Aneurysm embolization by rotational accumulation of mass
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61M-029/00
A61M-025/00
A61B-017/12
A61B-017/00
출원번호
US-0930303
(2011-01-03)
등록번호
US-8906057
(2014-12-09)
발명자
/ 주소
Connor, Robert A.
Janjua, Muhammad Tariq
출원인 / 주소
Aneuclose LLC
인용정보
피인용 횟수 :
9인용 특허 :
88
초록▼
This invention is a device and method for reducing blood flow into an aneurysm, especially a cerebral aneurysm, in order to promote therapeutic embolization of the aneurysm. The device comprises: at least one core member that is inserted into the aneurysm; and at least one longitudinal flexible memb
This invention is a device and method for reducing blood flow into an aneurysm, especially a cerebral aneurysm, in order to promote therapeutic embolization of the aneurysm. The device comprises: at least one core member that is inserted into the aneurysm; and at least one longitudinal flexible member that is wound repeatedly around the core member within the aneurysm. The longitudinal flexible member is wound around the core member until the rotational accumulation of the flexible member reduces blood flow into the aneurysm and promotes therapeutic embolization of the aneurysm.
대표청구항▼
1. A device to treat an aneurysm comprising: at least one core member including a distal end, that is inserted into the aneurysm; and at least one longitudinal flexible member, wherein the longitudinal flexible member is attached to the core member, wherein the longitudinal flexible member is wound
1. A device to treat an aneurysm comprising: at least one core member including a distal end, that is inserted into the aneurysm; and at least one longitudinal flexible member, wherein the longitudinal flexible member is attached to the core member, wherein the longitudinal flexible member is wound with multiple complete rotations around the at least one core member within the aneurysm, wherein the device is in a first state prior to insertion of the core member into the aneurysm wherein the longitudinal flexible member is wound a first number of complete rotations around the core member and this first number can be zero, wherein the device is in a second state after insertion of the core member into the aneurysm wherein the longitudinal flexible member is wound a second number of complete rotations around the core member and this second number is greater than the first number, and wherein accumulation of the at least one longitudinal flexible member within the aneurysm reduces blood flow into the aneurysm; anda guide loop that guides the longitudinal flexible member as the longitudinal flexible member winds around the core member and that encircles the core member, including the distal end of the core member, in a plane which is substantially parallel to the rotational axis of the core member while the longitudinal flexible member winds around the core member. 2. The device in claim 1 wherein the at least one longitudinal flexible member is wound repeatedly around the at least one core member by one or more rotations selected from the group consisting of: rotation of the at least one core member; and rotation of the longitudinal flexible member around the core member. 3. The device in claim 1 wherein the at least one longitudinal flexible member passes through at least one guiding structure to guide the longitudinal flexible member as it winds repeatedly around the core member and wherein the at least one guiding structure is selected from structures in the group consisting of: an arm, a wire, a cable, a catheter, a rod, a loop, a balloon, and a structure with shape memory. 4. The device in claim 1 wherein the at least one core member has a shape selected from the group consisting of: cylinder with rounded ends, figure-eight, hour glass, torus, ellipse, oval, sphere, cube, and fork with rounded prongs. 5. The device in claim 1 wherein the at least one longitudinal flexible member is selected from the group consisting of: biocompatible thread, biocompatible string, biocompatible filament, biocompatible tape, biocompatible wire, biocompatible coil, and string of connected biocompatible members. 6. The device in claim 1 wherein the at least one longitudinal flexible member adheres or otherwise attaches to itself as it winds around the at least one core member in order to prevent the longitudinal flexible member from unraveling after winding. 7. The device in claim 1 wherein the at least one longitudinal flexible member winds around a core member with a rotational axis with an orientation that is selected from the group consisting of: substantially perpendicular to the plane of the aneurysm neck; and substantially parallel to the plane of the aneurysm neck. 8. The device in claim 1 wherein aneurysms with different shapes and sizes can be optimally filled by varying the number, length, shape, detachment points, and/or material of the at least one core member and the at least one longitudinal flexible member. 9. A device to treat an aneurysm comprising: at least one core member including a distal end, that is inserted into the aneurysm; and at least one longitudinal flexible member, wherein the longitudinal flexible member is attached to the core member, wherein the longitudinal flexible member is wound with multiple complete rotations around the at least one core member within the aneurysm, wherein the device is in a first state prior to insertion of the core member into the aneurysm wherein the longitudinal flexible member is wound a first number of complete rotations around the core member and this first number can be zero, wherein the device is in a second state after insertion of the core member into the aneurysm wherein the longitudinal flexible member is wound a second number of complete rotations around the core member and this second number is greater than the first number, wherein the longitudinal flexible member accumulates around the core member in an outwardly-expanding manner, and wherein accumulation of the at least one longitudinal flexible member within the aneurysm reduces blood flow into the aneurysm, and wherein the at least one longitudinal flexible member is wound repeatedly around the at least one core member by one or more rotations selected from the group consisting of: rotation of the at least one core member; and rotation of the longitudinal flexible member around the core member; anda guide loop that guides the longitudinal flexible member as the longitudinal flexible member winds around the core member and that encircles the core member, including the distal end of the core member, in a plane which is substantially parallel to the rotational axis of the core member while the longitudinal flexible member winds around the core member. 10. The device in claim 9 wherein the at least one longitudinal flexible member passes through at least one guiding structure to guide the longitudinal flexible member as it winds repeatedly around the core member and wherein the at least one guiding structure is selected from structures in the group consisting of: an arm, a wire, a cable, a catheter, a rod, a loop, a balloon, and a structure with shape memory. 11. The device in claim 9 wherein the at least one core member has a shape selected from the group consisting of: cylinder with rounded ends, figure-eight, hour glass, torus, ellipse, oval, sphere, cube, and fork with rounded prongs. 12. The device in claim 9 wherein the at least one longitudinal flexible member adheres or otherwise attaches to itself as it winds around the at least one core member in order to prevent the longitudinal flexible member from unraveling after winding. 13. The device in claim 9 wherein the at least one longitudinal flexible member winds around a core member with a rotational axis with an orientation that is selected from the group consisting of: substantially perpendicular to the plane of the aneurysm neck; and substantially parallel to the plane of the aneurysm neck.
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