Abstract: Disclosed is an apparatus and method for facilitating the implantation and secure positioning of implantable medical devices within a subcutaneous pocket formed by a surgeon within the patient. Such apparatus and method are configured to address the above-described challenges of containing implantable medical devices within such subcutaneous pockets, and the spring-like leads or catheters that may be attached to them, during implantation.

Abstract: Disclosed is a modular system for providing electrical stimulation, in which a first modular electrode section has a contoured back end configured to engage a contoured front end of another electrode section or a tool that may be used to place the first modular electrode section in the patient's body. The contours of the modular electrode section allow the two components to engage with one another so as to prevent their separation in the horizontal plane, and a lead extending from the first modular electrode is configured to engage keels on the top surface of the second electrode portion or tool, with such keels providing a snap-type attachment between the lead and the second electrode portion or tool, such that the two components may be joined together but easily separated from one another through the intentional separation of the lead from the keels on the second electrode portion or tool.

Abstract: Disclosed is an implantable anchor for anchoring a catheter, including (by way of non-limiting example) an implantable lead, such as may be used for spinal cord stimulation, to the body of a patient, along with a method for its use. The anchor comprises an elongate body have a central lumen extending through the body from its proximal end to its distal end, which central lumen is configured to snugly receive the catheter body. In addition to the central lumen, a second lumen is provided in the proximal end of the anchor and is configured to receive an injector so that adhesive may be injected into the anchor surrounding at least a portion of the catheter body. In doing so, the anchor may be fixed to the catheter body, such that when the anchor is sutured in place within the patient's body, migration of the catheter may be avoided.

Abstract: A distributed system comprises a programming device and a remotely located server. During a programming session, the programming device transmits programs and rating information associated with the programs to the server. The server presents the rating information to a clinician to assist the clinician in selecting from among programs tested during the programming session. The programming device may also transmit patient information and device configuration information to the server for storage with selected programs and rating information within a database as part of a patient record. Programs and information received from a plurality of programming devices and for a plurality of patients may be stored in the database and analyzed by the server to provide responses to user queries made by clinicians via programming devices.

Abstract: A user, such as a clinician or the patient, uses a control device to manipulate at least one neurostimulation parameter. A mapping system uses a calibrated map to map the directional output of the control device to values of at least one stimulation parameter to allow the user to intuitively control the value of the parameter. In some embodiments, where a stimulation device is used to deliver spinal cord stimulation (SCS) therapy for example, the user manipulates a parameter to effect the location and/or strength of paresthesia experienced by the patient. In exemplary embodiments, the parameter values are combinations of electrodes, and the mapping system selects electrode combinations based on the output of the control device such that a direction of movement of paresthesia experienced by the patient corresponds to a direction of manipulation of a directional controller of the control device. The mapping system may calibrate the map based on patient paresthesia information received from a user.

Abstract: A distributed system comprises a programming device and a remotely located server. During a programming session, the programming device transmits programs and rating information associated with the programs to the server. The server presents the rating information to a clinician to assist the clinician in selecting from among programs tested during the programming session. The programming device may also transmit patient information and device configuration information to the server for storage with selected programs and rating information within a database as part of a patient record. Programs and information received from a plurality of programming devices and for a plurality of patients may be stored in the database and analyzed by the server to provide responses to user queries made by clinicians via programming devices.

Abstract: A watchdog unit receives stay-alive signals from a programming device during programming of an implantable medical device. The watchdog unit maintains a watchdog timer, and resets the timer upon receipt of each stay-alive signal. If the watchdog timer expires, the watchdog unit changes a mode of operation of the implantable device, e.g., places the implantable medical device into a known, safe state. For example, the watchdog unit may cause the implantable medical device to suspend delivery of therapy, perform a power-on reset, and/or recall a known, safe, therapy delivery program.

Abstract: A distributed system comprises a programming device and a remotely located server. During a programming session, the programming device transmits programs and rating information associated with the programs to the server. The server presents the rating information to a clinician to assist the clinician in selecting from among programs tested during the programming session. The programming device may also transmit patient information and device configuration information to the server for storage with selected programs and rating information within a database as part of a patient record. Programs and information received from a plurality of programming devices and for a plurality of patients may be stored in the database and analyzed by the server to provide responses to user queries made by clinicians via programming devices.

Abstract: A user, such as a clinician or the patient, uses a control device to manipulate at least one neurostimulation parameter. A mapping system uses a calibrated map to map the directional output of the control device to values of at least one stimulation parameter to allow the user to intuitively control the value of the parameter. In some embodiments, where a stimulation device is used to deliver spinal cord stimulation (SCS) therapy for example, the user manipulates a parameter to effect the location and/or strength of paresthesia experienced by the patient. In exemplary embodiments, the parameter values are combinations of electrodes, and the mapping system selects electrode combinations based on the output of the control device such that a direction of movement of paresthesia experienced by the patient corresponds to a direction of manipulation of a directional controller of the control device. The mapping system may calibrate the map based on patient paresthesia information received from a user.

Abstract: A watchdog unit receives stay-alive signals from a programming device during programming of an implantable medical device. The watchdog unit maintains a watchdog timer, and resets the timer upon receipt of each stay-alive signal. If the watchdog timer expires, the watchdog unit changes a mode of operation of the implantable device, e.g., places the implantable medical device into a known, safe state. For example, the watchdog unit may cause the implantable medical device to suspend delivery of therapy, perform a power-on reset, and/or recall a known, safe, therapy delivery program.

Abstract: Disclosed is a modular system for providing electrical stimulation to a patient's body, in which a first modular electrode section has a contoured back end configured to engage with a contoured front end of another electrode section or a tool that may be used to place the first modular electrode section in the patient's body. The contours of the back end of the first modular electrode section and of the front end of the second electrode section or tool allow the two components to engage with one another so as to prevent their separation in the horizontal plane (i.e., the plane that contains the top surfaces of the two components).

Abstract: Disclosed is an implantable anchor for anchoring a catheter, including (by way of non-limiting example) an implantable lead, such as may be used for spinal cord stimulation, to the body of a patient, along with a method for its use. The anchor comprises an elongate body have a central lumen extending through the body from its proximal end to its distal end, which central lumen is configured to snugly receive the catheter body. In addition to the central lumen, a second lumen is provided in the proximal end of the anchor and is configured to receive an injector so that adhesive may be injected into the anchor surrounding at least a portion of the catheter body. In doing so, the anchor may be fixed to the catheter body, such that when the anchor is sutured in place within the patient's body, migration of the catheter may be avoided.

Abstract: Disclosed is an electrode, such as an SCS paddle electrode, having a lead attached thereto along an interior portion of the electrode. The lead and electrode are configured such that the lead may be positioned generally coplanar with a top surface of the electrode, and may likewise be erected from such coplanar orientation up and away from the top surface of the electrode. Thus, the lead can maintain the typical configuration of emerging from the back end of the electrode, but because at least portions of the lead are not permanently bonded into the electrode paddle, the lead (when desired) can be pulled upward, with or without surrounding strain relief material, to emerge from the top surface of the paddle at an angle or curve to such top surface. This allows the base of the paddle to engage a bony opening, such as when the electrode is inserted into a patient's spine, skull, plane of fascia, etc.

Abstract: Disclosed is a shaped electrode and dissecting tool configured to aid in controlling the path of an electrode as it is moved into its intended position within the epidural space of a patient. The shaped electrode and dissecting tool is configured with a contoured leading edge having at least one concavity that aids in moving the electrode and dissecting tool through the intended tissues within the patient's body. A variety of concavity contours may be provided and used for particular surgical applications.

Abstract: Disclosed is an implantable medical device including a connector block that allows varied lead configurations to be used with a single connector block and implantable medical device assembly. The connector block is configured with one or more lead insertion lumens that are open at both ends, such that each end of the lead insertion lumen may receive a separate lead. The circuitry within the implantable medical device is configured to allow the delivery of electrical pulses from a pulse generator within the implantable medical device to two separate leads, or to a single lead (with a plug positioned within the opposite, open end of the insertion lumen), inserted within a single lead insertion lumen.

Abstract: Disclosed is an implantable medical device including a connector block that allows varied lead configurations to be used with a single connector block and implantable medical device assembly. The connector block is configured with one or more lead insertion lumens that are open at both ends, such that each end of the lead insertion lumen may receive a separate lead. The circuitry within the implantable medical device is configured to allow the delivery of electrical pulses from a pulse generator within the implantable medical device to two separate leads inserted within opposite ends of a single lead insertion lumen.

Abstract: A paddle lead includes a plurality of electrodes configured in at least three rows of three electrodes with the second, intermediate row operable to provide anode guarding. The paddle lead further includes a plurality of grooves disposed on a surface opposite the electrodes to facilitate the insertion of the paddle lead within a patient by inhibiting the veering of the paddle lead to one side or the other of the dorsal column as the paddle lead is advanced along the dorsal column midline during implantation.

Abstract: In one embodiment, a paddle lead comprises: a plurality of stimulating electrode contacts disposed, the plurality of stimulation electrode contacts being adapted to allow the stimulation paddle to flex transversely about a longitudinal axis; wherein the plurality of stimulation electrode contacts are arranged in at least first, second, and third rows that are disposed perpendicular to a longitudinal axis of the paddle; the first and third rows respectively having multiple electrode contacts electrically coupled to different conductors of the lead to enable the multiple electrode contacts of the first and third rows to function in independent cathode states, anode states, or high-impedance states; the second row being disposed between the first and third rows, the second row having multiple electrode contacts each electrically coupled to a common conductor to cause the multiple electrode contacts of the second row to function in a common cathode state, anode state, or high-impedance state.

Abstract: A programming device compares filter information to information that describes possible combinations of the electrodes within an electrode set implanted in a patient. The filter information describes at least one characteristic of valid, e.g., desired, electrode combinations, and in exemplary embodiments, is received from a user, e.g., a clinician, via a user interface of the programming device. The filter information can describe a number of electrodes in valid combinations, a fixed polarity for an electrode for valid combinations, or relational characteristics of the electrodes of valid combinations. The comparison process may be iterative. The programming device identifies a subset of the possible electrode combinations based on the comparison. By identifying the valid subset of electrode combinations based on the filter information, the programming device may reduce the amount of clinician and patient time required to program an implantable neurostimulator.