Abstract: A shunt rivet for implantation in the aorta and inferior vena cava to treat chronic obstructive pulmonary disease, and a method of treating chronic obstructive pulmonary disease.

Abstract: Devices, systems and methods are described for visualizing the anatomy of a patient. An expanding portion is configured to expand towards the tissue walls of a body space and be visible with one or more visualization instruments. Systems and methods are described which advance a probe from a first vessel toward a target in a second vessel.

Abstract: A locking component delivers and locks an attached medical device along a pre-deployed guide wire. The locking component can lock onto a flexible body member disposed on the guide wire, such as the distal helical tip coil of a conventional guide or a specially-designed guide wire. The locking component includes a tapered opening which temporarily compresses a portion of the helical coil and a locking recess in communication with the tapered opening for receiving the compressed coil. Compressed coils which enter the locking recess will spring back to their original shape (diameter) within the locking recess, locking the component to the coil.

Abstract: A shunt rivet for implantation in the aorta and inferior vena cava to treat chronic obstructive pulmonary disease, and a method of treating chronic obstructive pulmonary disease.

Abstract: A shunt rivet for implantation in the aorta and inferior vena cava to treat chronic obstructive pulmonary disease, and a method of treating chronic obstructive pulmonary disease.

Abstract: A shunt rivet for implantation between a first body space and a second body space in a patient, such as to treat chronic obstructive pulmonary disease.

Abstract: Methods are described for screening patients suffering from compromised cardiopulmonary function to determine if they will benefit from arteriovenous fistula therapy. Performance of an exercise regimen by the patients both in the presence and absence of supplemental oxygen is measured. Those patients whose performance improves in the presence of supplemental oxygen are considered likely candidates for benefitting from arteriovenous therapy.

Abstract: A shunt rivet for implantation in the aorta and inferior vena cava to treat chronic obstructive pulmonary disease, and a method of treating chronic obstructive pulmonary disease.

Abstract: A universal cutter for catheters includes a lead fixation feature having a deflectable lower portion and a hinge portion. The deflectable lower portion and the hinge portion of the lead fixation feature allow the cutter to hold and secure leads having varying outer diameters. The cutter holds the lead in place while a guide catheter is moved in a proximal direction toward a blade on the cutter to be split from about the lead.

Abstract: A shunt rivet for implantation in the aorta and inferior vena cava to treat chronic obstructive pulmonary disease, and a method of treating chronic obstructive pulmonary disease.

Abstract: An intravascular guide wire having at least two core materials joined together. There is a wire core having a proximal core section with a proximal end and a distal end and a distal core section with a proximal end and a distal end. The distal end of the proximal core section and the proximal end of the distal core section are formed into complementary shapes, and then placed into a flexible sleeve in opposing directions. Inside the flexible sleeve, the complementary shaped ends are joined together through bonding, welding, brazing, cementing, or soldering. The flexible sleeve can be either a stretched coil or a polyimide sleeve, each with an outer diameter similar to the outer diameter of the core wire, therefore the guide wire does not require additional grinding to reduce the outer diameter of the joined section.

Abstract: An intravascular guide wire having at least two core materials joined together without the use of a hypotube. There is a core having a proximal core section with a proximal end and a distal end and a distal core section with a proximal end and a distal end. The distal end of the proximal core section and the proximal end of the distal core section are ground into complementary shapes, and then placed into a fixture in opposing directions with a small gap in-between the ends to receive a mass of hardened material to wick therein. Once the proximal and distal core sections are bonded, welded, brazed, cemented, or soldered together, the guide wire is then ground to a required outer diameter, depending on the design needs of the specific guide wire.

Abstract: An intravascular guide wire having at least two core materials joined together. There is a wire core having a proximal core section with a proximal end and a distal end and a distal core section with a proximal end and a distal end. The distal end of the proximal core section and the proximal end of the distal core section are formed into complementary shapes, and then placed into a flexible sleeve in opposing directions. Inside the flexible sleeve, the complementary shaped ends are joined together through bonding, welding, brazing, cementing, or soldering. The flexible sleeve can be either a stretched coil or a polyimide sleeve, each with an outer diameter similar to the outer diameter of the core wire, therefore the guide wire does not require additional grinding to reduce the outer diameter of the joined section.

Abstract: An intravascular guide wire having at least two core materials joined together without the use of a hypotube. There is a core having a proximal core section with a proximal end and a distal end and a distal core section with a proximal end and a distal end. The distal end of the proximal core section and the proximal end of the distal core section are ground into complementary shapes, and then placed into a fixture in opposing directions with a small gap in-between the ends to receive a mass of hardened material to wick therein. Once the proximal and distal core sections are bonded, welded, brazed, cemented, or soldered together, the guide wire is then ground to a required outer diameter, depending on the design needs of the specific guide wire.

Abstract: An intravascular guide wire having at least two core materials joined together without the use of a hypotube. There is a core having a proximal core section with a proximal end and a distal end and a distal core section with a proximal end and a distal end. The distal end of the proximal core section and the proximal end of the distal core section are ground into complementary shapes, and then placed into a fixture in opposing directions with a small gap in-between the ends to receive a mass of hardened material to wick therein. Once the proximal and distal core sections are bonded, welded, brazed, cemented, or soldered together, the guide wire is then ground to a required outer diameter, depending on the design needs of the specific guide wire.