Low-profile dual-lumen perfusion balloon catheter with axially movable inner guide sheath

Claim 2

A dual-lumen perfusion balloon catheter comprising a dual-lumen catheter shaft, said catheter shaft at a distal end portion thereof carrying an expansible balloon section, an inflation lumen of said dual-lumen catheter shaft communicating internally of said balloon section, a guide wire and perfusion lumen of said catheter shaft traversing said balloon section, a pair of perfusion ports respectively located proximally and distally of said balloon section and both opening outwardly from and communicating with one another via said guide wire and perfusion lumen, a guide wire assembly including a distal end portion movably received in said guide wire and perfusion lumen and traversing said balloon section, and a tubular guide wire sheath member movably received in said guide wire and perfusion lumen and receiving said guide wire to traverse said perfusion ports while positively preventing said guide wire distal end portion from escaping the catheter via said perfusion ports.

Claim 3

The catheter of claim 1 further including said guide wire sheath member carrying a respective balloon member adjacent to a distal end thereof, said balloon member of said guide wire sheath member being of a diameter sufficiently small to pass into said guide wire and perfusion lumen proximally of said balloon section.

Claim 4

The catheter of claim 2 wherein said guide wire sheath member includes a seal section located distally of said balloon member, and said guide wire includes a valving collar sealingly receivable into said seal section to allow inflation of said balloon member by communication of pressurized fluid to said guide wire sheath member at a proximal end thereof.

Claim 5

The catheter of claim 3 wherein said valving collar includes a sleeve of polymeric material rotatably received on said guide wire in said distal end portion thereof with selected relative axial movement on said guide wire.

Claim 6

The invention of claim 4 wherein said polymeric material is selected from the group comprising: polyvinylchloride, polyamide, polyimide and fluoropolymer.

Claim 7

The invention of claim 3 wherein said valving collar is formed of metal.

Claim 8

The invention of claim 1 further comprising at least one radiopaque marker disposed adjacent to said distal end portion of said guide wire.

Claim 9

The invention of claim 7 wherein said radiopaque marker comprises a flexible metallic coil defining at least a part of said distal end portion of said guide wire.

Claim 10

The invention of claim 1 wherein said catheter shaft distal end portion defines an aperture opening outwardly from said guide wire and perfusion lumen, said distal end portion of said catheter shaft defining a mono-rail guide portion distally of said aperture.

Claim 11

The invention of claim 9 wherein said catheter shaft further defines an elongate guide wire sheath retention portion distally of said aperture and proximally of a proximal one of said pair of perfusion ports.

Claim 12

The invention of claim 10 wherein said catheter shaft further includes a proximal metallic hypo tube portion joining with a distal comparatively more flexible portion of said catheter shaft.

Claim 13

The invention of claim 1 wherein said guide wire sheath member and said guide wire assembly define cooperating means for joining a proximal end portion of said guide wire sheath member with an end of said guide wire assembly in end-to-end relation.

Claim 14

The invention of claim 12 wherein said cooperating means for joining includes said guide wire sheath member at a proximal end thereof carrying a resilient elastomeric member, said elastomeric member defining an opening into which an end of said guide wire assembly is insertable, and said guide wire assembly adjacent an end thereof defining a circumferential groove and an adjacent conical end surface portion allowing said end of said guide wire to be introduced forcefully into said opening of said elastomeric member so that the latter is received into said groove.

Claim 15

The invention of claim 1 wherein said catheter shaft and said expandable balloon section are formed of resilient polymeric material.

Claim 16

The invention of claim 14 wherein said polymeric material is selected from the group comprising homopolymers and copolymers of: polyvinylchoride, polyethylene, polyolefin, fluoropolymer, polyamide, polyester, polyimide, and polypropylene.

Claim 17

A low-profile dual-lumen dual-balloon catheter and guide wire combination comprising: a flexible, small diameter guide wire assembly having proximal and distal ends, with a valving portion of said distal end being of a larger diameter than the remainder of said guide wire; a flexible elongated tubular guide wire sheath having a proximal end and a distal end and a single axially extending fluid-conducting lumen adapted to receive said guide wire extending therethrough and opening on a distal end of said guide wire sheath; a balloon member disposed at a distal end portion of said guide wire sheath and in fluid communication with said lumen of said guide wire sheath, said distal opening of said guide wire sheath being provided with means for releasably engaging said enlarged diameter distal end valving portion of said guide wire assembly in sealing relationship; a catheter shaft having a pair of lumens extending therein, one of said pair of lumens slidably receiving said guide wire sheath and defining a distal end opening through which respective distal end portions of said guide wire and guide wire sheath are extendably distally of said catheter shaft, a balloon section carried on a distal end portion of said catheter shaft, and the other of said pair of lumens communicating with said balloon section; and a side wall of said catheter shaft defining a pair of perfusion ports respectively located distally and proximally of said balloon section; whereby said guide wire and sheath are retractable proximally of a proximal one of said pair of perfusion ports to allow perfusion blood flow through the full cross sectional area of said one catheter shaft lumen, and said guide wire sheath and guide wire together may be advanced across said perfusion ports while said sheath positively prevents escape of a distal end portion of said guide wire from said catheter shaft via said perfusion ports.

Claim 18

A low-profile dual-lumen dual-balloon catheter and guide wire combination comprising: a flexible, small diameter guide wire assembly having proximal and distal ends, with a valving portion of said distal end being of a larger diameter than the remainder of said guide wire; a flexible elongated tubular guide wire sheath having a proximal end and a distal end and a single axially extending fluid-conducting lumen adapted to receive said guide wire extending therethrough and opening on a distal end of said guide wire sheath; a balloon member disposed at a distal end portion of said guide wire sheath and in fluid communication with said lumen of said guide wire sheath, said distal opening of said guide wire sheath being provided with means for releasably engaging said enlarged diameter distal end valving portion of said guide wire assembly in sealing relationship; a catheter shaft having a pair of lumens extending therein, one of said pair of lumens slidably receiving said guide wire sheath and defining a distal end opening through which respective distal end portions of said guide wire and guide wire sheath are extendably distally of said catheter shaft, a balloon section carried on a distal end portion of said catheter shaft, and the other of said pair of lumens communicating with said balloon section; and a side wall of said catheter shaft defining a pair of perfusion ports respectively located distally and proximally of said balloon section; whereby said guide wire and sheath are retractable proximally of a proximal one of said pair of perfusion ports to allow perfusion blood flow through the full cross sectional area of said one catheter shaft lumen, and said guide wire sheath and guide wire together may be advanced across said perfusion ports while said sheath positively prevents escape of a distal end portion of said guide wire from said catheter shaft via said perfusion ports.

Claim 19

The invention of claim 16 wherein said larger diameter guide wire distal end valving portion is defined by a cylindrical collar member coupled to said guide wire distal end portion for relative rotational movement and a selected axial relative movement.

Claim 20

The invention of claim 16 wherein said means for releasably sealingly engaging said enlarged diameter distal end portion of said guide wire is a resilient sleeve-like seal portion of said guide wire sheath balloon member which extends from said distal opening thereof.

Claim 21

The invention of claim 18 wherein said resilient sleeve-like seal portion is formed from a lubricous polymeric material.

Claim 22

The invention of claim 16 wherein said catheter shaft and said balloon section are formed of resilient polymeric material.

Claim 23

In a medical treatment catheter including an elongate catheter shaft defining a guide wire and perfusion lumen extending therein, the guide wire and perfusion lumen receiving a guide wire assembly which in a first position thereof extends distally of a distal end of said catheter shaft, the catheter shaft at a distal end portion thereof carrying an inflatable dilatation balloon, the catheter shaft defining a pair of perfusion ports opening outwardly from said guide wire and perfusion lumen each on respective opposite distal and proximal sides of the dilatation balloon, the guide wire assembly being retractably proximally of said pair of perfusion ports to allow perfusion blood flow via the entire cross sectional area of said guide wire and perfusion lumen while said dilatation balloon is inflated, a method of preventing escape of a distal end of said guide wire from said catheter shaft via said pair of perfusion ports, said method comprising the steps of: providing a tubular guide wire sheath member receivably into said guide wire and perfusion lumen; disposing said guide wire assembly in said tubular guide wire sheath member; disposing said guide wire assembly and said guide wire sheath member together in said guide wire and perfusion lumen so that a distal end of said guide wire is extended beyond a distal end of said catheter shaft to guide advancement of said catheter; retracting said guide wire sheath member and said guide wire together proximally of said pair of perfusion ports to allow perfusion blood flow via the full cross sectional area of said guide wire and perfusion lumen when said dilatation balloon is inflated; and advancing said guide wire sheath and said guide wire assembly together across said pair of perfusion ports so that said guide wire sheath member positively prevents escape of a distal end portion of said guide wire assembly through said perfusion ports.

Claim 24

In a medical treatment catheter including an elongate catheter shaft defining a guide wire and perfusion lumen extending therein, the guide wire and perfusion lumen receiving a guide wire assembly which in a first position thereof extends distally of a distal end of said catheter shaft, the catheter shaft at a distal end portion thereof carrying an inflatable dilatation balloon, the catheter shaft defining a pair of perfusion ports opening outwardly from said guide wire and perfusion lumen each on respective opposite distal and proximal sides of the dilatation balloon, the guide wire assembly being retractably proximally of said pair of perfusion ports to allow perfusion blood flow via the entire cross sectional area of said guide wire and perfusion lumen while said dilatation balloon is inflated, a method of preventing escape of a distal end of said guide wire from said catheter shaft via said pair of perfusion ports, said method comprising the steps of: providing a tubular guide wire sheath member receivably into said guide wire and perfusion lumen; disposing said guide wire assembly in said tubular guide wire sheath member; disposing said guide wire assembly and said guide wire sheath member together in said guide wire and perfusion lumen so that a distal end of said guide wire is extended beyond a distal end of said catheter shaft to guide advancement of said catheter; retracting said guide wire sheath member and said guide wire together proximally of said pair of perfusion ports to allow perfusion blood flow via the full cross sectional area of said guide wire and perfusion lumen when said dilatation balloon is inflated; and advancing said guide wire sheath and said guide wire assembly together across said pair of perfusion ports so that said guide wire sheath member positively prevents escape of a distal end portion of said guide wire assembly through said perfusion ports.

Claim 25

In a medical treatment catheter including an elongate catheter shaft defining a guide wire and perfusion lumen extending therein, the guide wire and perfusion lumen slidably receiving a guide wire assembly which in a first position thereof extends distally of a distal end of said catheter shaft, the catheter shaft at a distal end portion thereof carrying an inflatable dilatation balloon, the catheter shaft defining a pair of perfusion ports opening outwardly from said guide wire and perfusion lumen each on respective opposite distal and proximal sides of the dilatation balloon, the guide wire assembly being retractably proximally of said pair of perfusion ports to allow perfusion blood flow via the entire cross sectional area of said guide wire and perfusion lumen while said dilatation balloon is inflated, a method of providing an extension of a guide member so that said catheter shaft may be retracted along said guide member and said extension together in preparation for the retracing along said extension and guide member of another subsequent catheter shaft to a treatment site, said method comprising the steps of: providing an elongate tubular guide wire sheath member slidably receivably into said guide wire and perfusion lumen; slidably disposing said guide wire assembly in said tubular guide wire sheath member; at a proximal end of said guide wire sheath member and at an end portion of said guide wire assembly providing cooperating engagement means for joining said guide wire assembly and said guide wire sheath member together in end-to-end relation; withdrawing said guide wire assembly from said guide wire sheath member while retaining the latter in place at a treatment site; joining together said guide wire sheath member and said guide wire assembly externally of a patient under treatment so that said guide wire assembly defines said extension of said guide wire sheath member; and employing said guide wire assembly as an extension of said guide wire sheath for retraction of said catheter shaft while retaining said guide wire sheath member at said treatment site.

Claim 26

In a medical treatment catheter including an elongate catheter shaft defining a guide wire and perfusion lumen extending therein, the guide wire and perfusion lumen slidably receiving a guide wire assembly which in a first position thereof extends distally of a distal end of said catheter shaft, the catheter shaft at a distal end portion thereof carrying an inflatable dilatation balloon, the catheter shaft defining a pair of perfusion ports opening outwardly from said guide wire and perfusion lumen each on respective opposite distal and proximal sides of the dilatation balloon, the guide wire assembly being retractably proximally of said pair of perfusion ports to allow perfusion blood flow via the entire cross sectional area of said guide wire and perfusion lumen while said dilatation balloon is inflated, a method of providing an extension of a guide member so that said catheter shaft may be retracted along said guide member and said extension together in preparation for the retracing along said extension and guide member of another subsequent catheter shaft to a treatment site, said method comprising the steps of: providing an elongate tubular guide wire sheath member slidably receivably into said guide wire and perfusion lumen; slidably disposing said guide wire assembly in said tubular guide wire sheath member; at a proximal end of said guide wire sheath member and at an end portion of said guide wire assembly providing cooperating engagement means for joining said guide wire assembly and said guide wire sheath member together in end-to-end relation; withdrawing said guide wire assembly from said guide wire sheath member while retaining the latter in place at a treatment site; joining together said guide wire sheath member and said guide wire assembly externally of a patient under treatment so that said guide wire assembly defines said extension of said guide wire sheath member; and employing said guide wire assembly as an extension of said guide wire sheath for retraction of said catheter shaft while retaining said guide wire sheath member at said treatment site.