摘要:
Optimization of evoked response detection in an automatic capture detection system employed by an implantable cardiac stimulation device is presented. Patient state information is used to determine the appropriate settings of variables that are associated with the evoked response signal detection algorithm. The variables used by the evoked response signal detection algorithm are first established for the patient in a variety of positions. During operation of the implantable cardiac stimulation device, the patient state is monitored and the variables used by the evoked response signal detection algorithm are adjusted accordingly.
摘要:
An implantable cardiac stimulation device and method automatically verify capture of one or both ventricular chambers by sensing a far-field signal in both atrial chambers. A far-field interval window is set following the delivery of the ventricular stimulation, during which a far-field signal is detected and compared to a signal representing a predetermined far-field R-wave that represents successful capture of one or both ventricular chambers. If the far-field signal is approximately equal to the predetermined far-field R-wave signal, then capture is verified. If capture is not verified, a threshold search is performed in the ventricle in which capture was lost.
摘要:
An implantable cardiac stimulation device is provided which alters the stimulation regime during determination of a capture threshold level. In order to avoid the potential for fusion beats which would interfere with a capture threshold level determination, a two-fold approach is used. First, the atrial refractoriness of the atrium of the patient's heart is extended by supplying a secondary atrial stimulation pulse during a prescribed time period following delivery of a primary atrial stimulation pulse. Second, the atrium is overdriven by providing an atrial stimulation pulse at a rate in excess of the intrinsic heart rate. Accordingly, the potential for fusion beats is significantly decreased and the reliability of the determined capture threshold level is increased. In a preferred embodiment, two closely placed stimulation pulses, i.e., a first primary atrial stimulation pulse and a secondary atrial stimulation pulse, are provided to an atrium of the patient's heart, and a second primary atrial stimulation pulse set to a test level is delivered faster than the heart's intrinsic rate. During this pacing regime, the potential for fusion beats is decreased and accordingly, sensing the presence or absence of evoked responses can accurately determine the capture threshold level.
摘要:
A pacemaker, or other implantable medical device, connected to heart tissue, detects atrial and ventricular electrical signals. The pacemaker analyzes the signals to determine whether the signals are representative of P-waves or R-waves according to atrial and ventricular sensitivity threshold values. Signals determined to be P-waves or R-waves are identified as sensed signals. Otherwise the signals are identified as not-sensed signals. The pacemaker further determines whether the sensed signals were detected during a refractory period or an alert period and its current tracking mode (e.g., VDD, DDD vs. DDI, VVI). Information pertaining to these atrial and ventricular signals is transmitted to an external programmer which generates representative histograms. The histograms present the number of counts detected within each of a set of high pass filtered amplitude ranges and further indicate the relative numbers of sensed vs. not-sensed counts. For the sensed counts, the histogram may further indicate the relative numbers of counts detected during refractory periods and alert periods. The histograms additionally show the applicable atrial or ventricular sensitivity threshold values to visually assist a physician in determining whether the threshold values are set properly. An auto-sensitivity adjustment system is also provided to determine optimal sensitivity threshold values.
摘要:
An implantable pacemaker automatically verifies atrial capture and performs atrial stimulation energy assessment when atrial capture is absent. The pacemaker delivers a stimulation pulse in the atrial chamber of the heart and samples the resulting far-field signal from the ventricular chamber during a predetermined far-field interval window. The pacemaker then compares the far-field signal sample to a predetermined far-field signal recognition template. If the far-field signal sample is approximately equal to the far-field signal recognition template, then atrial capture is deemed verified; otherwise, the pacemaker performs an atrial stimulation energy determination. Optionally, the pacemaker automatically determines the timing of the far-field interval window and defines the far-field signal recognition template.
摘要:
Techniques are provided for updating a morphology template used to discriminate abnormal cardiac rhythms. In one example, a non-weighted candidate morphology template is generated based on far-field R-wave morphology. A weighted candidate morphology template is generated based on an ensemble average of the non-weighted candidate morphology template and a previous (i.e. active) morphology template. The previous morphology template is then selectively updated based on a comparison of additional R-waves against both the non-weighted and the weighted candidate templates. Thereafter, abnormal cardiac rhythms such as ventricular tachycardia and supraventricular tachycardia are discriminated using the updated morphology template based on newly-detected far-field R-waves. These techniques provide a method for updating the morphology discrimination template in response to long-term changes in morphology due to cardiac remodeling or cardiac disease progression.
摘要:
Detection of T wave oversensing in an ICD is accomplished in order to prevent improper application of treatment to a patient. The ICD device senses for electrical impulses representing the R waves of a beating heart. In some instances the ICD device will sense T waves that it will assume to be R waves, because the ICD device expects or assumes that such sensed signals are R waves. Time intervals between each detected, assumed R waves are measured and a list of intervals is generated. The list is transformed into its frequency domain equivalent and analyzed for peaks and randomness criteria to determine whether T wave oversensing has occurred.
摘要:
A method for sensing cardiac activity in an atrium of a patient's heart includes delivering a pulse to the atrium using an electrode configuration that includes at least a cathode electrode; sensing cardiac activity in the atrium using a unipolar electrode configuration to provide a sensed signal wherein the unipolar electrode configuration does not include the cathode electrode; determining the duration during which the voltage of the sensed signal falls below a threshold voltage; and comparing the determined duration to a parameter to determine whether the pulse caused an atrial evoked response.
摘要:
A plurality of electrodes are implanted in, on or near the patient's heart and initially configured to define first circuits or vectors enabled for at least one of sensing and stimulating and second circuits or vectors which are idle for at least one of sensing and stimulating. Selected first circuits or second circuits are tested for fault indications related to one or both of sensing and stimulating and a status record is updated to indicate corresponding sensing fault indications and stimulating fault indications. If a sensing fault is found in one of the first circuits, the first circuit is redefined when enabled for sensing to include at least one electrode of a second circuit that does not have a record of a sensing fault indication. Likewise, if a stimulating fault is found in one of the first circuits, the first circuit is redefined when enabled for stimulating to include at least one electrode of a second circuit that does not have a record of a stimulating fault indication.
摘要:
An implantable cardiac stimulation device selects an arrhythmia therapy based upon the time of day. The device comprises an arrhythmia detector that detects an accelerated arrhythmia of a heart, and a data circuit that maintains a time record of cardiac cycle lengths developed during detected accelerated arrhythmias. A therapy circuit provides a selected therapy to the heart based upon the maintained time record of cardiac cycle lengths and the time of day.