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Predicting inappropriate S-ICD® episodes by simple 12-lead surface ECG parameters
Jan Wagner1, Benjamin Rath1, Kevin Willy1
1Department of Cardiology II - Electrophysiology, University Hospital Muenster, Muenster, Germany.
A preimplantation electrocardiogram (ECG) can predict inappropriate S-ICD® shocks. QRS-T wave discordance in lead I is a significant predictor, especially in hypertrophic cardiomyopathy patients.
Area of Science:
- Cardiology
- Biomedical Engineering
Background:
- Subcutaneous Implantable Cardioverter-Defibrillators (S-ICD®) offer protection against sudden cardiac death.
- Inappropriate shocks from S-ICD® systems are a concern, often caused by oversensing.
- Predictive markers for these inappropriate episodes are crucial for patient management.
Purpose of the Study:
- To evaluate the predictive role of a preimplantation 12-lead electrocardiogram (ECG) for inappropriate S-ICD® episodes.
- To identify specific ECG parameters associated with oversensing and subsequent inappropriate shocks.
Main Methods:
- A cohort of 116 patients with S-ICD® and at least 6 months follow-up was analyzed.
- Preimplantation 12-lead ECGs were assessed for QRS and T-wave amplitude, concordance/discordance, and QRS/T wave ratio using Datinf® Measure software.
- Results were correlated with occurrences of inappropriate S-ICD® episodes due to oversensing.
Main Results:
- Of 116 patients, 17 (14.7%) experienced 27 inappropriate shocks, primarily due to T-wave oversensing.
- Hypertrophic cardiomyopathy (HCM) was a significant risk factor (OR 6.16, p=0.004).
- QRS-T wave discordance in lead I independently predicted inappropriate shocks (OR 6.5, p=0.003); the combination of HCM and lead I discordance increased risk 8.4-fold (p=0.003).
Conclusions:
- Preimplantation ECG analysis, specifically QRS-T wave discordance in lead I, is a valuable tool for predicting inappropriate S-ICD® shocks.
- This finding holds particular importance for patients with hypertrophic cardiomyopathy.
- Identifying these ECG patterns can help mitigate the risk of inappropriate therapy in S-ICD® recipients.
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