Distal perfusion sheath
A distal perfusion sheath (DPS) is provided for cases where blood perfusion is needed for downstream arteries (distal) to the insertion point of the DPS within the target artery. The ability to provide distal perfusion with the DPS allows the DPS to be positioned in the target artery for long periods without causing lack of blood flow (ischemia) to an extremity that the target artery supplies. In embodiments, the DPS can still be used for surgical arterial access while allowing blood flow downstream. In addition, embodiments of the DPS configured with longer perfusion shunts can allow a contra-lateral extremity downstream to a large DPS to have blood flow while the sheath is in place.
1. A sheath for insertion into an artery, said sheath comprising:
an inner lumen;
an outer lumen surroundingly attached to said inner lumen with expandable scaffolds therebetween; and
a perfusion shunt in fluid communication with said outer lumen, said perfusion shunt configured for insertion into a distal portion of the artery beyond said sheath to provide blood flow from a proximal portion of the artery prior to said inserted sheath to the distal portion of the artery.
2. The sheath of claim 1 wherein said inner lumen and said outer lumen are concentric.
3. The sheath of claim 1 wherein said inner lumen and said outer lumen are eccentric.
4. The sheath of claim 1 wherein said inner lumen is configured for the insertion of at least one of: a catheter, guide wire, camera, or other device into said artery.
5. The sheath of claim 4 wherein said flush port controls fluids in said inner lumen.
6. The sheath of claim 1 wherein said inner lumen further comprises a hemostatic port and a flush port.
7. The sheath of claim 6 wherein said hemostatic port controls blood flow in said inner lumen, and is configured for insertion of a catheter, guide wire, camera, or other device into the artery.
8. The sheath of claim 1 wherein said scaffolds are expanded by injecting fluids into a port connected to said outer lumen.
9. The sheath of claim 8 wherein said biocompatible polyurethane materials are reinforced with metal.
10. The sheath of claim 8 wherein said biocompatible polyurethane materials are reinforced with Nitonal.
11. The sheath of claim 1 wherein said sheath is constructed with biocompatible polyurethane materials.
12. A method of using the sheath of claim 1 , the method comprising:
inserting said sheath in a patient artery;
inserting said perfusion shunt in said distal portion of said artery with a small incision (arteriotomy) in said distal portion of said artery just below said sheath;
securing said perfusion shunt to said distal portion of said artery with a vessel loop; and
inflating said scaffolds of said outer lumen.
13. A sheath for insertion into an artery, said sheath comprising:
an inner lumen with a proximal end configured for insertion into said artery, and a distal end that tapers outward;
an outer lumen concentrically attached to said inner lumen with expandable scaffolds;
a perfusion shunt in fluid communication with said outer lumen, said perfusion shunt configured for insertion into a distal portion of said artery beyond said sheath to provide blood flow from a proximal portion of said artery prior to said inserted sheath to said distal portion of said artery;
a plurality of guidewires within said inner lumen;
an engagement system with a series of wire-lock engagement points affixed to said distal end for individually engaging each of said plurality of guidewires; and
a rotatable hub at said distal end centered on a longitudinal axis of said sheath configured with a hemostatic valve at said center and a slit extending from said hemostatic valve to an outer edge of said hub.
14. The sheath of claim 13 wherein each of said plurality of guidewires is individually adjustable.
15. The sheath of claim 14 wherein in the event said guidewire is positioned in said hemostatic valve, said guidewire is free to move back and forth, or be twisted, along a longitudinal axis of said sheath.
16. The sheath of claim 13 wherein a guidewire from said plurality of guidewires is adjustable when said slit is aligned with an engagement point corresponding to said guidewire, and the engagement point is unlocked to provide movement of said guidewire to said hemostatic valve via said slit.
17. The sheath of claim 13 wherein said plurality of guidewires when engaged in said series of wire-lock engagement points are prevented from being dislodged when one guidewire from one of said plurality of guidewires is being used in said sheath.
18. The sheath of claim 13 wherein said engagement system secures said plurality of guidewires in independent positions in multiple target arteries.
19. The sheath of claim 13 wherein said sheath is constructed with biocompatible polyurethane materials.
20. The sheath of claim 19 wherein said biocompatible polyurethane materials are reinforced.