JP2022126737A - Fixing member for medical treatment - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a fixing member for medical treatment which is more comfort.

SOLUTION: A fixing member 10 for medical treatment comprises: a water curable core material 12; a protection material 13 for surrounding side end parts of the core material 12; and covering materials 11 for covering the core material 12 and the protection material 13. The thickness of the protection material 13 may be equal to or less than the thickness of the core material 12.

SELECTED DRAWING: Figure 1

COPYRIGHT: (C)2022,JPO&INPIT

Description

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a medical fixing material, and more particularly to a medical fixing material comprising a water-curable core material and a covering material covering the core material.

2. Description of the Related Art Conventionally, in the medical field, various medical fixing materials have been used for the purpose of treating fractures, sprains, and the like. As a medical fixing material, for example, a water-curable medical fixing material has been used in which a water-curable resin is applied to a glass fiber, a polyester non-woven fabric, or a polyester woven fabric to form a base material. Such a water-curable medical fixing material is known to be useful because of its high resistance to water and high mechanical strength.

However, in the case of a medical fixing material using a water-curable synthetic resin, it is conceivable that the synthetic resin may apply unfavorable pressure to the patient's skin, causing pain or injury.

Therefore, for example, Patent Document 1 discloses a base fabric, an aluminum casing provided directly on the base fabric, and an outer casing formed on the aluminum casing without being directly provided on the base fabric like a general orthopedic splint. A medical fixation material is disclosed comprising a surface layer and a skin protective layer.

Since such a medical fixing material employs glass fiber as the base fabric of the medical fixing material, it is thin and easy to shape to the affected part, so that the fixing force of the stay can be improved. In addition, if the medical fixing material can be made thinner, the degree of freedom in designing the brace can be improved.

Japanese Patent Publication No. 2010-520769

However, when the base fabric is formed of glass fibers or the like, the glass fibers protrude from the end face of the base fabric, causing a prickly sensation or sticking to the patient's skin. Therefore, in order to protect the patient's skin from the glass fiber, it is necessary to cover the end face with a cushion. There was a problem that discomfort occurred at the fixing point.

The present invention has been made in view of such circumstances, and an object of the present invention is to provide a medical fixing material with improved comfort.

In order to solve the above problems, the medical fixing material that is one embodiment of the present invention comprises a water-curable core material, a protective material that surrounds the side ends of the core material, and a covering material that covers the core material and the protective material. And prepare. The thickness of the protective material may be less than or equal to the thickness of the core material.
Further, the medical fixing material, which is one embodiment of the present invention, includes a water-curable core material containing glass fibers, and glass fibers surrounding the side ends of the core material and protruding from the side ends coming into contact with the skin. and a covering material covering the core material and the protective material.

ADVANTAGE OF THE INVENTION According to this invention, the medical fixing material which improved comfort can be provided.

1 is a schematic diagram showing a medical fixing material according to one embodiment of the present invention; FIG. FIG. 2 is an enlarged cross-sectional view of the medical fixing material of FIG. 1 taken along line AA. FIG. 2 is an exploded schematic view of the medical fixing material of FIG. 1; 1. It is a schematic diagram which shows the procedure which pours water into the medical fixing material of FIG. 1, and hardens it. 1. It is a schematic diagram which shows the procedure which mount|wears a human body with the medical fixing material of FIG. FIG. 2 is a schematic diagram showing a state in which the medical fixing material of FIG. 1 is attached to a human body; FIG. 2 is an enlarged view showing the thickness of each part of the medical fixing material of FIG. 1; 2 is a table showing the thickness of each part of the medical fixing material of FIG. 1; It is a table|surface which shows contrast with the Example of this invention, and a comparative example.

Preferred embodiments for carrying out the present invention will be described below with reference to the drawings. It should be noted that the embodiments described below are examples of representative embodiments of the present invention, and the scope of the present invention should not be construed narrowly. In addition, the present invention can also combine any of the following embodiments and modifications thereof with each other.

(1. Configuration example of medical fixing material)
FIG. 1 is a schematic diagram showing a medical fixing material (hydraulic stay) 10 according to one embodiment of the present invention. FIG. 2 is an enlarged cross-sectional view of the medical fixing material 10 taken along line AA of FIG. FIG. 3 is an exploded schematic view of the medical fixing material 10. As shown in FIG. The configuration of the medical fixing material 10 will be described with reference to FIGS. 1 to 3. FIG.

The medical fixing material 10 according to the present embodiment includes two upper and lower covering portions 11, a water-curable core material 12, and an end protection portion 13 which is a protective material for protecting the peripheral end portion of the core material 12. , is equipped with The covering portion 11 sandwiches the core material 12 and the edge protection portion 13 from above and below. As an example, the core material 12 is formed in a substantially rectangular shape, and the periphery of the edge is protected by the edge protection portion 13 . The edge protection portion 13 is joined to each side edge portion of the core material 12 by the joining portion 14, and is formed in a substantially rectangular shape as an example. The joint portion 14 bonds the upper and lower covering portions 11 to the core material 12 and the edge protection portion 13 . Furthermore, one or more cuts 15 are formed in the outer surface layer of the lower covering part 11 for injecting water into the medical fixing material 10 or for draining water from the medical fixing material 10 . It is Each part will be described in detail below.

(2. Coating part)
The covering portion 11 is a member that covers the upper and lower surfaces of the core material 12 . The material of the covering portion 11 can be, for example, polyester or polyolefin non-woven fabric or film that has been water-repellent (resin-repellent) processed with fluororesin. As a result, the covering portion 11 can be resin-repellent, such as preventing water-curable resin such as urethane resin from leaking out. Furthermore, the covering part 11 can also serve as a cushion when the medical fixing material 10 is attached to the human body.

Here, the fluorine-based resin is, for example, a copolymer whose main component is an acrylic acid derivative (perfluoromonomer) produced by esterifying a compound having a perfluoroalkyl group and a hydroxyl group with acrylic acid, methacrylic acid, or the like. In coalescence, oil-repellent treatment is performed with a fluorine-based treatment agent that uses monomers such as alkyl (meth)acrylate and vinyl chloride as copolymer components, and cross-linkable monomers such as 2-hydroxyethyl methacrylate and N-methylacrylamide. be able to.

Here, with respect to the nonwoven fabric, when the fiber bundles at the end surfaces of the base fabric that caused the tingling after the resin of the core material 12 was cured and the base fabric that did not cause the tingling were measured, the thickness of the fiber bundle of the base fabric causing the tingling was measured. was 350 μm or more. On the other hand, the thickness of the fiber bundle of the base fabric that did not cause irritation was 150 μm or less. From this result, it is conceivable that when the thickness of the fiber bundle is around 250 μm or more, prickness occurs after the resin of the core material 12 is cured.

Note that the medical fixing material 10 does not have a cushioning material between the covering portion 11 and the core material 12 . As a result, the medical fixing material 10 can be made thinner than conventional products.

(3. Core material)
The core material 12 is, for example, a sheet-like portion that provides strength to the medical fixing material (stay) 10 . In particular, the strength of the medical fixing material 10 is enhanced by the thickness and material of the core material 12 . As the material of the core material 12, for example, a base fabric (substrate) such as plastic fiber, glass fiber, etc., and urethane resin can be used. As a result, both the base fabric such as glass fiber and the urethane resin are inexpensive, so the medical fixing material 10 can be manufactured at low cost. The base fabric is a member for providing strength, and the urethane resin is a member for water hardening.

Since the medical fixing material 10 employs glass fiber as the base fabric of the core material 12, the thickness of the covering material 11 and the core material 12 can be reduced to make it easier to shape the affected part, thereby fixing the stay. can improve power. In addition, if the medical fixing material can be made thinner, the degree of freedom in designing the brace can be improved.

However, as shown in FIG. 2, if glass fibers 21, for example, are used as the base fabric of the core material 12, the glass fibers 21 protrude from the ends of the core material 12, causing irritation or sticking to the skin when worn. There is a risk that it may fall off. Therefore, it is necessary to protect the end face of the core material 12, but if the end of the covering material 11 is stretched to protect the end face of the core material 12, the entire medical fixing material 10 becomes thicker, and furthermore, the thickness increases. It becomes uneven and bumpy.

Moreover, the material of the core material 12 may be woven fabric, knitted fabric, non-woven fabric, or the like, and these may be used singly or in combination. Furthermore, fibers such as natural fibers and chemical fibers can be used for the core material 12, and the fibers include, for example, cotton, wool, rayon, polyamide fiber, polyester fiber, acrylic fiber, polyolefin fiber, and glass fiber. , carbon fiber, and other fibers.

(4. Edge protector)
The edge protection part 13 is a member that protects the edge face of the base fabric of the glass fiber in the core material 12 . The material of the edge protection part 13 has a coarse mesh structure, and for example, polyester nonwoven fabric can be used. The medical fixing material 10 can prevent the glass fibers 21 protruding from the end face of the core material 12 from coming into contact with the skin by providing the end protection part 13 .

By forming the edge protection part 13 to have a thickness equal to or smaller than that of the glass fiber base fabric, it is possible to reduce unevenness in the thickness direction of the medical fixing material 10, thereby making it easier to fit the affected part. , can improve fit and fixation.

(5. Joint)
The joining portion 14 is a member for bonding the covering portion 11, the core material 12, and the end protection portion 13, respectively. For example, a double-sided tape or an adhesive can be used as the material of the joint 14 .

(6. Notch of covering portion)
The notch 15 of the lower covering portion 11 is a portion that plays a role of pouring and draining water for hardening the core material 12 . The notch 15 is formed in a region between the side end portion of the core material 12 and the side end portion of the covering material 11, which is a portion of the outer surface layer of the covering portion 11 where the covering materials 11 are in contact with each other. This is because if there is a notch in the portion where the covering portion 11 and the core material 12 are in contact with each other, the resin will leak. In addition, by providing the notch 15 in the above portion, it is possible to prevent the resin from leaking and to facilitate the removal of moisture after the curing reaction has occurred.

Since the covering portion 11 of the medical fixing material 10 is water-repellent (resin-repellent), it is difficult for the internal moisture to escape to the outside. In addition, if water remains inside the medical fixing material 10, the affected area will be macerated (soggy). Therefore, by forming cuts 15 in the portion of the outer surface layer of the covering portion 11 where the covering materials 11 are in contact with each other, the water that has entered the interior of the medical fixing material 10 can be drained to the outside through the cuts 15. . Since the polyester nonwoven fabric of the edge protection portion 13 is not water-repellent, water can be drained from the edge protection portion 13 . Moreover, the part that plays a role of pouring water and draining water for hardening the core material 12 is not limited to the cut 15, and may be the shape of a hole or the like.

(7. An example of water hardening procedure)
FIG. 4 is a schematic diagram showing a procedure for pouring water into the medical fixing material 10 and hardening it. A procedure for curing the medical fixing material 10 will be described with reference to FIG.

FIG. 4A is a diagram showing the lower covering portion 11 with the upper covering portion 11 removed and a cut made. As an example, the lower covering portion 11 is formed with cuts 15 and cuts 45 at positions near the longitudinal side ends where the core material 12 and the end protection portion 13 are not adhered. FIG. 4B is a diagram showing how water is poured into the core material 12 from the cut 15 and drained from the cut 45 as an example of water pouring. FIG. 4C is a diagram showing how the core material 12 is hardened by draining excess water after pouring water.

First, it is confirmed that the cut 15 and the cut 45 are formed in the covering portion 11 of the medical fixing material 10 . Next, as shown in FIG. 4B , for example, water is injected into the covering portion 11 through the cut 15 . Excess water that is poured in more than the required amount is drained to the outside of the covering portion 11 through the cut 45, for example. After the core material 12 is sufficiently soaked in water, the medical fixing material 10 is squeezed to drain the water inside from the cuts 15 and 45 and the ends of the covering part 11, and the shape to be fixed is maintained for a while. put. As an example, the core material 12 hardens in about 10 minutes, but it takes about 24 hours to harden completely.

(8. Example of wearing a fixing material for medical use)
FIG. 5 is a schematic diagram showing the procedure for attaching the medical fixing material 10 to the human body. FIG. 6 is a schematic diagram showing a state in which the medical fixing material 10 is attached to the human body. A procedure for attaching the medical fixing material 10 to the human body will be described with reference to FIGS. 5 and 6. FIG. In this embodiment, as an example, a procedure for wearing the medical fixing material 10 around the wrist of a human body will be described.

First, as described above, the medical fixing material 10 is impregnated with water. Next, as shown in FIG. 5, the medical fixing material 10 impregnated with water is attached to the right wrist 51 from the palm side of the right hand of the human body, for example. At this time, the shape of the medical fixing material 10 is adjusted so that the medical fixing material 10 can accurately fix the affected part in the vicinity of the right wrist 51 . It should be noted that if the portion of the medical fixing material 10 that comes into contact with the thumb is cut off in a substantially semicircular shape in accordance with the shape of the palm, it can fit the right wrist 51 better. Then, as shown in FIG. 6, the medical fixing material 10 is fixed to the right wrist 51 with, for example, an elastic bandage 61 or a joint brace such as a supporter. In this manner, the medical fixing material 10 is formed by applying the covering material 11, which is a flexible material, to the affected area and hardening the core material 12 such as a stay while fitting the affected area.

With the above configuration and operation, the medical fixing material 10 of the present embodiment protects the peripheral edge of the core material 12 with the edge protection part 13, thereby reducing the thickness while maintaining the strength and improving the comfort. can be made

(9. Examples and Experimental Methods)
Next, an example of the medical fixing material 10 of this embodiment and an experimental method will be described with reference to FIGS. 7 and 8. FIG. FIG. 7 is an enlarged view showing the thickness of each part of the medical fixing material 10. As shown in FIG. FIG. 8 is a table showing the thickness of each part of the medical fixing material 10. As shown in FIG.

As shown in FIGS. 7 and 8, the thickness (1) of the cast core material 12 is preferably 2.0 mm to 10.0 mm, more preferably 4.0 mm to 6.0 mm.

In addition, the thickness of the covering material was conventionally about 2.5 mm to 3.0 mm, but in order to make the medical fixing material 10 thinner, the thickness (2) of the covering material 11 is reduced to 0.1 mm to 2.5 mm. is preferred, and 0.3 mm to 1.5 mm is more preferred. In addition, these thicknesses are set from Sontara 0.45 mm and ASP03290 2.5 mm as a result of measuring with a Peacock J-Bφ30 mm.

Further, the width (3) of the end protection portion 13 of the outer edge is preferably 2.0 mm to 8.0 mm, more preferably 4.0 mm to 6.0 mm. It is preferable that the thickness of the end protection portion 13, which is a protective material, be equal to or less than the thickness of the core material 12. As shown in FIG.

Next, the experimental methods of the present examples and comparative examples will be described.

For strength measurement, a three-point bending test (indentation test) is performed with an autograph, and the maximum pressure until breakage is 30 N / inch or more (Shimadzu Corporation "Autograph (registered trademark)" AG- 20KNI, 1kN load cell is used), and it is confirmed that it has enough strength to hold the joint by not breaking at 30N/inch.

Regarding the fixing force, each stay of the example and the comparative example was fixed to the wrist joint, and the braking angle (angle until the hand felt resistance by the stay when the wrist joint was bent) was measured. I'm sure it's not. In the comparative example, the braking angle is lowered by 5 degrees or more, and the result is that the feeling of fit is poor.

As for resin leakage, it was confirmed that no resin leakage occurred on the surface of the coating material 11 by applying heat to the stay.

Furthermore, the present inventors manufactured a hand-covering orthosis using the medical fixing material 10 according to the present embodiment, and performed wear evaluation. Several subjects were asked to wear the hand covering device according to the present embodiment, and an evaluation was requested. As a result, we got the answers that "it is easy to move fingers", "it does not get in the way", and "it fits in the hand". As a result, it was confirmed that the hand-covering orthosis according to the present embodiment was easy to wear and comfortable enough to be worn continuously.

(10. Comparison between Examples and Comparative Examples)
FIG. 9 is a table showing comparison between examples of the present invention and comparative examples. A comparison between an example of the present invention and a comparative example will be described with reference to FIG.

As shown in FIG. 9, the "number of layers (thickness) of the core material", the "width of the end protection part of the outer edge" and the "thickness of the covering material" of the medical fixing material were changed to obtain the results of Example (1). ) to (4) and comparative examples (1) to (4) were compared in wearing comfort. In all the examples and comparative examples (1) to (3) shown in FIG. 9, the coating material is subjected to a water-repellent (resin-repellent) treatment. In Comparative Example (4), the coating material was not treated with a water-repellent (resin-repellent) treatment. In the column of comfort in FIG. 9, "○" indicates comfortable, and "X" indicates uncomfortable.

Here, the “ratio” in the rightmost column of FIG. 9 represents the ratio of the thickness of the covering material to the thickness of the core material, that is, the value of (thickness of covering material)/(thickness of core material).

From the results shown in FIG. 9, when the thickness of the core material is thin (1 mm) as in Comparative Example (1), comfort cannot be obtained because the fixing force is insufficient when the medical fixing material is worn. In addition, as in Comparative Example (2), when the width of the edge protection part is long (10 mm), the amount of non-woven fabric that is not related to fixation increases when the medical fixation material is fitted to the affected area, resulting in comfort. can't get In addition, as in Comparative Example (3), when the covering material is thick (6 mm), it becomes difficult to fit the medical fixing material to the shape of the affected area, and comfort cannot be obtained when worn. In addition, as in Comparative Example (4), when the covering material is not treated with a water-repellent (resin-repellent) treatment, when the medical fixing material is attached, the core resin leaks from the covering material, which reduces comfort. can't get

On the other hand, from the results shown in FIG. 9, as in Examples (1) to (4), the thickness of the core material is 2 mm to 6 mm, the width of the edge protection part is 2 mm to 5 mm, and the thickness of the covering material It has been found that a medical brace can be worn comfortably when is in the range of 0.45 mm to 1.5 mm.

Further, from the results shown in FIG. 9, it was found that the medical fixing material could be worn comfortably when the ratio of the thickness of the covering material to the thickness of the core material was 1/20 or more and 1/4 or less. This is because if the ratio of the thickness of the covering material to the thickness of the core material is more than 1/4, the strength of the stay will be insufficient, and the fixing force will be insufficient when the medical fixing material is attached, making it difficult to fix. In addition, the overall thickness of the medical fixing material increases, making it difficult for the medical fixing material to fit the shape of the affected part, making it difficult to wear comfortably. If the ratio of the thickness of the covering material to the thickness of the core material is less than 1/20, the thickness of the core material will increase, making it difficult to shape the affected area when the medical fixing material is attached. This is because you will not be able to obtain In addition, the thickness of the covering material becomes thinner and the covering material is easily broken, and the breakage makes it easier for the resin to leak, making it difficult to obtain comfort.

The medical fixation material according to the present invention may have a core material such as a stay sandwiched between covering materials such as cushions impregnated with a curable resin into a base fabric (base material), and fix a fracture site or the like. can be used to

10 Medical fixing material (water hardening stay)
11 Coating part 12 Core material 13 Edge protection part 14 Joining part 15, 45 Cut 21 Glass fiber 51 Wrist 61 Bandage (cast material)

Claims (8)

a water-curable core material comprising glass fibers;
a protective material that surrounds the side ends of the core material and prevents the glass fibers protruding from the side ends from coming into contact with the skin;
a coating material covering the core material and the protective material;
medical fixation with The medical fixing material according to claim 1, wherein the thickness of the protective material is equal to or less than the thickness of the core material. 3. The medical fixing material according to claim 1, wherein the covering material covers upper and lower surfaces of the core material and the protective material. The medical fixation material according to any one of claims 1 to 3, wherein a thickness ratio of the covering material to the core material is 1/20 or more and 1/4 or less. The medical fixing material according to any one of claims 1 to 4, wherein the covering material is treated with resin repellency. 6. The medical fixing material according to claim 5, wherein the covering material is resin-repellent treated with a fluororesin. The medical fixation material according to any one of claims 1 to 6, wherein the covering material has one or more cuts in the outer surface layer. 8. The medical fixation material according to claim 7, wherein the notch is formed in a region between the side end portion of the core material and the side end portion of the covering material.

Images