Key result
Right bundle branch block (HR 2.553) and intraventricular conduction delay (HR 3.726) at admission were independent predictors of increased all-cause mortality in patients with dilated cardiomyopathy.
Why the study?
Does the presence of ventricular conduction block patterns (LBBB, RBBB, IVCD) increase all-cause mortality in hospitalized patients with dilated cardiomyopathy compared to those with narrow QRS?
Cohort (n=1,119)
No
Does the presence of ventricular conduction block patterns (LBBB, RBBB, IVCD) increase all-cause mortality in hospitalized patients with dilated cardiomyopathy compared to those with narrow QRS?
Hazard Ratio: 2.553 (95% CI 1.665–3.913)
Absolute Event Rate: 32.9% vs 19.9%
p-value: p=<0.001
In hospitalized patients with dilated cardiomyopathy, the presence of RBBB and IVCD at admission, but not LBBB, are independent predictors of increased all-cause mortality.
RBBB and IVCD on admission may aid mortality risk stratification in DCM; hypothesis-generating and requires prospective validation before changing practice.
BACKGROUND: Ventricular conduction blocks (VCBs) are associated with poor outcomes in patients with known cardiac diseases. However, the prognostic implications of VCB patterns in dilated cardiomyopathy (DCM) patients need to be evaluated. The purpose of this study was to determine all-cause mortality in patients with DCM and VCB. METHODS: This cohort study included 1119 DCM patients with a median follow-up of 34.3 (19.5-60.8) months, patients were then divided into left bundle branch block (LBBB), right bundle branch block (RBBB), intraventricular conduction delays (IVCD) and narrow QRS groups. The all-cause mortality was assessed using Kaplan-Meier survival curves and Cox regression. RESULTS: Of those 1119 patients, the all-cause mortality rates were highest in patients with IVCD (47.8, n = 32), intermediate in those with RBBB (32.9, n = 27) and LBBB (27.1 %, n = 60), and lowest in those with narrow QRS (19.9 %, n = 149). The all-cause mortality risk was significantly different between the VCB and narrow QRS group (log-rank χ2 = 51.564, P < 0.001). The presence of RBBB, IVCD, PASP ≥ 40 mmHg, left atrium diameter and NYHA functional class were independent predictors of all-cause mortality in DCM patients. CONCLUSIONS: Our findings indicate that RBBB and IVCD at admission,but not LBBB, were independent predictors of all-cause mortality in patients with DCM.
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Li et al. (2016) conducted a cohort in Dilated cardiomyopathy (n=1,119). Right bundle branch block (RBBB) vs. Narrow QRS was evaluated on All-cause mortality (HR 2.553, 95% CI 1.665-3.913, p=<0.001). Right bundle branch block (HR 2.553) and intraventricular conduction delay (HR 3.726) at admission were independent predictors of increased all-cause mortality in patients with dilated cardiomyopathy.
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