TY - JOUR
T1 - Cardiac resynchronization is pro-arrhythmic in the absence of reverse ventricular remodelling
T2 - A systematic review and meta-analysis
AU - Deif, Bishoy
AU - Ballantyne, Brennan
AU - Almehmadi, Fahad
AU - Mikhail, Michael
AU - McIntyre, William F.
AU - Manlucu, Jaimie
AU - Yee, Raymond
AU - Sapp, John L.
AU - Roberts, Jason D.
AU - Healey, Jeff S.
AU - Leong-Sit, Peter
AU - Tang, Anthony S.
PY - 2018/9/1
Y1 - 2018/9/1
N2 - Aims Cardiac resynchronization therapy (CRT) has been shown to reduce mortality and heart failure (HF) hospitalization but its effects on the rate of ventricular arrhythmias (VAs) appears to be neutral. We hypothesize that CRT with LV epicardial stimulation is inherently pro-arrhythmic and increases VA rates in the absence of reverse ventricular remodelling while conferring an anti-arrhythmic effect in mechanical responders. Methods In this systematic review and meta-analysis, we considered retrospective cohort, prospective cohort, and randomized and results controlled trials comparing VA rates between cardiac resynchronization therapy-defibrillator (CRT-D) non-responders, CRT-D responders and those with implantable cardioverter-defibrillator (ICD) only. Studies were eligible if they defined CRT-D responders using a discrete left ventricular volumetric value as assessed by any imaging modality. Studies were identified through searching electronic databases from their inception to July 2017. We identified 2579 citations, of which 23 full-text articles were eligible for final analysis. Our results demonstrated that CRT-D responders were less likely to experience VA than CRT-D non-responders, relative risk (RR) 0.49 [95% confidence interval (CI) 0.41–0.58, P < 0.01] and also less than patients with ICD only: RR 0.59 (95% CI 0.50–0.69, P < 0.01). However, CRT-D mechanical non-responders had a greater likelihood of VA compared with ICD only, RR 0.76 (95% CI 0.63–0.92, P = 0.004). Conclusion CRT-D non-responders experienced more VA than CRT-D responders and also more than those with ICD only, suggesting that CRT with LV epicardial stimulation may be inherently pro-arrhythmic in the absence of reverse remodelling.
AB - Aims Cardiac resynchronization therapy (CRT) has been shown to reduce mortality and heart failure (HF) hospitalization but its effects on the rate of ventricular arrhythmias (VAs) appears to be neutral. We hypothesize that CRT with LV epicardial stimulation is inherently pro-arrhythmic and increases VA rates in the absence of reverse ventricular remodelling while conferring an anti-arrhythmic effect in mechanical responders. Methods In this systematic review and meta-analysis, we considered retrospective cohort, prospective cohort, and randomized and results controlled trials comparing VA rates between cardiac resynchronization therapy-defibrillator (CRT-D) non-responders, CRT-D responders and those with implantable cardioverter-defibrillator (ICD) only. Studies were eligible if they defined CRT-D responders using a discrete left ventricular volumetric value as assessed by any imaging modality. Studies were identified through searching electronic databases from their inception to July 2017. We identified 2579 citations, of which 23 full-text articles were eligible for final analysis. Our results demonstrated that CRT-D responders were less likely to experience VA than CRT-D non-responders, relative risk (RR) 0.49 [95% confidence interval (CI) 0.41–0.58, P < 0.01] and also less than patients with ICD only: RR 0.59 (95% CI 0.50–0.69, P < 0.01). However, CRT-D mechanical non-responders had a greater likelihood of VA compared with ICD only, RR 0.76 (95% CI 0.63–0.92, P = 0.004). Conclusion CRT-D non-responders experienced more VA than CRT-D responders and also more than those with ICD only, suggesting that CRT with LV epicardial stimulation may be inherently pro-arrhythmic in the absence of reverse remodelling.
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U2 - 10.1093/cvr/cvy182
DO - 10.1093/cvr/cvy182
M3 - Review article
C2 - 30010807
AN - SCOPUS:85063284155
SN - 0008-6363
VL - 114
SP - 1435
EP - 1444
JO - Cardiovascular Research
JF - Cardiovascular Research
IS - 11
ER -