Method and apparatus for treating a desired area in the vascular system of a patient

Claim 1

An apparatus for inhibiting stenosis at a selected location in a human coronary vessel, said apparatus comprising: an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into a serpentine vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning at the selected location within a coronary vessel of the patient and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow a guidewire through the serpentine vascular system of a human patient and into the coronary vessel of the patient without displacing the guidewire from the treatment site, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guide wire therethrough to guide the distal end portion of said catheter to the selected location in the coronary vessel, and a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and a distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said loading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway, whereby a convenient radioactive element delivery system is provided that can be readily positioned at a site in a coronary vessel, for the prompt delivery of radioactive treating elements from the loading body, through the catheter and to the site to inhibit stenosis, and for the prompt retrieval of such elements through the catheter and into said loading body without undue risk to the user.

Claim 2

An apparatus for inhibiting stenosis at a selected location in a human coronary vessel, said apparatus comprising: an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into a serpentine vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning at the selected location within a coronary vessel of the patient and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow a guidewire through the serpentine vascular system of a human patient and into the coronary vessel of the patient without displacing the guidewire from the treatment site, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guide wire therethrough to guide the distal end portion of said catheter to the selected location in the coronary vessel, and a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and a distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said loading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway, whereby a convenient radioactive element delivery system is provided that can be readily positioned at a site in a coronary vessel, for the prompt delivery of radioactive treating elements from the loading body, through the catheter and to the site to inhibit stenosis, and for the prompt retrieval of such elements through the catheter and into said loading body without undue risk to the user.

Claim 10

A method for inhibiting stenosis at a selected site in a coronary vessel comprising: a) employing an elongated guidewire extending through the vascular system of the patient and into the coronary vessel to the site; (b) providing: (i) an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into the vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning within a coronary vessel of the patient at the selected site and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow the guidewire through the vascular system and into the coronary vessel of a patient, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guidewire therethrough to guide the distal end portion of said catheter to the selected site in the coronary vessel, and (ii) a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and a distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said loading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway; (c) advancing the distal end portion of the catheter over the guidewire to the location of the selected site in a coronary vessel; (d) moving the gate to the second position; (e) forcing fluid to flow in a first direction through said treating element passageway and said first and second lumen to move said treating elements to the distal end of said first lumen; (f) allowing said treating elements to remain at said distal end portion a sufficient time to provide a therapeutically effective dose of radiation to the selected site; (g) forcing fluid to flow in a reverse direction through the second and first lumen and the treating element passageway to return the treating elements to the treating element passageway in the loading device; (h) moving the gate to the first position to retain said treating elements in said loading body; (i) withdrawing the catheter from the patient's body; and (j) withdrawing the guidewire from the patient's body, whereby radiation is promptly, easily and accurately delivered to the selected site in a coronary vessel to inhibit stenosis without undue risk to the user.

Claim 11

A method for inhibiting stenosis at a selected site in a coronary vessel comprising: a) employing an elongated guidewire extending through the vascular system of the patient and into the coronary vessel to the site; (b) providing: (i) an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into the vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning within a coronary vessel of the patient at the selected site and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow the guidewire through the vascular system and into the coronary vessel of a patient, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guidewire therethrough to guide the distal end portion of said catheter to the selected site in the coronary vessel, and (ii) a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and a distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said loading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway; (c) advancing the distal end portion of the catheter over the guidewire to the location of the selected site in a coronary vessel; (d) moving the gate to the second position; (e) forcing fluid to flow in a first direction through said treating element passageway and said first and second lumen to move said treating elements to the distal end of said first lumen; (f) allowing said treating elements to remain at said distal end portion a sufficient time to provide a therapeutically effective dose of radiation to the selected site; (g) forcing fluid to flow in a reverse direction through the second and first lumen and the treating element passageway to return the treating elements to the treating element passageway in the loading device; (h) moving the gate to the first position to retain said treating elements in said loading body; (i) withdrawing the catheter from the patient's body; and (j) withdrawing the guidewire from the patient's body, whereby radiation is promptly, easily and accurately delivered to the selected site in a coronary vessel to inhibit stenosis without undue risk to the user.

Claim 12

A method for inhibiting stenosis at a selected site in a coronary vessel comprises: (a) employing an elongated guidewire extending through the vascular system of the patient and into the coronary vessel to the site; (b) providing: (i) an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into the vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning within a coronary vessel of the patient at the selected site and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow the guidewire through the vascular system and into a coronary vessel of a patient, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guidewire therethrough to guide the distal end portion of said catheter to the selected site in the coronary vessel, and (ii) a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of said treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and a distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said loading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway, and (iii) a source of blood compatible liquid communicating with said treating element passageway and comprising a fluid-filled cylinder and a manually movable piston within said cylinder to force liquid from said cylinder into said treating element passageway and said first and second lumen for moving said treating elements under the force of flowing fluid from said treating element passageway and through said first lumen to said distal end of said catheter to treat a desired area of coronary vessel with beta radiation to inhibit stenosis thereof; (c) advancing the distal end portion of the catheter over the guidewire to the location of the selected site in a coronary vessel; (d) moving the gate to the second position; (e) moving said piston to force fluid to flow through said treating element passageway, through said first lumen and into said second lumen to move said treating elements from said loading device to the selected site of the coronary vessel at the distal end of said catheter; (f) allowing said treating elements to remain at said distal end portion a sufficient time to expose the selected site to an effective amount of beta radiation to inhibit stenosis; (g) forcing fluid to flow in a reverse direction, through said second lumen and into said first lumen and said treating element passageway to return said treating elements to said treating element passageway in said loading device; (h) moving the gate to the first position to retain said treating elements in said loading body; (i) retracting said catheter over the guidewire and removing same from the patient's body; and (j) withdrawing the guidewire from the patient's body, whereby radiation is promptly, easily and accurately delivered to the selected site in a coronary vessel to inhibit stenosis without undue risk to the user.

Claim 13

A method for inhibiting stenosis at a selected site in a coronary vessel comprises: (a) employing an elongated guidewire extending through the vascular system of the patient and into the coronary vessel to the site; (b) providing: (i) an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into the vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning within a coronary vessel of the patient at the selected site and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow the guidewire through the vascular system and into a coronary vessel of a patient, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guidewire therethrough to guide the distal end portion of said catheter to the selected site in the coronary vessel, and (ii) a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of said treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and a distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said loading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway, and (iii) a source of blood compatible liquid communicating with said treating element passageway and comprising a fluid-filled cylinder and a manually movable piston within said cylinder to force liquid from said cylinder into said treating element passageway and said first and second lumen for moving said treating elements under the force of flowing fluid from said treating element passageway and through said first lumen to said distal end of said catheter to treat a desired area of coronary vessel with beta radiation to inhibit stenosis thereof; (c) advancing the distal end portion of the catheter over the guidewire to the location of the selected site in a coronary vessel; (d) moving the gate to the second position; (e) moving said piston to force fluid to flow through said treating element passageway, through said first lumen and into said second lumen to move said treating elements from said loading device to the selected site of the coronary vessel at the distal end of said catheter; (f) allowing said treating elements to remain at said distal end portion a sufficient time to expose the selected site to an effective amount of beta radiation to inhibit stenosis; (g) forcing fluid to flow in a reverse direction, through said second lumen and into said first lumen and said treating element passageway to return said treating elements to said treating element passageway in said loading device; (h) moving the gate to the first position to retain said treating elements in said loading body; (i) retracting said catheter over the guidewire and removing same from the patient's body; and (j) withdrawing the guidewire from the patient's body, whereby radiation is promptly, easily and accurately delivered to the selected site in a coronary vessel to inhibit stenosis without undue risk to the user.

Claim 14

A method for inhibiting stenosis at a selected site in a coronary vessel comprising: (a) employing an elongated guidewire extending through the vascular system of the patient and into the coronary vessel to the site; (b) providing: (i) an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into the vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning within a coronary vessel of the patient at the selected site and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow the guidewire through the vascular system and into a coronary vessel of a patient, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guidewire therethrough to guide the distal end portion of said catheter to the selected site in the coronary vessel, and (ii) a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said leading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway; (c) advancing the distal end portion of the catheter over the guidewire to the location of the selected site in a coronary vessel; (d) moving the gate to the second position; (e) forcing fluid to flow in a first direction through said treating element passageway and said first and second lumen to move said treating elements to the distal end of said first lumen; (f) allowing said treating elements to remain at said distal end portion a sufficient time to expose the selected site to an effective amount of beta radiation to inhibit stenosis; (g) retracting said catheter over the guidewire and removing same from the patient's body; and (h) withdrawing the guidewire from the patient's body, whereby radiation is promptly, easily and accurately delivered to the selected site in a coronary vessel to inhibit stenosis without undue risk to the user.

Claim 15

A method for inhibiting stenosis at a selected site in a coronary vessel comprising: (a) employing an elongated guidewire extending through the vascular system of the patient and into the coronary vessel to the site; (b) providing: (i) an elongated unitary flexible catheter, said catheter being of sufficiently small diameter for introduction into the vascular system of a human patient, said catheter including a distal end portion with a radiopaque marker for positioning within a coronary vessel of the patient at the selected site and a proximal end portion for remaining outside the patient's body, being sufficiently flexible to follow the guidewire through the vascular system and into a coronary vessel of a patient, including first and second parallel lumens extending substantially coextensively through said catheter between said proximal and distal end portions, said first and second lumens communicating with one another at said distal end portion and being otherwise closed to the exterior at said distal end portion to form a closed fluid-tight path, and including a third lumen open at said distal end portion for receiving the guidewire therethrough to guide the distal end portion of said catheter to the selected site in the coronary vessel, and (ii) a unitary, hand-holdable loading body at the proximal end of said catheter for holding, shielding and controlling movement of treating elements, said unitary loading body including: a treating element passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said first lumen, a return fluid passageway therein having an inlet end for communication with a source of blood-compatible fluid and an outlet end communicating with said second lumen, a plurality of cylindrical radioactive treating elements emitting beta radiation disposed in said treating element passageway of said loading body between said inlet and outlet ends, said treating elements being slidably movable through said treating element passageway and said first lumen for movement between said treating element passageway and distal end of said first lumen by the force of fluid flowing through said treating element passageway and said first and second lumens, said unitary loading body restricting passage of beta radiation from said radioactive treating elements through said loading body, and a gate within said leading body, said gate being movable between a first position blocking said treating element passageway at a location distal of said treating elements when disposed in said treating element passageway to prevent said treating elements from passing into said first lumen while allowing fluid to flow thereinto for priming and a second position permitting passage of said treating elements and fluid from and into said treating element passageway; (c) advancing the distal end portion of the catheter over the guidewire to the location of the selected site in a coronary vessel; (d) moving the gate to the second position; (e) forcing fluid to flow in a first direction through said treating element passageway and said first and second lumen to move said treating elements to the distal end of said first lumen; (f) allowing said treating elements to remain at said distal end portion a sufficient time to expose the selected site to an effective amount of beta radiation to inhibit stenosis; (g) retracting said catheter over the guidewire and removing same from the patient's body; and (h) withdrawing the guidewire from the patient's body, whereby radiation is promptly, easily and accurately delivered to the selected site in a coronary vessel to inhibit stenosis without undue risk to the user.