Abstract:
An implantable medical device, IMD, (100) conducts CRT settings searches at multiple CRT settings search periods during an optimization time period by testing different candidate CRT settings and selecting the optimal CRT setting based on output signals of a hemodynamic sensor (240). The respective optimal CRT settings determined during the optimization time period are employed in order to predict at least one future optimal CRT setting that can be used by the IMD (100) following the end of the optimization time period. The IMD (100) then generates and applies pacing pulses to a subject's (5) heart (10) according to a CRT setting of the at least one future optimal CRT setting. The embodiments therefore enable efficient cardiac resynchronization therapy without any sensor readings after the end of the optimization time period and can therefore provide cardiac resynchronization therapy even if the hemodynamic sensor (240) becomes inoperable.
Abstract:
An implantable medical device (100) is configured for generating a cardiogenic impedance signal representative of the cardiogenic impedance of at least a portion of a heart (10) of a subject (20) during multiple cardiac cycles. A transform processor (132) generates a spectrum signal by applying a time- to-frequency transform to the cardiogenic impedance signal. The spectrum signal is processed by a distribution processor (133) configured to calculate a distribution parameter indicative of a distribution in at least a portion of the spectrum signal. The calculated distribution parameter is of high diagnostic value and is employed by an arrhythmia classifier (134) in order to classify a detected arrhythmia of the heart (10), such as discriminate between hemodynamically stable or unstable arrhythmias and/or supraventricular or ventricular tachycardia.
Abstract:
A pulse generating implantable medical device comprising a power source for energizing the medical device, a control unit, a plurality of switching units (SW-RC-1, SW-STIM-1, SW-RT-1), a timing unit, a pulse generating unit adapted to generate one or many stimulation pulses to be applied to human or animal tissue via one or many stimulation electrodes, and a coupling capacitor in series with each stimulation electrode. A stimulation pulse is adapted to be applied during a stimulation pulse timing cycle that includes a stimulation phase and a recharge phase, and the timing of a stimulation pulse timing cycle is controlled by said control unit via the timing unit and said switching units. The implantable medical device further comprises an energy storage unit and, during the recharge phase, one or many of the switching units is adapted to establish electrical connection between said one or many stimulation electrodes and said energy storage unit in order to collect and store energy from applied stimulation pulses.
Abstract:
An implantable medical device, IMD, (100) comprises atrial and ventricular sensing units (125, 135) for sensing atrial or ventricular electric events. The IMD (100) also comprises atrial and ventricular pulse generators (120, 130) for generating atrial or ventricular pacing pulses. The ventricular sensing unit (135) is connectable to a multi-electrode lead (220) to individually sense electric events in a ventricle (14) using multiple electrode pairs (221, 223, 225) implanted at different ventricular sites. A controller (140) blanks the ventricular sensing unit (135) during a blanking period following delivery of an atrial stimulating pulse by the atrial pulse generator (120) and activates the ventricular sensing unit (135) at the expiry of the blanking period. Due to the lower propagation speed of PVC depolarization waves and the multi-site sensing, a PVC depolarization wave initiated at a ventricular site during the blanking period can be detected by the IMD (100).
Abstract:
An implantable medical device, IMD, (100) is connectable to at least one ventricular lead (210) having a ventricular basal electrode (214) and a ventricular apical electrode (212). The IMD (100) comprises a pulse generator (120) for generating pacing pulses applied to a heart (10) through the ventricular lead (210). The operation of this pulse generator (120) is controlled by a controller (130) that is configured to control the pulse generator to first deliver a pacing pulse to the ventricular basal electrode (214) to stimulate the basal portion of the ventricle (12, 14) before a pacing pulse is delivered to the apical portion of the ventricle (12, 14) by the ventricular apical electrode (212). This pulse sequence achieves a biologically more correct cardiac stimulation and a contraction pattern that reduces the risk for valvular regurgitation.
Abstract:
The invention relates to a medical implantable lead of the kind being adapted to be implanted into a human or animal body for monitoring and/or controlling of an organ inside the body. The lead comprises in a distal end a tubular header (3) inside which a shaft (7) is rotatable as well as extendable and retractable arranged and carries in a distal end a combined fixation means and electrode member in form of a helix (4), which is provided with a first contact surface being electrically connectible to a connector at the proximal end of the lead by means of an electric conductor (8), and which by means of the shaft is rotatable in relation to the lead and extendable out from the distal end to be able to fixate the distal end of the lead to the organ by being screwed into the tissue. The shaft also carries a second contact surface (13) being positioned on or adjacent a proximal portion of the helix and being connectible to a connector at the proximal end of the lead by means of an electric conductor (8). The lead comprises a conduction controlling means (14), which at least during an initial stage after implantation is capable of render the first contact surface electrically inactive and which is capable of render the first contact surface electrically active after the initial stage. By means of the inventive lead it is possible to detect whether the helix is sufficient screwed into the tissue (12) or not.
Abstract:
The present invention is directed to an implantable medical device and a method for power management for power efficient use of RF telemetry during, for example, conditions where long periods of continuous monitoring of the device and the patient is desired such as during MRI procedures. A protocol module adapted to, at receipt of a low power protocol indication, activate and use a low power protocol for communication between the device and external units. The protocol module is capable of switching between different communication protocols including a low power communication protocol and a default RF communication protocol depending on, for example, whether continuous long-term monitoring of the patient is performed. During the low power communication protocol, the protocol module is adapted to select parts of stored electrophysical and/or hemodynamical signal waveforms for telemetric transmission and to create communication packages having a predetermined length using the selected parts of the electrophysiological and/or hemodynamical signal waveform. Further, a transmitter is instructed to transmit the communication packages at predetermined transmission intervals and the telemetry module is instructed to power down the transmitter or set the transmitter in a lowest possible activation state during intermediate periods between the transmission intervals.
Abstract:
The present invention relates to a medical implantable lead having a coaxial structure, where an insulating tube arranged between an inner coil and an outer coil is provided with a periodically alternating capacitance along the length thereof in order to reduce lead tip heating during MRI scanning.
Abstract:
The present invention generally relates to implantable medical devices, such as bi-ventricular pacemakers, and, in particular, to techniques for such devices for detecting and monitoring mechanical dyssynchronicity of the heart. A dyssynchronicity measure indicating a degree of mechanical dyssynchronicity of a heart of a patient is calculated. A first intracardiac impedance set is measured using electrodes placed such that the first intracardiac impedance set substantially reflects a mechanical activity of the left side of the heart and a second intracardiac impedance set is measure using electrodes placed such that the second intracardiac impedance set substantially reflects a mechanical activity of the right side of the heart. The measure of a dyssynchronicity is calculated based on a resulting parameter set from a comparison between at least a subset of the first and the second impedance sets, respectively, the subsets containing information of the mechanical systole, wherein a reduced dyssynchronicity measure corresponds to an improved synchronicity between the right side and the left side of heart.
Abstract:
The invention relates to implantable medical devices, in particular to a implantable heart-stimulation device, a method for operating an implantable heart-stimulation device and a heart-stimulation system, wherein stimulation pulses are delivered via a plurality of stimulation channels to selected sites on or about a patient's heart via electrodes, and wherein coupling capacitors included in the stimulation channels are subsequently discharged through a sequence of temporally non-overlapping partial discharges of the respective coupling capacitors. By this configuration, the risk of charge neutrality of a stimulation channel not being maintained at the end of a stimulation sequence, comprising the delivery of stimulation pulses via stimulation channels, is reduced or eliminated.