• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The invention relates to a balloon catheter with a longitudinally extending shaft (2) which has at least a first and a second section (7, 8), the first section (7) being arranged distal to the second section (8) and being more flexible than the second section (8), wherein the shaft (2) has a first and a second tubular tube (10, 11) and a balloon (3) is arranged at the distal end of the first tube (10), which is pressurized with a through the fluid conveyed to the first tube (10) is expandable, and the second tube (11) is used to receive a guide wire, ends distal of the balloon (3) and has an opening at the distal end, wherein both the first and the second tube (10 , 11) run along the first and second sections (7, 8) and both the first and the second tube (10, 11) are more flexible in the first section (7) than in the second section (8), with between the first and the second section (7, 8) a transition section (9) is arranged in which the first tube (10) has the same material properties as in the first section (7) and the second tube (11) has the same material properties as in the second section (8) or the first tube (10) has the same material properties as in the second section (8) and the second tube (11) has the same material properties as in the first section (7).
    公开号:CH716028B1
    申请号:CH01406/19
    申请日:2019-11-07
    公开日:2020-10-15
    发明作者:Alexander Ruebben Dr
    申请人:Alexander Ruebben Dr；
    IPC主号:
    专利说明:

    The invention relates to a balloon catheter with a longitudinally extending shaft which has at least a first and a second section, the first section being arranged distal to the second section and being more flexible than the second section.
    The use of balloon catheters is now standard in everyday clinical practice. Their use in the context of intravascular interventions mostly relates to the widening of narrowed vascular sites, either with the help of the balloon catheter itself or in combination with other medical products such as balloon expandable stents. In percutaneous transluminal angioplasty, a balloon catheter is brought to the site of the stenosis via a guide wire and a guide catheter and expanded by supplying a fluid under pressure (approx. 4 to 12 bar). Deposits in the area of the stenosis are pressed into the vessel wall. In addition, a stent (vascular endoprosthesis) can be placed to keep the blood vessel open permanently. In order to prevent the reoccurrence of a stenosis due to vasoconstricting overgrowth of the enlarged area, drug-coated balloon catheters can also be used, which release an active ingredient such as paclitaxel at the area of the vasoconstriction during expansion. After the treatment and the subsequent folding of the balloon, the balloon catheter is withdrawn from the vascular system and removed.
    [0003] The femoral artery in the area of the groin is often chosen as the access point for balloon catheters. The femoral artery runs relatively superficially at least partially and is therefore easily accessible to the attending physician, both for treatments to be carried out in the coronary area and also for other areas of the vascular system such as the brain or extremities. In addition, relatively large-lumen catheters with large external diameters can be introduced via the femoral artery (inguinal artery).
    One problem with the introduction of balloon catheters is the conflict of objectives, on the one hand, to make the balloon catheter so that it can be advanced over relatively long distances, but on the other hand to have a sufficiently thin and flexible balloon catheter available so that it can also be introduced into narrow-lumen blood vessels. It is also important to make the balloon catheter as kink-proof as possible, so that the advancement of the balloon catheter from the proximal direction to the distal tip of the balloon catheter by the attending physician is transmitted without the advancement of the balloon catheter being endangered by kinking between the access point and the target position.
    With regard to good pushability and kink security, a relatively stiff balloon catheter would in principle be advantageous, but the greatest possible flexibility with regard to insertability into narrow-lumen, strongly twisted blood vessels. In order to do justice to these actually contradicting properties, balloon catheters are often relatively stiff in the proximal area and relatively flexible in the distal area. For example, a proximal portion made of a metal such as. B. stainless steel, while more distal sections made of a plastic material, often a polyamide, can be made.
    In this context, balloon catheters are also known which are constructed in a distal section from a particularly flexible material, in a central section from a material of medium flexibility and in a proximal section from a comparatively less flexible material. In principle, this fulfills the criterion of increasing flexibility from proximal to distal, but the transitions between the individual sections are potential weak points at which the balloon catheter can kink or kink when advancing in the distal direction.
    [0007] The object is therefore to provide a balloon catheter which overcomes this problem and in particular does not have any points where there is an increased risk of kinking.
    This object is achieved according to the invention by a balloon catheter with a longitudinally extending shaft which has at least a first and a second section, the first section being arranged distal to the second section and being more flexible than the second section, the shaft being a having a first and a second tubular tube and at the distal end of the first tube a balloon is arranged, which is expandable by the application of pressure with a fluid conducted through the first tube, and the second tube is used to receive a guide wire, ends distally of the balloon and at the distal end End has an opening, wherein both the first and the second tube run along the first and second section and both the first and the second tube are more flexible in the first section than in the second section, with a transition section between the first and the second section is arranged in thethe first tube has the same material properties as in the first section and the second tube has the same material properties as in the second section orthe first tube has the same material properties as in the second section and the second tube has the same material properties as in the first section.
    The invention is thus based on the idea of creating a transition section between the first and the second section, which on the one hand has an overall flexibility that lies between that of the first and that of the second section. This is achieved in that the material properties of the first tube differ from those of the second tube in the transition section. In addition, material is used either for the first or for the second tube whose properties correspond to those in the first or second section. In other words, the material properties overlap. It is true that both the first and the second tube are more flexible in the first section than in the second section, but the transition between the first, particularly flexible section and the second, less flexible section does not take place at a single position, but ultimately at two positions, namely the distal and the proximal end of the transition section. This considerably reduces the risk of kinking at the transition from the first to the second section.
    In the transition section, the material properties of the first and second tubes are designed to overlap. Either the material properties of the first tube in the transition section correspond to those in the first section, while the second tube has the material properties of the second section, or vice versa. This ensures that the material properties of one of the two tubes do not change at the distal and the proximal end of the transition section, so here there is a material constancy that makes kinking considerably less likely. Both at the distal and at the proximal end of the transition section, only the properties of one of the two tubes change, but not the properties of the other tube.
    Like conventional balloon catheters, the balloon catheter according to the invention has at least two tubes, namely a first tube, which is used to supply fluid for the purpose of expanding the balloon, and a second tube, which is provided for receiving a guide wire. The balloon is correspondingly arranged at the distal end of the first tube. When the balloon of the balloon catheter has reached its target position, the fluid is introduced through the first tube into the balloon in order to expand it and, for example, to press deposits on the vessels into the vessel wall or to expand a stent. The fluid is then withdrawn again through the first tube, whereupon the balloon deflates so that the balloon catheter can then be withdrawn from the blood vessel system in the proximal direction. The term tube is used in this context in the sense of a tube or a tube which extends at least partially through the balloon catheter in the longitudinal direction and has a lumen running through the interior of the tube. The tube can have the shape of a hollow cylinder with a circular or elliptical cross-section, but this is not absolutely necessary. Almost any other shapes are also conceivable when viewed in cross section. A circular or elliptical cross-section, however, has the advantage that one tube can be easily guided through the other tube, the second tube usually being placed through the first tube.
    The second tube is used to receive the guide wire. In contrast to the first tube, this one is not closed distally, but ends distal to the balloon and has an opening at the distal end. As a rule, the procedure is that the guide wire is first brought to the target position and then the balloon catheter is advanced over the guide wire to the target position, the guide wire sliding through the second tube.
    In connection with the second tube, essentially two different systems are known, namely over-the-wire (OTW) and rapid exchange (Rx) balloon catheters. The balloon catheter according to the invention can be in the form of both an OTW and an Rx balloon catheter. While in an OTW catheter the lumen for the guide wire extends over the entire length of the catheter from proximal to distal, the Rx catheter has a separate feed opening for the guide wire (Rx port), where the guide wire is clearly distal to the proximal End of the catheter emerges from the catheter. Correspondingly, in the case of an OTW balloon catheter, the tubes or the lumen extending through the tubes for the fluid supply and the guide wire run parallel or concentrically to one another from the proximal end of the catheter to the balloon, whereas in the case of an Rx catheter this only occurs between the Rx port and balloon is the case. The section between the Rx port and the proximal end, however, has only one tube for the fluid supply.
    In order to set the material properties in the first and second sections and in the transition section in the desired manner, the first and second tubes can be made of a first material in particular in the first section and the first and second tubes in the second section a second material, wherein the first material is more flexible than the second material and, in the transition section, the first tube is made of a different material than the second tube. For one of the two tubes the material between the first section and the transition section is thus kept constant, for the other tube between the transition section and the second section. In this way, the described overlapping transition between the material properties of the first and second tube is brought about.
    The first, particularly flexible or soft material, are thermoplastic elastomers, for example polyether block amides (PEBA). This is a thermoplastic elastomer that can be obtained by polycondensation of a carboxylic acid polyamide with a polyether with terminal OH groups. In particular, PEBA is sold by Arkema under the name PEBAX®. In this context, a flexible material is understood to be a material that adapts particularly well to the external conditions and can also follow fine ramifications of the vascular system, soft and flexible being used synonymously in this application.
    Alternatively, other polyamides can also be used as the first material for the balloon, for example those such as those sold by EMS-GRIVORY under the name Grilamid <®>. The use of a polyamide 12 (PA 12, Grilamid <®> L), a polyamide obtainable by the polycondensation of laurolactam, is particularly preferred. Other polyamides that can be used are polyamide 10.10 (PA 10.10, Grilamid <®> 1S), a polyamide obtainable by polycondensation of decanediamine and sebacic acid, polyamide 6.10 (PA 6.10, Grilamid <®> 2S), a polyamide obtainable by polycondensation of hexamethylenediamine and sebacic acid, or Polyamide 6.12 (PA 6.12, Grilamid <®> 2D), a polyamide obtainable by polycondensation of hexamethylenediamine and dodecanedioic acid.
    As a second material of medium flexibility, for. B. a polyamide such as nylon (polyhexamethylene adipamide) can be used. In particular, a material with a Shore D hardness in the range of approx72 can be used. For the second section, on the other hand, it is advisable to use materials with a Shore D hardness in the range of 80 - 85. The exact properties of the polymers can be adjusted by adding additives.
    The material from which the balloon itself is constructed can match or differ from the material of the first tube in the first section. For example, the balloon itself can also be made of nylon (polyhexamethylene adipic acid amide), which has proven itself as a material for balloons, even if the first tube in the first section is made of a more flexible material such as a polyether block amide. Other materials that can be used for the balloon are polyurethane, polyolefin copolymers, polyethylene, or silicone.
    Under balloon within the meaning of the invention, the element of a balloon catheter that can be expanded by supplying a fluid is understood, regardless of the shape of the expandable element or of what material it is made of. Typically the balloon has an elongated structure. The fluid can be gaseous or liquid. For example, water mixed with contrast medium or a saline solution mixed with contrast medium can serve as the fluid. The nominal pressure for expansion of the balloon can e.g. B. 4 to 12 bar, preferably 6 to 8 bar. At this pressure the balloon reaches its nominal diameter in the expanded state. The dimensions of the balloon can differ greatly depending on the area of application, the diameter in the expanded state can for example be between approx. 1 and approx. 50 mm, the length between approx. 5 and approx. 300 mm. Possibly. However, the dimensions can also deviate from this, for example when using the balloon / balloon catheter in urology or veterinary medicine.
    Typically, the deflated balloon of the balloon catheter is in a folded state. Depending on the size of the balloon, a different number of folds can be formed, which are then wound around the axis of the catheter in the same direction. This results in a significant reduction in the diameter.
    As an alternative or in addition to the variation of the material itself, the material thicknesses of the first and second tubes can also differ in the transition section. For example, the same material can be used for the first and the second section, but in a different thickness. In this case, both the first and the second tube in the first section are made of the material with a comparatively low material thickness, while the first and the second tube in the second section are made of the same (or a different) material, but with a higher material thickness are. In the transition section, an overlapping transition is again generated in such a way that the material properties of one tube match those in the first section and the material properties of the other tube match those in the second section. Thus, either the first tube in the first section and in the transition section has the same material thickness, while the second tube in the transition section and in the second section has the same material thickness, or the first tube has the same material thickness in the transition section and in the second section, while the second Tube has the same material thickness in the first section and in the transition section. The material thicknesses of the first and second tube do not necessarily have to match in a certain section; for example, the second tube in the first section can also have a smaller material thickness than the first tube. It is important, however, that the transition of the material thicknesses does not take place at a single point along the longitudinal axis of the balloon catheter for the first and second tubes, but rather offset from one another in the manner described.
    When bringing about a transition section by varying the material thicknesses can be used as the material for the first and second tube z. B. nylon (polyhexamethylene adipamide) can be used, with, unlike the variation of the material itself, the different properties are brought about by choosing a higher or lower material thickness.
    Under proximal is in the context of the invention in the direction of the exterior of the body, d. H. towards the attending physician, distal means the opposite direction, d. H. in the direction of the blood vessel to be treated. Radial is understood to mean the plane perpendicular to the longitudinal axis of the balloon catheter.
    The first and the second tube can run parallel to one another in the areas where both tubes are present, but it is preferred that the second tube extends at least partially through the first tube. Accordingly, there is a concentric course of the first and second tube. Usually the second tube is on the inside, i.e. H. the guide wire is guided through the inner second tube of the balloon catheter, while the first tube radially surrounds the second tube.
    A further, proximal section is preferably arranged proximally to the second section. This typically has less flexibility than the first or the second section, but makes up a considerable part of the total length of the balloon catheter. It is also possible to provide further sections between the second section and the proximal section. With regard to the proximal section, the focus is less on flexibility than on pushability and kink resistance. Correspondingly, the proximal section can be made from a metal, in particular from stainless steel, for example. However, it is also possible to provide a proximal section made of a polymer, this polymer typically being stiffer than the polymers used for the first and second sections and the transition section.
    At the proximal end of the balloon catheter, adjoining the shaft, a so-called catheter hub is usually provided, d. H. a connector for the device for fluid supply and pressurization. The connection can e.g. B. be a conventional Luer or Luer lock connection. In particular, it makes sense to provide two Luer lock connections, typically female connections, one of which is used to connect the first lumen to a balloon dilator and another to introduce the guide wire into the balloon catheter. The connections can be made from a polycarbonate, for example. The guide wire running through the balloon catheter can be held at its proximal end by a torquer, which facilitates the handling of the guide wire, which is usually very thin.
    So that the transition section can fulfill the desired role as a safeguard against undesired kinking of the balloon catheter, it should have a length of ≥ 3 cm, preferably 3 to 10 cm. A length of the transition section of 5 to 7 cm is particularly preferred. A transition section chosen too short would under certain circumstances no longer bring about the desired kink protection, whereas a transition section chosen too long would under certain circumstances no longer be suitable for introduction into narrow-lumen blood vessels.
    As the length of the first section 3 to 20 cm, in particular 5 to 15 cm, as the length of the second section 5 to 35 cm, in particular 20 to 30 cm have proven. In this context, the length of the first section is understood to mean the length from the distal tip of the balloon catheter to the beginning of the transition section. The total length of the balloon catheter is often more than 1 m, so that it can be introduced into the groin region and the balloon catheter can be advanced to a wide variety of locations in the blood vessel system. Often the proximal section alone is ≥ 1 m in length.
    A typical outer diameter of the first tube in the first section is 0.8-1.0 mm, in particular approximately 0.9 mm. The inside diameter is typically in a range of 0.7-0.8 mm. The outside diameter of the second tube can be 0.5-0.6 mm, for example, and the inside diameter of the second tube 0.4-0.5 mm. This is especially true when the second tube extends through the first tube. In the second section, the outer diameter of the first tube can be slightly higher than in the first section and, for example, be 0.9-1.1 mm. The inner diameter of the first tube in the second section is mostly 0.8-0.9 mm, while the second tube has dimensions that largely correspond to those in the first section.
    In order to prevent a renewed narrowing in the treated vessel section as a result of an initially successfully performed angioplasty, balloons with an active substance coating can be used. Restenosis is mostly due to cell proliferation in the corresponding vascular segment, i. H. Cells of the blood vessel grow into the vessel lumen and in turn ensure that the blood flow is impeded. To prevent this, balloon catheters coated with drugs that inhibit proliferation are increasingly used. Corresponding drugs usually have a particular effect on the Smooth Muscle Cells (SMC) and are intended to prevent restenosis caused by excessive growth of these cells. The drug is located on the outside of the balloon and is transferred from the balloon to or into the inner wall of the vessel during balloon dilation.
    The active ingredient used is in particular a medicament or medicament, preferably a medicament which has a proliferation-inhibiting effect and prevents the vasoconstricting overgrowth of the area enlarged by the balloon. It can also be a hormone-like or regulating active ingredient that can influence organ-specific effects or regulatory functions on certain cells. In particular, the active ingredient can be selected from: tretinoin, orphan receptor agonists, elena derivatives, corticosteroids, steroid hormones, paclitaxel, rapamycin, tacrolimus, hydrophobic proteins and substances that change cell proliferation. It is also possible to use mixtures of these active ingredients. In addition, it is also possible to use derivatives of the active substances mentioned, whereby derivatives are understood to mean in particular salts, esters and amides. Methylprednisolone, dexamethasone or estradiol, for example, can be used as steroid hormones. The use of paclitaxel, rapamycin or tacrolimus or corresponding derivatives is particularly preferred.
    In general, however, the term active ingredient is to be understood broadly, d. H. it can in principle be any coating on the balloon of the balloon catheter with which a certain effect is to be achieved at the target location. When introduced into blood vessels, this effect can consist in particular of inhibiting cell proliferation. In other areas of medicine, however, the desired effect can be different, for example in the area of urology for urinary catheters, where the coating is intended, in particular, to inhibit bacterial colonization. Here, for example, heparin can be used as an active ingredient.
    The coating of the surface of the balloon with the active ingredient is typically carried out in that the surface of the balloon is brought into contact with a solution of the active ingredient. This can be done in particular by immersing the balloon in the solution. Immersion usually takes a max. 1 min, typically 10 to 30 s. After immersion, the balloon should be withdrawn from the first solution at a speed of up to 10 mm / s. It is even more favorable if the extraction takes place at a speed of less than 5 mm / s, preferably at a speed between 0.5 mm / s and 2 mm / s. Slowly pulling it out results in slow drying of the surface.
    Before coating the balloon, it is useful to clean the surface of the balloon. This can be done, for example, with an appropriate solvent, for example the solvent also used for applying the active ingredient.
    The solution can be saturated with respect to the active ingredient, but this is not absolutely necessary. For example, methylene chloride, chloroform, alcohol, in particular ethanol, methanol or isopropanol, acetone, diethyl ether, liquid hydrocarbons such as pentane, hexane, heptane, cyclohexane or octane, toluene, tetrahydrofuran (THF) or ethyl acetate can be used as solvents. The use of solvent mixtures is also possible. It is preferably a solution of the active ingredient in methylene chloride.
    As an alternative to coating by dipping, this can also be done in other ways, for example by spraying.
    The balloon catheters according to the invention can be used in blood vessels, in particular in the field of angioplasty. In this case, the target location of the balloon is a blood vessel, blood vessels in different areas being possible, in particular coronary, intracranial and peripheral. However, it is also possible to use balloon catheters in other medical fields. One possible use is in urology, where balloon catheters are inserted into the urinary bladder as urinary catheters. The catheter is fixed with the balloon. Here the balloon can e.g. B. be provided with a coating that prevents bacterial colonization and incrustation, for example with heparin.
    In pneumology, balloon catheters can be used to expand or close a bronchus. Balloon catheters can also be used in gynecology. In the field of orthopedics, balloon catheters can be used to treat vertebral fractures by realigning the vertebrae by means of balloon expansion (balloon kyphoplasty). The balloon catheter according to the invention can in principle be used in all fields of medicine in which balloon catheters are used, the balloon catheter being of particular importance for the introduction into narrow-lumen blood vessels.
    In addition, the balloon catheter according to the invention can serve not only to remove stenoses and the local introduction of active substance, but also to place a stent (endoprosthesis) in the body lumen. Stents are tubular support structures that are implanted in a body lumen, for example a blood vessel, in order to keep this permanently open. Such stents can be self-expanding or can be expanded with the aid of a balloon. For this purpose, the stent is crimped onto the balloon and inserted into the body lumen with the aid of the balloon catheter. At the intended location, the balloon is then expanded by supplying a fluid, as a result of which the stent also expands and is anchored in the body lumen. At the same time, when the balloon according to the invention is used, the active substance is released onto the wall of the body lumen. Finally, the balloon is contracted again and removed from the body lumen while the stent remains in the body lumen.
    Radiopaque markings, which are used to visualize the catheter in the X-ray image, can be attached at various positions along the balloon catheter. In particular, markings made of platinum or a platinum alloy such as platinum-iridium can be involved.
    The invention is explained in more detail by way of example with reference to the accompanying figures. Show it:<tb> <SEP> Fig. 1: A balloon catheter according to the invention in side view;<tb> <SEP> Fig. 2 shows the distal part of the shaft of the balloon catheter from FIG. 1 in a longitudinal section.
    In Fig. 1, the balloon catheter 1 according to the invention is shown in a side view, wherein in the representation selected here right means proximal and left means distal. The balloon catheter 1 has a shaft 2 extending in the longitudinal direction, the outer diameter of which in the proximal section 6, which is shown here only in shortened form, is greater than further distal. The section of the shaft 2 in which the balloon 3 is arranged is marked with the letter A. A first lumen for the fluid supply and a second lumen for receiving the guide wire run through the shaft 2 (not shown here), the two lumens each being formed by a tube.
    Proximally adjoining the proximal section 6 of the shaft 2 are two catheter hubs in the form of Luer-Lock connections 4, 5, the connection 4 of the fluid supply into the first lumen by means of a balloon dilator and the connection 5 of the introduction of the guide wire serve in the second lumen.
    In Fig. 2 only the distal part of the shaft 2 is shown. A first tube 10 is designed so that it can accommodate the second tube 11, i. H. the second tube 11 runs in the longitudinal direction through the first tube 10. The first tube 10 is connected at its distal end to the balloon 3, which can be expanded by supplying fluid through the first tube 10. The second tube 11, however, has an opening at the distal end and is used to receive the guide wire, not shown here.
    The part of the shaft 2 shown here (without the proximal section 6 from FIG. 1) has a first section 7 and a second section 8, the first section 7 being arranged distal to the second section 8. However, the first and second sections 7, 8 do not directly adjoin one another; instead, there is a transition section 9 between the first section 7 and the second section 8. In the transition section 9, the first tube 10 in the example selected here is made of the same material as in the first Section 7, for example from PEBAX <®>. The second tube 11, however, is made in the transition section 9 from the same material as in the second section 8, for example from nylon. The transition from the stiffer to the more flexible material thus takes place for the first and the second tube 10, 11 at different points, in one case at the transition from the second section 8 to the transition section 9, in the other case at the transition from the transition section 9 to the first section 7 Properties of the respective other tube, however, remain unchanged at the corresponding points, so that the risk of kinking is significantly reduced. In the present example, the first tube 10 (including the balloon area) has a length of 15 cm at the distal end for the softer material and further proximally a length of 25 cm for the less soft material. The second tube 11, on the other hand, has a length of 10 cm at the distal end for the softer material and further proximally a length of 30 cm for the less soft material. The first section 7 thus has a length of 10 cm, the transition section 9 of 5 cm and the second section 8 a length of 25 cm.
    权利要求:
    Claims (14)
    [1]
    1. Balloon catheter with a longitudinally extending shaft (2) which has at least a first and a second section (7, 8), wherein the first section (7) is arranged distal to the second section (8) and is more flexible than the second section (8), wherein the shaft (2) has a first and a second tubular tube (10, 11) and a balloon (3) is arranged at the distal end of the first tube (10), which is pressurized with a through the first Tube (10) is expandable, and the second tube (11) is used to receive a guide wire, ends distal of the balloon (3) and has an opening at the distal end, wherein both the first and the second tube (10, 11 ) run along the first and second sections (7, 8) and both the first and the second tube (10, 11) are more flexible in the first section (7) than in the second section (8),characterized,that between the first and the second section (7, 8) a transition section (9) is arranged in which- The first tube (10) has the same material properties as in the first section (7) and the second tube (11) has the same material properties as in the second section (8) or- The first tube (10) has the same material properties as in the second section (8) and the second tube (11) has the same material properties as in the first section (7).
    [2]
    2. Balloon catheter according to claim 1, characterized in that in the first section (7) the first and the second tube (10, 11) are made of a first material and in the second section (8) the first and the second tube (10, 11) are made of a second material, the first material being more flexible than the second material and in the transition section (9) the first tube (10) being made of a different material than the second tube (11).
    [3]
    3. balloon catheter according to claim 2, characterized in that the first material is a thermoplastic elastomer.
    [4]
    4. balloon catheter according to claim 2 or 3, characterized in that the second material is a polyamide.
    [5]
    5. Balloon catheter according to one of claims 1 to 4, characterized in that the material thicknesses of the first and second tubes (10, 11) differ in the transition section (9).
    [6]
    6. balloon catheter according to one of claims 1 to 5, characterized in that the second tube (11) extends at least partially through the first tube (10).
    [7]
    7. Balloon catheter according to one of claims 1 to 6, characterized in that a proximal section (6) is arranged proximally of the second section (8).
    [8]
    8. balloon catheter according to claim 7, characterized in that the shaft (2) in the proximal section (6) is at least partially made of metal.
    [9]
    9. balloon catheter according to claim 8, characterized in that the shaft (2) in the proximal section (6) is at least partially made of stainless steel.
    [10]
    10. Balloon catheter according to one of claims 1 to 9, characterized in that the transition section (9) has a length of ≥ 3 cm, preferably 3 to 10 cm.
    [11]
    11. Balloon catheter according to one of claims 1 to 10, characterized in that the length of the first section (7) is 3 - 20 cm, in particular 5 - 15 cm.
    [12]
    12. Balloon catheter according to one of claims 1 to 11, characterized in that the length of the second section (8) is 5-35 cm, in particular 20-30 cm.
    [13]
    13. Balloon catheter according to one of claims 1 to 12, characterized in that the balloon (3) is coated with one or more active substances.
    [14]
    14. Balloon catheter according to claim 13, characterized in that the active ingredient used is selected from the group: tretinoin, orphan receptor agonists, elastin derivatives, corticosteroids, steroid hormones, paclitaxel, rapamycin, tacrolimus, hydrophobic proteins, heparin and / or hormone-like substances or substances that change cell proliferation.
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    DE102007006434A1|2008-08-14|Balloon catheter for use in stent, has fluid chamber connected with balloon unit in sections, where fluid communication connection is established between chamber and vessel during expansion of balloon unit
    DE102018123064A1|2020-03-19|Diameter reduction
    同族专利:
    公开号 | 公开日
    DE102019125858A1|2021-03-25|
    WO2021058236A1|2021-04-01|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    CN101001659A|2004-08-11|2007-07-18|株式会社钟化|Catheter|
    US20100016937A1|2008-07-18|2010-01-21|Yousef Alkhatib|Twisting Bifurcation Delivery System|
    DE102013021998A1|2013-12-30|2015-07-02|Alexander Rübben|balloon catheter|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE102019125858.8A|DE102019125858A1|2019-09-25|2019-09-25|Kink-proof balloon catheter|
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