Test box and integrated test pack for testing and evaluating dysphagia
By integrating the self-standing bag and container test box with preset consistency, the problem of allocation errors in swallowing dysphagia test is solved, and the accuracy and efficiency of the test results are improved.
Patent Information
- Application Number
- CN202421644208.2
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-11
- Publication Date
- 2025-09-05
- Estimated Expiration
- 2034-07-11
AI Technical Summary
In the prior art, the volume-viscosity swallowing test method of the dysphagia test has errors and differences in operating methods due to the temporary preparation of the test solution by the distributor, resulting in inaccurate test results and low efficiency.
A test box for dysphagia test evaluation is provided, integrating self-standing bags and containers with preset consistency, including test gels of different consistency, avoiding temporary preparation and improving accuracy and efficiency.
By integrating the test box and preset consistency gel, the accuracy and operating efficiency of materials during the test process can be ensured, artificial errors can be reduced, and the reliability and speed of test results can be improved.
Smart Images
Figure CN223299176U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of medical equipment, and in particular to a test box and an integrated test package for dysphagia testing and evaluation. Background Art
[0002] The volume-viscosity swallowing test (V-VST) is one of the most commonly used screening methods. It can clearly determine whether a subject has swallowing difficulties. However, during clinical application, the test solution must be prepared on-site by the preparer. Because thickener parameters are not quantified, there is a certain degree of error during preparation, resulting in failure to achieve the desired consistency. Furthermore, differences in the preparer's technique can lead to variations in the viscosity of the solution after each preparation, resulting in inaccurate test results and low test efficiency. Utility Model Content
[0003] In order to solve the problems of the prior art, the embodiments of the present application disclose a test box and an integrated test package for swallowing disorder testing and evaluation. The present application provides a test box for swallowing disorder testing and evaluation, comprising a first box body, a second box body, a third box body, a fourth box body and a fifth box body, wherein the second box body, the third box body, the fourth box body and the fifth box body are arranged in the first box body; the second box body and the third box body are arranged adjacent to each other for placing a self-supporting bag, which contains a test gel of a preset consistency; the fourth box body and the fifth box body are arranged adjacent to each other for placing a container, which is used to hold the test gel squeezed out of the self-supporting bag. The test box of the present application integrates the materials required in the testing process and is filled with a prepared test gel of a preset consistency, thereby avoiding the need for medical staff to temporarily configure the test gel during clinical use, thereby improving the accuracy and clinical operation efficiency. The technical solution of the embodiments of the present application is as follows:
[0004] In one aspect, the present application provides a test box for swallowing disorder testing and evaluation, comprising a first box body, a second box body, a third box body, a fourth box body, and a fifth box body, wherein the second box body, the third box body, the fourth box body, and the fifth box body are disposed in the first box body;
[0005] The second box body and the third box body are adjacently arranged and used to place a stand-up bag containing a test gel of a preset consistency;
[0006] The fourth box body and the fifth box body are adjacently arranged and used for placing a container, and the container is used for containing the test gel squeezed out of the self-supporting bag.
[0007] In some specific embodiments, the second box body and the third box body have the same specifications and are respectively filled with a plurality of the self-supporting bags;
[0008] The plurality of self-supporting bags are filled with the test gels of different preset consistencies.
[0009] In some specific embodiments, the fourth box body and the fifth box body have the same specifications and are respectively equipped with a plurality of the containers, and the number of the plurality of the containers matches the number of the plurality of stand-up bags.
[0010] In some specific embodiments, the stand-up bag includes a bag body, a bag bottom, a bag mouth and a bag cap, and the bag cap is arranged outside the bag mouth.
[0011] In some specific embodiments, the plurality of self-supporting bags have the same specifications and are arranged adjacent to each other in sequence;
[0012] Among them, between two adjacent self-supporting bags, the bag mouth of one of the self-supporting bags is arranged close to the bag bottom of the other self-supporting bag.
[0013] In some specific embodiments, the container comprises a container cover and a container body,
[0014] The cover is provided with a first fixing portion, and the container body is provided with a second fixing portion, and the first fixing portion is fixedly connected to the second fixing portion;
[0015] The container cover and the container body are connected by a buckle at one end away from the first fixing portion and the second fixing portion.
[0016] In some specific embodiments, the multiple containers have the same specifications and are arranged adjacent to each other in sequence;
[0017] Wherein, between two adjacent containers, the container cover of one container is arranged close to the bottom of the other container.
[0018] In some specific embodiments, the container is truncated cone-shaped.
[0019] In some specific embodiments, the first box body, the second box body, the third box body, the fourth box body and the fifth box body are made of white card.
[0020] On the other hand, the present application also provides an integrated test kit for swallowing disorder testing and evaluation, comprising a test gel and the above-mentioned test box, wherein the test gel is a set of configured gel combinations, and the test gel is disposed in the test box;
[0021] The gel combination includes a plurality of test gels of different preset consistencies.
[0022] By adopting the above technical solution, the present application provides a test box and integrated test package for swallowing disorder test and evaluation, which have the following beneficial effects:
[0023] The embodiments of the present application disclose a test box and an integrated test package for swallowing disorder testing and evaluation. The present application provides a test box for swallowing disorder testing and evaluation, comprising a first box body, a second box body, a third box body, a fourth box body and a fifth box body, wherein the second box body, the third box body, the fourth box body and the fifth box body are arranged in the first box body; the second box body and the third box body are arranged adjacent to each other for placing a self-supporting bag containing a test gel of a preset consistency; the fourth box body and the fifth box body are arranged adjacent to each other for placing a container for containing the test gel squeezed out of the self-supporting bag. The test box of the present application integrates the materials required in the test process and is filled with a prepared test gel of a preset consistency, thereby avoiding the need for the preparer to temporarily prepare the test gel during clinical use, thereby improving accuracy and clinical operation efficiency. BRIEF DESCRIPTION OF THE DRAWINGS
[0024] In order to more clearly illustrate the technical solutions in the embodiments of the present application, the following briefly introduces the drawings required for use in the description of the embodiments. Obviously, the drawings described below are only some embodiments of the present application. For ordinary technicians in this field, other drawings can be obtained based on these drawings without any creative work.
[0025] Figure 1 A schematic diagram of a test kit for swallowing disorder testing and evaluation provided in an embodiment of the present application;
[0026] Figure 2 A schematic diagram of a second box body or a third box body provided in an embodiment of the present application;
[0027] Figure 3 A schematic diagram of another second box body or a third box body provided in an embodiment of the present application;
[0028] Figure 4 A schematic diagram of a fourth box body or a fifth box body provided in an embodiment of the present application;
[0029] Figure 5 A schematic diagram of another fourth box body or fifth box body provided in an embodiment of the present application;
[0030] Figure 6 A schematic diagram of a stand-up pouch provided in an embodiment of the present application;
[0031] Figure 7 A schematic diagram of a container provided in an embodiment of the present application;
[0032] The following is a supplementary description of the accompanying drawings:
[0033] 1-first box body; 2-second box body; 3-third box body; 4-fourth box body; 5-fifth box body; 6-stand-up bag; 61-bag body; 62-bag bottom; 63-bag mouth; 64-bag cap; 7-container; 71-container cover; 72-container body. DETAILED DESCRIPTION
[0034] The following will be combined with the accompanying drawings in the embodiments of this application to clearly and completely describe the technical solutions in the embodiments of this application. Obviously, the embodiments described are only part of the embodiments of this application, not all of them. Based on the embodiments in this application, all other embodiments obtained by ordinary technicians in this field without making any creative work are within the scope of protection of this application.
[0035] References to "one embodiment" or "embodiment" herein refer to specific features, structures, or characteristics that may be included in at least one implementation of the present application. Throughout the description of this application, it should be understood that the terms "upper," "lower," "top," and "bottom," etc., indicating orientations or positional relationships, are based on the orientations or positional relationships shown in the accompanying drawings and are intended solely for ease of description and simplification. They do not indicate or imply that the devices or components referred to must have a specific orientation, be constructed, or operate in a specific orientation, and are therefore not to be construed as limiting the present application. Furthermore, the terms "first" and "second" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly specifying the number of the technical features indicated. Thus, a feature designated "first" or "second" may explicitly or implicitly include one or more of such features. Furthermore, the terms "first," "second," etc. are used to distinguish similar objects and are not necessarily used to describe a specific order or sequential sequence. It should be understood that such terms are interchangeable where appropriate, so that the embodiments of the present application described herein can be implemented in an order other than that illustrated or described herein.
[0036] When a numerical range is disclosed herein, the above range is considered to be continuous and includes the minimum and maximum values of the range, as well as every value between such minimum and maximum values. Further, when a range refers to an integer, every integer between the minimum and maximum values of the range is included. In addition, when multiple ranges are provided to describe a feature or characteristic, the ranges can be merged. In other words, unless otherwise indicated, all ranges disclosed herein should be understood to include any and all subranges included therein. For example, a specified range from "1 to 10" should be considered to include any and all subranges between a minimum of 1 and a maximum of 10. Exemplary subranges of the range 1 to 10 include, but are not limited to, 1 to 6.1, 3.5 to 7.8, 5.5 to 10, etc.
[0037] See also Figure 1 、 Figure 2 and Figure 4 , a test box for swallowing disorder test and evaluation according to an embodiment of the present application includes a first box body 1, a second box body 2, a third box body 3, a fourth box body 4 and a fifth box body 5, and the second box body 2, the third box body 3, the fourth box body 4 and the fifth box body 5 are arranged in the first box body 1; preferably, the first box body 1, the second box body 2, the third box body 3, the fourth box body 4 and the fifth box body 5 are all rectangular in shape, and the specifications of the first box body 1 are 192 mm in length, 74.5 mm in width and 163 mm in height, the second box body 2 and the third box body 3 have the same specifications, which are 72.5 mm in length, 64.5 mm in width and 160 mm in height, and the fourth box body 4 and the fifth box body 5 have the same specifications, which are 58 mm in length, 34.4 mm in width and 160 mm in height, and the second box body 2, the third box body 3, the fourth box body 4 and the fifth box body 5 are tightly arranged in the first box body 1, with high integration, and can integrate the materials required in the test process, thereby improving clinical operation efficiency.
[0038] The second and third boxes 2 and 3 are positioned adjacent to each other and are used to house a self-supporting bag 6 containing a test gel of a preset consistency. Specifically, the second and third boxes 2 and 3 are positioned horizontally adjacent to each other within the first box 1, each containing a test gel of a different preset consistency. Preferably, 20ml of each of three solutions of different viscosities and 20ml of purified water can be configured. The three solutions of varying consistencies are thickened using the same or different thickeners, with the viscosities meeting the JSDR 2013 grading standards: low viscosity 50-150mPa·s, medium viscosity 150-300mPa·s, and high viscosity 300-500mPa·s. During the test, medical staff can adjust the concentration of the test gel based on the patient's test performance and proceed to the next step of the test, effectively improving the efficiency of dysphagia testing.
[0039] The fourth box body 4 and the fifth box body 5 are arranged adjacent to each other and are used to place the container 7. The container 7 is used to contain the test gel squeezed out of the self-supporting bag 6. Specifically, the fourth box body 4 and the fifth box body 5 are arranged adjacent to each other along the axial direction in the first box body 1 and are used to place the container 7 respectively. During the test process, the medical staff directly pours the test gel contained in the self-supporting bag 6 into the container 7, which is convenient to use.
[0040] In some specific embodiments, see Figure 2 and Figure 3 The second box body 2 and the third box body 3 have the same specifications and are respectively equipped with multiple self-supporting bags 6; preferably, the second box body 2 and the third box body 3 are respectively equipped with three self-supporting bags 6, so that the self-supporting bags just fill the second box body 2 and the third box body 3, with high integration.
[0041] The plurality of self-supporting bags 6 are filled with test gels of different preset consistencies, which can effectively avoid the need for medical staff to temporarily prepare test gels during the test process, resulting in low efficiency of clinical operations. In addition, the thickener index in the test gel is not quantified, and there is an error in the amount of thickener used to a certain extent. In addition, the difference in the operating techniques of the preparer will lead to differences in the viscosity of the solution after each preparation, resulting in deviations in the evaluation effect.
[0042] In some specific embodiments, see Figure 4 and Figure 5 The fourth box body 4 and the fifth box body 5 have the same specifications and are respectively equipped with multiple containers 7. The number of the multiple containers 7 matches the number of the multiple self-supporting bags 6. During the test, medical staff can directly pour the test gel contained in the self-supporting bags 6 into the containers 7, which is convenient for use.
[0043] In some specific embodiments, see Figure 6 The stand-up bag 6 includes a bag body 61, a bag bottom 62, a bag mouth 63, and a bag cap 64. The bag cap 64 is arranged outside the bag mouth 63. Specifically, the bag body 61 is made of soft material, which is convenient for squeezing the test gel inside out of the bag mouth 63 and can prevent the test gel from flowing out when pouring, thereby avoiding waste.
[0044] In some specific embodiments, see Figure 2 and Figure 3 , multiple self-supporting bags 6 have the same specifications and are arranged adjacent to each other in sequence, with high integration and convenient storage.
[0045] Between two adjacent self-supporting bags 6, the mouth 63 of one self-supporting bag 6 is positioned adjacent to the bottom 62 of the other self-supporting bag 6. This arrangement of two adjacent self-supporting bags 6, one upside down and the other inverted, effectively ensures the stability of the self-supporting bags 6 and prevents the test gel from being damaged during transportation. The arrangement between adjacent self-supporting bags 6 may also be other arrangements, which are not limited in this application.
[0046] In some specific embodiments, see Figure 7 The container 7 includes a container cover 71 and a container body 72. The container cover 71 is provided with a first fixing portion, and the container body 72 is provided with a second fixing portion. The first fixing portion and the second fixing portion are fixedly connected. Preferably, the specification of the container 7 is 50ml and is made of plastic. By providing the container cover 71, it can be effectively ensured that the container 7 is not contaminated during transportation and the inner cavity of the container body 72 is kept clean.
[0047] The container cover 71 and the container body 72 are connected by a snap fastener at one end away from the first fixing portion and the second fixing portion, which is convenient to open and make use more convenient.
[0048] In some specific embodiments, see Figure 4 and Figure 5 , multiple containers 7 have the same specifications and are arranged adjacent to each other in sequence, with high integration and convenient storage.
[0049] Among them, between two adjacent containers 7, the container cover 71 of one container 7 is arranged close to the bottom of the other container 7. This "one upside-down, one inverted" arrangement between the two adjacent containers 7 can effectively ensure the stability of the containers 7 and make the arrangement more compact, thereby improving the capacity. The arrangement between adjacent containers 7 can also be other arrangements, which are not limited in this application.
[0050] In some specific embodiments, see Figure 7 , the shape of the container 7 is a truncated cone. Preferably, the shape of the container 7 is a truncated cone, and can also be other shapes, which is not limited in this application.
[0051] In some specific embodiments, see Figure 4 and Figure 5 The first box body 1, the second box body 2, the third box body 3, the fourth box body 4, and the fifth box body 5 are made of white card. Preferably, the first box body 1 is made of 400g white card, and the second box body 2, the third box body 3, the fourth box body 4, and the fifth box body 5 are made of 350g white card. The test kit of the present application has low cost, simple process, short production cycle, and is easy to mass produce and promote.
[0052] An integrated test kit for swallowing disorder testing and evaluation according to an embodiment of the present application includes a test gel and the above-mentioned test box. The test gel is a set of configured gel combinations, and the test gel is arranged in the test box to facilitate the integration of materials required during the test process and improve clinical operation efficiency.
[0053] The gel combination includes multiple groups of test gels with different preset consistencies. Preferably, the gel combination includes three groups of test gels with different preset consistencies, including a low viscosity of 50-150 mPa·s, a medium viscosity of 150-300 mPa·s, and a high viscosity of 300-500 mPa·s. This allows for mass production using a unified standard, which is beneficial for quality control, reducing deviations and risks in clinical testing, and promoting improvements in the taste of the test solution, thereby enhancing the subjective experience of the test subjects.
[0054] The embodiments of the present application disclose a test box and an integrated test package for swallowing disorder testing and evaluation. The present application provides a test box for swallowing disorder testing and evaluation, comprising a first box body, a second box body, a third box body, a fourth box body and a fifth box body, wherein the second box body, the third box body, the fourth box body and the fifth box body are arranged in the first box body; the second box body and the third box body are arranged adjacent to each other for placing a self-supporting bag containing a test gel of a preset consistency; the fourth box body and the fifth box body are arranged adjacent to each other for placing a container for containing the test gel squeezed out of the self-supporting bag. The test box of the present application integrates the materials required in the test process and is filled with a prepared test gel of a preset consistency, thereby avoiding the need for the preparer to temporarily prepare the test gel during clinical use, thereby improving accuracy and clinical operation efficiency.
[0055] The above description is merely an optional embodiment of the present application and is not intended to limit the present application. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principles of the present application shall be included in the scope of protection of the present application.
Claims
1. A test kit for swallowing disorder test assessment, characterized in that: It comprises a first box body (1), a second box body (2), a third box body (3), a fourth box body (4) and a fifth box body (5), wherein the second box body (2), the third box body (3), the fourth box body (4) and the fifth box body (5) are arranged in the first box body (1); The second box body (2) and the third box body (3) are arranged adjacent to each other and are used to place a self-supporting bag (6), wherein the self-supporting bag (6) is filled with a test gel of a preset consistency; The fourth box body (4) and the fifth box body (5) are arranged adjacent to each other and are used to place a container (7). The container (7) is used to contain the test gel squeezed out of the self-supporting bag (6).
2. A test kit for swallowing disorder test and evaluation according to claim 1, characterized in that: The second box body (2) and the third box body (3) have the same specifications and are respectively filled with a plurality of the self-supporting bags (6); The plurality of self-supporting bags (6) are respectively filled with the test gels of different preset consistencies.
3. A test kit for swallowing disorder testing and evaluation according to claim 1, characterized in that: The fourth box body (4) and the fifth box body (5) have the same specifications and are respectively equipped with a plurality of the containers (7), and the number of the plurality of the containers (7) matches the number of the plurality of self-supporting bags (6).
4. A test kit for swallowing disorder testing and evaluation according to claim 2, characterized in that: The self-supporting bag (6) comprises a bag body (61), a bag bottom (62), a bag mouth (63) and a bag cap (64), wherein the bag cap (64) is arranged outside the bag mouth (63).
5. A test kit for swallowing disorder testing and evaluation according to claim 4, characterized in that: The plurality of self-supporting bags (6) have the same specifications and are arranged adjacent to each other in sequence; Among them, between two adjacent self-supporting bags (6), the bag mouth (63) of one of the self-supporting bags (6) is arranged close to the bag bottom (62) of the other self-supporting bag (6).
6. A test kit for swallowing disorder testing and evaluation according to claim 3, characterized in that: The container (7) comprises a container cover (71) and a container body (72), the container cover (71) is provided with a first fixing portion, the container body (72) is provided with a second fixing portion, and the first fixing portion is fixedly connected to the second fixing portion; The container cover (71) and the container body (72) are connected via a buckle at one end away from the first fixing portion and the second fixing portion.
7. A test kit for swallowing disorder testing and evaluation according to claim 6, characterized in that: The multiple containers (7) have the same specifications and are arranged adjacent to each other in sequence; Wherein, between two adjacent containers (7), the container cover (71) of one container (7) is arranged close to the bottom of the other container (7).
8. A test kit for swallowing disorder test and evaluation according to claim 6 or 7, characterized in that: The container (7) is in the shape of a truncated cone.
9. The test kit for swallowing disorder test and evaluation according to claim 1, characterized in that: The material of the first box body (1), the second box body (2), the third box body (3), the fourth box body (4) and the fifth box body (5) is white card.
10. An integrated test package for swallowing disorder testing and evaluation, characterized in that: A test kit comprising a test gel and any one of claims 1 to 9, wherein the test gel is a set of fully configured gel combinations and the test gel is disposed in the test kit; The gel combination includes a plurality of test gels of different preset consistencies.