Devices and methods and agent-assisted medical procedures
Various embodiments of bulking or cushioning agents or material and related medical devices and methods are disclosed. For example, a method of performing a medical procedure in a tract of a body may include injecting a material in a liquid phase proximate a target site between a first tissue layer and a second tissue layer, allowing the material to transition from the liquid phase to the gel phase in response to a raise in temperature of the material to approximately at or above the predetermined temperature, and performing a surgical procedure on the target site. The material may have the liquid phase at temperatures below a predetermined temperature and a gel phase at temperature approximately at or above the predetermined temperature.
1. A system for performing a medical procedure, comprising:
an elongated member having a distal end configured to position a flowable material between a first tissue layer and a second tissue layer;
the flowable material contained in the elongated member, the material having a liquid phase below a predetermined temperature, and having a gel phase approximately at or above the predetermined temperature, wherein the gel phase of the flowable material when positioned between the first and second tissue layers elevates a portion of the first tissue layer above the second tissue layer; and
an end effector configured to perform the medical procedure on the elevated portion of the first tissue layer, wherein the end effector is an endoscopic resection device having a cutting member.
2. The system of claim 1 , wherein the elongated member comprises a needle.
3. The system of claim 1 , further comprising a handle at a proximal end of the elongated member, wherein the elongated member comprises a lumen extending between the proximal handle and the distal end, the flowable material contained in the lumen.
4. The system of claim 1 , wherein the predetermined temperature is a temperature of a body.
5. The system of claim 1 , wherein the flowable material comprises polyoxyethylene-polyoxyproplyene block copolymers.
6. The system of claim 1 , wherein the flowable material comprises poly(n-isopropyl acrylamide) or wherein the flowable material comprises thermally sensitive inorganic-organic hybrid gels or wherein the flowable material comprises polyvinyl alcohol.
7. The system of claim 1 , wherein the flowable material comprises a thermally sensitive block copolymer.
8. The system of claim 7 , wherein the thermally sensitive block copolymer comprises poly(N-isopropyl acrylamide-b-dl-lactide).
9. A system for performing a medical procedure, comprising:
an elongated member having a distal end configured to position a material between a first tissue layer and a second tissue layer;
the material contained in a lumen of the elongated member, the material having a first viscosity phase below a predetermined temperature, and having a second viscosity phase greater than the first viscosity phase approximately at or above the predetermined temperature, wherein the material when in the second viscosity phase and positioned between the first and second layers raises a portion of the first tissue layer above the second tissue layer; and
an end effector configured to perform the medical procedure on the raised portion of the first tissue layer, wherein the end effector is an endoscopic resection device having a cutting member.
10. The system of claim 9 , wherein the predetermined temperature is a temperature of a body.
11. The system of claim 9 , wherein the material comprises polyoxyethylene-polyoxyproplyene block copolymers.
12. A system for performing a medical procedure, comprising:
an elongated member having a distal end configured to position a material between a first tissue layer and a second tissue layer;
the material contained in a lumen of the elongated member, the material having a first viscosity state below a predetermined pH, and having a second viscosity state greater than the first viscosity state approximately at or above the predetermined pH, wherein the material when positioned between the first and second tissue layers and in the second viscosity state raises a portion of the first tissue layer above the second tissue layer; and
an end effector configured to perform the medical procedure on the raised portion of the first tissue layer, wherein the end effector is an endoscopic resection device having a cutting member.
13. The system of claim 12 , wherein the predetermined pH is approximately 7.4.
14. The system of claim 12 , wherein the material comprises polyoxyethylene-polyoxyproplyene block copolymers, and wherein the molecular weights of the block copolymers range from approximately 5,000 to approximately 25,000.