Laryngeal cancer atomization control method and atomization equipment

Abstract

The invention is suitable for the technical field of atomization control, and particularly relates to a laryngeal cancer atomization control method and atomization equipment, the atomization equipment is applied to the atomization equipment, the atomization equipment comprises a laryngeal cancer atomization device and a control device, the control device is in communication connection with the laryngeal cancer atomization device, and the method comprises the steps that the control device obtains contact information of a holding part of the laryngeal cancer atomization device; the control device determines holding information according to the contact information; the control device obtains historical information, matching is conducted on the basis of the holding information and the historical information, and control information is obtained under the condition that the holding information and the historical information are matched consistently; wherein the control information is used for indicating and controlling the laryngeal cancer atomization device to spray medicine, and the historical information is used for reflecting the holding condition of the hand of the owner under the condition that the owner holds the holding part of the laryngeal cancer atomization device. According to the laryngeal cancer atomization control method provided by the invention, the laryngeal cancer atomization device can be prevented from being mistakenly used due to contact by family members or children, and the probability of occurrence of dangers can be reduced.

Description

Technical Field

[0001] The present application belongs to the technical field of atomization control, and in particular, relates to a laryngeal cancer atomization control method and atomization equipment. Background Art

[0002] Nebulizers usually use spray equipment to convert drug solutions into approximate atomized droplets, and patients inhale these atomized drugs to achieve the therapeutic effect. The laryngeal cancer atomization control method refers to using atomization therapy to help laryngeal cancer patients relieve symptoms and improve respiratory function.

[0003] The nebulizer device in the related technology may be touched and used by non-patients (such as family members or children) in a home environment. If the non-patient starts the nebulizer device without understanding the correct usage method, the drug may be sprayed out, which may cause the non-patient to inhale the drug by mistake, causing unnecessary pharmacological reactions and affecting the non-patient's body. Summary of the invention

[0004] The embodiments of the present application provide a laryngeal cancer atomization control method and an atomization device, which can solve the problem of accidental inhalation of drugs due to non-patients touching the atomization device, leading to pharmacological reactions.

[0005] In a first aspect, an embodiment of the present application provides a laryngeal cancer atomization control method, which is applied to an atomization device, wherein the atomization device includes a laryngeal cancer atomization device and a control device, wherein the control device is communicatively connected to the laryngeal cancer atomization device, and the method includes: The control device acquires contact information of the gripping portion of the laryngeal cancer atomization device; wherein the contact information is used to indicate that the gripping portion of the laryngeal cancer atomization device is held by a hand; The control device determines the holding information according to the contact information; wherein the holding information is used to indicate whether the holder currently holding the holding part of the laryngeal cancer atomization device is holding it with the left hand or the right hand; The control device acquires historical information, and matches the historical information based on the holding information, and obtains control information when the holding information matches the historical information; wherein the control information is used to instruct the control of the laryngeal cancer atomizer to spray medicine, and the historical information is used to reflect the holding condition of the owner's hand when the owner is holding the holding part of the laryngeal cancer atomizer.

[0006] The laryngeal cancer atomization control method provided by the present application comprises the following steps: the control device obtains contact information of the gripping portion of the laryngeal cancer atomization device, and can detect whether the gripping portion of the atomization device is held by a person by obtaining the contact information of the gripping portion, and can detect whether the laryngeal cancer atomization device is picked up by a person; the control device determines the gripping information according to the contact information, and can determine the specific gripping situation of the gripping portion of the laryngeal cancer atomization device by the gripping information, and can serve as a basis for subsequent matching; the control device obtains historical information, and matches the gripping information with the historical information based on the gripping information, and obtains control information when the gripping information matches the historical information, and can match the gripping situation of the owner holding the laryngeal cancer atomization device according to the gripping state or habit reflected in the historical information, and can judge as accurately as possible whether the person currently holding the laryngeal cancer atomization device is the owner himself according to the matching situation, and decide whether to spray the medicine for the current operator or prohibit the spraying of the medicine according to the judgment result, so as to prevent the accidental use by family members or children due to contact, and prevent unnecessary pharmacological reactions caused by the accidental use, resulting in the body of non-patients being affected and the risk being increased.

[0007] In a second aspect, an embodiment of the present application provides a laryngeal cancer atomization control system, which is applied to an atomization device, wherein the atomization device includes a laryngeal cancer atomization device and a control device, wherein the control device is communicatively connected with the laryngeal cancer atomization device, and the system includes: An acquisition unit, used for the control device to acquire contact information of the gripping portion of the laryngeal cancer atomization device; wherein the contact information is used to indicate that the gripping portion of the laryngeal cancer atomization device is held by a hand; A detection unit, used for the control device to determine holding information according to the contact information; wherein the holding information is used to indicate whether the holder currently holding the holding portion of the laryngeal cancer atomization device is holding it with the left hand or the right hand; The result unit is used for the control device to obtain historical information, and match the historical information based on the holding information, and obtain control information when the holding information matches the historical information; wherein the control information is used to instruct the control of the laryngeal cancer atomizer to spray medicine, and the historical information is used to reflect the holding condition of the owner's hand when the owner holds the holding part of the laryngeal cancer atomizer.

[0008] In a third aspect, an embodiment of the present application provides a nebulization device, including a laryngeal cancer nebulization device and a control device, wherein the control device is communicatively connected to the laryngeal cancer nebulization device, and the control device includes a memory, a processor, and a computer program stored in the memory and executable on the processor, wherein the computer program, when executed by the processor, implements the method described in any one of the first aspects above.

[0009] In a fourth aspect, an embodiment of the present application provides a computer program product. When the computer program product runs on an atomization device, the atomization device executes the laryngeal cancer atomization control method described in any one of the first aspects above.

[0010] It can be understood that the beneficial effects of the second to fourth aspects mentioned above can be found in the relevant description of the first aspect mentioned above, and will not be repeated here. BRIEF DESCRIPTION OF THE DRAWINGS

[0011] In order to more clearly illustrate the technical solutions in the embodiments of the present application, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. 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 paying any creative work.

[0012] Figure 1 It is a flow chart of a laryngeal cancer atomization control method provided in one embodiment of the present application; Figure 2 It is a schematic diagram of the implementation flow of step S100 in the laryngeal cancer atomization control method provided in one embodiment of the present application; Figure 3 1 is a schematic diagram of the implementation flow of step S200 in the laryngeal cancer atomization control method provided in one embodiment of the present application; Figure 4 It is a schematic diagram of the implementation flow of step S300 in the laryngeal cancer atomization control method provided in one embodiment of the present application; Figure 5 It is a structural schematic diagram of a laryngeal cancer atomization control system provided in an embodiment of the present application; Figure 6 It is a schematic diagram of the structure of the control device of the atomization equipment provided in the embodiment of the present application. DETAILED DESCRIPTION

[0013] In the following description, specific details such as specific system structures, technologies, etc. are provided for the purpose of illustration rather than limitation, so as to provide a thorough understanding of the embodiments of the present application. However, it should be clear to those skilled in the art that the present application may also be implemented in other embodiments without these specific details. In other cases, detailed descriptions of well-known systems, devices, circuits, and methods are omitted to prevent unnecessary details from obstructing the description of the present application.

[0014] It should be understood that when used in the present specification and the appended claims, the term "comprising" indicates the presence of described features, wholes, steps, operations, elements and / or components, but does not exclude the presence or addition of one or more other features, wholes, steps, operations, elements, components and / or combinations thereof.

[0015] It should also be understood that the term “and / or” used in the specification and appended claims refers to any and all possible combinations of one or more of the associated listed items, and includes these combinations.

[0016] As used in the specification and appended claims of this application, the term "if" can be interpreted as "when" or "uponce" or "in response to determining" or "in response to detecting", depending on the context. Similarly, the phrase "if it is determined" or "if [described condition or event] is detected" can be interpreted as meaning "uponce it is determined" or "in response to determining" or "uponce [described condition or event] is detected" or "in response to detecting [described condition or event]", depending on the context.

[0017] In addition, in the description of the present application specification and the appended claims, the terms "first", "second", "third", etc. are only used to distinguish the descriptions and cannot be understood as indicating or implying relative importance.

[0018] References to "one embodiment" or "some embodiments" etc. described in the specification of this application mean that one or more embodiments of the present application include specific features, structures or characteristics described in conjunction with the embodiment. Therefore, the statements "in one embodiment", "in some embodiments", "in some other embodiments", "in some other embodiments", etc. that appear in different places in this specification do not necessarily refer to the same embodiment, but mean "one or more but not all embodiments", unless otherwise specifically emphasized in other ways. The terms "including", "comprising", "having" and their variations all mean "including but not limited to", unless otherwise specifically emphasized in other ways.

[0019] The nebulizer device in the related technology may be touched and used by non-patients (such as family members or children) in a home environment. If the non-patient starts the nebulizer device without understanding the correct usage method, the drug may be sprayed out, which may cause the non-patient to inhale the drug by mistake, causing unnecessary pharmacological reactions and affecting the non-patient's body.

[0020] In the method, the control device obtains contact information of the gripping portion of the laryngeal cancer atomizer device, and can detect whether the gripping portion of the atomizer device is held by a person by obtaining the contact information of the gripping portion, and can detect whether the laryngeal cancer atomizer device is picked up by a person; the control device determines the gripping information based on the contact information, and can determine the specific gripping situation of the gripping portion of the laryngeal cancer atomizer device through the gripping information, which can serve as a basis for subsequent matching; the control device obtains historical information, and matches the gripping information with the historical information based on the gripping information, and obtains control information when the gripping information matches the historical information, and can match the gripping situation of the owner holding the laryngeal cancer atomizer device according to the gripping state or habit reflected in the historical information, and judge as accurately as possible whether the person currently holding the laryngeal cancer atomizer device is the owner himself according to the matching situation, and decide whether to spray the medicine for the current operator or prohibit the spraying of the medicine according to the judgment result, so as to prevent the device from being contacted by family members or children and misuse, so as to prevent unnecessary pharmacological reactions caused by misuse, resulting in non-patient bodies being affected and increasing the risk.

[0021] The laryngeal cancer atomization control method provided in the embodiment of the present application can be applied to an atomization device. In this case, the atomization device is the executor of the laryngeal cancer atomization control method provided in the embodiment of the present application. The embodiment of the present application does not impose any restrictions on the specific type of the atomization device.

[0022] For example, the atomization device includes a laryngeal cancer atomization device and a control device, and the control device is in communication with the laryngeal cancer atomization device; the control device is integrated into a control panel on the control device, and can also be a mobile phone, a tablet computer, etc. The laryngeal cancer atomization device may include an atomization body, a sensing detection component, a drug storage space, and a reminder component, etc.; The sensing detection part may include a multi-area pressure sensor array, a finger posture recognition module and an oral state monitoring unit; the multi-area pressure sensor array may be a pressure sensor grid set in the first area (palm contact area) and the second area (finger contact area) of the grip part, which can accurately identify the coverage status and duration of the palm / finger. The capacitive fingerprint recognition array embeds a high-resolution capacitive sensor in the second area, identifies the thumb position through the fingerprint distribution pattern (which may be the difference in the mirror characteristics of the left and right fingerprints), and the micro TOF laser radar integrates a time-of-flight sensor at the root of the nozzle to measure the opening and closing of the oral cavity in real time (which may be calculated by the reflection distance). The drug storage space is a space for storing drugs; the reminder may be a speaker or any structure for playing sound. The laryngeal cancer atomization device may also include a human-computer interaction interface, such as a micro display screen for displaying operation settings.

[0023] In order to better understand the laryngeal cancer atomization control method provided in the embodiment of the present application, the specific implementation process of the laryngeal cancer atomization control method provided in the embodiment of the present application is exemplarily introduced below.

[0024] Figure 1 A schematic flow chart of a laryngeal cancer atomization control method provided in an embodiment of the present application is shown. The laryngeal cancer atomization control method comprises: S100, the control device obtains contact information of the gripping portion of the laryngeal cancer atomization device; wherein the contact information is used to indicate that the gripping portion of the laryngeal cancer atomization device is gripped by a hand.

[0025] It can be understood that the holding part being held by the hand can be understood as the holding part being covered by the hand in a certain area and the hand exerting a certain pressure on the holding part; covering a certain area can be that there are multiple sensing points on the holding part, and the multiple sensing points are arranged on the cancer atomization device. When the sensing points are in contact with the hand and the pressure meets the preset value, it is proved that the holding part is held by the hand; the sensing points can be respectively corresponding to the ventral surface of the fingertip of the thumb, the ventral surface of the fingertip of the index finger, the ventral surface of the fingertip of the middle finger, the ventral surface of the fingertip of the ring finger, the ventral surface of the fingertip of the little finger and the palm, among which the contact areas and pressures of the fingertip of the thumb, the ventral surface of the fingertip of the index finger, the ventral surface of the fingertip of the middle finger, the ventral surface of the fingertip of the ring finger, the ventral surface of the fingertip of the little finger and the palm are different respectively; the situation that the pressure meets the preset value can be The contact area size and contact pressure between the ventral surface of the thumb fingertip and the sensing point, the contact area size and contact pressure between the ventral surface of the index finger and the sensing point, the contact area size and contact pressure between the ventral surface of the middle finger and the sensing point, the contact area size and contact pressure between the ventral surface of the ring finger and the sensing point, the contact area size and contact pressure between the ventral surface of the little finger and the sensing point, and the contact area size and contact pressure between the palm of the hand and the sensing point, recorded when the owner uses it for the first time; wherein, the sensing points can be 12 sensing points, 6 sensing points are set on the left side of the cancer atomizer device, and the other 6 sensing points are set on the right side of the cancer atomizer device, and the 6 sensing points set on the left side of the cancer atomizer device are opposite to the 6 sensing points set on the right side of the cancer atomizer device.

[0026] In one possible implementation, see Figure 2 S100, obtaining contact information of a gripping portion of a laryngeal cancer atomization device, including: S110, detecting the coverage of the first area and the second area of ​​the gripping portion of the laryngeal cancer atomization device; wherein the first area is the area covered by the palm, the second area is the area covered by the fingers, and the coverage status is a covered state or an uncovered state.

[0027] It can be understood that it is possible to detect whether the area covered by the palm of the gripping portion of the laryngeal cancer atomization device is in a covered state or an uncovered state and whether the area covered by the fingers is in a covered state or an uncovered state.

[0028] S120, when the first area is covered by the palm of the current holder, detect the continuous coverage time of the palm to obtain first time information; wherein the first time information is used to indicate the time length of the first area covered by the palm.

[0029] It is understood that the continuous coverage time of the palm is the time the palm stays on the first area. The time may be a time set by the owner, such as 15 seconds, 30 seconds, 45 seconds, 60 seconds, 80 seconds or 120 seconds, but is not limited thereto.

[0030] Exemplarily, when the first area (ie, the area covered by the palm) is covered by the palm of the current holder, the continuous coverage time of the palm is detected to obtain a time length value, and the time length value is determined as the first time information.

[0031] S130, when the second area is covered by the finger of the current holder, detect the continuous covering time of the finger to obtain second time information; wherein the second time information is used to indicate the time length of the second area covered by the finger.

[0032] It can be understood that the continuous coverage time of the finger is the time the finger stays on the second area. The time can be a time set by the owner, for example, in addition to all the time examples described in step S120, the time can also be 10 seconds, 20 seconds, 40 seconds, 50 seconds, 90 or 110 seconds, etc. The time of 10 seconds, 20 seconds, 40 seconds, 50 seconds, 90 or 110 seconds can also be applied to step S120, but is not limited thereto.

[0033] Exemplarily, when the second area (ie, the area covered by the finger) is covered by the finger of the current holder, the continuous covering time of the finger is detected to obtain a time length parameter, and the time length parameter is determined as the first time information.

[0034] S140: When the duration indicated by the first time information and the duration indicated by the second time information are both greater than a preset coverage duration, contact information of the gripping portion of the laryngeal cancer atomization device is determined.

[0035] Exemplarily, when the duration indicated by the first time information is greater than the preset coverage duration, and when the duration indicated by the second time information is also greater than the preset coverage duration, it is determined that the holding portion of the laryngeal cancer atomization device is held by the hand.

[0036] With this arrangement, the preset coverage length can be used to more accurately determine whether the device is held by the operator, reducing brief touches or situations where the device is briefly picked up for the purpose of changing the placement of the laryngeal cancer atomizer and is mistakenly believed to need to be used, thereby improving the accuracy and precision of the judgment.

[0037] S200, the control device determines holding information according to the contact information; wherein the holding information is used to indicate whether the holder currently holding the holding part of the laryngeal cancer atomization device is holding it with the left hand or the right hand.

[0038] It can be understood that the holding habit of the current holder is determined to be left-hand holding or right-hand holding based on the contact information; determining whether the current holder's holding habit is left-hand holding or right-hand holding can be determined by the characteristics of the hand to determine whether the current holding hand is the left hand or the right hand; the hand characteristics can be the direction of the fingers or the ventral surface of the fingertips to determine the position of the laryngeal cancer atomization device covered.

[0039] In one possible implementation, see Figure 3 , S200, determining holding information according to the contact information, including: S210, based on the contact information, analyzing the finger positions of the current holder on the second area to obtain finger distribution information; wherein the finger distribution information is used to indicate the contact positions of the thumb, index finger, middle finger, ring finger and little finger on the second area.

[0040] It can be understood that when the gripping portion of the laryngeal cancer atomization device is held by a hand, the finger positions of the current holder on the second area are determined to obtain the finger distribution information.

[0041] Exemplarily, when the owner uses it, he will first set his own holding habits, which include whether to hold it with the right hand or the left hand, as well as the strength and coverage area of ​​the holding, etc.; for example, when the owner holds it with his left hand, the ventral surface of the fingertip is located on the right side of the holding part of the laryngeal cancer atomizer device, so the sensing point is on the right side, so the 6 sensing points on the right side are the sensing points set by the owner, and when the owner holds it with his right hand, the ventral surface of the fingertip is located on the left side of the holding part of the laryngeal cancer atomizer device, then the sensing point is on the left, so the 6 sensing points on the left side are the sensing points set by the owner; for example, when the owner holds it with his right hand, the 6 sensing points on the left are the sensing points set by the owner. If the non-owner uses it by mistake and holds it with his left hand, the fingers of the non-owner are located at the 6 sensing points on the right. Because the sensing points are different from the sensing points set by the owner (because the owner's are the sensing points on the left, and the non-owner's are on the right, which is inconsistent with the position of the sensing points set by the owner), it can be clearly determined that the operator is not the owner.

[0042] S220, obtaining tilt information according to the finger distribution information; wherein the tilt information is used to indicate the direction of the thumb.

[0043] It can be understood that the tilt information is used to indicate the direction of the thumb, which can be understood as after the ventral surface of the thumb tip contacts the sensing point, the tilt state of the thumb can be judged, and the direction of the thumb is determined by the tilt state of the thumb; after the ventral surface of the thumb tip contacts the sensing point, the tilt state includes the thumb being lower on the left and higher on the right and higher on the left and lower on the right. If the tilt state of the thumb judged when the ventral surface of the thumb tip contacts the sensing point is lower on the left and higher on the right, it can be determined that the thumb is facing the right side of the laryngeal cancer nebulizer device; if the tilt state of the thumb judged when the ventral surface of the thumb tip contacts the sensing point is higher on the left and lower on the right, it can be determined that the thumb is facing the left side of the laryngeal cancer nebulizer device.

[0044] S230: Determine holding information based on the direction of the thumb indicated by the tilt information.

[0045] For example, if the inclination state of the thumb judged to be lower on the left and higher on the right when the ventral surface of the thumb's fingertip contacts the sensing point, it can be determined that the thumb is facing the right side of the laryngeal cancer nebulizer device, and it can be determined that the person currently holding the gripping part of the laryngeal cancer nebulizer device as indicated by the holding information is holding it with the left hand; if the inclination state of the thumb judged to be higher on the left and lower on the right when the ventral surface of the thumb's fingertip contacts the sensing point, it can be determined that the thumb is facing the left side of the laryngeal cancer nebulizer device, and it can be determined that the person currently holding the gripping part of the laryngeal cancer nebulizer device as indicated by the holding information is holding it with the right hand.

[0046] With this setting, users can complete identity authentication by just holding the device without any additional operations, verify whether it is their own operation, simplify the process and improve compliance, prevent others from operating it incorrectly, prevent children or unauthorized persons from accessing the device, and reduce accidental risks; by judging whether the operation is performed by the left hand or the right hand, the accuracy of judging whether it is the owner's operation can be improved.

[0047] S300, the control device obtains historical information, and matches the historical information based on the holding information, and obtains control information when the holding information matches the historical information; wherein the control information is used to instruct the laryngeal cancer atomizer to spray medicine, and the historical information is used to reflect the holding condition of the owner's hand when the owner holds the holding part of the laryngeal cancer atomizer.

[0048] Exemplarily, historical information can be obtained through parameters set by the owner when using it for the first time; the holding information and historical information can be matched by matching the holding condition of the hand (left hand or right hand) of the holder who is currently holding the holding part of the laryngeal cancer atomizer device and the holding condition of the hand (left hand or right hand) of the owner when holding the holding part of the laryngeal cancer atomizer device as indicated by the historical information to see whether they are the same; if they are the same, the control information can be obtained.

[0049] With such arrangement, through the above steps, it is possible to determine as accurately as possible whether the person currently holding the laryngeal cancer atomizer device is the owner himself, and decide whether to spray the medicine or prohibit the current operator based on the judgment result. It can also prevent family members, children or other people from coming into contact with the device and misusing it, thereby preventing unnecessary harm, avoiding affecting the bodies of non-patients, and reducing the possibility of danger.

[0050] In one possible implementation, see Figure 4 S300, acquiring historical information, and matching the historical information based on the holding information, and obtaining control information when the holding information matches the historical information, including: S310, when the holding information and the historical information meet the matching condition, the matching status information is obtained; wherein the matching status information is used to indicate that the matching is successful, and the matching condition is that the holding condition of the holder who is currently holding the holding part of the laryngeal cancer atomizer device indicated by the holding information is the same as the holding condition of the owner when holding the holding part of the laryngeal cancer atomizer device reflected by the historical information.

[0051] Exemplarily, when the gripping condition of the holder currently holding the gripping part of the laryngeal cancer atomization device is the same as the gripping condition of the owner when holding the gripping part of the laryngeal cancer atomization device as reflected in the historical information, matching status information is obtained to prove that the matching is successful.

[0052] S320, based on the matching state information, perform a first detection on the hand of the current holder to obtain first detection information; wherein the first detection information is used to reflect the holding condition of the hand and the holding portion of the laryngeal cancer atomization device.

[0053] Exemplarily, when the matching status information indicates that the match is successful, the holding pressure of the hand of the current holder on the holding part of the laryngeal cancer atomization device is detected to obtain a detection pressure value, the detection pressure value is calculated with the pressure value applied by the owner to obtain a pressure result, the value of the pressure result is subjected to pressure analysis, and the analyzed result is determined as the first detection information.

[0054] In one possible implementation, see Figure 4 S320: Based on the matching state information, a first detection is performed on the hand of the current holder to obtain first detection information, including: S321, when the matching status information indicates that the matching is successful, detecting first pressure information of the current palm on the first area on the gripping portion of the laryngeal cancer atomization device; wherein the first pressure information is used to indicate the pressure value of the palm on the first area.

[0055] It can be understood that the first pressure information of the palm on the first area of ​​the gripping portion of the laryngeal cancer atomization device can be detected by a capacitive tactile sensor array, a pressure-variable sheet, or a piezoresistive sensor, etc., but not limited thereto. The capacitive tactile sensor array, the pressure-variable sheet, or the piezoresistive sensor can be respectively installed at the sensing point position, etc., but not limited thereto.

[0056] S322, detecting second pressure information of the current finger on the second area; wherein the second pressure information is used to indicate the pressure value of the finger on the second area.

[0057] It is understood that the second pressure information of the finger on the second area can be detected by a pressure-variable sheet or a piezoresistive sensor, but is not limited thereto. The micro piezoelectric sensor and the thin-film force-sensitive resistor can be respectively installed at the sensing point position, but is not limited thereto.

[0058] S323, comparing the first pressure information and the second pressure information with the first historical habit information to obtain first detection information; wherein the first historical habit is used to indicate the pressure value applied by the owner's palm to the first area and the pressure value applied by the owner's finger to the second area.

[0059] It can be understood that the first historical habit information can be the pressure value applied by the palm of the owner to the first area and the pressure value applied by the owner's finger to the second area set when the owner uses the laryngeal cancer atomization device for the first time.

[0060] Exemplarily, after obtaining the first pressure information and the second pressure information, the pressure value of the palm received on the first area indicated by the first pressure information and the pressure value applied to the first area by the palm of the owner indicated by the first historical habit information are calculated (the pressure value of the palm received on the first area indicated by the first pressure information is subtracted from the pressure value applied to the first area by the palm of the owner indicated by the first historical habit information), and a first result is obtained; secondly, the pressure value of the finger received on the second area indicated by the second pressure information and the pressure value applied to the second area by the finger of the owner indicated by the first historical habit information are calculated (the pressure value of the finger received on the second area indicated by the second pressure information is subtracted from the pressure value applied to the second area by the finger of the owner indicated by the first historical habit information), and a second result is obtained; if the first pressure information is negative, the pressure value of the palm received on the first area indicated by the second pressure information and the pressure value applied to the second area by the finger of the owner indicated by the first historical habit information are calculated; If the result is equal to 0 or within the error range of ±0.5 and the second result is equal to 0 or within the error range of ±0.5, it proves that the current operator is the owner; if the first result is not equal to 0 or the error range is greater than 0.5 or less than 0.5, and the second result is not equal to 0 or the error range is greater than 0.5 or less than 0.5, it proves that the current operator is not the owner; if the first result is equal to 0 or within the error range of ±0.5, and the second result is not equal to 0 or the error range is greater than 0.5 or less than 0.5, it proves that the current operator is not the owner; if the second result is equal to 0 or within the error range of ±0.5, and the first result is not equal to 0 or the error range is greater than 0.5 or less than 0.5, it proves that the current operator is not the owner; wherein the error range can be set according to the owner, for example, 0.3, 0.5, 0.8, 1, 2 or 5, etc., but not limited to this.

[0061] With such a setting, it is possible to determine whether the current operator is the owner by means of pressure, because each person has different strength, different habits in normal holding conditions, and different ages and genders will produce different holding pressures, and it is almost impossible to find the owner's strength when holding. Therefore, it is more accurate to determine whether the current operator is the owner, reduce misjudgments and improve accuracy.

[0062] S330, after the first detection is completed and the first detection information meets the requirements, a second detection is performed on the current holder to obtain second detection information; wherein the second detection information is used to reflect the situation between the oral cavity and the nozzle of the laryngeal cancer atomization device.

[0063] Exemplarily, when the first detection information meets the requirements, that is, when the pressure held by the current operator is the same as the pressure set by the owner, the state between the mouth of the current holder and the nozzle of the laryngeal cancer atomization device is detected to obtain the second detection information; this can be by detecting the angle between the mouth and the nozzle of the laryngeal cancer atomization device, etc., but is not limited to this.

[0064] In one possible implementation, see Figure 4 S330: After the first detection is completed and the first detection information meets the requirements, a second detection is performed on the current holder to obtain second detection information, including: S331, when the first detection information meets the requirements, the state of the current user's mouth is detected to obtain oral state information; wherein the oral state information is used to indicate the degree of opening of the current user's mouth.

[0065] It can be understood that the oral state information is used to indicate the degree of opening of the current user's oral cavity; the detection of the current user's oral state can be achieved by integrating a miniature infrared ranging sensor array near the mist outlet of the atomization device, and measuring the distance parameters in real time by transmitting and receiving infrared light signals; the distance parameters include maxillary distance, mandibular distance and opening width; among them, the maxillary distance can be aligned with the front of the upper jaw (hard palate area) by sensor A; the mandibular distance can be aligned with the front of the lower jaw (mental protrusion area) by sensor B; the opening width can be detected by the lateral sensor C to detect the distance between the left and right side walls of the oral cavity.

[0066] Then use the triangulation algorithm to calculate the opening angle , the formula is: arccos( ); Where L is the average anatomical distance between the upper and lower jaws (the preset value can be dynamically calibrated); and then calculated by the formula , that is, the degree of opening of the user's mouth as indicated by the oral status information.

[0067] S332, detecting the angle information between the nozzle of the laryngeal cancer atomizer and the oral cavity of the current user; wherein the angle information is used to indicate the angle value between the nozzle of the laryngeal cancer atomizer and the oral cavity of the current user.

[0068] For example, an angle sensor is installed at the connection between the nozzle and the grip of the atomizer device, which may be a potentiometer angle sensor or a magnetoelectric angle sensor. When the nozzle rotates, the resistance value or magnetic field signal of the angle sensor will change. By measuring this change and converting it into an electrical signal, the angle between the nozzle and the grip can be obtained through a signal processing circuit. This angle is the angle between the nozzle and the oral cavity. For example, the resistance value of the potentiometer angle sensor is With Angle Linear relationship , the resistance value is measured by measuring the circuit , we can calculate the angle = ,in, and is the calibration factor of the sensor; therefore, by the formula = The angle value between the nozzle of the laryngeal cancer atomizer and the oral cavity of the current user can be obtained.

[0069] S333, obtaining second detection information based on comparison of the oral state information with the angle information and the second historical habit information; wherein the second historical habit information is used to indicate the degree of opening of the owner's oral cavity and the angle value between the nozzle of the laryngeal cancer atomizer and the owner's oral cavity when the owner is using the laryngeal cancer atomizer.

[0070] It can be understood that the second historical habit information is used to indicate the degree of opening of the owner's mouth when the owner uses the laryngeal cancer atomizer, that is, the value of the degree of opening of the owner's mouth when the owner uses the laryngeal cancer atomizer.

[0071] Exemplarily, after obtaining the oral state information and the angle information, the degree of opening of the current user's oral cavity indicated by the oral state information is calculated with the degree of opening of the owner's oral cavity indicated by the second historical habit information (the degree of opening of the owner's oral cavity indicated by the second historical habit information is subtracted from the degree of opening of the current user's oral cavity indicated by the oral state information), and the oral result is obtained; secondly, the angle value between the nozzle of the laryngeal cancer atomizer device and the current user's oral cavity indicated by the angle information is calculated with the angle value between the nozzle of the laryngeal cancer atomizer device and the owner's oral cavity indicated by the second historical habit information (the angle value between the nozzle of the laryngeal cancer atomizer device and the owner's oral cavity indicated by the second historical habit information is subtracted from the angle value between the nozzle of the laryngeal cancer atomizer device and the current user's oral cavity indicated by the angle information). cavities), and obtain the angle result; if the oral result is equal to 0 or within the error range of ±1 and the angle result is equal to 0 or within the error range of ±1, it is proved that the current operator is the owner; if the oral result is not equal to 0 or the error range is greater than 1 or less than 1, and the angle result is not equal to 0 or the error range is greater than 1 or less than 1, it is proved that the current operator is not the owner; if the oral result is equal to 0 or within the error range of 1, the angle result is not equal to 0 or the error range is greater than 1 or less than 1, it is proved that the current operator is not the owner; if the angle result is equal to 0 or within the error range of ±1, the oral result is not equal to 0 or the error range is greater than 1 or less than 1, it is proved that the current operator is not the owner; wherein the error range can be set according to the owner, for example, 1, 1.5, 2 or 3, etc., but not limited to this.

[0072] With this arrangement, whether the current operator is the owner can be further determined through the oral state information and angle information. Since each person's oral structure, opening habits, and angle habits when using the atomizer are different, the identity of the current user can be further accurately verified. For example, some people may be accustomed to a larger oral opening angle, while others may be accustomed to a smaller opening angle; similarly, the angle at which each person points the nozzle of the atomizer at the oral cavity may be different. By comparing this personalized information with the pre-set historical habit information, the accuracy of identity authentication can be greatly improved, thereby ensuring that only the owner can correctly and safely use the laryngeal cancer atomizer. The multi-level identity authentication method not only enhances the safety of the device, but also reduces the risk.

[0073] S340: After the second detection is completed and the second detection information meets the requirements, a third detection is performed on the current holder to obtain control information.

[0074] Exemplarily, when the second detection information meets the requirements, the water temperature selected by the current holder is judged, and control information is obtained according to the judgment result; the judgment result is to process the water temperature selected by the current holder and the water temperature preset by the owner to obtain a processing result, and the processing result is confirmed as the control information.

[0075] In one possible implementation, see Figure 4 , S340, after the second detection is completed and the second detection information meets the requirements, a third detection is performed on the current holder to obtain control information, including: S341, when the second detection information meets the requirements, ask the current user to select the water temperature, and receive the water temperature information of the current user; wherein the water temperature information is used to indicate the water temperature selected by the current user, and the water temperature is the water temperature for gargling.

[0076] It can be understood that asking the current user to select the water temperature is to issue a request to select the water temperature when the second detection information meets the requirements. The current operator can be reminded by voice to select the water temperature or input the water temperature, and then the water temperature input or selected by the current operator is recorded.

[0077] S342, making a judgment based on the water temperature information and the preset water temperature value, if the mouthwash water temperature indicated by the water temperature information is the same as the preset water temperature value, obtaining control information.

[0078] Exemplarily, the water temperature currently selected by the user indicated by the water temperature information and the preset water temperature value (i.e., the water temperature selected by the owner at the first use or the water temperature set by the owner) are calculated to obtain the calculated difference. If the calculated difference is 0, it is proved that the mouthwash water temperature indicated by the water temperature information is the same as the preset water temperature value to obtain the control information. For example, the water temperature currently selected by the user indicated by the water temperature information is 45 degrees, and the preset water temperature value is 45 degrees. Then, the water temperature difference is obtained by subtracting the preset water temperature value from the water temperature value currently selected by the user indicated by the water temperature information, i.e., 45-45=0; therefore, the mouthwash water temperature indicated by the water temperature information is the same as the preset water temperature value to obtain the control information. In addition, the water temperature can be adjusted by the owner at will, and can be adjusted high in winter, such as 45 degrees, or adjusted low in summer, such as 20 degrees, etc., but is not limited thereto.

[0079] In a possible implementation, the method further includes: If the mouthwash water temperature indicated by the water temperature information is different from the preset water temperature value, a false touch information is obtained; wherein the false touch information is used to indicate a voice to remind the current operator to stop the operation.

[0080] It can be understood that the mouthwash water temperature indicated by the water temperature information is different from the preset water temperature value, which can be understood as the mouthwash water temperature is different from the preset water temperature value after comparison; illustratively, if the mouthwash water temperature indicated by the water temperature information is different from the preset water temperature value after comparison, then the current operator is judged to be a non-owner, so as to remind the current operator to stop the operation. For example, the water temperature selected by the current user indicated by the water temperature information is 45 degrees, and the preset water temperature value is 35 degrees, then the water temperature difference is obtained by subtracting the preset water temperature value from the water temperature value selected by the current user indicated by the water temperature information, that is, 45-35=10; therefore, the mouthwash water temperature indicated by the water temperature information is different from the preset water temperature value, so as to obtain the false touch information.

[0081] In a possible implementation, the method further includes: After the first detection is completed and the first detection information does not meet the requirements, or after the first detection is completed and the first detection information meets the requirements but the second detection is completed and the second detection information does not meet the requirements, a stop message is obtained; wherein the stop message is used to indicate an instruction to remind the current operator that operations are prohibited if they are not his / her own.

[0082] Exemplarily, after the first detection is completed and the first detection information does not meet the requirements, it indicates that the current operator is not the owner and a stop message is obtained; or after the first detection is completed and the first detection information meets the requirements but the second detection is completed and the second detection information does not meet the requirements, it indicates that the current operator is not the owner and a stop message is obtained.

[0083] In a possible implementation, the method further includes: 310A, when the holding condition of the holder who is currently holding the holding part of the laryngeal cancer atomizer device indicated by the holding information is different from the holding condition of the owner when holding the holding part of the laryngeal cancer atomizer device reflected by the historical information, a reminder message is obtained; wherein the reminder message is used to indicate a danger reminder to the current holder who is not the owner.

[0084] Exemplarily, the holding condition of the holder who is currently holding the holding part of the laryngeal cancer atomizer device as indicated by the holding information and the holding condition of the owner when holding the holding part of the laryngeal cancer atomizer device as reflected in the historical information are compared. After comparison, if the holding condition of the holder who is currently holding the holding part of the laryngeal cancer atomizer device as indicated by the holding information is different from the holding condition of the owner when holding the holding part of the laryngeal cancer atomizer device as reflected in the historical information, it is judged that the current operator is a non-owner, and a reminder message is obtained based on the judgment result to remind the current holder that he is not the owner of the danger.

[0085] 320A, based on the reminder information, if the holding condition of the holder currently holding the holding part of the laryngeal cancer nebulizer device indicated by the holding information is the same as the holding condition of the owner when holding the holding part of the laryngeal cancer nebulizer device reflected by the historical information, the locking information is obtained; wherein, the locking information is the instruction information prohibiting the laryngeal cancer nebulizer from spraying medicine.

[0086] Exemplarily, after the reminder message is issued, within a certain time (which can be 3 minutes, 5 minutes or 10 minutes), and after detecting that the current holder has adjusted the holding position multiple times and the holding condition of the holder currently holding the holding part of the laryngeal cancer nebulizer device indicated by the holding information is the same as the holding condition of the owner when holding the holding part of the laryngeal cancer nebulizer device reflected in the historical information, it is judged that the current operator is a non-owner and a locking information is obtained, and the laryngeal cancer nebulizer is prohibited from spraying medicine according to the locking information.

[0087] Such a setting, through the above description, can prevent non-owners from opening the laryngeal cancer nebulizer device by trying multiple times, can reduce the probability of danger, can improve the accuracy of judgment, and avoid non-owners from misusing the laryngeal cancer nebulizer device as much as possible, thereby reducing the impact on the non-owner's physical health due to misuse, thereby improving the safety of the laryngeal cancer nebulizer device.

[0088] It should be understood that the size of the serial numbers of the steps in the above embodiments does not mean the order of execution. The execution order of each process should be determined by its function and internal logic, and should not constitute any limitation on the implementation process of the embodiments of the present application.

[0089] Corresponding to the laryngeal cancer atomization control method described in the above embodiment, the embodiment of the present application also provides a laryngeal cancer atomization control system, and each unit of the system can implement each step of the laryngeal cancer atomization control method. Figure 5A structural block diagram of a laryngeal cancer atomization control system provided in an embodiment of the present application is shown. For ease of explanation, only the parts related to the embodiment of the present application are shown.

[0090] Reference Figure 5 , the laryngeal cancer atomization control system includes: An acquisition unit, used to control the device to acquire contact information of the gripping portion of the laryngeal cancer atomization device; wherein the contact information is used to indicate that the gripping portion of the laryngeal cancer atomization device is held by a hand; The detection unit is used to control the device to determine the holding information according to the contact information; wherein the holding information is used to indicate whether the holder who is currently holding the holding part of the laryngeal cancer atomization device is holding it with the left hand or the right hand; The result unit is used to control the device to obtain historical information, and match the historical information based on the holding information, and obtain control information when the holding information matches the historical information; wherein the control information is used to instruct the control of the laryngeal cancer atomizer to spray medicine, and the historical information is used to reflect the holding condition of the owner's hand when the owner holds the holding part of the laryngeal cancer atomizer.

[0091] It should be noted that the information interaction, execution process, etc. between the above-mentioned systems / units are based on the same concept as the method embodiment of the present application. Their specific functions and technical effects can be found in the method embodiment part and will not be repeated here.

[0092] Those skilled in the art can clearly understand that, for the convenience and simplicity of description, only the division of the above-mentioned functional units and modules is used as an example for illustration. In practical applications, the above-mentioned function allocation can be completed by different functional units and modules as needed, that is, the internal structure of the system can be divided into different functional units or modules to complete all or part of the functions described above. The functional units and modules in the embodiment can be integrated in a processing unit, or each unit can exist physically separately, or two or more units can be integrated in one unit. The above-mentioned integrated unit can be implemented in the form of hardware or in the form of software functional units. In addition, the specific names of the functional units and modules are only for the convenience of distinguishing each other, and are not used to limit the scope of protection of this application. The specific working process of the units and modules in the above-mentioned system can refer to the corresponding process in the aforementioned method embodiment, which will not be repeated here.

[0093] The present application also provides an atomization device, Figure 6 This is a schematic diagram of the structure of a control device for an atomization device provided in one embodiment of the present application. Figure 6 As shown, the control device 6 of this embodiment includes: at least one processor 60 ( Figure 6 Only one is shown), at least one memory 61 ( Figure 6 Only one is shown in the figure) and a computer program 62 stored in the at least one memory 61 and executable on the at least one processor 60. When the processor 60 executes the computer program 62, the control device 6 implements the steps in any of the above-mentioned laryngeal cancer atomization control method embodiments, or the control device 6 implements the functions of each module / unit in the above-mentioned system embodiments.

[0094] Exemplarily, the computer program 62 may be divided into one or more modules / units, which are stored in the memory 61 and executed by the processor 60 to complete the present application. The one or more modules / units may be a series of computer program instruction segments capable of completing specific functions, which are used to describe the execution process of the computer program 62 in the control device 6.

[0095] The control device 6 may be a computing device such as a desktop computer or a notebook. The control device may include, but is not limited to, a processor 60 and a memory 61. Those skilled in the art will appreciate that Figure 6 It is only an example of the control device 6 and does not constitute a limitation on the control device 6. It may include more or fewer components than shown in the figure, or a combination of certain components, or different components. For example, it may also include input and output devices, network access devices, buses, etc.

[0096] The processor 60 may be a central processing unit (CPU), or other general-purpose processors, digital signal processors (DSP), application-specific integrated circuits (ASIC), field-programmable gate arrays (FPGA) or other programmable logic devices, discrete gate or transistor logic devices, discrete hardware components, etc. A general-purpose processor may be a microprocessor or any conventional processor, etc.

[0097] In some embodiments, the memory 61 may be an internal storage unit of the control device 6, such as a hard disk or memory of the control device 6. In other embodiments, the memory 61 may also be an external storage device of the control device 6, such as a plug-in hard disk, a smart media card (SMC), a secure digital (SD) card, a flash card, etc. equipped on the control device 6. Further, the memory 61 may also include both an internal storage unit and an external storage device of the control device 6. The memory 61 is used to store an operating system, an application program, a boot loader (BootLoader), data, and other programs, such as the program code of the computer program. The memory 61 may also be used to temporarily store data that has been output or is to be output.

[0098] An embodiment of the present application further provides a computer-readable storage medium, wherein the computer-readable storage medium stores a computer program, and when the computer program is executed by a processor, the steps in any of the above method embodiments are implemented.

[0099] An embodiment of the present application provides a computer program product. When the computer program product runs on an atomization device, the atomization device implements the steps in any of the above method embodiments.

[0100] If the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer-readable storage medium. Based on this understanding, the present application implements all or part of the processes in the above-mentioned embodiment method, which can be completed by instructing the relevant hardware through a computer program, and the computer program can be stored in a computer-readable storage medium. When the computer program is executed by the processor, the steps of the above-mentioned various method embodiments can be implemented. Among them, the computer program includes computer program code, and the computer program code can be in source code form, object code form, executable file or some intermediate form. The computer-readable medium may at least include: any entity or device that can carry the computer program code to the atomization device, a recording medium, a computer memory, a read-only memory (ROM, Read-Only Memory), a random access memory (RAM, Random Access Memory), an electric carrier signal, a telecommunication signal, and a software distribution medium. For example, a USB flash drive, a mobile hard disk, a magnetic disk or an optical disk. In some jurisdictions, according to legislation and patent practice, computer-readable media cannot be electric carrier signals and telecommunication signals.

[0101] In the above embodiments, the description of each embodiment has its own emphasis. For parts that are not described or recorded in detail in a certain embodiment, reference can be made to the relevant descriptions of other embodiments.

[0102] Those of ordinary skill in the art will appreciate that the units and algorithm steps of each example described in conjunction with the embodiments disclosed herein can be implemented in electronic hardware, or a combination of computer software and electronic hardware. Whether these functions are performed in hardware or software depends on the specific application and design constraints of the technical solution. Professional and technical personnel can use different methods to implement the described functions for each specific application, but such implementation should not be considered to be beyond the scope of this application.

[0103] In the embodiments provided in the present application, it should be understood that the disclosed laryngeal cancer atomization control system, device and method can be implemented in other ways. For example, the laryngeal cancer atomization control system and device embodiments described above are merely schematic. For example, the division of the modules or units is only a logical function division. There may be other division methods in actual implementation, such as multiple units or components can be combined or integrated into another system, or some features can be ignored or not executed. Another point is that the mutual coupling or direct coupling or communication connection shown or discussed can be an indirect coupling or communication connection through some interfaces, devices or units, which can be electrical, mechanical or other forms.

[0104] The units described as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, that is, they may be located in one place or distributed on multiple network units. Some or all of the units may be selected according to actual needs to achieve the purpose of the solution of this embodiment.

[0105] The embodiments described above are only used to illustrate the technical solutions of the present application, rather than to limit them. Although the present application has been described in detail with reference to the aforementioned embodiments, a person skilled in the art should understand that the technical solutions described in the aforementioned embodiments may still be modified, or some of the technical features may be replaced by equivalents. Such modifications or replacements do not deviate the essence of the corresponding technical solutions from the spirit and scope of the technical solutions of the embodiments of the present application, and should all be included in the protection scope of the present application.

Claims

1. A laryngeal cancer atomization control method, characterized in that: Applied to an atomization device, the atomization device includes a laryngeal cancer atomization device and a control device, the control device is communicatively connected with the laryngeal cancer atomization device, and the method includes: The control device acquires contact information of the gripping portion of the laryngeal cancer atomization device; wherein the contact information is used to indicate that the gripping portion of the laryngeal cancer atomization device is held by a hand; The control device determines the holding information according to the contact information; wherein the holding information is used to indicate whether the holder currently holding the holding part of the laryngeal cancer atomization device is holding it with the left hand or the right hand; The control device acquires historical information, and matches the historical information based on the holding information, and obtains control information when the holding information matches the historical information; wherein the control information is used to instruct the control of the laryngeal cancer atomizer to spray medicine, and the historical information is used to reflect the holding condition of the owner's hand when the owner is holding the holding part of the laryngeal cancer atomizer.

2. The laryngeal cancer atomization control method according to claim 1, characterized in that: The step of obtaining contact information of the gripping portion of the laryngeal cancer atomization device includes: Detecting the coverage of a first area and a second area of ​​the grip of the laryngeal cancer atomization device; wherein the first area is an area covered by a palm, the second area is an area covered by a finger, and the coverage status is a covered state or an uncovered state; In the case that the first area is covered by the palm of the current holder, detecting the continuous coverage duration of the palm to obtain first time information; wherein the first time information is used to indicate the duration of the first area being covered by the palm; In the case where the second area is covered by the finger of the current holder, detecting the continuous covering time of the finger to obtain second time information; wherein the second time information is used to indicate the time length of the second area covered by the finger; When the duration indicated by the first time information and the duration indicated by the second time information are both greater than the preset coverage duration, the contact information of the gripping portion of the laryngeal cancer atomization device is determined.

3. The laryngeal cancer atomization control method according to claim 2, characterized in that: The determining the holding information according to the contact information includes: Based on the contact information, analyzing the finger positions of the current holder on the second area to obtain finger distribution information; wherein the finger distribution information is used to indicate the contact positions of the thumb, index finger, middle finger, ring finger and little finger on the second area; Obtaining tilt information according to the finger distribution information; wherein the tilt information is used to indicate the direction of the thumb; The holding information is determined based on the direction of the thumb indicated by the tilt information.

4. The laryngeal cancer atomization control method according to claim 2, characterized in that: The acquiring of historical information, and matching the historical information based on the holding information, and obtaining control information when the holding information and the historical information match each other, includes: When the holding information and the historical information meet the matching condition, the matching status information is obtained; wherein the matching status information is used to indicate that the matching is successful, and the matching condition is that the holding condition of the holder who is currently holding the holding part of the laryngeal cancer atomization device indicated by the holding information is the same as the holding condition of the owner when holding the holding part of the laryngeal cancer atomization device reflected by the historical information; Based on the matching status information, a first detection is performed on the hand of the current holder to obtain first detection information; wherein the first detection information is used to reflect the holding condition of the hand and the holding part of the laryngeal cancer atomization device; After the first detection is completed and the first detection information meets the requirements, a second detection is performed on the current holder to obtain second detection information; wherein the second detection information is used to reflect the situation between the oral cavity and the nozzle of the laryngeal cancer atomization device; After the second detection is completed and the second detection information meets the requirements, a third detection is performed on the current holder to obtain control information.

5. The laryngeal cancer atomization control method according to claim 4, characterized in that: The first detection of the hand of the current holder based on the matching state information to obtain first detection information includes: When the matching status information indicates that the matching is successful, detecting first pressure information of the palm on the first area on the gripping portion of the laryngeal cancer atomization device; wherein the first pressure information is used to indicate the pressure value of the palm on the first area; Detecting second pressure information of the current finger on the second area; wherein the second pressure information is used to indicate the pressure value of the finger on the second area; The first pressure information and the second pressure information are compared with first historical habit information to obtain first detection information; wherein the first historical habit is used to indicate the pressure value applied by the owner's palm to the first area and the pressure value applied by the owner's fingers to the second area.

6. The laryngeal cancer atomization control method according to claim 4, characterized in that: After the first detection is completed and the first detection information meets the requirements, a second detection is performed on the current holder to obtain second detection information, including: In the case where the first detection information meets the requirements, the state of the current user's mouth is detected to obtain oral state information; wherein the oral state information is used to indicate the degree of opening of the current user's mouth; Detecting the angle information between the nozzle of the laryngeal cancer atomizer and the oral cavity of the current user; wherein the angle information is used to indicate the angle value between the nozzle of the laryngeal cancer atomizer and the oral cavity of the current user; Based on the comparison of the oral state information with the angle information and the second historical habit information, the second detection information is obtained; wherein, the second historical habit information is used to indicate the degree of opening of the owner's mouth and the angle value between the nozzle of the laryngeal cancer atomizer device and the owner's mouth when the owner uses the laryngeal cancer atomizer device.

7. The laryngeal cancer atomization control method according to claim 4, characterized in that: After the second detection is completed and the second detection information meets the requirements, a third detection is performed on the current holder to obtain control information, including: If the second detection information meets the requirements, the current user is asked to select a water temperature, and the water temperature information of the current user is received; wherein the water temperature information is used to indicate the water temperature selected by the current user, and the water temperature is the water temperature for gargling; A judgment is made based on the water temperature information and a preset water temperature value, and if the mouthwash water temperature indicated by the water temperature information is the same as the water temperature threshold, control information is obtained; The method further comprises: If the mouthwash water temperature indicated by the water temperature information is different from the preset water temperature value, false touch information is obtained; wherein, the false touch information is used to indicate a voice to remind the current operator to stop the operation.

8. The laryngeal cancer atomization control method according to claim 4, characterized in that: The method further comprises: After the first detection is completed and the first detection information does not meet the requirements, or after the first detection is completed and the first detection information meets the requirements but the second detection is completed and the second detection information does not meet the requirements, a stop message is obtained; wherein the stop message is used to indicate an instruction to remind the current operator that operations are prohibited unless the operator is himself.

9. The laryngeal cancer atomization control method according to claim 4, characterized in that: The method further comprises: When the gripping condition of the holder who is currently holding the gripping part of the laryngeal cancer atomizer indicated by the gripping information is different from the gripping condition of the owner when holding the gripping part of the laryngeal cancer atomizer reflected by the historical information, a reminder message is obtained; wherein the reminder message is used to indicate that a danger reminder is given to the current holder who is not the owner; Based on the reminder information, if the holding condition of the holder currently holding the holding part of the laryngeal cancer nebulizer device indicated by the holding information is the same as the holding condition of the owner when holding the holding part of the laryngeal cancer nebulizer device reflected by the historical information, the locking information is obtained; wherein, the locking information is the instruction information prohibiting the laryngeal cancer nebulizer from spraying medicine.

10. An atomization device, comprising a laryngeal cancer atomization device and a control device, wherein the control device is in communication with the laryngeal cancer atomization device, the control device comprises a memory, a processor, and a computer program stored in the memory and executable on the processor, characterized in that: When the processor executes the computer program, the method according to any one of claims 1 to 9 is implemented.

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