Drop-off sample testing methods, apparatuses, medical testing devices, and readable storage media

Abstract

The application relates to a sample delivery detection method and device, a medical detection equipment and a readable storage medium. The method is applied to the medical detection equipment and comprises the following steps: in response to a login operation triggered by a login object, obtaining an identity of the login object; in the case that the identity is a sample delivery personnel, querying sample delivery order information of the login object; according to the sample delivery order information, determining an order initiator; receiving a reagent tube sample provided by the login object through the medical detection equipment, and detecting the reagent tube sample to generate a detection result report corresponding to the order initiator. The method can improve the sample detection efficiency.

Description

Technical Field

[0001] This application relates to the field of testing equipment technology, and in particular to a method, apparatus, medical testing equipment, and readable storage medium for sample delivery testing. Background Technology

[0002] With the development of medical testing technology, many medical tests can be performed by consumers themselves by purchasing simple reagents. However, many medical tests still require professional medical personnel or medical testing equipment.

[0003] For medical tests that are difficult to perform with simple reagents, consumers currently need to go to the hospital when they experience discomfort and require medical testing. They need to swipe their ID card, fill in the testing information, and then collect samples themselves or have them collected by medical staff. They then have to wait for the medical staff to complete the testing before they can obtain a test report. The testing process is cumbersome and inefficient. Summary of the Invention

[0004] Therefore, it is necessary to provide a sample delivery and testing method, apparatus, medical testing equipment, and readable storage medium that can improve the efficiency of sample testing in addressing the aforementioned technical problems.

[0005] Firstly, this application provides a method for testing samples submitted on behalf of another party, including:

[0006] In response to a login operation triggered by a login object, obtain the login object's identity identifier;

[0007] If the identity is identified as a delivery person, the delivery order information of the logged-in user can be retrieved;

[0008] Based on the delivery order information, determine the recipient of the order;

[0009] The medical testing equipment collects the reagent tube samples provided by the logged-in user, tests the reagent tube samples, and generates a test result report corresponding to the user who initiated the order.

[0010] In one embodiment, the method further includes:

[0011] Obtain the reagent binding information of the order initiator and the sample tube identifier of the reagent tube provided by the logged-in object;

[0012] If the reagent to be used exists in the reagent binding information and the sample tube identifier matches the reagent to be used, then the step of testing the reagent tube sample using medical testing equipment is performed.

[0013] In one embodiment, the method further includes:

[0014] If there is no reagent to be used in the reagent binding information, or if the reagent to be used does not match the sample tube identifier, the holder of the reagent tube sample can be found by querying the sample tube identifier.

[0015] Send a transfer confirmation request to the holder for the transfer of the reagent tube sample to the order initiator;

[0016] In response to the confirmation instruction for the transfer confirmation request, the sample tube identifier of the reagent tube sample is bound to the order initiating object, the reagent binding information of the order initiating object is determined, and the step of testing the reagent tube sample through medical testing equipment is executed.

[0017] In one embodiment, after sending a transfer confirmation request for the reagent tube sample to the holder, the method further includes:

[0018] If a rejection instruction is received for the transfer confirmation request, or if no confirmation instruction for the transfer confirmation request is received within the predetermined waiting period, the reagent tube sample will be refused.

[0019] In one embodiment, the medical testing device is equipped with a first scanning component pointing towards the external environment; acquiring the sample tube identifier of the reagent tube sample provided by the logged-in user includes:

[0020] The first scanning component is used to collect the first scan data of the reagent tube sample.

[0021] The first scan data is identified to obtain the sample tube identifier of the reagent tube sample.

[0022] In one embodiment, the storage compartment of the medical testing device is equipped with a second scanning component; the method for acquiring the sample tube identifier of the reagent tube sample provided by the logged-in user also includes:

[0023] The medical testing equipment is controlled to store the reagent tube samples provided by the logged-in user into the storage compartment.

[0024] The second scanning component collects second scanning data from the reagent tube samples in the storage compartment.

[0025] The second scan data is identified to obtain the sample tube identifier of the reagent tube sample.

[0026] In one embodiment, the method further includes:

[0027] If the device contains reagent tube samples, perform the device locking operation.

[0028] After the reagent tube sample has been tested, unlock the device.

[0029] Secondly, this application also provides a sample delivery and testing device for use in medical testing equipment, comprising:

[0030] The information acquisition module is used to obtain the identity identifier of the login object in response to the login operation triggered by the login object;

[0031] The order query module is used to retrieve the delivery order information of the logged-in user when the user's identity is identified as a delivery person.

[0032] The object determination module is used to determine the order initiator based on the delivery order information;

[0033] The sample testing module is used to collect reagent tube samples provided by the logged-in user through medical testing equipment, test the reagent tube samples, and generate a test result report corresponding to the order initiator.

[0034] Thirdly, this application also provides a medical testing device, including a memory and a processor, wherein the memory stores a computer program, and the processor executes the computer program to perform the following steps:

[0035] In response to a login operation triggered by a login object, obtain the login object's identity identifier;

[0036] If the identity is identified as a delivery person, the delivery order information of the logged-in user can be retrieved;

[0037] Based on the delivery order information, determine the recipient of the order;

[0038] The medical testing equipment collects the reagent tube samples provided by the logged-in user, tests the reagent tube samples, and generates a test result report corresponding to the user who initiated the order.

[0039] Fourthly, this application also provides a computer-readable storage medium having a computer program stored thereon, which, when executed by a processor, performs the following steps:

[0040] In response to a login operation triggered by a login object, obtain the login object's identity identifier;

[0041] If the identity is identified as a delivery person, the delivery order information of the logged-in user can be retrieved;

[0042] Based on the delivery order information, determine the recipient of the order;

[0043] The medical testing equipment collects the reagent tube samples provided by the logged-in user, tests the reagent tube samples, and generates a test result report corresponding to the user who initiated the order.

[0044] Fifthly, this application also provides a computer program product, including a computer program that, when executed by a processor, performs the following steps:

[0045] In response to a login operation triggered by a login object, obtain the login object's identity identifier;

[0046] If the identity is identified as a delivery person, the delivery order information of the logged-in user can be retrieved;

[0047] Based on the delivery order information, determine the recipient of the order;

[0048] The medical testing equipment collects the reagent tube samples provided by the logged-in user, tests the reagent tube samples, and generates a test result report corresponding to the user who initiated the order.

[0049] The aforementioned sample delivery testing method, apparatus, medical testing equipment, and readable storage medium, in response to a login operation triggered by a logged-in user, obtain the user's identity identifier. If the identifier indicates the user is a delivery person, the system retrieves the user's delivery order information. Based on this order information, the system identifies the order initiator, collects the reagent tube samples provided by the logged-in user using the medical testing equipment, tests the samples, and generates a test result report corresponding to the order initiator. This application, by using the user's identity identifier, can determine whether the logged-in user is a delivery person, thereby retrieving their delivery order information, identifying the order initiator, testing the reagent tube samples, and generating a test result report corresponding to the order initiator. Therefore, this application eliminates the need for complex testing procedures; based on the delivery person's order information, it can identify the correspondence between the collected reagent tube samples and the tested personnel, effectively improving the efficiency of sample testing. Attached Figure Description

[0050] To more clearly illustrate the technical solutions in the embodiments of this application or related technologies, the drawings used in the description of the embodiments of this application or related technologies will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this application. For those skilled in the art, other related drawings can be obtained based on these drawings without creative effort.

[0051] Figure 1 This is a diagram illustrating the application environment of a sample delivery and testing method in one embodiment.

[0052] Figure 2 This is a flowchart illustrating a sample delivery and testing method in one embodiment;

[0053] Figure 3 This is a flowchart illustrating the sample delivery and testing method in another embodiment;

[0054] Figure 4 This is a flowchart illustrating the sample delivery and testing method in yet another embodiment;

[0055] Figure 5 This is a structural block diagram of the sample delivery and testing device in one embodiment;

[0056] Figure 6 This is an internal structural diagram of a medical testing device in one embodiment. Detailed Implementation

[0057] To make the objectives, technical solutions, and advantages of this application clearer, the following detailed description is provided in conjunction with the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative and not intended to limit the scope of this application.

[0058] It should be noted that the terms "first," "second," etc., used in this application can be used to describe various elements, but these elements are not limited by these terms. These terms are only used to distinguish the first element from the second element. The terms "comprising" and "having," and any variations thereof, used in this application, are intended to cover non-exclusive inclusion. The term "multiple" used in this application refers to two or more. The term "and / or" used in this application refers to one of the embodiments, or any combination of multiple embodiments.

[0059] It should be noted that the user information (including but not limited to user device information, user personal information, etc.) and data (including but not limited to data used for analysis, stored data, and displayed data) involved in this application are all information and data authorized by the user or fully authorized by all parties, and the collection, use, and processing of related data must comply with relevant regulations. It is understood that the user information and data involved in this application have all undergone anonymization processing to ensure that the relevant data complies with relevant privacy requirements.

[0060] The sample detection method provided in this application embodiment can be applied to, for example... Figure 1In the application environment shown, the medical testing device 102 communicates with the server 104 via a network. A data storage system can store the data that the server 104 needs to process. The data storage system can be integrated onto the server 104, or it can be located in the cloud or on other network servers. The server 104 can store identity information corresponding to different objects. The medical testing device 102 can obtain the identity identifier of the logged-in object by responding to a login operation triggered by the logged-in object. If the identity identifier is a delivery person, it can query the delivery order information of the logged-in object and determine the order initiator based on the delivery order information. Then, the medical testing device 102 tests the reagent tube sample and generates a test result report corresponding to the order initiator. The medical testing device 102 can be, but is not limited to, various medical devices that can be used to test one or more test reagents. The server 104 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.

[0061] In one exemplary embodiment, such as Figure 2 As shown, a method for sample delivery and testing is provided, which can be applied to... Figure 1 Taking the medical testing device 102 as an example, the explanation includes the following steps S110 to S130. Wherein:

[0062] Step S110: In response to the login operation triggered by the login object, obtain the identity identifier of the login object.

[0063] In this embodiment, the login object is an object that is logged in, either on the execution subject (medical testing equipment) or on a terminal device communicating with the execution subject. The login operation can be scanning a QR code, entering an account password, or remote authorization, among other methods.

[0064] It should be noted that the identity identifier can be a label that describes the identity of the logged-in object, such as a regular user, a delivery person, or an administrator.

[0065] This embodiment can display a login interface in response to the selection and detection operation of the login object. The login object can then log in by entering its username and password, scanning a QR code, or performing other login operations on the interface. Furthermore, this embodiment can obtain the login object's identity information (such as username, anonymized real-name authentication information, and identity identifier) ​​in response to the login operation triggered by the login object, and then determine the corresponding identity identifier based on the login object's identity information.

[0066] Step S120: If the identity is identified as a delivery person, retrieve the delivery order information of the logged-in user.

[0067] The delivery order information describes the current delivery order made by the delivery person, and may include the order initiator (i.e., the person who placed the order), the description of the item to be delivered, the delivery person's information, the delivery time, the delivery address, etc.

[0068] If the identity is identified as a delivery person, it means that the logged-in user is not the person being tested, but a delivery person (such as a food delivery worker or courier) delivering the test tube samples. In this embodiment, the delivery order information of the logged-in user can be obtained by sending a query request to the delivery person's order dispatch platform (i.e., the network platform that issues delivery orders to delivery persons).

[0069] Furthermore, in this embodiment, if the identity identifier is not that of a delivery person, the reagent binding information of the logged-in object and the sample tube identifier of the reagent tube sample provided by the logged-in object can be obtained. If there is a reagent to be used in the reagent binding information of the logged-in object and the sample tube identifier matches the reagent to be used, the step of testing the reagent tube sample through medical testing equipment is executed.

[0070] Step S130: Determine the order initiator based on the delivery order information.

[0071] This embodiment can determine the order initiator based on delivery order information. For example, if the delivery person's dispatch platform and the server connected to the medical testing equipment are on the same data platform, or share data, this embodiment can determine the order initiator by traversing the delivery order information. If the delivery person's dispatch platform and the server connected to the medical testing equipment are on different data platforms, or share data, this embodiment can determine the person initiating the delivery order by traversing the delivery order information, and then match this person information with the identity information of various objects on the server connected to the medical testing equipment, identifying the object matching the person information as the order initiator.

[0072] Step S140: Collect the reagent tube samples provided by the logged-in object using medical testing equipment, test the reagent tube samples, and generate a test result report corresponding to the order initiator.

[0073] This embodiment utilizes medical testing equipment to collect reagent tube samples provided by a logged-in user, performs testing on the samples, and generates a test result report corresponding to the logged-in user. For example, if the medical testing equipment is set to test only specified reagent tubes, this embodiment can perform testing on the reagent tube samples according to a predetermined testing operation corresponding to the specified reagent tube, generate a test result report corresponding to the logged-in user, and send the test result report to the logged-in user. For example, if the medical testing equipment can test at least two types of reagent tubes, this embodiment can identify the reagent tube samples to obtain sample tube identifiers, query the reagent tube type corresponding to the sample tube identifier, perform testing on the reagent tube samples according to the testing operation corresponding to the reagent tube type, generate a test result report corresponding to the logged-in user, and send the test result report to the logged-in user. It is understood that if the reagent tube sample has a bound object in this embodiment, the test result report can be sent to the bound object, which can be the logged-in user or other objects. If the reagent tube sample does not have a bound object, the test result report can be sent to the logged-in user. The test result report can be sent via SMS, software push notifications, email, etc.

[0074] Furthermore, this embodiment can update the reagent status of the reagent to be used in the reagent binding information after the reagent tube sample is stored. For example, this embodiment can mark the corresponding reagent to be used in the reagent binding information as used based on the stored reagent tube sample. Of course, this embodiment can also update the reagent status of the corresponding reagent to be used in the reagent binding information after testing the reagent tube sample; this embodiment does not limit this.

[0075] In some embodiments, the method further includes:

[0076] Step S210: With the reagent tube sample contained, perform the device locking operation.

[0077] Step S220: After the reagent tube sample is tested, unlock the device.

[0078] It should be noted that the device lock operation is used to at least prevent the storage of other reagent tube samples. For example, the device lock operation may be to display a designated lock interface on the medical testing device, which is used to refuse to respond to any operation attempts targeting that medical testing device. The device lock operation may also prevent the opening of the storage compartment, prevent the ejection of the storage device, etc.

[0079] In this embodiment, since neither the logged-in user needs to participate in the testing of the reagent tube samples nor the acquisition of the test result report, the logged-in user can leave directly after providing the reagent tube samples to the medical testing equipment. Therefore, to avoid confusion in the test results caused by other users placing other reagent tube samples during the testing process, this embodiment can perform a device lock operation after receiving the reagent tube samples provided by the logged-in user to prevent the receipt of reagent tube samples provided by other users. The device lock operation can be released after the reagent tube sample testing is completed. For reagent tube samples that have completed testing, this embodiment can place the tested reagent tube samples in a designated recycling device or store them in a designated sample storage location.

[0080] In this embodiment, when reagent tube samples are stored, a device locking operation is performed. After the reagent tube samples are tested, the device locking operation is released. This helps to ensure the orderly conduct of reagent tube sample testing and reduces the chance of confusion in the test results.

[0081] In the aforementioned sample delivery testing method, the login identifier of the logged-in user is obtained in response to a login operation triggered by the logged-in user. If the identifier indicates the user is a delivery person, the delivery order information of the logged-in user is retrieved. Based on the delivery order information, the order initiator is determined. The medical testing equipment is used to collect the reagent tube samples provided by the logged-in user, and the reagent tube samples are tested to generate a test result report corresponding to the order initiator. This application can determine whether the logged-in user is a delivery person by using the login identifier, thereby retrieving the login user's delivery order information, determining the order initiator, testing the reagent tube samples, and generating a test result report corresponding to the order initiator. Therefore, this application eliminates the need for a complex testing process. Based on the delivery order information of the delivery person, the correspondence between the collected reagent tube samples and the tested personnel can be identified, effectively improving the efficiency of sample testing.

[0082] In one exemplary embodiment, such as Figure 3 As shown, the method further includes steps S310 to S320. Wherein:

[0083] Step S310: Obtain the reagent binding information of the order initiator and the sample tube identifier of the reagent tube sample provided by the login object;

[0084] Step S320: If the reagent to be used exists in the reagent binding information and the sample tube identifier matches the reagent to be used, perform the step of testing the reagent tube sample using medical testing equipment.

[0085] The reagent binding information describes the association between the order initiator and the test reagent information. For example, the test reagent information may include the reagent's identification information, quantity, purchase time, and type. The reagent identification information may include the test kit box identifier and the reagent tube identifier within the kit. It is understood that the box identifier and tube identifier can use barcodes, QR codes, unique strings, or other identification formats. The reagent to be used is the test reagent bound to the order initiator and in an unused state. The reagent tube sample is the sampled reagent tube.

[0086] This embodiment can query the reagent binding information corresponding to the order initiator based on the identity information of the order initiator. Since the reagent tube identification information can be printed or affixed to the reagent tube in the form of a QR code, barcode, etc., this embodiment can scan the reagent tube sample using a scanning component (such as a camera or barcode scanner) of the medical testing equipment to obtain the sample scan data. Then, the sample scan data is identified to obtain the sample tube identification of the reagent tube sample. For example, the scanning component of the medical testing equipment is positioned to point towards the outside of the medical testing equipment, so that the reagent tube sample displays its identification information on the outside of the medical testing equipment, thus achieving the acquisition of the sample tube identification. Of course, the scanning component can also be placed inside the storage compartment of the medical testing equipment. For example, when the medical testing device is equipped with a first scanning component pointing towards the external environment, since the sample tube identifier of the reagent tube sample can be obtained without placing the sample tube sample into the storage compartment of the medical testing device, this embodiment can control the medical testing device to perform storage operations such as opening or popping out the storage compartment to store the reagent tube sample provided by the order initiator when the reagent binding information contains a reagent to be used and the reagent to be used matches the sample tube identifier. The storage compartment is a mechanism in the medical testing device used to store reagent tube samples. When the storage compartment of the medical testing device is equipped with a second scanning component, since the reagent tube sample needs to be stored in the storage compartment beforehand to obtain the reagent tube identifier, no further storage operation is required when the reagent binding information contains a reagent to be used and the reagent to be used matches the sample tube identifier.

[0087] Furthermore, in this embodiment, if a reagent to be used exists in the reagent binding information and the sample tube identifier matches the reagent to be used, the step of testing the reagent tube sample using medical testing equipment is executed. This application, through the reagent binding information of the order initiator, can determine whether the order initiator has a reagent to be used bound to it, and whether the sample tube identifier of the reagent tube sample matches the reagent to be used. This further verifies the correspondence between the reagent tube sample provided by the logged-in object and the sampled person, ensuring the accuracy of sample testing.

[0088] In some embodiments, the medical testing device is configured with a first scanning component pointing towards the external environment; acquiring the sample tube identifier of the reagent tube sample provided by the logged-in object includes:

[0089] Step S410: First scanning data is acquired by targeting the reagent tube sample with the first scanning component;

[0090] Step S420: Identify and identify the first scan data to obtain the sample tube identifier of the reagent tube sample.

[0091] The medical testing equipment is equipped with a first scanning component that points to the external environment, which refers to the environment outside the medical testing equipment. This allows the first scanning component to obtain the sample tube identification of the reagent tube provided by the user without needing to collect the sample tube. The first scanning component can be a laser scanning component, a linear CCD (Charge-Coupled Device) scanning component, or an image scanning component, and can be selected according to specific needs; this embodiment does not impose any restrictions on this.

[0092] Since the first scanning component of the medical testing equipment is oriented towards the external environment, this embodiment can remind the logged-in user to place the reagent tube sample within the scanning range of the first scanning component through voice, text, or images. Thus, this embodiment can acquire first scan data by targeting the reagent tube sample with the first scanning component, identify the first scan data, and obtain the sample tube identifier for the reagent tube sample.

[0093] The medical testing device in this embodiment is equipped with a first scanning component that points to the external environment, thereby enabling direct and rapid acquisition of the sample tube identification of the reagent tube sample provided by the logged-in object. It is also more suitable for medical testing devices that cannot release the stored reagent tube sample.

[0094] In some embodiments, the storage compartment of the medical testing device is equipped with a second scanning component; acquiring the sample tube identifier of the reagent tube sample provided by the logged-in user further includes:

[0095] Step S510: Control the medical testing equipment to collect the reagent tube sample provided by the logged-in user into the collection compartment;

[0096] Step S520: The second scanning component collects second scanning data for the reagent tube sample in the storage compartment.

[0097] Step S530: Identify and label the second scan data to obtain the sample tube identifier of the reagent tube sample.

[0098] The medical testing equipment includes a second scanning component within its storage compartment. This compartment is used to store reagent tube samples, allowing the second scanning component to obtain the sample tube identification after storing the sample provided by the registered user. The second scanning component can be a laser scanning component, a linear CCD (Charge-Coupled Device) scanning component, or an image scanning component, and can be selected according to specific needs; this embodiment does not impose any restrictions on this.

[0099] Since the second scanning component of the medical testing equipment is located inside the equipment's storage compartment, this embodiment can remind the user to place the reagent tube sample in the storage compartment via voice, text, or images. Furthermore, this embodiment can control the medical testing equipment to store the reagent tube sample provided by the user in the storage compartment, and use the second scanning component to collect second scan data of the sample in the storage compartment. This second scan data is then identified to obtain the sample tube identifier.

[0100] The medical testing equipment in this embodiment is equipped with a second scanning component in its storage compartment, which can reduce the interference of the external environment on the sample tube markings for identifying reagent tube samples.

[0101] In one exemplary embodiment, such as Figure 4 As shown, the method further includes steps S610 to S630. Wherein:

[0102] Step S610: If there is no reagent to be used in the reagent binding information, or if the reagent to be used does not match the sample tube identifier, query the holder of the reagent tube sample according to the sample tube identifier.

[0103] Step S620: Send a transfer confirmation request to the holder for the transfer of the reagent tube sample to the order initiator;

[0104] Step S630: In response to the confirmation instruction for the transfer confirmation request, the sample tube identifier of the reagent tube sample is bound to the order initiating object, the reagent binding information of the order initiating object is determined, and the step of testing the reagent tube sample through medical testing equipment is executed.

[0105] The object holding the reagent tube sample is the object bound to the reagent tube sample. The transfer confirmation request may include description information of the reagent tube sample and description information of the order initiating object.

[0106] In this embodiment, if the reagent to be used is not found in the reagent binding information, or if the reagent to be used does not match the sample tube identifier, it indicates that the order initiator has not bound an unused test reagent, or that the order initiator has not bound a reagent tube sample corresponding to the sample tube identifier. Therefore, this embodiment can query the holder of the reagent tube sample based on the sample tube identifier. A transfer confirmation request for the reagent tube sample is then sent to the holder. The holder can respond to the confirmation instruction in response to the transfer confirmation request. In this embodiment, in response to the confirmation instruction for the transfer confirmation request, the sample tube identifier of the reagent tube sample is bound to the order initiator, confirming it as the reagent binding information of the order initiator, and the step of testing the reagent tube sample using medical testing equipment is executed.

[0107] Furthermore, if there is no corresponding holder for the reagent tube sample, it means that the reagent tube sample is not bound to any object. In this embodiment, the sample tube identifier of the reagent tube sample can be directly bound to the order initiating object, and the reagent binding information of the order initiating object can be determined. Then, the step of testing the reagent tube sample through medical testing equipment can be executed.

[0108] In real-world scenarios, the person holding the reagent sample (the person who binds the reagent) and the person who initiates the order (the person being sampled) may not be the same person. For example, person A (the person holding the reagent) may bind multiple purchased test reagents to themselves, but these test reagents may actually be used by person B (the person who initiates the order). This embodiment uses a transfer confirmation request to establish a binding relationship between the reagent sample and the actual person being sampled, effectively improving the authenticity of the correspondence between the reagent sample and the person being sampled during the reagent testing process.

[0109] In some embodiments, after sending a transfer confirmation request for the reagent tube sample to the holder, the method further includes:

[0110] Step S640: If a rejection instruction for the transfer confirmation request is received, or if no confirmation instruction for the transfer confirmation request is received within a predetermined waiting period, the reagent tube sample is rejected.

[0111] In this embodiment, if a rejection instruction for the transfer confirmation request is received, or if no confirmation instruction for the transfer confirmation request is received within a predetermined waiting period, it indicates that the holder has refused the transfer of the reagent tube sample, and this embodiment can refuse to accept the reagent tube sample. For example, if the reagent tube sample has already been accepted, this embodiment can open or pop out the storage compartment and prompt the logged-in user to retrieve the reagent tube sample. If the reagent tube sample has not been accepted, this embodiment can close or cancel the pop-out of the storage compartment and prompt the logged-in user that the holder of the reagent tube sample has refused permission to transfer the reagent tube sample.

[0112] In this embodiment, if a rejection instruction for a transfer confirmation request is received, or if a confirmation instruction for a transfer confirmation request is not received within a predetermined waiting period, the reagent tube sample will be refused to be accepted, thereby preventing the reagent tube sample from being mistakenly bound.

[0113] It should be understood that although the steps in the flowcharts of the above embodiments are shown sequentially according to 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 above embodiments may include multiple steps or multiple stages. These steps or stages are not necessarily completed at the same time, but can be executed at different times. The execution order of these steps or stages is not necessarily sequential, but can be performed alternately or in turn with other steps or at least some of the steps or stages in other steps. It is understood that the steps in different embodiments can be freely combined as needed, and all non-contradictory solutions formed by such combinations are within the scope of protection of this application.

[0114] Based on the same inventive concept, this application also provides a sample delivery testing device for implementing the sample delivery testing method described above. The solution provided by this device is similar to the solution described in the above method; therefore, the specific limitations in one or more embodiments of the sample delivery testing device provided below can be found in the limitations of the sample delivery testing method described above, and will not be repeated here.

[0115] In one exemplary embodiment, such as Figure 5 As shown, a sample delivery and testing device 700 is provided, applied to medical testing equipment, including: an information acquisition module 710, an order query module 720, a target identification module 730, and a sample testing module 740, wherein:

[0116] The information acquisition module 710 is used to acquire the identity identifier of the login object in response to the login operation triggered by the login object;

[0117] The order query module 720 is used to query the delivery order information of the logged-in user when the user's identity is identified as a delivery person.

[0118] The object determination module 730 is used to determine the order initiator object based on the delivery order information;

[0119] The sample testing module 740 is used to collect reagent tube samples provided by the logged-in object through medical testing equipment, test the reagent tube samples, and generate a test result report corresponding to the order initiator.

[0120] In some embodiments, the sample detection module 740 is further configured to:

[0121] Obtain the reagent binding information of the order initiator and the sample tube identifier of the reagent tube provided by the logged-in object. If there is a reagent to be used in the reagent binding information and the sample tube identifier matches the reagent to be used, execute the step of testing the reagent tube sample through medical testing equipment.

[0122] In some embodiments, the sample delivery and testing device 700 further includes a reagent transfer module for:

[0123] If the reagent to be used is not found in the reagent binding information, or if the reagent to be used does not match the sample tube identifier, the holder of the reagent tube sample is found based on the sample tube identifier. A transfer confirmation request for the transfer of the reagent tube sample to the order initiator is sent to the holder. In response to the confirmation instruction for the transfer confirmation request, the sample tube identifier of the reagent tube sample is bound to the order initiator, and the reagent binding information of the order initiator is determined. Then, the step of testing the reagent tube sample through medical testing equipment is executed.

[0124] In some embodiments, the reagent transfer module is further configured to:

[0125] If a rejection instruction is received for the transfer confirmation request, or if no confirmation instruction for the transfer confirmation request is received within the predetermined waiting period, the reagent tube sample will be refused.

[0126] In some embodiments, the medical testing device is configured with a first scanning component pointing towards the external environment; the information acquisition module 710 is further configured to:

[0127] The first scanning component collects first scanning data from the reagent tube sample, identifies and marks the first scanning data to obtain the sample tube identifier of the reagent tube sample.

[0128] In some embodiments, a second scanning component is disposed within the storage compartment of the medical testing device; the information acquisition module 710 is further configured to:

[0129] The medical testing equipment controls the collection of reagent tube samples provided by the logged-in user into the collection compartment. The second scanning component collects second scanning data of the reagent tube samples in the collection compartment, identifies the second scanning data, and obtains the sample tube identification of the reagent tube samples.

[0130] In some embodiments, the sample delivery and testing device 700 further includes a device locking module for:

[0131] When reagent tube samples are stored, perform the device lock operation; after the reagent tube samples have been tested, release the device lock operation.

[0132] Each module in the aforementioned sample delivery and testing device can be implemented entirely or partially through software, hardware, or a combination thereof. These modules can be embedded in the processor of the medical testing equipment in hardware form or independent of it, or stored in the memory of the medical testing equipment in software form, so that the processor can call and execute the corresponding operations of each module.

[0133] In one exemplary embodiment, a medical testing device is provided. This medical testing device can be a terminal, and its internal structure diagram can be as follows: Figure 6As shown, the medical testing device includes a processor, memory, input / output interface, communication interface, display unit, and input device. The processor, memory, and input / output interface are connected via a system bus, and the communication interface, display unit, and input device are also connected to the system bus via the input / output interface. The processor provides computational and control capabilities. The memory includes non-volatile storage media and internal memory. The non-volatile storage media stores the operating system and computer programs. The internal memory provides the environment for the operation of the operating system and computer programs in the non-volatile storage media. The input / output interface is used for exchanging information between the processor and external devices. The communication interface is used for wired or wireless communication with external terminals; wireless communication can be achieved through Wi-Fi, mobile cellular networks, Near Field Communication (NFC), or other technologies. When the computer program is executed by the processor, it implements a sample testing method. The display unit is used to form a visually visible image and can be a display screen, projection device, or virtual reality imaging device. The display screen can be an LCD screen or an e-ink screen. The input device of the medical testing equipment can be a touch layer covering the display screen, or buttons, a trackball, or a touchpad located on the outer casing of the medical testing equipment, or an external keyboard, touchpad, or mouse. Furthermore, the medical testing equipment may include a scanning component for acquiring scanning data of the reagent tube sample provided by the registered user to identify the sample tube identifier. The medical testing equipment may also include a detection execution component for detecting the reagent tube sample. The medical testing equipment may also include a storage compartment for storing the reagent tube sample.

[0134] Those skilled in the art will understand that Figure 6 The structure shown is merely a block diagram of a portion of the structure related to the present application and does not constitute a limitation on the medical testing equipment to which the present application is applied. Specific medical testing equipment may include more or fewer components than those shown in the figure, or combine certain components, or have different component arrangements.

[0135] In one exemplary embodiment, a computer device is provided, including a memory and a processor, wherein the memory stores a computer program, and the processor executes the computer program to implement the steps in the embodiments described above.

[0136] In one embodiment, a computer-readable storage medium is provided having a computer program stored thereon, which, when executed by a processor, implements the steps in the above embodiments.

[0137] In one embodiment, a computer program product is provided, including a computer program that, when executed by a processor, implements the steps described in the above embodiments.

[0138] Those skilled in the art will understand that all or part of the processes in the methods of the above embodiments can be implemented by a computer program instructing related hardware. This computer program can be stored in a non-volatile computer-readable storage medium. When executed, the computer program can include the processes of the embodiments of the above methods. Any references to memory, databases, or other media used in the embodiments provided in this application can include at least one of non-volatile memory and volatile memory. Non-volatile memory can include read-only memory (ROM), magnetic tape, floppy disk, flash memory, optical memory, high-density embedded non-volatile memory, resistive random access memory (ReRAM), magnetic random access memory (MRAM), ferroelectric random access memory (FRAM), phase change memory (PCM), graphene memory, etc. Volatile memory can include random access memory (RAM) or external cache memory, etc. By way of illustration and not limitation, RAM can take many forms, such as Static Random Access Memory (SRAM) or Dynamic Random Access Memory (DRAM). The databases involved in the embodiments provided in this application may include at least one type of relational database and non-relational database. Non-relational databases may include, but are not limited to, blockchain-based distributed databases. The processors involved in the embodiments provided in this application may be general-purpose processors, central processing units, graphics processing units, digital signal processors, programmable logic devices, quantum computing-based data processing logic devices, artificial intelligence (AI) processors, etc., and are not limited to these.

[0139] The technical features of the above embodiments can be combined in any way. For the sake of brevity, not all possible combinations of the technical features in the above embodiments are described. However, as long as there is no contradiction in the combination of these technical features, they should be considered to be within the scope of this application.

[0140] The above embodiments are merely illustrative of several implementation methods of this application, and their descriptions are relatively specific and detailed. However, they should not be construed as limiting the scope of this application. It should be noted that those skilled in the art can make various modifications and improvements without departing from the concept of this application, and these all fall within the protection scope of this application. Therefore, the protection scope of this application should be determined by the appended claims.

Claims

1. A method for testing samples delivered on behalf of others, characterized in that, Applied to medical testing equipment, the method includes: In response to a login operation triggered by a login object, obtain the identity identifier of the login object; If the identity is identified as a delivery person, the delivery order information of the logged-in user can be retrieved. Based on the delivery order information, determine the recipient of the order; The medical testing equipment collects the reagent tube samples provided by the logged-in user, tests the reagent tube samples, and generates a test result report corresponding to the order initiator.

2. The method according to claim 1, characterized in that, The method further includes: Obtain the reagent binding information of the order initiating object, and the sample tube identifier of the reagent tube sample provided by the login object; If a reagent to be used exists in the reagent binding information and the sample tube identifier matches the reagent to be used, the steps of collecting the reagent tube sample provided by the logged-in object through the medical testing device and testing the reagent tube sample are performed.

3. The method according to claim 2, characterized in that, The method further includes: If there is no reagent to be used in the reagent binding information, or if the reagent to be used does not match the sample tube identifier, the holder of the reagent tube sample can be found based on the sample tube identifier. Send a transfer confirmation request to the holder for the transfer of the reagent tube sample to the order initiator; In response to the confirmation instruction for the transfer confirmation request, the sample tube identifier of the reagent tube sample is bound to the order initiating object, the reagent binding information of the order initiating object is determined, and the steps of receiving the reagent tube sample provided by the logged-in object through the medical testing equipment and testing the reagent tube sample are executed.

4. The method according to claim 3, characterized in that, After sending a transfer confirmation request for the reagent tube sample to the holder, the method further includes: If a rejection instruction is received for the transfer confirmation request, or if no confirmation instruction is received for the transfer confirmation request within a predetermined waiting period, the reagent tube sample shall be refused.

5. The method according to claim 2, characterized in that, The medical testing equipment is equipped with a first scanning component that points towards the external environment; Obtaining the sample tube identifier of the reagent tube sample provided by the logged-in object includes: First scanning data is obtained by using the first scanning component to scan the reagent tube sample; The first scan data is identified to obtain the sample tube identifier of the reagent tube sample.

6. The method according to claim 2, characterized in that, The medical testing equipment is equipped with a second scanning component in its storage compartment; the method for acquiring the sample tube identifier of the reagent tube sample provided by the logged-in user also includes: The medical testing equipment is controlled to collect the reagent tube samples provided by the logged-in user into the storage compartment. The second scanning component collects second scanning data from the reagent tube samples in the storage compartment. The second scan data is identified to obtain the sample tube identifier of the reagent tube sample.

7. The method according to any one of claims 1 to 6, characterized in that, The method further includes: With the reagent tube sample contained therein, perform a device locking operation; After the reagent tube sample has been tested, the device lock operation is released.

8. A sample delivery and testing device, characterized in that, The device is used in medical testing equipment and includes: The information acquisition module is used to acquire the identity identifier of the login object in response to the login operation triggered by the login object; The order query module is used to query the delivery order information of the logged-in object when the identity is identified as a delivery person; The object determination module is used to determine the order initiating object based on the delivery order information; The sample testing module is used to collect reagent tube samples provided by the logged-in user through the medical testing equipment, test the reagent tube samples, and generate a test result report corresponding to the order initiator.

9. A medical testing device, comprising a memory and a processor, wherein the memory stores a computer program, characterized in that, When the processor executes the computer program, it implements the steps of the method according to any one of claims 1 to 7.

10. A computer-readable storage medium having a computer program stored thereon, characterized in that, When the computer program is executed by a processor, it implements the steps of the method according to any one of claims 1 to 7.

Images