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68 Routine cardiac implantable electronic device checks are not required after direct current cardioversion
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  1. Clare Stodart,
  2. Benedict Wiles,
  3. Phillip Banks,
  4. Sian Mackay,
  5. John Paisey
  1. University Hospital Southampton NHS Foundation Trust

Abstract

Background At our institution, Cardiac Implantable Electronic Devices (CIEDs) are routinely checked after elective direct current cardioversion procedures (DCCV) to ensure that the leads and generator have not been damaged. Anecdotally, this was perceived to be an unnecessary intervention. A comprehensive assessment of the impact of DCCV on device parameters and programming would allow either a change in practice to be safely undertaken, or to justify this ongoing use of resources.

Method We retrospectively evaluated the routine post procedure device checks performed on consecutive patients with CIEDs undergoing elective DCCV at our institution between 2013 and 2019. Lead parameters (impedance, high voltage impedance, amplitude and capture threshold) recorded immediately post DCCV, were compared to the previous recorded values for each device. Atrial threshold and P wave amplitudes were not assessed as they would have been significantly altered by conversion of atrial dysrhythmia to sinus rhythm, rather than by the procedure itself. Where values could not be determined at either of the two device checks (pre or post DCCV), for example no R wave amplitude due to absence of underlying rhythm, this parameter was excluded from the data set. Values before and after DCCV were compared using a paired samples t test. Lead thresholds were assessed in volts, provided the pre and post DCCV checks used the same pulse width. The incidence of programming changes as a direct result of DCCV was also calculated.

Results A total of 53 patients were identified for analysis (60.3% male, mean age 73 +/- 15 years). All patients underwent an elective DCCV receiving up to 3 shocks (starting at 150J) with defibrillation pads placed in conventional positions (either anterior-posterior or anterolateral) >8cm from the CIED generator. Device types were dual chamber pacemaker 51%, single chamber pacemaker 11%, CRT-D 11%, DR-ICD 9%, CRT-P 8%, VR-ICD 6% and S-ICD 4%. CIED manufacturers were Medtronic 66%, Boston Scientific 21%, Abbott 11%, and Microport (Sorin) 2%. The mean time between pre DCCV and post DCCV device checks was 4.7 +/- 2.7 months.

The mean changes in lead parameters (presented with 95% confidence intervals) were as follows; impedance -7.4 ohms (-22.0 to +7.3, p=0.32, n=90), high voltage impedance -0.2 ohms (-3.7 to +3.4, p=0.92, n=17), amplitude -0.1 mV (-0.7 to + 0.6, p=0.80, n=38) and lead threshold -0.01 V (-0.07 to +0.04, p=0.64, n=57). The incidence of device reprogramming as a result of DCCV was found to be 0% (n=53).

Conclusion DCCV is not associated with statistically significant changes in lead impedance, amplitude or threshold across a range of CIED devices. DCCV is not associated with a need for alterations in device programming post procedure. Providing the standard protocol and pad positions (anterior-posterior or anterolateral, >8cm from CIED generator) for DCCV in patients with CIEDs are followed, there is therefore no requirement for a routine CIED check post DCCV.

Conflict of Interest None

  • Cardioversion
  • Pacemaker
  • Defibrillator

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