Induction type anal bag for severely ill patient

Abstract

An induction type anal bag for a severely ill patient comprises a bag body, a check valve and a drain valve. The check valve is an inductive one-way valve and is connected with an artificial anus of a patient through a connecting pipe; a temperature sensor, a smell sensor and a humidity sensor are arranged on the check valve; the rear end of the check valve is connected with an inlet pipe; the inlet pipe is connected with an inlet hole of the bag body; the drain valve is arranged at the bottom of the bag body; and the rear end of the drain valve is connected with the drain pipe. By detecting the temperature, the humidity, the smell components and the characteristics of various different smell components in the connecting pipe, on-off of the check valve is controlled, and the excretion accuracy and the intelligent degree of the critical patient are improved.

Description

Technical Field

[0001] The utility model relates to the field of medical auxiliary products, in particular to an induction anal bag for seriously ill patients. Background Art

[0002] An anal bag (also known as an "anal bag") is a medical aid used to collect fecal matter discharged from an artificial anus (also known as a stoma). When doctors treat patients with certain intestinal diseases (such as inflammatory bowel disease or colon cancer), part of the intestine is removed and the remaining intestine is connected to the patient's abdominal skin, creating an external opening in the process.

[0003] The use of anal bags requires attention to hygiene and regular care, including regular replacement of the anal bag, timely cleaning of the skin around the anal bag and the stoma, and the use of correct hygiene techniques when handling the anal bag and excrement. Timely and correct use and care will reduce the risk of skin problems and infections, thereby improving the patient's quality of life.

[0004] The existing artificial anus bag is not highly intelligent. When using the existing artificial anus bag, seriously ill patients find it difficult to accurately judge the timing of discharging the excrement discharged from the artificial anus into the anus bag. At the same time, the odor in the artificial anus bag storing the excrement will also be emitted, affecting the patient's living environment. Utility Model Content

[0005] The purpose of the present application is to provide an induction anal bag for seriously ill patients to solve the technical problems described in the background technology.

[0006] The technical solutions adopted in this application are as follows:

[0007] An induction anal bag for seriously ill patients comprises: a bag body, a stop valve and a discharge valve; the stop valve is an induction one-way valve, connected to the patient's artificial anus through a connecting pipe; a temperature sensor, an odor sensor and a humidity sensor are arranged on the stop valve; the rear end of the stop valve is connected to an inlet pipe, which is connected to an inlet hole of the bag body; the discharge valve is arranged at the bottom of the bag body, and the rear end of the discharge valve is connected to the discharge pipe; a control module is used to issue control instructions to each functional module; the temperature sensor, the odor sensor and the humidity sensor are all connected to a first communication module, the second communication module is electrically connected to the control module, and the first communication module and the second communication module are in communication connection with each other.

[0008] Preferably, the induction anal bag for seriously ill patients further comprises: medical staff can communicate with the second communication module via a mobile terminal.

[0009] Preferably, a storage plate is provided on the top of the accommodating cavity, and the storage plate and the top of the bag body form a cavity for placing a micro pump, and the micro pump is connected to a double-cavity air tube; one end of the double-cavity air tube is connected to the accommodating cavity, and the other end is connected to a deodorizing box; an odor adsorbent wrapped in non-woven fabric is provided in the deodorizing box.

[0010] Preferably, a connecting plate is provided on the top of the bag body, and the deodorizing box is mounted on the connecting plate by a detachable connection method in the form of a thread or a buckle; the front end of the double-cavity air tube is mounted on the storage plate, and the rear end is mounted on the connecting plate.

[0011] Preferably, the deodorizing box is installed on the bag body in a detachable connection manner.

[0012] Preferably, an adhesive disc is provided on the bag body, which is fixedly connected to the bag body. The adhesive disc can be attached to the patient's skin, and medical staff can also use the adhesive disc to fix the induction anal bag of a seriously ill patient on a mounting frame around the patient.

[0013] Preferably, a liquid filter plate is provided at the front end of the double-lumen air tube to prevent excrement in the accommodating cavity from entering the double-lumen air tube.

[0014] Preferably, a volume detection sensor may be disposed in the cavity formed by the storage plate and the top of the bag body.

[0015] Preferably, a double-cavity connecting tube is installed on the top connecting plate of the bag body, the double-cavity connecting tube is connected to the double-cavity air tube, and the other end of the double-cavity connecting tube is connected to the air purification device.

[0016] The present application relates to an induction anal bag for seriously ill patients, and the advantages and positive effects of the present application are:

[0017] 1. By detecting the temperature, humidity, odor components in the connecting pipe, as well as the characteristics of various odor components, the on-off of the stop valve is controlled, thereby improving the accuracy and intelligence of excretion for critically ill patients.

[0018] 2. The micro pump connected to the double-cavity air tube allows the gas to enter the deodorizing box through the double-cavity air tube when it is working, and returns to the containing cavity after being adsorbed and deodorized by the odor absorbent, thereby removing the odor of the excrement in the containing cavity; the cavity formed by the storage plate and the top of the bag body is not connected to the containing cavity and the deodorizing box, so that the operation of the micro pump placed in the cavity is not affected by the excrement gas and liquid.

[0019] 3. The deodorizing box is installed on the bag body in a detachable connection. Regularly replacing the odor absorbent in the deodorizing box can maintain the odor removal effect of the deodorizing box on the induction anal bag of seriously ill patients. BRIEF DESCRIPTION OF THE DRAWINGS

[0020] One or more embodiments are exemplarily described by corresponding drawings, which do not constitute limitations on the embodiments. Elements with the same reference numerals in the drawings represent similar elements, and the figures in the drawings do not constitute proportional limitations unless otherwise stated.

[0021] Figure 1 The present invention is a schematic structural diagram of an embodiment of an induction anal bag for seriously ill patients.

[0022] Figure 2 The present invention is a schematic structural diagram of a deodorizing box of an induction anal bag for seriously ill patients according to an embodiment of the present invention.

[0023] Figure 3 The present invention is a schematic structural diagram of another embodiment of an induction anal bag for seriously ill patients.

[0024] Figure 4 The present invention is a functional module diagram of an embodiment of an induction anal bag for seriously ill patients. DETAILED DESCRIPTION

[0025] The technical solutions in the embodiments of the present application will be described below in conjunction with the accompanying drawings.

[0026] In the embodiments of the present application, prefixes such as "first" and "second" are used only to distinguish different description objects, and have no limiting effect on the position, order, priority, quantity or content of the described objects. The use of prefixes such as ordinal numbers to distinguish description objects in the embodiments of the present application does not constitute a limitation on the described objects. For the statement of the described objects, please refer to the description in the context of the claims or embodiments, and no unnecessary limitation should be constituted due to the use of such prefixes. In addition, in the description of the present embodiment, unless otherwise specified, the meaning of "multiple" is two or more.

[0027] The directions or positional relationships indicated by the terms "upper", "lower", "left", "right", "front", "back", "top", "bottom", "inside" and "outside" in the embodiments of the present application are based on the directions or positional relationships shown in the accompanying drawings and are only for the convenience of describing the present application and simplifying the description. They do not indicate or imply that the referred device or element must have a specific direction, be constructed and operated in a specific direction. Therefore, they should not be understood as limitations on the present application.

[0028] In the description of the present invention, it is also necessary to explain that, unless otherwise clearly specified and limited, the terms "setting", "installation" and "connection" should be understood in a broad sense. For example, "connection" can be a fixed connection, a detachable connection or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium, or it can be the internal connection of two components. For ordinary technicians in this field, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

[0029] As the instruction manual Figure 1-4 As shown: an inductive anal bag for seriously ill patients, comprising: a bag body 100, a stop valve 200, and an excretion valve 121; the stop valve 200 is an inductive one-way valve that can prevent excrement from flowing back, and the stop valve 200 is connected to the patient's artificial anus through a connecting tube 210; the stop valve 200 is provided with a temperature sensor 201, an odor sensor 202, and a humidity sensor 203, the temperature sensor 201 is used to detect the temperature in the connecting tube 210, the odor sensor 202 is used to detect the odor components in the connecting tube 210, and the characteristics of multiple different odor components, the humidity sensor 203 is used to detect the humidity in the connecting tube 210, and the control module 300 Receive the corresponding data transmitted by the temperature sensor 201, the odor sensor 202 and the humidity sensor 203, and control the on-off of the stop valve 200 according to the temperature, humidity, odor components, and characteristics of various different odor components in the connecting tube 210. At the same time, the temperature, humidity, odor components, and characteristics of various different odor components in the connecting tube 210 can also assist medical staff in diagnosing the patient's physical condition according to the corresponding numerical values; the rear end of the stop valve 200 is connected to the inlet tube 220, and the inlet tube 220 is connected to the inlet hole 102 of the bag body 100; the drain valve 121 is arranged at the bottom of the bag body 100, and the rear end of the drain valve 121 is connected to the drain pipe 120.

[0030] The working principle of an inductive anal bag for seriously ill patients is as follows: when the temperature sensor 201, the odor sensor 202 and the humidity sensor 203 detect that the corresponding values ​​in the connecting tube 210 reach the threshold, the control module 300 sends a control instruction to the stop valve 200, the stop valve 200 opens, and the patient's excrement enters the accommodating chamber 101 formed by the bag body 100. When the excrement in the accommodating chamber 101 reaches a certain value, the medical staff can open the discharge valve 121, and the excrement in the accommodating chamber 101 is discharged through the discharge pipe 120.

[0031] In this embodiment, by detecting the temperature, humidity, odor components, and characteristics of a variety of different odor components in the connecting tube, the on-off of the stop valve is controlled, thereby improving the accuracy and intelligence of excretion for critically ill patients.

[0032] Specifically, an induction anal bag for seriously ill patients includes: a control module 300, which is used to issue control instructions to each functional module; a temperature sensor 201, an odor sensor 202 and a humidity sensor 203 are all connected to a first communication module 310, and a second communication module 311 is electrically connected to the control module 300. The first communication module 310 and the second communication module 311 are communicatively connected to transmit data such as temperature, humidity, odor components, and characteristics of multiple different odor components in a connecting tube 210 collected by the temperature sensor 201, the odor sensor 202 and the humidity sensor 203, and at the same time, transmit control instructions to the stop valve to control the on and off of the stop valve.

[0033] Specifically, the storage module 320 is electrically connected to the control module 300 and is used to store data such as the operating program and operating status of the induction anal bag for seriously ill patients.

[0034] Specifically, the medical staff can communicate with the second communication module 311 through the mobile terminal, so as to control the operation of the induction anal bag of the seriously ill patient through the mobile terminal, and can also receive the warning information sent by the control module 300 through the mobile terminal.

[0035] Specifically, the material, length, and thickness of the connecting tube 210, the inlet tube 220, and the discharge tube 120 are determined according to the specific installation and use environment of the induction anal bag.

[0036] Specifically, a storage plate 110 is provided on the top of the accommodating chamber 101, and the storage plate 110 and the top of the bag body 100 form a cavity for placing a micro pump 112, and the micro pump 112 is connected to the double-cavity air tube 111; one end of the double-cavity air tube 111 is connected to the accommodating chamber 101, and the other end is connected to the deodorizing box 211; the deodorizing box 211 is provided with an odor absorbent 215 wrapped in non-woven fabric, which is used to absorb the odor of excrement in the accommodating chamber 101.

[0037] In this embodiment, the micro pump 112 connected to the double-cavity air tube 111, when in operation, allows the gas to enter the deodorizing box 211 through the double-cavity air tube 111, and then returns to the accommodating chamber 101 after being adsorbed and deodorized by the odor adsorbent 215, thereby removing the odor of the excreta in the accommodating chamber 101; the cavity formed by the storage plate 110 and the top of the bag body 100 is not connected to the accommodating chamber 101 and the deodorizing box 211, so that the operation of the micro pump 112 placed in the cavity is not affected by the excreta gas and liquid.

[0038] Specifically, the micro pump 112 is electrically connected to the control module 300 and receives a control instruction from the control module 300 to switch between the inflation / stop working states.

[0039] Specifically, a connecting plate 113 is provided on the top of the bag body 100 , and the deodorizing box 211 is installed on the connecting plate 113 by a detachable connection method (thread, snap, etc.); the front end of the double-chamber air tube 111 is installed on the storage plate 110 , and the rear end is installed on the connecting plate 113 .

[0040] In this embodiment, the deodorizing box 211 is installed on the bag body 100 in a detachable manner. The odor adsorbent 215 in the deodorizing box 211 is replaced regularly to maintain the odor removal effect of the deodorizing box 211 on the induction anal bag of seriously ill patients.

[0041] Specifically, an adhesive disc 230 is provided on the bag body 100, and the adhesive disc 230 is fixedly connected to the bag body 100. The adhesive disc 230 can be attached to the patient's skin, and medical staff can also use the adhesive disc 230 to fix the induction anal bag of a seriously ill patient on the mounting frame around the patient.

[0042] Specifically, a liquid filter plate is disposed at the front end of the double-lumen air tube 111 to prevent excrement in the accommodating cavity 101 from entering the double-lumen air tube 111 .

[0043] In another embodiment, a double-cavity connecting tube 221 is installed on the top connecting plate 113 of the bag body 100, the double-cavity connecting tube 221 is connected to the double-cavity air tube 111, and the other end of the double-cavity connecting tube 221 is connected to the air purification device 240. The air purification device 240 absorbs and purifies the odor of excrement in the accommodating cavity 101 through the double-cavity connecting tube 221 and the double-cavity air tube 111.

[0044] In another embodiment, a volume detection sensor (not shown in the figure) may be further provided in the cavity formed by the storage plate 110 and the top of the bag body 100, for detecting the volume of excrement in the accommodating chamber 101. When the volume of excrement in the accommodating chamber 101 exceeds a threshold value, the control module 300 sends a warning message to the medical staff, so that the medical staff can open the discharge tube 120 in time to discharge the excrement in the accommodating chamber 101.

[0045] In the description of this specification, the description with reference to the terms "one embodiment", "some embodiments", "example", "specific example", or "some examples" means that the specific features, structures, materials or characteristics described in conjunction with the embodiment or example are included in at least one embodiment or example of the utility model. In this specification, the schematic representation of the above terms does not necessarily refer to the same embodiment or example. Moreover, the specific features, structures, materials or characteristics described can be combined in any one or more embodiments or examples in a suitable manner.

[0046] The above-mentioned embodiments only express several implementation methods of the utility model, and the descriptions are relatively specific and detailed, but they cannot be understood as limiting the scope of the utility model patent. It should be pointed out that for ordinary technicians in this field, several modifications and improvements can be made without departing from the concept of the utility model, which all belong to the protection scope of the utility model. Therefore, the protection scope of the utility model patent shall be based on the attached claims.

Claims

1. An induction anal bag for seriously ill patients, characterized in that: include: The bag body (100), the stop valve (200), and the discharge valve (121); the stop valve (200) is an inductive one-way valve, and the stop valve (200) is connected to the patient's artificial anus through a connecting tube (210); the stop valve (200) is provided with a temperature sensor (201), an odor sensor (202), and a humidity sensor (203); the rear end of the stop valve (200) is connected to an inlet tube (220), and the inlet tube (220) is connected to an inlet hole (102) of the bag body (100); the discharge valve (121) is connected to the inlet hole (102) of the bag body (100); The valve (121) is arranged at the bottom of the bag body (100), and the rear end of the discharge valve (121) is connected to the discharge pipe (120); the control module (300) is used to issue control instructions to each functional module; the temperature sensor (201), the odor sensor (202) and the humidity sensor (203) are all connected to the first communication module (310), the second communication module (311) is electrically connected to the control module (300), and the first communication module (310) and the second communication module (311) are communicatively connected with each other.

2. The induction anal bag for seriously ill patients as claimed in claim 1, characterized in that: The induction anal bag for seriously ill patients also includes: medical staff can communicate with the second communication module (311) through a mobile terminal.

3. The induction anal bag for seriously ill patients as claimed in claim 2, characterized in that: A storage plate (110) is arranged on the top of the accommodating cavity (101); the storage plate (110) and the top of the bag body (100) form a cavity for accommodating a micro pump (112); the micro pump (112) is connected to a double-cavity air tube (111); one end of the double-cavity air tube (111) is connected to the accommodating cavity (101), and the other end is connected to a deodorizing box (211); an odor absorbent (215) wrapped in non-woven fabric is arranged in the deodorizing box (211).

4. The induction anal bag for seriously ill patients as claimed in claim 3, characterized in that: A connecting plate (113) is provided on the top of the bag body (100), and the deodorizing box (211) is mounted on the connecting plate (113) by a detachable connection method in the form of a thread or a buckle; the front end of the double-cavity air tube (111) is mounted on the storage plate (110), and the rear end is mounted on the connecting plate (113).

5. The induction anal bag for seriously ill patients as claimed in claim 4, characterized in that: The deodorizing box (211) is installed on the bag body (100) in a detachable connection manner.

6. The induction anal bag for seriously ill patients as claimed in claim 5, characterized in that: An adhesive disc (230) is arranged on the bag body (100), and the adhesive disc (230) is fixedly connected to the bag body (100). The adhesive disc (230) can be attached to the skin of a patient, and medical staff can also fix the induction anal bag of a seriously ill patient on a mounting frame around the patient through the adhesive disc (230).

7. The induction anal bag for seriously ill patients as claimed in claim 6, characterized in that: A liquid filter plate is provided at the front end of the double-lumen air tube (111) to prevent excrement in the accommodating cavity (101) from entering the double-lumen air tube (111).

8. The induction anal bag for seriously ill patients as claimed in claim 7, characterized in that: A volume detection sensor may also be arranged in the cavity formed by the storage plate (110) and the top of the bag body (100).

9. The induction anal bag for seriously ill patients as claimed in claim 2, characterized in that: A double-cavity connecting tube (221) is installed on the top connecting plate (113) of the bag body (100), the double-cavity connecting tube (221) is connected to the double-cavity air tube (111), and the other end of the double-cavity connecting tube (221) is connected to the air purification device (240).

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