KR20190048423A - Pigeon breast correction apparatus using pressure controller and manufacturing method for pigeon breast correction thereof - Google Patents

Abstract

The present invention relates to a pigeon breast treatment device including an air pad (100) for pigeon breast treatment, and a pressure control part (300) capable of adjusting the pressure of the air pad (100), wherein a pressure value set by using the physical conditions of a user is transmitted to and received from the pressure control part (300). To this end, the pigeon breast treatment device comprises: the air pad (100) manufactured according to the body of individual users, having, therein, an air bag for introducing air into the air bag, and having a longitudinal length greater than the lateral length thereof; the pressure control part (300) for controlling the pressure inside the air pad (100); a hose (200) for connecting the air pad (100) to the pressure control part (300) and transmitting the air pressure controlled by the pressure control part (300) to the air pad (100); and a transmission part (400) for newly setting the pressure inside the air pad (100) using the pressure inside the air pad (100) and the physical condition of the user and transmitting the set value. Through the above configuration, the pigeon breast treatment device may apply uniform pressure on the pigeon breast region of the user.

Description

TECHNICAL FIELD [0001] The present invention relates to a pectoral treatment apparatus using a pressure control unit, and a method of manufacturing a pectoral apparatus using the pressure control unit. [0002] PIGEON BREAST CORRECTION APPARATUS USING PRESSURE CONTROLLER AND MANUFACTURING METHOD FOR PIGEON BREAST CORRECTION THEREOF [

The present invention relates to a pectoral apparatus, which comprises a pressure controller (300) including an air pad (100) for treatment of a pectoral muscle and capable of adjusting the pressure of the air pad (100), and a pressure value And is configured to be able to transmit and receive to and from the pressure control unit 300.

In general, the pectoral bones are more than the sternum of the chest, which means that the central part of the chest protrudes excessively. There is no problem in general life, but it is accompanied by external problems. In some patients, breathing difficulty or arrhythmia may occur in some patients.

Until now, it is a common procedure to treat as surgical correction. It is performed by separating ribs and ribs connected to the sternum in the middle of the chest, correcting the shape, and then fixing it again. However, such surgical correction has a problem that a relatively large scar remains, a long treatment time is required, and the cost is high.

Current techniques for non-surgical correction methods are disclosed in Korean Patent Registration No. 10-0584184 entitled " Pancreas Calibrator & Method ", and Registration No. 10-1081150 " Chest Wall Assist Device ".

Korean Patent Registration No. 10-0584184 entitled " Pancreatometer & Usage Method " is composed of a chest pressing part having a chest pressing plate and a back receiving part. The chest pressing part and the back receiving part are connected to each other, And a shoulder strap extending over both shoulders of the wearer. However, since the chest pressure plate is fixed to the center of the chest of the wearer, it is difficult to change the pressing position according to the degree of correction, and only the connecting strap is provided as a means for adjusting the degree of compression of the chest, Therefore, it is difficult to precisely control the degree of compression individually. In addition, since the pectoral rectifier has a shoulder strap, it is not only troublesome to wear the pectoral rectifier but also causes a cosmetic problem and a manufacturing cost to increase.

No. 10-1081150 entitled " chest wall orthosis " can greatly improve the efficiency of treatment by varying the position, number, and spacing of the chest compression plate of the chest wall orthosis, and can control the degree of protrusion of the chest compression plate The degree of compression of the lesion can be precisely and easily adjusted, and the calibration position can be changed according to the degree of correction. However, the above-mentioned " chest wall orthosis " includes various types of chest compression plates depending on the shape and shape of the affected part to be compressed, and a chest compression plate having a suitable shape is selected according to the shape and shape of the ring part to be compressed, And adjusting the number or position of the chest pressure plate according to the position of the affected part, there was a limitation in accurately and precisely fitting the brace to the body structure of the pectoral patient. In addition, according to the judgment of the user, the degree of protrusion of the chest plate is adjusted, and it is difficult and troublesome to judge the proper time to adjust the degree of protrusion of the chest press plate.

In addition, since the connection part is disposed at the side of the body, the wear of the chest wall orthosis to the body is revealed to the outside, and the body is in inconvenience and inconvenience due to interference with the chest wall assistant during various body operations .

Korean Registered Patent Publication No. 10-1081150 " Fresh Breast Straightener and its Use Method " Korea Patent Registration No. 10-0584184 " Chest wall aids "

SUMMARY OF THE INVENTION The present invention has been made in order to solve the above problems, and it is an object of the present invention to manufacture a pectoral treatment apparatus in which the pressure of the air pad 100 is adjustable.

It is also an object of the present invention to manufacture a pectoral apparatus which can be adjusted by measuring pressure in real time.

In addition, the object of the present invention is to provide an external information transmitting / receiving unit 340 for measuring the pressure of a patient's chest and judging the pressure according to a set value according to a treatment purpose of a patient, To produce a therapeutic device.

According to an aspect of the present invention, there is provided an air pad, which is manufactured in accordance with an individual body of a user and has an air bag for allowing air to flow therein, ; A pressure control unit 300 for controlling the internal pressure of the air pad 100; A hose 200 connecting the air pad 100 to the pressure control unit 300 and transmitting the air pressure controlled by the pressure control unit 300 to the air pad 100; And a transmitter 400 for setting a pressure inside the air pad 100 using a pressure inside the air pad 100 and a user's body condition and transmitting the set value, Thereby uniformly applying pressure to the user's new breast portion.

According to the solution of the above-mentioned problems, the present invention can automatically adjust the pressure of the air pad 100 provided for treating the chest.

In addition, the present invention can manufacture a pectoral apparatus which can be controlled by measuring pressure in real time.

In addition, the present invention includes a pectoral apparatus provided with an external information transmitting / receiving unit 340 for measuring the pressure of the patient's chest and then determining the pressure based on a set value according to a treatment purpose of a patient, Can be manufactured.

In addition, the present invention can manufacture a pectoral apparatus capable of pressing only the area of the chest without pressing the entire chest of the user.

In addition, the present invention provides a brace suitable for a user according to a shape derived from a simulation after performing a tomogram of a user's chest, simulating a state after wearing the pectoral apparatus according to the present invention through a computer based on the photographed image, There is an effect of increasing the efficiency.

Further, according to the present invention, a shape memory alloy wire having elastic (super elastic) behavior characteristics of the present invention pseudo-elastic deforms according to a change of a thoracic volume by a user's breathing to pressurize a body part of a user, There is an effect of minimizing the occurrence of the problem.

1 is a view showing a pectoral treatment apparatus using a pressure control unit 300 according to the present invention.
2 is a detailed view showing the configuration of the pressure control unit 300. As shown in FIG.
3 is a detailed view of the pressure control unit 300 and the transmitter unit 400. As shown in FIG.
4 is a detailed view of the configuration of the transmitting portion 400. As shown in Fig.
5 is a flowchart illustrating a method of manufacturing a pectoral apparatus using the pressure control unit 300 according to the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In FIGS. 1 to 4, the same reference numerals are assigned to components performing the same function. In the drawings and the detailed description, detailed description of specific elements and functions of elements not directly related to the technical features of the present invention will be omitted. .

1 to 4, a pectoral apparatus using a pressure control unit 300 according to a preferred embodiment of the present invention includes an air pad 100, a hose 200, a pressure control unit 300, and a transmitter unit 400 So as to uniformly apply pressure to the user's new breast portion, and can be manufactured in a customized manner.

First, as shown in FIG. 1, the air pad 100 forms an air bag so that air can be introduced into the air pad 100, and the air pad 100 is seated on the user's new breast portion. More specifically, the air pad 100 is manufactured in accordance with the user's individual body, and has an air bag for introducing air into the air bag 100, and has a longer length than a horizontal length.

The transverse length is preferably 1.3 to 1.5 times the length of the user's paw, and the length to length ratio is preferably 1: 3 to 1: 4. When the length to length ratio is less than 1: 3, the therapeutic effect may be insignificant because the size is smaller than the user's pectoral region. If the length to length ratio is more than 1: 4, It is preferable that the treatment is performed under the above conditions since the therapeutic effect may be lowered because the treatment area may be relatively less stressed during the treatment.

In addition, it is preferable that air is not leaked through the air pad 100 by fixing the air electrode 100 with the shape memory alloy wire along the outer peripheral surface of the air pouch. The shape memory alloy wire according to the preferred embodiment of the present invention is pseudo-elastic deformed according to the change of the thoracic volume by the user's breathing to adjust the air pressure uniformly to the air pad 100, So that the user's breast portion can be efficiently pressed.

On the other hand, the shape memory alloy wire is alloyed with Ni (nickel) and Ti (titanium) at a ratio of 50:50, and is formed so as to exhibit pseudoelastic behavior through a heat treatment and a training process. In other words, the transformation between the austenite and martensite phases occurs smoothly at room temperature, and in particular, causes shape memory to return to the austenite at martensite at room temperature Both the austenite transformation start temperature and the completion temperature are controlled to be lower than room temperature to form pseudoelastic behavior.

The shape-memory alloy wire subjected to the heat treatment in this way undergoes a training process in which it is repeatedly repeatedly deformed and restored at a temperature exceeding the austenite transformation completion temperature, and a transformation from austenite to martensite is further And finally austenite to martensite phase transformation takes place when tensile stress is applied at room temperature and finally shows a strain of about 5% or more, and the degree of stress change during the deformation is very small, And when the stress is removed, the martensite to austenite transformation occurs, and the shrinkage of about 5% or more can be seen. Since the stress is removed and the process of restoring is very small, the stress is changed little by the phase transformation and shrinks by adding a constant stress. As a result, the wire contracts and expands at the user's inhale and exhalation, There is an effect that can be done. Therefore, it is preferable that the shape memory alloy wire used in the present invention is produced such that a phase transformation from austenite to martensite takes place and the shrinkage ratio is 5 to 10%.

Next, the pressure control unit 300 controls the internal pressure of the air pad 100 as shown in FIG. 2, the pressure control unit 300 includes an electronic air pump 310, a pressure measurement sensor 320, a processor 330, and a receiving unit 340. [

First, the electronic air pump 310 is an air supply source for flowing air into or out of the air pad 100. 1, the electronic air pump 310 is disposed on the rear surface of the pressure control unit 300 and connected to the second hose 220 to be described later, Air flows in and out.

Next, the pressure measurement sensor 320 measures the pressure of the air pad 100. As shown in FIG. 1, the pressure measurement sensor 320 may be connected to the first hose 210 to measure a pressure of air entering or exiting the air pad 100.

Next, the processor 330 controls the air pressure in the air pad 100 through the control of the electromagnetic air pump 310, and reads the output of the pressure measurement sensor 320 to convert the pressure into a pressure value.

The receiving unit 340 receives the set value transmitted by the transmitting unit 400 to be described later and outputs the pressure value measured by the pressure measuring sensor 320 and converted by the processor 330 To the transmitter section (400). As shown in FIG. 1, the receiver 340 is provided on the rear side of the pressure measurement sensor 320 and the processor 330, so that the pressure value can be transmitted to the receiver 340.

3, the receiving unit 340 can receive the pressure value and the set value by the transmitting unit 400 and Bluetooth or Wi-Fi.

1, the hose 200 connects the air pad 100 and the pressure control unit 300 and connects the air pressure controlled by the pressure control unit 300 to the air pad 100 100). More specifically, the hose 200 is connected to the pressure control unit 300 at the air pad 100, and the pressure control unit 300 is divided into two hoses 210 and 220.

The first hose 210 is connected to the pressure measurement sensor 320 at the air pad 100 to measure a pressure inside the air pad 100. The first hose 210 is divided into two branches and connected to the rear and side surfaces of the pressure control unit 300, respectively. Further, the pressure control unit 300 is divided into two branches on the rear surface of the pressure control unit 300 so as to be connected to the electromagnetic air pump 310, respectively.

The second hose 220 is connected to the electronic air pump 310 at the air pad 100 to control the inflow of air into or out of the air pad 100.

Next, the transmitter 400 newly sets the internal pressure of the air pad 100 using the pressure inside the air pad 100 and the user's body condition, (300). More specifically, as shown in FIG. 4, the transmitter 400 includes a pressure determiner 410 and a pressure commander 420.

The pressure determination unit 410 newly sets the pressure inside the air pad 100 for treating the user's breast by using the pressure value measured by the pressure measurement sensor 320 and the user's body condition And calculates the set value.

The pressure command unit 420 transmits the set value set by the pressure determination unit 410 to the reception unit 340.

3, the pressure of the user's breast is feedback-controlled by the pressure controller 300 and the transmitter 400, so that the treatment efficiency can be further increased, and the pressure can be measured and adjusted in real time have.

As shown in FIG. 5, the method for manufacturing a custom-made pectoral apparatus will now be described in more detail.

First, a first step S100 is a photographing step of taking tomographic images of the chest of the user. More specifically, the photographing step S100 creates a three-dimensional shape information of the user's pectoral region by tomographing the pectoral region including the chest of the user. The generated user's pectoral region three-dimensional shape information is input to the computer.

Next, in a second step S200, an orthosis image of the user's pectoral region is generated through a computer to simulate the post-wearing state of the user. And simulating the state of wear of the wearer such as whether the wearer matches the body of the user, that is, the chest and the pectoral region of the user through the simulation.

Next, the third step S300 is a model making step of manufacturing the air pad 100. After the simulation step, the three-dimensional shape information of the user's parentheses is used to obtain a model .

Next, in a fourth step (S400), the treatment instrument model prepared in the model making step is formed by adjusting the size and shape in association with the user's new breast part.

As described above, the therapeutic device model is manufactured such that the horizontal length is 1.3 to 1.5 times the length of the user's paw, and the ratio of the vertical length to the horizontal length is 1: 3 to 1: 4 desirable.

Next, the fifth step (S500) fixes the shape memory alloy wire along the inner side edge of the medical instrument model produced by the molding step.

More specifically, the shape memory alloy wire manufacturing step S500 is performed by alloying Ni (nickel) and Ti (titanium) at a ratio of 50:50. After the heat treatment and the training process, % Shrinkage ratio.

The shape memory alloy wire is manufactured by first heat-treating at a temperature equal to or higher than the completion of the austenite transformation, forming the shape of the air pad 100, maintaining the shape at room temperature for 10 to 12 hours, Training course. The heat treatment and the training process to be held at room temperature are repeatedly performed five to six times so that transformation from austenite to martensite can be more smoothly performed and tensile stress is applied at room temperature .

 The heat treatment is preferably performed at 800 to 850 占 폚. If the heat treatment is less than 800 ° C, the hardness is low and the phase transformation is insignificant, so that the shrinkage percentage may not be 5 to 10%. If the heat treatment is performed at 850 ° C or more, the shrinkage stress of the air pad 100 is insufficient, It may be difficult to apply a constant pressure to the catalyst layer.

In addition, when the shape memory alloy wire is kept at room temperature for less than 10 hours, the degree of change of stress may be very small, and a constant stress may not be added at the time of tensile. If the shape memory alloy wire is held at room temperature for more than 12 hours, The expansion of the air pad 100 manufactured by the present invention may be difficult.

In addition, when the shape memory alloy wire is not trained at room temperature and is carried out at a temperature lower than room temperature or at a temperature higher than room temperature, the use life of the manufactured air pad 100 may be lowered, .

According to the solution of the above-mentioned problems, the present invention can automatically adjust the pressure of the air pad 100 provided for treating the chest.

In addition, the present invention can manufacture a pectoral apparatus which can be controlled by measuring pressure in real time.

In addition, the present invention includes a pectoral apparatus provided with an external information transmitting / receiving unit 340 for measuring the pressure of the patient's chest and then determining the pressure based on a set value according to a treatment purpose of a patient, Can be manufactured.

In addition, the present invention can manufacture a pectoral apparatus capable of pressing only the area of the chest without pressing the entire chest of the user.

In addition, the present invention provides a brace suitable for a user according to a shape derived from a simulation after performing a tomogram of a user's chest, simulating a state after wearing the pectoral apparatus according to the present invention through a computer based on the photographed image, There is an effect of increasing the efficiency.

Further, according to the present invention, a shape memory alloy wire having elastic (super elastic) behavior characteristics of the present invention pseudo-elastic deforms according to a change of a thoracic volume by a user's breathing to pressurize a body part of a user, There is an effect of minimizing the occurrence of the problem.

Although the patient-customized panty therapy aid using the shape memory alloy according to the preferred embodiment of the present invention as described above and the method of manufacturing the same have been shown and described with reference to the above description and drawings, It will be understood by those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the invention.

100. Air pad
200. Hose
210. First Hose
220. 2nd Hose
300. Pressure control section
310. Electronic air pump
320. Pressure sensor
330. Processor
340. Receiver
400. The transmitter
410. Pressure determination unit
420. Pressure command section
S100. A photographing step of photographing a chest of a user and generating three-dimensional shape information of a user's pectoral region;
S200. A simulation step of producing an orthosis image through a computer by using the three-dimensional shape information of the user's pectoral region and simulating a post-wearing state of the user;
S300. A modeling step of fabricating a model of a medical device corresponding to an actual user's pectoral region using the user's pectoral region three-dimensional shape information after the simulation step;
S400. A shaping step of adjusting the size and shape of the therapeutic device model produced in the model making step by associating with the user's new breast part;
S500. A wire manufacturing step of fixing the shape memory alloy wire along the inner side edge of the medical instrument model produced by the molding step;

Claims (5)

An air pad 100 manufactured according to an individual body of the user and having an air bag for introducing air into the air bag, the air pad 100 being longer than the horizontal length;
A pressure control unit 300 for controlling the internal pressure of the air pad 100;
A hose 200 connecting the air pad 100 to the pressure control unit 300 and transmitting the air pressure controlled by the pressure control unit 300 to the air pad 100; And
A transmitter 400 for newly setting a pressure inside the air pad 100 using the pressure inside the air pad 100 and the user's body condition and transmitting the set value to the pressure controller 300 And a pressure sensor for detecting a pressure of the user's chest, the pressure sensor comprising: The method according to claim 1,
Wherein the air pad (100) has a length to length ratio of 1: 3 to 1: 4. The pressure controller (300) The method according to claim 1,
The pressure control unit 300,
An electronic air pump 310 for supplying air to the air pad 100;
A pressure measuring sensor 320 measuring the pressure of the air pad 100;
A processor 330 for reading the output of the pressure measurement sensor 320 and converting the output to a pressure value; And
And a receiving unit (340) for receiving the set value transmitted by the transmitting unit (400) and transmitting the pressure value converted by the processor (330) to the transmitting unit (400) A pectoral apparatus using the control unit 300 The method according to claim 1,
The transmitting unit 400 includes:
A pressure determination unit 410 for newly setting a pressure inside the air pad 100 using the pressure inside the air pad 100 and the user's body condition; And
And a pressure instruction unit (420) for transmitting a set value set by the pressure determination unit (410). The pressure control unit (300) The method according to claim 1,
The pancreatic apparatus manufactured by the user custom-
A photographing step of photographing the chest of the user and generating three-dimensional shape information of a user's pectoral region;
A simulation step of producing an orthosis image through a computer by using the three-dimensional shape information of the user's pectoral region and simulating a post-wearing state of the user;
A modeling step of fabricating a model of a medical device corresponding to an actual user's pectoral region using the user's pectoral region three-dimensional shape information after the simulation step;
A shaping step of adjusting the size and shape of the therapeutic device model produced in the model making step by associating with the user's new breast part; And
And a wire manufacturing step of fixing the shape memory alloy wire along the inner side edge of the treatment instrument model manufactured by the molding step. [7] The method for manufacturing a pectoral treatment apparatus using the pressure control part 300

Images