Adjustable treatment chamber catheter

Claim 3

The method as set forth in claim 1, further including the step of inserting a guiding catheter from a point of entry into the body to a region near the treatment site and continuing with the step of guiding the treatment chamber catheter through the guiding catheter and then into the biological conduit.

Claim 4

The method as set forth in claim 2, further including the point of entry being the groin, a distal end of the guiding catheter being advanced into the aorta, and the treatment site being located in a peripheral blood vessel of the heart.

Claim 5

The method as set forth in claim 1, further including a step, immediately following the step of loosening friable material at the treatment site, of operating the catheter member including the burden loosening means to reduce the size of the loosened biological material for stabilizing the treatment site.

Claim 6

The method as set forth in claim 4, further including the steps of inserting an adjunctive catheter device for treatment into the sealed treatment chamber through the access lumen and operating the inserted device within the sealed treatment chamber to provide a predetermined adjunctive treatment.

Claim 7

The method as set forth in claim 5, wherein the predetermined adjunctive treatment includes one or more of the following: balloon angioplasty, rotational atherectomy, transluminal extraction, and directional atherectomy.

Claim 8

The method as set forth in claim 4, wherein the step of operating the catheter member including the burden loosening means includes the steps of rotating and reciprocally sliding the intermediate coaxial catheter member axially with respect to the inner coaxial catheter member.

Claim 9

The method as set forth in claim 1, wherein the selected treatment site is a saphenous vein graft.

Claim 12

The treatment method as set forth in claim 9, wherein the adjunctive treatment includes introducing a medicating fluid into the sealed treatment chamber via the infusion means, confining the medicating fluid at the treatment site, and removing the fluid from the treatment chamber via the aspiration means.

Claim 13

The treatment method as set forth in claim 10, further including the steps of preventing the fluid from being diluted and carried away in the bloodstream by confining the medicating fluid within the fluid sealed treatment chamber.

Claim 14

The treatment method as set forth in claim 9, wherein the adjunctive treatment includes balloon angiolplasty, rotational atherectomy, transluminal extraction, and directional coronary atherectomy.

Claim 15

The treatment method as set forth in claim 9, further including the steps of repositioning the sealed treatment chamber to another treatment site by deflating the balloons, guiding the treatment chamber catheter to the other treatment site, and resuming with the step of establishing a sealed treatment chamber of appropriate length.

Claim 16

The treatment method as set forth in claim 9, further including the steps of preventing debris from entering the bloodstream and causing myocardial infarction by trapping the debris between the inflated balloons within the fluid sealed treatment chamber.

Claim 19

The treatment method as set forth in claim 15, further including the step of removing the confined medication and biological debris from the sealed treatment chamber via the aspiration means.

Claim 20

The treatment method as set forth in claim 16, wherein the provided treatment chamber catheter includes means for deflating the inflated sealing members, and further including the steps of deflating the inflatable sealing members and removing the treatment chamber catheter from the biological conduit.

Claim 21

The treatment method as set forth in claim 15, further including the step of inserting a guiding catheter from a point of entry into the body to a region near the treatment site and continuing with the step of guiding the treatment chamber catheter through the guiding catheter and then into the biological conduit.

Claim 22

A fluid sealed treatment chamber catheter for insertion into a biological conduit, and defining an adjustable length treatment chamber, comprising: an inner coaxial catheter member having proximal and distal ends and including multiple lumens extending between the ends; an outer coaxial catheter member having proximal and distal ends and including multiple lumens, the outer coaxial catheter member enclosing a portion of the inner coaxial catheter member, one lumen of the outer coaxial catheter member having a diameter and the inner coaxial catheter member having a diameter and said lumen having a diameter substantially larger than the diameter of the enclosed portion of inner coaxial catheter member; a distal sealing member disposed near the distal end of the inner coaxial catheter member, the distal sealing member being inflatable and having an interior in fluid communication with a lumen of the inner catheter member, said lumen being sealed near the distal end of the inner coaxial catheter member permitting infusion of a fluid via said communicating lumen to inflate and aspiration of said fluid to deflate said distal sealing member; a proximal sealing member disposed near the distal end of the outer coaxial catheter member, the proximal sealing member being inflatable and having an interior in fluid communication with a lumen of the outer catheter member, said lumen being sealed near the distal end of the outer coaxial catheter member permitting infusion of a fluid via said communicating lumen to inflate and aspiration of said fluid to deflate said proximal sealing member; a guide wire located within a lumen and extending along a portion of, and being axially slidable with respect to the inner coaxial catheter member, the guide wire extending distally of the distal end of the inner coaxial member, said guide wire lumen forming a fluid seal with the guide wire at the distal end to the inner coaxial catheter member, the guide wire being slidable within said fluid seal, said lumen including an opening located near a proximal end of the distal sealing member; and a catheter member extending through a lumen of the outer coaxial catheter member from the proximal end to a location between the sealing members, said catheter member being rotatable and axially slidable with respect to the outer catheter member and having burden loosening members disposed near its distal end and adapted for loosening friable material.

Claim 23

A fluid sealed treatment chamber catheter for insertion into a biological conduit, and defining an adjustable length treatment chamber, comprising: an inner coaxial catheter member having proximal and distal ends and including multiple lumens extending between the ends; an outer coaxial catheter member having proximal and distal ends and including multiple lumens, the outer coaxial catheter member enclosing a portion of the inner coaxial catheter member, one lumen of the outer coaxial catheter member having a diameter and the inner coaxial catheter member having a diameter and said lumen having a diameter substantially larger than the diameter of the enclosed portion of inner coaxial catheter member; a distal sealing member disposed near the distal end of the inner coaxial catheter member, the distal sealing member being inflatable and having an interior in fluid communication with a lumen of the inner catheter member, said lumen being sealed near the distal end of the inner coaxial catheter member permitting infusion of a fluid via said communicating lumen to inflate and aspiration of said fluid to deflate said distal sealing member; a proximal sealing member disposed near the distal end of the outer coaxial catheter member, the proximal sealing member being inflatable and having an interior in fluid communication with a lumen of the outer catheter member, said lumen being sealed near the distal end of the outer coaxial catheter member permitting infusion of a fluid via said communicating lumen to inflate and aspiration of said fluid to deflate said proximal sealing member; a guide wire located within a lumen and extending along a portion of, and being axially slidable with respect to the inner coaxial catheter member, the guide wire extending distally of the distal end of the inner coaxial member, said guide wire lumen forming a fluid seal with the guide wire at the distal end to the inner coaxial catheter member, the guide wire being slidable within said fluid seal, said lumen including an opening located near a proximal end of the distal sealing member; and a catheter member extending through a lumen of the outer coaxial catheter member from the proximal end to a location between the sealing members, said catheter member being rotatable and axially slidable with respect to the outer catheter member and having burden loosening members disposed near its distal end and adapted for loosening friable material.

Claim 24

The fluid sealed treatment chamber as set forth in claim 19, further including perfusion means for allowing a biological fluid to bypass the sealed treatment chamber.

Claim 25

An adjustable treatment catheter for insertion into a biological conduit, comprising: inner and outer coaxial catheter members, both members having a distal end and a proximal end and being independently slidable with respect to each other; two expandable sealing members, one sealing member being disposed near the distal end of each catheter member; means for expanding the sealing members to form a pair of seals with the biological conduit, and adjustable length treatment chamber being defined within the conduit and between the seals; burden loosening means for loosening friable material, burden loosening means positioned within the sealed treatment chamber; and perfusion means for bypassing a fluid within the biological conduit around the sealed treatment chamber.

Claim 26

An adjustable treatment catheter for insertion into a biological conduit, comprising: inner and outer coaxial catheter members, both members having a distal end and a proximal end and being independently slidable with respect to each other; two expandable sealing members, one sealing member being disposed near the distal end of each catheter member; means for expanding the sealing members to form a pair of seals with the biological conduit, and adjustable length treatment chamber being defined within the conduit and between the seals; burden loosening means for loosening friable material, burden loosening means positioned within the sealed treatment chamber; and perfusion means for bypassing a fluid within the biological conduit around the sealed treatment chamber.