WO2014103907A1 - カテーテル用バルーン、カテーテル及びカテーテル用バルーンを作製する方法 - Google Patents
カテーテル用バルーン、カテーテル及びカテーテル用バルーンを作製する方法 Download PDFInfo
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- WO2014103907A1 WO2014103907A1 PCT/JP2013/084196 JP2013084196W WO2014103907A1 WO 2014103907 A1 WO2014103907 A1 WO 2014103907A1 JP 2013084196 W JP2013084196 W JP 2013084196W WO 2014103907 A1 WO2014103907 A1 WO 2014103907A1
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- Prior art keywords
- balloon
- catheter
- band
- pressure
- diameter
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1002—Balloon catheters characterised by balloon shape
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1027—Making of balloon catheters
- A61M25/1029—Production methods of the balloon members, e.g. blow-moulding, extruding, deposition or by wrapping a plurality of layers of balloon material around a mandril
-
- 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
- A61F2/2427—Devices for manipulating or deploying heart valves during implantation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1002—Balloon catheters characterised by balloon shape
- A61M2025/1004—Balloons with folds, e.g. folded or multifolded
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1027—Making of balloon catheters
- A61M25/1029—Production methods of the balloon members, e.g. blow-moulding, extruding, deposition or by wrapping a plurality of layers of balloon material around a mandril
- A61M2025/1031—Surface processing of balloon members, e.g. coating or deposition; Mounting additional parts onto the balloon member's surface
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M2025/1043—Balloon catheters with special features or adapted for special applications
- A61M2025/1084—Balloon catheters with special features or adapted for special applications having features for increasing the shape stability, the reproducibility or for limiting expansion, e.g. containments, wrapped around fibres, yarns or strands
Definitions
- causes of stenotic aortic lesions include acquired calcification, rheumatic aortic stenosis, and congenital aortic stenosis.
- calcifying aortic stenosis when the lesion becomes worse, the calcification of the leaflets progresses, the leaflets gradually harden, and the range of movement is gradually limited, which can cause heart failure. Therefore, in the case of severe valve leaflet stenosis, treatment by surgery is necessary.
- a highly elastic material such as latex or silicone may be used as the balloon material, and the entire balloon is made extensible.
- a highly elastic material such as latex or silicone
- the outer diameter after contraction becomes small it has an advantage that it can be easily removed.
- a balloon made of a highly elastic material such as latex or silicone can have an arbitrarily large diameter, there has been a problem that an apparatus or means for accurately controlling the expanded outer diameter of the extensible balloon is required.
- the existing balloon is cylindrical or egg-shaped, and blood and blood vessel walls are slippery, so it is easy to move. There was a problem that attention was required.
- the present invention employs the following means in order to achieve the above-described object.
- the catheter balloon of the present invention includes a cylindrical balloon portion formed in a non-extensible or low-extensible state, and an elastic body wound around the balloon portion and having a diameter shorter than the expanded diameter of the balloon portion. And a band portion comprising:
- the balloon portion may be made of a non-stretchable material or a low-stretchable material.
- the expansion ratio of the outer diameter may be 10% or less.
- the balloon for a catheter when the balloon portion is below a predetermined pressure, only the portion to which the band portion is not attached is inflated to form a substantially bowl shape, and at a predetermined pressure or higher.
- the band part may also expand.
- the balloon portion is inflated only at a portion where the band portion is not attached at a pressure lower than a predetermined pressure, and has a substantially bowl shape, at a pressure higher than the predetermined pressure.
- the band portion may also expand and become substantially cylindrical.
- a production method for producing a balloon for a catheter includes: (1) A step of disposing a tubular band around a tubular member made of a non-stretchable or low-stretchable material (2) From the step of heating these and expanding the tubular member into a cylindrical shape while hot-drawing It is characterized by becoming.
- a balloon for a catheter can be produced in one step, and the band part and the balloon part can be thermally welded over the entire surface.
- a step of attaching a stretchable band to a processed cylindrical material There may be.
- the method of attaching the stretchable band to the processed cylindrical material may be adhesion, heat welding, or the like.
- the expansion outer diameter of the extensible balloon can be easily controlled in the treatment of calcification, rheumatic and congenital aortic stenosis. Further, it is possible to provide a catheter balloon that can effectively prevent balloon migration and can be easily fixed at a predetermined position, a catheter, and a method for manufacturing the catheter balloon.
- FIG. 1A is a schematic diagram showing a state where the shoulder portion of the catheter balloon 10 according to the embodiment is expanded
- FIG. 1B is a schematic diagram showing a state where the balloon portion and the band portion according to the embodiment are disassembled.
- FIG. FIG. 2 is a view showing a variation of the state in which the band portion 30 of the catheter balloon 10 according to the embodiment is expanded.
- Drawing 3 is a figure showing a process of the 1st manufacturing method of balloon 10 for catheters concerning an embodiment. 4 is an enlarged cross-sectional view taken along a line BB in FIG.
- Drawing 5 is a figure showing a process of the 2nd manufacturing method of balloon 10 for catheters concerning an embodiment.
- Drawing 6 is a figure showing a process of a usage method of balloon 10 for catheters concerning an embodiment.
- FIG. 7 is a graph showing changes in the balloon internal pressure and the outer diameter of the catheter balloon.
- FIG. 1 is a schematic view showing a state where the shoulder portion of the balloon for catheter of the present invention is expanded
- FIG. 2 is a schematic view showing a state where the balloon portion and the band portion are disassembled.
- expansion means that the balloon simply opens due to an increase in internal pressure, and does not substantially mean that the balloon itself expands and expands.
- Extension means that the band itself is extended to increase the diameter.
- the catheter balloon 10 of the present embodiment is made of a cylindrical balloon portion 20 made of a non-extensible material or a low-extensible material, and a material made of a stretchable elastic body.
- the band part 30 is provided.
- the band portion 30 has a diameter shorter than the expanded diameter of the balloon portion 20 in a state where no expansion force is applied, and is wound around the middle of the balloon portion 20. For this reason, the balloon 10 for the catheter is intentionally made thin without intentionally expanding the portion of the cylindrical portion 21 of the balloon portion 20 around which the band portion 30 is wound. easily expanded.
- the balloon part 20 is formed in a hollow bag shape formed in a conical shape so that the middle abdomen is formed in a cylindrical shape and both ends are squeezed.
- the balloon itself is formed to be non-extensible or low-extensible, and is formed so as not to expand more than a certain amount even when the inside is pressurized.
- Various known materials can be used as the material used for the balloon unit 20. For example, nylon, polyvinyl chloride, polyethylene, polyurethane, polyether block amide copolymer, olefin-based polymers such as polyethylene terephthalate and polypropylene, or a copolymer made of a combination thereof can be used.
- a non-stretchable material or a low-stretchable material is used for the material itself forming the balloon portion 20.
- the balloon part 20 does not necessarily need to be a single material, and may be a two-layered material made of different materials for the inner layer and the outer layer.
- Such a two-layer balloon can be produced by molding a tube produced by two-layer extrusion.
- a material having high compatibility with the band portion 30 described later is employed for the outer layer, the materials can be easily fixed to each other by being welded to the band portion 30. By adopting an expansion rate in such a range, overexpansion can be prevented.
- the balloon portion 20 is formed to a length of 30 mm to 80 mm, preferably 50 to 70 mm, and the maximum expansion diameter is preferably formed to 10 mm to 25 mm. Depending on the size of the maximum expansion diameter of the balloon part 20, in addition to the artery and vein, it can be used for a body opening and other hollow organs of the human body.
- the band part 30 is a ring-shaped member having extensibility, and is wound around the balloon part 20 to hold a part of the balloon part 20 at a diameter smaller than the maximum expansion diameter within a certain pressure range, Stretches in a range above a certain pressure.
- silicone, polyurethane and other elastomeric polymers are preferably used, but are not limited thereto.
- the band portion 30 has a thickness of 20 ⁇ m to 100 ⁇ m, preferably 50 to 70 ⁇ m, a width of 3 to 30 mm, preferably 5 to 15 mm, and a diameter of 3 mm to 20 mm. The diameter should be smaller than the maximum expansion diameter of the balloon 20 to be installed.
- a part of the diameter of the balloon part 20 is held thin by the band part 30, so that it is below a predetermined pressure, that is, below the pressure for expanding or inflating the band part 30.
- a predetermined pressure that is, below the pressure for expanding or inflating the band part 30.
- the band portion 30 needs to stretch the material itself, the band portion 30 is held at the diameter before expansion of the band portion 30 with almost no stretching. For this reason, below the fluid pressure at which the band portion 30 expands, the waist portion 22 at the center of the balloon portion 20 is thin and the shoulder portion 23 is thick as a whole, as shown in FIG. Therefore, the valve leaflet or the annulus is fitted to the waist portion, so that the balloon portion can be easily disposed at a predetermined position and can be prevented from moving. By further injecting an expansion fluid from this state and increasing the internal pressure of the balloon portion 20, the band portion 30 disposed in the waist portion 22 is expanded and the diameter is expanded.
- the shoulder part 23 does not expand or only expands slightly after the equilibrium state. Furthermore, by injecting an expansion fluid and increasing the internal pressure of the balloon part 20, the band part 30 expands, and the diameter of the balloon part 20 of the waist part 22 is expanded. As shown in FIG. The waist portion 22 of the portion 20 is expanded to the same extent as the diameter of the shoulder portion 23. However, since the balloon part 20 is non-extensible or low-extensible, the balloon part 20 is only slightly expanded further. Therefore, it is prevented that the diameter continues to expand like an extensible balloon and easily bursts.
- the expansion pressure at this time varies depending on the width, thickness, circumferential length, or material of the band portion 30.
- the waist portion 22 of the balloon portion 20 may be adjusted to expand slightly smaller than the diameter of the shoulder portion 23. By adjusting in this way, it is possible to prevent the catheter balloon 10 from migrating.
- the part 30 may be formed in a ring shape, and this band part may be inserted into the balloon part 20 and fixed as shown in FIG.
- the fixing of the band part 30 to the balloon part 20 is mainly selected from adhesion or welding, but is not limited to this. In the case of heat welding, it is preferable to use materials having high compatibility for the balloon part 20 and the band part 30, respectively. At this time, as described above, a highly compatible material may be used only for the outer layer of the balloon portion 20. By adopting such a two-layer structure, the stretching performance and the welding performance can be assigned to each layer, so that the respective physical properties are easily satisfied. Further, the portion for fixing the band portion 30 to the balloon portion 20 may be fixed to the front surface of the balloon portion 20, and as shown in FIG.
- the balloon portion 20 to which the band portion 30 is fixed in this manner has a thin waist portion and a thick shoulder portion 23. Then, as shown in FIG. 3D, the shoulder portion 23 is folded so as to be completed.
- the balloon part 20 produced as described above is arranged at the distal end of the catheter body to serve as a catheter.
- a tip 40 attached to the distal tip of the catheter body, an inner tube 50 having a guide wire lumen 51 connected to the tip 40, and the guide wire lumen.
- a balloon portion 20 provided around 51 and an outer tube 60 having an expansion fluid injection lumen 61 communicating with a balloon lumen 52 of the balloon portion 20 are provided.
- the balloon unit 20 is inflated by the expansion fluid that has passed through the expansion fluid injection lumen 61.
- the catheter 100 is introduced through the femur, brachial artery or left subclavian artery by the Seldinger method.
- antegrade insertion is possible by inserting directly into the aortic valve via a surgical incision.
- a case where the catheter balloon 10 is indwelled in the transcatheter aortic valve replacement will be described as an example in which the catheter balloon 10 is indwelled by the transfemoral approach.
- a variety of different placement techniques are possible in accordance with the present invention.
- the catheter balloon 10 is advanced in a retrograde manner to the target position.
- the distal end side shoulder 23 of the catheter balloon 10 is positioned in the left ventricular outflow tract, and the waist 22 is positioned at the leaflet 91 of the aorta 90. Detained.
- the pressure in the balloon portion 20 is further increased, and the expansion fluid is introduced so as to be in the range of 0.5 atm to 5.0 atm, preferably 1.0 to 3.0 atm.
- the waist part 22 is expanded and pushing to the outer side of a leaflet is started. The expansion of the waist portion 22 pushes and opens the leaflet, and pulverizes the calcified portion.
- the diameter of the waist portion 22 gradually increases.
- the shoulder portion 23 in which the band portion 30 is not installed It is expanded to almost the same as the outer diameter of. Since the outer diameter of the waist part 22 is produced with the same dimension as the shoulder part 23, it is not expanded further, and the possibility of damaging surrounding tissues due to excessive expansion can be completely prevented. Since the blockage of blood flow is limited to a short time, the balloon unit 20 is deflated in a short time. Further, when expanding, by introducing a contrast agent into the balloon unit 20, X-ray imaging can be performed in an expanded state, so that the length of the expanded valve leaflet can be estimated.
- Example 2 The experimental results of pressure and outer diameter in the examples are shown below.
- a present Example shows only 1 aspect to the last, and is not limited to this raw material and form.
- Balloon part having a 15 mm outer diameter balloon part 20 made of low-stretch nylon and a band part 30 made of polyurethane as an extensible material and made of polyurethane and having a width of 3 mm, 5 mm and 10 mm respectively.
- the expansion fluid was injected into 20 and the inner pressure of the balloon part 20 and the change in the outer diameter of the waist part 22 and the shoulder part 23 to which the band part 30 was attached were measured.
- the expansion fluid was injected into the balloon part 20, and the measurement of the outer diameter of each part was started from the time when pressure began to be applied.
- the pressure was 11.46 mm at a pressure of 0.046 MPa, 13.4 mm at a pressure of 0.156 MPa, and 14.3 mm at a pressure of 0.221 MPa.
- the shoulder portion was 14.3 mm at a pressure of 0.046 MPa, 14.8 mm at a pressure of 0.156 MPa, and 15.1 mm at a pressure of 0.221 MPa. The resulting graph is shown in FIG.
- a pressure higher than the extension force of the band part 30 is required, but this pressure can be changed depending on the material, dimensions, etc. of the band part 30. Recognize. Further, as the pressure increases, the diameter of the shoulder portion 23 also expands slightly. However, since a non-stretchable material is used, the expansion rate is 10% or less, and it can be seen that there is no significant change. As the pressure continues to increase, the band portion 30 is stretched and the shoulder portion 23 approaches the outer diameter, but depending on the material or dimensions of the band portion 30, the band portion 30 is completely the same as the outer diameter of the shoulder portion 23 It can be seen that the diameter is slightly smaller. Thereby, since the slight unevenness
- the catheter balloon 10 and the catheter 100 according to the present embodiment have been described by taking transcatheter aortic valve replacement as an example.
- transcatheter aortic valve replacement for example, for use in valvuloplasty of a stenotic aortic valve or a pulmonary valve, Can be used to patent any stenotic contraction. It can also be used during pre-dilatation of the aortic valve leaflet prior to placement of a percutaneous aortic valve or other artificial device used for aortic valve repair, replacement or implantation.
- the blood vessels to be used include all blood vessels of the body including coronary arteries, peripheral arteries, veins, esophagus, trachea, intestinal blood vessels, bile ducts and ureters of the body.
Abstract
Description
を備えたことを特徴とする。これにより、前述した効果を有するカテーテルを提供することができる。
(1)非伸張性又は低伸張性の素材からなる管状部材の周囲にチューブ状のバンド部を配置する工程
(2)これらを加熱し、管状部材を熱延伸しつつ円筒形に膨張させる工程
からなることを特徴とする。
かかる作製方法によれば、一工程でカテーテル用バルーンを作製することができ、また、バンド部とバルーン部とが全面に亘って熱溶着させることができる。
(1)非伸張性又は低伸張性の素材からなる管状部材を加熱し、熱延伸しつつ円筒異形に膨張させる工程
(2)加工した円筒形素材に伸縮性のバンドを取り付ける工程
からなるものであってもよい。この場合加工した円筒形素材に伸縮性のバンドを取り付ける方法としては、接着、熱溶着などであってもよい。
第1製造方法は、最初にバルーン部20を作製し、その後にバルーン部20にバンド部30を取り付ける方法である。バルーン部20を作製する方法としては、ブロー成形によって成形してもよいし、押出成形によって作製されたチューブを加熱した後、拡張するように延伸して成形してもよい。一方、バンド部30は、帯状の伸張性のシートを用意することができれば、製造方法は特に限定するものではない。例えば、押出成形されたチューブを延伸して作製したり、ディッピングにより成形したりしてもよい。作製されたバルーン部20にバンド部30を固定するに際しては、枚葉状のバンド部30をバルーン部20に巻き付けるようにして固定してもよいし、図3(A)に示すように、あらかじめバンド部30をリング状に成形し、このバンド部を図3(B)に示すようにバルーン部20に挿入して固定してもよい。バンド部30のバルーン部20への固定は、主として接着又は溶着が選択されるがこれに限定されるものではない。熱溶着する場合には、バルーン部20とバンド部30とはそれぞれ相溶性の高い材料を使用することが好ましい。この際に前述したようにバルーン部20の外層のみに相溶性の高い素材を採用してもよい。かかる2層構造とすることによって、伸張性能と溶着性能とをそれぞれの層に割り振ることができるため、それぞれの物性を満たしやすくなる。さらに、バルーン部20にバンド部30を固定する箇所は、バルーン部20の前面に固定してもかまわないし、図4に示すように、翼状に折り畳んだ(いわゆる傘のように折り畳んだ)際の各翼の先端又は中間部に均等に固定してもよい。このように均等に固定することにより、拡張時のウエスト部22が不均一に拡張されることを極力避けることができる。こうしてバンド部30が固定されたバルーン部20は、図3(C)に示すように、ウエスト部が細くなり、ショルダー部23が太い瓢箪状に形成される。そして、図3(D)に示すように、ショルダー部23を巻くようにして折り畳んで完成する。
第2製造方法は、バルーン部20とバンド部30の両方を同時に成形する方法であり、ブロー成形によって作製する方法である。先ず、図5(A)に示すように、ブロー成形前の管状部材であるパリソン25の周囲にバンド部30の材料となるチューブが配置されるように固定する。この状態のまま図5(B)に示すように、バルーン部20とともにバンド部30をブロー成形により拡張延伸し、図5(C)に示すように、同時に成形時の加熱により熱溶着によって一体化させる。かかる方法を採用することにより、一工程でカテーテル用バルーン10を作製することができ、また、バンド部30とバルーン部20とが全面に亘って熱溶着し易くなる。
以下、実施例における圧力と外径の実験結果を示す。なお、本実施例は、あくまで1態様を示すにすぎず、本素材、形態に限定されるものではない。低伸張性のナイロンで作製された外径15mmのバルーン部20に伸張性の材質としてポリウレタンで作製された外径が9mmでそれぞれ幅3mm、5mm及び10mmに形成したバンド部30を取り付けたバルーン部20に拡張流体を注入していき、バルーン部20の内圧とバンド部30を装着したウエスト部22とショルダー部23との外径の変化を測定した。バルーン部20内に拡張流体を注入し、圧力がかかり始める時点から各部の外径の計測を開始し、その後は定量ずつ流体を注入し、その都度圧力と外径を測定した。ただし、圧力は、バンド部30の伸張性素材のクリープ現象により経時的に低下するため、ある程度時間が経過し、安定した状態の圧力を記録した。このときの測定結果は、以下のとおりである。バンド幅3mmの場合、圧力0.032MPaで12.6mm、圧力0.150MPaで14.3mmであった。バンド幅5mmの場合、圧力0.024MPaで12.0mm、圧力0.1450MPaで14.2mm、圧力0.180MPaで14.5mmであった。バンド幅10mmの場合、圧力0.046MPaで11.1mm、圧力0.156MPaで13.4mm、圧力0.221MPaで14.3mmであった。一方ショルダー部は、圧力0.046MPaで14.3mm、圧力0.156MPaで14.8mm、圧力0.221MPaで15.1mmであった。結果のグラフを図7に示す。
Claims (6)
- 非伸張性又は低伸張性に形成された円筒形のバルーン部と、
前記バルーン部に巻回されており、前記バルーン部の拡張径よりも短い直径を有する弾性体からなるバンド部と、
を備えたことを特徴とするカテーテル用バルーン。 - 前記バルーン部は、所定の圧力未満においては、前記バンド部が取り付けられていない部分のみが膨張して略瓢箪形の形態をなし、
所定の圧力以上においては、前記バンド部のみが膨張し径が拡大し、略円筒形となることを特徴とする請求項1記載のバルーン。 - 前記バルーン部は、所定の圧力未満においては、前記バンド部が取り付けられていない部分のみが膨張して略瓢箪形の形態をなし、
所定の圧力以上の圧力をかけた場合であっても、瓢箪形であることを特徴とする請求項1又は2に記載のカテーテル用バルーン。 - 前記バンド部の内層を形成する素材と、前記バルーンの外層を形成する素材は、相溶性であることを特徴とする請求項1から3のいずれか1項に記載のカテーテル用バルーン。
- アウターチューブと、
前記アウターチューブの拡張流体注入用ルーメンと連通する請求項1から4のいずれか1項に記載のカテーテル用バルーンと、
を備えたことを特徴とするカテーテル。 - 請求項1から4のいずれか1項に記載のカテーテル用バルーンを作製する作製方法において、以下の工程からなることを特徴とする作製方法。
(1)非伸張性又は低伸張性の素材からなる管状部材の周囲にチューブ状のバンド部を配置する工程
(2)これらを加熱し、管状部材を熱延伸しつつ円筒形に膨張させる工程
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13867162.3A EP2939701A4 (en) | 2012-12-25 | 2013-12-20 | CATHETER BALLOON, CATHETER AND METHOD FOR MANUFACTURING CATHETER BALLOON |
US14/414,800 US20150174383A1 (en) | 2012-12-25 | 2013-12-20 | Catheter balloon, catheter, and method of manufacturing the catheter balloon |
CN201380039868.6A CN104507525A (zh) | 2012-12-25 | 2013-12-20 | 导管球囊、导管及制造导管球囊的方法 |
KR1020157001003A KR20150018887A (ko) | 2012-12-25 | 2013-12-20 | 카테터용 벌룬, 카테터 및 카테터용 벌룬을 제작하는 방법 |
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JP2012-281704 | 2012-12-25 | ||
JP2012281704A JP2014124264A (ja) | 2012-12-25 | 2012-12-25 | カテーテル用バルーン、カテーテル及びカテーテル用バルーンを作製する方法 |
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WO2014103907A1 true WO2014103907A1 (ja) | 2014-07-03 |
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PCT/JP2013/084196 WO2014103907A1 (ja) | 2012-12-25 | 2013-12-20 | カテーテル用バルーン、カテーテル及びカテーテル用バルーンを作製する方法 |
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US (1) | US20150174383A1 (ja) |
EP (1) | EP2939701A4 (ja) |
JP (1) | JP2014124264A (ja) |
KR (1) | KR20150018887A (ja) |
CN (1) | CN104507525A (ja) |
WO (1) | WO2014103907A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022101862A1 (en) * | 2020-11-13 | 2022-05-19 | Nagajyothi, K. | Pressure induced deflatable foley's catheter |
Families Citing this family (13)
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JP2016168151A (ja) * | 2015-03-12 | 2016-09-23 | 株式会社東海メディカルプロダクツ | バルーンカテーテル |
EP3326678A4 (en) | 2015-07-22 | 2019-04-17 | Olympus Corporation | ENDOSCOPIC TREATMENT INSTRUMENT |
CN107847719B (zh) * | 2015-07-28 | 2020-10-16 | 奥林巴斯株式会社 | 内窥镜用处置器具 |
KR101675698B1 (ko) * | 2015-10-30 | 2016-11-11 | 김주현 | 경막 협착 또는 추간공 협착 치료를 위한 의료장치 |
US10272228B1 (en) | 2016-05-17 | 2019-04-30 | Aspisafe Solutions Inc. | Expandable intubation assemblies |
JP6742885B2 (ja) * | 2016-10-27 | 2020-08-19 | テルモ株式会社 | バルーンカテーテル |
JPWO2019163502A1 (ja) * | 2018-02-26 | 2021-02-04 | 日本ゼオン株式会社 | 内視鏡用バルーンカテーテル |
CN109907870A (zh) * | 2019-03-22 | 2019-06-21 | 佘彩芹 | 葫芦形空心避孕器 |
CN111588970B (zh) * | 2020-05-29 | 2022-09-16 | 成都赛拉诺医疗科技有限公司 | 扩张球囊装置及扩张球囊装置的制作方法 |
CN112827057B (zh) * | 2020-12-31 | 2023-04-14 | 先健科技(深圳)有限公司 | 球囊导管 |
CN115253035B (zh) * | 2021-11-05 | 2024-02-23 | 首都医科大学宣武医院 | 用于切割斑块的介入手术的导管球囊及导管 |
DE102022134125A1 (de) | 2021-12-23 | 2023-06-29 | Japan Lifeline Co., Ltd | Katheter, ballonexpansionsverfahren, ballonkompressionsverfahren |
JP2024049770A (ja) | 2022-09-29 | 2024-04-10 | 日本ライフライン株式会社 | カテーテル挿入器具、カテーテル装置 |
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- 2013-12-20 US US14/414,800 patent/US20150174383A1/en not_active Abandoned
- 2013-12-20 KR KR1020157001003A patent/KR20150018887A/ko not_active Application Discontinuation
- 2013-12-20 CN CN201380039868.6A patent/CN104507525A/zh active Pending
- 2013-12-20 EP EP13867162.3A patent/EP2939701A4/en not_active Withdrawn
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WO2022101862A1 (en) * | 2020-11-13 | 2022-05-19 | Nagajyothi, K. | Pressure induced deflatable foley's catheter |
Also Published As
Publication number | Publication date |
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KR20150018887A (ko) | 2015-02-24 |
JP2014124264A (ja) | 2014-07-07 |
CN104507525A (zh) | 2015-04-08 |
EP2939701A1 (en) | 2015-11-04 |
US20150174383A1 (en) | 2015-06-25 |
EP2939701A4 (en) | 2016-10-12 |
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