Implants and methods for percutaneous perforation closure
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61B-017/00
A61B-050/33
A61B-017/22
A61B-050/30
A61B-090/00
출원번호
US-0781628
(2013-02-28)
등록번호
US-9737286
(2017-08-22)
발명자
/ 주소
Grant, Peter
Martin, Christopher
Dunning, Michael
Ryan, Damien
Dolphin, Joseph
Hession, Micheál
Pawlikowski, Bartosz
McGoldrick, Mark
Brett, Ger
McCartin, Michael
Regan, Des
Murphy, Matthew
출원인 / 주소
Vivasure Medical Limited
대리인 / 주소
Choate, Hall & Stewart LLP
인용정보
피인용 횟수 :
0인용 특허 :
140
초록▼
A device for sealing an aperture in a tissue includes: a foot including a distal portion configured to be disposed distal to the tissue when the device is implanted in a position to seal the aperture; and a flexible wing positionable against a distal surface of the tissue adjacent the aperture such
A device for sealing an aperture in a tissue includes: a foot including a distal portion configured to be disposed distal to the tissue when the device is implanted in a position to seal the aperture; and a flexible wing positionable against a distal surface of the tissue adjacent the aperture such that the flexible wing is disposed between the distal portion of the foot and the distal surface adjacent the aperture.
대표청구항▼
1. A device for sealing an aperture in a tissue, the device comprising: a foot including a distal portion configured to be disposed distally beyond a distal surface of the tissue when the device is in a sealing position, and a proximal portion having a longitudinal axis and configured to extend prox
1. A device for sealing an aperture in a tissue, the device comprising: a foot including a distal portion configured to be disposed distally beyond a distal surface of the tissue when the device is in a sealing position, and a proximal portion having a longitudinal axis and configured to extend proximally through the aperture and proximally beyond a proximal surface of the tissue when the device is in the sealing position;a thin flexible wing having at least one surface and a longitudinal plane, the thin flexible wing positionable against the distal surface of the tissue adjacent the aperture such that the thin flexible wing is disposed between the anterior distal portion of the foot and the distal surface of the tissue when the device is in the sealing position, wherein the at least one surface has a wettability that is increased from a base state of a material from which the thin flexible wing is formed; andan elongated retention member comprising a first portion and a second portion supported and housed by the proximal portion of the foot, the elongated retention member slideably moveable with respect to the proximal portion of the foot from a first position to a second position,wherein the elongated retention member, when in the first position is substantially straight with the first portion and the second portion aligned and extended substantially parallel to the longitudinal axis of the proximal portion of the foot, andwherein the elongated retention member, when in the second position is curved with the first portion substantially parallel to the longitudinal axis of the proximal portion of the foot and the second portion substantially parallel to the longitudinal plane of the thin flexible wing and positioned against the proximal surface of the tissue adjacent the aperture. 2. The device according to claim 1, wherein the device is configured to seal a surgical perforation in a cavity such as a gastrointestinal tract, heart, peritoneal cavity, esophagus, vagina, rectum, trachea, bronchi, or a blood vessel. 3. The device according to claim 1, wherein the device is configured to seal a surgical perforation in an artery, and the thin flexible wing is positionable against an internal luminal surface of the artery adjacent to the surgical perforation. 4. The device according to claim 1, wherein the foot is configured to provide support to the tissue in regions of the distal surface that surround the aperture. 5. The device according to claim 1, wherein the distal portion of the foot has an elongated shape. 6. The device according to claim 5, wherein the device is configured to seal a surgical perforation having a diameter that is less than a length of the distal portion of the foot. 7. The device according to claim 5, wherein the distal portion of the foot has two opposed lateral projections that extend outwardly from the longitudinal axis of the elongated shape. 8. The device according to claim 7, wherein the lateral projections are rounded. 9. The device according to claim 7, wherein the foot has a transverse width measured from an outer edge of one of the lateral projections to an outer edge of the other lateral projection that is constant along at least a portion of the lateral projections. 10. The device according to claim 1, wherein the distal portion of the foot is rectangular. 11. The device according to claim 1, wherein the distal portion of the foot is circular. 12. The device according to claim 1, wherein the device is comprises a recessed surface disposed in the distal portion of the foot and into which the thin flexible wing is received and crimped to provide an effective fluid seal between the wing and the distal portion of the foot. 13. The device according to claim 12, wherein the crimping of the thin flexible wing is achieved using at least one of (a) mechanical crimping, (b) chemical crimping, and (c) thermal crimping. 14. The device according to claim 1, further comprising a passageway extending through at least one of the foot and the thin flexible wing and configured to receive a guidewire therethrough, such that the entire device is freely movable along the guidewire. 15. The device according to claim 14, wherein the elongated retention member further comprises a closure member configured to move from the first position to the second position after complete removal of the guidewire, the movement of the closure member from the first position to the second position causing the passageway to be sealed. 16. The device according to claim 15, wherein the passageway includes an enlarged portion configured to maintain a seal via coagulation. 17. The device according to claim 16, wherein the enlarged portion is tapered. 18. The device according to claim 1, wherein at least one of the foot, the thin flexible wing, and the elongated retention member is formed at least in part of a material having an inherent viscosity in a range from 0.5 to 7.0 dl/g. 19. The device according to claim 1, wherein the longitudinal axis of the proximal portion of the foot is flexible with respect to a longitudinal axis of the distal portion of the foot. 20. The device according to claim 1, wherein the longitudinal axis of the proximal portion of the foot forms an angle in a range from 10 to 70 degrees with respect to a longitudinal axis of the distal portion of the foot. 21. The device according to claim 1, wherein the longitudinal axis of the proximal portion of the foot forms an angle of 30 degrees with respect to a proximal surface of the distal portion of the foot. 22. The device according to claim 1, wherein the distal portion of the foot has a length this is greater than a diameter of the aperture. 23. The device according to claim 1, wherein the proximal portion is flexible relative to the distal portion of the foot. 24. The device according to claim 1, wherein the distal portion of the foot is configured to reinforce the thin flexible wing to facilitate sealing of the aperture. 25. The device according to claim 1, wherein the elongated retention member is configured to provide a safety mechanism against the foot being fully pushed or pulled distally through the aperture. 26. The device according to claim 1, further comprising a guide channel configured to receive a guide wire. 27. The device according to claim 26, wherein the elonngated retention member is configured to block the guide channel when the elongated retention member is in the second position. 28. The device according to claim 26, wherein the elongated retention member is configured to leave the guide channel open when the elongated retention member is the first position. 29. A device for sealing an aperture in a tissue, the device comprising: a foot including a distal portion configured to be disposed distally beyond a distal surface of the tissue when the device is in a sealing position, and a proximal portion having a longitudinal axis and configured to extend proximally through the aperture and proximally beyond a proximal surface of the tissue when the device is in the sealing position;a thin flexible wing having at least one surface and a longitudinal plane, the thin flexible wing positionable against the distal surface of the tissue adjacent the aperture such that the thin flexible wing is disposed between the anterior distal portion of the foot and the distal surface of the tissue when the device is in the sealing position, wherein the at least one surface has a wettability that is increased from a base state of a material from which the thin flexible wing is formed; andan elongated retention member comprising a first portion and a second portion supported and housed by the proximal portion of the foot, the elongated retention member slideably moveable with respect to the proximal portion of the foot from a first position to a second position,wherein the elongated retention member, when in the first position is substantially straight with the first portion and the second portion aligned and extended substantially parallel to the longitudinal axis of the proximal portion of the foot,wherein the elongated retention member, when in the second position is curved with the first portion substantially parallel to the longitudinal axis of the proximal portion of the foot and the second portion substantially parallel to the longitudinal plane of the thin flexible wing and positioned against the proximal surface of the tissue adjacent the aperture, andwherein the device is formed of a polymer adapted to remain shelf stable and functional for sealing after terminal sterilization. 30. The device according to claim 29, wherein the polymer is adapted to remain shelf stable and functional for sealing after terminal sterilization using at least one of (a) ethylene oxide, (b) electron-beam, (c) gamma irradiation, and (d) nitrous oxide. 31. A device for sealing an aperture in a tissue, the device comprising: a foot including a distal portion configured to be disposed distally beyond a distal surface of the tissue when the device is in a sealing position, and a proximal portion having a longitudinal axis and configured to extend proximally through the aperture and proximally beyond a proximal surface of the tissue when the device is in the sealing position;a thin flexible wing having at least one surface and a longitudinal plane, the thin flexible wing positionable against the distal surface of the tissue adjacent the aperture such that the thin flexible wing is disposed between the anterior distal portion of the foot and the distal surface of the tissue when the device is in the sealing position, wherein the at least one surface has a wettability that is increased from a base state of a material from which the thin flexible wing is formed; andan elongated retention member comprising a first portion and a second portion supported and housed by the proximal portion of the foot, the elongated retention member slideably moveable with respect to the proximal portion of the foot from a first position to a second position,wherein the elongated retention member, when in the first position is substantially straight with the first portion and the second portion aligned and extended substantially parallel to the longitudinal axis of the proximal portion of the foot,wherein the elongated retention member, when in the second position is curved with the first portion substantially parallel to the longitudinal axis of the proximal portion of the foot and the second portion substantially parallel to the longitudinal plane of the thin flexible wing and positioned against the proximal surface of the tissue adjacent the aperture, andwherein at least one of the foot and the flexible wing, and the elongated retention member is formed at least in part of a polymer that is biodegradable. 32. The device according to claim 31, wherein the entire device is formed of a polymer that is biodegradable. 33. The device according to claim 31, wherein the polymer comprises Polydioxanone, Poly-L-lactide, Poly-D-lactide, Poly-DL-lactide, Polyglycolide, ε-Caprolactone, Polyethylene glycol, or combinations thereof. 34. The device according to claim 31, wherein the polymer comprises polydioxano
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