Self-test kit for rapid detection of gynecological inflammation

Abstract

The utility model relates to a self-test kit for rapidly detecting gynecological inflammation. The self-test kit comprises a detection card (chromatographic biological detection test paper is fixed in the detection card), a sample tube containing a biological diluent, a sampling cotton swab and a dropper. A panel of the detection card is provided with a detection area (sample dropping hole) and a display area, and the display area is provided with four color block display windows from No.1 to No.4 which respectively correspond to four self-test judgment results of normal, mild symptom, inflammation and severe. The detection card, the biological diluent sample tube, the sampling cotton swab and the dropper are independently sealed and packaged and are integrally arranged in a box. Due to the characteristic of independent packaging, pollution and misoperation can be reduced to the maximum extent. In the detection process, the self-test judgment of the inflammation degree is performed according to a visual comparison mode, and the detection kit is marked with a corresponding detection result, so that errors can be reduced, and the accuracy of the self-test result is improved. The gynecological inflammation detection device can rapidly detect the gynecological inflammation degree and has the advantages of being easy to operate, clean, sanitary, convenient to popularize and the like.

Description

Technical Field

[0001] The utility model relates to a gynecological inflammation self-test product, in particular to a self-test kit for rapid detection of gynecological inflammation. Background Art

[0002] Gynecological inflammation is a common disease among women. It mainly refers to acute or chronic inflammation of the female reproductive organs after being invaded and infected by various pathogens, such as vaginitis, cervicitis, metritis, pelvic inflammatory disease, etc. At the same time, gynecological inflammation will spread and cross-infect. In the early stage of inflammation, patients ignore the disease, or are reluctant to go to the hospital for a comprehensive examination, which leads to further deterioration of the disease and causes a variety of health problems, such as infertility, etc. In severe cases, cancer may occur. It is extremely harmful to women's health.

[0003] At present, the clinical detection methods for gynecological inflammation include secretion smear microscopy detection, which determines the cleanliness of the vagina according to the count of different bacterial species, as well as B-ultrasound detection, endoscopy, laparoscopy and other technologies for comprehensive detection of genitals such as the vagina and uterus. The above detection methods can accurately detect inflammation, but this depends on professional equipment and a comprehensive examination by a doctor. It is especially inconvenient for women living in remote areas. Although there are multi-detection kits on the market, they also require multiple sampling and cumbersome operations, which are not friendly to older women.

[0004] There are also some gynecological inflammation detection cards or test strips on the market. On the one hand, the detection card absorbs the secretion liquid to the detection strip through chromatography, and waits for the detection strip to develop color before comparing it with the standard card. However, this process is limited by the state of the secretion. If the secretion is too thick, it will not be able to be chromatographed smoothly, and it will not be possible to further determine the severity of the disease. Therefore, it will bring certain inconveniences and errors. Utility Model Content

[0005] The purpose of the utility model is to solve the above-mentioned problems existing in the prior art and to provide a self-test kit for rapid detection of gynecological inflammation. Through self-testing of vaginal microenvironment secretions, the presence of inflammation can be determined quickly, efficiently and accurately, and effective assistance can be provided for early detection, early diagnosis and early treatment of gynecological diseases.

[0006] A large number of studies have shown that the occurrence of inflammation is often accompanied by changes in the local microenvironment such as pH value. At the same time, abnormal leucorrhea is also an important reference indicator for the clinical diagnosis of gynecological inflammation. The normal pH of leucorrhea is slightly acidic at 3 to 5, but when inflammation occurs due to infection by foreign bacteria, the pH value of leucorrhea will increase. Therefore, by detecting the pH value of leucorrhea, rapid self-examination of gynecological inflammation can be achieved. Rapid detection can be achieved under the condition of protecting the privacy of patients to the greatest extent, so as to achieve the fundamental purpose of early detection and early treatment.

[0007] Technical solution of utility model

[0008] A self-test kit for rapid detection of gynecological inflammation comprises a test card (with an embedded chromatographic biological test paper), a sample tube containing a biological diluent, a sampling cotton swab, and a dropper. The test card, biological diluent sample tube, sampling cotton swab, and dropper are packaged in independent sealed packages.

[0009] A chromatographic biological test paper is fixed inside the test card, and a test area and a display area are arranged on the panel of the test card. The test area is used to drop the sample liquid to be tested, and the display area is provided with display windows No. 1 to No. 4. The display windows are provided with corresponding self-test judgment results, which correspond to normal, mild, inflammation and severe respectively.

[0010] The sampling cotton swab is a medical sampling swab used for extracting vaginal secretions.

[0011] The biological diluent is physiological saline, which is used to wash off and dilute the vaginal secretions on the cotton swab.

[0012] The dropper is a plastic dropper, which is used to absorb the vaginal secretions after washing in the sample tube and drip them into the detection area in the detection card.

[0013] Advantages and benefits

[0014] The detection card, sampling cotton swab, biological dilution sample tube and dropper in the utility model are all separately and independently sealed and packaged. Due to the characteristics of the independent sealed packaging, contamination and erroneous operation can be reduced to the greatest extent.

[0015] During the testing process, the self-test judgment of the degree of inflammation is based on visual comparison, and the test kit is marked with the corresponding test results, which can reduce errors and improve the accuracy of the self-test results.

[0016] The overall detection process takes a short time and has the characteristics of simple operation, clean and sanitary, and easy to popularize. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] Figure 1The utility model is a schematic diagram of the self-test kit for rapid detection of gynecological inflammation, which includes: (1) a sampling cotton swab, (2) a biological dilution sample tube, (3) a dropper, and (4) a test card (with a chromatographic biological test paper fixed inside);

[0018] Figure 2 It is a structural diagram of the test card in the test kit of the utility model and a schematic diagram of the interpretation of the test results. DETAILED DESCRIPTION

[0019] The embodiments of the utility model are described in detail below in conjunction with the accompanying drawings.

[0020] like Figure 1 The schematic diagram of the composition of the self-test kit for rapid detection of gynecological inflammation is shown, including the main body of the test kit test card, sampling cotton swabs, biological diluent sample tubes, droppers and instructions, and the test card, sampling cotton swabs, biological diluent sample tubes and droppers are independently sealed and packaged.

[0021] The detection kit is attached Figure 1 , which is equipped with: (1) sampling cotton swab, (2) biological dilution sample tube, (3) dropper, (4) detection card (with chromatography biological detection paper fixed inside), and 4 color block display windows are set in the detection area, and the 4 display windows are provided with corresponding result judgments, including normal, mild, inflammation, and severe.

[0022] The sampling cotton swab is shown in the attached Figure 1 , are medical sampling sticks and biological diluent sample tubes (filled with physiological saline), which are used to extract and elute vaginal secretions respectively.

[0023] The chromatographic bioassay test paper inside the test card is attached. Figure 2 The pH color change range of the chromatographic bioassay paper corresponding to normal values ​​is: 3.8≤pH≤4.4, set as window 1; the pH color change range of the chromatographic bioassay paper corresponding to mild values ​​is: 4.4≤pH≤5.4, set as window 2; the pH color change range of the chromatographic bioassay paper corresponding to inflammation is: 5.5≤pH≤6.5, set as window 3; the pH color change range of the chromatographic bioassay paper corresponding to severe values ​​is: pH≥6.5, set as window 4.

[0024] When using the utility model gynecological inflammation rapid detection kit, first tear open the waterproof sealed packaging bag, use a medical sampling stick to extract vaginal secretions, and insert the cotton swab stained with secretions into the biological diluent sample tube and stir to elute the secretions and fully mix with the diluent, wait for 15 to 30 seconds, and use a dropper to drop the mixed liquid to be tested mixed with secretions in the sample tube into the drop sample hole (5 to 7 drops) in the detection area of ​​the test card. After the mixed liquid is adsorbed to the 4 color block display windows above, the result is interpreted. The interpretation time should be controlled within 10 to 15 minutes. Figure 2 shown.

[0025] When using the utility model gynecological inflammation rapid detection kit for detection, if the detection kit only displays light yellow in window No. 1, the detection sample is "normal"; if the detection kit displays light green in window No. 2, the detection sample is "mild"; if the detection kit displays blue in windows No. 1 to 3, the detection sample is "inflammation"; if the detection kit displays blue in windows No. 1 to 3 and dark green in window No. 4, the detection sample is "severe", such as Figure 2 shown.

[0026] The detection kit, sampling cotton swab, biological dilution sample tube and dropper of the utility model are all separately packaged. Due to the characteristics of independent packaging, contamination and misoperation are reduced to the greatest extent. During the detection process, the self-test determination of the degree of inflammation is based on visual comparison, and the detection kit is marked with the corresponding test results, which can reduce errors and improve the accuracy of the self-test results.

Claims

1. A self-test kit for rapid detection of gynecological inflammation, comprising a test kit card and a sample tube, characterized in that: The sample tube contains a biological diluent, the test card has a chromatographic biological test strip fixed inside, and the test card panel is provided with a test area and a display area corresponding to the test strip. The test area is used to drip the sample liquid to be tested, and the display area is provided with four color block display windows No. 1 to No. 4, which respectively correspond to the four self-test judgment results of normal, mild, inflammation and severe.

2. The self-test kit for rapid detection of gynecological inflammation according to claim 1, characterized in that: The test kit also includes a sampling cotton swab and a dropper, and the test card, sample tube, sampling cotton swab and dropper are packaged in independent sealed packages.

3. The self-test kit for rapid detection of gynecological inflammation according to claim 1, characterized in that: The four color block display windows in the display area of ​​the detection card respectively correspond to the pH color change range of the chromatographic bioassay test paper, 3.8≤pH≤4.4 for normal, 4.4≤pH≤5.4 for mild symptoms, 5.5≤pH≤6.5 for inflammation, and pH≥6.5 for severe symptoms.

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