CN211381514U - Atrial septal defect stoma plugging device - Google Patents

Atrial septal defect stoma plugging device Download PDF

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Publication number
CN211381514U
CN211381514U CN201920932677.7U CN201920932677U CN211381514U CN 211381514 U CN211381514 U CN 211381514U CN 201920932677 U CN201920932677 U CN 201920932677U CN 211381514 U CN211381514 U CN 211381514U
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atrial septal
septal defect
waist
stoma
tray body
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CN201920932677.7U
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张刚成
荆志成
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Wuhan Xinwei Medical Technology Co ltd
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Wuhan Maidi Weien Medical Technology Co ltd
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Abstract

The utility model discloses an atrial septal defect makes a mouthful plugging device relates to medical instrument technical field, has solved the unable complete cure of traditional ASD plugging device and has had the problem of the high pulmonary artery resistance patient of shunting to the left in the right side, and its technical scheme main points are: the waist-shaped table comprises a left table body, a waist body and a right table body which are coaxially arranged, wherein two ends of the waist body are respectively fixedly connected with the left table body and the right table body; the central shafts of the left tray body, the waist body and the right tray body are provided with stoma through holes in a penetrating way; the diameter of left side disk body equals with the diameter of right disk body, and the face that deviates from of left side disk body and right disk body is equipped with first die and second die respectively, has and provides the passageway of intervention operation approach for right heart catheter inspection in the atrial septal defect treatment process, can carry out effective treatment to left side cardiac diastole insufficiency and the patient of pulmonary hypertension heart failure.

Description

Atrial septal defect stoma plugging device
Technical Field
The utility model relates to the technical field of medical equipment, more specifically say, it relates to atrial septal defect makes a mouthful plugging device.
Background
Atrial Septal Defects (ASD) are a common congenital heart disease, which is a congenital abnormality in which the septum between the left and right atria is underdeveloped, causing abnormal shunting of blood flow in the heart. Atrial septal defects can be divided into two major types, secondary pore type defects and primary pore type defects, and the former are the majority. About 10-15% of the congenital heart disease, and the ratio of male to female is 1: 2.
An Atrial Septal Defect (ASD) occluder is a specially designed instrument for occluding atrial septal defects. The physician will select the appropriate occluder for a particular atrial septal defect and the selected occluder will be implanted through the catheter to the defect site and permanently left at the defect site. The technology is firstly used in clinic in 1976. Until now in the late eighties, with the continuous improvement of occluders, the technology has become mature day by day, especially under the guidance of the rapidly developed two-dimensional and three-dimensional transesophageal echocardiography technology. The therapeutic measures are to adopt a transfemoral femoral vein puncture method, send the stopper into the atrium, fix the stopper at the Atrioventricular Septal Defect (ASD) lesion, block left-right shunt of the atrial level and restore the normal blood circulation path.
Atrial septal defects, however, are prone to endocardial infection, which affects cardiac function. Under the condition, if the problems of obvious pulmonary hypertension and the like do not exist, the defect part is generally only required to be blocked or repaired by interventional therapy, the wound is small, the patient can be discharged after observing for 2 days after the blockage, and the postoperative recovery is quicker. However, if the patient with high pulmonary artery resistance has a right-left shunt due to the combination of the congenital heart disease (such as ASD) and pulmonary hypertension, the traditional ASD occluder cannot completely cure the patient, and the correction of the cardiac deformity cannot reduce the pulmonary artery pressure, and can also cause the pulmonary artery pressure of the patient to rise sharply or even die suddenly. Therefore, how to design an atrial septal defect stoma occluder is a problem which is urgently needed to be solved at present, and provides a basic condition for treating patients with left diastolic dysfunction and pulmonary hypertension heart failure.
SUMMERY OF THE UTILITY MODEL
The utility model aims at providing an atrial septal defect makes a mouthful occluder has and provides the passageway of interveneeing the operation approach for right heart catheter inspection in the atrial septal defect treatment process, can carry out the effect of treatment to left heart diastole insufficiency and the patient of pulmonary hypertension heart failure.
The above technical purpose of the present invention can be achieved by the following technical solutions: the atrial septal defect stoma occluder comprises a left tray body, a waist body and a right tray body which are coaxially arranged, wherein two ends of the waist body are fixedly connected with the left tray body and the right tray body respectively; the central shafts of the left tray body, the waist body and the right tray body are provided with stoma through holes in a penetrating way; the diameter of the left tray body is equal to that of the right tray body, and a first riveting head and a second riveting head are respectively arranged on the deviating surfaces of the left tray body and the right tray body.
By adopting the technical scheme, the occluder is implanted into the atrial septal defect, so that the left disk body and the right disk body are respectively positioned at two sides of the atrial septal defect and the waist body passes through the atrial septal defect, a channel for interventional operation access is conveniently provided for right heart catheter examination, and patients with left cardiac diastolic dysfunction and pulmonary hypertension heart failure can be treated; the left tray body and the right tray body with equal diameters are utilized, so that the permanent retention of the occluder at the atrial septal defect is more stable; the position of the plugging device can be conveniently adjusted by utilizing the first riveting head and the second riveting head.
The utility model discloses further set up to: the left tray body, the waist body and the right tray body are all nickel-titanium alloy wire knitted bodies.
By adopting the technical scheme, the plasticity of the plugging device is convenient to enhance.
The utility model discloses further set up to: the waist body comprises a first spiral body and a second spiral body which are opposite in spiral direction, and the first spiral body and the second spiral body are woven in a crossed mode.
By adopting the technical scheme, the sealing performance of the stoma through hole is convenient to enhance by utilizing the first spiral body and the second spiral body.
The utility model discloses further set up to: the diameter of the stoma through hole is 5-12 mm.
By adopting the technical scheme, the application range of the stoma through hole is convenient to enhance.
The utility model discloses further set up to: the diameter of the stoma through hole is 5mm, 6mm, 8mm, 10mm or 12 mm.
By adopting the technical scheme, the right heart catheter is convenient to match with the existing right heart catheter.
The utility model discloses further set up to: the first rivet head and the second rivet head are arranged in a centrosymmetric mode deviating from a central point.
By adopting the technical scheme, the position of the plugging device can be flexibly adjusted from multiple directions.
The utility model discloses further set up to: the first rivet head and the second rivet head are both stainless steel bodies.
Through adopting above-mentioned technical scheme, prevent that condition such as first die and second die corrosion, oxidation from taking place.
To sum up, the utility model discloses following beneficial effect has: implanting the occluder into the atrial septal defect, so that the left disc body and the right disc body are respectively positioned at two sides of the atrial septal defect and the waist body passes through the atrial septal defect, thereby being convenient for providing a channel for interventional operation access for right heart catheter examination and being capable of treating patients with left cardiac diastolic dysfunction and pulmonary hypertension heart failure; the left tray body and the right tray body with equal diameters are utilized, so that the permanent retention of the occluder at the atrial septal defect is more stable; the first rivet head and the second rivet head are utilized, so that the position of the plugging device can be flexibly adjusted from multiple directions; the sealing performance of the stoma through hole is enhanced by utilizing the first spiral body and the second spiral body.
Drawings
Fig. 1 is a schematic view of the overall structure in an embodiment of the present invention;
fig. 2 is an exploded view of the waist body in the embodiment of the present invention.
In the figure: 1. a left tray body; 2. a right tray body; 3. a waist body; 4. an ostomy through-hole; 5. a first rivet head; 6. a second rivet head; 7. a first spiral body; 8. a second spiral body.
Detailed Description
The present invention will be described in further detail with reference to the accompanying fig. 1-2.
Example (b): atrial septal defect stoma occluder, as shown in figure 1, including coaxial left disk body 1, waist body 3 and the right disk body 2 that sets up, 3 both ends of waist body respectively with left disk body 1 and right disk body 2 integrated into one piece. A stoma through hole 4 is arranged through the central shaft of the left tray body 1, the waist body 3 and the right tray body 2. The diameter of the left tray body 1 is equal to that of the right tray body 2, and the deviating surfaces of the left tray body 1 and the right tray body 2 are respectively provided with a first rivet head 5 and a second rivet head 6. The occluder is implanted into the atrial septal defect, the left disk body 1 and the right disk body 2 are respectively positioned at two sides of the atrial septal defect and the waist body 3 passes through the atrial septal defect, so that a channel for interventional operation access is conveniently provided for right heart catheter examination, and patients with left cardiac diastolic dysfunction and pulmonary hypertension heart failure can be treated. The left tray body 1 and the right tray body 2 with equal diameters are utilized, so that the permanent retention of the occluder at the atrial septal defect is more stable. The position of the plugging device can be conveniently adjusted by utilizing the first riveting head 5 and the second riveting head 6.
In this embodiment, the left tray body 1, the waist body 3 and the right tray body 2 are all woven from nitinol wires, which is convenient for enhancing the plasticity of the plugging device.
As shown in fig. 2, the waist body 3 includes a first spiral body 7 and a second spiral body 8 with opposite spiral directions, and the first spiral body 7 and the second spiral body 8 are woven in a crossing manner. The sealing performance of the stoma via 4 is facilitated by the first and second screws 7, 8.
The diameter of the stoma via 4 is 5-12mm, which facilitates enhancing the application range of the stoma via 4.
In this embodiment, the stoma via 4 has a diameter of 5mm, 6mm, 8mm, 10mm or 12mm, which is convenient for matching with an existing right heart catheter.
As shown in fig. 1, the first rivet head 5 and the second rivet head 6 are arranged in a central symmetry manner deviating from a central point, so that the position of the plugging device can be flexibly adjusted from multiple directions.
In this embodiment, the first rivet head 5 and the second rivet head 6 are made of stainless steel, so as to prevent corrosion, oxidation and the like of the first rivet head 5 and the second rivet head 6.
The working principle is as follows: the occluder is implanted into the atrial septal defect, the left disk body 1 and the right disk body 2 are respectively positioned at two sides of the atrial septal defect and the waist body 3 passes through the atrial septal defect, so that a channel for interventional operation access is conveniently provided for right heart catheter examination, and patients with left cardiac diastolic dysfunction and pulmonary hypertension heart failure can be treated. The left tray body 1 and the right tray body 2 with equal diameters are utilized, so that the permanent retention of the occluder at the atrial septal defect is more stable. By utilizing the first rivet head 5 and the second rivet head 6, the position of the plugging device can be flexibly adjusted from multiple directions.
The present embodiment is only for explaining the present invention, and it is not limited to the present invention, and those skilled in the art can make modifications to the present embodiment without inventive contribution as required after reading the present specification, but all of them are protected by patent laws within the scope of the claims of the present invention.

Claims (7)

1. Atrial septal defect makes a mouthful plugging device, characterized by: the waist-shaped table comprises a left table body (1), a waist body (3) and a right table body (2) which are coaxially arranged, wherein two ends of the waist body (3) are fixedly connected with the left table body (1) and the right table body (2) respectively; a stoma through hole (4) is arranged in a penetrating way on the central shaft of the left tray body (1), the waist body (3) and the right tray body (2); the diameter of the left tray body (1) is equal to that of the right tray body (2), and the deviating surfaces of the left tray body (1) and the right tray body (2) are respectively provided with a first rivet head (5) and a second rivet head (6).
2. The atrial septal defect stoma occluder of claim 1, wherein: the left tray body (1), the waist part body (3) and the right tray body (2) are all nickel-titanium alloy wire knitted bodies.
3. The atrial septal defect stoma occluder of claim 1, wherein: the waist body (3) comprises a first spiral body (7) and a second spiral body (8) which are opposite in spiral direction, and the first spiral body (7) and the second spiral body (8) are woven in a crossed mode.
4. The atrial septal defect stoma occluder of claim 1, wherein: the diameter of the stoma through hole (4) is 5-12 mm.
5. The atrial septal defect stoma occluder of claim 4, wherein: the diameter of the stoma through hole (4) is 5mm, 6mm, 8mm, 10mm or 12 mm.
6. The atrial septal defect stoma occluder of claim 1, wherein: the first rivet head (5) and the second rivet head (6) are arranged in a centrosymmetric mode deviating from a central point.
7. The atrial septal defect stoma occluder of claim 1, wherein: the first rivet head (5) and the second rivet head (6) are both stainless steel bodies.
CN201920932677.7U 2019-06-20 2019-06-20 Atrial septal defect stoma plugging device Active CN211381514U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201920932677.7U CN211381514U (en) 2019-06-20 2019-06-20 Atrial septal defect stoma plugging device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201920932677.7U CN211381514U (en) 2019-06-20 2019-06-20 Atrial septal defect stoma plugging device

Publications (1)

Publication Number Publication Date
CN211381514U true CN211381514U (en) 2020-09-01

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Application Number Title Priority Date Filing Date
CN201920932677.7U Active CN211381514U (en) 2019-06-20 2019-06-20 Atrial septal defect stoma plugging device

Country Status (1)

Country Link
CN (1) CN211381514U (en)

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Effective date of registration: 20231030

Address after: No. 4, 4th Floor, Building 12, Block B, No. 818 Gaoxin Avenue, Donghu New Technology Development Zone, Wuhan City, Hubei Province, 430000

Patentee after: Wuhan Xinwei Medical Technology Co.,Ltd.

Address before: Room 17, 3rd Floor, Building 2 and 3, Yinhai Huating, No.1 Xiaohongshan Te, Wuchang District, Wuhan City, Hubei Province, 430000

Patentee before: WUHAN MAIDI WEIEN MEDICAL TECHNOLOGY CO.,LTD.

TR01 Transfer of patent right