Microfabricated catheter having an intermediate preferred bending section
The present disclosure relates to devices and methods for accessing a targeted vessel, such as a coronary artery, near the aortic root. A catheter device includes a proximal section, an intermediate section, and a distal section. The intermediate section includes a more proximal section (a proximal-intermediate section) and a more distal section (a distal-intermediate section). The proximal-intermediate section is microfabricated to enable preferred bending along a single plane. The distal-intermediate section is more rigid than the proximal-intermediate section and the distal section. In use, the proximal-intermediate section abuts against the aortic wall and bends to allow the distal-intermediate section to extend across the aortic root toward a targeted vessel on the opposite side of the aorta.
1. An interventional device, comprising:
an elongated member extending between a proximal end and a distal end, the elongated member including
a proximal section;
a distal section including a microfabricated region comprising a cut arrangement for increasing the flexibility of the distal section, wherein the microfabricated region of the distal section has greater flexibility than the proximal section; and
an intermediate section between the proximal section and the distal section, the intermediate section comprising a proximal-intermediate section extending distally from the proximal section and a distal-intermediate section extending proximally from the distal section,
wherein the proximal-intermediate section includes a microfabricated cut arrangement enabling preferential flexing in one plane, and
wherein the distal-intermediate section omits cuts and is more rigid than the proximal-intermediate section, at least a portion of the proximal section, and the microfabricated region of the distal section.
2. The device of claim 1 , wherein the proximal section includes a microfabricated region having a cut arrangement for increasing the flexibility of the microfabricated region.
3. The device of claim 2 , wherein the proximal section includes a braided region.
4. The device of claim 3 , wherein the braided region is proximal of the microfabricated region of the proximal section.
5. The device of claim 2 , wherein longitudinal spacing between cuts of the microfabricated region of the proximal section grows progressively narrower toward the intermediate section.
6. The device of claim 1 , wherein the microfabricated cut arrangement of the proximal-intermediate section includes cuts arranged on a single side to leave a resulting spine.
7. The device of claim 1 , wherein at least the distal section and intermediate section are formed from a single integral piece of stock material.
8. The device of claim 1 , wherein at least the distal section, the intermediate section, and a portion of the proximal section are formed from a single integral piece of stock material.
9. The device of claim 1 , further comprising an outer laminate and/or an inner liner.
10. The device of claim 9 , wherein the outer laminate and/or the inner liner extend distally beyond the distal section to form an atraumatic distal tip.
11. The device of claim 1 , wherein the intermediate section is configured in size and shape for placement at the aortic root, with the proximal-intermediate section providing a bend at one wall of the aortic root and the distal-intermediate section extending across the aortic root toward an opposite wall.
12. An interventional device, comprising:
an elongated member extending between a proximal end and a distal end, the elongated member including:
a proximal section comprising a microfabricated region with a first cut arrangement with cuts arranged on multiple sides;
a distal section comprising a microfabricated region with a second cut arrangement with cuts arranged on multiple sides and that provides greater flexibility than the first cut arrangement; and
an intermediate section between the proximal section and the distal section, the intermediate section comprising a proximal-intermediate section extending distally from the proximal section and a distal-intermediate section extending proximally from the distal section,
wherein the proximal-intermediate section includes a microfabricated cut arrangement with cuts arranged on a single side to leave a resulting spine and to enable preferential flexing, and
wherein the distal-intermediate section is more rigid than the proximal-intermediate section and the distal section, and
wherein the distal section is capable of lateral bending relative to the distal-intermediate section.
13. The device of claim 12 , wherein the distal-intermediate section omits cuts.
14. The device of claim 12 , wherein the proximal section includes a braided region proximal of the microfabricated region of the proximal section.
15. The device of claim 12 , wherein longitudinal spacing between cuts of the microfabricated region of the proximal section grows progressively narrower toward the intermediate section.
16. The device of claim 12 , further comprising an outer laminate and/or an inner liner, wherein the outer laminate and/or the inner liner extend distally beyond the distal section to form an atraumatic distal tip.