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Safety threshold of R-wave amplitudes in patients with implantable cardioverter defibrillator

Authors

J M Lillo-Castellano, Manuel Marina-Breysse, Alfonso Gómez-Gallanti, J B Martínez-Ferrer, Javier Alzueta, Luisa Pérez-Álvarez, Arcadi Alberola, Ignacio Fernández-Lozano, Anibal Rodríguez, Rosa Porro, Ignacio Anguera, Adolfo Fontenla, J J González-Ferrer, Victoria Cañadas-Godoy, Nicasio Pérez-Castellano, Daniel Garófalo, Óscar Salvador-Montañés, Conrado J Calvo, Jorge G Quintanilla, Rafael Peinado, Inmaculada Mora-Jiménez, Julián Pérez-Villacastín, J L Rojo-Álvarez, David Filgueiras-Rama

Journal Paper

http://doi.org/10.1136/heartjnl-2016-309295

Publisher URL

https://journals.bmj.com/

Publication date

October 2016

A safety threshold for baseline rhythm R-wave amplitudes during follow-up of implantable cardioverter defibrillators (ICD) has not been established. We aimed to analyse the amplitude distribution and undersensing rate during spontaneous episodes of ventricular fibrillation (VF), and define a safety amplitude threshold for baseline R-waves.

METHODS:
Data were obtained from an observational multicentre registry conducted at 48 centres in Spain. Baseline R-wave amplitudes and VF events were prospectively registered by remote monitoring. Signal processing algorithms were used to compare amplitudes of baseline R-waves with VF R-waves. All undersensed R-waves after the blanking period (120 ms) were manually marked.

RESULTS:
We studied 2507 patients from August 2011 to September 2014, which yielded 229 VF episodes (cycle length 189.6±29.1 ms) from 83 patients that were suitable for R-wave comparisons (follow-up 2.7±2.6 years). The majority (77.6%) of VF R-waves (n=13953) showed lower amplitudes than the reference baseline R-wave. The decrease in VF amplitude was progressively attenuated among subgroups of baseline R-wave amplitude (≥17; ≥12 to <17; ≥7 to <12; ≥2.2 to <7 mV) from the highest to the lowest: median deviations -51.2% to +22.4%, respectively (p=0.027). There were no significant differences in undersensing rates of VF R-waves among subgroups. Both the normalised histogram distribution and the undersensing risk function obtained from the ≥2.2 to <7 mV subgroup enabled the prediction that baseline R-wave amplitudes ≤2.5 mV (interquartile range: 2.3-2.8 mV) may lead to ≥25% of undersensed VF R-waves.

CONCLUSIONS:
Baseline R-wave amplitudes ≤2.5 mV during follow-up of patients with ICDs may lead to high risk of delayed detection of VF.