Electrical scalpel

Patient

This 67-year-old man received a Lumax 340 HF-T triple chamber defibrillator in the context of dilated cardiomyopathy with left bundle branch block, before undergoing prostate surgery.

Main programmed settings

  • VF zone at 231 bpm and VT1 zone at 150 bpm
  • 8 /12 cycles in the VF zone and 26 cycles in the VT1 zone were needed for the diagnosis
  • Maximum sensitivity programmed at 0.5 mV
  • VF zone: ATP one shot and 8 shocks of maximum strength (40 J); VT1 zone: 3 bursts of ATP, followed by 3 ramps, followed by a single 15-J shock and 7 shocks of maximum strength
  • Pacing mode: DDIR RV pacing at 50 bpm, (very high LV threshold)


Trace

Programmer tracing

  1. atrial and RV only paced rhythm;
  2. rapid, polymorphous signals are visible on the 3 channels;
  3. detection at the atrial (Ars) and ventricular (VF) channels;
  4. episode of VF detected after 8 VF classified cycles;
  5. charge of the capacitors;
  6. end of oversensing;
  7. interruption of the charge after 3 consecutive VP cycles;
  8. competition between VF redetection (8/12 cycles in the VF zone) and end of episode (12/16 VS or VP cycles) counters;
  9. further oversensing;
  10. VF redetection counter full (8/10 cycles in the VF zone); charge of the capacitors;
  11. short charge;
  12. end of charge;
  13. at the end of the charge, delivery of an electrical shock on the first short (VF or VT1) or long (VS or VP) cycle following the charge; this is the second charge for a single episode (the first was interrupted) and the electrical shock was delivered despite the slow rhythm. The” PSh DDI” labeling after the shock explains that the defibrillator operated in the programmed post-shock pacing mode (DDI) for a programmable duration (nominal = 10 sec);
  14. end of episode.

Comments

When a recipient of defibrillator undergoes surgery, the surgeon must be advised a) to use the electrical scalpel in the bipolar mode, b) to use it for very short periods of time, and c) to place the plates of the scalpel away from the pulse generator of the defibrillator.

To completely eliminate the risk of clinically significant interference, pacing must be programmed to an asynchronous mode (available from the Lumax 740 model and subsequent models) and detection and therapies must be turned off. This burdensome strategy mandates the pre-operative programming and the postoperative interrogation and re-programming of the device with verification of the thresholds.

One other option consists in placing a magnet over the pulse generator to inhibit all therapies. The magnet also prevents the memorization of artifacts interpreted as arrhythmic episodes, avoiding the need to delete the genuine episodes that occurred before exposure to the interferences (since this is a looping memory of finite storage capacity). The magnet effect is reversible, and the therapies and memorization of the episodes resume upon removal of the magnet. The patient, who is no longer protected by the defibrillator, must be monitored throughout the procedure. The use of a magnet must not prevent a full postoperative interrogation of the device.

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