MEDICAL FIXATION APPARATUS FOR LESION
20200138617 ยท 2020-05-07
Inventors
Cpc classification
A61F13/048
HUMAN NECESSITIES
A61F13/041
HUMAN NECESSITIES
International classification
Abstract
The present invention relates to a medical fixation apparatus for a lesion. According to an embodiment, a medical cast comprises: an expansion band having a predetermined length; a pair of elastic fibers which are coupled to opposite widthwise edges of the expansion band, are coated with a water-curable synthetic resin, and can surround a body part; and a plurality of coupling units, which have a flat shape and, when the pair of elastic fibers surround a body part, are arranged at a predetermined interval along an edge at which the pair of elastic fibers face each other to connect the pair of elastic fibers.
Claims
1. A medical fixation apparatus for a lesion, comprising: an extendable band having a predetermined length; a pair of elastic fiber respectively coupled to both width-directional edges of the extendable band, applied with water-curable synthetic resin, and being able to surround a body part; and a plurality of flat coupler units disposed with predetermined gaps along edges where the pair of elastic fibers face each other to connect the pair of elastic fibers when the body part is surrounded with the pair of elastic fibers.
2. The medical fixation apparatus of claim 1, wherein the coupler unit is composed of a male coupler and a female coupler that are made of a material having predetermined elasticity, the male coupler is composed of a flat body and a locking portion protruding from a side of the body in a fish spear shape, the female coupler is composed of a flat body and an insertion portion formed on a side of the body and being locked to the locking portion, and a width of a rear end of the locking portion is larger than a width of the insertion portion, and the male coupler and the female coupler are not separated after being fastened to each other.
3. The medical fixation apparatus of claim 2, wherein a connection block having a locking protrusion on a bottom is further disposed in the body of the female coupler to be able slide out, and an accommodating portion that can be coupled to the connection block is further formed at the body of the male coupler.
4. The medical fixation apparatus for a lesion of claim 1, wherein the coupler units are coupled to an outer side of the elastic fibers not to come in contact with a skin.
5. A medical fixation apparatus for a lesion, comprising: an elastic fiber applied with water-curable synthetic resin and being placed on a lesion; a plurality of fixing bands having an adjustable length; and flat coupler units disposed at a width-directional edge of the elastic fiber, an end of the fixing band, the other edge of the elastic fiber, and the other end of the fixing band so that the elastic fiber placed on a lesion can be fixed to a patient body by the fixing bands.
6. The medical fixation apparatus for a lesion of claim 5, wherein the fixing band is composed of a first band with a Velcro portion on a front and a second band with a Velcro portion on a bottom, and the first and second bands are combined in a single unit.
7. The medical fixation apparatus of claim 5, wherein the coupler unit is composed of a male coupler and a female coupler that are made of a material having predetermined elasticity, the male coupler is composed of a flat body and a locking portion protruding from a side of the body in a fish spear shape, the female coupler is composed of a flat body and an insertion portion formed on a side of the body and being locked to the locking portion, and a width of a rear end of the locking portion is larger than a width of the insertion portion, and the male coupler and the female coupler are not separated after being fastened to each other.
8. A medical fixation apparatus for a lesion, comprising: an elastic fiber having a plurality of hooks at a width-directional edge, applied with water-curable synthetic resin, and being placed on a lesion; a plurality of fixing bands having a Velcro portion on a front thereof; and flat coupler units disposed at the other width-directional edge of the elastic fiber and an end of the fixing band such that the end of the fixing band can be coupled to the elastic fiber.
9. The medical fixation apparatus of claim 8, wherein the coupler unit is composed of a male coupler and a female coupler that are made of a material having predetermined elasticity, the male coupler is composed of a flat body and a locking portion protruding from a side of the body in a fish spear shape, the female coupler is composed of a flat body and an insertion portion formed on a side of the body and being locked to the locking portion, and a width of a rear end of the locking portion is larger than a width of the insertion portion, and the male coupler and the female coupler are not separated after being fastened to each other.
Description
DESCRIPTION OF DRAWINGS
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
MODE FOR INVENTION
[0032] Hereafter, various embodiments are described in detail with reference to the accompanying drawings.
First Embodiment
[0033] As shown in
[0034] The extendable band 10 is made of a rubber material such as Neoprene and has a predetermined width and length. When the medical fixation apparatus 100 for a lesion is applied, the extendable band 10 is usually positioned outside a joint. The extendable band 10 can be easily cut by scissors or a knife, and when curing is finished, the medical fixation apparatus 100 for a lesion can be easily separated by cutting the extendable band 10.
[0035] The elastic fiber 20 is provided in pair and they are coupled (sewn) to both width-directional edges of the extendable band 10. Water-curable synthetic resin is applied (permeated) in the fiber tissues of the elastic fiber 20, so when water (moisture) is provided, the elastic fiber 20 hardens. The pair of elastic fibers 20 surrounds a body part with a fracture, dislocation, a sprain, etc. with the extendable band 10 positioned outside a joint therebetween.
[0036] That is, when a lesion is surrounded with the elastic fibers 20 wetted with water or sprayed with water, the elastic fibers 20 fix the lesion while hardening.
[0037] Further, the elastic fibers 20 may be a polyester knit, a glass fiber knit, a natural fiber, or a synthetic fiber, or may be a knit of natural yarns such as a urethane yarn or a rubber yarn. However, the elastic fiber 20 may be woven in a net shape to be able to elastically extend when they are pulled regardless of the material.
[0038] The coupler unit 30 is formed flat, and a plurality of coupler units 30 is provided with predetermined gaps along the edges that face each other when the pair of elastic fibers 20 surrounds a body part and connects the pair of elastic fibers 20 to each other.
[0039] In the process of manufacturing the medical fixation apparatus 100 for a lesion, a process of putting the elastic fibers 20 sewn with the coupler units 30 in a solution containing water-curable synthetic resin and then squeezing the solution by pressing the elastic fibers 20 with rollers. However, when the coupler units 30 are formed flat with a thickness similar to the thickness of the elastic fibers 20, the possibility of damage to the coupler units 30 due to rollers is remarkably reduced. Further, the operation of the rollers is not interfered with by the coupler units 30, so the water-curable synthetic resin uniformly permeates into the elastic fibers 20.
[0040] The coupler units 30 are composed of male couplers 32 and female couplers 34, and the male couplers 32 and the female couplers 34 are not separated after being fastened, unless they are forcibly damaged. Accordingly, it is possible to easily find out whether the medical fixation apparatus 100 for a lesion has been unexpectedly separated through whether the coupler units 30 have been damaged.
[0041] In more detail, the coupler units 40 are made of synthetic resin (plastic etc.) having predetermined elasticity, and may be coupled to the outer side of the elastic fibers 20 not to come in contact with a skin after an operation.
[0042] As shown in
[0043] The width of the rear portion of the locking portion 32b is larger than the width of the insertion portion 34b.
[0044] That is, when the male coupler 32 is pushed into the female coupler 34, the rear end of the locking portion 32b is locked and fastened in the insertion portion 34b, and the fastened couplers 32 and 34 are not separated unless the locking portion 32b is forcibly damaged. The coupler units 30 having this configuration normally operate even if they are stained with water-curable synthetic resin. After curing, it is possible to easily separate the coupler units 30 by cutting the locking portions 32b.
[0045] On the other hand, unlike Velcro or a slide fastener, flows can pass through the spaces between the coupler units 30 having predetermined gaps. Accordingly, the pair of elastic fibers 20 may have lengths such that they do not completely meet each other to improve ventilation.
[0046] Referring to
[0047] Accordingly, when the splint is unavoidably separated by breaking (cutting) the locking portions 32b of the male couplers 32 due to bathing or additional radiography, the male couplers 32 and the female couplers 34 can be reused.
Second Embodiment
[0048] As shown in
[0049] A groove in which the connector 40 can be inserted is formed in the coupler units 30t and the coupler units 30t are connected through the connector 40. The coupler units 30t may be formed as flat and thin as possible.
[0050] Latchet protrusions 40c are formed at both end portions of the connector 40 so that the connector 40 inserted in the coupler units 30t is not unexpectedly removed.
[0051] As described, when it is required to unavoidably separate the medical fixation apparatus 200 for a lesion and the put it on again, it is possible to pull or reinsert the connector 40 out of or into the coupler units 30t by removing the latchet protrusions 40c with scissors or a knife.
[0052] The connector 40 may be composed of a band section 40a made of an elastic fiber and a pair of columns 40b coupled to both width-directional edges of the band section 40a to be inserted into the coupler units 30t.
[0053] After an operation, the band section 30a faces the extendable band 10. The band section 40a and the extendable band 40 partially reduce excessive pressure that may be applied to a lesion. After curing, it is possible to easily separate the medical fixation apparatus 200 for a lesion by cutting the band section 40a and the extendable band 40 with a knife or scissors.
[0054] According to the medical fixation apparatuses 100 and 200 for a lesion that have the configurations described above, there is little concern of damage to the coupler units 30 and 30t due to rollers in the manufacturing process because they are formed flat.
[0055] Further, since the functions of the coupler units 30 and 30t are not largely deteriorated for the structures even if they are stained with water-curable synthetic resin, there is an effect in that it is to possible to easily apply the apparatus to a patient.
[0056] Further, it is possible to easily find out whether the cast has been unexpectedly separated through whether the coupler units 30 or the connector 40 has been damaged.
Third Embodiment
[0057] As shown in
[0058] Water-curable synthetic resin has been applied (permeated) between the fiber tissues of the elastic fiber 1, so the water-curable synthetic resin hardens when water (moisture) is applied. The elastic fiber 1 is put on a body part with a fracture, dislocation, a sprain, etc.
[0059] That is, when the elastic fibers 1 wetted with water or sprayed with water is brought in close contact with a lesion, the elastic fiber 1 fixes the lesion while hardening.
[0060] Further, the elastic fiber 1 may be a polyester knit, a glass fiber knit, a natural fiber, or a synthetic fiber, or may be a knit of natural yarns such as a urethane yarn or a rubber yarn. However, the elastic fiber 20 may be woven in a net shape to be able to elastically extend when they are pulled regardless of the material
[0061] The fixing bands 2 can be adjusted in length and are coupled to the elastic fiber 1 by the coupler units 3 to be described below. It is possible to easily apply the medical fixation apparatus 300 for a lesion by putting the elastic fiber 1 on an injured body B and the coupling the fixing bands 2 to the elastic fiber 1. Further, the fixing bands 2 are not coupled to the elastic fiber 1 and are separately sold, so there is no concern that the fixing bands 2 lose their functions (Velcro function etc.) by being soaked in water-curable synthetic resin in the manufacturing process.
[0062] The fixing bands 2 are each composed of a first band 2a with a Velcro portion on the front and a second band 2b with a Velcro portion on the bottom, and the first and second bands 2a and 2b are combined in a single unit.
[0063] According to common medical casts, it is required to prevent a patient from freely separating the medical casts, but a medical fixation apparatus for a lesion that is temporarily put on before a cast is applied may be formed in a structure that can be freely separated to be able to check the state (swelling) of a lesion.
[0064] On the other hand, as shown in
[0065] Further, when the fixing band 2 is made of an elastic rubber material, the length may not need to be adjusted.
[0066] The coupler unit 3 is formed flat with a thickness similar to the thickness of the elastic fiber 1 and is disposed at a width-directional edge of the elastic fiber 1, an end of the fixing band 2, the other edge of the elastic fiber 1, and the other end of the fixing band 2 so that the elastic fiber 1 placed on a lesion can be fixed by a plurality of fixing bands.
[0067] In the process of applying (coating) water-curable synthetic resin to the elastic fiber 1, a process of putting the elastic fiber 1 sewn with the coupler units 3 in a solution containing water-curable synthetic resin and then squeezing the solution by pressing the elastic fiber 1 with rollers. However, when the coupler units 3 are formed flat with a thickness similar to the thickness of the elastic fiber 1, the possibility of damage to the coupler units 3 due to rollers is remarkably reduced. Further, the operation of the rollers is not interfered with the coupler units 3, so the water-curable synthetic resin uniformly permeates into the elastic fiber 1.
[0068] As shown in
[0069] The male coupler 32 is composed of a flat body 32a and a locking portion 32b protruding from a side of the body 32a in a fish spear shape (or an arrow shape), and the female coupler 34 is composed of a flat body 34a and an insertion portion 34b formed on a side of the body 34a and being locked to the locking portion 32b of the male coupler 32.
[0070] The width of the rear end of the locking portion 32b is larger than the width of the insertion portion 34b. That is, when the male coupler 32 is pushed into the female coupler 34, the rear end of the locking portion 32b is locked and fastened in the insertion portion 34b.
[0071] The coupler unit 3 may be made of synthetic resin (plastic etc.) having predetermined elasticity and may be coupled to the outer side of the elastic fiber 10 not to be in contact with a skin after an operation.
[0072] Further, when the female couplers 34 are disposed at both edges of the elastic fiber 1 and the male couplers 32 are disposed at both ends of the fixing band 2, there is an effect in that it is possible to more easily apply the medical fixation apparatus 300 for a lesion.
[0073] The coupler unit 3 having the structure described above normally operates even if it is stained with water-curable synthetic resin. Accordingly, there is no need for covering the couplers (32 or 34) on the elastic fiber 1 with a separate vinyl in the process of applying (coating) water-curable synthetic resin to the elastic fiber 1. Further, there is no need for taking special care to prevent the coupler unit 3 from being stained with synthetic resin during an operation.
Fourth Embodiment
[0074] As shown in
[0075] A plurality of hooks 4 is disposed at a width-directional edge of the elastic fiber 1. The hooks 4 are formed flat with a thickness similar to the thickness of the elastic fiber 1 and allow fixing bands 2f to be hooked.
[0076] The fixing bands 2f have a Velcro portion on the front.
[0077] The coupler unit 3 is disposed at the other width-directional edge of the elastic fiber 1 and an end of the fixing band 2f such that the end of the fixing band 2f can be coupled to the elastic fiber 1.
[0078] As shown in
[0079] According to the medical fixation apparatuses 300 and 400 for a lesion that have the configurations described above, the coupler unit 3 is formed flat with a thickness similar to the thickness of the elastic fiber 1, so there is little concern of damage in a process of rolling the elastic fiber 1.
[0080] Further, since the coupler unit 3 does not interfere with rolling, a product with water-curable synthetic resin uniformly applied (coated) to the elastic fiber 1 can be manufactured.
[0081] Further, since the function of the coupler unit 3 is not largely deteriorated even if it is stained with water-curable synthetic resin, there is no need for covering the coupler unit 3 with a separate vinyl cover in the manufacturing process and the apparatus can be easily applied to a patient.
TABLE-US-00001 <Description of the Reference Numerals in the Drawings> 100, 100: Medical fixation apparatus for 10: Extendable band a lesion 20: Elastic fiber 30, 30: Coupler unit 32: Male coupler 32a: Body 32b: Locking portion 32c: Accommodating portion 34: Female coupler 34a: Body 34b: Insertio nportion 34c: Connection block 34d; Locking protrusion 40: Connector 40a: Band section 40b: Column 40c: Latchet protrusion