[Technical Field]
[0001] The present invention relates to a piston cover of a cardiopulmonary resuscitation
device, and more specifically, to a piston cover of a cardiopulmonary resuscitation
device capable of continuously providing a cushioning effect that relieves and distributes
pressure applied to a chest of a patient during an emergency treatment process for
the patient.
[Background Art]
[0002] In the related art, various types of cardiopulmonary resuscitation (CPR) devices
are known. One of the devices is driven by compressed air or breathing gas (Jolife
AB, Lund, Sweden; LucasTM). A unique advantage of the cardiopulmonary resuscitation
device is light weight thereof, which makes it portable. Another advantage is the
elastic properties of compressed air, which makes gas-driven cardiopulmonary resuscitation
devices less likely to cause damage to a chest of a patient than devices with rigid
compression means. The known device may be used as an emergency device in life-saving
situations. Furthermore, in a known device, the motive gas may be supplied from a
hospital air supply line which may be desirable for uninterrupted bursts of cardiopulmonary
resuscitation when a patient is admitted.
[0003] However, even when elastic properties of compressed air are used, since a material
of a compression means itself is hard, when the compression means compresses a chest
of a patient, strong pressure is applied to the chest of the patient, which may cause
rib fractures and hemothorax during cardiopulmonary resuscitation.
[Disclosure]
[Technical Problem]
[0004] Accordingly, an object of the present invention is to provide a piston cover of a
cardiopulmonary resuscitation device capable of continuously providing a cushioning
effect for relieving and distributing pressure applied to a chest of a patient during
a chest compression process of the patient in order to improve the conventional compression
means.
[0005] However, the technical problems to be achieved in the present invention are not limited
to the technical problems mentioned above, and other technical problems not mentioned
can be clearly understood by a person having ordinary knowledge in the technical field
to which the present invention belongs from the description below.
[Technical Solution]
[0006] In order to achieve the above purpose, in a cover fit-coupled to a piston 310 for
compressing a chest of a patient provided in a cardiopulmonary resuscitation device
according to one exemplary embodiment of the present invention, the cover may include:
a first pad 600 in which a first pad upper portion 610 and a first pad lower portion
620 are integrally formed with each other, the first pad upper portion including a
pair of grooves 6024a and 6024b formed between a first piston fitting portion 611a
and a second piston fitting portion 611b, and between a third piston fitting portion
611c and a fourth piston fitting portion 611d forming a piston fitting hole 6110 and
a piston fitting portion 611 in which a fastening member formed in a part of an outer
peripheral surface of the piston 310 is inserted into the pair of grooves 6024a and
6024b when the piston 310 is fit-coupled to the piston fitting hole 6110, and the
first pad lower portion compressing a chest compression point of the patient with
a lower surface of the first pad lower portion while generating a negative pressure
when the piston 310 is expanded and pulling the chest of the patient with the lower
surface and moving the chest upward through the negative pressure when the piston
310 is contracted; and a first plate 700 including a protruding member 720 fit-coupled
to the first pad lower portion 620 and fit-coupled to the first pad lower portion
620 to form an interspace A.
[0007] In addition, in a cover fit-coupled to a piston 310 for compressing a chest of a
patient provided in a cardiopulmonary resuscitation device according to another exemplary
embodiment of the present invention, the cover may include: a second pad 800 in which
a second pad upper portion 810 and a second pad lower portion 820 are integrally formed
with each other, the second pad upper portion including a pair of grooves 8024a and
8024b formed between a first piston fitting portion 811a and a second piston fitting
portion 811b, and between a third piston fitting portion 811c and a fourth piston
fitting portion 811d forming a piston fitting hole 8110 and a piston fitting portion
811 in which a fastening member formed in a part of an outer peripheral surface of
the piston 310 is inserted into the pair of grooves 8024a and 8024b when the piston
310 is fit-coupled to the piston fitting hole 8110, and the second pad lower portion
compressing a chest compression point of the patient with a lower surface of the second
pad lower portion while generating a negative pressure when the piston 310 is expanded
and pulling the chest of the patient with the lower surface and moving the chest upward
through the negative pressure when the piston 310 is contracted; and a second plate
900 including a first protruding member 920 and a second protruding member 930 fit-coupled
to the second pad lower portion 820 and fit-coupled to the second pad lower portion
820 to form interspaces A and B.
[Advantageous Effects]
[0008] The cover of the present invention has the effect of preventing rib fractures and
hemothorax from occurring during a chest compression process by continuously providing
a cushioning effect of relieving and distributing the pressure applied to a chest
of a patient during the chest compression process of the patient, to the patient.
[0009] However, the effects obtainable from the present invention are not limited to the
effects mentioned above, and other effects not mentioned will be clearly understood
by those skilled in the art to which the present invention belongs from the description
below.
[Description of Drawings]
[0010]
FIG. 1 is a perspective view of a cardiopulmonary resuscitation device according to
one exemplary embodiment of the present invention.
FIG. 2 is a schematic view of the cardiopulmonary resuscitation device illustrated
in FIG. 1.
FIG. 3 is a perspective view of a first pad constituting a cover according to one
exemplary embodiment of the present invention.
FIG. 4 is a cross-sectional view taken along line A-A of FIG. 3.
FIG. 5 is a perspective view of a first pad lower portion included in an area B illustrated
in FIG. 4.
FIG. 6 is a plan view of the first pad lower portion included in the area B illustrated
in FIG. 4.
FIG. 7 is a perspective view of a second pad constituting a cover according to another
exemplary embodiment of the present invention.
FIG. 8 is a cross-sectional view taken along line C-C of FIG. 7.
FIG. 9 is a perspective view of a second pad lower portion included in an area D illustrated
in FIG. 8.
FIG. 10 is a plan view of the second pad lower portion included in the area D illustrated
in FIG. 8.
[Best Mode]
[0011] Hereinafter, with reference to the attached drawings, exemplary embodiments of the
present invention will be described in detail so that those skilled in the art can
easily implement the present invention. However, since the description of the present
invention is merely an exemplary embodiment for structural and functional explanation,
the scope of the rights of the present invention should not be construed as being
limited by the exemplary embodiments described in the text. That is, since the exemplary
embodiments can be variously modified and can have various forms, the scope of the
rights of the present invention should be understood to include equivalents that can
realize the technical idea. In addition, the purpose or effect presented in the present
invention does not mean that a specific exemplary embodiment must include all of them
or only such effects, and therefore the scope of the rights of the present invention
should not be understood as being limited thereby.
[0012] The meanings of terms described in the present invention should be understood as
follows.
[0013] The terms "first", "second", or the like are intended to distinguish one component
from another, and the scope of the right should not be limited by these terms. For
example, the first component may be referred to as the second component, and similarly,
the second component may also be referred to as the first component. When a component
is referred to as being "connected" to another component, it should be understood
that it may be directly connected to the other component, but there may also be another
component therebetween. Meanwhile, when a component is referred to as being "directly
connected" to another component, it should be understood that there is no other component
in between. Moreover, other expressions that describe the relationship between components,
such as "between" and "directly between" or "adjacent to" and "directly adjacent to",
should be interpreted in the same way.
[0014] A singular expression should be understood to include the plural expression unless
the context clearly indicates otherwise, and the terms "include" or "have" should
be understood to specify the presence of a stated feature, number, step, operation,
component, part, or combination thereof, but not to exclude the possibility of the
presence or addition of one or more other features, numbers, steps, operations, components,
parts, or combinations thereof.
[0015] All terms used herein, unless otherwise defined, have the same meaning as commonly
understood by a person of ordinary skill in the art to which the present invention
belongs. Terms defined in commonly used dictionaries should be interpreted as having
a meaning consistent with the contextual meaning of the relevant art, and shall not
be interpreted as having an ideal or overly formal meaning unless explicitly defined
in the present invention.
[0016] FIG. 1 is a perspective view of a cardiopulmonary resuscitation device according
to one exemplary embodiment of the present invention, and FIG. 2 is a schematic view
of the cardiopulmonary resuscitation device illustrated in FIG. 1.
[0017] Referring to FIG. 1 and FIG. 2, the cardiopulmonary resuscitation device of the present
invention includes a base plate 100, a support 200, and a hood 300 for compressing
a chest of a patient.
[0018] The base plate 100 is formed in a shape to support a back of a patient requiring
cardiopulmonary resuscitation, and includes a sliding guide 110 for sliding the support
200 and the hood 300 and a stopper 120 for fixing the positions of the support 200
and the hood 300.
[0019] In the base plate 100, an internal space into which a frame 115 provided in the sliding
guide 110 can be inserted to adjust the height of a piston 310 is formed on a side
portion of the base plate 100.
[0020] The sliding guides 110 are provided on both sides of the base plate 100, and one
end and the other end of the support 200 are coupled to be slidable, allowing the
support 200 to slide forward or backward.
[0021] As illustrated in (b) of FIG. 2, which is an enlarged view of an area A illustrated
in (a) of FIG. 2, the sliding guide 110 is provided with the frame 115 that is inserted
into or withdrawn from the inside of the base plate 100, thereby allowing the distance
between both ends of the support 200 to be adjusted, thereby adjusting the height
of the piston 310.
[0022] In this case, the reason why the height of the piston 310 is adjusted is to prevent
a situation in which a chest of a specific patient cannot be compressed by the piston
310 because each patient has a different body shape.
[0023] The stopper 120 is provided in the sliding guide 110 and is formed in a form that
can be connected to one end and the other end of the support 200 to connect one end
and the other end of the support 200, and fixes the positions of the support 200 and
the hood 300 through connection to one end and the other end of the support 200.
[0024] The support 200 is coupled to the sliding guide 110 to move a lower end of the piston
310 to a position where the lower end compresses the chest of the patient, and in
one exemplary embodiment of the present invention, the shape for supporting the hood
300 may be arched, but is not limited thereto.
[0025] One end and the other end of the support 200 are movably coupled to the pair of sliding
guides 110, and thus, the support may slide forward or backward with the sliding guide
110 as an axis, or a distance between both ends of the support may be adjusted by
inserting and withdrawing the frame 115.
[0026] It is preferable that the forward and backward sliding movement of the support 200
and the distance adjustment between both ends are performed before the piston 310
compresses the chest of the patient, and when the support 200 moves to a position
for the piston 310 to compress and relax the chest of the patient, one end and the
other end are fastened by the pair of stoppers 120.
[0027] The support 200 is configured in a form in which one end and the other end are attached
to and detached from the pair of sliding guides 110, and can be attached to and detached
from the pair of sliding guides 110. Through attachment and detachment, the support
is attached to and detached from the base plate 100 together with the hood 300 and
may be used as a separate device.
[0028] The hood 300 is coupled to one side of the support 200, more specifically, to the
center portion (arch crown) of the arch-shaped support 200, and includes the piston
310 for compressing the chest of the patient and a control unit 320 for contracting
or expanding the piston 310.
[0029] In the hood 300, the control unit 320 may be exposed to the outside or installed inside.
[0030] The piston 310 is separated from the chest of the patient before compressing the
chest of the patient, and may repeat a process of being operated by the control unit
320 to compress the chest of the patient and then being separated to relax the chest
of the patient.
[0031] The piston 310 may be operated based on a compression continuous mode that continuously
compresses the chest of the patient according to a chest compression mode set through
the control unit 320, or a compression 30 : 2 mode that performs chest compression
and artificial respiration of the patient simultaneously by performing 2 artificial
respirations after performing 30 chest compressions of the patient, and thus, the
chest compressionbased emergency treatment can be provided to the patient.
[0032] The control unit 320 may control the operation of the cardiopulmonary resuscitation
device as well as the operation of the piston 310, and may be provided with a plurality
of buttons for this purpose.
[0033] The plurality of buttons is not illustrated in the drawings, but as a specific example,
the plurality of buttons may include a power button for turning the cardiopulmonary
resuscitation device on/off, a stop button for stopping the operation of the piston
310, a compression mode setting button for causing the piston 310 to perform chest
compression (CPR) of a patient or for setting the chest compression mode of the piston
310, a compression depth setting button for setting the chest compression depth of
the piston 310, and a compression speed setting button for setting the chest compression
speed (number of times) of the piston 310.
[0034] The above control unit 320 performs a self-test to determine whether the settings
are initialized and normal operation is possible when an input signal is input to
the power button and the cardiopulmonary resuscitation device is turned on. When the
cardiopulmonary resuscitation device is on, in a case where the input signal is input
to the power button again, the settings are initialized and the cardiopulmonary resuscitation
device is turned off.
[0035] The control unit 320 controls the operation of the piston 310 so that the chest of
the patient is repeatedly compressed and relaxed when the chest compression mode set
through the compression mode setting button is the compression continuous mode. Meanwhile,
when the chest compression mode set through the compression mode setting button is
the compression 30 : 2 mode, the operation of the piston 310 may be controlled so
that two artificial respirations are performed after the chest of the patient is compressed
30 times.
[0036] The control unit 320 may control the operation of the piston 310 so that the chest
of the patient is compressed to at least one depth of 4 cm, 4.5 cm, 5 cm, and 5.5
cm when the input signal is input to the compression depth setting button, and further,
may control the operation of the piston 310 so that the chest of the patient is compressed
to 5 cm when the input signal is input to the compression depth setting button in
an initialization state, thereafter, the chest of the patient is compressed to 5.5
cm when the signal is input, the chest of the patient is compressed to 4 cm when the
signal is input again, and the chest of the patient is compressed to 4.5 cm when the
signal is input again.
[0037] The control unit 320 may control the operation of the piston 310 so that the chest
of the patient is compressed at least one of 100, 110, and 120 times when the input
signal is input to the compression speed setting button, and further, may control
the operation of the piston 310 so that the chest of the patient is compressed 110
times when the input signal is input to the compression speed setting button in the
initialization state, the chest of the patient is compressed 120 times when the signal
is input again, and the chest of the patient is compressed 100 times when the signal
is input again.
[0038] The cardiopulmonary resuscitation device may include a cover that is mounted on the
lower end of the piston 310, is made of a material having a different hardness from
that of the piston 310 of a hard material, and can continuously provide a cushioning
effect that relieves and distributes the pressure applied to the chest of the patient.
[0039] According to one exemplary embodiment of the present invention, as illustrated in
FIGS. 3 to 6, the cover may include a first pad 600 to which the lower end of a piston
310 is fit-coupled to directly compress the chest of the patient, and a first plate
700 which is fit-coupled to the first pad 600 to form the interspace A and disposed
inside the first pad 600.
[0040] FIG. 3 is a perspective view of a first pad constituting a cover according to one
exemplary embodiment of the present invention, FIG. 4 is a cross-sectional view taken
along line A-A of FIG. 3, FIG. 5 is a perspective view of a first pad lower portion
included in an area B illustrated in FIG. 4, and FIG. 6 is a plan view of the first
pad lower portion included in the area B illustrated in FIG. 4.
[0041] Referring to FIGS. 3 to 6, the first pad 600 has an outer shape including a first
pad upper portion 610 to which the lower end of the piston 310 is fit-coupled and
a first pad lower portion 620 for compressing the chest of the patient with the lower
surface of the first pad lower portion, and the first pad upper portion 610 may have
a piston fitting portion 611 formed therein.
[0042] The first pad upper portion 610 forms a piston fitting hole 6110 by the piston fitting
portion 611 that is integrally formed in a shape bent from the first pad lower portion
620, and the piston 310 may be fastened to the first pad upper portion 610 when the
lower end portion of the piston comes into contact with the first plate 700, and then
a fastening member (not illustrated) formed in a part of the outer peripheral surface
is inserted into the piston fitting hole 6110 through rotation of the cover.
[0043] The piston fitting portion 611 forms the piston fitting hole 6110, and the lower
end of the piston 310 may be fit-coupled to the first pad upper portion 610 through
the piston fitting hole 6110.
[0044] Moreover, the piston fitting portion 611 is a part formed by being bent from the
first pad upper portion 610 to form the piston fitting hole 6110 into which the piston
310 can be inserted, and may include a first piston fitting portion 611a, a second
piston fitting portion 611b, a third piston fitting portion 611c, and a fourth piston
fitting portion 611d.
[0045] In addition, the piston fitting portion 611 has a pair of grooves 6024a and 6024b formed
between the first piston fitting portion 611a and the second piston fitting portion
611b and between the third piston fitting portion 611c and the fourth piston fitting
portion 611d, and when the piston 310 is fit-coupled to the piston fitting hole 6110,
the fastening member formed in a part of the outer peripheral surface of the piston
310 may be inserted into the pair of grooves 6024a and 6024b.
[0046] That is, the piston 310 may be fastened to the first pad 600 by the fastening member
being inserted into the pair of grooves 6024a and 6024b while the lower end portion
of the piston comes into contact with the first plate 700.
[0047] Moreover, the piston fitting portion 711 may have a lower portion that may expand
(or flow) toward the outside of the first pad upper portion 610 so that the fastening
member of the piston 310 may be inserted into or withdrawn from the pair of grooves
6024a and 6024b during the process of engaging and disengaging the fastening member
of the piston 310 and the pair of grooves 6024a and 6024b, and for this purpose, an
expansion space 7101 may be formed in the interspace between the piston fitting portion
and the first pad upper portion 610.
[0048] The first pad upper portion 610 may be made of at least one of polyurethane, polypropylene,
and biocompatible silicone, which are materials with high hardness, so that the contraction
and expansion of the piston 310 and the force therefor can be transmitted to the cap
regardless of various external forces that may be applied from the outside.
[0049] In addition, the first pad upper portion 610 may have a hardness of 40 to 60 shore
A in the case of biocompatible silicone, and a hardness of 25 to 30 asker C in the
case of other materials. In one exemplary embodiment of the present invention, the
asker C hardness may be measured by an asker hardness tester that applies a predetermined
shape of indenter to the surface of a sample with the force of a spring and measures
the hardness based on the depth into which the indenter is indented into the sample
in a state where the resistance of the sample and the force of the spring are balanced,
and the shore hardness measures the height of the rebound when an object with a small
diamond fixed to the end of the object is dropped from a certain height.
[0050] The first pad lower portion 620 is the part of the area B of FIG. 4, may be formed
integrally with the first pad upper portion 610, and may directly contact the chest
compression point of the patient and compress the chest of the patient when the piston
310 is extended toward the chest of the patient.
[0051] The first pad lower portion 620 has an outer shape formed by a housing 621, and the
housing 621 may be provided with a plurality of air flow holes 623 and a seating portion
624.
[0052] In addition, the housing 621 includes an outer housing 621a and an inner housing
621b integrally formed with each other, and the lower surface of the housing comes
into contact with the chest of the patient.
[0053] Moreover, the housing 621 has a protruding member insertion hole 622 formed at the
boundary between the outer housing 621a and the inner housing 621b to enable the fit-coupling
of the protruding member 720 provided in the first plate 700.
[0054] The protruding member insertion hole 622 may be formed in a circular shape at the
boundary between the outer housing 621a and the inner housing 621b to enable the fit-coupling
of the protruding member 720.
[0055] The outer housing 621a and inner housing 621b may be implemented in a bellows shape
to allow for a change in the volume of the interspace A.
[0056] In addition, the upper portions of the outer housing 621a and the inner housing 621b
are fit-coupled to the bottom portion 710 of the first plate 700, and an adhesive
means (for example, an adhesive) may be provided (or applied) to the upper portions
of the outer housing 621a and the inner housing 621b so that the fit-coupling structure
of the first pad 600 and the first plate 700 is maintained. However, the adhesive
means is not limited to being provided on the upper portions of the outer housing
621a and the inner housing 621b, and may be provided on the bottom portion 710.
[0057] In addition, the outer housing 621a and the inner housing 621b have side walls that
form the protruding member insertion hole 622 protruding upward, thereby generating
the interspace A between the inner housing 621b and the first plate 700 in the fit-coupling
structure of the first pad 600 and the first plate 700.
[0058] The inner housing 621b has a plurality of air flow holes 623 formed on the lower
surface so that when pressure is transmitted from the chest of the patient to the
lower surface during the chest compression process of the patient, a change in volume
occurs through the air flow in the interspace A.
[0059] The volume of the interspace A between the upper side of the inner housing 621b and
the first plate 700 may decrease when air flows outward along the air flow hole 623
by the piston 310 that expands during the chest compression process of the patient,
and in contrast, when the piston is separated from the chest of the patient after
the compressing the chest of the patient is completed, the volume of the interspace
may increase according to the air introduced through the air flow hole 623.
[0060] The inner housing 621b has the lower surface that comes into contact with the chest
of the patient during the chest compression process of the patient, and as the piston
310 expands, air flows outward from the interspace A, and thus, the volume of the
interspace A decreases. Therefore, when the seating portion 624 provided in the interspace
A comes into contact with the bottom portion 710 of the first plate 700, a negative
pressure is generated in the interspace A, and when the piston 310 is contracted after
the negative pressure is generated in the interspace A, the lower surface that comes
into contact with the chest compression point of the patient may move upward while
pulling the chest of the patient.
[0061] As such, the first pad lower portion 620 is made of at least one of ethylene-vinyl
acetate, polyethylene, polyethylene-polypropylene blend, polystyrene, neoprene, chloroprene,
polyurethane, and biocompatible silicone, and due to the characteristics of these
materials, the first pad lower portion may be implemented as a shape that conforms
to the shape of the chest of the patient.
[0062] Moreover, in the first pad lower portion 620, the biocompatible silicone may have
a hardness of 10 to 30 shore A, and other materials may have a hardness of 10 to 20
asker C.
[0063] Meanwhile, the first pad lower portion 620 needs to conform to the chest of the patient
when compressing the chest of the patient, and accordingly, the lower surface of the
inner housing 621b that comes into contact with the chest compression point of the
patient is preferably made of biocompatible silicone that easily conforms to the chest
of the patient among applicable materials, thereby continuously providing a cushioning
effect that relieves and distributes the pressure applied to the chest of the patient,
thereby preventing rib fractures and hemothorax from occurring during the chest compression
process of the patient.
[0064] When the first plate 700 is fit-coupled to the first pad lower portion 620, the bottom
portion 710 faces the seating portion 624 with the interspace A therebetween.
[0065] The lower surface of the bottom portion 710 may come into contact with the seating
portion 624 when the volume of the interspace A decreases during the process of compressing
the chest of the patient.
[0066] The protruding member 720 that can be fit-coupled to a protruding member insertion
hole 622 to be fit-coupled to the first pad lower portion 620 protrudes from the bottom
portion 710 of the first plate 700.
[0067] The protruding member 720 may protrude in a circular shape to be fit-coupled into
the protruding member insertion hole 622.
[0068] As such, the cover of the present invention is not limited to being implemented only
through the fit-coupling of the first pad 600 and the first plate 700, and may also
be implemented by fit-coupling of a second pad 800 that is a modified version of the
first pad 600 and a second plate 900 that is a modified version of the first plate
700.
[0069] Hereinafter, a cover according to another exemplary embodiment of the present invention
implemented through the fit-coupling of the second pad 800 and the second plate 900
will be described in detail.
[0070] FIG. 7 is a perspective view of a second pad constituting the cover according to
another exemplary embodiment of the present invention, FIG. 8 is a cross-sectional
view taken along line C-C of FIG. 7, FIG. 9 is a perspective view of a second pad
lower portion included in an area D illustrated in FIG. 8, and FIG. 10 is a plan view
of the second pad lower portion included in the area D illustrated in FIG. 8.
[0071] Referring to FIGS. 7 to 10, the second pad 800 has an outer shape including a second
pad upper portion 810 to which the lower end of the piston 310 is fit-coupled and
a second pad lower portion 820 for compressing the chest of the patient with the lower
surface of the second pad lower portion, and the second pad upper portion 810 may
have a piston fitting portion 811 formed therein.
[0072] The second pad upper portion 810 forms a piston fitting hole 8110 by the piston fitting
portion 811 that is integrally formed in a shape bent from the second pad lower portion
820, and the piston 310 may be fastened to the second pad upper portion 810 when the
lower end portion of the piston comes into contact with the second plate 900, and
then a fastening member (not illustrated) formed in a part of the outer peripheral
surface is inserted into the piston fitting hole 8110 through rotation of the cover.
[0073] The piston fitting portion 811 forms the piston fitting hole 8110, and the lower
end of the piston 310 may be fit-coupled to the second pad upper portion 810 through
the piston fitting hole 8110.
[0074] Moreover, the piston fitting portion 811 is a part formed by being bent from the
second pad upper portion 810 to form the piston fitting hole 8110 into which the piston
310 can be inserted, and may include a first piston fitting portion 811a, a second
piston fitting portion 811b, a third piston fitting portion 811c, and a fourth piston
fitting portion 811d.
[0075] In addition, the piston fitting portion 811 has a pair of grooves 8024a and 8024b formed
between the first piston fitting portion 811a and the second piston fitting portion
811b and between the third piston fitting portion 811c and the fourth piston fitting
portion 811d, and when the piston 310 is fit-coupled to the piston fitting hole 8110,
the fastening member formed in a part of the outer peripheral surface of the piston
310 may be inserted into the pair of grooves 8024a and 8024b.
[0076] That is, the piston 310 may be fastened to the second pad 800 by the fastening member
being inserted into the pair of grooves 8024a and 8024b while the lower end portion
of the piston comes into contact with the second plate 900.
[0077] Moreover, the piston fitting portion 811 may have a lower portion that may expand
(or flow) toward the outside of the second pad upper portion 810 so that the fastening
member of the piston 310 may be inserted into or withdrawn from the pair of grooves
8024a and 8024b during the process of engaging and disengaging the fastening member
of the piston 310 and the pair of grooves 8024a and 8024b, and for this purpose, an
expansion space 8101 may be formed in the interspace between the piston fitting portion
and the second pad upper portion 810.
[0078] The second pad upper portion 810 may be made of at least one of polyurethane, polypropylene,
and biocompatible silicone, which are materials with high hardness, so that the contraction
and expansion of the piston 310 and the force therefor can be transmitted to the cap
regardless of various external forces that may be applied from the outside.
[0079] In addition, the second pad upper portion 810 may have a hardness of 40 to 60 shore
A in the case of biocompatible silicone, and a hardness of 25 to 30 asker C in the
case of other materials.
In one exemplary embodiment of the present invention, the asker C hardness may be measured
by an Asker hardness tester that applies a predetermined shape of indenter to the
surface of a sample with the force of a spring and measures the hardness based on
the depth into which the indenter is indented into the sample in a state where the
resistance of the sample and the force of the spring are balanced, and the shore hardness
measures the height of the rebound when an object with a small diamond fixed to the
end of the object is dropped from a certain height.
[0080] The second pad lower portion 820 is the part of the area D of FIG. 8, may be formed
integrally with the second pad upper portion 810, and may directly contact the chest
compression point of the patient and compress the chest of the patient when the piston
310 is extended toward the chest of the patient.
[0081] The second pad lower portion 820 has an outer shape formed by a housing 821, and
the housing 821 may be divided into a first housing 821a and a second housing 821b
formed integrally with each other, and may include a plurality of air flow holes 823,
a first seating portion 824, a second seating portion 825, and a partition 826.
[0082] The first housing 821a includes a first protruding member insertion hole 822a into
which the first protruding member 920 of the second plate 900 is to be fit-coupled,
thereby enabling the fit-coupling of the second pad 800 and the second plate 900.
[0083] The first housing 821a may be divided into a plurality of interspaces A in which
negative pressure is generated through a plurality of partitions 826. Therefore, when
the volume of the interspaces A is reduced by receiving pressure from the chest of
the patient, not only may all of the plurality of lower surfaces move toward the bottom
portion 910 of the second plate 900, but also only some of the lower surfaces that
come into contact with the chest compression point of the patient and receives a pressure
of a certain strength or greater from the chest of the patient among the plurality
of lower surfaces may move toward the bottom portion 712.
[0084] It is preferable that the first protruding member insertion hole 822a is formed in
a circular shape on the first housing 821a so that the first protruding member 920
can be fit-coupled to the first protruding member insertion hole.
[0085] The second housing 821b is connected to the first housing 821a through the plurality
of partitions 826 in the structure of the housing 821, and includes a second protruding
member insertion hole 822b into which the second protruding member 930 of the second
plate 900 is to be fit-coupled, so that the fit-coupling of the second pad 800 and
the second plate 900 are implemented together with the first housing 821a.
[0086] It is preferable that the second protruding member insertion hole 822b is formed
in a circular shape on the second housing 821b so that the second protruding member
930 can be fit-coupled to the second protruding member insertion hole.
[0087] The side walls of the first housing 821a and the second housing 821b may protrude
upward so that the interspaces A and B are generated between the bottom portion 910
of the second plate 900 and the first housing and the second housing in the fit-coupling
structure of the second pad 800 and the second plate 900.
[0088] In addition, the first housing 821a and the second housing 821b may be implemented in
a bellows shape so that the volumes of the interspaces A and B can be changed.
[0089] In addition, the upper portions of the first housing 821a and the second housing 821b
are coupled to the bottom portion 910 of the second plate 900, and an adhesive means
(for example, an adhesive) may be provided (or applied) to the upper portions of the
first housing 821a and the second housing 821b so that the fit-coupling structure
of the second pad 800 and the second plate 900 is maintained. However, the adhesive
means is not limited to being provided on the upper portions of the first housing
821a and the second housing 821b, and may be provided on the bottom portion 910.
[0090] The plurality of air flow holes 823 is formed on the lower surfaces of the first
housing 821a and the second housing 821b, respectively, and may include a plurality
of first air flow holes 823a formed on the lower surface of the first housing 821a
and a plurality of second air flow holes 823b formed on the lower surface of the second
housing 821b.
[0091] The first and second air flow holes 823a and 823b may reduce the volumes of the interspaces
A and B by causing the air in the interspace A between the bottom portion 910 of the
second plate 900 and the first housing 821a and the interspace B between the bottom
portion 910 and the second housing 821b to flow outward during the process of compressing
the chest of the patient through the expansion of the piston 310.
[0092] A plurality of first seating portions 824 may be formed to be provided in the interspaces
A of the first housing 821a divided into a plurality of portions through the plurality
of partitions 826, and when the air in the interspace A flows outward from the plurality
of first air flow holes 823a and the volume of the interspace A decreases, the first
seating portions come into contact with the bottom portion 910 of the second plate
900 so that the interspace A may be in a negative pressure state.
[0093] As a specific example, when a peripheral portion of the lower surface of the bottom
portion 910 which surrounds the center portion of the lower surface of the bottom
portion 910 of the second plate 900 and is parallel to the first seating portion 824
in a vertical direction moves downward due to downward pressure applied from the fastening
member provided on the piston 310 through the expansion of the piston 310, the first
seating portion 824 comes into contact with the peripheral portion of the lower surface
of the bottom portion 910. Accordingly, the partitioned interspace A may be in a negative
pressure state.
[0094] The second seating portion 825 may be provided in the interspace B of the second
housing 821b, and when the air in the interspace B partitioned by the plurality of
second air flow holes 823b flows to the outside and the volume of the interspace B
decreases, the second seating portion comes into contact with the bottom portion 910
of the second plate 900 so that the interspace B may be in a negative pressure state.
[0095] As a specific example, when the center portion of the lower surface of the bottom
portion 910 that is parallel to the second seating portion 825 in the vertical direction
in the bottom portion 910 of the second plate 900 is moved downward due to the downward
pressure applied through the expansion of the piston 310, the second seating portion
825 comes into contact with the center portion of the lower surface of the bottom
portion 910. Accordingly, the interspace B may be in a negative pressure state.
[0096] It is preferable that the plurality of partitions 826 is provided to partition the
interspace A of the first housing 821a into a plurality of portions, and each partition
826 may be provided in a shape that connects the first housing 821a and the second
housing 821b.
[0097] As such, the second pad lower portion 820 is made of at least one of ethylene-vinyl
acetate, polyethylene, polyethylene-polypropylene blend, polystyrene, neoprene, chloroprene,
polyurethane, and biocompatible silicone, and due to the characteristics of these
materials, the second pad lower portion 820 may be implemented as a shape that conforms
to the shape of the chest of the patient.
[0098] Moreover, in the second pad lower portion 820, the biocompatible silicone may have
a hardness of 10 to 30 shore A, and other materials may have a hardness of 10 to 20
asker C.
[0099] Meanwhile, the second pad lower portion 820 needs to conform to the chest of the
patient when compressing the chest of the patient, and accordingly, the lower surfaces
of the first and second housings 821a and 821b that come into contact with the chest
compression point of the patient are preferably made of biocompatible silicone that
easily conforms to the chest of the patient among applicable materials, thereby continuously
providing a cushioning effect that relieves and distributes the pressure applied to
the chest of the patient, thereby preventing rib fractures and hemothorax from occurring
during the chest compression process of the patient.
[0100] When the second plate 900 is fit-coupled to the second pad lower portion 820, the
bottom portion 910 faces the first seating portion 824 and the second seating portion
825 with the interspaces A and B therebetween.
[0101] The lower surface of the bottom portion 910 may come into contact with the seating
portion 624 when the volumes of the interspaces A and B decrease during the process
of compressing the chest of the patient.
[0102] The second plate 900 includes the first protruding member 920 that can be fit-coupled
to the first protruding member insertion hole 822a so as to be fit-coupled to the
second pad lower portion 820, and the second protruding member 930 that is positioned
closer to the center portion of the bottom portion 910 than the first protruding member
920 and can be fit-coupled to the second protruding member insertion hole 822b.
[0103] The first protruding member 920 may protrude in a circular shape from the bottom
portion 910 so as to be fit-coupled into the first protruding member insertion hole
822a.
[0104] The second protruding member 930 may protrude in a circular shape from the bottom
portion 910 so as to be fit-coupled into the second protruding member insertion hole
822b.
[0105] The cover according to another exemplary embodiment of the present invention has
an advantage in that the fit-coupling structure between the pad and the plate is reinforced
by implementing the fit-coupling between the second pad 800 and the second plate 900
through a relatively large number of protruding members 920 and 930 compared to the
cover according to one exemplary embodiment of the present invention.
[0106] The detailed description of the preferred exemplary embodiments of the present invention
disclosed above has been provided to enable those skilled in the art to implement
and practice the present invention. While the above has been described with reference
to preferred exemplary embodiments of the present invention, it will be understood
by those skilled in the art that various modifications and changes can be made to
the present invention without departing from the scope of the present invention. For
example, those skilled in the art can utilize each of the configurations described
in the above-described exemplary embodiments in a manner that combines them. Accordingly,
the present invention is not intended to be limited to the exemplary embodiments illustrated
herein, but is to be accorded the widest scope consistent with the principles and
novel features disclosed herein.
[0107] The present invention can be embodied in other specific forms without departing from
the technical spirit and essential characteristics of the present invention. Therefore,
the above detailed description should not be construed as restrictive in all aspects
but should be considered as illustrative. The scope of the present invention should
be determined by reasonable interpretation of the appended claims, and all changes
coming within the equivalent scope of the present invention are intended to be included
in the scope of the present invention. The present invention is not intended to be
limited to the exemplary embodiments set forth herein but is to be accorded the widest
scope consistent with the principles and novel features disclosed herein. In addition,
claims that do not have an explicit citation relationship in the claims may be combined
to constitute an exemplary embodiment or may be included as a new claim by post-application
amendment.
[0108] The piston cover of the cardiopulmonary resuscitation device of the present invention
can continuously provide a cushioning effect to the patient to relieve and distribute
the pressure applied to the chest of the patient during the chest compression process
of the patient, thereby preventing rib fractures and hemothorax from occurring during
the chest compression process. Therefore, the present invention has industrial applicability.
1. A piston cover fit-coupled to a piston (310) for compressing a chest of a patient
provided in a cardiopulmonary resuscitation device, the piston cover comprising:
a first pad (600) in which a first pad upper portion (610) and a first pad lower portion
(620) are integrally formed with each other, the first pad upper portion including
a pair of grooves (6024a and 6024b) formed between a first piston fitting portion
(611a) and a second piston fitting portion (611b), and between a third piston fitting
portion (611c) and a fourth piston fitting portion (611d) forming a piston fitting
hole (6110) and a piston fitting portion (611) in which a fastening member formed
in a part of an outer peripheral surface of the piston (310) is inserted into the
pair of grooves (6024a and 6024b) when the piston (310) is fit-coupled to the piston
fitting hole (6110), and the first pad lower portion compressing a chest compression
point of the patient with a lower surface of the first pad lower portion while generating
a negative pressure when the piston (310) is expanded and pulling the chest of the
patient with the lower surface and moving the chest upward through the negative pressure
when the piston (310) is contracted; and
a first plate (700) including a protruding member (720) fit-coupled to the first pad
lower portion (620) and fit-coupled to the first pad lower portion (620) to form an
interspace (A).
2. The piston cover of claim 1, wherein the first pad lower portion (620) includes
a housing (621) including an outer housing (621a) and an inner housing (621b) of which
upper portions are coupled to a bottom portion (710) of the first plate (700) and
which are integrally formed with each other,
a plurality of air flow holes (623) formed on a lower surface of the inner housing
(621b) so that air in an interspace (A) between the inner housing (621b) and the bottom
portion (710) flows, and
a seating portion (624) provided in the interspace (A) to comes into contact with
the bottom portion (710) when the air in the interspace (A) flows outward through
the air flow holes (623) and volume of the interspace (A) decreases.
3. The piston cover of claim 2, wherein the first pad lower portion (620) includes a
protruding member insertion hole (622) to which the protruding member (720) is fit-coupled
at a boundary between the outer housing (621a) and the inner housing (621b).
4. The piston cover of claim 3, wherein in the outer housing (621a) and the inner housing
(621b), side walls forming the protruding member insertion hole (622) protrude upward
so that the interspace (A) is generated between the bottom portion (710) and the outer
housing and inner housing in a fit-coupling structure of the first pad (600) and the
first plate (700).
5. The piston cover of claim 4, wherein the inner housing (621b) generates a negative
pressure in the interspace (A) when the volume of the interspace (A) is reduced so
that the bottom portion (710) and the seating portion (624) provided in the interspace
(A) come into contact with each other and pulls the chest of the patient with a lower
surface of the inner housing when the piston (310) is contracted after the negative
pressure is generated in the interspace (A) to move the chest upward.
6. The piston cover of claim 1, wherein the first pad lower portion (620) is made of
at least one of ethylene-vinyl acetate, polyethylene, polyethylene-polypropylene blend,
polystyrene, neoprene, chloroprene, polyurethane, and biocompatible silicone, and
the biocompatible silicone has a hardness of 10 to 30 shore A, and at least one of
ethylene-vinyl acetate, polyethylene, polyethylene-polypropylene blend, polystyrene,
neoprene, chloroprene, and polyurethane has a hardness of 10 to 20 asker C.
7. The piston cover of claim 6, wherein in the first pad lower portion (620), a lower
surface that compresses the chest compression point of the patient is made of the
biocompatible silicone.
8. The piston cover of claim 1, wherein the first pad (600) is made of at least one of
polyurethane, polypropylene, and biocompatible silicone.
9. A piston cover fit-coupled to a piston (310) for compressing a chest of a patient
provided in a cardiopulmonary resuscitation device, the piston cover comprising:
a second pad (800) in which a second pad upper portion (810) and a second pad lower
portion (820) are integrally formed with each other, the second pad upper portion
including a pair of grooves (8024a and 8024b) formed between a first piston fitting
portion (811a) and a second piston fitting portion (811b), and between a third piston
fitting portion (811c) and a fourth piston fitting portion (811d) forming a piston
fitting hole (8110) and a piston fitting portion (811) in which a fastening member
formed in a part of an outer peripheral surface of the piston (310) is inserted into
the pair of grooves (8024a and 8024b) when the piston (310) is fit-coupled to the
piston fitting hole (8110), and the second pad lower portion compressing a chest compression
point of the patient with a lower surface of the second pad lower portion while generating
a negative pressure when the piston (310) is expanded and pulling the chest of the
patient with the lower surface and moving the chest upward through the negative pressure
when the piston (310) is contracted; and
a second plate (900) including a first protruding member (920) and a second protruding
member (930) fit-coupled to the second pad lower portion (820) and fit-coupled to
the second pad lower portion (820) to form interspaces (A and B).
10. The piston cover of claim 9, wherein the second pad lower portion (820) includes
a first housing (821a) of which an upper portion is coupled to a bottom portion (910)
of the second plate (900) and which forms a first protruding member insertion hole
(822a) to which the first protruding member (920) is to be fit-coupled,
a second housing (821b) of which an upper portion is coupled to the bottom portion
(910) of the second plate (900) and which forms a second protruding member insertion
hole (822b) to which the second protruding member (930) is to be fit-coupled,
a plurality of air flow holes (823) in which a plurality of first air flow holes (823a)
that allow air in the interspace (A) between the first housing (821a) and the bottom
portion (910) to flow, and a plurality of second air flow holes (823b) that allow
air in the interspace (B) between the second housing (821b) and the bottom portion
(910) to flow are formed on lower surfaces of the first housing (821a) and the second
housing 821b,
a plurality of partitions (826) configured to partition the interspace (A) of the
first housing (821a) into a plurality of portions,
a plurality of first seating portions (824) provided in each of the interspaces (A)
partitioned into the plurality of portions by the partitions (826) to come into contact
with the bottom portion (910) when the air in the interspace (A) flows outward through
the first air flow hole (823a) and volume of the interspace (A) decreases, and
a second seating portion (825) provided in an interspace (B) to come into contact
with the bottom portion (910) when the air in the interspace (B) flows outward through
the second air flow hole (823b) and volume of the interspace (B) decreases.
11. The piston cover of claim 10, wherein in the first housing (821a) and the second housing
(821b), side walls forming the first protruding member insertion hole (822a) and the
second protruding member insertion hole (822b) protrude upward so that the interspaces
(A and B) are generated between the bottom portion (910) and the first housing and
second housing in a fit-coupling structure of the second pad (800) and the second
plate (900).
12. The piston cover of claim 11, wherein the first housing (821a) and the second housing
(821b) generate a negative pressure in the interspaces (A and B) when volumes of the
interspaces (A and B) are reduced so that the bottom portion (910), the first seating
portion (824), and the second seating portion (825) come into contact with each other
and pulls the chest of the patient with lower surfaces of the first housing and the
second housing when the piston (310) is contracted after the negative pressure is
generated in the interspaces (A and B) to move the chest upward.
13. The piston cover of claim 9, wherein the second pad lower portion (820) is made of
at least one of ethylene-vinyl acetate, polyethylene, polyethylene-polypropylene blend,
polystyrene, neoprene, chloroprene, polyurethane, and biocompatible silicone, and
the biocompatible silicone has a hardness of 10 to 30 shore A, and at least one of
ethylene-vinyl acetate, polyethylene, polyethylene-polypropylene blend, polystyrene,
neoprene, chloroprene, and polyurethane has a hardness of 10 to 20 asker C.
14. The piston cover of claim 13, wherein in the second pad lower portion (820), a lower
surface that compresses the chest compression point of the patient is made of the
biocompatible silicone.
15. The piston cover of claim 9, wherein the second pad (800) is made of at least one
of polyurethane, polypropylene, and biocompatible silicone.