• Carmine Muto, Francesco Solimene, Paolo Gallo, Maurizio Nastasi, Concetto La Rosa, Raimondo Calvanese, Raffaele Iengo, Michelangelo Canciello, Raffaele Sangiuolo, Igor Diemberger, Carmine Ciardiello, and Bernardino Tuccillo.
• Ospedale S.Maria di Loreto Mare, Napoli, Italy. carminemuto@libero.it
• Circ Arrhythm Electrophysiol. 2013 Jun 1; 6 (3): 538-45.

BackgroundCurrent recommendations require a QRS duration of ≥120 ms as a condition for prescribing cardiac resynchronization therapy (CRT). This study was designed to test the hypothesis that patients with heart failure (HF) of ischemic origin, current indications for defibrillator implantation, and QRS <120 ms may benefit from CRT in the presence of marked mechanical dyssynchrony.Methods And ResultsPatients with intraventricular dyssynchrony on echocardiography were randomly assigned to CRT or dual-chamber defibrillator implantation (CRT defibrillator and dual-chamber implantable cardioverter-defibrillator arm, respectively). The primary end point was the HF clinical composite response, which scores patients as improved, unchanged, or worsened. The secondary end point was the cumulative survival from HF hospitalization and HF death. An additional secondary end point was the composite of HF hospitalization, HF death, and spontaneous ventricular fibrillation. Twenty-three of 56 patients with CRT defibrillator showed an improvement in their clinical composite response at 1 year, compared with 9 of 55 patients with dual-chamber implantable cardioverter-defibrillator (41% versus 16%; P=0.004). After a median follow-up of 16 months, the CRT defibrillator arm showed a nonsignificant higher survival from HF hospitalization and HF death (P=0.077), and a significantly higher survival from the combined end point of HF hospitalization, HF death, and spontaneous ventricular fibrillation (P=0.028).ConclusionsIn this comparison of CRT defibrillator and dual-chamber implantable cardioverter-defibrillator, CRT improved clinical status in some patients with ischemic cardiomyopathy, mild-to-moderate symptoms, narrow QRS duration, and mechanical dyssynchrony on echocardiography.Clinical Trial RegistrationURL: http://clinicaltrials.gov. Unique identifier: NCT01577446.

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