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Published on: May 13, 2019
Effect of left ventricular outflow tract obstruction on clinical outcome in hypertrophic cardiomyopathy
Martin S Maron1, Iacopo Olivotto, Sandro Betocchi
1Division of Cardiology, Tufts-New England Medical Center, Boston, USA.
Insights
Left ventricular outflow tract obstruction in hypertrophic cardiomyopathy significantly increases the risk of death and severe heart failure symptoms. This finding highlights the importance of identifying and managing this obstruction for improved patient outcomes.
Area of Science:
- Cardiology
- Internal Medicine
- Clinical Research
Background:
- Hypertrophic cardiomyopathy (HCM) is a complex cardiac condition.
- The impact of left ventricular outflow tract obstruction (LVOTO) on HCM outcomes is not fully understood.
- Clarifying the role of LVOTO is crucial for patient management.
Purpose of the Study:
- To investigate the influence of resting left ventricular outflow tract obstruction on morbidity and mortality in patients with hypertrophic cardiomyopathy.
- To determine if LVOTO is an independent predictor of adverse clinical outcomes in HCM.
Main Methods:
- A large cohort of 1101 consecutive patients with hypertrophic cardiomyopathy was assessed.
- Patients were followed for a mean of 6.3 years.
- The study evaluated the association between LVOTO (peak instantaneous gradient ≥30 mm Hg at rest) and clinical outcomes, including death and heart failure progression (New York Heart Association class III or IV).
Main Results:
- 273 patients (25%) had resting LVOTO.
- Patients with LVOTO had a significantly higher probability of death related to HCM (RR, 2.0; P=0.001).
- LVOTO was independently associated with increased risk of death or progression to severe heart failure (RR, 1.6-2.7; P<0.02), particularly in patients ≥40 years old.
Conclusions:
- Resting left ventricular outflow tract obstruction is a significant, independent predictor of adverse outcomes in hypertrophic cardiomyopathy.
- LVOTO is associated with a higher risk of death and progression to severe heart failure.
- These findings underscore the clinical importance of identifying and addressing LVOTO in HCM patients.
Background:
The influence of left ventricular outflow tract obstruction on the clinical outcome of hypertrophic cardiomyopathy remains unresolved.
Methods:
We assessed the effect of outflow tract obstruction on morbidity and mortality in a large cohort of patients with hypertrophic cardiomyopathy who were followed for a mean (+/-SD) of 6.3+/-6.2 years.
Results:
Of the 1101 consecutive patients, 273 (25 percent) had obstruction of left ventricular outflow under basal (resting) conditions with a peak instantaneous gradient of at least 30 mm Hg. A total of 127 patients (12 percent) died of hypertrophic cardiomyopathy, and 216 surviving patients (20 percent) had severe, disabling symptoms of progressive heart failure (New York Heart Association [NYHA] functional class III or IV). The overall probability of death related to hypertrophic cardiomyopathy was significantly greater among patients with outflow tract obstruction than among those without obstruction (relative risk, 2.0; P=0.001). The risk of progression to NYHA class III or IV or death specifically from heart failure or stroke was also greater among patients with obstruction (relative risk, 4.4; P<0.001), particularly among patients 40 years of age or older (P<0.001). Age-adjusted multivariate analysis confirmed that outflow tract obstruction was independently associated with an increased risk of both death related to hypertrophic cardiomyopathy (relative risk, 1.6; P=0.02) and progression to NYHA class III or IV or death from heart failure or stroke (relative risk, 2.7; P<0.001). The likelihood of severe symptoms and death related to outflow tract obstruction did not increase as the gradient increased above the threshold of 30 mm Hg.
Conclusions:
In patients with hypertrophic cardiomyopathy, left ventricular outflow tract obstruction at rest is a strong, independent predictor of progression to severe symptoms of heart failure and of death.
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