Drug coated balloon catheter

1. A balloon catheter comprising:

an inner shaft member having a proximal end portion, a distal end portion, and a length therebetween, the inner shaft member defining a guidewire lumen therein, the guidewire lumen having a distal port;

an outer shaft member movable relative to the inner shaft member between an initial delivery condition and a deployed condition, the distal port of the guidewire lumen being exposed to an environment external to the outer shaft member when the inner shaft member is in the initial delivery condition relative the outer shaft member, the outer shaft member having a proximal end portion, a distal end portion, and a length therebetween;

an annular flow passage disposed between the inner and outer shaft members;

a flexible membrane attached to and extending between the distal end portion of the inner shaft member and the distal end portion of the outer shaft member; and

wherein the flexible membrane includes an inner surface and an outer surface, the inner surface configured in fluid communication with the annular flow passage, and further wherein the outer shaft member and the inner shaft member define a chamber in the initial delivery condition configured to receive the flexible membrane rolled in a generally axial direction therein.

2. The balloon catheter of claim 1 wherein the outer shaft member is axially movable relative to the inner shaft member.

3. The balloon catheter of claim 2 including a dynamic seal disposed between the inner shaft member and the outer shaft member to maintain a sealed environment of the annular flow passage during movement of the outer shaft relative to the inner shaft.

4. The balloon catheter of claim 1 wherein the outer surface of the flexible membrane is attached to the inner surface of the outer shaft member and the outer surface of the flexible membrane is attached to the outer surface of the inner shaft member.

5. The balloon catheter of claim 1 wherein the outer shaft member is rotatably movable relative to the inner shaft member.

6. The balloon catheter of claim 5 including a dynamic seal disposed between the inner shaft member and the outer shaft member to maintain a sealed environment of the annular flow passage during movement of the outer shaft relative to the inner shaft.

7. The balloon catheter of claim 1 including a retrieval element attached to the inner shaft member.

8. A method of treating a luminal system of a patient comprising:

providing a balloon catheter including:

an inner shaft member having a proximal end portion, a distal end portion, and a length therebetween, the inner shaft member defining a guidewire lumen therein, the guidewire lumen having a distal port;

an outer shaft member movable relative to the inner shaft member between an initial delivery condition and a deployed condition, the outer shaft member having a proximal end portion, a distal end portion, and a length therebetween, with an annular flow passage disposed between the inner and outer shaft members, the distal port of the guidewire lumen being exposed to an environment external to the outer shaft member when the inner shaft member is in the initial delivery condition relative the outer shaft member;

a flexible membrane extending between the distal end portion of the inner shaft member and the distal end portion of the outer shaft member, the flexible membrane having an inner surface and an outer surface with the inner surface in fluid communication with the annular flow passage, and further wherein the outer shaft member and the inner shaft member define a chamber in the initial delivery condition configured to receive the flexible membrane rolled in a generally axial direction therein;

positioning the balloon catheter at a desired deployment site;

moving the outer shaft member relative to the inner shaft member; and

introducing inflation fluid into the annular flow passage, simultaneously or sequentially with said relative movement, to deploy the flexible membrane into an expanded configuration to treat the luminal system of a patient.

9. The method of claim 8 wherein initial deployment of the flexible membrane at least partially occludes the luminal system of the patient prior to full expansion of the flexible membrane.

10. A balloon catheter comprising:

an inner shaft member having a proximal end portion, a distal end portion, and a length therebetween, the inner shaft member defining a guidewire lumen therein, the guidewire lumen having a distal port;

an outer shaft member movable relative to the inner shaft member between an initial delivery condition and a deployed condition, the distal port of the guidewire lumen being exposed to an environment external to the outer shaft member when the inner shaft member is in the initial delivery condition relative the outer shaft member, the outer shaft member having a proximal end portion, a distal end portion, and a length therebetween;

an annular flow passage disposed between the inner and outer shaft members;

a flexible membrane attached to and extending between the distal end portion of the inner shaft member and the distal end portion of the outer shaft member; and

wherein the flexible membrane includes an inner surface and an outer surface, the flexible membrane being free of perforations therethrough, the inner surface configured in fluid communication with the annular flow passage, and further wherein the outer shaft member and the inner shaft member define a chamber in the initial delivery condition configured to receive the flexible membrane rolled in a generally axial direction therein.

11. The balloon catheter of claim 10 wherein the flexible membrane includes a therapeutic agent disposed on the outer surface thereof.

12. The balloon catheter of claim 1 wherein the flexible membrane includes a therapeutic agent disposed on the outer surface thereof when the inner shaft member is in the initial delivery condition.