IT201900000677A1 - DEVICE AND METHOD OF PERSONALIZED NON-INVASIVE TREATMENT OF SKIN IMPLEMENTS - Google Patents

Description

Description of the invention entitled:

"DEVICE AND METHOD FOR PERSONALIZED NON-INVASIVE TREATMENT OF SKIN IMPLEMENTS"

Description

Field of technique

The present invention operates in the field of aesthetic medicine, sports and in the field of rehabilitation, in particular it describes a device suitable for recognizing and treating, by means of compressive microvibration, some pathologies such as cellulite, tissue recompaction, lymphatic and venous stasis, edematosis, muscle and scar contractures, neck shoulder syndrome and pubalgia. Other fields of application of this device are treatments for sportsmen before and after surgery, sports massage, lymphatic drainage and the treatment of pains of various genesis.

Known art

The so-called cellulite, also called "gynoid lipodystrophy", "edematous fibrous panniculopathy", "edematous adiposis", "edematous-fibrosclerotic panniculopathy", "dermopanniculosis deformans", "status protrusus cutis", and "liposclerosis", is a topographical manifestation of skin associated with depressions or introflexions, frequent in the pelvic and abdominal area, in the hips, buttocks and thighs. It can also occur associated with nodules in the subcutaneous adipose tissue and, in more rare cases, with a suspected inflammatory state.

The great confusion about the name to be given to cellulite reflects the difficulty of correctly understanding the nature of the phenomenon. Despite the great interest in treating this condition and the huge market for topical treatments aimed at improving its appearance, cellulite is still an enigmatic condition for medical researchers.

The high incidence (80-90%) in the female population that presents the imperfections of cellulite in post-pubertal age, in addition to the fact that it occurs without symptoms, make it considered a normal physiological condition. It can instead be considered within a pathological picture noting that, yes, it is a normal condition for many women, but not for all, and that in its most serious forms it manifests itself with painful nodules on palpation that make us suspect inflammatory processes, moreover it is generally associated with an excessive accumulation of subcutaneous adipose tissue whose relationship with cardiovascular risk is not clear.

Dozens of different causes have been hypothesized such as: metabolic disorders, nutritional disorders, specific subcutaneous architectures, alterations in the structure of the connective tissue, hormonal factors, genetic factors, disorders of the microcirculatory system, alterations in the lymphatic system, alterations in the extracellular matrix, inflammations.

The classifications of cellulite are as follows:

- edematous: that is associated with an accumulation of fluids, especially around the ankles, calves, thighs and arms.

- fibrous: that is associated with an increase in trabecular structures and connective tissue septa that divide the subcutaneous adipose tissue into different lobes; fibrous cellulite is characterized by small nodules that are not perceptible to the touch except as subcutaneous roughness and orange peel skin.

- sclerotic: that is associated with a hardening of the tissues associated with large nodules and plaques; this form can be very painful.

Several measures can help prevent cellulite. Some attention to nutrition, constant physical activity, the use of comfortable and not too tight clothes, shoes with not excessively high heels and changes in posture are the easiest remedies to implement to prevent this annoying disorder.

The huge market for treatments to reduce cellulite ranges from topical products to liposuction, although many of these treatments lack evidence of efficacy. The most common are listed:

● topical products or creams and the like to be applied manually to the affected area consistently and daily for long periods of time;

● massages;

● pressotherapy: treatment that is based on the external pressure of the patient's limbs or his abdominal area through specific equipment;

● mesotherapy: technique for administering drugs by intraepidermal, superficial and deep intradermal and subcutaneous or hypodermic routes, it has the advantages of being able to use reduced doses of the active ingredient that have a prolonged effect over time;

● emulsiolipolysis: a drug therapy achievable by district injection with hypothalamic phospholipids, carnitine, aminophylline, lidocaine 2%, physiological solution;

● lipoapoptosis: a drug therapy achievable by district injection with vitamin C, trivalent iron, 2% lidocaine, water for injections;

● carboxytherapy: treatment that originates from thermal medicine and consists in the administration of carbon dioxide subcutaneously; ● osmotic lipoclasia: skin biostimulation with platelet-rich plasma; ● oxygenoclasia: technique of introducing pure medical oxygen through a small needle into excess fat;

● endermologie system: technique designed in France in the 1970s in which a vacuum system and a plurality of rollers, mounted on a handpiece, exert pressure and lifting on the skin, causing a redistribution of subcutaneous fat.

● ultrasound therapy: treatment based on the effect produced by mechanical vibrations applied to the external tissues of the body using an ultrasonic transducer.

● laser therapy: treatment that acts at various depth levels based on the power of the rays transmitted.

● diathermy: practice, without scientific validation, which supports healing properties induced by the increase in the temperature of some non-superficial areas of the body caused by the passage of electric current.

As can be seen from the above list, which is not exhaustive, the market is saturated with treatments, among which there are some without certain results. The ineffectiveness is often due to the fact that, as explained above, the cause of cellulite and the disorders it entails are not certain.

There are also several patents that claim treatments for the treatment of cellulite such as US 2002147467 which provides first an exfoliating treatment to maximize the absorption of substances applied to the skin, then the administration of mechanical vibrations associated with electrical pulsations in the affected area.

EP 1844750, on the other hand, claims an instrument for aesthetic treatments, therefore not of a medical nature, which reduces cellulite through ultrasonic vibrations with a frequency between 25 kHz and 50 kHz.

GB 2303552 describes a medical device capable of reducing cellulite through ultrasounds at a frequency of about 3.3 MHz which reach a depth of 1.27 - 2.54 cm from the surface of the skin without overheating the part.

The patent, extended worldwide, WO2007122656, owned by the market leader in the sector of anti-cellulite and anti-blemish therapies and skin disorders in general, claims a computer-controlled vibratory device, used to treat parts of the body, whose characteristic primary is to apply massages by inducing mechanical oscillations by means of a plurality of massage elements which are rotatably mounted about their own axis in a roller driven by an electric motor. The rotation of the roller around its shaft is controlled by the operator through an electronic control unit, selecting a program suitable for the treatment to be performed. The device described in this patent performs a massage based on the resistance opposed by the muscles located under the adipose layer. The purpose of the present invention is to propose a device and a method of compressive microvibration customized on the ailments suffered by each patient which carries out four actions in a synergistic way, acting on the vascular system at the microcirculation level, on the lymphatic system, on tissue re-compacting and on the analgesic effect, also involving a muscular effect. The operation of this device relies on a sensor capable of detecting the type of disturbance and a dedicated software that determines the best therapy to be followed on a case-by-case basis.

Description of the invention

According to the present invention, a device is provided and a method of use thereof is described for the non-invasive diagnosis and treatment of skin imperfections and disorders according to personalized methods for each patient.

The device comprises a transportable console equipped with at least one pair of recesses, possibly heated by a resistance inside the recess which, operating by infrared light, also has a bactericidal function, which are configured to each house a corresponding handpiece.

The handpieces are the instrument through which an operator performs the treatment on the skin tissues of a patient.

Advantageously, the presence of at least one larger handpiece, of larger dimensions, is provided for carrying out the treatment on the body, while the smaller handpiece, of smaller dimensions, is specifically configured for the treatment of the face or other anatomical parts with an articulated conformation. Each handpiece includes a rotating cylinder on whose external surface a plurality of independent rotating elements are movably connected. In some preferred embodiments, the rotating elements of the larger handpiece are spheres, ovoids or cylinders, arranged in a bee cell, made of gel with a hardness between 5 shore and 100 shore, preferably 35 shore. The rotating elements of the smaller handpiece, on the other hand, are spheres, ovoids or cylinders, arranged in a "V" shape, made of hypoallergenic silicone with a surface treatment designed to obtain a predetermined surface roughness. The roughness is intended to obtain a peeling and stretching effect on the patient's skin.

The preferred embodiment of the smaller handpiece, that is the one dedicated to facial treatments, provides that the rotating elements of the cylinder are arranged in such a way as to impart a converging or diverging force with respect to the centreline of the cylinder itself which constitutes the neutral point. Precisely in correspondence with this point, advantageously, a ring nut is provided which, by rotating around the longitudinal axis of said cylinder, is able to modify the angle of incidence of said rotating elements, or to cause them to compress or expand the epidermis of the patient. This feature has evident wrinkle smoothing effects, with efficacy comparable to hyaluronic acid or botulinum injections, but obtaining the same advantageous result without infiltrations, injections or other invasive interventions.

The rotating elements of the larger handpiece, on the other hand, in an even more advantageous embodiment, have an external surface equipped with a plurality of recesses in the shape of a spherical cap designed to create a suction effect when pressed on the patient's epidermis. In other words, they have a "golf ball" geometry. When the recesses are pressed against the patient's epidermis, they adhere to them thanks to the suction effect due to the geometry of the rotating elements. When the cylinder, by rotating, causes the recesses attached "suction cup" to the patient's skin to detach, a suction of the tissues is generated which has beneficial effects on the treatment of the imperfections associated with the disorders that cause cellulite.

Advantageously, the treatment is performed thanks to the simultaneous rotation, vibration and pressure that the operator applies perpendicular to the patient's tissues, compressing them.

The pressure is regulated by the experience of the operator, or, in a more equipped version of the present invention, by a light indicator placed on the handle of the handpieces on the side in view of the operator when in action. Said indicator light consists of a plurality of warning lights or LED lights designed to turn on progressively as the pressure exerted by the operator on the patient's body increases and vice versa.

The rotation and vibration frequency is adjusted by the operator through the communication interface, preferably integrated into the console and possibly also replicated on the back of the handpieces, which acts on a rotation and vibration adjustment device integrated in each handpiece.

Eventually it will be possible to independently adjust the rotation frequency and the vibration frequency of the cylinders of the handpieces.

The method of using the device involves the following stages:

(A) first phase of parameter setting, in which the operator sets, through the communication interface, an admissible frequency range of vibrations based on the characteristics of the patient's tissue, his age and his musculature. The frequency of the vibrations is always between 20 Hz and 700 Hz, preferably between 40 Hz and 355 Hz;

(B) second test phase, in which, by grasping the handle of the handpiece dedicated to the region to be treated (larger handpiece if on the body, minor handpiece if on the face), the operator extracts it from the relative recess of the console and places it with the cylinder in contact with the skin tissue to be treated. An electric energy absorption sensor, possibly combined with pressure and / or engine rpm sensors, with which both handpieces are advantageously equipped, sends the detected data to a control unit integrated in the treatment device. Said control unit, comparing the electrical energy absorption data and the rotation and vibration frequency data set by the operator, communicates, through the communication interface, the correctness or otherwise of the frequency range of the rotations and vibrations set by said control unit. operator. For example, if the cylinder absorbs an amount of electricity exceeding a certain preset threshold, it means that the frequency range set by the operator is too low for the characteristics of the patient's skin tissue. Evidently the operator's assessment was wrong. At this point, the communication interface will notify the operator that the frequency range of rotations and vibrations is different or unsuitable for the condition of the disturbance detected by the device on the patient's body, also indicating the recommended value.

(C) Third phase of administration of the therapy, in which said operator runs through the areas of the patient's body or face to be treated with the selected handpiece, applying a predetermined pressure perpendicular to the patient's skin tissue. During the third phase of administration of the therapy, if the electric energy absorption sensor, possibly combined with pressure and / or engine rpm sensors, of the handpiece in use should detect an area with greater mechanical resistance, for example a muscle contracture , the control unit which processes the data sent by said electrical energy absorption sensor, sends a command to increase the rotation frequency and vibrations to a frequency adjustment device of the handpiece in use, until a mechanical resistance is detected minor.

(D) fourth phase of checking the homogeneity of the treatment on the entire area affected by the disorder or skin blemish. In the simplest version of the treatment device, this last phase is performed through the visual analysis, by the operator, of skin redness due to the vascularization of the tissue induced by the treatment.

Alternatively, the fourth control step can be advantageously carried out in a more scientific manner. In this case, the device advantageously also comprises a temperature sensor on each handpiece, suitable for detecting the skin temperature of the patient, sending the data to said control unit which reproduces the data on said communication interface also signaling the value of the increase. of temperature from the beginning of the treatment. In this way, a constant increase equates to the homogeneity of the treatment that the operator can control based on reliable scientific data.

Even more advantageous embodiments of the handpieces provide for the provision on them of at least one of the following equipment:

- a common quick release mechanism designed to allow stable disconnection and re-connection between a handpiece and its cylinder and therefore allow total sanitation between one treatment and the next;

- a pair of side indicators, placed on both sides of the relative handpiece, designed to emit light signals to the operator to indicate the direction of discharge for the purpose of proper lymphatic drainage;

- a display designed to replicate said communication interface on the side of the handpiece in view of the operator;

- an internal resistance able to raise its temperature, when not in use, up to a predetermined temperature that can be set through said communication interface;

- the oversized handle to make the handpiece ergonomically more comfortable to hold.

The advantages of the present invention are clear in the light of the preceding description and will be even more so thanks to the attached figures and the description of the preferred embodiment.

Description of the figures

The invention will be described below in at least one preferred embodiment for explanatory and non-limiting purposes with the aid of the attached figures, in which:

- FIGURE 1 shows a general view of the console 1 with the two recesses 1.1-1.2 for the two handpieces 3-4, the communication interface 2 and the control unit 5 schematized in a symbolic way inside the body of the console 1.

- FIGURE 2 illustrates in detail the external structure of the two handpieces 3-4 with all the equipment that allows the operator performing the treatment not to make mistakes and to act effortlessly. Fig. 2 (a) shows a side view, while Fig. 2 (b) shows the front view, that is of the side of the handpiece 3-4 that is in view of the operator while he is carrying out the treatment on the patient's body or face .

- FIGURE 3 illustrates the arrangement of the spheres on the two handpieces 3-4. Fig. 3 (a) shows the honeycomb arrangement of the spheres 3.6 of the cylinder 3.7 of the first handpiece 3. Fig. 3 (b), on the other hand, shows the disposition of the spheres 4.6 of the cylinder 4.7 of the second handpiece 4 equipped with ring nut 4.7.1.

- FIGURE 4 schematically shows the relationship between the electrical energy absorption sensors 3.1-4.1 of the two handpieces 3-4 which communicate the data detected to the control unit 5 which, in turn, acts on the relative frequency adjustment devices.

Detailed description of the invention

With reference to FIG. 1, the personalized and non-invasive treatment device of the present invention is represented in a three-dimensional view.

It is equipped with a console 1 equipped with wheels and handles for easy transport and electrical connection means for powering the integrated components. At the top, said console 1 is equipped with a pair of recesses 1.1-1.2, one of which is suitable for housing a larger handpiece 3 and one, smaller, suitable for housing a smaller handpiece 4.

The difference in size between the handpieces 3-4 is due to several factors, but mainly to the fact that the larger handpiece 3 is specifically designed to perform treatments on larger areas of the patient's body, while the smaller handpiece 4 is suitable for be applied on the face or on other anatomical parts with an articulated conformation.

Both said handpieces 3-4 contain a relative cylinder 3.7-4.7 which rotates and turns at predetermined frequencies. On the external surface of each cylinder 3.7-4.7 there are movably engaged rotating balls 3.6-4.6 independent of each other.

Another difference between the 3-4 handpieces is represented by the type of said spheres 3.6-4.6. Both types of spheres have hardness between 5 shore and 100 shore, preferably 35 shore, but, while the spheres 3.6 of the major handpiece 3 are made of gel and are arranged in a honeycomb cell, the spheres 4.6 of the minor handpiece 4 are made of silicone, they are arranged in a “V” shape and have a surface finish that makes them rough in order to perform a peeling and stretching of the patient's facial skin.

Finally, the minor handpiece 4 is characterized by the fact that the spheres 4.6 which are located in the upper portion of the cylinder 4.7 rotate in the opposite direction to the spheres 4.6 located in the lower portion of the cylinder 4.7. This means that, with respect to a neutral point, towards which the thrust of the spheres 4.6 converges or from which it diverges, a distension or re-compacting effect of the skin tissue is obtained. Right at this neutral point there is a ring 4.7.1 which, if rotated by the operator acting on the handpiece 4, changes the rotation angle of the spheres 4.6, obtaining the convergent or divergent effect.

The operation of the device object of the present invention is semi-automatic since it makes use of an advanced software capable of setting the treatment parameters in real time, following any change in the mechanical characteristics of the skin tissue subjected to treatment.

This is made possible by the fact that each 3-4 handpiece is equipped with an electrical energy absorption sensor 3.1-4.1, possibly combined with pressure and / or engine rpm sensors, which detects the amount of electrical energy absorbed by the related handpiece 3-4 to obtain the desired rotation and vibration frequency. This absorption varies according to the mechanical resistance of the patient's skin tissue. Said sensors 3.1-4.1 send the detected data to a control unit 5 programmed with the aforementioned software which processes them and verifies that the resistance, the desired rotation and vibration frequency is not excessive or too low for the mechanical resistance of the fabric on which it acts. called handpiece 3-4.

To adjust in real time the frequency of this rotation and of this vibration, the control unit 5 acts on a device for adjusting the rotation and vibration 3.2-4.2 integrated in each of said handpieces 3-4.

Let's assume now that we need to perform a relaxing treatment on the back of a patient, let's say a sportsman, suffering from muscle contractures.

The operator first performs a parameter setting phase, selecting a frequency range of rotations and vibrations (always between a minimum of 20 Hz, preferably 40 Hz and a maximum of 700 Hz, preferably 355 Hz). The range is set via a special communication interface 2, integrated in said console 1. The operator, based on his experience, selects the frequency according to age, musculature and the ailment suffered. In the example under consideration this will be quite high.

At this point a second test phase follows in which, by grasping the larger handpiece 3 and placing its cylinder 3.7 in contact with a point on the patient's back, the electrical energy absorption sensor 3.1, possibly combined with pressure sensors and / or of engine revolutions, of the larger handpiece 3 sends the data detected to the control unit 5. The latter, by comparing the electrical energy absorption data and the rotation and vibration frequency data set by the operator, communicates, via the 'communication interface 2 the correctness or otherwise of the frequency range of rotations and vibrations set by the operator.

Now the therapy can be administered, in the third stage of the treatment method. In this phase, the operator runs the entire back of the patient with the larger handpiece 3, applying a predetermined pressure perpendicular to the patient's skin tissue. The applied pressure force is communicated to the operator by a light indicator 3.4 consisting of a plurality of warning lights or LED lights designed to turn on progressively as the pressure exerted by the operator on the patient's body increases and vice versa.

During this third phase of therapy administration, if the electrical energy absorption sensor 3.1 should detect an area with greater mechanical resistance, typically due to a muscle contracture, the control unit 5 which processes the data sent by said absorption sensor electrical energy 3.1, sends a command to increase the frequency of rotations and vibrations to the frequency adjustment device 3.2 of the larger handpiece 3, until a lower mechanical resistance is detected.

The therapy causes the vascularization of the tissues and therefore the raising of their temperature and the consequent redness. Thanks to the visual analysis of the patient's back, the operator will be able to check the homogeneity of the therapy on the entire area to be treated.

At the end of the treatment, thanks to a quick release mechanism 3.9 placed on the side of the handle 50 of the handpiece 3, it is possible to disconnect the cylinder 3.7 inside the handpiece 3 so as to be able to extract the cylinder 3.7 and sanitize it in all its parts, spheres 3.6 including.

Finally, it is clear that modifications, additions or variants that are obvious for a person skilled in the art can be made to the invention described so far, without thereby departing from the scope of protection that is provided by the attached claims.

Claims (11)

Claims 1. Non-invasive personalized treatment device for skin disorders and imperfections, suitable for the diagnosis and treatment of skin disorders and imperfections based on the characteristics of each patient, characterized by the fact that it includes: - a console (1) equipped with wheels and handles for easy transport and electrical connection means for powering the components integrated in the console (1) itself, comprising at least a pair of recesses (1.1-1.2) suitable for housing in reversibly, a corresponding pair of handpieces (3-4); - said at least one pair of handpieces (3-4), of which a major handpiece (3) and a minor handpiece (4): said major handpiece (3) being able to be grasped by the handle (50) by an operator to performing microvibration treatment on a patient's body; said minor handpiece (4) being able to be grasped by the handle (51) by an operator to perform the microvibration treatment on a patient's face; said treatment being administered thanks to the simultaneous rotation and vibration of each internal cylinder (3.7-4.7) relating to each handpiece (3-4) which rotates and vibrates at a predetermined frequency; each of said cylinders (3.7-4.7) being equipped, on its external surface, with a plurality of independent rotating elements (3.6-4.6) movably connected to said cylinder (3.7-4.7) adapted to be pressed on the patient's body or face , to obtain the desired massaging effect; - at least one rotation and vibration adjustment device (3.2-4.2) integrated in each handpiece (3-4), adapted to govern the frequency of said rotations and vibrations of said cylinder (3.7-4.7) of said handpieces (3- 4); - at least one electric energy absorption sensor (3.1-4.1) for each handpiece (3-4), able to detect the quantity of electric energy absorbed by each handpiece (3-4) to obtain the desired rotation and vibration of the relative rotating elements (3.6-4.6); said electric energy absorption sensors (3.1-4.1) being able to communicate the data detected to - a control unit (5) programmed with a dedicated software able to process the data coming from said electric energy absorption sensors (3.1-4.1) and to act accordingly, in real time, on said frequency regulation devices ( 3.2-4.2) of each handpiece (3-4) to obtain an immediate variation of the rotation and vibration frequency of said cylinders (3.7-4.7), within a predetermined range between 20 Hz and 700 Hz, preferably between 40 Hz and 355 Hz, depending on the mechanical resistance offered by the patient's skin tissue in contact with one of said handpieces (3-4); - a communication interface (2), preferably integrated in said console (1) designed to allow an operator to receive in real time the information regarding the treatment in progress and to set the desired parameters including the frequency of the vibrations and rotations to be administered to the patient through said handpieces (3-4). 2. Non-invasive personalized treatment device for skin disorders and imperfections, according to the preceding claim 1, characterized in that said rotating elements (3.6) of said cylinder (3.7) integrated in said major handpiece (3) consist of spheres, ovoids or cylinders, arranged in a honeycomb cell, made of gel with a hardness between 5 shore and 100 shore, preferably 35 shore. 3. Device for personalized non-invasive treatment of skin disorders and imperfections, according to any one of the preceding claims, characterized in that said rotating elements (4.6) of said cylinder (4.7) integrated in said of said minor handpiece (4) consist from spheres, ovoids or cylinders, arranged in a "V" shape, made of hypoallergenic silicone with a surface treatment suitable for obtaining a predetermined surface roughness, said rotating elements (4.6) having a hardness between 5 shore and 100 shore, preferably 35 shore. 4. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized in that, through said communication interface (2), the operator can independently adjust the rotation frequency and the frequency of vibration of the cylinders (3.7-4.7) of said handpieces (3-4). 5. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized in that each of said handpieces (3-4) comprises: - a common quick release mechanism (3.9-4.9) adapted to allow stable disconnection and re-connection between a handpiece (3-4) and the relative cylinder (3.7-4.7); - a pair of side indicators (3.3-4.3), placed on both sides of the relative handpiece (3-4), designed to emit light signals to the operator to indicate the direction of discharge for the purpose of proper lymphatic drainage; - a light indicator (3.4-4.4) consisting of a plurality of warning lights or LED lights designed to turn on progressively as the pressure exerted by the operator on the patient's body increases and vice versa; - a display (3.8-4.8) designed to replicate said communication interface (2) on the side of the handpiece (3-4) in view of the operator. 6. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized in that said cylinder (4.7) of said minor handpiece (4) is equipped with a ring nut (4.7.1) which , by rotating around the longitudinal axis of said cylinder (4.7), it is able to modify the angle of incidence of said rotating elements (4.6) on the patient's body, or to cause them to impart a convergent or divergent force with respect to a neutral point coinciding with the position of said ring nut (4.7.1). 7. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized in that said rotating elements (3.6-4.6) of said major handpiece (3) and / or said minor handpiece (4 ) have an external surface provided with a plurality of recesses in the shape of a spherical cap designed to create a suction effect when pressed on the patient's epidermis. 8. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized in that said recesses (1.1-1.2) of said console (1) are equipped with an internal resistance suitable to heat said handpieces (3-4) when placed in the relative recesses (1.1-1.2) up to a predetermined temperature that can be set through said communication interface (2). 9. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized by the fact that said handpieces (3-4) are equipped with an internal resistance capable of raising their temperature, when not in use, up to a preset temperature settable through said communication interface (2); said internal resistance, working with infrared light, also has a bactericidal function. 10. Non-invasive personalized treatment device for skin disorders and imperfections, according to any one of the preceding claims, characterized in that at least one of said handpieces (3-4) is equipped with at least one temperature sensor suitable for detecting the skin temperature of the patient, sending the data to said control unit (5) which reproduces the data on said communication interface (2) also signaling the value of the temperature increase from the beginning of the treatment. 11. Method of personalized non-invasive treatment of skin disorders and imperfections, suitable for the diagnosis and treatment of skin disorders and imperfections based on the characteristics of each patient, characterized by the use of a treatment device according to any of the preceding claims and by understanding the following stages: (A) first phase of parameter setting, in which an operator sets, via a communication interface (2) of the treatment device, an admissible frequency range of rotations and vibrations based on the characteristics of the patient's tissue, his age and his musculature; the frequency of the vibrations being between 20 Hz and 700 Hz, preferably between 40 Hz and 355 Hz; (B) second test phase, in which, by grasping a handpiece (3-4) of said treatment device, and placing its cylinder (3.7-4.7) in contact with the patient's body or face, an absorption sensor electric power (3.1-4.1) of said handpiece (3-4) sends the data detected to a control unit (5) integrated in the treatment device; said control unit (5) comparing the data of electric energy absorption and the data of the frequency of vibrations and rotations set by the operator, communicates, through the communication interface (2) the correctness or otherwise of the frequency range of the vibrations and rotations set by said operator; (C) third stage of administration of the therapy, in which said operator runs through the areas of the patient's body or face to be treated with a handpiece (3-4), applying a predetermined pressure perpendicular to the patient's skin tissue; during said third phase of therapy administration, if the electrical energy absorption sensor (3.1-4.1) of the handpiece (3-4) in use should detect an area with greater mechanical resistance, for example a muscle contracture, called control unit (5) which processes the data sent by said electric energy absorption sensor (3.1-4.1), sends a command to increase the frequency of vibrations and rotations to a frequency adjustment device (3.2-4.2) of the handpiece (3 -4) in use, until a lower mechanical resistance is detected; (D) fourth phase of monitoring the homogeneity of the treatment on the entire area affected by the disorder or skin blemish, this phase can be performed through a visual analysis of the skin redness due to the vascularization of the tissue induced by the treatment, by the 'operator, or this phase can be performed by monitoring the skin temperature increase, due to the vascularization of the tissue induced by the treatment, performed by the control unit (5) which processes the temperature data detected by the temperature sensor of the handpiece (3-4) in use.