JP2023067028A - Detection information notification system using stoma apparatus, drowsiness detection tool used for detection information notification system, heat stroke detection tool, and stoma apparatus - Google Patents

Abstract

To make it possible, when a subject uses a stoma pouch, to grasp pouch replacement time constantly and also to grasp detection information detected from other body parts.SOLUTION: Replacement notification detection information is reported with a wearing position of a stoma apparatus worn by a subject and the detection information is enabled to be confirmed by a device around the subject. Thereby, the subject is enabled to recognize the replacement notification detection information attached to the subject's body without worrying about surroundings. Especially, replacement timing of a stoma pouch and a stoma face plate is enabled to be grasped constantly, which makes it possible to hold a sense of security in a daily life. Monitoring from another body wearing tool attached to the body is enabled at the same time and transmission of detection information to surroundings can be performed in response to abnormal detection information detected by the body wearing tool, which makes it possible to obtain a sense of further security.SELECTED DRAWING: Figure 1

Description

The present invention is a technology for detecting the replacement timing of an ostomy faceplate and an ostomy pouch in an ostomy appliance worn by a subject and notifying the subject, and at the same time, detecting abnormalities in other body information worn by the subject. It is a technology to notify by

Japanese Utility Model Laid-Open No. 62-21003 discloses a diaper cover that changes colors for babies.
Japanese Unexamined Patent Application Publication No. 2000-185065 discloses an excretion sensor system that uses vibration to notify the user of the need to urinate.
Japanese Unexamined Patent Application Publication No. 2002-017765 discloses a face plate for containing and sending excrement.
Japanese Unexamined Patent Application Publication No. 2011-019726 discloses a diaper change detection sensor and a dedicated attachment adapter.
Japanese Patent Application Laid-Open No. 2008-011865 discloses a technique of collecting and managing a plurality of pieces of biometric information in one terminal.
Japanese Patent Application Laid-Open No. 2020-174974 shows a heat stroke detection device with an oxygen sensor on the arm, and when heat stroke symptoms are detected by the oxygen sensor, the heat stroke detection device issues an LED, sounds a buzzer warning sound, and furthermore A technology has been disclosed to display the heat stroke prediction level on the smartphone as well.
Japanese Patent Laid-Open No. 11-151298 discloses that as an auxiliary device for preventing doze, a transmissive sensor or a reflective sensor is provided at or near the glasses to constantly monitor the movement of the eye, and if the movement is excessive, these sensors detect it. There is disclosed a technique for notifying by a buzzer or vibration.
However, in a situation where biometric information can be confirmed by a state sensor in the vicinity of a detection device attached to a subject, there is no prior art that allows a terminal at a distant position to check the biometric information as well.
In addition, a device that manages a plurality of biological information obtained from a subject in one device is confirmed in the prior art, but there is a prior art that notifies the abnormal situation only when the biological information indicates an abnormal value. Not found.
In addition, there are various prior arts of ostomy appliances, and various prior arts of diaper excretion management for infants and elderly people, but these are prior arts for confirming those who are close to them, and the subjects themselves No prior art has been confirmed that makes it possible to confirm the replacement timing of the ostomy appliance.

Japanese Utility Model Laid-Open No. 62-21003 Japanese Patent Application Laid-Open No. 2000-185065 Japanese Patent Application Laid-Open No. 2002-017765 Japanese Unexamined Patent Application Publication No. 2011-019726 Japanese Patent Application Laid-Open No. 2008-011865 Japanese Patent Application Laid-Open No. 2020-174974 JP-A-11-151298

The invention of the present application is an invention for the following problems that cannot be solved by these prior arts.
The origin of the invention was the need to make it easier to check the replacement timing of the ostomy appliance.
Since excretion from the stoma cannot be controlled by the patient himself/herself, excrement accumulates in the ostomy pouch while sleeping, exceeding the storage capacity of the ostomy pouch and overflowing from the back side of the ostomy face plate, causing leakage.
In addition, even if the storage capacity of the ostomy pouch is not exceeded, water as excrement from around the stoma will gradually enter between the subject's body and the ostomy faceplate from around the stoma, causing the manufacturer's limit of use. The ostomy appliance should be replaced when the depth reaches approximately 10 mm from the end of the stoma. The spread from around the stoma to the outer circumference is not visible. In addition, even if the stoma faceplate is touched by hand, it is thick and it is difficult to judge when to replace it.
With the current ostomy appliance, the replacement timing of the ostomy appliance must be determined empirically in light of the subject's living conditions, which is psychologically unfavorable. Therefore, there is a demand for a technique for conveying this information to subjects in a more comprehensible manner.
As I explored this technology, I noticed that various devices have been developed in the world that constantly detect and report the current state of the body. Frequent urination sensor, blood sugar sensor, heat stroke sensor, blood oxygen saturation sensor, etc., are installed and operated with detection tools and devices incorporating the above sensors in various shapes in various parts of the subject's body as necessary. It is
However, the information sensed by each sensor is individually reported to the subject and the persons surrounding the subject.
Therefore, there is a demand for technical development that can collectively operate the reporting forms of these various state sensors and biosensors.
Returning to the original topic, when confirming the timing of changing the ostomy appliance (ostomy pouch and ostomy faceplate) from the device, the subject was always aware of the ostomy pouch and ostomy pouch in the ostomy appliance in their daily activities. There is a situation where it is necessary to change the ostomy faceplate at the right time, and there are also surrounding eyes. If the information can be obtained, it should be communicated to the subject near the time of wearing it, or communicated to another terminal held by the subject, or in the worst case, to be communicated to a third party.
In this application, we are developing a technique to solve these many problems with new ideas.

A sensor is provided on the ostomy faceplate of the ostomy appliance that the subject wears on the body to check the state of excrement, and this sensor detects the replacement timing of the ostomy faceplate as the value of the water content of the excrement or the amount of dye. By making it possible, the subject will be able to easily know when to replace the pouch for smart and the faceplate for stoma.

When the stoma faceplate is attached to the stoma of the subject with a skin protective agent interposed therebetween, a first wiring and a second wiring are provided on the skin protective agent side of the stoma faceplate as a means for detecting the excretions as a water content value. As a result, it is possible to detect the water content of the excrement from the electrical resistance value between the first wiring and the second wiring. The subject can know when to replace the face plate.
In this case, if the wiring shape of the first wiring and the second wiring is arranged in an annular shape so as to machine the stoma mounting opening of the stoma face plate, the detection accuracy is further improved.

As a means for detecting the excreta as a value of the amount of staining to the skin protective agent of the stoma faceplate, a space for confirming the degree of staining is provided in the skin protective agent, and the amount of staining in the space for confirming the degree of staining is detected. It is possible to know when to replace the ostomy pouch and the ostomy faceplate.
For this reason, detection is facilitated by constructing a stain confirmation window at a position corresponding to the stain confirmation space of the stoma faceplate with a transparent member. If the amount of light applied is measured, the progress of staining can be detected electrically, and the timing for exchanging the ostomy pouch and the ostomy faceplate can be notified to surrounding devices and appliances.

In recent years, various biological information has been collected on the subject's body, such as a cerebral infarction detection device, a sleepiness detection device, a frequent urination detection device, a blood sugar level detection device, a heat stroke detection device, and a blood oxygen saturation detection device, in addition to this stoma device. There is an increasing number of situations where biosensors that acquire
Under such circumstances, smartphones are also held by their own sides.
For this reason, not only notification information that indicates when to replace the ostomy pouch and ostomy faceplate detected by the ostomy appliance, but also notification information obtained from the biological information from the above-mentioned various detection tools can be collectively confirmed on the smartphone. becomes possible.
In addition, depending on the urgency at that time, it is also possible to transmit the notification information to an emergency contact designated by the subject.
Furthermore, in addition to smartphones, it is also possible to utilize eyeglasses, which are drowsiness detection tools worn by the subject, as a terminal for notifying the drowsiness detection information obtained from the subject.

As a result, when the subject needs to take some kind of treatment for the body, the subject can directly know the situation near the wearing device, and indirectly, the notification device held by the subject can inform the individual. It is possible to obtain notification information about the need for treatment at a site. In addition, when the subject himself/herself cannot take care of the need, it is also possible to notify the person concerned of the subject himself/herself about the current situation and ask for help from the outside.

The figure which shows the whole view of this invention Explanatory diagram of general specifications for ostomy appliances FIG. 2 is a front view for explaining the ostomy appliance for detecting the amount of excreted water according to the present invention; Fig. 2 is a cross-sectional view of the ostomy appliance for detecting the amount of excreted water of the present invention taken along the line BB'; Circuit diagram and operation diagram of the pouch replacement detection device for detecting the amount of excreted water of the present invention A block diagram of a pouch exchange detection device for detecting the amount of excreted water of the present invention provided with a detection information transmission unit Functional layout diagram of the pouch exchange detection device for detecting the amount of excreted water of the present invention Fig. 2 is a diagram for explaining the ostomy appliance for detecting the amount of excretion stain of the present invention; A configuration diagram in which a detection information transmission unit is attached to the pouch replacement detection device for detecting the amount of excrement staining of the present invention Functional layout diagram of the pouch exchange detection device for detecting the amount of excrement staining of the present invention Explanatory diagram of reporting other sensor information to the sleepiness detector Explanatory diagram for reporting other sensor information to the heat stroke detector

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.
The drawings are examples for explanation, and the present invention is not limited to the following embodiments.

FIG. 1 is a diagram showing an overall view of the present invention.
In FIG. 1, (1-A) is a diagram for explaining the ostomy appliance for reporting the amount of excreted water, in which the ostomy pouch (4) attached to the ostomy faceplate base (8) and the ostomy faceplate (1a2) are exchanged. FIG. 10 is an explanatory diagram of an ostomy appliance (1a) that detects timing as a value of water content in excrement and notifies a subject of the detected replacement notification detection information.
The ostomy appliance (1a) in Fig. 1 (1-A) surrounds the stoma (3) of the subject's body (2) so that the stoma mounting opening (8a) of the ostomy appliance (1a) is positioned on the stoma (3). The ostomy faceplate (1a2) comprises a skin protective agent (7), an ostomy faceplate base (8), a detection information notification unit (11) for notifying replacement notification detection information, and detection information transmission. By attaching the ostomy pouch (4) to the attachment portion provided on the stoma faceplate base (8), excretions are delivered to the subject's body (2). It is to be expanded as a replaceable cattle and manure section.
Here, the replacement timing of the ostomy pouch (4) and the ostomy faceplate (1a2) is determined by connecting the water amount detection wiring (9) to the skin protective agent (7) side of the ostomy faceplate (8) of the ostomy appliance (1a). As a state sensor (10) composed of a first electrode (9a) and a second electrode (9b), the replacement timing of the ostomy pouch (4) and the ostomy face plate (1a2) is detected, and a detection information reporting unit (11 ), and the detection information transmission unit (12) transmits the replacement notification detection information to the external terminal.
The details of the ostomy appliance for informing the water content of excrement will be described with reference to FIGS. 3 to 7. FIG.

In addition, (1-C) of Fig. 1 is a diagram for explaining the ostomy appliance for detecting the amount of excrement stain, and shows the ostomy pouch (4) attached to the ostomy faceplate (1a2) and the ostomy faceplate (1a2). FIG. 2 is an explanatory diagram of an ostomy appliance (1a) that detects replacement timing as a dye amount value of excrement and notifies a subject of the detected replacement notification detection information.
The ostomy appliance (1a) in (1-C) of Fig. 1 is arranged such that the stoma mounting opening (8a) of the stoma face plate (1a2) is attached to the stoma (3) so as to surround the stoma (3) of the subject's body (2). The ostomy faceplate (1a2) comprises a skin protective agent (7), an ostomy faceplate base (8), a detection information notification unit (11) for notifying replacement notification detection information, and detection information transmission. The ostomy pouch (4) is attached to the subject's body (2) at the mounting portion of the stoma faceplate base (8) provided on the stoma faceplate (1a2). It is to be expanded as a storage unit that can exchange excrement.
Here, the exchange timing of the ostomy pouch (4) and the ostomy faceplate (1a2) is determined by the dyeing degree confirmation space (7c) provided in the skin protective agent (7) of the ostomy faceplate (1a2) and the ostomy faceplate base. Replacement of the ostomy pouch (4) and the ostomy faceplate (1a2) is performed by observing the dyeing degree through the dyeing degree confirmation window (8b) provided in (8). The timing is detected and notified by the detection information notification unit (11), and the replacement notification detection information is electrically detected to transmit the replacement notification detection information to the external terminal of the detection information transmission unit (12). showing.
The details of the ostomy appliance for informing the water content of excrement will be described with reference to FIGS. 8 to 10. FIG.

(1-B) of FIG. 1 is a diagram for explaining the notification of the human body biosensor, and transmission of detection information of the ostomy appliance (1a) described in (1-A) and (1-C) of FIG. Part (12) and physical information from the body attachment (1) worn on the body (2) of the subject in (1-B) of FIG. It is possible to report and confirm the situation etc. as a detection information notification device (5), and to notify the emergency center (5a) to call 119 as necessary.
In (1-B) of FIG. 1, a stoma appliance (1a), a drowsiness detector (1b), and a heatstroke detector (1c) are attached to the subject's body (2) as examples of body attachments (1). As an example of the body attachment (1), there are other devices for detecting various biological information such as a cerebral infarction detection device, a frequent urination detection device, a blood sugar level detection device, and a blood oxygen saturation detection device. It is also conceivable to wear equipment.
Details for explaining the notification of the human body sensor will be explained with reference to FIGS. 11 and 12. FIG.

Thus, in FIG. 1, a state sensor (10) provided on the ostomy faceplate (1a2) indicates the exchange timing of the stoma pouch (4) when the subject wears the stoma faceplate (1a2) on the subject's body (2). , the detection information notification unit (11) notifies the subject of the replacement timing of the ostomy pouch (4) and the ostomy face plate (1a2), and the detection information transmission unit (12) sends information to a smartphone (5b) or the like. It is possible to notify the notification information to other terminals.
In addition, biometric information from another body attachment (1) attached to the body (2) of the subject can be similarly notified to a smart phone (5b) or the like. In the device (1) as well, the device (1b) exchanges the ostomy pouch (4) and the stoma faceplate (1a2) exchange timing notification detection information and the heat stroke detection device (1c) biometric information, etc. It is possible to notify the detection information notification unit (11) of the drowsiness detector (1b) together.

FIG. 2 is an explanatory diagram of general specifications of the ostomy appliance.
(2-A) of FIG. 2 is a diagram for explaining a case where the stoma faceplate (1a2) is attached to the subject's body. The stoma face plate (1a2) is attached to the stoma (3), which is an outlet for discharged feces and urine, and the stoma pouch (4) is attached.
The ostomy faceplate (1a2) has a stoma attachment opening (8a) in the center so that it can be easily attached to the stoma (3). 6) shows an example in which the stoma faceplate (1a2) is attached to the subject's body (2) at a position surrounding the stoma (3).
The ostomy pouch (4), which is an extension for the subject's body (2) as an exchangeable storage section for excrement, is attached to the subject's body (2) via the ostomy face plate (1a2). be.

Further, in FIG. 2, (2-B) is a diagram illustrating the general structure of the stoma faceplate (1a2).
In (2-B), the ostomy faceplate (1a2) explained in (2-A) was explained as an integral structure, but in (2-B), the skin protective agent is applied to the ostomy faceplate base (8). The illustration shows that (7) and tape (6) are stacked to form a stoma faceplate (1a2).
The skin protectant (7) here consists of a polymer (7a) and a colloid (7b).
(2-A) and (2-B) in Fig. 2 are examples of commercially available ostomy faceplates (1a2). The equipment (1a) is introduced as an example.

FIG. 3 is a front view for explaining the ostomy appliance (1a) for detecting the amount of excreted water according to the present invention.
In FIG. 3, the ostomy appliance (1a) of the present invention has a face plate base (8) for stoma and a skin protective agent (7) on the body (2) side of the subject as described in (1-A) of FIG. is provided, and a first wiring (9a) and a second wiring (9b) are formed in a ring shape around the stoma mounting opening (8a) on the surface of the stoma faceplate base (8) on the side of the skin protective agent (7). It is provided as a moisture amount detection wiring (9), and is composed of a state sensor (10) for detecting the pouch replacement timing with this moisture amount detection wiring (9).
By attaching the stoma pouch (4) to the stoma attachment opening (8a), the stoma face plate (1a2) functions as a fitting function.
FIG. 4 shows a cross-sectional view taken along line BB' indicated by a dashed line in the center of FIG.

FIG. 4 is a cross-sectional view of the ostomy appliance for detecting the amount of excreted water of the present invention taken along the line BB'.
In FIG. 3 above, the fitting part of the ostomy faceplate base (8) and the ostomy pouch (4) hidden by the ostomy pouch (4) placed overlapping the ostomy faceplate base (8) and pouch replacement A device (13) can be seen.
In FIG. 4, the stoma mounting opening (8a) of the stoma faceplate base (8) is applied so as to surround the stoma (3) surgically provided in the center of the body (2) of the subject from the upper side of the figure, and the subject is A cross-sectional view is shown in which the ostomy faceplate (1a2) is attached with the skin protectant (7) sandwiched between the body (2) and the ostomy faceplate base (8).
Here, a first wiring (9a) and a second wiring (9b) are annularly provided on the skin protective agent (7) side of the stoma faceplate base (8) so as to surround the stoma mounting opening (8a). However, in the cross-sectional view of FIG. 4, it can be confirmed that the first wiring (9a) and the second wiring (9b) are arranged symmetrically on the left and right sides of the stoma (3).
Around the ostomy mounting opening (8a) of the ostomy face plate base (8), an uneven member for fitting the ostomy pouch (4) is arranged, and the ostomy pouch (4) is placed on the ostomy face plate base (8). is detachably connected.
Furthermore, the first wiring (9a) and the second wiring (9b) of the stoma faceplate base (8) are provided as electrodes (14) as (+ side electrode) and (- side electrode) outside the stoma face plate base (8). are externally provided and are connected correspondingly to the electrodes of the pouch replacement detection device (13).
Although the pouch replacement detection device (13) is shown hidden under the ostomy pouch (4) in the figure, the ostomy pouch (4) is a soft bag, so the subject can use it whenever necessary. The status of the pouch change detection device (13) under the ostomy pouch (4) is visible at all times.
Ostomy pouches (4) are a matter of course, but ostomy appliances (1a) such as ostomy face plates (1a2) are sanitary consumables.
However, the pouch replacement detection device (13) containing an electric circuit, which will be described later, is an expensive module component, and is operated in a reusable structure.

Next, this pouch replacement detection device (13) will be described.
FIG. 5 is a circuit diagram (5-B) and an operation diagram (5-A) of the pouch exchange detector (13) for detecting the amount of excreted water of the present invention.
The circuit diagram shown in (5-B) of FIG. 5 will be explained.
The first wiring (9a) and the second wiring (9b) in the lower left of FIG. 5 (5-B) are electrodes provided in the stoma face plate (1a2), and the resistance described When the amount of water in excrement between the faceplate (1a2) and the skin seeps into the skin protective agent of the stoma faceplate (1a2), it is detected as a change in resistance value (RL).
As a value, the resistance value of RL is ∞ when the water content is zero, but it changes to a small value such as 40 MΩ and 21 MΩ when the water content increases.
In (5-B), this resistance value change is accepted by a Schmitt type 2NAND gate (Q1 gate) while reducing noise with R1, Tr1, C2, and R2, High output at 0.65V or less, 1.25V or more Design the circuit by adjusting the resistance value of R2 so that the output becomes Low at . (When power supply voltage is 3V)
As a result, the blue LED provided after passing through the 2NAND gate Q2 can be turned on and off under predetermined conditions.
In addition, the output of the Q2 gate is connected to the UM66, which is a three-terminal melody IC, and when the Q1 output is Low, the melody can be played from the speaker through the parts of Tr2, Tr3, C4, and R6.
Then, when the input of Q3 is low, Q4 can function to turn on the red LED.
(5-A) in FIG. 5 shows this movement as an operation diagram.
In (5-A), the ON/OFF state of the blue LED, red LED, and melody IC when the value of RL appearing between the first wire (9a) and the second wire (9b) changes from ∞ to 40MΩ21MΩ. shows the passage of time.
In this way, in this circuit, the pouch exchange timing on the ostomy face plate (1a2) is regarded as the value of RL appearing between the first wiring (9a) and the second wiring (9b), and the blue LED, red LED, and melody IC It is possible to inform the subject by the sound emitted by the
For reference, in (5-B), the input voltage of Q1 is 0.65V or less according to the 74HC132 data sheet, and it has been explained above that it becomes H output, and 1.25V or more, it becomes L output. The resistance value is x ≈ 40 MΩ when Vin = 0.65 or less, and x ≈ 21 MΩ when Vin = 1.25 or more. The operation is explained assuming that the resistance value is

FIG. 6 is a configuration diagram in which a detection information transmission unit is provided in the pouch exchange detection device (13) for detecting the amount of excreted water of the present invention.
Fig. 6 shows, on the left, the first wiring (9a) and the second wiring (9a) of the moisture detection wiring (9) provided in the combination of the skin protective agent (7) of the ostomy faceplate (1a2) and the ostomy faceplate base (8). Wiring (9b) and a virtual water content detection resistor RL generated therebetween are connected to the pouch exchange detection device (13).
In FIG. 6, the pouch replacement detection device (13) is explained as being processed by a one-chip microcomputer instead of a circuit composed of individual parts as shown in (5-B) of FIG.
The 1-chip microcomputer has built-in AD conversion logic as an input, and a built-in circuit that can be connected to the detection information reporting unit (11) such as an LED, vibrator, and speaker as an output.
In addition, it has a function to connect to a microcomputer such as RBT-001, which is a Bluetooth (registered trademark) functional component, and to control the functional component that transmits replacement notification detection information to the outside by the microcomputer program.
The value of the moisture content detection resistor RL between the first wiring (9a) and the second wiring (9b) input in FIG. Notify the subject of the replacement timing of the ostomy faceplate (1a2) using the LED, vibrator, and speaker of the detection information notification unit (11) in accordance with the replacement notification detection information corresponding to the amount of water detected by the program becomes possible.
In addition, the replacement notification detection information is notified to various terminals such as smartphones and other biometric information detectors nearby through the RBT-001, which is a Bluetooth functional component.
Here, RBT-001, which is a Bluetooth functional component, is a commercially available communication module for electronic work, but it can also be realized by connecting other communication units.

Further, FIG. 7 illustrates a functional layout diagram of the pouch replacement detection device (13) for detecting the amount of excreted water of the present invention.
The pouch exchange detection device (13) in FIG. 7 is an enlarged view of the pouch exchange detection device (13) shown in FIG.
In FIG. 7, the leftmost + and - two electrodes (14) are contact points electrically connected to the first wiring (9a) and second wiring (9b) of the smart face plate (8) in FIG.
On the right side of FIG. 7, the detection information reporting unit (11), a blue LED, a red LED, a speaker (represented by SP in the figure), and a vibrator (represented by a vibrator in the figure) are arranged.
The subject should set the driving time of the vibrator to be the same as the driving time of the speaker, or set the condition so that the subject can easily recognize it.
For the movement of these detection information notifying units (11), the operation diagram of (5-A) in FIG. 5 should be referred to.
Also, the Bluetooth, which is the detection information transmission unit (12), is arranged in a corner of the pouch exchange detection device (13), and it becomes possible to transmit exchange notification detection information to an external terminal.
How to set and operate the built-in 1-chip microcomputer in this pouch exchange detection device (13) is arbitrarily decided by the designer at the time of product development, so the explanation here is omitted. However, there is no problem if switches for various settings are provided on the back side of the pouch replacement detection device (13).
Since this pouch replacement detector (13) is more expensive than the smart faceplate (1a2), which is a consumable item, it is made to be easily attachable to and detachable from the smart faceplate (1a2).

FIG. 8 is a view for explaining the ostomy appliance for detecting the amount of excretion stain of the present invention.
The top view of FIG. 8 (8-A) is a front view of the ostomy appliance for detecting the amount of excretion stain of the present invention, and the skin protective agent (7) is placed in the center of the ostomy faceplate base (8). It is a figure pasted around the stoma mounting opening (8a) of the faceplate base (8).
As shown in FIG. 8 (8-A), the ostomy appliance for detecting the amount of excreted stain has a plurality of stain confirmation spaces (7c) and stain confirmation windows (8b) arranged so as to overlap each other. Here, the number and shape of the dyeing confirmation space (7c) and the dyeing confirmation window (8b) may be shapes other than those shown.
In (8-A) of FIG. 8, a cross-sectional view showing this state on the broken line BB' is shown below.
Next, details of the smart face plate (1a2) for detecting the amount of excrement stain will be described with reference to this sectional view.
In this cross-sectional view, the subject's body (2), stoma pouch (4), and pouch exchange detection device (13), which are omitted in the above figure, are also shown. If you compare this figure with FIG. 4, which shows the cross-sectional view of the ostomy appliance for detecting the amount of discharged water, it will be easier to understand the structure of the smart faceplate (1a2) for detecting the amount of excrement. think.
In the cross-sectional view of FIG. 8 (8-A), the stoma mounting opening (8a) is aligned with the stoma (3) on the subject's body (2), and the stoma faceplate base (8) is attached to it. It shows a situation in which a skin protective agent (7) is placed on the skin, and an ostomy pouch (4) is detachably provided in the center of an ostomy faceplate base (8).
However, the stoma faceplate base (8) is provided with a plurality of transparent stain confirmation windows (8b), and the skin protective agent (7) is similarly provided with a stain confirmation space (7c). The stain confirmation window (8b) and the stain confirmation space (7c) are arranged in a vertically overlapping position, and the ostomy faceplate (8) and the skin protective agent (7) are laminated together for use.
By doing so, it is possible to check the degree of staining in the staining degree confirmation space (7c) when the water of the excrement exuding from the stoma (3) has soaked into the skin protective agent (7), and the stoma faceplate can be used. The test subject can detect the water content of the excrement seeping from the stoma (3) through the stain confirmation window (8b) that covers the stain confirmation space (7c) with the transparent member of the base (8). becomes.
Between the ostomy faceplate base (8) and the skin protective agent (7), or between the skin protective agent (7) and the skin protective agent (7), a skin protective seal (17) colored with a conspicuous color other than the skin color is applied in order to distinguish it from the subject's skin color. One idea is to use

An example of the material for the skin protective agent (7) and the skin protective seal (17) is introduced for reference. The display material of the first example is made by impregnating paper or the like with a solution of cobalt chloride dissolved in alcohol and drying it. It is a blue one, or it is a blue one that is impregnated with polyvinyl alcohol (PVA) glue and dried. This display material changes color from blue to pink or red depending on the water content in the urine.
The display material of the second example is pH test paper. Since human urine normally has a weakly acidic pH≈6, this display material is discolored by urine.
The display material of the third example is a type of pH test paper, and is a blue one obtained by impregnating a paper or the like with an alcoholic solution of bromothymol blue (BTB), which is made basic by adding a little sodium hydroxide, and then drying. is. This display material changes color from blue to yellow due to acid in urine.

Thus, the test subject can visually check the water content of excrement seeping out from the stoma (3) through the dyeing confirmation window (8b) provided in the stoma face plate (8).
Then, the color change of the stain confirmation window (8b) can be detected as an electrical displacement amount by the pouch exchange detection device (13), and the subject can be notified of the situation by digital processing. becomes.
This pouch exchange module (13) will be described in detail later with reference to FIGS. 9 and 10. FIG.
(8-B) of FIG. 8 shows how this staining degree becomes darker with the passage of time. Please understand that ◯ in the figure represents a sample of the change in color density seen from the dyeing degree confirmation window (8b).
When the subject is concerned about the stoma replacement timing of the ostomy faceplate (1a2), he/she can judge by using the color of the stain confirmation window (8b) under the ostomy faceplate (1a2) as an electrical displacement amount. becomes.

FIG. 9 is a diagram showing the configuration of a pouch replacement detection device (13) for detecting the amount of excrement staining according to the present invention, with a detection information transmitting unit.
Fig. 9 shows, on the left, a stain confirmation space (7c) in the skin protective agent (7) of the stoma faceplate (1a2) and a stain confirmation window (8b) in the stoma faceplate base (8). It shows the status of the presence sensor (10).
The subject can always visually observe the change in color of the stain confirmation window (8b), which is the state sensor (10), as described with reference to FIG. 8 (8-B).
In FIG. 9, this visible color change is converted into an electric quantity through a dyeing sensor (15) by a pouch replacement detector (13) and then converted into a digital value by an A/D conversion logic of a one-chip microcomputer. there is
Here, the dyeing sensor (15) is a commonly used color sensor, and includes an LED that emits light to the dyeing degree confirmation window (8b) according to the change in color that can be confirmed in the dyeing degree confirmation window (8b), It consists of a photosensor that receives the light reflected from the stain confirmation window (8b).
The 1-chip microcomputer has built-in AD conversion logic as an input, and a built-in circuit that can be connected to the detection information reporting unit such as an LED, vibrator, and speaker for the output.
In addition, it also has a function to connect to a microcomputer such as the RBT-001, which is a Bluetooth functional component, and control the functional component that transmits replacement notification detection information to the outside by the microcomputer program.
Therefore, the pouch exchange detection device (13) in Fig. 9 is converted into a digital number by the AD conversion logic built into the 1-chip microcomputer, and exchange notification corresponding to the color change of the amount of dye detected by the program in the 1-chip microcomputer. It is possible to notify the subject of the replacement timing of the ostomy faceplate (1a2) along with the detection information using the LED, vibrator, and speaker as the detection information notification unit (11).
In addition, the replacement notification detection information can be sent to various terminals such as smartphones and other biometric information detection devices nearby through the RBT-001, which is a Bluetooth functional component.
Here, RBT-001, which is a Bluetooth functional component, is a commercially available communication module for electronic work, but it can also be realized by connecting other communication units.

Further, FIG. 10 illustrates a functional layout diagram of the pouch exchange detection device (13) for detecting the amount of excretion stain of the present invention.
The pouch replacement detection device (13) in FIG. 10 is an enlarged view of the pouch replacement detection device (13) shown in FIG.
In FIG. 10, the dyeing degree S on the left, that is, the dyeing degree sensor (15) is a sensor composed of an LED and a sensor. The change in color of excrement exuded from (7) is identified by a sensor by irradiating the staining confirmation space (8b) surface with light from the LED through the staining confirmation space (8b) of the stoma face plate base (8). It is something to do.
On the right side of FIG. 10, the detection information reporting unit (11), a blue LED, a red LED, a speaker (indicated by SP in the figure), and a vibrator (indicated by vibrator in the figure) are arranged.
The subject should set the driving time of the vibrator to be the same as the driving time of the speaker, or set the condition so that the subject can easily recognize it.
For the operation of the detection information reporting unit (11), the content explained in the operation diagram of (5-A) of FIG.
Also, the Bluetooth, which is the detection information transmission unit (12), is arranged in a corner of the pouch exchange detection device (13), and it becomes possible to transmit exchange notification detection information to an external terminal.
How to set and operate the built-in 1-chip microcomputer in this pouch exchange detection device (13) is arbitrarily decided by the designer at the time of product development, so the explanation here is omitted. However, there is no problem if switches for various settings are provided on the back side of the pouch replacement detection device (13).
Since this pouch replacement detection device (13) is more effective than the consumable smart face plate (1a2), it is made to be easily attachable to and detachable from the smart face plate (1a2).
By configuring the pouch replacement detection device (13) with such a structure, the replacement timing of the ostomy pouch (4) can be adjusted to the first electrode (9a) and the second electrode (9b) described in FIGS. is used as the state sensor (10), and the color change in the staining degree confirmation space (7c) described in FIGS. The sensor (15) can be built in by a realization method such as functioning as the state sensor (10).

FIG. 11 is an explanatory diagram for informing the drowsiness detector of other sensor information. In a life scene where the subject wears a recent wearable terminal, the test subject wears, for example, a sleepiness detection device (1b) and a heat stroke detection device (1c) in addition to the stoma device (1a) of the present invention. A case is also considered.
Therefore, FIG. 11 shows an example of cooperation between the ostomy faceplate (1a2) of the present invention and these wearable terminals, which is a case where the stoma faceplate (1a2) knows when to replace the ostomy pouch with the drowsiness detector (1b). introduce.
Before that, FIG. 11 shows how the drowsiness detector (1b) is connected to the stoma face plate (1a2) of the present application by a communication means such as Bluetooth.
In addition, a general drowsiness detection device (1b) is a doze prevention auxiliary device in Japanese Patent Application Laid-Open No. 11-151298 of Prior Patent Document 7, which is provided with a transmission type sensor or a reflection type sensor at or near the glasses to constantly monitor the eyes. A technology has been disclosed in which the movement of the body is monitored, and if the movement is excessive, these sensors detect it and notify the user with a buzzer or vibration, so please refer to it.
However, Japanese Patent Application Laid-Open No. 11-151298 only reports the information of one's own drowsiness detector (1b), and other biological information and the exchange timing of the ostomy pouch (4) from the ostomy faceplate (1a2) of the present application. is not intended to inform
The pouch replacement detection device (13) attached to the ostomy faceplate (1a2) of the present application is provided in the pouch replacement detection device (13) as described in FIGS. Although it is possible to notify the subject using the detection information notifying unit (11) such as an LED, speaker, or vibrator, if the subject is concentrating on some action, it may be difficult to notice. Even so, if the sound from the speaker or the strength of the vibrator is increased, it will be an annoyance to the surroundings, which is not preferable.
In such a case, if the subject wears the drowsiness detection device (1b) as another body attachment (1), the stoma faceplate (1a2) of the present application can be detected from the drowsiness detection device (1b) as well. It is possible to notify the replacement timing of the pouch (4).
In Fig. 11, as an example of the drowsiness detection device (1b), a transmission reflection sensor (eyelid sensor) or the like is attached to the glasses to monitor how the eyelids are closed, or a tilt sensor is attached to monitor the tilt of the neck. Drowsiness detection is performed by monitoring whether the subject is attacked by sleepiness.
And if drowsiness is detected, drowsiness is detected in the test subject by the detection information notification unit (11) such as a vibrator or LED provided in the drowsiness detector (1b)! Please be careful~! A detection information notification unit (11) provided on the glasses or the like informs the subject of the current state. If the drowsiness detector (1b) is provided with a detection information transmission unit (12), the drowsiness detection information can be transmitted to the terminal of the driver management department (5a) to detect the driver's health. Management can be managed.
In particular, if the subject is a driver of some kind of office, monitoring the subject's drowsiness is important information for the driver management department (5a).
The communication means of the detection information transmission unit (12) of the drowsiness detection tool (1b) is likely to be Bluetooth in many cases. Information will be reported from the subject's smartphone (5b) to the driver management department (5a) by communication.
In FIG. 11, by incorporating the notification information receiving unit (16) in such a sleepiness detection device (1b), the detection information transmission unit (12) of the other body attachment (1) worn by the subject drowsiness detection information can be received.
As a result, for example, the notification information from the drowsiness detection device (1b) is notified by blinking a yellow LED in the field of view of the eyeglasses, which is the drowsiness detection device (1b) of the subject, and the exchange timing of the ostomy pouch (4) of the present application is indicated by red. It is possible to notify the subject by blinking the LED, and furthermore, caution information from the heat stroke detector (1c) can be notified to the subject in the visual field of the glasses by blinking the blue LED. By taking such measures, notification information from the mounting position of the ostomy faceplate (1a2) and the exchange timing of the ostomy pouch (4) can be sent from the ostomy faceplate (1a2) to the smartphone (5b) near the subject. It becomes possible to secure notification means other than means for notification.

FIG. 12 is an explanatory diagram for informing the heat stroke detector of other sensor information.
Furthermore, as another example of a life scene in which the subject wears a recent wearable terminal, the ostomy faceplate (1a2) uses the heat stroke detection device (1c) to determine the replacement timing of the stoma pouch (4). I'll give you an example I know.
Before that, FIG. 12 shows how the heat stroke detector (1c) is connected to the stoma face plate (1a2) of the present application by a communication means such as Bluetooth.
In addition, a general heat stroke detector (1c) is a heat stroke detection device provided with an oxygen sensor on the arm in Japanese Patent Application Laid-Open No. 2020-174974 of Prior Patent Document 6, and heat stroke symptoms were detected by the oxygen sensor. In such a case, technology has been disclosed that causes the heat stroke detection device to emit an LED and sound a buzzer warning sound, and that information is also displayed on a smartphone as a heat stroke prediction level, so please refer to it.
However, Japanese Patent Application Laid-Open No. 2020-174974 only reports the information of the heat stroke detection device (1c) of the user, and other biological information and replacement of the ostomy pouch (4) from the ostomy faceplate (1a2) of the present application. It does not indicate timing.
The pouch replacement detection device (13) attached to the ostomy faceplate (1a2) of the present application is provided in the pouch replacement detection device (13) as described in FIGS. It is possible to notify the subject with the detection information notification unit (11) such as an LED, a speaker, or a vibrator,
When the subject is concentrating on some action, it may be difficult to notice. Even so, if the sound from the speaker or the strength of the vibrator is increased, it will be an annoyance to the surroundings, which is not preferable.
In such a case, if the subject wears the heat stroke detection device (1c) as another body attachment (1), the heat stroke detection device (1c) and the ostomy faceplate (1a2) of the present application can be detected. It is possible to notify the replacement timing of the stoma pouch (4).
In Fig. 12, an oxygen sensor (10) or the like is attached to the arm as an example of a heat stroke detector (1c), and the blood oxygen saturation level Spo2 is measured by an infrared light reflection receiving method to measure the degree of heat stroke. A detector is shown.
And if heat stroke is detected, the heat stroke is detected in the test subject by the detection information reporting unit (11) such as a vibrator or LED provided in the heat stroke detector (1c)! Please be careful~! The present condition is communicated to the subject from the detection information reporting unit (11) provided on a bracelet or the like. If the heatstroke detection tool (1c) is provided with a detection information transmission unit (12), the detection information can be sent to an emergency center (5a) such as 119, so that emergency transport procedures can be performed. It becomes possible to
It seems that the communication means of the detection information transmission unit (12) of the heat stroke detection tool (1c) is often Bluetooth, but in this case, the information is shared with the smartphone (5b) owned by the subject by Bluetooth, The information is reported from the subject's smartphone (5b) to the emergency center (5a) by communication.
In FIG. 12, by incorporating the notification information receiving unit (16) in such a heatstroke detecting device (1c), the detection information transmitting unit (12) of the other body attachment (1) worn by the subject is detected. It is possible to receive heat stroke detection information from.
As a result, for example, the notification information from the heat stroke detection device (1c) is notified by rapidly vibrating the bracelet, which is the heat stroke detection device (1c), of the subject. The exchange timing of (4) can be notified slowly with a beep, beep, beep, and furthermore, caution information from the drowsiness detector (1b) can be notified to the subject's bracelet in a different vibration pattern. By taking such measures, notification information from the mounting position of the ostomy faceplate (1a2) and the exchange timing of the ostomy faceplate (1a2) can be sent from the ostomy faceplate (1a2) to the smartphone (5b) near the subject. It becomes possible to secure notification means other than means for notification.

Other body attachment devices (1) to be worn by subjects exist in various fields such as cerebral infarction detection device, frequent urination detection device, blood sugar level detection device, blood oxygen saturation detection device, etc. The replacement timing of the ostomy pouch (4) detected by the face plate (1a2) can also be notified by other detectors worn by the subject. It is also possible to notify the smart phone (5b) held by the caregiver or an emergency center (5a) such as a facility of the replacement timing of the ostomy faceplate (1a2).

The ostomy appliance will now be described.
A product in which the ostomy pouch (4) and the ostomy faceplate (1a2) are integrated is called one product, and a product in which the ostomy pouch and the ostomy faceplate are separate and independent is called a two product.

As explained above, various information occurring in the subject's body is reported to the subject himself/herself, and furthermore, according to the degree of urgency, the subject's condition is reported to the partner who is permitted by the subject. It becomes easier to take countermeasures for health maintenance and management required for each change and age.

1 Body fitting 1a Ostomy appliance 1a2 Ostomy face plate 1b Drowsiness detector
1c heatstroke detector 2 subject's body 3 stoma 4 stoma pouch 5 detection information reporting device 5a emergency center 5b smartphone 6 tape 7 skin protective agent 7a polymer 7b colloid 7c stain confirmation space 8 stoma faceplate base 8a stoma mounting opening 8b Dyeing degree confirmation window 9 Moisture content detection wiring 9a First wiring 9b Second wiring 10 State sensor 11 Detection information reporting unit 12 Detection information transmitting unit 13 Pouch replacement detection device 14 Electrode 15 Dyeing sensor 16 Detection information receiving unit 17 Skin protection sticker

A sensor is provided on the ostomy faceplate of the ostomy appliance that the subject wears on the body to check the state of excrement. By making it possible to detect the amount of stain as a value, the subject can easily know when to replace the ostomy pouch .

(1-B) of FIG. 1 is a diagram for explaining the notification of the human body biosensor, and transmission of detection information of the ostomy appliance (1a) described in (1-A) and (1-C) of FIG. Part (12) and physical information from the body attachment (1) worn on the body (2) of the subject in (1-B) of FIG. It is possible to report and confirm the situation etc. as a detection information notification device (5), and to notify the emergency center (5a) to call 119 as necessary. In (1-B) of FIG. 1, a stoma appliance (1a) , a sleepiness detection device (1b), and a heatstroke detection device (1c) are attached to the subject's body (2) as examples of the body attachment device (1). As an example of the body attachment (1), there are other devices for detecting various biological information such as a cerebral infarction detection device, a frequent urination detection device, a blood sugar level detection device, and a blood oxygen saturation detection device. It is also conceivable to wear equipment.
Details for explaining the notification of the human body sensor will be explained with reference to FIGS. 11 and 12. FIG.

FIG. 6 is a configuration diagram in which a detection information transmission unit is provided in the pouch replacement detection module for detecting the amount of excreted water according to the present invention.
Fig. 6 shows, on the left, the first wiring (9a) and the second wiring of the moisture detection wiring (9) provided in the combination of the skin protective agent (7) and the stoma faceplate (8) of the ostomy appliance (1a). (9b) and a situation in which the virtually generated moisture detection resistor RL is connected to the pouch exchange module (13).
In FIG. 6, the pouch exchange module (13) is explained as being processed by a one-chip microcomputer instead of a circuit composed of individual parts as shown in FIG. 5 (5-B).
The 1-chip microcomputer has built-in AD conversion logic as an input, and a built-in circuit that can be connected to the detection information reporting unit such as an LED, vibrator, and speaker for the output.
In addition, it also has a function to connect to a microcomputer such as the RBT-001, which is a Bluetooth functional component, and control the functional component that transmits detection information to the outside by the microcomputer program.
The value of the moisture content detection resistor RL between the first wiring (9a) and the second wiring (9b) input in FIG. It is possible to notify the subject of the replacement timing of the ostomy pouch (4) using the LED, vibrator, and speaker, which are the detection information notification unit (11), along with the detection information corresponding to the amount of water detected by the program. becomes.
In addition, the detection information can be transmitted to various terminals such as smartphones and other biometric information detection devices nearby through the RBT-001, which is a Bluetooth functional component.
Here, RBT-001, which is a Bluetooth functional component, is a commercially available communication module for electronic work, but it can also be realized by connecting other communication units.

Further, FIG. 7 illustrates a functional layout diagram of the pouch replacement detection module for detecting the amount of excreted water of the present invention. The pouch exchange detection module (13) in FIG. 7 is an enlarged view of the pouch exchange detection module (13) shown in FIG. In FIG. 7, the leftmost + and - two electrodes (14) are contact portions electrically connected to the first wiring (9a) and the second wiring (9b) of the stoma face plate (8) in FIG.
On the right side of Fig. 7, the detection information reporting unit (11), a blue LED, a red LED, a speaker (represented by SP in the figure), and a vibrator (represented by a vibrator in the figure) are arranged.
The test subject should set the driving time of the vibrator to be equal to the driving time of the speaker, or set the condition so that the test subject can easily recognize it.
For the movement of these detection information notifying units (11), the operation diagram of (5-A) in FIG. 5 should be referred to.
In addition, the Bluetooth, which is the detection information transmission unit (12), is arranged in a corner of the pouch replacement detection module (13), making it possible to transmit detection information to an external terminal.
How to set and operate the built-in 1-chip microcomputer in this pouch exchange detection module (13) is arbitrarily decided by the designer at the time of product development, so the explanation here is omitted. However, there is no problem if switches for various settings are provided on the back side of the pouch replacement detection module.
Since this pouch replacement detection module (13) is more effective than the consumable ostomy appliance (1a) , it is made to be easily attachable to and detachable from the ostomy appliance (1a) .

FIG. 8 is a view for explaining the ostomy appliance for detecting the amount of excretion stain of the present invention.
The top view of FIG. 8 (8-A) is a front view of the ostomy appliance for detecting the amount of excretion stain of the present invention, and the skin protective agent (7) is placed in the center of the ostomy faceplate (8). It is a figure pasted around the stoma mounting opening (8a) of the face plate (8).
As shown in FIG. 8 (8-A), the ostomy appliance for detecting the amount of excreted stain has a plurality of stain confirmation spaces (7c) and stain confirmation windows (8b) arranged so as to overlap each other.
Here, the number and shape of the dyeing confirmation space (7c) and the dyeing confirmation window (8b) may be shapes other than those shown.
In (8-A) of FIG. 8, a cross-sectional view showing this state on the broken line BB' is shown below.
Next, details of the ostomy appliance (1a) for detecting the amount of excretion stain will be described with reference to this cross-sectional view.
In this cross-sectional view, the subject's body (2), stoma pouch (4), and pouch replacement detection module (13), which are omitted in the above figure, are also shown. If this figure can be compared with FIG. 4, which shows the cross-sectional view of the ostomy appliance for detecting the amount of discharged water, the structure of the ostomy appliance (1a) for detecting the amount of excrement stains can be understood more easily. think.
In the cross-sectional view of FIG. 8 (8-A), the stoma mounting opening (8a) is aligned with the stoma (3) on the subject's body (2), and the stoma face plate (8) is attached to it. It shows a situation in which a skin protective agent (7) is placed and a stoma pouch (4) is detachably provided in the center of a stoma faceplate (8).
However, the stoma faceplate (8) is provided with a plurality of transparent stain confirmation windows (8b), and the skin protective agent (7) is similarly provided with a stain confirmation space (7c). The stain confirmation window (8b) and the stain confirmation space (7c) are arranged in a vertically overlapping position, and the ostomy faceplate (8) and the skin protective agent (7) are laminated together for use.
By doing so, it is possible to check the degree of staining in the staining degree confirmation space (7c) when the water of the excrement exuding from the stoma (3) has soaked into the skin protective agent (7), and the stoma faceplate can be used. The test subject can see the water content of excrement seeping out of the stoma (3) through the stain confirmation window (8b), which is a lid of the stain confirmation space (7c) with the transparent member (8). Become.
Between the stoma faceplate (8) and the skin protective agent (7), or on the skin protective agent (7), a skin protective seal (6) colored with a conspicuous color other than the skin color is placed to distinguish it from the subject's skin color. One idea is to use

Further, FIG. 10 illustrates a functional layout diagram of the pouch replacement detection module for detecting the amount of excretion stain of the present invention.
The pouch exchange detection module (13) in FIG. 10 is an enlarged view of the pouch exchange detection module (13) shown in FIG.
In FIG. 10, the dyeing degree S on the left, that is, the dyeing degree sensor (15) is a color sensor composed of an LED and a photosensor (phototransistor), and the dyeing degree confirmation window (7c ), the surface of the dyeing confirmation space (8b) is irradiated with light from the LED through the dyeing confirmation space (8b) of the stoma face plate (8) to detect the color change of the excrement exuded from the skin protective agent (7). Then, the light is received by the photosensor.
On the right side of FIG. 10, a blue LED, a red LED, a speaker (represented by SP in the figure) and a vibrator (represented by a vibrator in the figure) are arranged as the detection information reporting unit (11).
The test subject should set the driving time of the vibrator to be equal to the driving time of the speaker, or set the condition so that the test subject can easily recognize it.
For the operation of the detection information reporting unit (11), the content explained in the operation diagram of (5-A) of FIG.
In addition, the Bluetooth, which is the detection information transmission unit (12), is arranged in a corner of the pouch replacement detection module (13), making it possible to transmit detection information to an external terminal.
How to set and operate the built-in 1-chip microcomputer in this pouch replacement detection module (13) is up to the designer to decide arbitrarily during product development.
Although the explanation here is omitted, there is no problem if the switches for various settings are provided on the back side of the pouch replacement detection module.
Since this pouch replacement detection module (13) is more effective than the consumable ostomy appliance (1a) , it is made to be easily attachable to and detachable from the ostomy appliance (1a) .
By configuring the pouch replacement detection module (13) with such a structure, the replacement timing of the ostomy pouch (4) can be adjusted to the first electrode (9a) and the second electrode (9b) described in FIGS. is used as the state sensor (10), and the color change in the staining degree confirmation space (7c) described in FIGS. The sensor (15) can be built in by a realization method such as functioning as the state sensor (10).

Claims (9)

A state sensor is provided on the ostomy faceplate of the ostomy appliance attached to the subject, and the state sensor detects the exchange timing of the ostomy faceplate and the ostomy pouch attached to the ostomy faceplate as the value of the water content of the excrement or the value of the dye amount. Ostomy appliance that detects and notifies detected replacement notification detection information. The state sensor is configured by attaching the stoma faceplate to the stoma of the subject with a skin protective agent interposed therebetween, and providing a first wiring and a second wiring on the skin protective agent side of the stoma faceplate to detect the moisture content of excrement. 2. The ostomy appliance according to claim 1, wherein the value of is detected by the electrical resistance value between the first wiring and the second wiring, and the replacement notification detection information detected by the state sensor is notified. The ostomy faceplate has an ostomy mounting opening for mounting the ostomy faceplate on the stoma of the subject, and the first wiring and the second wiring are provided in an annular shape surrounding the ostomy mounting opening. The stoma appliance according to claim 2. 2. The state sensor according to claim 1, wherein the stoma faceplate is attached to the stoma of the subject with a skin protective agent interposed therebetween, and a dye level confirmation space is provided in the skin protective agent to detect the amount of stain in the dye level confirmation space. Ostomy appliances as described. 5. The method according to claim 4, wherein the stain confirmation space is a through space formed in the skin protective agent, and a position corresponding to the containment space of the ostomy face plate provided on the skin protective agent is transparent. stoma appliance. 6. The ostomy faceplate or any one of claims 1 to 5, wherein a detection information transmission unit for wirelessly transmitting replacement notification detection information detected by the state sensor to the outside of the ostomy appliance is provided on the ostomy faceplate or in the vicinity of the ostomy faceplate. The ostomy appliance described in 1. The subject also wears a biosensor other than the smart equipment, and detection information outputting the detection information from the biosensor together with the detection information from the detection information transmission unit according to claim 6 to the subject's terminal. notification system. The biosensor is a biosensor provided in at least one of a cerebral infarction detection device, a drowsiness detection device, a frequent urination detection device, a blood sugar level detection device, a heat stroke detection device, and a blood oxygen saturation detection device. 8. The detection information notification system according to claim 7. 9. The detection information notification system according to claim 7 or 8, wherein the subject's terminal is a detection tool incorporating the biosensor.

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