Chapter 3 · Oversensing · Case 12
The benefits of induction at the end of implantation
Patient and episode
Patient
- Patient implanted with a dual-chamber defibrillator with a Fidelis lead undergoing a box change (Evera XT DR); induction protocol at the end of the procedure.
The recording
Tap a number on the trace, or an entry in the list below
Rate / interval plot

EGM

- What do you think of this interval plot? The plot initially shows an induction protocol with rapid pacing burst; the fact that the low-amplitude electric shock is delivered on the T wave is not indicated on the graph; induction of a probable ventricular arrhythmia detected in the VF zone (appearance compatible with a real ventricular arrhythmia); the first shock delivered (35 Joules) significantly alters the ventricular cycles, with evidence of a cloud of points (very short cycles and longer cycles with great variability); the second shock does not alter the appearance of the ventricular cycles.
- What type of procedure is involved? The EGM shows rapid ventricular pacing followed by a low-amplitude shock delivered on the T wave (in the vulnerable period) due to an induction protocol at the end of implantation to check for correct defibrillator function.
- What is the effect of the first low output shock? The electric shock induces rapid ventricular tachycardia, which is detected in the VF zone.
- What is the effect of the second high output shock? The electric shock terminates the ventricular arrhythmia but is followed by the over-detection of anarchic signals with saturation of the amplifiers, suggesting a diagnosis of lead dysfunction.
Points to remember
- This plot shows the value of inducing ventricular arrhythmia when changing leads, particularly when the patient is implanted with a lead known to have an increased rate of dysfunction.
- Lead fracture was unmasked in this patient following detection of an episode of induced VF and the delivery of an electric shock; the electric shock delivered sometimes stretches a lead which had already been stretched and weakened beforehand and causes a definitive fracture; the stimulation impedances were strictly normal prior to this episode and no episode of oversensing had previously been recorded in the device memory; therefore there was no warning sign of lead dysfunction and no other indication for this patient to have an induction protocol performed when the box was changed.
- This young patient had the faulty lead removed and a new ipsilateral lead implanted.
Practice out loud
Just describe the tracing. What do you think is going on? Describing the numbers can help.
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From Medtronic ICD — clinical cases by P. Bordachar, A. Thiyagarajah, L. Fontagne, M. Strik, S. Ploux. Published by Cardiocases. Every numbered marker on a recording is explained in the list beneath it; tap a marker on the trace or an entry in the list.
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