59 results about "Pacemaker leads" patented technology

An introducer system for implantation of pacemaker leads into the venous system of the human heart through the coronary sinus is comprised of a flexible, elongate, outer elongate element having a first shape or bias along a portion. The first shape on the outer element may be prebiased or may be initially straight and subsequently biased once deployed in the body chamber. A flexible, elongate, telescopic inner elongate element has a second shape or bias on its distal portion and has the first shape or bias on a more proximal portion. The inner elongate element is telescopically disposed in the outer sheath. The outer and inner elongate elements are rotatable with respect to each other, such that when the inner elongate element is distally extended from the outer sheath, there exists an angular orientation between the inner and outer sheaths which is congruent, when there is at least partial alignment between the distal portion of the outer elongate element and the more proximal portion of the inner sheath, both having the first shape or bias. This results in the rotation of the distal second shape or curve of the inner elongate element into a predetermined three dimensional location.

An apparatus and method for placing a device in a body area of a patient, by: tracking the device over a 3-dimensional model of the body area; activating the device at different locations in the body area; measuring the response signal or parameter caused by the activation; storing the locations as well as the response signals; choosing an optimal location for the device base in the stored response signals and navigating the device to the optimal location.

A pressure capsule embedded in a pacemaker lead to monitor intracardiac chamber pressure is described. This pressure monitor capsule provides highly accurate pressure readings while insuring a high integrity seal against bodily fluids and tissue growth. The capsule is intended to be embedded into a pacemaker cardiac lead or a catheter with the distal (Tip) isolation diaphragm sensing pressure, coupling the pressure through an air column to a protected sensing MEMS device and providing a secure fluid seal to the lead walls. The proximal (Back) end of the capsule provides the electrical interface through the lead to the pacemaker pulse generator.

A method for capturing dislodged vegetative growth during a surgical procedure is provided. The method includes maneuvering, into a circulatory system, a first cannula having a distal end and an opposing proximal end, such that the first cannula is positioned to capture the vegetative growth en bloc. A second cannula is positioned in fluid communication with the first cannula, such that a distal end of the second cannula is situated in spaced relation to the distal end of the first cannula. A suction force is provided through the distal end of the first cannula so as to capture the vegetative growth. Fluid removed by the suction force is reinfused through the distal end of the second cannula. Subsequent to becoming dislodged, the vegetative growth is caputred by the first cannula. A method for capturing a vegetative growth during removal of a pacemaker lead is also provided.

The current invention is an intracardiac pressure guided pacemaker. It has a sensor in pacemaker lead to sense intracardiac pressure, which is used to find the best pacing location in the cardiac chamber and to adjust the timing of pacing signal. It will optimize pacing location and pacing timing and, therefore, optimize resychronization of the contraction of myocardium and interaction between different cardiac chambers. This will improve cardiac function at the same working condition without increase in oxygen demand from myocardium. The pacemaker has a computer program, which, based on intracardiac pressure, can adjust pacing parameters of the pacemaker to optimize resynchronization of the myocardium and interaction between different cardiac chambers automatically at different heart rate and in certain time interval specified by care provider. This also can be achieved by using an interrogator manually. The pacemaker can also store profiles of pacing parameter and intracardiac pressure, which can be retrieved for review to help optimize cardiac performance.

A method for capturing dislodged vegetative growth during a surgical procedure is provided. The method includes maneuvering, into a circulatory system, a first cannula having a distal end and an opposing proximal end, such that the first cannula is positioned to capture the vegetative growth en bloc. A second cannula is positioned in fluid communication with the first cannula, such that a distal end of the second cannula is situated in spaced relation to the distal end of the first cannula. A suction force is provided through the distal end of the first cannula so as to capture the vegetative growth. Fluid removed by the suction force is reinfused through the distal end of the second cannula. Subsequent to becoming dislodged, the vegetative growth is caputred by the first cannula. A method for capturing a vegetative growth during removal of a pacemaker lead is also provided.

A pacemaker lead (18) is implanted by using a two anchor system. One anchor (916) to first secure the position of an introducer (14) through which the pacemaker lead will be implanted, and a second anchor (20) used for implanting the distal tip of the pacemaker lead (18). Examples of the anchors included various types of mechanical anchors or mechanical anchor combinations such as a suction anchor, a barbed needle, or a needle and balloon combination. The anchors can be used in the pericardial space in the heart by disposing an elongate instrument into the venous system of the heart; puncturing the venous system at a predetermined position; disposing the elongate instrument into the pericardial space at a predetermined location in the pericardial space; and implanting a pacemaker lead at the predetermined position.

A catheter system suitable for implanting pacemaker leads. A guide catheter is provided with steering capability, and the necessary steering components are modified to permit the catheter to be sliced during withdrawal, so that the proximal forced applied to the pacemaker lead is minimized and the lead is less likely to be dislodged.

An introducer system for use with a pacemaker lead includes a plastic sheath compatible for insertion within a body, a first end configured for insertion into the body with a second end extending out of the body. A central lumen of the sheath is configured to permit introduction of the lead and includes a flexible, kink-resistant section smooth on its outer surface with a helical pleat defining a helical groove enabling a conductor extending from the mapping probe to the pacing system analyzer to be received in the helical groove of the sheath. A mapping probe at the first end of the sheath is connectable to a pacing system analyzer for seeking a location on the myocardial surface of the heart or an endocardial location at which optimal pacing parameters can be achieved prior to implantation of the lead.

A lockout connector arrangement for implantable medical devices having at least one port for receiving a non-cardiac lead connector selectively permits only certain electrical leads to be connected to the implantable medical device. A lead connector pin of a non-cardiac lead connector is specially designed to be larger than a DF-1 lead connector pin, but smaller than an IS-1 lead connector pin. A corresponding header of implantable pulse generator has a connector port for a non-cardiac lead with a proximal-most portion that is larger than the DF-1 lead connector pin, but smaller than the IS-1 lead connector pin; and otherwise generally consistent with the other dimensions of an ISO standard IS-1 pacemaker lead connector.

A pacemaker lead (18) is implanted by using a two anchor system. One anchor (916) to first secure the position of an introducer (14) through which the pacemaker lead will be implanted, and a second anchor (20) used for implanting the distal tip of the pacemaker lead (18). Examples of the anchors include various types of mechanical anchors or mechanical anchor combinations such as a suction anchor, a barbed needle, or a needle and balloon combination. The anchors can be used in the pericardial space in the heart by disposing an elongate instrument into the venous system of the heart; puncturing the venous system at a predetermined position; disposing the elongate instrument into the pericardial space at a predetermined location in the pericardial space; and implanting a pacemaker lead at the predetermined position.

A left ventricular stimulation lead construction and a technique for lead placement that provides for improved anchoring and positioning of the electrode located on the distal end of the lead, while also including a method for readjusting the positioning of the lead as necessary. The lead includes a small diameter guide wire wherein the distal end of the guide wire serves as an anchor for the pacing lead. The lead structure includes a central hollow lumen to allow passage of the guide wire and a locking mechanism positioned on the proximal end of the pacing lead to fix the ends of the guide wire and pacing lead relative to one another. The method provides for advancing the guide wire until it is anchored, positioning the pacing lead along the guide wire into the desired position relative to the cardiac tissue, releasably fixing the lead relative to the guide wire, wherein the guide wire is permanently retained to serve as an anchor.

An implantable medical device has a medical unit, such as a pacemaker lead, and a casing at least partially enclosing the medical unit. The casing is formed of a base polymer such as a polyurethane, a polyurethane copolymer, a fluoropolymer and a polyolefin or a silicone rubber. The casing has biologically active agents covalently bonded to the base polymer. The biologically active agents can be attached to the base polymer as surface active end groups. As an alternative, the biologically active may be attached to a backbone the base polymer. As yet a further alternative, the biologically active agents may be attached to surface modifying end groups, which are in turn attached to the base polymer. Examples of suitable biologically active agents are microbial peptide agents, detergents, non-steroidal anti-inflammatory drugs, cations, amine-containing organosilicones, diphosphonates, fatty acids and fatty acid salts.

A pressure capsule embedded in a pacemaker lead to monitor intracardiac chamber pressure is described. This pressure monitor capsule provides highly accurate pressure readings while insuring a high integrity seal against bodily fluids and tissue growth. The capsule is intended to be embedded into a pacemaker cardiac lead or a catheter with the distal (Tip) isolation diaphragm sensing pressure, coupling the pressure through an air column to a protected sensing MEMS device and providing a secure fluid seal to the lead walls. The proximal (Back) end of the capsule provides the electrical interface through the lead to the pacemaker pulse generator.

An apparatus and method for placing a device in a body area of a patient, by: tracking the device over a 3-dimensional model of the body area; activating the device at different locations in the body area; measuring the response signal or parameter caused by the activation; storing the locations as well as the response signals; choosing an optimal location for the device base in the stored response signals and navigating the device to the optimal location.

A device for removing from a patient a previously implanted elongated structure, such as a pacemaker lead or a defibrillator lead, that may be encapsulated in biological tissue of the patient. In one form, the device comprises a sheath member having an inside dimension greater than the outside dimension of the elongated structure, and a gripping member positioned about the sheath member. The gripping member has a longitudinal passage extending substantially therethrough, which longitudinal passage is dimensioned to encircle at least a portion of the elongated structure. A proximal portion of the gripping member may extend outwardly beyond the proximal end of the elongated structure and outwardly of at least the vascular system of the patient. The gripping member may comprise a first configuration having a first diameter that is greater than the outside dimension of the elongated structure, and a second configuration having a second diameter that is substantially the same as the outside dimension of the elongated structure.

The present invention is a splitable / peelable reinforced flexible tubular body (10) for a catheter or sheath (12). The body (10) comprises a proximal end (14), a distal end (16), a wall structure (18), and a lumen (20) defined by the wall structure (18). The wall structure (18) extends between the ends and includes a reinforcement layer (22) within the wall structure (18) and a separation line (26) extending longitudinally along the wall structure (18). The separation line (26) is adapted to facilitate the splitting / peeling of the wall structure (18) to allow a medical device such as a pacemaker lead to be removed from within the tubular body (10).

The invention provides a cardiac balloon catheter and methods of using the same in the process of venography in the coronary sinus and pulmonary vein of the heart. The catheter has a flexible body containing a curved distal portion, at least three lumens running the length of the body each with a port of entry at the proximal end, an inflatable balloon located proximally of the curved distal portion of the body and port of exit of at least one of the lumens located at a distal end. Optionally, the catheter may contain up to ten pairs of bipolar electrodes. The invention provides methods for using the catheter to generate a geographic may of a venous structure of the heart and to generate an electrical map of the electrical conduction patterns of the heart for locating an aberrant electrical conduction pattern. Additionally, the invention catheter can be used in placement of pacemaker leads in the left ventricle for biventricular pacing of the heart.

Methods and devices for separating an implanted object, such as a pacemaker lead, from tissue surrounding such object in a patient's vasculature system. Specifically, the surgical device includes a handle, an elongate inner sheath and a circular cutting blade that extends from the distal end of the sheath upon actuating the handle. The circular cutting blade is configured to engage the tissue surrounding an implanted lead and cut such tissue in a coring fashion as the surgical device translates along the length of the lead, thereby allowing the lead, as well as any tissue remaining attached to the lead, to enter the device's elongate shaft. The surgical device has a barrel cam cylinder in the handle assembly that imparts rotation of the blade and a separate cam mechanism in the tip of outer sheath assembly that imparts and controls the extension and retraction of the blade. The barrel cam cylinder and cam mechanism cooperate to cause the blade to rotate in a first direction and extend from and retract in the outer sheath due to a first actuation of the handle and to rotate in a second direction and extend and retract in the outer sheath due to a second actuation of the handle. The inner sheath and outer sheath are constructed of laser-cut hypotubes, thereby allowing the surgical device, particularly the sheath assembly, to have a smaller profile for navigating smaller sized vasculature.

To provide radio-frequency (RF) bandstop filtering within an implantable lead, such as a pacemaker lead, one or more segments of the tip and ring conductors of the lead are formed as insulated coils to function as inductive band stop filters. By forming segments of the conductors into insulated coils, a separate set of discrete or distributed inductors is not required, yet RF filtering is achieved to, e.g., reduce lead heating during magnetic resonance imaging (MRI) procedures. To enhance the degree of bandstop filtering at the RF signal frequencies of MRIs, additional capacitive elements are added. In one example, the ring electrode of the lead is configured to provide capacitive shunting to the tip conductor. In another example, a capacitive transition is provided between the outer insulated coil and proximal portions of the ring conductor. In still other examples, conducting polymers are provided to enhance capacitive shunting. The insulated coils may be spaced at ¼ wavelength locations.

The present invention is a splittable multi-piece hemostasis valve that is held together in an assembled condition via a binder formed about the assembled valve. The binder may be a sleeve of thin polymer material shrink-wrapped about the valve. When the valve needs to be split in order to clear a medical device such as a pacemaker lead, the sleeve is split and the valve is disassembled.

An implantable lead assembly for a body implantable medical system adapted to transmit electrical signals between a proximal end portion of the lead assembly and a distal end portion of the lead assembly to thereby stimulate selected body tissue includes an elongated insulative sheath of flexible resilient material having at least one longitudinally extending lumen, an electrical conductor received within the lumen of the insulative sheath and extending between a proximal end and a distal end, and at least one elongated super plastic element slidably received within the lumen of the insulative sheath, the super plastic element being bendable to configure the lead assembly to negotiate tortuous turns in the vasculature of the body. An electrical connector is coupled to the proximal end of the conductor for releasable attachment to a stimulating pulse generator and an electrode is coupled to the distal end of the conductor.

An implantable medical device, perhaps a pacemaker lead, has a medical unit and a casing at least partially enclosing the medical unit. The casing is formed of a base polymer having surface modifying pendant groups formed of an acrylamide polymer or an acrylamide copolymer, perhaps polyisopropyl acrylamide. The base polymer may be a polyurethane, polyimide, fluoropolymer or polyolefin, for example.

A pacemaker is provided. The pacemaker includes a pulse generator and an electrode line connecting with the pulse generator. The electrode line includes a conductor, an insulation layer and a shielding layer. The insulation layer is located on an outer surface of the conductor. The shielding layer is located on an outer surface of the first insulation layer. The shielding layer is a carbon nanotube structure having a plurality of radioactive particles therein.

The present invention is a splittable multi-piece hemostasis valve that is held together in an assembled condition via a binder formed about the assembled valve. The binder may be a sleeve of thin polymer material shrink-wrapped about the valve. When the valve needs to be split in order to clear a medical device such as a pacemaker lead, the sleeve is split and the valve is disassembled.

An introducer system is used for implantation of pacemaker leads into the venous system of the human heart through the coronary sinus. The system is comprised of three telescopic components, an inner telescoping core, a precurved inner telescoping sheath, and an outer telescoping sheath, introducer, guide or catheter. In an embodiment where a core is used it is torsionally stiff. In an embodiment where no core is used, the inner sheath is torsionally stiff. In either case, the member which is torsionally stiff is torqueable. In general, the inner sheath and outer guide will be both laterally and torsionally flexible, while the core will be torsionally stiff. The core and inner sheath, when curved together in the venous system and proximally coupled, will be sufficiently bound to each other that proximal rotation of the core will be coupled to and cause distal rotation of the inner sheath.

Methods and devices for separating an implanted object, such as a pacemaker lead, from tissue surrounding such object in a patient's vasculature system. Specifically, the surgical device includes a handle, an elongate inner sheath and a circular cutting blade that extends from the distal end of the sheath upon actuating the handle. The circular cutting blade is configured to engage the tissue surrounding an implanted lead and cut such tissue in a coring fashion as the surgical device translates along the length of the lead, thereby allowing the lead, as well as any tissue remaining attached tothe lead, to enter the device's elongate shaft. The surgical device has a barrel cam cylinder in the handle assembly that imparts rotation of the blade and a separate cam mechanism in the tip of outer sheath assembly that imparts and controls the extension and retraction of the blade. The barrel cam cylinder and cam mechanism cooperate to cause the blade to rotate in a first direction and extendfrom and retract in the outer sheath due to a first actuation of the handle and to rotate in a second direction and extend and retract in the outer sheath due to a second actuation of the handle. Theinner sheath and outer sheath are constructed of laser-cut hypotubes, thereby allowing the surgical device, particularly the sheath assembly, to have a smaller profile for navigating smaller sized vasculature.