Modulation of inflammatory response following endovascular treatment
A method of treating an aortic aneurysm of a patient with an endovascular graft system and mitigating post implant syndrome associated therewith comprises placing at least one prosthesis across an aneurysmal space. The prosthesis comprises a double-walled filling structure and a stent-graft. The stent graft is radially expanded at a first pressure and the filing structure is filled with a first filing agent to contact a thrombus in the aortic aneurysmal space. After the first filling agent is removed, the filling structure is filled with a second filling agent to contact the thrombus. Next the stent-graft is expanded at a second pressure causing the filing structure to place an effective amount of pressure on the thrombus and substantially mitigating the effects of post implant syndrome associated with the prosthesis.
1. A method of treating an aortic aneurysm of a patient with an endovascular graft system and mitigating post implant syndrome inflammation resulting therefrom, comprising:
placing at least one prosthesis in an aortic aneurysmal space, said prosthesis comprising a stent-graft and a double-walled filling structure, wherein the filling structure comprises an outer wall, an inner wall, and a fillable space between the outer wall and the inner wall;
radially expanding the stent-graft with an expansion balloon at a first pressure of at least about 180 mm Hg;
filling the filling structure with a first filling agent such that the filling structure expands and contacts a thrombus disposed in the aneurysmal space;
removing the first filling agent from filling structure;
filling the filling structure with a second filling agent such that the filling structure expands and contacts the thrombus;
radially expanding the stent-graft with an expansion balloon at a second pressure thereby causing the filling structure with the second filling agent to place an effective amount of pressure on the thrombus;
wherein the effective amount of pressure placed on the thrombus mitigates the effects of post implant syndrome associated with the prosthesis by reducing inflammation in the aneurysm.
2. The method of claim 1 , further comprising the step of introducing the first filling agent into the fillable space, prior to radially expanding the stent-graft, such that the filling structure expands and contacts the thrombus disposed in the aortic aneurysmal space.
3. The method of claim 2 , comprising radially expanding the stent-graft with an expansion balloon at the second pressure thereby causing the filling structure with the first filling agent to place an effective amount of pressure between about 190 mm Hg and about 300 mm Hg, on the thrombus, wherein said second pressure is greater than the first pressure.
4. The method of claim 1 , wherein the expansion balloon is maintained in an expanded state at the first pressure for at least 30 seconds.
5. The method of claim 1 , wherein the expansion balloon is maintained in an expanded state at the second pressure for at least 30 seconds.
6. The method of claim 1 , wherein the expansion balloon is maintained in an expanded state at the first pressure, second pressure or both for about 1 minute to about 10 minutes.
7. The method of claim 1 , wherein the pressure of the expansion balloon is cycled between the first pressure and the second pressure for at least 30 seconds.
8. The method of claim 3 , wherein pressure of the expansion balloon is cycled between the first pressure and the second pressure for at least one minute.
9. The method of claim 1 , further comprising measuring, with at least one sensor, the pressure profile of the aneurysm to be treated before placement of the prosthesis.
10. The method of claim 1 , further comprising measuring, with at least one sensor, the pressure profile of the aneurysm to be treated after placing the prosthesis.
11. The method of claim 1 , further comprising measuring, with at least one sensor, the pressure profile of the aortic aneurysm to be treated and adjusting the first pressure, second pressure, or both to exceed a maximum pressure measured inside the aneurysm.
12. The method of claim 1 , wherein the filling structure comprises a channel which allows biological fluid from the thrombus or aneurysm wall to escape distally.
13. The method of claim 1 , further comprising mechanically aspirating the thrombus in the aortic aneurysmal space.
14. The method of claim 1 , further comprising delivering an agent that promotes maturation of thrombus.
15. The method of claim 1 , comprising placing an effective amount of pressure between about 190 mm Hg and about 300 mm Hg on the thrombus to displace biological fluid from the thrombus or aneurysm wall.
16. The method of claim 15 , wherein the biological fluid comprises pro-inflammatory agents.
17. The method of claim 15 , further comprising placing an effective amount of pressure on the thrombus or aneurysm wall to promote biological remodeling in the aortic aneurysmal space.
18. The method of claim 17 , wherein the biological remodeling comprises producing new fluid pathways between the aortic aneurysm space and a circulatory system of the patient.
19. The method of claim 17 , wherein the biological remodeling comprises forming new vasculature.
20. The method of claim 1 , further comprising anchoring or sealing the prosthesis proximally and distally.
21. The method of claim 1 , wherein the outer surface of the outer wall of the filling structure comprises a therapeutic agent.
22. The method of claim 1 , further comprising introducing a therapeutic agent into the aortic aneurysmal space before filling the filling structure.