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
• • 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
• • 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
  • A61B17/12136—Balloons
• • 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
• • 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
  • A61B2017/1205—Introduction devices
• • 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
  • A61B2017/1205—Introduction devices
  • A61B2017/12054—Details concerning the detachment of the occluding device from the introduction device
  • A61B2017/12063—Details concerning the detachment of the occluding device from the introduction device electrolytically detachable

Definitions

• the present invention relates to a device tor treating aneurysms and in pa ⁇ icular to a device for use in the endovascular treatment of intracra ⁇ ial aneurysms.
• U.S. 5,334.210 discloses a vascular occlusion assembly which comprises a bag made of rip stop nylon material so as to prevent the passage of blood.
• the bag has a predetermined diamond shape and thus would not be suitable for conforming to aneurysms.
• the heavy and non-stretch nature of the material of the bag would make it difficult to steer through fine intracranial blood vessels. No guide wire is provided and the bag is attached and detached by a frictional arrangement.
• WO96/01591 also discloses a self-expanding vascular occlusion device.
• a pre- moulded basket of metal fabric is collapsed for passage through a catheter, placed in location by a guide wire affixed to the basket, and subsequently expanded within a channel in a patient's body. Since the passage of a metallic body is traumatic to patients, the basket moves along the interior of the catheter.
• Devices in accordance with the present invention are especially suitable for use with a Guglielmi Detachable Coil arrangement (GD coil) as disclosed in Guglielmi G.. Vinuela F.. Duckwiler G.. Dion J.. et al. Endovascular treatment of posterior circulation aneurysms using electrically detachable coils. J Neurosurgery. 77: 515-524, 1992.
• GD coil Guglielmi Detachable Coil arrangement
• Saccular intracra ⁇ ial (cerebral) aneurysms occur when regions of weakness in the wall of intracranial arteries result in the development of balloon-like swellings on the sides of the arteries. They are important because they are prone to burst and cause haemorrhage over the surface of the brain (subarachnoid haemorrhage). This can result in death in over 30% of patients within 24 hours and a further 25-30% will die within the next four weeks without some form of surgical intervention.
• the conventional treatment of cerebral aneurysms was to perform a neuro-surgical operation to place a clip across the neck of the aneurysm, analogous to tying the neck of a balloon.
• the GD coil has proved very successful especially for aneurysms of the posterior intracranial circulation. It is often used in the treatment of aneurysms which are thought to be inoperable by other means.
• the GD coil is not wimout problems, however, and amongst these are: 1. Relatively poor results in large ( > lcm diameter) or giant ( > 2.5cm diameter) aneurysms, generally because of a tendency for the coil mass to pack down and for the neck region of the aneurysm to enlarge with time after treatment.
• the present invention seeks to overcome, or reduce, one or more of the above problems.
• a device for treating aneurysms comprising a catheter and. removably attached to one end of the cameter, a bag arranged to be inserted in an aneurysm and of a material which is permeable to at least some of the components of the blood.
• connection of the catheter to the bag is such that, with the bag inside the aneurysm, one or more GD coils, or other suitable inserts, can be placed inside the bag before it is disconnected from the catheter.
• the bag may be provided with a guide wire to assist insertion of the bag and the catheter.
• the bag may also comprise one or more marker rings, and the guide wire may have a shoulder which engages one of the rings in the manner of a one-way drive.
• the material of the bag is preferably flexible and stretchable in the manner of nylon stockings so that it can conform to the interior size and shape of the aneurysm.
• the material is non- metallic and may be made from natural or synthetic fibre material.
• the material of the bag may be such as to encourage clotting or. alternatively, to discourage clotting.
• the bag may be provided as part of a kit of parts including a bag. a catheter to which the bag is removably attached, and a guide wire.
• a device for treating aneurysms comprising a catheter and, removably attached to one end of the catheter, a bag arranged to be inse ⁇ ed in an aneurysm and of a material which is flexible and locally stretchable.
• a device for introducing an annular or pan-annular member into a patient comprising a catheter having an element at or adjacent one end thereof with at least one electrode extending along the cameter to said element, said element being connected to said member by two or more spaced struts, die struts being arranged to be removed eiectrolyticaJly when an electric current is passed through said electrode.
• the element on the catheter is preferably also annular or pan-annular so that the struts provide a stable arrangement for maintaining the member and the element reiatively fixed, e.g. with their planes substantially parallel.
• a fourth aspect of die present invention there is provided an arrangement for introducing a bag into a patient, wherein the bag includes a substantially annular opening and a guide wire is provided with a first ponion which passes freely through the opening and a second po ⁇ ion which does not, whereby die guide wire constitutes a one-way drive means for introduction of the bag.
• the first ponion may be a narrow end po ⁇ ion on the end of a shaft which constitutes the second po ⁇ ion, the po ⁇ ions defining a step or shoulder therebetween.
• the second po ⁇ ion may be constituted by a widened section of sho ⁇ extent, e.g. a ball-shaped member on a guide wire of otherwise uniform thinner cross-section.
• the opening in the bag may be provided by a marker ring.
• Figure I is a sectional view of a conventional GD coil inside an intra-cranial aneurysm
• Figure 2 is a view of the aneurysm of Figure I after it has been packed with GD coils;
• Figure 3 is a view of a device in accordance with a first embodiment of the present invention inside an intra-cranial aneurysm;
• Figure 4 is an enlarged view of the device of Figure 3;
• Figure 5 is a similarly enlarged view of the device of Figures 3 and 4, but in a collapsed state for inse ⁇ ion;
• Figure 6 shows a modified device in accordance with die present invention.
• Figure 7 shows a device in accordance with a second embodiment of the present invention.
• each device 10 comprises a coil IS welded or soldered by means of a single connection on to a pushing steel wire 1 1 which is very thin just proximal to a solder joint 12.
• the wire is electrically insulated up to a point approximately 1mm from the joint 12.
• the device 10 is introduced into the aneurysm 20 via a catheter 14. Normal cranial arteries are indicated at 21.
• Platinum markers 16 on the catheter 14 and the pushing wire 1 1, when aligned, indicate that the coil 18 is in an ideal position for detachment.
• a small positive voltage (approximately 3.5V) is applied to the proximal end of the wire.
• the negative terminal is attached to an earthing needle in the patient's groin.
• a current of 1mA passes which causes electrolytic erosion of the distal end of the pushing wire and detachment of die coil 18 in approximately 2 minutes. Fu ⁇ her coils 18 are inse ⁇ ed in sequence until the aneurysm is well packed and it becomes difficult to inse ⁇ any more, see Fig. 2.
• Figures 3 to 5 show a device 30 in accordance with the present invention comprising a bag or envelope 31 forming a liner and removably attached by means of two steel detachment struts 32 to the distal end of a catheter 14.
• the basis concept of this embodiment is to inse ⁇ the bag 31 into the aneurysm 20 before inse ⁇ i ⁇ g the GD coils.
• the bag 31 is an approximately spherical envelope of material which is porous to liquids, including blood. It is provided in a range of sizes which can be matched to die aneurysm 20. It is inse ⁇ ed into the aneurysm 20 on die end of the catheter 14 and remains attached to the catheter while GD coils 18 (or o ier materials) are inse ⁇ ed into it. thus expanding it against the walls of the aneurysm. When the coil mass is complete and detached, die bag 31 is detached from its delivery cadieter 14 and die cadieter wididrawn.
• a guide wire 40 normally employed to inse ⁇ just a catheter, is here used to direct the bag 31 at die end of catheter i 4 to die site of the aneurysm 20.
• the guide wire has a tip 41 of na ⁇ ow cross-section forming a shoulder 42 with the remainder of the wire.
• Tip 41 may have a lengdi of approximately 1 to 2 cm and is more flexible than die remainder of the wire to assist inse ⁇ ion.
• the wire cross-sections are such that wire 40 can pass freely through a platinum base (or south-polar) marker ring 36 of bag 31 , but only tip 41 can pass through a platinum apical (or north-polar) marker ring 46.
• the guide wire operates as a one-way drive for inse ⁇ ing the bag 31 and the attached cadieter 14. Inse ⁇ ion is facilitated by the wider pan of wire 40 keeping the bag stretched longitudinally and thus stretching the bag into a relatively long narrow configuration. This facilitates navigation in the blood vessels and guidance into die aneurysm. Alignment of bag base marker 36 and cameter marker 16 is useu to ensure correct location of die bag 31. When die bag is correctly positioned, the guide wire 40 is withdrawn ieaving the bag attached to the cadieter 1 -
• GD coils 18 attached to respective pusher wires 1 1 are then introduced sequentially along cadieter 14 and inse ⁇ ed in the bag 31 as in ie previously-known method.
• the bag dien expands to conform to the interior of die aneurysm as shown in Fig. 3.
• the catheter detachment mechanism is a modification of die GD coil attachment, and electrolytic detachment is possible.
• the bag has attached to its base a small ring (not shown) of platinum or other suitable material, and of die same or similar diameter as die cadieter. This ring is mounted on top of the distal marker ring 16 of die delivery catheter and is attached to it by the two thin steel struts 32.
• the distal marker ring 16 is in turn connected to a fine electrode 49 embedded in the wall of the delivery catheter Detachment is by electrolysis of the steel struts 32 in much die same way as a GD coil is detached.
• the mate ⁇ al of die bag 3 is a very fine knitted, braided or woven fabric allowing some degree of local stretch.
• the bag is as non-bulk> as possible m its collapsed state, to pass through the guide catheter and blood vessels, but has to be able to expand :o the size of the aneurysm. possibly up to 3cm diameter, idiout significant resistance untii it reaches its design size.
• a preferred material is 5-den ⁇ er nylon.
• the bag is strong enough to contain d e coils 18 and prevent them prolapsing out of me neck of die aneurysm 20.
• die entire oag 31 is arranged to be located wi in die aneurysm, leaving the blood vessels 21 completely clear.
• the bag 31 strengthens the aneurysm walls to reduce the risk of aneurysm rupture, bridges its neck and contains the coils, facilitating insertion of the coils 18 and reducing the chance of coil prolapse.
• the bag 31 is of stretchy material and is not self-expanding; aldiough it is of approximately spherical shape, it conforms to die shape of die pa ⁇ icular aneurysm. panicularlv upon die inse ⁇ ion of coils 18.
• Fu ⁇ her. die bag induces fibrosis in die aneurysm walls, strengthening diem permanently and also forms a framework for endothelial cells to grow across the neck of die aneurysm. thus restoring normal blood flow in die parent a ⁇ ery. It allows better treatment of giant aneurysms and reduces die likelihood of regrowdi of the aneurysm.
• die guide wire 40 can have a sho ⁇ region 50 of increased width, e.g. of the type known as a "ball". This is provided between the tip 41 and the shaft of the guide wire.
• the microcati eter 14 has a helical electrode 59 embedded in its wall for electrolysing d e struts 32.
• die way in which die device 30 is inserted may be changed and die marker rings 36, 46 may be of the same diameter or the end of cadieter 14 may be arranged to pass through the base marker 36 but not the apex marker 46.
• rings include rings of any shape and also to pa ⁇ - ⁇ ngs.
• struts 32 may be provided including one. or diree or more.
• mechanical attachment and detachment devices might be employed or a frictional attachment followed by detachment by pulling die catheter 14 out or pushing off die bag 31.
• the material of the bag 31 may be a very fine version of the types of material used to make tights. Natural fibres such as silk, or man-made fibres such as nylon. Lycra. Dacron or Teflon may be appropriate. Porous membranes such as Gore-Tex may be considered. (Gore-Tex is conventionally thought of as impermeable to water-based liquids: however if it is pre-wetted widi alcohol and the alcohol is then replaced with water, water will pass freely dirough it. Plasma will also pass through it though the cellular elements of blood will not). Although the chosen material may act as a framework for the invasion by fibroblasts or endothelial cells, it is possible to impregnate die fabric with other materials, e.g.
• the bag may be in the form of a bailoon. e g. of Dacron sheet material. having a plurality of perforations. This has the advantages of being strong, smoodi and lightweight and compact. However, it may not be sufficiently elastic to conform to the shape of a particular aneurysm
• Electrodes 49, 59 can be of braided conductive material embedded in die catheter wall.
• a device 130 has a microcatheter 1 14 which together with its marker ring 1 16 can actually pass through die south-polar ring 136 of die liner bag 131.
• the ring 136 is free to move to and fro along the distal end region of the catheter 114.
• a detachable ring 1 17, which is too wide to pass dirough south-polar ring 136. is attached to catheter marker ring by two electrolysable struts 172.
• Ball 150 of the guide wire 140 is too broad to pass dirough the north-polar ring 146. but sufficiently narrow to pass dirough the detachable ring 1 17.
• die terminal marker 1 16 and the cadieter 1 14 Again guide wire 140 has a relatively flexible tip 141
• catheter 1 14 has an electrode (not shown) embedded in its walls for removing struts 172 when desired.
• die device 130 is assemoled with ring 1 17 inside bag 131. so that the bag 131 is loosely retained on the distal end or tr-e cadieter
• the device is steered into die aneurysm widi die bag 131.
• die catheter 1 14 and the guide w re 140 in approximately tr.e relative positions shown.
• aldiough die catheter could ce advanced .lightly relative to the bag
• the detachable ring 117 can be pushed right up against die no ⁇ h-Dolar ring 146 or die bag.
• the guide wire 140 is then wmdrawn rrom die catheter, and die cameter is retracted slightly so that its distal end lies near the centre or the bag. Coils 18 can tren be deployed through the catheter and into the bag insice the aneurysm. As the bag 131 is filled, the catheter can be urged towards the south-polar ring 136. but ring 1 1 7 prevents the catheter from leaving die bag.
• ring 1 17 When the bag has been filled, the struts 1 " 2 are electrolysed away so that ring 1 17 is detached.
• Catheter 1 14 is dien withdrawn from bag 131 and removed from tr.e patient.
• the south-polar ring 136 ensures diat ring 1 T is retained inside the bag widi the coiis 18: accordingly, ring 1 17 should be made of an appropriate material.
• An advantage of this embodiment is that it is more easily steerable towards and into the aneurysm. Also, it permits a more accurate control of the position of the release of the coils 18 within the bag 131.
• the bags 31, 131 may be filled with elements other than GD coils, e.g. elements of different shapes and/or elements which contain or include a material which can initiate a healing response.
• the inserts could include detachable or pushable platinum coiis, injectable panicles or materials which are injected as a liquid but which solidify in d e bag. These materials may or may not include a bio-active material to induce a healing response.
• the bags 31, 131 are made of a suitable material widi a suitable porosity, there may be no need to fill them with elements 18 and it may be enough to cause die bags to inflate within the aneurysm. Also, die bags may be impermeable to all components of blood.
• the above-described devices can also be used with aneurysms located elsewhere in die body.

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• Health & Medical Sciences (AREA)
• Surgery (AREA)
• Life Sciences & Earth Sciences (AREA)
• Heart & Thoracic Surgery (AREA)
• Molecular Biology (AREA)
• Vascular Medicine (AREA)
• Engineering & Computer Science (AREA)
• Biomedical Technology (AREA)
• Reproductive Health (AREA)
• Medical Informatics (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Animal Behavior & Ethology (AREA)
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• Veterinary Medicine (AREA)
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• Media Introduction/Drainage Providing Device (AREA)

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Cited By (51)

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Citations (5)

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• 1997
  • 1997-07-18 GB GB9715241A patent/GB9715241D0/en not_active Ceased
• 1998
  • 1998-07-20 AU AU84524/98A patent/AU8452498A/en not_active Abandoned
  • 1998-07-20 DE DE69804621T patent/DE69804621T2/de not_active Expired - Lifetime
  • 1998-07-20 EP EP98935171A patent/EP0996371B1/en not_active Expired - Lifetime
  • 1998-07-20 WO PCT/GB1998/002165 patent/WO1999003404A1/en not_active Ceased
  • 1998-07-20 JP JP2000502713A patent/JP4070404B2/ja not_active Expired - Fee Related
  • 1998-07-20 US US09/463,069 patent/US6585748B1/en not_active Expired - Fee Related
  • 1998-07-20 ES ES98935171T patent/ES2175739T3/es not_active Expired - Lifetime

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