Microorganism detection system and method for displaying microorganism detection information

Abstract

The embodiment of the application discloses a kind of microbial detection system and the display method of microbial detection information, microbial detection system includes at least one microbial detection device, display device and control component, control component is used to control display device to show sample list area, sample list area is used to show the sample list of part or all samples in microbial detection system;Control component determines target sample in sample list according to first interactive instruction, and controls display device to show the patient information and sample information of target sample in sample detail area, and shows the detection result of all culture bottles of target sample in sample result area;Also determine target culture bottle in the detection result of all culture bottles according to second interactive instruction, and control display device to show the result details of target culture bottle in result detail area.Based on this, the embodiment of the application can intuitively show the clinical value reference information of patient, and facilitate detection personnel to judge the accuracy of sample detection result.

Description

Technical Field

[0001] This application relates to the field of medical device technology, and in particular to a microbial detection system and a method for displaying microbial detection information. Background Technology

[0002] A blood culture testing facility is a microbiological testing device used to detect the presence of bacteria in blood samples. It plays a crucial role in determining the presence of bacteria in a patient's blood for accurate diagnosis. During use, blood culture testing facilities incubate and test blood samples. For example, by incubating and testing the blood sample, a microbial growth curve is obtained, allowing doctors to make diagnoses based on this curve.

[0003] Currently, blood culture testing employs a "double-bottle, double-sided" blood collection method. This involves collecting blood from both upper limb veins of the subject, with two culture bottles taken from each side: one for anaerobic bacteria culture and the other for aerobic bacteria culture. This method aims to improve the detection rate of pathogenic microorganisms and ensure a comprehensive assessment of potential infections. However, existing sample testing instruments typically display results only for a single culture bottle, providing limited information. Many factors influence sample testing results, including but not limited to sampling timing, patient antibiotic use, contamination during sample processing, and transport time. Therefore, the current method of displaying sample testing results cannot intuitively reflect the true state of the patient's body, easily leading to misinterpretation of the results by testing personnel. Summary of the Invention

[0004] The following is an overview of the subject matter described in detail in this application. This overview is not intended to limit the scope of the claims.

[0005] This application provides a microbial detection system and a method for displaying microbial detection information, which can intuitively display the clinical value reference information of patients and facilitate the testing personnel to judge the accuracy of sample test results.

[0006] In a first aspect, embodiments of this application provide a microbial detection system, comprising:

[0007] At least one microbial detection device, said microbial detection device being used to detect samples;

[0008] The display device includes a display area, the display area including a sample information management interface, the sample information management interface including a sample list area, a sample details area, a sample result area, and a result details area;

[0009] A control component is configured to control the display device to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system; the control component is further configured to acquire a first interaction instruction, determine a target sample in the sample list according to the first interaction instruction, and control the display device to display the patient information and sample information of the target sample in the sample details area, and display the test results of all culture bottles of the target sample in the sample result area; the control component is further configured to acquire a second interaction instruction, determine a target culture bottle from the test results of all culture bottles according to the second interaction instruction, and control the display device to display the result details of the target culture bottle in the result details area.

[0010] In one embodiment of this application, the at least one microbial detection device includes at least one blood culture instrument. The blood culture instrument includes an incubation module and a detection module. The incubation module is used to load at least one culture bottle corresponding to the sample and to culture the microorganisms in the culture bottle. The detection module is used to detect the growth of the microorganisms in the culture bottle to obtain the sample detection information.

[0011] The sample list displays at least the blood culture samples detected by the blood culture instrument. The sample information displayed in the sample details area is the sample information of the target blood culture sample determined according to the first interactive command. The culture bottle detection results displayed in the result details area are the blood culture bottle detection results corresponding to the target blood culture sample.

[0012] In one embodiment of this application, the patient information includes at least one of the following:

[0013] Clinical diagnostic information;

[0014] Medication information;

[0015] Patient type information;

[0016] Patient's department information;

[0017] Gender information;

[0018] Age information;

[0019] Birth time information;

[0020] Patient identification information;

[0021] Medical history information;

[0022] Allergy history information;

[0023] Historical information on drug resistance;

[0024] Patient notes.

[0025] In one embodiment of this application, the sample information includes at least one of the following:

[0026] Information on the department where the sample was submitted for testing;

[0027] Sample source information;

[0028] Sample identification information;

[0029] Sample type information;

[0030] Sample category information;

[0031] Sample sampling time;

[0032] Sample loading time;

[0033] Sample transport time;

[0034] Sample review time;

[0035] Sample validity information;

[0036] Sample review information;

[0037] Sample processing status information;

[0038] Sample notes.

[0039] In one embodiment of this application, the sample result area is further used to display at least one of the following culture flask information:

[0040] Culture bottle labeling information;

[0041] Information on culture flask type;

[0042] Information on the status of the culture flask;

[0043] Location information of the culture flask;

[0044] Reloading information for culture flasks;

[0045] Information on the detection time of the culture flask;

[0046] Time required to complete the testing of the culture flask.

[0047] In one embodiment of this application, the result details area is further used to display at least one of the following information:

[0048] The growth curve of the microorganisms in the culture flask;

[0049] Culture bottle labeling information;

[0050] Information on culture flask type;

[0051] Information on the status of the culture flask;

[0052] Location information of the culture flask;

[0053] Reloading information for culture flasks;

[0054] The sample size information of the culture flask;

[0055] Loading time information for culture flasks;

[0056] Information on the delayed loading time of the culture flask;

[0057] Information on the detection time of the culture flask;

[0058] Information on the detection interval of the culture flask;

[0059] Information on the detection time of the culture flask;

[0060] Unloading time information for culture flasks;

[0061] Information on the expiration date of culture flasks;

[0062] Time required to complete the testing of the culture flask;

[0063] Information on the longest detection time for sample bottles;

[0064] Preliminary negative test results.

[0065] In one embodiment of this application, the result details area is further used to display the delayed loading time of the selected target culture flask. When the delayed loading time is greater than a preset time, the delayed loading time is highlighted in the result details area. Preferably, the preset time is 2 hours.

[0066] In one embodiment of this application, determining the target sample in the sample list according to the first interactive instruction includes at least one of the following:

[0067] The first interactive instruction includes a filtering instruction and a sample selection instruction. After the control component filters the samples in the sample list area according to the filtering instruction, it displays the filtered sample list. The control component determines the target sample from the filtered sample list according to the sample selection instruction.

[0068] The first interactive instruction is a filtering instruction. The control component filters the samples in the sample list area according to the filtering instruction. The target sample is determined in the filtered sample list according to a preset rule. Preferably, the preset rule is that the first sample in the sample list is the target sample, or the abnormal sample in the sample list is the target sample.

[0069] The first interactive instruction is a sample selection instruction, and the control component determines the target sample from the sample list according to the selection instruction;

[0070] The first interactive instruction is sample information input by the user, and the control component determines the target sample from the sample list based on the sample information;

[0071] The first interactive instruction is sample information obtained by scanning and identifying the sample. The control component searches for and determines the target sample in the sample list based on the sample information.

[0072] In one embodiment of this application, the control component is further configured to control the display device to display a diagram of the operating path of the selected sample and / or the selected culture flask between different detection devices.

[0073] In one embodiment of this application, the operation path diagram is displayed synchronously with the sample information of the selected sample in the display area, and / or synchronously with the detection results of the selected culture flask in the display area;

[0074] Alternatively, the result details area includes a first control, and the control component, in response to receiving a user's trigger information for the first control, controls the display device to display a path diagram of the target culture flask. Preferably, the path diagram is displayed via a separate pop-up window and / or in the result details area; wherein the path diagram includes loading and unloading time information of different testing devices for the target culture flask, and / or includes the location identifier of the current position of the target culture flask, and / or includes information on the departments the target culture flask passes through during its operation, and / or includes information on the testing devices.

[0075] In one embodiment of this application, in the sample list area, samples with abnormal results are highlighted, and / or, in the sample list area, samples with abnormal results are highlighted, and / or, in the sample result area, the test results of culture bottles with abnormal results are highlighted, and / or, in the result details area, abnormal culture bottle information is highlighted.

[0076] In the sample list area, the selected sample is highlighted; and / or, in the sample result area, the selected culture flask is highlighted; and / or, in the sample list area, the sample pointed to by the cursor is highlighted; and / or, in the sample result area, the culture flask pointed to by the cursor is highlighted. Wherein, in the sample list area, if the selected target sample is a sample with abnormal results, then both highlighting the target sample and highlighting the abnormal results are performed; and / or, if the selected target sample is a normal sample, then both highlighting the target sample and highlighting the normal results are performed; and / or, if the selected target sample is a sample with abnormal results, then both highlighting the target sample and highlighting the sample with abnormal results are performed.

[0077] And / or, if the sample pointed to by the cursor is a sample with abnormal results, then the sample is highlighted with a first pointing; and / or, if the sample pointed to by the cursor is a normal sample, then the sample is highlighted with a second pointing; if the sample pointed to by the cursor is a sample with abnormal results, then the sample is highlighted with a third pointing.

[0078] In one embodiment of this application, the sample information displayed in the sample details area is the sample information corresponding to the target detection item, and / or, the culture bottle detection result displayed in the sample result area is the detection result corresponding to the target detection item;

[0079] The target detection item is either a detection item selected by the user or a detection item determined by the control component according to preset rules, wherein the preset rules are one of the following:

[0080] Default detection items;

[0081] The latest tested item in the sample;

[0082] The earliest item tested in the sample;

[0083] The testing items include at least one of the following:

[0084] Blood culture test;

[0085] Antimicrobial susceptibility testing;

[0086] Mass spectrometry detection.

[0087] In one embodiment of this application, the display area further displays a plurality of detection item selection controls corresponding to different detection items. The control component obtains the user's operation information on the detection item selection controls and determines the target detection item based on the operation information. Preferably, each of the detection item selection controls is arranged and displayed in the display area in the style of a label.

[0088] Secondly, embodiments of this application provide a method for displaying microbial detection information. The microbial detection system includes at least one microbial detection device and a display device. The display area includes a sample information management interface, which includes a sample list area, a sample details area, a sample result area, and a result details area. The display method includes:

[0089] The display device is controlled to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system;

[0090] Obtain a first interaction instruction, and determine the target sample from the sample list according to the first interaction instruction;

[0091] The display device is controlled to display patient information and sample information of the target sample in the sample details area, and to display the test results of all culture bottles of the target sample in the sample results area;

[0092] Obtain a second interactive instruction, and determine the target culture flask from the detection results of all culture flasks according to the second interactive instruction;

[0093] The display device is controlled to display the result details of the target culture flask in the result details area.

[0094] In one embodiment of this application, it further includes:

[0095] Obtain the delayed loading time of the target culture flask;

[0096] The delayed loading time is displayed in the results details area. If the delayed loading time is greater than a preset time, the delayed loading time is highlighted in the results details area. Preferably, the preset time is 2 hours.

[0097] In one embodiment of this application, determining the target sample in the sample list according to the first interactive instruction includes at least one of the following:

[0098] The first interactive instruction includes a filtering instruction and a sample selection instruction. After the control component filters the samples in the sample list area according to the filtering instruction, it displays the filtered sample list. The control component determines the target sample from the filtered sample list according to the sample selection instruction.

[0099] The first interactive instruction is a filtering instruction. The control component filters the samples in the sample list area according to the filtering instruction. The target sample is determined in the filtered sample list according to a preset rule. Preferably, the preset rule is that the first sample in the sample list is the target sample, or the abnormal sample in the sample list is the target sample.

[0100] The first interactive instruction is a sample selection instruction, and the control component determines the target sample from the sample list according to the selection instruction;

[0101] The first interactive instruction is sample information input by the user, and the control component determines the target sample from the sample list based on the sample information;

[0102] The first interactive instruction is sample information obtained by scanning and identifying the sample. The control component searches for and determines the target sample in the sample list based on the sample information.

[0103] In one embodiment of this application, the sample information management interface is further configured to display a path diagram of the target sample and / or the target culture flask moving between different detection devices. The path diagram is displayed synchronously with the sample information of the target sample in the display area, and / or synchronously with the detection results of the target sample in the display area. Preferably, the path diagram includes loading time information and unloading time information of the target culture flask by different detection devices, and / or includes a location identifier marking the current position of the target culture flask, and / or includes information on the departments through which the target culture flask passes during its movement, and / or includes information on the detection devices.

[0104] In one embodiment of this application, the result details area includes a first control, and the display method further includes:

[0105] The system obtains user trigger information for the first control and displays the operation path diagram of the target culture flask in response to the trigger information. Preferably, the operation path diagram is displayed through a separate pop-up window and / or in the result details area.

[0106] In one embodiment of this application, controlling the display device to display patient information and sample information of the target sample in the sample details area, and to display the test results of all culture bottles of the target sample in the sample results area, includes:

[0107] Determine the target detection items corresponding to the target sample;

[0108] The sample details area displays patient information corresponding to the target sample and sample information corresponding to the target detection item.

[0109] The display of the detection results of all culture flasks of the target sample in the sample result area includes:

[0110] The sample results area displays the detection results of all culture bottles corresponding to the target detection item for the target sample;

[0111] The target detection items include at least one of the following:

[0112] Blood culture test;

[0113] Drug allergy testing;

[0114] Mass spectrometry detection.

[0115] In one embodiment of this application, the sample information management interface further includes multiple detection item selection controls distributed to correspond to different detection items. Preferably, each of the detection item selection controls is arranged and displayed in the display area in the style of a label. Determining the target detection item corresponding to the target sample includes one of the following:

[0116] Obtain user operation information on the detection item selection control, and determine the target detection item based on the operation information.

[0117] Alternatively, the target detection item is determined according to a preset rule, wherein the preset rule is one of the following: the default detection item, the latest detected item of the sample, and the earliest detected item of the sample.

[0118] The embodiments of this application include at least the following beneficial effects:

[0119] On one hand, an embodiment of this application provides a microbial detection system, including at least one microbial detection device, a display device, and a control component. The microbial detection device is used to detect samples. The display device includes a display area, which includes a sample information management interface. The sample information management interface includes a sample list area, a sample details area, a sample result area, and a result details area. The control component is used to control the display device to display the sample list area, which displays a sample list of some or all samples in the microbial detection system. The control component is also used to acquire a first interactive instruction, determine a target sample in the sample list according to the first interactive instruction, and control the display device to display the patient information and sample information of the target sample in the sample details area, and to display the detection results of all culture bottles of the target sample in the sample result area. The control component is also used to acquire a second interactive instruction, determine the target culture bottle from the detection results of all culture bottles according to the second interactive instruction, and control the display device to display the result details of the target culture bottle in the result details area. In this embodiment, the sample list area, sample details area, sample result area, and result details area can be displayed simultaneously on the sample information management interface, so that medical personnel can quickly obtain all clinical value reference information of the patient. Compared to existing technologies that only display the test results of a single culture flask of the target sample, requiring users to navigate to other flasks to view their results, this application embodiment displays the test results of all culture flasks of the target sample on a single interface. This is more intuitive and convenient, eliminating the need for medical personnel to perform multiple operations to view the results of all flasks. Furthermore, it displays patient and sample information for the target sample, providing more comprehensive information. The result details area displays detailed results for the target culture flasks, directly reflecting the patient's actual condition and preventing misinterpretation by testing personnel, thus facilitating the assessment of the accuracy of the sample test results. Therefore, this application embodiment can intuitively display the patient's clinical value reference information, making it easier for testing personnel to determine the accuracy of the sample test results.

[0120] On the other hand, one embodiment of this application provides a method for displaying microbial detection information. The microbial detection system includes at least one microbial detection device and a display device. The display area includes a sample information management interface, which includes a sample list area, a sample details area, a sample result area, and a result details area. The display method includes: controlling the display device to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system; obtaining a first interaction instruction and determining a target sample in the sample list according to the first interaction instruction; controlling the display device to display patient information and sample information of the target sample in the sample details area, and displaying the test results of all culture bottles of the target sample in the sample result area; obtaining a second interaction instruction and determining the target culture bottle from the test results of all culture bottles according to the second interaction instruction; and controlling the display device to display the result details of the target culture bottle in the result details area. In this embodiment, the sample list area, sample details area, sample result area, and result details area can be displayed simultaneously on the sample information management interface, so that medical personnel can quickly obtain all clinical value reference information of the patient. Compared to existing technologies that only display the test results of a single culture flask of the target sample, requiring users to navigate to other flasks to view their results, this application embodiment displays the test results of all culture flasks of the target sample on a single interface. This is more intuitive and convenient, eliminating the need for medical personnel to perform multiple operations to view the results of all flasks. Furthermore, it displays patient and sample information for the target sample, providing more comprehensive information. The result details area displays detailed results for the target culture flasks, directly reflecting the patient's actual condition and preventing misinterpretation by testing personnel, thus facilitating the assessment of the accuracy of the sample test results. Therefore, this application embodiment can intuitively display the patient's clinical value reference information, making it easier for testing personnel to determine the accuracy of the sample test results.

[0121] Other features and advantages of the embodiments of this application will be set forth in the following description, and will be apparent in part from the description, or may be learned by practicing the embodiments of this application. The objects and other advantages of the embodiments of this application may be realized and obtained by means of the structures particularly pointed out in the description, claims and drawings. Attached Figure Description

[0122] The accompanying drawings are used to provide a further understanding of the technical solutions of this application and constitute a part of the specification. They are used together with the embodiments of this application to explain the technical solutions of this application and do not constitute a limitation on the technical solutions of this application.

[0123] Figure 1 This is a structural block diagram of a microbial detection system provided in one embodiment of this application;

[0124] Figure 2This is a schematic diagram of a sample information management interface provided in one embodiment of this application;

[0125] Figure 3 This is a schematic diagram of the operation path displayed in the sample information management interface according to one embodiment of this application;

[0126] Figure 4 This is a schematic diagram of a detection item label provided in one embodiment of this application;

[0127] Figure 5 This is a flowchart of a method for displaying microbial detection information according to an embodiment of this application;

[0128] Figure 6 This is a flowchart of steps S201 to S202 provided in one embodiment of this application;

[0129] Figure 7 This is a flowchart of steps S301 to S303 provided in one embodiment of this application. Detailed Implementation

[0130] The present application will be further described below with reference to the accompanying drawings and specific embodiments. The described embodiments should not be considered as limitations on the present application, and all other embodiments obtained by those skilled in the art without inventive effort are within the scope of protection of the present application.

[0131] In the following description, references are made to “some embodiments,” which describe a subset of all possible embodiments. However, it is understood that “some embodiments” may be the same subset or different subsets of all possible embodiments and may be combined with each other without conflict.

[0132] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this application belongs. The terminology used herein is for the purpose of describing embodiments of this application only and is not intended to limit this application.

[0133] The terms “first,” “second,” “third,” “fourth,” etc. (if present) in the specification and accompanying drawings of this application are used to distinguish similar objects and are not necessarily used to describe a specific order or sequence. It should be understood that such data can be interchanged where appropriate so that embodiments of the application described herein can be implemented, for example, in orders other than those illustrated or described herein. Furthermore, the terms “comprising” and “having,” and any variations thereof, are intended to cover a non-exclusive inclusion; for example, a process, method, system, product, or apparatus that comprises a series of steps or units is not necessarily limited to those steps or units explicitly listed, but may include other steps or units not explicitly listed or inherent to such processes, methods, products, or apparatuses.

[0134] A blood culture testing facility is a microbiological testing device used to detect the presence of bacteria in blood samples. It plays a crucial role in determining the presence of bacteria in a patient's blood for accurate diagnosis. During use, blood culture testing facilities incubate and test blood samples. For example, by incubating and testing the blood sample, a microbial growth curve is obtained, allowing doctors to make diagnoses based on this curve.

[0135] Currently, blood culture testing employs a "double-bottle, double-sided" blood collection method. This involves collecting blood from both upper limb veins of the subject, with two culture bottles taken from each side: one for anaerobic bacteria culture and the other for aerobic bacteria culture. This method aims to improve the detection rate of pathogenic microorganisms and ensure a comprehensive assessment of potential infections. However, existing sample testing instruments typically display results only for a single culture bottle, providing limited information. Many factors influence sample testing results, including but not limited to sampling timing, patient antibiotic use, contamination during sample processing, and transport time. Therefore, the current method of displaying sample testing results cannot intuitively reflect the true state of the patient's body, easily leading to misinterpretation of the results by testing personnel.

[0136] Based on this, this application provides a microbial detection system and a method for displaying microbial detection information, which can intuitively display the clinical value reference information of patients and facilitate the testing personnel to judge the accuracy of sample test results.

[0137] This application provides a microbial detection system that can intuitively display the clinical value reference information of patients, facilitating the assessment of the accuracy of sample test results by testing personnel. For example... Figure 1 The diagram shown is a structural block diagram of a microbial detection system. The microbial detection system 100 may include at least one microbial detection device 110, a display device 120, and a control component 130.

[0138] It should be noted that, Figure 1 The structure shown is for illustrative purposes only and may include more... Figure 1 The more or fewer components shown, or having the same Figure 1 The different configurations shown. Figure 1 The components shown can be implemented in hardware and / or software.

[0139] The microbial detection device 110 is used to detect samples. The microbial detection device 110 includes, but is not limited to, medical testing devices such as blood culture instruments, mass spectrometers, and drug sensitivity identification equipment. Different microbial detection devices 110 can be placed in different departments of hospitals or testing institutions. Samples include, but are not limited to, blood samples, urine samples, stool samples, sputum samples, fluid samples, and secretion samples.

[0140] like Figure 2 As shown, the display device 120 includes a display area, which includes a sample information management interface 121. The sample information management interface 121 includes a sample list area 122, a sample details area 123, a sample result area 124, and a result details area 125. Specifically, the sample list area 122 displays a list of some or all samples in the microbial detection system; the sample details area 123 displays patient and sample information for the target sample; the sample result area 124 displays the test results for all culture bottles of the target sample; and the result details area 125 displays the result details for the target culture bottle. The sample list area 122, sample details area 123, sample result area 124, and result details area 125 are displayed simultaneously on the sample information management interface 121, forming a patient-centered integrated layout of sample information. This facilitates reference by medical personnel and allows testing personnel to efficiently assess the accuracy of sample test results.

[0141] Regarding the display layout of the sample list area 122, sample details area 123, sample results area 124, and results details area 125 on the sample information management interface 121, the sample list area 122 and sample details area 123 can be displayed on the left side of the sample information management interface 121, and the sample results area 124 and results details area 125 can be displayed on the right side of the sample information management interface 121. The sample list area 122 and sample details area 123 can be arranged horizontally, and the sample results area 124 and results details area 125 can be arranged vertically, so that medical staff can view the information according to the information flow of the sample list area 122, sample details area 123, sample results area 124, and results details area 125, which is more in line with reading habits. However, it should be noted that the embodiments of this application are not limited to the display layout described above. Regardless of the display layout, the sample list area 122, sample details area 123, sample results area 124, and results details area 125 can be displayed simultaneously on the sample information management interface 121, so that medical personnel can quickly obtain all the clinical value reference information of the patient. It should be noted that the clinical value reference information may include, but is not limited to, clinical diagnostic information, drug use, transportation time, delayed loading time, sample volume, and expiration date.

[0142] The control component 130 is used to control the display device 120 to display the sample list area 122, which is used to display a sample list of some or all samples in the microbial detection system. The control component 130 is also used to acquire a first interactive instruction, determine the target sample in the sample list according to the first interactive instruction, and control the display device 120 to display the patient information and sample information of the target sample in the sample details area 123, and to display the test results of all culture bottles of the target sample in the sample result area 124. The control component 130 is also used to acquire a second interactive instruction, determine the target culture bottle from the test results of all culture bottles according to the second interactive instruction, and control the display device 120 to display the result details of the target culture bottle in the result details area 125. In other words, for example, when medical personnel select a target sample from the sample list, the sample details area 123 will display the patient information and sample information of the target sample, and the sample results area 124 will display the test results of all culture bottles of the target sample. Compared with the prior art, which only displays the test results of a single culture bottle of the target sample and requires page jump to view other culture bottles, this embodiment can display the test results of all culture bottles of the target sample on the same interface, which is more intuitive and convenient, and does not require medical personnel to perform multiple operations to view the test results of all culture bottles. Moreover, it can also display the patient information and sample information of the target sample, and the displayed information is more comprehensive. For another example, when medical personnel select a target culture bottle from the test results of all culture bottles, the result details area 125 will display the result details of the target culture bottle. This can intuitively reflect the true state of the patient's body, avoid misjudgment of the test results by the testing personnel, and thus facilitate the testing personnel to judge the accuracy of the sample test results.

[0143] Based on this, the microbial detection system of this application embodiment can intuitively display the clinical value reference information of patients, making it convenient for testing personnel to judge the accuracy of sample test results.

[0144] In one embodiment, at least one microbial detection device 110 includes at least one blood culture instrument. The blood culture instrument includes an incubation module and a detection module. The incubation module is used to load at least one culture bottle corresponding to the sample and to culture the microorganisms in the culture bottle. The detection module is used to detect the growth of the microorganisms in the culture bottle to obtain sample detection information.

[0145] Taking a blood culture instrument as an example, the microbial detection device 110 can include an incubation module and a detection module. The incubation module can culture microorganisms in the culture bottle, and the detection module can detect the growth of microorganisms in the culture bottle to obtain sample detection information.

[0146] The sample list displays at least the blood culture samples detected by the blood culture analyzer. The sample information displayed in the sample details area 123 is the sample information of the target blood culture sample determined according to the first interactive command. The test results of the culture bottles displayed in the result details area 125 are the test results of the blood culture bottles corresponding to the target blood culture sample. It should be noted that, in addition to displaying blood culture samples detected by the blood culture analyzer, the sample list can also display samples from the mass spectrometer and samples for drug sensitivity testing.

[0147] In one embodiment, such as Figure 2 As shown, patient information includes, but is not limited to: clinical diagnosis information, medication information, patient type information, patient department information, gender information, age information, date of birth information, patient identity information, medical history information, allergy history information, drug resistance history information, and patient remarks information. For clinical diagnosis information, for example, if the instrument has not reported a positive result for 5 days, but clinical indications suggest a bloodstream infection caused by a specific pathogen, the culture time for that specific pathogen needs to be extended. For medication information, it can display drug usage details, such as antimicrobial drug usage, including the type of antimicrobial drug used, dosage, and method of administration. If the instrument reports a positive result, but Gram staining does not reveal the pathogen, it may be due to the slow growth of certain bloodstream pathogens or the clinical use of antimicrobial drugs.

[0148] In one embodiment, such as Figure 2 As shown, the sample information includes, but is not limited to: sample sending department information, sample source information, sample identification information, sample type information, sample category information, sample sampling time, sample processing time, sample handling time, sample review time, sample validity period information, sample review information, sample processing status information, and sample remarks information.

[0149] In one embodiment, such as Figure 2 As shown, the sample result area 124 is also used to display at least one of the following culture bottle information: culture bottle identification information, culture bottle type information, culture bottle detection status information, culture bottle location information, culture bottle reloading information, culture bottle detection time information, and culture bottle detection completion time.

[0150] In one embodiment, such as Figure 2As shown, the results details area 125 also displays at least one of the following information: the growth curve of microorganisms in the culture bottle, culture bottle identification information, culture bottle type information, culture bottle detection status information, culture bottle location information, culture bottle reloading information, culture bottle sample volume information, culture bottle loading time information, culture bottle delayed loading time information, culture bottle detection time information, culture bottle detection interval time information, culture bottle detection time information, culture bottle unloading time information, culture bottle expiration date information, culture bottle detection completion time, longest detection time for sample bottles, and preliminary negative count information. Regarding the sample volume information for the culture bottle, for example, taking blood culture as an example, the blood volume should ideally be 1 / 10 of the culture medium. For adults, a single blood sample volume is 5–10 ml, and for infants and young children, it is 1–2 ml. If the adult blood sample volume is ≤5 mL, it may lead to false negatives or delayed microbial growth; if the adult blood sample volume is ≥10 mL, it may lead to false positives. Information regarding the expiration date of culture flasks, such as a message indicating that the culture flask has expired or is about to expire, may affect the final culture results.

[0151] In one embodiment, the result details area 125 is also used to display the delayed loading time of the selected target culture flask. When the delayed loading time is greater than a preset time, the delayed loading time is highlighted in the result details area 125. Preferably, the preset time is 2 hours.

[0152] There are time-sensitive requirements for the transport of culture flasks. Generally, the transport time plus the loading time should be ≤2 hours. In special circumstances, after communication with the clinician, the time may be appropriately delayed, but the delay should not exceed 2 hours, otherwise it may lead to false negatives and inaccurate results. Based on this, the result details area 125 of this embodiment can also display the delayed loading time of the selected target culture flask. Taking a preset time of 2 hours as an example, if the delayed loading time is greater than 2 hours, the delayed loading time will be highlighted in the result details area 125 to remind medical personnel that the target culture flask has been delayed and the result may be inaccurate. The highlighting method can be different colors, different fonts, or other conspicuous markings. In short, it is only necessary to make the abnormality clearly noticeable to medical personnel at a glance.

[0153] In one embodiment, determining a target sample in the sample list according to a first interactive instruction includes at least one of the following:

[0154] The first interactive instructions include a filtering instruction and a sample selection instruction. After the control component 130 filters the samples in the sample list area 122 according to the filtering instruction, it displays the filtered sample list. The control component 130 selects the target sample from the filtered sample list according to the sample selection instruction.

[0155] Medical staff can first filter the samples in sample list area 122 using the filtering operation. For example, medical staff can click... Figure 2 The filter control in the upper right corner displays a list of filtered samples. You can then select from the filtered sample list, for example, select the target sample.

[0156] The first interactive instruction is a filtering instruction. The control component 130 filters the samples in the sample list area 122 according to the filtering instruction. The target sample is determined in the filtered sample list according to a preset rule. Preferably, the preset rule is that the first sample in the sample list is the target sample, or the abnormal sample in the sample list is the target sample.

[0157] Medical staff can filter samples in sample list area 122 using only the filtering operation, and display the samples in the filtered sample list according to preset rules. For example, if the preset rule is that the first sample in the sample list is the target sample, then the first sample is displayed at the beginning of the sample list as the target sample; or if the preset rule is that abnormal samples in the sample list are the target samples, then the abnormal samples are displayed at the beginning of the sample list as the target samples.

[0158] The first interactive instruction is a sample selection instruction, and the control component 130 determines the target sample from the sample list according to the selection instruction.

[0159] Medical personnel can select a target sample from the sample list, for example, by directly selecting the target sample from the sample list.

[0160] The first interactive instruction is the sample information input by the user, and the control component 130 determines the target sample from the sample list based on the sample information.

[0161] Medical staff can also find target samples in the sample list by directly entering sample information. For example, medical staff can... Figure 2 Enter the sample information in the sample query in the upper right corner to find the target sample in the sample list.

[0162] The first interactive instruction is to scan the sample to obtain sample information, and the control component 130 searches for and determines the target sample in the sample list based on the sample information.

[0163] In some cases, the sample itself may have a label with an identification code, including but not limited to a QR code or barcode. In this case, medical personnel can obtain the sample information by directly scanning the code and then find the target sample in the sample list based on that information.

[0164] In one embodiment, the control component 130 is further configured to control the display device 120 to display a diagram 126 showing the operation path of the selected sample and / or the selected culture flask between different detection devices.

[0165] The transport path diagram 126 illustrates the movement of selected samples and / or culture flasks between different testing devices, facilitating medical staff's monitoring of the time required for each step and the inter-departmental transport process. This allows for tracing the historical location of selected samples and / or culture flasks, and enables medical staff to quickly ascertain their current location when necessary, facilitating immediate retrieval for further testing, thus significantly improving testing efficiency. For example, as... Figure 3 As shown, the operation path diagram 126 can be displayed in the form of a subway map. In the operation path diagram 126, each node represents a different transfer location. Different transfer locations can be marked with location information, detection equipment model information, transfer-in time information, and transfer-out time information. Based on the transfer-in time information and transfer-out time information of each node, the time consumption between nodes can be obtained. Based on this, the entire operation path diagram 126 can intuitively display the relevant information of the entire transfer path.

[0166] In one embodiment, the operation path diagram 126 is displayed synchronously in the display area with the sample information of the selected sample, and / or synchronously in the display area with the detection results of the selected culture flask.

[0167] Regarding the specific display position of the operation path diagram 126 in the display area, it can be displayed synchronously with the sample information of the selected sample, or it can be displayed synchronously with the detection results of the selected culture flask. This embodiment does not impose specific limitations on this. In this case, the operation path diagram 126 is displayed in the display area in a simultaneous display mode.

[0168] In one embodiment, the result details area 125 includes a first control, and the control component 130 controls the display device 120 to display the operation path diagram 126 of the target culture flask in response to receiving the user's trigger information for the first control.

[0169] In addition to the simultaneous display, the operation path diagram 126 can also be displayed in other non-simultaneous ways. The result details area 125 includes a first control. When the first control is triggered, the control display device 120 will display the operation path diagram 126 of the target culture flask. For example, when a medical professional clicks the first control, the operation path diagram 126 of the target culture flask will be displayed as a pop-up window; or, for example, when a medical professional moves the mouse to the area where the first control is located, the operation path diagram 126 of the target culture flask will be displayed as a floating window.

[0170] In one embodiment, such as Figure 3 As shown, the operation path diagram 126 can be displayed in a separate pop-up window and / or in the result details area 125. The operation path diagram 126 can be displayed not only in a separate pop-up window but also in the result details area 125. Of course, the operation path diagram 126 can also be displayed in other areas of the sample information management interface 121.

[0171] In one embodiment, such as Figure 3 As shown, the operation path diagram 126 may include loading time information and unloading time information of the target culture bottle by different testing devices. The loading time information is used to indicate the time when the target culture bottle is loaded into the testing device, and the unloading time information is used to indicate the time when the target culture bottle is unloaded from the testing device; and / or, it may include a location identifier of the current position of the target culture bottle, which indicates the location of the target culture bottle; and / or, it may include information about the departments through which the target culture bottle passes during its operation, such as inpatient departments and laboratories; and / or, it may include testing device information, which indicates attribute information such as the model of the testing device.

[0172] In one embodiment, the culture bottle information in the result details area 125 can provide a sample transport path diagram 126 displayed in a subway map format, allowing medical personnel to quickly identify the current location of the sample and trace its historical location. The sample transport node changes with the actual number of transfers; if it is only loaded once (i.e., no transport occurs), this function will not be displayed. The transport path diagram 126 displays the sample's path nodes and current location. Since blood culture has high requirements for transport time, prolonged transport time can affect sample results. The transport path diagram 126 provided in this embodiment allows users to easily view the entry and exit times of each stage, as well as the transport stages and dwell times between departments during the process. For example, based on the displayed sample entry and exit times at each node, the time spent between nodes can be calculated or directly displayed.

[0173] Based on this, the operational path diagram 126 displays the sample transport path and current location, allowing for tracing of historical locations, monitoring transport time, and delaying loading time to reduce the impact of long transport times on sample results. It also facilitates medical staff in analyzing and solving problems, improving their work efficiency and enhancing their user experience.

[0174] In one embodiment, samples with abnormal results are highlighted in the sample list area 122, and / or, samples with abnormal results are highlighted in the sample list area 122, and / or, in the sample result area 124, the test results of culture bottles with abnormal results are highlighted, and / or, in the result details area 125, abnormal culture bottle information is highlighted. Here, samples with abnormal results refer to samples with abnormal detection, such as positive samples; samples with abnormal results refer to samples that are inherently abnormal or have been abnormally processed; highlighting includes, but is not limited to, different color displays, highlighting, and marking displays, to allow medical personnel to clearly observe samples with abnormal results and / or abnormal samples at a glance in the sample list area 122, sample result area 124, and result details area 125.

[0175] In one embodiment, such as Figure 2 As shown, in the sample list area 122, the selected sample is highlighted, and / or in the sample result area 124, the selected culture flask is highlighted, and / or in the sample list area 122, the sample pointed to by the cursor is highlighted, and / or in the sample result area 124, the culture flask pointed to by the cursor is highlighted; wherein, in the sample list area 122, if the selected target sample is a sample with abnormal results, the target sample is highlighted and the result abnormality is highlighted simultaneously, and / or, if the selected target sample is a normal sample, the target sample is highlighted and the normality is highlighted simultaneously, and / or, if the selected target sample is a sample with abnormal results, the target sample is highlighted and the sample abnormality is highlighted simultaneously.

[0176] In the sample list area 122, when a medical staff member clicks to select a sample, that sample will be highlighted; or, when a medical staff member hovers the mouse cursor over a sample, that sample will be highlighted. In the sample result area 124, when a medical staff member clicks to select a culture flask, that culture flask will be highlighted; or, when a medical staff member hovers the mouse cursor over a culture flask, that culture flask will be highlighted. If the sample selected by the medical staff member happens to be an abnormal sample, both selection and abnormal result highlighting will be applied simultaneously. That is, if selection highlighting is enabled and abnormal result highlighting is displayed in red, then the sample will be highlighted in red. If the sample selected by the medical staff member is a normal sample, both selection and normal result highlighting will be applied simultaneously. That is, if selection highlighting is enabled and normal result highlighting is displayed in green, then the sample will be highlighted in green. If the sample selected by the medical staff happens to be an abnormal sample, then both the selected sample and the abnormal sample will be highlighted. In other words, if the selected sample is highlighted and the abnormal sample is highlighted in yellow, then the sample will be highlighted in yellow.

[0177] In one embodiment, if the sample pointed to by the cursor is a sample with abnormal results, the sample is highlighted in a first pointing manner; and / or, if the sample pointed to by the cursor is a normal sample, the sample is highlighted in a second pointing manner; and if the sample pointed to by the cursor is a sample with abnormal results, the sample is highlighted in a third pointing manner. That is, when medical personnel point the mouse cursor to samples with abnormal results, normal samples, and samples with abnormal results, the corresponding pointing highlighting is different. The specific difference could be a different color, a different level of highlighting, or a different identifier; this embodiment does not limit this.

[0178] In one embodiment, the sample information displayed in the sample details area 123 is the sample information corresponding to the target detection item, and / or, the culture bottle detection result displayed in the sample result area 124 is the detection result corresponding to the target detection item.

[0179] The target detection item is the detection item selected by the user or the detection item determined by the control component 130 according to preset rules. These preset rules include, but are not limited to: default detection item, the most recent detection item for the sample, and the earliest detection item for the sample. The detection items include, but are not limited to: blood culture detection, drug sensitivity testing, and mass spectrometry detection. For example, if the preset rule is the default detection item, assuming the default detection item is blood culture detection, the sample information displayed in the sample details area 123 is the sample information corresponding to the blood culture detection, and the culture bottle detection result displayed in the sample result area 124 is the detection result corresponding to the blood culture detection. As another example, if the preset rule is the most recent detection item for the sample, assuming the most recent detection item is blood culture detection, the sample information displayed in the sample details area 123 is the sample information corresponding to the blood culture detection, and the culture bottle detection result displayed in the sample result area 124 is the detection result corresponding to the blood culture detection. For example, if the preset rule is the earliest tested item of the sample, and assuming that the earliest tested item of the sample is blood culture test, then the sample information displayed in the sample details area 123 is the sample information corresponding to the blood culture test, and the culture bottle test result displayed in the sample result area 124 is the test result corresponding to the blood culture test.

[0180] In one embodiment, the display area also displays multiple test item selection controls corresponding to different test items. The control component 130 obtains the user's operation information on the test item selection controls and determines the target test item based on the operation information. Preferably, each test item selection control is arranged and displayed in the display area in the style of a label.

[0181] like Figure 4 As shown, different tests have different labels, including but not limited to blood culture label 127, mass spectrometry (i.e., identification) label 128, and drug sensitivity label 129. The selection controls for each test can be arranged and displayed in the display area according to the label style. Medical personnel can select tests by operating the selection controls, and the corresponding results are displayed based on the currently selected test, such as user selection or default selection.

[0182] Based on this, the microbial detection system provided in this application includes at least one microbial detection device, a display device, and a control component. The microbial detection device is used to detect samples. The display device includes a display area, which includes a sample information management interface. The sample information management interface includes a sample list area, a sample details area, a sample result area, and a result details area. The control component is used to control the display device to display the sample list area, which displays a sample list of some or all samples in the microbial detection system. The control component is also used to acquire a first interactive instruction, determine a target sample in the sample list according to the first interactive instruction, and control the display device to display the patient information and sample information of the target sample in the sample details area, and to display the detection results of all culture bottles of the target sample in the sample result area. The control component is also used to acquire a second interactive instruction, determine a target culture bottle from the detection results of all culture bottles according to the second interactive instruction, and control the display device to display the result details of the target culture bottle in the result details area. In this application embodiment, the sample list area, sample details area, sample result area, and result details area can be displayed simultaneously on the sample information management interface, so that medical personnel can quickly obtain all clinical value reference information of the patient. Compared to existing technologies that only display the test results of a single culture flask of the target sample, requiring users to navigate to other flasks to view their results, this embodiment displays the test results of all culture flasks of the target sample on a single interface. This is more intuitive and convenient, eliminating the need for medical personnel to perform multiple operations to view the results of all flasks. Furthermore, it displays patient and sample information for the target sample, providing more comprehensive information. The result details area displays detailed results for the target culture flasks, directly reflecting the patient's actual condition and preventing misinterpretation by testing personnel, thus facilitating the assessment of the accuracy of the sample test results. Therefore, this embodiment can intuitively display the patient's clinical value reference information, making it easier for testing personnel to determine the accuracy of the sample test results.

[0183] This application also provides a method for displaying microbial detection information. The microbial detection system includes at least one microbial detection device and a display device. The display area includes a sample information management interface, which includes a sample list area, a sample details area, a sample result area, and a result details area. Figure 5 As shown, the display method includes the following steps:

[0184] Step S101: Control the display device to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system;

[0185] Step S102: Obtain the first interaction instruction, and determine the target sample in the sample list according to the first interaction instruction;

[0186] Step S103: Control the display device to display the patient information and sample information of the target sample in the sample details area, and to display the test results of all culture bottles of the target sample in the sample results area;

[0187] Step S104: Obtain the second interactive instruction, and determine the target culture flask from the detection results of all culture flasks according to the second interactive instruction;

[0188] Step S105: Control the display device to display the result details of the target culture flask in the result details area.

[0189] This display method can be applied to microbial detection systems, which may include at least one microbial detection device and a display device.

[0190] Microbial testing devices are used to test samples. These devices include, but are not limited to, medical testing equipment such as blood culture instruments, mass spectrometers, and drug sensitivity testing equipment. Different microbial testing devices can be placed in different departments of hospitals or testing institutions. Samples include, but are not limited to, blood samples, urine samples, stool samples, sputum samples, fluid samples, and secretion samples.

[0191] like Figure 2 As shown, the display device includes a display area, which includes a sample information management interface 121. The sample information management interface 121 includes a sample list area 122, a sample details area 123, a sample result area 124, and a result details area 125. Specifically, the sample list area 122 displays a list of some or all samples in the microbial detection system; the sample details area 123 displays patient and sample information for the target sample; the sample result area 124 displays the test results for all culture bottles of the target sample; and the result details area 125 displays the result details for the target culture bottle. The sample list area 122, sample details area 123, sample result area 124, and result details area 125 are displayed simultaneously on the sample information management interface 121, forming a patient-centered integrated layout of sample information. This facilitates reference by medical personnel and allows testing personnel to efficiently assess the accuracy of sample test results.

[0192] Regarding the display layout of the sample list area 122, sample details area 123, sample results area 124, and results details area 125 on the sample information management interface 121, the sample list area 122 and sample details area 123 can be displayed on the left side of the sample information management interface 121, and the sample results area 124 and results details area 125 can be displayed on the right side of the sample information management interface 121. The sample list area 122 and sample details area 123 can be arranged horizontally, and the sample results area 124 and results details area 125 can be arranged vertically, so that medical staff can view the information according to the information flow of the sample list area 122, sample details area 123, sample results area 124, and results details area 125, which is more in line with reading habits. However, it should be noted that the embodiments of this application are not limited to the display layout described above. Regardless of the display layout, the sample list area 122, sample details area 123, sample results area 124, and results details area 125 can be displayed simultaneously on the sample information management interface 121, so that medical personnel can quickly obtain all the clinical value reference information of the patient. It should be noted that the clinical value reference information may include, but is not limited to, clinical diagnostic information, drug use, transport time (delayed loading time), sample volume, and expiration date.

[0193] Specifically, the control display device 120 displays a sample list area 122, which is used to display a sample list of some or all samples in the microbial detection system; by acquiring a first interactive instruction, the target sample is determined in the sample list according to the first interactive instruction, and the control display device 120 displays the patient information and sample information of the target sample in the sample details area 123, and displays the test results of all culture bottles of the target sample in the sample result area 124; and by acquiring a second interactive instruction, the target culture bottle is determined from the test results of all culture bottles according to the second interactive instruction, and the control display device 120 displays the result details of the target culture bottle in the result details area 125. In other words, for example, when medical personnel select a target sample from the sample list, the sample details area 123 will display the patient information and sample information of the target sample, and the sample results area 124 will display the test results of all culture bottles of the target sample. Compared with the prior art, which only displays the test results of a single culture bottle of the target sample and requires page jump to view other culture bottles, this embodiment can display the test results of all culture bottles of the target sample on the same interface, which is more intuitive and convenient, and does not require medical personnel to perform multiple operations to view the test results of all culture bottles. Moreover, it can also display the patient information and sample information of the target sample, and the displayed information is more comprehensive. For another example, when medical personnel select a target culture bottle from the test results of all culture bottles, the result details area 125 will display the result details of the target culture bottle. This can intuitively reflect the true state of the patient's body, avoid misjudgment of the test results by the testing personnel, and thus facilitate the testing personnel to judge the accuracy of the sample test results.

[0194] In one embodiment, at least one microbial detection device includes at least one blood culture instrument. The blood culture instrument includes an incubation module and a detection module. The incubation module is used to load at least one culture bottle corresponding to the sample and to culture the microorganisms in the culture bottle. The detection module is used to detect the growth of the microorganisms in the culture bottle to obtain sample detection information.

[0195] Taking a blood culture instrument as an example, a microbial detection device can include an incubation module and a detection module. The incubation module can culture microorganisms in the culture bottle, and the detection module can detect the growth of microorganisms in the culture bottle to obtain sample detection information.

[0196] The sample list displays at least the blood culture samples detected by the blood culture analyzer. The sample details area displays the sample information of the target blood culture sample determined according to the first interactive command. The results displayed in the results details area are the test results of the blood culture bottles corresponding to the target blood culture sample. It should be noted that, in addition to displaying blood culture samples detected by the blood culture analyzer, the sample list can also display samples detected by mass spectrometry and samples for drug susceptibility testing.

[0197] In one embodiment, patient information includes, but is not limited to: clinical diagnosis information, medication information, patient type information, patient department information, gender information, age information, date of birth information, patient identity information, medical history information, allergy history information, drug resistance history information, and patient remarks information. For clinical diagnosis information, for example, if the instrument has not reported a positive result for 5 days, but clinical indications suggest a bloodstream infection caused by a specific pathogen, the culture time for the specific pathogen needs to be extended. For medication information, it can display drug usage details, such as antimicrobial drug usage, including the type of antimicrobial drug used, dosage, and method of administration. If the instrument reports a positive result, but Gram staining does not reveal the pathogen, it may be due to the slow growth of certain bloodstream infection pathogens or the clinical use of antimicrobial drugs.

[0198] In one embodiment, the sample information includes, but is not limited to: sample sending department information, sample source information, sample identification information, sample type information, sample category information, sample sampling time, sample processing time, sample transport time, sample review time, sample validity period information, sample review information, sample processing status information, and sample remarks information.

[0199] In one embodiment, the sample result area is also used to display at least one of the following culture bottle information: culture bottle identification information, culture bottle type information, culture bottle detection status information, culture bottle location information, culture bottle reloading information, culture bottle detection time information, and culture bottle detection completion time.

[0200] In one embodiment, the result details area is also used to display at least one of the following information: the growth curve of microorganisms in the culture bottle, culture bottle identification information, culture bottle type information, culture bottle detection status information, culture bottle location information, culture bottle reloading information, culture bottle sample volume information, culture bottle loading time information, culture bottle delayed loading time information, culture bottle detection time information, culture bottle detection interval time information, culture bottle detection time information, culture bottle unloading time information, culture bottle expiration date information, culture bottle detection completion time, longest detection time for sample bottles, and preliminary negative count information. Regarding the sample volume information of the culture bottle, for example, taking blood culture as an example, the blood volume should preferably be 1 / 10 of the culture medium. For adults, the blood volume per sample is 5-10 ml, and for infants, it is 1-2 ml. If the blood volume per sample for adults is ≤5 mL, it may lead to false negatives or delayed microbial growth; if the blood volume per sample for adults is ≥10 mL, it may lead to false positives. Regarding the expiration date information of the culture bottle, for example, an expired or soon-to-expire indication of the loaded culture bottle may affect the final culture results.

[0201] Based on this, the microbial detection system of this application embodiment can intuitively display the clinical value reference information of patients, making it convenient for testing personnel to judge the accuracy of sample test results.

[0202] In one embodiment, such as Figure 6 As shown, the display method also includes the following steps:

[0203] Step S201: Obtain the delayed loading time of the target culture flask;

[0204] Step S202: Display the delayed loading time in the result details area. If the delayed loading time is greater than a preset time, highlight the delayed loading time in the result details area. Preferably, the preset time is 2 hours.

[0205] There are time-sensitive requirements for the transport of culture flasks. Generally, the transport time plus the loading time should be ≤2 hours. In special circumstances, after communication with the clinician, an appropriate delay may be made, but the delay should not exceed 2 hours, otherwise it may lead to false negatives and inaccurate results. Based on this, the delayed loading time of the target culture flask is obtained and displayed in the results details area. That is, the results details area can also display the delayed loading time of the selected target culture flask. Taking a preset time of 2 hours as an example, if the delayed loading time is greater than 2 hours, the delayed loading time will be highlighted in the results details area to remind medical staff that the target culture flask has been delayed and its results may be inaccurate. The highlighting method can be different colors, different fonts, or other eye-catching markings. In short, it only needs to be clear enough for medical staff to notice the abnormality at a glance.

[0206] In one embodiment, determining a target sample in the sample list according to a first interactive instruction includes at least one of the following:

[0207] The first interactive instructions include filtering instructions and sample selection instructions. After the control component filters the samples in the sample list area according to the filtering instructions, it displays the filtered sample list. The control component selects the target sample from the filtered sample list according to the sample selection instructions.

[0208] Medical staff can first filter the samples in the sample list area using the filtering function. For example, medical staff can click... Figure 2 The filter control in the upper right corner displays a list of filtered samples. You can then select from the filtered sample list, for example, select the target sample.

[0209] The first interactive instruction is a filtering instruction. The control component filters the samples in the sample list area according to the filtering instruction. The target sample is determined in the filtered sample list according to a preset rule. Preferably, the preset rule is that the first sample in the sample list is the target sample, or the abnormal sample in the sample list is the target sample.

[0210] Medical staff can filter samples in the sample list area using only the filtering operation, and the filtered samples will be displayed in the sample list according to preset rules. For example, if the preset rule is that the first sample in the sample list is the target sample, then the first sample will be displayed at the beginning of the sample list as the target sample; or if the preset rule is that the abnormal sample in the sample list is the target sample, then the abnormal sample will be displayed at the beginning of the sample list as the target sample.

[0211] The first interactive instruction is a sample selection instruction, and the control component determines the target sample from the sample list according to the selection instruction.

[0212] Medical personnel can select a target sample from the sample list, for example, by directly selecting the target sample from the sample list.

[0213] The first interactive instruction is the sample information input by the user. The control component determines the target sample from the sample list based on the sample information.

[0214] Medical staff can also find target samples in the sample list by directly entering sample information. For example, medical staff can... Figure 2 Enter the sample information in the sample query in the upper right corner to find the target sample in the sample list.

[0215] The first interactive instruction is to scan and identify the sample information. The control component then searches for and determines the target sample in the sample list based on the sample information.

[0216] In some cases, the sample itself may have a label with an identification code, including but not limited to a QR code or barcode. In this case, medical personnel can obtain the sample information by directly scanning the code and then find the target sample in the sample list based on that information.

[0217] In one embodiment, the sample information management interface is also used to control the display device to display the operation path diagram of the target sample and / or target culture flask moving between different detection devices.

[0218] A transport path diagram is used to illustrate the transport route of the target sample and / or culture bottle between different testing devices, making it easy for medical staff to view the time of each step and the transfer between departments. On the one hand, it allows tracing the historical location of the target sample and / or culture bottle; on the other hand, medical staff can quickly know the current location of the target sample and / or culture bottle when necessary, facilitating immediate retrieval for further testing, thus greatly improving testing efficiency. For example, ... Figure 3 As shown, the operation path diagram can be displayed in the style of a subway map. In the operation path diagram, each node represents a different transfer location. Different transfer locations can be marked with location information, detection equipment model information, transfer-in time information, and transfer-out time information. Based on the transfer-in time information and transfer-out time information of each node, the time consumption between nodes can be obtained. Based on this, the entire operation path diagram can intuitively display the relevant information of the entire transfer path.

[0219] In one embodiment, the operation path diagram is displayed synchronously with the sample information of the target sample in the display area, and / or, synchronously with the detection results of the target culture flask in the display area.

[0220] Regarding the specific display position of the operation path diagram in the display area, it can be displayed synchronously with the sample information of the target sample, or it can be displayed synchronously with the detection results of the target culture flask. This embodiment does not impose specific limitations on this. In this case, the operation path diagram is displayed in the display area in a simultaneous display mode.

[0221] In one embodiment, the result details area includes a first control, and the display method further includes the following steps:

[0222] The system obtains user trigger information for the first control and displays the operation path diagram of the target culture flask in response to the trigger information. Preferably, the operation path diagram is displayed through a separate pop-up window and / or in the result details area.

[0223] By acquiring and responding to user trigger information for the first control, the control display device displays the operational path diagram of the target culture flask. Besides on-screen display, the operational path diagram can also be displayed in other non-on-screen ways. The result details area includes the first control; when the first control is triggered, the control display device displays the operational path diagram of the target culture flask. For example, when a medical professional clicks the first control, the operational path diagram of the target culture flask is displayed as a pop-up window; or, for instance, when a medical professional moves the mouse over the area where the first control is located, the operational path diagram of the target culture flask is displayed as a floating window.

[0224] In one embodiment, the operation path diagram can be displayed via a separate pop-up window and / or in the result details area. The operation path diagram can be displayed not only via a separate pop-up window but also in the result details area. Of course, the operation path diagram can also be displayed in other areas of the sample information management interface.

[0225] In one embodiment, the operation path diagram may include loading time information and unloading time information of the target culture flask by different testing devices. The loading time information is used to indicate the time when the target culture flask is loaded into the testing device, and the unloading time information is used to indicate the time when the target culture flask is unloaded from the testing device. And / or, it may include a location identifier of the current position of the target culture flask, which indicates the location of the target culture flask. And / or, it may include department information that the target culture flask passes through during its operation, which may include, for example, inpatient departments, laboratories, etc. And / or, it may include testing device information, which indicates attribute information such as the model of the testing device.

[0226] In one embodiment, the culture bottle information in the results details area can provide a sample transport path diagram displayed in a subway map format, allowing medical staff to quickly identify the current location of the sample and trace its historical location. The sample transport nodes change with the actual number of transfers; if a sample is only loaded once (i.e., no transport occurs), this function will not be displayed. The transport path diagram displays the sample's path nodes and current location. Since blood cultures have strict requirements on transport time, prolonged transport can affect sample results. The transport path diagram provided in this embodiment allows users to easily view the entry and exit times of each stage, as well as the transport stages and dwell times between departments. For example, based on the displayed sample entry and exit times at each node, the time spent between nodes can be calculated or directly displayed.

[0227] Based on this, a transport path diagram is used to display the sample transport route and current location, trace historical locations, monitor transport time, and delay loading time to reduce the impact of long transport times on sample results. This also facilitates medical staff in analyzing and solving problems, improving their work efficiency and enhancing their user experience.

[0228] In one embodiment, such as Figure 7 As shown, step S103, controlling the display device to display the patient information and sample information of the target sample in the sample details area, and to display the test results of all culture bottles of the target sample in the sample results area, includes the following steps:

[0229] Step S301: Determine the target detection items corresponding to the target sample;

[0230] Step S302: Display the patient information corresponding to the target sample and the sample information corresponding to the target detection item in the sample details area;

[0231] Step S303: Display the detection results of all culture flasks of the target sample in the sample result area.

[0232] First, determine the target testing items corresponding to the target sample. Target testing items include, but are not limited to, blood culture testing, drug sensitivity testing, and mass spectrometry testing. Taking blood culture testing as an example, the sample details area displays the patient information corresponding to the target sample and the sample information corresponding to the blood culture test. The sample results area displays the test results of all culture bottles of the target sample. Patient information includes, but is not limited to, clinical diagnosis information, medication information, patient type information, patient department information, gender information, age information, date of birth information, patient identity information, medical history information, allergy history information, drug resistance history information, and patient remarks. Sample information includes, but is not limited to, the department that submitted the sample, sample source information, sample identification information, sample type information, sample category information, sample sampling time, sample processing time, sample transfer time, sample review time, sample expiration date information, sample review information, sample processing status information, and sample remarks. In addition to displaying the test results of all culture bottles of the target sample, the sample results area can also display at least one of the following culture bottle information: culture bottle identification information, culture bottle type information, culture bottle test status information, culture bottle location information, culture bottle reloading information, culture bottle test time information, and culture bottle test completion time.

[0233] In one embodiment, step S303, displaying the detection results of all culture flasks of the target sample in the sample result area, includes:

[0234] The sample results area displays the test results of all culture bottles corresponding to the target test items for the target sample; among which, the target test items include, but are not limited to: blood culture test, drug allergy test, and mass spectrometry test.

[0235] Taking blood culture detection as an example, the sample results area displays the detection results of all culture bottles corresponding to the blood culture detection for the target sample.

[0236] In one embodiment, the sample information management interface also includes multiple test item selection controls distributed to correspond to different test items. Preferably, each test item selection control is arranged and displayed in the display area in the style of a label.

[0237] Step S301: Determine the target detection item corresponding to the target sample, including one of the following:

[0238] Obtain user operation information on the detection item selection control, and determine the target detection item based on the operation information;

[0239] Alternatively, the target detection item can be determined according to preset rules, where the preset rules are one of the following: default detection item, the latest detection item of the sample, and the earliest detection item of the sample.

[0240] The sample information management interface also includes multiple test item selection controls distributed to correspond to different test items. Preferably, each test item selection control is arranged and displayed in the display area in the style of a label, so that medical staff can operate the corresponding test item selection control according to the style of the label, and select the corresponding target test item according to the operation information.

[0241] In one embodiment, the target test item can be determined based on the user's operation information on the test item selection control. Different test items have different labels, including but not limited to blood culture labels, drug sensitivity labels, and mass spectrometry labels. Each test item selection control can be arranged and displayed in the display area according to the label style. Medical personnel can select test items by operating the test item selection control, and the corresponding results are displayed according to the currently selected test item, such as user selection or default selection.

[0242] In one embodiment, a target detection item can also be determined according to preset rules, wherein the preset rules are one of the following: default detection item, the latest detection item of the sample, and the earliest detection item of the sample. The target detection item is a detection item selected by the user or a detection item determined by the control component according to preset rules, wherein the preset rules include, but are not limited to: default detection item, the latest detection item of the sample, and the earliest detection item of the sample; the detection item includes, but is not limited to: blood culture detection, drug sensitivity detection, and mass spectrometry detection. For example, when the preset rule is the default detection item, assuming the default detection item is blood culture detection, the sample information displayed in the sample details area is the sample information corresponding to blood culture detection, and the culture bottle detection result displayed in the sample result area is the detection result corresponding to blood culture detection. As another example, when the preset rule is the latest detection item of the sample, assuming the latest detection item of the sample is blood culture detection, the sample information displayed in the sample details area is the sample information corresponding to blood culture detection, and the culture bottle detection result displayed in the sample result area is the detection result corresponding to blood culture detection. For example, if the preset rule is the earliest tested item in the sample, and assuming that the earliest tested item in the sample is blood culture, then the sample information displayed in the sample details area is the sample information corresponding to the blood culture test, and the culture bottle test results displayed in the sample results area are the test results corresponding to the blood culture test.

[0243] Based on this, the microbial detection information display method provided in this application embodiment includes a microbial detection system comprising at least one microbial detection device and a display device. The display area includes a sample information management interface, which includes a sample list area, a sample details area, a sample result area, and a result details area. The display method includes: controlling the display device to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system; obtaining a first interaction instruction and determining a target sample in the sample list according to the first interaction instruction; controlling the display device to display patient information and sample information of the target sample in the sample details area, and displaying the detection results of all culture bottles of the target sample in the sample result area; obtaining a second interaction instruction and determining the target culture bottle from the detection results of all culture bottles according to the second interaction instruction; and controlling the display device to display the result details of the target culture bottle in the result details area. In this application embodiment, the sample list area, sample details area, sample result area, and result details area can be displayed simultaneously on the sample information management interface, so that medical personnel can quickly obtain all clinical value reference information of the patient. Compared to existing technologies that only display the test results of a single culture flask of the target sample, requiring users to navigate to other flasks to view their results, this embodiment displays the test results of all culture flasks of the target sample on a single interface. This is more intuitive and convenient, eliminating the need for medical personnel to perform multiple operations to view the results of all flasks. Furthermore, it displays patient and sample information for the target sample, providing more comprehensive information. The result details area displays detailed results for the target culture flasks, directly reflecting the patient's actual condition and preventing misinterpretation by testing personnel, thus facilitating the assessment of the accuracy of the sample test results. Therefore, this embodiment can intuitively display the patient's clinical value reference information, making it easier for testing personnel to determine the accuracy of the sample test results.

[0244] The terms “first,” “second,” “third,” “fourth,” etc. (if present) in the specification and accompanying drawings of this application are used to distinguish similar objects and are not necessarily used to describe a specific order or sequence. It should be understood that such data can be interchanged where appropriate to describe embodiments of this application, for example, those that can be implemented in orders other than those illustrated or described herein. Furthermore, the terms “comprising” and “having,” and any variations thereof, are intended to cover a non-exclusive inclusion; for example, a process, method, system, product, or apparatus that comprises a series of steps or units is not necessarily limited to those steps or units explicitly listed, but may include other steps or units not explicitly listed or inherent to such processes, methods, products, or apparatuses.

[0245] It should be understood that in this application, "at least one (item)" means one or more, and "more than" means two or more. "And / or" is used to describe the relationship between related objects, indicating that three relationships can exist. For example, "A and / or B" can represent three cases: only A exists, only B exists, and both A and B exist simultaneously, where A and B can be singular or plural. The character " / " generally indicates that the preceding and following related objects are in an "or" relationship. "At least one (item) of the following" or similar expressions refer to any combination of these items, including any combination of single or plural items. For example, at least one (item) of a, b, or c can represent: a, b, c, "a and b", "a and c", "b and c", or "a and b and c", where a, b, and c can be single or multiple.

[0246] It should be understood that in the description of the embodiments of this application, "multiple" means two or more, "greater than", "less than", "exceeding" etc. are understood to exclude the number itself, and "above", "below", "within" etc. are understood to include the number itself.

[0247] In the several embodiments provided in this application, it should be understood that the disclosed systems, apparatuses, and methods can be implemented in other ways. For example, the apparatus embodiments described above are merely illustrative; for instance, the division of units is only a logical functional division, and in actual implementation, there may be other division methods. For example, multiple units or components may be combined or integrated into another system, or some features may be ignored or not executed. Furthermore, the coupling or direct coupling or communication connection shown or discussed may be through some interfaces, or indirect coupling or communication connection between apparatuses or units, and may be electrical, mechanical, or other forms.

[0248] The units described as separate components may or may not be physically separate. The components shown as units may or may not be physical units; that is, they may be located in one place or distributed across multiple network units. Some or all of the units can be selected to achieve the purpose of this embodiment according to actual needs.

[0249] Furthermore, the functional units in the various embodiments of this application can be integrated into one processing unit, or each unit can exist physically separately, or two or more units can be integrated into one unit. The integrated unit can be implemented in hardware or as a software functional unit.

[0250] If the integrated unit is implemented as a software functional unit and sold or used as an independent product, it can be stored in a computer-readable storage medium. Based on this understanding, the technical solution of this application, in essence, or the part that contributes to the prior art, or all or part of the technical solution, can be embodied in the form of a software product. This computer software product is stored in a storage medium and includes several instructions to cause a computer device (which may be a personal computer, server, or network device, etc.) to execute all or part of the steps of the methods of the various embodiments of this application. The aforementioned storage medium includes various media capable of storing program code, such as USB flash drives, portable hard drives, read-only memory (ROM), random access memory (RAM), magnetic disks, or optical disks.

[0251] It should also be understood that the various implementation methods provided in this application can be combined arbitrarily to achieve different technical effects.

[0252] The above provides a detailed description of the preferred embodiments of this application. However, this application is not limited to the above-described embodiments. Those skilled in the art can make various equivalent modifications or substitutions without departing from the spirit of this application. All such equivalent modifications or substitutions are included within the scope defined by the claims of this application.

Claims

1. A microbial detection system, characterized in that, include: At least one microbial detection device, said microbial detection device being used to detect samples; The display device includes a display area, the display area including a sample information management interface, the sample information management interface including a sample list area, a sample details area, a sample result area, and a result details area; A control component is configured to control the display device to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system; the control component is also configured to acquire a first interaction instruction, determine a target sample in the sample list according to the first interaction instruction, and control the display device to display the patient information and sample information of the target sample in the sample details area, and display the detection results of all culture bottles of the target sample in the sample results area; The control component is also used to acquire a second interactive instruction, determine a target culture flask from the detection results of all culture flasks according to the second interactive instruction, and control the display device to display the result details of the target culture flask in the result details area.

2. The microbial detection system according to claim 1, characterized in that, The at least one microbial detection device includes at least one blood culture instrument, which includes an incubation module and a detection module. The incubation module is used to load at least one culture bottle corresponding to the sample and to culture the microorganisms in the culture bottle. The detection module is used to detect the growth of the microorganisms in the culture bottle to obtain the sample detection information. The sample list displays at least the blood culture samples detected by the blood culture instrument. The sample information displayed in the sample details area is the sample information of the target blood culture sample determined according to the first interactive command. The culture bottle detection results displayed in the result details area are the blood culture bottle detection results corresponding to the target blood culture sample.

3. The microbial detection system according to claim 1, characterized in that, The patient information includes at least one of the following: Clinical diagnostic information; Medication information; Patient type information; Patient's department information; Gender information; Age information; Birth time information; Patient identification information; Medical history information; Allergy history information; Historical information on drug resistance; Patient notes.

4. The microbial detection system according to claim 1 or 3, characterized in that, The sample information includes at least one of the following: Information on the department where the sample was submitted for testing; Sample source information; Sample identification information; Sample type information; Sample category information; Sample sampling time; Sample loading time; Sample transport time; Sample review time; Sample validity information; Sample review information; Sample processing status information; Sample notes.

5. The microbial detection system according to claim 1, characterized in that, The sample results area is also used to display at least one of the following culture flask information: Culture bottle labeling information; Information on culture flask type; Information on the status of the culture flask; Location information of the culture flask; Reloading information for culture flasks; Information on the detection time of the culture flask; Time required to complete the testing of the culture flask.

6. The microbial detection system according to any one of claims 1 to 3, characterized in that, The results details area is also used to display at least one of the following information: The growth curve of the microorganisms in the culture flask; Culture bottle labeling information; Information on culture flask type; Information on the status of the culture flask; Location information of the culture flask; Reloading information for culture flasks; The sample size information of the culture flask; Loading time information for culture flasks; Information on the delayed loading time of the culture flask; Information on the detection time of the culture flask; Information on the detection interval of the culture flask; Information on the detection time of the culture flask; Unloading time information for culture flasks; Information on the expiration date of culture flasks; Time required to complete the testing of the culture flask; Information on the longest detection time for sample bottles; Preliminary negative test results.

7. The microbial detection system according to any one of claims 1 to 3, characterized in that, The results details area is also used to display the delayed loading time of the target culture flask. When the delayed loading time is greater than a preset time, the delayed loading time is highlighted in the results details area. Preferably, the preset time is 2 hours.

8. The microbial detection system according to any one of claims 1 to 3, characterized in that, Determining the target sample in the sample list according to the first interactive instruction includes at least one of the following: The first interactive instruction includes a filtering instruction and a sample selection instruction. After the control component filters the samples in the sample list area according to the filtering instruction, it displays the filtered sample list. The control component determines the target sample from the filtered sample list according to the sample selection instruction. The first interactive instruction is a filtering instruction. The control component filters the samples in the sample list area according to the filtering instruction. The target sample is determined in the filtered sample list according to a preset rule. Preferably, the preset rule is that the first sample in the sample list is the target sample, or the abnormal sample in the sample list is the target sample. The first interactive instruction is a sample selection instruction, and the control component determines the target sample from the sample list according to the selection instruction; The first interactive instruction is sample information input by the user, and the control component determines the target sample from the sample list based on the sample information; The first interactive instruction is sample information obtained by scanning and identifying the sample. The control component searches for and determines the target sample in the sample list based on the sample information.

9. The microbial detection system according to any one of claims 1 to 3, characterized in that, The control component is also used to control the display device to display the operation path diagram of the selected sample and / or the selected culture flask moving between different detection devices.

10. The microbial detection system according to claim 9, characterized in that, The operation path diagram is displayed synchronously in the display area with the sample information of the selected sample and / or synchronously in the display area with the detection results of the selected culture flask; Alternatively, the result details area includes a first control, and the control component, in response to receiving a user's trigger information for the first control, controls the display device to display a diagram of the operation path of the target culture flask. Preferably, the operation path diagram is displayed through a separate pop-up window and / or in the result details area. The operation path diagram includes loading and unloading time information of different detection devices for the target culture bottle, and / or, location identifier of the current position of the target culture bottle, and / or, department information passed through by the target culture bottle during operation, and / or, detection device information.

11. The microbial detection system according to any one of claims 1 to 3 and 5, characterized in that, In the sample list area, samples with abnormal results are highlighted, and / or, in the sample list area, samples with abnormal results are highlighted, and / or, in the sample result area, the test results of culture bottles with abnormal results are highlighted, and / or, in the result details area, abnormal culture bottle information is highlighted. In the sample list area, the selected sample is highlighted; and / or, in the sample result area, the selected culture flask is highlighted; and / or, in the sample list area, the sample pointed to by the cursor is highlighted; and / or, in the sample result area, the culture flask pointed to by the cursor is highlighted. Wherein, in the sample list area, if the selected target sample is a sample with abnormal results, then both highlighting the target sample and highlighting the abnormal results are performed; and / or, if the selected target sample is a normal sample, then both highlighting the target sample and highlighting the normal results are performed; and / or, if the selected target sample is a sample with abnormal results, then both highlighting the target sample and highlighting the sample with abnormal results are performed. And / or, if the sample pointed to by the cursor is a sample with abnormal results, then the sample is highlighted with a first pointing; and / or, if the sample pointed to by the cursor is a normal sample, then the sample is highlighted with a second pointing; if the sample pointed to by the cursor is a sample with abnormal results, then the sample is highlighted with a third pointing.

12. The microbial detection system according to any one of claims 1 to 3 and 5, characterized in that, The sample information displayed in the sample details area is the sample information corresponding to the target detection item, and / or the culture bottle detection results displayed in the sample results area are the detection results corresponding to the target detection item; The target detection item is either a detection item selected by the user or a detection item determined by the control component according to preset rules, wherein the preset rules are one of the following: Default detection items; The latest tested item in the sample; The earliest item tested in the sample; The testing items include at least one of the following: Blood culture test; Antimicrobial susceptibility testing; Mass spectrometry detection.

13. The microbial detection system according to claim 12, characterized in that, The display area also displays multiple test item selection controls corresponding to different test items. The control component obtains the user's operation information on the test item selection controls and determines the target test item based on the operation information. Preferably, each test item selection control is arranged and displayed in the display area in the style of a label.

14. A method for displaying microbial detection information, characterized in that, The microbial detection system includes at least one microbial detection device and a display device. The display area includes a sample information management interface, which includes a sample list area, a sample details area, a sample result area, and a result details area. The display method includes: The display device is controlled to display the sample list area, which is used to display a sample list of some or all samples in the microbial detection system; Obtain a first interaction instruction, and determine the target sample from the sample list according to the first interaction instruction; The display device is controlled to display patient information and sample information of the target sample in the sample details area, and to display the test results of all culture bottles of the target sample in the sample results area; Obtain a second interactive instruction, and determine the target culture flask from the detection results of all culture flasks according to the second interactive instruction; The display device is controlled to display the result details of the target culture flask in the result details area.

15. The display method according to claim 14, characterized in that, Also includes: Obtain the delayed loading time of the target culture flask; The delayed loading time is displayed in the results details area. If the delayed loading time is greater than a preset time, the delayed loading time is highlighted in the results details area. Preferably, the preset time is 2 hours.

16. The display method according to claim 14 or 15, characterized in that, Determining the target sample in the sample list according to the first interactive instruction includes at least one of the following: The first interactive instruction includes a filtering instruction and a sample selection instruction. After the control component filters the samples in the sample list area according to the filtering instruction, it displays the filtered sample list. The control component determines the target sample from the filtered sample list according to the sample selection instruction. The first interactive instruction is a filtering instruction. The control component filters the samples in the sample list area according to the filtering instruction. The target sample is determined in the filtered sample list according to a preset rule. Preferably, the preset rule is that the first sample in the sample list is the target sample, or the abnormal sample in the sample list is the target sample. The first interactive instruction is a sample selection instruction, and the control component determines the target sample from the sample list according to the selection instruction; The first interactive instruction is sample information input by the user, and the control component determines the target sample from the sample list based on the sample information; The first interactive instruction is sample information obtained by scanning and identifying the sample. The control component searches for and determines the target sample in the sample list based on the sample information.

17. The display method according to claim 14, characterized in that, The sample information management interface is also used to display the operation path diagram of the target sample and / or the target culture bottle moving between different detection devices. The operation path diagram is displayed synchronously with the sample information of the target sample in the display area, and / or synchronously with the detection results of the target sample in the display area. Preferably, the operation path diagram includes the loading time information and unloading time information of the target culture bottle by different detection devices, and / or includes a location identifier marking the current position of the target culture bottle, and / or includes the department information passed through by the target culture bottle during operation, and / or includes the detection device information.

18. The display method according to claim 17, characterized in that, The result details area includes a first control, and the display method further includes: The system obtains user trigger information for the first control and displays the operation path diagram of the target culture flask in response to the trigger information. Preferably, the operation path diagram is displayed through a separate pop-up window and / or in the result details area.

19. The display method according to claim 14, characterized in that, The control of the display device to display patient and sample information of the target sample in the sample details area and to display the test results of all culture bottles of the target sample in the sample results area includes: Determine the target detection items corresponding to the target sample; The sample details area displays patient information corresponding to the target sample and sample information corresponding to the target detection item. The display of the detection results of all culture flasks of the target sample in the sample result area includes: The sample results area displays the detection results of all culture bottles corresponding to the target detection item for the target sample; The target detection items include at least one of the following: Blood culture test; Drug allergy testing; Mass spectrometry detection.

20. The display method according to claim 19, characterized in that, The sample information management interface also includes multiple detection item selection controls distributed to correspond to different detection items. Preferably, each of the detection item selection controls is arranged and displayed in the display area in the style of a label. Determining the target detection item corresponding to the target sample includes one of the following: Obtain user operation information on the detection item selection control, and determine the target detection item based on the operation information; Alternatively, the target detection item is determined according to a preset rule, wherein the preset rule is one of the following: the default detection item, the latest detected item of the sample, and the earliest detected item of the sample.

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