Key result
Late gadolinium enhancement extension on CMR positively correlated with the ESC sudden cardiac death risk prediction model (r = 0.7, P < 0.001).
Why the study?
Does late gadolinium enhancement extension on CMR correlate with the ESC sudden cardiac death risk model in patients with hypertrophic cardiomyopathy?
Observational (n=77)
Does late gadolinium enhancement extension on CMR correlate with the ESC sudden cardiac death risk model in patients with hypertrophic cardiomyopathy?
LGE extension on CMR correlates with the ESC sudden cardiac death risk model in HCM patients and may provide incremental value for ICD decision-making, particularly in intermediate-risk patients.
Answers are grounded in this paper and cite their sources.
LGE extent on CMR was associated with ESC SCD risk in HCM; leaves open incremental value for ICD decisions in intermediate-risk patients.
BACKGROUND: Hypertrophic cardiomyopathy (HCM) remains the most common cause of sudden cardiac death (SCD) in the young; however, current strategies do not identify all HCM patients at risk. A novel validated algorithm was proposed by the last European Society of Cardiology guidelines to guide implantable cardioverter-defibrillator (ICD) therapy. Recently, extensive myocardial fibrosis was independently associated with increased risk of SCD events. This study aimed to establish the relation between myocardial fibrosis (late gadolinium enhancement [LGE] extension) and the novel SCD risk-prediction model in a real population of HCM to evaluate its potential additional value in the different risk groups. HYPOTHESIS: There is a significant association between LGE extension and the novel SCD risk calculator that may help conflicting ICD decisions. METHODS: Seventy-seven patients with HCM underwent routine clinical evaluation, echocardiography, and cardiac magnetic resonance study. Their SCD risk at 5 years was calculated using the new model. RESULTS: Extension of LGE positively correlated with SCD risk prediction (r = 0.7, P < 0.001). Low-, intermediate-, and high-risk groups according to the model showed significantly different extent of LGE (5% ± 6% vs 18% ± 9% vs 17% ± 4%; P < 0.001). Four patients (6%) in the low-risk group and 5 (62%) in the intermediate-risk group showed extensive areas of LGE. All patients except 1 (86%) at highest risk (n = 6) showed extensive areas of LGE. CONCLUSIONS: LGE extension is concordant with the novel SCD-risk model defining low- and high-risk groups; it may provide additional information, allowing better discrimination to support implantable cardioverter-defibrillator decision. LGE quantification holds promise for SCD stratification in HCM.
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Hinojar et al. (2017) conducted an observational in Hypertrophic cardiomyopathy (n=77). Late gadolinium enhancement (LGE) on CMR vs. ESC sudden-death risk model groups was evaluated on Correlation between LGE extension and SCD risk prediction (r = 0.7, p=<0.001). Late gadolinium enhancement extension on CMR positively correlated with the ESC sudden cardiac death risk prediction model (r = 0.7, P < 0.001).
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