WO2004073528A1 - 塞栓形成用体内留置具 - Google Patents
塞栓形成用体内留置具 Download PDFInfo
- Publication number
- WO2004073528A1 WO2004073528A1 PCT/JP2004/001864 JP2004001864W WO2004073528A1 WO 2004073528 A1 WO2004073528 A1 WO 2004073528A1 JP 2004001864 W JP2004001864 W JP 2004001864W WO 2004073528 A1 WO2004073528 A1 WO 2004073528A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- coil
- metal
- wire
- indwelling device
- axial extension
- 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.)
- Ceased
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
- A61B17/1214—Coils or wires
- A61B17/12154—Coils or wires having stretch limiting means
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
- A61B17/1214—Coils or wires
- A61B17/12145—Coils or wires having a pre-set deployed three-dimensional shape
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
- A61B17/12109—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel
- A61B17/12113—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel within an aneurysm
Definitions
- the present invention relates to an in-vivo indwelling device for forming an embolus, and more particularly, to an in-vivo indwelling device for forming an embolus used for, for example, modifying or blocking blood flow, and embolizing a lesion.
- vascular embolization in which an in-vivo indwelling device for embolization is placed in an aneurysm is known as a less invasive treatment for aneurysms and the like.
- the embolization device placed inside the aneurysm becomes a physical obstacle to blood flow, and a thrombus is formed around the embolization device. The risk of ruptured aneurysms can be reduced.
- an in-vivo indwelling device for embolization that is to be indwelled at a predetermined site in a blood vessel such as an aneurysm is an in-vivo indwelling device for embolization formed of a metal coil (hereinafter, also referred to as an “embolic-forming coil”).
- a metal coil hereinafter, also referred to as an “embolic-forming coil”.
- Such an embolization coil is used by being introduced into an aneurysm via an appropriate catheter by an extruding means (inductor) detachably connected to the end thereof, detached at a predetermined site, and placed there. Is done.
- embolization coil is required to have various characteristics such as the following characteristics.
- a gap may be created due to a change in shape over time and reperfusion may occur (compaction). From the viewpoint of maximizing the embolization rate per unit volume (the occupation rate of the embolization coil in a given position) as much as possible. It is necessary to have the property.
- the coil body Prevents the coil body from being extended indefinitely so that it can be pushed out of the catheter, placed in a predetermined location, and then recovered and repositioned to correct its position. Or, it has a function of suppressing, that is, it is difficult to collect the coil main body or damage the application site by stretching the coil main body, for example, by catching on the distal edge of the catheter.
- the configuration must be such that such a problem does not occur because there is a danger that it will occur.
- the present invention has been made in view of the above circumstances, and an object of the present invention is to ensure that it can be introduced and retained at a predetermined site in the body, and that, for example, after it has been placed, Even in the case of performing a re-deployment operation for collecting and correcting the position, the re-deployment operation of the in-dwelling device can be executed reliably, and therefore, the embolus forming body having high safety and high operability can be placed in the body. To provide tools.
- the invention's effect is to ensure that it can be introduced and retained at a predetermined site in the body, and that, for example, after it has been placed, Even in the case of performing a re-deployment operation for collecting and correcting the position, the re-deployment operation of the in-dwelling device can be executed reliably, and therefore, the embolus forming body having high safety and high operability can be placed in the body.
- the wire itself has high level flexibility by comprising the wire which comprises an axial direction expansion regulating member by the thing of a diameter of a specific magnitude
- the axial extension restricting member is disposed inside the coil main body, and the axial extension restricting member itself is made of a material having a high tensile breaking strength, thereby extending the coil main body in the axial direction. Therefore, for example, after being placed in the body, When performing the re-placement operation to remove and correct the position, the coil body is pulled into the catheter in a state where the coil body is prevented from being further extended by the axial extension restricting member.
- the re-placement operation including recovery can be performed reliably, and the in-vivo placement device can be configured as having high safety.
- FIG. 1 is an explanatory cross-sectional view schematically showing the configuration of an example of the embolus forming indwelling device of the present invention.
- FIG. 2 is an explanatory view for explaining a method of measuring the flexibility of the in-vivo indwelling device according to the present invention.
- FIG. It is sectional drawing.
- FIG. 4 is an explanatory cross-sectional view schematically showing the configuration of still another example of the in-vivo embolization device according to the present invention.
- FIG. 5 is an explanatory cross-sectional view schematically showing the configuration of still another example of the in-vivo embolization device according to the present invention.
- FIG. 1 is an explanatory cross-sectional view schematically showing the configuration of an example of the embolus forming indwelling device of the present invention.
- the in-vivo indwelling device for embolization (hereinafter simply referred to as “in-vivo indwelling device”) 10 includes a metal coil 11 constituting a flexible coil body, and a distal end of the metal coil 11.
- the portion is provided with a rounded head 12, and a proximal end of the metal coil 11 is provided with, for example, a rod-shaped holding member 13 for holding the metal coil 11.
- a part of the metal coil 11 is fixed to the inner peripheral surface at the proximal end of the metal coil 11, and is located outside the proximal edge of the metal coil 11 1 in the coil axial direction (to the right in FIG. 1). It is provided so as to protrude and extend.
- the holding member 13 holds the metal coil 11 so that it can be connected to or detached from an appropriate delivery wire, a catheter, or the like.
- the metal coil 11 constituting the indwelling device 10 is formed by winding a metal wire in a spiral shape. It can be selected from those that have no adverse effect on the body (biocompatible ones). For example, tungsten, titanium, gold, platinum and their alloys, stainless copper, etc. it can.
- the metal coil 11 constituting the indwelling device 10 is supposed to have flexibility or flexibility, and differs depending on the material of the metal wire constituting the metal coil 11. It is preferable that it has the following configuration.
- the diameter (element diameter) of the metal wire constituting the metal coil 11 is 10 to 120 m
- the coil diameter of the metal coil 11 is 100 to 400 ⁇
- the coil length is 2 ⁇ 500 mm, number of turns per unit length (l mm) :! ⁇ 100.
- an axial extension restricting member 20 composed of one metal wire 21 has one end and the other end.
- the metal coil 11 is fixed to the distal end and the proximal end of the metal coil 11 and extends in the coil axial direction of the metal coil 11 in a state where the entire coil forms a helical structure. It is arranged so that it can be extended within the range.
- hatched portions by the dot pattern indicate fixed portions of the metal wires 21.
- the metal wire 21 constituting the axial extension restricting member 20 is constituted by a material having a tensile rupture strength larger than at least a minimum stress required for the metal coil 11 to be permanently deformed by extension in the coil axis direction.
- the metal wire is made of a high metal wire, the wire diameter of which is made as small as possible in the axial expansion regulating member 20 so as to secure the desired strength.
- the metal wire 21 has a tensile strength at break of, for example, 700 N / mm 2 or more, more preferably 900 to 500 N, which is specific to the metal wire constituting the metal wire 21. / mm composed by two things.
- Specific examples of such a metal wire include, for example, tungsten, titanium, gold, platinum and their alloys, stainless steel, etc., among which, compared to other metal materials. It is preferable to use tungsten or a tungsten alloy from the viewpoint of high strength and excellent workability.
- the metal wire 21 is formed of a wire having a diameter (elementary wire diameter) of 25 ⁇ or less, more preferably 5 to 20 ⁇ m.
- the wire constituting the metal wire 21 may be, for example, a round wire, a square wire, a flat wire, or any other wire having a cross-sectional shape.
- the axial extension restricting member 20 of the indwelling device 10 has a tensile breaking strength of, for example, 0.1 N or more when the configuration of the material and the wire diameter of the metal wire 21 is specified. It is more preferable that the tensile strength at break is 0.2 to 1 N.
- the “tensile breaking strength [N]” is a value specific to the axial extension regulating member in which the material and the configuration of the metal wire 21 and the like, for example, are specified. It is indicated by the maximum load required to break the directional extension restricting member.
- the tensile breaking strength of the entire axial extension restricting member 20 of the indwelling device 10 shown in FIG. 1 substantially corresponds to the tensile breaking strength inherent to the metal wire constituting the metal wire 21.
- the metal wire 21 preferably has a total length of 0.1 to 30.0% larger than the coil length of the metal coil 11 in a normal state, and more preferably 0.1 to 30.0%. 3.0% larger.
- Means for fixing the tip of metal wire 2 1 to head 1 2 and the rear end of metal wire 2 1 and holding The means for fixing to the member 13 is not particularly limited, and, for example, bonding with an adhesive, welding, pressure bonding, physical connection, and other means can be used.
- the flexibility of the indwelling device 10 as a whole is preferably 3 OmNZmm or less, more preferably 1 to 25 mNZmm.
- “flexibility” in the present specification is indicated by a compression modulus measured as follows.
- the in-vivo indwelling device 10 is fixed in such a manner that the coil axis of the metal coil 11 extends in, for example, a vertical direction (vertical direction in FIG. 2).
- a method is used in which a load is gradually applied to the tool 10 from above in the coil axis direction, and the stress when the tip 1 pitch of the metal coil 11 is pressed and bent is measured as the compression modulus. be able to.
- the axial extension restricting member 20 constituting the indwelling device 10 of the present invention comprises a stranded wire 21 A formed by loosely twisting a plurality of metal wires, as shown in FIG.
- the material constituting each of the metal wires those exemplified as the material constituting the metal wire 21 in the indwelling device 10 shown in FIG. 1 can be used.
- each of the metal wires constituting the machine wire 21A uses the same metal wire as the metal wire 21 in the indwelling device 10 shown in FIG. Wire diameter) can be smaller than that of the metal wire 21 in the indwelling device 10 shown in FIG.
- the size of the diameter of each metal wire varies depending on the number and material of the metal wires to be twisted.
- the tensile break strength of the entire machine wire 21A is, for example, 0.1 N. It can be set appropriately as described above.
- the ⁇ loosely twisted state '' means that the pitch p of the stranded wire 21 A represented by the length between two points where the metal wires cross each other in FIG. 3 is, for example, 0. 0.5 to 3.0 mm, more preferably 0.1 to 1.5 mm, or 100 to 69 ON / mm 2 , more preferably 15 to 15 mm when twisting metal wires.
- the axial extension restricting member 20 can have high flexibility while ensuring the intended strength. It can be configured as having.
- the axial extension regulating member 20 constituting the indwelling device 10 of the present invention can be made of a fibrous polymer material, such as polyethylene terephthalate (PET).
- PET polyethylene terephthalate
- a polyester resin such as polypropylene (PP) and a polyamide resin such as nylon.
- the in-dwelling device 10 of the present invention includes, as shown in FIG. 4, an axial extension regulating member 30 composed of a single fiber element 31 made of, for example, a resin.
- the proximal edge of the metal coil 11 is not fixed to the metal coil 11 except that it is fixed to the head 12, and the other end is unrelated to the metal coil 11. It is provided so as to protrude further and extend outward in the coil axis direction.
- a locking member 25 which prohibits the metal coil 11 from extending beyond a certain extent in the coil axis direction.
- the configuration provided can be adopted.
- the resin constituting the fiber 31 element can be selected from those that do not adversely affect the human body when left in the human body for a long period of time.
- Bul-based polymers such as alcohol, polychlorinated butyl, and poly-acetate butyl; for example, olefin-based polymers such as ethylene butyl alcohol, polyethylene, and polypropylene; and polymers or copolymers such as nylon, polyester, polystyrene, and polyurethane;
- naturally-occurring polymers such as cellulose, chitin and chitosan can be exemplified.
- the diameter of the fiber element 31 constituting the axial extension restricting member 30 is the minimum size required for the metal coil 11 to have the expected tensile breaking strength in the coil axial direction of the metal coil 11. And more specifically, for example, a wire having a diameter of 25 ⁇ m or less, more preferably a diameter of 5 to 20 ⁇ .
- a plurality of wires having a unit wire diameter (diameter of each wire) of 5 to: : 5 ⁇ , more preferably 5 to: 10 ⁇ m are arranged in the coil axis direction. It is preferable that they are arranged side by side.
- the length of the fiber element 31 is preferably 0.1 to 30.0% larger than the coil length of the metal coil 11 in a normal state, and more preferably 0.1%. ⁇ 3.0% larger.
- the shape of the locking member 25 is not particularly limited as long as it has a shape larger than the inner diameter of the metal coil 11 and does not damage the application site. For example, it is formed of a smooth hemisphere having an outer diameter larger than the coil diameter of the metal coil 11.
- the locking member 25 is provided at an outer position from the proximal edge of the metal coil 11 in a normal state by, for example, 0.1 to 30.0% of the coil length. Is preferred.
- the fiber element 31 constituting the axial extension regulating member 30 is not fixed to the metal coil 11 at all.
- the metal coil 11 is disposed inside the metal coil 11 so as to protrude from both edges of the metal coil 11 and extend outward in the coil axis direction. It is possible to adopt a configuration in which locking members 25 and 25 for inhibiting extension of the coil 11 beyond a certain level are provided.
- the in-dwelling device 10 as described above can be used in a state where it has a linear shape.
- a linear metal coil 11 may be used.
- the coil body is further spirally wound to form a secondary coil, for example, shaped into an "S" or "J" shape, a three-dimensional structure, or other secondary forms It is preferable to use it in the state where it was done.
- the secondary coil diameter can be, for example, 1 to 45 mm.
- an appropriate catheter is percutaneously inserted into the blood vessel using a puncture needle, and the catheter is arranged so that the tip of the force catheter reaches the entrance of the aneurysm.
- the in-dwelling device 10 shaped in various forms is detachably attached to the tip of the guidewire, the in-dwelling device 10 is stretched linearly to a primary form (shown in FIGS. 1 to 4).
- the guide wire is inserted into the catheter to be advanced, and the indwelling device 10 is pushed out from the distal end of the catheter to be placed in the aneurysm.
- the method of attaching the indwelling device 10 to the guidewire is as follows: (1) A structure in which the holding member 13 in the indwelling device 10 and the guidewire are mechanically engaged to be mechanically attached and detached. Method, (2) For example, by supplying a monopolar high-frequency current, A method of causing the holding member 13 in 10 to be heated and melted and cut by a high-frequency current, thereby performing electrolytic separation by energization so as to be separated from the guide wire.
- the indwelling device 10 When the indwelling device 10 is pushed out of the catheter, it is restored to a secondary coil shape and takes on a three-dimensionally entangled shape. In this state, after confirming by radioscopy that the indwelling device 10 is completely inserted into the aneurysm, the indwelling device 10 is separated from the distal end of the guidewire and is left.
- the indwelling device 10 can be configured as having high flexibility, whereby high operability can be obtained when performing the indwelling operation,
- the device can be reliably introduced and retained at a predetermined site via an appropriate catheter, and the force of re-placement including recovery of the device 10 can be reliably performed. It can be configured as having high safety.
- the axial direction expansion restriction member 20 is connected to the coil shaft.
- the axial extension regulating member 20 itself has high flexibility. Therefore, the metal wire 21 can be deformed following the extension of the metal coil 11 in the coil axial direction. Specifically, the axial extension regulating member 20 is formed.
- the metal wire 21 When the metal coil 11 is extended in the coil axis direction, the metal wire 21 is provided in a state where the metal wire 21 can be extended within a range regulated with respect to the coil axis direction of the metal coil 11.
- Metal wire 2 1 is metal By being pulled in the coil axis direction with the extension of the coil 11, the metal wire 21 can be stretched to a state in which the metal wire 21 is tensioned with respect to the metal coil 11.
- the indwelling device 1 0 can be configured as having high flexibility.
- the indwelling operation as described above in order to place the indwelling device 10 in the body at an appropriate position, the indwelling device 10 disposed in the body is collected by being pulled back into the catheter.
- the metal wire 21 is provided inside the metal coil 11 and the metal wire 21 By constructing itself from a material having a high tensile breaking strength, the extension of the metal coil 11 in the coil axis direction can be regulated.
- the metal wire 21 is moved to a state of tension with respect to the metal coil 11 when performing the re-placement operation, the metal coil 11 1 Since the metal coil 11 is pulled into the catheter in a state where it is prevented from being further extended in the axial direction, the re-placement operation including the collection of the in-vivo in-dwelling device 10 can be performed reliably.
- the indwelling device 10 can be configured as having high safety.
- the firer element 31 constituting the axial extension restricting member 30 has a configuration in which only one end is fixed to the metal coil 11 and the locking member 25 is provided at the other end.
- the metal coil 11 is Since the degree of freedom is high with respect to the fiber element 31, the flexibility of the metal coil 11 is not hindered by the fiber element 31, and the indwelling device 10 has high flexibility. Therefore, high operability can be obtained when performing the indwelling operation, and the indwelling device 10 can be surely introduced into a predetermined site via an appropriate catheter and indwelled.
- the locking member 25 As a result of the restriction of the extension of the metal coil 11 in the coil axis direction by the locking member 25, for example, after being once placed inside the body via an appropriate catheter, it is recovered and repositioned to correct the position.
- the rigidity of the fiber element 31 prevented the metal coil 11 from extending further in the coil axis direction. In this state, the metal coil 11 is pulled into the catheter, so that the indwelling operation including recovery of the indwelling device 10 can be reliably performed, and the indwelling device 10 is configured as having high safety. be able to.
- the axial extension restricting member 20 is constituted by the stranded wire 21 A formed by twisting a plurality of metal wires 1 (see FIG. 3).
- the diameter of each of the metal wires constituting the stranded wire 21 A can be reduced, As a result, the flexibility of the metal wire itself is increased, and the axial extension restricting member 20 can be configured to have the intended strength and to have higher flexibility while ensuring the intended strength.
- the directional extension restricting member 20 is made of a tungsten wire or a tungsten alloy wire, the tungsten or the tungsten alloy itself has extremely high strength, so that it is compared to other biocompatible metal wires.
- the diameter can be reduced, so that the axial extension restricting member 20 is surely configured as having both high strength and high flexibility. It can be.
- the axial extension regulating member 20 is formed by winding a metal wire in a spiral shape to form a coil, or by forming a metal wire into a jig. It can be constituted by one shaped in a zag or ribbon shape or the like.
- the metal coil 11 should be stretched in the coil axis direction to a certain size or less, and the metal wire should be attached to the metal wire so that the indwelling device has a predetermined flexibility.
- the coil diameter, coil length and other configurations of the coil to be formed can be set.
- the coil main body is not limited to a metal coil, but may be, for example, a resin coil.
- the coil body is composed of a material in which a fiber material such as polyester is woven into the coil body in a loop shape, a material in which the surface of the coil body is covered with a fiber material woven in a cylindrical shape, and the like. According to the coil body having such a configuration, the ability to form an embolus at a predetermined site can be further improved.
- a description will be given of an example of an experiment conducted to reduce the effect of the indwelling device according to the present invention.
- Metal coil made of platinum-tungsten alloy wire with a wire diameter of 50 ⁇ : 250 Coil length: 3 O mm, number of windings per 1 mm: 20) Inside the wire diameter 2
- a 30.3 mm long tungsten wire with a spiral structure is inserted and arranged in an axial extension regulating member.
- the outer surface at both ends of the tungsten wire and the metal are removed.
- the tungsten wire is in a state of being stretched in the axial direction of the coil as shown in Fig. 1 by a simple wire structure.
- An indwelling device was manufactured. This is called “Indwelling device 1”
- Example 2 In Manufacturing Example 1, except that the axial extension restricting member was constituted by a stranded wire formed by loosely twisting three tungsten wires each having a wire diameter of 10 im and a total length of 30.6 mm. In the same manner as in Example 1, a stranded wire indwelling device as shown in Fig. 3 was manufactured. This will be referred to as “detainer 2”.
- the stranded wire is formed by twisting tungsten wires by applying a tension (torsional stress) of 500 N / mm 2 , and the pitch of the stranded wire is 0.7 mm.
- a metal coil (coil diameter: 300 ⁇ m, coil length: 15 O mm, number of windings per mm: 3 3) formed of a tungsten wire rod with an element wire diameter of 30 zm, a diameter of 20 mm
- an axial extension restricting member composed of a fiber element made of polyvinyl alcohol (PVA) with ⁇ and length of 16 O mm.
- PVA polyvinyl alcohol
- the fiber element was disposed without being fixed to the metal coil, and was connected to each of the fiber elements located 5 mm outside the coil axis direction from both ends of the metal coil.
- An in-dwelling device having a configuration as shown in FIG. 5 was manufactured in the same manner as in Production Example 3 except that a stopper member was provided. This will be referred to as “detainer 4”.
- Production Example 1 the same procedure as in Production Example 1 was carried out except that the material constituting the axial extension regulating member was changed according to Table 1 below.
- a wire-structured indwelling device was manufactured. These are referred to as “detainer 5” to “detainer 7”.
- the numerical values in the lower part of the materials indicate the tensile breaking strength (N / mm 2 ) specific to the constituent material described in claim 1.
- Production Example 1 a simple wire structure was adopted in the same manner as in Production Example 1, except that the axial extension regulating member was composed of a simple wire of 30 m in length and 30.3 mm in total length. Manufactured an indwelling device. This is referred to as “comparative indwelling device 1”.
- the axial extension restricting member was formed of a tungsten wire having the same total length (30 mm) as the coil length of the metal coil in a normal state, and the tungsten wire was tensioned with respect to the metal coil.
- An indwelling device having a simple wire structure was manufactured in the same manner as in Production Example 1 except that the device was fixed with. This is referred to as “Reference detainer 2”.
- the tensile breaking strength of the axial extension restricting member is the tensile pressure! ⁇
- a test machine “Strograph E-L” manufactured by Toyo Seiki Seisaku-sho, Ltd.
- the axial extension restricting member can be configured to have a sufficiently high tensile breaking strength.
- the extension of the coil in the axial direction of the coil beyond a certain level can be restricted, and the indwelling device can be configured to have high flexibility. ⁇ It was confirmed that high level and safety could be obtained.
- the metal coil is deformed in the elastic region, and the original state is obtained by releasing the load on the metal coil.
- the characteristics of the metal coil are practically not impaired, it is desirable that the metal coil be in a state where the elongation is as small as possible when performing the re-placement operation.
- the indwelling devices 1 to 7 according to the present invention since the elongation rate of the metal coil can be set to about: to 3%, it is considered that the indwelling operation can be reliably performed. .
- the comparative indwelling device 1 has a configuration in which the diameter of the axial extension regulating member is relatively large, so that the flexibility of the entire indwelling device is low. It is assumed that it may be difficult to do so reliably.
- the axial extension restricting member has a sufficiently high tensile breaking strength, and is provided in a state of being tensioned with respect to the metal coil. Is not extended in the coil axis direction, but it is assumed that the flexibility of the entire indwelling device is low, and it may be difficult to reliably perform the indwelling operation of the indwelling device in the body.
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Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04712700.6A EP1595506A4 (en) | 2003-02-20 | 2004-02-19 | DEVICE FOR FORMING AN EMBOLUS |
| US10/545,992 US20060173488A1 (en) | 2003-02-20 | 2004-02-19 | Indwelling instrument for forming embolus |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003-042724 | 2003-02-20 | ||
| JP2003042724A JP2004261234A (ja) | 2003-02-20 | 2003-02-20 | 塞栓形成用体内留置具 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2004073528A1 true WO2004073528A1 (ja) | 2004-09-02 |
Family
ID=32905364
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2004/001864 Ceased WO2004073528A1 (ja) | 2003-02-20 | 2004-02-19 | 塞栓形成用体内留置具 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20060173488A1 (ja) |
| EP (1) | EP1595506A4 (ja) |
| JP (1) | JP2004261234A (ja) |
| WO (1) | WO2004073528A1 (ja) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016140314A1 (ja) * | 2015-03-03 | 2016-09-09 | 株式会社カネカメディックス | 血管塞栓用具、およびその製造方法 |
| WO2016140313A1 (ja) * | 2015-03-03 | 2016-09-09 | 株式会社カネカメディックス | 血管塞栓用具、およびその製造方法 |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2549371T3 (es) | 2004-08-25 | 2015-10-27 | Microvention, Inc. | Sistema de separación térmica para dispositivos implantables |
| WO2010014075A1 (en) * | 2007-07-27 | 2010-02-04 | Microvention, Inc. | Detachable coil incorporating stretch resistance |
| EP2231030B1 (en) | 2007-12-21 | 2019-02-27 | MicroVention, Inc. | System and method for locating detachment zone of a detachable implant |
| CA2710781C (en) | 2007-12-21 | 2016-09-27 | Microvention, Inc. | A system and method of detecting implant detachment |
| CN102405023A (zh) * | 2009-04-20 | 2012-04-04 | 株式会社钟化 | 栓塞线圈 |
| JPWO2011030820A1 (ja) * | 2009-09-09 | 2013-02-07 | 株式会社カネカ | 塞栓コイル |
| JP5899200B2 (ja) | 2010-04-14 | 2016-04-06 | マイクロベンション インコーポレイテッド | インプラント送達デバイス |
| EP4151164A1 (en) | 2014-04-11 | 2023-03-22 | Microvention, Inc. | Implant delivery system |
| US10639456B2 (en) | 2015-09-28 | 2020-05-05 | Microvention, Inc. | Guidewire with torque transmission element |
| EP3682818B1 (en) * | 2017-09-12 | 2023-11-08 | Kaneka Corporation | Indwelling device for embolization |
| US11439404B2 (en) * | 2017-09-12 | 2022-09-13 | Kaneka Corporation | Indwelling device for embolization and method for manufacturing the same |
| US12114863B2 (en) | 2018-12-05 | 2024-10-15 | Microvention, Inc. | Implant delivery system |
| CN115957421A (zh) * | 2021-10-11 | 2023-04-14 | 先健科技(深圳)有限公司 | 鞘管及输送装置 |
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- 2004-02-19 EP EP04712700.6A patent/EP1595506A4/en not_active Withdrawn
- 2004-02-19 US US10/545,992 patent/US20060173488A1/en not_active Abandoned
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| JP2002507902A (ja) * | 1997-06-20 | 2002-03-12 | ターゲット セラピューティクス,インコーポレイテッド | 伸長抵抗性血管閉塞コイル(▲ii▼) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016140314A1 (ja) * | 2015-03-03 | 2016-09-09 | 株式会社カネカメディックス | 血管塞栓用具、およびその製造方法 |
| WO2016140313A1 (ja) * | 2015-03-03 | 2016-09-09 | 株式会社カネカメディックス | 血管塞栓用具、およびその製造方法 |
| JPWO2016140314A1 (ja) * | 2015-03-03 | 2018-02-08 | 株式会社カネカメディックス | 血管塞栓用具、およびその製造方法 |
| US11291798B2 (en) | 2015-03-03 | 2022-04-05 | Kaneka Medix Corporation | Vascular embolization device and production method therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1595506A4 (en) | 2013-07-03 |
| EP1595506A1 (en) | 2005-11-16 |
| US20060173488A1 (en) | 2006-08-03 |
| JP2004261234A (ja) | 2004-09-24 |
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