Abstract: In one embodiment, a method for fabricating a neurostimulation stimulation lead comprises: providing a plurality of ring components and hypotubes in a mold; placing an annular frame with multiple lumens over distal ends of the plurality of hypotubes to position a portion of each hypotube within a respective lumen of the annular frame; molding the plurality of ring components and the hypotubes to form a stimulation tip component for the stimulation lead, wherein the molding fills interstitial spaces between the plurality of ring components and hypotubes with insulative material; and forming segmented electrodes from the ring components after performing the molding.

Abstract: A delivery device for installing a medical device in a patient comprising a body portion having a proximal end and a distal end, the distal end having a chisel shaped tip, a receptacle disposed in the distal end of the body portion for receiving a medical device for implanting in the patient, a handle disposed at the proximal end of the body portion for facilitating advancement of the proximal end of the body portion into the patient.

Abstract: A device includes a handle, an expandable structure including a plurality of splines extending from a proximal hub to a distal hub, a first electrode on a first spline of the plurality of splines, an outer tube extending from the handle to the proximal hub, and a shaft extending through the outer tube from the handle to the distal hub. The expandable structure has a collapsed state and a self-expanded state. The handle is configured to retract the shaft. Retracting the shaft may expand the expandable structure outward of the self-expanded state.

Abstract: Ablation systems and methods of the present disclosure are directed toward delivering pulsed radiofrequency (RF) energy to target tissue. The pulsations of the RF energy, combined with cooling at a surface of the target tissue, can advantageously promote local heat transfer in the target tissue to form lesions having dimensions larger than those that can be safely formed in tissue using non-pulsed RF energy under similar conditions.

Abstract: Methods of treating acute heart failure in a patient in need thereof. Methods include inserting a therapy delivery device into a pulmonary artery of the patient and applying a therapy signal to autonomic cardiopulmonary fibers surrounding the pulmonary artery. The therapy signal affects heart contractility more than heart rate. Specifically, the application of the therapy signal increases heart contractility and treats the acute heart failure in the patient. The therapy signal can include electrical or chemical modulation.

Abstract: A spine of an electrode assembly is constructed by simultaneously deploying a plurality of individual bobbins of lead wire radially around the longitudinal axis of a polymeric tube. A free end of lead wire from each bobbin is electrically connected to a respective electrode and the electrodes are sequentially installed from a distal first location on the polymeric tube to a proximal location. Each lead wire may be helically wound around the polymeric tube between the electrode to which the lead wire is electrically connected and a proximally adjacent electrode, such that each lead wire between adjacent pairs of electrodes has an alternating direction of winding.

Abstract: Guidewires and methods for transmitting electrical stimuli to a heart and for guiding and supporting the delivery of elongate treatment devices within the heart are disclosed. A guidewire can comprise an elongate body, including first and second elongate conductors, and at least first and second electrodes. A distal end portion of the elongate body can include a preformed bias shape, such as a pigtail-shaped region, on which the first and second electrodes can be located. The preformed bias shape can optionally be non-coplanar relative to an intermediate portion of the elongate body. The first and second elongate conductors can be formed of a single structure or two or more electrically connected structures. The conductors can extend from proximal end portions to distal end portions that electrically connect to the first and second electrodes.

Abstract: A torque limiting mechanism between a medical device and an implantation accessory is disclosed. In a particular embodiment, a delivery system for a leadless active implantable medical device includes a delivery catheter and a torque shaft disposed within the delivery catheter. The delivery system also includes a docking cap having a distal end for engaging an attachment mechanism of the leadless active implantable medical device. The delivery system also includes a torque limiting component coupled to a distal end of the torque shaft and a proximal end of the docking cap.

Abstract: A distal-end assembly of a medical device, the distal-end assembly includes a flexible substrate and electrical conductors. The flexible substrate is configured to be coupled to a distal end of an insertion tube. The electrical conductors are disposed on the flexible substrate and are shaped to form: (i) one or more electrodes, configured to exchange electrical signals with a proximal end of the medical device, and (ii) one or more printed filters, which are disposed adjacently to at least one of the electrodes and are configured to filter signals in a predefined frequency range from the electrical signals exchanged between the at least one of the electrodes and the proximal end.

Abstract: Provided are an implanted medical device (1) and preparation method thereof, and an implanted medical device preform for preparing the implanted medical device (1). The implanted medical device (1) comprises a metal basal body (21) and a polymer film layer (22) covering the surface of the metal basal body (21) and preventing endothelium growth and covering, wherein at least a part of the surface of the metal basal body (21) is provided with a surface-modified layer (211) which contains doped ions, and the metal basal body (21) is connected to the polymer film layer (22) by the doped ions. Since the metal basal body (21) may be bonded to the polymer film layer (22) by the doped ions, the polymer film layer (22) is unlikely to separate during delivery, therefore effectively preventing endothelium growth and covering in vivo.

Abstract: A guiding catheter and method of its use are presented wherein the catheter includes an elongate catheter shaft having a proximal region and a distal region and a length. The shaft defines a distal region and includes a distal tip. The distal region defines an arc of approximately 180 degrees and having a radius of 0.3 inches to 0.6 inches. The distal tip forms a half turn of a left-hand helix having a pitch of 0 inches to 0.4 inches. The unique shape of the distal region allows the distal tip be perpendicularly aligned with the septal wall of the right atrium at the His bundle location when the catheter is advanced therein.

Abstract: A device for producing a trabecular fiber within a ventricle of a heart. The device includes a substrate and a first tissue anchor connected to the substrate. The substrate is formed of a non-rigid material.

Abstract: Ablation probe tips (108, 148, 320, 360) and physical and virtual stents (110) for use in tooth bud ablation procedures that result in tooth agenesis as well as tooth bud ablation methods are described herein.

Abstract: A lead body having a defibrillation electrode positioned along a distal portion of the lead body is described. The defibrillation electrode includes a plurality of electrode segments spaced a distance apart from each other. At least one of the plurality of defibrillation electrode segments includes at least one coated portion and at least one uncoated portion. The at least one coated portion is coated with an electrically insulating material configured to prevent transmission of a low voltage signal (e.g., a pacing pulse) while allowing transmission of a high voltage signal (e.g., a cardioversion defibrillation shock). The at least one uncoated portion is configured to transmit both low voltage and high voltage signals. The lead may also include one or more discrete electrodes proximal, distal or between the defibrillation electrode segments.

Abstract: A tube or skeleton for a steerable catheter includes a cylindrical body structured to permit bending in at least one bending direction and to resist bending in directions transverse to the bending direction. The cylindrical body may include a laser cut metal tube, wires bent and connected to one another, or one or more coiled wires with axial support wires attached to the coil to define one or more bending directions to form bending segments. The skeleton includes axially stiff portions that resist compression when a pull wire is pulled to cause bending movement. The axially stiff portions may include a backbone, an alignment of pivot structures, connected axially extending portions of wire elements, or axially extending support wires or rods. Two or more bending portions may be provided, each with different bending directions. Complex bending shapes may be provided by arranging the segments in rotated positions along the skeleton.

Abstract: A curved laser probe with single-use optic fiber may include a reusable handle, an optic fiber fixture, and a single-use optic fiber. The single-use optic fiber may include an optic fiber having an optic fiber distal end and an optic fiber proximal end. The optic fiber may be disposed in a first transitory connector having a first transitory connector distal end and a first transitory connector proximal end wherein the optic fiber distal end extends a fixed distance from the transitory connector distal end. The optic fiber may be disposed in a second transitory connector having a second transitory connector distal end and a second transitory connector proximal end wherein the optic fiber proximal end extends a fixed distance from the second transitory connector distal end. The first transitory connector may be inserted in the reusable handle and the second transitory connector may be inserted in the optic fiber fixture.

Abstract: The present invention relates to medical devices and methods for treating a lesion such as a vascular stenosis using non-thermal irreversible electroporation (NTIRE). Embodiments of the present invention provide a balloon catheter type NTIRE device for treating a target lesion comprising a plurality of electrodes positioned along the balloon that are electrically independent from each other so as to be individually selectable in order to more precisely treat an asymmetrical lesion in which the lesion extends only partially around the vessel.

Abstract: A system and method for extra cardiac defibrillation is disclosed. In a particular embodiment, an extra cardiac implantable cardioverter defibrillator system includes an implantable defibrillator having a metal case and a defibrillation lead. The defibrillation lead has a connector at its proximal end for coupling to the implantable defibrillator and a first defibrillation coil electrode at a distal portion of the lead. The first defibrillation electrode configured to be disposed in an inferior vena cava.

Abstract: A medical device for assisting a function of the heart is provided. The heart is placed in the thorax, the thoracic diaphragm is dividing the thorax from the abdomen and the pericardium is surrounding the heart and is attached to the thoracic diaphragm at a pericardial contacting section of the thoracic diaphragm. The medical device comprises a diaphragm passing part adapted to pass from the abdomen, through the thoracic diaphragm at the pericardial contacting section, into the pericardium, wherein said diaphragm passing part is adapted to allow the thoracic diaphragm to move during respiration, when implanted.

Abstract: Implantable leadless cardiac pacing systems and methods for providing substernal pacing using the leadless cardiac pacing systems are described. In one embodiment, an implantable leadless cardiac pacing system includes a housing, a first electrode on the housing, a second electrode on the housing, and a pulse generator within the housing and electrically coupled to the first electrode and the second electrode. The housing is implanted substantially within an anterior mediastinum of a patient and the pulse generator is configured to deliver pacing pulses to a heart of the patient via a therapy vector formed between the first and second electrodes.

Abstract: Embodiments include a temporarily or permanently implantable medical device, wherein the medical device includes a housing connected to at least one elongate electrical function conductor to transmit therapy signals or diagnosis signals or both. The medical device includes at least one electrode pole connected to the at least one elongate electrical function conductor, via which electrode pole electric current is delivered to adjacent bodily, or electrode pole electrical potentials are sensed in surrounding tissue, or both. The medical device includes, in the housing, an electrical component as a line extension, wherein the electrical component is connected to the at least one elongate electrical function conductor and includes an electric length that is at least a quarter of a wavelength ? (lambda) of electromagnetic waves in a radio frequency range, such as of MRI scanners.

Abstract: A medical device may include a sheath, and an elongate member disposed within a distal portion of the sheath, the elongate member configured to reciprocally move between a sheathed configuration and a deployed configuration. The elongate member may be substantially linear and disposed within the sheath while in the sheathed configuration and extend distally from the sheath in a first direction in the deployed configuration. The elongate member may include a first bend disposed distal to the distal portion of the sheath, the first bend directing the elongate sheath in a second direction that is substantially opposite to the first direction, and a second bend distal to the first bend, the second bend directing the elongate sheath in a third direction substantially transverse to the first and second directions.

Abstract: The present invention enables a core wire that contains a plurality of strands and a bonding object to be bonded more reliably using an ultrasonic bonding device that cantilever supports a pressing portion that performs ultrasonic bonding. A bonding object (for example, a terminal) is supported as on a stage, a core wire is overlaid on the bonding object, and the core wire and the bonding object are ultrasonically bonded in a state where the core wire is pressed toward the bonding object, using a pressing portion that is supported in cantilever fashion. During ultrasonic bonding, a pressing surface of the pressing portion is inclined in a pressing direction progressively toward a side where the pressing portion is cantilever supported, and also a bonding surface of the bonding object is inclined in the pressing direction progressively toward the side where the pressing portion is cantilever supported.

Abstract: Methods, systems and probe devices for detecting EMG activity are used in aiding the diagnosis of Obstruction Sleep Apnea (OSA). A probe comprises an elongated member configured with a size and shape for placement adjacent at least one of the soft palate and pharyngeal wall of the patient after insertion of the probe into the patient. The probe includes at least one sensor configured to sense at least EMG activity of muscle layers of at least one of the soft palate and pharyngeal wall and output sensor signals corresponding thereto.

Abstract: A method for attaching an electrode to cabling, including providing a cable having a plurality of insulated wires coiled around a central core. The method further includes removing insulation from each wire in a set of the coiled wires so as to provide a respective access channel to a respective section of a respective conductor of each wire in the set while the respective section remains coiled on the central core. The method further includes fastening a respective electrode to the respective access channel while the respective section remains coiled on the central core.

Abstract: Implantable devices and systems include one or more leads adapted to be emplaced in the internal thoracic vein (ITV) of a patient. The lead may include features to adapt the lead for such placement. An associated device for use with the lead may include operational circuitry adapted for use with a lead having an electrode for sensing and/or therapy purposes coupled thereto. Methods for implantation and use of such devices and systems are disclosed as well.

Abstract: Implantable medical leads and implantable lead extensions include a shield. The implantable medical lead is coupled to the implantable lead extension. Stimulation electrodes of the implantable medical lead contact stimulation connectors within a housing of the implantable extension to establish a conductive pathway for stimulation signals from filars of the implantable extension to filars of the implantable medical lead. Continuity is established between the shield of the implantable medical lead and the implantable extension by providing a radio frequency conductive pathway within the housing. The radio frequency conductive pathway extends from a shield of the implantable extension to a shield connector that contacts a shield electrode of the implantable medical lead. The radio frequency conductive pathway may have various forms such as a jumper wire or an extension of the shield within the implantable extension.

Abstract: An electrode device is disclosed comprising: an elongate, implantable body comprising elastomeric material, a plurality of electrodes positioned along a length of the implantable body; an electrical connection comprising one or more conductive elements extending through the elastomeric material and electrically connecting to the electrodes; and a reinforcement device extending through the elastomeric material. The length of the implantable body is extendible by placing the implantable body under tension. The reinforcement device limits the degree by which the length of the implantable body can extend under tension. At least one of the electrodes can extend circumferentially around a portion of the implantable body. A delivery device and method of delivery for an electrode device is also disclosed.

Abstract: Neuromodulation catheters with shafts for enhanced flexibility and control and methods of making and using the catheters. A neuromodulation catheter can include an elongated shaft having a distal end portion and a mandrel extending at least along the distal end portion. The mandrel can have an at least substantially solid core. The neuromodulation catheter can further include a transition member and a neuromodulation assembly coupled to the transition member. The transition member can have a proximal portion, a distal portion, and a guide wire lumen extending through the proximal and distal portions. The neuromodulation assembly can extend distally from the distal portion of the transition member, and the mandrel can extend proximally from the proximal portion of the transition member.

Abstract: Microelectronic packages, modules, systems, and other assemblies containing enhanced electromagnetic (EM) shield structures are provided, as are methods for fabricating electromagnetically-shielded microelectronic assemblies. In an embodiment, the electromagnetically-shielded microelectronic assembly includes first and second signal paths, which carry different electrical signals during operation of the microelectronic assembly. An EM shield structure is positioned between the first and second signal paths. The EM shield structure includes, in turn, a magnetic shield portion adjacent (e.g., in contact with and/or directly or indirectly bonded to) an electrical shield portion. The magnetic shield portion has a first magnetic permeability and a first electrical conductivity, while the electrical shield portion has a second magnetic permeability less than the first magnetic permeability and having a second electrical conductivity greater than the first electrical conductivity.

Abstract: A dilator comprises a guide extending through a tube, and a slidable sleeve exterior to the tube, such that a slit in the tube extending from a first end of the tube to a second end of the tube, opposite of the first end, is closed by a force applied via the slidable sleeve. When closed, the slit does not interfere with the tube being used as a dilator to dilate tissues of a patient through which the guide extends. When opened, the slit allows the tube to be placed onto the guide or removed from the guide.

Abstract: A temporary implantable medical device lead includes a connector, a helically coiled conductor and a first mechanical element. The connector is configured to connect the lead to an external control module. The helically coiled conductor has a proximal end mechanically and electrically connected to the connector. The conductor includes a plurality of filars mechanically and electrically connected to the connector. The first mechanical element includes a metal tube having a plurality of longitudinally spaced grooves formed along an exterior of the tube. The plurality of longitudinally spaced grooves receives at least some of the plurality of filars. The at least some of the plurality of filars electrically connected to the first mechanical element such that the first mechanical element is configured as an electrode to deliver electrical stimulation to portions or systems of a body from the external control module.

Abstract: A retractable lead system is provided that includes a cup, a spherical contact, and a plunger. The cup is disposed proximate a vacuum end of the retractable lead system, and defines a cavity and a contact reception seat. The contact reception seat defines a spherical portion having a contact reception spherical radius. The spherical contact is disposed within the contact reception seat, and defines a contact spherical radius that corresponds to the contact reception spherical radius. The spherical contact is configured to be electrically coupled to an interior lead disposed within a vacuum environment. The plunger includes an ambient contact and a retractable contact disposed on opposite ends of the plunger. The plunger is configured to be actuated between an open position at which the retractable contact is retracted from the spherical contact and a closed position at which the retractable contact is coupled with the spherical contact.

Abstract: An implantable medical device includes ventricular and atrial portions, and a flexible leadlet that extends therebetween. An open channel of the atrial portion, formed along a core thereof, is sized to receive the leadlet therein, when the leadlet is folded over on itself. An interventional medical system includes the device and a delivery tool; a tubular sidewall of the tool defines a lumen and has a tether extending therein. A slot formed in the sidewall extends proximally from an open end thereof, coincident with a distal opening of the lumen. When the atrial portion is contained within the lumen, a segment of the leadlet extends alongside the atrial portion; another segment of the leadlet, being folded over on itself, proximal to the atrial portion, has the tether engaged therewith. The slot may allow passage of the leadlet therethrough, when the atrial portion is positioned for deployment through the distal opening.

Abstract: A medical lead is configured to be implanted into a patient's body and comprises a lead body, and an electrode coupled to the lead body. The electrode comprises a first section configured to contact the patient's body, and a second section capacitively coupled to the first section and configured to be electrically coupled to the patient's body.

Abstract: An implantable medical lead may include a lead body, a substrate, and an elastic deflection component. The lead body includes a proximal end configured to couple to an implantable pulse generator, a distal end opposite the proximal end, and an electrical conductor extending through the lead body. The substrate is at the distal end and supports an array of electrodes. The elastic deflection component physically and electrically connects the electrical conductor and an electrode of the array of electrodes. The elastic deflection component is configured to compensate for at least one of tension forces or compression forces transferred from the electrical conductor to the electrode of the array of electrodes.

Abstract: A system for artificial stimulation of the heart of a subject is provided, the system comprising a controller comprising a receiver for receiving signal data, a processor for processing received signal data, and a transmitter for transmitting signal data; a sensing stent for location in the proximal coronary sinus of the subject, the sensing stent electrode comprising a sensing electrode assembly for sensing atrial and/or ventricular signals from the heart of the subject and a transmitting assembly for transmitting signal data to the receiver of the controller; and a stimulation stent for location in a vein of the subject distal of the sensing stent, the stimulation stent comprising a receiver for receiving signal data from the transmitter of the controller and an electrode assembly for providing a stimulating electrical signal to the heart of the subject in response to the data received.

Abstract: A device and method for providing cardiac pacing of triangle of Koch and bundle of His zones by multiple electrodes inserted using in a single conduit are provided. The method includes providing a single conduit with multiple electrodes, positioning electrodes in the target zone of a heart, selecting acceptable electrodes as active based on a predetermined criteria and providing cardiac stimulation for multiple chambers of the heart from a single location.

Abstract: An implantable medical device (IMD) may include a housing having a proximal end and a distal end and a set of one or more electrodes connected to but spaced apart from the housing. The IMD may further include a controller disposed within the housing, wherein the controller is configured to sense cardiac electrical signals, and deliver electrical stimulation pulses via the first set of one or more electrodes. In some embodiments, a first portion of the housing is configured to be disposed at least partly within a coronary sinus of a patient's heart and a second portion of the housing is configured to be disposed at least partly within a right atrium of the patient's heart.

Abstract: Sensing devices and methods of implanting sensing devices within an anatomical vessel network of a patient are provided. In one method, a fixation element (e.g., a stent or coil) of the sensing device is expanded into firm contact with a wall of a main anatomical vessel (e.g., a right pulmonary artery), and a stabilization element of the sensing device is placed into contact with a wall of an anatomical vessel branch of the main anatomical vessel. In another method, a first fixation element of the sensing device is expanded into firm contact with the wall of the main anatomical vessel (e.g., a right pulmonary artery) at a longitudinal location proximal to the anatomical vessel branch, and a second fixation element of the sensing device is expanded into firm contact with the wall of the main anatomical vessel at a longitudinal location distal to the anatomical vessel branch.

Abstract: An implantable neural tissue electrode assembly includes a cylindrical electrode lead with at least one electrode contact on the outer surface of the electrode lead. An active distal end fixation anchor is located at the distal end of the electrode lead and is adapted to fasten to adjacent tissue by rotation in a fastening direction. A passive rear fixation anchor is located on the outer surface of the electrode lead offset a longitudinal distance back from the distal end and has at least one curved blade with a blade tip directed away from rotation in the fastening direction. The rear fixation anchor is adapted to permanently fasten to adjacent tissue by rotation opposite to the fastening direction so that the blade tip cuts into the adjacent tissue, and the electrode assembly is adapted such that physiological induced strains are distributed along the electrode lead.

Abstract: An implantable medical device having a housing that encloses a pulse generator and a sensing module includes a housing-based cathode electrode electrically coupled to the pulse generator and to the sensing module. A sensing extension extending from the housing proximal end includes an anode electrode electrically coupled to the sensing module for sensing cardiac electrical signals. The sensing extension includes a flotation member that causes the sensing extension to extend away from the housing along a direction of flowing blood when the implantable medical device is deployed within a cardiovascular system of a patient.

Abstract: An ablation catheter adapted for use with a guide wire has a 3-D shaped portion that carries ring electrodes for ablating a vessel or tubular region, including the renal artery. The 3-D shaped portion, for example, a helical portion, enables the ring electrodes to contact an inner surface of the vessel at a plurality of locations at different depths along the vessel to form a conduction block without forming a closed conduction loop which would otherwise increase the risk of stenosis of the vessel. In one embodiment, the catheter has a lumen with entry and exit ports to allow the guide wire to pass through the lumen but bypass the 3-D shaped portion. In another embodiment, the catheter has outer bands providing side tunnels through which the guide wire can pass through.

Abstract: The disclosure is directed to programming implantable stimulators to deliver stimulation energy via one or more implantable leads having complex electrode array geometries. The disclosure also contemplates guided programming to select electrode combinations and parameter values to support efficacy. The techniques may be applied to a programming interface associated with a clinician programmer, a patient programmer, or both. A user interface permits a user to view electrodes from different perspectives relative to the lead. For example, the user interface provides a side view of a lead and a cross-sectional view of the lead. The user interface may include an axial control medium to select and/or view electrodes at different axial positions along the length of a lead, and a rotational control medium to select and/or view electrodes at different angular positions around a circumference of the lead.

Abstract: A catheter system including an accelerometer-based sensing assembly is provided. In particular the present teachings relate to an accelerometer based assembly used to determine contact between a catheter and surrounding proximate tissue, such as cardiac tissue. An embodiment of such a system may, for example, be used for visualization, mapping, ablation, or other methods of diagnosis and treatment of tissue and/or surrounding areas.

Abstract: A medical electrical lead and a method of its use. The lead has an elongated lead body having an outer circumference and provided with an electrode. A push tube is mounted circumferentially around the lead body and the lead body is longitudinally movable with respect thereto. A fixation helix is mounted to the push tube, extending along a generally helical axis around the outer circumference of the lead body. The lead may be employed by advancing the lead to a desired location for the fixation helix and then rotating the push tube to secure the helix to tissue. The lead body may then be moved longitudinally with respect to the push tube to place the electrode in a desirable location.

Abstract: Partitioning devices that may be secured and sealed within a heart chamber for separating a patient's heart chamber into a productive portion and a non-productive portion are described herein. The partitioning devices described herein may include a membrane with a plurality of inflatable elements. The membrane may include a valve disposed in a central region of the membrane with a plurality of inflation channels extending radially from the valve. These devices may be secured within the heart chamber by sealing them to the wall of the heart chamber, for example, by inflating the plurality of inflatable elements on the periphery of the device. The non-productive portion may be filled with a material, including occlusive materials. Sealing and/or filling the non-productive portion formed by the devices described herein may help prevent leakage from the non-productive region.

Abstract: The invention relates to an electrical multichannel system (100) and to a neural stimulation and/or recording device comprising such a system. The multichannel system comprises a plurality of application components (130), e.g. stimulation electrodes, and associated access points (120) that are connected by a plurality of electrical lines (110). The resistances of these lines are adjusted to given target values, for example to equal values, by incorporating appropriate tuning sections (140) into the electrical lines. The lines may for example comprise different geometries and/or materials in the tuning sections.

Abstract: A catheter may include an outer layer defining a plurality of apertures therethrough, and a body defining at least one longitudinal lumen therein. The body may be within the outer layer, and the apertures may be radially outward of the lumen. The catheter may also include a plurality of electrodes positioned in or on the catheter, with each electrode being electrically exposed through an aperture of the plurality of apertures. A ribbon cable may extend through the lumen and include a plurality of leads, with the plurality of leads being electrically connected to the plurality of electrodes. The plurality of leads and electrodes may be formed by the deposition of conductive inks or paints, or by the electrodeposition of copper or other conductive metals or materials.

Abstract: A system and method are presented that electrically stimulates the phrenic nerve whereby said stimulation results in muscle activation of the diaphragm as observed by a measurement of work or power of breathing associated with the inspiratory portion of a stimulated breath.