Abstract: An implantable medical device (IMD) may include a communication module, a therapy control module, a firmware control module, and a service application. The communication module is configured to wirelessly communicate over an RF link with an external device. The therapy control module is configured to deliver therapy to the patient, and may include a reprogrammable therapy logic circuit configured to operate the therapy control module in a reprogrammable mode of operation, and base-therapy state machine (BTSM) logic circuit configured to operate the therapy control module in a base therapy mode of operation. The firmware control module may include CPU and a memory. The service application may be stored in the memory. The firmware control module is configured to launch the service application, and the BTSM logic circuit provides a base level of sensing and pacing therapy while the communications module in parallel maintains the RF link with the external device.

Abstract: An implantable medical device (IMD) may include a communication module, a therapy control module, a firmware control module, and a service application. The communication module is configured to wirelessly communicate over an RF link with an external device. The therapy control module is configured to deliver therapy to the patient, and may include a reprogrammable therapy logic circuit configured to operate the therapy control module in a reprogrammable mode of operation, and base-therapy state machine (BTSM) logic circuit configured to operate the therapy control module in a base therapy mode of operation. The firmware control module may include CPU and a memory. The service application may be stored in the memory. The firmware control module is configured to launch the service application, and the BTSM logic circuit provides a base level of sensing and pacing therapy while the communications module in parallel maintains the RF link with the external device.

Abstract: An implantable bi-ventricular heart stimulating device and system, suitable for treating congestive heart failure, have a control circuit with first and second pacing circuits and first and second sensing circuits. The device operates with time cycles corresponding to normal heart cycles. The control circuit determines: (a) whether a signal typical of an evoked response to a pacing pulse delivered by the first pacing circuit is sensed within a first time interval and (b) whether a signal typical for an R-wave transferred from the second ventricle, or from some other part of the heart, to the first ventricle is detected within a first time window. The operation of the device depends on whether the conditions (a) and (b) are fulfilled.

Abstract: An implantable bi-ventricular heart stimulating device (10) has a control circuit with first and second sensing circuits for respectively sensing in the two ventricles and first and second stimulation circuits for respectively stimulating the two ventricles. The control circuit determines whether a signal, sensed by said second sensing circuit, occurs essentially simultaneously with a signal sensed by the first sensing circuit. Furthermore, the control circuit determines whether a further signal is sensed by said second sensing circuit within a predetermined time interval which follows after the signal sensed by the second sensing circuit but within the same time cycle as that signal. If this occurs, the control circuit determines whether the sensed signals represent actual cardiac events, or are likely the result of far field detection.

Abstract: A heart stimulator has a pulse generator which emits stimulation pulses of different amplitudes, which are delivered to a patient's heart via a lead connected to the pulse generator. The pulse generator is controlled by a control unit, in a procedure for determining a stimulation threshold value, to emit stimulation pulses of successively unidirectionally changing amplitudes. Each stimulation pulse is followed by a test pulse having a predetermined high, constant amplitude delivered in a period corresponding to the refractory period after the preceding stimulation pulse. Each test pulse has an amplitude sufficient to capture a non-refractory heart. A measurement unit is connected to the electrode lead, and measures a signal picked up by the lead after each test pulse. The measured signals are supplied to a comparator, which compares the signals following the test pulses with each other.

Abstract: A heart stimulator has a pulse generator which emits stimulation pulses for delivery to the heart of a patient through a lead connected to the pulse generator and introduced into the heart. The heart stimulator has an evoked response detector which includes a measuring unit for measuring electrode signals picked up by the lead. An averaging unit is supplied with the electrode signals and forms an average value of the amplitude of the respective electrode signals for each heartbeat. A comparator in the evoked response detector compares the average value for each heartbeat with two predetermined limit values and emits a signal indicating that the electrode signal results from a fusion beat if the average values are between the two limit values.

Abstract: An implantable bi-ventricular heart stimulating device (10) has a control circuit with first and second sensing circuits for respectively sensing in the two ventricles and first and second stimulation circuits for respectively stimulating the two ventricles. The control circuit determines whether a signal, sensed by said second sensing circuit, occurs essentially simultaneously with a signal sensed by the first sensing circuit. Furthermore, the control circuit determines whether a further signal is sensed by said second sensing circuit within a predetermined time interval which follows after the signal sensed by the second sensing circuit but within the same time cycle as that signal. If this occurs, the control circuit determines whether the sensed signals represent actual cardiac events, or are likely the result of far field detection.

Abstract: An implantable bi-ventricular heart stimulating device and system, suitable for treating congestive heart failure, have a control circuit with first and second pacing circuits and first and second sensing circuits. The device operates with time cycles corresponding to normal heart cycles. The control circuit determines: (a) whether a signal typical of an evoked response to a pacing pulse delivered by the first pacing circuit is sensed within a first time interval and (b) whether a signal typical for an R-wave transferred from the second ventricle, or from some other part of the heart, to the first ventricle is detected within a first time window. The operation of the device depends on whether the conditions (a) and (b) are fulfilled.

Abstract: A heart stimulator has an evoked response detector which determines evoked response in the presence of polarization. To determine the magnitude of the polarization for different stimulation amplitudes, the electrode signals picked up by a lead after the delivery of a stimulation pulse having a selected amplitude are measured. A polarization signal is obtained from the picked up signals, and this polarization signal, with modification, is subtracted from signals picked up following subsequently emitted stimulation pulses. Dependent on the subtraction result, a determination is made as to whether an evoked response has occurred.

Abstract: An evoked response detector for a heart stimulator determines evoked response in the presence of polarization. The heart stimulator has a pulse generator which produces stimulation pulses of varying amplitudes, and a lead adapted for introduction into the heart of a patient is connected to the pulse generator for delivering stimulation pulses to the heart. The evoked response detector includes measuring and memory circuitry for measuring and storing the electrode signals picked up by the lead in response to the delivered stimulation pulses, at least one of these stimulation pulses having a sufficiently high amplitude for obtaining capture. Each measured electrode signal contains two signal components, one of these signal components being proportional to the amplitude of the associated stimulation pulse and the other signal component being substantially constant, independent of the associated stimulation pulse amplitude.

Abstract: A medical implant contains a magnetic field detector with a sensor whose capacitance changes in the presence of a magnetic field with a predefined strength, and a capacitance-controlled unit connected to the sensor. The capacitance-controlled unit sends a measurement signal to a detection unit. If a measurement signal parameter affected by capacitance exhibits a specific change over a predefined period of time, a detection signal is generated by the detection unit to indicate the presence of a magnetic field. The sensor's capacitance also changes when the sensor moves, and this is utilized for measuring activity in an activity measurement circuit connected to the capacitance-controlled unit and for generating an activity signal on the basis of the measurement signal.