Duet stent deployment system and method of performing a transjugular intrahepatic portosystemic shunting procedure using same
US-2016242943-A1 · Aug 25, 2016 · US
US11141238B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11141238-B2 |
| Application number | US-201815904841-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 26, 2018 |
| Priority date | Feb 27, 2017 |
| Publication date | Oct 12, 2021 |
| Grant date | Oct 12, 2021 |
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The present disclosure relates to the field of endoscopy. Specifically, the present disclosure relates to systems and methods which allow the distal portion of a catheter to be visualized within the body using a colored marker and one or more secondary markers. In particular, the present disclosure relates to systems and methods which indicate when a medical device is properly positioned for deployment within a body lumen.
Opening claim text (preview).
What is claimed is: 1. A system, comprising: an outer catheter, the outer catheter including: a proximal end; a distal end; and a lumen extending therebetween, wherein a distal portion of the outer catheter includes a visual marker and at least one imageable marker; and an inner catheter slidably disposed within the lumen of the outer catheter; a stent disposed over the inner catheter, the stent being configured to transition from a first configuration to a second configuration when not disposed within the lumen of the outer catheter, the stent comprising a proximal retention member and a distal retention member when in the second configuration; wherein the outer catheter is proximally retractable together with the inner catheter and the stent with respect to a reference position within a body lumen; wherein the visual marker of the outer catheter is positioned along the outer catheter and with respect to the stent such that visual confirmation within the body lumen of the visual marker proximal to the reference position denotes that the entire proximal retention member is deployable proximally relative to the reference position. 2. The system of claim 1 , wherein the at least one imageable marker is disposed within the visual marker. 3. The system of claim 1 , wherein the at least one imageable marker is disposed on or within a distal portion of the outer catheter which corresponds to an approximate midpoint of the stent when loaded within the outer catheter lumen in the first configuration. 4. The system of claim 1 , wherein the at least one imageable marker is disposed on or within a distal portion of the outer catheter which corresponds to an approximate distal end of the stent when loaded within the outer catheter lumen in the first configuration. 5. The system of claim 1 , wherein the at least one imageable marker comprises a plurality of imageable markers disposed about a circumference of the outer catheter. 6. The system of claim 1 , wherein the visual marker includes a colored marker. 7. The system of claim 1 , wherein the at least one imageable marker includes a light sensor. 8. The system of claim 1 , wherein the at least one imageable marker includes an echogenic material. 9. A system, comprising: an outer catheter, comprising: a proximal end, a distal end, and a lumen extending therebetween; wherein a distal portion of the outer catheter includes at least one imageable marker; a visual marker positioned along the distal portion of the outer catheter; an inner catheter slidably disposed within the outer catheter lumen; and a stent disposed over a distal portion of the inner catheter, wherein the stent is configured to move between a first configuration when disposed within the outer catheter lumen, and a second configuration when not disposed within the outer catheter lumen, and wherein, when in the second configuration, a distal end portion of the stent forms a distal retention member and a proximal end portion of the stent forms a proximal retention member; and wherein the outer catheter is retractable proximally relative to the inner catheter and with respect to a reference position within a patient's body, and wherein visual confirmation within the patient's body of the visual marker at or proximal to the reference position denotes that the entire proximal retention member is clear of the reference position in order to deploy entirely proximally to the reference position. 10. The system of claim 9 , wherein the at least one imageable marker is disposed within the visual marker. 11. The system of claim 9 , wherein the at least one imageable marker is disposed on or within a distal portion of the outer catheter which corresponds to an approximate midpoint of the stent. 12. The system of claim 9 , wherein the at least one imageable marker is disposed on or within a distal portion of the outer catheter which corresponds to an approximate distal end of the stent. 13. The system of claim 9 , wherein the at least one imageable marker comprises a plurality of radiopaque markers disposed about a circumference of the outer catheter. 14. The system of claim 9 , wherein the visual marker includes a colored marker. 15. The system of claim 9 , wherein the at least one imageable marker includes a light sensor. 16. The system of claim 9 , wherein the at least one imageable marker includes an echogenic material. 17. The system of claim 9 , wherein the stent is a self-expanding stent.
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