Abstract: A medical system comprises an implantable medical device having a power source, the implantable medical device configured for monitoring a quantity of the stored energy in the power source, generating a battery status signal based on the monitored quantity of stored energy, and for transcutaneously transmitting a communication initiation signal and the battery status signal. The medical system further comprises an external device configured for transcutaneously receiving the communication initial signal and the battery status signal from the rechargeable implantable medical device, changing from a relatively low energy consumption state to a relatively high energy consumption state in response to the received communication initiation signal, and for generating a user-discernible signal in response to the received status signal.

Abstract: A method of determining desynchronization between a first implantable medical device and a second implantable medical device. The method includes receiving a synchronization query from the first device at the second device, that is transmitted in response to the first device detecting a predetermined transition of a first clock of the first device, the first clock having a first pulse rate. The method further includes determining a number of pulses of a second clock of the second device occurring between reception of the synchronization query and a predetermined transition of a third clock of the second device, the third clock having the first pulse rate. The second clock has a second pulse rate higher than the first pulse rate. The method further includes determining the desynchronization between the first device and the second device based on the determined number of pulses of the second clock.

Abstract: A computer-implemented system is provided for distributing product updates to medical devices. An update interface residing on a distribution platform is configured to distribute product updates and maintain a log of such distributions in an audit database. A configuration device in data communication with the update interface registers itself with the update interface and downloads product updates from the update interface, such that the registration includes providing identifying information for the configuration device and a user of the configuration device. A medical device in data communication with the configuration device registers itself with the configuration device and downloads a particular product update from the configuration device, such that the configuration device creates a record of the particular product update and communications the record of the particular product update to the update interface.

Abstract: Channel assessment and selection for wireless communication is made between two or more medical devices, such as between an implantable medical device (IMD) and a non-implanted medical device, between two IMDs, or between two non-implanted medical devices. A telemetry module of a medical device operating in accordance with the techniques of this disclosure obtains measured ambient power levels on a plurality of channels of a frequency band regulation, such as the ten channels of the MICS band regulation. The telemetry module computes channel assessment values for at least a portion of the plurality of channels based on the measured ambient power levels on at least one other channel of the plurality of channels and selects a channel to transmit on based on the channel assessment values.

Abstract: A system including an external medical data telemetry device to communicate with an implantable medical device (IMD). The external medical data telemetry device includes a processor, a reconfigurable radio-frequency (RF) transceiver circuit, at least one far-field antenna, and a user interface. The reconfigurable RF transceiver circuit modulates an outgoing IMD data signal and demodulates an incoming IMD data signal using a modulation type that is selectable from a plurality of modulation types by the processor. The processor selects the modulation type using information entered by a user through the user interface.

Abstract: A therapy program is modified to decompose an electrical stimulation signal defined by the therapy program into a plurality of subsignals based on a comparison between an energy associated with the stimulation signal and a threshold value. An electrical stimulation signal defined by a therapy program may be decomposed into a plurality of subsignals when an electrical stimulation energy of the stimulation signal exceeds the maximum energy output of the medical device or of a channel of the medical device. The energy associated with each one of the subsignals may be less than the energy threshold value of the medical device.

Abstract: An implantable pulse generator includes a current steering capability that allows a clinician or patient to quickly determine a desired electrode stimulation pattern, including which electrodes of a group of electrodes within an electrode array should receive a stimulation current, including the amplitude, width and pulse repetition rate of such current. Movement of the selected group of electrodes is facilitated through the use of remotely generated directional signals, generated by a pointing device, such as a joystick. As movement of the selected group of electrodes occurs, current redistribution amongst the various electrode contacts takes place. The redistribution of stimulus amplitudes utilizes re-normalization of amplitudes so that the perceptual level remains fairly constant. This prevents the resulting paresthesia from falling below the perceptual threshold or above the comfort threshold.

Abstract: Embodiments of the invention relate to a wireless physiological monitoring system. The system includes at least one wireless sensor and a monitoring device which are linked to one another of a wireless fashion for measuring physiological signals of a patient. The at least one wireless sensor is located on the patient and may comprise a wireless surface electrode assembly or a wireless needle assembly. The system may also comprise a wireless stimulator synchronized with the wireless sensor for performing certain diagnostic tests, such as nerve conduction velocity tests, for example. The wireless sensor preferably includes active, reference and common conductors. The common conductor can be used to measure the common mode voltage of the patient in the vicinity of the testing, and this voltage can then be subtracted from the measured active and reference voltages.

Abstract: An implantable medical device (IMD) comprises a transmitting/receiving (T/R) device for transmitting medical data sensed from a patient to, and for receiving control signals from, a medical expert (a human medical professional and/or a computerized expert system) at a remote location; an electronic medical treatment device for treating the patient in response to control signals applied thereto; and a sensor circuit, having a sensor circuit output, for producing sensor circuit output signal(s) representing medical data sensed from the patient. The IMD also includes logic device which analyzes the sensor circuit output signal(s) to detect a medical abnormality and, upon detecting an abnormality, either sends a notification signal representing a medical state of said patient to the medical expert at the remote location or sends a local treatment device control signal to the medical treatment device, or does both.

Abstract: An implantable medical device including a data communication device that includes a device to alter and/or generate an oscillatory electric field imposed on body tissue surrounding the implantable medical device when the implantable medical device is in its implanted state. The device that alters an oscillatory electric field modulates an impedance of body tissue surrounding the implantable medical device when the implantable medical device is in its implanted state and within an oscillatory electric field. The device that alters an oscillatory electric field includes a device that generates an oscillatory electric field that is phase-synchronized with an oscillatory electric field imposed on body tissue surrounding the implantable medical device when the implantable medical device is in its implanted state.

Abstract: An electrical stimulation system provides stimulation therapy to a patient. The system includes a neurostimulation lead that contacts patient tissue and couples with an implantable stimulation device, such as an implantable pulse generator, that receives stimulation parameters for providing stimulation therapy to a patient. The implantable stimulation device includes a header with a plurality of connector assemblies that receive an end of the neurostimulation lead, and a case containing a charging coil and a telemetry coil coupled to programming circuitry on a printed circuit board, which is in turn coupled to the connector assemblies via a feedthrough assembly. The telemetry coil receives data from an external programmer and transmits the data to the programming circuitry, which in turn uses the data to communicate to the connector assemblies and the neurostimulation lead to provide stimulation therapy to a patient.

Abstract: A system to increase the reliability of the electrical connections between the electrodes and the battery/controlling electronics of an electrical stimulating device as DBS (Deep Brain Stimulator), heart pacemakers and the like. We disclose a redundant male/female connector and/or a set of redundant wires to improve the reliability of the connections between the electrodes at a first location and the battery/controlling electronics at a second location. The redundant male/female connector serves as a backup for a potential loss of electrical continuity due to the adverse effect of body fluids, and the redundant wires serve as a backup for potential loss of electrical continuity due to repetitive muscle movement causing wire movement and stress. DBS connecting wires, that ran behind the ear down the neck of the patient, are subjected to repetitive stresses due to neck twisting and therefore at high risk of breaking.

Abstract: An implantable medical device including a data communication device that includes a device that alters an oscillatory electric field imposed on body tissue surrounding the implantable device. The device that alters an oscillatory electric field modulates an impedance of a conductive medium surrounding the implantable device when the implantable device is within an oscillatory electric field. The device that alters an oscillatory electric field includes a device that generates an oscillatory electric field that is phase-synchronized with an oscillatory electric field imposed on a conductive medium surrounding the implantable device.

Abstract: Far field telemetry operations are conducted between an external device and an implantable medical device while power is being transferred to the implantable medical device for purposes of recharging a battery of the implantable medical device. The far field operations may include exchanging recharge information that has been collected by the implantable medical device which allows the external device to exercise control over the recharge process. The far field operations may include suspending far field telemetry communications for periods of time while power continues to be transferred where suspending far field telemetry communications may include powering down far field telemetry communication circuits of the implantable medical device for periods of time which may conserve energy. The far field operations may further include transferring programming instructions to the implantable medical device.

Abstract: Systems and methods for monitoring the acoustic coupling of medical devices is disclosed. An illustrative system for monitoring the acoustic coupling of an acoustic transducer attached to a patient's body includes a signal generator adapted to supply an electrical signal to the transducer, a circuit configured to measure at least one electrical parameter of the transducer, and a processor adapted to evaluate the degree of acoustic coupling of the transducer to the body based on the measured electrical signal. The processor can measure the frequency response of the acoustic transducer to the electrical signal, a time domain response of the acoustic transducer to the electrical signal, or a combination of both.

Abstract: A communication device for an implantable medical device may include: an input/output interface configured to communicate with a wireless communication device; a communication interface configured to communicate with a remote system; and a processor configured to perform an analysis of data received from the wireless communication device via the input/output interface and associated with the implantable medical device. The communication device may include a user interface configured to receive data input by a user. A communication system may include a wireless communication device and the aforementioned communication device.

Abstract: A medical device communication system includes a receiver adapted to receive radio frequency (RF) signals and configured to operate in a first mode to poll for an RF signal for a first time interval to detect an element of a valid input signal during the first time interval. In response to detecting the element of a valid input signal in the first time interval, the receiver operates in a second mode to poll for the RF signal for a second time interval to analyze the RF signal over the second time interval to detect a valid modulation of the RF signal. In response to detecting a valid modulation of the RF signal during the second time interval, the receiver is enabled to establish a communication session with a transmitting device.

Abstract: An implantable electroacupuncture device (IEAD) treats a disease or medical condition of a patient through application of stimulation pulses applied at a specified acupoint or other target tissue location. In a preferred implementation, the IEAD is an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years.

Abstract: A particular method of providing power to an implantable medical device includes providing a first signal to a primary coil that is inductively coupled to a secondary coil of an implantable medical device. The method also include determining a first alignment difference between a voltage corresponding to the first signal and at least one of a current corresponding to the first signal and a component voltage at a component of a primary coil circuit. The method further includes determining a frequency sweep range based on the first alignment difference. The method also includes performing a frequency sweep over the frequency sweep range.

Abstract: A therapy system for applying an electrical signal to a target nerve includes an electrode, an implantable component and an external component. The electrode has an impedance of at least about 2000 ohms. The electrical signal is applied using constant current or constant voltage.

Abstract: An arteriovenous graft system is described. The arteriovenous graft system includes an arteriovenous graft that is well suited for use during hemodialysis. In order to minimize or prevent arterial steal, at least one valve device is positioned at the arterial end of the arteriovenous graft. In one embodiment, for instance, the arteriovenous graft system includes a first valve device positioned at the arterial end and a second valve device positioned at the venous end. In one embodiment, the valve devices may include an inflatable balloon that, when inflated, constricts and closes off the arteriovenous graft. If desired, a single actuator can be used to open and close both valve devices.

Abstract: An improved external charger for charging the battery within or providing power to an implantable medical device is disclosed. The improved external charger includes circuitry for detecting the temperature of the external charger and for controlling charging to prevent exceeding a maximum temperature. The external charger in some embodiments includes a user interface for allowing a patient to set the external charger's maximum temperature. The user interface can be used to select either constant maximum temperatures, or can allow the user to choose from a number of stored charging programs, which programs can control the maximum temperature to vary over time. Alternatively, a charging program in the external charger can vary the maximum temperature set point automatically. By controlling the maximum temperature of the external charger during charging in these manners, the time needed to charge can be minimized while still ensuring a temperature that is comfortable for that patient.

Abstract: Deep brain electrodes are remotely sensed and activated by means of a remote active implantable medical device (AIMD). In a preferred form, a pulse generator is implanted in the pectoral region and includes a hermetic seal through which protrudes a conductive leadwire which provides an external antenna for transmission and reception of radio frequency (RF) pulses. One or more deep brain electrode modules are constructed and placed which can transmit and receive RF energy from the pulse generator. An RF telemetry link is established between the implanted pulse generator and the deep brain electrode assemblies. The satellite modules are configured for generating pacing pulses for a variety of disease conditions, including epileptic seizures, Turrets Syndrome, Parkinson's Tremor, and a variety of other neurological or brain disorders.

Abstract: Method and systems for optimizing acoustic energy transmission in implantable devices are disclosed. Transducer elements transmit acoustic locator signals towards a receiver assembly, and the receiver responds with a location signal. The location signal can reveal information related to the location of the receiver and the efficiency of the transmitted acoustic beam received by the receiver. This information enables the transmitter to target the receiver and optimize the acoustic energy transfer between the transmitter and the receiver. The energy can be used for therapeutic purposes, for example, stimulating tissue or for diagnostic purposes.

Abstract: A device according to some embodiments of the present disclosure includes a housing configured to retain a battery, a primary antenna associated with the housing, and at least one processor in electrical communication with the battery and the primary antenna. In some embodiments, the at least one processor may be configured to cause transmission of a primary signal from the primary antenna to an implantable device during a treatment session of at least three hours in duration, wherein the primary signal is generated using power supplied by the battery and includes a pulse train, the pulse train including a plurality of modulation pulses.

Abstract: A method for defining connections between a plurality of lead bodies and a plurality of output ports of a neurostimulator, and an external control device for performing the method are disclosed. The external control device includes a user interface and control circuitry. The method includes displaying the lead bodies and the output ports of the neurostimulator; selecting a first one of the lead bodies; dragging a connector from the first lead body to a first one of the output ports of the neurostimulator; and dropping the connector onto the first output port of the neurostimulator, thereby defining a connection between the first lead body and the first output port of the neurostimulator. In another embodiment, a method includes defining the connection between the first lead body and the first output port, and graphically displaying the connection between the first lead body and the first output port of the neurostimulator.

Abstract: Controlling the interaction between an external device and an implanted device, including a method of controlling interaction between an external device and an implanted device, the method including at least the steps of: establishing communications between the implanted device and the external device; the external device determining an identification of the implant and comparing the identification with identifications in a stored list; if the device matches one of said identifications, then using a corresponding set of operating parameters to interact with said implant; and otherwise, not interacting with said device.

Abstract: An implantable medical device includes a transcutaneous capacitive data link circuit. The link circuit include: a first pair of capacitors each having an external electrode configured to be externally positioned on a recipient and an internal electrode configured to be internally positioned in the recipient; a first voltage driver having positive and negative terminals each connected to one of the external electrodes, and configured to generate a first voltage drive signal responsive to a first input control signal; and a first differential amplifier circuit connected to the internal electrodes, configured to generate a first output data signal representative of the first input control signal.

Abstract: A biostimulator system comprises one or more implantable devices and an external programmer configured for communicating with the implantable device or devices via bidirectional communication pathways comprising a receiving pathway that decodes information encoded on stimulation pulses generated by ones of the implantable device or devices and conducted through body tissue to the external programmer.

Abstract: This disclosure describes a chopper mixer telemetry circuit for use in a wireless receiver. The receiver may be located in an implantable medical device (IMD) or external programmer. The chopper mixer telemetry circuit may include a mixer amplifier that operates as a synchronous demodulator to provide selective extraction of wireless signals received from a transmitter while suppressing out-of-band noise that can undermine the reliability of the telemetry link between an IMD or programmer and another device. The mixer amplifier may utilize parallel signal paths to convert the received telemetry signal into an in-phase (I) signal component and a quadrature (Q) signal component and recombine the I and Q signal components to reconstruct the total signal independently of the phase mismatch between the transmitter and receiver. Each signal path may include a chopper-stabilized mixer amplifier that amplifies telemetry signals within a desired band while suppressing out-of-band noise.

Abstract: Apparatus for monitoring vital signs of one or more living subjects comprises a monitoring station and at least one sensor in communication with the monitoring station. The sensor comprises an antenna system, an ultra wideband radar system coupled to the antenna system, a signal processor and a communication system. The signal processor is connected to receive a signal from the ultra wideband radar system and configured to extract from the signal information about one or more vital signs of a person or animal in a sensing volume corresponding to the antenna system. The communication system is configured to transmit the information to the monitoring station.

Abstract: A data collection system collects and stores physiological data from an ambulatory patient at a high resolution and/or a high data rate (“more detailed data”) and sends a low-resolution and/or downsampled version of the data (“less detailed data”) to a remote server via a wireless network. The server automatically analyzes the less detailed data to detect an anomaly, such as an arrhythmia. A two-tiered analysis scheme is used, where the first tier is more sensitive and less specific than the second tier. If the more sensitive analysis detects or suspects the anomaly, the server signals the data collector to send more detailed data that corresponds to a time period associated with the anomaly. The more specific second tier analyses the more detailed data to verify the anomaly. The server may also store the received data and make it available to a user, such as via a graphical or tabular display.

Abstract: A method of medical diagnosis and monitoring using equipment that has wireless electrodes, which are attached to the surface of the skin of the patient. The method comprises collection of data from a patient, converting the data to digital form and transmitting the digital data wirelessly from a patient to a base station located away from the patient where in the wireless transmission between the patient and base station is bi directional.

Abstract: By a medical implant transceiver implantable within a body of a living organism, a portion of a signal is received from a medical controller transceiver external to the body of the living organism. Based on directions within the portion of the signal, a time duration is determined, after which a subsequent portion of the signal is to be transmitted from the medical controller transceiver. The directions include a value indicative of the time duration. The time duration differs based on the value. The subsequent portion is to be transmitted from the medical controller transceiver after an end of the portion. The medical implant transceiver enters into an inactive state for the time duration and awakens after the time duration has elapsed.

Abstract: Systems and methods for programming and logging medical device and patient data are provided. The systems include a handheld device, which is capable of communicating with a medical device, and a base station, which provides connectivity for the handheld device to accomplish various functions such as recharging, programming, data back-up and data entry. The methods comprise the steps of detecting a medical device, obtaining and recording information from the medical device. Additionally, medical device parameters may be modified and the recorded information may be archived for future reference.

Abstract: A method and external control device for preventing frequency locking in a multi-channel neurostimulation system and external control device is provided. A plurality of pulsed electrical waveforms is provided. Each of the pulsed electrical waveforms has a period and a pulse width. The greatest common divisor of the periods of the pulsed electrical waveforms is computed, and the sum of the pulse widths of the pulsed electrical waveforms is computed. A plurality of timing channels in the neurostimulation system is allowed to be programmed with the pulsed electrical waveforms if the greatest common divisor is equal to or greater than the sum.

Abstract: A system and method for receiving telemetry data from implantable medical devices such as cardiac pacemakers with improved noise immunity is disclosed. Ambient noise levels and signal strength are monitored and used to adaptively adjust the detection sensitivity of the receiver. Filtering of the received signal is performed to remove both broadband and narrowband noise. Removal of narrowband noise is accomplished with notch filters that are dynamically adjusted in accordance with a detected noise spectrum.

Abstract: A neural prosthesis includes a centralized device that can provide power, data, and clock signals to one or more individual neural prosthesis subsystems. Each subsystem may include a number of individually addressable, programmable modules that can be dynamically allocated or shared among neural prosthetic networks to achieve complex, coordinated functions or to operate in autonomous groups.

Abstract: Implantable subcutaneous device of biocompatible material that can receive data and energy by electromagnetic coupling with at least one external device is disclosed. The implantable device bears an airtight housing and a magnet that can hold the other external device centered with the implantable device. The housing bears a hollow crown containing at least electronic device(s) and a coil, and a bottom sealing the opening of the crown in an airtight manner. The magnet has dimensions compatible with a central housing formed by the so-called internal wall of the crown and in which it is positioned.

Abstract: An ingestible therapy activator system and method are provided. In one aspect, the ingestible therapy activator includes an ingestible device having an effector module to send an effector instruction and a responder module associated with a therapeutic device. The responder module may receive and process the effector instruction, resulting in a response by the therapeutic device. Examples of responses by therapeutic device include activating a therapy, deactivating a therapy, modulating a therapy, and discontinuing a therapy.

Abstract: A system for treating a medical condition in a living body, comprising two subsystems, an implant subsystem and an electrical stimulation unit subsystem. The implant subsystem comprises at least one electrostimulation module, contains at least one electrically conductive electrode and, preferably, an anchoring member. The electrical stimulation unit, adapted for producing and controlling electrical waveforms, is connected to the electrodes. The implant subsystem is implanted adjacent to at least one of the following structures: the carotid sinus nerve, aortic nerve, common carotid artery, external carotid artery, internal carotid artery, carotid artery bifurcation, carotid body, aortic body or aortic arch receptors.

Abstract: A wearable device for facilitating neurophysiological treatment of a patient harboring an implanted neural stimulator is provided. The wearable device includes a transmitting antenna configured to accept one or more input signals and to transmit one or more electromagnetic signals to a neural stimulator that is implanted in a patient's body. The wearable device further includes a control circuitry configured to provide the one or more input signals to the transmitting antenna. The wearable device further includes a battery that provides electrical power to at least the control circuitry. The wearable device is configured to be worn outside the patient's body.

Abstract: A non-implantable communication unit conducts wireless communication with an implantable medical device (IMD). The communication unit comprises a request processor for generating power down requests destined to the IMD and triggering temporary power down of the IMD radio equipment. When the communication unit receives a data packet from the IMD or a connected programmer it determines the size of the data packet. A timer processor sets a timer to a value defined based on the determined size. A processor controller selectively controls the operation of request processor to generate or stop generating the power down requests based on a current value of the timer. Power down of the IMD radio equipment is thereby prevented if it is likely that the IMD comprises data to transmit to the communication unit as predicted based on data packet sizes.

Abstract: A telemetry wake-up circuit is electrically disposed between a telemetry transceiver associated with an AIMD, and an RF tag. The RF tag may be remotely interrogated to generate a signal to which the telemetry wake-up circuit is responsive to switch the telemetry transceiver from a sleep mode to an active telemetry mode. In the sleep mode, the telemetry transceiver draws less than 25,000 nanoamperes from the AIMD, and preferably less than 500 nanoamperes.

Abstract: In an example, an apparatus can include an implantable medical device comprising a housing, an implantable telemetry circuit carried within the housing, a dielectric compartment mechanically coupled to the housing, the dielectric compartment including first and second substantially parallel face portions and a third face portion extending between the first and second face portions, and an implantable telemetry antenna, located at least partially within the dielectric compartment. The implantable telemetry circuit can be electrically coupled to the implantable telemetry antenna and configured to wirelessly transfer information electromagnetically using the implantable telemetry antenna. In an example the implantable telemetry antenna comprises a spiral conductor portion extending along the first, second, and third face portions. In an example the spiral conductor includes a cross section having a lateral width that can be greater than a sidewall height of the cross section.

Abstract: The present disclosure involves a method of providing graphical representations of medical devices and connections between the medical devices. A graphical representation of a lead is displayed. The lead is configured to deliver electrical stimulation to a patient via one or more of a plurality of electrode contacts. A graphical representation of one of: an implantable pulse generator (IPG) or a lead connector block is displayed. The IPG and the lead connector block are each configured for coupling with the lead. In response to a user input, a graphical representation of a connection is generated. The connection is between the lead and one of: the IPG or the lead connector block. An actual connection between the lead and one of: the IPG or the lead connector block is monitored. A status of the actual connection between the lead and one of: the IPG or the connector block is then reported.

Abstract: An implanted medical device can be detected within an effective proximity of an electronic device by an IMD safety control module coupled with the electronic device, in response to the performance of a function by the electronic device. Performance of the function by the electronic device can be known to have the potential to cause adverse effects to operation of and/or a treatment provided by the implanted medical device within the effective proximity. The implanted medical device can be an active implanted medical device having wireless communication capabilities. Performance of the function by the electronic device can be disabled. Resolution from an operator of the electronic device can be requested. Upon receipt of the resolution, performance of the function by the electronic device can be enabled.

Abstract: A system for event-based synchronized multimedia playback, comprising a media source device and a plurality of destination devices, each destination device comprising a local clock, and a synchronization module on one of the devices. The synchronization module transmits common events, En, each with a unique event number, to each of the plurality of destination devices. Each destination device records time Dxn when event En is received and transmits an acknowledgement message back to the synchronization module comprising time Dxn and event number n. The synchronization module determines phase and frequency differences between clocks of respective destination devices; computes a frequency adjustment to compensate for phase and rate differences; and directs each respective destination device to adjust its clock phase and frequency accordingly. Each destination device adjusts its local clock as directed or may perform a sample rate conversion on sample data in order to enable synchronized media playback.

Abstract: The invention relates to an implantable pulse generator (100), IPG, for stimulation of a neurological cellular mass comprising a casing (2) that at least partially encloses the pulse generating module (PGM) (4) and that is transparent to radio-frequency electromagnetic fields, or wherein the pulse generating module (4) includes a controller circuit (18) provided as two or more circuit boards (20, 22), co-operatively connected, one such circuit board being an interface circuit board, where at least one component of the controller circuit (8) is located on the interface circuit board (20), and feed through wires for connector block (6) are connected thereto (20), and one of the opposing surfaces of the interface circuit board (20) is aligned over apertures (48, 50, 52) in the PGM housing for the feed through wires.

Abstract: An improved external charger for an implantable medical device is disclosed in which charging is at least partially controlled based on a sensed pressure impingent on its case, which pressure is indicative of the pressure between the external charger and a patient's tissue. The improved external charger includes pressure detection circuitry coupled to one or more pressure sensors for controlling the external device in accordance with the sensed impingent pressure. The sensed pressure can be used to control charging, for example, by suspending charging, by adjusting a maximum set point temperature for the external charger based on the measured pressure, or by issuing an alert via a suitable user interface. By so controlling the external charger on the basis of the measured pressure, the external charger is less likely to create potentially problematic or uncomfortable conditions for the user.