Reveal Linq and false diagnosis of bradycardia

Tracing
N° 17
Manufacturer Medtronic Device ILR Field Reveal Linq
Patient

Same patient as in tracing 15.

Graph and trace

This episode is classified as Brady (4 consecutive RR cycles with interval> 1500 ms);

  1. on the tracing, there is a sinus rhythm with a large variability in R-wave amplitude; undersensing of small-amplitude complexes occurring after a more voluminous complex;
  2. after 4 long RR pseudo-intervals (> 1500 ms), diagnosis of bradycardia;
  3. the bradycardia episode ends after four consecutive R-waves detected with a ventricular interval less than or equal to the programmed interval.
Comments

This episode corresponds to a false diagnosis of bradycardia in conjunction with undersensing of R-waves. The most frequent causes of false diagnoses of a pause by the device are

  1. the loss of contact between the sensing electrodes of the device and muscle tissue; this is most often reflected in the absence of changes in RR intervals before and after the pause and by an abrupt deviation of the recorded signal followed by a gradual return to the reference value;
  2. a defect in small-amplitude R-wave sensing as in this example.

Different settings are available for programming in order to prevent the repetitive recording of false pauses. The sensitivity is not fixed during the cardiac cycle but rather adapts according to the amplitude of the detected R-wave with various programmable parameters. The sensing of an R-wave triggers a programmable blanking period (nominal value 150 ms) without possible sensing to prevent double counting of the R-wave. The sensing threshold is then set to 65% (non-programmable value) of the measured value of the R-wave. It should be noted that this threshold cannot exceed 0.65 mV. If an R-wave exceeds 1 mV, the sensing threshold is automatically set to 0.65 mV. The sensing threshold remains fixed for a programmable period (Stability threshold duration before decay, nominal value 150 ms). At the end of this time interval, the sensitivity increases (the threshold decreases) linearly for one second to reach 30% of the amplitude of the R-wave (non-programmable values). The sensitivity remains fixed until 1.5 seconds after the sensing of the previous R-wave. The sensitivity then increases up to 20% of the maximum value of the R-wave and then linearly thereafter until a new R-wave is sensed or the programmed minimum threshold is reached. The sensing threshold never falls below the programmed sensitivity setting (nominal value 0.035 mV). In order to avoid undersensing issues, it is possible to shorten the blanking value (poorly effective in this setting), to reduce the stability time of the threshold before decay or to reduce the programmed sensitivity value by verifying that the new programming is not associated with oversensing (P-wave, T-wave, myopotentials).

Various modifications have been made to the new devices in an attempt to reduce the false diagnoses of bradycardia or tachycardia which can saturate the device's memory.

  1. The use of a new titanium nitride coating could optimize the recording reliability of electrocardiographic signals, increase the signal-to-noise ratio and reduce oversensing of parasitic signals.
  2. To limit the risk of undersensing in a patient with ventricular extrasystoles (beat-to-beat amplitude change) or with small-amplitude R-waves, a new smart filtering algorithm has been integrated. When a pause is diagnosed, a second filter operates with the aim of reclassifying undersensed intervals and rejecting false positives (false pause diagnoses).
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