling needle. When there is an abnormality, the current time information is obtained and combined with the abnormality to generate maintenance information for the current time period. Medical staff can determine the cause of the abnormality based on the displayed maintenance information and take further maintenance measures for the sampling needle according to the cause of the abnormality, thereby improving the efficiency of sampling needle maintenance. 2. After addressing and eliminating personnel-related abnormalities in the sampling needle, these abnormalities may also trigger blood and equipment malfunctions. For example, a personnel abnormality might occur when personnel fail to clean the sampling needle promptly after use, causing residual blood to coagulate and clog the needle tip, thus leading to equipment malfunction. Alternatively, a personnel abnormality might occur when blood is not promptly placed in the designated storage location after collection, resulting in blood clots and thus blood abnormalities. Therefore, it is necessary to determine whether personnel abnormalities will cause blood or equipment malfunctions. If personnel abnormalities will cause blood abnormalities, these should be addressed, such as promptly screening for blood clots and placing the blood in the designated storage location. If personnel abnormalities will cause equipment malfunctions, these should be addressed to ensure the equipment functions normally during subsequent blood collection processes, thereby further reducing the occurrence of sampling needle clogging. Attached Figure Description

[0031] Figure 1 This is a flowchart illustrating the method for managing sampling needles according to an embodiment of this application; Figure 2 This is a block diagram of the sampling needle management device according to an embodiment of this application; Figure 3 This is a schematic diagram of an electronic device according to an embodiment of this application. Detailed Implementation

[0032] The following is in conjunction with the appendix Figure 1-3 This application will be described in further detail.

[0033] After reading this specification, those skilled in the art may make modifications to this embodiment without contributing any inventive step, but such modifications are protected by patent law as long as they fall within the scope of the claims of this application.

[0034] To make the objectives, technical solutions, and advantages of the embodiments of this application clearer, the technical solutions of the embodiments of this application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of this application, not all embodiments. Based on the embodiments of this application, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of this application.

[0035] Furthermore, the term "and / or" in this article is merely a description of the relationship between related objects, indicating that three relationships can exist. For example, A and / or B can represent: A existing alone, A and B existing simultaneously, or B existing alone. Additionally, the character " / " in this article, unless otherwise specified, generally indicates that the preceding and following related objects have an "or" relationship.

[0036] The embodiments of this application will now be described in further detail with reference to the accompanying drawings.

[0037] This application provides a method for managing sampling needles, executed by an electronic device. This electronic device can be a server or a terminal device. The server can be a standalone physical server, a server cluster or distributed system composed of multiple physical servers, or a cloud server providing cloud computing services. The terminal device can be a smartphone, tablet, laptop, desktop computer, etc., but is not limited to these. The terminal device and the server can be directly or indirectly connected via wired or wireless communication. This application does not impose any limitations on this. Figure 1 As shown, the method includes: Step S10: When a data acquisition command is detected, the sampling data information of the sampling needle is acquired.

[0038] Specifically, intelligent data acquisition devices, monitors, and sensors are used to acquire sampling data from the sampling needle.

[0039] The intelligent data acquisition device includes an AD converter, an MCU chip, and a current acquisition chip.

[0040] Step S11: Determine whether there is any abnormality in the sampling needle based on the sampling data information.

[0041] Specifically, the normal sampling status of the sampling needle is obtained by statistical analysis of the historical information of the sampling needle. If the sampling data of the sampling needle differs from the normal status, it can be determined that there is an abnormality in the display case.

[0042] Step S12: If there is an abnormality in the sampling needle, obtain the current time information and generate maintenance information based on the current time information and the abnormality in the sampling needle.

[0043] Specifically, when the sampling needle is abnormal, the current time information is captured so that medical staff can determine the time point when the sampling needle abnormality occurred, and then maintenance information for the sampling needle is generated based on the abnormality.

[0044] Step S13: Control the display of maintenance information.

[0045] Specifically, maintenance information is obtained through a controller, a service, and a DAO. The data access layer is only responsible for interacting with the database and reading data. The service layer needs to write logic code according to the actual business requirements of the system. The business logic layer calls the relevant methods of the data access layer to interact with the database and feeds back the execution results to the controller. The controller sends the location information to the view renderer to render the maintenance information and display it.

[0046] This application provides a method for managing sampling needles. When managing and maintaining the sampling needles, the method determines whether there are any abnormalities in the sampling needles based on the sampling data information. When there are abnormalities, the method obtains the current time information and combines the current time information with the abnormality information to generate maintenance information for the current time period. Medical staff determine the cause of the abnormality based on the displayed maintenance information and take further maintenance measures for the sampling needles based on the cause of the abnormality, thereby improving the efficiency of sampling needle maintenance.

[0047] One possible implementation of this application embodiment is that step S10 specifically includes step S101 (not shown in the figure) and step S102 (not shown in the figure), wherein, Step S101: Obtain device status information, blood test information, and personnel identification information.

[0048] Among them, personnel identification information includes personnel location information and personnel behavior information, equipment status information includes sensor status information and sampling needle status information, and blood detection information is the blood information collected by the sampling needle.

[0049] Specifically, the blood test information is acquired by installing a pressure sensor, a common-mode amplifier circuit, and a differential amplifier circuit inside the sampling needle. The pressure sensor is a Honeywell 26PCDFG6G bridge-type dual-output pressure sensor. The output stages of the pressure sensor are connected to two parallel common-mode amplifier circuits, and the output stages of both common-mode amplifier modules are connected to a differential amplifier circuit. The output stage of the differential amplifier circuit is connected to an AD converter, and the output stage of the AD converter is connected to an MCU chip. After the two common-mode amplifier circuits amplify the pressure signal detected by the pressure sensor, the pressure signal is sent to the differential amplifier circuit for secondary amplification. The AD converter converts the secondary amplified pressure signal into a digital signal and sends it to the MCU chip for integration processing to obtain the blood clot status. The MCU chip then sends the blood clot status to the electronic device, thereby acquiring the blood test information.

[0050] Based on the characteristics of the pressure sensor, the voltage potential of the connecting resistor in the common-mode amplifier circuit is zero. According to the negative feedback characteristics of the integrated operational amplifier, the final amplification factor of the signal can be easily obtained.

[0051] The equipment status information is acquired through several methods: a current sampling resistor is connected in series on the power supply line of the pressure sensor; a MAX4080 current acquisition chip is used to monitor the working status of the pressure sensor in real time and feed it back to the MCU chip; the MCU chip determines the working status of the voltage sensor by detecting the data acquired by the MAX4080 current acquisition chip. Additionally, a monitoring camera is used to acquire images of the sampling needles, which are then input into a pre-trained neural network for training. This generates sampling needle features from multiple images, which are then analyzed sequentially to determine if the sampling needles exhibit abnormalities such as bending or wear.

[0052] The methods for obtaining personnel identification information include: installing multiple monitors in the sampling chamber where the sampling needles are placed, and the monitors recognizing the faces of the personnel using the sampling needles to obtain personnel identification information.

[0053] Step S102: Organize the equipment status information, blood test information, and personnel identification information to generate sampling data information.

[0054] One possible implementation of this application embodiment includes step S111 (not shown in the figure), step S112 (not shown in the figure), step S113 (not shown in the figure), step S114 (not shown in the figure), step S115 (not shown in the figure), step S116 (not shown in the figure), and step S117 (not shown in the figure), wherein, Step S111: Determine whether the sampler has a device malfunction based on the device status information.

[0055] The specific steps for determining whether a display case has an equipment malfunction based on equipment status information include: Determine the status of the sampling needle and pressure sensor based on the equipment status information; Determine if any equipment status does not meet the preset safety standards; Specifically, the preset safety standard is the normal parameter data standard of the sampling needle and pressure sensor. For example, a known pressure is applied to the pressure sensor, and the pressure detected by the pressure sensor is verified to be the same as the known pressure. Alternatively, based on the current value collected by the current acquisition chip and the fixed resistance value, the real-time power of the pressure sensor is determined, and the real-time power is compared with the standard power in the normal parameter data standard to determine whether the current pressure sensor meets the preset safety standard.

[0056] If the device status does not meet the preset safety standard, it is determined that there is a device malfunction in the sampling needle, and step S112 is executed; If the status of the non-existent equipment does not meet the preset safety standard, it is determined that there is no equipment abnormality in the sampling needle, and step S113 is executed; Step S112: If there is a device malfunction in the sampling needle, then it is determined that there is a first malfunction in the sampling needle.

[0057] Step S113: If there is no equipment malfunction in the sampling needle, then determine whether there is a blood malfunction based on the blood test information.

[0058] The specific steps for determining whether there are blood abnormalities based on blood test information include: Based on blood test information, determine the blood parameters in the blood; Determine if any blood parameters do not meet the preset blood parameter thresholds; Specifically, the sampling needle is equipped with a pressure sensor, a common-mode amplifier circuit, and a differential amplifier circuit. The pressure sensor is a Honeywell 26PCDFG6G bridge-type dual-output pressure sensor. The output stages of the pressure sensor are connected to two parallel common-mode amplifier circuits, and the output stages of both common-mode amplifier modules are connected to a differential-mode amplifier circuit. The output stage of the differential-mode amplifier circuit is connected to an AD converter, and the output stage of the AD converter is connected to an MCU chip. After the two common-mode amplifier circuits amplify the pressure signal detected by the pressure sensor, the pressure signal is sent to the differential-mode amplifier circuit for secondary amplification. The AD converter converts the secondary amplified pressure signal into a digital signal and sends it to the MCU chip for integration processing to obtain the blood clot status. The MCU chip sends the blood clot status to the electronic device, thereby obtaining blood detection information.

[0059] If any blood parameters do not meet the preset blood parameter threshold, it is determined that there is a blood abnormality in the sampling needle, and step S114 is executed. If no blood parameters do not meet the preset blood parameter threshold, it is determined that there is no blood abnormality in the sampling needle, and step S115 is executed.

[0060] Step S114: If there is a blood abnormality, then it is determined that there is a second abnormality in the sampling needle.

[0061] Step S115: If there is no abnormality in the blood, determine whether there is a personnel abnormality in the sampling needle based on the personnel identification information.

[0062] The process involves determining whether there are any abnormalities in the sampling needle based on personnel identification information. Specific steps include: Based on personnel identification information, determine personnel location information and personnel behavior information; The location information of the sampling needle is determined based on the personnel location information; Based on the preset sampling needle management specifications, determine the behavioral norms for location information; Determine whether a person's behavior conforms to behavioral norms; If the behavior does not comply with the code of conduct, it is determined that there is an abnormality in the sampling needle, and step S116 is executed; If the behavior is in compliance with the code of conduct, it is determined that there is no abnormality in the sampling needle, and step S117 is executed; Specifically, the location of a person is determined by the person's location information. The locations of each department are known, such as Department 1, Department 2, and Department 3. Different preset sampling needle management specifications are formulated for different departments. For example, the preset sampling needle management specifications for Department 1 are that the sampling needle should be cleaned in time after use and placed in an environment with a temperature of minus ten degrees Celsius.

[0063] Step S117: If there is a personnel abnormality in the sampling needle, then it is determined that there is a third abnormality in the sampling needle.

[0064] If there is no abnormality in the sampling needle in step S118, then it is determined that there is no abnormality in the sampling needle.

[0065] One possible implementation of this application embodiment includes steps S14 (not shown in the figure), S15 (not shown in the figure), S16 (not shown in the figure), and S17 (not shown in the figure) after step S13, wherein... Step S14: Determine whether personnel abnormalities in the sampling needle will cause blood abnormalities and equipment abnormalities.

[0066] Step S15: If a person's abnormality would cause blood abnormality, a blood restoration plan is generated to restore the blood to normal.

[0067] Step S16: If personnel abnormality causes equipment abnormality, then handle the equipment abnormality to ensure that the sampling needle equipment is functioning normally.

[0068] Step S17: If personnel abnormality can cause both blood abnormality and equipment abnormality, the equipment abnormality should be dealt with first to ensure that the equipment in the sampling needle is normal. Determine whether the blood abnormality is related to the equipment abnormality. If not, the blood abnormality should be restored according to the blood restoration plan.

[0069] Specifically, after addressing and eliminating personnel-related abnormalities in the sampling needle, these abnormalities may also trigger blood and equipment malfunctions. For example, a personnel abnormality might occur when personnel fail to clean the sampling needle promptly after use, causing residual blood to coagulate and clog the needle tip, thus leading to equipment malfunction. Alternatively, a personnel abnormality might occur when blood is not promptly placed in the designated storage location after collection, resulting in blood clots and thus blood abnormalities. Therefore, it is necessary to determine whether personnel abnormalities will cause blood or equipment malfunctions. If personnel abnormalities will cause blood abnormalities, these should be addressed, such as promptly screening for blood clots and placing the blood in the designated storage location. If personnel abnormalities will cause equipment malfunctions, these should be addressed to ensure the equipment functions normally during subsequent blood collection processes, thereby further reducing the occurrence of sampling needle clogging.

[0070] The above embodiments describe a sampling needle management method from the perspective of process flow. The following embodiments describe a sampling needle management device from the perspective of virtual module or virtual unit. For details, please refer to the following embodiments.

[0071] This application provides a sampling needle management device, such as... Figure 2 As shown, the device 20 may specifically include: an acquisition module 21, a judgment module 22, an information generation module 23, and a control and display module 24, wherein, The acquisition module 21 is used to acquire the sampling data information of the sampling needle when a data acquisition command is detected; The judgment module 22 is used to determine whether there is an abnormality in the sampling needle based on the sampling data information; The information generation module 23, when there is an abnormality in the sampling needle, obtains the current time information and generates maintenance information based on the current time information and the abnormality of the sampling needle; The control display module 24 is used to control and display maintenance information.

[0072] In one possible implementation of this application embodiment, when acquiring sampling data information from the sampling needle, the acquisition module 21 is specifically used for: Acquire device status information, blood test information, and personnel identification information. Personnel identification information includes personnel location information and personnel behavior information. Device status information includes sensor status information and sampling needle status information. Blood test information is the blood information collected by the sampling needle. The equipment status information, environmental monitoring information, and personnel identification information are organized to generate sampling data.

[0073] In another possible implementation of this application embodiment, when the determination module 22 determines whether there is an abnormality in the sampling needle based on the sampling data information, it is specifically used for: Determine whether the sampler is malfunctioning based on the device status information; If the sampling needle is faulty, then the sampling needle is identified as having the first fault. If there is no equipment malfunction in the sampling needle, then determine whether there is any blood abnormality based on the blood test information; If the blood test shows abnormalities, then the sampling needle is confirmed to have a second abnormality. If no abnormalities are found in the blood, the presence of any abnormalities in the sampling needle is determined based on the personnel identification information. If there is an abnormality in the sampling needle, then it is determined that there is a third abnormality in the sampling needle; If there are no abnormalities in the sampling needle, then it is determined that there are no abnormalities in the sampling needle.

[0074] In another possible implementation of this application embodiment, when the determination module 22 determines whether the sampler has a device malfunction based on the device status information, it is specifically used for: Determine the status of the sampling needle and pressure sensor based on the equipment status information; Determine if any equipment status does not meet the preset safety standards; If the equipment status does not meet the preset safety standards, it is determined that there is an equipment malfunction in the sampling needle; If the status of the non-existent equipment does not meet the preset safety standards, then it is determined that there is no equipment malfunction in the sampling needle.

[0075] In another possible implementation of this application embodiment, when the determination module 22 determines whether there is a blood abnormality based on the blood test information, it is specifically used for: Based on blood test information, determine the blood parameters in the blood; Determine if any blood parameters do not meet the preset blood parameter thresholds; If any blood parameters do not meet the preset blood parameter threshold, it is determined that there is a blood abnormality in the sampling needle; If no blood parameters do not meet the preset blood parameter threshold, it is determined that there is no blood abnormality in the sampling needle.

[0076] In another possible implementation of this application embodiment, when the judgment module 22 determines whether there is a personnel abnormality in the sampling needle based on the personnel identification information, it is specifically used for: Based on personnel identification information, determine personnel location information and personnel behavior information; The location information of the sampling needle is determined based on the personnel location information; Based on the preset sampling needle management specifications, determine the behavioral norms for location information; Determine whether a person's behavior conforms to behavioral norms; If the behavior does not comply with the code of conduct, it is determined that there is an abnormality in the sampling needle. If the behavior conforms to the code of conduct, it is determined that there is no abnormality in the personnel of the sampling needle.

[0077] In another possible implementation of this application embodiment, the device 20 further includes: a linkage judgment module, a first processing module, a second processing module, and a third processing module, wherein, The linkage judgment module is used to determine whether personnel abnormalities in the sampling needle will cause blood abnormalities or equipment malfunctions; The first processing module is used to generate a blood restoration plan when a person's abnormality causes a blood abnormality, so as to restore the blood to normal. The second processing module is used to handle equipment malfunctions caused by personnel abnormalities, so as to ensure that the sampling needle equipment functions normally. The third processing module is used to handle the equipment abnormality first when personnel abnormality can cause both blood abnormality and equipment abnormality, so as to restore the equipment in the sampling needle to normal, determine whether the blood abnormality is related to the equipment abnormality, and if not, restore the blood abnormality according to the blood restoration plan.

[0078] Those skilled in the art will understand that, for the sake of convenience and brevity, the specific working processes of the systems, devices, and units described above can be referred to the corresponding processes in the foregoing method embodiments, and will not be repeated here.

[0079] This application also describes an electronic device from the perspective of a physical device, such as... Figure 3 As shown, Figure 3 The illustrated electronic device 300 includes a processor 301 and a memory 303. The processor 301 and the memory 303 are connected, for example, via a bus 302. Optionally, the electronic device 300 may also include a transceiver 304. It should be noted that in practical applications, the transceiver 304 is not limited to one type, and the structure of this electronic device 300 does not constitute a limitation on the embodiments of this application.

[0080] Processor 301 may be a CPU (Central Processing Unit), a general-purpose processor, a DSP (Digital Signal Processor), an ASIC (Application Specific Integrated Circuit), an FPGA (Field Programmable Gate Array), or other programmable logic devices, transistor logic devices, hardware components, or any combination thereof. It can implement or execute the various exemplary logic blocks, modules, and circuits described in conjunction with the disclosure of this application. Processor 301 may also be a combination that implements computational functions, such as including one or more microprocessor combinations, a combination of a DSP and a microprocessor, etc.

[0081] Bus 302 may include a pathway for transmitting information between the aforementioned components. Bus 302 may be a PCI (Peripheral Component Interconnect) bus or an EISA (Extended Industry Standard Architecture) bus, etc. Bus 302 can be divided into address bus, data bus, control bus, etc. For ease of representation, Figure 3 The bus is represented by a single thick line, but this does not mean that there is only one bus or one type of bus.

[0082] The memory 303 may be a ROM (Read Only Memory) or other type of static storage device capable of storing static information and instructions, RAM (Random Access Memory) or other type of dynamic storage device capable of storing information and instructions, or an EEPROM (Electrically Erasable Programmable Read Only Memory), CD-ROM (Compact Disc Read Only Memory) or other optical disc storage, optical disc storage (including compressed optical discs, laser discs, optical discs, digital universal optical discs, Blu-ray discs, etc.), magnetic disk storage media or other magnetic storage devices, or any other medium capable of carrying or storing desired program code in the form of instructions or data structures and accessible by a computer, but not limited thereto.

[0083] The memory 303 is used to store application code that executes the solution of this application, and its execution is controlled by the processor 301. The processor 301 is used to execute the application code stored in the memory 303 to implement the content shown in the foregoing method embodiments.

[0084] Electronic devices include, but are not limited to: mobile terminals such as mobile phones, laptops, digital radio receivers, PDAs (personal digital assistants), PADs (tablet computers), PMPs (portable multimedia players), and in-vehicle terminals (such as in-vehicle navigation terminals), as well as fixed terminals such as digital TVs and desktop computers. Servers can also be included. Figure 3 The electronic device shown is merely an example and should not impose any limitation on the functionality and scope of use of the embodiments of this application.

[0085] It should be understood that although the steps in the flowcharts of the accompanying figures are shown sequentially as indicated by the arrows, these steps are not necessarily executed in the order indicated by the arrows. Unless explicitly stated herein, there is no strict order restriction on the execution of these steps, and they can be executed in other orders. Moreover, at least some steps in the flowcharts of the accompanying figures may include multiple sub-steps or multiple stages. These sub-steps or stages are not necessarily completed at the same time, but can be executed at different times, and their execution order is not necessarily sequential, but can be performed alternately or in turn with other steps or at least some of the sub-steps or stages of other steps.

[0086] The above are only some embodiments of this application. It should be noted that for those skilled in the art, several improvements and modifications can be made without departing from the principle of this application, and these improvements and modifications should also be considered within the scope of protection of this application.

Claims

1. A method for managing sampling needles, characterized in that, include: When a data acquisition command is detected, the sampling data information of the sampling needle is acquired; Determine whether the sampling needle is abnormal based on the sampling data information; If the sampling needle is abnormal, the current time information is obtained, and maintenance information is generated based on the current time information and the abnormality of the sampling needle. The control displays the maintenance information; The sampling data information obtained from the sampling needle includes: The system acquires device status information, blood detection information, and personnel identification information. The personnel identification information includes personnel location information and personnel behavior information. The device status information includes sensor status information and sampling needle status information. The blood detection information is the blood information collected by the sampling needle. The device status information, the blood test information, and the personnel identification information are processed to generate sampling data information; The process of determining whether the sampling needle is abnormal based on the sampling data information includes: Determine whether the sampling needle is malfunctioning based on the device status information. If the sampling needle has a device malfunction, then the sampling needle is determined to have a first malfunction; If the sampling needle does not have any equipment malfunction, then the presence of blood abnormalities in the blood is determined based on the blood test information. If the blood sample shows an abnormality, then the sampling needle is determined to have a second abnormality. If the blood sample does not show any abnormalities, then the presence of any abnormalities in the sampling needle is determined based on the personnel identification information. If there is an abnormality in the sampling needle, then it is determined that there is a third abnormality in the sampling needle; If there is no abnormality in the sampling needle, then it is determined that there is no abnormality in the sampling needle; The determination of whether the sampling needle is malfunctioning based on the device status information includes: Based on the device status information, determine the device status of the sampling needle and the pressure sensor; Determine if any equipment status does not meet the preset safety standards; If the device status does not meet the preset safety standard, it is determined that the sampling needle has a device malfunction. If no device status does not meet the preset safety standard, then it is determined that the sampling needle does not have any device malfunction. The determination of whether the blood has any abnormalities based on the blood test information includes: Based on the blood test information, determine the blood parameters in the blood; Determine whether any of the blood parameters do not meet the preset blood parameter thresholds; If any of the blood parameters do not meet the preset blood parameter threshold, then it is determined that the sampling needle has a blood abnormality. If no blood parameter does not meet the preset blood parameter threshold, then it is determined that the sampling needle does not have the blood abnormality. The determination of whether there is any abnormality in the sampling needle based on the personnel identification information includes: Based on the personnel identification information, determine the personnel location information and personnel behavior information; The location information of the sampling needle is determined based on the personnel location information; The behavior specifications for the location information are determined according to the preset sampling needle management specifications; Determine whether the person's behavior conforms to the behavioral norms; If the behavior does not conform to the stated code of conduct, it is determined that there is an abnormality in the personnel present when sampling. If the behavior conforms to the aforementioned behavioral guidelines, it is determined that there is no abnormality in the personnel present when sampling.

2. The method of claim 1, wherein, The method further includes: Determine whether personnel abnormalities related to the sampling needle will cause abnormalities in the blood and equipment. If the abnormality of the person would cause the abnormality of the blood, a blood restoration plan will be generated to restore the blood to normal. If the abnormality of the personnel would cause the abnormality of the equipment, the abnormality of the equipment would be handled to ensure that the sampling needle equipment is functioning normally. If the personnel abnormality can simultaneously cause the blood abnormality and the equipment abnormality, the equipment abnormality is dealt with first to restore the equipment in the sampling needle to normal operation. It is then determined whether the blood abnormality is related to the equipment abnormality. If not, the blood abnormality is restored according to the blood restoration plan.

3. A sampling needle management device, characterized in that, include: The acquisition module is used to acquire the sampling data information of the sampling needle when a data acquisition command is detected; The judgment module is used to determine whether there is any abnormality in the sampling needle based on the sampling data information; The information generation module acquires the current time information when the sampling needle is in an abnormal condition, and generates maintenance information based on the current time information and the abnormal condition of the sampling needle. The control display module is used to control the display of the maintenance information; Specifically, when acquiring sampling data information from the sampling needle, the acquisition module is used for: The system acquires device status information, blood detection information, and personnel identification information. The personnel identification information includes personnel location information and personnel behavior information. The device status information includes sensor status information and sampling needle status information. The blood detection information is the blood information collected by the sampling needle. The device status information, the blood test information, and the personnel identification information are processed to generate sampling data information; Specifically, when the judgment module determines whether there is an abnormality in the sampling needle based on the sampling data information, it is used for: Determine whether the sampling needle is malfunctioning based on the device status information. If the sampling needle has a device malfunction, then the sampling needle is determined to have a first malfunction; If the sampling needle does not have any equipment malfunction, then the presence of blood abnormalities in the blood is determined based on the blood test information. If the blood sample shows an abnormality, then the sampling needle is determined to have a second abnormality. If the blood sample does not show any abnormalities, then the presence of any abnormalities in the sampling needle is determined based on the personnel identification information. If there is an abnormality in the sampling needle, then it is determined that there is a third abnormality in the sampling needle; If there is no abnormality in the sampling needle, then it is determined that there is no abnormality in the sampling needle; Specifically, when the judgment module determines whether the sampling needle is malfunctioning based on the device status information, it is used for: Based on the device status information, determine the device status of the sampling needle and the pressure sensor; Determine if any equipment status does not meet the preset safety standards; If the device status does not meet the preset safety standard, it is determined that the sampling needle has a device malfunction. If no device status does not meet the preset safety standard, then it is determined that the sampling needle does not have any device malfunction. Specifically, when the judgment module determines whether there is a blood abnormality in the blood based on the blood detection information, it is used for: Based on the blood test information, determine the blood parameters in the blood; Determine whether any of the blood parameters do not meet the preset blood parameter thresholds; If any of the blood parameters do not meet the preset blood parameter threshold, then it is determined that the sampling needle has a blood abnormality. If no blood parameter does not meet the preset blood parameter threshold, then it is determined that the sampling needle does not have the blood abnormality. Specifically, when the judgment module determines whether there is any abnormality in the sampling needle based on the personnel identification information, it is used for: Based on the personnel identification information, determine the personnel location information and personnel behavior information; The location information of the sampling needle is determined based on the personnel location information; The behavior specifications for the location information are determined according to the preset sampling needle management specifications; Determine whether the person's behavior conforms to the behavioral norms; If the behavior does not conform to the stated code of conduct, it is determined that there is an abnormality in the personnel present when sampling. If the behavior conforms to the aforementioned behavioral guidelines, it is determined that there is no abnormality in the personnel present when sampling.

4. An electronic device, characterized in that, The electronic device includes: At least one processor; Memory; At least one application, wherein the at least one application is stored in memory and configured to be executed by at least one processor, said at least one application being configured to: perform the sampling needle management method according to any one of claims 1 to 2.

5. A computer-readable storage medium having a computer program stored thereon, characterized in that, When the computer program is executed in the computer, it causes the computer to perform the sampling needle management method according to any one of claims 1 to 2.

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