Method for preparing and employing an implant delivery apparatus
View Patent ↗A method for pre-loading an implant delivery apparatus and for delivering an implant is provided. An implant is mounted within the distal end of an elongated section of a delivery apparatus. After the implant is mounted within the elongated section, fluid is drawn into a chamber within the delivery apparatus that is proximal to the implant. This is accomplished by drawing fluid, such as a biocompatible liquid, into the chamber by applying pressure to a port. The fluid is trapped inside the chamber forming a liquid column. The elongated section is advanced through a lumen or passageway delivering the implant to a desired location. A shaft, which is in communication with the fluid column, is held stationary and the elongated section retracted deploying the implant. As the elongated section is retracted, the implant exerts forces upon the elongated section that are transmitted to the fluid column which resists buckling.
1. A method for preparing an implant delivery apparatus for delivering an implant within a lumen comprising:
a) mounting an implant on a support,
b) mounting the support within a distal region of a hollow elongated member wherein the elongated hollow member has a first seal located in the distal region and a second seal located in a proximal region, the first seal and the second seal forming a chamber there between, the chamber being located proximal the implant, wherein the first and second seals permit fluid to flow in a first direction only; and
c) simultaneously drawing a liquid proximally past the first and second seal to form a liquid column within the chamber, the liquid column being adapted to receive compressive loads that are transmitted proximally along the fluid column.
2. The method of claim 1 wherein the elongated member comprises a substantially tubular sheath.
3. The method of claim 1 wherein the implant comprises a self-expanding stent.
4. The method of claim 2 wherein the proximal region has an expanded diameter and forms a handle and the distal region is elongated and has a diameter that allows for passage through a lumen of a human body.
5. The method of claim 4 wherein the handle includes a port in fluid communication with the inside of the elongated member.
6. The method of claim 5 wherein a biocompatible, incompressible fluid is present between the first and second seals prior to sterilization.
7. The method of claim 5 wherein a shaft is fixedly attached to the second seal and the first seal is formed from the proximal end of the support, the distal end of the support having a fluted tip allowing for fluid passage into the elongated member.
8. The method of claim 7 further comprising the steps of:
submersing the distal end of the elongated member in a biocompatible fluid;
applying a vacuum to the fluid port whereby the first and second seals allow fluid to flow towards the proximal end of the elongate member; and
withdrawing the vacuum whereby the first and second seals retain the biocompatible fluid there between and form the fluid column.
9. A method for preparing an implant delivery apparatus for delivering an implant within a lumen comprising:
a) mounting an implant within a distal region of a hollow elongated member;
b. placing a first seal located in the distal region and a second seal in a proximal region of the elongated member, the first seal and the second seal forming a chamber there between, the chamber being located proximal the implant, wherein the first and second seals permit fluid to flow in a first direction only; and
c) simultaneously drawing a liquid proximally past the first and second seal forming a liquid column within the chamber, the liquid column being adapted to receive compressive loads that are transmitted proximally along the fluid column.
10. The method of claim 9 wherein the elongated member comprises a substantially tubular sheath.
11. The method of claim 9 wherein the implant comprises a self-expanding stent.
12. The method of claim 10 wherein the proximal region has an expanded diameter and forms a handle and the distal region is elongated and has a diameter that allows for passage through a lumen of a human body.
13. The method of claim 12 wherein the handle includes a first port in fluid communication with the inside of the elongated member.
14. The method of claim 13 wherein the elongated member includes a guidewire lumen said lumen in fluid communication with a region between the first and second seals and the distal end of the elongated member.
15. The method of claim 14 further comprising the steps of:
submersing the distal end of the elongated member in a biocompatible liquid;
applying a vacuum to the first port whereby the liquid is drawn through the lumen into the region between the first and second seals; and
withdrawing the vacuum whereby the first and second seals retain the biocompatible liquid there between forming the fluid column.
16. The method of claim 13 wherein a third seal is mounted within the elongated member distal to the first seal.
17. The method of claim 16 wherein the elongated member includes a second port in fluid communication with a region between the first seal and the third seal.
18. The method of claim 17 further comprising the steps of:
submersing the distal end of the elongated member in a biocompatible liquid such that the second port is located within the liquid;
applying a vacuum to the first port whereby the liquid is drawn through the second port and into the region between the first and second seals; and
withdrawing the vacuum whereby the first and second seals retain the biocompatible liquid there between forming the fluid column.