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Myocardial bridging in adult patients with hypertrophic cardiomyopathy
Paul Sorajja1, Steve R Ommen, Rick A Nishimura
1Division of Cardiovascular Disease and Internal Medicine, Mayo Clinic and Foundation, 200 SW First Street, Rochester, MN 55905, USA.
Insights
Myocardial bridging in adult hypertrophic cardiomyopathy (HCM) patients does not increase the risk of sudden cardiac death or other mortality. This finding suggests bridging is not a significant prognostic factor in this population.
Area of Science:
- Cardiology
- Cardiovascular Research
- Clinical Investigation
Background:
- Myocardial bridging is linked to adverse outcomes in pediatric hypertrophic cardiomyopathy (HCM).
- The prognostic significance of myocardial bridging in adult HCM patients remains unclear.
Purpose of the Study:
- To investigate the association between myocardial bridging and mortality risk in adult patients diagnosed with HCM.
- To determine if myocardial bridging impacts sudden cardiac death and overall mortality in this patient group.
Main Methods:
- Retrospective analysis of coronary angiograms from 425 adult HCM patients.
- Assessment for myocardial bridging and comparison of survival rates between patients with and without bridging.
- Clinical follow-up to evaluate all-cause mortality, cardiac death, and sudden cardiac death.
Main Results:
- Myocardial bridging was identified in 15% (64 patients) of the study cohort.
- No significant difference in survival free of all-cause mortality, cardiac death, or sudden cardiac death was observed between groups.
- Neither the presence nor characteristics of myocardial bridging predicted a poorer outcome in univariate or multivariate analyses.
Conclusions:
- Adult patients with HCM and diagnosed myocardial bridging do not face an elevated risk of death, including sudden cardiac death.
- Myocardial bridging appears to be a benign finding in adult HCM patients regarding mortality risk.
Objectives:
This investigation examined the risk of sudden cardiac death and other mortality in adult patients with hypertrophic cardiomyopathy (HCM) who have myocardial bridging diagnosed at coronary angiography.
Background:
Several reports have associated myocardial bridging with an adverse prognosis in pediatric HCM patients, but the prognosis of myocardial bridging in adult patients with HCM is unknown.
Methods:
The coronary angiograms of 425 patients with HCM (mean age 60 +/- 15 years [range 18 to 89 years]) at the Mayo Clinic were examined for the presence of myocardial bridging. Clinical follow-up was conducted to assess mortality. Survival of patients with bridging was compared with HCM patients who also underwent angiography but who did not have evidence of bridging.
Results:
A total of 64 patients (15%) had myocardial bridging. The mean follow-up for the entire study was 6.8 +/- 5.4 years. There was no difference in survival free of all-cause mortality (5-year estimate, bridging vs. no bridging, 91% vs. 85%; p = 0.42), all cardiac death (93% vs. 89%; p = 0.60), and sudden cardiac death (95% vs. 97%; p = 0.72). Univariate and multivariate proportional hazards models also did not identify the presence of bridging or specific characteristics of the degree or extent of bridging with a poor outcome.
Conclusions:
This study observed no increased risk of death, including sudden cardiac death, among adult patients with HCM who had myocardial bridging diagnosed at coronary angiography.
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