Abstract: A database methodology that concerns the mapping of any arbitrary object into a plurality of regions, enabling the assignment of multiple region-specific attributes thereto and facilitating the concurrent, graphical presentation of any assigned attributes. Attribute storage, manipulation, and presentation are driven by the individual regions and characteristics of the object.

Abstract: An implantable stimulation system including epidural lead for spinal cord stimulation that includes a paddle having a curved proximal end and lateral winged tips and an array of electrodes coupled to conductors within a lead body. The conductors couple to a pulse generator or other stimulation device. The curved and winged paddle provides more complete electrical stimulation coverage to targeted human tissue by minimizing the potential gap between electrodes and targeted fibers.

Abstract: A system and/or method treating for a neurological disorder by brain region stimulation. The system and/or method comprises a probe and a device to provide stimulation. The probe has a stimulation portion implanted in communication with a predetermined brain region site. The stimulation portion of the probe may be implanted in contact with a predetermined brain region.

Abstract: The invention is directed to a dose control apparatus. The apparatus has two armatures pressed against a valve seat by at least one spring. A coil induces a magnetic field that motivates the armatures against the force of the spring, thereby opening the valve. The armatures may move along a common axis in opposite directions. The apparatus may also include a core located between the armatures and a casing about the coil. The core and casing act to guide the magnetic field, reducing the power requirements for creating the field. Current may be periodically reversed in the coil to provide a degaussing field. In addition, a signal may be produced by the coil in the presence an externally applied magnetic field such as an MRI. An opposing magnetic field may be produced by the coil or the current provided to the coil may be adjusted.

Abstract: The application relates to a stimulation device with power conservation functionality. In implantable devices, power supplies may be limited. Replenishing these power supplies may require costly surgery or periodic recharging depending on the model. A method may be implemented that skips or drops periodic pulses without apparently changing the frequency of the pulses. In this manner, the dropped pulses may be undetected by the patient. On the other hand, the dropped pulse represents power savings. Dropping one in ten pulses may lead to a 10% energy savings. The stimulation device may implement the method with one or more counters implemented in hardware or software.

Abstract: In one embodiment, an implantable medical device comprises: a rechargeable battery for powering the implantable medical device; an antenna for receiving RF power; and circuitry for charging the rechargeable battery using power received via the antenna, wherein the circuitry for charging comprises control circuitry that causes the circuitry for charging to recharge the rechargeable battery using multiple current levels applied in succession, and wherein the circuitry for charging switches from at least one of the current levels to another current level when a charging voltage of the rechargeable battery reaches a threshold value that is varied by the control circuitry over a lifespan of the rechargeable battery.

Abstract: The invention relates to multi-stable valves and methods for their use. The multi-stable valves may include a movable physical stop and a position arm. The physical stop may be placed in the path of the arm effectively locking the valve in at least one position upon deactivation of the valve's motivating forces. The valve may be, for example, a micro valve or a microelectromechanical device. Such a valve may be used in implantable drug infusion applications and other applications having limitations on available energy. In one exemplary embodiment, the valve comprises a membrane separating two channels. The membrane may be lifted by activation of a piezo material, opening the channels for fluid flow. A physical stop may be moved into place and the piezo material deactivated, bringing to rest the arm on the physical stop. In this manner, the valve is stabilized in the open position without requiring continuous supply of energy.

Abstract: One embodiment includes a tubular housing for electrically connecting an implantable stimulation device to an implantable electrical stimulation lead. The tubular housing includes a tubular outer segment including a first material, a tubular middle segment inside the outer segment in contact with the outer segment including a second material, and a tubular inner segment inside the middle segment in contact with the middle segment including a third material. A circumferential groove in the inner segment exposes a portion of the middle segment to an axial hole through the tubular housing. The groove is adapted to receive a coiled spring. The groove enables transmission of stimulation pulses from the exposed portion of the middle segment, through the coiled spring, to the stimulation lead inserted through the axial hole for stimulation of tissue in a patient.

Abstract: The invention relates to an actuation system and method for an implantable infusion pump. In an example, a working fluid is placed in an actuator. Upon actuation, the working fluid is driven into a piston cylinder. Upon deactuation, the actuator draws the fluid from the cylinder through a restrictor at a rate dictated by the motivating force, fluid viscosity, and restriction. Driving of the piston may produce a bolus dosage or fill a supplemental flow chamber for subsequent delivery. The exemplary system may be configured by selecting a fluid volume and a viscosity. These, in combination, produce a prescribed fluid delivery rate (or recharge rate) and cumulative flow volume provided to a patient over a time period or in a bolus dose. The system may also be configured to limit the total dosage of a bolus injection, or the rate of a supplemental dosage. In this manner, the system is safe, preventing overdose.

Abstract: In one embodiment, a neurostimulation lead, comprises: a lead body, the lead body comprising an inner insulator, an outer insulator positioned around the inner insulator, wherein the outer insulator and the inner insulator are fused together; at least one conductor that is wound between the inner insulator and the outer insulator; and at least one electrode that is electrically coupled to the at least one conductor.

Abstract: A device and method for generating electrical stimulation. The implantable device includes a programmable switching device or array that receives at least one pulse generator output coupled through at least one coupling capacitor. The switching device selectively connects at least one pulse generator output to a plurality of electrode terminals via at least one coupling capacitor. Electrical stimulation signals may be applied directly from the electrode terminals, or are applied through a lead or lead extension having corresponding electrodes electrically connected to the electrode terminals.

Abstract: According to one embodiment, an electrode for use in electrostimulation is provided, where the electrode comprises a notch that operates to substantially eliminate gaseous material from being trapped about the electrode during a molding process of an electrostimulation lead.

Abstract: According to one embodiment, a neurological stimulation system includes an electrical stimulation lead suited for implantation into the epidural space overlying the medulla for stimulation of nerve tissue in the brain stem. The lead includes a plurality of electrodes suited to be positioned in the epidural space overlying the medulla and to deliver stimulation energy to the nerve tissue. The system also includes a stimulation source suited for implantation into the person's body and operable to generate signals for transmission to the electrodes of the lead positioned in the epidural space overlying the medulla to cause the electrodes to deliver stimulation energy to the nerve tissue. In a particular embodiment, the lead may be suited for implantation posteriorly on, in, or near the brain stem overlying the medulla. In a particular embodiment, the lead may be inserted through an open craniotomy or a burr hole located approximately over the junction of the occiput and the first or second cervical vertebrae.

Abstract: Categories are established for use in physiological monitoring devices and these categories are prioritized such that data indicative of a critical event self-triggers a communication to an external receiver for the purpose of re-transmitting the critical data for use by a clinician. The categories can be established by the clinician and, if desired, the precise monitored data parameters can be assigned to specific categories. Far-field transmission can be used to send certain stored data to an external receiver, provision is made for externally charging the device batteries.

Abstract: A low power (and lower cost) implementation for amplifier used in delivering a stimulation pulse is provided according to embodiments through use of a pre-charge period for each pulse. For example, a voltage at a variable output terminal of a digital-to-analog converter is increased on the leading edge of PULSE and INVERTCLK signals to result in an output of an operational amplifier increasing to a predetermined voltage prior to output of a stimulation pulse, according to an embodiment. A shunt path may be implemented to shunt current away from a load during the pre-charge period.

Abstract: Techniques are disclosed which provide a substantially constant battery reserve capacity with respect to therapeutic medical devices. Accordingly, a battery control system may be operable to maintain a substantially constant reserve capacity throughout the life of the battery. The battery reserve capacity activation threshold may be set and continuously or periodically updated so that a battery's remaining capacity equals the predetermined reserve capacity when the measured parameter reaches the activation threshold, thereby allowing a maximum amount of a battery's total capacity to be employed for therapeutic use and reserve only that portion of that capacity determined to provide for a desired level and/or period of device function after reaching the reserve threshold.

Abstract: A stimulation system includes a stimulation source, an implantable stimulation lead, an implantable sensing device, and a controller. The stimulation source generates and transmits stimulation pulses to stimulation electrodes on the stimulation lead. The stimulation electrodes deliver the stimulation pulses to target nerve tissue in a nerve pathway to cause paresthesia in a portion of the person's body. Each stimulation pulse induces an action potential in a number of nerve fibers in the nerve pathway. The sensing device includes sensing electrodes positioned proximate the nerve pathway that detect compound action potentials of nerve fibers stimulated by the stimulation pulses. The controller modifies the stimulation pulses generated by the stimulation source and delivered to the target nerve tissue by the stimulation electrodes based on the detected compound action potentials to maintain a substantially constant level of paresthesia in the portion of the person's body.

Abstract: An implantable lead, and method of manufacturing same, and a system and method for stimulation. The lead has proximal and distal ends having, respectively, a connector portion with a terminal and an electrode. An optically switched device is electrically connected to the electrode and to the terminal. An optical fiber is optically coupled to the connector portion at one end and to the optically switched device at another end. The optically switched device conducts a stimulus from the terminal to the electrode in response to an optical signal transmitted over the optical fiber.

Abstract: In one embodiment, a device is provided for partially shielding electrical energy emitted from an electrical stimulation lead implanted in a human's body to enable stimulation of the human's nerve tissue, the lead including one or more electrodes operable to stimulate the nerve tissue. The device includes an anterior concave surface adapted to contact and at least partially surround a posterior side of the lead such that the lead is positioned between the anterior concave surface and the nerve tissue when the device and the lead are implanted in the body. The device includes a posterior convex surface coupled to the anterior concave surface and adapted to contact the body tissue opposite the nerve tissue. The device is adapted to partially shield electrical energy emitted from one or more electrodes on a posterior side of the lead when the device and the lead are implanted in the body to reduce a quantity of electrical energy reaching the body tissue opposite the nerve tissue.