WO2005007075A2 - Adaptive resynchronization therapy system - Google Patents

Adaptive resynchronization therapy system Download PDF

Info

Publication number
WO2005007075A2
WO2005007075A2 PCT/IL2004/000659 IL2004000659W WO2005007075A2 WO 2005007075 A2 WO2005007075 A2 WO 2005007075A2 IL 2004000659 W IL2004000659 W IL 2004000659W WO 2005007075 A2 WO2005007075 A2 WO 2005007075A2
Authority
WO
WIPO (PCT)
Prior art keywords
module
adaptive
learning
sensor
algorithmic
Prior art date
Application number
PCT/IL2004/000659
Other languages
French (fr)
Other versions
WO2005007075A3 (en
WO2005007075B1 (en
Inventor
Rami Rom
Original Assignee
Ai-Semi Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ai-Semi Ltd. filed Critical Ai-Semi Ltd.
Priority to EP04744999A priority Critical patent/EP1696999A4/en
Priority to US10/565,279 priority patent/US7657313B2/en
Publication of WO2005007075A2 publication Critical patent/WO2005007075A2/en
Publication of WO2005007075A3 publication Critical patent/WO2005007075A3/en
Publication of WO2005007075B1 publication Critical patent/WO2005007075B1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/365Heart stimulators controlled by a physiological parameter, e.g. heart potential
    • A61N1/36514Heart stimulators controlled by a physiological parameter, e.g. heart potential controlled by a physiological quantity other than heart potential, e.g. blood pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/365Heart stimulators controlled by a physiological parameter, e.g. heart potential
    • A61N1/368Heart stimulators controlled by a physiological parameter, e.g. heart potential comprising more than one electrode co-operating with different heart regions
    • A61N1/3684Heart stimulators controlled by a physiological parameter, e.g. heart potential comprising more than one electrode co-operating with different heart regions for stimulating the heart at multiple sites of the ventricle or the atrium
    • A61N1/36843Bi-ventricular stimulation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/3627Heart stimulators for treating a mechanical deficiency of the heart, e.g. congestive heart failure or cardiomyopathy
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/365Heart stimulators controlled by a physiological parameter, e.g. heart potential
    • A61N1/36514Heart stimulators controlled by a physiological parameter, e.g. heart potential controlled by a physiological quantity other than heart potential, e.g. blood pressure
    • A61N1/36521Heart stimulators controlled by a physiological parameter, e.g. heart potential controlled by a physiological quantity other than heart potential, e.g. blood pressure the parameter being derived from measurement of an electrical impedance
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/365Heart stimulators controlled by a physiological parameter, e.g. heart potential
    • A61N1/36514Heart stimulators controlled by a physiological parameter, e.g. heart potential controlled by a physiological quantity other than heart potential, e.g. blood pressure
    • A61N1/36564Heart stimulators controlled by a physiological parameter, e.g. heart potential controlled by a physiological quantity other than heart potential, e.g. blood pressure controlled by blood pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/365Heart stimulators controlled by a physiological parameter, e.g. heart potential
    • A61N1/368Heart stimulators controlled by a physiological parameter, e.g. heart potential comprising more than one electrode co-operating with different heart regions
    • A61N1/3682Heart stimulators controlled by a physiological parameter, e.g. heart potential comprising more than one electrode co-operating with different heart regions with a variable atrioventricular delay
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/365Heart stimulators controlled by a physiological parameter, e.g. heart potential
    • A61N1/368Heart stimulators controlled by a physiological parameter, e.g. heart potential comprising more than one electrode co-operating with different heart regions
    • A61N1/3684Heart stimulators controlled by a physiological parameter, e.g. heart potential comprising more than one electrode co-operating with different heart regions for stimulating the heart at multiple sites of the ventricle or the atrium

Definitions

  • the present invention relates generally to medical devices implementing a closed loop processing employing feed back control mechanism. More specifically invention deals with adaptive cardiac pacemaker and ICD devices.
  • Implanted pacemakers and intracardiac cardioverter defibrillators deliver therapy to patients suffering from various heart-diseases (Clinical Cardiac Pacing and Defibrillation -2 nd edition, Ellenbogen, Kay, Wilkoff, 2000). It is known that the cardiac output depends strongly on the left heart contraction in synchrony with the right heart (see US 6,223,079). Congestive heart failures (CHF) is defined generally as the inability of the heart to deliver enough blood to meet the metabolic demand. Often CHF is caused by electrical conduction defects. The overall result is a reduced blood stroke volume from the left side of the heart. For
  • CHF patients a permanent pacemaker with electrodes in 3 chambers, that are used to re-synchronize the left heart contraction to the right heart is an effective therapy, ("Device Therapy for Congestive Heart Failure", K. Ellenbogen et al , Elsevier Inc. (USA), 2004).
  • the resynchronization task demands exact pacing management of the heart chambers such that the overall stroke volume is maximized for a given heart rate (HR), where it is known that the key point is to bring the left ventricle to contract in synchrony with the right ventricle.
  • HR heart rate
  • the re-synchronization task is patient dependent, and with each patient the best combination of pacing time intervals that restores synchrony are changed during the normal daily activities of the patient. For these reasons, next generation cardiac re-synchronization therapy devices should have online adaptive capabilities according to Hemodynamic performance.
  • CRT cardiac resynchronization therapy
  • Fig. 1 is a schematic general description of an adaptive CRT system of the present invention
  • FIG. 2A is a schematic major component layout of an adaptive CRT device of the invention
  • Fig. 2B is a schematic major processor output connections of the processing modules of the invention
  • Fig. 3 is a neural network - micro controller architecture of a device of the invention
  • Fig.4 is a state machine representation of a neuron of the learning module of the invention.
  • Fig. 5A is a synapse of the invention implemented as a state machine
  • Fig. 5B shows a timing diagram of the dynamic synapse.
  • Fig. 6A is a synaptic weights adaptation rules of the present invention.
  • Fig. 6B is a flow chart for determining the state of a spike and the stored value at the pacing register with respect to the hemodynamic performance function of the heart;
  • Fig. 7 is a block diagram of an adaptive rate responsive pacemaker using right ventricular and right atrial leads as sensors and pacing the right atria.
  • a device of the invention is a feed - back controlled system for delivering input to the patienfs body, in a manner which takes account of the body's significant physiological status relating to the delivered input.
  • a system of the invention is an adaptive, hemodynamic sensitive device, for regulating the heart rhythmic contraction.
  • Fig. 1 to which reference is now made a schematic description of the system of the invention shows its main building blocks.
  • Sensors 20 feed physiological information into a learning which is typically neural network module 22 and to the algorithmic module 24.
  • Algorithmic module 24 receives processed data from the neural network module and supervises the adaptation of the neural network module 22.
  • Pulse generator 26 issues impulses at time and places as controlled only by algorithmic module 24.
  • the system as described above forms a unitary block implanted in the patient's heart, a cardiac pacemaker or defibrillator, with sensors positioned at critical sites, and pulsing electrodes applied at strategic sites in or about the heart.
  • a cardiac pacemaker or defibrillator with sensors positioned at critical sites, and pulsing electrodes applied at strategic sites in or about the heart.
  • only the pacing module is implanted, whereas the neural network module is not implanted in the patienfs body, but is communicable through a communications link. Accordingly, the neural network module receives through a typically wireless link, information regarding hemodynamic condition of the patient and the electrical behaviour of the heart.
  • the main two modules in which the invention is implemented are the algorithmic module and the neural network module.
  • both modules are implemented as software modules typically in one processor, whereas in other embodiments two different processors are employed, for the algorithmic and for the neural network module, respectively.
  • a clinician programs the AV delay parameter and the W interval parameter of the pacemaker using a programmer as with the prior art methods.
  • the initial programmed values are used as a safety limits and a hemodynamic baseline for the present invention adaptive CRT device.
  • the neural network module working with the deterministic algorithmic module optimises the AV delay and W interval continuously and generates hemodynamic performance measured for example as cardiac output at all heart conditions. Whenever the neural network module fails to find a set of parameters that generates a better hemodynamic performance compared to the baseline value obtained with the initial programmed values, the adaptive CRT device switches back to pacing with the programmed fixed values.
  • Artificial neural networks are known to have advantages over standard algorithmic processing in performing tasks such as adaptive control and pattern recognition. However, artificial neural networks are not deterministic and may lead to quite unexpected results. In the case of cardiac pacemakers and other life saving medical appliances, the occurrence of results beyond acceptable limits. Thus, a limit setting device, is employed in the embodiments of the present invention for confining the range of parameters provided by the neural network. Typically, artificial neural networks are designed and trained for a specific task. Unsupervised learning networic architectures are very limited and are not used in many applications. Applications based on artificial neural networks that use supervised learning are far more successful then solely unsupervised autonomous networks. In accordance with the present invention, algorithmic module is used as a supervisor for the artificial neural network module.
  • the present invention preferably employs spiking neuronal networks, hereinafter referred to as SNN.
  • SNN spiking neuronal networks
  • Basic models of spiking neurons are reviewed by Wulfram Gerstner in Chapter 1 of "Pulsed Neural Network", edited by Wolfgang Maass and Christofer M. Bishop, The MIT Press, London England (2001).
  • Computing methods for use with spiking neurons are presented by Wolfgang Maass in Chapter 2, of the same publication.
  • SNN have often been implemented in VLSI which was also reflected in specific design schemes.
  • Adaptive cardiac resynchronisation processor elements The adaptive CRT device aims at optimizing pacing parameters, AV delay and W interval online, responding to the output of a hemodynamic sensor.
  • the two parameters optimise the diastolic filling time and ensure mechanical synchronization of both ventricles.
  • a schematic block diagram describing the pacemaker/ICD device in accordance with a preferred embodiment of the invention is shown in Figs. 2A and 2B.
  • implanted or external sensors 50 monitor the electrical and hemodynamic activity of the patienfs heart.
  • the monitored signals are amplified and pre - processed by an analogue circuit 52 the output of which is digitized by A/D module 54 and processed by a digital processor 56.
  • microprocessor 56 two sub - units are linked, as described schematically in Fig. 2B.
  • An algorithmic module 58 performing an algorithmic process and neural network (NN) processor 60 performs a continuous adaptation process in connection with the algorithm, based on the changing circumstances detected by sensors 50.
  • a pulse generator of the pacemaker CD device 62 is driven by the processor 56.
  • processor 56 is implemented as a VLSI device.
  • the NN module carries out spiking NN (SNN) processes, whereas the algorithmic module performs as a master module.
  • the master processor manages the pulse generator in order to deliver pacing or shock therapy, ensuring a safe operation of the system by an algorithm with a limiting high and low thresholds, limiting rates, limiting intervals and limiting amplitudes.
  • the NN module or slave processor's task is to generate predictions for the optimal intervals for resynchronization of the left ventricle contraction with the right ventricle contraction at all heart rates, i.e the programmable parameters AV delay and W interval, to be described below.
  • a spiking neuron network (SNN) architecture is implemented in silicon for the following reasons: 1.
  • SNN architectures specialize in continuous detection and classification of temporal sequences.
  • the inputs to the SNN in the present invention are three intracardiac electrograms (IEGM) coming from the implanted electrodes in the right atria, right ventricle and outside of the left ventricle, and one or more inputs from hemodynamic sensors that are either implanted or non-invasive. All inputs described above deliver a continuous temporal signal that the SNN processors is required to process online.
  • IEGM intracardiac electrograms
  • SNN architecture has a massive parallel computation capability that allows a design of a processor with extremely low clock frequency such as 1 -10 KHz and low power consumption.
  • SNN architecture performs local computation in each neuron and synapse module and stores data locally with no need to access external, on - chip or off - chip memory modules and hence allows to scale up to a massive parallel computation power with extremely low power dissipation.
  • a description of a preferred embodiment using specially designed SNN processor with novel learning rules is described below with reference to Figs 3 - 8.
  • Fig. 3 shows the spiking neural network (SNN) processor architecture.
  • the SNN processor 66 has an input layer, 70, a middle layer, 72, and an output neuron layer 74.
  • a control block, 76 performs calculations needed for the synaptic weights adaptation rules of the SNN processor in co-operation with the microcontroller module, 78, that are forwarded to the SNN middle and output layers.
  • the input layer 70 receives inputs from the 3 implanted electrodes 80 from tiie heart chambers, data from hemodynamic sensors 82 such as impedance sensor from the right and left ventricles and pressure sensor.
  • the three implanted electrodes are known collectively as intra-cardiac electrograms (IEGM) which deliver also pacing signals to the heart chambers.
  • IEGM intra-cardiac electrograms
  • the micro-controller can forward to the NN module processed data representing dynamic sensors such as the heart rate and a time derivative of a pressure sensor signal (dp/dt).
  • the input layer 70 of the invention typically contains integrate and fire (l&F) neuron modules, that transform the input signals to a trains of spikes that enter the spiking neuron network of the middle layer. A description of the l&F neuron is given below.
  • the middle layer is a network of l&F neurons containing several layers of neurons and synapses modules that connect each neuron to several neurons in an adjacent layer. All the neurons of the middle layer network are connected to tiie output layer.
  • the output layer there are two l&F neurons, two registers and a large number of synapse modules that connect each l&F neuron to all neurons of the middle layer.
  • One l&F neuron affects the pacing of the right ventricle the second affects the pacing of the left ventricle.
  • the two registers store the pacing interval values to be forwarded to the micro-controller.
  • Fig. 4 shows an exemplary digital l&F neuron implemented as a state machine, described hereinafter.
  • the l&F neuron is driven by excitatory and inhibitory synapses and has an internal membrane potential register (not shown).
  • the neuron has three states, namely SUM state 84, FIRE state 86, and REFRACTORY state 88.
  • SUM state the neuron sums the input excitatory post-synaptic responses (EPSR) and inhibitory post-synaptic responses (IPSR) and accumulates the result in a membrane potential register.
  • ESR excitatory post-synaptic responses
  • IIPSR inhibitory post-synaptic responses
  • the synaptic module is also preferably implemented as a state machine as shown in Fig. 5A.
  • the synapse has five states, namely IDLE, 90, PRE_HEBB 92.PSR 94, HEBB 96, and POST_HEBB 98.
  • a PSR post-synaptic response
  • W a stored synaptic weight
  • Fig. 5B shows the three Hebb sates described above, demonstrating output neuron spikes occurrences at three different states. In the first case designated by graph 120 the output neuron spike occurs at the pre-HEBB state.
  • the post-spike occur at the HEBB state
  • the spike occurs at the post- HEBB state.
  • the identity of the state at which the spike has occurred is stored at the synapse every cardiac cycle and it affects the synaptic weights adaptation rules as described below.
  • the synaptic weights adaptation rules of the present invention are a combination of Hebb rule and a feedback control obtained by interaction with the environment.
  • Hebb rule asserts that when a post-synaptic neuron fires after it was excited by a synaptic PSR, the synapse weight is strengthened.
  • the environment is represented by the signals of the IEGM and by a hemodynamic sensors signal.
  • Hebb rule is implemented as described next. Of the five states described in Fig. 5A to which reference is again made, three are Hebbian, namely PRE_HEBB, HEBB and POST.HEBB. In Fig 5B each synapse receiving an output neuron spike stores the corresponding state, i.e.
  • a clinician programs the AV delay parameter and the W interval parameter of the pacemaker as in prior art CRT devices, using accepted parameters of the art, which generates a numerical baseline representation of the sensed hemodynamic performance using the programmed parameters above.
  • the present invention's SNN processor starts operating in normal CRT mode pacing with the programmed intervals and the two l&F neurons of the output layer learns to fire at the programmed time stored. When the l&F neurons has learned to fire at the expected time, the processor switches to adaptive CRT mode in which the AV delay and W intervals are changed dynamically.
  • a numerical representation of the sensed hemodynamic performance is obtained in each cardiac cycle and the synaptic weights of the SNN processor adapts accordingly to deliver the AV delay and W intervals that results in the best hemodynamic performance. Whenever the hemodynamic performance is lower then the recorded baseline value, a switch back to the normal CRT mode pacing with the initial AV delay and W interval values programmed by the clinician occurs. It is expected that the SNN processor will work most of the time in the adaptive CRT mode facilitating optimal hemodynamic performance.
  • the synaptic weight adaptation rules applied during the normal CRT mode takes into consideration two different occurrences. One, the deviation of the spike of the output neuron from the programmed value in terms of time. Two, the sampled Hebb states stored at each synapse as shown in Fig. 5B to which reference is again made.
  • the synaptic weights adaptation rule generates a shift of the firing time of the l&F neuron in the direction of the programmed time.
  • the synaptic weights adaptation rule are as follows:-
  • synapses that were at PRE_HEBB state increment their weights
  • synapses that were at HEBB or POST_HEBB states decrement their weight
  • synapses that were at HEBB or POST_HEBB states increment their weight.
  • the SNN processor adapts its synaptic weights continuously interacting with the environment through the electric and hemodynamic sensors.
  • Fig. 6A helps to explain the adaptive CRT mode synaptic weights adaptation rule.
  • the output neuron fires at a time T measured from the sensed right atrial contraction every cardiac cycle, 200.
  • the time T is compared, at step 202, with the time P stored at the pacing register of the output layer. If T > P the pacing register value is increased at step 204. Else, it is decreased at step 206.
  • the pacemaker paces the heart with the updated values, stored at the pacing register.
  • a numerical representation of the sensed hemodynamic performance is calculated with the updated pacing values and is compared, at steps 204 and 206,
  • the stroke volumes, SV of the left or right ventricle is used as the hemodynamic performance criterion.
  • Four possible states are defined by comparing the new stroke volumes with the previous stroke volumes.
  • Fig 6B. shows the adaptive CRT mode learning profile for the synaptic adaptation rules.
  • the numerical representation of the hemodynamic performance has a maximal value 220 at some pacing time interval.
  • the task performed in the adaptive CRT mode is to modify the synaptic weight such that the value stored at the pacing register is the value that maximizes the hemodynamic performance. After a spike occurs, a corresponding state is determined as relates to the stored pacing register value stored.
  • Spike 250 relates to the recorded pacing register 252 stored, defining a state 3.
  • spike 260 relates to pacing register 258 defining state 2.
  • the synaptic weight adaptation value is calculated in each synapse and its value depends on the flow diagram state and on the Hebb state stored at each synapse as was shown in Fig. 5A to which reference is again made.
  • the state associated with a spike is classified as 1 or 3 as in Fig. 6B to which reference is again made, the firing intervals are to be increased.
  • the firing intervals ae When the flow diagram state is classified as 2 or 4 the firing intervals ae to be decreased.
  • the synaptic weights are modified in each synapse separately in order to affect the firing time of the l&F neuron. Synapse in a PRE_HEBB state and is to increase its weight will cause the l&F neuron to increase firing intervals. A synapse in a POST_HEBB state and is to increase its weight will cause the l&F neuron to decrease firing intervals.
  • the hemodynamic performance is a physiological parameter such as stroke volumes of each ventricle or a processed data such as the time derivative of a pressure sensor signal.
  • the external adaptive CRT device receives lEGMs and hemodynamic data using a communications channel, preferably a neural network module, or other learning modules, processes the data in the external device.
  • the external adaptive CRT device is not implanted in the patienfs body, and it transmits to a biventricular pacemaker or defibrillator implanted in the patienfs body the optimal pacing parameters, AV delay and W interval, to the pacemaker on-line.
  • the diagnostics and rehabilitation procedure can be supervised by a clinician at a cardiac rehabilitation centre.
  • the system of the invention facilitates diagnostics and rehabilitation procedure of some form to be carried out at the patient environment (home, office etc) without the supervision of a clinician.
  • the hemodynamic sensor used is an implanted sensor such as a pressure sensor, or a non-invasive hemodynamic sensor such as impedance sensors (such as BioZ ® sensor of CardioDynamics Inc. San Diego, California, USA) or an echocardiograph.
  • impedance sensors such as BioZ ® sensor of CardioDynamics Inc. San Diego, California, USA
  • an echocardiograph the images of the wall motion are to be transformed to a numeric hemodynamic performance function to be used for optimisation by the present invention external adaptive CRT device.
  • the system of the present invention uses the information derived from the hemodynamic sensor in two complementary ways.
  • the specific hemodynamic condition correlates with a specific hemodynamic performance representation, and two, a classification of the heart's condition is performed.
  • the optimal AV delay and W interval are learned and updated continuously.
  • the adaptive CRT device improves gradually the patient hemodynamic performance and hence the adaptive CRT device of the invention allows a gradual cardiac rehabilitation. This work scheme constitutes a potential clinical improvement in hemodynamic performance such as the cardiac output.
  • Consistent delivery of CRT Atrial event tracking is an important issue in cardiac timing cycles in general which has also strong implication on CRT devices, as described in "Device Therapy for Congestive Heart Failure" by K. Ellenbogen et al, Elsevier Inc. (USA), 2004.
  • CRT is not delivered consistently due to loss of atrial tracking for hours and even for days as can be seen by pacemaker diagnostics in patients' follow-ups.
  • Loss of atrial tracking occurs due to several reasons, for example, surpassing the programmed maximal tracking rate (MTR) during exercise.
  • MTR programmed maximal tracking rate
  • the adaptive CRT device of the present invention is expected to overcome the problem of loss of CRT delivery at the MTR.
  • the adaptive CRT device thus produces optimal pacing parameters that obviate the need for the MTR limit.
  • Prediction of the desired optimal rate response to the physiological demand in response to all the patient conditions is a complex task.
  • the currently used motion sensors do not respond to physiological/mental stress or anxiety which are not accompanied by an increase in the upper body motion.
  • motion sensors respond to non-physiological events such as a bus ride, a plane take-off, operating a household drill, and other events external to the body and metabolic sensors are too slow to respond.
  • An adaptive rate response pacemaker in accordance with the present invention senses the ventricle contraction and paces the right atria, with the same SNN architecture of the present invention for adaptive CRT device presented above (using only one output neuron).
  • the SNN processor predicts the optimal timing for pacing the right atria such that the maximal dp/dt obtained with a ventrical pressure sensor is optimized in all heart conditions.
  • Fig. 7 a block diagram is shown representing an adaptive rate responsive pacemaker based on the present invention.
  • the sensors used are right atrial lead 280, right ventricle lead 282, and a pressure sensor, not shown.
  • the advantage of the adaptive rate response pacemaker of the present invention is in the online, continuous adaptation to the patient hemodynamic needs with an algorithm that maximizes the hemodynamic performance as seen through a maximal dp/dt values.
  • pacemakers with auto-capture functions preserve energy and hence have a longer battery life. They also have the advantage of causing less patient discomfort due to an excessive heart stimulation.
  • compiling the auto-capture function is a complex task due to the high variability of the heart electrical activity signals, and in particular, to the so called "fusion" phenomenon, exhibiting overlaps in time of the evoked response and internal beat.
  • capture management is even more important issue, since it is harder to capture the left ventricle comparing to the right ventricle. Usually, a higher pulse energy is used for the left ventricle and still it is not guaranteed that the left ventricle is consistently captured.
  • the pacing interval delivered to the ventricles are not constant we can predict the time difference between the evoked response in the current cardiac cycle and the evoked response of the next cardiac cycle. If the sensed event matches the prediction, it is verified as an evoked response and capture is verified. If the event is not predicted, the beat is an intrinsic one.
  • the ability to differentiate between evoked response beat from intrinsic beat using the adaptive CRT device algorithm can be used to manage the pulse energy in order to save battery energy while ensuring capture.
  • closed loop medical devices delivering physiologically active agents can benefit from the combined system of a learning module and deterministic module that serve also as a supervisor for the learning module as presented in this invention.
  • the architecture guarantees safe operation and at the same time allow adaptive, sensitive to the patient system. It is expected to improve performance of various closed loop, feed back controlled therapeutic medical device such as Insulin pump, controlled drug delivery systems, brain stimulation devices, etc.
  • the cardiac pacemakers and ICD devices is only one implementation of the invention.

Landscapes

  • Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Physiology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Biophysics (AREA)
  • Radiology & Medical Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Hematology (AREA)
  • Electrotherapy Devices (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A system including a learning module (22) and an algorithmic module for learning a physiological aspect of a patient body and regulating the delivery of a physiological agent to the body.

Description

ADAPTIVE RESYNCHRONIZATION THERAPY SYSTEM
FIELD OF THE INVENTION The present invention relates generally to medical devices implementing a closed loop processing employing feed back control mechanism. More specifically invention deals with adaptive cardiac pacemaker and ICD devices.
BACKGROUND OF THE INVENTION
Implanted pacemakers and intracardiac cardioverter defibrillators (ICD) deliver therapy to patients suffering from various heart-diseases (Clinical Cardiac Pacing and Defibrillation -2nd edition, Ellenbogen, Kay, Wilkoff, 2000). It is known that the cardiac output depends strongly on the left heart contraction in synchrony with the right heart (see US 6,223,079). Congestive heart failures (CHF) is defined generally as the inability of the heart to deliver enough blood to meet the metabolic demand. Often CHF is caused by electrical conduction defects. The overall result is a reduced blood stroke volume from the left side of the heart. For
CHF patients a permanent pacemaker with electrodes in 3 chambers, that are used to re-synchronize the left heart contraction to the right heart is an effective therapy, ("Device Therapy for Congestive Heart Failure", K. Ellenbogen et al , Elsevier Inc. (USA), 2004). The resynchronization task demands exact pacing management of the heart chambers such that the overall stroke volume is maximized for a given heart rate (HR), where it is known that the key point is to bring the left ventricle to contract in synchrony with the right ventricle. Clearly, the re-synchronization task is patient dependent, and with each patient the best combination of pacing time intervals that restores synchrony are changed during the normal daily activities of the patient. For these reasons, next generation cardiac re-synchronization therapy devices should have online adaptive capabilities according to Hemodynamic performance.
Currently available cardiac resynchronization therapy (CRT) devices have drawbacks that prevent the achievement of an optimally delivered CRT and are listed:-
1. Programming and troubleshooting CRT device - Optimizing the CRT device using echocardiography is expansive, time consuming and operator dependent. The clinician should optimize both the atriaventricular delay (AV delay), in order to achieve maximal diastolic filling time, and the interventricular delay (W interval) in order to achieve resynchronisation of heart chambers contractions.
2. Consistent Delivery of CRT - There are several reasons why CRT is not delivered consistently, and some times is not delivered at all for hours. Examples are failure to optimise the AV delay and low maximal tracking rate.
3. Follow Ups - The clinician must perform the complex task of optimization and programming of the CRT device, first at implantation and then at each follow-up.
4. CRT non-responders, significant number of patients do not respond to CRT after implantation. Artificial neural networks are known to have advantages over standard algorithmic processing in performing tasks such as adaptive control and pattern recognition. Spiking neural networks architectures are a unique form of artificial neural networks that are inspired by the biological nerve system. Spiking neurons architectures, applications and learning rules are reviewed by Wolfgang Maass et. al. "Pulsed Neural Network", The MIT Press, London England (2001). Rate responsive heart stimulation device using neural networks has been proposed in US Patent 5,782,885
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a schematic general description of an adaptive CRT system of the present invention;
FIG. 2A is a schematic major component layout of an adaptive CRT device of the invention; Fig. 2B is a schematic major processor output connections of the processing modules of the invention;
Fig. 3 is a neural network - micro controller architecture of a device of the invention; Fig.4 is a state machine representation of a neuron of the learning module of the invention.
Fig. 5A is a synapse of the invention implemented as a state machine;
Fig. 5B shows a timing diagram of the dynamic synapse.
Fig. 6A is a synaptic weights adaptation rules of the present invention. Fig. 6B is a flow chart for determining the state of a spike and the stored value at the pacing register with respect to the hemodynamic performance function of the heart;
Fig. 7 is a block diagram of an adaptive rate responsive pacemaker using right ventricular and right atrial leads as sensors and pacing the right atria.
DETAILED DESCRIPTION OF THE PRESENT INVENTION
General System Architecture A device of the invention is a feed - back controlled system for delivering input to the patienfs body, in a manner which takes account of the body's significant physiological status relating to the delivered input.
A system of the invention is an adaptive, hemodynamic sensitive device, for regulating the heart rhythmic contraction. In Fig. 1 to which reference is now made, a schematic description of the system of the invention shows its main building blocks. Sensors 20 feed physiological information into a learning which is typically neural network module 22 and to the algorithmic module 24. Algorithmic module 24 receives processed data from the neural network module and supervises the adaptation of the neural network module 22. Pulse generator 26 issues impulses at time and places as controlled only by algorithmic module 24.
In a preferred embodiment of the invention, the system as described above forms a unitary block implanted in the patient's heart, a cardiac pacemaker or defibrillator, with sensors positioned at critical sites, and pulsing electrodes applied at strategic sites in or about the heart. In other embodiments, only the pacing module is implanted, whereas the neural network module is not implanted in the patienfs body, but is communicable through a communications link. Accordingly, the neural network module receives through a typically wireless link, information regarding hemodynamic condition of the patient and the electrical behaviour of the heart.
The main two modules in which the invention is implemented are the algorithmic module and the neural network module. In some embodiments, both modules are implemented as software modules typically in one processor, whereas in other embodiments two different processors are employed, for the algorithmic and for the neural network module, respectively.
In accordance with the present invention implementing an adaptive CRT device, a clinician programs the AV delay parameter and the W interval parameter of the pacemaker using a programmer as with the prior art methods.
The initial programmed values are used as a safety limits and a hemodynamic baseline for the present invention adaptive CRT device. The neural network module working with the deterministic algorithmic module optimises the AV delay and W interval continuously and generates hemodynamic performance measured for example as cardiac output at all heart conditions. Whenever the neural network module fails to find a set of parameters that generates a better hemodynamic performance compared to the baseline value obtained with the initial programmed values, the adaptive CRT device switches back to pacing with the programmed fixed values.
Artificial neural networks are known to have advantages over standard algorithmic processing in performing tasks such as adaptive control and pattern recognition. However, artificial neural networks are not deterministic and may lead to quite unexpected results. In the case of cardiac pacemakers and other life saving medical appliances, the occurrence of results beyond acceptable limits. Thus, a limit setting device, is employed in the embodiments of the present invention for confining the range of parameters provided by the neural network. Typically, artificial neural networks are designed and trained for a specific task. Unsupervised learning networic architectures are very limited and are not used in many applications. Applications based on artificial neural networks that use supervised learning are far more successful then solely unsupervised autonomous networks. In accordance with the present invention, algorithmic module is used as a supervisor for the artificial neural network module. As a neural network module, the present invention preferably employs spiking neuronal networks, hereinafter referred to as SNN. Basic models of spiking neurons are reviewed by Wulfram Gerstner in Chapter 1 of "Pulsed Neural Network", edited by Wolfgang Maass and Christofer M. Bishop, The MIT Press, London England (2001). Computing methods for use with spiking neurons are presented by Wolfgang Maass in Chapter 2, of the same publication. SNN have often been implemented in VLSI which was also reflected in specific design schemes.
Adaptive cardiac resynchronisation processor elements The adaptive CRT device aims at optimizing pacing parameters, AV delay and W interval online, responding to the output of a hemodynamic sensor. The two parameters optimise the diastolic filling time and ensure mechanical synchronization of both ventricles. A schematic block diagram describing the pacemaker/ICD device in accordance with a preferred embodiment of the invention is shown in Figs. 2A and 2B. In Fig. 2A implanted or external sensors 50 monitor the electrical and hemodynamic activity of the patienfs heart. The monitored signals are amplified and pre - processed by an analogue circuit 52 the output of which is digitized by A/D module 54 and processed by a digital processor 56. In the microprocessor 56 two sub - units are linked, as described schematically in Fig. 2B. An algorithmic module 58 performing an algorithmic process and neural network (NN) processor 60 performs a continuous adaptation process in connection with the algorithm, based on the changing circumstances detected by sensors 50. A pulse generator of the pacemaker CD device 62 is driven by the processor 56. In some embodiments of the invention processor 56 is implemented as a VLSI device.
In a preferred embodiment of the invention the NN module carries out spiking NN (SNN) processes, whereas the algorithmic module performs as a master module. In a preferred embodiment of the invention, the master processor manages the pulse generator in order to deliver pacing or shock therapy, ensuring a safe operation of the system by an algorithm with a limiting high and low thresholds, limiting rates, limiting intervals and limiting amplitudes. The NN module or slave processor's task is to generate predictions for the optimal intervals for resynchronization of the left ventricle contraction with the right ventricle contraction at all heart rates, i.e the programmable parameters AV delay and W interval, to be described below.
The Spiking Neural Network module
In a preferred embodiment of the present invention a spiking neuron network (SNN) architecture is implemented in silicon for the following reasons: 1. SNN architectures specialize in continuous detection and classification of temporal sequences. The inputs to the SNN in the present invention are three intracardiac electrograms (IEGM) coming from the implanted electrodes in the right atria, right ventricle and outside of the left ventricle, and one or more inputs from hemodynamic sensors that are either implanted or non-invasive. All inputs described above deliver a continuous temporal signal that the SNN processors is required to process online.
2. SNN architecture has a massive parallel computation capability that allows a design of a processor with extremely low clock frequency such as 1 -10 KHz and low power consumption.
3. SNN architecture performs local computation in each neuron and synapse module and stores data locally with no need to access external, on - chip or off - chip memory modules and hence allows to scale up to a massive parallel computation power with extremely low power dissipation. A description of a preferred embodiment using specially designed SNN processor with novel learning rules is described below with reference to Figs 3 - 8.
Fig. 3 shows the spiking neural network (SNN) processor architecture. The SNN processor 66 has an input layer, 70, a middle layer, 72, and an output neuron layer 74. A control block, 76, performs calculations needed for the synaptic weights adaptation rules of the SNN processor in co-operation with the microcontroller module, 78, that are forwarded to the SNN middle and output layers. The input layer 70 receives inputs from the 3 implanted electrodes 80 from tiie heart chambers, data from hemodynamic sensors 82 such as impedance sensor from the right and left ventricles and pressure sensor. The three implanted electrodes are known collectively as intra-cardiac electrograms (IEGM) which deliver also pacing signals to the heart chambers. The micro-controller can forward to the NN module processed data representing dynamic sensors such as the heart rate and a time derivative of a pressure sensor signal (dp/dt). The input layer 70 of the invention typically contains integrate and fire (l&F) neuron modules, that transform the input signals to a trains of spikes that enter the spiking neuron network of the middle layer. A description of the l&F neuron is given below. The middle layer is a network of l&F neurons containing several layers of neurons and synapses modules that connect each neuron to several neurons in an adjacent layer. All the neurons of the middle layer network are connected to tiie output layer.
In the output layer there are two l&F neurons, two registers and a large number of synapse modules that connect each l&F neuron to all neurons of the middle layer. One l&F neuron affects the pacing of the right ventricle the second affects the pacing of the left ventricle. The two registers store the pacing interval values to be forwarded to the micro-controller.
Fig. 4 shows an exemplary digital l&F neuron implemented as a state machine, described hereinafter. The l&F neuron is driven by excitatory and inhibitory synapses and has an internal membrane potential register (not shown). The neuron has three states, namely SUM state 84, FIRE state 86, and REFRACTORY state 88. In the SUM state, the neuron sums the input excitatory post-synaptic responses (EPSR) and inhibitory post-synaptic responses (IPSR) and accumulates the result in a membrane potential register. When the membrane potential reaches a threshold value, the state-machine makes a transition to the FIRE state, generating an output spike following which, the state-machine proceeds to the REFRACTORY state. The state machine waits for a fixed pre-defined time in the refractory state and returns to the SUM state. The synaptic module is also preferably implemented as a state machine as shown in Fig. 5A. The synapse has five states, namely IDLE, 90, PRE_HEBB 92.PSR 94, HEBB 96, and POST_HEBB 98. When a spike is received from a pre-synaptic neuron, a transition to the PRE_HEBB state occurs. After a predefined time delay, transition to a post-synaptic response (PSR) state takes place and a PSR is emitted. The PSR is proportional to a stored synaptic weight, W, and it is a decaying function of time. After one clock period at the PSR state, the state machine enters the HEBB state. After time delay the state machine transit to a POST__HEBB state and finally it return to IDLE state. Fig. 5B shows the three Hebb sates described above, demonstrating output neuron spikes occurrences at three different states. In the first case designated by graph 120 the output neuron spike occurs at the pre-HEBB state. In the second case designated by graph 122 the post-spike occur at the HEBB state, and in the third case designated by graph 124, the spike occurs at the post- HEBB state. The identity of the state at which the spike has occurred is stored at the synapse every cardiac cycle and it affects the synaptic weights adaptation rules as described below.
The synaptic weights adaptation rules
The synaptic weights adaptation rules of the present invention are a combination of Hebb rule and a feedback control obtained by interaction with the environment. Hebb rule asserts that when a post-synaptic neuron fires after it was excited by a synaptic PSR, the synapse weight is strengthened. The environment is represented by the signals of the IEGM and by a hemodynamic sensors signal. In the present invention Hebb rule is implemented as described next. Of the five states described in Fig. 5A to which reference is again made, three are Hebbian, namely PRE_HEBB, HEBB and POST.HEBB. In Fig 5B each synapse receiving an output neuron spike stores the corresponding state, i.e. PRE_HEBB, HEBB or POST_HEBB. The way these states enter the synaptic weights adaptation rules is explained below with reference to Figs. 6A- B. As described above, a clinician programs the AV delay parameter and the W interval parameter of the pacemaker as in prior art CRT devices, using accepted parameters of the art, which generates a numerical baseline representation of the sensed hemodynamic performance using the programmed parameters above. The present invention's SNN processor starts operating in normal CRT mode pacing with the programmed intervals and the two l&F neurons of the output layer learns to fire at the programmed time stored. When the l&F neurons has learned to fire at the expected time, the processor switches to adaptive CRT mode in which the AV delay and W intervals are changed dynamically. A numerical representation of the sensed hemodynamic performance is obtained in each cardiac cycle and the synaptic weights of the SNN processor adapts accordingly to deliver the AV delay and W intervals that results in the best hemodynamic performance. Whenever the hemodynamic performance is lower then the recorded baseline value, a switch back to the normal CRT mode pacing with the initial AV delay and W interval values programmed by the clinician occurs. It is expected that the SNN processor will work most of the time in the adaptive CRT mode facilitating optimal hemodynamic performance.
The synaptic weight adaptation rules applied during the normal CRT mode, takes into consideration two different occurrences. One, the deviation of the spike of the output neuron from the programmed value in terms of time. Two, the sampled Hebb states stored at each synapse as shown in Fig. 5B to which reference is again made. The synaptic weights adaptation rule generates a shift of the firing time of the l&F neuron in the direction of the programmed time. The synaptic weights adaptation rule are as follows:-
When the output neuron spike occurs before the programmed time, synapses that were at PRE_HEBB state increment their weights, and synapses that were at HEBB or POST_HEBB states decrement their weight. When the output spike occurs after the programmed time, synapses that were at PRE_HEBB state decrement their weight, and synapses that were at HEBB or POST_HEBB states increment their weight.
Within the adaptive CRT mode the SNN processor adapts its synaptic weights continuously interacting with the environment through the electric and hemodynamic sensors. Fig. 6A helps to explain the adaptive CRT mode synaptic weights adaptation rule. The output neuron fires at a time T measured from the sensed right atrial contraction every cardiac cycle, 200. The time T is compared, at step 202, with the time P stored at the pacing register of the output layer. If T > P the pacing register value is increased at step 204. Else, it is decreased at step 206. At the next cardiac cycle the pacemaker paces the heart with the updated values, stored at the pacing register. A numerical representation of the sensed hemodynamic performance is calculated with the updated pacing values and is compared, at steps 204 and 206, In one example the stroke volumes, SV, of the left or right ventricle is used as the hemodynamic performance criterion. Four possible states are defined by comparing the new stroke volumes with the previous stroke volumes. Fig 6B. shows the adaptive CRT mode learning profile for the synaptic adaptation rules. The numerical representation of the hemodynamic performance has a maximal value 220 at some pacing time interval. The task performed in the adaptive CRT mode is to modify the synaptic weight such that the value stored at the pacing register is the value that maximizes the hemodynamic performance. After a spike occurs, a corresponding state is determined as relates to the stored pacing register value stored. Spike 250 relates to the recorded pacing register 252 stored, defining a state 3. Spike 254 accordingly, as relates to pacing register 252 defines a state 1, spike 256 as relates to pacing register 258 defines state 4, spike 260 relates to pacing register 258 defining state 2. After the state associated with a spike is determined, the synaptic weight adaptation value is calculated in each synapse and its value depends on the flow diagram state and on the Hebb state stored at each synapse as was shown in Fig. 5A to which reference is again made. When the state associated with a spike is classified as 1 or 3 as in Fig. 6B to which reference is again made, the firing intervals are to be increased. When the flow diagram state is classified as 2 or 4 the firing intervals ae to be decreased. The synaptic weights are modified in each synapse separately in order to affect the firing time of the l&F neuron. Synapse in a PRE_HEBB state and is to increase its weight will cause the l&F neuron to increase firing intervals. A synapse in a POST_HEBB state and is to increase its weight will cause the l&F neuron to decrease firing intervals.
The synaptic weights adaptation rules described above, for both the normal and the adaptive CRT modes, occur simultaneously at each output neuron, in which a different optimized function is defined for each output neuron. The hemodynamic performance is a physiological parameter such as stroke volumes of each ventricle or a processed data such as the time derivative of a pressure sensor signal.
External Adaptive CRT Device
Another preferred embodiment of the present invention is an externally adaptive CRT device for diagnostics and cardiac rehabilitation. The external adaptive CRT device receives lEGMs and hemodynamic data using a communications channel, preferably a neural network module, or other learning modules, processes the data in the external device. In this case the external adaptive CRT device is not implanted in the patienfs body, and it transmits to a biventricular pacemaker or defibrillator implanted in the patienfs body the optimal pacing parameters, AV delay and W interval, to the pacemaker on-line. The diagnostics and rehabilitation procedure can be supervised by a clinician at a cardiac rehabilitation centre. The system of the invention, facilitates diagnostics and rehabilitation procedure of some form to be carried out at the patient environment (home, office etc) without the supervision of a clinician. The hemodynamic sensor used is an implanted sensor such as a pressure sensor, or a non-invasive hemodynamic sensor such as impedance sensors (such as BioZ® sensor of CardioDynamics Inc. San Diego, California, USA) or an echocardiograph. In the case of an echocardiograph, the images of the wall motion are to be transformed to a numeric hemodynamic performance function to be used for optimisation by the present invention external adaptive CRT device.
Benefits of the adaptive CRT device
Adaptive CRT Device cardiac rehabilitation capability
The system of the present invention uses the information derived from the hemodynamic sensor in two complementary ways. One, the specific hemodynamic condition correlates with a specific hemodynamic performance representation, and two, a classification of the heart's condition is performed. For each heart condition, the optimal AV delay and W interval are learned and updated continuously. The adaptive CRT device improves gradually the patient hemodynamic performance and hence the adaptive CRT device of the invention allows a gradual cardiac rehabilitation. This work scheme constitutes a potential clinical improvement in hemodynamic performance such as the cardiac output.
Consistent delivery of CRT Atrial event tracking is an important issue in cardiac timing cycles in general which has also strong implication on CRT devices, as described in "Device Therapy for Congestive Heart Failure" by K. Ellenbogen et al, Elsevier Inc. (USA), 2004. In existing CRT devices, CRT is not delivered consistently due to loss of atrial tracking for hours and even for days as can be seen by pacemaker diagnostics in patients' follow-ups. Loss of atrial tracking occurs due to several reasons, for example, surpassing the programmed maximal tracking rate (MTR) during exercise. The MTR is especially important for CRT patients since when they start to exercise their cardiac output is too low for their metabolic demand, and therefore the heart rate starts increasing in order to increase cardiac output. When the patient heart rate reaches the programmed MTR ( typically about 120 BPM), the implanted pacemaker stops delivery of CRT pacing and the cardiac output drops. The adaptive CRT device of the present invention, is expected to overcome the problem of loss of CRT delivery at the MTR. The classification mechanism explained above corresponding to the hemodynamic performance (maximal dp/dt for exmple), that produce the optimal AV delay and W interval for each heart condition, potentially replaces the need to use the existing MTR limit since the optimal pacing intervals at each state are learned and stored at the spiking neuron network synapse weights. The adaptive CRT device thus produces optimal pacing parameters that obviate the need for the MTR limit.
Adaptive Rate Response
Prediction of the desired optimal rate response to the physiological demand in response to all the patient conditions is a complex task. The currently used motion sensors do not respond to physiological/mental stress or anxiety which are not accompanied by an increase in the upper body motion. On the other hand, motion sensors respond to non-physiological events such as a bus ride, a plane take-off, operating a household drill, and other events external to the body and metabolic sensors are too slow to respond. An adaptive rate response pacemaker in accordance with the present invention, senses the ventricle contraction and paces the right atria, with the same SNN architecture of the present invention for adaptive CRT device presented above (using only one output neuron). The SNN processor predicts the optimal timing for pacing the right atria such that the maximal dp/dt obtained with a ventrical pressure sensor is optimized in all heart conditions. In Fig. 7 a block diagram is shown representing an adaptive rate responsive pacemaker based on the present invention. The sensors used are right atrial lead 280, right ventricle lead 282, and a pressure sensor, not shown. The advantage of the adaptive rate response pacemaker of the present invention is in the online, continuous adaptation to the patient hemodynamic needs with an algorithm that maximizes the hemodynamic performance as seen through a maximal dp/dt values.
Adaptive Capture Management
As discussed in US Patent 6,456,881 , pacemakers with auto-capture functions preserve energy and hence have a longer battery life. They also have the advantage of causing less patient discomfort due to an excessive heart stimulation. However, compiling the auto-capture function is a complex task due to the high variability of the heart electrical activity signals, and in particular, to the so called "fusion" phenomenon, exhibiting overlaps in time of the evoked response and internal beat. For CRT devices, capture management is even more important issue, since it is harder to capture the left ventricle comparing to the right ventricle. Usually, a higher pulse energy is used for the left ventricle and still it is not guaranteed that the left ventricle is consistently captured. Since with the adaptive learning the pacing interval delivered to the ventricles are not constant we can predict the time difference between the evoked response in the current cardiac cycle and the evoked response of the next cardiac cycle. If the sensed event matches the prediction, it is verified as an evoked response and capture is verified. If the event is not predicted, the beat is an intrinsic one. The ability to differentiate between evoked response beat from intrinsic beat using the adaptive CRT device algorithm can be used to manage the pulse energy in order to save battery energy while ensuring capture.
Other closed loop medical devices delivering physiologically active agents can benefit from the combined system of a learning module and deterministic module that serve also as a supervisor for the learning module as presented in this invention. The architecture guarantees safe operation and at the same time allow adaptive, sensitive to the patient system. It is expected to improve performance of various closed loop, feed back controlled therapeutic medical device such as Insulin pump, controlled drug delivery systems, brain stimulation devices, etc. Hence, the cardiac pacemakers and ICD devices is only one implementation of the invention.

Claims

1. An adaptive feed-back controlled system for regulating a physiological function of a body, comprising: • at least one sensor for continuously monitoring a significant physiological performance; • a learning neural network module for receiving and processing information of said at least one sensor and for learning at least one physiological aspect of said body; • a deterministic algorithmic module receiving parameters from said neural network module and for supervising online said learning module, and • a therapeutic delivering means connected to said deterministic algorithmic module and wherein said .
2. A system according to claim 1 wherein said modules and therapeutic delivery means are implanted, constituting an adaptive cardiac resynchronization therapy device, delivering biventricular pacing with adaptive AV delay and W interval, modified continuously with correlation to the hemodynamic performance of the heart.
3. A system according to Claim 1 wherein said neural network network module employs a spiking neuron network architecture.
4. A system according to Claim 3 wherein said neural network network module employs a spiking neuron network architecture implemnted as a silicon processor operating at with extremely low clock frequency.
5. A system according to claim 1 wherein said neural networks module is external.
6. A system according to claim 1 wherein said at least one sensor is a non invasive sensor.
7. A system according to claim 1 wherein said therapeutic delivery system is connected to said algorithmic module via a wireless communications link.
8. A system according to claim 1 wherein said therapeutic delivery means are at least one selected from the group consisting of pacemaker, defibrillator, brain stimulator and controlled drug delivery systems.
9. A method for regulating a controlled delivery of a physiologically active agent to a patient comprising the steps of: • obtaining continuous signal from at least one sensor monitoring said patient; • processing said continuous signal by an algorithmic processing module and a learning module, and wherein said learning modules carries out adaptive learning in connection with said at least one sensor is first supervised by applying an accepted set of parameters , and • affecting a delivery module in accordance with said processing, wherein said affect either results from said algorithmic process or from said learning processing.
10. A method for regulating a controlled delivery of a physiologically as in claim 9 wherein said learning module is a neural network module.
11. A method for regulating a controlled delivery of a physiologically as in claim 10 wherein said synaptic weight change is a Hebbian.
12. A method for adaptive biventricular pacing control comprising the steps of: • programming initial AV (atriaventricular) delay parameter and W (interventricular delay) interval parameter of an algorithmic module; • operating in normal CRT mode wherein an algorithmic deterministic module for controlling delivery of pulses, wherein pacing is carried out according to said parameters and wherein learning operation with said parameters takes place, and • transition to adaptive CRT mode wherein said AV delay and W interval change dynamically in order to achieve optimal hemodynamic performance, and wherein said adaptive mode is limited to perform in a predefined low limit of hemodynamic performance.
13. A method for adaptive biventricular pacing control as in claim 12 wherein the condition of the heart is classified continuously based on the information of a hemodynamic sensor wherein a maximal tracking rate is surpassed.
14. A method for adaptive biventricular pacing control as in claim 13 wherein said information relates to implanted ventricular pressure sensor.
5. A method for adaptive biventricular pacing control as in claim 13 wherein said information relates to ventricular impedance implanted sensor.
PCT/IL2004/000659 2003-07-21 2004-07-20 Adaptive resynchronization therapy system WO2005007075A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP04744999A EP1696999A4 (en) 2003-07-21 2004-07-20 Adaptive resynchronization therapy system
US10/565,279 US7657313B2 (en) 2003-07-21 2004-07-20 Adaptive cardiac resynchronization therapy system

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US48908003P 2003-07-21 2003-07-21
US60/489,080 2003-07-21
US50204203P 2003-09-10 2003-09-10
US60/502,042 2003-09-10

Publications (3)

Publication Number Publication Date
WO2005007075A2 true WO2005007075A2 (en) 2005-01-27
WO2005007075A3 WO2005007075A3 (en) 2005-04-14
WO2005007075B1 WO2005007075B1 (en) 2005-05-12

Family

ID=34083494

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IL2004/000659 WO2005007075A2 (en) 2003-07-21 2004-07-20 Adaptive resynchronization therapy system

Country Status (3)

Country Link
US (1) US7657313B2 (en)
EP (1) EP1696999A4 (en)
WO (1) WO2005007075A2 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1848499A2 (en) * 2004-12-12 2007-10-31 Ai-Semi Ltd. Optimizing and monitoring adaptive cardiac resynchronization therapy devices
EP1858580A2 (en) * 2005-02-28 2007-11-28 A.I. Medical Semiconductor Adaptive cardiac resyncronization therapy and vagal stimulation system
WO2008010220A2 (en) 2006-07-17 2008-01-24 A. I. Medical Semiconductor Intelligent control system for adaptive cardiac resynchronization therapy device
WO2010109448A1 (en) * 2009-03-22 2010-09-30 Ai Medical Semiconductor Ltd. Optimal deep brain stimulation therapy with q learning
US7963924B2 (en) 2006-10-25 2011-06-21 Sorin Crm Sas Heart simulator
US8396550B2 (en) 2008-10-29 2013-03-12 Sorin Crm Sas Optimal cardiac pacing with Q learning
US9020217B2 (en) 2008-09-25 2015-04-28 Cae Healthcare Canada Inc. Simulation of medical imaging
US9089710B2 (en) 2012-12-28 2015-07-28 Cardiac Pacemakers, Inc. Systems and methods to optimize pacing fusion with native activation
US9446246B2 (en) 2008-11-07 2016-09-20 Pacesetter, Inc. Identification of electro-mechanical dysynchrony with a non-cardiac resynchronization therapeutic device

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9089709B2 (en) 2004-12-12 2015-07-28 Sorin Crm Sas System and method for the visualization and optimization of cardiac resynchronization therapy
US8870742B2 (en) 2006-04-06 2014-10-28 Ethicon Endo-Surgery, Inc. GUI for an implantable restriction device and a data logger
WO2008130293A1 (en) * 2007-04-24 2008-10-30 St. Jude Medical Ab Implantable heart stimulating device
US8986253B2 (en) 2008-01-25 2015-03-24 Tandem Diabetes Care, Inc. Two chamber pumps and related methods
US8408421B2 (en) 2008-09-16 2013-04-02 Tandem Diabetes Care, Inc. Flow regulating stopcocks and related methods
AU2009293019A1 (en) 2008-09-19 2010-03-25 Tandem Diabetes Care Inc. Solute concentration measurement device and related methods
WO2011014704A2 (en) 2009-07-30 2011-02-03 Tandem Diabetes Care, Inc. Infusion pump system with disposable cartridge having pressure venting and pressure feedback
US8639328B2 (en) 2010-10-29 2014-01-28 Medtronic, Inc. Cardiac therapy based upon impedance signals
US8606387B2 (en) * 2010-11-18 2013-12-10 Taiwan Semiconductor Manufacturing Company, Ltd. Adaptive and automatic determination of system parameters
US8812414B2 (en) 2011-05-31 2014-08-19 International Business Machines Corporation Low-power event-driven neural computing architecture in neural networks
US9053428B2 (en) 2011-07-21 2015-06-09 Qualcomm Incorporated Method and apparatus of robust neural temporal coding, learning and cell recruitments for memory using oscillation
US9147155B2 (en) * 2011-08-16 2015-09-29 Qualcomm Incorporated Method and apparatus for neural temporal coding, learning and recognition
US8909576B2 (en) * 2011-09-16 2014-12-09 International Business Machines Corporation Neuromorphic event-driven neural computing architecture in a scalable neural network
US9092735B2 (en) 2011-09-21 2015-07-28 Qualcomm Incorporated Method and apparatus for structural delay plasticity in spiking neural networks
US9111224B2 (en) 2011-10-19 2015-08-18 Qualcomm Incorporated Method and apparatus for neural learning of natural multi-spike trains in spiking neural networks
US20130110190A1 (en) 2011-10-31 2013-05-02 Medtronic, Inc. Method to assess hemodynamic performance during cardiac resynchronization therapy optimization using admittance waveforms and derivatives
US9367797B2 (en) 2012-02-08 2016-06-14 Jason Frank Hunzinger Methods and apparatus for spiking neural computation
US9111225B2 (en) 2012-02-08 2015-08-18 Qualcomm Incorporated Methods and apparatus for spiking neural computation
US9180242B2 (en) 2012-05-17 2015-11-10 Tandem Diabetes Care, Inc. Methods and devices for multiple fluid transfer
US9555186B2 (en) 2012-06-05 2017-01-31 Tandem Diabetes Care, Inc. Infusion pump system with disposable cartridge having pressure venting and pressure feedback
US9715327B2 (en) 2012-06-07 2017-07-25 Tandem Diabetes Care, Inc. Preventing inadvertent changes in ambulatory medical devices
US9064215B2 (en) 2012-06-14 2015-06-23 Qualcomm Incorporated Learning spike timing precision
US9173998B2 (en) 2013-03-14 2015-11-03 Tandem Diabetes Care, Inc. System and method for detecting occlusions in an infusion pump
US9558443B2 (en) 2013-08-02 2017-01-31 International Business Machines Corporation Dual deterministic and stochastic neurosynaptic core circuit
US9789319B2 (en) 2013-11-21 2017-10-17 Medtronic, Inc. Systems and methods for leadless cardiac resynchronization therapy
EP2896428B1 (en) 2014-01-16 2016-11-09 Sorin CRM SAS Neural network assembly for evaluating and adapting an anti-tachycardia therapy by an implantable defibrillator
US9387330B2 (en) 2014-01-17 2016-07-12 Medtronic, Inc. Cardiac resynchronization therapy optimization based on intracardiac impedance and heart sounds
US9199086B2 (en) 2014-01-17 2015-12-01 Medtronic, Inc. Cardiac resynchronization therapy optimization based on intracardiac impedance
US10481565B2 (en) * 2014-11-11 2019-11-19 Applied Brain Research Inc. Methods and systems for nonlinear adaptive control and filtering
US9561376B2 (en) * 2015-01-29 2017-02-07 Pacesetter, Inc. Systems and methods for estimating intracardiac distance using sensed electrical pulses
US9965267B2 (en) 2015-11-19 2018-05-08 Raytheon Company Dynamic interface for firmware updates
US10473758B2 (en) 2016-04-06 2019-11-12 Raytheon Company Universal coherent technique generator
CN105999549B (en) * 2016-06-07 2018-10-16 创领心律管理医疗器械(上海)有限公司 Reduce and diagnose the Medical Devices of unnecessary cardiac pacing
US20180078773A1 (en) * 2016-09-21 2018-03-22 Cardiac Pacemakers, Inc. Multi-device cardiac resynchronization therapy with mode switching timing reference
WO2019183514A1 (en) 2018-03-23 2019-09-26 Medtronic, Inc. Vfa cardiac therapy for tachycardia
WO2019183512A1 (en) 2018-03-23 2019-09-26 Medtronic, Inc. Vfa cardiac resynchronization therapy
EP3768369A1 (en) 2018-03-23 2021-01-27 Medtronic, Inc. Av synchronous vfa cardiac therapy
US10596383B2 (en) 2018-04-03 2020-03-24 Medtronic, Inc. Feature based sensing for leadless pacing therapy
WO2020065582A1 (en) 2018-09-26 2020-04-02 Medtronic, Inc. Capture in ventricle-from-atrium cardiac therapy
US11951313B2 (en) 2018-11-17 2024-04-09 Medtronic, Inc. VFA delivery systems and methods
US11679265B2 (en) 2019-02-14 2023-06-20 Medtronic, Inc. Lead-in-lead systems and methods for cardiac therapy
WO2020177720A1 (en) * 2019-03-06 2020-09-10 Enteromed Ltd Devices, systems, and methods for delivering therapy to intestinal muscle
US11697025B2 (en) 2019-03-29 2023-07-11 Medtronic, Inc. Cardiac conduction system capture
US11213676B2 (en) 2019-04-01 2022-01-04 Medtronic, Inc. Delivery systems for VfA cardiac therapy
US11712188B2 (en) 2019-05-07 2023-08-01 Medtronic, Inc. Posterior left bundle branch engagement
US12017073B2 (en) 2019-05-16 2024-06-25 Enteromed Ltd Devices, systems, and methods for delivering therapy to a sacral nerve
US11305127B2 (en) 2019-08-26 2022-04-19 Medtronic Inc. VfA delivery and implant region detection
US11813466B2 (en) 2020-01-27 2023-11-14 Medtronic, Inc. Atrioventricular nodal stimulation
US11911168B2 (en) 2020-04-03 2024-02-27 Medtronic, Inc. Cardiac conduction system therapy benefit determination
US11813464B2 (en) 2020-07-31 2023-11-14 Medtronic, Inc. Cardiac conduction system evaluation

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5782885A (en) 1996-02-12 1998-07-21 Pacesetter Ab Rate responsive heart stimulation device using neural network and IEGM classifier
US5871507A (en) 1997-06-06 1999-02-16 Pacesetter Ab Implantable cardiac assist device having differential signal detection between unipolar atrial and ventricular leads using signal morphology analysis
US6223079B1 (en) 1997-12-15 2001-04-24 Medtronic, Inc Bi-ventricular pacing method
US6456881B1 (en) 2000-08-02 2002-09-24 Pacesetter, Inc. System and method of identifying fusion for dual-chamber automatic capture stimulation device

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04279175A (en) * 1990-07-03 1992-10-05 Telectronics Nv Arhythmia controller and arhythmia detecting method
US5251626A (en) * 1990-07-03 1993-10-12 Telectronics Pacing Systems, Inc. Apparatus and method for the detection and treatment of arrhythmias using a neural network
US5800467A (en) * 1995-12-15 1998-09-01 Pacesetter, Inc. Cardio-synchronous impedance measurement system for an implantable stimulation device
US5995871A (en) * 1997-10-29 1999-11-30 Uab Research Foundation System and method for cardioversion using scan stimulation
US5980571A (en) * 1997-12-11 1999-11-09 Colin Corporation Substitute-heart control apparatus
US6242988B1 (en) * 1999-09-29 2001-06-05 Lucent Technologies Inc. Spiking neuron circuit
US7280989B1 (en) * 2000-01-28 2007-10-09 Arizona Board Of Regents Phase-locked loop oscillatory neurocomputer
US6594524B2 (en) * 2000-12-12 2003-07-15 The Trustees Of The University Of Pennsylvania Adaptive method and apparatus for forecasting and controlling neurological disturbances under a multi-level control
US6704599B2 (en) * 2001-05-09 2004-03-09 Cardiac Pacemakers, Inc. Timing refractory period for cardiac resynchronization pacing

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5782885A (en) 1996-02-12 1998-07-21 Pacesetter Ab Rate responsive heart stimulation device using neural network and IEGM classifier
US5871507A (en) 1997-06-06 1999-02-16 Pacesetter Ab Implantable cardiac assist device having differential signal detection between unipolar atrial and ventricular leads using signal morphology analysis
US6223079B1 (en) 1997-12-15 2001-04-24 Medtronic, Inc Bi-ventricular pacing method
US6456881B1 (en) 2000-08-02 2002-09-24 Pacesetter, Inc. System and method of identifying fusion for dual-chamber automatic capture stimulation device

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
"Clinical Cardiac Pacing and Defibrillation", 2000
K. ELLENBOGEN ET AL.: "Device Therapy for Congestive Heart Failure", 2004, ELSEVIER INC.
See also references of EP1696999A4
WOLFGANG MAASS: "Pulsed Neural Network", 2001, THE MIT PRESS

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1848499A4 (en) * 2004-12-12 2009-12-02 Ai Semi Ltd Optimizing and monitoring adaptive cardiac resynchronization therapy devices
EP1848499A2 (en) * 2004-12-12 2007-10-31 Ai-Semi Ltd. Optimizing and monitoring adaptive cardiac resynchronization therapy devices
EP1858580A4 (en) * 2005-02-28 2011-08-03 A I Medical Semiconductor Adaptive cardiac resyncronization therapy and vagal stimulation system
EP1858580A2 (en) * 2005-02-28 2007-11-28 A.I. Medical Semiconductor Adaptive cardiac resyncronization therapy and vagal stimulation system
WO2008010220A2 (en) 2006-07-17 2008-01-24 A. I. Medical Semiconductor Intelligent control system for adaptive cardiac resynchronization therapy device
EP2046445A2 (en) * 2006-07-17 2009-04-15 A.I. Medical Semiconductor Intelligent control system for adaptive cardiac resynchronization therapy device
EP2046445A4 (en) * 2006-07-17 2013-02-13 A I Medical Semiconductor Intelligent control system for adaptive cardiac resynchronization therapy device
US7963924B2 (en) 2006-10-25 2011-06-21 Sorin Crm Sas Heart simulator
US9020217B2 (en) 2008-09-25 2015-04-28 Cae Healthcare Canada Inc. Simulation of medical imaging
US8396550B2 (en) 2008-10-29 2013-03-12 Sorin Crm Sas Optimal cardiac pacing with Q learning
US9446246B2 (en) 2008-11-07 2016-09-20 Pacesetter, Inc. Identification of electro-mechanical dysynchrony with a non-cardiac resynchronization therapeutic device
WO2010109448A1 (en) * 2009-03-22 2010-09-30 Ai Medical Semiconductor Ltd. Optimal deep brain stimulation therapy with q learning
US8774923B2 (en) 2009-03-22 2014-07-08 Sorin Crm Sas Optimal deep brain stimulation therapy with Q learning
US9089710B2 (en) 2012-12-28 2015-07-28 Cardiac Pacemakers, Inc. Systems and methods to optimize pacing fusion with native activation

Also Published As

Publication number Publication date
US20060235477A1 (en) 2006-10-19
EP1696999A2 (en) 2006-09-06
EP1696999A4 (en) 2008-05-28
WO2005007075A3 (en) 2005-04-14
US7657313B2 (en) 2010-02-02
WO2005007075B1 (en) 2005-05-12

Similar Documents

Publication Publication Date Title
US20060235477A1 (en) Adaptive resynchronization therapy system
US7894902B2 (en) Adaptive cardiac resyncronization therapy and vagal stimulation system
US8301250B2 (en) Intelligent control system for adaptive cardiac resynchronization therapy device
US8588907B2 (en) Closed-loop control of intermittent excitatory cardiac stimulation for therapeutic effect
US5814077A (en) Pacemaker and method of operating same that provides functional atrial cardiac pacing with ventricular support
EP1680179B1 (en) Pacing system for diastolic dysfunction
US8509895B2 (en) Ventricle pacing during atrial fibrillation episodes
US7890172B2 (en) Pacing output configuration selection for cardiac resynchronization therapy patients
EP0536720B1 (en) System for terminating a pacemaker-mediated tachycardia during rate adaptive pacing
EP2010279B1 (en) Pacing therapy for diastolic heart failure
US9295847B2 (en) Monitoring right ventricular hemodynamic function during pacing optimization
NL8100636A (en) METHOD FOR MAXIMIZING STROKE VOLUME BY ATRIOVENTRICULAR STIMULATION USING AN IMPLANTED CARDIOVERTOR / STIMULATOR AND APPARATUS FOR APPLYING THIS METHOD
US10092756B2 (en) System for stimulation therapy of the vagus nerve by implementation of a state transition model
JP4347699B2 (en) Pacemaker with adaptive arrhythmia detection window
US10124173B2 (en) System for stimulation therapy of the vagus nerve by implementation of a self-adaptive state transition model based on physical or physiological levels
US20100256700A1 (en) Method and apparatus for organ specific inflammation therapy
US9789320B2 (en) Method and apparatus for ambulatory optimization of multi-site pacing using heart sounds
US9981132B2 (en) System for stimulation therapy of the vagus nerve by implementation of a state transition model with a learning phase
WO2016061176A1 (en) System for optimizing multi-site pacing using heart sounds
US10099056B2 (en) System for stimulation therapy of the vagus nerve by implementation of a state transition model operating at multiple temporal or spatial resolutions
Goldschlager Advances in DDD Pacing: Progrès en Stimulation DDD

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
B Later publication of amended claims

Effective date: 20050411

WWE Wipo information: entry into national phase

Ref document number: 2006235477

Country of ref document: US

Ref document number: 10565279

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 2004744999

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2004744999

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 10565279

Country of ref document: US