Catheter balloons
View Patent ↗The present invention relates to catheter balloons wherein the balloon are constructed of hydrophilic energy conductive polymers. It also relates to catheter balloons that self-anchor at a target site in a patient's body. Finally, it relates to catheter balloons with very small cross-sectional profiles at the distal end.
1. A medical probe, comprising:
an elongate shaft; and
an inflatable balloon distally located on the elongate shaft, the inflatable balloon comprising a hydrophilic polymer being electrically conductive and having a tensile strength of at least 3000 psi when hydrated with an electrolytic solution, wherein the balloon is configured to inflate to specified equilibrium dimensions when subjected to about one atmosphere of internal pressure; and
an electrically non-conductive polymer mask adhered to a surface of the balloon to create a pattern of electrically conductive and electrically non-conductive areas when the hydrophilic polymer is hydrated with the electrolytic solution, wherein the electrically non-conductive polymer has physical and chemical characteristics compatible with those of the hydrophilic polymer.
2. The medical probe of claim 1 , wherein the inflatable balloon is an ablation balloon.
3. The medical probe of claim 2 , wherein the electrically conductive areas of the balloon have a wall thickness of from about 0.0005″ to about 0.005″.
4. The medical probe of claim 1 , wherein the hydrophilic polymer has an elasticity that permits the balloon to inflate to dimensions greater than its equilibrium dimensions under more than one atmosphere of internal pressure without failing.
5. The medical probe of claim 4 , wherein the balloon can be inflated to dimensions at least 50% greater than its equilibrium dimensions.
6. The medical probe of claim 1 , wherein the hydrophilic polymer, when hydrated, comprises from 10 volume percent to about 40 volume percent water.
7. The medical probe of claim 6 , wherein the hydrophilic polymer, when hydrated, comprises about 20% volume percent water.
8. The medical probe of claim 1 , wherein the electrically non-conductive polymer comprises an electrically non-conductive homopolymeric or co-polymeric thermoplastic polyurethane.
9. The medical probe of claim 8 , wherein the electrically non-conductive polyurethane is a polyether-based aliphatic polyurethane.
10. The medical probe of claim 1 , wherein the electrically non-conductive polymer is an aliphatic urethane.
11. A medical probe comprising:
an elongate shaft;
an inflatable balloon distally located on the elongate shaft, the balloon having a first diameter, a second diameter, and a third diameter located between the first and second diameters, wherein the third diameter is less than both the first and second diameters, the first diameter is coupled to the third diameter by a distal-facing sloping surface, and the second diameter is coupled to the third diameter by a proximal-facing sloping surface;
an electrically non-conductive polymer mask adhered to the distal-facing surface of the balloon to create a pattern of electrically conductive and electrically non-conductive areas when the hydrophilic polymer is hydrated with the electrolytic solution, wherein the electrically non-conductive polymer has physical characteristics compatible with those of the hydrophilic polymer; and
a therapeutic element located on the distal-facing sloping surface.
12. The medical probe of claim 11 , wherein the electrically non-conductive polymer comprises an electrically non-conductive homopolymeric or co-polymeric thermoplastic polyurethane.
13. The medical probe of claim 12 , wherein the electrically non-conductive polyurethane is a polyether-based aliphatic polyurethane.
14. The medical probe of claim 11 , wherein the electrically non-conductive polymer is an aliphatic urethane.
15. The medical probe of claim 11 , wherein the electrically conductive areas of the balloon have a wall thickness of from about 0.0005″ to about 0.005″.
16. The medical probe of claim 11 , wherein the balloon is an ablation balloon.
17. The medical probe of claim 8 , or claim 11 , wherein the balloon is an RF ablation balloon.
18. The medical probe of any of claim 11 or claim 20 , wherein the elongate shaft is configured to be intravascularly introduced into a patient.
19. The medical probe of claim 18 , wherein the elongated shaft is configured to be introduced within a heart of the patient.
20. A medical probe, comprising:
an elongate shaft;
an inflatable member distally located on the elongate shaft, the inflatable member having a proximal end, a distal end, a lumen extending therebetween, and an electrically conductive region; and
an electrode carried by the elongate member, the electrode configured for being in direct electrical contact with electrically conductive fluid within the inflatable member, the electrode located within the lumen of the inflatable member and proximal to the electrically conductive region of the inflatable member.
21. The medical probe of claim 20 , wherein the inflatable member comprises hydrophilic polymer being electrically conductive and having a tensile strength of at least 3000 psi when hydrated within an electrolytic solution.
22. The medical probe of claim 21 , wherein the hydrophilic polymer comprises a homopolymeric or co-polymeric thermoplastic polyurethane when hydrated with the electrolytic solution.
23. The medical probe of claim 22 , wherein the thermoplastic polyurethane is a polyether-based aliphatic polyurethane.
24. The medical probe of claim 21 , further comprising an electrically non-conductive polymer mask adhered to a surface of the inflatable member to create a pattern of electrically conductive and electrically non-conductive areas when the hydrophilic polymer is hydrated with the electrolytic solution, wherein the electrically non-conductive polymer has physical and chemical characteristics compatible with those of the hydrophilic polymer.
25. The medical probe of claim 20 , wherein the inflatable member is configured to inflate to specified equilibrium dimensions when subjected to about one atmosphere of internal pressure.
26. A method of treating an ostium of a blood vessel, comprising:
inserting the medical probe of claim 11 through the ostium into the blood vessel;
inflating the balloon, so that expansion of the second diameter dilates the blood vessel, thereby causing a wall of the blood vessel to apply pressure to the proximal-facing sloped surface and to pull the distal-facing sloped surface into intimate contact with tissue in the vicinity of the ostium; and
operating the therapeutic element to provide therapy to the ostium.