Programmer for biostimulator system

Information

  • Patent Grant
  • 7945333
  • Patent Number
    7,945,333
  • Date Filed
    Friday, October 13, 2006
    18 years ago
  • Date Issued
    Tuesday, May 17, 2011
    13 years ago
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.
Description
BACKGROUND

Cardiac pacing electrically stimulates the heart when the heart's natural pacemaker and/or conduction system fails to provide synchronized atrial and ventricular contractions at appropriate rates and intervals for a patient's needs. Such bradycardia pacing provides relief from symptoms and even life support for hundreds of thousands of patients. Cardiac pacing may also give electrical overdrive stimulation intended to suppress or convert tachyarrhythmias, again supplying relief from symptoms and preventing or terminating arrhythmias that could lead to sudden cardiac death.


Cardiac pacing is usually performed by a pulse generator implanted subcutaneously or sub-muscularly in or near a patient's pectoral region. The generator usually connects to the proximal end of one or more implanted leads, the distal end of which contains one or more electrodes for positioning adjacent to the inside or outside wall of a cardiac chamber. The leads have an insulated electrical conductor or conductors for connecting the pulse generator to electrodes in the heart. Such electrode leads typically have lengths of 50 to 70 centimeters.


Known pulse generators can include various sensors for estimating metabolic demand, to enable an increase in pacing rate proportional and appropriate for the level of exercise. The function is usually known as rate-responsive pacing. For example, an accelerometer can measure body motion and indicate activity level. A pressure transducer in the heart can sense the timing between opening and closing of various cardiac valves, or can give a measure of intracardiac pressure directly, both of which change with changing stroke volume. Stroke volume increases with increased activity level. A temperature sensor can detect changes in a patient's blood temperature, which varies based on activity level. The pacemaker can increase rate proportional to a detected increase in activity.


Pulse generator parameters are usually interrogated and modified by a programming device outside the body, via a loosely-coupled transformer with one inductance within the body and another outside, or via electromagnetic radiation with one antenna within the body and another outside.


Although more than five hundred thousand pacemakers are implanted annually, various well-known difficulties are present.


The pulse generator, when located subcutaneously, presents a bulge in the skin that patients can find unsightly or unpleasant. Patients can manipulate or “twiddle” the device. Even without persistent twiddling, subcutaneous pulse generators can exhibit erosion, extrusion, infection, and disconnection, insulation damage, or conductor breakage at the wire leads. Although sub-muscular or abdominal placement can address some of concerns, such placement involves a more difficult surgical procedure for implantation and adjustment, which can prolong patient recovery.


A conventional pulse generator, whether pectoral or abdominal, has an interface for connection to and disconnection from the electrode leads that carry signals to and from the heart. Usually at least one male connector molding has at least one terminal pin at the proximal end of the electrode lead. The at least one male connector mates with at least one corresponding female connector molding and terminal block within the connector molding at the pulse generator. Usually a setscrew is threaded in at least one terminal block per electrode lead to secure the connection electrically and mechanically. One or more O-rings usually are also supplied to help maintain electrical isolation between the connector moldings. A setscrew cap or slotted cover is typically included to provide electrical insulation of the setscrew. The complex connection between connectors and leads provides multiple opportunities for malfunction.


For example, failure to introduce the lead pin completely into the terminal block can prevent proper connection between the generator and electrode.


Failure to insert a screwdriver correctly through the setscrew slot, causing damage to the slot and subsequent insulation failure.


Failure to engage the screwdriver correctly in the setscrew can cause damage to the setscrew and preventing proper connection.


Failure to tighten the setscrew adequately also can prevent proper connection between the generator and electrode, however over-tightening of the setscrew can cause damage to the setscrew, terminal block, or lead pin, and prevent disconnection if necessary for maintenance.


Fluid leakage between the lead and generator connector moldings, or at the setscrew cover, can prevent proper electrical isolation.


Insulation or conductor breakage at a mechanical stress concentration point where the lead leaves the generator can also cause failure.


Inadvertent mechanical damage to the attachment of the connector molding to the generator can result in leakage or even detachment of the molding.


Inadvertent mechanical damage to the attachment of the connector molding to the lead body, or of the terminal pin to the lead conductor, can result in leakage, an open-circuit condition, or even detachment of the terminal pin and/or molding.


The lead body can be cut inadvertently during surgery by a tool, or cut after surgery by repeated stress on a ligature used to hold the lead body in position. Repeated movement for hundreds of millions of cardiac cycles can cause lead conductor breakage or insulation damage anywhere along the lead body.


Although leads are available commercially in various lengths, in some conditions excess lead length in a patient exists and is to be managed. Usually the excess lead is coiled near the pulse generator. Repeated abrasion between the lead body and the generator due to lead coiling can result in insulation damage to the lead.


Friction of the lead against the clavicle and the first rib, known as subclavian crush, can result in damage to the lead.


In many applications, such as dual-chamber pacing, multiple leads can be implanted in the same patient and sometimes in the same vessel. Abrasion between the leads for hundreds of millions of cardiac cycles can cause insulation breakdown or even conductor failure.


Data stored in memory of implanted pulse generators is typically made available to a physician or other personnel for collection and/or analysis. For example, information is sought regarding system performance and trouble-shooting relating to the device, lead system, and/or patient in an acute, clinical setting. The information is generally supplied via a telemetry capability between the external programmer and the implanted device. In addition, an external programmer can be used to adjust parameters of multi-function implantable medical devices, such as pacing rate, pulse amplitude, sensed signal gain, and pulse timing and coordination.


Typically, an external programmer used during a telemetry procedure is positioned remotely from the patient. A programming head of the programmer such as a wand or other external device, containing an antenna or coil, is connected to the remainder of the programmer via a stretchable coil cable and is positioned over the patient's implanted device site for programming or telemetry interrogation of the implanted device.


Communication between the implanted medical device and the external programmer is facilitated by receiving and transmitting circuitry included within the implanted medical device and external programmer. Bandwidth is generally kept low to minimize power consumed by the implanted medical device. Power consumption is a consideration in designing implantable medical devices since the devices are typically powered by a depletable energy source, such as a primary battery. Replacement of an implanted medical device due to battery depletion can be costly and inconvenient.


Therefore, minimization of power consumption by the implanted medical device is a design and operational consideration. To facilitate power consumption management, transmitter and receiver circuitry can be powered down when not in use but are to be awakened when desired to enable communication. Awakening can occur periodically, in which the implantable device checks for a communication signal at regular intervals. The awakening process can otherwise be achieved by using electromagnetic energy coupled to the receiving antenna or coil to facilitate the wake up function. Awakening techniques result in a complicated telemetry protocol, which generally results in longer linkup times. In addition, the awakening techniques employ a relatively large antenna or coil, which is undesirable and inconsistent with a physically compact implanted medical device.


In addition to power reduction and small size, another design criterion for implanted medical devices is accurate communication of data. Communication often occurs in environments such as hospitals and doctors' offices, which can be noisy due to the presence of other electronic and electromagnetic sources. To achieve robustness of the link, bandwidth is generally kept low, with small packet sizes. To assure that data are transmitted accurately, the antenna or coil in the implantable device is typically positioned to maximize signal strength, both transmitted and received.


SUMMARY

According to an embodiment of a biostimulator system, one or more implantable devices and an external programmer are 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.





BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the invention relating to both structure and method of operation may best be understood by referring to the following description and accompanying drawings, in which similar reference characters denote similar elements throughout the several views:



FIGS. 1A and 1B are pictorial diagrams showing embodiments of biostimulator systems comprising two leadless cardiac pacemakers secured to internal and to exterior surfaces of the heart, respectively, and an external programmer and two surface electrodes;



FIG. 2 is a schematic block diagram depicting an embodiment of an external programmer that can be used in a biostimulator system and adapted to communicate via conductive techniques;



FIG. 3 is a time waveform graph showing a sample of modulated communication transmitted from an external programmer to a system of one or more leadless cardiac pacemakers;



FIG. 4 is a time waveform graph illustrating a conventional pacing pulse;



FIG. 5 is a time waveform graph depicting a pacing pulse adapted for communication as implemented for an embodiment of the illustrative pacing system;



FIG. 6 is a time waveform graph showing a sample series of pacing pulses in which information is encoded by altering the interval between individual pulses; and



FIGS. 7A through 7E are schematic flow charts depicting techniques that can be used in various embodiments of methods for communicating in an implantable biostimulator system.





DETAILED DESCRIPTION

An external programmer can be used with a system of one or more leadless cardiac pacemakers. Individual leadless cardiac pacemakers can be implanted adjacent to the inside or outside wall of a cardiac chamber. The programmer uses a minimum of two electrodes in electrical contact with the skin to communicate with each pacemaker through conduction. Information is passed from programmer to implant through a modulation technique designed to avoid stimulation of skeletal muscles. Communication from implant to programmer is performed by encoding information on the pacing pulses.


The programmer includes a user interface to display status and settings information for one or more individual implantable pacemakers, and enables the user to change programmable parameters on an individual implantable pacemaker. The programmer also can display the electrocardiogram sensed from the same two external electrodes on the skin. The programmer can perform tasks including electrocardiogram sensing, retrieving status information from implantable pacemakers, and changing configuration parameters of the implantable pacemakers simultaneously through the same set of electrodes.


Use of conducted communication of information improves over standard methods of communication in several aspects. For example, the illustrative conductive techniques enable communication without requiring a programmer head to be held undesirably close to the patient or to be held in a precise position relative to the implant site for an extended period of time. The illustrative conductive communication also enables power consumption to be reduced due to substantially lower current requirements and eliminating peak power demands currently imposed by existing inductive and radio frequency (RF) systems. Also, the conductive communication technique uses elements generally already existing in the implanted pulse generator, such as the therapeutic electrodes that function as an input-output device, enabling elimination of a coil or antenna that are conventionally used for communication and reducing complexity and component count significantly.


Referring to FIGS. 1A and 1B, schematic pictorial views depict embodiments of biostimulator systems 100A, 100B that communicate via conductive communication. The biostimulator systems 100A, 100B comprise one or more implantable devices 102 and an external programmer 104 configured for communicating with the one or more implantable devices 102 via bidirectional communication pathways comprising a receiving pathway that decodes information encoded on stimulation pulses generated by one or more of the implantable devices 102 and conducted through body tissue to the external programmer 104.


According to the illustrative arrangement, the bidirectional communication pathways can be configured for communication with multiple leadless cardiac pacemakers 102 via two or more electrodes 106 and conduction through body tissue.


In accordance with various biostimulator system embodiments, an external device or module 104 is connected by a communication transmission channel and has transmitting and receiving functional elements for a bidirectional exchange of information with one or more implanted medical devices 102. The communication channel includes two or more electrodes 106 which can be affixed or secured to the surface of the skin. From the point of the skin, the communication transmission channel is wireless, includes the ion medium of the intra- and extra-cellular body liquids, and enables electrolytic-galvanic coupling between the surface electrodes and the implantable modules 104.


In the biostimulator systems 100A, 100B, the bidirectional communication pathways can further comprise a transmitting pathway that passes information from the external programmer 104 to one or more of the implantable devices 102 by direct conduction through the body tissue by modulation that avoids skeletal muscle stimulation using modulated signals at a frequency in a range from approximately 10 kHz to 100 kHz.


Information transmitted from the external programmer 104 to the implanted devices 102 is conveyed by modulated signals at the approximate range of 10 kHz to 100 kHz which is a medium-high frequency. The signals are passed through the communication transmission channel by direct conduction. A modulated signal in the frequency range has a sufficiently high frequency to avoid any depolarization within the living body which would lead to activation of the skeletal muscles and discomfort to the patient. The frequency is also low enough to avoid causing problems with radiation, crosstalk, and excessive attenuation by body tissue. Thus, information may be communicated at any time, without regard to the heart cycle or other bodily processes. No restriction is imposed regarding location of electrode placement on the body because low signal attenuation enables the signal to travel throughout the body and to be received by the implanted devices 102.


In some embodiments, the bidirectional communication pathways can further comprise a receiving pathway including a low-pass filter adapted to separate the electrocardiogram from the information signals. The same surface electrodes 106 that are used to transmit the information through the communication channel may also be used to detect a patient's electrocardiogram. Electrocardiogram frequencies are generally between 1 and 100 Hz, far lower than the 10 kHz to 100 kHz range of frequencies used to transmit information through the communication transmission channel. Therefore, the electrocardiogram can be separated from the information signal by a low-pass filter and can optionally be displayed by the programmer 104. In addition to low-pass filtering, blanking techniques that are typical in processing of cardiac signals can be used when the communication channel is active to prevent noise or erroneous signals from the communication channel affecting the electrocardiogram channel.


Because a plurality of implantable devices 102 can be present, communication of information from the programmer is detected by all devices, enabling information to be sent to each implanted device without sending the same information multiple times.


In various embodiments and applications, the bidirectional communication pathways can further comprise a transmitting pathway that passes information from the programmer 104 to the one or more implantable devices 102 in a common communication event whereby information is sent to one or more target devices of the implantable devices 102 using a selected technique. For example, information specific to a single implantable device or a subset of implantable devices having a unique address can be assigned to the single implantable device or the subset of implantable devices and encoded in the information. In another technique, information can designate a specific function that is executed by a particular implantable device or a particular subset of implantable devices. The information is passed to one or more implantable devices without sending individual address information for activating execution by the particular implantable device or the particular subset of implantable devices alone. In another technique, information can designate a specific function that is executed by a particular implantable device or a particular subset of implantable devices that have programming specific to the function adapted to recognize the received information is relevant to the function.


Specifically, information that is specific to a single implanted device or a subset of devices can be sent. A unique address can be assigned to each device or subset. The address can be encoded in the information sent to the plurality of devices, and any individual device can make use only of information that matches either the address or the address of the subset to which the particular device belongs.


In another technique, if each implanted device 102 or subset of devices 102 serves a specific function, which is different from other implanted devices, then information may be passed to the specific device or subset without the additional overhead of a group or individual address. For example, the device or subset can be responsible for only a specific function. When the programmer transmits information to the entire group, but the information is relevant to only the device or subset of that group, then any devices that cannot make use of the information may ignore the information. Each device has unique programming specific to a particular function and can recognize whether received information is relevant to the function. Devices operative in conjunction with the technique can be non-generic and perform specific functions, or can be generic devices with general functionality that can be made more specific by programming. Accordingly, functionality of a device can be defined at manufacture or may be defined at implantation or thereafter. The function of each device can be defined at the time of manufacture and the devices labeled or marked such that the associated function can be known upon inspection.


In some embodiments, the one or more implantable devices 102 can comprise one or more leadless cardiac pacemakers that generate cardiac pacing pulses and encode information onto the generated cardiac pacing pulses by selective alteration of pacing pulse morphology that is benign to therapeutic effect and energy cost of the pacing pulse. The cardiac pacing pulses conduct into body tissue via the electrodes for antenna-less and telemetry coil-less communication. For information transmitted from the implanted leadless cardiac pacemaker 102 to the external programmer 104, a communication scheme can be used in which the information is encoded on the pacing pulse. The pulse morphology is altered to contain the encoded information without altering the therapeutic benefits of the pacing pulse. The energy delivered by the pacing pulse remains essentially the same after the information is encoded. The external programmer 104 receives the pacing pulses through the associated surface electrodes 106. Encoded information is drawn from the pacing pulses and can contain state information of the implantable leadless cardiac pacemaker, such as battery voltage, lead impedance, sensed electrocardiogram amplitude, pacemaker current drain, programmed parameters, or other parameters.


The leadless cardiac pacemaker or pacemakers 102 can be configured to detect a natural cardiac depolarization, time a selected delay interval, and deliver an information-encoded pulse during a refractory period following the natural cardiac depolarization. By encoding information in a pacing pulse, power consumed for transmitting information is not significantly greater than the power used for pacing. Information can be transmitted through the communication channel with no separate antenna or telemetry coil. Communication bandwidth is low with only a small number of bits encoded on each pulse.


In some embodiments, information can be encoded using a technique of gating the pacing pulse for very short periods of time at specific points in the pacing pulse. During the gated sections of the pulse, no current flows through the electrodes of a leadless cardiac pacemaker. Timing of the gated sections can be used to encode information. The specific length of a gated segment depends on the programmer's ability to detect the gated section. A certain amount of smoothing or low-pass filtering of the signal can be expected from capacitance inherent in the electrode/skin interface of the programmer as well as the electrode/tissue interface of the leadless cardiac pacemaker. A gated segment is set sufficiently long in duration to enable accurate detection by the programmer 104, limiting the amount of information that can be transmitted during a single pacing pulse. Accordingly, a technique for communication can comprise generating stimulation pulses on stimulating electrodes of an implanted biostimulator and encoding information onto generated stimulation pulses. Encoding information onto the pulses can comprise gating the stimulation pulses for selected durations at selected timed sections in the stimulation pulses whereby gating removes current flow through the stimulating electrodes and timing of the gated sections encodes the information.


Another method of encoding information on pacing pulses involves varying the timing between consecutive pacing pulses in a pulse sequence. Pacing pulses, unless inhibited or triggered, occur at predetermined intervals. The interval between any two pulses can be varied slightly to impart information on the pulse series. The amount of information, in bits, is determined by the time resolution of the pulse shift. The steps of pulse shifting are generally on the order of microseconds. Shifting pulses by up to several milliseconds does not have an effect on the pacing therapy and cannot be sensed by the patient, yet significant information can be transmitted by varying pulse intervals within the microsecond range. The method of encoding information in variation of pulses is less effective if many of the pulses are inhibited or triggered. Accordingly, a technique for communication can comprise generating stimulation pulses on stimulating electrodes of an implanted biostimulator and encoding information onto generated stimulation pulses comprising selectively varying timing between consecutive stimulation pulses.


Alternatively or in addition to encoding information in gated sections and/or pulse interval, overall pacing pulse width can be used to encode information.


The three described methods of encoding information on pacing pulses can use the programmer 104 to distinguish pacing pulses from the patient's normal electrocardiogram, for example by recognition of the specific morphology of the pacing pulse compared to the R-wave generated during the cardiac cycle. For example, the external programmer 104 can be adapted to distinguish a generated cardiac pacing pulse from a natural cardiac depolarization in an electrocardiogram by performing comparative pattern recognition of a pacing pulse and an R-wave produced during a cardiac cycle.


The illustrative external programmer 104 and associated operating methods or techniques enable presentation to the user of information gathered from the implanted biostimulator or leadless cardiac pacemakers 102 using conductive communication. Some of the information to be presented may include battery voltage, lead impedance, electrocardiogram amplitude, or current drain of the device. The information can be presented in addition to other information such as parameters to be set and programmed into the leadless cardiac pacemaker. The information can be presented to a user on a display screen. Some embodiments or configurations of an external programmer 104 can include a secondary link, for example either wireless or through a cable, to another display device, such as a handheld computer or terminal. The secondary link can also include communication over a local area network or the internet for display at a remote terminal.



FIG. 1A depicts a sample configuration involving the external programmer 104 and two endocardially implanted leadless cardiac pacemakers 102. The external programmer 104 is physically connected to the skin surface via two electrodes 106, which serve three functions. First, the electrodes 106 transmit encoded information from the programmer 104 to the implanted leadless cardiac pacemakers 102 using a modulated signal at a medium frequency 10 kHz to 100 kHz. Second, the electrodes 106 receive information from individual leadless cardiac pacemakers 102 by detecting encoded information in the pacing pulses of the leadless cardiac pacemakers 102. Third, the electrodes 106 receive surface electrocardiogram for display and analysis by the programmer 104.


In FIG. 1A, the two leadless cardiac pacemakers 102 are implanted endocardially. Thus, in a biostimulator system 100A or 100B an implantable device 102 may comprise one or more leadless cardiac pacemakers that can be implanted adjacent to an inside or an outside wall of a cardiac chamber. Referring to FIG. 1B, a similar system is represented with a difference that the two leadless cardiac pacemakers 102 are implanted by affixing to the exterior surface of the heart. The electrodes 106 and programmer 104 function similarly in arrangements shown in FIGS. 1A and 1B whether the leadless cardiac pacemakers 102 are implanted endocardially or epicardially (on the external heart surface). No restriction is imposed that the leadless cardiac pacemakers are all implanted inside or all implanted outside the heart. One or more may be implanted endocardially along with others implanted on the outer surface of the heart. The functioning of the programmer 104 is substantially the same. Although two electrodes 106 are shown in FIGS. 1A and 1B, two is generally the minimum number for adequate conductive communication. More electrodes can be used, enabling an electrocardiogram (ECG) to be sensed at multiple vectors for better analysis. More than two electrodes also enable a choice of vectors for conducted communication with the leadless cardiac pacemakers, thereby maximizing the signal to noise ratio of the system. FIGS. 1A and 1B each depict two leadless cardiac pacemakers 102. One, two, or more leadless cardiac pacemakers can be implanted, depending on the number of pacemakers appropriate for effective therapy.


In various embodiments, the external programmer 104 can be configured to perform one or more operations such as electrocardiogram sensing, retrieving status information from implanted pacemakers, modifying configuration parameters of multiple implanted pacemakers simultaneously in information passed through a common electrode set, displaying electrocardiograms, displaying information received from the at least one implantable device, and others.


In various embodiments, a pacemaker 102 can manage power consumption to draw limited power from an internal battery, thereby reducing device volume. Each circuit in the pacemaker can be designed to avoid large peak currents. For example, cardiac pacing can be achieved by discharging a tank capacitor (not shown) across the pacing electrodes. Recharging of the tank capacitor is typically controlled by a charge pump circuit. In a particular embodiment, the charge pump circuit can be throttled to recharge the tank capacitor at constant power from the battery. The one or more leadless cardiac pacemakers can be configured to charge the tank capacitor in preparation for stimulation pulse generation, time one or more windows between pulse generation, disable charging of the tank capacitor during the one or more timed windows, and enable a receive amplifier in the implanted biostimulator while the tank capacitor is disabled.


In some embodiments, the external programmer 104 can detect a stimulation pulse from a leadless cardiac pacemaker 102 and transmit data after a selected delay to coincide with a window that the leadless cardiac pacemaker's receiving amplifier is enabled.


The implantable devices 102 can encode and/or decode information using various techniques such as encoding the information using pacing pulse width, binary-coded notches in a pacing pulse, modulation of off-time between pacing pulses, or other suitable encoding techniques. The external programmer 104 can encode and/or decode information using on-off keying encoding and modulation techniques depicted in FIG. 3. However, any other appropriate method can be used whereby a modulated bit-stream can be generated at a medium high frequency, for example frequency-shift keying, frequency modulation, or amplitude shift keying.


Referring to FIG. 2, a schematic block diagram shows an embodiment of an external programmer 204 adapted for communicating with an implanted biostimulator system using conducted communication. The external programmer 204 comprises an interface 208 configured for coupling to at least two electrodes 206 that make electrical contact with body skin for communicating with one or more implanted biostimulators. The external programmer 204 further comprises bidirectional communication pathways 210R and 210T coupled to the interface 208 and configured for bidirectional communication with the one or more implanted biostimulators. The communication pathways comprise a receiving pathway 210R that decodes information encoded on stimulation pulses generated by the one or more implanted biostimulators and conducted through body tissue.


The bidirectional communication pathways 210R and 210T are configured for communication with one or more leadless cardiac pacemakers via the electrodes 206 and conduction through body tissue.


The external programmer 204 can have bidirectional communication pathways 210R and 210T that further comprise a transmitting pathway 210T that passes information from the programmer 204 to one or more implanted biostimulators by conduction through the body tissue using modulation that avoids skeletal muscle stimulation.


In some arrangements, the bidirectional communication pathways 210R and 210T can be further specified to comprise a transmitting pathway that passes information from the programmer 204 to the one or more implanted biostimulators by direct conduction using modulated signals at a frequency in a range from approximately 10 kHz to 100 kHz. Also in some arrangements, the two or more electrodes 206 and the bidirectional communication pathways 210R and 210T can be configured for bidirectional information signal communication and for sensing an electrocardiogram.


Also in some embodiments, the bidirectional communication pathways 210R and 210T can further comprise a transmitting pathway 210T that passes information from the programmer 204 to multiple implanted devices in a common communication event. In some embodiments or selected operating conditions, the transmitting pathway 210T can be arranged to pass information from the programmer 204 to multiple implanted devices in a common communication event whereby information specific to a single implanted device or a subset of implanted devices have a unique address assigned to the single implanted device or the subset of implanted devices and encoded in the information. The transmitting pathway 210T can also be arranged to pass information from the programmer 204 to multiple implanted devices in a common communication event whereby information designates a specific function that is executed by a particular implanted device or a particular subset of implanted devices. The information is passed to the multiple implanted devices without individual address information for activating execution by the particular implanted device or the particular subset of implanted devices alone. The transmitting pathway 210T can also be arranged, either alone or in combination with other techniques, to pass information from the programmer 204 to multiple implanted devices in a common communication event whereby information designates a specific function that is executed by a particular implanted device or a particular subset of implanted devices that comprise programming specific to the function adapted to recognize the received information is relevant to the function.


In the illustrative embodiment, the bidirectional communication pathways 210R and 210T comprise the two or more electrodes 206 forming a conductive communication path between the programmer 204 and the skin surface, and a transmitting pathway 210T. The transmitting pathway 210T comprises a processor 212, a command/message encoder 230, a modulator 232, and an amplifier 236. The processor 212 is configured to communicate information to one or more implanted leadless cardiac pacemakers. The command/message encoder 230 is coupled to the processor 212 via a parallel interface and configured to encode and serialize data into a bit stream. Information encoding can be selected from encoding techniques such as on-off keying, frequency-shift keying, frequency modulation, and amplitude shift keying. The modulator 232 is coupled to the command/message encoder 230 and receives and modulates the serialized data using a frequency in a range from approximately 10 kHz to approximately 100 kHz. The amplifier 236 is coupled to the modulator 232 and increases signal amplitude to a level suitable for robust conducted communication.


The bidirectional communication pathways 210R and 210T further comprise a receiving pathway 210R including a low-pass filter 214 adapted to separate the electrocardiogram from the information signals.


In various embodiments and arrangements, the bidirectional communication pathways 210R and 210T further comprise a receiving pathway 210R that receives information at the programmer 204 from the one or more implanted biostimulators by conduction through the body tissue. The receiving pathway 210R can decode information, for example by decoding data that is encoded by the biostimulators using pacing pulse width, using binary-coded notches in a pacing pulse, using modulation of off-time between pacing pulses, or other suitable techniques for encoding data in the biostimulators.


In the illustrative embodiment, the bidirectional communication pathways 210R and 210T couple to the two or more electrodes 206 forming a conductive communication path between the programmer 204 and the skin surface, and a receiving pathway 210R. The receiving pathway 210R comprises an electrocardiogram (ECG) amplifier/filter 214, an analog-to-digital converter (ADC) which is not shown in FIG. 2, and the processor 212. The electrocardiogram (ECG) amplifier/filter 214 includes a differential band-pass amplifier configured to select and amplify signals in a frequency range from approximately 1 Hz to approximately 100 Hz. The analog-to-digital converter (ADC) is configured to digitize the filtered and amplified signal. The processor 212 is coupled to the ADC and configured to receive and optionally display ECG data, and configured to decode information encoded into cardiac pacing pulses.


The programmer 204 may further comprise a processor 212 coupled to the bidirectional communication pathways and configured to manage communication with one or more biostimulators, for example leadless cardiac pacemakers. Leadless cardiac pacemakers can be implanted adjacent to an inside or an outside wall of a cardiac chamber as depicted in FIGS. 1A and 1B.


As depicted in FIG. 2, external electrodes 206 enable a conductive communication path between the programmer 204 and the skin surface. Electrocardiogram (ECG) signals enter an ECG amplifier/filter 214, which can include a differential band-pass amplifier. In general, an ECG signal has spectral components in a range between 1 Hz and 100 Hz. Band-pass filter poles for the ECG amplifier/filter 214 can be selected such that sufficient signal energy is passed within the 1 Hz to 100 Hz range, while filtering other signals that are not associated with cardiac activity. The ECG signal can be amplified and digitized using an analog-to-digital converter (ADC). Once digitized, the signal is passed to the processor, for example central processing unit (CPU) 212.


In some embodiments, the electrodes 206 can be implemented with more than two electrodes to enable an electrocardiogram (ECG) to be sensed at multiple vectors and further to enable selection from among the multiple vectors for conducted communication with implanted leadless cardiac pacemakers so that system signal-to-noise ratio can be improved or maximized.


The CPU 212 receives and optionally displays ECG data using a display interface 216 and can also display other data acquired from the implanted leadless cardiac pacemaker acquired through the encoded pacing pulses, such as battery voltage, lead impedance, sensed cardiac signal amplitude, or other system status information. The CPU 212 also can accept input from a user via a keyboard and/or touch-screen interface 218. Some examples of user input are selected pacing rate or pacing pulse amplitude for implanted leadless cardiac pacemakers. The CPU 212 can also communicate over a network interface 220 to other data entry or display units, such as a handheld computer or laptop/desktop unit. The network interface 220 can be cabled or wireless and can also enable communication to a local area network or the internet for greater connectivity.


The processor 212 is coupled to the bidirectional communication pathways and configured to perform one or more of various operations such as electrocardiogram sensing, retrieving status information from implanted pacemakers, modifying configuration parameters of multiple implanted pacemakers within a single or multiple cardiac cycles in information passed through a common electrode set, and other operations. A display interface 216 coupled to the processor 212 can be configured to display an electrocardiogram sensed from the electrodes 206. In some arrangements or embodiments, a secondary link 220 can be coupled to the processor 212 and configured for unidirectional or bidirectional wireless or cable transmission to and/or from a remote display and/or data-entry device to display an electrocardiogram sensed from the at least two electrodes, and/or to control the programmer and/or at least one implanted biostimulator.


The CPU 212 can execute operations based on firmware stored in non-volatile memory (Flash) 222. The non-volatile memory 222 can also be used to store parameters or values that are to be maintained when power is removed. The CPU 212 uses volatile memory or random access memory (RAM) 224 as general storage for information such as ECG data, status information, swap memory, and other data. A battery and supply regulator 226 gives a constant voltage supply to the programmer 204 during normal operation. A clock module 228 generates a system clock signal used by the CPU 212 and by interface blocks for timing.


The CPU 212, during operation to communicate information to one or more implanted leadless cardiac pacemakers, sends the information over a parallel interface to a command/message encoder 230, which serializes the data into a bit stream. Serialized data is sent to a modulator 232. The serialized bit-stream is modulated, for example using a frequency between 10 kHz and 100 kHz. An optional separate modulator clock 234 supplies a timing signal at a selected carrier frequency that may be used by the modulator 232. An amplifier 236 sets signal amplitude to a level that enables robust conducted communication. A sample of a modulated bit-steam is shown in FIG. 3 wherein logic high is shown as a medium high frequency sine wave. An encoding and modulation technique depicted in FIG. 3 is on-off keying. However, any other appropriate method whereby a modulated bit-stream can be generated at a medium high frequency may be used, for example frequency shift keying, frequency modulation, or amplitude shift keying.


Because multiple biostimulator devices can be implanted, communication of information from the programmer 204 can be detected by all devices, enabling information to be sent to each implanted device without sending the same information multiple times.


If information for communication is specific to a single implanted device or a subset of devices, a unique address can be assigned to each device or subset. The address is encoded in the information sent to the plurality of devices, and any individual device can have the option to make use of information that either matches the address or the address of the subset to which the particular device belongs.


If each implanted device or a subset of devices performs a specific function which is different from other implanted devices, then information can be passed to the specific device or subset without the additional overhead of a group or individual address. For example, when the device or subset is responsible for only a specific function. When the programmer 204 transmits information to the entire group, but the information is relevant to only the device or subset of that group, then any devices that cannot make use of the information may ignore the information as superfluous. The technique presumes that each device have unique programming specific to the associated function, and each device have capability to recognize whether or not received information is relevant to the function. Devices using the illustrative technique are not generic. The function of each device can be defined at the time of manufacture or at the time of implant or thereafter. The devices are labeled or marked such that the associated function can be known upon inspection.


To reduce the peak current for operation of the leadless cardiac pacemakers, a technique can be used in which a window or multiple windows occur between subsequent pacing pulses during which the leadless cardiac pacemaker does not charge pacing tank capacitor in preparation for the next pacing pulse. Instead the pacemaker enables an internal receiving amplifier. Because the programmer 204 can sense pacing pulses from the implanted devices, the programmer 204 can time data transmission to coincide with the pre-defined synchronous window or windows. A reduced peak current capability occurs because the charger and receiving amplifier, both power intensive elements, never have to be operated together. Because the data transmission is generally very short compared to the period between pacing pulses, the window technique should not significantly lower the ability of the leadless cardiac pacemaker to charge the pacing tank capacitor effectively between pacing pulses.


Referring again to FIG. 2, data acquired by the programmer 204 from a specific implanted leadless cardiac pacemaker is received at the surface electrodes 206 and passes to an amplifier/filter 240, which functions to remove noise from the incoming signal. Any filtering performed by the amplifier/filter 240 is designed to leave encoded pulses intact as much as possible. A message decoder 238 determines whether the received signal is actually a pacing pulse or another signal, such as a cardiac R-wave.



FIG. 4 shows a sample pacing pulse, for example a typical output-pulse waveform for a conventional pacemaker. The approximately-exponential decay is due to discharge of a capacitor in the pacemaker through the approximately-resistive load presented by the electrodes/tissue interface and leads. Typically the generator output is capacitor-coupled to one electrode to ensure net charge balance. The pulse duration is shown as T0 and is typically 500 microseconds. When the pacemaker 102 is supplying a pacing pulse but is not sending data for communication, the waveform can resemble that shown in FIG. 4.


To encode data on the pacing pulse, specific portions of the pulse are gated. Timing of the gated segments defines the specific data carried by the pacing pulse. FIG. 5 is a time waveform graph showing a sample output-pulse waveform of the illustrative pacemaker that communicates signals using conduction during a time when the pacemaker is sending data for communication and also delivering a pacing pulse.



FIG. 5 shows that the pulse generator 102 has divided the output pulse into shorter pulses 501, 502, 503, 504; separated by notches 505, 506, and 507. The pulse generator 102 times the notches 505, 506, and 507 to fall in timing windows W1, W2, and W4 designated 508, 509, and 511 respectively. Note that the pacemaker 102 does not form a notch in timing window W3 designated 510. The timing windows are each shown separated by a time T1, approximately 100 microseconds in the example.


As controlled by a processor in a leadless cardiac pacemaker 102, a pulse generator in the pacemaker selectively generates or does not generate a notch in each timing window 508, 509, 510, and 511 so that the device 102 encodes four bits of information in the pacing pulse. A similar scheme with more or fewer timing windows can send more or fewer bits per pacing pulse. The width of the notches is small, for example approximately 15 microseconds, so that the delivered charge and overall pulse width, specifically the sum of the widths of the shorter pulses, in the pacing pulse is substantially unchanged from that shown in FIG. 4. Accordingly, the pulse shown in FIG. 5 can have approximately the same pacing effectiveness as that shown in FIG. 4, according to the law of Lapique which is well known in the art of electrical stimulation.


In a leadless cardiac pacemaker, a technique can be used to conserve power when detecting information carried on pacing pulses from other implanted devices. The leadless cardiac pacemaker can have a receiving amplifier that implements multiple gain settings and uses a low-gain setting for normal operation. The low-gain setting could be insufficiently sensitive to decode gated information on a pacing pulse accurately but could detect whether the pacing pulse is present. If an edge of a pacing pulse is detected during low-gain operation, the amplifier can be switched quickly to the high-gain setting, enabling the detailed encoded data to be detected and decoded accurately. Once the pacing pulse has ended, the receiving amplifier can be set back to the low-gain setting. For usage in the decoding operation, the receiving amplifier is configured to shift to the more accurate high-gain setting quickly when activated. Encoded data can be placed at the end of the pacing pulse to allow a maximum amount of time to invoke the high-gain setting.


As an alternative or in addition to using notches in the stimulation pulse, the pulses can be generated with varying off-times, specifically times between pulses during which no stimulation occurs. The variation of off-times can be small, for example less than 10 milliseconds total, and can impart information based on the difference between a specific pulse's off-time and a preprogrammed off-time based on desired heart rate. For example, the device can impart four bits of information with each pulse by defining 16 off-times centered on the preprogrammed off-time. FIG. 6 is a graph showing a sample pulse generator output which incorporates a varying off-time scheme. In the figure, time Tp represents the preprogrammed pulse timing. Time Td is the delta time associated with a single bit resolution for the data sent by the pulse generator. The number of Td time increments before or after the moment specified by Tp gives the specific data element transmitted. The receiver of the pulse generator's communication has advance information of the time Tp. The communication scheme is primarily applicable to overdrive pacing in which time Tp is not dynamically changing or altered based on detected beats.



FIG. 6 shows the technique of conveying information by modulating the off-time between pacing pulses. Alternatively or in addition to the two illustrative coding schemes, overall pacing pulse width can be used to impart information. For example, a paced atrial beat may exhibit a pulse width of 500 microseconds and an intrinsic atrial contraction can be identified by reducing the pulse width by 30 microseconds. Information can be encoded by the absolute pacing pulse width or relative shift in pulse width. Variations in pacing pulse width can be relatively small and have no impact on pacing effectiveness.


The illustrative example avoids usage of radiofrequency (RF) communication to send pacing instructions to remote electrodes on a beat-to-beat basis to cause the remote electrodes to emit a pacing pulse. RF communication involves use of an antenna and modulation/demodulation unit in the remote electrode, which increase implant size significantly. Also, communication of pacing instructions on a beat-to-beat basis increases power requirements for the main body and the remote electrode. In contrast, the illustrative system and stimulator do not require beat-to-beat communication with any controlling main body.


The illustrative leadless pacemaker 102 includes an internal power source that can supply all energy for operations and pulse generation. In contrast, some conventional implanted pulse generators have remote pacing electrodes that receive some or all energy from an energy source through an RF induction technique, an energy transfer scheme that employs a large loop antenna on the remote electrode which increases size significantly. In addition, energy transfer with the RF induction technique is inefficient and is associated with a significant increase in battery size of the energy source. In contrast, the illustrative leadless pacemaker 102 uses an internal battery and does not require energy to be drawn from outside sources. Also in the conventional system, the energy source receives sensing information by RF communication from the remote electrodes and sends pacing instructions to the electrodes on a beat-to-beat basis in a configuration that uses an addressing scheme in which the identity of specific remote pacing electrodes is stored in the energy source memory. The conventional method can also be inefficient due to overhead for transmitting an identification number from/to a generic pacing electrode at implant and/or during sensing. The illustrative leadless pacemaker 102 avoids such overhead through a structure in which pulse generation functionality is independent within a single implantable body.


Another conventional technology uses a system of addressable remote electrodes that stimulate body tissue without requiring a main body to send commands for individual stimulations. The remote electrodes are specified to be of a size and shape suitable for injection rather than for endocardial implantation. A controller sets operating parameters and sends the parameters to remote electrodes by addressable communication, enabling the remote electrodes function relatively autonomously while incurring some overhead to controller operations. However, the remote electrodes do not sense or monitor cardiac information and rely on the main body to provide sensing functionality. In contrast, the illustrative leadless pacemaker 102 combines pacing and sensing of intrinsic cardiac activity in a single implantable body.


To ensure the leadless cardiac pacemaker functions correctly, a specific minimum internal supply voltage is maintained. When pacing tank capacitor charging occurs, the supply voltage can drop from a pre-charging level which can become more significant when the battery nears an end-of-life condition and has reduced current sourcing capability. Therefore, a leadless cardiac pacemaker can be constructed with a capability to stop charging the pacing tank capacitor when the supply voltage drops below a specified level. When charging ceases, the supply voltage returns to the value prior to the beginning of tank capacitor charging.


In another technique, the charge current can be lowered to prevent the supply voltage from dropping below the specified level. However, lowering the charge current can create difficulty in ensuring pacing rate or pacing pulse amplitude are maintained, since the lower charge current can extend the time for the pacing tank capacitor to reach a target voltage level.


Schemes can be implemented for transmitting data from the implant to the programmer that do not significantly increase the current consumption of the pacemaker. For example, the pacemaker could transmit data continuously in a loop, with no consumption penalty.


The method of encoding data using modulation of off-time between pacing pulses is less effective if pulses are inhibited, since data can be transmitted using only pacing pulses generated by the pacemaker. When data are encoded in binary-coded notches in the pacing pulse or by varying pacing pulse width, if a therapeutic pacing pulse is inhibited, then the leadless cardiac pacemaker can still generate a non-therapeutic pulse during the refractory period of the heart after the sensed beat, although the pacing pulse has the sole purpose of transmitting data to the programmer or optionally to at least one other implanted biostimulator.


Referring to FIGS. 7A through 7E, schematic flow charts depict techniques that can be used in various embodiments of methods for communicating in an implantable biostimulator system. According to FIG. 7A, an illustrative method 700 comprises monitoring 702, at an external programmer, electrical signals conducted through body tissue to body surface electrodes and detecting 704 pulses generated by a body-implanted biostimulator. The external pacemaker decodes 706 information encoded into the generated pulse by the body-implanted biostimulator.


Referring to FIG. 7B, a method 710 can further comprise generating 712 cardiac pacing pulses at an implanted leadless cardiac pacemaker. Information is encoded 714 onto generated cardiac pacing pulses at the implanted leadless cardiac pacemaker by selective alteration of pacing pulse morphology that is benign to therapeutic effect and energy cost of the pacing pulse. In various embodiments, the implanted leadless cardiac pacemaker can encode the information using one or more techniques such as encoding using pacing pulse width, using binary-coded notches in a pacing pulse, and using modulation of off-time between pacing pulses. The cardiac pacing pulses are conducted 716 into body tissue via electrodes for antenna-less and telemetry coil-less communication. The information encoded onto generated cardiac pacing pulses can include pacemaker state information, battery voltage, lead impedance, sensed cardiac signal amplitude, pacemaker current drain, programmed parameters, and the like.


Referring to FIG. 7C, a method 720 can further comprise generating 722 cardiac pacing pulses at an implanted leadless cardiac pacemaker and encoding 724 information onto generated cardiac pacing pulses at the implanted leadless cardiac pacemaker by selective alteration of pacing pulse morphology that is benign to therapeutic effect and energy cost of the pacing pulse. The implanted leadless cardiac pacemaker detects 726 a natural cardiac depolarization and inhibits 728 cardiac pacing pulse delivery with delay for delivery during a refractory period following the natural cardiac depolarization. The cardiac pacing pulses are conducted 730 into body tissue via electrodes for antenna-less and telemetry coil-less communication.


Referring to FIG. 7D, various embodiments of a method 740 can comprise charging 742 a tank capacitor in preparation for stimulation pulse generation. Stimulation pulses are generated 744 on stimulating electrodes of an implanted biostimulator and information encoded 746 onto generated stimulation pulses. One or more windows can be timed 748 between pulse generations. Charging of the tank capacitor is disabled 750 during the one or more timed windows and a receiving amplifier in the implanted biostimulator is enabled 752 while the tank capacitor is disabled. The external programmer senses 754 the stimulation pulses generated by the implanted biostimulator and transmits 756 information from the external programmer to the implanted biostimulator to coincide with the one or more timed windows. For example, the external programmer can detect a stimulation pulse from the implanted biostimulator, time a selected delay interval, and transmit data after the selected delay to coincide with a window that the implanted biostimulator's receive amplifier is enabled.


Referring to FIG. 7E, various embodiments of a method 760 can comprise physically connecting 762 the external programmer to a body surface via two or more body surface electrodes and communicating 764 information among the external programmer and one or more implanted leadless cardiac pacemakers. Encoded information is transmitted 766 from the external programmer to the implanted leadless cardiac pacemakers via the body surface electrodes using a modulated signal at a frequency in a range of approximately 10 kHz to approximately 100 kHz. The external programmer receives 768 the information via the body surface electrodes from one or more of the implanted leadless cardiac pacemakers by detecting information encoded into generated pacing pulses. The external programmer can also receive 770 a surface electrocardiogram via the body surface electrodes for display and analysis.


Terms “substantially”, “essentially”, or “approximately”, that may be used herein, relate to an industry-accepted tolerance to the corresponding term. Such an industry-accepted tolerance ranges from less than one percent to twenty percent and corresponds to, but is not limited to, component values, integrated circuit process variations, temperature variations, rise and fall times, and/or thermal noise. The term “coupled”, as may be used herein, includes direct coupling and indirect coupling via another component, element, circuit, or module where, for indirect coupling, the intervening component, element, circuit, or module does not modify the information of a signal but may adjust its current level, voltage level, and/or power level. Inferred coupling, for example where one element is coupled to another element by inference, includes direct and indirect coupling between two elements in the same manner as “coupled”.


While the present disclosure describes various embodiments, these embodiments are to be understood as illustrative and do not limit the claim scope. Many variations, modifications, additions and improvements of the described embodiments are possible. For example, those having ordinary skill in the art will readily implement the steps necessary to provide the structures and methods disclosed herein, and will understand that the process parameters, materials, and dimensions are given by way of example only. The parameters, materials, and dimensions can be varied to achieve the desired structure as well as modifications, which are within the scope of the claims. Variations and modifications of the embodiments disclosed herein may also be made while remaining within the scope of the following claims. Phraseology and terminology employed herein are for the purpose of the description and should not be regarded as limiting. With respect to the description, optimum dimensional relationships for the component parts are to include variations in size, materials, shape, form, function and manner of operation, assembly and use that are deemed readily apparent and obvious to one of ordinary skill in the art and all equivalent relationships to those illustrated in the drawings and described in the specification are intended to be encompassed by the present description. Therefore, the foregoing is considered as illustrative only of the principles of structure and operation. Numerous modifications and changes will readily occur to those of ordinary skill in the art whereby the scope is not limited to the exact construction and operation shown and described, and accordingly, all suitable modifications and equivalents may be included.

Claims
  • 1. An external programmer adapted for communicating with an implanted biostimulator system comprising: an interface configured for coupling to at least two electrodes adapted to make electrical contact with body skin for communicating with at least one implanted biostimulator;bidirectional communication pathways coupled to the interface configured for bidirectional communication with the at least one implanted biostimulator and comprising a receiving pathway and a processor configured to sense an electrocardiogram with the at least two electrodes and to decode information encoded on pulses generated by the at least one implanted biostimulator and conducted through body tissue and received by the receiving pathway with the at least two electrodes.
  • 2. The programmer according to claim 1 wherein: the bidirectional communication pathways further comprise a transmitting pathway, the processor being further configured to pass information from the transmitting pathway and the at least two electrodes to the at least one implanted biostimulator by conduction through the body tissue by modulation that avoids skeletal muscle stimulation.
  • 3. The programmer according to claim 1 wherein the processor is further configured to manage communication with at least one leadless cardiac pacemaker.
  • 4. The programmer according to claim 1 wherein the processor is further configured to manage communication with at least one leadless cardiac pacemaker implanted adjacent to an inside or an outside wall of a cardiac chamber.
  • 5. The programmer according the claim 1 wherein the processor is further configured to perform at least one operation of operations comprising retrieving status information from implanted pacemakers, and modifying configuration parameters of multiple implanted pacemakers within a single or multiple cardiac cycles in information passed through the at least two electrodes; and the programmer further comprising a display interface coupled to the processor and configured to display an electrocardiogram sensed from the at least two electrodes.
  • 6. The programmer according to claim 1 wherein the processor is further configured to perform at least one operation of operations comprising retrieving status information from implanted pacemakers, and modifying configuration parameters of multiple implanted pacemakers within a single or multiple cardiac cycles in information passed through the at least two electrodes; and the programmer further comprising a secondary link coupled to the processor and configured for wireless or cable transmission to a remote display device to display an electrocardiogram sensed from the at least two electrodes.
  • 7. The programmer according to claim 1 further comprising: the bidirectional communication pathways configured for communication with a plurality of leadless cardiac pacemakers via the at least two electrodes and conduction through body tissue.
  • 8. The programmer according to claim 1 further comprising: the bidirectional communication pathways further comprising a transmitting pathway that passes information from the programmer to the at least one implanted biostimulator by direct conduction using modulated signals at a frequency in a range from approximately 10 kHz to 100 kHz.
  • 9. The programmer according to claim 1 further comprising: the at least two electrodes and the bidirectional communication pathways configured for bidirectional information signal communication, the bidirectional communication pathways comprising a receiving pathway including a low-pass filter adapted to separate the electrocardiogram signals from information signals.
  • 10. The programmer according to claim 1 further comprising: the at least two electrodes and the bidirectional communication pathways configured for bidirectional information signal communication, the receiving pathway including a low-pass filter adapted to separate electrocardiogram signals from information signals and a blanking controller configured to blank noise and unwanted signals from electrocardiogram signals when the communication channel is active.
  • 11. The programmer according to claim 1 wherein: the at least two electrodes comprise more than two electrodes enabling the electrocardiogram (ECG) to be sensed at multiple vectors and selection from among the multiple vectors for conducted communication with the at least one leadless cardiac pacemaker whereby system signal-to-noise ratio can be maximized.
  • 12. The programmer according to claim 1 further comprising: the bidirectional communication pathways further comprising a transmitting pathway that passes information from the programmer to a plurality of implanted devices in a common communication event.
  • 13. The programmer according to claim 1 further comprising: the bidirectional communication pathways further comprising a transmitting pathway that passes information from the programmer to a plurality of implanted devices in a common communication event whereby information specific to a single implanted device or a subset of implanted devices have a unique address assigned to the single implanted device or the subset of implanted devices and encoded in the information.
  • 14. The programmer according to claim 1 further comprising: the bidirectional communication pathways further comprising a transmitting pathway that passes information from the programmer to a plurality of implanted devices in a common communication event whereby information designates a specific function that is executed by a particular implanted device or a particular subset of implanted devices, the information being passed to the implanted device plurality without individual address information for activating execution by the particular implanted device or the particular subset of implanted devices alone.
  • 15. The programmer according to claim 1 further comprising: the bidirectional communication pathways further comprising a transmitting pathway that passes information from the programmer to a plurality of implanted devices in a common communication event whereby information designates a specific function that is executed by a particular implanted device or a particular subset of implanted devices that comprise programming specific to the function adapted to recognize the received information is relevant to the function.
  • 16. The programmer according to claim 1 further comprising: the at least two electrodes forming a conductive communication path between the programmer and a skin surface; andthe receiving pathway comprising: an electrocardiogram (ECG) amplifier/filter comprising a differential band-pass amplifier configured to select and amplify signals in a frequency range from approximately 1 Hz to approximately 100 Hz;an analog-to-digital converter (ADC) configured to digitize the filtered and amplified signal; andthe processor coupled to the ADC and configured to receive and optionally display ECG data.
  • 17. The programmer according to claim 1 further comprising: the at least two electrodes forming a conductive communication path between the programmer and a skin surface; andthe bidirectional communication pathways further comprising a transmitting pathway comprising: a processor configured to communicate information to at least one implanted leadless cardiac pacemaker;a command/message encoder coupled to the processor and configured to encode and serialize data into a bit stream, the encoding being selected from a group of encoding techniques consisting of on-off keying, frequency-shift keying, frequency modulation, and amplitude shift keying;a modulator coupled to the command/message encoder that receives and modulates the serialized data using a frequency in a range from approximately 10 kHz to approximately 100 kHz; andan amplifier coupled to the modulator that increases signal amplitude to a level suitable for robust conducted communication.
  • 18. The programmer according to claim 1 further comprising: the receiving pathway that decodes information encoded using pulse width.
  • 19. The programmer according to claim 1 further comprising: the receiving pathway configured to decode information encoded using binary-coded notches in a pulse.
  • 20. The programmer according to claim 1 further comprising: the receiving pathway configured to decode information encoded using modulation of off-time between pulses.
CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority to and incorporates herein by reference in its entirety for all purposes, Provisional U.S. Patent Application Nos. 60/726,706 entitled “LEADLESS CARDIAC PACEMAKER WITH CONDUCTED COMMUNICATION,” filed Oct. 14, 2005; 60/761,531 entitled “LEADLESS CARDIAC PACEMAKER DELIVERY SYSTEM,” filed Jan. 24, 2006; 60/729,671 entitled “LEADLESS CARDIAC PACEMAKER TRIGGERED BY CONDUCTED COMMUNICATION,” filed Oct. 24, 2005; 60/737,296 entitled “SYSTEM OF LEADLESS CARDIAC PACEMAKERS WITH CONDUCTED COMMUNICATION,” filed Nov. 16, 2005; 60/739,901 entitled “LEADLESS CARDIAC PACEMAKERS WITH CONDUCTED COMMUNICATION FOR USE WITH AN IMPLANTABLE CARDIOVERTER-DEFIBRILLATOR,” filed Nov. 26, 2005; 60/749,017 entitled “LEADLESS CARDIAC PACEMAKER WITH CONDUCTED COMMUNICATION AND RATE RESPONSIVE PACING,” filed Dec. 10, 2005; and 60/761,740 entitled “PROGRAMMER FOR A SYSTEM OF LEADLESS CARDIAC PACEMAKERS WITH CONDUCTED COMMUNICATION,” filed Jan. 24, 2006; all by Peter M. Jacobson.

US Referenced Citations (472)
Number Name Date Kind
3199508 Roth Aug 1965 A
3212496 Preston Oct 1965 A
3218638 Honig Nov 1965 A
3241556 Zacouto Mar 1966 A
3478746 Greatbatch Nov 1969 A
3603881 Thornton Sep 1971 A
3727616 Lenzkes Apr 1973 A
3757778 Graham Sep 1973 A
3823708 Lawhorn Jul 1974 A
3830228 Foner Aug 1974 A
3835864 Rasor et al. Sep 1974 A
3870051 Brindley Mar 1975 A
3872251 Auerbach et al. Mar 1975 A
3905364 Cudahy et al. Sep 1975 A
3940692 Neilson et al. Feb 1976 A
3943926 Barragan Mar 1976 A
3943936 Rasor et al. Mar 1976 A
3946744 Auerbach Mar 1976 A
3952750 Mirowski et al. Apr 1976 A
4027663 Fischler et al. Jun 1977 A
4072154 Anderson et al. Feb 1978 A
4083366 Gombrich et al. Apr 1978 A
4102344 Conway et al. Jul 1978 A
4146029 Ellinwood, Jr. Mar 1979 A
4151513 Menken et al. Apr 1979 A
4151540 Sander et al. Apr 1979 A
4152540 Duncan et al. May 1979 A
4173221 McLaughlin et al. Nov 1979 A
4187854 Hepp et al. Feb 1980 A
4210149 Heilman et al. Jul 1980 A
4223678 Langer et al. Sep 1980 A
4250888 Grosskopf Feb 1981 A
4256115 Bilitch Mar 1981 A
4296756 Dunning et al. Oct 1981 A
4310000 Lindemans Jan 1982 A
4318412 Stanly et al. Mar 1982 A
4336810 Anderson et al. Jun 1982 A
4350169 Dutcher et al. Sep 1982 A
4374382 Markowitz Feb 1983 A
4406288 Horwinski et al. Sep 1983 A
4411271 Markowitz Oct 1983 A
4418695 Buffet Dec 1983 A
4424551 Stevenson et al. Jan 1984 A
4428378 Anderson et al. Jan 1984 A
4440173 Hudziak et al. Apr 1984 A
4442840 Wojciechowicz, Jr. Apr 1984 A
4453162 Money et al. Jun 1984 A
4481950 Duggan Nov 1984 A
4513743 van Arragon et al. Apr 1985 A
4516579 Irnich May 1985 A
4522208 Buffet Jun 1985 A
4524774 Hildebrandt Jun 1985 A
4531527 Reinhold, Jr. et al. Jul 1985 A
4543955 Schroeppel Oct 1985 A
4550370 Baker Oct 1985 A
4552127 Schiff Nov 1985 A
4552154 Hartlaub Nov 1985 A
4562846 Cox et al. Jan 1986 A
4586508 Batina et al. May 1986 A
4606352 Geddes et al. Aug 1986 A
4607639 Tanagho et al. Aug 1986 A
4612934 Borkan Sep 1986 A
4625730 Fountain et al. Dec 1986 A
4679144 Cox et al. Jul 1987 A
4681111 Silvian Jul 1987 A
4681117 Brodman et al. Jul 1987 A
4702253 Nappholz et al. Oct 1987 A
4719920 Alt et al. Jan 1988 A
4722342 Amundson Feb 1988 A
4750495 Moore et al. Jun 1988 A
4763340 Yoneda et al. Aug 1988 A
4763655 Wirtzfeld et al. Aug 1988 A
4787389 Tarjan Nov 1988 A
4791931 Slate Dec 1988 A
4793353 Borkan Dec 1988 A
4794532 Leckband et al. Dec 1988 A
4802481 Schroeppel Feb 1989 A
4809697 Causey et al. Mar 1989 A
4827940 Mayer et al. May 1989 A
4830006 Haluska et al. May 1989 A
4844076 Lesho et al. Jul 1989 A
4846195 Alt Jul 1989 A
4860750 Frey et al. Aug 1989 A
4875483 Vollmann et al. Oct 1989 A
4880004 Baker, Jr. et al. Nov 1989 A
4883064 Olson et al. Nov 1989 A
4886064 Strandberg Dec 1989 A
4896068 Nilsson Jan 1990 A
4903701 Moore et al. Feb 1990 A
4905708 Davies Mar 1990 A
4926863 Alt May 1990 A
4987897 Funke Jan 1991 A
5010887 Thornander Apr 1991 A
5012806 De Bellis May 1991 A
5014700 Alt May 1991 A
5014701 Pless et al. May 1991 A
5031615 Alt Jul 1991 A
5040533 Fearnot Aug 1991 A
5040534 Mann et al. Aug 1991 A
5040536 Riff Aug 1991 A
5042497 Shapland Aug 1991 A
5052399 Olive et al. Oct 1991 A
5058581 Silvian Oct 1991 A
5065759 Begemann Nov 1991 A
5076270 Stutz, Jr. Dec 1991 A
5076272 Ferek-Petric Dec 1991 A
5085224 Galen et al. Feb 1992 A
5086772 Larnard et al. Feb 1992 A
5088488 Markowitz et al. Feb 1992 A
5095903 DeBellis Mar 1992 A
5109845 Yuuchi et al. May 1992 A
5111816 Pless et al. May 1992 A
5113859 Funke May 1992 A
5113869 Nappholz et al. May 1992 A
5133350 Duffin Jul 1992 A
5135004 Adams et al. Aug 1992 A
5170784 Ramon et al. Dec 1992 A
5170802 Mehra Dec 1992 A
5179947 Meyerson et al. Jan 1993 A
5184616 Weiss Feb 1993 A
5193539 Schulman et al. Mar 1993 A
5193540 Schulman et al. Mar 1993 A
5193550 Duffin Mar 1993 A
5217010 Tsitlik et al. Jun 1993 A
5247945 Heinze et al. Sep 1993 A
5259394 Bens Nov 1993 A
5267150 Wilkinson Nov 1993 A
5282841 Szyszkowski Feb 1994 A
5284136 Hauck et al. Feb 1994 A
5291902 Carman Mar 1994 A
5300093 Koestner et al. Apr 1994 A
5304206 Baker, Jr. et al. Apr 1994 A
5304209 Adams et al. Apr 1994 A
5313953 Yomtov et al. May 1994 A
5318596 Barreras et al. Jun 1994 A
5324316 Schulman et al. Jun 1994 A
5331966 Bennett et al. Jul 1994 A
5333095 Stevenson et al. Jul 1994 A
5342401 Spano et al. Aug 1994 A
5354317 Alt Oct 1994 A
5358514 Schulman et al. Oct 1994 A
5373852 Harrison et al. Dec 1994 A
5383912 Cox et al. Jan 1995 A
5383915 Adams Jan 1995 A
5404877 Nolan et al. Apr 1995 A
5405367 Schulman et al. Apr 1995 A
5406444 Selfried et al. Apr 1995 A
5411532 Mortazavi May 1995 A
5411535 Fujii et al. May 1995 A
5411537 Munshi et al. May 1995 A
5417222 Dempsey et al. May 1995 A
5419337 Dempsey et al. May 1995 A
5431171 Harrison et al. Jul 1995 A
5446447 Carney et al. Aug 1995 A
5456261 Luczyk Oct 1995 A
5466246 Silvian Nov 1995 A
5469857 Laurent et al. Nov 1995 A
5480415 Cox et al. Jan 1996 A
5481262 Urbas et al. Jan 1996 A
5522876 Rusink Jun 1996 A
5531779 Dahl et al. Jul 1996 A
5539775 Tuttle et al. Jul 1996 A
5549654 Powell Aug 1996 A
5549659 Johansen et al. Aug 1996 A
5551427 Altman Sep 1996 A
5556421 Prutchi et al. Sep 1996 A
5562717 Tippey et al. Oct 1996 A
5571143 Hoegnelid et al. Nov 1996 A
5571148 Loeb et al. Nov 1996 A
5579775 Dempsey et al. Dec 1996 A
5586556 Spivey et al. Dec 1996 A
5591217 Barreras Jan 1997 A
5598848 Swanson et al. Feb 1997 A
5649952 Lam Jul 1997 A
5650759 Hittman et al. Jul 1997 A
5654984 Hershbarger et al. Aug 1997 A
5662689 Elsberry et al. Sep 1997 A
5669391 Williams Sep 1997 A
5674259 Gray Oct 1997 A
5676153 Smith et al. Oct 1997 A
5693076 Kaemmerer Dec 1997 A
5694940 Unger et al. Dec 1997 A
5694952 Lidman et al. Dec 1997 A
5697958 Paul et al. Dec 1997 A
5702427 Ecker et al. Dec 1997 A
5725559 Alt et al. Mar 1998 A
5728154 Crossett et al. Mar 1998 A
5730143 Schwarzberg Mar 1998 A
5735880 Prutchi et al. Apr 1998 A
5738102 Lemelson Apr 1998 A
5740811 Hedberg et al. Apr 1998 A
5741314 Daly et al. Apr 1998 A
5766231 Erickson et al. Jun 1998 A
5792205 Alt et al. Aug 1998 A
5810735 Halperin et al. Sep 1998 A
5814076 Brownlee Sep 1998 A
5814087 Renirie Sep 1998 A
5814089 Stokes et al. Sep 1998 A
5824016 Ekwall Oct 1998 A
5871451 Unger et al. Feb 1999 A
5876353 Riff Mar 1999 A
5876425 Gord et al. Mar 1999 A
5891178 Mann et al. Apr 1999 A
5899928 Sholder et al. May 1999 A
5935079 Swanson et al. Aug 1999 A
5954761 Machek et al. Sep 1999 A
5957861 Combs et al. Sep 1999 A
5984861 Crowley Nov 1999 A
5987352 Klein et al. Nov 1999 A
5995876 Kruse et al. Nov 1999 A
5999857 Weijand et al. Dec 1999 A
6002969 Machek et al. Dec 1999 A
6004269 Crowley et al. Dec 1999 A
6061596 Richmond et al. May 2000 A
6080187 Alt et al. Jun 2000 A
6093146 Filangeri Jul 2000 A
6096065 Crowley Aug 2000 A
6102874 Stone et al. Aug 2000 A
6112116 Fischell et al. Aug 2000 A
6115628 Stadler et al. Sep 2000 A
6115630 Stadler et al. Sep 2000 A
6115636 Ryan Sep 2000 A
6119031 Crowley Sep 2000 A
6125290 Miesel Sep 2000 A
6125291 Miesel et al. Sep 2000 A
6128526 Stadler et al. Oct 2000 A
6129751 Lucchesi et al. Oct 2000 A
6132390 Cookston et al. Oct 2000 A
6132456 Sommer et al. Oct 2000 A
6134459 Roberts et al. Oct 2000 A
6134470 Hartlaub Oct 2000 A
6141584 Rockwell et al. Oct 2000 A
6141588 Cox et al. Oct 2000 A
6141592 Pauly Oct 2000 A
6144866 Miesel et al. Nov 2000 A
6148230 KenKnight Nov 2000 A
6152882 Prutchi Nov 2000 A
6163723 Roberts et al. Dec 2000 A
6164284 Schulman et al. Dec 2000 A
6167310 Grevious Dec 2000 A
6178349 Kieval Jan 2001 B1
6178356 Chastain et al. Jan 2001 B1
6185443 Crowley Feb 2001 B1
6185452 Schulman et al. Feb 2001 B1
6185464 Bonner et al. Feb 2001 B1
6190324 Kieval et al. Feb 2001 B1
6198952 Miesel Mar 2001 B1
6201993 Kruse et al. Mar 2001 B1
6208894 Schulman et al. Mar 2001 B1
6208900 Ecker et al. Mar 2001 B1
6223081 Kerver Apr 2001 B1
6230059 Duffin May 2001 B1
6236882 Lee et al. May 2001 B1
6240321 Janke et al. May 2001 B1
6243608 Pauly et al. Jun 2001 B1
6248080 Miesel et al. Jun 2001 B1
6263245 Snell Jul 2001 B1
6265100 Saaski et al. Jul 2001 B1
6266554 Hsu et al. Jul 2001 B1
6272379 Fischell et al. Aug 2001 B1
6280409 Stone et al. Aug 2001 B1
6289229 Crowley Sep 2001 B1
6306088 Krausman et al. Oct 2001 B1
6310960 Saaski et al. Oct 2001 B1
6315721 Schulman et al. Nov 2001 B2
6324418 Crowley et al. Nov 2001 B1
6324421 Stadler et al. Nov 2001 B1
RE37463 Altman Dec 2001 E
6343227 Crowley Jan 2002 B1
6343233 Werner et al. Jan 2002 B1
6347245 Lee et al. Feb 2002 B1
6358202 Arent Mar 2002 B1
6361522 Scheiner et al. Mar 2002 B1
6363282 Nichols et al. Mar 2002 B1
6364831 Crowley Apr 2002 B1
6381492 Rockwell et al. Apr 2002 B1
6381493 Stadler et al. Apr 2002 B1
6381494 Gilkerson et al. Apr 2002 B1
6383209 Crowley May 2002 B1
6385593 Linberg May 2002 B2
6386882 Linberg May 2002 B1
6397100 Stadler et al. May 2002 B2
6402689 Scarantino et al. Jun 2002 B1
6405073 Crowley et al. Jun 2002 B1
6405083 Rockwell et al. Jun 2002 B1
6409674 Brockway et al. Jun 2002 B1
6409675 Turcott Jun 2002 B1
6412490 Lee Jul 2002 B1
6418346 Nelson et al. Jul 2002 B1
6423056 Ishikawa et al. Jul 2002 B1
6424866 Mika et al. Jul 2002 B2
6428484 Battmer et al. Aug 2002 B1
6434429 Kraus et al. Aug 2002 B1
6438410 Hsu et al. Aug 2002 B2
6438417 Rockwell et al. Aug 2002 B1
6442433 Linberg Aug 2002 B1
6444970 Barbato Sep 2002 B1
6445953 Bulkes et al. Sep 2002 B1
6458145 Ravenscroft et al. Oct 2002 B1
6459928 Mika et al. Oct 2002 B2
6459937 Morgan et al. Oct 2002 B1
6466820 Juran et al. Oct 2002 B1
6468263 Fischell et al. Oct 2002 B1
6470215 Kraus et al. Oct 2002 B1
6471645 Warkentin et al. Oct 2002 B1
6472991 Schulman et al. Oct 2002 B1
6477424 Thompson et al. Nov 2002 B1
6480733 Turcott Nov 2002 B1
6482154 Haubrich et al. Nov 2002 B1
6484055 Marcovecchio Nov 2002 B1
6484057 Ideker et al. Nov 2002 B2
6490487 Kraus et al. Dec 2002 B1
6496715 Lee et al. Dec 2002 B1
6500168 Jellie Dec 2002 B1
6501983 Natarajan et al. Dec 2002 B1
6512949 Combs et al. Jan 2003 B1
6512959 Gomperz et al. Jan 2003 B1
6522926 Kieval et al. Feb 2003 B1
6522928 Whitehurst et al. Feb 2003 B2
6539257 KenKnight Mar 2003 B1
6556860 Groenewegen Apr 2003 B1
6558321 Burd et al. May 2003 B1
6564807 Schulman et al. May 2003 B1
6567680 Swetlik et al. May 2003 B2
6571120 Hutten May 2003 B2
6574509 Kraus et al. Jun 2003 B1
6574511 Lee Jun 2003 B2
6580946 Struble Jun 2003 B2
6580948 Haupert et al. Jun 2003 B2
6584351 Ekwall Jun 2003 B1
6584352 Combs et al. Jun 2003 B2
6589187 Dirnberger et al. Jul 2003 B1
6592518 Denker et al. Jul 2003 B2
6594523 Levine Jul 2003 B1
6597948 Rockwell et al. Jul 2003 B1
6597952 Mika et al. Jul 2003 B1
6609023 Fischell et al. Aug 2003 B1
6611710 Gomperz et al. Aug 2003 B2
6615075 Mlynash et al. Sep 2003 B2
6622043 Kraus et al. Sep 2003 B1
6647292 Bardy et al. Nov 2003 B1
6648823 Thompson Nov 2003 B2
6649078 Yu Nov 2003 B2
6654638 Sweeney Nov 2003 B1
6658285 Potse et al. Dec 2003 B2
6658297 Loeb Dec 2003 B2
6658301 Loeb et al. Dec 2003 B2
6659959 Brockway et al. Dec 2003 B2
6669631 Norris et al. Dec 2003 B2
6681135 Davis et al. Jan 2004 B1
6684100 Sweeney et al. Jan 2004 B1
6687540 Marcovecchio Feb 2004 B2
6687546 Lebel et al. Feb 2004 B2
6689117 Sweeney et al. Feb 2004 B2
6690959 Thompson Feb 2004 B2
6694191 Starkweather et al. Feb 2004 B2
6695885 Schulman et al. Feb 2004 B2
6697672 Andersson Feb 2004 B2
6699200 Cao et al. Mar 2004 B2
6702857 Brauker et al. Mar 2004 B2
6704602 Berg et al. Mar 2004 B2
6711440 Deal et al. Mar 2004 B2
6721597 Bardy et al. Apr 2004 B1
6728572 Hsu et al. Apr 2004 B2
6728574 Ujhelyi et al. Apr 2004 B2
6731976 Penn et al. May 2004 B2
6731979 MacDonald May 2004 B2
6733485 Whitehurst et al. May 2004 B1
6735474 Loeb et al. May 2004 B1
6738670 Almendinger et al. May 2004 B1
6741877 Shults et al. May 2004 B1
6741886 Yonce May 2004 B2
6746404 Schwartz Jun 2004 B2
6754538 Linberg Jun 2004 B2
6760620 Sippens Groenewegen Jul 2004 B2
6764446 Wolinsky et al. Jul 2004 B2
6768923 Ding et al. Jul 2004 B2
6783499 Schwartz Aug 2004 B2
6785576 Verness Aug 2004 B2
6786860 Maltan et al. Sep 2004 B2
6792314 Byers et al. Sep 2004 B2
6799069 Weiner et al. Sep 2004 B2
6804559 Kraus et al. Oct 2004 B1
6804561 Stover Oct 2004 B2
6809507 Morgan et al. Oct 2004 B2
6811533 Lebel et al. Nov 2004 B2
6813519 Lebel et al. Nov 2004 B2
6821154 Canfield et al. Nov 2004 B1
6823217 Rutten et al. Nov 2004 B2
6824512 Warkentin et al. Nov 2004 B2
6829508 Schulman et al. Dec 2004 B2
6839596 Nelson et al. Jan 2005 B2
6848052 Hamid et al. Jan 2005 B2
6850801 Kieval et al. Feb 2005 B2
6862465 Shults et al. Mar 2005 B2
6862480 Cohen et al. Mar 2005 B2
6865420 Kroll Mar 2005 B1
6869404 Schulhauser et al. Mar 2005 B2
6871099 Whitehurst et al. Mar 2005 B1
6878112 Linberg et al. Apr 2005 B2
6879695 Maltan et al. Apr 2005 B2
6879855 Schulman et al. Apr 2005 B2
6882875 Crowley Apr 2005 B1
6889081 Hsu May 2005 B2
6893395 Kraus et al. May 2005 B1
6895279 Loeb et al. May 2005 B2
6895281 Amundson et al. May 2005 B1
6896651 Gross et al. May 2005 B2
6897788 Khair et al. May 2005 B2
6901294 Whitehurst et al. May 2005 B1
6901296 Whitehurst et al. May 2005 B1
6907285 Denker et al. Jun 2005 B2
6907293 Grill et al. Jun 2005 B2
6912420 Scheiner et al. Jun 2005 B2
6917833 Denker et al. Jul 2005 B2
6925328 Foster et al. Aug 2005 B2
6931327 Goode, Jr. et al. Aug 2005 B2
6999821 Jenney et al. Feb 2006 B2
7001372 Richter Feb 2006 B2
7023359 Goetz et al. Apr 2006 B2
7146222 Boling Dec 2006 B2
7146225 Guenst et al. Dec 2006 B2
7164950 Kroll et al. Jan 2007 B2
7181505 Haller et al. Feb 2007 B2
7187971 Sommer et al. Mar 2007 B2
7200437 Nabutovsky et al. Apr 2007 B1
7289853 Campbell et al. Oct 2007 B1
7363090 Halperin et al. Apr 2008 B2
7558631 Cowan et al. Jul 2009 B2
7565195 Kroll et al. Jul 2009 B1
7630767 Poore et al. Dec 2009 B1
7634313 Kroll et al. Dec 2009 B1
20020116028 Greatbatch et al. Aug 2002 A1
20020147488 Doan et al. Oct 2002 A1
20030163184 Schiener Aug 2003 A1
20040011366 Schulman et al. Jan 2004 A1
20040143262 Visram et al. Jul 2004 A1
20040147973 Hauser Jul 2004 A1
20040167587 Thompson Aug 2004 A1
20040172116 Seifert et al. Sep 2004 A1
20040193223 Kramer et al. Sep 2004 A1
20040249417 Ransbury et al. Dec 2004 A1
20040260349 Stroebel Dec 2004 A1
20050038474 Wool Feb 2005 A1
20050096702 Denker et al. May 2005 A1
20050131478 Kim et al. Jun 2005 A1
20050149138 Min et al. Jul 2005 A1
20050165465 Pianca et al. Jul 2005 A1
20050267555 Marnfeldt et al. Dec 2005 A1
20050288722 Eigler et al. Dec 2005 A1
20060085039 Hastings et al. Apr 2006 A1
20060085041 Hastings et al. Apr 2006 A1
20060085042 Hastings et al. Apr 2006 A1
20060121475 Davids et al. Jun 2006 A1
20060135999 Bodner et al. Jun 2006 A1
20060136004 Cowan et al. Jun 2006 A1
20060161222 Haubrich et al. Jul 2006 A1
20060241705 Neumann et al. Oct 2006 A1
20060247750 Seifert et al. Nov 2006 A1
20070088394 Jacobson Apr 2007 A1
20070088396 Jacobson Apr 2007 A1
20070088397 Jacobson Apr 2007 A1
20070088398 Jacobson Apr 2007 A1
20070088400 Jacobson Apr 2007 A1
20070088418 Jacobson Apr 2007 A1
20070276004 Hirsch et al. Nov 2007 A1
20070293904 Gelbart et al. Dec 2007 A1
20080004535 Smits Jan 2008 A1
20080119911 Rosero May 2008 A1
20080269591 Halperin et al. Oct 2008 A1
20090082828 Ostroff Mar 2009 A1
20090171408 Solem Jul 2009 A1
Foreign Referenced Citations (5)
Number Date Country
1741465 Jan 2007 EP
WO 9837926 Sep 1998 WO
WO 2006065394 Jun 2006 WO
WO 2007047681 Apr 2007 WO
WO 2007059386 May 2007 WO
Related Publications (1)
Number Date Country
20070088405 A1 Apr 2007 US
Provisional Applications (7)
Number Date Country
60726706 Oct 2005 US
60729671 Oct 2005 US
60737296 Nov 2005 US
60739901 Nov 2005 US
60749017 Dec 2005 US
60761531 Jan 2006 US
60761740 Jan 2006 US