EP2693937A1

EP2693937A1 - Device for training the application of compression material

Info

Publication number: EP2693937A1
Application number: EP12715058.9A
Authority: EP
Inventors: Brigitte Nink-Grebe
Original assignee: Medi GmbH and Co KG
Current assignee: Medi GmbH and Co KG
Priority date: 2011-04-07
Filing date: 2012-04-10
Publication date: 2014-02-12
Also published as: RU2013143750A; WO2012136845A1; DE102011016379A1; DE102011016379B4

Abstract

The invention relates to the training and monitoring of a correct application of compression material. A training extremity (1) made of hard material is provided with multiple pressure measuring sensors (S1-S16), the sensor surface (10) of which substantially lies on the surface level (11) of the training extremity (1). A layer which is made of flexible cushioning material (12) and over which the compression material (14) is to be applied is applied over the training extremity (1) and over each sensor surface (10). A display device (4) displays the pressure values measured by the pressure measuring sensors (S1-S16) in real time.

Description

Device for training the application of

compression material

description

The invention relates to a device for training the application of compression material.

In the treatment of various diseases, such as

Lymphatic and venous disorders, the compression treatment has proven to be the most effective form of therapy. Doctors, nurses and Physiotherapeu ^¬ th the body part to be treated, in particular the arm or leg of a patient with different compression materials wrapped. It is important that the compression material exerts a pressure on the underlying tissue, which is within ^¬ certain limits. The targeted application of medical replacement bandages serves to support the interstitial tissue pressure for improved reabsorption of accumulated fluid. The effectiveness of this measure depends essentially on the applied Pressure profile, wherein the pressure intensity and the local course of the contact pressures are relevant both for the therapy success ^¬ as well as for the prevention of consequential damage. Local pressure on the damaged Ge ^¬ tissues and vascular system is applied by application of medical compression means, with the aim to support the terstitiellen in ^¬ pressure tissue locally, so that the venous and lymphatic return flow is conveyed. In this case, contact pressure and pressure curve under compression are decisive for the success of the therapy.

Actually applied to a limb pressure ^¬ intensity depends not only on the experience of the therapist also on the compression used materials, bandaging techniques and other different mechanisms of action. While in the relaxed muscles only the contact pressure of the compression means acts (resting pressure), the muscle contraction resulting from active movement to a pressure increase of the interstitial tissue (working pressure), whereby the venous and lymphatic return flow is additionally supported.

In order to achieve maximum therapeutic success, it is necessary for each patient to individually adapt a stage-specific pressure profile with controlled pressure progression. Improper bandaging or improper compression stockings can not only hinder the healing process, but also harbor further health risks such as tissue necrosis or nerve damage. Within the framework of guidelines or industrial quality seals, concrete pressure specifications have already been defined, ^both for compression stockings and for ^replacement bandages. However, these published pressure figures are still different in different European countries and there is no standard international standardization.

The current state of scientific knowledge with regard to diagnosis and therapy, for example of lymphedema, is summarized in a national German guideline and contains differentiated general and theoretical recommendations on the type, extent, duration and intensity of the compression treatment. However, there is no standard training or testing standard for practical user training and control. Technical skills such as the acquisition of the bandage technique, the sensitization with regard to an adequate bandage pre-stretching for uniform pressure distribution result primarily from subjective empirical values and can not be distributed ^across users due to a lack of standardized teaching methods. Although the relevance of adjusting a stage-appropriate pressure profile with a controlled pressure curve is undisputed, the measurement of pressures and pressure gradients has so far only been performed directly on the patient.

Thus, DE 39 33 827 AI proposes to measure the pressure acting on a tissue external pressure by pressure transducer which occurs between the tissue and the external pressure ago calling surface. As a donor electromechanical flexible film is proposed. The GE- measured pressures are ge ^¬ stores in a recording device and output in graphic or numeric form on a monitor.

DE 10 2007 020 247 A1 describes a device for measuring a contact pressure of a medical compression means with sensors, which consist of a textile carrier and fluid cells with a pressure-deforming membrane, wherein between the membrane and the pressure sensor, a stored fluid is present , The fluid cells represent an increase and thus influence once again the pressure to be measured in terms of a false-positive pressure increase.

DE 195 05 765 C2 describes a device for contact pressure measurement of medical compression stockings and bandages with a pneumatic sensor system which can be attached between the body part to be examined and the compression measure. The pneumatic sensor system has a pressure transducer and a closed volume, so that an increasing inside of the closed volume air pressure increase can be detected. With an inflator, the ge ^¬ connected volume of the sensor system is filled ection by linear Luftvolumenin. Pressure measuring signals of the sensor system to an electronic evaluation and display system are continuously fed, comprising a nonlinear be true ^¬ from the external pressure of the acquisition of compression ^¬ dependent calibration of the sensor system. The problem with the known devices is that they are designed for direct application to the patient and sionsmaßnahme remain on the patient over the dwell time of Kompres including their electrical supply cable to the sensors, which is unreasonable for the patient. Also, it is not reasonable for patients to be available for training and exercise purposes of medical professionals available and, if necessary, several times to endure the procedure of attaching sensors and the application of Kom ^¬ pressionsmaterials.

The object of the invention is therefore to provide a device for training the application of Kompressionsmateri al, which makes it possible outside a patient Pa as realistic as possible simulation of the application of compression material to allow and to obtain accurate readings.

This object is achieved by the attached in claim 1 given features. Advantageous embodiments and further developments of the invention can be found in the dependent claims.

The basic idea of the invention is a Trai- ningsextremität such as an arm or a leg of a hard material, particularly plastic material watch before ^¬ on which a plurality of pressure sensors mounted. The sensor surfaces of these pressure sensors are essentially at the level of the surface of the training extremity. A flexible cushioning layer is applied above the training extremity and over the sensor surfaces. Preferably, this is Cushion layer made of synthetic or Flies- Filterma ^¬ terialien. The sensors are electrically connected to a display device which displays the pressure values measured by the pressure measuring sensors.

The sensor surfaces of the pressure measuring sensors can protrude slightly and in particular about 1 to 2 mm above the level of hard training extremity. The pole ^¬ termaterial leads the compression practical as well pERSonal pergewebe more laterally on the sensor surfaces. By the padding material, an in-tissue pressure distribution is achieved. The pressure measuring sensors are preferably designed such that they measure pressures which act perpendicular to the sensor surface and also pressures which act tangentially to the sensor surface, wherein al ^¬ le possible intermediate values can be detected.

Preferably, over the cushion material, a water ^¬ tight, sterilizable and disinfectant-resistant coating is applied may preferably insist on chloroprene rubber.

The metrological connections of the pressure measuring sensors are arranged inside the hollow training extremity and therefore do not influence the measurement result.

The metrological connections of the pressure measuring sensors can be separated by means of sockets and plugs. Preferably, the respective pressures in real time are measured, registered and Darge ^¬ up on a monitor. In an evaluation such as a computational ^¬ ner, can freely selectable pressure reference values as desired be deposited. Deviations from a position-specific defined target pressure value can be achieved by signal colors z. B. in the traffic light system with the colors red, yellow and green.

Preferably, the training extremity has a releasable support to secure it to a stationary object such as a table. The holder has a rotatable axis by means of which the Trai ^¬ ningsextremität can be adjusted at least between a horizontal and a vertical position.

In the following the invention will be explained in more detail using an exemplary embodiment in conjunction with the drawing. It shows:

Fig. 1 is a schematic side view of

Device according to the invention;

FIG. 2 is an enlarged sectional view of a section of the training ^extreme in the area of a pressure-measuring sensor; FIG.

Figure 3 is an illustration of a monitor at a ^¬ set of the device according to the invention.

FIG. 4 is an excerpt of a table of measurements obtained by the device from various therapists; FIG.

Fig. 5 to diagrams of the pressure in dependence FIG. 7 shows the distance of the pressure measuring sensors relative to the distal end of the training extremity, which were determined by three different therapists.

Fig. 1 shows schematically a training extremity 1 in side view. Along the Trainingsextremität 1 are a plurality of sensors Sl to S16 are mounted whose be fed from ^¬ output signals via an electrical line or of generalized on metrological terminals 2 an evaluation unit, which here consists of a computer 3 and a monitor. 4 The pressure measuring sensors S 1 to S 16 are attached at different points of the training extremity 1, namely at predefined distances a measured from the distal end 5 in the direction of the proximal end 6 of the training extremity 1.

Attached to the proximal end 6 of the training extremity is a holding device 7, with which the training extremity 1 is attached to a stationary object, such as a patient. can be attached to a table. The holding device 7 has a lockable pivoting mechanism 8, by means of which the training extremity 1 is opposite to the stationary object, such as e.g. The table (not shown) can be pivoted, at least between a vertical and a horizontal position.

In Fig. 1, is depicted Trainingsextremität 1 in two Be ^¬ side views in order to illustrate that the pressure measurement sensors S are arranged distributed around the circumference of the Trainingsextremität 1 to S16. The Trainingsextremität 1 consists material such as polyethylene of hard art and is modeled on the physio logical ^¬ dimensions of a human. When replicating an arm or a leg, joints may be provided in the area of elbows or knees, which allow a straight-line flexion of the training extremity. In the example of FIG. 1, a corresponding joint is brought 9 at the location of a knee joint to ^¬. The multicore cable 2, which connects the sensors S 1 to S 16 to the computer 3, is arranged inside the hollow training extremity 1. So be ^¬ not prevent the line 2 the compression process and does not falsify the measurement result. In the sectional view of FIG. 2, a section of the material of the training ^extremity 1 is to be seen. In an opening of this material, a pressure ^¬ measuring sensor S is used, the pressure measuring surface 10 is substantially in a plane 11, which is defined by the surface of the training extreme in the area of Sen ^¬ sensor S. In this case, the pressure measuring surface 10 slightly above this plane 11 vorste ^¬ hen and that in the order of 1 to 2 mm. The entire surface of the training extremity 1 is coated with a padding material 12, which also covers the sensors S and their pressure measuring surface 10. The cushion material 12 is flexible and thus komprimier ^¬ bar and forms a result body tissue, such as skin and subcutaneous tissue layers after. It has in practice a thickness of about 15 mm. The material can ^¬ example, a Flies- or filter fabric to be. There are other upholstery materials are sorted ^¬ but possible. Depending on used cushioning material may be further applied to the outer upper surface of the cushion material 12 ^¬

Layer 13 may be applied to a coating which consists of waterproof, wipe-disinfectant and disinfectant-resistant material, for example, chlorine rubber in question, which is commercially available under the brand name "Neoprene". On the outermost layer 12 or 13, a pressure dressing 14 is then applied, which is to be applied so that a physiologically correct pressure is applied. This pressure is measured by the sensors S and reported via the line 2 to the computer 3.

The sensors S are preferably constructed in chip technology. They have a pressure / voltage converter 15, which is arranged between a pressure measuring disk 10 and a base 16, which is here re ^¬ alisiert by a housing wall. The pressure gauge 10 and the base 16 are clamped by springs 17 against each other. The pressure voltage converter 15 has a spherical segment-shaped sensor surface 18 which engages an adjusting disc 19, a ^¬ namely in a spherical cap adapted to the sensor surface recess, wherein the readjustment ^¬ disc 19 is connected to the pressure measuring disk 10th By the springs 17, of which preferably four are provided, all of which have substantially the same force, the pressure measuring disc 10 can tilt about the center of the spherical cap-shaped sensor surface 18 and thus also measure forces that do not occur perpendicular to the center of the pressure measuring surface ^¬ . Also, the sensor S can thus measure forces that are aligned obliquely or tangentially to the plane 11. At this point it should be noted that this sensor type however, it is preferred that other types of

Pressure measuring sensors can be used.

The described type of sensor is otherwise described in the non-prepublished patent application DE 10 2010 005 792.

When creating a pressure bandage 14, the precisely measured ^¬ nen pressure values of the sensors S are displayed to S16 in real time on the monitor 4 so that the therapist can immediately see whether he applies the pressure bandage "right."

As shown in FIG. 3, two views of the training extremity 1 are shown on the monitor 4, with a view of the sensors S1 to S16 in la ^¬ court and with the respectively measured pressure value of the corresponding sensor. The measured values of the sensors S1 to S16 are compared with predetermined values and depending on the comparison, the displayed pressure value is displayed in color. For example, too high pressures in the color red, too low pressures in the color yellow and correct pressures in the color green are shown. The user has the possibility of further measured values to save to document training resulting ^¬ nisse and training results. Thus, the therapist can immediately recognize the quality of his Druckapplikati ^¬ on and correct and optimize during the bandaging process.

With the holding means 7 and the turning mechanism 8, the Trainingsextremität can be respectively inserted so ^¬ represents 1, the ergonomically most favorable for the attachment of the compression means position einge- is taken. As a mobile device, the Trai- can ningsextremität for training and practice purposes each be transported ^¬ time and is available as training and test standard available.

The table of FIG. 4 shows a section of ge ^¬ measured pressure values of sensors Sl to S7 for different therapists. Double-hatched boxes indicate that the measured pressure is higher than the setpoint, and simply hatched boxes indicate that it is lower than a setpoint range. The chart, prepared with experienced therapists, illustrates dramatically that no therapist was able to apply a completely correct pressure bandage.

The diagrams of FIGS. 5 to 7 show graphically the pressure curves for three selected ^{therapies of} the table of FIG. 4, namely the therapists 3, 8, and 12. The shaded area indicates a band or a permissible value range for the desired values , The position of the individual sensors with respect to their distance a from the distal end of the training extremity is shown in the x-axis. It can be seen that the therapist 3 (FIG. 5) lies above or below the desired value band in the region of the sensors S1, S2 and S3, while the other sensors are within the ^band . At therapist 8 (Figure 6), only two sensors are within the setpoint band while the remaining values are above.

With Therapist 12, the pressure readings of most sensors are extremely above the set point band. These trained therapist measurements clearly demonstrate the urgent need for better training and education of therapists in the application of pressure bandages, which is realized by the device of the invention.

Claims

claims

Device for training the application of compression material,

with a Trainingsextremität (1) of hard Ma ^¬ TERIAL,

at least three pressure measuring sensors (S1-S16) whose sensor surface (10) lies substantially at the level (11) of the surface of the training extremity (1),

with a layer of a flexible Polsterma ^¬ TERIAL (12) overlying the Trainingsextremität (1) and over the sensor surfaces (10) of the pressure sensors (S1-S16) is applied and

with a display device (4) indicating pressure values measured by the pressure measuring sensor (S1-S16).

Apparatus according to claim 1, characterized in that the padding material (12) consists of fleece ^¬ or filter fabric.

Apparatus according to claim 1 or 2, characterized in that above the layer of cushion ^¬ material (12) an outer surface layer (13) is applied from cleanable and disinfectable material.

Device according to claim 3, characterized in that the outer surface layer (13) consists of cleanable and disinfectable Clor rubber.

Device according to one of claims 1 to 4, characterized in that the training extremity (1) is hollow inside and that metrological connections (2) of the pressure measuring sensors (S1-S16) are arranged in the interior of the training extremity (1).

Device according to one of claims 1 to 5, characterized in that the sensor surfaces (10) of the pressure measuring sensors (S1-S16) are at most 1 to 2 mm above the level (11) of the training extremity (1).

Device according to one of claims 1 to 6, characterized in that the pressure measuring sensors (S1-S16) pressure / voltage converter (15) which are arranged between the pressure measuring surface (10) and a base (16), wherein the pressure / Voltage converter (14) has a spherical cap-shaped sensor surface (18) which engages in an adapted recess of the pressure measuring surface (10) or an adjusting disk (19).

Apparatus according to claim 7, characterized in that the pressure measuring surface (10) and the base (16) by springs (17) are braced against each other.

Device according to one of claims 5 to 8, characterized in that all pressure measuring sensors (S1-S16) can be connected to the measuring connections (2) via plug / socket connections.

10. Device according to one of claims 1 to 9, character- ized in that the training extremity (1) has a holding device (7) with a lockable pivot mechanism (8).

Device according to one of claims 1 to 10, characterized in that measured values of the pressure measuring sensors (S1-S16) are displayed in real time on the display device (4).

Device according to one of claims 1 to 11, characterized in that reference values for pressures of the pressure measuring sensors (S1-S16) are stored in a computer (3), that the measured pressure values of the pressure measuring sensors (S1-S16) are compared with the reference values and that Deviations of the measured values from the reference values are signaled on the display device.

Device according to claim 12, characterized in that the deviations of the measured values vo are the reference values indicated by color representation, in particular by Far ^¬ ben red, yellow and green.