Method and apparatus for treating a carotid artery
US-9526504-B2 · Dec 27, 2016 · US
US2016166754A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016166754-A1 |
| Application number | US-201414908597-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 31, 2014 |
| Priority date | Jul 31, 2013 |
| Publication date | Jun 16, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Unitary body systems and devices and methods to use the same for retroperfusion. In an exemplary device embodiment of the present disclosure, the device comprises a unitary body having a wall and a lumen defined therethrough, a first portion terminating at a first end and configured for at least partial placement within a mammalian artery, a first one-way valve positioned at or near an end of the first portion opposite the first end, a second portion terminating at a second end and configured for at least partial placement within a mammalian vein, and a second one-way valve positioned at or near an end of the second portion opposite the second end.
Opening claim text (preview).
1 . A perfusion device, comprising: a unitary body having a wall and a lumen defined therethrough; a first portion terminating at a first end and configured for at least partial placement within a mammalian artery; a first one-way valve positioned at or near an end of the first portion opposite the first end; a second portion terminating at a second end and configured for at least partial placement within a mammalian vein; and a second one-way valve positioned at or near an end of the second portion opposite the second end. 2 . (canceled) 3 . (canceled) 4 . The device of claim 1 , wherein the first portion has a first length, wherein the second portion has a second length, and wherein the first length is less than the second length. 5 . (canceled) 6 . (canceled) 7 . (canceled) 8 . (canceled) 9 . The device of claim 1 , wherein in use at least part of the first portion is configured to be positioned within a subclavian artery or axiallary artery, and wherein at least part of the second portion is configured to be positioned within a subclavian vein or an axillary vein for use and/or treatment at or near the heart. 10 . The device of claim 1 , wherein in use at least part of the first portion is configured to be positioned within an iliac artery, and wherein at least part of the second portion is configured to be positioned within a saphenous vein or a femoral vein. 11 . (canceled) 12 . The device of claim 1 , wherein one or more portions of the unitary body is/are flexible. 13 . The device of claim 1 , wherein the unitary body is able to deform easily without collapsing so that the lumen remains open to allow blood to flow from the first end, through the body, and out of the second end when in use. 14 . The device of claim 1 , wherein the unitary body comprises a coil-reinforced wall having one or more coils. 15 . (canceled) 16 . The device of claim 1 , further comprising: a balloon positioned within or coupled to the second portion. 17 . (canceled) 18 . (canceled) 19 . (canceled) 20 . (canceled) 21 . (canceled) 22 . The device of claim 1 , further comprising: a flarable tip defined at or coupled to the second end of the device. 23 . (canceled) 24 . (canceled) 25 . (canceled) 26 . (canceled) 27 . (canceled) 28 . (canceled) 29 . (canceled) 30 . (canceled) 31 . The device of claim 1 , wherein the second portion comprises a first tapered portion. 32 . (canceled) 33 . (canceled) 34 . (canceled) 35 . The device of claim 1 , wherein the device is configured so that the second portion is sized and shaped to facilitate implantation within the mammalian vein. 36 . The device of claim 1 , wherein the device is configured so that the second portion is sized and shaped to reduce a risk of rupture of the mammalian vein. 37 . (canceled) 38 . (canceled) 39 . (canceled) 40 . (canceled) 41 . (canceled) 42 . (canceled) 43 . (canceled) 44 . (canceled) 45 . (canceled) 46 . (canceled) 47 . The device of claim 1 , wherein when the first portion is immediately adjacent to the second portion, the first portion meets the second portion at a central junction. 48 . The device of claim 47 , wherein part of the first portion adjacent to the central junction is flexible. 49 . (canceled) 50 . (canceled) 51 . (canceled) 52 . (canceled) 53 . (canceled) 54 . The device of claim 1 , wherein when the device comprises a segment between the first one-way valve and the second one way-valve, the device is configured so that a first angle ranging from above 0° to 180° can be formed relative to the first portion and the segment and/or a second angle ranging from above 0° to 180° can be formed relative to the second portion and the segment. 55 . (canceled) 56 . (canceled) 57 . The device of claim 22 , wherein the second portion comprises one or more tapered portions. 58 . (canceled) 59 . (canceled) 60 . (canceled) 61 . The device of claim 1 , forming part of a system, the system further comprising at least one other item selected from the group consisting of one or more of a first guide wire, a second guide wire, a splittable introducer sheath, and/or a data wire. 62 . (canceled) 63 . (canceled) 64 . (canceled) 65 . (canceled) 66 . (canceled) 67 . (canceled) 68 . A method, comprising the step of positioning the device of claim 1 within a mammalian patient so that the first portion is positioned within an artery and so that the second portion is positioned within a vein. 69 . The method of claim 68 , wherein the positioning step is performed by positioning a first portion of a perfusion device within the artery, wherein a first guidewire is positioned through part of the first portion of the device into the artery, and positioning a second portion of a perfusion device within the vein, wherein a second guidewire is positioned through part of the second portion of the device into the vein. 70 . The method of claim 69 , wherein the positioning step is further performed by advancing a first dilator over the first guidewire before positioning the first portion of the perfusion device into the artery and by advancing a second dilator over the second guidewire before positioning the second portion of the perfusion device into the vein.
Reperfusion, e.g. of the coronary vessels, e.g. retroperfusion · CPC title
Blood vessels · CPC title
Guide wires · CPC title
Dilators made of swellable material {(balloon catheters for angioplasty A61M25/104)} · CPC title
Check- or non-return valves · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.