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QRS Fragmentation and the Risk of Sudden Cardiac Death in MADIT II

Andrew BrenyoCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, NY 14642, USA. [email protected]Grzegorz PietrasikCardiology Division, University at Buffalo, Buffalo, New York, USAAlon BarsheshetCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, New York, USADavid T. HuangCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, New York, USABronislava PolonskyCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, New York, USAScott McNittCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, New York, USAArthur J. MossCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, New York, USAWojciech ZarębaCardiology Division, Department of Medicine, University of Rochester Medical Center, Rochester, New York, USA
2012en
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BACKGROUND: QRS fragmentation (fQRS) has been reported as a useful ECG parameter in predicting mortality in high-risk postinfarction patients. Its prognostic value for sudden cardiac death (SCD) and ventricular arrhythmias in ischemic cardiomyopathy (ICM) remains unknown. METHODS: MADIT II enrollment 12-lead ECGs were analyzed for fQRS defined as RSR' patterns (≥1 R' or notching of S or R wave) in patients with a normal QRS duration and >2 notches on the R or S wave in patients with abnormal QRS duration, present in 2 contiguous leads. Exclusion criteria included a paced rhythm and an uninterpretable or incomplete ECG. Study endpoints included SCD, SCD or appropriate implantable cardioverter defibrillator (ICD) shock, and total mortality (TM). RESULTS: Of the 1,232 ECGs reviewed, 1,040 were of suitable quality for fQRS analysis. QRS fragmentation was found in 33% of patients in any leads, in 10% of patients in anterior leads, in 8% of patients in lateral leads and in 21% of patients in inferior leads. Anterior and lateral location of QRS fragmentation was not associated with follow-up events. Inferior location of fQRS was found to be predictive of SCD/ICD shock (hazard ratio [HR] 1.46, P = 0.032), SCD (HR 2.05, P = 0.007), and TM (HR 1.44, P = 0.036). This association was driven primarily by the increase in events found in LBBB patients: SCD/ICD shock (HR 2.05, P = 0.046), SCD (HR 4.24, P = 0.002), and TM (HR 2.82, P = 0.001). CONCLUSIONS: Fragmented QRS, especially identified in inferior leads, is predictive of SCD, SCD or appropriate ICD shock, and all-cause mortality in patients with ICM. Identifying inferior fQRS in patients with LBBB is of particular prognostic significance and should reinforce the use of ICD therapy in this high-risk group.

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