Pacemaker compression and stabilization support

Abstract

The present invention relates to a support for compressing and stabilizing a pacemaker and, more specifically, to a support for compressing and stabilizing a pacemaker, the support comprising: a compression fixing part closely contacting an affected part in a human body, into which a pacemaker is inserted; a first fixing belt having one end coupled to the compression fixing part and the other end coupled to the compression fixing part through a gap between a shoulder and an armpit of a patient, the armpit being opposite to the shoulder; and a second fixing belt having one end coupled to the compression fixing part and the other end coupled to one end again via an armpit and the opposite armpit of the patient, wherein the compression fixing part presses the affected part through the first fixing belt and the second fixing belt, thereby stabilizing the pacemaker inserted into the body and stably implementing the function of the pacemaker at the inserted position.

Description

Pacemaker compression and stabilization support

[0001] The present invention relates to a support for compressing and stabilizing a pacemaker, and more specifically, to a pacemaker compression and stabilization support, which includes a compression fixing part that is in close contact with a wound site where a pacemaker is inserted into a body, a first fixing belt having one end connected to the compression fixing part and the other end connected to the compression fixing part through a patient's shoulder and the opposite armpit, and a second fixing belt having one end connected to the compression fixing part and the other end connected to the other end through a patient's armpit and the opposite armpit, thereby stabilizing a pacemaker inserted into a body and enabling the pacemaker to stably perform its function at the inserted location.

[0002] The heart consists of two atria and two ventricles, and is connected to four blood vessels, including the aorta, vena cava, pulmonary artery, and pulmonary vein, to serve as a passage for blood movement.

[0003] The heart is divided into the right atrium and right ventricle on one side and the left atrium and left ventricle on the other, based on the interventricular septum in the center. The tricuspid valve exists between the right atrium and right ventricle, and the mitral valve exists between the left atrium and left ventricle.

[0004] As the heart repeatedly contracts and relaxes, it acts as a pump, forcing blood through the blood vessels. During systole, blood within the heart advances through the blood vessels. In the right heart, blood flows from the right ventricle to the pulmonary artery, and in the left heart, from the left ventricle to the aorta.

[0005] However, if the membrane between the atrium and ventricle does not function properly, blood in the ventricles will flow backward during the heart's systole. When the tricuspid valve between the right atrium and right ventricle does not function properly, causing blood to flow backward from the right ventricle into the right atrium, this is called "tricuspid regurgitation." When the mitral valve between the left atrium and left ventricle does not function properly, causing blood to flow backward from the left ventricle into the left atrium, this is called "mitral regurgitation."

[0006] Tricuspid regurgitation usually occurs in patients with mitral regurgitation, and in patients with heart valve disease, it can cause atrial fibrillation, arrhythmia, and heart failure as heart function declines, which can be treated by implanting a pacemaker.

[0007] In relation to the above, since the first artificial pacemaker was introduced by Furman and Robinson in 1958, pacemakers have been used as a primary treatment for patients with bradycardia. Recently, pacemakers have been used as a primary treatment for arrhythmia diseases such as complete atrioventricular block, severe atrioventricular block, and symptomatic sinus syndrome. Pacemaker therapy is a treatment method that artificially generates electrical impulses through an artificial pacemaker when the electrical impulses in the heart cannot flow normally.

[0008] To explain further, the pacemaker is fixed to the muscle layer by making an incision in the skin, and the fixed position must be maintained during the procedure until the incised skin wound heals, so that the main body and delivery tube do not move and the function of the heartbeat can be stably implemented.

[0009] To do this, the pacemaker should be fixed by rolling up a soft gauze about the size of two adult fists and placing it on top of the skin incision to secure it in place after the procedure, then wrapping an elastic bandage around the gauze and between the shoulder, arm, and armpit to secure it in place for about three weeks or more.

[0010] However, the method of fixing the pacemaker using gauze and elastic bandages as described above is done manually by medical staff, causing a lot of discomfort and anxiety about stability in patients, and there are many difficulties in the process of managing the patient after the treatment by medical staff, i.e., wrapping and removing the elastic bandage.

[0011] The present invention is a technology devised to solve the problems of the above-described prior art, and the conventional method of fixing a pacemaker using gauze and an elastic bandage causes a lot of inconvenience and instability to patients, and causes a lot of difficulty to medical staff in the process of managing after treatment. Therefore, the main purpose of the present invention is to provide a pacemaker compression and stabilization support that stably compresses the affected area where the pacemaker is inserted into the body through a compression fixing part that is in close contact with the affected area where the pacemaker is inserted into the body, a first fixing belt having one end connected to the compression fixing part and the other end connected to the compression fixing part through the patient's shoulder and armpit, and a second fixing belt having one end connected to the compression fixing part and the other end connected to the one end through the patient's both armpits, thereby fixing and positioning the pacemaker inserted into the body at the inserted position, thereby stably implementing the function of the pacemaker.

[0012] In order to achieve the above-described purpose, the present invention proposes a pacemaker compression and stabilization support device comprising: a compression fixing part (100) positioned on the upper surface of a skin incision formed at a location where a pacemaker is inserted and having a lower portion in close contact with the skin incision; a first fixing belt (200) having elasticity and having one end joined to the front of the compression fixing part (100); and a second fixing belt (300) having elasticity and having one end joined to the rear of the compression fixing part (100); wherein the other end of the first fixing belt (200) is joined to the other side of the compression fixing part (100) through the left shoulder and right armpit of the patient, and the other end of the second fixing belt (300) is joined to one end through the left armpit and right armpit of the patient.

[0013] In addition, the pressure fixing member (100) of the present invention is characterized by comprising: a pressure member (110) formed in a disk shape so that the lower part is in close contact with the skin incision site, and a fastening member (112) having a screw thread formed on the outer periphery is protruded at the upper part; a fastening member (120) through which the fastening member (112) is elevated and is connected to one end of the first fixing belt (200) at the front, the other end of the first fixing belt (200) is connected to the other side, and one end of the second fixing belt (300) is connected to the rear; and a rotating member (130) that is rotatably connected to the upper part of the fixing member (120) and is connected to the fastening member (112) so as to elevate the fastening member (112) as it rotates.

[0014] In addition, the fixed member (120) of the present invention is characterized in that it includes a hook member (122) that is formed protrudingly at the upper portion and has a hook step (122a) formed at the inner upper portion; and the rotating member (130) is characterized in that it includes a hook projection (132); that is formed protrudingly at the lower outer periphery to correspond to the hook step (122a).

[0015] In addition, the above-mentioned hooking member (122) of the present invention is characterized in that it is formed in an arc shape while protruding from the upper portion of the above-mentioned fixing member (120).

[0016] In addition, the screw thread formed on the outer periphery of the fastening member (112) of the present invention is configured to include at least one guide groove (112a) formed in the longitudinal direction of the fastening member (112); and the fixing member (120) is characterized in that it is configured to include a through hole (121); formed in a shape corresponding to the outer periphery of the fastening member (112).

[0017] In addition, the guide groove (112a) of the present invention is characterized in that it includes an indicator mark (112a-1) formed so as to check the protruding length of the fastening member (112).

[0018] In addition, the fastening member (112) of the present invention is configured to include a joining groove (114) formed at the upper portion, and the pressing fixing member (100) is configured to include a detachment prevention cover (140) whose lower portion is joined to the joining groove (114) of the fastening member (112) and whose upper diameter is formed to be larger than the diameter of the fastening member (112).

[0019] In addition, the pressure member (110) of the present invention is characterized in that it is configured to include a first buffer member (116) that is attached and coupled to the lower surface and has elasticity.

[0020] In addition, the first buffer member (116) of the present invention is characterized in that it includes a buffer groove (116a) formed on the lower surface.

[0021] In addition, the first buffer member (116) of the present invention is characterized in that it is formed to have a diameter smaller than the diameter of the pressing member (110), and the pressing member (110) is characterized in that it is configured to include a plurality of second buffer members (118) that are attached to and combined with the lower surface and arranged around the periphery of the first buffer member (116).

[0022] The pacemaker compression and stabilization support according to the present invention presented as above can obtain the effect of stabilizing and stabilizing the pacemaker by applying pressure to the skin incision, i.e., the affected area, where the pacemaker is inserted, through a compression fixing part that is in close contact with the affected area where the pacemaker is inserted into the body, a first fixing belt having one end connected to the compression fixing part and the other end connected to the compression fixing part through the patient's shoulder and armpit, and a second fixing belt having one end connected to the compression fixing part and the other end connected to the one end through the patient's both armpits.

[0023] In addition, the present invention installs a movable compression member on a fixed member, and installs a rotating member for elevating the compression member on the compression member, so that the compression force, i.e., the applied pressure, can be adjusted through the rotating member and the compression member, thereby obtaining the effect of more efficiently compressing the skin incision site, i.e., the affected area, where the pacemaker is inserted.

[0024] In addition, the present invention forms a guide groove without a screw thread on the outer periphery of the fastening member of the pressure member, and forms a through hole corresponding to the outer periphery of the fastening member in the fixing member, thereby obtaining an effect of allowing the pressure member to be raised and lowered stably.

[0025] In addition, the present invention forms a marking scale in a guide groove on the outer periphery of a fastening member without threads, and the compressive force by the compressing member can be predicted through the marking scale, and accordingly, the compressive force applied to the skin incision site where the pacemaker is inserted, i.e., the affected area, can be easily predicted, and thus, when reinstalled, an effect of forming a compressive force similar to the previous compressive force can be obtained.

[0026] In addition, the present invention can obtain an effect of minimizing discomfort by attaching and joining a first buffer member that is in close contact with the skin incision site, i.e., the affected area, where the pacemaker is inserted, to the lower surface of the compression member, and naturally compressing the skin incision site, i.e., the affected area, where the pacemaker is inserted, through the first buffer member so that the compression force can be applied evenly.

[0027] In addition, the present invention can obtain the effect of enabling smooth recovery of the affected area by allowing geothermal heat to be generated in a damaged blood vessel that occurs when a pacemaker is inserted into the body through a second cushioning member that is attached and combined to the lower surface of the compression member and arranged to be positioned outside the first cushioning member.

[0028] FIG. 1 is a front view and a right side view showing a state in which a pacemaker compression and stabilization support (hereinafter referred to as “support”) according to a preferred embodiment of the present invention is worn.

[0029] Figure 2 is a rear view and a left side view showing a state in which a support according to a preferred embodiment of the present invention is worn.

[0030] Fig. 3 is a perspective view showing a pressure fixing part according to a preferred embodiment of the present invention.

[0031] Figure 4a is an exploded perspective view showing a pressure fixing part according to a preferred embodiment of the present invention.

[0032] Figure 4b is an exploded bottom perspective view showing a pressure fixing part according to a preferred embodiment of the present invention.

[0033] Figure 5 is a bottom perspective view and bottom view showing a pressure member according to a preferred embodiment of the present invention.

[0034] Figure 6 is a side view and a cross-sectional side view showing a pressure fixing part according to a preferred embodiment of the present invention.

[0035] *Detailed explanation of the main symbols in the drawing*

[0036] 100: Pressure fixing unit

[0037] 110: Pressure member 112: Fastening member

[0038] 112a: Guide groove 112a-1: Marking scale

[0039] 114: Joint groove 116: First buffer member

[0040] 116a: Buffer groove 118: Second buffer member

[0041] 120: Fixed member 121: Through hole

[0042] 122: Hook member 122a: Hook step

[0043] 130: Rotating member 132: Hook

[0044] 140: Anti-fall cover

[0045] 200: 1st fixed belt

[0046] 300: Second fixed belt

[0047] The present invention relates to a support for compressing and stabilizing a pacemaker, and more specifically, to a compression and stabilization support for a pacemaker, which comprises: a compression fixing part (100) that is in close contact with a skin incision site where a pacemaker is inserted into a body, i.e., an affected area; a first fixing belt (200) having one end connected to the compression fixing part (100) and the other end connected to the compression fixing part (100) through a patient's shoulder and the opposite armpit; and a second fixing belt (300) having one end connected to the compression fixing part (100) and the other end connected to the compression fixing part (100) through both armpits of a patient, thereby stabilizing a pacemaker inserted into a body easily, and thereby stabilizing a pacemaker inserted into a body at an inserted position, i.e., fixing until a wound is healed, so that the pacemaker's function can be stably implemented.

[0048] The pacemaker compression and stabilization support of the present invention as described above comprises: a compression fixing part (100) positioned on the upper surface of a skin incision formed at a location where a pacemaker is inserted and having a lower portion in close contact with the skin incision; a first fixing belt (200) having elasticity and having one end joined to the front of the compression fixing part (100); and a second fixing belt (300) having elasticity and having one end joined to the rear of the compression fixing part (100); wherein the other end of the first fixing belt (200) is joined to the other side of the compression fixing part (100) through the left shoulder and right armpit of the patient, and the other end of the second fixing belt (300) is joined to one end through the left armpit and right armpit of the patient.

[0049] In addition, the pressure fixing member (100) of the present invention is characterized by comprising: a pressure member (110) formed in a disk shape so that the lower part is in close contact with the skin incision site, and a fastening member (112) having a screw thread formed on the outer periphery is protruded at the upper part; a fastening member (120) through which the fastening member (112) is elevated and is connected to one end of the first fixing belt (200) at the front, the other end of the first fixing belt (200) is connected to the other side, and one end of the second fixing belt (300) is connected to the rear; and a rotating member (130) that is rotatably connected to the upper part of the fixing member (120) and is connected to the fastening member (112) so as to elevate the fastening member (112) as it rotates.

[0050] In addition, the fixed member (120) of the present invention is characterized in that it includes a hook member (122) that is formed protrudingly at the upper portion and has a hook step (122a) formed at the inner upper portion; and the rotating member (130) is characterized in that it includes a hook projection (132); that is formed protrudingly at the lower outer periphery to correspond to the hook step (122a).

[0051] In addition, the above-mentioned hooking member (122) of the present invention is characterized in that it is formed in an arc shape while protruding from the upper portion of the above-mentioned fixing member (120).

[0052] In addition, the screw thread formed on the outer periphery of the fastening member (112) of the present invention is configured to include at least one guide groove (112a) formed in the longitudinal direction of the fastening member (112); and the fixing member (120) is characterized in that it is configured to include a through hole (121); formed in a shape corresponding to the outer periphery of the fastening member (112).

[0053] In addition, the guide groove (112a) of the present invention is characterized in that it includes an indicator mark (112a-1) formed so as to check the protruding length of the fastening member (112).

[0054] In addition, the fastening member (112) of the present invention is configured to include a joining groove (114) formed at the upper portion, and the pressing fixing member (100) is configured to include a detachment prevention cover (140) whose lower portion is joined to the joining groove (114) of the fastening member (112) and whose upper diameter is formed to be larger than the diameter of the fastening member (112).

[0055] In addition, the pressure member (110) of the present invention is characterized in that it is configured to include a first buffer member (116) that is attached and coupled to the lower surface and has elasticity.

[0056] In addition, the first buffer member (116) of the present invention is characterized in that it includes a buffer groove (116a) formed on the lower surface.

[0057] In addition, the first buffer member (116) of the present invention is characterized in that it is formed to have a diameter smaller than the diameter of the pressing member (110), and the pressing member (110) is characterized in that it is configured to include a plurality of second buffer members (118) that are attached to and combined with the lower surface and arranged around the periphery of the first buffer member (116).

[0058] Hereinafter, the present invention will be described in detail with reference to drawings 1 to 6 illustrating embodiments of the present invention.

[0059] First, the front, rear, upper, lower, one side, and the other side mentioned in the present invention refer to the patient's head direction as the front, the leg direction as the rear, the chest direction as the upper side, the back direction as the lower side, the left side of the patient as the one side, and the right side of the patient as the other side, considering the case where the patient is lying down, as shown in Drawing 1, and the first fixing belt (200) and the second fixing belt (300) to be described in detail later are referred to by dividing them into one end and the other end based on the longitudinal direction, unlike the standard shown in Drawing 1.

[0060] The compression fixing member (100), which is a main component of the present invention, is positioned on the upper surface of the skin incision (hereinafter also referred to as the 'incised part') formed at the location where the pacemaker is inserted into the patient's body, that is, on the skin surface, and the lower part thereof is in close contact with the skin incision. By positioning the upper part of the skin incision and compressing the skin incision through the first fixing belt (200) and the second fixing belt (300), which will be described in detail later, the position of the pacemaker inserted into the body is stabilized without moving.

[0061] Specifically, the compression fixing member (100) of the present invention is formed in a disk shape, and includes a compression member (110) having a lower portion that is in close contact with the skin incision site and a fastening member (112) having screw threads formed on the outer periphery and protruding at the upper portion; a fastening member (120) that penetrates the fastening member (112) so as to be able to rise and fall, has one end of a first fixing belt (200) to be described in detail later coupled at the front, has the other end of the first fixing belt (200) coupled at the other side, and has one end of a second fixing belt (300) to be described in detail later coupled at the rear; and a rotating member (130) that is rotatably coupled to the upper portion of the fixing member (120) and raises and lowers the fastening member (112) as it is rotated by being fastened to the fastening member (112).

[0062] The above-mentioned compression member (110) is formed in a circular shape and is stably and closely attached to the upper portion of the skin incision, so as to be in close contact with the skin incision, that is, the entire affected area or more than 80% of the affected area, thereby allowing the pacemaker inserted into the body to be compressed at the inserted location.

[0063] The above fastening member (112) allows the pressure member (110) to be raised or lowered through the rotating member (130) so that the pressure member (110) is spaced apart from or closely brought into contact with the fixing member (120), thereby allowing the pressure force to be adjusted without adjusting the length of the first fixing belt (200) and the second fixing belt (300) after the fixing member (120) is fixed through the first fixing belt (200) and the second fixing belt (300), which will be described in detail later.

[0064] In addition, the screw thread formed on the outer periphery of the fastening member (112) is configured to include at least one guide groove (112a) formed in the longitudinal direction of the fastening member (112), and the guide groove (112a) enables the fastening member (112) to be raised and lowered by minimizing lateral movement when the fastening member (112) is raised and lowered by penetrating the fixing member (120), thereby realizing the effect of more stable raising and lowering.

[0065] At this time, the fixed member (120) is configured to include a through hole (121) formed in a shape corresponding to the outer circumference of the fastening member (112), and the inner circumference of the through hole (121) and the outer circumference of the guide groove (112a) are in close contact, so that the fastening member (112) is stably raised and lowered by the rotation of the rotating member (130), and accordingly, the pressing member (110) is raised and lowered together, so that the pressing force can be adjusted.

[0066] In addition, the above guide home (112a) is configured to include an indicator mark (112a-1) formed on the outer periphery, and the indicator mark (112a-1) allows the protrusion length of the fastening member (112) to be confirmed by protruding through the fixing member (120).

[0067] In addition, the above-mentioned indicator scale (112a-1) can be adjusted to a protrusion length similar to the protrusion length of the previous fastening member (112) when re-wearing the support of the present invention, thereby enabling the skin incision to be pressed with a similar compressive force as when the support of the present invention was previously worn, thereby realizing the effect of providing the most comfortable and stable compressive force to the patient.

[0068] Meanwhile, the pressure member (110) may be configured to include a first buffer member (116) made of a synthetic resin material having elasticity that is attached and combined to the lower surface and is in close contact with the skin incision site. The first buffer member (116) may be made of a synthetic resin material having elasticity, such as silicone or rubber, for example, and is in close contact with the skin incision site so that the pressure force by the pressure member (110) can be evenly applied to the entire skin incision site.

[0069] In addition, the first buffer member (116) is configured to include a buffer groove (116a) formed on the lower surface, and the buffer groove (116a) is formed in the shape of a dimple of a golf ball, and as the skin incision site, i.e., the affected area, is pressed, the lower surface of the first buffer member (116) is pressed outward and inward, thereby expanding the area, so that the affected area can be pressed more evenly and stably, and is positioned at the center of the skin incision site so that the compressive force at the center of the skin incision site can be applied weakly compared to the overall compressive force, so that the skin incision site can be protected.

[0070] At this time, it is preferable that the first buffer member (116) is formed with the same diameter as the diameter of the pressure member (110) when the second buffer member (118), which will be described in detail later, is not attached to the lower surface of the pressure member (110).

[0071] In connection with the above, the pressure member (110) is configured to include a plurality of second buffer members (118) that are attached and combined to the lower surface, but are positioned on the outside of the first buffer member (116), that is, arranged and combined around the periphery of the first buffer member (116).

[0072] Accordingly, the first buffer member (116) is formed to have a diameter smaller than the diameter of the pressing member (110) so that the second buffer member (118) can be attached to and combined with the lower surface of the pressing member (110).

[0073] The second buffer member (118) is combined with the lower surface of the compression member (110) so that a perimeter spaced apart from the center of the skin incision is compressed, and a plurality of members are arranged in a circular shape, thereby achieving the effect of stopping bleeding in the damaged blood vessels of the skin incision and allowing the damaged blood vessels to recover smoothly.

[0074] At this time, the lower part of the second buffer member (118) is formed in a curved shape to achieve the effect of allowing the damaged blood vessels of the skin incision site to be naturally and stably stopped from bleeding.

[0075] In addition, the reason why the second buffer member (118) is composed of multiple pieces and spaced apart is to ensure smooth blood circulation in unbroken blood vessels and stable recovery of the affected area.

[0076] That is, when the pacemaker has been inserted into the body for less than a reference date (approximately 3 to 5 days), that is, when the blood vessel around the skin incision is damaged, the medical staff can use the compression member (110) to which the second buffer member (118) is attached and combined to compress and stabilize the pacemaker, and when the pacemaker has been inserted into the body for more than a reference date, that is, when the blood vessel around the skin incision is damaged and ruptured, the medical staff can use the compression member (110) to which only the first buffer member (116) is attached and combined to compress the pacemaker more stably and firmly.

[0077] The above fixing member (120) is formed with a through hole (121) as described above so that the fastening member (112) of the pressure member (110) can be raised and lowered, and one end of a first fixing belt (200) to be described in detail later is coupled to the front, and the other end of the first fixing belt (200) is coupled to the other side, while one end of a second fixing belt (300) to be described in detail later is coupled to the rear, so that the pressure fixing member (100) of the present invention is stably positioned on the upper surface of the skin incision formed at the location where the pacemaker is inserted by the first fixing belt (200) and the second fixing belt (300).

[0078] In addition, the fixing member (120) is installed so that the fastening member (112) can be raised and lowered, thereby allowing the support of the present invention to be adjusted to the pressing force by the pressing member (110) even when the patient wears it.

[0079] In addition, the above-mentioned fixing member (120) is formed with a coupling hole (not shown in the drawing) on ​​the front, the other side, and the rear, respectively, so that one end and the other end of the first fixing belt (200) and one end of the second fixing belt (300), which will be described in detail later, can be coupled, so that one end and the other end of the first fixing belt (200) and one end of the second fixing belt (300) can pass through and then be coupled.

[0080] The above-mentioned rotating member (130) is rotatably coupled to the upper portion of the above-mentioned fixed member (120), and has screw threads formed on the inner circumference corresponding to the screw threads formed on the outer circumference of the above-mentioned fastening member (112), so that the above-mentioned fastening member (112) is raised and lowered as it is fastened to the above-mentioned fastening member (112) and rotated.

[0081] That is, since the rotating member (130) is rotatably connected to the upper portion of the fixed member (120), it does not rise and fall when rotated, so that the fastening member (112) is raised and lowered by rotation, and medical staff or patients can easily adjust the pressure by rotating the rotating member (130).

[0082] At this time, the rotating member (130) may be configured to include a plurality of grip grooves (not shown in the drawing) formed on the outer periphery, and an effect of allowing medical staff or patients to easily rotate the member can be obtained through the grip grooves.

[0083] In addition, the above-mentioned rotating member (130) may be configured to include at least one pair of gripping projections (not shown in the drawing) that are formed protrudingly on the outer periphery, and the gripping projections, together with the gripping groove, realize the effect of allowing medical staff or patients to more easily rotate the above-mentioned rotating member (130).

[0084] In connection with the above, a structure in which the rotating member (130) is rotatably coupled to the fixed member (120) will be described. The fixed member (120) is configured to include a hook member (122) that is formed protrudingly at the upper portion and has a hook step (122a) formed at the inner upper portion, and the rotating member (130) is configured to include a hook protrusion (132) that is formed protrudingly to correspond to the hook step (122a) at the lower outer periphery, and the rotating member (130) is rotatably coupled to the hook member (122) by the hook step (132).

[0085] That is, the rotating member (130) is rotatably coupled when the upper portion of the hook (132) is hooked to the lower portion of the hook step (122a) of the hook member (122) that is protruded from the fixed member (120) and the hook step (122a) is positioned between the upper surface of the fixed member (120) and the hook step, and thus, when fastened to the fastening member (112), the fastening member (112) is raised and lowered when rotated.

[0086] At this time, the above-mentioned hooking member (122) is formed in an arc shape and is partially opened, so that the hooking projection (132) of the above-mentioned rotating member (130) is easily coupled between the upper surface of the above-mentioned fixed member (120) and the above-mentioned hooking step (122a), and then the above-mentioned fastening member (112) is coupled to the above-mentioned rotating member (130) and is fixed.

[0087] In connection with the above, the fastening member (112) is configured to include a joining groove (114) formed at the upper portion, and the pressure fixing member (100) of the present invention is configured to include a detachment prevention cover (140) whose lower portion is joined to the joining groove (114) of the fastening member (112) and whose upper diameter is formed to be larger than the diameter of the fastening member (112).

[0088] That is, when the rotation member (130) is rotated to lower the fastening member (112), the lower surface of the anti-separation cover (140) comes into contact with the upper surface of the rotation member (130), thereby preventing the fastening member (112) from being lowered any further, thereby preventing the rotation member (130) and the fastening member (112) from being separated, thereby allowing the support of the present invention to be maintained in a stably installed state.

[0089] At this time, the rotary member (130) is configured to include a mounting groove (not shown in the drawing) formed on the upper surface to correspond to the diameter of the detachment prevention cover (140), and the mounting groove allows the detachment prevention cover (140) to be inserted into the upper portion of the rotary member (130), thereby making it easier to check the lowering length, i.e., the lowered state, of the fastening member (112), thereby realizing the effect of enabling a faster judgment of the pressing state of the pressing member (110).

[0090] The first fixing belt (200), which is a main component of the present invention, is made of an elastic material, and one end is connected to the front of the pressure fixing part (100), that is, the front of the fixing member (120), so that the upper part and the other side of the pressure fixing part (100) can be fixed in position in close contact with the skin incision site, that is, the affected area.

[0091] The first fixed belt (200) of the present invention has a female Velcro (not shown in the drawing) formed on the upper surface, and a male Velcro (not shown in the drawing) formed on one end and the other end of the upper surface, respectively, and as shown in Drawing 1, one end is passed through a joining hole formed in the front of the fixed member (120) described above, and then one end of the male Velcro is attached and coupled to the female Velcro and fixed, and the other end is passed through a joining hole formed on the other side of the fixed member (120), and then the male Velcro of the other end is attached and coupled to the female Velcro and fixed.

[0092] Accordingly, the first fixing belt (200) of the present invention forms a compressive force by connecting one end to the front of the fixing member (120) and then pulling the other end to connect it to the other side of the fixing member (120), thereby allowing the front and other side of the pressure fixing member (100) to be fixed in a state where the compressive force is formed on the affected area.

[0093] To explain further, the first fixing belt (200) is connected at one end to the front of the fixing member (120) and then the other end is connected to the other side of the compression fixing member (100) through the patient's left shoulder and right armpit, thereby allowing the compression fixing member (100) to be more firmly maintained in an installed state.

[0094] The second fixing belt (300), which is a main component of the present invention, is made of an elastic material and has one end joined to the rear of the compression fixing part (100), that is, the rear of the fixing member (120), so that the rear of the compression fixing part (100) can be fixed in a position in close contact with the skin incision site, that is, the affected area, so that the position of the compression fixing part (100) can be stably and firmly maintained together with the first fixing belt (200).

[0095] The second fixed belt (300) of the present invention has a female Velcro (not shown in the drawing) formed on the upper surface, and a male Velcro (not shown in the drawing) formed on one end of the upper surface and the other end of the lower surface, respectively, and as shown in Drawing 1, one end is passed through a joining hole formed on the rear of the fixing member (120) described above, and then the male Velcro of one end of the upper surface is attached and coupled to the female Velcro and fixed, and the male Velcro of the other end of the lower surface is attached and coupled to the female Velcro of one end of the upper surface and fixed.

[0096] Accordingly, the second fixing belt (300) of the present invention forms a compressive force by connecting one end to the rear of the fixing member (120) and then pulling the other end to connect it to the other end, thereby allowing the rear of the compressive fixing member (100) to be fixed in a state where the compressive force is formed on the affected area, thereby allowing the position of the compressive fixing member (100) to be maintained in a state where the compressive force is formed at the correct position together with the first fixing belt (200).

[0097] In addition, the second fixing belt (300) is connected at one end to the rear of the fixing member (120) and then the other end is connected to the other end via the left and right armpits of the patient, thereby allowing the pressure fixing member (100) to be more firmly maintained in the installed state.

[0098] At this time, if the patient's left shoulder is uncomfortable, it will be obvious that the pressure fixing member (100) can be rotated so that the other end of the first fixing belt (200) passes through the patient's right shoulder and left armpit and is connected to the other side (one side when rotated) of the pressure fixing member (100), and the other end of the second fixing belt (300) passes through the patient's right armpit and right armpit and is connected to one end.

[0099] The above has been described with reference to a preferred embodiment of the present invention, and the present invention is not limited to the above embodiment, and a person having ordinary skill in the art to which the present invention pertains can make various changes without departing from the gist of the present invention through the above embodiment.

Claims

1. A pressure fixing member (100) positioned on the upper surface of the skin incision formed at the location where the pacemaker is inserted and having the lower part in close contact with the skin incision; and A first fixing belt (200) having elasticity and having one end connected to the front of the above-mentioned pressure fixing member (100); and It is configured to include a second fixing belt (300) having elasticity and having one end joined to the rear of the above-mentioned pressure fixing member (100); The above first fixed belt (200) The other end is connected to the other side of the above-mentioned compression fixing device (100) through the patient's left shoulder and right armpit. The above second fixed belt (300) A pacemaker compression and stabilization support characterized in that one end is connected to the other end through the patient's left and right armpits.

2. In paragraph 1, The above pressure fixing member (100) A compression member (110) formed in a disc shape, the lower part of which is in close contact with the skin incision, and a fastening member (112) having screw threads formed on the outer periphery thereof is protruded at the upper part; and A fixing member (120) through which the fastening member (112) is liftable, one end of the first fixing belt (200) is coupled to the front, the other end of the first fixing belt (200) is coupled to the other side, and one end of the second fixing belt (300) is coupled to the rear; and A pacemaker compression and stabilization support, characterized in that it comprises a rotating member (130) that is rotatably connected to the upper portion of the fixed member (120) and is connected to the fastening member (112) to raise and lower the fastening member (112) as it rotates.

3. In paragraph 2, The above fixed member (120) It is composed of a catch member (122) that is formed protrudingly at the top and has a catch step (122a) formed at the inner top; The above rotating member (130) A pacemaker compression and stabilization support, characterized in that it comprises a hook projection (132) formed to protrude in correspondence with the hook step (122a) on the lower outer periphery.

4. In paragraph 3, The above-mentioned hanging member (122) A pacemaker compression and stabilization support characterized by being formed in an arc shape and protruding from the upper portion of the above-mentioned fixed member (120).

5. In paragraph 2, The screw thread formed on the outer periphery of the above fastening member (112) It is configured to include at least one guide groove (112a) formed in the longitudinal direction of the above fastening member (112); The above fixed member (120) A pacemaker compression and stabilization support, characterized in that it comprises a through hole (121) formed in a shape corresponding to the outer periphery of the above fastening member (112).

6. In paragraph 5, The above guide home (112a) A pacemaker compression and stabilization support, characterized in that it comprises a marking scale (112a-1) formed to enable checking the protruding length of the above-mentioned fastening member (112).

7. In paragraph 2, The above fastening member (112) It is composed of a joining groove (114) formed on the upper side; The above pressure fixing member (100) A pacemaker compression and stabilization support, characterized in that it comprises a detachment prevention cover (140) whose lower part is joined to the joining groove (114) of the above-mentioned fastening member (112) and whose upper diameter is formed to be larger than the diameter of the above-mentioned fastening member (112).

8. In paragraph 2, The above pressure member (110) A pacemaker compression and stabilization support, characterized in that it comprises a first cushioning member (116) that is attached and bonded to the lower surface and has elasticity.

9. In paragraph 8, The above first buffer member (116) A pacemaker compression and stabilization support, characterized in that it comprises a buffer groove (116a) formed on the lower surface.

10. In paragraph 9, The above first buffer member (116) It is characterized in that it is formed to have a diameter smaller than the diameter of the above pressure member (110), The above pressure member (110) A pacemaker compression and stabilization support, characterized in that it comprises a plurality of second buffer members (118) that are attached to and combined on the lower surface and arranged and combined around the periphery of the first buffer member (116).

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