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Published on: February 28, 2012
Defibrillation Testing During Implantation of Subcutaneous Implantable Cardioverter Defibrillators
Fawzi Kerkouri1, Romain Eschalier2, Samir Fareh3
1Division of Cardiology, European Georges Pompidou Hospital, Paris, France; Department of Cardiology, University Hospital of Brest, Brest, France; Université Paris Cité, Inserm U970, Paris Cardiovascular Research Center, Paris, France; University of Brest, Laboratoire ORPHY EA 4324, Brest, France.
Defibrillation testing (DT) during subcutaneous implantable cardioverter-defibrillator (S-ICD) implantation is often unnecessary. Omitting DT in most S-ICD patients does not increase mortality or shock risks, suggesting selective testing is sufficient.
Area of Science:
- Cardiology
- Medical Devices
- Electrophysiology
Background:
- Defibrillation testing (DT) is recommended for subcutaneous implantable cardioverter-defibrillator (S-ICD) implantation despite limited evidence.
- The necessity of DT in S-ICD recipients requires further investigation.
Purpose of the Study:
- To evaluate the long-term impact of performing defibrillation testing (DT) during S-ICD implantation.
- To determine if omitting DT affects patient outcomes.
Main Methods:
- The HONEST study is a nationwide, observational cohort of S-ICD recipients in France (2012-2019).
- Propensity score-weighted analyses compared outcomes between patients who underwent DT and those who did not.
- Five-year endpoints were centrally adjudicated.
Main Results:
- Defibrillation testing (DT) was performed in 82.6% of 4,924 patients, decreasing over time.
- Nontested patients had distinct demographic and clinical characteristics.
- DT omission was not associated with increased risks of overall mortality, cardiovascular mortality, sudden cardiac death, or inappropriate shocks.
- Rates of ineffective shocks or undetected ventricular arrhythmias were similar between groups.
Conclusions:
- Defibrillation testing (DT) can be safely omitted in the majority of S-ICD recipients.
- Selective DT may be considered for specific higher-risk patient subgroups.
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