CN117244184A - Wearable low-intensity pulse ultrasonic device and treatment system - Google Patents
Wearable low-intensity pulse ultrasonic device and treatment system Download PDFInfo
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- CN117244184A CN117244184A CN202311202186.4A CN202311202186A CN117244184A CN 117244184 A CN117244184 A CN 117244184A CN 202311202186 A CN202311202186 A CN 202311202186A CN 117244184 A CN117244184 A CN 117244184A
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- 238000011282 treatment Methods 0.000 title claims abstract description 165
- 238000007789 sealing Methods 0.000 claims abstract 5
- 238000002560 therapeutic procedure Methods 0.000 claims description 16
- 239000000919 ceramic Substances 0.000 claims description 13
- 238000002604 ultrasonography Methods 0.000 claims description 9
- 230000008859 change Effects 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 230000007274 generation of a signal involved in cell-cell signaling Effects 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- 230000001225 therapeutic effect Effects 0.000 claims description 3
- 230000007774 longterm Effects 0.000 abstract description 2
- 230000000694 effects Effects 0.000 description 11
- 239000000523 sample Substances 0.000 description 7
- 238000010586 diagram Methods 0.000 description 6
- 230000009286 beneficial effect Effects 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 230000008901 benefit Effects 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 208000034657 Convalescence Diseases 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229910002113 barium titanate Inorganic materials 0.000 description 2
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 2
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- ZBSCCQXBYNSKPV-UHFFFAOYSA-N oxolead;oxomagnesium;2,4,5-trioxa-1$l^{5},3$l^{5}-diniobabicyclo[1.1.1]pentane 1,3-dioxide Chemical compound [Mg]=O.[Pb]=O.[Pb]=O.[Pb]=O.O1[Nb]2(=O)O[Nb]1(=O)O2 ZBSCCQXBYNSKPV-UHFFFAOYSA-N 0.000 description 2
- 238000000554 physical therapy Methods 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 238000011269 treatment regimen Methods 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N7/00—Ultrasound therapy
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Radiology & Medical Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Percussion Or Vibration Massage (AREA)
Abstract
The invention discloses a wearable low-intensity pulse ultrasonic device and a treatment system, comprising a host and a treatment head, wherein the host comprises a host upper cover, a key sealing piece, a screen component, a fastener, an upper cover sealing piece, a lower cover sealing piece, a host circuit board, a battery component, a lower cover and keys; the treatment head comprises an upper cover, a treatment head circuit board, a vibrator and a lens; compared with the traditional floor type equipment and desktop level equipment, the invention adopts unfocused low-power equipment, thereby reducing the risk of household use; lower power, reduced risk of long-term use; the portable wearing is low in profile and portable, and can carry out the treatment when the human body is stationary or does not strenuous exercise; the system has a function of setting local treatment parameters, simultaneously has the functions of receiving the input of the on-line digital electronic prescription and modifying the local parameters, and simultaneously uploads the treatment data to the cloud.
Description
Technical Field
The invention relates to the technical field of medical equipment, in particular to a wearable low-intensity pulse ultrasonic device and a treatment system.
Background
The ultrasonic physiotherapy equipment on the current market is divided into two forms, one is a relatively large floor type equipment, the equipment is operated and used by a professional doctor in a hospital department, patients need to go to the hospital for treatment regularly, the other is a small-size desktop-level equipment, the hospital department is operated and used by the professional doctor, and the equipment can be extended to a family scene and used by the patients. The former is more powerful and some are focused ultrasound energy, which has a higher risk and must be handled by a professional physician; the patient needs to go to the department at regular intervals to treat, can't carry and wear the treatment, and is very inconvenient, and the latter volume is still great, can't satisfy and carry and wear the demand, simultaneously, as a therapeutic equipment of medical treatment, its treatment parameter when the operation of the patient oneself at home of arbitrary, and doctor's advice compliance can't track, record, confirm, probably can cause new use risk. The information and the data cannot be summarized and stored, and are reported to doctors or families, and the information acquired by the doctors during re-diagnosis is incomplete or misjudged. Such as the treatment time or intensity of the patient's use, the deficiency or excess may be ineffective or cause complications. If the patient does not execute the treatment calendar/the use frequency according to the doctor's advice, the expected effect is not achieved, the treatment scheme or parameters cannot be dynamically adjusted in time according to the state of the patient, and the patient is required to go to the hospital to receive on-site review or treatment at regular intervals.
Disclosure of Invention
The invention aims to provide a wearable low-intensity pulse ultrasonic device and a treatment system, which are used for solving the problems that the prior ultrasonic physiotherapy equipment provided in the background art is large in size, and cannot hide the carrying and wearing use requirements of patients and record and adjust the treatment scheme requirements.
In order to achieve the above purpose, the invention adopts the following technical scheme:
a wearable low-intensity pulse ultrasonic device, comprising a host 1 and a therapy head 2, wherein the host 1 comprises a host upper cover 1, a key seal 102, a screen assembly 103, a fastener 104, an upper cover seal 105, a lower cover seal 105, a host circuit board 106, a battery assembly 107, a lower cover 108 and keys 111; the therapy head 2 includes an upper cover 201, a therapy head circuit board 202, a vibrator 203, and a lens 204.
The lower cover of the host 1 is provided with a charging interface 110 and a USB interface 109, and the USB interface 109 is connected with the treatment head 2 through a wiring.
The vibrator 203 is arranged close to the lens 204, and the front end of the lens 204 is a convex lens; the treatment head 2 adopts low-dose sonic energy signals, and can adopt discontinuous pulse signals, so that the vibrator 203 does not continuously work; the energy of pulse signals for driving the vibrator 203 to resonate is low, so that the vibrator works at a low sound intensity of 0.1-5W/m 2 Within the range; the pulse signal frequencyThe rate may be 1, 1.5, 3MHz, the pulse width is 20-200 us, the pulse repetition frequency is 0.1-3 KHz, the waveform is not limited to triangular wave, but may be other types of sine wave, cosine wave, square wave, rectangular wave, pulse wave, sawtooth wave, the vibrator 203 is a vertical effect vibrator sintered into a circular sheet by a voltage ceramic vibrator, the material of the vertical effect vibrator may be but is not limited to: barium titanate (BaTiO 3), lead zirconate titanate (PbZrTiO 3) or lead magnesium niobate (PbNbMgO 3) are sintered, the thickness direction of the vibrator is a polarization direction, the transmission direction of sound waves after the vibrator resonates is parallel to the direction of an electric field, the sound waves are not focused on one point after being transmitted, and the convex lens scatters the sound waves.
The host circuit board 106 is provided with a Bluetooth/wifi connection module, an interface identification module, a signal generation module and a boosting module.
The treatment system of the wearable low-intensity pulse ultrasonic device is characterized in that a host 1 is connected with mobile phone software of a patient through a Bluetooth/wifi function, uploads relevant treatment information to the mobile phone of the patient and receives data and control signals sent by a mobile phone end of the patient; the doctor can issue an electronic treatment prescription through the computer terminal/mobile phone terminal, and then upload the prescription to the server and then issue the prescription to the host 1 through the software of the mobile phone terminal of the patient.
The host 1 is set to have the same operation parameters as the doctor prescription for patient treatment; the doctor evaluates the rehabilitation condition of the patient through the periodic outpatient consultation or the on-line consultation of the patient, and then prescribes a proper electronic prescription.
The host 1 stores a plurality of treatment prescription schemes of the same model of functional headend, and also stores one/more treatment prescription schemes of a plurality of models of functional headend.
The treatment head 2 is bound with the mobile phone APP, the host computer recognizes the model of the treatment head 2 after the treatment head 2 is connected with the mobile phone after the binding, the treatment parameter setting in the mobile phone can be automatically matched with the functional head end of the connected corresponding model, and the treatment parameter feedback is displayed on the interface of the mobile phone for a user to start/pause treatment.
The user can be reminded in advance of the start of the treatment by the cellphone app at a certain time before the start of the treatment, the benefit of this is obviously beneficial for the user to follow the regular, compliance of the order. The information forming log of the treatment completion can be presented in a calendar form in the mobile phone app, and further statistics data such as total times/total time of treatment, compliance rate of actual treatment and prescription can be summarized for patient tracking and backtracking.
The information of treatment completion can be transmitted to a doctor after being uploaded to a server by the mobile phone APP through a network, and the doctor can track the treatment progress of a patient in real time. When the patient carries out network review or off-line outpatient review, a doctor can call the treatment log information, and judge whether a treatment prescription is complied or not, whether a scheme is really beneficial to the rehabilitation of the patient, whether a treatment scheme is to be further adjusted, and a parameter range value which is specifically adjusted by the scheme according to the actual physical sign condition of the patient; the doctor can change the original treatment scheme to form a new treatment prescription and reset the treatment scheme in the patient treatment host according to the above procedure.
The main process of issuing an electronic prescription comprises the following steps:
the Bluetooth/wifi module is mounted on the pcb of the host, and the host is connected and bound with the mobile phone App through the Bluetooth/wifi module. The App port has a doctor end and a patient client port.
(1) The doctor prescribes an electronic prescription (patient base information data, serial numbers of the host and the treatment head to which the patient is bound, frequency of the treatment head, intensity of treatment, single time of treatment, total time or number of treatments, spectral characteristics of the treatment head drive signal, calendar or cycle plan of treatment) through the doctor port.
(2) After the patient is connected with the Bluetooth/wifi of the host computer through the patient client, the electronic prescription data in the app system can be issued to the host computer system through the Bluetooth/wifi.
(3) The host circuit has the software and hardware functions (frequency specification of the treatment head, manufacturing and failure time of the treatment head, time or number of times the treatment head can be used) to identify the treatment head.
Alternatively, one or more electronic prescriptions for different frequency treatment heads may be present in the host computer at the same time, and the inserted treatment heads are identified by the automatic identification function of the host computer, and the corresponding electronic treatment prescriptions are implemented.
Optionally, the host has an initial default treatment regimen (e.g., after any specification of treatment head is identified as available, treatment can be performed at a default sound intensity, for a default time).
Optionally, the host has a setup function or developer mode that can modify the default treatment intensity and treatment time of the system.
Optionally, a calendar program is provided in the host and at the app end, records patient usage records, and summarizes the total treatment time/number for a certain period of time to evaluate compliance with the treatment plan in the doctor's prescription.
Optionally, the host computer or the app end has a reminding function, which can remind the patient of the treatment action in a future treatment calendar in the treatment calendars to be followed.
Optionally, the ultrasound therapy system of the present invention has a probe mode, based on the sensitivity of the piezoelectric ceramic and the positive piezoelectric effect: the treatment head 2 is placed at the patient to drive the piezoelectric ceramic resonance to emit sound waves with characteristic signal characteristics and to recover and evaluate echo signals. This mode is used periodically throughout the convalescence period to probe for echo signals and record and upload. The doctor can evaluate the rehabilitation condition of the patient more systematically according to the emission recovery intensity of the signal, the change trend or the echo signal comparison of normal tissues at the same position of the human body and the data information of the treatment calendar and report of the patient uploaded by the system.
This probing pattern may be at the end of each treatment session or may occur regularly during each treatment session.
The flow of the probe mode is as follows;
1. the specific signal drives the piezoelectric ceramic vibrator to be in an inverse piezoelectric effect state;
2. the vibrator generates ultrasonic waves.
3. Ultrasound enters the damaged tissue of the human body.
4. The damaged tissue reflects the ultrasound waves.
5. The echo makes the piezoelectric ceramic vibrator deform and is in positive piezoelectric effect state.
6. And charging and discharging the vibrator.
7. And detecting a charge and discharge signal.
8. The charge-discharge signal is recorded, and the data (average value, maximum value, minimum value, etc.) is processed.
9. Report information (e.g., curves, bar graphs drawn with the mean, or maximum, or minimum, or their weighted indices for each probing mode) is formed.
Compared with the prior art, the invention has the following beneficial effects:
compared with the traditional floor type equipment and desktop level equipment, the invention adopts unfocused low-power equipment, and reduces the risk of household use. Lower power, reducing the risk of long-term use.
1. The portable wearing, low profile and portability can carry out the portable treatment when the human body is stationary or does not strenuous exercise, and is more suitable for the situations of home and appearance; expanding the treatment scene from a hospital department to long-time continuous and regular treatment at home and out;
2. parameter information control and acquisition functions used by the system; the system itself has a local treatment parameter setting function. Meanwhile, the system can receive the on-line digital electronic prescription to import and modify local parameters, and upload the treatment data to the cloud end, so that the monitoring, tracking and retrospective analysis of the patient himself, the family and medical staff are facilitated. The patient is facilitated to treat according to the established electronic prescription and the compliance of the treatment is identified.
3. Acquisition of patient recovery state and dynamic adjustment of treatment protocol; based on the sensitivity of the piezoelectric ceramic and the positive piezoelectric effect, the ultrasonic therapy system of the invention has a probe mode:
4. through offline review, or treatment history data uploaded to the cloud by the system, or the above-mentioned exploration mode data, a doctor can scientifically evaluate the recovery state of the patient, so as to determine whether to change the treatment prescription. The digital electronic prescription adjusted in combination with the actual recovery of the patient can be more adapted to the actual condition of the patient, helping the patient to recover faster and preventing the risk of excessive treatment.
Drawings
FIG. 1 is a schematic view of the whole structure of an ultrasonic device according to the present invention
FIG. 2 is a schematic diagram of a host splitting structure according to the present invention;
FIG. 3 is a schematic view of a split structure of a therapeutic head according to the present invention;
FIG. 4 is a schematic diagram of a host structure according to the present invention;
FIG. 5 is a schematic view of a lens-scattered sound wave of the present invention;
FIG. 6 is a schematic diagram of the treatment head of the present invention transmitting and receiving sound waves;
FIG. 7 is a schematic diagram of the system operation of the present invention;
FIG. 8 is a schematic flow chart of the complementary digital electronic prescription and implementation of the present invention;
FIG. 9 is a schematic diagram of a host interface of the present invention;
FIG. 10 is a schematic diagram of a discontinuous signal wave of the present invention;
fig. 11 is a schematic view of a thin circular piezoelectric ceramic according to the present invention.
In the figure: 1. a host; 101. a host upper cover; 102. a key seal; 103. a screen assembly; 104. a fastener; 105. upper and lower cap seals; 106. a host circuit board; 107. a battery assembly; 108. a lower cover; 109. a USB interface; 110. a charging interface; 111. a key; 2. a treatment head; 201. an upper cover; 202. a treatment head circuit board; 203. a vibrator; 204. and a lens.
Detailed Description
The technical solutions of the present invention will be clearly and completely described below with reference to the accompanying drawings, and it is apparent that the described embodiments are only some embodiments of the present invention, but not all embodiments, and all other embodiments obtained by persons skilled in the art without making creative efforts based on the embodiments in the present invention are all within the protection scope of the present invention.
A wearable low-intensity pulse ultrasonic device, comprising a host 1 and a therapy head 2, wherein the host 1 comprises a host upper cover 1, a key seal 102, a screen assembly 103, a fastener 104, an upper cover seal 105, a lower cover seal 105, a host circuit board 106, a battery assembly 107, a lower cover 108 and keys 111; the therapy head 2 includes an upper cover 201, a therapy head circuit board 202, a vibrator 203, and a lens 204.
The lower cover of the host 1 is provided with a charging interface 110 and a USB interface 109, and the USB interface 109 is connected with the treatment head 2 through a wiring.
The vibrator 203 is arranged close to the lens 204, and the front end of the lens 204 is a convex lens; the treatment head 2 adopts low-dose sonic energy signals, and can adopt discontinuous pulse signals, so that the vibrator 203 does not continuously work; the energy of pulse signals for driving the vibrator 203 to resonate is low, so that the vibrator works at a low sound intensity of 0.1-5W/m 2 Within the range; the pulse signal frequency can be 1, 1.5 and 3MHz, the pulse width is 20-200 us, the pulse repetition frequency is 0.1-3 KHz, the waveform is not limited to triangular wave, but can be sine wave, cosine wave, square wave, rectangular wave, pulse wave and saw tooth wave of other types, the vibrator 203 is a longitudinal effect vibrator sintered into a circular sheet by a voltage ceramic vibrator, and the material of the longitudinal effect vibrator can be but is not limited to: barium titanate (BaTiO 3), lead zirconate titanate (PbZrTiO 3) or lead magnesium niobate (PbNbMgO 3) are sintered, the thickness direction of the vibrator is a polarization direction, the transmission direction of sound waves after the vibrator resonates is parallel to the direction of an electric field, the sound waves are not focused on one point after being transmitted, and the convex lens scatters the sound waves.
The host circuit board 106 is provided with a Bluetooth/wifi connection module, an interface identification module, a signal generation module and a boost module
The treatment system of the wearable low-intensity pulse ultrasonic device is characterized in that a host 1 is connected with mobile phone software of a patient through a Bluetooth/wifi function, uploads relevant treatment information to the mobile phone of the patient and receives data and control signals sent by a mobile phone end of the patient; the doctor can issue an electronic treatment prescription through the computer terminal/mobile phone terminal, and then upload the prescription to the server and then issue the prescription to the host 1 through the software of the mobile phone terminal of the patient.
The host 1 is set to have the same operation parameters as the doctor prescription for patient treatment; the doctor evaluates the rehabilitation condition of the patient through the periodic outpatient consultation or the on-line consultation of the patient, and then prescribes a proper electronic prescription.
The host 1 stores a plurality of treatment prescription schemes of the same model of functional headend, and also stores one/more treatment prescription schemes of a plurality of models of functional headend.
The treatment head 2 is bound with the mobile phone APP, the host computer recognizes the model of the treatment head 2 after the treatment head 2 is connected with the mobile phone after the binding, the treatment parameter setting in the mobile phone can be automatically matched with the functional head end of the connected corresponding model, and the treatment parameter feedback is displayed on the interface of the mobile phone for a user to start/pause treatment.
The user can be reminded in advance of the start of the treatment by the cellphone app at a certain time before the start of the treatment, the benefit of this is obviously beneficial for the user to follow the regular, compliance of the order. The information forming log of the treatment completion can be presented in a calendar form in the mobile phone app, and further statistics data such as total times/total time of treatment, compliance rate of actual treatment and prescription can be summarized for patient tracking and backtracking.
The information of treatment completion can be transmitted to a doctor after being uploaded to a server by the mobile phone APP through a network, and the doctor can track the treatment progress of a patient in real time. When the patient carries out network review or off-line outpatient review, a doctor can call the treatment log information, and judge whether a treatment prescription is complied or not, whether a scheme is really beneficial to the rehabilitation of the patient, whether a treatment scheme is to be further adjusted, and a parameter range value which is specifically adjusted by the scheme according to the actual physical sign condition of the patient; the doctor can change the original treatment scheme to form a new treatment prescription and reset the treatment scheme in the patient treatment host according to the above procedure.
The main process of issuing an electronic prescription comprises the following steps:
the Bluetooth/wifi module is mounted on the pcb of the host, and the host is connected and bound with the mobile phone App through the Bluetooth/wifi module. The App port has a doctor end and a patient client port.
(4) The doctor prescribes an electronic prescription (patient base information data, serial numbers of the host and the treatment head to which the patient is bound, frequency of the treatment head, intensity of treatment, single time of treatment, total time or number of treatments, spectral characteristics of the treatment head drive signal, calendar or cycle plan of treatment) through the doctor port.
(5) After the patient is connected with the Bluetooth/wifi of the host computer through the patient client, the electronic prescription data in the app system can be issued to the host computer system through the Bluetooth/wifi.
(6) The host circuit has the software and hardware functions (frequency specification of the treatment head, manufacturing and failure time of the treatment head, time or number of times the treatment head can be used) to identify the treatment head.
Alternatively, one or more electronic prescriptions for different frequency treatment heads may be present in the host computer at the same time, and the inserted treatment heads are identified by the automatic identification function of the host computer, and the corresponding electronic treatment prescriptions are implemented.
Optionally, the host has an initial default treatment regimen (e.g., after any specification of treatment head is identified as available, treatment can be performed at a default sound intensity, for a default time).
Optionally, the host has a setup function or developer mode that can modify the default treatment intensity and treatment time of the system.
Optionally, a calendar program is provided in the host and at the app end, records patient usage records, and summarizes the total treatment time/number for a certain period of time to evaluate compliance with the treatment plan in the doctor's prescription.
Optionally, the host computer or the app end has a reminding function, which can remind the patient of the treatment action in a future treatment calendar in the treatment calendars to be followed.
Optionally, the ultrasound therapy system of the present invention has a probe mode, based on the sensitivity of the piezoelectric ceramic and the positive piezoelectric effect: the treatment head 2 is placed at the patient to drive the piezoelectric ceramic resonance to emit sound waves with characteristic signal characteristics and to recover and evaluate echo signals. This mode is used periodically throughout the convalescence period to probe for echo signals and record and upload. The doctor can evaluate the rehabilitation condition of the patient more systematically according to the emission recovery intensity of the signal, the change trend or the echo signal comparison of normal tissues at the same position of the human body and the data information of the treatment calendar and report of the patient uploaded by the system.
This probing pattern may be at the end of each treatment session or may occur regularly during each treatment session.
The flow of the probe mode is as follows;
1. the specific signal drives the piezoelectric ceramic vibrator to be in an inverse piezoelectric effect state;
2. the vibrator generates ultrasonic waves.
3. Ultrasound enters the damaged tissue of the human body.
4. The damaged tissue reflects the ultrasound waves.
5. The echo makes the piezoelectric ceramic vibrator deform and is in positive piezoelectric effect state.
6. And charging and discharging the vibrator.
7. And detecting a charge and discharge signal.
8. The charge-discharge signal is recorded, and the data (average value, maximum value, minimum value, etc.) is processed.
9. Report information (e.g., curves, bar graphs drawn with the mean, or maximum, or minimum, or their weighted indices for each probing mode) is formed.
The foregoing has shown and described the basic principles, principal features and advantages of the invention. It will be understood by those skilled in the art that the present invention is not limited to the foregoing embodiments, and that the foregoing embodiments and description are merely preferred embodiments of the invention, and are not intended to limit the invention, but that various changes and modifications may be made therein without departing from the novel spirit and scope of the invention, which is defined by the appended claims. The scope of the invention is defined by the appended claims and equivalents thereof.
Claims (10)
1. The wearable low-intensity pulse ultrasonic device is characterized by comprising a host (1) and a treatment head (2), wherein the host (1) comprises a host upper cover (1), a key sealing piece (102), a screen assembly (103), a fastener (104), an upper cover sealing piece (105), a host circuit board (106), a battery assembly (107), a lower cover (108) and keys (111); the treatment head (2) comprises an upper cover (201), a treatment head circuit board (202), a vibrator (203) and a lens (204).
2. The wearable low-intensity pulse ultrasonic device according to claim 1, wherein a charging interface (110) and a USB interface (109) are arranged on the lower cover of the main machine (1), and the USB interface (109) is connected with the treatment head (2) through a wiring.
3. The wearable low-intensity pulsed ultrasound device of claim 1, wherein the vibrator (203) is disposed proximate to the lens (204), the front end of the lens (204) being a convex lens; the treatment head (2) adopts low-dose sound wave energy signals, and can adopt discontinuous pulse signals to enable the vibrator (203) to work discontinuously; the energy of pulse signals which can drive the vibrator (203) to resonate is lower, so that the piezoelectric ceramics work at a smaller sound intensity of 0.1-5W/m 2 Within the range; the pulse signal frequency can be 1, 1.5 and 3MHz, the pulse width is 20-200 us, the pulse repetition frequency is in the range of 0.1-3 KHz, the waveform is not limited to triangular waves, and the pulse signal frequency can be sine waves, cosine waves, square waves, rectangular waves, pulse waves and saw-tooth waves of other types.
4. The wearable low-intensity pulsed ultrasound device of claim 1, wherein the host circuit board (106) has thereon a bluetooth/wifi connection module, an interface identification module, a signal generation module, and a boost module.
5. The treatment system of the wearable low-intensity pulse ultrasonic device is characterized in that a host (1) is connected with mobile phone software of a patient through a Bluetooth/wifi function, uploads relevant treatment information to the mobile phone of the patient and receives data and control signals sent by the mobile phone end of the patient; the doctor can issue an electronic treatment prescription through the computer terminal/mobile phone terminal, and then upload the prescription to the server and then issue the prescription to the host (1) through the software of the mobile phone terminal of the patient.
6. The system of claim 5, wherein the host computer (1) is configured to provide the same operating parameters as the doctor's prescription for patient treatment; the doctor evaluates the rehabilitation condition of the patient through the periodic outpatient consultation or the on-line consultation of the patient, and then prescribes a proper electronic prescription.
7. The system of claim 5, wherein the host (1) stores a plurality of treatment prescription protocols for the same model of functional head end and one/more treatment prescription protocols for multiple models of functional head end.
8. The system of claim 5, wherein the therapy head (2) is bound to a mobile phone APP, the host recognizes the model of the therapy head (2) after the binding, the therapy parameter setting in the mobile phone automatically matches the function head end of the corresponding model connected, and the therapy parameter feedback is displayed on the interface of the mobile phone for the user to start/pause the therapy.
9. The system of claim 5, wherein the user can be reminded of starting the treatment at a certain time by the mobile app before starting the treatment, and the log of the completion of the treatment can be presented in a calendar form in the mobile app, and further statistics (such as total number of treatments/total time, compliance rate of actual treatment and prescription) can be summarized for patient tracking and backtracking.
10. The therapeutic system of the wearable low-intensity pulsed ultrasonic device of claim 9, wherein the information of the completion of the therapy is uploaded to the server by the mobile phone APP through the network and then transmitted to the doctor, and the doctor can track the progress of the therapy of the patient in real time; when the patient carries out network review or off-line outpatient review, a doctor can call the treatment log information, and judge whether the treatment scheme is to be further adjusted or not and the parameter range value which is specifically adjusted by combining the actual physical sign condition of the patient; the doctor can change the original treatment scheme to form a new treatment prescription and reset the treatment scheme in the patient treatment host according to the above procedure.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202311202186.4A CN117244184A (en) | 2023-09-18 | 2023-09-18 | Wearable low-intensity pulse ultrasonic device and treatment system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202311202186.4A CN117244184A (en) | 2023-09-18 | 2023-09-18 | Wearable low-intensity pulse ultrasonic device and treatment system |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN117244184A true CN117244184A (en) | 2023-12-19 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202311202186.4A Pending CN117244184A (en) | 2023-09-18 | 2023-09-18 | Wearable low-intensity pulse ultrasonic device and treatment system |
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| Country | Link |
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| CN (1) | CN117244184A (en) |
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2023
- 2023-09-18 CN CN202311202186.4A patent/CN117244184A/en active Pending
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