WO2025170191A1 - Pacemaker compression and stabilization support - Google Patents
Pacemaker compression and stabilization supportInfo
- Publication number
- WO2025170191A1 WO2025170191A1 PCT/KR2024/095255 KR2024095255W WO2025170191A1 WO 2025170191 A1 WO2025170191 A1 WO 2025170191A1 KR 2024095255 W KR2024095255 W KR 2024095255W WO 2025170191 A1 WO2025170191 A1 WO 2025170191A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compression
- pacemaker
- fixing
- fastening member
- fixing belt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
Definitions
- 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.
- 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.
- the heart 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.
- 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.
- pacemakers have been used as a primary treatment for patients with bradycardia.
- artificial 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Figure 5 is a bottom perspective view and bottom view showing a pressure member according to a preferred embodiment of the present invention.
- 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.
- 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.
- 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).
- 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).
- 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).
- the first buffer member (116) be 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) and is not combined.
- 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.
- 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.
- 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).
- the fixing member (120) is installed so that the fastening member (112) can be raised and lowered, thereby allowing the pressure force by the pressure member (110) to be adjusted even when the support of the present invention is worn by a patient.
- 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.
- 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.
- 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.
- 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).
- 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.
- 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).
- 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.
- 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.
- 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.
- 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.
- 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.
Landscapes
- Health & Medical Sciences (AREA)
- Cardiology (AREA)
- Animal Behavior & Ethology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
Abstract
Description
본 발명은 심박동기를 압박 및 안정화시키는 지지대에 관한 것으로, 보다 상세하게 설명하면, 심박동기가 체내에 삽입된 환부에 밀접되는 압박고정부와, 상기 압박고정부에 일단이 결합되고 환자의 어깨와 반대편 겨드랑이 사이를 거쳐 상기 압박고정부에 타단이 결합되는 제1고정벨트 및 상기 압박고정부에 일단이 결합되고, 환자의 겨드랑이와 반대편 겨드랑이를 거쳐 타단이 다시 일단에 결합되는 제2고정벨트를 통해 상기 압박고정부가 환부에 압박되도록 함으로써, 체내에 삽입된 심박동기를 안정화시켜 삽입된 위치에서 심박동기의 기능이 안정적으로 구현될 수 있도록 하는 심박동기 압박 및 안정 지지대에 관한 것이다.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.
심장은 2개의 심방과 2개의 심실로 이루어지며 대동맥, 대정맥, 폐동맥, 폐정맥 등 4가지 혈관과 연결되어 혈액의 이동통로가 된다.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.
심장 중앙의 심실중격을 기준으로 한쪽은 우심방과 우심실, 다른 한쪽은 좌심방과 좌심실로 나누어진다. 우심방과 우심실 사이에는 삼첨판막이 존재하고, 좌심방과 좌심실 사이에는 승모판막이 존재한다.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.
심장은 수축과 이완작용을 반복함에 따라 심장이 펌프 역할을 하여, 혈액이 혈관을 따라 흐르게 된다. 심장의 수축기에는 심장 내의 혈액이 혈관으로 전진하는 데, 오른쪽심장에서는 우심실에서 폐동맥으로, 왼쪽 심장에서는 좌심실에서 대동맥으로 혈액이 이동하게 된다.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.
그러나, 심방과 심실 사이의 막이 제대로 작동하지 않으면, 심장의 수축기에 심실의 혈액이 역류하게 된다. 우심방과 우심실 사이의 삼첨판막이 제대로 작동하지 않아 우심실의 피가 우심방으로 역류하면 '삼첨판막 역류증'이라 하고, 좌심방과 좌심실 사이의 승모판막이 제대로 작동하지 않아 좌심실의 피가 좌심방으로 역류하면 '승모판막 역류증'이라 한다.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."
삼첨판막 역류증은 보통 승모판막 역류증이 있는 환자에게 발생하며, 심장판막 질환이 있는 환자는 심장기능이 떨어지게 되면서 심방세동, 부정맥, 심부전증 등을 유발할 수 있으며 이는 심박동기를 체내에 삽입하여 치료할 수 있다.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.
상기와 연관하여, 1958년 Furman과 Rovinson 등에 의해 처음으로 인공 심박동기(Pacemaker)가 도입된 이후, 심박동기는 서맥성 부정맥 환자의 주요한 치료법으로 사용되고 있다. 최근 인공 심박동기는 완전 방실 차단이나 고도 방실 차단, 증상을 동반한 동기능 부전 증후군과 같은 부정맥 질환의 주요한 치료로 사용되고 있다. 심박동기 치료는 정상적으로 심장의 전기 자극이 흘러가지 못하여 인위적으로 인공 심박동기에 의해 전기 자극을 만들어 주는 치료 방법이다.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, artificial 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.
부가하여 설명하면, 심박동기는 피부를 절개하여 근육층에 고정하는데, 절개된 피부의 상처가 회복되기까지 시술시 고정된 위치를 유지해야 본체와 전달관이 이동하지 않고 심장 박동의 기능을 안정적으로 구현할 수 있다.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.
이를 위해 심박동기는 시술 후 피부 절개지를 고정하기 위해 약 어른 주먹 두개 정도의 부드러운 거즈를 둥그렇게 뭉쳐서 피부 절개지의 상부에 밀착시킨 후 탄력 붕대를 상기 거즈를 포함하여 어깨와 팔과 겨드랑이 사이로 감아 고정시키고, 약 3주 이상을 고정해야 한다.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.
그러나, 상기와 같은 거즈와 탄력 붕대를 이용한 심박동기의 고정방법은 의료진들의 수작업으로 이루어지기 때문에 환자들이 많은 불편과 안정성에 대한 불안을 초래하고 있고, 의료진들의 처치 후 관리하는 과정 즉, 탄력 붕대를 감고 푸는 과정에서 많은 어려움이 있다.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.
본 발명은 상술한 종래기술에 따른 문제점을 해결하고자 안출된 기술로서, 종래의 거즈와 탄력 붕대를 이용한 심박동기의 고정방법은 환자들이 많은 불편과 안정성에 대한 불안을 초래하고, 의료진들의 처치 후 관리하는 과정에서 많은 어려움이 발생하는 바, 심박동기가 체내에 삽입된 환부에 밀접되는 압박고정부와, 상기 압박고정부에 일단이 결합되고 환자의 어깨와 겨드랑이를 거쳐 타단이 상기 압박고정부에 결합되는 제1고정벨트 및 상기 압박고정부에 일단이 결합되고 환자의 양쪽 겨드랑이를 거쳐 타단이 일단에 결합되는 제2고정벨트를 통해 심박동기가 삽입된 환부를 안정적으로 압박하여 체내에 삽입된 심박동기가 삽입된 위치에 고정되어 자리잡도록 함으로써, 심박동기의 기능이 안정적으로 구현될 수 있도록 하는 심박동기 압박 및 안정 지지대를 제공하는 것을 주된 목적으로 하고 있다.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.
본 발명은 상기와 같은 소기의 목적을 실현하고자, 심박동기가 삽입된 위치에 형성된 피부 절개지의 상부 표면에 위치되어 상기 피부 절개지에 하부가 밀접되는 압박고정부(100);와 상기 압박고정부(100)의 전방에 일단이 결합되고, 탄성을 가지는 제1고정벨트(200); 및 상기 압박고정부(100)의 후방에 일단이 결합되고, 탄성을 가지는 제2고정벨트(300);를 포함하여 구성되고, 상기 제1고정벨트(200)는 타단이 환자의 왼쪽 어깨와 오른쪽 겨드랑이를 거쳐 상기 압박고정부(100)의 타측에 결합되며, 상기 제2고정벨트(300)는 타단이 환자의 왼쪽 겨드랑이와 오른쪽 겨드랑이를 거쳐 일단에 결합되는 것을 특징으로 하는 심박동기 압박 및 안정 지지대를 제시한다.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.
또한, 본 발명의 상기 압박고정부(100)는 원판 형태로 형성되어 하부가 상기 피부 절개지에 밀접되고, 외주연에 나사산이 형성된 체결부재(112)가 상부에 돌출형성되는 압박부재(110);와 상기 체결부재(112)가 승강 가능하도록 관통되고, 전방에 상기 제1고정벨트(200)의 일단이 결합되며, 타측에 상기 제1고정벨트(200)의 타단이 결합되는 한편, 후방에 상기 제2고정벨트(300)의 일단이 결합되는 고정부재(120); 및 상기 고정부재(120)의 상부에 회전 가능하도록 결합되고, 상기 체결부재(112)에 체결되어 회전됨에 따라 상기 체결부재(112)를 승강시키는 회전부재(130);를 포함하여 구성되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 고정부재(120)는 상부에 돌출형성되고, 내측 상부에 걸림단턱(122a)이 형성되는 걸림부재(122);를 포함하여 구성되고, 상기 회전부재(130)는 하부 외주연에 상기 걸림단턱(122a)과 대응되도록 돌출형성되는 걸림돌기(132);를 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 걸림부재(122)는 상기 고정부재(120)의 상부에 돌출형성되되, 호 형상으로 형성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 체결부재(112)의 외주연에 형성되는 나사산은 상기 체결부재(112)의 길이방향으로 형성되는 적어도 하나의 가이드홈(112a);을 포함하여 구성되고, 상기 고정부재(120)는 상기 체결부재(112)의 외주연과 대응되는 형상으로 형성되는 관통홀(121);을 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 가이드홈(112a)은 상기 체결부재(112)의 돌출길이를 확인할 수 있도록 형성되는 표시눈금(112a-1);을 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 체결부재(112)는 상부에 형성되는 결합홈(114);을 포함하여 구성되고, 상기 압박고정부(100)는 상기 체결부재(112)의 결합홈(114)에 하부가 결합되고, 상부 직경이 상기 체결부재(112)의 직경보다 크게 형성되는 이탈방지커버(140);를 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 압박부재(110)는 하부면에 부착되어 결합되고, 탄성을 가지는 제1완충부재(116);를 포함하여 구성되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 제1완충부재(116)는 하부면에 형성되는 완충홈(116a);을 포함하여 구성되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 제1완충부재(116)는 상기 압박부재(110)의 직경보다 작은 직경을 가지도록 형성되는 것을 특징으로 하고, 상기 압박부재(110)는 하부면에 부착되어 결합되되, 상기 제1완충부재(116)의 둘레에 배열되어 결합되는 복수 개의 제2완충부재(118);를 포함하여 구성되는 것을 특징으로 한다.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).
상기와 같이 제시된 본 발명에 의한 심박동기 압박 및 안정 지지대는 심박동기가 체내에 삽입된 환부에 밀접되는 압박고정부와, 상기 압박고정부에 일단이 결합되고 환자의 어깨와 겨드랑이를 거쳐 타단이 상기 압박고정부에 결합되는 제1고정벨트 및 상기 압박고정부에 일단이 결합되고 환자의 양쪽 겨드랑이를 거쳐 타단이 일단에 결합되는 제2고정벨트를 통해 심박동기가 삽입된 피부 절개지 즉, 환부를 가압 즉, 압박하여 상기 심박동기가 체내에서 안정적으로 고정되어 안정화될 수 있도록 하는 효과를 얻을 수 있다.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.
또한, 본 발명은 고정부재에 승강 가능한 압박부재를 설치하고, 상기 압박부재를 승강시키는 회전부재를 상기 압박부재에 설치하여 상기 회전부재와 압박부재를 통해 압박력 즉, 가압력을 조절할 수 있어 보다 효율적으로 심박동기가 삽입된 피부 절개지 즉, 환부를 압박할 수 있는 효과를 얻을 수 있다.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.
또한, 본 발명은 압박부재의 체결부재의 외주연에 나사산이 형성되지 않는 가이드홈을 형성하고, 고정부재에 상기 체결부재의 외주연과 대응되는 관통홀을 형성함으로써, 상기 압박부재가 안정적으로 승강되도록 하는 효과를 얻을 수 있다.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.
또한, 본 발명은 체결부재의 외주연에 나사산이 형성되지 않은 가이드홈에 표시눈금을 형성하고, 상기 표시눈금을 통해 압박부재에 의한 압박력을 예상할 수 있으며, 이에 따라 심박동기가 삽입된 피부 절개지 즉, 환부를 압박하는 압박력을 쉽게 예측 가능함으로써, 재설치시 이전의 압박력과 유사한 압박력을 형성할 수 있는 효과를 얻을 수 있다.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.
또한, 본 발명은 압박부재의 하부면에 심박동기가 삽입된 피부 절개지 즉, 환부와 밀접되는 제1완충부재를 부착하여 결합하고, 상기 제1완충부재를 통해 자연스럽게 심박동기가 삽입된 피부 절개지 즉, 환부를 압박하여 압박력이 고르게 작용될 수 있도록 함으로써, 불편함을 최소화할 수 있는 효과를 얻을 수 있다.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.
또한, 본 발명은 압박부재의 하부면에 부착되어 결합되되, 상기 제1완충부재의 외측에 위치되도록 배열되어 결합되는 제2완충부재를 통해 심박동기의 체내 삽입시 발생된 파손된 혈관의 지열이 이루어질 수 있도록 함으로써, 환부의 회복이 원활하게 이루어질 수 있도록 하는 효과를 얻을 수 있다.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.
도 1은 본 발명의 바람직한 실시예에 의한 심박동기 압박 및 안정 지지대(이하, '지지대'라 한다.)가 착용된 상태를 나타낸 정면도 및 우측면도.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.
도 2는 본 발명의 바람직한 실시예에 의한 지지대가 착용된 상태를 나타낸 배면도 및 좌측면도.Fig. 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.
도 3은 본 발명의 바람직한 실시예에 의한 압박고정부를 나타낸 사시도.Figure 3 is a perspective view showing a pressure fixing part according to a preferred embodiment of the present invention.
도 4a는 본 발명의 바람직한 실시예에 의한 압박고정부를 나타낸 분해 사시도.Figure 4a is an exploded perspective view showing a pressure fixing part according to a preferred embodiment of the present invention.
도 4b는 본 발명의 바람직한 실시예에 의한 압박고정부를 나타낸 분해 저면 사시도.Figure 4b is an exploded bottom perspective view showing a pressure fixing part according to a preferred embodiment of the present invention.
도 5는 본 발명의 바람직한 실시예에 의한 압박부재를 나타낸 저면 사시도 및 저면도.Figure 5 is a bottom perspective view and bottom view showing a pressure member according to a preferred embodiment of the present invention.
도 6은 본 발명의 바람직한 실시예에 의한 압박고정부를 나타낸 측면도 및 측단면도.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.
*도면의 주요부호에 대한 상세한 설명**Detailed explanation of the main symbols in the drawing*
100 : 압박고정부100: Pressure fixing unit
110 : 압박부재 112 : 체결부재110: Pressure member 112: Fastening member
112a : 가이드홈 112a-1 : 표시눈금112a: Guide groove 112a-1: Marking scale
114 : 결합홈 116 : 제1완충부재114: Joint groove 116: First buffer member
116a : 완충홈 118 : 제2완충부재116a: Buffer groove 118: Second buffer member
120 : 고정부재 121 : 관통홀120: Fixed member 121: Through hole
122 : 걸림부재 122a : 걸림단턱122: Hook member 122a: Hook step
130 : 회전부재 132 : 걸림돌기130: Rotating member 132: Hook
140 : 이탈방지커버140: Anti-fall cover
200 : 제1고정벨트200: 1st fixed belt
300 : 제2고정벨트300: Second fixed belt
본 발명은 심박동기를 압박 및 안정화시키는 지지대에 관한 것으로, 보다 상세하게 설명하면, 심박동기가 체내에 삽입된 피부 절개지 즉, 환부에 밀접되는 압박고정부(100)와, 상기 압박고정부(100)에 일단이 결합되고 환자의 어깨와 반대편 겨드랑이 사이를 거쳐 상기 압박고정부(100)에 타단이 결합되는 제1고정벨트(200) 및 상기 압박고정부(100)에 일단이 결합되고, 환자의 두 겨드랑이를 거쳐 상기 압박고정부(100)에 타단이 결합되는 제2고정벨트(300)를 통해 상기 압박고정부(100)가 환부에 안정적으로 압박되도록 함으로써, 체내에 삽입된 심박동기의 안정화가 용이하고, 이에 따라 체내에 삽입된 심박동기가 삽입된 위치에서 안정화 즉, 상처가 회복될 때까지 고정되도록 하여 심박동기의 기능이 안정적으로 구현될 수 있도록 하는 심박동기 압박 및 안정 지지대에 관한 것이다.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.
상기와 같은 본 발명의 심박동기 압박 및 안정 지지대는 심박동기가 삽입된 위치에 형성된 피부 절개지의 상부 표면에 위치되어 상기 피부 절개지에 하부가 밀접되는 압박고정부(100);와 상기 압박고정부(100)의 전방에 일단이 결합되고, 탄성을 가지는 제1고정벨트(200); 및 상기 압박고정부(100)의 후방에 일단이 결합되고, 탄성을 가지는 제2고정벨트(300);를 포함하여 구성되고, 상기 제1고정벨트(200)는 타단이 환자의 왼쪽 어깨와 오른쪽 겨드랑이를 거쳐 상기 압박고정부(100)의 타측에 결합되며, 상기 제2고정벨트(300)는 타단이 환자의 왼쪽 겨드랑이와 오른쪽 겨드랑이를 거쳐 일단에 결합되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 압박고정부(100)는 원판 형태로 형성되어 하부가 상기 피부 절개지에 밀접되고, 외주연에 나사산이 형성된 체결부재(112)가 상부에 돌출형성되는 압박부재(110);와 상기 체결부재(112)가 승강 가능하도록 관통되고, 전방에 상기 제1고정벨트(200)의 일단이 결합되며, 타측에 상기 제1고정벨트(200)의 타단이 결합되는 한편, 후방에 상기 제2고정벨트(300)의 일단이 결합되는 고정부재(120); 및 상기 고정부재(120)의 상부에 회전 가능하도록 결합되고, 상기 체결부재(112)에 체결되어 회전됨에 따라 상기 체결부재(112)를 승강시키는 회전부재(130);를 포함하여 구성되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 고정부재(120)는 상부에 돌출형성되고, 내측 상부에 걸림단턱(122a)이 형성되는 걸림부재(122);를 포함하여 구성되고, 상기 회전부재(130)는 하부 외주연에 상기 걸림단턱(122a)과 대응되도록 돌출형성되는 걸림돌기(132);를 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 걸림부재(122)는 상기 고정부재(120)의 상부에 돌출형성되되, 호 형상으로 형성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 체결부재(112)의 외주연에 형성되는 나사산은 상기 체결부재(112)의 길이방향으로 형성되는 적어도 하나의 가이드홈(112a);을 포함하여 구성되고, 상기 고정부재(120)는 상기 체결부재(112)의 외주연과 대응되는 형상으로 형성되는 관통홀(121);을 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 가이드홈(112a)은 상기 체결부재(112)의 돌출길이를 확인할 수 있도록 형성되는 표시눈금(112a-1);을 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 체결부재(112)는 상부에 형성되는 결합홈(114);을 포함하여 구성되고, 상기 압박고정부(100)는 상기 체결부재(112)의 결합홈(114)에 하부가 결합되고, 상부 직경이 상기 체결부재(112)의 직경보다 크게 형성되는 이탈방지커버(140);를 포함하여 구성되는 것을 특징으로 한다.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).
또한, 본 발명의 상기 압박부재(110)는 하부면에 부착되어 결합되고, 탄성을 가지는 제1완충부재(116);를 포함하여 구성되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 제1완충부재(116)는 하부면에 형성되는 완충홈(116a);을 포함하여 구성되는 것을 특징으로 한다.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.
또한, 본 발명의 상기 제1완충부재(116)는 상기 압박부재(110)의 직경보다 작은 직경을 가지도록 형성되는 것을 특징으로 하고, 상기 압박부재(110)는 하부면에 부착되어 결합되되, 상기 제1완충부재(116)의 둘레에 배열되어 결합되는 복수 개의 제2완충부재(118);를 포함하여 구성되는 것을 특징으로 한다.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).
이하, 본 발명의 실시예를 도시한 도면 1 내지 6을 참고하여 본 발명을 구체적으로 설명하면 다음과 같다.Hereinafter, the present invention will be described in detail with reference to drawings 1 to 6 illustrating embodiments of the present invention.
먼저, 본 발명에서 언급되는 전방, 후방, 상부, 하부, 일측, 타측은 도면 1에 도시된 바와 같이, 환자가 누워 있는 경우를 고려하여 환자의 머리방향이 전방, 다리방향이 후방, 가슴방향이 상부, 등방향이 하부, 환자의 왼측을 일측, 환자의 오른쪽을 타측으로 지칭하고, 이후에 자세히 설명될 제1고정벨트(200)와 제2고정벨트(300)는 도면 1에 도시된 기준과 다르게 길이방향을 기준으로 일단과 타단으로 구분하여 지칭한다.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.
본 발명의 주요 구성요소인 압박고정부(100)는 심박동기가 환자의 체내에 삽입된 위치에 형성되는 피부 절개지(이하, '환부'라고도 한다.)의 상부 표면 즉, 피부 표면에 위치되어 상기 피부 절개지에 하부가 밀접되는 것으로, 이후에 자세히 설명될 제1고정벨트(200)와 제2고정벨트(300)를 통해 상기 피부 절개지의 상부에 위치되어 상기 피부 절개지를 압박함으로써, 체내에 삽입된 심박동기의 위치가 이동되지 않고 안정화될 수 있도록 한다.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.
구체적으로, 본 발명의 압박고정부(100)는 원판 형태로 형성되어 하부가 상기 피부 절개지에 밀접되고, 외주연에 나사산이 형성된 체결부재(112)가 상부에 돌출형성되는 압박부재(110)와, 상기 체결부재(112)가 승강 가능하도록 관통되고, 전방에 이후에 자세히 설명될 제1고정벨트(200)의 일단이 결합되며, 타측에 상기 제1고정벨트(200)의 타단이 결합되는 한편, 후방에 이후에 자세히 설명될 제2고정벨트(300)의 일단이 결합되는 고정부재(120) 및 상기 고정부재(120)의 상부에 회전 가능하도록 결합되고, 상기 체결부재(112)에 체결되어 회전됨에 따라 상기 체결부재(112)를 승강시키는 회전부재(130)를 포함하여 구성된다.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).
상기 압박부재(110)는 원판 형태로 형성되어 상기 피부 절개지의 상부에 안정적으로 밀접되어 상기 피부 절개지 즉, 환부 전체 혹은 환부의 80% 이상과 밀접됨으로써, 체내에 삽입된 심박동기가 삽입된 위치에서 압박될 수 있도록 한다.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.
상기 체결부재(112)는 상기 압박부재(110)가 고정부재(120)로부터 이격되거나 밀접되도록 상기 압박부재(110)가 회전부재(130)를 통해 승강되도록 함으로써, 상기 고정부재(120)가 이후에 자세히 설명될 제1고정벨트(200)와 제2고정벨트(300)를 통해 고정된 후 상기 제1고정벨트(200)와 제2고정벨트(300)의 길이조절을 하지 않고도 압박력을 조절할 수 있도록 한다.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.
부가하여, 상기 체결부재(112)의 외주연에 형성되는 나사산은 상기 체결부재(112)의 길이방향으로 형성되는 적어도 하나의 가이드홈(112a)을 포함하여 구성되는데, 상기 가이드홈(112a)은 상기 체결부재(112)가 상기 고정부재(120)를 관통하여 승강될 때, 측방향으로의 유동을 최소화하여 승강될 수 있도록 함으로써, 보다 안정적으로 승강되도록 하는 효과를 실현케 한다.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.
이때, 상기 고정부재(120)는 상기 체결부재(112)의 외주연과 대응되는 형상으로 형성되는 관통홀(121)을 포함하여 구성되고, 상기 관통홀(121)의 내주면과 상기 가이드홈(112a)의 외주연이 밀접됨으로써, 회전부재(130)의 회전에 의해 상기 체결부재(112)가 안정적으로 승강되고, 이에 따라 상기 압박부재(110)가 함께 승강되어 압박력을 조절할 수 있다.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.
아울러, 상기 가이드홈(112a)은 외주연에 형성되는 표시눈금(112a-1)을 포함하여 구성되는데, 상기 표시눈금(112a-1)은 상기 체결부재(112)가 상기 고정부재(120)를 관통하여 돌출된 돌출길이를 확인할 수 있도록 한다.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).
부가하여 설명하면, 상기 표시눈금(112a-1)은 본 발명의 지지대를 재착용할 때, 이전의 체결부재(112)의 돌출길이와 유사한 돌출길이로 조절될 수 있도록 함으로써, 이전에 본 발명의 지지대를 착용할 때와 유사한 압박력으로 피부 절개지를 압박할 수 있도록 하여 환자에게 가장 편하고 안정적인 압박력을 제공할 수 있도록 하는 효과를 실현케 한다.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.
한편, 상기 압박부재(110)는 하부면에 부착되어 결합되고, 하부가 상기 피부 절개지와 밀접되는 탄성을 가지는 합성수지 재질로 이루어진 제1완충부재(116)를 포함하여 구성될 수 있는데, 상기 제1완충부재(116)는 일예로 실리콘 또는 고무 등과 같은 탄성을 가지는 합성수지 재질로 이루어질 수 있고, 상기 피부 절개지와 밀접되어 상기 압박부재(110)에 의한 압박력이 고르게 피부 절개지 전체에 작용될 수 있도록 한다.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.
아울러, 상기 제1완충부재(116)는 하부면에 형성되는 완충홈(116a)을 포함하여 구성되는데, 상기 완충홈(116a)은 골프공의 딤플 형상으로 형성되고, 피부 절개지 즉, 환부에 압박됨에 따라 상기 제1완충부재(116)의 하부면이 외측과 내측으로 압박되어 면적이 확장됨으로써, 환부가 보다 고르고 안정적으로 압박될 수 있도록 하며, 피부 절개지의 중심에 위치되어 피부 절개지의 중심의 압박력이 전체적인 압박력에 비해 약하게 작용될 수 있도록 하여 상기 피부 절개지가 보호될 수 있도록 한다.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.
이때, 상기 제1완충부재(116)는 이후에 자세히 설명될 제2완충부재(118)가 압박부재(110)의 하부면에 부착되어 결합되지 않는 경우 상기 압박부재(110)의 직경과 동일한 직경으로 형성되는 것이 바람직하다.At this time, it is preferable that the first buffer member (116) be 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) and is not combined.
상기와 연관하여, 상기 압박부재(110)는 하부면에 부착되어 결합되되, 상기 제1완충부재(116)의 외측에 위치되도록 즉, 상기 제1완충부재(116)의 둘레에 배열되어 결합되는 복수 개의 제2완충부재(118)를 포함하여 구성된다.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).
이에 따라, 상기 제1완충부재(116)는 상기 제2완충부재(118)가 상기 압박부재(110)의 하부면에 부착되어 결합될 수 있도록 상기 압박부재(110)의 직경보다 작은 직경을 가지도록 형성된다.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).
상기 제2완충부재(118)는 피부 절개지의 중심으로부터 이격된 둘레가 압박되도록 하되, 복수 개가 원형으로 이격되어 배열되도록 상기 압박부재(110)의 하부면에 결합됨으로써, 피부 절개지의 파손된 혈관을 지혈하여 파손된 혈관의 회복이 원활하게 이루어질 수 있도록 하는 효과를 실현케 한다.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.
이때, 상기 제2완충부재(118)의 하부는 만곡된 형상으로 형성되어 피부 절개지의 파손된 혈관이 자연스럽고 안정적으로 지혈될 수 있도록 하는 효과를 실현케 한다.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.
부가하여, 상기 제2완충부재(118)가 복수 개로 구성되어 이격되는 이유는 파손되지 않은 혈관들의 혈액순환이 원활하게 이루어져 환부의 회복이 안정적으로 이루어질 수 있도록 하기 위함이다.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.
즉, 의료진은 심박동기가 체내에 삽입된 기간이 기준일(약 3 내지 5일)을 경과하지 않았을 때, 즉, 피부 절개지 주위의 혈관이 파손된 상태일 때는 상기 제2완충부재(118)가 부착되어 결합된 압박부재(110)를 사용하여 심박동기를 압박 및 안정화 시키고, 심박동기가 체내에 삽입된 기간이 기준일을 경과하였을 때, 즉, 피부 절개지 주위의 혈관의 파손이 회복되었다고 파단될 때는 상기 제1완충부재(116)만 부착되어 결합된 압박부재(110)를 사용하여 심박동기를 보다 안정적이고 견고하게 압박시킬 수 있다.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.
상기 고정부재(120)는 상기 압박부재(110)의 체결부재(112)가 승강 가능하도록 앞서 설명된 관통홀(121)이 형성되고, 전방에 이후에 자세히 설명될 제1고정벨트(200)의 일단이 결합되며, 타측에 상기 제1고정벨트(200)의 타단이 결합되는 한편, 후방에 이후에 자세히 설명될 제2고정벨트(300)의 일단이 결합되어 상기 제1고정벨트(200)와 제2고정벨트(300)에 의해 본 발명의 압박고정부(100)가 심박동기가 삽입된 위치에 형성된 피부 절개지의 상부 표면에 안정적으로 위치되도록 한다.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).
또한, 상기 고정부재(120)는 상기 체결부재(112)가 승강 가능하도록 설치됨에 따라 본 발명의 지지대가 환자에 착용된 상태에서도 상기 압박부재(110)에 의한 압박력을 조절할 수 있도록 한다.In addition, the fixing member (120) is installed so that the fastening member (112) can be raised and lowered, thereby allowing the pressure force by the pressure member (110) to be adjusted even when the support of the present invention is worn by a patient.
아울러, 상기 고정부재(120)는 이후에 자세히 설명될 제1고정벨트(200)의 일단과 타단 및 제2고정벨트(300)의 일단이 결합될 수 있도록 전방과 타측 및 후방에 각각 결합홀(도면 미표시)이 형성되어 상기 제1고정벨트(200)의 일단과 타단 및 제2고정벨트(300)의 일단이 관통된 후 결합될 수 있도록 한다.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.
상기 회전부재(130)는 상기 고정부재(120)의 상부에 회전 가능하게 결합되고, 내주연에 상기 체결부재(112)의 외주연에 형성된 나사산과 대응되는 나사산이 형성되어 상기 체결부재(112)에 체결되어 회전됨에 따라 상기 체결부재(112)를 승강시킨다.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.
즉, 상기 회전부재(130)는 상기 고정부재(120)의 상부에 회전 가능하게 결합됨에 따라, 회전될 때 승강되지 않음으로, 회전에 의해 상기 체결부재(112)가 승강되고, 의료진 또는 환자는 상기 회전부재(130)를 회전시켜 쉽게 압박력을 조절할 수 있는 효과를 얻을 수 있다.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).
이때, 상기 회전부재(130)는 외주연에 형성되는 복수 개의 파지홈(도면 미표시)을 포함하여 구성될 수 있고, 상기 파지홈을 통해 의료진 또는 환자가 용이하게 회전시킬 수 있는 효과를 얻을 수 있다.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.
또한, 상기 회전부재(130)는 외주연에 돌출형성되는 적어도 한 쌍의 파지돌기(도면 미표시)를 포함하여 구성될 수 있고, 상기 파지돌기는 상기 파지홈과 함께 의료진 또는 환자가 상기 회전부재(130)를 보다 용이하게 회전시킬 수 있는 효과를 실현케 한다.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).
상기와 연관하여, 상기 회전부재(130)가 상기 고정부재(120)에 회전가능하도록 결합되는 구조를 설명하면, 상기 고정부재(120)는 상부에 돌출형성되고, 내측 상부에 걸림단턱(122a)이 형성되는 걸림부재(122)를 포함하여 구성되고, 상기 회전부재(130)는 하부 외주연에 상기 걸림단턱(122a)과 대응되도록 돌출형성되는 걸림돌기(132)를 포함하여 구성되며, 상기 회전부재(130)는 상기 걸림돌기(132)가 걸림부재(122)에 회전가능하게 결합된다.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).
즉, 상기 회전부재(130)는 걸림돌기(132)의 상부가 상기 고정부재(120)에 돌출형성된 걸림부재(122)의 걸림단턱(122a)의 하부에 걸려 상기 고정부재(120)의 상부면과 상기 걸림단턱(122a)의 사이에 상기 걸림돌기(132)가 위치됨에 따라 회전가능하게 결합되고, 이에 따라 상기 체결부재(112)와 체결되면 회전시 상기 체결부재(112)가 승강된다.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.
이때, 상기 걸림부재(122)는 호 형상으로 형성되어 일부가 개방됨에 따라 상기 회전부재(130)의 걸림돌기(132)가 상기 고정부재(120)의 상부면과 상기 걸림단턱(122a)의 사이에 용이하게 결합되고, 이후 상기 체결부재(112)가 상기 회전부재(130)에 결합됨에 따라 고정된다.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.
상기와 연관하여, 상기 체결부재(112)는 상부에 형성되는 결합홈(114)을 포함하여 구성되고, 본 발명의 압박고정부(100)는 상기 체결부재(112)의 결합홈(114)에 하부가 결합되고, 상부 직경이 상기 체결부재(112)의 직경보다 크게 형성되는 이탈방지커버(140)를 포함하여 구성된다.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).
즉, 상기 이탈방지커버(140)는 상기 회전부재(130)를 회전시켜 상기 체결부재(112)를 하강시킬 때 하부면이 상기 회전부재(130)의 상부면과 접촉됨으로써, 상기 체결부재(112)가 더이상 하강되지 않도록 하여 상기 회전부재(130)와 체결부재(112)가 분리되는 것을 방지하여 본 발명의 지지대가 안정적으로 설치된 상태를 유지할 수 있도록 한다.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.
이때, 상기 회전부재(130)는 상부면에 상기 이탈방지커버(140)의 직경과 대응되도록 형성되는 안착홈(도면 미표시)을 포함하여 구성되는데, 상기 안착홈은 상기 이탈방지커버(140)가 상기 회전부재(130)의 상부에 내입되도록 하여 상기 체결부재(112)의 하강 길이 즉, 하강된 상태를 보다 쉽게 확인할 수 있도로 함으로써, 압박부재(110)의 압박 상태를 보다 빠르게 판단할 수 있도록 하는 효과를 실현케 한다.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).
본 발명의 주요 구성요소인 제1고정벨트(200)는 탄성을 가지는 재질로 이루어지고, 상기 압박고정부(100)의 전방 즉, 상기 고정부재(120)의 전방에 일단이 결합되는 것으로, 상기 압박고정부(100)의 상부 및 타측이 피부 절개지 즉, 환부에 밀접된 상태로 위치가 고정될 수 있도록 한다.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.
이러한 본 발명의 제1고정벨트(200)는 상부면에 암벨크로(도면 미표시)가 형성되고, 상부면 일단과 타단에 각각 수벨크로(도면 미표시)가 형성되어 도면 1과 같이 앞서 설명된 상기 고정부재(120)의 전방에 형성된 결합홀에 일단이 관통된 후 일단의 수벨크로가 암벨크로에 부착결합되어 고정되고, 상기 고정부재(120)의 타측에 형성된 결합홀에 타단이 관통된 후 타단의 수벨크로가 암벨크로에 부착결합되어 고정된다.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.
이에 따라, 본 발명의 제1고정벨트(200)는 일단을 상기 고정부재(120)의 전방에 결합시킨 후 타단을 당겨 상기 고정부재(120)의 타측에 결합시킴으로써, 압박력을 형성함과 동시에 상기 압박고정부(100)의 전방 및 타측이 환부에 압박력이 형성된 상태로 고정될 수 있도록 한다.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.
부가하여 설명하면, 상기 제1고정벨트(200)는 일단이 상기 고정부재(120)의 전방에 결합된 후 타단이 환자의 왼쪽 어깨와 오른쪽 겨드랑이를 거쳐 상기 압박고정부(100)의 타측에 결합됨으로써, 보다 견고하게 상기 압박고정부(100)가 설치된 상태를 유지할 수 있도록 한다.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.
본 발명의 주요 구성요소인 제2고정벨트(300)는 탄성을 가지는 재질로 이루어지고, 상기 압박고정부(100)의 후방 즉, 상기 고정부재(120)의 후방에 일단이 결합되는 것으로, 상기 압박고정부(100)의 후방이 피부 절개지 즉, 환부에 밀접된 상태로 위치가 고정될 수 있도록 하여 상기 제1고정벨트(200)와 함께 상기 압박고정부(100)의 위치가 안정적이고 견고하게 유지될 수 있도록 한다.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).
이러한 본 발명의 제2고정벨트(300)는 상부면에 암벨크로(도면 미표시)가 형성되고, 상부면 일단과 하부면 타단에 각각 수벨크로(도면 미표시)가 형성되어 도면 1과 같이 앞서 설명된 상기 고정부재(120)의 후방에 형성된 결합홀에 일단이 관통된 후 상부면 일단의 수벨크로가 암벨크로에 부착결합되어 고정되고, 하부면 타단의 수벨크로가 상부면 일단의 암벨크로에 부착결합되어 고정된다.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.
이에 따라, 본 발명의 제2고정벨트(300)는 일단을 상기 고정부재(120)의 후방에 결합시킨 후 타단을 당겨 일단에 결합시킴으로써, 압박력을 형성함과 동시에 상기 압박고정부(100)의 후방이 환부에 압박력이 형성된 상태로 고정될 수 있도록 하여 상기 제1고정벨트(200)와 함게 상기 압박고정부(100)의 위치가 정확한 위치에 압박력이 형성되는 상태에서 유지될 수 있도록 한다.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).
부가하여 설명하면, 상기 제2고정벨트(300)는 일단이 상기 고정부재(120)의 후방에 결합된 후 타단이 환자의 왼쪽 겨드랑이와 오른쪽 겨드랑이를 거쳐 일단에 결합됨으로써, 보다 견고하게 상기 압박고정부(100)가 설치된 상태를 유지할 수 있도록 한다.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.
이때, 환자의 왼쪽 어깨가 불편한 경우 상기 압박고정부(100)를 회전시켜 상기 제1고정벨트(200)의 타단이 환자의 오른쪽 어깨와 왼쪽 겨드랑이를 거쳐 상기 압박고정부(100)의 타측(회전시 일측)에 결합되고, 상기 제2고정벨트(300)의 타단이 환자의 오른쪽 겨드랑이와 오른쪽 겨드랑이를 거쳐 일단에 결합되도록 할 수 있음은 자명할 것이다.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.
상기는 본 발명의 바람직한 실시예를 참고로 설명하였으며, 본 발명은 상기의 실시예에 한정되지 아니하고, 상기의 실시예를 통해 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자가 본 발명의 요지를 벗어나지 않는 범위에서 다양한 변경으로 실시할 수 있는 것이다.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 (10)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020240017134A KR102813148B1 (en) | 2024-02-05 | 2024-02-05 | Pacemaker pressure and stabilization support fixture |
| KR10-2024-0017134 | 2024-02-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2025170191A1 true WO2025170191A1 (en) | 2025-08-14 |
Family
ID=95936001
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/KR2024/095255 Pending WO2025170191A1 (en) | 2024-02-05 | 2024-02-16 | Pacemaker compression and stabilization support |
Country Status (2)
| Country | Link |
|---|---|
| KR (1) | KR102813148B1 (en) |
| WO (1) | WO2025170191A1 (en) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR200381454Y1 (en) * | 2005-01-19 | 2005-04-12 | 정명자 | Styptic Belt |
| JP2011528569A (en) * | 2008-05-06 | 2011-11-24 | メリット・メディカル・システムズ・インコーポレーテッド | Radial artery compression device |
| KR101796213B1 (en) * | 2016-06-22 | 2017-11-09 | 재단법인 아산사회복지재단 | Medical apparatus for hemostasis of central venous line insertion site |
| JP2018019988A (en) * | 2016-08-05 | 2018-02-08 | 国立大学法人 熊本大学 | Wound compression device |
| JP7303580B2 (en) * | 2019-04-16 | 2023-07-05 | 依奈徳医療技術（上海）有限公司 | hemostatic belt |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101955291B1 (en) | 2017-10-25 | 2019-03-08 | (주) 타우피엔유메디칼 | A device to treat heart valve regurgitation and fix the pacemaker lead |
-
2024
- 2024-02-05 KR KR1020240017134A patent/KR102813148B1/en active Active
- 2024-02-16 WO PCT/KR2024/095255 patent/WO2025170191A1/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR200381454Y1 (en) * | 2005-01-19 | 2005-04-12 | 정명자 | Styptic Belt |
| JP2011528569A (en) * | 2008-05-06 | 2011-11-24 | メリット・メディカル・システムズ・インコーポレーテッド | Radial artery compression device |
| KR101796213B1 (en) * | 2016-06-22 | 2017-11-09 | 재단법인 아산사회복지재단 | Medical apparatus for hemostasis of central venous line insertion site |
| JP2018019988A (en) * | 2016-08-05 | 2018-02-08 | 国立大学法人 熊本大学 | Wound compression device |
| JP7303580B2 (en) * | 2019-04-16 | 2023-07-05 | 依奈徳医療技術（上海）有限公司 | hemostatic belt |
Also Published As
| Publication number | Publication date |
|---|---|
| KR102813148B1 (en) | 2025-05-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2019103540A1 (en) | Cerclage atrial defibrillator | |
| WO2018143560A1 (en) | Tool for tricuspid regurgitation operation | |
| Fitzpatrick et al. | Recurrent symptoms after ventricular pacing in unexplained syncope | |
| KAPLAN et al. | Closed-Chest Cardiac Massage for Circulatory Arrest: Effectiveness in 100 Consecutive Cases | |
| HARRIS et al. | Epicardial pacing to control arrhythmias following cardiac surgery | |
| WO2025170191A1 (en) | Pacemaker compression and stabilization support | |
| US12357832B1 (en) | Multifunctional pacemaker wire conversion device and application method thereof | |
| Bach et al. | Cardiac arrhythmias from a malpositioned Greenfield filter in a traumatic quadriplegic | |
| WO2019190060A1 (en) | Capture catheter for sensing myocardial electrical signal | |
| WO2021010679A2 (en) | Cerclage operation device provided with position fixing device | |
| O'Toole et al. | Emergency transcutaneous pacing in the management of patients with bradyasystolic rhythms | |
| CN218890064U (en) | Transitional pacemaker | |
| CN213047689U (en) | Adjustable elastic fixing chest strap for cardiothoracic surgery | |
| Ciesla et al. | Lines, tubes, catheters, and physiologic monitoring in the ICU | |
| RU2036670C1 (en) | Method of temporary electric stimulation of heart | |
| Rein et al. | Noninvasive external pacing in the newborn | |
| Furman et al. | An Intracardiac Pacemaker for Stokes–Adams Seizures. | |
| CN221557270U (en) | Nasal cannula fixing device | |
| RU2815893C2 (en) | Fastening system for electrostimulation generator | |
| CN218106532U (en) | Oxygen supply device | |
| CN213346611U (en) | Head fixing device for interventional operation | |
| Heller | Nursing the Patient With an ARTIFICIAL PAGEMAKER | |
| CN216755200U (en) | Temporary pacemaker electrode fixing device | |
| Kavan et al. | Electroencephalographic Patterns During Intracardiac Surgery Using Cardiopulmonary Bypass: A Comparison of Two Anesthetic Agents | |
| KLEINSCHMIDT et al. | The Bland‐White‐Garland syndrome. Clinical picture and anaesthesiological management |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 24924131 Country of ref document: EP Kind code of ref document: A1 |